TW201118162A - Method and apparatus for the treatment of material and fuel - Google Patents

Method and apparatus for the treatment of material and fuel Download PDF

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TW201118162A
TW201118162A TW98139745A TW98139745A TW201118162A TW 201118162 A TW201118162 A TW 201118162A TW 98139745 A TW98139745 A TW 98139745A TW 98139745 A TW98139745 A TW 98139745A TW 201118162 A TW201118162 A TW 201118162A
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solid
reactor
reaction
heat exchanger
water
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TW98139745A
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TWI427142B (en
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Dominik Peus
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Antacor Ltd
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

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  • Processing Of Solid Wastes (AREA)

Abstract

The invention relates to a method and apparatuses for the production of materials or fuels, humus, Maillard or Maillard-like reaction products from a solid-fluid mixture of water and a carbon-containing component and for the treatment thereof, wherein the the solid-fluid mixture is treated at a temperature of over 100 DEG C and a pressure of over 5 bar. Feed materials are thereby fed continuously to a first reactor via a heat exchanger, and the reaction mixture is fed from one to a following reactor in a batch mode, and reaction products are continuously discharged from a last reactor.

Description

201118162 六、發明說明: 【發明所屬之技術領域】 本發明係有關於一種方法及裝置,用以從水和含碳化合物 的固·液混合物產生材料或燃料、腐殖質,梅納德反 應或是類梅納德(Millard-like)反應產物並用以處理該等產物, 其中固-液混合物是在超過l〇〇°C之溫度及超過5巴(bar)之壓 力下進行處理。進料原料係以連續的方式饋入第一反應器,反 應混合物以批量模式由一個反應器進入下一個反應器,而反應 的產物係以連續的方式由最後一個反應器釋出。 【先前技術】 一在1913年,在Friedrich Bergius的博士後論文陳述“利 用高壓在化學程序中煤炭的再生之發展程序,,(the use 〇f high pressures in chemical processes and a reproduction of the development processes 〇f coal)中第一次指出,在未添加催化劑 的實驗至反應中’在溫度為245°C至接近340°C之Pal反將办 氣排出的反應條件下,可以由木材或是纖維素中得到煤炭。 而在元素分析(element analysis)中量測到碳的含量通常高於 。而纖維素的放熱反應的計算則是利用貝爾吉斯(Bergius') 方法,此貝爾吉斯方法在2006年7月已由在potsdamer的 Max-Planck_inStitute flir K〇n〇id _ Grenz他也如加灿卿的 Markus Antonietti教授所證實,Markus如恤祕教授不但發 現並且以實驗室的規模公開此放熱反應的計算方法,同時將 其命名為水熱碳化法(hydrothermal carbonizatioii>。 在水熱碳化法中,生物質(bi〇mass)置放在實驗室的壓力 鍋^,且壓力鍋的條件為壓力為1〇巴、溫度為18〇。〇,並且 在半,的時間内將生物質轉化為近似碳(carb〇n_like)的材料, 或者是在最初的步驟中將生物質與水混合在一起。 對於藉由燃料的產物作為能源回收而言,潮濕的生物質 在長時間的條件下須具有一致性,但是由於缺乏效率,因此 3 201118162 在使用上有其限制。燃燒石化能源(fossile energy carrier)造成 的二氧化碳排放被視為主要要為氣候改變負責。 在德國專利DE 19723510案指出,生物的殘留物的處理 裝置係包含圓筒狀的反應器,其中食物廢料係在一溫度壓力 下以水解程序(temperature pressure hydrolysis process)或是熱 致水解(thermal pressure hydrolysis)進行。反應器係為具有可加 熱殼體表面(heatable casing surface)之迴路式反應器(ι00ρ reactor)。藉由泵來確認懸浮液混合之後,在反應器中產生流 【發明内容】 本發明的目的係發展出一種方法,藉由本方法,可經濟 且高效能地從固-液混合物中製造燃料、腐殖質、含碳材料以 及梅納德或是類梅納德反應產物,此種方法尤適用於工業規 本發明的目的可由獨立§青求項的主題達成,進一步的發 展可由附屬之請求項而更臻顯明。 根據本發明的方法係使含碳固液混合物及/或進料原料在處 理及/或反應的過程之前及/或其期間被額外處理,中間次級產 物及/或最終產物則被調整狀態(c〇nditi〇ned)或處理。在 理或是反應舞及/或反應的再加卫的麵巾,祕固_液、昆人 物有目的的前置步驟或是預處理及固_液混合物的進一 ^ ,序’中間產物、次級產物及/或最終產物,_料 二碳材料及/或麵德反應麵獅德反應絲 有成本效益的方式大幅增加。 八 在^質的積極利用的過程中,為了植物 有4程度的二氧化碳化會釋放至大氣中。因ί ΐ 政二二:料的利用對二氧化碳較無影響,故對氣候無室。此外 產在例如農業的有效利用面積上' 腐殖質 作為-氧化叙庫(C〇2藏)。若無此等考量及若無非石 201118162 化燃料的積極增加利用及可再生的原物料之下,京都協議 (Kyoto agreement)中所明訂的氣候保護以及其他目標都將難 以達成。 在本發明的方法中,利用生物質產生燃料,碳量會在轉 化的程序中減少,碳量的比例相較於其他的方法會小得多。 在有序(orderly)轉化程序的過程中,會有少量碳或者是沒 有任何碳量損失。而在酒精發酵(alcohdic fermentati(m)程序中 有^過30%的碳量損失、轉換成沼氣(bi〇gas)大約有5〇%的碳 量^失、木質碳化處理(W〇〇d Carb〇niZati〇npr〇cess)約有 7〇〇/〇 的碳董損失’以及堆肥處理(compostingprocess)有超過90〇/0 。藉此’碳就可以以二氧化碳或是甲獅ethane) ,形式釋放出去,此等氣體視為溫室(greenh〇use)氣體且對於 =是有害的。本發_綠就非是此鋪況,在本發明所 =的方法t,二氧化碳減量幾乎是沒錢只有最小的排 狄重。 以 根據本發明所揭露的方法係具有高效率。相對來說,^ 生物或是析出物㈣㈣内的能她匕較: :3%至5%的能4效益有_估計淨效率 露之方法’只有非常少或甚至於沒有 鑛嫩備(biQgas pi㈣ 本發質轉換成燃料的大多數方法相比,在 :前ίΓΓ的程序中,水是科缺少的。‘到 化成能量的方法的限制在於缺乏效率、可祕 物質的能量利用的最主要的挑戰i 中,含量。然而,在本發明所揭露的方法 201118162 效益。 當處理固-液混合物’如生物質,係在高溫及高壓下進 而進行的處理反應器可以具有特定的特性。因此,在反應 的内側表面可以具是防雜的表面,或者是因為極端的 而在内側表面設有適當的塗層。此外,也提供一種固·液混合 物的混合裝置。 13 本發明係有關於-種方法’用於從含碳gj •液混合物產 材料及/或燃料、腐殖質及/或之梅納德反應產物或類梅納德反 應產物,其中固-液混合物在溫度超過10(rc及壓力超過^巴 下且在至少1個小時的期間進行處理。 根據本發明所述之更進一步的實施例的目的,本方法係 在半連續式或是連續式的方式進行。其意指尤其在反應的過 程當中,固·液混合物的處理不是以不連續的方式(亦即以批 量模式(batchmode))進行。其溫度和壓力比為主要維持在一 操作範圍内,以最佳化反應空間之利用並使滯留時 短。進料原料、催化劑、製程水以及未轉化的進料 其它的中間產物可視需要移除或再利用,而雜質 (contraries)、反應產物、中間產物、次級產物及/或最終產 物可以在程序進行時由反應空間中移除。這些以及進一步的 方法步驟,如所述之製程水、廢水、排出氣體、反應產物、 中間產物、次級產物及/或最終產物的調整及/或清除以同時 在連續式反應器中進行或是延遲進行亦或是間隔進行。 。在本發明更進一步的實施例的目的,係將溫度調整在 160p以上’或者是介於16(TC及300°c之間、或者是介於 185°C及225°C之間,及/或使得溫度可以被自動控制。 y 在本發明更進一步的實施例的目的,係將壓力調整在7 巴以上、或是在1〇巴及34巴、10巴及17巴、17巴及26巴 或在26巴及34巴之間。在本發明的更進一步的實施例的目 的’處理時間至少2小時、3至60小時、5至30小時或是3〇 至60小時’尤其是在6至12小時或12至24小時。在本發 6 201118162 明更進一步的實施例的目的,根據進料原料的型式,及/或固_ 液混合物及/或欲反應產物來選擇處理時間或是條件。在本發 明的更進一步的實施例的目的,係預處理至少一種進料原料 及/或固-液混合物,其預處理方式最佳的方式是藉由脫水 (dewatering)、碎磨(comminution)、在辅助原料下預培養 (preincubation)、混合及/或預熱。 部份預處理可以在酸性環境或是酸性介質中進行培養, 其酸驗值(pH-value)係低於6、5、4、3或是低於2。在增加碎 磨度及降低pH值之後使得每一個步驟所需要的時間減少。在 酸pH值的條件下的培養可在粉碎之後進行。 本發明的更一進步的實施例的目的在於在處理之前、處 理過程中及/或進行處理之後,將進料原料及/或固_液混合物 碎磨,較佳方式為切碎或是礙碎。這些碎磨的固_液混合物的 粒徑係應低於10公分(cm)、或是低於】公分或低於2毫米 (mm) 〇 在處理之前或者是處理的過程中,將至少一種加水或不 加水的催化劑及/或水溶液加入固—液混合物中或者至少一種 ^料原料内。其中催化劑包含一種或是數種不同的成份。將 這些成份結合以形成一催化劑混合物。催化劑的成份可以是 叛酸(carboxylic add) ’尤其在較佳模式中可使用質子酸㈣她 acid)。使用二級(di-)或三級繞酸此⑹以及以上所 有等級之羧酸或是酒石酸(tartaric acid)以及檸檬酸(citric acid) 士證明是特別有利。檸檬酸及酒石酸係為結晶且無毒性。而 這兩種酸類都存在於水果中(檸檬含有檸檬酸,葡萄含有酒石 酸)但疋也可以使用無機酸’例如硫酸細血如acid)。酸類 可以作為催化劑的成份’同時在生物質培養步驟中以產生酸 性介質(acid medium)。 此外’更特別的是,催化劑或是催化劑混合物可以包含 或夕種金屬及/或金屬化合物細伽丨C0mp0und),尤其為另 外附加。上述金屬可以是化學元素週期表中亞族Ia、IIa、Iva、 7 201118162201118162 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to a method and apparatus for producing a material or fuel, a humus, a Maynard reaction or the like from a solid-liquid mixture of water and a carbon-containing compound. The Millard-like reaction product is used to treat the products, wherein the solid-liquid mixture is treated at a temperature in excess of 10 ° C and a pressure in excess of 5 bar. The feed material is fed to the first reactor in a continuous manner, and the reaction mixture is passed from one reactor to the next in batch mode, and the product of the reaction is released from the last reactor in a continuous manner. [Prior Art] In 1913, the postdoctoral thesis of Friedrich Bergius stated "the use of high pressures in chemical processes and a reproduction of the development processes 〇f For the first time in coal), in the experiment without reaction, the reaction can be obtained from wood or cellulose under the reaction conditions of Pal at a temperature of 245 ° C to nearly 340 ° C. Coal. The carbon content is usually higher in elemental analysis, while the exothermic reaction of cellulose is calculated using the Bergis method, which was used in 2006. The month has been confirmed by Potsdamer's Max-Planck_inStitute flir K〇n〇id _ Grenz, who is also known as Professor Markus Antonietti of Cancan, who has not only discovered and published the calculation of this exothermic reaction on a laboratory scale. At the same time, it was named hydrothermal carbonizatioii. In the hydrothermal carbonization method, biomass (bi〇mass) was placed in the experiment. The pressure cooker ^, and the condition of the pressure cooker is a pressure of 1 bar, a temperature of 18 〇. 〇, and convert the biomass to a material of approximately carbon (carb〇n_like) in a half time, or in the initial step The biomass is mixed with water. For the recovery of fuel products as energy, wet biomass must be consistent under long-term conditions, but due to lack of efficiency, 3 201118162 has its use. Limitation. The carbon dioxide emissions from burning fossile energy carriers are considered to be mainly responsible for climate change. In German patent DE 19723510, the biological residue treatment device consists of a cylindrical reactor in which food The waste is carried out under a temperature pressure by a temperature pressure hydrolysis process or a thermal pressure hydrolysis. The reactor is a loop reactor having a heatable casing surface (ι00ρ) Reactor. After the suspension is confirmed by the pump, a flow is generated in the reactor. The object of the invention is to develop a process by which fuel, humus, carbonaceous material and Maynard or Maynard-like reaction products can be produced economically and efficiently from a solid-liquid mixture, in particular Applicable to Industrial Regulations The purpose of the present invention may be achieved by the subject matter of the independent § 青青, and further developments may be more apparent from the accompanying claims. The process according to the invention is such that the carbon-containing solid-liquid mixture and/or the feedstock are additionally treated before and/or during the process of treatment and/or reaction, and the intermediate secondary product and/or the final product are adjusted ( C〇nditi〇ned) or processed. A facial mask that is re-enhanced in reaction or reaction and/or reaction, a solid pre-step or a pre-treatment and a solid-liquid mixture. The product of the grade and / or the final product, the material of the two carbon materials and / or the surface reaction surface of the Lions reaction yarn has increased substantially in a cost-effective manner. VIII In the process of active use of the quality, 4 degrees of carbon dioxide will be released into the atmosphere for the plant. Because ί ΐ 政 2: The use of materials has no effect on carbon dioxide, so there is no room for climate. In addition, it is produced on the effective use area of agriculture, for example, as a humus as a oxidized sultan (C〇2 藏). Without such considerations and without the active use of non-stone 201118162 chemical fuels and renewable raw materials, the climate protection and other targets set out in the Kyoto agreement will be difficult to achieve. In the method of the present invention, using biomass to produce fuel, the amount of carbon is reduced in the conversion process, and the proportion of carbon is much smaller than other methods. During the orderly conversion process, there will be a small amount of carbon or no loss of carbon. In the alcoholic fermentation (alcohdic fermentati (m) program, there is a carbon loss of 30%, conversion to biogas (bi〇gas), about 5% of carbon loss, wood carbonization treatment (W〇〇d Carb 〇niZati〇npr〇cess) about 7 〇〇 / 〇 carbon Dong loss 'and composting process (composting process) has more than 90 〇 / 0. This can be released in the form of carbon dioxide or lion ethane These gases are considered greenhouse gases and are harmful to =. The present invention is not the case of this method. In the method t of the present invention, the carbon dioxide reduction is almost no money and only the minimum weight. The method disclosed in accordance with the present invention is highly efficient. Relatively speaking, ^ bio or precipitates (4) (4) can be compared with her: : 3% to 5% can be 4 benefits have _ estimated net efficiency exposure method 'only very little or even no mine tenderness (biQgas pi (four) Compared with most methods of converting this hair into fuel, water is lacking in the process of the former. The limitation of the method of turning into energy is the lack of efficiency, the most important challenge of the energy utilization of the secret substance. i. content. However, the method disclosed in the present invention 201118162 benefits. When treating a solid-liquid mixture such as biomass, the treatment reactor which is further subjected to high temperature and high pressure can have specific characteristics. Therefore, in the reaction The inner side surface may have a surface that is anti-hybrid or, because of the extreme, a suitable coating on the inner side surface. In addition, a mixing device for the solid-liquid mixture is also provided. 13 The present invention relates to a method- For the production of materials and / or fuels, humus and / or Menard reaction products or Menard-like reaction products from carbon-containing gj • liquid mixtures, wherein the solid-liquid mixture at temperatures above 10 (rc and pressure) The treatment is carried out in excess of at least one hour and for a period of at least one hour. According to a further embodiment of the invention, the method is carried out in a semi-continuous or continuous manner, which means in particular in the reaction In the process, the treatment of the solid-liquid mixture is not carried out in a discontinuous manner (that is, in batch mode). The temperature and pressure ratio are mainly maintained within an operating range to optimize the utilization of the reaction space. And the residence time is short. The feedstock, catalyst, process water, and other intermediates of the unconverted feed may be removed or reused as needed, while the contraries, reaction products, intermediates, secondary products, and/or ultimately The product may be removed from the reaction space as the process proceeds. These and further process steps, such as the described process water, wastewater, vent gas, reaction products, intermediates, secondary products, and/or final product adjustments and/or Or scavenging to be carried out simultaneously in a continuous reactor or delayed or at intervals. For the purposes of still further embodiments of the present invention, Adjust the temperature above 160p' or between 16 (TC and 300 °c, or between 185 °C and 225 °C, and / or make the temperature can be automatically controlled. y in the present invention The purpose of further embodiments is to adjust the pressure above 7 bar, or between 1 bar and 34 bar, 10 bar and 17 bar, 17 bar and 26 bar or between 26 bar and 34 bar. The purpose of a further embodiment is that the treatment time is at least 2 hours, 3 to 60 hours, 5 to 30 hours or 3 to 60 hours 'especially 6 to 12 hours or 12 to 24 hours. In this issue 6 201118162 For purposes of still further embodiments, the processing time or conditions are selected based on the type of feedstock material, and/or the solid-liquid mixture and/or the product to be reacted. For the purposes of still further embodiments of the present invention, at least one feedstock and/or solid-liquid mixture is pretreated, the preferred way of which is by dewatering, comminution, Preincubation, mixing and/or preheating under auxiliary materials. Partial pretreatment can be carried out in an acidic or acidic medium with a pH-value of less than 6, 5, 4, 3 or less than 2. The time required for each step is reduced after increasing the degree of grinding and lowering the pH. The cultivation under the conditions of the acid pH can be carried out after the pulverization. A further progressive embodiment of the invention aims to pulverize the feed material and/or the solid-liquid mixture before, during and/or after the treatment, preferably by chopping or smashing. . The particle size of these ground solid-liquid mixtures should be less than 10 cm (cm), or less than [cm] or less than 2 mm (mm). At least one water is added before or during the treatment. The catalyst and/or aqueous solution without or without water is added to the solid-liquid mixture or at least one of the raw materials. The catalyst contains one or several different components. These ingredients are combined to form a catalyst mixture. The composition of the catalyst may be carboxylic add', especially in the preferred mode, the protic acid (tetra) her acid may be used. It is particularly advantageous to use a secondary (di-) or tertiary acid to acid (6) and all of the above grades of carboxylic acid or tartaric acid and citric acid. Citric acid and tartaric acid are crystalline and non-toxic. Both of these acids are present in fruits (lemon contains citric acid and grapes contain tartaric acid) but strontium can also use inorganic acids such as sulfuric acid such as acid. The acid can act as a component of the catalyst' simultaneously in the biomass culture step to produce an acid medium. Furthermore, more particularly, the catalyst or catalyst mixture may comprise, or in addition to, the metal and/or metal compound fine oxime C0mp0und). The above metals may be subgroups Ia, IIa, Iva, 7 201118162 of the periodic table of the chemical elements.

Va、Via 及 Vila 的過渡金屬(transition metal),例如鐵(iron)、 鎳(nickel)、銘(cobalt)、銅(copper)、鋅(zinc)、錄(rhodium)、 把(palladium)、銀(silver)、飢(vanadium)、絡(chromium)、鶴 (tungsten)、鉬(molybdenum)及/或鈦(titanium),已證明鐵或鐵 鹽(iron salt)尤其有利。亦可使用這些金屬的金屬氧化物,例 如氧化飢(vanadium oxide, V2O5)、氧化銅(copper oxide, CuO)、氧化鋅(zinc oxide)及 / 或氧化絡(chromium oxide, Ci*2〇3)。在化學元素週期表中,主要族群中的金屬如氧化鋁 (aluminum oxide,Al2〇3) ’也可以以有利方式作為催化劑。 此外’或是取而代之’生物催化劑(bi〇catalysts)也可以在固-液混合物處理之前使用,以便加速固-液混合物轉化成燃料、 含碳混合物、腐殖質及/或梅納德或類梅納德反應產物。藉 此,例如酵素(enzyme)、微生物(micro-organism)(特別是指細 菌(bacteria)及/或菌類(ftmgi))、植物細胞(vegetabie ceu)、動物 細胞及/或是細胞是在自由或固定的形態下使用。由於在固一 液混合物處理過程中的極端條件,只有生物催化劑可以在處 理固-液混合物的過程中使用,尤其是反應及/或次級產物的 預處理或狀況調整。 本發明更進一步的實施例的目的在於,在處理前及/或在 處理過程中,混合至少一種進料原料及/或混合固_液混合 物’其混合的方式較佳為攪動(stirring)、混合、懸浮 (suspending)、及/或攪拌(agitating)。藉此,可以利用一個或 是組合多個混合裝置進行混合,尤其是不同的混合裝置的組 合,可以是至少一個喷射真空泵(jetvacuumpump)、液體喷射 混合器(liquid jet mixer)或是喷嘴(nozzle)。根據本發明,混合 裝置較佳在進行混合時,在反應空間中不需要任何活動式的 部件。 本發明更進一步的實施例的目的在於,在處理之後將反 應^物以乾燥器或是不同乾燥方法之組合進行乾燥處理,其 乾燥處理的方法包括對流式(convection)或是接觸式乾燥裝置 201118162 或是流動式及/或帶狀及/或流體化床乾燥裝置(fluidized bed drier) ° 本發明更進一步的實施例的目的在於,將在本方法中所 累積的製程水(process water)移除’其移除的方式較佳係藉由 至少一種固-液分離裝置將製程水清除或是送回(retum)至反 應混合物。而固-液分離裝置可以是微過濾裝置(micr〇_)、超 過濾裝置(ultra-)或是奈米過濾裝置(nanoflltrati〇n)及逆滲透 (reverse osmosis)法或是結合上述各種的裝置,包含具有陶瓷 過濾元件(ceramic filter element)或是具有旋轉盤(rotational disk)及/或分離薄膜式過濾器(centrifugal membrane filter)的裝 置。 本發明更進一步的實施例的目的在於,以機械、化學或 是生物的方式清潔已累積的廢水。 本發明更進一步的實施例的目的在於,以機械、化學及/ 或生物的方式清潔或處理,在處理、加工及/或調整的過程中 累積的排出氣體。 本發明有關於一種方法,特別是對於不同反應、中間產 物、次級產物及/或最終產物的工業生產之連續式或半連續式 程^。反應產物、中間產物、次級產物及最終產物可以包含 的範,從煤炭(Peat-)或是泥炭(turf-)的燃料與褐煤(lignite)到 類煤炭燃料(coal-like fUd)、腐殖質、梅納德或類梅納德反應 產物、如隔熱材料、奈米海綿(nano sponge)、丸狀物(pellet)、 纖維(fiber)、繞線(^able)、活性炭(active coal)或是吸附炭 (sorption coal)類材料、木炭取代材料substitute i^atenal)等之含碳材料具有高度壓縮碳產物及材料,且特別的 是對於石墨及含石墨或是近似石墨的產物的進料原料以及碳 纖維及複合式進料原料及纖維複合材料(fiber composite material)。 a y本發明更進一步的實施例的目的在於,固-液混合物含有 部份的生物質。藉由壓力和熱量的供給而利用水熱碳化法的 9 201118162 原理,使得在最初去聚合(depolymerize)及水解(hydrolyze)具溼 度的生物質時,可以根據本發明之有效及高度經濟的方法釋 放出熱量。產生的單體(monomer)的聚合作用(polymerization) 會讓含碳反應產物在幾個小時内被發展。在較短的反應時間 之後,在其他進程之初或在反應的進一步進程期間,生物質 產生具有增加的含碳量之燃料,可以適用於能量的產生。 根據本發明的方法,本發明還提供不同的反應產物、中 間產物、次級產物及最終產物的製作,其包括燃料的產生、 由煤炭(peat-)及褐煤(lignite)到類煤炭燃料(coal-like fiiel),腐 殖質、梅納德或類梅納德反應產物,如隔熱材料、奈米海綿 (nano sponge)、丸狀物(pellet)、纖維(fiber)、纜線(cable)、活 性炭(active coal)或是吸附炭(sorption coal)類材料、木炭取代 材料(charcoal substitute material)等之含碳材料具有高度壓縮 碳產物及材料,且特別的是對於石墨及含石墨或是近似石墨 的產物的進料原料以及碳纖維及複合式進料原料及纖維複合 材料(fiber composite material)。 根據本發明,其方法在最初的步驟時,由生物質產生能 量、,其中根據本發明的方法所產生的燃料,可以藉由調整此 燃料而作為發電(energy generation)之用。調整狀態可以包含 產生粉狀的丸狀物或是炭碑(briqUette)或是腐殖質狀的燃料。 本實施例的優點在於提供一種對於發電及特別是對於燃燒而 使用已調整狀態的燃料。根據本發明,可實現一種方法,當 ,用根據本發明所產生的燃料時,該方法係產生不同形式二 能源的方法’該等不同形式的能源包括熱能及/或電流或是兩 ,的組合。根據本發明,對於不同的再生能源所產生 ,的能源其具料種組合方式,其包含再生祕、燃燒石 水力、太及/或風力以及先騎述之各種能源的儲 及能齡統可以進—步的使用具有其他_體、液 體及乳體燃料,及使用根據本發明的方法所產生的燃料。 本發明更進-步有關於—種產生能源的方法,車交佳 201118162 法是利用蒸汽渦輪(steam turbine)及/或燃氣輪機(gas turbine),當包括使用根據本發明之燃料的方法,結合可儲存 式風力能源’特別的是指加壓空氣(pressurized air)或是可調度 型混合風電系統(Dispatchable Wind Power System, DWPS)。 本發明更進一步的是有關於根據本發明所產生之材料或 是燃料的使用,係用於由生物質產生能源。 本發明還提供一種在工業規模的條件下以實現固_液混 合物的有效處理之裝置。 本發明的更進一步之實施例的目的,係提供一種由圓筒 本體(cylindrical basic body)及/ 或在财壓(pressure-resistant)條 件下所構成之反應器。 本發明的更進一步之實施例的目的,係提供一種包含錐 形(cone-shaped)基體的反應器,其中錐形基體的角度相對於反 應器之軸(axis)之角度約為45度或小於40度或小於35度。 本發明的更進一步之較佳的實施例的目的,係在反應器 的内部空間(inner space) ’特別是底層或是器壁的部份以及與 介質接觸的設備部件、由熱交換器(heat exchanger)以及其他裝 置及谷器係由防熱(heat-resistant)及防餘(corrosion-resistant)及 防水(water-repellant)材料所構成,其中防熱(heat-resistant)及防 蝕(corrosion-resistant)及防水(water-repellant)材料可以是經塗 佈之金屬(coated metal) ’特別是貴金屬(noble metal)、陶兗材 料或是具有琺瑯質(enamel)的材料。反應器的内部空間特別是 指底層或是器壁(wall)的區域以及係與反應混合物接觸的底 座以及其他元件係完全或是部份經過表面處理及/或以塗層材 料塗佈,其用以防止或是減少結塊(caking)或是反應混合物成 份的沉積。塗佈材料較佳包含防蝕、耐磨及/或防水材料,特 別是指金屬或陶瓷材料及合金、特別是指鉻、鎳、鉬、鈦、 鋁、鈮及矽材、鐵、鈷、鎢、硼及碳,以及特別是指鈦_銘化 合物。尤其是指提供塗層材料藉由塗佈方法施加,例如電鑛 (plating) ’特別較佳是指談鍵法(figjjje职如叩)例如高速火談 11 201118162 熔射法(high-velocity oxyfUel,HVOF)。 本發明的更進一步的實施例的目的,係在反應器的内部 空間設置一薄膜部件。此薄膜部件具有穿孔,每一個穿孔的 距離小於10 mm ’較佳的距離是小於6皿η,更佳的距離是小 於4 rmn。若薄膜部件是以片狀金屬所構成,因為有穿孔,亦 可以稱為片狀金屬薄膜。而一些薄膜元件可以用於反應器中。 本發明的更進一步的實施例的目的,薄膜部件的穿孔直 徑小於400um,特別是小於looum,更特別的是小於35um。 本發明的更進一步的實施例的目的,薄膜部件的孔洞係 為漏斗的形狀。 本發明的更進一步的實施例的目的,在被穿孔的薄膜部 件f反應器壁之間具有一空腔。薄膜部件連接於反應器内壁 使知空腔分成兩個彼此隔開的區域。如美國公開文獻US_a_4 700 445中所述,在此實施例中,其優點在於假設至少一空腔 具有一排出開口(outletopening),其薄臈部件與反應器内壁之 間的連接方式係利用點或是線的方式焊接,藉此界定出流體 通道的焊接區域可以藉由在部件之間或在平板之間射入高壓 介質而被擴展或是被支撐(pill〇wed),藉此調和液體(tempering liquid)或熱交換介質可以通過在出口及入口或者是聯結之間 的通道流經。在此公開文件中,反應器的雙層壁可同時作為 熱交換器。 ^ 本發明的更進-步的實施例的目的,係提供設計為雙層 壁形式之反應器内壁,藉此在内侧壁及外側壁之間至少具有 個空腔。如美國公開文獻US-A-4 700 445中所述,雙壁声 或是片狀平板可以糊適合的方式連接至空腔,使得空腔^ 成兩個區域。其中之-個區域係具有—人口以及另一個· 具有-出口或是聯結的部份。在制壁之間的連接可以 利用點或是線性焊接,藉此非焊接區域可 ^焊接區域可以藉由在部件之間或在平板之隨 質,被擴展或是支撐,藉此調和液體(temperingliquid)或熱交 12 201118162 換介質可以通過在出口及入口或者是聯結之間的通道流經。 在此公開文獻中,反應器的雙層壁可同時作為熱交換器。 本發明的更進一步的實施例的目的,其反應器是疊接 式、管式(tube) μ盾環式反應器(CyCie react〇r)、迴路式(ι〇〇ρ) 及/或攪動式(stirring)反應器及/或較佳的是薄膜反應器及/或 流體化床反應器。至少一種反應器或是不同的反應器的組合 具有至少一種特性且較佳的組合方式是疊接式、管式、循環 式反應器及較佳的是迴路式或是擾動式反應器,尤其是至少 一個薄膜反應器及/或至少一個循環式流體化床層產生裝置。 本發明的更進一步的實施例的目的,係提供具有調和或 是熱交換系統的反應器,其與至少一控制單元連接。調和系 統至少以有利方式包含旋入式加熱器(screwh heater),至少一 加熱(heating)及冷卻線圈(coding c〇il)、至少一半管式線圈焊 接在反應器壁、至少一熱交換器管或平板及/或至少一薄膜部 件或具穿孔之底層及/或内壁。調和系統包含反應器的雙層壁 或疋雙管結構。本發明的更進一步的有利的實施例的目的, 介質所通過的反應器的所有的裝置,包括具有穿孔的薄膜部 件、喷射真空泵或疋液體射流混合器、栗^jump)及喷嘴(n〇zzle) 也可以是調和系統中之部件。 、本發明也提供具有非機械式組合之裝置,意指盡可能的 沒有任何機械的及/或活動式之元件。 本發明的更進一步的實施例的目的,係提供一種混合裝 置用以混合、攪動、攪拌反應器的内容物。為了將動能(kinetic energy)傳遞至反應器的内容物’可使用機械式攪動及具有或 不具有活動式元件之混合系統。 一本發明的更進一步的實施例的目的,係提供不具有活動 式元件及包含至少一個噴射真空泵或液體喷射混合器、至少 一液體栗及/或至少一喷嘴之混合裝置。 ^發明的更進一步的實施例的目的,提供一混合裝置特 別的是在抽吸區(suctionregion)中設置一混合裝置,其設計是 13 201118162 使在此真空區發生的擾流(turbulence)及剪應力負載(shear load)將固體碎磨以及打散(de_aggi〇merate)。 本發明的更進一步的實施例的目的,提供一種碎磨裝 置’更特別的是在反應器中將固體碎磨,其碎磨裝置至少包 含碾磨機(mill)及/或切碎機(ch〇pper)。 本發明的更進一步的實施例的目的,係提供一種乾燥裝 置’其包含至少一個對流式乾燥器(convecti〇n drier)或是接觸 式乾燥器(contact drier),或流動式(flow)及/或帶式乾燥器 (belt drier) ° 本發明的更進一步的實施例的目的,提供在運轉的過程 中调整製程水。其更佳的裝置是製程水調整設備(process water conditioning plant),其至少包含一篩選器(Sieve)、一過濾器、 一水力旋流器(hydrocyclone)、一離心機(centrifUge)或是電子/ 電磁分離裝置(electrical or magnetic separation device) 〇 製程水 調整作用主要將固體由反應混合物中分離出來。製程水調整 設備包含至少一製程水貯存器及/或至少一固-液分離裝置。 在本發明之有利的實施例中,其製程水調整裝置包含至少一 篩選器、過渡器、離心機、水力旋流器(hydrocyclone unit)、 及支援力場(force field supported)分離裝置之或是這些裝置的 組合。製程水調整設備可以由不同或相同分離裝置組成。 程序調整設備也包含至少一過遽設備,特別的是旋轉盤 過濾器(rotational disk filter),較佳是使用陶瓷的旋轉盤。 本發明的更進一步的實施例的目的,係提供一種生物廢水 調整設備(biological waste water conditioning plant),其包含至 少一生物反應器(bioreactor)、特別是指生物薄膜反應器 (biomembrane reactor)。其生物反應器中更包含至少迴路式反 應器(loop reactor)。 本發明的更進一步的實施例的目的,提供一個迴路式反 應器’其至少包含用以混合氣體和液體之一喷嘴(nozzle)。 本發明的更進一步的實施例的目的,係提供一迴路式反 201118162 應器,係具有一管子,且讓流體由上往下流動。 本發明的更進一步的實施例的目的,係提供一空氣清潔 裝置,其特別是包含至少一用於清潔程序上的及/或排放 (outlet air)空氣之空氣清潔裝置,尤其是指空氣過濾器(ak filter)。 利用根據本發明之裝置用以產生燃料、含碳材料及實用 性材料(utility material)的裝置,腐殖質及/或生物質的梅納德 或類梅納德反應產物亦可提供。 本發明還建立一種可以在工業級規模中,對於生物質的 燃料了以有效的產生能源’其中對能源生成(energy generati〇n) k供至少^—種配置。 本發明的更進一步的有利的實施例的目的,其能源產生 的配置包含燃燒設備,係利用來自生物質的固體燃料,其中 在根據本發明所揭露之處理生物質的裝置所產生的燃料可以 直接巧燒,且此燃料可以用於產生燃燒氣體及水蒸汽。燃燒 ,置係與渦輪及產生器連接,使得可由在燃燒設備中產生的 氟體及水蒸汽產生電流。藉由本發明的設置,能以最高可能 效率在混合軌體-航·程序中產生·,可財現超過 43%的效率、較佳騎過46%、铺_是舰概至。 ,了防止腐_現象’藉由將高溫煙道氣體淨化㈣fl 使討以制齡的環境承 少為備反應1 ’其設備反應器的溫度至 進行操作,其產生的方式係根據本發明的 巴雜件下進行生婦喊=及^ 物的f間產物、次級產物及/或最終產 能源產生的配置方式可以包含丸狀式爐㈣w oven)或是 15 201118162 碳灰燃燒電力設備,其中可提供循環式加壓流體化床燃燒複 合循環技術(circulating pressurized fluidized bed combustion combined cycle,PFBC)或是燃燒碳複合式循環電力技術,如加 Μ 粉煤燃燒(pressurized pulverized coal combustion,PPCC)。 能源產生的配置可以包含一碳燃料電池(carbon fUel cell)。 本發明的更進一步的實施例的目的,提供一種用以處理 生物質的裝置,其包含至少一用以收納生物質的反應器,及 至少一用以處理生物質及/或調整反應產物及/或次級產物之 裝置。 本發明的更進一步的實施例的目的,係提供一種管式反 應裝置、循環式反應裝置,特別有利的是指迴路式反應裝置、 攪伴式反應裝置及/或更佳的是薄膜式反應式或流體化床反 應器。其反應器更佳的是包含至少一薄膜部件及/或用以產生 循環式流體化床層的裝置。同時,反應器的溫度係至少為 l〇〇°C及壓力係高於5巴。 在本發明更進一步的實施例的目的,提供數個用於容納 及處理生物質的反應器以增加設備的容量(capacity)或是流 速。且這些反應器可以以串聯的方式連接。 本發明的更進一步的實施例的目的,反應器設有調和系 統’其與至少一控制單元連接。調和系統可以包含旋入式加 熱器(screw-in heater)、至少一加熱及冷卻線圈(heating⑹ cooling c〇il)、至少一半管式線圈以焊接的方式設置在反應器 壁上、及/或至少一熱交換管或熱交換板。調和系統也可以包 含雙層壁的反應器或雙管件(d〇ubie tube)構造之反應器。 本發明的更進一步的實施例的目的,提供一種混合裝置 用以混合、攪動、攪拌反應器的内容物。反應器可以設有混 合、攪動、攪拌及/或清潔裝置。在本發明的更進一步的實施 例’提供一種碎磨裝置特別是指在反應器裝將固體碎磨,其 碎磨裝置包含至少一碾磨機或至少一切碎機 (chopper) ° 201118162 番,ΐΐϊ明的更進一步的實施例的目的,提供一種乾燥裝 裝晉至少一對流式乾燥裝置或是接觸式乾燥 裝置,較佳為流動式及/或帶式乾燥裝置。 娜tit明的更進—步的實施例的目的,在運轉的過程中 調整,程水。此裝置為製程水調整設備,其可以包含至少一 篩選器、一過濾器、一水力旋流器、一離心 2分,裝置。製程水調整作用將固體由反應混合:疋中二離/ 出來。製程水調整設備包含至少一個製程水貯存器及/戋至少 2罢液λ離裝置。f本發明的有利的實施例中,其製程水調 裝包3至少一篩選器、過濾器、離心分離器,水力旋流 器、電氣或是磁性分離裝置或是這些裝置的組合。程序調整 裝置可以包含不同或相同的分離裝置的組合。製程水調整設 ,可以包含至少-個過攄設備’特別是具有陶賴,也可^ 疋具有轉盤過濾裝置及/或具有離心薄膜式過濾裝置。 在本發明的更進一步的實施例的目的,提供一種生物 ,物理裝置或疋水調整設備或是這些裝置的組合,更好的 ^包含至少二©-較離裝置、-生物反應H,更好的是生物 溥膜反應器(biomembrane reactor)、逆滲透膜(reverse 〇麵sis) ’微過濾(microflltrati〇n),超過濾⑽邮丨⑽㈣及/或 濕式氧化作用(wet oxidation)。生物反應器包含至少一迴路式 反應器。 在本發明的更進一步的實施例的目的,提供一種空氣清 潔裝置,其特別是包含至少一個清潔程序及/或空氣放 置,尤其是空氣過濾裝置。 本發明所使用的設備係用於能源的生成,尤其是電流。 本發明提供一種材料及/或燃料,且與已知的燃料材料相 比,根據本發明揭露的方法形成的材料,其具有較佳的特性。 本發明欲解決的目的在於由生物質產生燃料或是材料, ,相較=生物質來說,根據成份(乾質量(dry mass))的質量分 率,其碳分率係比生物質高1%至300%。根據本案的材料及/ 17 201118162 或燃料包含泥碳的燃料、褐煤到類煤炭燃料、腐殖質、梅納 德或類梅納德反應產物,及含碳材料例如隔熱材料、奈米海 綿(nano sponge)、丸狀物(pellet)、纖維(fiber)、纜線(cable)、 純、最純的煤及超純煤是活性炭(active coal)或是吸附炭 (sorption coal)類材料、木炭取代材料(charcoal substitute material),高度壓縮碳產物及材料,特別的是對於石墨及含石 墨或是近似石墨的產物的進料原料以及碳纖維及複合式進料 原料及纖維複合材料(fiber composite material)。 相較於生物質,基於成份的質量分率(乾質量),根據本 發明的燃料及/或材料其包含的碳分率係增加了 10%至 300%、50%至 300%或 100%至 300%,尤其是 200%至 300%。 或者,相較於生物質,基於成份的質量分率(乾質量),根 據本發明的燃料及/或材料其包含的碳分率增加了 5%至 200%、10%至 150%或 1〇 至 120%,尤其是由 5〇%至 1〇〇%。 相較於進料原料,基於成份的質量分率(乾質量),根據本 發明的燃料及/或材料還分別包含5〇%至90%、55%至80%或 超過98%的碳分率。 在^案的目的之進一步實施例,分別根據成份的質量分 率(乾質量)與生物質比較’燃料及/或材料的氫分率減少了 1% 至 300%、5%至 200%及 20 至 1〇〇〇/0。 質本哲發曰^目的之進一步實施例,分別根據成份的 質篁刀率(乾質虿)與進料原料比較,燃料及/或材料 減少了 1〇/〇至3_、5%至·%及15至·/〇。叶㈣刀羊 ^目、的之進—步實施例’分別根據成份的質量分 別料及/或材料的氮分率減少了 1%至300%、特 疋、。至2j0%、尤其較佳的是15%至1〇〇%。 $ 質量為基礎’根據本發明的燃料及/或材料可以句人 :較最初燃料值,尤其是生物質。3 _铜材料因為 1.成 201118162 境友善的燃燒特性,例如由於降低灰分、較低的氯、硝酸鹽、 硫、及重金屬含量、及灰塵或粒子,細微的灰塵及包括氮和 氧化硫之氣體有毒物質具有較低的擴散。 根據本發明的燃料及/或材料,相較於生物質或是石化固 體或生物質燃料而言,更包含具有相對高反應性及低的燃燒 起始溫度。 當根據本發明之燃料及/或材料變成足夠多孔性時,比具 有相當的燃料值或是含碳量之固體燃料更可以用較低的消耗 能量進行碾碎。 根據本發明材料及/或燃料的小粒徑,因而可具有大的表 面積,特別的是其粒徑約由2 um至50 mm,粒徑也可以低於 1mm ’及也可以低於2〇〇 um。根據本案的燃料和材料,由於 粒徑小且具有大的表面積,因此可以容易的進行乾燥。 根據本發明材料及/或燃料包含梅納德或類梅納德反應產 物。 在本發明的一目的之實施例中,根據一方法產生生物質 ,材料和燃料其包含至少下列步驟:在溫度高於1〇〇〇c,壓力 尚於5巴及處理時間至少一小時來處理生物質及生物質的處 理及/或反應產物、中間產物、次級產物及/或最終產物的調整。 。溫度可以調整至超過16〇°c,也可以調整介於16〇它及 3〇〇°C之間,及也可以調整在185〇c及225〇c之間。其壓力可 以調整至少7巴,也可以介於10巴及34巴之間,也可以在 10巴及17巴之間、18巴至26巴或27巴及34巴之間。處理 時間至少2小時,最佳的是3小時至6〇小時,也可以是5小 時至30小時或31小時至6〇小時,更特別的是ό小時至12 小時或13小時至24小時。在生物質處理之後,利用乾燥裝 置將反應產物乾燥,其乾燥裝置可以是對流式乾燥裝置或是 巧觸式乾燥裝置’且具有流動式及/或帶式及/或流體化床乾 燥裝置,直到達到6%至25%、10%至20〇/〇或是12°/。至15% 之期望的剩餘濕度含量。 201118162 如上所述的方法之反應產物、中間產物、次級產物及最 終產物包含的範圍由泥碳的燃料、褐煤到類煤炭燃料、腐殖 質、梅納德或類梅納德反應產物,及含碳材料例如如隔熱材 料、奈米海綿(nano Sp〇nge)、丸狀物(pellet)、纖維(flber)、繞 線(cable)、最純的煤及超純煤或是活性炭(active coal)或是吸 附炭(sorption coal)類材料、木炭取代材料(charcoal substitute material) ’高度壓縮碳產物及材料,特別的是對於石墨及含石 墨或是近似石墨的產物的進料原料以及碳纖維及複合式進料 原料及纖維複合材料(fiber composite material)所構成。 本發明更進一步有關於產生材料或是燃料是根據本發明 所述之由生物質的能源生成所產生。 生物質·相對於石化燃料、包含從長遠來看可作為國内 能源載體供應的可再生原料,以及液體和固體有機物質及生 物及生化程序產品以及其轉化產品,該等產品對於本方法具 有足夠高的含碳量,或者也可以藉由根據本發明包含燃料的 方法對其組成以及特性處理為具有經濟價值上的利用性的 反應、中間產物、次級產物及最終產物。進料原料例如在下 列之中:碳水化合物(carbohydrate)、糖(sugar)及澱粉(starch)、 農業的(agricultural)及林業(forestry)的產物’尤其是指耕種的 能源植物(energy plant)(如快速成長的樹種、蘆葦(reed)、或是 全穀植物(whole grain plants)等等)、大豆(soy)、甘蔗(sugar cane) 及穀草(grain straw)以及生物殘餘物(bi〇genous residual)、廢棄 物質(waste substance)及次級產物、植物或是不同來源的植物 殘留物(如草邊、造景栽培物等等);農業的廢棄物包括稻草 (straw)、甘蔗葉(sugar cane leave)、廢棄的穀物(wastegrain)、 4伤未銷售的農產品例如:蕃搞或是甜菜(犯牌beet)、分解青 貯匈料部份及其它飼料殘留物、修剪的草(grass clipping)、穀 稻、菜葉、甘蔗葉、含碳殘留物及具有有機廢棄物之廢棄原 料、家庭及工廠的廢棄物高熱量分率(殘留物)、爛泥(sludg^)'、' 不同型式及級別的木材其包括林木(forest w〇〇d)、木材 20 201118162 (timber)、舊豕倶、木屑(saw residues)及由食品工薇所產生的 廢棄物其包括蔚餘和食物垃圾、廢棄植物(waste vegetable)、 廢棄油脂及紙張和紙漿(paper and pulp)、紡織品特別是指天然 纖維及天然聚合物及動物排泄物其包括··液體糞便、馬翼及家 禽類的排泄物。屍體及特別是指動物的屍體都可以算作是生 物質之列。 對本案來說,進料原料及/或固-液混合物之處理,係可 以認知為對固-液混合物的所有影響或效果,其可以將固一液 /昆合物轉化成反應產物,尤其是提供能量用於起始及維持轉 化反應,包含處理固-液混合物在溫度超過1〇(rc及壓力超過 5巴的條件下進行。 對本案而言,生物質及/或固-液混合物的生物質的加 工,是在化學轉化步驟之前及之後,以不同的步驟處理進料 原料、反應產物及/或中間產物。其加工包括了所有的步驟、 程序以及對反應參與物的影響或作用,其包括預處理及/或 處理。 對預處理來說,所有的影響或是作用係理解為對於固一液 混合物從開始轉化反應直到反應空間的填充程序的結束及以 開始能源供應是有影響的。特別的是,在反應空間内或是在 反應空間的外部,進料原料的預熱以及反應混合物的主要成 份(亦即有超過2/3的反應混合物之成份)被碎磨為粒徑大小 至10 mm以下係視為預處理。 、對本案而言,固-液混合物均為懸浮液、分散物及其它 分散系統’其包括含液體之固體,特別是生物質。根據本發 明的方法發現,特別是對於這些固_液混合物而言,在反應係 在物理或是化學方式下進行時,其液相含量的增加或是溶劑 及/或固_物理献學反應侧赠糾_液分離或是且有 =量固體部份賴化率。在此份說明書中進制料或&質 為s液體或不含液體之固體係作為固液混合物的製造。 對本發明的反應產物及/或次級產物的重新調整作用及 21 201118162 ,整作絲說,其包括轉化反狀:她趋及/或最終產物 的所有影響和_ ’储由這些方法^制期望的或是 的形式。 對本發明的半連續式或連續方法來說,應理解為實驗工 ^站及/或工魏模之反應產物、巾間聽、魏產物及最炊 ίΐίϊϊ則其中至少滿足如下所述之—個規則或是兩個或 1 姨ίί在至。少―麵力容^、反絲或是賴組成内溫度持 、,,只地鬲於40 C至90 C經過至少兩個反應週期、更佳的溫产 由60C至70C及/或是高於在至少丨巴之絕對壓力下的製程 水的彿點溫度(boiling temperature),與反應混合物直接的接觸 超過-分鐘,使得延長的皮膚直接細(例如把手放在 接觸反應絲物之容H皿壁较容器壁上)超過—分鐘而不 會增加可見的皮膚發紅只有使關助裝置、隔熱物 的裝置才有可能。 2. 尤其在至少-健力nm、反應时是設備組成中,壓力 持續地咼於1巴絕對壓力或是環境壓力經過至少兩個反應週 期。至少兩個容器,至少該等反應器中的其中一個以可g現 傳輸、壓力等化或是儲存壓縮介質(media)的方式下連接。 3. 進料原料、固-液混合物、反應產物、次級產物、中間產物 的加工及/或最終產物或其它反應參與物的加工在多個或是 在一個設備中多於一個容器或器皿中進行。 〆 4. 進行加工的容器或器皿均為設備所必需或主要的組件其 整體體積至少為500公升’因此至少一個容器無法僅利用人 工移動,而僅能利用附加的辅助裝置移動。 5·在一個反應週期中,使用已預處理之含碳固-液混合物及/ 或不同種類的進料原料、生物質或是含碳化合物,尤其是不 同的組合以及不同的濃度。 八 6.不同進料原料之固_液混合物、反應產物、次級產物、中間 產物及/或最終產物及/或其它反應參與物,包括催化劑及/或 22 201118162 或=調和介質,例如水(特別*製程水)及/或氣體(特 工/σ絲體)細啊、時滯(time_laPsed)、連續、 L =或疋區間式供應至反應混合物或是由反應混合物中移 出H狀f序在壓力容11、反應1或*其它他設備組成 t二i>lGCJL 7GC或是高於在1巴絕對壓力之製程水 的满點 >皿度時進行’或是t至少— 巴絕對壓力時進行。 ^ 1 ,連貫性程序巾’尤其是在單_賴巾處理反應混合物。 细應週期之前或是在反應職期間,將動能導入進料原 料或疋反應混合物使之運轉,其翻是_任何類型之至少 -獅或是混合系統或是結合獅或混合彡統,較佳的是指 至少一種非機械式攪動或混合系統,藉此,當使用單一系統 時’不需要具有磁性祕至唯—的轉軸關時仍可以以電力 的方式操作。 9. 在反應週期之前或是在反應週期期間,特別是利用至少一 和系統或是結合不同的系統或裝置,將熱能導入原料中 或疋將熱能由補巾驅散,藉此若是賴單-紐,則不應 是要-般常帛_(_)及/或棚—些手餘(han 隔、 離之非阻障式聯結熱傳送裝置且以電力來驅動。 10. 根據本發明所述之連續式方法其特徵在於:請求項i、 36、50、72、98、103、113、115、122 及 143 及這些獨立項 j附屬項。另外’對於連續的方式可以由包含於其中的特性 得^進二步的規則,其中含碳進料原料係以連續的方式經由 熱交換器進人第-反應||,及反航合物細批量方式傳送 至後續的反應器以及反應產物以連續的方式由最後一個反應 器釋出。由連續方式可以得到,以上所述之請求項 护 些裝置和元件所結合而得到的特徵。 3 在一容器可理解為内侧具有一空腔,頂部可開啟或關 。其特別是用以將内容物與其環境分離。進行轉化反應的 容器(轉化反應即固-液混合物的處理及/或固—液混合物的加 23 201118162 ’其是由對外側封閉之反應 工)’例如為壓力容器或反應器 空間或是壓力容器空間所構成。 於其中進行決定性反應步驟之容器係特別是描述為反 應器。決足性反應步驟係特別理解為例如在溫度和壓力範圍 運轉至較大的程度的步驟,其必須平均轉化至少1〇%至3〇% 的進料原料變成如上所叙反應錄、巾間產物、次級產物 或最終產物其中之一。 _藉由已存在的空間區域且在一個反應或壓力的容器空間 來定義反應m或是壓力容n賴,其巾反應條件可測地彼 此有偏差。偏差的反應條件經由一結構性、機械性且根據流 體及/或相、化學的、電子的、電化學或其它類型的影響而發 生。為了此目的之裝置還不只於用於實驗室目的之壓力鍋 gutoclave)其配置有電力操作攪動裝置或是具有磁性耦接之 單一轉轴的混合系統裝置,且外部反應器壁的壓縮負載平滑 内側之壁側熱交換藉由電熱外殼容器,其可以一些握把隔離。 反應週期(reaction cycle),反應的週期可以理解為單一轉 化反應的持續期間,其開始係將起始產物導入反應空間内以 及供應能量以使轉化反應開始。一週期由反應過程開始到在 反應混合物中有期望的反應產物的存在,不加後處理或調 整’或是直到反應過程完成,。 ^據流體、熱力性質(thermically)或是根據結構以機械方 式或是利用超音波(ultrasonic)將能量傳送至混合物,從而藉由 攪動或攪拌致使反應器内容物運動的裝置,視為攪動或是混 合系統。攪動或攪拌導致於反應器内容物的運動。經由如泵 (pump)、液體蒸汽混合物或是喷射真空泵、喷灑閥(spray valve) 或是喷射喷嘴(jet nuzzle)以及機械和熱力混合裝置等之裝置 以使反應混合物運動或是沿著壓力梯度引導反應混合物亦是 此等系統中的一部分。 用以執行本發明之方法之設備由至少兩個裝置或是元件 所構成。至少兩個容器或器皿、至少該等反應器中的一個係 24 201118162 力等,„壓縮介質的方式連接 。設備不 的狀況;疋本=2;⑵J容器’在此組件失效 兩個π八―會到限制,特別是考慮到至少 至少十健分_成本效益。 ⑦的裝置或元件為一般使用,則採用連貫性程 2<^ent pn)cess)。與乾燥物質相 而線=:是空芩二以通的方法 妒,μ」始或疋起始’或者是反餘序關始或是起 二·徵在於達成反應程序的至少―個目標參數,包括壓 =>皿度’其中水熱碳化法之轉化反應可以在超過至少一個 的,進行。反應程序的結束其特徵係在於:在清空 參Β之别’係持續維持反應程序中的至少其中一個目標 =針的反應錄、㈣產贼是魏產械是參與 體、液體及⑽物質,其係處於或已經處於操作 间於5巴、溫度高於100。〇,與其停留在反應空間 的長度無關。 液混合祕全毅縣液、分餘及其它 刀=系統,其包括含液體之固體、特別是生物質。根據本案 =置尤其是用糊-液混合物,在反絲种,其增加液相 ίϊ溶劑的含量’及/或是導致於溶紙/朗_物理或化 ^一化’其可改善固_液分離物或是變化率 呈 較高固體含量。 $ 入懸浮液及分散物係均為非均相(heterogeneous)之固-液混 :物/液體和物體的非均相(或無法混合(immiscible))物質混 :物係理解為懸浮液。懸浮液具有至少一個固相及至少一個 液相。膠狀的分散物、膠質粒子(micelle)、氣泡(vesicie)、乳 25 201118162 膠(emulsion)、膠體(gel)及氣膠(aerosol),例如,乳膠或發泡 (foam),均屬分散系統’亦即為小顆粒以及連續分散介質的 二元混合物(binary mixture)。 類梅納德反應產物在本案中應理解為化合物其係為梅納 德反應產物的中間產物、次級產物、最終產物及反應參與物, 且其可以具有相似的化學、物理或是生物特性。由重新排列 主要阿瑪得利產物(primary阿馬多里product)的而產生的高 度糖基化終產物(Advanced glyCati〇n end products,AGE)亦屬 此等化合物,且更進一步反應至梅納德反應的最終產物。高 巧糖基化終產物可與其它的蛋白質經由重新排列及聚合作用 形成交聯(crosslink)。由於發展路徑之故,高度糖基化終產物 有多種不同且複雜的的形式,藉此,至目前已檢測出的形式 有 Νε-叛甲基離氨基酸(>^(carb〇xymethyl)lysine (CML))、 糖氨酸(ftirosine)及戊糖素(pentosidine)。 類聚四氟乙稀(Polytetrafluoroethylene,PTFE)物質應理 解為具有至少一個或是一些聚四氟乙烯的特性之類似、相關 或是非相關種類的物質及化合物,該等特性例如:反應惰性、 極低摩擦係數、極低折料、冑熱阻、表面污染物的低黏附 持久性或是平坦表面。 燃料是一種用於能量產生及藉由化學、電學或是其他方 法轉化成能量的物質。 材料或疋實用性材係藉由進一步的加工、處理或是調整 或是處理成產物,或成為最終產物之工作對象之物質。 本案的目的係更詳細例示如下。 根據本發明的方法中進料原料或是生物質的材料轉化的 程序可以大略區分為下列幾個階段: 1·加熱階段(heating Phas吵生物質係處於一溫度和壓 力下去聚合作用階段(dep〇lymerjzati〇n沖咖)係藉 由,源的供鋼始進行。制是指具有高碳水化合物 含量之生物質,在加熱階段過程中,初始已產生膨脹 26 201118162 反應(swelling reaction)。水藉此容置於細胞壁(cell wall)内的多醋(p〇lysaccharides)之間。在膨脹程序 中,凝膠狀(gelatinous)(在進一步過程中為膠狀)結 構亦暫時形成,其會在去聚合作用階段中的進一步過 程中再次分解。 2. 去聚合作用階段(depolymerization phase):在此,原 始結構蛋白會分解,特別是指植物或是木質纖維素 (lignocellulose)生物質,其主要由聚合結構蛋白纖維 素(polymerized structural protein cellulose)、半纖維素 (hemicellulose)及木質素(lignin)組成。單體(monomer) 及寡聚物(oligomere)碳化合物形式。抵抗性及交聯結 構蛋白的比例愈高’及進料原料的表面愈小,則去解 聚合階段需要更多的時間。同時,水解結果係指在化 學化合物被與水的反應所破壞的化學反應。碳化合 物、非植物及非結構化蛋白質及脂肪分別的比例愈 尚’木質素-纖維素生物質的比例愈低,此階段進行 得愈快。接近此階段的終點,熱能釋放增加並形成類 似於原料油的物質。 3. 重構階段(restructuring phase):單體化及非交聯之碳 化合物係被重新結構化及交聯。凝聚物形式巨觀而言 類似於進料原料的最初始粗糙結構,但是失去與上層 結構之内凝聚力且因此也失去其阻抗力及堅固性。具 有較高的脆性(brittleness)及多孔性之新形成的結構 由粒徑為數百個微米至5奈米的小顆粒徑組成,且在 中間及最終狀態為更小的粒徑。新的碳化合物的形式 係相似於天然煤炭。其包含不同的碳化合物以及烯類 衍生物、,其中含碳量增加及與氫氣與氧氣分率有關 的元素(乾質量)的百分質量分率減少。相較於石化燃 料’其中一個較容易區分的特徵係為在反應產物的液 相及固相中有梅納德反應產物的存在。 27 201118162 4. 穩定階段(stabilization phase):雖然去極性化 (depolarization)及聚合作用階段以放熱方式進行,在 此階段大幅度減少熱能釋放’並在穩定階段完成反應 且最後停止反應不再繼續。 反應產物的特性例如:純度(degree of purity)、形式 (form)、結構、密度、力學阻力(mechanical resistance)或力學 強度(mechanical strength)、粒徑(particle size)、表面結構、組 成、燃燒(combustion)特性、燃燒值(fUel value)及能源含量 (energy content)係視方法或反應條件而定,也就是依憑用於控 制根據本案之方法(亦即加工程序)的參數。反應過程或是 加工程序係尤其受下列處理或是反應條件或標準影響: 1·析出物或是進料原料的組成及特性包括:密度、粒 徑、含水度、純度、含碳量、無機物含量及含驗量。 2. 固相及液相之間的關係或是乾質量(dry mass)及製藉 水之間的關係。 3. 溫度、壓力及這些參數的變異限制(variationlimit)。 4·催化劑(catalysts):選擇、組成、濃度、粒徑、混合 比例及供應時間。在反應進行後期藉由提供催化劑或 是催化劑混合物,可以加速、操縱或引導反應。藉此 可以影響反應產物的特性。對於反應產物的形成及結 構而言,顆粒大小的金屬催化劑是必要的部份。反應 時間相當大的程度是由酸的強度(pK值)來決定^ ‘ 5. 熱交換或是調和系統及溫度調整的時間、酸鹼值、濃 度比,以及在製程水中的這些性質。 6. 例如經由水解(hydrolysis)而造成在反應混合物的物 質或是化學變化:尤其是在轉化反應過程中增加密度 及多孔性。 又 7. 聚合作用期間’聚合作用進行愈快,反應產物愈純。 8. 混合或攪動反應器内容物及轉移能量至其中的方法 與方式,以及流速、剪應力及混合間隔與時間。 28 201118162 9. 製程水:驗鹽的濃度、酸、例如氯(ehl〇rine)、硫㈣⑽ 專元素及其鹽類及金屬及包括含碟&h〇Sph〇r〇us)及 氣化物(nitrate)化合物的無機物。在運轉過程中以及 運轉過程外之製程水的清潔方法。 10·雜質(contraries)的濃度,雜質例如為沙,或會造成阻 礙、怠速、延遲反應進行,或是導致產生不要的次級 產物或是沉殿物(precipitation)的物質。 11. 實行的類型包含在此所述方法步驟的強度以及持續 期間。 12. 調和及混合系統的選擇、組合、協同作用及控制。 13. 製程水調整的選擇、組合、功效及效率,及包括藉由 製程水及物質的供應或是回收而對可變反應容積做 所需調整之考量的指引。 ^ 更進一步的方法步驟可如下所述: 1·進料原料的供應,包括生物質、進料原料、催化劑及 水。 2. 預處理。 3. 進料原料傳送至一傳送系統及/或容器内。 4. 適用於個別的加工或是處理步驟,將進料原料傳送至 容器内。 5. 進料原料的除水及/或乾燥。 6. 進料原料或許還有催化劑的碎磨。 7·金屬及雜質的移除。 8.利用催化劑,特別是酸,進行培養。 9· 一種或是幾種另外的催化劑的添混。 10. 生物質的預熱。 jL例如當導入反應器内時的壓緊(compaction)。 2·導入壓力容器或反應空間。 13. 加熱。 14. 製程水調整及空氣清潔。 29 201118162 15. 由反應空間移除反應產物。 16. 由反應混合物中分離出反應產物、 物及/或最終產物。 m 17. 所需反應產物的乾燥。 18. 所需反應產物的碎磨。 丄9.所需反應產物的冷卻。 20. 調整。 21. 忐源回收,特別是經由熱循環或熱交換。 在化學轉化程序之前及之後,係在祠的步射處理進 ^料及反應產物、巾間產物、次級絲及/或最終產物。 該等加工步驟是針虹業或是技術層次的㈣轉換。因此, =應理解為超出利时刀進行人工分解或是人卫碎磨 方法巾’生物f的加工及/或反應物及/或次級 產物的重整不?、可姻電子獅獅或齡纽,其具 性耦合之轉軸’並具有特徵為反應器外壁之承受壓縮之 光 ' 内側藉由電熱殼體容器(electrically heated casing c=a^ier)(其可藉由一些手握把隔離)以進行壁侧熱傳導。 對於半連續式或是連續式方法而言,於以上第9點及 第10 2所述之攪動或混合系統及/或是調和系統的標準。 通常可以在貯存生物質之前進行碎磨,且特別的是在實 際的轉化程序之前,更特綱是在生物質加人反毅間之前 或β之後進行碎磨。就研磨裝置而言,通常是用例如碾磨 :濕式研磨器來艰磨。根據進料原料及所需的顆粒大小 ίίί使/用不同類型的細切、研磨或溼式研磨。顆粒大小影 ^應進行。因此,棘大小愈小,麟雜喊雜愈大。 J應參與物的表面積愈大,化學轉化愈快。碎狀後的生物 的顆粒小可以小於1〇公分、也可以小於1公分,亦可 2毫f。在碎磨過程中的能量、時間及原料成果係視程 f程序而定’特別是與進料原料的形態、顆粒大小及滯留長 度有關。 30 201118162 f pH健於6、傭5、也可岐低於4、_是低於 可以低於2之雜魏或是雜介質巾的培養係為預 H的1分i步驟所需要的時間係隨著碎磨的 P酸性下 少。例如可以在進行碎磨之後,在阳值為 此^係在配置有雙層壁或是另—翻㈣統之隔熱培 ^ |§皿t細。此調和纽之使用主要是經由來自根據本 ,之產生程序或其絲序的程序熱献賴,或是利用部份 純化及加熱_程水。培養職至少1()分鐘至6()分鐘、! 小日|至10小時或是10小時至6(H、時。視進料原料及其他 預處理步驟而定’預培養可以減少相當的反應時間。在理想 的條件下,節省了超過3〜1〇%、10〜20%或更多的時間。 因為水是在實行反應期間化學性產生的,且由進料原料 刀離出來水的谷積係隨著程序進行而增加。對於例如在後 續的反應器皿中的反應空間所需要的反應容量會隨著水的 回收而降低。因此’在反應進行期間,以反應器串接(cascade) 的概念來說,每一個個別反應器的容積減少。可以在轉化反 應結束之後或者是在轉化反應的過程中取得製程水。在反應 過程中製程水的回收係發生在溫度高於18〇〇c且壓力超過5 巴、。此對於固-液分離之方法及裝置而言係為特定的要求。 在近期·^出的方法中’篩選程序(粗筛(c〇arse sieving)、細筛 (fine sieving))、過滤程序及/或藉由氣旋式㈣咖批)、動力式 (dynamic)、靜電式(static)、真空式、壓力式及消毒過濾式之 離〜力/冗積程序,特別是橫流過濾(cr〇ss n〇w其包 含微過濾、超過濾、奈米過濾及逆滲透法尤佳。更佳的是使 用以由力场支持的水力旋流器(hydrocyclone)、離心式、分 離裝置的方法及功能性原理為基礎,及/或利用過濾方法的 裝置。較佳的過濾方法特別的是能以水熱碳化法的反應條件 加以使用者。旋轉盤過濾裝置或離心薄膜過濾裝置較佳係用 於固-液分離。不同固-液分離方式可以相互結合。在第一反 31 201118162 應器之後的各反應E可以與g]-液分離裝置i^接。目_液分離 j續式或是p撕式的方式進行,進行時間為在反應器内停 =時間的至少二十分U可以根據需柄及所使用之裝 3效能純行調整。回_製程水係姐在—隔離的防餘 谷器或是壓力器皿内。 為使製程水濃縮(enriehing),巾可於s轉程序從未處理 的製程水之貯存射直接移除。—方面係由林發明的說明 書中所述的-倾是數個驗分離裝置使製程水_ ,及在 另一方面例如是在蒸發器(evap〇mt〇r)藉由蒸發水 (^vaporatingwater)而使製程水濃縮。蒸發程序所產生的水蒸 氡係在程序的其他位置朗,例如當進人熱交換_之前對進 料原料進行加熱,經由熱交換ϋ料對齡加熱或是運轉將 反應產物麟n例如妓獅獅機(airagitatormill) 或是在此份說明書中於其它部份所述之其它的乾燥裝置。 為使製程水濃縮,至少移除1%〜5%、5%^20%或 2()%~70°/H $ 了&目# ’在此份說明書巾所述的其它方 法也可以使用’例如逆滲透,然而其缺點在於由於溫度敏感 型薄膜的關係而必須降低更多溫度。製程水係貯存在一隔離 且防蝕之器皿或是如果可能的話,設計為可排除空氣之壓力 容器之製程水貯存槽。 濃縮製程水係部份用於進料原料的預培養、預熱、可泵 送固-液混合物的產生,用於在反應混合物中的吸^,用於 在設備的反應器内將供應的進料原料之塗佈或添混,以及返 回至正在運轉的程序中,在設備内或是設備的外進一步的程 序處理中係作為熱載體介質(heat carrier me(jium)及/或作為 肥料成份。對於各別的使用’可以在溫度超過丨它至5〇。〇之 各個溫度取得製程水。Transition metal of Va, Via, and Vila, such as iron, nickel, cobalt, copper, zinc, rhodium, palladium, silver Iron, vanadium, chromium, tungsten, molybdenum and/or titanium have proven to be particularly advantageous for iron or iron salts. Metal oxides of these metals may also be used, such as vanadium oxide (V2O5), copper oxide (CuO), zinc oxide, and/or chromium oxide (Ci*2〇3). . In the periodic table of the chemical elements, a metal such as alumina (Al2?3) in the main group can also be used as a catalyst in an advantageous manner. In addition, 'or instead' biocatalysts (bi〇catalysts) can also be used prior to solid-liquid mixture treatment to accelerate the conversion of solid-liquid mixtures into fuels, carbon-containing mixtures, humus and/or Maynard or Maynard-like reaction product. Thereby, for example, enzymes, micro-organisms (especially bacteria and/or fungi (ftmgi)), plant cells (vegetabie ceu), animal cells and/or cells are free or Used in a fixed form. Due to the extreme conditions in the treatment of the solid-liquid mixture, only the biocatalyst can be used in the treatment of the solid-liquid mixture, especially the pretreatment or conditioning of the reaction and/or secondary products. A further embodiment of the present invention is directed to mixing at least one feedstock material and/or mixing solid-liquid mixture prior to treatment and/or during processing. The manner of mixing is preferably a stirring, mixing , suspending, and/or agitating. Thereby, the mixing can be carried out by one or a combination of a plurality of mixing devices, in particular a combination of different mixing devices, which can be at least one jet vacuum pump, liquid jet mixer or nozzle. . According to the present invention, the mixing device preferably does not require any movable components in the reaction space when mixing. A further embodiment of the invention aims to dry the reaction after treatment with a dryer or a combination of different drying methods, the drying process comprising a convection or contact drying device 201118162 Or a fluidized and/or ribbon and/or fluidized bed drier. A further embodiment of the invention aims to remove process water accumulated in the process. The manner of removal is preferably to remove or reduct the process water to the reaction mixture by at least one solid-liquid separation device. The solid-liquid separation device may be a microfiltration device (micr〇_), an ultrafiltration device (ultra-) or a nanofiltration device (nanoflltrati〇n) and a reverse osmosis method or a combination of the above various devices. Included is a device having a ceramic filter element or having a rotating disk and/or a centrifugal membrane filter. A further embodiment of the invention aims to clean accumulated wastewater in a mechanical, chemical or biological manner. A further embodiment of the invention aims to clean or treat, in a mechanical, chemical and/or biological manner, the exhaust gases accumulated during processing, processing and/or conditioning. The present invention relates to a process, particularly a continuous or semi-continuous process for the industrial production of different reactions, intermediates, secondary products and/or final products. Reaction products, intermediates, secondary products, and final products can range from coal (Peat-) or peat (turf-) fuels to lignite (coal-like fUd), humus, Maynard or Maynard-like reaction products, such as insulating materials, nano sponges, pellets, fibers, ^able, active coal, or A carbonaceous material such as a sorption coal-based material or a charcoal-substituting material has a highly compressed carbon product and material, and particularly a feedstock for graphite and a graphite-containing or graphite-like product. Carbon fiber and composite feedstock and fiber composite material. A y A further embodiment of the invention has the object that the solid-liquid mixture contains a portion of the biomass. By using the pressure and heat supply, the 9 201118162 principle of hydrothermal carbonization allows for efficient and highly economical release according to the present invention when initially depolymerizing and hydrolyzing biomass with humidity. Exhaust heat. The polymerization of the resulting monomer causes the carbon-containing reaction product to develop within a few hours. After a short reaction time, biomass produces an increased carbon content fuel at the beginning of other processes or during further progress of the reaction, which may be suitable for energy production. According to the process of the present invention, the present invention also provides for the production of different reaction products, intermediates, secondary products, and final products, including fuel production, from coal (peat-) and lignite (lignite) to coal-like fuels (coal). -like fiiel), humic, Maynard or Maynard-like reaction products such as insulating materials, nano sponges, pellets, fibers, cables, activated carbon (active coal) or sorption coal-based materials, charcoal substitute materials, etc., carbonaceous materials having highly compressed carbon products and materials, and particularly for graphite and graphite-containing or graphite-like Feedstock feedstock for the product as well as carbon fiber and composite feedstock materials and fiber composite materials. According to the invention, the method produces energy from biomass at the initial step, wherein the fuel produced by the method according to the invention can be used for energy generation by adjusting the fuel. The adjustment state may include the production of powdered pellets or a charcoal (briqUette) or humus-like fuel. An advantage of this embodiment is that it provides a fuel that uses an adjusted state for power generation and particularly for combustion. According to the present invention, a method can be implemented which, when using the fuel produced according to the present invention, is a method of producing two forms of energy in different forms. The different forms of energy include thermal energy and/or current or a combination of two. . According to the present invention, the energy generated by different renewable energy sources has a combination of materials, including regenerative secrets, combustion stone water power, too and/or wind power, and storage and energy ages of various energy sources. The use of the steps has other _ body, liquid and milk fuels, and the fuel produced using the method according to the invention. The present invention further relates to a method for generating energy, and the method of using the steam turbine and/or gas turbine, when using a method according to the present invention, can be combined. Storage wind energy 'specially refers to pressurized air or Dispatchable Wind Power System (DWPS). The invention further relates to the use of materials or fuels produced in accordance with the present invention for the production of energy from biomass. The present invention also provides an apparatus for achieving efficient treatment of a solid-liquid mixture under industrial scale conditions. It is an object of still further embodiments of the present invention to provide a reactor constructed from a cylindrical basic body and/or under pressure-resistant conditions. It is an object of still further embodiments of the present invention to provide a reactor comprising a cone-shaped substrate wherein the angle of the tapered substrate is about 45 degrees or less relative to the axis of the reactor. 40 degrees or less than 35 degrees. A further preferred embodiment of the invention is directed to the inner space of the reactor 'particularly the bottom layer or part of the wall and the parts of the apparatus in contact with the medium, by heat exchanger (heat The exchangers and other devices and troughs are constructed of heat-resistant and corrosion-resistant and water-repellant materials, among which heat-resistant and corrosion-resistant and The water-repellant material may be a coated metal 'especially a noble metal, a pottery material or a material having an enamel. The internal space of the reactor, especially the area of the bottom layer or the wall, and the base and other components that are in contact with the reaction mixture are completely or partially surface treated and/or coated with a coating material. To prevent or reduce the caking or deposition of components of the reaction mixture. The coating material preferably comprises an anti-corrosive, wear-resistant and/or waterproof material, in particular a metal or ceramic material and alloy, in particular chromium, nickel, molybdenum, titanium, aluminum, niobium and tantalum, iron, cobalt, tungsten, Boron and carbon, and especially titanium. In particular, it is provided that the coating material is applied by a coating method, such as electroplating, which is particularly preferably referred to as a high-velocity oxyfUel, such as a high-speed oxyfUel (figjjje). HVOF). A further embodiment of the invention aims to provide a film member in the interior of the reactor. The film member has perforations, each of which has a distance of less than 10 mm ′. The preferred distance is less than 6 η, and the better distance is less than 4 rmn. If the film member is made of a sheet metal, it may be referred to as a sheet metal film because of the perforation. Some thin film components can be used in the reactor. For the purpose of a further embodiment of the invention, the perforation diameter of the film member is less than 400 um, in particular less than looum, more particularly less than 35 um. For the purpose of still further embodiments of the present invention, the holes of the film member are in the shape of a funnel. It is an object of a further embodiment of the invention to have a cavity between the walls of the perforated film member f reactor. The membrane member is attached to the inner wall of the reactor to divide the cavity into two spaced apart regions. In the embodiment disclosed in US Pat. Wire welding, whereby the weld zone defining the fluid passage can be expanded or supported by injecting a high pressure medium between the components or between the plates, thereby tempering the liquid Or the heat exchange medium can flow through the passage between the outlet and the inlet or the junction. In this publication, the double wall of the reactor can serve as a heat exchanger at the same time. The purpose of a further embodiment of the present invention is to provide a reactor inner wall designed in the form of a double wall whereby at least a cavity is formed between the inner and outer side walls. As described in U.S. Patent No. 4,700, 445, the double-walled or sheet-like plate can be attached to the cavity in a paste-like manner such that the cavity is formed into two regions. One of these areas has a population and another one with an exit or a link. The connection between the walls can be made by point or linear welding, whereby the non-welded area can be expanded or supported by the element or between the plates, thereby tempering the liquid (temperingliquid) ) or hot cross 12 201118162 The changing medium can flow through the passage between the outlet and the inlet or the junction. In this publication, the double wall of the reactor can serve as a heat exchanger at the same time. A further embodiment of the invention is directed to a reactor, a tube, a CyCie reactor, a loop (ι), and/or a stirrer. The reactor and/or preferably a thin film reactor and/or a fluidized bed reactor. At least one reactor or a combination of different reactors has at least one characteristic and a preferred combination is a spliced, tubular, cyclic reactor and preferably a loop or disturbance reactor, especially At least one membrane reactor and/or at least one circulating fluidized bed production unit. It is an object of still further embodiments of the present invention to provide a reactor having a tempering or heat exchange system coupled to at least one control unit. The blending system comprises, at least in an advantageous manner, a screwh heater, at least one heating and cooling coil, at least half of the tubular coil welded to the reactor wall, at least one heat exchanger tube Or a flat sheet and/or at least one film member or a perforated bottom layer and/or inner wall. The blending system comprises a double wall or a double tube structure of the reactor. For the purpose of a further advantageous embodiment of the invention, all of the means of the reactor through which the medium passes, including a membrane member having perforations, a jet vacuum pump or a helium liquid jet mixer, a pump, and a nozzle (n〇zzle) ) It can also be a component in a blending system. The present invention also provides a device having a non-mechanical combination, meaning that there are as many mechanical and/or movable components as possible. It is an object of still further embodiments of the present invention to provide a mixing apparatus for mixing, agitating, and agitating the contents of a reactor. Mechanical agitation and a mixing system with or without moving elements can be used to transfer kinetic energy to the contents of the reactor. It is an object of a further embodiment of the invention to provide a mixing device that does not have a movable element and that includes at least one jet vacuum pump or liquid jet mixer, at least one liquid pump and/or at least one nozzle. The object of a further embodiment of the invention is to provide a mixing device, in particular in the suction region, which is designed to be 13 201118162 to cause turbulence and shearing in this vacuum zone. A shear load breaks and breaks up the solids (de_aggi〇merate). It is an object of a further embodiment of the invention to provide a grinding device 'more particularly to grind the solids in a reactor, the grinding device comprising at least a mill and/or a chopper (ch) 〇pper). It is an object of still further embodiments of the present invention to provide a drying apparatus that includes at least one convective drier or contact drier, or flow and/or Or belt drier ° It is an object of still further embodiments of the present invention to provide for the adjustment of process water during operation. A preferred device is a process water conditioning plant comprising at least one filter (Sieve), a filter, a hydrocyclone, a centrifuge (centrifuge) or an electron/ Electrical or magnetic separation device The process of water conditioning mainly separates solids from the reaction mixture. The process water conditioning apparatus comprises at least one process water reservoir and/or at least one solid-liquid separation device. In an advantageous embodiment of the invention, the process water regulating device comprises at least one filter, a transition device, a centrifuge, a hydrocyclone unit, and a force field supported separation device or A combination of these devices. The process water conditioning device can be composed of different or identical separation devices. The program adjustment device also includes at least one filter device, in particular a rotary disk filter, preferably a ceramic rotary disk. It is an object of still further embodiments of the present invention to provide a biological waste water conditioning plant comprising at least one bioreactor, particularly a biomembrane reactor. The bioreactor further comprises at least a loop reactor. It is an object of still further embodiments of the present invention to provide a loop reactor which includes at least one nozzle for mixing a gas and a liquid. It is an object of a still further embodiment of the present invention to provide a one-circuit reverse type 201118162 having a tube and allowing fluid to flow from top to bottom. It is an object of a further embodiment of the invention to provide an air cleaning device, in particular comprising at least one air cleaning device for cleaning and/or outlet air, in particular an air filter. (ak filter). The use of a device according to the invention for producing fuel, carbonaceous materials and a utility material, a humus and/or biomass Maynard or Maynard-like reaction product may also be provided. The present invention also establishes an energy efficient generation of energy for biomass fuels on an industrial scale, where at least one configuration is provided for energy generation. It is an object of a further advantageous embodiment of the invention that the energy-generating configuration comprises a combustion apparatus that utilizes solid fuel from biomass, wherein the fuel produced by the apparatus for treating biomass according to the present invention can be directly It is burned and this fuel can be used to generate combustion gases and water vapor. The combustion, the system is coupled to the turbine and the generator such that current can be generated by the fluorine and water vapor generated in the combustion equipment. With the arrangement of the present invention, it is possible to produce in the hybrid rail-air program with the highest possible efficiency, and it is possible to achieve an efficiency of more than 43%, a better ride of 46%, and a shop. The method of preventing rot- _ phenomenon 'by purifying the high-temperature flue gas (4) fl to reduce the temperature of the equipment to the reaction 1 'the temperature of the equipment reactor to operate, which is produced according to the invention Under the miscellaneous items, the configuration of the raw materials, secondary products and/or final energy production may include a pellet furnace (four) w oven or 15 201118162 carbon ash burning power equipment, among which Circulating pressurized fluidized bed combustion combined cycle (PFBC) or combustion carbon composite cycle power technology, such as pressurized pulverized coal combustion (PPCC). The energy generated configuration can include a carbon fUel cell. It is an object of still further embodiments of the present invention to provide a device for treating biomass comprising at least one reactor for containing biomass, and at least one for treating biomass and/or adjusting reaction products and/or Or a device for secondary products. It is an object of still further embodiments of the present invention to provide a tubular reaction apparatus, a circulating reaction apparatus, and particularly advantageously a loop type reaction apparatus, a stirred reaction apparatus, and/or more preferably a thin film type reaction type. Or a fluidized bed reactor. More preferably, the reactor comprises at least one membrane component and/or means for producing a circulating fluidized bed. At the same time, the temperature of the reactor is at least l ° ° C and the pressure system is higher than 5 bar. For the purposes of still further embodiments of the present invention, several reactors for containing and processing biomass are provided to increase the capacity or flow rate of the apparatus. And these reactors can be connected in series. For the purposes of still further embodiments of the present invention, the reactor is provided with a blending system' which is coupled to at least one control unit. The blending system can include a screw-in heater, at least one heating and cooling coil (heating (6) cooling c〇il), at least half of the tubular coils are placed on the reactor wall in a welded manner, and/or at least A heat exchange tube or heat exchange plate. The blending system can also comprise a double wall reactor or a double tube (d〇ubie tube) reactor. It is an object of still further embodiments of the present invention to provide a mixing apparatus for mixing, agitating, and agitating the contents of the reactor. The reactor can be provided with mixing, agitation, agitation and/or cleaning means. In a still further embodiment of the present invention, a grinding device is provided, in particular, in which the solids are ground in a reactor, and the grinding device comprises at least one mill or at least all choppers. It is an object of still further embodiments to provide a dry pack of at least one pair of flow dryers or contact dryers, preferably flow and/or belt dryers. Natit's more advanced step-by-step embodiment is adjusted during the operation, Cheng Shui. The apparatus is a process water conditioning apparatus which may include at least one filter, a filter, a hydrocyclone, a centrifugation, and a device. The process water adjustment function mixes the solids from the reaction: the two are separated/exited. The process water conditioning apparatus includes at least one process water reservoir and/or at least 2 strike λ separation devices. In an advantageous embodiment of the invention, the process water conditioning package 3 is at least one of a filter, a filter, a centrifugal separator, a hydrocyclone, an electrical or magnetic separation device or a combination of these devices. The program adjustment device may comprise a combination of different or identical separation devices. The process water adjustment device may comprise at least one boring device, in particular, having a terrarium, or a turret filter device and/or a centrifugal membrane filter device. For the purpose of still further embodiments of the present invention, there is provided a biological, physical device or hydrophobic adjustment device or a combination of these devices, preferably comprising at least two separate devices, a biological reaction H, preferably It is a biomembrane reactor, a reverse osmosis membrane, a microfiltration (microflltrati〇n), an ultrafiltration (10), a postal (10) (four), and/or a wet oxidation. The bioreactor comprises at least one loop reactor. In an object of a further embodiment of the invention, an air cleaning device is provided, which in particular comprises at least one cleaning program and/or air placement, in particular an air filtration device. The apparatus used in the present invention is used for energy generation, especially current. The present invention provides a material and/or fuel which, in contrast to known fuel materials, has a preferred property in accordance with the methods disclosed herein. The object of the present invention is to produce a fuel or a material from biomass. The carbon fraction is higher than the biomass according to the mass fraction of the component (dry mass) compared to the biomass. % to 300%. According to the material of this case and / 17 201118162 or fuel containing peat fuel, lignite to coal-like fuel, humus, Maynard or Maynard reaction products, and carbonaceous materials such as insulation, nano sponge (nano sponge ), pellets, fibers, cables, pure, purest coal and ultra-pure coal are active coal or sorption coal materials, charcoal replacement materials (charcoal substitute material), a highly compressed carbon product and material, particularly a feedstock for graphite and graphite or near graphite products, as well as carbon fiber and composite feedstocks and fiber composite materials. Compared to biomass, based on the mass fraction (dry mass) of the component, the fuel and/or material according to the present invention comprises a carbon fraction which is increased by 10% to 300%, 50% to 300% or 100% to 300%, especially 200% to 300%. Alternatively, the fuel and/or material according to the present invention has a carbon content increase of 5% to 200%, 10% to 150% or 1%, based on the mass fraction (dry mass) of the component compared to the biomass. Up to 120%, especially from 5% to 10,000%. The fuel and/or material according to the present invention further comprises a carbon fraction of 5% to 90%, 55% to 80% or more than 98%, respectively, based on the mass fraction (dry mass) of the component compared to the feed material. . In a further embodiment of the purpose of the method, the hydrogen fraction of the fuel and/or material is reduced by 1% to 300%, 5% to 200%, and 20, respectively, based on the mass fraction (dry mass) of the component and the biomass. To 1〇〇〇/0. According to a further embodiment of the quality of the product, the fuel and/or material is reduced by 1 〇 / 〇 to 3 _, 5% to · % according to the sizing rate of the component (dry 虿) compared with the feed material. And 15 to ·/〇. The leaf (four) knife and sheep, the step-by-step example, respectively, reduce the nitrogen content of the component according to the mass fraction of the component and/or the material by 1% to 300%, especially. Up to 2j0%, particularly preferably 15% to 1%. $Quality based on the fuel and/or material according to the invention can be compared to the initial fuel value, especially biomass. 3 _ copper material because 201118162 Friendly combustion characteristics, such as low ash, lower chlorine, nitrate, sulfur, and heavy metal content, and dust or particles, fine dust and gas toxic substances including nitrogen and sulfur oxides have lower diffusion . The fuel and/or material according to the present invention further comprises a relatively high reactivity and a low combustion onset temperature as compared to biomass or petrochemical solids or biomass fuels. When the fuel and/or material according to the present invention becomes sufficiently porous, it can be crushed with a lower energy consumption than a solid fuel having a comparable fuel value or carbon content. According to the small particle size of the material and/or fuel according to the invention, it is therefore possible to have a large surface area, in particular a particle size of from about 2 um to 50 mm, a particle size of less than 1 mm ' and also less than 2 〇〇. Um. According to the fuel and material of the present invention, since the particle diameter is small and has a large surface area, drying can be easily performed. The material and/or fuel according to the invention comprises a Maynard or Maynard-like reaction product. In an embodiment of the invention, the biomass, material and fuel are produced according to a method comprising at least the following steps: treating at a temperature above 1 〇〇〇c, at a pressure of 5 bar and at a treatment time of at least one hour. Adjustment of biomass and biomass treatment and/or reaction products, intermediates, secondary products and/or final products. . The temperature can be adjusted to more than 16 〇 ° C, or it can be adjusted between 16 〇 and 3 〇〇 ° C, and can also be adjusted between 185 〇 c and 225 〇 c. The pressure can be adjusted to at least 7 bar, or between 10 bar and 34 bar, or between 10 bar and 17 bar, between 18 bar and 26 bar or between 27 bar and 34 bar. The treatment time is at least 2 hours, preferably 3 hours to 6 hours, or 5 hours to 30 hours or 31 hours to 6 hours, more particularly ό hours to 12 hours or 13 hours to 24 hours. After the biomass treatment, the reaction product is dried by means of a drying device, which may be a convection drying device or a tactile drying device and has a flow and/or belt and/or fluidized bed drying device until 6% to 25%, 10% to 20 〇/〇 or 12°/. The desired residual moisture content to 15%. 201118162 The reaction products, intermediates, secondary products and final products of the process as described above range from peat fuel, lignite to coal-like fuels, humus, Maynard or Maynard-like reaction products, and carbonaceous Materials such as, for example, insulating materials, nano sponges, pellets, flers, cables, purest coals and ultrapure coals or active coals Or sorption coal-based materials, charcoal substitute materials, 'highly compressed carbon products and materials, especially for graphite and graphite or near graphite products, and carbon fiber and composite The feed material and the fiber composite material are composed. The invention further relates to the production of materials or fuels produced by the energy production of biomass in accordance with the present invention. Biomass · Relative to fossil fuels, including renewable raw materials that can be supplied as domestic energy carriers in the long run, as well as liquid and solid organic substances and biological and biochemical process products and their conversion products, which are sufficient for this method The high carbon content, or the composition and characteristics of the fuel-containing process according to the invention, can also be treated as economically valuable reactions, intermediates, secondary products and final products. Feedstocks are, for example, in the following: carbohydrates, sugars and starches, agricultural and forestry products, especially the cultivated energy plant ( Such as fast-growing tree species, reeds, or whole grain plants, etc., soy, sugar cane and grain straw, and bio residues (bi〇genous residual) ), waste substances and secondary products, plants or plant residues from different sources (such as grass borders, landscaping cultures, etc.); agricultural waste includes straw, sugar cane (sugar cane) Leave), abandoned grain (wastegrain), 4 unsold agricultural products such as: Fan or beet (beet), decomposition of silage Hungarian parts and other feed residues, grass clipping, valley Rice, vegetable leaves, sugar cane leaves, carbon residue and waste materials with organic waste, household and factory waste high calorie fraction (residue), sludge (sludg^)', 'different types and grades of wood It includes forests (forest W〇〇d), wood 20 201118162 (timber), old sputum, saw residues and waste produced by food weiwei, including yuyu and food waste, waste vegetable, waste oil and Paper and pulp, textiles, in particular, natural fibers and natural polymers and animal wastes, including liquid feces, horse wings and poultry excrement. The body and especially the body of the animal can be counted as a biomass. In the present case, the treatment of the feedstock and/or the solid-liquid mixture can be recognized as all effects or effects on the solid-liquid mixture, which can convert the solid/kun compound into a reaction product, especially Providing energy for the initiation and maintenance of the conversion reaction, including treatment of the solid-liquid mixture at temperatures above 1 Torr (rc and pressures in excess of 5 bar. In this case, the biomass and/or solid-liquid mixture is produced. The processing of the material is to treat the feedstock, reaction products and/or intermediates in different steps before and after the chemical conversion step. The processing includes all the steps, procedures and effects or effects on the reaction participants. Including pretreatment and/or treatment. For pretreatment, all effects or effects are understood to be influential for the end of the filling process from the start of the conversion reaction until the reaction space is completed and to start the energy supply. In particular, in the reaction space or outside the reaction space, the preheating of the feedstock and the main components of the reaction mixture (ie more than 2/3 of the reaction mixture) The composition of the compound is ground to a particle size of 10 mm or less as a pretreatment. In this case, the solid-liquid mixture is a suspension, dispersion and other dispersion system. In particular, biomass. It has been found in the process according to the invention, in particular for these solid-liquid mixtures, that the liquid phase content is increased or solvent and/or solid when the reaction system is carried out physically or chemically. _Physical study response side of the _ liquid separation or there is = the amount of solid part of the rate of lasing. In this specification, the material or & s liquid or liquid-free solid system as a solid-liquid mixture Manufacture. Re-adjustment of the reaction product and/or secondary product of the present invention and 21 201118162, the entire crepe says that it includes a transformational reversion: she tends to/or all effects of the final product and _ 'store by these methods The desired or the form of the invention. For the semi-continuous or continuous method of the present invention, it should be understood that the reaction product of the experimental station and/or the worker Wei mold, the towel, the Wei product and the most 炊 ΐ ΐ 其中 are at least satisfied. As follows a rule or two or 1 姨ίί at the end. Less - face force ^, reverse wire or Lai composition internal temperature holding,, only 鬲 40 C to 90 C after at least two reaction cycles, Better temperature production from 60C to 70C and / or higher than the boiling temperature of the process water at an absolute pressure of at least 丨, direct contact with the reaction mixture for more than - minutes, so that the extended skin is directly Fine (for example, placing the handle on the wall of the reaction vessel with the H vessel wall more than the container wall) for more than - minutes without increasing the visible redness of the skin, only the device for shutting down the device and the insulator is possible.  Especially at least - the strength of the nanometer, the reaction is the composition of the device, the pressure is continuously at 1 bar absolute or the ambient pressure is passed through at least two reaction cycles. At least two containers, at least one of the reactors, are connected in a manner that can be transported, pressure equalized, or stored in a compressed medium. 3.  The processing of the feedstock, solid-liquid mixture, reaction product, secondary product, intermediate product, and/or final product or other reaction participants is carried out in a plurality or in more than one vessel or vessel in one apparatus. 〆 4.  The containers or vessels to be processed are all necessary or essential components of the apparatus and have an overall volume of at least 500 liters. Thus at least one of the containers cannot be moved by humans only, but can only be moved by means of additional auxiliary means. 5. In a reaction cycle, a pretreated carbon-containing solid-liquid mixture and/or different kinds of feed materials, biomass or carbon-containing compounds, especially different combinations and different concentrations are used. Eight 6. Solid-liquid mixtures, reaction products, secondary products, intermediates and/or final products and/or other reaction partners of different feed materials, including catalysts and/or 22 201118162 or = blending media, such as water (special * process) Water) and / or gas (Agent / σ filament) fine, time lag (time_laPsed), continuous, L = or 疋 interval supply to the reaction mixture or remove the H-like f sequence from the reaction mixture in the pressure capacity 11, Reaction 1 or * other equipment consists of t 2 i > lGCJL 7GC or higher than the full point of the process water at 1 bar absolute pressure > or t at least - absolute pressure. ^1, a coherent procedural towel', especially in a single slap towel treatment reaction mixture. Before the fine cycle or during the reaction period, the kinetic energy is introduced into the feed material or the reaction mixture to make it run. It is at least a lion or a hybrid system of any type or a combination of a lion or a mixed system. It refers to at least one non-mechanical agitation or mixing system whereby electrical operation can still be performed when a single system is used, which does not require a magnetically-secure shaft. 9.  Before the reaction cycle or during the reaction cycle, in particular using at least one system or a combination of different systems or devices, the thermal energy is introduced into the raw material or the thermal energy is dissipated by the patch, whereby if it is a single-new It should not be - as usual - _ (_) and / or shed - some hand (han separated, separated from the non-blocking junction heat transfer device and driven by electricity.  The continuous method according to the present invention is characterized by requesting items i, 36, 50, 72, 98, 103, 113, 115, 122 and 143 and these independent items j. In addition, 'for a continuous manner, the two-step rule can be obtained from the characteristics contained therein, wherein the carbon-containing feed material is fed into the first reaction-through|| in a continuous manner via a heat exchanger, and The batch is transferred to the subsequent reactor and the reaction product is released from the last reactor in a continuous manner. It can be obtained in a continuous manner, and the above-mentioned claims protect the features obtained by combining the devices and components. 3 In a container, it can be understood that there is a cavity on the inside and the top can be opened or closed. It is used in particular to separate the contents from their environment. a vessel for the conversion reaction (conversion reaction, ie treatment of the solid-liquid mixture and/or addition of the solid-liquid mixture 23 201118162 'which is a reactor closed to the outside), such as a pressure vessel or reactor space or a pressure vessel The space is formed. The vessel in which the decisive reaction step is carried out is specifically described as a reactor. The decision-making step is to be understood in particular to mean, for example, a step of operating to a greater extent in the temperature and pressure ranges, which must have an average conversion of at least 1% to 3% of the feed material to become a reaction, inter-race product as described above. One of the secondary products or the final product. _ By the existing spatial region and in a reaction or pressure vessel space to define the reaction m or the pressure capacity, the reaction conditions of the towel can be measured to be biased. The reaction conditions of the deviation occur via a structural, mechanical and fluid, and/or phase, chemical, electronic, electrochemical or other type of influence. The device for this purpose is not only for the pressure cooker for laboratory purposes, it is equipped with a power operated agitation device or a hybrid system device with a magnetically coupled single shaft, and the compression load of the external reactor wall is smooth inside. The wall side heat exchange is by means of an electrically heated outer casing which can be isolated by some grips. The reaction cycle, the period of the reaction, can be understood as the duration of a single conversion reaction, which begins by introducing the starting product into the reaction space and supplying energy to initiate the conversion reaction. One cycle begins with the reaction process until there is a desired reaction product in the reaction mixture, without post-treatment or adjustment' or until the reaction process is completed. a device that is fluidically, thermodynamically or thermally transferred to a mixture mechanically or by ultrasound, thereby causing the contents of the reactor to move by agitation or agitation, as agitation or Hybrid system. Stirring or agitation results in movement of the contents of the reactor. Moving the reaction mixture or along a pressure gradient via a device such as a pump, a liquid vapor mixture or a jet vacuum pump, a spray valve or a jet nuzzle, and a mechanical and thermal mixing device The lead reaction mixture is also part of these systems. The apparatus for carrying out the method of the invention consists of at least two devices or elements. At least two containers or vessels, at least one of the reactors 24 201118162, etc., „compressed medium connected. The condition of the equipment is not; 疋本=2; (2) J container 'in this component fails two π eight ― Will be limited, especially considering at least ten health points _ cost-effective. 7 devices or components for general use, the use of coherence 2 <^ent pn)cess). Line with dry matter =: is empty 芩 以 以 通 μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ μ Including pressure = > dish degree 'where the conversion reaction of the hydrothermal carbonization method can be carried out in excess of at least one. The end of the reaction procedure is characterized by: in the emptying of the ginseng, the system maintains at least one of the targets in the reaction program = the reaction record of the needle, and (4) the thief is the genus, the body, the liquid, and the (10) substance. The system is at or already in operation at 5 bar and the temperature is above 100. Oh, it has nothing to do with the length of the reaction space. Liquid Mixing Secrets Yi County Liquid, Residual and Other Knife = System, which includes solids containing liquids, especially biomass. According to the present invention, in particular, a paste-liquid mixture is used, in the case of a reverse-filament type, which increases the content of the solvent, and/or causes the dissolution of the paper/language/physical or chemical properties, which improves the solid-liquid. The isolate or rate of change has a higher solids content. The suspensions and dispersions are all heterogeneous solid-liquid mixtures: heterogeneous (or immiscible) substances mixed with liquids and objects: systems are understood to be suspensions. The suspension has at least one solid phase and at least one liquid phase. Colloidal dispersions, micelles, vesicies, milk 25 201118162 emulsions, gels and aerosols, for example, latex or foam, are dispersion systems 'Also is a binary mixture of small particles and a continuous dispersion medium. The Maynard-like reaction product is understood in the present context to be a compound which is an intermediate, secondary product, final product and reaction partner of the Maynard reaction product, and which may have similar chemical, physical or biological properties. Advanced glyCati〇n end products (AGE) produced by rearranging the main Amadori product, also belonging to these compounds, and further reacting to Mena The final product of the German reaction. The high glycosylation end product can form a crosslink with other proteins via rearrangement and polymerization. Due to the developmental path, highly glycosylation end products have many different and complex forms, whereby the form that has been detected so far has Νε-rebellion methyl amino acid (>^(carb〇xymethyl)lysine ( CML)), ftirosine and pentosidine. A polytetrafluoroethylene (PTFE) material is understood to be a similar, related or unrelated species of matter and compounds having at least one or some properties of polytetrafluoroethylene, such as: reaction inertness, very low friction Coefficient, very low drawency, thermal resistance, low adhesion durability of surface contaminants or flat surfaces. Fuel is a substance used for energy production and converted into energy by chemical, electrical or other methods. The material or 疋 practical material is a substance that is processed, processed, or otherwise processed or processed into a product, or a work object of the final product. The purpose of this case is illustrated in more detail below. The process of converting the feedstock or biomass material according to the method of the present invention can be roughly divided into the following stages: 1. Heating stage (heating Phas noisy biomass is in a temperature and pressure down polymerization stage (dep〇 Lymerjzati〇n) is based on the supply of steel from the source. The system refers to biomass with a high carbohydrate content, which initially has an expansion during the heating phase. 26 201118162 Swelling reaction. Containing between p〇lysaccharides in the cell wall. In the expansion procedure, gelatinous (gelatinous in a further process) structure is also temporarily formed, which will be depolymerized. Decomposition in a further process in the action phase. 2. Depolymerization phase: where the original structural protein decomposes, in particular a plant or lignocellulose biomass, which is mainly composed of a polymeric structure. Composition of polymerized structural protein cellulose, hemicellulose, and lignin. Monomers and oligomers (oligomere) in the form of carbon compounds. The higher the ratio of resistant and crosslinked structural proteins' and the smaller the surface of the feedstock, the more time is required to depolymerize. At the same time, the hydrolysis results are referred to in chemical compounds. The chemical reaction destroyed by the reaction of water. The higher the ratio of carbon compounds, non-plants and unstructured proteins and fats, the lower the proportion of lignin-cellulosic biomass, the faster this stage is carried out. At the end point, the release of heat energy increases and forms a substance similar to the feedstock oil. 3. Restructuring phase: The cyclized and non-crosslinked carbon compounds are restructured and crosslinked. Similar to the initial rough structure of the feedstock, but losing cohesion with the superstructure and thus losing its resistance and robustness. The newly formed structure with higher brittleness and porosity consists of It has a small particle diameter of several hundred micrometers to 5 nanometers and a smaller particle size in the middle and final state. The new carbon compound is similar in form to natural coal. Containing different carbon compounds and olefin derivatives, the percentage of mass of carbon and the elemental (dry mass) associated with hydrogen and oxygen fraction is reduced. Compared with fossil fuels, one of them is easier to distinguish. Characterized by the presence of a Maynard reaction product in the liquid and solid phases of the reaction product. 27 201118162 4. Stabilization phase: although the depolarization and polymerization phases are carried out exothermically, At this stage, the heat release is greatly reduced' and the reaction is completed in the stabilization phase and finally the reaction is stopped. Characteristics of the reaction product such as: degree of purity, form, structure, density, mechanical resistance or mechanical strength, particle size, surface structure, composition, combustion ( The combustion characteristics, the fUel value and the energy content depend on the method or reaction conditions, that is, on the parameters used to control the method according to the present invention (ie, the processing program). The reaction process or processing procedure is particularly affected by the following treatments or reaction conditions or standards: 1. The composition and characteristics of the precipitate or feedstock include: density, particle size, water content, purity, carbon content, inorganic content And including the test. 2. The relationship between the solid phase and the liquid phase is the relationship between the dry mass and the borrowed water. 3. Temperature, pressure and variation limits for these parameters. 4. Catalysts: selection, composition, concentration, particle size, mixing ratio, and supply time. The reaction can be accelerated, manipulated or directed by providing a catalyst or a mixture of catalysts later in the reaction. Thereby, the characteristics of the reaction product can be affected. A particle size metal catalyst is an essential part for the formation and structure of the reaction product. The considerable degree of reaction time is determined by the strength of the acid (pK value). ‘ 5. Heat exchange or blending system and temperature adjustment time, pH, concentration ratio, and these properties in process water. 6. The substance or chemical change in the reaction mixture is caused, for example, by hydrolysis: in particular, density and porosity are increased during the conversion reaction. 7. During the polymerization period, the faster the polymerization proceeds, the more pure the reaction product. 8. Methods and means of mixing or agitating the contents of the reactor and transferring energy thereto, as well as flow rate, shear stress, and mixing interval and time. 28 201118162 9. Process water: salt concentration, acid, such as chlorine (ehl〇rine), sulfur (4) (10) elements and their salts and metals and including dish & 〇Sph〇r〇us) and gasification ( Nitrate) An inorganic substance of a compound. The cleaning method of the process water during the operation and outside the operation process. 10. Concentration of contaminants, such as sand, may cause obstruction, idling, delayed reaction, or substances that cause unwanted secondary products or precipitation. 11. The type of implementation includes the strength and duration of the method steps described herein. 12. Selection, combination, synergy and control of blending and mixing systems. 13. Selection, composition, efficacy and efficiency of process water adjustment, and guidance on the need to make adjustments to the variable reaction volume through the supply or recovery of process water and materials. ^ Further method steps can be as follows: 1. Supply of feedstock, including biomass, feedstock, catalyst and water. 2. Pretreatment. 3. The feedstock is transferred to a transfer system and/or container. 4. Apply to individual processing or processing steps to transfer the feedstock to the vessel. 5. Water removal and/or drying of the feedstock. 6. The feedstock may also have a crushing of the catalyst. 7. Removal of metals and impurities. 8. Culturing using a catalyst, particularly an acid. 9. Addition of one or several additional catalysts. 10. Preheating of biomass. jL is, for example, a compaction when introduced into the reactor. 2. Introduce the pressure vessel or reaction space. 13. Heating. 14. Process water adjustment and air cleaning. 29 201118162 15. The reaction product is removed from the reaction space. 16. The reaction product, product and/or final product is separated from the reaction mixture. m 17. Drying of the desired reaction product. 18. Grinding of the desired reaction product.丄 9. Cooling of the desired reaction product. 20. Adjustments. 21. Recycling of plutonium, especially via thermal cycling or heat exchange. Prior to and after the chemical conversion process, the feed and reaction products, the inter-cloth product, the secondary filaments, and/or the final product are processed in a crucible. These processing steps are either a rainbow or a technical level (four) conversion. Therefore, = should be understood as the artificial decomposition of the knife or the processing of the bio-f and/or the reorganization of the reactants and/or secondary products. , can be married to the electronic lion or age, its characteristic coupling shaft 'and has the characteristics of the outer wall of the reactor to withstand the compression of light' inside the electric heated casing (electrically heated casing c = a ^ ier) Wall-side heat conduction is performed by some hand grips. For semi-continuous or continuous processes, the agitation or mixing system and/or the standard of the blending system described in points 9 and 10 above. It is usually possible to grind before storage of the biomass, and in particular before the actual conversion procedure, it is more specifically to grind before or after the addition of the biomass. In the case of grinding devices, it is often difficult to grind with, for example, a milling:wet grinder. Depending on the feedstock and the desired particle size, different types of fine cut, grind or wet grind are used. Particle size should be performed. Therefore, the smaller the size of the spine, the bigger the screaming. The larger the surface area of J should be, the faster the chemical conversion. The particles of the shredded organism may be less than 1 cm, or less than 1 cm, or 2 m. The energy, time and raw material results in the grinding process are determined by the process f program, in particular, depending on the form, particle size and retention length of the feed material. 30 201118162 f pH is healthy at 6, commission 5, can also be less than 4, _ is less than 2 can be less than 2, Wei Wei or miscellaneous media towel, the culture system is the time required for the pre-H 1 minute i step As the ground P is less acidic. For example, after grinding, in the positive value, the system is equipped with a double wall or another (four) system of insulation. The use of this blend is mainly due to the heat from the program according to the procedure for generating the program or its sequence, or the use of partial purification and heating. Training for at least 1 () minutes to 6 () minutes,! Small day|to 10 hours or 10 hours to 6 (H, hour. Depending on the feed material and other pretreatment steps) Pre-culture can reduce the equivalent reaction time. Under ideal conditions, save more than 3~1 〇%, 10~20% or more. Since water is chemically generated during the reaction, and the water leaving the feedstock knives is increased as the program proceeds. For example, in the subsequent The reaction capacity required for the reaction space in the reaction vessel will decrease with the recovery of water. Therefore, during the reaction, the volume of each individual reactor is reduced in terms of the cascade of reactors. Process water is obtained after the end of the conversion reaction or during the conversion reaction. During the reaction, the recovery of the process water occurs at a temperature higher than 18 〇〇c and the pressure exceeds 5 bar. This is a method for solid-liquid separation. And the device is a specific requirement. In the recent method, 'screening program (c〇arse sieving, fine sieving), filtration program and / or by cyclone (four) coffee Batch), dynamic (dyn Amic), electrostatic, vacuum, pressure and sterilizing filter-to-force/hybrid programs, especially cross-flow filtration (cr〇ss n〇w which includes microfiltration, ultrafiltration, nanofiltration and The reverse osmosis method is particularly preferred. More preferably, it is based on a hydrocyclone supported by a force field, a centrifugal method, a separation device, and a functional principle, and/or a device using a filtration method. In particular, the filtration method can be applied to the user by the reaction conditions of the hydrothermal carbonization method. The rotary disk filtration device or the centrifugal membrane filtration device is preferably used for solid-liquid separation. Different solid-liquid separation methods can be combined with each other. One reaction 31 201118162 Each reaction E after the reactor can be connected with the g]-liquid separation device. The liquid separation is performed in the form of a continuous or p-tear method, and the operation time is stopped in the reactor. At least two tenths of U can be adjusted according to the required handle and the 3 performances used. Back to the process water system sister - in the isolation of the anti-grain or pressure vessel. For the process water enrichment (enriehing), towel Process water that can be processed from s to unprocessed The storage shot is directly removed. The aspect is described in the specification of the invention of the forest - the tilting is a plurality of inspection and separation devices to make the process water_, and on the other hand, for example, in the evaporator (evap〇mt〇r) Evaporating water (^vaporating water) to concentrate the process water. The steam evaporating process generated by the evaporation process is in other positions of the program, for example, heating the feed material before entering the heat exchange, and charging the feed through the heat exchange Heating or running the reaction product, such as an airagitator mill or other drying device described elsewhere in this specification. To concentrate the process water, remove at least 1% to 5%. 5%^20% or 2()%~70°/H $ &目# 'Other methods described in this specification sheet can also be used 'eg reverse osmosis, however, the disadvantage is due to temperature sensitive film The relationship must be reduced by more temperature. The process water system is stored in an isolated and corrosion resistant vessel or, if possible, a process water storage tank that is designed to exclude air pressure vessels. The concentrated process water system is used for pre-carrying, preheating, and pumpable solid-liquid mixture production of the feedstock for the absorption in the reaction mixture for use in the reactor of the plant. The coating or addition of the feedstock, and returning to the running process, is used as a heat carrier medium (and/or as a fertilizer component) in the equipment or in further processing outside the equipment. For each use, 'process water can be obtained at temperatures above 丨 to 5 〇.

董^於進料原料的預培養、預熱、可泵送固-液混合物的產 生或疋對於在設備的反應器中供應的進料原料的塗佈或是 添混,較佳為使用溫度為25°C至50°C、50°C至70°C或是i〇°C 32 201118162 製程水。對於這些目的而言,其 ^ ί ί 妓储4歧低於2。 溫产Urt—步在設備内或是設備外部之程序,較佳使用 熱而=然而為了該等上 料轉,溫度超過靴内供應的進 戋者在蒸發或利用另一種方式排除某個量的水, itr、f 酸作輸匕劑得到需要的PH值,其沸 水水対槪舰份的程度使其彿點高於 2?9〇C ° ^^^Phoric acid) 麻:/皿:糸在213 C。儘管沸點較高,即使很難避免催化 點之5水由製程水散逸,仍可以藉由以低於酸的沸 ^ 有效’如硫倾(二價)胁點或是分解溫度 =;GGC’氯化鐵(三價)之彿點溫度高於12G〇c(昇華), =疋氣化鐵(二價)之軸溫度為娜。。藉自製程水的濃縮 可以減少一種或是數種催化劑成份。 m製Ϊ水蒸汽係用在程序中的其它位置,例如在進入熱交 、器之前先對進料原料進行加熱、經由熱交換器程序之熱油 (j^rmal oil)的加熱或是用於操作乾燥反應產物的裝置,例如 空氣攪拌礙磨機(air agitator mill)及/或在此份說明書中先前 所述之乾燥裝置。根據應用來進行製程水蒸汽的清潔。 在本案中所述’可以用數個泵在溫度高於250°C之條件 下來運送濃縮製程水’其泵可以是渦輪泵(helical displacement pump)。其溫度係在環境壓力下經由熱交換器而 降低,或是在進料送入無壓裝置&ressureless appaj^s)或是 送入混合裝置之前降低溫度,使得固_液混合物的溫度為 50°C 〜60。(:或是 60。(:〜80〇C。 特別的是由生物質中分離出金屬、無機物或是沙類之物 33 201118162 質以及其它雜質。此等方法及程序係用於例如在沼氣廠 (biogas plant)中建立生物質及有機廢棄物的處理範圍。 在預培養之後’可以在酸性介質中,加入含有添加水 或是不含添加水之傕化劑及/或在水溶液中的催化劑。催化 劑可以包含至少一種或是數種不同的成份。這些成份在一起 形成催化劑混合物。催化劑的成份可以是例如包含酸。反應 程序在相當大的程度上係受到催化劑的選擇、組成、濃度、 顆粒大小、混合比以及供應的時間影響。因此這些取決於催 化劑的因素對於最終產物的形成、設計及特性有很大的影 響。對於最終的形式及結構或是反應產物,金屬催化劑的顆 粒大小形成必要的部份。而反應時間是亦由酸的強度(成值) 來決定,例如,當使用粒徑小於十微米時,特別是200奈米 至1〇〇〇奈米,及特別較佳是10奈米至199奈米時,形成最 終產物可均勻化形態纖維狀奈米結構的機率會增加。顆粒大 小愈小,可以定義出愈精確及均勻的新碳化合物之纖維狀結 構。然而,對於已定義之奈米結構之產生來說,碳水化合物 含量、顆粒大小及顆粒大小均勻的程度對於反應進行的趨勢 都發揮了作用。藉由催化劑及催化劑混合物供應時間的安排 可加速反應或是引導反應。根據期望的最終產物,在反應程 序中較晚的時間將催化劑導入也是有用的。無機酸也可以作 為酸,特別是礦物酸(mineralacids),特別較佳的是強酸,以 及其具有盡可能低的PK值。所使用的這些酸及酸的反應物 係為非毒性且具有最小的腐蝕性。此外,在反應物中測不出 ,,酸以及這些酸的成份會被純化或是盡可能以簡易的方 式處理。亦作為食物添加劑的硫酸滿足大部分要求,因而特 別適合。不同的酸類也可以結合在一起。羧酸(carb〇xylic aCld、S)e’尤其是質子酸(Protonacid)是可以作為一種選擇使來 用或,額外添加使用。使用二元-鲮酸或是三元羧酸及以上 所有羧酸、酒石酸(tartaric acid)及檸檬酸(citric acid)已經證 明特別有利。檸檬酸及、為結晶狀且無雜。這兩種 34 201118162 念2果中自然、產生(柑橘類水果如檸檬含有捧檬酸, 作為摧化劑成份的酸同時可用於產生培 養步驟之酸性介質。酸的濃度尤其係與ρκ值有關,且大約 為0.1至3之容量百分比、〇 6至2之容量百分比,尤其較 佳為0.3至1之容量百分比。進料原料以酸預培養係可&少 反應時間。預培養的時間愈長,酸性愈強及酸的濃度愈高, 反應時間愈短。除了其他的成份,催化劑或是催化物 可以包含一種或是多種金屬。較佳係使用過渡金屬(transLn metal)例如鐵、鎳、鈷、銅、鉻、鶴、鉬、或是鈦,夢此, 鐵已經可以證明尤其有利。在導入反應器之前可以進行添加 催化劑,也可以在此方法的其他的時間内添加催加劑。此 外’不同的催化劑混合物或是組成可以在不同時間添加於反 應混合物。 ' 生物質係徹底地與催化劑或是催化劑混合物混合。接 著,催化劑與生物質一起形成一反應混合物。其混合^序可 以選擇性的在反應器内進行。反應混合物的壓縮作用可以在 一個或是數個步驟中,在反應器内或是反應器外進行。高度 壓縮是有利的,其特別是指反應空間較佳的使用。由期望= 反應物及反應程序至反應器的可傳送性來決定壓縮量。舉例 而言,反應混合物也可以在預處理之後導入反應器内。 在反應成伤導入壓力容器空間之前例如可發生預熱步 驟。所有的反應物可以進行預熱。在這些進料原料之中了特 別是生物質,可以加熱至接近60。(:至90〇C。例如藉由供應 熱能而進行預熱步驟,尤其是加入溫度接近沸點的製程水'二 預熱的生物質懸浮液、壓力在絕對壓力為丨巴之條件下的 其他水,或是藉由供應製程水蒸汽或是其它熱源載體。由熱 交換程序所產生的熱能也可以選擇性或是附加的在此步^ 中使用。 而反應時間係與期望的反應產物有關,其介於1小時至 60小時、特別的是介於3小時及40小時之間、更特別的是 35 201118162 在5小時及18小時之間。當不再有明顯的焓(enthyalpy;) 釋放時’反應時間可以視為結束’或是反應視為為終止。最 小限度的預處理及/或省略個別的預處理步驟時,會使反應 時間增加至超過60小時。反應時間係與各自的進料原料以 及組成尤其有關。表面積愈大、顆粒大小愈小、木質素(lignin) 或是纖維素(cellulose)比例愈小及碳水化合物比愈大,則在 去聚合作用階段的熱能釋放愈快,愈快達到穩定階段,而減 少反應時間或是滯留時間。各別的進料原料的轉化時間愈 短,則例如導入在反應器中已經運轉的反應的延遲會愈長。 由較大比例的脂肪或是非植物及非交聯性的例如動物性蛋 白質或是細菌蛋白質亦可使反應時間縮短。在反應程序中熱 能釋放的終止係為轉化程序結束的指標。 根據本案,溫度可以高達300。(:。但是溫度在185。(:至 205°C之間也是有利的,特別是在215°C,及更特別的較佳 是在225°C。 根據本案’在沒有空氣的狀況下,壓力介於7巴至90巴 之間。較佳的是壓力介於11巴及18巴之間,也可以介於18 巴及26巴之間’也可以是介於26巴至34巴之間。 【實施方式】 本發明之裝置包含一反應器,此反應器可以根據反應器 内的程序的進行、使用固體的種類和量及/或所需的反應產物 而以不同的方式來開發。根據本案,至少其中之一反應器可 以是疊接式反應器(cascadereactor)、管式反應器、循環式反應 器(circuit reactor)、迴路式反應器(i〇〇p react〇r)、薄膜式反應 器、體化床及/或攪動式器皿或是攪動式器皿反應器、或是 具有單獨特性的反應器、或是具有這些反應器的不同特性的 、板合1反應器的流體化床較佳是循環式。根據本案之一反應 器或是不同反應器之組合,可在設備中以用於不同的處理時 間及加工步驟。此外,可以根據所需壓力將反應器設計成壓 36 201118162 力器皿。而壓力器皿形式係根據加工程序以及所使用的混合 技術來設計。 ^ t發1之目的的進一步之實施例中,反應器係形成為具 有循%式流體化床(circulating fluidized bed)之多重薄膜流體 化床反應器(multi-membrane fluidized bed reactor)的類型。此 反應器係結合各種薄膜反應器及流體化床反應器的優點。在 本文中,流體化床應理解為固體顆粒的壓載物(ballasting)或是 聚集物,該等固體顆粒係藉由向上的流體流動而被帶入流體 化狀態。在本文中,所謂的『流體化』(fluidized)係促使(前 者)壓載物於此時具有類流體的特性(例如,水的特性)。根 據^案,固:液混合物出現在反應器内。如果固體細粒或是微 粒壓載物藉由氣體或是液體(所謂的流體介質(liquid medium))由下往上通過,則被攪動。流體介質需要以足夠高 的速度通過以提升顆粒,以將之攪動。所需的能量輸入取決 於反應條件。當反應完成時,由於攪動作用,固相的顆粒可 以部份但連續的方式由反應空間中輕易移除。新鮮的固體原 料可以對應地再予填加。調整流體的流速,以使攪動固體的 方式至少是可以形成一靜止的流體化床。而在此狀態的流體 流速低於顆粒的沉降速度。藉由結合個別相鄰的顆粒,其流 體阻力係高於單一顆粒的流體阻力。因此可以形成具有分明 表面(defined surface)的懸浮層。而流體的流速可以隨著對薄膜 元件施加高壓而增加。相當多顆粒藉由較高的流體流動從基 巧區(basezone)釋出,而上層邊界崩解。一定比例的固體仍會 落回在流體化床中之基底區。在密集(dense)區域上方所謂的 自由空間(free space)中形成流動’其中固體在相當寬的核心中 提升為薄薄的懸浮液,而固體會在反應器的邊緣以高速叢集 式落下。藉由定位至少四個液體流動混合器(liquid stream mixer)(其分布的方式在直徑方面盡可能平均且在垂直距離也 是盡可能平均),以及額外的混合裝置(其包括就在基底金屬 片(base metal sheet)上之表面)’抑制了凝聚物以及層邊界的形 37 201118162 成,使得顆粒的均質授動可進行。 +當適當使用時,特別是利用薄膜部件時,下列好處可 以藉由根據本發明之反應器達成,其中: 1. 藉由加速推進劑(propellant)以及流體流動產生的 亂流,使得在連續的流體及分散的固相之間產生 高的相對速度。 2. 頻繁的顆粒-顆粒撞擊及顆粒-壁面的撞擊。 3. 顆粒的加強混合。 4. 反應混合物與流體的熱交換加速。 5. 沉積的最小化。 6. 在反應過程中例如水及反應物的劑量受到控制。 根據本案之反應器可以具有一個或是多個下列的特性。 反應器可以包含至少一壓力容器及至少一個用於固_液分離 之裝置,且也稱為薄膜反應器(membrane react〇r)。反應器可 以具有至少一個粗篩及/或細篩的過濾裝置或是兩種裝置的 組合,其亦可合併成一過濾裝置。至少其中一個壓力容器可 以具有一攪動及/或混合系統,也可以稱為攪動容器反應器 (stirringvesselreactor)。壓力容器或反應器的總反應空間之體 積可為0.5立方公尺至1〇,〇〇〇立方公尺(cubicmeter),也可以 疋5立方公尺至2,000立方公尺及或者是5〇立方公尺至5〇〇 立方公尺。其設備的所有容器包含壓力容器或反應器的反應 空間、料斗(hopper)及儲存空間之體積可為〇·5立方公尺至 10,000立方公尺,也可以是1〇 〇〇〇立方公尺至7〇 〇〇〇立方公 尺及也可以是50,0〇0立方公尺至500,000立方公尺。視進料 原料及生物質而定’生物質的含水量可高達佔總重量的95〇/〇 或是更多。因為此原因,在轉化程序之前先完成除水程序會 是有用的。由於許多生物質的高含濕度及低毛重(packed weight),可傳送度有所限制,使得在反應空間中初始的固體 比例可接近5%及30%之間。反應產物的產率會在相對於總反 應空間體積的單一百分比數字左右。因此,較大的反應空間 38 201118162 ,積係有必要的。由數個壓力容器或反應器連接在一起可以 传到大的反應空間體積。藉由連接這些反應器,其方法例如 疊接式,及/或不同反應器型式的結合,由改善加工程序的控 制’可得到更優的滞留時間分配及較高的操作容量。同時, 可^及,同反應階段及部份步驟的不同需求。更合適的熱交 =係在管式反應H巾進行,在獅式容H或是_式反應器 中I進行較佳的混合以及再混合。藉由將反應器的整個體積 而刀成數個壓力器皿,係可以改善具有壓力器皿之個別設備 之傳送能力。藉由連接數個壓力器皿或反應器,可促成實現 連續,或半連續式程序。驗收容在反應n巾職或包含在 ^應,中之壓縮程序氣體的至少—壓力容器可以使用於且整 :至設備中。在程序氣體排放至大氣環境中或者是送入在設 ί外部或内部之自有的峨程序之前,在-自有的清潔程 ^你|如一空氣清潔設備(air cleaning卩1刪中加以清潔。程序 ,體,,人與濕式氧錄序_樣的氧化程序巾,其以壓縮空 =進行操作。若翻收與雌序連接,麟歧在程序氣體 中可氧化的成份可轉化成熱能且經由熱交換程序回收。 藉由在加工程序過程連續分離或是取回單一反應物,例 曰ί ’可以在方法實行_增加固體部分。根據反應程序或 =理條件’ g]體的含量可以由原來的15%增加至20%或 π t、f別是增加至31%〜45%,及更特別岐46%至70。/。 =時’母個反應器之體積可峨著反應發展同時減少。同時, 化的進料原料,而可以在給定的反應器體積 較尚的刼作效能。將數個反應器以串聯的方式連接,豆 2用^valve)加以分離,進一步使得可以為了增加產量的目、 庫物力器皿内添加或是再添加新鮮進料原料、反 f物或疋催化劑。反應混合物係由壓力H皿傳送至下一個壓 ί Κΐΐίίί續程歸理_健件獨行。反應器及 錄線係^減 39 201118162 ’較佳的材料為不銹鋼。其反應器的壁 ΐΐΐΓρ计,慮為7巴至20巴之間,較佳的是在20 J至咒巴之間、更特別的是在30巴至40巴之間;其溫度是 ^ 160 c ^ 230 c之間、特別的是26(rc及更特別的是3〇(rc。 至少一個壓力容器、反應器或是設備組件中的溫 义其在,> _反應週期巾係持續高於贼至卿、特別的 疋由60 C至7〇C及/或高於製程水在丨巴之絕對壓力下之沸點 溫度’這使得延長直接皮膚接觸,例如以手直接接觸容器壁 與反應混合物超過_分鐘以上而不會增加皮膚發紅,只有在 藉由辅助裝置、隔離物質或是附加的裝置才有可能。 >根據本案所述之反應器可以包含一垂直筒狀本體。其直 徑-高度比(cUameter-heightratio)至少為 1:0.5、1:2、1:5 或是更 大。上基慮係為一近似球形之基座。在上層部份,特別是上半 ep及特別疋在上層的2/3的部份,為圓錐形狀,其直徑是朝著 底層而逐漸增加。相對於反應器軸,圓錐形狀的基座的角度為 45度、,獅是小於4G度、及更制的是小於%度。由例 如反應器壁至基底區的轉變係為圓形用以減少擾亂流體。對於 反應混合物的供應而言,喷嘴的設置是可變的,其例如可以設 置在壓力容器上半部,較佳是上三分之一。該供應係經由閥 (valve),通過大約在基底或圓錐形基底中央之輸出喷嘴來進 行。反應器的組件和喷嘴可以藉由焊接連接在一起。另外,可 裝設蓋子。藉由優先利用液體流動(liquid stream)混合器或喷射 真空泵及全喷射式噴嘴(fUll jet nozzles),其直徑·高度比可以接 近1:2至1:3 ’也可以是1:4至1:5 ’及也可以是ι:5至1:6。 薄膜反應器係為可結合至少化學反應與薄膜方法或與固 -液分離作用之裝置。藉此,兩種程序可以整合在一起,而可 以發展協同作用。兩種程序可以同時容置在單一殼體或是設備 中。在化學反應過程中,至少轉換其中一個化學反應物的成 份。藉由使用薄膜反應器,反應產物、中間產物、次級產物及 最終產物可以選擇性的由反應混合物中移除,而析出物可以受 201118162 控制的方式加人,或者是加強與析出物的接 及祕錄,尤妓水鱗續式 反應混σ物中移除。因此,可達成明顯的產量增加。 的介質或是物質’_是可分解的氧紐對於反_序及腐^ 的減少而有所幫助,由域的化學雜變化,包括特別是在 聚合作用過程巾密度的變化促進固_液分離侧^藉此, 在反應混合物中可以得到較高的固體濃度。根據固體的含量及 轉化程序的狀態,將反應混合物傳送至迴路式反應器中。藉 此’反應混合物軸向地在第一方向上以及相反的第二方向流過 ^向轴向内筒區段。當使用迴路式反應器時,内管可以設置熱 交換元件以加速熱交換且使得反應器的直徑可以更大。内管^ 稱為插入管或導管。導管的餘會影響迴触的縣力以及偏 ^(deflection)損失。當長度不變,迴流的偏轉損失及摩擦力隨 著直徑的減少而增加。當所選擇的直徑太大的時候,則迴流會 整個崩潰。插入管的直徑則大約為反應器直徑的1/4至I〆〗, 至多是反應器直徑的一半。導管可以設置在距離反應器基座 1/3或是1/4的位置。 在反應混合物中呈現還原關係(recjuctive reiati〇nship)。由 於酸性環境’腐钮性物質例如氯(chl〇rine)的存在,高溫及高壓 下,在操作條件下與反應混合物接觸的表面有腐儀的風險。藉 此,特別是經過長時間的操作下,經過局部的腐蝕可以呈現其 耐磨性。依據使腐钮作用最小化的直徑,可以使用堅固安裝的 薄膜部件或疋流體透析裝置(fluid-permeable cartridge)。 薄膜元件由穿孔元件(perforated element)所構成,特別的 是可以讓氣體及液體通過該元件之金屬平板。流體及氣體透 析裝置(gas-permeable cartidge)大部份也是由有孔金屬組件所 構成’藉由該裝置’已純化的推進劑(pr〇pellant)、溶劑或是 水可流至反應器空間中。當薄膜部件或是流體透析式裝置分 別使用時’不但是與各自的反應容器的直徑及容限度 (tolerance)有關,也與其形式及腐蝕負載有關。塑膠、金屬、 201118162 硬性金屬(hard metal)、陶瓷材料及聚四氟乙烯 (polytetrafluoroethylene)及特別是不銹鋼(stainless sted)及特 別是用於薄膜部件之不鏽鋼的合金被視為可能的材料,或是 塗層物質或是載體材料(carrier material)。塗層通常不只是簡 單之可移除的聚四氟乙烯筒匣,例如在實驗室規模中,此種 裝置可以以壓力鋼的方式來使用。而化學、機械、熱力學及 熱機方式均可以用於施加塗層。要施加材料,載體材料及/ 或黏著劑因而以氣體、溶化或是固體的方式呈現。較佳為使 用直流電(Galvanic spraying或是火焰喷射法(flame spraying),例如高速火焰熔射法(HV〇F)。可以施加塗層的 一種技術是電鍍。 取代電鍵法或是除電鑛之外附加的是在設備的一個戋是 數個容器的内部空間可以配置一筒匣(cartridge)。特別的是反 應器的内壁特別可排有薄膜部件。此筒匣主要具有圓筒狀且 可承載於格栅上,此格柵是指像網狀的結構。 或者,不銹鋼殼體,相較於熱交換平板系統,係設置在 ,,器或是筒H的外部或内部的補鋼層上。鋼板係以點或 f的方式焊接’藉此藉由在部件之間或在平板之間射入高 質’界定流體通道的未焊接的區域可被觀或是被「支 撐」(pillowed) ’調和液體(tempering Uquid)或熱交換介質可以 經此通過流體通道。不同的介質可以通過這些空腔。這些介 質可以作為熱_,其可以是充分加I的製程水、淡如也 water)或是水蒸汽或是熱油。 為y,不錄鋼殼體(其轉為反應器空間)的壓力負載最 p,夕用、些裝置,藉由這些裝置’在空腔及反應器空 二二成的壓力差盡可能小。利用雷射裝置(lasermean)在 孔以防止或是降低在空腔内的可能壓力差。其 :?| :二二,形式係與在_元件或是在筒11裡的相對應。 離係盡可能的彼此分開,使得抵達反應空間的介質 蓋可能少。 42 201118162 在殼體上或是在容器上的孔洞之距離至少10公分至2〇 公分,其也可以至少為60公分,及至少150公分。藉由出 現在殼體環路的過壓讓介質經由在内部反應器空間或是在 反應器壁與筒匣之間的空腔中的孔洞抵達内部反應空間。利 用雷射接合將單獨的點或是線焊接迴路連接而產生流通道 (flowpassage),而可以確保調和介質均勻分佈在殼體内。而 在調和系統内的壓力係超過在反應器内的壓力達6巴。在筒 匣的外殼直接鄰靠於壓力容器的内側。或者,可鄰靠穿孔的 格栅或是網狀結構。筒匣包括規則性的孔洞其直徑約為2〇 微米至70微米。 當使用電鍍的金屬平板時,在單側或是雙側電鍍 (plating)之外及/或在發生磨損徵兆之後,可以施加一内殼 體,其设體可以藉由焊接的方式連接及較佳的是利用雷射 焊接方式連接。同時,如上之具有筒匣的外殼體的空腔可 以為了内殼體的使用而形成。其内殼體的厚度為1 mm至 1.5 mm,也可以是1.5 mm至2 mm,或者是2 mm至2.5 mm。壓力損失被最小化,且藉由輸入尽輸出噴嘴的尺寸及 數量而又更加被最小化。 由鋼或特別是由不銹鋼所製成之筒匣,或者是薄膜部 件、反應器、由介質接觸之管件、熱交換器或是配件係由鋼或 尤其是不銹鋼所構成,以及用於本實施例為奥氏體鋼 (austenitic steels)或是增加鉻及鉬含量之6、7及8族之鋼或者 是雙鍊鋼(duplex steels)(其中德國工業標準(DIN)名稱為 1.457 卜 1.4404、1.4435、1.4539、1.4439、1.4462、1.4529、 1.4501)。在更進一步之實施例中,使用更高要求的反應條件 例如:銅、鎳合金、高钥含鎳合金,如2.4610,及鈦。筒匿的 壁厚度係設計為使筒匣可暴露在壓力差為2巴、特別是4巴 及特別是6巴。 尤其在基底區,會有因為沉降及重力作用而聚集固體部 份,具有結塊及堵塞的危險。這些妨礙了順暢的熱交換及劣化 43 201118162 在反應混合物中析出物的接觸,而阻礙反應的控制。因此,在 這些部伤中所使用的薄膜部件係特別加工,尤其是在基底或是 壁的區域’但是至少在圓錐區域JL較佳是下1/3冑份,特別的 是會發生沉積及結塊的區域。這些金屬平板的處理如在金屬平 板上以規則的距離鑽孔,特別是距離在1〇 mm以下,也可以 低於6 mm及低於4 mm。 利用雷射裝置在_部件或是在酿上的孔聽藉由雷 射在元件缺件上鑽孔’且具有之直㈣條微米及1〇 微米之間的,也可以是介於100微米幾2〇微米之間也可以 介於50微米及25微米之間。此孔洞較佳是漏斗形狀 (flmnel-shaped),因此孔洞的直徑出口處至少為入口處兩倍。 藉此’可,成扇型流動,使熱傳遞最佳化。細的轴向係幾 乎與反應器的軸向平行及/或垂直於穿孔薄膜部件件的表 面。加熱、冷卻以及充份處理過的製程水、淡水或是水蒸汽 係藉由過壓通過孔獅從空腔流至壓力容器的崎空間了因 此孔洞係可伽為喷嘴。同時上述紐係侧為調和物以及 推進物。製程水_是淡水必須加以充分處理以使之可以通過 孔/同或疋熱父換系統。對補給水以及容器水有效的標1目 的在於用於調整。 ”八 由反應器的内部空間所密封之空腔係在反應器壁及薄膜 部件之間,作為溶劑、水或是水蒸汽的引導。由高的孔洞中 排出’製程水的過舰是足夠高而能防止反應混合物的渗 透。薄膜部件或是筒匣壁的強度係設計為使得壁的強度完全 符合在内侧以及外侧的藶力差的需求。薄膜或是其與壓力容 器壁形成的空腔可以分割成複數區域,該等區域例如包含在 圓錐體或是在基底區之同々表面。此特徵為獨的壓力級。 不同壓力級例如由閥或是分離式泵送系統所實現。因而可以 _對由於重力所引發的崎作用造成的賊及結塊。藉由 以致的壓力所調整的孔洞直徑得到可比較的效果。例如在 較強的沉降作用的區域中的直徑可較大。 201118162 取代塗層或是使用避免腐钱作用的附加物質,對於内部 f間’尤其是基底或是壓力容__體及底座及其它與反 應混合物接觸部件,可以加喊祕理㈣⑽顿㈣。此 尤其可以藉由降低表面祕度而得到。取而代之或是除了表 面處理之外,研磨製造方法可以在一般的預處理之後使用, ,可以是電化學研磨方法、或者也可以是在電解液中金屬的 %極研磨’該電解液係特別相關於材料而加以調整。 在化學轉化反應過程中,錢料原料中含有的能量接近 0至34%以熱的形式釋放出去。此能源經由熱交換裝置用於 =在程序巾歧程料之具有熱需求的其姉序。例如此 :能可用於預熱生物質或是在程序内或纽備中的反應空 i 外或是在設備外,此能量可以用於加熱室、機器 或疋作為其它程相程序熱。關㈣賴獅,不只是會 ^入,動化學轉化程序_的舰,也會釋放放熱反應的熱 =。藉此可以消除不受控熱點_ sp〇t)的發展及反應器的失 二°,用至少-個,較佳為更多個,或是不同調和系統的組 口’其係以機械式、電子式或是化學的方式驅動。此外,或 取,代之’對町所述的製程水系統,反應器的調和系統例 如,層壁結構、旋入式散熱器(screw_in radiat〇r)、加熱線圈 ^卻線圈或是在反絲所使㈣散熱鰭片(fm)或是^外侧 接之半管式線畴所構成。取而代之或細加的,根據 、、了構及所_的材料’可_敝鮮板彡_細exchanger pate system)。製程水及/或熱油較佳帛作為通過且接近反應 器的内部空間的熱源載體或是用於調和系統而之調和介質。 個別的調和系統的組合、配置、設計及控制是由加工程 ^尤其是根據進料原料的組成所決定。在反應料側及反 應器内所有的製程水系統均可㈣於調和H在另一方面 於進行’係意指在反應器外的熱交換程序,以及另一方 J藉,調和製程水的導人,像是對於液體射流或是喷射真空 7而&所期望的材料如用於混合裝置、泵及/或喷嘴之稀釋、 45 201118162 調和、抽吸介質或是推進劑。混合製程水及淡水可以適合最 佳的反應器調和。藉此,加工程序可藉由例如降低特定無機 物質的濃度而再最佳化。此導入的物質較有利的是調和介 $,尤其是注入就溫度而言為關鍵性位置的調和水或是再循 環製程水。調和係經由加工程序附加地控制。除了進料原料 的組合之外、pH值樣品製備及催化劑,取決於轉化特性的進 料原料的延時導入是溫度控制一個重要的因素。 在方法的進行過程’進料原料或反應混合物黏度、密度 及大小及其他特性會改變。這些改變係由於含碳進料原料的& 學反應及結構上的改變,這些也可以是去聚合作用及之後進料 原料的更改結構(restructure)的原因。藉此,與加工程序有關, 產生混合程序的不同需求。根據程序、進料原料、固體濃度及 對反應產物的需求,混合及/或流體分佈係盡可能的均勻^具 均質性。為了熱交換以及增強對於析出接觸的目的,及為了 j吏 例如仍為交聯的高含量木質素(Hgin)或是纖維素(cdlul〇se)的 層更徹底瓦解、反應物及大部份的催化劑混合物的平均分佈及 反應混合物的排出的目的,以連續的方式或是間歇式進行攪拌 作用(agitation)或懸浮作用(SUSpensi〇n)。同時,沉降物分解, 鬆動,且消除栓塞及凝結形成。因而以總體正面的方式影響反 應進行。其意指,混合程序愈完全愈均勻,反應進行愈快,且 使反應產物同質性愈高。在反應空間中,可以使用具^有及/或 不具有活動式之部件的至少一個或數個、且尤其是不同混合系 統的組合。在反應空間中,一個或是更多或是不同攪拌器的組 合’可以作為具有活動式部件之混合^。攪拌器更配置有具有 至少一個及較佳的是兩個或是數個軸,使得可藉由相同的馬達 及反應器入口來驅動更多攪拌器。相較於能量供應或相較於混 合時間來說’相對低的能量要求是這賴拌系⑽優點。相較 於在反應空ΡΘ巾不具有活動式部件之混合纽來說,除了高成 本之外,主要的缺點在於容易故障及較高的維修費用。 喷射真空泵(jet vacuum pump)或是液體射流混合器(liquid 46 201118162 jet mixer)二泵及喷嘴(n〇zzle)係為液體喷射系統』过 system)這些裝置通常不具有任何活動式部件因此只需要 ^少的保養嘴體喷射系統可作用為混合系、统因為其適於經 ^推進物(propellant)將動能導入反應器中,這些推進物也可以 4為加熱或是冷卻之用,以便於使反應器内容物懸浮或是均勻 液體儒綠蚊進-步_點包括小尺寸、流路與流動 係之擾亂最小化及密封系統(sealjjjg SyStem)的避免。傳 ^系統經常使用的碎流板(streambreaker)是多餘的。的 在這些系統使用時,不會有碎流板_條件流體不作用區(dead Z〇ne)存在。同時,避免了浮動(floating)(固體的浮動),藉此 以降低進氣(air intake)的危險。該等液體喷射流系統可以由 一個共同的或是數個製程水貯存器饋給。這些液體喷射系统可 以彼此獨立控制,使不同量的推進物及/或由調和物可以通 過二為了料作用及_化,更佳的是將推進物及/或調和物 ^幾乎連續纽/或叫關方式加人。紐喷⑽統且尤其 疋,真空粟或液體噴混合器的置放選擇,係使得液體流路的 ,成產生例如垂直迴路流動的形式。反應器的直徑_高度比為 夕’迴,流動以「8」的形式形成,或是以對應的高度,更 =迴路係械+於垂直方向橫向流動。液體翁混合_或是喷射 真空泵較佳設置在反應器的上半部,尤其是在上1/3,藉此推 ^物射流躺下联乎與反應㈣軸向平行。數個㈣喷射混 :器或疋喷射真空果可與較大或是較高的反應H以串聯的方 式,接’特別的是控度-高度比為1:3,這意思是指這些是在不 =度以㈣的方式連接,使得各自後續的混合裝置使加速的 ^體再加速。在大直徑’特別是超過—公尺的直徑,數個液體 喷射混合H或喷躲在-種方式設置在_方向,使得在一個 有效地加齡賴喷射。若是在—個高度使用超過兩個 液體喷射混合H或是喷射真H,數個紐喷射混合器各自相 1 其加速的流體會向下至反應器的基底。—個或是數個液體 、射混合器或是喷射真空栗就設置在圓錐型或是基底區上 201118162 方’使得流體被導向成切線地經過基底部或是圓錐形的壁。- 數她體喷射混合ϋ或是喷射真空泵餘置在圓錐型 底區中*出口噴嘴旁’使得流體直接以切線的*式經過 與基底部或是圓錐型的壁。 ,利用㈣喷射祕或是喷射真空泵的亂流或是f應力負 *^©@_(de_aggl()mer時藉由在亂流及剪應力負載最大 的區域使_加的碎躲置,尤其是在進人σ、減或是排出 開口等處使用,可以預定的方式消除結塊(dump)及凝結物的 形成。在進入、抽吸開口有阻塞傾向的位置,可設置其本身的 〒程水供,,而製程水僅需為了此目的粗略處理。例如韩選 器、過濾器及溥膜係用於粗略處理。相較於推進物及調和物的 製程水處S,粗略處理為較快速及幾乎直接沒有或僅有實質上 很低的保留體積。或者’有聰和沉·險的混合器之進入或 抽吸開口,使之遠離本身推進物流動環路及/或配置短期流路 反轉^構(short-term flow reversal mechanism)。為控制這些喷 嘴,係採用流量計(fl0wmeter)、壓力表(man〇meter)及閥 (valve) ’其藉由例如在抽吸區中的壓力改變來反應阻塞。對於 有堵塞和沉積危險的抽吸槽(sucti〇n sl〇t)或抽吸開口,混合的 反應混合物供應可以藉由一種分割式推進物流體供應來實 現:一。部份是直接由反應器中吸取,另一部份是經過粗濾並由 反應器上部吸取。經由閥來控制及切換推進物流體供應,以便 例如當操作問題發生時或是經處理之淨化水的程度達到較低 程度的時候,可以節省推進物。 在容器的内部空間甲的預定位置上可以使用噴嘴。其中 尤其是欲防止沉澱及結塊的不作用(dead)區域或是範圍。'相 較於反應器的内部壓力,所有液體喷射系統中有連續壓力差, 用以防止反應混合物返回至混合器、泵及噴嘴。減速或滯留加 速固體反應物的沉澱或沉降過程序’其因而逐漸累積在反應器 下部。 在化學轉化程序中,沉澱物和結塊會形成在反應器的器 48 201118162 iiiS(rrting)及與反應混合物所接觸到的部件上。在 反應=内谷物傳送至另—鑛力容器之後可 而ίίΐ低實質操作溫度。例如可移動及可控制之高嘴可 置。此清絲置可明由手_續_、水間 二或ίΐί影機的控制之下實行。清潔裝置可以利用遠= f的麼力和溫度以得到最佳的清潔結果,且不ί 材料綱。對於喷射介質的表面清潔而言: 尤其適合:作為喷出物的乾冰顆粒係以 每秒300公尺(300m/s) ’且以高動能撞擊污垢 =i r)。藉將之冷卻至負8(rc;污垢層收縮且變脆。 ΐί ί賴擴張達700倍,使得污垢層由表面 ,,置。對環境有害的有機溶劑及齒化碳水化合物 步決定性的優點是由乾冰顆粒分解於空氣中產生 變成多餘的。乾冰喷射器較佳 & ^_ve_kelsystem)。此乾冰喷射器經 ^在=位置的手洞導入反應器中,並靠入先前設置的固持系 ^乾^顆粒藉由旋轉喷散裝置㈣ating s卿 欲加以清潔之處。 】 液體或疋氣體狀態的介質例如水、再調整或已處理的 程水或氣體如水蒸汽對喷射真空泵或液體喷射混合器而言,可 以作為推進物。*反絲中時或就在之後,製程 經過篩選、碱及麟雜質,使得混合裝置、栗及喷嘴不^ 阻檔且反應H管件、雜纽其它底座的磨損可最小化 劑的溫度鋪触換之魏行調整’使得其導人肋控制程 溫度。推/調和介質係以與在反應!!⑽壓力相當的 通過反應器的外側。若製程水的調和系統功能已失,則推進 /調和介質就會以與反應器_溢度相#的溫度通過反應 的外侧。取代製程水’淡水、水蒸汽或來自其它程序的水均可The pre-culture, preheating, pumpable solid-liquid mixture production or enthalpy of the feed material is applied or mixed for the feed material supplied in the reactor of the apparatus, preferably at a use temperature of 25 ° C to 50 ° C, 50 ° C to 70 ° C or i 〇 ° C 32 201118162 process water. For these purposes, its ^ ί 妓 4 4 is lower than 2. Warming Urt—steps in the equipment or outside the equipment, preferably using heat = however, for these feeds, the temperature exceeds the supply of the booter in the boot to evaporate or use another way to exclude a certain amount Water, itr, f acid as a transport agent to obtain the required pH value, the boiling water level of the ship is such that the point is higher than 2?9〇C ° ^^^Phoric acid) Hemp: / dish: 糸213 C. Although the boiling point is high, even if it is difficult to avoid the 5 points of the catalytic point from being dissipated by the process water, it can still be effective by lowering the boiling point of the acid such as sulfur (bivalent) stress point or decomposition temperature =; GGC 'chlorine The temperature of the Buddha's point of the iron (trivalent) is higher than 12G 〇c (sublimation), and the temperature of the axis of the bismuth iron (divalent) is Na. . The concentration of self-made water can reduce one or several catalyst components. The m steam is used in other locations in the process, such as heating the feed material before entering the heat exchanger, heating the heat oil via the heat exchanger program or using A device for drying the reaction product, such as an air agitator mill and/or a drying device as previously described in this specification. Process water vapor cleaning according to the application. In the present case, it is described that a plurality of pumps can carry concentrated process water at a temperature higher than 250 ° C. The pump can be a helical displacement pump. The temperature is lowered by the heat exchanger at ambient pressure, or the temperature is lowered before the feed is fed to the pressureless device & resupless device or sent to the mixing device, so that the temperature of the solid-liquid mixture is 50. °C ~ 60. (: or 60. (: ~80〇C. Especially the separation of metal, inorganic or sand from the biomass 33 201118162 and other impurities. These methods and procedures are used, for example, in biogas plants The treatment range of biomass and organic waste is established in the (biogas plant). After the pre-culture, the catalyst containing the added or non-added water and/or the aqueous solution may be added to the acidic medium. The catalyst may comprise at least one or several different components which together form a catalyst mixture. The composition of the catalyst may, for example, comprise an acid. The reaction procedure is to a considerable extent dependent on the choice of catalyst, composition, concentration, particle size. , mixing ratio, and time impact of supply. Therefore, these factors depending on the catalyst have a great influence on the formation, design and properties of the final product. For the final form and structure or reaction product, the particle size of the metal catalyst is formed. Part, and the reaction time is also determined by the strength (value) of the acid, for example, when the particle size is small. At ten micrometers, especially from 200 nanometers to 1 nanometer, and particularly preferably from 10 nanometers to 199 nanometers, the probability of forming a final product to homogenize the fibrous nanostructure of the morphology is increased. The smaller the smaller, the more precise and uniform the fibrous structure of the new carbon compound can be defined. However, for the production of defined nanostructures, the degree of uniformity of carbohydrate content, particle size and particle size is a trend for the reaction. Both of them play a role. The catalyst and catalyst mixture supply time can accelerate the reaction or guide the reaction. According to the desired final product, it is also useful to introduce the catalyst at a later time in the reaction procedure. The inorganic acid can also be used as an acid. In particular, mineral acids, particularly preferred are strong acids, and they have as low a PK value as possible. The reactants of these acids and acids used are non-toxic and minimally corrosive. The reactants are not detected, and the acid and the components of these acids are purified or treated as easily as possible. The sulfuric acid of the agent satisfies most of the requirements and is therefore particularly suitable. Different acids can also be combined. The carboxylic acid (carb〇xylic aCld, S)e', especially protonic acid, can be used as an option or It is particularly advantageous to use binary-decanoic acid or tricarboxylic acid and all of the above carboxylic acids, tartaric acid and citric acid. Citric acid is crystalline and free of impurities. These two types of fruit are produced naturally (the citrus fruits such as lemons contain citric acid, and the acid used as the catalyzing component can also be used to generate the acidic medium for the culture step. The concentration of the acid is especially related to the ρκ value, and About 0. The percentage of capacity of 1 to 3, the percentage of capacity of 〇 6 to 2, particularly preferably 0. A percentage of capacity from 3 to 1. The feed material is pre-cultured with an acid and can be used with less reaction time. The longer the pre-culture time, the stronger the acidity and the higher the acid concentration, and the shorter the reaction time. The catalyst or catalyst may contain one or more metals in addition to other components. It is preferred to use a transLn metal such as iron, nickel, cobalt, copper, chromium, crane, molybdenum, or titanium, and it has been found that iron has proven to be particularly advantageous. The catalyst may be added prior to introduction into the reactor, or a catalyst may be added during other times of the process. Further, the different catalyst mixtures or compositions can be added to the reaction mixture at different times. The biomass is thoroughly mixed with the catalyst or catalyst mixture. The catalyst then forms a reaction mixture with the biomass. The mixing sequence can be selectively carried out in the reactor. The compression of the reaction mixture can be carried out in one or several steps, either in the reactor or outside the reactor. High compression is advantageous, and in particular refers to the preferred use of the reaction space. The amount of compression is determined by the desired = reactant and the transferability of the reaction procedure to the reactor. For example, the reaction mixture can also be introduced into the reactor after pretreatment. For example, a preheating step can occur before the reaction is introduced into the pressure vessel space. All reactants can be preheated. Among these feedstocks, especially biomass, can be heated to near 60. (: to 90 ° C. For example, by supplying heat energy, the preheating step, especially the addition of a process water having a temperature close to the boiling point, a two preheated biomass suspension, and other water at a pressure of absolute pressure Or by supplying process water vapor or other heat source carrier. The heat energy generated by the heat exchange process can also be selectively or additionally used in this step. The reaction time is related to the desired reaction product, Between 1 hour and 60 hours, especially between 3 hours and 40 hours, more particularly 35 201118162 between 5 hours and 18 hours. When there is no more obvious en (enthyalpy;) release The reaction time can be regarded as the end 'or the reaction is considered to be terminated. The minimum pretreatment and / or omission of the individual pretreatment steps will increase the reaction time to more than 60 hours. The reaction time is related to the respective feed materials. And the composition is especially relevant. The larger the surface area, the smaller the particle size, the smaller the proportion of lignin or cellulose, and the larger the carbohydrate ratio, the heat in the depolymerization stage. The faster the release, the faster the stabilization phase is achieved, and the reaction time or residence time is reduced. The shorter the conversion time of the individual feed materials, the longer the delay in the reaction that has been introduced into the reactor, for example. A large proportion of fat or non-plant and non-crosslinking, such as animal protein or bacterial protein, can also shorten the reaction time. The termination of thermal energy release in the reaction program is an indicator of the end of the conversion process. According to the case, the temperature can be as high as 300. (:. But the temperature is between 185. (: to 205 ° C is also advantageous, especially at 215 ° C, and more particularly preferably at 225 ° C. According to the present case 'in the absence of air The pressure is between 7 and 90 bar. It is preferred that the pressure is between 11 and 18 bar, or between 18 and 26 bar, or between 26 and 34 bar. [Embodiment] The apparatus of the present invention comprises a reactor which can be developed in different ways depending on the progress of the procedure in the reactor, the type and amount of solids used, and/or the desired reaction product. According to the case At least one of the reactors may be a cascade reactor, a tubular reactor, a circuit reactor, a loop reactor (i〇〇p react〇r), a membrane reactor , a fluidized bed and/or an agitated vessel or an agitated vessel reactor, or a reactor having separate characteristics, or a fluidized bed having a different characteristics of the reactor, the plated 1 reactor is preferably Circulating. According to one of the reactors or a combination of different reactors, it can be used in the equipment for different processing time and processing steps. In addition, the reactor can be designed to press 36 201118162 according to the required pressure. The pressure vessel format is designed according to the processing procedure and the mixing technique used. In a further embodiment of the purpose of the invention, the reactor is of the type formed as a multi-membrane fluidized bed reactor having a circulating fluidized bed. This reactor combines the advantages of various thin film reactors and fluidized bed reactors. As used herein, a fluidized bed is understood to mean ballasting or aggregates of solid particles that are brought into a fluidized state by upward fluid flow. In this context, the so-called "fluidized" causes the (previous) ballast to have fluid-like properties (e.g., water properties) at this time. According to the case, the solid: liquid mixture appears in the reactor. If the solid fine particles or the particulate ballast are passed from bottom to top by a gas or a liquid (so-called liquid medium), they are agitated. The fluid medium needs to pass at a sufficiently high rate to lift the particles to agitate them. The energy input required depends on the reaction conditions. When the reaction is complete, the solid phase particles can be easily removed from the reaction space in a partial but continuous manner due to agitation. Fresh solid raw materials can be refilled accordingly. The flow rate of the fluid is adjusted so that the manner in which the solids are agitated is at least a static fluidized bed. The fluid flow rate in this state is lower than the sedimentation velocity of the particles. By combining individual adjacent particles, the fluid resistance is higher than the fluid resistance of a single particle. It is thus possible to form a suspension layer having a defined surface. The flow rate of the fluid can be increased as high pressure is applied to the membrane element. Quite a few particles are released from the basezone by higher fluid flow, while the upper boundary collapses. A certain proportion of solids will still fall back into the basement zone in the fluidized bed. A flow is formed in a so-called free space above the dense area where the solids are lifted into a thin suspension in a relatively wide core, and the solids fall off at high speed clusters at the edges of the reactor. By positioning at least four liquid stream mixers (the distribution of which is as uniform as possible in diameter and at the same vertical distance as possible), as well as additional mixing devices (which include the base metal sheet ( The surface on the base metal sheet) 'suppresses the shape of the agglomerate and the layer boundary, so that the homogenization of the particles can be carried out. + When properly used, especially when using film components, the following benefits can be achieved by the reactor according to the invention, wherein:  By accelerating the propellant and the turbulence created by the fluid flow, a high relative velocity is produced between the continuous fluid and the dispersed solid phase. 2.  Frequent particle-particle impact and particle-wall impact. 3.  Enhanced mixing of the granules. 4.  The heat exchange of the reaction mixture with the fluid is accelerated. 5.  Minimize deposition. 6.  The dosage of, for example, water and reactants is controlled during the reaction. The reactor according to the present invention may have one or more of the following characteristics. The reactor may comprise at least one pressure vessel and at least one means for solid-liquid separation, and is also referred to as a membrane reactor. The reactor may have at least one coarse screen and/or fine screen filter unit or a combination of both units, which may also be combined into one filter unit. At least one of the pressure vessels may have an agitation and/or mixing system, which may also be referred to as a stirring vessel reactor. The volume of the total reaction space of the pressure vessel or reactor may be zero. From 5 m3 to 1 〇, the cubic meter can also be from 5 m3 to 2,000 m3 and or from 5 m3 to 5 m3. The volume of the reaction space, hopper and storage space of all the vessels of the equipment containing the pressure vessel or reactor may range from 立方5 m ^ 3 to 10,000 m ^ 3 or 1 〇〇〇〇 m ^ 3 to 7 〇〇〇〇 m ^ 3 and can also be 50,0 〇 0 m ^ 3 to 500,000 m ^ 3 . Depending on the feedstock and biomass, the biomass can have a water content of up to 95 〇/〇 or more based on the total weight. For this reason, it is useful to complete the water removal process before the conversion process. Due to the high moisture content and low packed weight of many biomasses, the transportability is limited so that the initial solids ratio in the reaction space can be close to between 5% and 30%. The yield of the reaction product will be around a single percentage number relative to the total reaction space volume. Therefore, a larger reaction space 38 201118162, the system is necessary. It can be transferred to a large reaction space volume by several pressure vessels or reactors connected together. By connecting these reactors, methods such as splicing, and/or combinations of different reactor types, improved retention time distribution and higher operating capacity can be achieved by improved control of the processing program. At the same time, it can meet the different needs of the reaction phase and some of the steps. A more suitable heat exchange is carried out in a tubular reaction H-belt, with better mixing and remixing in a lion-type H or _ reactor. By singulating the entire volume of the reactor into a plurality of pressure vessels, the transfer capability of individual equipment having pressure vessels can be improved. By connecting several pressure vessels or reactors, a continuous, or semi-continuous procedure can be facilitated. At least the pressure vessel contained in the reaction n or the compression process gas contained in the reactor can be used and integrated into the equipment. Before the program gas is discharged into the atmosphere or sent to the outside or inside of the facility, it can be cleaned in the air cleaning unit (air cleaning equipment). Procedure, body, human and wet oxygen recording sequence-like oxidation procedure towel, which operates with compression null =. If the retraction is connected with the female sequence, the oxidizable component of the process gas in the process gas can be converted into heat energy and Recycling via a heat exchange program. By continuously separating or retrieving a single reactant during the processing procedure, an example can be performed in the method to increase the solid portion. The content of the body can be determined by the reaction procedure or the condition The original 15% increase to 20% or π t, f is increased to 31% ~ 45%, and more specifically 岐 46% to 70. / = = when the size of the mother reactor can be reduced while the reaction develops At the same time, the raw material of the feed can be used in a given reactor volume. The several reactors are connected in series, and the beans 2 are separated by ^valve, which further makes it possible to increase The output of the product, the storage of the material and the material Or add fresh feed material, catalyst anti f or piece goods. The reaction mixture is transferred from the pressure vessel to the next pressure. 续 Κΐΐ ί ί 续 _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ Reactor and Recording System Reduction 39 201118162 ‘The preferred material is stainless steel. The wall ΐΐΐΓ of the reactor is considered to be between 7 and 20 bar, preferably between 20 J and the bar, more particularly between 30 and 40 bar; the temperature is ^ 160 c ^ 230 c, especially 26 (rc and more particularly 3 〇 (rc. at least one pressure vessel, reactor or equipment component in the temperature sense, > _ reaction cycle system is consistently higher than Thief to Qing, special 疋 from 60 C to 7 〇 C and / or higher than the boiling temperature of the process water under the absolute pressure of 丨 ' 'This makes prolonged direct skin contact, for example, by hand directly contacting the container wall and the reaction mixture exceeds More than _ minutes without increasing the redness of the skin, only by auxiliary devices, spacers or additional devices. > The reactor according to the present invention may comprise a vertical cylindrical body. Diameter-height The ratio (cUameter-heightratio) is at least 1:0. 5, 1:2, 1:5 or greater. The upper base is an approximately spherical base. In the upper part, especially the upper half ep and especially the 2/3 part of the upper layer, it has a conical shape whose diameter gradually increases toward the bottom layer. The angle of the conical shaped base is 45 degrees with respect to the reactor axis, the lion is less than 4G degrees, and the lion is less than % degrees. The transition from, for example, the reactor wall to the substrate zone is circular to reduce disruption of the fluid. For the supply of the reaction mixture, the arrangement of the nozzles is variable, which may for example be arranged in the upper half of the pressure vessel, preferably in the upper third. The supply is via a valve through an output nozzle approximately at the center of the substrate or conical substrate. The components of the reactor and the nozzles can be joined together by welding. In addition, a cover can be installed. By preferentially utilizing a liquid stream mixer or a jet vacuum pump and a full jet nozzle (fUll jet nozzles), the diameter to height ratio can be close to 1:2 to 1:3 ' or 1:4 to 1: 5 'and can also be ι: 5 to 1:6. The thin film reactor is a device that can combine at least a chemical reaction with a thin film method or with a solid-liquid separation. In this way, the two programs can be integrated and synergies can be developed. Both programs can be housed in a single housing or device at the same time. During the chemical reaction, at least one of the chemical reactants is converted. By using a thin film reactor, the reaction product, intermediate product, secondary product, and final product can be selectively removed from the reaction mixture, and the precipitate can be added in a manner controlled by 201118162, or the reinforcement can be added to the precipitate. And the secret record, especially the water scale continuous reaction mixed σ removal. Therefore, a significant increase in production can be achieved. The medium or substance '_ is a decomposable oxygen-nucleus that contributes to the reduction of the anti-sequence and the rot, and the chemical heterogeneous changes in the domain, including the change in the density of the towel during the polymerization process, promote solid-liquid separation. By this, a higher solid concentration can be obtained in the reaction mixture. The reaction mixture is passed to a loop reactor depending on the amount of solids and the state of the conversion procedure. By this, the reaction mixture flows axially in the first direction and in the opposite second direction toward the axially inner cylindrical section. When a loop reactor is used, the inner tube can be provided with a heat exchange element to accelerate heat exchange and make the diameter of the reactor larger. The inner tube ^ is called an insertion tube or a catheter. The remainder of the catheter will affect the county power of the return and the loss of the deflection. When the length is constant, the deflection loss and friction of the reflow increase as the diameter decreases. When the selected diameter is too large, the reflow will collapse. The diameter of the insertion tube is approximately 1/4 to 1 直径 of the diameter of the reactor, and at most half of the diameter of the reactor. The conduit can be placed 1/3 or 1/4 of the base of the reactor. A reduction relationship (recjuctive reiati〇nship) is present in the reaction mixture. Due to the presence of an acidic environment, such as chr〇rine, there is a risk of corrosion of the surface in contact with the reaction mixture under operating conditions at elevated temperatures and pressures. Therefore, especially after a long period of operation, the wear resistance can be exhibited by local corrosion. Depending on the diameter that minimizes the action of the button, a rigidly mounted film member or a fluid-permeable cartridge can be used. The membrane element consists of a perforated element, in particular a metal plate that allows gas and liquid to pass through the element. Most of the gas-permeable cartidge is also made up of porous metal components. The purified propellant (pr〇pellant), solvent or water can flow into the reactor space. . When film components or fluid dialysis devices are used separately, they are not only related to the diameter and tolerance of the respective reaction vessels, but also to their form and corrosion loading. Plastics, metals, 201118162 hard metal, ceramic materials and polytetrafluoroethylene and especially stainless steel (stainless sted) and especially alloys for thin film parts are considered as possible materials, or The coating material is either a carrier material. The coating is usually not just a simple removable Teflon cartridge, for example on a laboratory scale, the device can be used in the form of pressure steel. Chemical, mechanical, thermodynamic and thermal methods can be used to apply the coating. To apply the material, the carrier material and/or the adhesive are thus presented as a gas, a melt or a solid. It is preferred to use direct current (Galvanic spraying or flame spraying), such as high-speed flame spraying (HV〇F). One technique that can apply a coating is electroplating. Instead of or in addition to electric ore. It is possible to arrange a cartridge in the inner space of one of the containers of the device. In particular, the inner wall of the reactor may be specially provided with a film member. The cartridge is mainly cylindrical and can be carried on the grid. On the grid, the grid refers to a mesh-like structure. Alternatively, the stainless steel casing is disposed on the outer or inner steel layer of the vessel or the cylinder H compared to the heat exchange panel system. Soldering in a point or f manner, whereby the unwelded area defining the fluid passage between the components or between the plates can be viewed or "pillowed" by the liquid ( Tempering Uquid) or heat exchange medium can pass through the fluid passage. Different media can pass through these cavities. These media can be used as heat, which can be fully added process water, light water, or steamed. Or hot oil. For y, the pressure load of the unrecorded steel casing (which is converted into the reactor space) is the most p, and the devices are used, and the pressure difference between the cavity and the reactor is as small as possible. A laser device is used in the hole to prevent or reduce the possible pressure difference in the cavity. Its :?| : 22, the form corresponds to the _ component or the tube 11. The separations are separated from each other as much as possible so that the media cover that reaches the reaction space may be small. 42 201118162 The distance between the holes in the casing or on the container is at least 10 cm to 2 cm, which may also be at least 60 cm and at least 150 cm. The medium is allowed to reach the internal reaction space via a hole in the inner reactor space or in the cavity between the reactor wall and the cartridge by an overpressure occurring in the casing loop. Laser joints are used to connect individual points or wire-welded circuits to create flowpassage, which ensures uniform distribution of the media in the housing. The pressure in the blending system exceeds the pressure in the reactor by up to 6 bar. The outer casing of the cartridge is directly adjacent to the inside of the pressure vessel. Alternatively, it may be adjacent to a perforated grid or a mesh structure. The cartridge includes regular pores having a diameter of from about 2 microns to about 70 microns. When an electroplated metal plate is used, an inner casing may be applied outside of the one-sided or double-side plating and/or after the occurrence of signs of wear, the body of which may be joined by soldering and preferably. It is connected by laser welding. At the same time, the cavity of the outer casing having the cartridge as described above can be formed for the use of the inner casing. The inner casing has a thickness of 1 mm to 1. 5 mm, it can be 1. 5 mm to 2 mm, or 2 mm to 2. 5 mm. The pressure loss is minimized and is further minimized by the size and number of input output nozzles. a cartridge made of steel or, in particular, stainless steel, or a film component, a reactor, a tube in contact with a medium, a heat exchanger or an accessory, consisting of steel or especially stainless steel, and used in the present embodiment Austenitic steels or grade 6, 7 and 8 steels of chromium and molybdenum or duplex steels (where German Industrial Standard (DIN) is 1. 457 Bu 1. 4404, 1. 4435, 1. 4539, 1. 4439, 1. 4462, 1. 4529, 1. 4501). In still further embodiments, more demanding reaction conditions are used, such as: copper, nickel alloys, high-key nickel-containing alloys, such as 2. 4610, and titanium. The wall thickness of the tube is designed such that the cartridge can be exposed to a pressure difference of 2 bar, in particular 4 bar and especially 6 bar. Especially in the base zone, there is a risk of agglomeration and blockage due to sedimentation and gravity. These hinder smooth heat exchange and deterioration. 43 201118162 The contact of precipitates in the reaction mixture hinders the control of the reaction. Therefore, the film components used in these partial injuries are specially processed, especially in the area of the substrate or the wall 'but at least in the conical region JL is preferably the lower 1/3 ,, in particular, deposition and knotation occur. The area of the block. These metal plates are treated such that they are drilled at regular distances on a metal plate, especially at distances below 1 mm, or below 6 mm and below 4 mm. Using a laser device to drill a hole in a component by a laser or a hole in the brewing hole, and having a straight (four) micrometer and a thickness of 1 micron, or between 100 micrometers It can also be between 50 microns and 25 microns between 2 microns. The hole is preferably flmnel-shaped so that the diameter exit of the hole is at least twice the entrance. By this, a fan-shaped flow is made to optimize heat transfer. The fine axial direction is almost parallel to the axial direction of the reactor and/or perpendicular to the surface of the perforated film member. The heated, cooled, and fully treated process water, fresh water, or water vapor is passed through the pores through the hole lions to the space of the pressure vessel, so that the holes can be condensed into nozzles. At the same time, the above-mentioned side of the new line is a blend and a propellant. Process water _ is that fresh water must be adequately treated so that it can be replaced by a hole/same or hot father. The target for the supply of water and the water of the container is for adjustment. "The cavity sealed by the internal space of the reactor is between the reactor wall and the membrane member as a guide for solvent, water or water vapor. The passage of the process water from the high hole is high enough. It can prevent the penetration of the reaction mixture. The strength of the film member or the wall of the cylinder is designed such that the strength of the wall completely meets the requirements of the difference in the force between the inside and the outside. The film or the cavity formed by the wall of the pressure vessel can be Divided into a plurality of regions, for example, contained in a cone or on the same surface of the base region. This feature is a unique pressure level. Different pressure levels are implemented, for example, by a valve or a separate pumping system. Thieves and agglomerates caused by the effect of gravity caused by gravity. The diameter of the hole adjusted by the resulting pressure gives a comparable effect. For example, the diameter in the region of stronger sedimentation can be larger. 201118162 Substituting The layer is either an additional substance that avoids the use of money, for the internal f-parts, especially the substrate or the pressure-capacitor and the base and other parts in contact with the reaction mixture, You can call the secret (4) (10) (4). This can be obtained especially by reducing the surface secret. Instead of or in addition to the surface treatment, the grinding method can be used after general pretreatment, which can be an electrochemical grinding method. Or it may be a % pole grinding of the metal in the electrolyte. The electrolyte is specifically related to the material. During the chemical conversion reaction, the energy contained in the raw material is close to 0 to 34% and is released in the form of heat. Go out. This energy is used by the heat exchange device to = the order of heat demand in the process towel. For example: it can be used to preheat the biomass or in the process or in the reactor or It is outside the equipment, this energy can be used to heat the room, machine or sputum as other process phase heat. Off (four) Lai lion, not only will, the chemical conversion program _ the ship, will also release the heat of the exothermic reaction = In this way, the development of the uncontrolled hot spot _ sp〇t) and the loss of the reactor can be eliminated, and at least one, preferably more, or a group of different harmonic systems can be eliminated. ,Electricity Or chemically driven. In addition, or take, instead of the process water system described in 'Taicho, the reactor's blending system, for example, the wall structure, screw-in radiator (screw_in radiat〇r), heating coil ^The coil is either made up of the (4) heat sink fins (fm) or the half-pipe line domain connected to the outside of the reverse wire. Instead of or in addition, the material according to the structure, the structure, and the Process water and/or hot oil is preferably used as a heat source carrier passing through and close to the internal space of the reactor or a blending medium for a blending system. Combination of individual blending systems , configuration, design and control are determined by the addition of engineering, especially according to the composition of the feedstock. All process water systems on the reaction side and in the reactor can be used to reconcile H on the other hand. Refers to the heat exchange process outside the reactor, and the other party, to reconcile the process water, such as for liquid jets or jet vacuums 7 & the desired materials such as for mixing devices, pumps and / or Dilution of the nozzle, 45 201118162 And, pumping medium or propellant. Mixed process water and fresh water are suitable for optimum reactor blending. Thereby, the processing procedure can be re-optimized by, for example, reducing the concentration of the specific inorganic substance. The introduced material is advantageously a blending medium, in particular a blending water or a recirculating process water that is critical in terms of temperature. The blending system is additionally controlled via a processing program. In addition to the combination of feed materials, pH sample preparation and catalysts, the delayed introduction of feed materials depending on the conversion characteristics is an important factor in temperature control. The process feedstock or reaction mixture viscosity, density and size, and other characteristics may vary during the course of the process. These changes are due to the &study and structural changes of the carbonaceous feedstock, which may also be the reason for the depolymerization and subsequent restructure of the feedstock. This, in connection with the machining process, creates different requirements for the mixing process. The mixing and/or fluid distribution is as uniform as possible, depending on the procedure, feedstock feedstock, solids concentration and demand for the reaction product. For the purpose of heat exchange and enhancement for the purpose of precipitation contact, and for the purpose of, for example, the cross-linked high-content lignin (Hgin) or cellulose (cdlul〇se) layer is more completely disintegrated, reactants and most For the purpose of the average distribution of the catalyst mixture and the discharge of the reaction mixture, agitation or suspension (SUSpensi〇n) is carried out in a continuous manner or in a batch manner. At the same time, the sediment decomposes, loosens, and eliminates embolization and condensation formation. The reaction is thus affected in a positive overall manner. This means that the more complete and uniform the mixing procedure, the faster the reaction proceeds and the higher the homogeneity of the reaction product. In the reaction space, a combination of at least one or several, and in particular different, mixing systems with and/or without moving parts can be used. In the reaction space, a combination of one or more or different agitators can be used as a mixture with movable components. The agitator is further provided with at least one and preferably two or more shafts so that more agitators can be driven by the same motor and reactor inlet. The relatively low energy requirement compared to the energy supply or compared to the mixing time is the advantage of this simmering system (10). In addition to the high cost, the main disadvantage is that it is easy to malfunction and high maintenance cost compared to the hybrid button in which the reaction empty towel does not have movable parts. Jet vacuum pump or liquid jet mixer (liquid 46 201118162 jet mixer) two pumps and nozzles (n〇zzle) are liquid injection systems "systems" These devices usually do not have any moving parts and therefore only need ^Less maintenance nozzle injection system can function as a mixing system, because it is suitable for introducing kinetic energy into the reactor via propellant, these propellants can also be used for heating or cooling, so as to facilitate The reactor contents are suspended or evenly liquided. The steps of the ruthenium include small size, minimization of flow and flow systems, and avoidance of the sealing system (sealjjjg SyStem). The streambreaker that is often used by the system is redundant. In the use of these systems, there will be no flow plate _ conditional fluid inactive zone (dead Z〇ne). At the same time, floating (floating of solids) is avoided, thereby reducing the risk of air intake. The liquid jet systems can be fed by a common or several process water reservoirs. These liquid ejecting systems can be controlled independently of each other so that different amounts of propellant and/or confluent can pass through the two materials, and it is better to have the propellant and/or the confluent ^ almost continuous / or called The way of closing is added. The neospray (10) system and especially the helium, the placement of the vacuum mill or the liquid jet mixer, is such that the liquid flow path is in the form of, for example, a vertical loop flow. The diameter_height ratio of the reactor is ’'back, and the flow is formed in the form of "8", or at a corresponding height, more = loop mechanical + lateral flow in the vertical direction. Liquid Mixing - or Jet The vacuum pump is preferably placed in the upper half of the reactor, especially in the upper third, whereby the jet of radiation is lying parallel to the axial direction of the reaction (4). Several (four) jet mixing: or squirting vacuum can be combined with a larger or higher reaction H in series, in particular, the control-height ratio is 1:3, which means that these are Not = degrees are connected in a (four) manner such that each subsequent mixing device re-accelerates the accelerated body. In the large diameter 'especially more than - metric diameter, several liquid jets are mixed with H or sprayed in a way that is set in the _ direction so that the spray is effectively applied at an age. If more than two liquid jets are used at a height to mix H or jet true H, the fluids of each of the several jet mixers will accelerate down to the base of the reactor. One or several liquids, jet mixers or jet vacuum pumps are placed on the conical or base area. The 201118162 square causes the fluid to be directed tangentially through the base or conical wall. - The number of her body jet mixing or the jet vacuum pump is placed in the conical bottom zone * next to the outlet nozzle so that the fluid passes directly through the base or conical wall in a tangential manner. Use (4) jet turbulence or turbulent flow of jet vacuum pump or f stress negative *^©@_(de_aggl() mer to hide the _ plus in the area where the turbulent flow and shear stress are the most loaded, especially It can be used in a predetermined manner to eliminate the formation of dumps and condensate in the sigma, subtraction or discharge opening, etc. In the position where the inlet and suction openings have a tendency to block, the turbulent water can be set. For the process, the process water only needs to be roughly processed for this purpose. For example, the Han selector, the filter and the ruthenium film are used for rough processing. Compared with the process water S of the propellant and the blend, the rough treatment is faster and almost straightforward. No or only a substantially low retention volume. Or 'into the inlet or suction opening of a convergent and dangerous mixer, away from its propellant flow loop and/or short-term flow reversal In order to control these nozzles, a flow meter (fl0wmeter), a pressure gauge (manometer), and a valve (valve) are used to react to the blockage by, for example, a change in pressure in the suction zone (short-term flow reversal mechanism). For pumping with clogging and sedimentation hazards The tank (sucti〇n sl〇t) or the suction opening, the mixed reaction mixture supply can be achieved by a split propellant fluid supply: one is directly absorbed by the reactor and the other is passed through The coarse filter is taken up by the upper part of the reactor. The propellant fluid supply is controlled and switched via a valve to save propellant, for example, when operational problems occur or when the degree of treated purified water is low. Nozzles can be used in the predetermined position of the internal space A. Among them, in particular, it is intended to prevent the dead zone or range of precipitation and agglomeration. 'Compared with the internal pressure of the reactor, there is continuous pressure in all liquid injection systems. Poor, to prevent the reaction mixture from returning to the mixer, pump and nozzle. Deceleration or retention accelerates the precipitation or settling of the solid reactants. It thus gradually accumulates in the lower part of the reactor. In the chemical conversion process, precipitates and agglomerates Will be formed in the reactor 48 201118162 iiiS (rrting) and the parts in contact with the reaction mixture. In the reaction = the inner grain is transferred to - After the mineral container, the actual operating temperature can be lowered. For example, the movable and controllable high mouth can be set. This clearing can be carried out under the control of the hand_continuation_, water room 2 or ίΐί. The cleaning device can use the force and temperature of far = f to get the best cleaning result, and the material is not. For the surface cleaning of the spray medium: Especially suitable: dry ice particles as the effluent are 300 per second. Metric (300m/s) 'and hits dirt with high kinetic energy = ir). Cool it to minus 8 (rc; the dirt layer shrinks and becomes brittle. ΐί ί 扩张 expands 700 times, making the dirt layer from the surface, set. The environmentally harmful organic solvent and the toothed carbohydrate step-determining advantage is Decomposition by dry ice particles in the air becomes redundant. Dry ice blasters are preferred & ^_ve_kelsystem. The dry ice blaster is introduced into the reactor through a hand hole at the = position, and leans into the previously set holding system to dry the granules by rotating the scatter device (4). Liquid or helium gas medium such as water, reconditioned or treated process water or gas such as water vapor can be used as a propellant for jet vacuum pumps or liquid jet mixers. * When the yarn is in the middle or just after the process, the process is screened, alkali and lining impurities, so that the mixing device, the chestnut and the nozzle are not blocked, and the wear of the H-tube and the other base of the hybrid can minimize the temperature of the agent. The Wei line adjustment makes it guide the rib to control the temperature. The push/tune media is passed through the outside of the reactor at a pressure equivalent to the reaction!! (10). If the process of the process water blending system has been lost, the propellant/conditioning medium will pass through the outside of the reaction at the temperature of the reactor_fluid phase #. Replace process water 'fresh water, steam, or water from other processes

C 49 201118162 以作為推進物、加熱或是冷卻物。 在製程水中的材料係與進料原料的混合物及包含催化劑 之加工程序有關。事先與生物質結合的材料是藉由程序性碎裂 而分解。在化學轉換程序中,許多的元素包含氣、硫、硝酸鹽 及它們的鹽類及金屬,特別是重金屬及無機物及鹼金屬例如鉀 或鈉及鹼金屬的鹽類在某部份進入水相。一部份再一次在固相 結合。剩餘的部份係留在液相中。與液相結合的材料部份亦與 濃度差有關,這是指已經在液相中所呈現的濃度。達到某些^ 料沉澱醜和在濃度增加下魏。錢·及化合物例酸 巧及氯化物會因沉澱為鹽類且因此不利影響加工程序於反應 器組件。在液相中,有機碳化合物的部份為每公升50克以上。 沒有再循環的製程水的化學需氧量(chemical 〇xygen demand, COD)已經高於5 mg ο,,明顯已超過法定導入界限值。一▲ 了解的是化學需氧量(CQD)是將狀義的· 機物含量化學氧化所需的氧量。 寸置甲斤有有 /取決於進料原料的濕度含量及包含固_液比的加工程序, 再猶環的製程水部份為職至35%、也可以是35%至6〇%或 ^可以是是6G%至85%。製财幾乎完全騎回,其意指, 製,水環路關或限制只有以針對節省淡水及降低廢水體積 的受限方式才有可能。除了有機碳化合物的累積之外,大量的 無機材料例如硫化物、猶m魏這些的化合物濃 j。無機雜質濃度加速腐如在反應器中石灰沉澱物會妨礙流 ϊϊίΐΐ雜備例如栗、閥及喷嘴。因而增加反應器設計的 硫酸鹽會沉澱。累積的時間歧飽和的時間與進 料原料的材料組成及加工程序有關。 轉化程序通常持續數個小時。在這段時間,與材料 的獅辦料發生’需要考_這些,以使加工程 ίίί Γt前兩到三個程序階段以間隔方式提供各種不同的 ㈣i L減期望的反應產物’例如在將近最後_程序階段 〜束時收回反應產物。在程序進行過程中取回献提供推進劑 50 201118162 或調和物例如氣體、水’制是製程水及/絲序氣體/合成氣 體及催化劑。會攪亂化學反應、混合及流動的過程的反應劑及 特別是次級產物被移除。 . 不同的方法可用於固體材料的沉積及特別是在反應混合 • 物中的反應產物。固-液分離係用於液相的分離,藉此可以得 到^體,濃縮。不同的篩選程序(粗篩、細篩)、過濾程序及/ 或藉由氣旋(cyclone)利用離心力的沉積可以相互結合以用 於固體的分離。為了降低在程序過程中的過濾或篩選的負擔, 在預處理的範圍中進行一個或數個過濾程序或是篩選程序。 由這兩種方法,至少一個粗濾或一個細濾或是這兩個方法 的,合可實行。藉由過濾方法,特別是微過濾及/或超過濾法 或是兩者的結合,總有機碳化合物的1/3至2/3的量可以由製 程水中移除。較佳的是在操作條件下進行固_液分離,且通常 不只是使用如實驗室規模之較簡易的濾紙來進行。使用方法的 選擇係取決於化學組成、顆粒大小分佈、密度、顆粒形式、堅 硬度及溶解度等等,並包含電流及負載,不同的密度及離心力 及不同的粒子大小的使用。 動態的、靜止的、真空、加壓及無菌過濾,在這些當中 特別的是橫流過渡(cross flow filtration)包含可用的微過濾、超 過濾、奈米過濾及逆滲透方法係裝置所使用的其中一些。較佳 是使用利用水力旋流器、離心器、電子式或磁式分離裝置及/ 或過濾方法之方法或是功能原理的裝置。其中較佳的過濾方法 特別疋可以用於水熱碳化法(hydrothermal carbonization)之反 應條件者。對於固-液分離,由其是在操作條件下,較佳是使 用旋轉盤過濾、器或離心薄膜過渡裝置。用於孔洞的形成較佳的 • 材料係由金屬且尤其是陶瓷所構成。多孔形成材料的形式較佳 是圓盤狀。根據所利用的過濾方法及導入的材料,過濾裝置的 孔洞尺寸及在滤液中的固體量並非總是成比例。這對於使用陶 瓷材料作為過濾元件特別適用。將水相以過濾或是未過濾的方 式導入製程水貯存器中。欲加以分離的固體的特性,以及選來 51 201118162 ,行分離的方法是根據加工程序及所需要的反應產物的特性 f選擇。程序進行得愈深入,反應產物的密度愈高,愈容易完 2離程序。錄雛衫疑條件τ進行。麵液中的 固體含量通常是按孔洞尺寸的比例下沉,且可以藉由超過遽的 使用而有顯著的增加,並可以超過2/3至4/5。將一或數個固 液分離裝置整合至排除泥沙或其他雜質的程序,該等泥沙或雜 I具有高密度或是高重量,可以在生物f的處理過程中加以分 固體的離心力分離的原理的利用,對於製程水的清潔特別 有利,其製程水作為推進物喷射介質以保護泵、混合器及喷嘴。 在程序過程中,由反應器的上半部,特別的是由上方的 Λ處if別較佳的是由反應器上方的1/4處的一個或數個位 …收回製程水以再調整或處理。再調整或已處理的製程水係回 ,至設備的水環路中作為再循環。纟少一個及特別是數個製程 ^貯存器可以用於每-麵職反應器献麟數個已經社 二的反應器。不同的清潔步驟係在個別的製程水貯存器之^ 行。個別的製程水貯存器或是共用的製程水貯存器的容量 近$部反應H的總體積的35%至85% ^製程水貯存 了、 ,器的溫度和麗力負载而設計,使得降壓程度及熱交換裝置不 j可或缺。—製程水清潔整合於所賴備的水環路中。不同 =處理或再機方法取決於再調整程序水的制。不同 t化學及生物方法及裝置為此侧使用或是組合起來使用。C 49 201118162 Used as a propellant, heating or cooling. The materials in the process water are related to the mixture of feed materials and the processing procedures including the catalyst. Materials that are previously associated with biomass are broken down by procedural fragmentation. In the chemical conversion process, many elements include gases, sulfur, nitrates and their salts and metals, especially heavy metals and inorganics, and alkali metals such as potassium or sodium and alkali metal salts enter the aqueous phase in some parts. Part of it is combined again in the solid phase. The remaining part is retained in the liquid phase. The portion of the material that is combined with the liquid phase is also related to the difference in concentration, which is the concentration that has been exhibited in the liquid phase. Achieve some ugly precipitation and increase in concentration under the Wei. The acid and the compound are sour and chloride can precipitate as a salt and thus adversely affect the processing procedure in the reactor assembly. In the liquid phase, the portion of the organic carbon compound is 50 grams or more per liter. The chemical 〇xygen demand (COD) of the process water without recirculation has been higher than 5 mg ο, which clearly exceeds the statutory import limit. One ▲ understands that chemical oxygen demand (CQD) is the amount of oxygen required to chemically oxidize the organic matter content. There is / depending on the moisture content of the feed material and the processing procedure including the solid-liquid ratio, and the process water part of the loop is 35%, or 35% to 6〇% or ^ It can be 6G% to 85%. The production of money is almost completely back riding, which means that the system, the water loop or the restriction is only possible in a limited way to save fresh water and reduce the volume of wastewater. In addition to the accumulation of organic carbon compounds, a large number of inorganic materials such as sulfides and compounds such as sulphide are concentrated. The concentration of inorganic impurities accelerates as the lime deposits in the reactor can interfere with the flow of impurities such as pumps, valves and nozzles. Thus, the sulfate that increases the reactor design will precipitate. The cumulative time-saturation time is related to the material composition and processing procedure of the feedstock. The conversion process usually lasts for hours. During this time, the material of the lion is in charge of 'required test _ these, so that the first two to three program stages of the addition process ίίί Γt provide a variety of different (four) i L minus expected reaction products in the interval - for example, near the end _ Program stage ~ bundle to recover the reaction product. Retrieving propellant during the process of the process 50 201118162 or blends such as gas, water, are process water and / silk gas / synthesis gas and catalyst. The reactants and especially the secondary products that will disturb the chemical reaction, mixing and flowing processes are removed. Different methods are available for the deposition of solid materials and especially for the reaction products in the reaction mixture. The solid-liquid separation is used for the separation of the liquid phase, whereby the body can be obtained and concentrated. Different screening procedures (coarse screen, fine screen), filtration procedures, and/or deposition by centrifugal force by cyclone can be combined with each other for separation of solids. In order to reduce the burden of filtering or screening during the process, one or several filters or filters are performed in the scope of the pre-processing. By these two methods, at least one coarse filter or one fine filter or both can be implemented. The amount of 1/3 to 2/3 of the total organic carbon compound can be removed from the process water by filtration, particularly microfiltration and/or ultrafiltration or a combination of the two. It is preferred to carry out the solid-liquid separation under the operating conditions, and usually not only using a simple filter paper such as a laboratory scale. The choice of method of use depends on chemical composition, particle size distribution, density, particle form, hardness and solubility, etc., and includes the use of current and load, different densities and centrifugal forces, and different particle sizes. Dynamic, static, vacuum, pressurized and sterile filtration, among which cross flow filtration includes some of the available microfiltration, ultrafiltration, nanofiltration and reverse osmosis systems. . Preferably, a device utilizing a hydrocyclone, a centrifuge, an electronic or magnetic separation device and/or a filtration method or a functional principle is used. Among them, the preferred filtration method is particularly suitable for use in the reaction conditions of hydrothermal carbonization. For solid-liquid separation, it is preferred to use a rotating disk filter, centrifuge or centrifugal membrane transition device under operating conditions. For the formation of holes, the material is preferably made of metal and especially ceramic. The form of the porous forming material is preferably a disk shape. The size of the pores of the filtration device and the amount of solids in the filtrate are not always proportional, depending on the filtration method employed and the material being introduced. This is especially true for the use of ceramic materials as filter elements. The aqueous phase is introduced into the process water reservoir in a filtered or unfiltered manner. The nature of the solid to be separated, and the selection of 51 201118162, the method of separation is based on the processing procedure and the characteristics of the desired reaction product f. The deeper the procedure is, the higher the density of the reaction product, and the easier it is to complete the procedure. Recorded the suspected condition τ. The solids content in the face fluid typically sinks in proportion to the size of the pores and can be significantly increased by over the use of hydrazine and can exceed 2/3 to 4/5. Integrating one or several solid-liquid separation devices into a process for removing sediment or other impurities having a high density or a high weight, which can be separated by centrifugal force separation during the treatment of the biological f The use of the principle is particularly advantageous for the cleaning of process water, which acts as a propellant spray medium to protect the pump, mixer and nozzle. During the procedure, the process water is re-adjusted from the upper half of the reactor, especially from the top of the reactor, preferably by one or more of the 1/4 points above the reactor. deal with. The re-adjusted or treated process water is returned to the water loop of the equipment for recycling. One less and especially several processes ^ The reservoir can be used in several reactors for each-face-reactor. The different cleaning steps are performed in separate process water reservoirs. The capacity of the individual process water reservoir or the shared process water reservoir is approximately 35% to 85% of the total volume of the reaction H. The process water is stored, the temperature of the device and the Lili load are designed to make the pressure drop. The degree and heat exchange device are not available. - Process water cleaning is integrated into the water loop that it is prepared for. The difference = processing or re-machine method depends on the system of re-adjusting the program water. Different t chemical and biological methods and devices are used for this side or in combination.

有氧及厭氧高效能生物反應器(anaerobic high perf__ biQ 生物膜反應1(biG membrane m論s)、厭氧及推動 式泥漿法(anaerobic and animate sluny meth〇ds)。以上 程水循環應該可以相當地降低在猶 f中有機化口物的含置,但必須測量返回的製程水量 二解的有機物質及高鹼金屬的濃度或無機物材料濃; (如鈣)有關。為了能收回盡可能高處部份的製程水,係g 同的方法及裝置特別有效的組合。 用於機械式廢水清潔的農置係為過滤器,較佳是微過滤 52 201118162 器,及尤其是一種超過滤器,且適用於以上所述的固-液分離 方法。其内建立了磁H的固_液分離裝置較佳是—旋轉盤過 遽器及尤其是細顏猶||。對_程水或是廢水的生物清 潔,疋使用-種裝置’其最快滿足清潔或是處理複雜的需求。 例如,最佳的是使用具有鋼材結構之裝置,例如生物薄膜方法 中的高效能生物反應器,較佳是有氧製程水處理,特別是一迴 路式反應器。在此設計中,迴路式反應器其設計具有一有效的 喷嘴以混合固體及液相。取而代之或是附加的,對於有氧法, 用於厭氧製程水處理之反應器或者是逆電滲析(reverse dectrodialysis)也可以使用,特別是為了回收硝酸鹽、蒸餾、 蒸發及/或離子交換法及活性碳。 臭氧暴露(odor exposure)造成對固體的儲存及輸送及設 備、建築物及輸送設備的設計的需求。臭氧暴露的強度會隨著 儲存時間而減少。建築物或是儲存及輸送空間,特別的是用於 燃料者係設計為不透线或是不透臭氧,使得承載的空氣無法 散逸。建築物的通路藉由閘門加以密閉。設置一個或是數個化 學及/或生物空氣清潔設備,使得臭氧暴露對於僱員、供應商 及居民可以降低至最小量。 反應產物的冷卻,特別是在1巴之絕對壓力低於沸點溫 又,通吊疋在反應空間外部進行,也可以在用於液化 jevolatihzation)的裝置中進行。由此釋放的熱能可以經由熱交 換程序用於其他程序。 一個或是數個碎磨步驟可以在反應產物冷卻作用之前、 或在冷卻作用進行的過程中、或是在冷卻作用之後進行。使用 碾碎(mill)或是壓碎②代沾化幻的方式是較佳的。 由^應混合物中分離出固相通常是在第一步驟以機械的 進行在第一步驟係在熱分離裝置(thermal separation device)中進行。 曰使用靜態濃縮器(static thickener)在重力作用下降低含水 罝’有或無機械式旋轉裝置或是清污機(rakingmachine),例如 53 201118162 ©^AmH(stationary thickener)(throughput 裝置(dosing device)控制供應量。此 ^ 料裝置可以均勻的分配濃縮混合物及以相應的高體積 =數個機H缩H可以直接整合至乾縣置。圓錐形結構 Ϊ優雜在於魏鱗置可以直接軌混合物。相對應於 量?調整可喊料部的設備。或者也可將欲濃縮的混合 ,力下導入一孤形篩面(arched sieve surface)或是一曲 二二選,(CUrVed SCreen)。其造成離心力擠壓一部份的液體通 j選器的槽孔遗_混合物縣賴過程最後被送進乾燥 攻^。一水力旋流器提供更有利的分離方式,其中固體和液體 係a由離〜加速加以分離。在潛流(皿derfl〇w)中濃 ,應至乾縣置,而已處理或是已淨化之液體於溢^ (overflow)離開水力旋流[藉由設在前面並已調整之濃縮 器及插入定量給料裝置來確保對乾燥裝置連續及最適的供 ,。對於利肖剪切離心分離機(shearcentrifijge)進行乾燥來說 疋特別的重要。剪切離心分離機具有高的操作安全性及適用於 粒狀固體的除濕及清洗。 除了經常為了能量之故須在乾燥之前連接的機械裝置之 外’較佳是使用熱乾燥法。供應至乾燥程序的量其重量大於一 么斤。。連續式的操作對於填充操作(charge叩erati〇n)而言較 佳。乾燥程序=至少-個或是數個乾燥器進行或是利用不同的 分離及/或乾縣置的組合來進行^例如使用職式乾燥器 (correctiondrier)來乾燥反應產物以及次級產物。藉此欲加 以乾燥的東西與熱乾燥氣體接觸。在此的缺點是,所使用的氣 體需排$出去,且通常需要由粉塵分離器(dust separators)進行 清潔。氣體可能在冷凝之後喊濕度。例如—流體化床乾燥器 可以作為對。流式乾燥器。根據現有的或是所需要_粒大小^ 使用喷^11、喷嘴塔(nozzle tower)或H賦錢器(fl〇w 拖盤汾吵)、滾桶(d_)或是穿隨 式乾燥器(tunneldrier),連續式程序為有利的。 54 201118162 μ當使用接觸式賴11時,基本上只有翻表面可用於熱 總一帶式(belt)、真空帶式(vacuumbelt)、滾桶式(dmm)、 心dscrew)、圓濟式(Cyiin(jer)、滾筒式㈣㈣或帶式乾燥器 ^dt如句子特別的是使用一種真空滾桶過濾器(vacuum drum 1 ter)或乾燥器。為了得到較低的濕度含量,根據其產量,可 選擇性的或是附加的使用盤式乾燥器(disk把沉)。乾燥程序 了以藉由熱亂體介質(h〇t gaseous medium)實施,例如空氣J:滿 度。介於6如,J机之間,較佳為饥到赃之間,^圭: 7〇C到85°C之間。取而代之的是,在上述所有的熱乾燥裝置 中使用過熱水蒸汽(overheated water vapour)及特別較佳的是 溫度在130°C至18(TC之水蒸汽。 一組合的機械-熱力法(mechanicai—thennai meth〇(j)可以用 於分離或是賴。相較讀制方法,麵·熱力法的優點是 ^物具有明顯較低的殘留濕度,藉此產物的可傳輸性或是可輸 送性可以得到提高,尤其是具有細顆粒或是奈米系統之產物。 更進一步的優點在於:藉由冷凝蒸氣(condensating steam)將 反應產物中部份的污染物沖走。其蒸氣的使用作為更進一步驅 動除濕作用而增進以過滤方式運作之離心機的效能。肇因於冷 凝刖端的機械式位移機制與慣性力協同作用,在實際上導致粗 縫的毛細管系統之完全消耗。在這些方法中,蒸例如氣壓力過 濾便是利用此機制。其利用飽和或是過熱蒸氣除去氣體壓差, 而不是使用加壓的空氣。使用蒸氣麗力疊合離心除濕尤佳。在 一方法空間中,根據本案,結合蒸氣壓力及離心除濕作用的程 序將反應產物之較細的分散固體由懸浮液中傳送至乾燥、純化 及自由流動之最終產物(free flowing end produei)。 根據本案之反應產物的殘餘濕度含量較有利的是約6〇/。 至25% ’也可以是10%至20%或也可以是12%至15%。 在轉化反應之後’反應混合物係呈現為懸浮液。其中, 後續的反應產物、中間產物、次級產物及/或最終產物的結構 是與進料原料有關。 ' 55 201118162 燃料的分類是由煤炭類(peat-like)、所有褐煤類(lignite-like) 到煤炭類燃料(coal-likefbel)、腐殖質、梅納德或類梅納德反應 產物、含碳材料如隔熱材料、奈米海綿(nano sponge)、丸狀物 (pellet)、纖維(fiber)、纜線(cable)、活性煤炭(active coal)或是 吸附煤炭(sorption coal)類材料、木炭取代材料(charcoal substitute material)等之含碳材料具有高度壓縮碳產物及材 料’且特別的是對於石墨及含石墨或是類石墨的產物的進料原 料以及碳纖維及複合式進料原料及纖維複合材料(flber composite material)。 根據本案’純的、最純的及超純的煤炭類材料屬於產物。 相較於進料原料,這些材料有利的特性主要是因為礦物性物質 的減少。純煤主要理解為煤炭的可燃燒部份,及最純煤亦理 解為活性煤炭或是木炭。超純煤的礦物含量例如低於0.1的重 量百分比以下。 第1圖係顯示具有反應器2之裝置1。反應器2由具有一 反應空間4之圓筒狀本體3所構成。反應空間4用以容納固_ 巧混合物例如生物質。反應器2包含用於固-液混合物之填充 器5及出口分支6,而中間產物、次級產物或是最終產物可以 由該出口分支6從反應空間4移除。其反應器2更包含用於混 合固-液混合物之裝置。在此實施例中,此混合裝置為所示之 授動裝置7 ’在處理及/或加工巾可__裝置將固-液混合 ^進行混合。反應器2更包含一圓筒狀導管或是插入管8,其 導引或是控制固-液混合物在反應空間4中的流動。及麻器2 另外包含-顿妓減賴儒絲^ 混合裝置。反應器2更配置有一過濾裝置1〇,藉由該裝置, ,體成份保留在反應空間4内。經由過濾裝置1〇及管線u, 其製程水或是工業用水可以由反應空間4中取回並且送入一 中。工^水可以供應至儒真纹或液體喷射混 ° °° ,藉此經由管線1送至在反應空間4中的固—液人 3’或是可以經由細渡器14作為淨水導人另—個貯存^ ^口内。 56 201118162 淨水或是處理過的水可由該另-貯存!!15經由管線16返回反 應器2或是經由管線17提供至廢水。 第2圖係顯示根據第!圖之反應器2的器壁區域的截面。 反應器壁20係為雙層壁的方式形成,在此反應器壁由一外 壁層21及一内壁層22組成。内壁層22在反應空間4的邊緣 ,,一薄膜部件(membranePart)23,其可以是穿孔的金屬片或 是薄膜金屬片,並且是一熱交換板。薄膜部件23可以安裝在 反應器2内或是利用焊接的方式安裝在内壁層22上。外壁層 21及内壁層22彼此之間有一距離使得一空腔24存在於外壁 層21及内壁層22之間。在熱交換設備中,在此空腔%中可 以有熱油以作為熱能的傳遞。將熱油加熱且將熱油導入空腔 内,而對反應器2的内部空間加熱。此係在一封閉迴路中 進行。相較於水,熱油的優點在於熱油有顯著較高的沸點,因 而可達300。(:之溫度。在薄膜部件23與内壁22之間具有另一 25。此空腔25用以容納淨水而例如可以作為調和系統。 若薄膜部件23係為一薄膜金屬片或是一具穿孔熱交換板,在 ^腔25内的壓力需至少稍微高於在反應空間4内的壓力,使 得沒有反應混合物的成份可以到達空腔25。由於在反應空間4 中極端的反應條件’内壁22,主要是薄膜部件23,是由耐蝕 材料所構成或至少塗佈有耐银材料。 第3圖表示一設備之實施例之範例示意圖。 燃料或在裝置中產生的反應產物的燃燒作用,根據燃料 的種類’在例如丸狀式燃燒爐(pellet如⑽⑶)、丸狀式容器 (pellet vessel)或是附加的燃燒裝置中進行,較佳是有自動燃料 供應。 對於能源產生的配置可以例如包含一燃燒設備。在丸狀 式燃燒爐中的燃燒盤(combustion disk)的形式和尺寸調整至灰 分(ash c〇ment)。根據此發明,由於使用此裝置而具有較低的 灰分’較小的燃燒盤的尺寸已經足夠。為了防止在燃燒盤結 塊,根據本案之燃燒設備或是丸狀式燃燒爐配置有一自動裝置 57 201118162 用於由燃燒盤移除灰分。 由粉塵狀燃料(dust-like fUel)中所產生能源的過程中,根 據本案之粉塵燃燒裝置包含一燃煤發電設備(coal power plant) ’或是具有至少一蒸汽渦輪之煤粉燃燒或是超臨界燃煤 發電設備(supercritical coal-fired power plant)。為了得到高效 率’燃燒程序在超過600°C之盡可能高的溫度下進行、或是超 過650°C ’且在另一實施例的範例中其溫度係超過7〇〇。〇。更 進一步的可以利用現代發電設備技術以增加在高溫區域的效 ,’以致對於目前產量可以實現具有盡可能高之效能的氣體蒸 汽渦輪程序’係效能高達超過43%、或是超過46%、或是在 更進一步的實施例中的範例為49%至55%。 .採用整合式煤戾氣化技術之整合式氣化循環技術 (integrated gasificationcombined cycle,IGCC)適用於根據本案 的方法所產生的燃料之燃燒,流體化床燃燒技術亦可,特別的 是t麗流體化床複循環發電技術(PFBC)及尤其是具有燃燒 煤峡複彳盾環能源例如加廢式粉煤燒作用(pressurized pulverized coal combustion ; PPCC)之燃燒發電設備。 ^燃燒程序應具有高於1000。(:之燃料進氣溫度、較佳的是 ,^12GG°C,尤佳是高於14G0°C。在高溫下燃料氣體的清除 係设計為利用燃料氣體的低溫電漿特性,使得顆粒的含量及腐 蝕物質的含量特別是鈉及鉀化合物和腐蝕性燃料氣體降低至 一程度,使得燃料氣體可以立即被送入氣體渦輪。 根據本案,藉由在設備中設置用於燃料氣體内液體熔渣 的为離裝置’可實現顆粒含量小於3mg/m3 i.n、且直徑d小於 3微米、鹼含量v為0.01 mg/m3 i.n.。 由粉塵狀燃料中產生電流或是能源的另種方式為使用碳 燃料電池(carbon fbel cell)。相較於氫燃料電池(hydr〇gen cell) ’ 1燃料電池具有兩個明顯的優點。在其他方面,碳的充 ,狀態是氫分子的兩倍大^炭燃料電池在反應前或是反應後的 乳體體積具有姻的大小,但是氫罐電池在兩種狀況體積就 58 201118162 不同。此意味著前者的熵(entropy)幾乎不會有變化,因此,整 個燃料值可以完全的轉換成電能。藉此碳燃料電池的利用率在 理論上可高於氫燃料電池達60%。要得到所需的碳粒子密度 是「項挑戰。根據本案之設備提供產生粒子大小為用於碳燃料 電池之奈米範圍的煤類燃料的可能性。 與其他產生能源的方法的共同作用可以藉由共同使用能 源產生裝置來建立’特別的是渦輪例如蒸汽渦輪、例如在風塔 内使用的氣體或是風力渦輪。可調度型混合風電系統 (Dispatchable Wind Power System,DWPS)在這些可更新能源 中通用的渦輪及特別是蒸汽或是氣體渦輪是最常使用。壓 縮空氣在充氣室(plenum chamber)中進行減壓。藉由壓縮空氣 導入渦輪使得效率增加至超過20°/。至200°/。或是40%至 170°/。’在實施例的另一範例是增加至ι5〇%。 根據本案在裝置中藉由已產生的燃料的使用而產生的能 源,特別的是以熱能及/或電能的形式,至少一部份可以是下 列其中一種設計: •遠端及近端加熱網絡; •進料原料、水(包含製程水)、反應物、中間產物、次級產 物及/或最終產物,特別的是燃料、含碳材料、腐殖質及/或生 物質的梅納德或類梅納德反應產物的加工及處理程序,其包含 碎磨、乾燥、脫水、調整、移除金屬及雜質的清潔及/或乾燥 ^序,特別的是含金屬物質,例如藉由氣旋式分離裝置' 培^ 器、擾動或混合系統、栗、加熱、水蒸汽的供應、熱交換程序、 壓縮、傳送及輸送程序、製程水、水及廢水調整&處理及空氣 清潔或處理、固液分離程序、冷卻及對於更進一步程序的調整 及能源再生。 •用於金屬、食物的生產、加工及處理的工業操作,金屬方 面尤其是紹、碎鐵,食物方面特別是牛奶加工^酒製造、溫 室或非溫室園藝操作以及肉製品加工。 •用於肥料及肥料工具的加工及生產的操作、輪胎回收設 59 201118162 備(tire recycling plant)的操作。 •化學工業的操作及生產設備,尤其是氣態或液態形式之空 氣成份及其它物質的產品的加工及生產,其他物質包括氧氣、 氮氣及氬氣。 •水清潔及去鹽設備(desalinization plants),特別的是利用逆滲 透;或是 •榨油廠(oil mill)、精煉廠、乙醇生產設備。 對於熱及能源交換及為了共同作用潛在性,根據本發明 所述的設備產生的燃料及/或反應產物的利用可以與不同的電 力設備及能源產生程序一起操作。為此,以下所述特別適用: 燃煤發電設備(coal-fired power plants),其中的整合性氣 化復循環發電技術(integrated gasification eombined eyde, IGCC)還有流體化床燃燒技術、尤其是結合了加壓流體化床燃 燒復循環之程序(circulating pressurized fluidized bed combustion combined cycle, PFBC)及特別是結合能源設備及煤 石反燃燒循%此源例如加壓式粉煤燒(pressurized pUiverized coal combustion (PPCC)。 •燃氣發電設備(gas power plant); •採用不同燃料之燃料電池’其燃料包含甲醇、煤、油及 氣體; ' •生物質發電設備(biomass power plant);或是 •太陽能發電設備(solar power plant)。 第3圖顯示一種用於能源產生的設備,其具有用以處理 生物質之裝置1及及用於能源產生之配置2。裝^ 1包含兩個 反應器3、4,以串聯的方式連接,其各具有一圓筒形本體, 包含一反應空間5並表現為一種壓力容器的形式。反應空間5 作為容納包括生物質的進料原料之用。裝置丨更進一^的包含 以切碎機(ch〇Pper)6及碾磨機_1)7的形式之碎磨裝置。生物 質首先供應至切碎機6以進行較粗的碎磨(如箭頭8所示),及 接著送入碾磨機7以進行更進一步的碎磨。以此方法製備的生 201118162 物質接著在-混合裝置9内集中混合,藉此辅助材料例如催化 劑亦可加入(如箭頭ίο所示)。接著藉由泵送裝置 apparatus)ll經由管線12將生物質供至反應器3、4,並進一 步在例如7巴之壓力以及例如至少16〇ΐ:<高溫下,於反應器 空間5中進行處理。在反應空間5中所需溫度的調整藉由調和 系統13來確認。調和系統13例如可以包含用以加埶冷栌一 裝置,其利用泵14熱交換供應至反應器3、4内或反應; 3、4。生物質饋入連續配置的反應器3、4係藉由閥裝置(v=ve device)15、16 來控制。 在生物質處理之後’反應產物由反應器3、4中取出並提 供至分離裝置20,其將固體反應產物由液體成份中分離出 來。液體成份係供應至一廢水調整設備(waste water conditioningplant)21内,並以與環境相容的方式進行清潔。仍 然潮濕的固體反應產物經由液化裝置22送入乾燥裝置μ,並 將這些固體反應產物乾燥至達到所需要的殘餘濕度含量。經乾 燥的反應產物通常是粉煤或是類似的燃料。燃料暫時儲在力一 燃料儲存器24’該燃料儲存器24設置在裝置'及配置2之間。 用於能量產生之配置2包含一燃燒設備3〇,其用於燃燒 裝置1產生的燃料。燃燒作用的熱能用於燃燒設備30以加熱 ,或是在管件31中產生水蒸汽,以及藉由此方法所產生的^ 蒸汽來驅動渦輪32。渦輪32的旋轉能量可以提供至產生器 (genemt〇r)33並藉此轉換成電能,其例如可以送/電力網絡 (electricity netw〇rk)(如箭頭34所示)。在燃燒設備3〇的燃燒期 間產生的燃料氣體經由煙囪(chiinney)3 6排放至開放空氣中之 前,係以一清潔方法35加以處理,其包括例如一燃料氣體的 脫硫作用(desulphurization)及一燃料氣體N0X移除裝置。 在該方法進行或在化學轉化程序的過程中,有機材料及 無機材料由進料原料中移除,且因此可以供用及易於存取。可 ,取性的改善部份是由於先前難以取得的或是化學性結合材 料的分解而有部份成為液相。其發生的程度與反應或是處理條 61 201118162 件有關。除了有機分解及未分解物質之外,無機物質例如鹼、 金屬、鹽及包含腐殖酸類物質之酸、鈣、鎂、氣、鐵、鋁、磷: 钟、納、氮及其化合物也屬於被移除或是可供用及更容易取' 的物質。 $ 反應產物的固體碳成份在轉化反應之後呈現為材料及/ 燃料且具有下列特徵,其中: 材料及/或燃料的成份可以由反應程序來控制。個別材料 的濃度無法立即選擇性地並與其他材料無關地任意改變。然 而,不同的材料群組及參數可以在相同的方向來改變。例如^ 低硫的含量的過城中,氯及灰分同時降低。 藉由元素分析不同的量測中’對於草(grass)、切割籬笆(cut hedges (thuja))及甜菜(sugar beet)而言,碳分率超過50%至63% 的元素(乾質量)的百分質量分率,且因而高於進料原料的質量 分率約20%至60%。氧分率降低至一半及氮分率約1/4及氫分 率係降低至約1/4。 相較於生物質,材料及/或燃料的碳分率增加1〇%至 300%、也可以是50%至3〇〇%或1〇〇%至3〇〇%,尤其是2〇〇% 至300%。 八 相較於進料原料,燃料及/或材料的碳分率增加5%至 20〇G/°、特別的是10%至150%,尤其較佳的是10至120%, 尤其是由50%至100%。 原料及/或燃料的碳分率通常在40%至95%之間,也可 以是50。/❶至鄕,或是55%至80%。視反應程序及進料原料 而定’碳分率也可以達得高於98°/〇之較高純度。 相較於進料原料,燃料及/或材料的氫分率減少1%至 300%、5%至200%或者也可以是20%至1〇〇%。 相較於進料原料,燃料及/或材料的氧分率係減少1%至 300%、也可以是5%至200%或是15%至1〇〇%。 相較於進料原料,燃料及/或材料的氮分率係減少1%至 300%、也可以是5%至200%、或者也可以是15%至100%。 62 201118162 相較於進料原料,燃料及/或材料的硫分率也可以是生 物質的分率且減少1%至300%、也可以是5%至200%或是 200%至600%或是400%至超過1800%。 相較於進料原料,燃料及/或材料的灰分分率可以是生 物質的分率且減少1%至100%,也可以是101%至1000〇/〇、 或也可以是1000%至超過3000〇/〇。 相較於進料原料’燃料及/或材料的微粒物質也可以是 生物質的分率且減少1%至200%、也可以是201%至 1500%、或也可以是1501%至2000%。 在燃燒過程中,藉由製程水的高分率,可倍數減少無機 物材料及灰份及微粒細塵部份,例如幅度可達3〇〇百分比以 上。上述物質分率以及多種其它物質的稀釋,係藉由製程水 的比例的增加而發生’這些物質原來包含在進料原料中並在 轉化^應過程中被移除並被分解。亦可以說是這些物質被沖 洗乾淨,使得可溶解物質的分率實際上可以根據在固相中的 供應的製程水的比例來降低。 =使不考慮催化劑成份或是次佳的反應條件主導,仍然 可以得到較高的碳分率,其超過進料原料的的碳分率5%至 10^以上。對生物質適當處理及加工程序,可以得55%至 77/。的碳分率。在合適的加工程序中,適合的進料原料包含 催化劑混合物的調整,可以得到及以上的碳量。藉 些數值可以與石化燃料比較。 在轉化反應器結束之後,材料及/或燃料的碳分率已經 確實增加’但是能量含量或是燃料值降低達36%。因為在反 應中釋放熱量,故為放熱反應(饮〇也6〇11311^(^〇11)。在相反 面’至少65%的乾的生物質的原始燃料值與進料原料的質量 重量有關。 β若使用含碳水化合物之生物質例如穀類(grain)、玉米或 是糖類係作為進料原料,材料的燃料值及/或燃料的燃料值 約為65%至85%,在另一實施例的範例中相較於進料原料, 63 201118162 為7()%至8G%°在進料原料中具有愈少的碳水化人 =的含量,在轉化反應過程帽放的能量愈低。相較於二 原料,此同時使反應產物有愈高的燃料值。 寸 述根據所使用的生物質,其反應產物的能量如下列範例所 若木質纖維生物質例如切枝切葉類或是收穫 為進料原料’其材料及域燃料的轉值約7()%至9〇% 起始物質的質量重量有關,也可以是的75%至85%。” 若是具有低碳水化合物、纖維素或是木質素 質例如清錢是污水縣係作為鱗 的燃料值係約m至95%,與起始物質的質 J“科 也可以是85%至90%。 純的、最關或是超義⑽衫财 作為化學基質及祕·財鱗1麵—步泣= 為碳燃料電池中的燃料。 4疋并 偏ίί材f在反應程序中由固相分解變成水相並出現在 j水中。多數的無機物例如磷、硫還有硝酸鹽可以由製程 =回,。這些東西可以作為肥料、在其他程序的原料或是 材料。為了確保自然的循環,無機成份最好可以由液相中分 :出以再返回用於生物質自然發展的表 面。藉由使先則為生產程序從生物質中中萃取出來之生 =包含的營養物返虹表面,航可轉持—接近封閉的循 壞。 由去聚合作収新的聚合⑽戦讀·學碳化合 物及結構。特別岐,由其形成的凝結物可以以相較於大多 已知固體石化燃料為低的能量輸人進行碎磨。更進一步,褐 μ < m狀_㈣ϋ是根據進料原料,也許是由 於梅納德反應產物的形成。 在反之前許多進料原料的密度低於水。在反應程 序的過程中其密度持續增加’視進料補及反絲序而定, 64 201118162 達到可與黑煤相當的密度。當大部份進料原料的密度在2〇〇 kg/m3至600 kg/m3,及密度偶爾會達到8〇〇 kg/m3 (乾重 量)’反應產物的密度可以達到高於9〇〇 kg/m3至12〇〇 kg/m3,偶爾也會到達125〇1^/1113至135〇kg/m3,這是假 設在反應產物的顆粒之間的空氣被移除或是藉由擠出 況。 藉由反應產物的小顆粒尺寸的優點,相較於進料原料造 成*較大的表面積。這會造成在相同的濕度含量下,比含有相 當碳量的自然存在碳化合物較容易乾燥。在同時,大的表面 積貢獻一較低的點燃溫度。 反應產物獨特的特性存在於梅納德或類梅納德反應產 物及液相及固相。強濃的氣味形成隨著進料原料改變。基本 上氣味的形成與梅納德反應產物的形成有關。 與其他天_在且具有相當的碳量之碳化合物相比 較,具有改善的導電性。 •泥煤到黑煤類燃料。 •比相同碳分率之傳統或是石化燃料具有較少的揮發性 成份。 旦·燃燒形成較低的灰分、較低的氮量、硫量、硝酸鹽含 里、重金屬及反應性的物質,亦即相較於具有同樣高碳分率 的石化燃料有較低的自燃溫度。 •相較於具有同樣高碳分率的石化燃料,在燃燒作用中, 燃料氣體的組成有利且有較低的損害。 總之,相較於傳統的燃料而言,上述新的反應產物的特 徵以及其對環境和驗較友善的特性可以制許多優點。相 較於傳統由生物質能源回收來說,對於由生物質之材料及/ 或燃料的工業製造的目而言,其處理方式更有效率且更具有 經濟巧。、在生物質的f量轉化巾,幾乎沒有任何碳量損 失吊在進料原料中有超過95%的碳通過進入反應產物的 固體成份+,其可轉為能源隨。麵的碳化合物變成液 65 201118162 ==:¾:其事 ,料原料中大約1%_4%的碳係變鎌相。其分率與加 齡物的液體 s碳之奈料料及結構藉纟反絲縣形成,特別 f由進料補及催倾的域及麵來形成。材料部份是具 2使用的材料及表晴性。在這些#中例如奈米海綿可以 作為水的貯存器或是隔離材料。 —戶^明的梅納德反應在加熱程序中例如蛋白質、含蛋白及 富有碳水化合物的食物在溫度超過13(rc烘焙、煎(fry)、烘 烤(roast)、燒烤(gnu)及油炸。在所謂的梅納德反應的過程 中,紅到黃棕色、有時候是黑色的聚合物,褐斑(melan〇idines) 來自夕種增味劑還有碳水化合物及氨基酸。特別的是許多黑 色褐班在烘及烤的過程當中於高溫下形成,發生,但是反應 也y以藉由較兩的壓力來加速達成。藉此這些在產物中形成 相§於食物的一部份,例如麵包、咖啡、麥芽、堅果或是玉 米片及例如產生提高至30%的咖啡。 在一第一非酵素反應(non_enzymaticreacti〇n)中,梅納德 反應的進料析出物形成一席夫域(Schiffbase)。此步驟的進行 係在數分鐘内或是長達數個小時且為可逆,因為席夫域是非常 不穩定的化合物。席夫域的量與葡萄糖的濃度直接相關,當葡 萄糖由反應中移除或是濃度較低時,隨著產物在幾分鐘内衰變 (decay)。不穩定的席夫域更進一步轉換成更穩定的阿馬多里 (阿馬多里)產物。此程序顯著較慢,但是其較不可逆,而阿 馬多里產物會累積。初步的阿馬多里產物會自行重新排列及更 進一步地反應成梅納德反應的最終產物反應,為高度糖基化最 終產物(advanced glycation end product,AGE)。高度糠基化最終 產物可以經由重新排列及聚合作用與其它的蛋白質形成交 聯。由於發展路徑之故,有多種不同及複雜的形式之高度糖基 66 201118162 化最終產物,目前已檢測至的形式有Νε-(羧甲基)離氨基酸 (Ns-(carboxymethyl) lysine) (CML)、糖氨酸(fUrosine)及戊糖 素(pentosidine)。 梅納德或類梅納德反應產物在水熱碳化法過程中以高 濃度形成。在固體中(在其它固體之間)及在液相中(例如製程 水)’有相對高濃度指示劑CML,其濃度通常介於0.3-2 mmol/ mol lysine。通常在反應產物液相中,亦即在製程水中 的濃度,呈現出比固相中更高的濃度。濃度或是濃度比係根 據固-液比率及進料原料的組成及加工程序來決定。抗氧化 劑(Antioxidant)及化學預防劑(chemo-preventive )特性係分 派予CML。其假設相較於或是相似特性可以在水熱碳化法 的其他中間產物、次級產物或是反應產物其包括梅納德或是 類梅納德反應產物中找到。 梅納德或類梅納德反應產物係利用過濾、超過濾及/或 層析法(chromatographic method)等進行隔離,特別的是利用 管柱層析法(column chromatography.)。 ,較於具有較高燃料質的反應產物而言,根據本發明之 方法藉由水熱碳化法產生的腐殖質具有相對較短的滯留時 間。其通常仍然包括進料原料的含纖維材料(其中包含木質 素及纖維素)。生物聚合物未完全去聚合化。根據本案所形 成的腐殖質係具有至少30%至45%的碳分率及至少15 MJ/kg至24 MJ/kg的熱值,並易於燃燒。 根據本發明的方法所產生的腐殖質可以部份具有與天 然腐瘦質類似的特性及部份也可以具有與泥煤或泥炭 似的特性: •保護土地以防止雨水的侵蝕,因為水可以均勻且深度 地滲透; 又 •降低風的侵蝕; 67 201118162 •傲食碰_地min worm)及其他有用的土壤有機體; .在夏天降低土地溫度及在冬天增加土地溫度; •對植物供應養份,養分緩慢釋出,使植物可以處理; 量;·使土地可以縣、纟帛i儲存水份且限纖發至一最小 過程藉由加人石灰及有機肥料喻制在土财的化學變化 出無·機釋物放出及有機酸使具有高度含驗性的土地被中和以釋放 合物在可變化及可用的形式下儲存氨(ammonia)及其它氮化 县的不像舰^的有用舰,其係經過很 長的時間自然形成: 熱腐^^增加水結合能力,並鶴超過天 巧予質或疋泥煤。其可以是數倍,通常是G3至Μ U倉8τϊΐΐ多或是更高。產生的腐殖質具有多孔結 ί 的木f素、纖維素及半球狀纖維素及 與間、或是〇.5%至2%之間,其降解速ί ϊ 冰度、含氧量、酸度及環境生物活性及其 調ΐ 3件有關:根據本發明腐殖質的ρΗ值藉由後處理來 至5至6或是6至7。雜腐殖f的後處理可以在程序 ^入驗基如氫氧化納_)戦緩衝劑 儲存之前、當中或是之後藉由清洗ί 據ΡΗ值^°。輪4結合,所添加邮灰4基本上是根 本案的方法的反應產物之上述特徵對燃燒特性來說是 68 201118162 有效的。 藉由最佳化加工程序,在腐殖質中的某些物質可以濃 縮,特別是藉由在反應混合物中固相及液相之間的濃度差。 這在腐殖質被使用作為二氧化碳((^(^庫/碳庫(carb〇n sink) 或是肥料時很理想。不同於此,在將根據本案產生之腐殖質 摻雜至產物的加工中,特定物質的濃縮就是不希望有的。此 外’避免大量的無機物及鹼性物質及其它對產物利用有害的 物質之濃縮。根據本案,產生的腐殖質為一均勻的腐殖^及 燃料’其特性可以被計算’並可經由進料原料的組成及催化 劑與加工程序加以控制。根據本案產生的腐殖質可以在數小 時内產生。因此根據本案之方法比其他已知的腐殖質的製造 方法快,後者通常需要花費數個星期或數個月。 5據本案之方法’其產生的材料及/或燃料包含泥炭 _:)或是煤炭或是近似泥炭或是近似煤炭材料,其 具有下列特性: 、 本案的方法’由生物f巾得到舰炭(祕) 到類黑煤燃料(coal-like fUel)。 •燃料值與加ji程序有關,制的是反麟間。姆料值 隨者反應時間或是在反應器内的滞留時間而增加。 揮發性比成Ϊ相闕碳分率之傳統或是石化燃料具有較少的 能量率為〇.7至〇.95。碳水化合物含量愈低, 90竓至95% :木質素或是細菌的生物質。 •』目=於具有總量的相#之碳分率的石化燃料,此燃料 為更具/舌性及具有較低的自燃溫度。 •如爾、或煤炭等;δ化燃料具有與藉由根據本案之 所產生的燃料確實相似_料值,但其組成及雜“ 69 201118162 料明顯不同。 不同類型及種類的石化燃料具有非常不同的化學組成 及特性,且與礦區及來源的點有關,使得每一個種類的煤具 有獨特和明確的特徵。例如石化Lausitz原料褐煤的燃料值 為8,700 kJ/kg ’水含量約為56%、硫含量約為0.7%、及灰 分約4.5%。根據本案,材料或燃料的水含量、硫含量及灰 分都較低’而燃料值通常明確地高於2〇,〇〇〇 kj/kg。1千瓦 (kilowatt)的石化Lausitz原料褐煤可以產生,與水含量無 關。相對之下,根據本案,從同量的然後可以產生超過& 的電流量。 σ 相較於石化燃料,根據本案之材料及/或燃料中有很強 可以檢驗出的梅納德反應產物濃度。Νε_ (羧曱基)離氨基 酸(NKcarboxymethyl) lysine ) (CML)本身可作為指示劑 1 在反應產物的液相中且在固相中也可以偵測到此種化合 物。量測到0.2至1.5 mmol/mol以上濃度之離氨基酸 (lysine) ’藉此相較於固相,可以在液相中量測到較高的部 份。濃度的分佈與進料原料、反應條件及加工程序有關。° 在採礦之後,與採礦深度有關,石化燃料以塊狀的或是 相對剛度壓縮之結塊形式呈現,必須以高能量進行碎磨。更 進步,須以磨煤機將之乾燥並碾磨至細顆粒褐煤或是粉 煤。相較於此,材料及/或燃料在製程尾端之後呈現粒徑大 亡f於1 mm至30 nm的顆粒,且由於其具有較大的表;而 谷易進行乾燥。藉此,用於調整施用的能量及尤其是燃料的 乾燥相較於固體石化燃料來說是相當低。 .....’ 不只疋相較於煤的石化燃料種類、也與大部份目前可用 ^可回收原料的燃料相比較’本燃料的特性尤其有利。下列 ^數中的至少,,但通常是數個或是全部係更適合於燃 辦粗寺進料原料相比或是其他石化燃料或是生物質 ,,,、枓·減少的灰分、較少的氣、硝酸鹽、硫重金屬及較低的 201118162 粉末、微塵及氣體有毒㈣之散發,紐有麵 燃料的品質及燃燒特性雜進料原料或是進料原 糊,與催嫩合物相,、且與 右勒ίΐΐΐΐ肪以及能源含量的進料原料使得燃料具 可達翻翻於污泥的程序中,熱值 取ί具有燃料值為17-20 MJ/kg之進料原料相比,且有婵 職g _4断概之後’其灰錢少 料值值為17-20腿g之進料原料,具有燃 t g峨料進行雜之後,其硫含量降低達 氣體^於進料原料,具有較低的較細的微粒物質及較低的 燃燒程序步驟、調整相關的燃料品質及 嫩石化燃料 相較純的及近似超純的材料屬於產物。 物質的減ό、站性^二料有利的特徵主要的歸因於無機物 亦理解為‘神V。、相t理解為煤之可燃燒部份,最純的煤 百分比厌。,煤的無機物含量例如低於ο.1的重量 71 201118162 末所法’煤碑由反應產物產生的顆粒及粉 燃燒快速_及優良的 合於的橫截面其深度約為1至2公分且其傾斜角度 」“夾故盖之間’其點燃作用可以藉由空氣在燃燒腔中 Si -較大的蚊的面積致使煤碑有較佳的 •根據本案所提供的礙磨粉末對纖維素或是 成份之最魏合比例係支觸雜及機侧。、 命+ i f5熱值為25 MJ/kg至30 MJ/kg之粉末或燃料顆粒 二 ^7,(dllpped wood)或是木片(w〇〇d chip)的比例為 53 : H % : 42或是較佳為64 : 36。因此切木或是木 片的3水量大約為H)%。其顆粒不會大於2咖,也小於 1.5mm及小可以小於1瓜瓜。 •熱值為22MJ/kg至25 MJ/kg之粉末或是燃料顆粒與 稻草(straw)的比例是在61 : 39、也可以是在恥:料或是在 72 : 28。因此切木或是木片的含水量大約是1〇%。其顆粒藉 此不會大於2mm、也可以小於h5mm或尤其是小於lmn^ .相對於以上所述之比例,含等量的纖維素及木質素之 具有泥炭或是泥煤之粉末被加工成煤磚。 .泥炭或是泥煤也可以等量的纖維素及木質素單獨的加 工變成煤磚。 •根據本案之方法產生的粉末及含纖維素及含木質素其 他材料或,泥炭或是泥煤是集中一起混合或是單獨混合,'例 如在具有篩網為2mm之Conidur排放篩選器之衝擊垂片礙 磨機(impact tab mill)中進行。 •形成壓力咼於100 MPa,也可以高於12〇 Mpa及也 72 201118162 可以高於140 MPa。 •加壓操作(pressing operation)係在溫度接近⑹它及應 不超過90°C下進行。 其尺寸大小為250 X 60 X 50 mm,。 •煤磚的堆密度(bulk density)約為0.95 g/m3.至1.15 g/mJ ° 根據本發明所述之方法由反應產物所產生的丸狀物 (pellets): 、·巧據本案所述之方法所產生的丸狀物,濕式結丸之後 成團乾燥的方法較佳。此方法適用於以相對低的能源施用由 具有不同熱值(heating value)之燃料產生丸狀物。 •良好的燃燒使得標準的自動化燃燒系統可以以丸狀物 達到。 •對於小的燃燒站可以滿足界定排放標準。 .其必要條件是燃料的外觀係為一小型的形式且盡可能 的均勻。 •丸狀物的直徑為3 mm至7mm,較佳是4mm至6mm。 其長度在5公分及45公分之間。丸狀物具有高阻抗或堅硬 度,其在處理的過程只會產生極少量的粉塵,且具有高的防 水性及可以妥善分配。 •連續的將丸狀物送入全自動丸狀物爐器或是容器内及 在受控制之方式進行燃燒。 •藉由盡可能完全的均勻燃燒·可達到高熱效能,與最 少的無機污染物或是燃料氣體排放。 •在熱值高於25MJ/kg以及也可以高於27MJ/kg時, 使用結合材料(bonding material)及燃燒促進劑(combustion accelerator),特別的是壁紙膏(waiipaperpaste)、草皮、稻草 73 201118162 及其它木質纖維素生物質。 或是木 如壁紙f齡質生物f大約達鄕,可以藉由例 h n或是木片或是其他木質纖維質生物質的水含量因 此可以約為12-14%。 ,·藉此顆粒不會大於2聰、也可以小於1.5mm及也可 以小於1mm 〇 上述之比例’具有泥炭的粉末或是燃料顆粒 ”等里的纖維素及木質素含量被加卫成丸狀物。 •根據本案的方法所述之泥炭或腐殖質可以單獨與等量 纖維素及木質素加工成丸狀物。 .粉末及含纖維素及含木質伽加的材料或是泥炭或泥 煤係集中混合在-城是義合,例如在具有2mm之 康尼杜(Conidur)釋放筛選器之耐衝擊垂片碾磨機(impact tab mill)中進行混合。 •加壓的壓力向於1〇〇 MPa,也可以高於12〇 Mpa且 也可以rlj於140 MPa。 •加壓溫度係接近8〇t:且應不超過90〇C。 •對於丸狀物最重要的調整,特別是相較於石化燃料的 丸狀物,是來自改善的燃燒特性及在煤灰的燒結作用(sinter behavior)、灰處理方法(通常是較低的灰分)及燃燒盤的尺寸 的領域内。 74 201118162 能源可以彻根據本案之方法所產生醜 =有利的實施例中產生。根據本騎產生燃料的燃^行 與在不同的裝置内進行的調整作用有關。 以丸狀物_式’鋪通常是社狀物爐具、丸狀物 器或延長_燒111進行,並具有自動轉供應。有商章 應的燃燒設備通常都可以使用。為了增加峨的特性,ϋ =的領域中’根據本案之燃燒設備可以調整至改變之燃燒特 •根據灰分調整燃燒盤的形式和尺寸。灰分愈小,可使 用愈小的燃燒盤直徑以產生較佳的燃燒。 " •建議採用由燃燒盤中移除灰分用之自動裝置以防止燃 燒盤的結塊個。此結塊通料麟的自然發生 丸狀物的大小,特別是褐煤。 ‘”'付 * ·根據本案所述之粉末或是燃料的燃燒係在具有至少一 個蒸汽渦輪之燃煤電廠中進行。為了達到高效率,辦爐 在溫度高於·C,特別是高於65()ΐ及; 進行。 更進一步可以藉由例如現代電廠技術增加在高溫區域 的效能’使得有足夠高效率之結合氣體蒸汽渦輪技術能進可 能實現。電流產生的效率可以高於43%、也可以高於46% 或是高於49%至55%。 ' •具有整合之煤碳氣化的煤炭氣化複合循環發電技術 (IGCC) it用於根據本案之方法所產生的燃料的燃燒,i 流體化床燃燒技術亦可’特別的是具有循環加壓式流體化床 複循^發電技術(PFBC)之複合程序及尤其是具有燃煤^ 合循環電力之聯合電廠,例如加壓粉煤燃燒(PPCC)。 •燃燒程序包含氣體進入溫度大於1〇〇〇〇c,也可以大 於1200°c以及也可以大於1400。〇 75 201118162 .咼溫氣體清潔方法係以此方式設計,使其粒子含量及 ,钱性活性物質的含量,特別是鈉及鉀化合物,以及腐蝕性 氣體降低至一個程度,使得燃料氣體可以立即送進氣體渦輪 (gas turbine) ’較佳是利用燃料氣體的低溫電漿特性。 •顆粒含量小於3 mg/m3 i n、且直徑d小於3微米、驗含量 小於0.01 mg/m3 i.n.之容量百分比,可以藉由用以分離燃料氣 體内的液體熔渣之分離器來實現。 β .根據本案所述之方法,更進一步對於由燃料(特別的 是粉末)產生電流或能源的方法係碳燃料電池之用途。 处、·藉由共用的能源產生裝置,特別的是渦輪較佳的是用 於能源產生的蒸汽渦輪或是氣體渦輪可以藉由其 及/或其缝驗生紐而產生朗_。 _胃 .•在這些可再生能源中之可調度型混合風電系統 (Disputable Wind Power System,DWPS),其中渦輪共用, 特別是蒸汽渦輪或是氣咖輪,為有㈣。壓縮空氣在調麗 室(plenumchamber)中進行減壓。而後將壓縮空氣額外地 已在操作中的渦輪内。 •若壓縮空氣導入正在運轉的渦輪中,其效率增加 20%至200〇/〇或是4〇%至170%,及也可以是6〇%至15〇%。 .經由壓縮空氣導入已經在操作的渦輪而增加效率,效 lUT超過2〇%至2〇〇%或是4〇%至17〇%,及也可以是6〇%至 ,據,此份書中的裝置所述之實施例,不同的程序 以個單元中結合。碎磨及混合可_如在單一礙 進行或疋在一空處擾流礙磨機恤加此此⑽中 在此說明書情有的裝置或是設傷係配置 程序猶脑具有錄度,Μ具有鱗上的 f 76 201118162 方法或是程序步驟而言 的可能性。對以上所述所有的步驟、 同樣可行的。 量進㈣轉錢反應器批Aerobic and anaerobic high-performance bioreactors (anaerobic high perf__ biQ biofilm reaction 1 (biG membrane m s), anaerobic and animate sluny meth〇ds. The above water cycle should be comparable To reduce the content of organic matter in the jujube, but it is necessary to measure the amount of organic matter and the alkalinity of the organic matter and the concentration of the inorganic material in the returned process water; (such as calcium). In order to recover as high as possible Part of the process water is a particularly effective combination of the same method and device. The agricultural system used for mechanical waste water cleaning is a filter, preferably a microfiltration 52 201118162, and especially an ultra filter, and is applicable. In the above-mentioned solid-liquid separation method, the solid-liquid separation device in which the magnetic H is established is preferably a rotating disk filter and, in particular, a fine water or a wastewater. Clean, 疋 use - a device that 's quick to meet the needs of cleaning or handling complex. For example, it is best to use a device with a steel structure, such as a high-performance bioreactor in a biofilm process, preferably Oxygen process water treatment, especially one-circuit reactor. In this design, the loop reactor is designed with an effective nozzle to mix the solid and liquid phases. Instead, or for the aerobic method, for the anoxic method. Oxygen process water treatment reactors or reverse dectrodialysis can also be used, especially for the recovery of nitrates, distillation, evaporation and/or ion exchange processes and activated carbon. Odor exposure causes solids The need for storage and transportation and the design of equipment, buildings and conveyors. The intensity of ozone exposure will decrease with storage time. Buildings or storage and transportation spaces, especially for fuels, are designed to be impervious. Or impervious to ozone, so that the air carried can not be dissipated. The passage of the building is sealed by the gate. One or several chemical and / or biological air cleaning equipment is provided, so that ozone exposure can be reduced for employees, suppliers and residents. To a minimum amount. The cooling of the reaction product, especially at an absolute pressure of 1 bar below the boiling point temperature, Externally, it can also be carried out in a device for liquefaction jevolatihzation). The heat energy thus released can be used for other procedures via the heat exchange program. One or several grinding steps can be carried out before the cooling of the reaction product, during the cooling process, or after the cooling. It is preferred to use a mill or crush 2 generation. The separation of the solid phase from the mixture is usually carried out mechanically in the first step in a first step in a thermal separation device.曰 Use a static thickener to reduce the water 重力 'with or without a mechanical rotating device or a raking machine, for example 53 201118162 ©^AmH(stationary thickener)(through device (dosing device) Control the supply. This material device can evenly distribute the concentrated mixture and can be directly integrated into the dry county with the corresponding high volume = several machines H. The conical structure is superior to the Wei scale and can be a direct rail mixture. Corresponding to the quantity? Adjust the equipment of the shouting part. Or you can also introduce the mixing to be concentrated into an isolated sieve surface or a curved selection (CUrVed SCreen). Centrifugal force squeezes a part of the liquid through the slot of the j-selector. The mixture process is finally sent to the dry attack. A hydrocyclone provides a more favorable separation method, in which the solid and liquid systems are separated by ~ Accelerate to separate. In the submerged flow (dump 〇fl〇w), it should be concentrated to the county, and the treated or purified liquid leaves the hydrocyclone in the overflow [by the front and adjusted concentration And The dosing device is inserted to ensure continuous and optimum supply to the drying device. It is particularly important for the drying of the shearing centrifuge. The shearing centrifuge has high operational safety and is suitable for use. Dehumidification and cleaning of granular solids. In addition to the mechanical means that must be connected before drying for energy reasons, it is preferred to use a thermal drying method. The amount supplied to the drying process is greater than one kilogram. Continuous The operation is preferably for a filling operation (charge 叩 〇 〇 。 。 。 。 = = = = = = = = = = = = = = = = = = = = 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 A correction drier is used to dry the reaction product as well as the secondary product, whereby the material to be dried is contacted with the hot dry gas. The disadvantage here is that the gas used is to be discharged, and usually requires a dust separator ( Dust separators). The gas may scream humidity after condensation. For example, a fluidized bed dryer can be used as a pair of flow dryers. Or what you need _ grain size ^ use spray ^11, nozzle tower or H money machine (fl〇w drag disk noisy), drum (d_) or wear drier (tunneldrier) The continuous procedure is advantageous. 54 201118162 μ When using the contact type, basically only the turning surface can be used for the heat total belt, vacuum belt, drum (dmm), heart dscrew ), Cyiin (jer), drum type (four) (four) or belt dryer ^dt, in particular, the use of a vacuum drum filter (vacuum drum 1 ter) or dryer. In order to obtain a lower moisture content, depending on the yield, a disc dryer (disk sink) may be used selectively or additionally. The drying procedure is carried out by means of a h〇t gaseous medium, such as air J: fullness. Between 6 and J machines, preferably between hungry and sturdy, ^gui: between 7〇C and 85°C. Instead, overheated water vapour is used in all of the above thermal drying devices and particularly preferably at a temperature of 130 ° C to 18 (TC steam). A combined mechanical-thermal method (mechanicai - Thennai meth〇(j) can be used for separation or reliance. Compared with the reading method, the surface-heat method has the advantage of having a significantly lower residual humidity, whereby the product can be transported or transportable. It is improved, especially with fine particles or a product of the nano system. A further advantage is that some of the contaminants in the reaction product are washed away by condensing steam. The use of steam is further driven. The dehumidification enhances the efficiency of the centrifuge operating in the filtration mode. The mechanical displacement mechanism of the condensing tip cooperates with the inertial force to cause complete consumption of the capillary system which actually causes the coarse slit. In these methods, for example, steaming Gas pressure filtration uses this mechanism. It uses saturated or superheated steam to remove the gas pressure difference instead of using pressurized air. In particular, in a method space, according to the present case, in combination with the process of vapor pressure and centrifugal dehumidification, the finely dispersed solids of the reaction product are transferred from the suspension to the final product of drying, purification and free flow (free Flowing end produei) The residual moisture content of the reaction product according to the present invention is advantageously about 6 〇 /. to 25% 'may also be 10% to 20% or may be 12% to 15%. After the conversion reaction' The reaction mixture is presented as a suspension, wherein the structure of the subsequent reaction product, intermediate product, secondary product and/or final product is related to the feed material. ' 55 201118162 The classification of fuel is made by coal (peat-like) , all lignite-like to coal-like fuel (coal-likefbel), humus, Maynard or Maynard-like reaction products, carbonaceous materials such as thermal insulation materials, nano sponges, pellets a carbonaceous material such as a pellet, a fiber, a cable, an active coal, or a sorption coal-based material or a charcoal substitute material. Highly compressed carbon products and materials' and in particular feedstock materials for graphite and graphite or graphite-like products, as well as carbon fiber and composite feedstocks and flber composite materials. According to the present case, 'pure, The purest and ultrapure coal-based materials are products. The advantageous properties of these materials are mainly due to the reduction of mineral matter compared to the feedstock. Pure coal is mainly understood as the combustible part of coal, and the purest coal is also understood to be active coal or charcoal. The mineral content of the ultrapure coal is, for example, less than a weight percentage of 0.1. Figure 1 shows a device 1 with a reactor 2. The reactor 2 is composed of a cylindrical body 3 having a reaction space 4. The reaction space 4 is used to contain a solid mixture such as biomass. Reactor 2 contains a filler 5 and an outlet branch 6 for the solid-liquid mixture, from which the intermediate product, secondary product or final product can be removed from the reaction space 4. Its reactor 2 further comprises means for mixing the solid-liquid mixture. In this embodiment, the mixing device is shown in the illustrated transfer device 7' where the treatment and/or processing of the towel can be mixed by solid-liquid mixing. The reactor 2 further comprises a cylindrical conduit or insertion tube 8 which directs or controls the flow of the solid-liquid mixture in the reaction space 4. And the numerator 2 also contains a - 妓 妓 赖 儒 ^ ^ ^ mixing device. The reactor 2 is further provided with a filter device 1 by which the body composition remains in the reaction space 4. The process water or industrial water can be retrieved from the reaction space 4 and sent to one via the filtration unit 1 and the line u. The water can be supplied to the Confucian or liquid jet mixing °°, thereby being sent to the solid-liquid person 3' in the reaction space 4 via the line 1 or can be used as a clean water guide through the finer 14 - a storage ^ ^ mouth. 56 201118162 Purified or treated water can be stored separately! ! 15 is returned to reactor 2 via line 16 or to wastewater via line 17. Figure 2 shows the basis according to the first! A cross section of the wall region of the reactor 2 of the drawing. The reactor wall 20 is formed as a double wall, and the reactor wall is composed of an outer wall layer 21 and an inner wall layer 22. The inner wall layer 22 is at the edge of the reaction space 4, and a membrane part 23, which may be a perforated metal piece or a thin film metal piece, and is a heat exchange plate. The film member 23 may be mounted in the reactor 2 or may be attached to the inner wall layer 22 by soldering. The outer wall layer 21 and the inner wall layer 22 have a distance from each other such that a cavity 24 exists between the outer wall layer 21 and the inner wall layer 22. In the heat exchange apparatus, hot oil may be present in this cavity % as heat energy transfer. The hot oil is heated and the hot oil is introduced into the cavity to heat the internal space of the reactor 2. This is done in a closed loop. The advantage of hot oil over water is that the hot oil has a significantly higher boiling point and can therefore reach 300. (The temperature: there is another 25 between the film member 23 and the inner wall 22. This cavity 25 is for accommodating clean water and can be used, for example, as a blending system. If the film member 23 is a film metal sheet or a perforation The heat exchange plate, the pressure in the chamber 25 needs to be at least slightly higher than the pressure in the reaction space 4, so that no components of the reaction mixture can reach the cavity 25. Due to the extreme reaction conditions in the reaction space 4, the inner wall 22, Mainly the film member 23, which is composed of a corrosion resistant material or at least coated with a silver resistant material. Fig. 3 is a schematic view showing an example of an embodiment of a device. The combustion of a fuel or a reaction product produced in the device, according to the fuel The type 'is carried out, for example, in a pellet burner (pellet such as (10) (3)), a pellet vessel or an additional combustion device, preferably with an automatic fuel supply. The configuration for energy generation may, for example, comprise a combustion The form and size of a combustion disk in a pellet burner is adjusted to ash c。ment. According to the invention, due to the use of the device The lower ash 'small burner disk size is sufficient. To prevent agglomeration in the combustion disk, the combustion apparatus or the pellet burner according to the present invention is provided with an automatic device 57 201118162 for removing ash from the combustion disk. In the process of generating energy in a dust-like fuel (dust-like fUel), the dust burning device according to the present invention comprises a coal-fired power plant or a pulverized coal combustion with at least one steam turbine or supercritical Supercritical coal-fired power plant. In order to achieve high efficiency 'the combustion procedure is carried out at temperatures as high as possible above 600 ° C, or exceeds 650 ° C ' and in an example of another embodiment Its temperature system is more than 7 〇〇. 〇. Further use of modern power generation equipment technology to increase the efficiency in high temperature areas, so that the current production can achieve the highest possible efficiency of the gas steam turbine program 'system performance up to 43%, or more than 46%, or in the further examples, the example is 49% to 55%. Using integrated coal enthalpy gasification technology The integrated gasification combined cycle (IGCC) is suitable for the combustion of fuel produced according to the method of the present invention, and the fluidized bed combustion technology can also be used, in particular, the fluidized bed double cycle power generation technology (PFBC) and especially It is a combustion power generation equipment with a combustion coal gorge recirculating shield ring energy such as pressurized pulverized coal combustion (PPCC). ^ The combustion procedure should have a higher than 1000. (: The fuel intake temperature, preferably, is 12 GG ° C, and particularly preferably higher than 14 G0 ° C. The fuel gas removal system at high temperatures is designed to utilize the low temperature plasma characteristics of the fuel gas to make the particles The content of the content and the corrosive substance, in particular the sodium and potassium compounds and the corrosive fuel gas, are reduced to such an extent that the fuel gas can be immediately sent to the gas turbine. According to the present case, the liquid slag for the fuel gas is provided in the apparatus. The separation device can achieve a particle content of less than 3 mg/m3 in, a diameter d of less than 3 μm, and an alkali content of 0.01 mg/m3 in. Another way to generate electricity or energy from a dusty fuel is to use carbon fuel. Carbon fbel cell. Compared with hydrogen fuel cell, the fuel cell has two distinct advantages. In other respects, the carbon is charged twice as large as the hydrogen molecule. The volume of the milk before or after the reaction has the size of the marriage, but the hydrogen tank battery is different in the two condition volumes 58 201118162. This means that the entropy of the former is hardly changed, therefore, The fuel value can be completely converted into electrical energy. The utilization rate of the carbon fuel cell can theoretically be higher than that of the hydrogen fuel cell by 60%. To obtain the required carbon particle density is a "challenge. According to the equipment provided in this case. The particle size is the possibility of a coal-based fuel for the nano range of carbon fuel cells. The synergy with other energy-generating methods can be established by using a common energy generating device, in particular a turbine such as a steam turbine, for example Gas used in wind towers or wind turbines. Dispatchable Wind Power System (DWPS) is the most commonly used turbine and especially steam or gas turbine in these renewable energy sources. The depressurization is carried out in a plenum chamber. The efficiency is increased by more than 20°/. to 200°/. or 40% to 170°/ by the introduction of compressed air into the turbine. Another example in the embodiment is an increase. To ι5〇%. According to the present invention, the energy generated by the use of the generated fuel in the device, in particular in the form of heat and/or electric energy, at least Some may be one of the following designs: • distal and proximal heating networks; • feedstock, water (including process water), reactants, intermediates, secondary products, and/or final products, particularly fuel, Processing and processing procedures for Maynard or Maynard-like reaction products containing carbonaceous materials, humus and/or biomass, including grinding, drying, dewatering, conditioning, removal of metals and impurities, and/or drying^ In particular, metal-containing substances, such as by cyclone separation devices, perturbations or mixing systems, pumping, heating, steam supply, heat exchange procedures, compression, transfer and transfer procedures, process water, water And wastewater conditioning & treatment and air cleaning or treatment, solid-liquid separation procedures, cooling and adjustment for further procedures and energy regeneration. • Industrial operations for the production, processing and processing of metals and foods, especially for metal, especially for crushed iron, food, especially for milk processing, wine processing, greenhouse or non-greenhouse gardening, and meat processing. • Operation and production operations for fertilizers and fertilizer tools, tire recycling 59 201118162 Tire recycling plant operation. • The operation and production equipment of the chemical industry, especially the processing and production of air and other substances in gaseous or liquid form. Other substances include oxygen, nitrogen and argon. • Water cleaning and desalinization plants, especially using reverse osmosis; or • oil mill, refinery, ethanol production equipment. For heat and energy exchange and for synergistic potential, the utilization of fuel and/or reaction products produced by the apparatus according to the present invention can be operated with different power equipment and energy generation programs. To this end, the following applies in particular: coal-fired power plants, in which integrated gasification eombined eyde (IGCC) and fluidized bed combustion technology, especially Circulating pressurized fluidized bed combustion combined cycle (PFBC) and in particular combined energy equipment and coal-fired anti-combustion cycle, such as pressurized pUiverized coal combustion (pressurized pUiverized coal combustion (pressurized pUiverized coal combustion) PPCC) • Gas power plant; • Fuel cell with different fuels whose fuel contains methanol, coal, oil and gas; ' • Biomass power plant; or • Solar power A solar power plant. Figure 3 shows a device for energy production with a device 1 for processing biomass and a configuration for energy generation 2. The device 1 comprises two reactors 3, 4 Connected in series, each having a cylindrical body containing a reaction space 5 and acting in the form of a pressure vessel. The space 5 serves as a feed material for containing biomass. The apparatus further includes a grinding device in the form of a chopper (Pong) 6 and a mill 1) 7. The biomass is first supplied to the shredder 6 for coarser grinding (as indicated by arrow 8) and then to the mill 7 for further grinding. The raw material 201118162 prepared in this way is then concentratedly mixed in the mixing device 9, whereby an auxiliary material such as a catalyst can also be added (as indicated by the arrow ίο). The biomass is then supplied to the reactors 3, 4 via line 12 by means of a pumping device apparatus 11 and further at a pressure of, for example, 7 bar and for example at least 16 Torr: <Processing in reactor space 5 at elevated temperatures. The adjustment of the required temperature in the reaction space 5 is confirmed by the blending system 13. The blending system 13 may, for example, comprise means for applying a cold head, which is supplied to the reactors 3, 4 or reacted by heat exchange with a pump 14; The biomass feed into the continuously arranged reactors 3, 4 is controlled by valve means (v = ve device) 15, 16. After the biomass treatment, the reaction product is taken out from the reactors 3, 4 and supplied to a separation device 20, which separates the solid reaction product from the liquid component. The liquid components are supplied to a waste water conditioning plant 21 and cleaned in an environmentally compatible manner. The still moist solid reaction product is sent to the drying unit μ via the liquefaction unit 22, and these solid reaction products are dried to the desired residual moisture content. The dried reaction product is typically pulverized coal or a similar fuel. The fuel is temporarily stored in the force-fuel reservoir 24' which is disposed between the device 'and the configuration 2. The configuration 2 for energy generation comprises a combustion device 3〇 for burning the fuel produced by the device 1. The heat of combustion is used to burn the apparatus 30 for heating, or to generate water vapor in the tube member 31, and to drive the turbine 32 by the steam generated by the method. The rotational energy of the turbine 32 can be provided to a generator 33 and thereby converted to electrical energy, which can for example be sent to an electricity network (as indicated by arrow 34). The fuel gas generated during the combustion of the combustion apparatus 3 is discharged to the open air via chitoney 36, and is treated by a cleaning method 35, which includes, for example, a desulfurization of a fuel gas and a Fuel gas NOX removal device. The organic material and the inorganic material are removed from the feedstock during the process or during the chemical conversion process and are therefore available for use and easy to access. The improvement in availability is partly due to the previously difficult to obtain or partial decomposition of the chemically bonded material. The extent of its occurrence is related to the reaction or treatment strip 61 201118162. In addition to organic decomposition and undecomposed substances, inorganic substances such as alkalis, metals, salts, and acids, calcium, magnesium, gas, iron, aluminum, and phosphorus containing humic acids: bells, nanoparticles, nitrogen, and their compounds also belong to Remove or use materials that are easier to take. The solid carbon component of the reaction product appears as a material and/or fuel after the conversion reaction and has the following characteristics, wherein: the composition of the material and/or fuel can be controlled by a reaction procedure. The concentration of individual materials cannot be arbitrarily changed immediately and independently of other materials. However, different material groups and parameters can be changed in the same direction. For example, in the low-sulfur content of the city, chlorine and ash are simultaneously reduced. By elemental analysis of different measurements of 'grass, cut hedges (thuja) and sugar beets, elements with a carbon content of more than 50% to 63% (dry mass) The percent mass fraction, and thus the mass fraction of the feedstock, is from about 20% to about 60%. The oxygen fraction was reduced to half and the nitrogen fraction was about 1/4 and the hydrogen fraction was reduced to about 1/4. Compared to biomass, the carbon content of materials and/or fuels increases by 1% to 300%, and may also be 50% to 3% or 1% to 3%, especially 2%. Up to 300%. The carbon fraction of the fuel and/or material is increased by 5% to 20 〇G/°, particularly 10% to 150%, particularly preferably 10 to 120%, especially 50%, compared to the feed material. % to 100%. The carbon content of the feedstock and/or fuel is usually between 40% and 95%, and may also be 50. /❶ to 鄕, or 55% to 80%. Depending on the reaction procedure and the feedstock, the carbon fraction can also be higher than 98°/〇. The hydrogen fraction of the fuel and/or material is reduced by 1% to 300%, 5% to 200% or may also be 20% to 1% compared to the feedstock. The oxygen fraction of the fuel and/or material is reduced by 1% to 300%, and may also be 5% to 200% or 15% to 1% compared to the feed material. The nitrogen content of the fuel and/or material is reduced by 1% to 300%, may be 5% to 200%, or may be 15% to 100%, as compared to the feed material. 62 201118162 The sulfur content of the fuel and / or material may also be the fraction of biomass and may be reduced by 1% to 300%, may also be 5% to 200% or 200% to 600% or compared to the feed material. It is 400% to over 1800%. The ash content of the fuel and/or material may be a fraction of biomass and may be reduced by 1% to 100%, or may be 101% to 1000 Å/〇, or may also be 1000% to over, compared to the feed material. 3000 〇 / 〇. The particulate matter relative to the feed material 'fuel and/or material may also be a fraction of biomass and may be reduced by 1% to 200%, may also be 201% to 1500%, or may be 1501% to 2000%. In the combustion process, the high content of the process water can be used to reduce the inorganic materials and the ash and fine dust fractions, for example, up to 3%. The above fractions of matter and the dilution of various other substances occur by an increase in the proportion of process water. These materials were originally contained in the feedstock and were removed and decomposed during the conversion process. It can also be said that these substances are washed away so that the fraction of soluble substances can actually be reduced according to the proportion of process water supplied in the solid phase. = Even if the catalyst composition is not considered or the suboptimal reaction conditions are dominant, a higher carbon fraction can still be obtained, which exceeds the carbon content of the feedstock by 5% to 10^. Proper handling and processing of biomass can range from 55% to 77%. Carbon fraction. In a suitable processing procedure, a suitable feedstock comprises an adjustment of the catalyst mixture to obtain and above the amount of carbon. These values can be compared to fossil fuels. After the end of the conversion reactor, the carbon fraction of the material and/or fuel has indeed increased 'but the energy content or fuel value has decreased by 36%. Because of the release of heat in the reaction, it is an exothermic reaction (drinking is also 6〇11311^(^〇11). On the opposite side, at least 65% of the raw biomass of the dry biomass is related to the mass of the feedstock. β If a carbohydrate-containing biomass such as grain, corn or sugar is used as the feed material, the fuel value of the material and/or the fuel value of the fuel is about 65% to 85%, in another embodiment In the example, compared to the feedstock, 63 201118162 is 7 ()% to 8G% °. The less carbon hydration in the feedstock, the lower the energy of the cap during the conversion reaction. The second raw material, at the same time, the higher the fuel value of the reaction product. Depending on the biomass used, the energy of the reaction product is as follows: if the lignocellulosic biomass such as cut and leaf is harvested or harvested as feed The conversion of the raw material 'the material and the domain fuel is about 7 ()% to 9 %. The mass of the starting material is related to the weight of the starting material, which can also be 75% to 85%." If it has low carbohydrate, cellulose or wood quality For example, clear money is the fuel value of the sewage county as a scale. 95%, with the quality of the starting substance J "can also be 85% to 90%. Pure, most critical or super-sense (10) shirt as a chemical substrate and secrets, 1 scale - step weep = carbon fuel The fuel in the battery. 4疋 and biased material f in the reaction process from the solid phase decomposition into the water phase and appear in j water. Most inorganic substances such as phosphorus, sulfur and nitrate can be processed by the process = back. As a fertilizer, a raw material or a material in other processes. In order to ensure natural circulation, the inorganic component may preferably be separated from the liquid phase to return to the surface for the natural development of the biomass. The raw material extracted from the biomass = the nutrients contained in the surface of the rainbow, the aeronautical can be transferred - close to the closed cycle. The polymerization by depolymerization (10) reading and learning carbon compounds and structures. The condensate formed therefrom can be ground by a lower energy input than most known solid fossil fuels. Further, brown μ < m-form_(tetra)ϋ is based on the feedstock, perhaps due to the formation of the Maynard reaction product. Many of the feed materials have a lower density than water before the reverse. The density continues to increase during the course of the reaction. Depending on the feed replenishment and the reverse order, 64 201118162 achieves a density comparable to that of black coal. When the density of most of the feed materials is between 2〇〇kg/m3 and 600kg/m3, and the density occasionally reaches 8〇〇kg/m3 (dry weight), the density of the reaction product can reach more than 9〇〇kg. /m3 to 12 〇〇kg/m3, and occasionally also reach 125〇1^/1113 to 135〇kg/m3, which is assumed to be that air between the particles of the reaction product is removed or by extrusion. By virtue of the small particle size of the reaction product, a larger surface area is created compared to the feed material. This results in easier drying at the same moisture content than naturally occurring carbon compounds containing a comparable amount of carbon. At the same time, the large surface area contributes a lower ignition temperature. The unique properties of the reaction product are found in Maynard or Maynard-like reaction products and in liquid and solid phases. Strong odor formation changes with the feedstock. Basically, the formation of odor is related to the formation of the Maynard reaction product. It has improved conductivity compared to other carbon compounds which have a comparable amount of carbon. • Peat to black coal fuel. • Less volatile than conventional or fossil fuels of the same carbon fraction. Dan. Combustion produces lower ash, lower nitrogen, sulfur, nitrate, heavy metals and reactive substances, ie lower auto-ignition temperature than fossil fuels with the same high carbon fraction. . • The composition of the fuel gas is favorable and has less damage in combustion than in fossil fuels with the same high carbon fraction. In summary, the characteristics of the new reaction products described above, as well as their environmentally friendly and friendly properties, can provide a number of advantages over conventional fuels. Compared to traditional biomass energy recovery, it is more efficient and economical to process for biomass-based materials and/or fuels. In the biomass conversion paper, there is almost no carbon loss. More than 95% of the carbon in the feed material passes through the solid component + which enters the reaction product, which can be converted into energy. The surface of the carbon compound becomes liquid 65 201118162 ==:3⁄4: The matter is about 1%_4% of the carbon-based ruthenium phase in the raw material. The fraction and the liquid s carbon of the ageing material are formed by the anti-filament county, and the f is formed by the domain and surface of the feed and the recharge. The material part is the material used for 2 and the surface clarity. In these #, for example, a nano sponge can be used as a reservoir for water or as a barrier material. - The Meiner reaction of the households in the heating process such as protein, protein-containing and carbohydrate-rich foods at temperatures above 13 (rc baking, fry, roast, grilled (gnu) and fried During the so-called Maynard reaction, red to yellow-brown, sometimes black, brown spots (melan〇idines) come from scented flavor enhancers as well as carbohydrates and amino acids. Especially many black The browning is formed at high temperatures during the baking and roasting process, but the reaction is also accelerated by more than two pressures, whereby these form part of the product in the product, such as bread, Coffee, malt, nuts or corn flakes and, for example, coffee that is increased to 30%. In a first non-enzymatic reaction (non_enzymaticreacti〇n), the feed precipitate of the Maynard reaction forms a Schiffbase This step is performed in a few minutes or as long as several hours and is reversible because the Schiff field is a very unstable compound. The amount of the Schiff field is directly related to the concentration of glucose, when glucose is shifted from the reaction. Divide or At lower concentrations, as the product decays within a few minutes, the unstable Schiff field is further converted to a more stable product of the Amadori (Amadori). This procedure is significantly slower, but It is more irreversible, and the Amadori product will accumulate. The initial Amadori product will rearrange itself and further react to the final product reaction of the Maynard reaction, which is the highly glycated end product (advanced glycation end) Product, AGE). Highly thiolated final products can be crosslinked with other proteins via rearrangement and polymerization. Due to the developmental pathway, there are many different and complex forms of highly glycosylation. The detected forms are Νε-(carboxymethyl) lysine (CML), glycosine (fUrosine) and pentosidine. Maynard or Maynard-like reaction The product is formed at a high concentration during the hydrothermal carbonization process. There is a relatively high concentration of indicator CML in the solid (between other solids) and in the liquid phase (eg process water), usually at a concentration of 0.3-2. Mmmol/ mol lysine. Generally, the concentration in the liquid phase of the reaction product, that is, in the process water, is higher than that in the solid phase. The concentration or concentration ratio is based on the solid-liquid ratio and the composition of the feedstock. Determined by the processing program. Antioxidant and chemo-preventive properties are assigned to CML, which assumes that other intermediates, secondary products, or other products in the hydrothermal carbonization process can be compared to similar or similar properties. The reaction product is found in the Maynard or Maynard-like reaction product. The Maynard or Maynard-like reaction product is isolated by filtration, ultrafiltration and/or chromatographic methods, in particular by column chromatography. The humus produced by the hydrothermal carbonization process according to the method of the present invention has a relatively short residence time compared to a reaction product having a higher fuel quality. It typically still includes the fibrous material of the feedstock (which contains lignin and cellulose). The biopolymer is not completely depolymerized. The humic system formed according to the present invention has a carbon fraction of at least 30% to 45% and a calorific value of at least 15 MJ/kg to 24 MJ/kg and is easily burned. The humus produced by the method according to the invention may have some properties similar to those of natural rot, and some may also have characteristics similar to peat or peat: • protect the land from rainwater, since the water may be uniform and Deep penetration; • Reduce wind erosion; 67 201118162 • Amazing food worms and other useful soil organisms; Lowering land temperature in summer and increasing land temperature in winter; • Supplying nutrients to plants, nutrients Slow release, so that plants can be treated; Quantity; · Make the land can be stored in the county, 纟帛i water and limit the fiber to a minimum process by adding lime and organic fertilizer to make a chemical change in the soil Machine release and organic acid make the highly testable land neutralized to release the compound in a variable and usable form to store ammonia (Ammonia) and other useful ships of the nitriding county. It takes a long time to form naturally: hot rot ^ ^ increase water binding capacity, and cranes over Tian Qiao pre-quality or peat. It can be several times, usually G3 to Μ U bin 8 ϊΐΐ or more. The resulting humus has a porous layer of woody cellulose, cellulose and hemispherical cellulose and between, or between 5% and 2%, its degradation rate, ice, oxygen, acidity and environment Biological activity and its regulation 3 related: The ρ Η value of the humus according to the present invention is post-treated to 5 to 6 or 6 to 7. The post-treatment of the humic acid f can be carried out by washing the ΡΗ value ^ ° before, during or after the storage of the reagents such as sodium hydroxide. The combination of the wheel 4 and the added ash 4 is basically the reaction product of the method of the present invention. The above characteristics are effective for the combustion characteristics of 68 201118162. By optimizing the processing procedure, certain materials in the humus can be concentrated, particularly by the difference in concentration between the solid and liquid phases in the reaction mixture. This is ideal when humus is used as carbon dioxide ((^( 库 / sink sink sink sink 或是 或是 或是 或是 或是 或是 或是 或是 或是 或是 或是 或是 或是 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 Concentration is undesired. In addition, 'avoid a large amount of inorganic and alkaline substances and other substances that are harmful to the use of the product. According to the case, the humus produced is a uniform humification and fuel' characteristics can be calculated 'Can be controlled by the composition of the feedstock and the catalyst and processing procedures. The humus produced according to this case can be produced in a few hours. Therefore, the method according to the present method is faster than other known methods of manufacturing humus, which usually requires a number of Weeks or months. 5 According to the method of the present case, the materials and/or fuels produced include peat _: or coal or similar peat or similar coal materials, which have the following characteristics: The biological f towel gets the charcoal (secret) to the coal-like fUel. • The fuel value is related to the ji procedure. The reaction time increases with the residence time in the reactor. The volatility is lower than that of conventional or fossil fuels with a ratio of carbon to 石化.7 to 〇.95. The lower the temperature, 90竓 to 95%: lignin or bacterial biomass. • The target is a petrochemical fuel with a total carbon phase of the phase, which is more/tongue and has a lower Auto-ignition temperature: • ar, or coal; δ fuel has a similar value to the fuel produced by the case, but its composition and miscellaneous “69 201118162 material is significantly different. Different types and types of fossil fuel It has very different chemical composition and characteristics, and is related to the mining area and the point of origin, so that each type of coal has unique and clear characteristics. For example, the petrochemical Lausitz raw material lignite has a fuel value of 8,700 kJ/kg and the water content is about 56. %, sulfur content is about 0.7%, and ash is about 4.5%. According to the case, the water content, sulfur content and ash content of the material or fuel are lower' and the fuel value is usually clearly higher than 2〇, 〇〇〇kj/kg 1 kilowatt (kilowatt) petrochemical L The ausitz raw lignite can be produced independently of the water content. In contrast, according to the case, the same amount can then produce more than & the amount of σ compared to fossil fuels, according to the material and / or fuel in this case The concentration of the Maynard reaction product can be detected. Νε_ (NKcarboxymethyl) lysine (CML) itself can be used as indicator 1 in the liquid phase of the reaction product and can also be detected in the solid phase. To this compound, a concentration of 0.2 to 1.5 mmol/mol or more of the lysine is measured, whereby a higher fraction can be measured in the liquid phase than the solid phase. The concentration distribution is related to the feedstock, reaction conditions and processing procedures. ° After mining, depending on the depth of the mining, fossil fuels are in the form of massive or relatively rigidly compressed agglomerates that must be ground with high energy. More progress must be dried and milled to fine-grained lignite or pulverized coal by a coal mill. In contrast, the material and/or fuel exhibits particles having a particle size of 1 mm to 30 nm after the end of the process, and because of its large surface, the grain is easily dried. Thereby, the dryness for adjusting the applied energy and especially the fuel is quite low compared to solid fossil fuels. .....' The characteristics of this fuel are particularly advantageous compared to the type of fossil fuel used in coal and the fuel that is currently available in recyclable materials. At least one of the following numbers, but usually several or all are more suitable for burning crude temple feed materials or other fossil fuels or biomass,,, 枓·reduced ash, less Gas, nitrate, sulfur heavy metals and lower 201118162 powder, fine dust and gas toxic (4) emissions, the quality of the noodle fuel and combustion characteristics of the feed material or feed raw paste, and the tender composition, And the feed material with the right amount of energy and the energy content allows the fuel to reach the process of turning over the sludge, and the calorific value is compared with the feed material having a fuel value of 17-20 MJ/kg, and After the dereliction of g _4 breaks the summary, its gray money is less than the value of 17-20 leg g of feed material, after burning tg dip, the sulfur content is reduced to gas ^ in the feed material, with Low fine particulate matter and lower combustion procedure steps, adjustment of associated fuel quality, and lean petrochemical fuel are products that are relatively pure and nearly ultrapure. The favorable characteristics of material reduction and stationability are mainly attributed to inorganic matter, which is also understood as 'God V. Phase is understood to be the combustible part of coal, and the purest coal percentage is disgusting. The inorganic content of the coal is, for example, less than the weight of ο.1. 71 201118162 The method of the last method is to burn the particles and the powder produced by the reaction product quickly and have a good cross section with a depth of about 1 to 2 cm and The angle of inclination "between the caps" can be ignited by the air in the combustion chamber. Si - the area of the larger mosquitoes makes the coal pens better. According to the case, the powder is impregnated on cellulose or The most suitable proportion of the ingredients is the contact and the machine side., the life + i f5 calorific value is 25 MJ/kg to 30 MJ/kg of powder or fuel particles 2, 7, (dllpped wood) or wood chips (w〇 The ratio of 〇d chip) is 53 : H % : 42 or preferably 64 : 36. Therefore, the amount of 3 water for cutting wood or wood chips is about H)%. The particles are not more than 2 coffees and less than 1.5 mm. Small can be less than 1 melon. • The calorific value is 22MJ/kg to 25 MJ/kg or the ratio of fuel particles to straw is 61:39, or it can be shame: or 72: 28. Therefore, the water content of the cut wood or the wood chip is about 1%. The particles are not more than 2mm, or less than h5mm or especially less than lmn^. Relative to the above ratio, powders containing peat or peat containing equal amounts of cellulose and lignin are processed into briquettes. Peat or peat can also be equivalent to cellulose and lignin alone. The processing becomes a briquettes. • The powder produced according to the method of this case and other materials containing cellulose and lignin or peat or peat are mixed together or mixed separately, 'for example, Conidur with a screen of 2 mm The impact filter is carried out in an impact tab mill. • The pressure is set at 100 MPa, which can be higher than 12 〇Mpa and also 72 201118162 can be higher than 140 MPa. • Press operation It is carried out at temperatures close to (6) and should not exceed 90 ° C. Its size is 250 X 60 X 50 mm. • The bulk density of briquettes is about 0.95 g/m3. to 1.15 g/ mJ ° Pellets produced from the reaction product according to the method of the present invention: The pellets produced by the method described in the present invention are preferably dried in a pellet after wet pelleting. This method is suitable for applying relatively low energy Pellets are produced from fuels with different heating values. • Good combustion allows standard automated combustion systems to be achieved in pellets. • For small combustion stations, defined emission standards can be met. The appearance of the fuel is in a small form and as uniform as possible. • The diameter of the pellets is from 3 mm to 7 mm, preferably from 4 mm to 6 mm. Its length is between 5 cm and 45 cm. The pellets have a high impedance or hardness, which produces only a very small amount of dust during the treatment process, and has high water repellency and can be properly dispensed. • Continuously feed the pellets into a fully automatic pill oven or vessel and burn in a controlled manner. • High heat performance with minimal inorganic pollutants or fuel gas emissions by burning as completely as possible. • When the calorific value is higher than 25MJ/kg and can also be higher than 27MJ/kg, use bonding material and combustion accelerator, especially wallpaper (waiipaperpaste), turf, straw 73 201118162 and Other lignocellulosic biomass. Or wood, such as the wallpaper f-aged organism f, can reach about 12-14% by example h n or the water content of wood chips or other lignocellulosic biomass. , the cellulose and lignin content in the ratio of the above-mentioned ratio 'peat powder or fuel granules', etc. are reinforced into pellets, so that the granules are not more than 2 sag, or less than 1.5 mm, and may be less than 1 mm. • Peat or humus as described in the method of the present invention can be processed into pellets separately with equal amounts of cellulose and lignin. Powder and cellulose-containing and woody gamma-containing materials or peat or peat concentrates The mixing is in the city, for example in an impact tab mill with a 2 mm Conidur release filter. • The pressure of the pressure is 1 〇〇. MPa, can also be higher than 12〇Mpa and rlj at 140 MPa. • The pressure temperature is close to 8〇t: and should not exceed 90〇C. • The most important adjustment for the pellet, especially compared to The pellets of fossil fuels are derived from improved combustion characteristics and in the field of sinter behavior of coal ash, ash treatment (usually lower ash) and the size of the combustion disc. 74 201118162 Energy can be thoroughly According to the method of this case, the ugly = there is Produced in the preferred embodiment. The fuel produced according to the ride is related to the adjustment performed in different devices. The pill _ type is usually a stove, a pill or an extension. _ Burning 111 is carried out and has automatic transfer supply. Combustion equipment with commercial seals can usually be used. In order to increase the characteristics of 峨, in the field of ϋ = 'The combustion equipment according to this case can be adjusted to the change of combustion · According to ash Adjust the form and size of the combustion disc. The smaller the ash, the smaller the diameter of the combustion disc can be used to produce better combustion. " • It is recommended to use an automatic device for removing ash from the combustion disc to prevent agglomeration of the combustion disc. The size of the naturally occurring pellets of this agglomerate, especially lignite. '"'pay* The combustion of the powder or fuel according to the present case is in a coal-fired power plant with at least one steam turbine. get on. In order to achieve high efficiency, the furnace is operated at a temperature higher than ·C, especially higher than 65 (). Further, by increasing the performance in high temperature regions by, for example, modern power plant technology, it is possible to achieve a sufficiently efficient combined gas turbine technology. The efficiency of current generation can be higher than 43%, or higher than 46% or higher than 49% to 55%. ' Coal gasification combined cycle power generation technology (IGCC) with integrated coal-carbon gasification is used for the combustion of fuel produced according to the method of the present case, i fluidized bed combustion technology can also be 'specifically with cyclic pressure A combined procedure for fluidized bed recirculation and power generation (PFBC) and, in particular, a combined power plant with coal-fired combined cycle power, such as pressurized pulverized coal combustion (PPCC). • The combustion program contains a gas entry temperature greater than 1 〇〇〇〇 c, or greater than 1200 ° C and may also be greater than 1400. 〇75 201118162 . The temperature gas cleaning method is designed in such a way that the particle content and the content of the active substance, especially the sodium and potassium compounds, and the corrosive gas are reduced to such an extent that the fuel gas can be immediately sent. The gas turbine 's preferably utilizes the low temperature plasma characteristics of the fuel gas. • The percentage of the volume of the particles having a particle content of less than 3 mg/m3 i n and a diameter d of less than 3 μm and a content of less than 0.01 mg/m3 i.n. can be achieved by a separator for separating the liquid slag in the fuel gas. β. According to the method described in the present invention, the method of generating a current or energy from a fuel (particularly a powder) is a use of a carbon fuel cell. By means of a shared energy generating device, in particular a turbine, preferably a steam turbine or a gas turbine for energy generation can be produced by and/or its seam inspection. _ Stomach. • Among these renewable energy sources, the Disputable Wind Power System (DWPS), in which the turbine is shared, especially the steam turbine or the gas coffee wheel, is (4). The compressed air is depressurized in a plenum chamber. The compressed air is then additionally inside the turbine that is already in operation. • If compressed air is introduced into a running turbine, its efficiency increases by 20% to 200〇/〇 or 4〇% to 170%, and may also be 6〇% to 15〇%. The efficiency is increased by introducing compressed air into the already operating turbine, and the efficiency lUT exceeds 2% to 2% or 4% to 17%, and may also be 6% to, according to this book. The device described in the embodiment, the different programs are combined in units. Grinding and mixing can be carried out in a single obstacle or in a space where the turbulence is impeded. In this (10), the device or the setting system of the injury system has a record. The possibility of the method or procedure step on the f 76 201118162. All the steps described above are equally feasible. Volume into (four) transfer money reactor batch

〇eil彡,亚田該處將進料送入混合容器(6)。 藉由;〇eil彡, Yatian sent the feed to the mixing vessel (6). By

送臀谷益0广培養容器(8)可以使催化劑滯留在材料上一 段時間。容If⑺及⑻係為雙層壁且具有熱水連接_ water connectlon),使得材料可以預熱至50°C至60〇C。 …乾』的進料原料的培養材料係經由輸送裝置(9)及(1〇) 饋3 ’彳物樹為—螺奴輸魏置(se_ eonveyor)或是輸 送帶(conveyor belt),在高於製程水的蒸汽麗的壓力下,由第 -進料股經由進難置(21)送進反應肋。進料裝置⑼由一 力式輸送裝置(force conveyor)所構成,例如是一注射器 (injeCt〇r)、雙螺旋擠壓器(double screw extruder)、偏心式螺旋 泵(eccentric ?piml pump)、活塞式泵_〇n pump)及螺旋式位 ^果(spiral displacement pump),其可以各自配置或不配置螺 旋式壓縮機(spiral compressor)或是雙螺旋式壓縮機(double spiml compressor)。進料裝置(21)可以附加設置一關閉裝置 77 201118162 (shutoff device)。進料裝置(21)確保由具有高於反應器内壓之 壓力位準之股I進入反應器(19)内,並防止反衝(ba 進料裝置。 )返八 具有相對於全體積為3%至5〇%之固體含量之可杲送進料 原料經由股II與製程水(4)及催化劑(15)在混合容器(1々中混 合,且;^經由適用的輸送裝置(1Ό送入反應器中,該輸送装置 可以設計為例如一活塞⑼如的、螺旋式位移泵(spi如 displacement pump)或偏心式螺旋泵(eccentric spiralpump)。其 ^料經由熱交換單元(18)加熱至少到溫 C至220C或是220C至250。(:。以此種方式由進料股!預處理 的進料原料,以並行的方法或是事後經由先前饋送至或存在 於輸送器的進料原料而由進料股Π引導。其進料股1的質量流 率與進料股II的質量流率的比例或是現有與饋送之進料原^ 的比例例如1:20、1:5、1:1或是ι〇:ι。 現有或饋送之材料的均勻混合經由一混合或是攪動裝置 (20)在第一反應器中發生。隨反應發生的加熱及放熱反應的釋 出經由一熱交換裝置(22)發生,該熱交換裝置與反g器的 雙層壁(23)連接,及/或經由其它熱交換器,該等熱交換器 係提供於反應器、或是與反應混合物連接。這些熱交'換器可 以例如以螺旋(spiral)、管式(tubular)、管束式(bundle)或是^旋 式熱交換器(spiral heat exchangers)。在所需要的滯留時間之 後,利用一壓降將反應器的内容物傳送至第二反應器(24)。 可以附帶使用用於加速流體之輸送手段。在流動方向上 處於第一反應器後方之壓力容器具有較小的體積。因為製程 水係利用在此說明書中的另一部份所說明的裝置來收回,藉 此反應混合物的體積可以減少。因此在程序的進一步進程需 要較少的反應器體積或是較小的反應空間。製程水的回收同 時也可以使得合併不同平行反應器或反應混合物縮小的反應 體積可行’其在單一反應器以平行的方式或是時間延遲的方 78 201118162 式合併,其反應階段偏離達5〇。/0的總反應時間,或是反應時 間偏離達至50%。此反應器的體積比它所接收的反應混合物 來處的所有反應器的體積總和低5%、1〇%或2〇〇/0。 • 反應器(24)也可以配置一熱交換器(22)、攪動裝置(20)及 雙層壁(23)’並使溫度在滯留時間固定維持在反應所需要的位 準。經由熱交換器(22)釋放所釋出的反應熱,藉此可以達到冷 卻:在反應器(24)之滯留時間結束之後,材料經由熱交換 器單元(25)在液化容器(26)中進行液化。此材料可以經由攪 動裝置(20)、熱交換器(22)及雙層壁(23)進行熱處理。熱交換 器(27)確保材料冷卻至低於水的蒸發溫度的溫度。藉此,其流 體及壓力液化經由逆向導向的液化泵控制,該液化泵可以由 力式輸送器、偏離式螺旋泵、螺旋式位移泵或活塞式薄膜泵 形成。 、 濕式進料原料儲存在液化容器(29)中。累積的熱可以經由 雙層壁釋出。過量的製程水經由後續的固_液分離裝置(3〇)進 行分離,而固-液分離裝置係設計為一玻璃瓶(decanter)、離心 機、氣旋式(cyclone)、過濾空腔壓搾裝置(fllter chamber device)、過濾裝置或是有相同的目的或在此份說明書中其它 部份所述的用以分離或乾燥之裝置,而製程水再次可供用於 根據本發明之方法的其他程序。最終產物暫時儲存在儲器 (31)中赠更進-步的使用。 ,第一反應器或是數個第一反應器的進料亦可經由單一進 料股來進行,亦即,單獨經由進料股I或進料股^或是與第二 進料股無關。如果是饋入『濕』的進料原料的時候,^是沒 問題的。但是當反應器填滿了『乾』的及自由流動的進料原 料時,需考慮到有足夠的水供應。製程水或是濃縮的製程水 在溫度超過6(TC、10(TC、16(TC或20(TC使用是為有利的,其 中低於自由流動量或是為『乾』進料原料之填加位準達5%、 10/〇、40%或60%的填加是足夠的。在反應器内製程水的填 79 201118162 加高度與進料原料的容積密度(bulk density)及其他的濃 (consistency )等等有關。 汽又 ,據^發明’為了增加進料原料的產量或是燃料或材料 巧J ’盡可能的將g]體的含量調高是必需的。對於使 3罝最大化的限制因素-方面在於主要是濕的生物質 J性,另-W在於與連接反應器之乾生物質的泵無“ 性·’應考慮的是,對於乾的生物質亦必須進行預 小通常足夠。在填充方法之過程中黏= 物=度減小,降低至超過進料原料』=的 黏度的3/4、或超過1/2或是1/5。然而 株殘留材料及農產品的積極利用及環境衛生條 θ 處理獲得增加的重要性。藉由位於發酵i 解(thenTi里羞生的方法上游的水解且特別是所謂的熱 其疋=木質纖維素的生物f的崩解,例如木材、草及樹枝 言(mi_ganisms)及燃料製造而 ί/ii藉 給予經濟及安全的選擇性例如動物勝食 責;情法的利用’動物膳食難以生產繼昂 處理所叙轉綠之翻,錢廢棄物的 致生物質的使用相對於用以產生相 法i,(fernter)之前’預處理生物質的各種方 料原料瘦由二/所明的熱致水解在幾年前已經發展,進 原枓由迴路式反應器(loop reactor)(如公開文件 201118162 ㈣ϋΓ述或水解應(如公開文件卿28815所述) 引導以及加熱至18〇t。微生物水解係建 (如公開文件DE伽391_)巾進行。 &式反應器 解而去SI: 一气設備係為了在溫度靴的熱壓力水 2 :此期的兩效益產能’實際上無法呈現廣泛的 番raJ歧的没備已經不能持續的得到期望的固體含 ί中2、、Ό ^ f在形成為管式交換11的熱交換 器中發,。II些持續多年的問題僅能藉由降低固體含量避 免’而H樣降了低轉献加紐料的產率使 經濟可利雜實際上無法_。 午做此技術的 _ ίίίί 2素之生物f的生物f的沉降(sed—) 作用及t合物結構_脹侧及在農作物中的澱粉的這些作 熱;?Γ?爾低估。膨脹係-種固體本體:暴 始蒸 時的可逆體積增加。聚合物結構的藉 由含水而膨脹。_及化學_脹鱗是魏_。在物理 如水會在木片的孔洞及空隙中。在水及木片之 „表面張力稱為毛細作用力(c 理,還有化學輕程序,其中水是加入親水結f tt 氫氧基(0Hgn)up)。献_氫鍵架橋而產 作'。在植物結構中,水儲存在細胞壁的多醣 Γ 之間。在膨服過程中,凝膠_tine)、在 峰、膠體結構(c〇u〇idai stmcture)會暫時產 進—步熱時會再次分解。—些蛋白物質例如骨頭及 皮膚廢物的膠狀物質而可以在水中進行膨脹。 澱粉在自然界中產生且以殿粉細粒的形式出現,其可以 i=L==°f/M_(suspend) °其主要是在溫度介 於47c及57C之間進仃。在較高的溫坑至阶之間 t細粒會練。轉糖(amylase)及錢麟(amylGpectine、 成的殿粉愈剩愈少,例如馬鈴薯㈣論)澱粉祕穴及小)麥The gluten-rich 0-wide culture vessel (8) allows the catalyst to remain on the material for a period of time. The contents If (7) and (8) are double-walled and have a hot water connection _ water connectlon so that the material can be preheated to 50 ° C to 60 ° C. The culture material of the feed material of the "dry" is fed through the conveying device (9) and (1〇) 3 'the tree of the tree is the se_ eonveyor or the conveyor belt, at a high The reaction ribs are fed from the first-feed strands via the inlet (21) under the pressure of the steam of the process water. The feeding device (9) is composed of a force conveyor, such as a syringe (injeCt〇r), a double screw extruder, an eccentric ?piml pump, a piston Pump _〇n pump) and spiral displacement pump, which may or may not be equipped with a spiral compressor or a double spiml compressor. The feeding device (21) can additionally be provided with a closing device 77 201118162 (shutoff device). The feed device (21) ensures that the strand I having a pressure level higher than the internal pressure of the reactor enters the reactor (19) and prevents backflushing (ba feed means.) Back eight has a relative volume of 3 The solid content of the feedable feedstock from % to 5% by weight is mixed with the process water (4) and the catalyst (15) in a mixing vessel (1 Torr) and passed through a suitable conveying device (1 Ό feed) In the reactor, the conveying device can be designed, for example, as a piston (9), such as a spiral displacement pump (spi), or an eccentric spiral pump. The material is heated via the heat exchange unit (18) to at least Temperature C to 220 C or 220 C to 250. (: In this way, the feed stock pretreated by the feed stock! is fed in parallel or afterwards via the feed material previously fed to or present in the conveyor. Guided by the feed strand, the ratio of the mass flow rate of the feed strand 1 to the mass flow rate of the feed strand II or the ratio of the existing feed to the feed is, for example, 1:20, 1:5, 1: 1 or ι〇: ι. Uniform mixing of existing or fed materials via a mixing or agitation device (20) at first The occurrence of heating and exothermic reaction with the reaction takes place via a heat exchange device (22) which is connected to the double wall (23) of the reverse g and/or via other heat exchanges The heat exchangers are provided in the reactor or connected to the reaction mixture. These heat exchangers can be, for example, spiral, tubular, bundle or ^-rotating Spiral heat exchangers. After the required residence time, the contents of the reactor are transferred to the second reactor (24) using a pressure drop. The means for accelerating the fluid can be used in conjunction with the flow. The pressure vessel in the direction behind the first reactor has a smaller volume because the process water is retracted using the apparatus described in another part of this specification, whereby the volume of the reaction mixture can be reduced. Further processes require less reactor volume or smaller reaction space. The recovery of process water can also result in a smaller reaction volume for combining different parallel reactors or reaction mixtures. 'It is combined in a single reactor in a parallel manner or in a time-delayed manner. The reaction phase deviates by up to 5 〇. The total reaction time of /0 or the reaction time deviates to 50%. The volume is 5%, 1% or 2〇〇/0 lower than the total volume of all reactors in the reaction mixture it receives. • The reactor (24) can also be equipped with a heat exchanger (22), agitating device (20) and the double wall (23)' and maintain the temperature in the residence time at the level required for the reaction. The released reaction heat is released via the heat exchanger (22), thereby achieving cooling: in the reaction After the residence time of the device (24) is over, the material is liquefied in the liquefaction vessel (26) via the heat exchanger unit (25). This material can be heat treated via agitation means (20), heat exchanger (22) and double wall (23). The heat exchanger (27) ensures that the material cools to a temperature below the evaporation temperature of the water. Thereby, the fluid and pressure liquefaction are controlled via a reverse-directed liquefaction pump which can be formed by a force conveyor, a deviating screw pump, a screw displacement pump or a piston diaphragm pump. The wet feedstock is stored in a liquefaction vessel (29). The accumulated heat can be released via the double wall. The excess process water is separated by a subsequent solid-liquid separation device (3〇), and the solid-liquid separation device is designed as a decanter, a centrifuge, a cyclone, and a filter cavity press device ( The fllter chamber device, the filter device or the device for separation or drying, which has the same purpose or described elsewhere in this specification, is again available for use in other processes for the method according to the invention. The final product is temporarily stored in the reservoir (31) for further use. The feed to the first reactor or the several first reactors can also be carried out via a single feed strand, i.e., independently via the feed strand I or the feed strand or independently of the second feed strand. If it is feeding the "wet" feed material, ^ is no problem. However, when the reactor is filled with “dry” and free-flowing feedstock, it is necessary to consider that there is sufficient water supply. Process water or concentrated process water at temperatures above 6 (TC, 10 (TC, 16 (TC or 20 (TC or 20 is advantageous for use, where less than free flow or feed for "dry" feedstock) Filling up to 5%, 10/〇, 40% or 60% is sufficient. Filling the process water in the reactor 79 201118162 plus height and bulk density of the feedstock and other concentrates ( Consistency and so on. Vapor, according to the invention, in order to increase the output of the feedstock or the fuel or material, it is necessary to increase the content of the g] as much as possible. The limiting factor - the aspect is mainly wet biomass J, and the other is that the pump with the dry biomass connected to the reactor has no "sex". It should be considered that the dry biomass must also be pre-small enough. During the filling method, the viscosity = the degree of decrease is reduced to more than 3/4 of the viscosity of the feed material, or more than 1/2 or 1/5. However, the residual material of the strain and the active use of agricultural products And the importance of the environmental sanitation θ treatment is increased by the fact that it is located in the fermenting solution Upstream hydrolysis and especially the so-called disintegration of the bio-f of lignocellulose = lignocellulose, such as wood, grass and twigs and fuel manufacturing, while ί/ii gives economic and safety options such as animal wins The use of the law; the use of the law of the 'animal diet is difficult to produce, following the treatment of the green, the greening of the money, the use of biomass of money waste relative to the use of the phase method i, (fernter) before the 'pretreatment of biomass The thermal hydrolysis of various raw materials and raw materials has been developed a few years ago, and the original reactor is looped by a loop reactor (as disclosed in the public document 201118162 (4) or hydrolyzed (such as Public Documentary 28815). Said) Guided and heated to 18 〇t. Microbial hydrolysis system (such as the public document DE gamma 391_) towel. & type reactor to go to SI: gas equipment for the heat of the temperature in the boots 2: this period The two benefit-capacity's are actually unable to present a wide range of deficiencies that have been unsustainable and have been unable to sustain the desired solids. 2, Ό ^ f is emitted in a heat exchanger formed into a tubular exchange 11, II Some problems that last for many years can only By reducing the solids content to avoid 'and the H-like drop of the low-transfer donation of the feedstock yields the economy can be practically impossible. _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ —) Role and t-structure _ bulging side and the heat of the starch in the crop; Γ 尔 尔 underestimate. Expansion system - kind of solid body: reversible volume increase at the beginning of steaming. Watery and swell. _ and chemical _ bulging scale is Wei _. In the physical, such as water will be in the holes and voids of the wood chips. The surface tension in water and wood chips is called capillary force (c, and there is a chemical light procedure in which water is added to the hydrophilic knot f tt hydroxyl (0Hgn) up). In the plant structure, water is stored between the polysaccharides of the cell wall. During the expansion process, the gel _tine, the peak, and the colloidal structure (c〇u〇idai stmcture) will be temporarily produced. Decomposition - Some protein substances such as bones and skin waste are colloidal substances that can be expanded in water. Starch is produced in nature and appears in the form of fine powder of the temple powder, which can be i=L==°f/M_(suspend ° ° It is mainly between the temperature of 47c and 57C. In the higher temperature pit to the order between the fine particles will be trained. Amylase and Qian Lin (amylGpectine, into the temple powder Less, such as potato (four) on the starch secret point and small) wheat

Q 81 201118162 殿粉(wheat starch)為67.5。(:。其溶液的黏度因此大幅增加, 凝膠形成。傳統上凝膠也可以稱為膠體(glue),這些凝朦的作 用類似膠體。殿粉膨脹及凝膠形成的整個過程因此稱為膠化 (gelation)。澱粉膠體具有不同的硬化能力(stiffening capacity),其與澱粉的種類有關^膨脹作用藉由壓力及熱量再 次增加,且在熱致水解的條件下加速進行。 、,由文獻巾可以知道丨崎在不同的生物質巾變異很大。在 玉米青貯(maize silage)其例如可以是相對於乾物質為12及 M4重量百分比之間。玉米青貯膠的應化能力係大於小麥殿粉 膠且及大於馬鈴魏娜^玉米青貯為—種常祕產生生物 質的生物質,水解程序尤其需要考慮到其高硬化能力,以避 免熱交換系統的阻塞。 應考慮低的澱粉量例如低於5%可以改善在某些條件下 ,可泵送性,特別是在固定的溫及壓力比的條件下。然而隨 著熱致水解’壓力和溫度快速的增加時,體積增加且因此流 動阻力(flow resistance)增加必須預先考慮。具有高澱粉含量例 如相對於乾物質超過10-30%、30-50%或是超過5〇。/。的進料原 ^是生物質係直接經由用於『乾』生物質的股⑽㈣)導入 第一反應器,亦即進料股丨,並在該處塗佈來自股〗〗的液體加 熱。生物質,及/或與之混合。具有相對於乾質量為3%、5%或 10 /。以下之低澱粉含量的生物質或進料原料經由進料股Η導 入,該等生物質或進料原料可以同時有或沒有預處理而加以 果送。 ^積及阻塞的形成的增加原因可能是各種因素的組合。 在熱交換器中的程序氣體形成以及澱粉膨脹在體積增加發揮 ^要的作用。理想地,係假設—管式反應H巾有塞離opper 〇W):,此’可預期根據氣體形成或是膨脹,體積會增加, 璺力Jk著增加。還會因為輸送的產物(g〇〇ds)的澱粉膨脹增加 的黏度而額外增加。因此,流體阻力也會增加。 82 201118162 “ίί於紐力树财賴結财,級直管管件的長 量,過去形成為管狀反應器的熱交換器係以水平的方 i二’ 重力°為改善生物質的熱致水解或是加 ^序尤其疋考慮到相對於固體含量的較高產率,在本 述^用於水解或是用於加熱生物質的方法,其特徵在 ϋ固^混°通過熱交換ii加熱,且固液混合物絲本上以平 ίΐϊ重力的方式被料通過对觸管件,以避免結塊及/或 可流_賴料本身係向下移動及不需要考量到重力以 擊二:防止結塊及阻塞。於此’熱交換裝置係 士 *Γδ十,在實施例中,管件轴向的角度相對於水平面 3。ί度y度或大於10度。熱交換器由至少20%、40%或 。、垂直f件部件所構成。垂直管 =附击其,的角度相對於垂直面係為7載〇度以 二又垂直疋指對垂直方向角度低於45度,在實施例中, 垂直管件部件_直方向的肢最多1〇度。 ^ ΐίί f1 ^如f式反絲或是録狀反應11或是板式 或疋料熱交換器敝合所組成。熱交換器係以模 ίΪ Γί及可以由不同的模組、單元或是區段構成。模 以的方式互相排列’使數個熱_單元能 伽ίΐϊ11的調和系統係由雙層麵構成,其_由熱能 ^過。熱能載體介f可例如為熱油、水蒸汽或是來 it ϊϊϊ之方法或其它程序的製程水。可以組合不同的 载體;1質。介質的目標溫度㈣et temPerature)在60°C及 r + «HI。在第—區段或是第—模_溫制如6G°C至100 i=?=i12G°C ’在第二區段或是第二模組之溫度例如 間或12叱及_之間’在第三區段之溫度 ’丨;40C及180C之間或是16〇。(:及2〇(TC之間,及在第四區 83 201118162 严之溫〒介於18。。。及細^之間、22(Γ(:及“。。。之 〇Q 81 201118162 The wheat starch is 67.5. (: The viscosity of the solution is thus greatly increased, and the gel is formed. Traditionally, the gel can also be called a glue, and these gels act like colloids. The whole process of swelling and gel formation is called glue. Gelation. Starch colloids have different stiffening capacities, which are related to the type of starch. The swelling effect is increased again by pressure and heat, and accelerated under conditions of thermal hydrolysis. It can be known that Miyazaki varies greatly in different biomass towels. In corn silage, for example, it can be between 12 and M4 by weight relative to dry matter. The ability of corn silage is greater than that of wheat powder. Glue and larger than Ma Ling Wei Na ^ corn silage is a kind of biomass that often produces biomass. The hydrolysis process especially needs to consider its high hardening ability to avoid the blockage of the heat exchange system. Consider low starch content such as low 5% can improve pumpability under certain conditions, especially at fixed temperature to pressure ratios. However, with thermal hydrolysis, 'pressure and temperature are fast When increasing, the volume increases and therefore the flow resistance increases must be considered in advance. The feed has a high starch content, for example more than 10-30%, 30-50% or more than 5 相对 relative to the dry matter. It is the biomass system that is directly introduced into the first reactor via the strand (10) (four) for "dry" biomass, that is, the feed strand, and where the liquid from the strand is coated. Biomass, and/or mixed with it. It has a 3%, 5% or 10 / relative to the dry mass. The following low starch content biomass or feedstock is introduced via the feed strands, which may be fed with or without pretreatment. The increase in the formation of the product and the blockage may be due to a combination of various factors. The formation of the program gas in the heat exchanger and the expansion of the starch play a major role in increasing the volume. Ideally, it is assumed that the tubular reaction H towel has a plug away from the opper 〇W): this can be expected to increase in volume depending on the gas formation or expansion, and the force Jk increases. It is also additionally increased by the increased viscosity of the starch of the delivered product (g〇〇ds). Therefore, the fluid resistance will also increase. 82 201118162 “ ίί 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽 纽It is a method of adding, in particular, a higher yield relative to the solid content, which is used in the present invention for hydrolysis or for heating biomass, and is characterized in that it is heated by heat exchange ii and solidified. The liquid mixture is passed through the pair of pipe fittings in a flat gravity to avoid agglomeration and/or flow. The material itself moves downwards and does not need to be considered to be gravity. To prevent agglomeration and blockage In this embodiment, the heat exchanger device is at least 20 degrees, 40% or more. In the embodiment, the axial direction of the pipe member is relative to the horizontal plane 3. The degree of y is greater than or equal to 10 degrees. The heat exchanger is at least 20%, 40% or . Vertical f-pieces. Vertical pipe = attached to it, the angle is 7 degrees relative to the vertical plane, and the vertical angle is less than 45 degrees in the vertical direction. In the embodiment, the vertical pipe part _ Straight limbs up to 1 degree. ^ ΐίί f1 ^ such as f-type reverse wire or The reaction 11 is formed by a combination of a plate or a heat exchanger. The heat exchanger is modulo and can be composed of different modules, units or sections. The heat _ unit energy gamma 11 blending system consists of two layers, which are made up of thermal energy. The thermal energy carrier f can be, for example, hot oil, water vapor or a method of process or other process water. Combine different carriers; 1 quality. The target temperature of the medium (4) et temPerature) at 60 ° C and r + «HI. In the first section or the first mode _ temperature system such as 6G ° C to 100 i =? = i12G °C 'between the temperature of the second section or the second module, for example between 12 叱 and _ 'in the temperature of the third section 丨; between 40C and 180C or 16 〇. (: and 2 〇 (between TC, and in the fourth district 83 201118162 Yan Wenwen is between 18... and fine ^, 22 (Γ (: and "..

Cf3500之間。熱載體介質的溫度可變化達2〇°c、4〇〇c或是 =°C。熱交換H的單元、模组或是區段以串聯的方式連接使 得固-液的溫度在達到最高溫度例如22〇〇c至26叱之後,可以 Πΐΐ低的入口溫度或是出口溫度。對應於區域衛生 有—水解反應器,其可以使材料保持在 正負2C至8C的程度及確保滯留時間為例如至少%分鐘。 有雙職狀贱触轉之設備。該用於 含有^齡量之崎,例如姆⑽ 之固體。於此,『乾』的生物曾键在尤祖1 板出料容器(2)。進料原料經由輸送裝置送磨 輸旋式輸送裝置或是一輸送帶並由= 合。其混合 轉嶋自貯存器(4)及 二製器中徹底混 催化劑滯留在材料上一 ⑻ 有熱水連接,可使材料預熱至50。(:至60。(;:。〜/、 『乾』的進料物質的已培養材料經由輸 ,進反應器進料裝置⑼内。進料裝置包含、^ (stoppmg apparatus)。進料裝置使培養的材 f 口反應器之壓力之股!送入反應器(19),並防止裝 量之可泵 具有相對於整體體積具有3%至·之固體含 84 201118162 送進料原料係經由進料股II與製程水(4)及催化劑(15)在混合 容器(14)中混合、培養(16),並經由合適的輸送裝置(17)送入 反應器中’(該輸送裝置(17)例如活塞、螺旋式位移、或是偏 離式螺旋泵)。該材料經由熱交換單元(18)加熱到至少i8〇°c至 200°C。在水解反應器(21)中,來自進料股π之流體、可泵送 生物質與來自進料股〗之乾的生物質混合。該材料可以附帶地 經由熱交換器(22)及雙層壁(2〇)而被熱影響。 。反應器(21)之滞留時間過了之後,材料的液化經由熱交 換單元(23)進入液化容器(25)内。熱交換器(23)讀保材料冷卻 至低於水的蒸發溫度。因此通道及壓力液化係由逆向導向之 液化栗(backward-oriented devolatilization pump)控制,其係設 計為力式輸送裝置、偏離式螺旋、螺旋式位移、或是 膜式果。 * 一濕的進料原料係儲存在液化容器(25)内。累積的熱可以 經,雙層壁釋放。過量的製程水經由後續的固-液分離裝置㈣ 進行分離’而固液分離裝置係設計為一玻璃瓶((1隨咏)、離 心機、氣旋式(cyclone)、過濾空腔加壓裝置脚er如她沉 P_ng device)、過濾裝置或是用於類似目的或在此說明 其=部份所述的裝置,而製程水可再提供用於在本發明所述 ^一ί中的其他程序。最終產物暫時儲存在儲存器(27)中以便 進一步使用。 调如連續方式廣泛操作。亦即,進料原料經由一反應 至^ i=由材料通過所需時間的熱交換被送去加工的時間 器十分之六°相__對於填加至熱交換 序,或是在以分支(。跑)方式填加至液化容器 (m來°因此’設備的產量經由輸送I置(17)及導入裝置 置受到=丨。逆向導向式液化1(24)之旋轉速度在設備不同位 閱可^代液隨著設備中存在的壓力而蒸發。 85 201118162 液化裝置或疋液化果藉由溫度及/或麗力來控經 ,的降低可以獲得在熱錢II巾較長师留時fa卜介質的溫 度因而降低。依之後的裝置中或是後續_序中所需J調整 溫,I例如,若將反應混合物更進一步的導入具有環境壓力 的容器時’必雜溫度調整至低於軸,卿免 非控制的蒸發程序。根據說明#的另—部份所述之實施例, 饋送至另-個乾縣序’會需要高於雜的溫度0控制液化 泵2得麵的殘留壓力(remaining residual pressure)足夠用 5、2 於後項程序或裝置巾的輸送。剩餘賊_力例如低於10、 r。或1巴。 … 股用於触搞之設制設計_於根據 本f明所奴方法之雙股進難置的設計在某些點上具有相 t二ίϊ置及設計形式可以互換。所有與雙股進料原料 連接的裝置盡可能在技術及在崎方面練纽度上 ,制、調整、自動化。這對於所有提到的程序、方法或 序步驟同樣是有效的。 ~ 在,方法的過程中可峨察得_度的降低,作為水 抒的量度。固·液混合物的黏度當固_液混合物通過水解 ’轉低至少3/4、1/2或是1/5之進料原料的黏度。 里必須盡可能調高以增加進料原料的產量或是增加 ,料的產率。最大化固體含量的限制因素—方面主要是^ 果送性,及與泵無關而與導人反應器連接之稱、 微乾的生物質的可輸送性。 根據發明之申請專利範圍第37項及第38項所述之方法, ^ 了陶紐料的產生’,產生懸浮液献分散物。 ,關於^的製造方法’該物件為根射請專利範圍第取 項之前文之含碳材料之缺空至少部份具有包含陶 (ceramic)及含碳材料或是其它的物質之結構。 全部的或部份陶瓷材料之物品的製造,例如組件或是耗 86 201118162 ^^^^ 夕⑽麵—㈣’在目前來說非常複雜, T種強度非常高的物f,難以塑造或是以機械 1蚨後加工。奴化矽為非毒性高溫陶瓷,尤其因為它本身的 優異特性轉有高利益,例如具有賴^―樣的硬度、光學 穿透性(optical transparence)、半導體特性、高熱傳導性、化與 耐文性’因此在許多不同的工程領域中使用,例如耐火 材料(refractoiy material)的製造、隔熱體及作為半導體材料。 碳化矽物件的製造係具有高經濟重要性。 導材十 4 _碳化矽的物質係通常由傳統的燒結法形成,其中利用不 同的結合劑(bonding agent)在高溫下烘烤細密研磨的碳化矽 粉末。此程序的缺點在於除了需要高溫及長的燒結時間之 外,所產生的物件具有多孔性,使得只能用在特定應用中。 、由公開文件DE3322060已知另一種用於製造碳化石夕的方 法’其中產生的含碳材料的物體,例如石墨,在量測與形狀 為精確,然後,在長時間的退火(anneaiing)處理中,藉由檐 加工’使該物體至少接近該表面的碳由碳化矽來取代^於此, 在退火期間將物質擠壓成二氧化石夕的粒狀材料,及例如在退 火期間將氫氣導引遍於粒狀材料。藉此,可以產生具有值得 注意的氧化矽之氣體,此氣體可以擴散進入物體鄰近表面之 含碳材料,且與物體的碳反應,使得碳化矽形成在物體的基 ^(matrix)内。藉此,可以在至少鄰近表面處完成達成物體的 碳與碳化矽交換,從而達成物體鄰近表面區域的相當改善。 利用此程序方法的缺點在於其氧化矽氣體的產生複雜,且難 以保持及配給在此氣體中所需的氧化矽的量。因此本發明的 目的係提供陶曼材料尤其是碳化;g夕之物體的改善的製造方 法’其中含碳材料的物體或是多孔性陶竟物質,尤其是碳化 矽’可以以簡單及安全的方式完全或是部份轉化成碳化矽。 藉由產生水與含碳組成的固_液混合物作為產生隔熱材 料及/或陶瓷材料的起始或是附加物質,可以得到附帶的物質 87 201118162 懸浮液或是分散物,其巾m合物在溫度超過励。c及壓 f ^ 巴下進行處理。可能藉㈣浮液(suspensiGn)的高純度 量排除。硫及灰分伽為附加物㈣浮液或分散 ,的純度的特徵化,其它參數,例如驗金屬、氯、碳、辦、 鎮、鉻、銅、!S、鋅亦同。藉由增加純化水或是製程水 =加’上述物質的含量在含碳固-液混合物中係相應 ^低。藉由,侧外崎洗步驟以增加在固·液齡物中碳的 巧’其經岭壓及溫度來發展更高的效率。藉此,相對於 ^碳成份_縣始含量,魏合物的獻/歧分降低至 y 50 Α或75/ί>。相對於含碳成份的個別原始含量,硫及灰份可 降低超過80%、90%或是99%。或是叫财絲達,在與清 洗程序有_反雜序的過財’硫及灰分連續降低,且趨 近程序結束時,其降低至超過進料原料的硫及灰分之2/1〇、 1/12或是ι/loo 〇 物是酸性的,這是因為在酸性介質中預培養及添加 ㈣為催化劑,因此驗性溶液提供本身製造喊材料。利 用溶膠·凝縣將雜附加㈣祕液或是分餘加入至鹼 性溶膠中賊_序_。雜合物及含錢或無機魏鹽 及/或二氧化矽之溶膠經由此處理方法以及更進一步的方法步 ,產生。轉為水賴之水溶液。碳成敍魏鹽成份用於 製造凝膠。郷域至碳切㈣產生碳切氣體渗透 所提供的多孔賴型。賴魏含純化碳、純碳、高純碳 趙純磁。 特別重要的是碳是細分割為高碳化矽粒狀材料,當粒狀 材,被加熱時,二氧化矽立即與此碳反應,藉此形成含碳化 石(氣體’較佳的是主要是純碳化魏體。碳在二氧化石夕中的 分佈可以由在附加的物質懸浮液或分散物中的碳顆粒的小尺 寸達成,藉此含碳化矽氣體的形成在大幅低於碳化石夕的正常 昇華溫度下發生,尤其溫度已經是在1700°C及1900t之間。 88 201118162 此,在更進—步的述的方式直接擴散至物體。藉 m·炭ί二物體藉,,代物體中來自碳基質㈣⑽ 於心dn刺的。藉此,在碳化碎中碳的基質的主要成 乂換’而基f的主要成份的結構廣泛保留,且物體的 特性已以所述的方式愤變及改善。 且物體的 狀材程序中產生富射㈣〇n顧础㈣粒 =序產生富碳二氧化矽粒狀材料,可以以非常▲確以及 2以立即與碳及其它欲加人的物質反應並立即可用於接 近物體表面的擴散程序。 、 、由公開文件DE 102006055469已知用於產生一物體的方 法其中物體由含碳材料之碳化石夕結構的至少部分空缺所產 ^,其中根據所植的最終㈣及/綠後的尺寸在第一'步驟 ^造含碳材料之物體,且接著該含碳材料之物體至少局部以 富碳二氧化矽粒狀材料圍繞,及在退火溫度下, ,,财進行至少-次退火,其中二氧切=材蔓= 放出含奴化矽氣體,其滲透物體且將部份的或全部的含碳 料轉換成碳化梦。 如果溶膠-凝膠程序利用可溶解的水解無機或有機矽酸 鹽作為起始物質以產生富碳二氧化矽粒狀材料是有利的。多 種的可行的起始物質係包含於其中,可適用作為矽提供物以 ^/成粒狀材料,及可以適用在溶膠_凝膠程序中。以下所述明 確述及的物質僅是先前所述物質分類的特別較佳的者,不能 被視為欲使用的物質之總結表列。水溶性鹼性矽酸鹽如水玻 89 201118162 璃可以作為採用無機矽酸鹽之溶膠-凝膠程序之起始物質。 本接續方法之特徵在於申請專利範圍第丨、36、5〇、72、 98 103、、115及143項及其附屬項。對於接續方法更進 了步的規範可以由在此包含的特性衍生,其中含碳進料原料 係連^供應至第一反應器,且反應混合物係以批量方式由一 反,器導向下—個反應器,而反應產物係連續的由最後的反 ,'器中釋出。以上所述之巾請專利範圍更進—步包含用於執 行本接續方法之設備與裝置之特徵與特徵組合。 、 【圖式簡單說明】 第1圖顯示根據本案之反應器的縱截面示意圖,其並 據本案之設備的其他組件; 第2圖顯示根據第1圖之反應器壁區域之截面; 第3圖以例示方式顯示設備之示意圖; 【主要元件符號說明】 1 料斗 2 底板出料容器 3 碎磨裝置 4 貯存器(製程水) 5 催化劑 6 混合容器 7 輪送裝置 8 培養容器 9 輪送裝置 10 輪送裝置 14 混合容器 15 催化劑 第4圖顯示設備之另一示意圖;以及 第5圖顯示設備之又一示意圖。 201118162 17 輸送裝置 18 熱交換單元 19 反應器、導入裝置 20 混合或攪動裝置 21 進料裝置 22 熱交換裝置 23 雙層壁、熱交換單元 24 第二反應器 25 熱交換單元、液化容器 26 液化容器、固-液分離裝置 27 熱交換器、儲存器 29 液化容器 30 固-液分離裝置 31 儲存器 91Between Cf3500. The temperature of the heat carrier medium can vary by up to 2 °c, 4〇〇c or = °C. The units, modules or sections of the heat exchange H are connected in series such that the temperature of the solid-liquid can be lowered to the inlet or outlet temperature after reaching a maximum temperature of, for example, 22 〇〇 c to 26 。. Corresponding to the zone sanitation-hydrolysis reactor, it is possible to maintain the material at a positive or negative 2C to 8C level and to ensure a residence time of, for example, at least % minutes. There are dual-purpose smashing devices. This is used for solids containing a certain amount of age, such as m (10). Here, the "dry" creature has been in the Yuzu 1 plate discharge container (2). The feed material is fed to the rotary conveyor or a conveyor belt via a conveyor and is controlled by =. The mixture is transferred from the reservoir (4) and the second reactor. The catalyst is completely mixed on the material. (8) There is a hot water connection to preheat the material to 50. (: to 60. (;:: ~ /, "dry" feed material of the feed material is fed into the reactor feed device (9). The feed device contains, (stoppmg apparatus). The feed device makes The pressure of the cultured material f-reactor is fed to the reactor (19) and prevents the chargeable pump from having a solid content of 3% to 8% relative to the overall volume. 201118162 The feed material is fed through the feed. The strand II is mixed with the process water (4) and the catalyst (15) in a mixing vessel (14), incubated (16), and fed into the reactor via a suitable conveying device (17) (the conveying device (17), for example Piston, helical displacement, or offset helical pump.) The material is heated via a heat exchange unit (18) to at least i8 〇 ° c to 200 ° C. In the hydrolysis reactor (21), from the feed π The fluid, pumpable biomass is mixed with the dry biomass from the feed stock. The material can be additionally thermally affected via the heat exchanger (22) and the double wall (2〇). After the residence time has elapsed, the liquefaction of the material enters the liquefaction vessel (25) via the heat exchange unit (23). The heat exchanger (23) reads The material is cooled to a temperature below the evaporation temperature of the water. Therefore, the channel and pressure liquefaction are controlled by a backward-oriented devolatilization pump designed as a force transfer device, an off-axis spiral, a helical displacement, or It is a membrane type fruit. * A wet feed material is stored in the liquefaction vessel (25). The accumulated heat can be released through the double wall. The excess process water is separated by the subsequent solid-liquid separation device (4). The solid-liquid separation device is designed as a glass bottle ((1), centrifuge, cyclone, filter cavity press device er, such as P_ng device), filter device or for similar purposes or The apparatus described in the section is described herein, and the process water may be further provided for other procedures in the present invention. The final product is temporarily stored in the reservoir (27) for further use. Widely operated in a continuous manner, that is, the feedstock is sent to the processing time via a reaction to a heat exchange of the material for a desired period of time, a phase of six __ for the addition to the heat exchange sequence, Or in points The branch (.running) method is added to the liquefaction vessel (m to ° so the yield of the equipment is received by the transport I (17) and the induction device is received = 丨. The reverse directional liquefaction 1 (24) rotation speed is different in the device The liquid can be evaporated with the pressure existing in the equipment. 85 201118162 The liquefaction device or the liquefied fruit can be controlled by temperature and / or Lili, and the reduction can be obtained when the hot money II towel is longer. The temperature of the medium is thus lowered. The temperature is adjusted according to the J required in the subsequent device or in the subsequent step, for example, if the reaction mixture is further introduced into the container having the ambient pressure, the temperature must be adjusted to be lower than the axis. Qing is exempt from the controlled evaporation process. According to the embodiment described in the other part of the description #, feeding to another dry county order 'will require a temperature higher than the miscellaneous temperature 0 to control the residual pressure of the liquefied pump 2 enough to use 5, 2 The delivery of the latter procedure or device towel. The remaining thief _ force is, for example, less than 10, r. Or 1 bar. ... The design of the stock for the touch _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ All the equipment connected to the double-feed raw materials are as much as possible in terms of technology and kiosk, system, adjustment and automation. This is also valid for all mentioned procedures, methods or sequence steps. ~ In the process of the method, the decrease in _ degree can be observed as a measure of water sputum. The viscosity of the solid-liquid mixture is reduced by the hydrolysis of the solid-liquid mixture by at least 3/4, 1/2 or 1/5 of the feed material. It must be adjusted as high as possible to increase the yield of the feedstock or increase the yield of the feed. The limiting factor for maximizing the solids content - in terms of the nature of the delivery, and the connection to the pilot reactor independent of the pump, the transportability of the micro-dry biomass. According to the method of claims 37 and 38 of the invention, the production of the ceramic material produces a suspension dispersion. , the manufacturing method of ^, the object is the root shot, the patent scope is taken. The void of the carbonaceous material before the at least part has a structure including ceramic and carbonaceous materials or other substances. The manufacture of all or part of the ceramic material, such as the assembly or the consumption of 86 201118162 ^^^^ eve (10) surface - (four) ' is very complicated at present, T is very high intensity f, difficult to shape or Mechanical processing after 1 。. Nucleation is a non-toxic high-temperature ceramic, especially because of its excellent properties, such as hardness, optical transparence, semiconductor properties, high thermal conductivity, and resistance to text. 'Therefore it is used in many different engineering fields, such as the manufacture of refractoiy materials, insulators and as semiconductor materials. The manufacture of tantalum carbide articles is of high economic importance. The material of the conductive material 1,4-carbene is usually formed by a conventional sintering method in which finely ground cerium carbide powder is baked at a high temperature by using a different bonding agent. A disadvantage of this procedure is that in addition to the high temperatures and long sintering times required, the resulting articles are porous so that they can only be used in certain applications. Another method for producing a carbonaceous material, the method of producing a carbonaceous material, such as graphite, is known in the publication DE3322060, which is accurate in measurement and shape, and then, in an anneaiing treatment for a long period of time. Substituting the carbon of the object at least close to the surface by yttrium processing, squeezing the material into a granulated material of the oxidized stone during annealing, and guiding the hydrogen gas, for example, during annealing Through the granular material. Thereby, a gas having an interesting yttrium oxide which can diffuse into the carbonaceous material adjacent to the surface of the object and react with the carbon of the object such that the lanthanum carbide is formed in the matrix of the object can be produced. Thereby, the exchange of carbon and niobium carbide of the object can be accomplished at least adjacent the surface, thereby achieving a considerable improvement in the area of the adjacent surface of the object. A disadvantage of using this procedural method is that the production of cerium oxide gas is complicated, and it is difficult to maintain and ration the amount of cerium oxide required in this gas. The object of the present invention is therefore to provide an improved manufacturing method for a Tauman material, in particular carbonization; an object in which a carbonaceous material or a porous ceramic material, in particular a tantalum carbide, can be used in a simple and safe manner. Completely or partially converted to tantalum carbide. By adding a solid-liquid mixture of water and carbon as a starting or additional substance for generating a heat insulating material and/or a ceramic material, an incidental substance 87 201118162 suspension or dispersion can be obtained, and the composition thereof The temperature exceeds the excitation. c and pressure f ^ bar for processing. It may be excluded by the high purity of (iv) floating liquid (suspensiGn). Sulfur and ash are added as additives (IV) float or dispersion, the purity of the characteristics, other parameters, such as metal, chlorine, carbon, office, town, chromium, copper,! S, zinc is also the same. By increasing the amount of purified water or process water = plus the content of the above substances is correspondingly low in the carbon-containing solid-liquid mixture. The higher efficiency is developed by the side-sanding step to increase the carbon pressure in the solid-liquid age. Thereby, the contribution/disambiguation of the Wei compound is reduced to y 50 Α or 75/ί> with respect to the content of the carbon component. Sulfur and ash can be reduced by more than 80%, 90% or 99% relative to the individual raw content of the carbonaceous component. Or it is called Weisha, in the process of cleaning with the _ anti-hybrid, the sulfur and ash continuously decrease, and when it approaches the end of the program, it is reduced to more than 2/1〇 of the sulfur and ash of the feed material. The 1/12 or ι/loo mash is acidic because the pre-culture and addition of the (4) catalyst in the acidic medium provides an assay solution that provides the material itself. Use sol·Jingxian to add miscellaneous (4) secret liquid or fraction to the alkaline sol in the thief _ order _. The hybrid and the sol containing the rich or inorganic Wei salt and/or cerium oxide are produced via this treatment method and further method steps. Turn into an aqueous solution of water. The carbon-based salt component is used to make gels. The 郷 domain to carbon cut (4) produces a porous slag type provided by carbon gas permeation. Lai Wei contains purified carbon, pure carbon and high purity carbon. It is particularly important that the carbon is finely divided into high-carbonized cerium-like materials. When the granular material is heated, the cerium oxide reacts with the carbon immediately, thereby forming a carbon-containing fossil (the gas 'is preferably mainly pure Carbonized Wet body. The distribution of carbon in the day of the dioxide can be achieved by the small size of the carbon particles in the additional substance suspension or dispersion, whereby the formation of the cerium-containing cerium gas is substantially lower than that of the carbonized stone. At sublimation temperature, especially the temperature is already between 1700 ° C and 1900 t. 88 201118162 This, in a more advanced way, directly spreads to the object. By borrowing from m · char ί, the object comes from The carbon matrix (4) (10) is punctured in the heart dn. By this, the main enthalpy of the matrix of carbon in the carbonized smash is replaced by the structure of the main component of the base f, and the characteristics of the object have been angered and improved in the manner described. And the object's shape program produces a rich shot (4) 〇 n Gu Chu (four) granules = order to produce carbon-rich cerium oxide granular material, can be very ▲ and 2 to immediately react with carbon and other substances that want to add people Immediately available for access to surface surfaces The method for producing an object is known from the publication DE 10 2006 055 469, wherein the object is produced from at least part of the vacancy of the carbonaceous material of the carbonaceous material, wherein the final (four) and/or green The size of the object in the first step is to form a carbonaceous material, and then the object of the carbonaceous material is at least partially surrounded by the carbon-rich ceria particulate material, and at the annealing temperature, at least - annealed , where dioxobic = vine = release sulphide-containing gas, which penetrates the object and converts some or all of the carbon-containing material into a carbonization dream. If the sol-gel procedure utilizes soluble hydrolyzable inorganic or organic citric acid It is advantageous to use a salt as a starting material to produce a carbon-rich ceria particulate material. A variety of viable starting materials are included therein, which are suitable as a ruthenium supply, and can be applied to a sol. In the gel procedure, the substances explicitly mentioned below are only the particularly preferred ones of the previously classified substances and cannot be regarded as a summary list of the substances to be used. Glass 89 201118162 Glass can be used as the starting material for the sol-gel procedure using inorganic citrate. This continuation method is characterized by the scope of patent applications Nos. 36, 5, 72, 98, 103, 115 and 143 and Its subsidiary item. The specification for further continuation of the continuation method can be derived from the properties contained herein, wherein the carbonaceous feedstock feedstock is supplied to the first reactor, and the reaction mixture is passed in a batch manner. Guided to the next reactor, and the reaction product is continuously released from the final counter. The above-mentioned towel is more patented and includes the features and equipment of the device and device for performing the connection method. Characteristic combination. [Simplified description of the drawing] Fig. 1 is a schematic longitudinal sectional view of the reactor according to the present invention, and other components of the apparatus according to the present invention; Fig. 2 shows a cross section of the reactor wall area according to Fig. 1; Fig. 3 is a schematic view showing the apparatus in an exemplary manner; [Explanation of main components] 1 Hopper 2 Floor discharge container 3 Grinding device 4 Reservoir (process water) 5 Catalyst 6 Mixing container 7 Feeding device 8 feeding the culture vessel 9 feeding apparatus 10 further device 14 of the mixing container 15 a schematic view of FIG. 4 shows the catalyst; and still another schematic view of the display apparatus 5. 201118162 17 Conveying device 18 Heat exchange unit 19 Reactor, induction device 20 Mixing or agitating device 21 Feeding device 22 Heat exchange device 23 Double wall, heat exchange unit 24 Second reactor 25 Heat exchange unit, liquefaction container 26 Liquefaction container , solid-liquid separation device 27 heat exchanger, reservoir 29 liquefaction vessel 30 solid-liquid separation device 31 reservoir 91

Claims (1)

201118162 七、申請專利範圍: 1. 一種用於由水及一含碳成份之固-液混合物產生並處理材料 或燃料、腐殖質、梅納德或類似反應物之方法’其中該固_液混人 物係在超過100°c之溫度及超過5巴(巴)之壓力下處其特 於: 、 起始物質係於至少十分之六的反應時間經由一熱交換器連續 饋入一第一反應器内,且該反應混合物以批量模式進入」下一^ 反應器,且反應產物於至少十分之六的反應時間由一最後反應 連續釋出。 2. 如申請專利範圍第1項所述之方法,其中一批量至少為個別 先刖反應器的10至25之質量百分比或是至少25之質量百&amp;比的 反應器容量》 3. 如申請專利範圍第1項或第2項所述之方法,其中用於避免 返混之一批量係保留在一封閉式反應器中至少百分之一的反應時 間’該封閉式反應器在流動方向上設置至少在該第一反應器之^。 4. 如申請專利範圍第3項所述之方法,包含經由二壓力閥 (pressure valve)或關閉閥(shut_〇ff valve)等封閉組件控 式反應器之封閉。 j 5. 如申請專利範_ 1項至第4項之其中一項所述之方法,其 中在^留時_間…批不超過6〇%之容量係饋人該封閉式 反應器。 6. 如申請專利範圍第i項至第5項之其中一項所述之方法,其 中具有相似長度之殘餘反應時間的複數批量,從至少兩個反器 合併起來進入下一個反應器。 &quot; 7. 如申請專利範圍帛6項所述之方法,其中該合併批量的殘餘 反。應時間#偏離超職等被合併之批量之最長殘留反應時間的 8. 如申請專利範圍帛!項至第7項之其令一項所述之方法,其 中該最後反應器為另一熱交換器。 9. 如申請專利範圍帛i項至第8項之其中一項所述之方法,其 92 201118162 ^熱交換器可以是具有調和系統之管式反應器、雙管熱交換器、 管束式(tubular bundle)熱交換器或一板式熱交換器或上述之組合。 10. 如申請專利範圍第1項至第9項之其中一項所述之方法,其 中用於加熱該起始物質之熱交換器在至少十分之六的反應時間由 該起始物質流經。 11. 如申請專利範圍第8項所述之方法,其中用於冷卻該反應混 合物之該另一熱交換裝置在至少十分之六的反應時間由該起始物 質流經。 12·如申請專利範圍第1項至第11項之其中一項所述之方法,其 中虽該反應混合物被導引由一反應器流動至下一個反應器時,該 反應混合物被導引通過·—熱交換器。 13.如申請專利範圍第1項至第12項之其中一項所述之方法,其 中該反應混合物被導引通過一熱交換器以減壓(decompressio 如申請專利範圍帛項所述之方法,其中該熱交換器在至少 2分之六的反麟間由反應參無流經聽為觀應混合物減 15.如申請專利範圍帛】項至第14項之其中一項所述之方法,盆 中該熱交換⑽由數侧貞似單元構成及/或具有模喊構。’、 :==5=項所述之方法’其中該熱賴器之該等 項所述之方法’其中該模組 18. ^申請專利範圍第i項至第17項之其中一項所述 該管式反應器的調和系統(temperi 、 2申請專利範圍第18項所述之方法,其中 經該管式反應器之該雙層壁之中間空間。”、戰’丨質係机 20·如申請專利範圍帛19項所述之方法 熱油、水蒸汽或是製程水(p聰ss water)。〜、'此载體)丨質為 21.如申請專利範圍第19項或第2〇項 熱能載體介質係組合起來。 玫之方法,其中不同的 93 201118162 22.如申請專利範圍第19項至第21項之其中一項所述之方法, 其中流經該熱交換器之熱能載體介質的最終溫度係介於6〇 350°C之間。 23. 如申請專利範圍第15項至第22項之其中一項所述之方法, 其中該熱交換器係由不同的模組、單元或是區段所構成。 24. 如申凊專利範圍第23項所述之方法,其中在該熱交換器之第 一區塊或是第一模組的溫度為仞它至1〇〇°c或是⑻:至12〇它, 在第二。區段或是第二模組之溫度介於丨㈨力及14〇〇c之間或是介 於120。(:及16(TC之間,在第三區段之溫度介於14(rc及丨⑽它之 間巧介於160°C及200。(:之間,及在第四區段之溫度介於丨奶它及 220°C之間、20(TC及24(TC之間或是介於240〇C及350。(:之間。 25. 。如申,專利範圍第22項或第23項所述之方法,其中該熱交 f器之該。等單元、模組或區段係串聯連接以使在到達例如為;2〇 至26(TC之高溫或是峰值溫度之後,固·液混合物的溫度 為較低的入口溫度或是出口溫度。 I6·如申請專利範圍第1項至第25項之其中一項所述之方法,豆 。中該熱交換器係配置有一保持通道,使得溫度可以維 1 C至8。〇之一致位準。 27.如申請專利範圍第1項至第26項之其中一項所述之方法,其 =在該反舰合物在通過熱交換ϋ之後,該反航合物係導入^ $搜動(stirring)或混合系統之反應器,或是高度至少為‘ 兩倍之反應器以混合或是分散。 申請專利範圍帛1項至第27項之其中一項所述之方法,其 〒該等成份由起始物質、水祕化劑組成。 t如申請專利範圍®1項至第28項之其中一項所述之方法,其 化批量的胸咖綱係收喊份、反敲物、製程水或i 如申請專利範圍第Μ項所述之方法,其中在至少百分之 =留時間㈣該等成份、反應產物、製程水或該催化劑。 如申請專利範圍第29項或第30項所述之方法,其中在一批 94 201118162 量在該反應器的滯留時間期間,在至少百分之一的滯留時間加入 反應產物、製程水或催化劑。 32. 如申凊專利範圍第31項所述之方法,其中係處理所加的製程 水。 33. 如申請專利範圍第32項所述之方法,其中所加的製程水的處 理包含至少一固-液分離或其他水調整措施。 34. 如申凊專利範圍第1項至第33項之其中一項所述之方法,其 中該方法係在排除氧氣下進行。 、 35. 如申請專利範圍第1項至第34項之其中一項所述之方法,其 中由水及含碳成份組成之該固_液混合物的處理為水解。 36. —種根據如申請專利範圍第丨項至第35項之其中一項所述之 方,所製成之可泵送祕财液或齡散物,其巾藉由溫度超過 l〇〇°C及壓力超過5巴之條件下處理水及含碳成份之固-液混合物 產生該可泵送燃料懸浮液或分散物,其特徵在: 山於該懸浮液或該分散物包含至少4〇%之固體量及至少的 碳含量。 37 一種根據如申請專利範圍第丨項至第35項之其中一項所述之 方,製成之附加的浮液或該分散物,其中藉由在溫度超過1〇〇它 及壓力超過5巴之條件下處理水及含碳成份之固_航合物產生 ^洋液或分散物’且_加_浮液或分散物用以製造 材,其特徵在於: 八,懸浮液或該分散物包含至少4〇%之固體量及至少5〇%的碳 !!二種利用水及-含碳成份ϋ混合物作為起始物質或附 =物質^產生隔熱材料及/或陶兗材料之方法,其中在溫度超過 00 C及麗力超過5巴之條件下處理該固_液混合物,其特徵在於 減份的各細含量,該固·液混合的硫及/或灰份 3日 申請相細第38項所述之方法,其帽混合物為酸性, 且陶瓷材料係藉由鹼性溶膠(sol)產生。 Θ文注 95 201118162 40. 如申請專利範圍第37項所述之方法,1中以 (sol-gel)法细騎崎細魄漏,其 酸性懸浮㈣狀起始輯錄序。 爾^膠中加入 41. 如申請專利範圍第39項或第4〇項所述之方法,其中 二^㈣該溶膠包含有滅無機魏鹽(Silieate)l二t 餐敎杨料絲_水玻璃 如申請專利範圍第41項或第42項所述之方法 有碳化合物及矽酸鹽化合物之凝膠。 ϋ3 ===第43瓣檐,包含加麵勝至形成 利侧44細之方法,包含細碳切氣趙 牴如申請專利範圍f44項或第45項所述之方法,其中 矽氣體滲透既有的多孔性模型。 47. 如申請專繼in第46項所述之方法,其中賴型包含石墨。 48. 如申請專利範圍第!項至第47項之其中一項所述之方法,其 中所製成的材料為碳化矽,特別是指碳化矽或是矽碳化矽(SiSicj。 =· 一種麟處•舰合物之裝置,制_液混合物為水及含 碳成份之固-液混合物,該裝置在超過1〇〇〇c之溫度及超過5巴之 壓力下處理該固-液混合物,該裝置包含一反應器,其特徵在於: 一進裝置包含一泵用以輸送具有固體含量係至少為10質量 百刀比或至15質量百分比之固-液混合物,或一熱交換器,其 中管軸對水平面的角度量大於1〇度。 ' ' 一種用於處理固-液混合物之裝置,該固-液混合物為水及含 ,成份之固-液混合物,該裝置在超過1〇(rc之溫度及超過5巴之 壓力下處理該固-液混合物,該裝置包含一反應器,其特徵在於: 一水解裝置包含一泵用以輸送具有至少】〇質量百分比或至少 15質量百分比之一固體含量之一固_液混合物,或一熱交換器, 96 201118162 其中管軸對水平面的角度量大於10度。 51. 如申請專利範圍第49項或第50項所述之裝置,其中該果為 偏心式螺旋泵(eccentric spiral pump)或是活塞式泵(piston pui^ : 52. 如申請專利範圍第51項所述之裝置,其中該泵係為1〇 130巴之壓力設計。 53. 如申請專利範圍第49項至第52項之其中一項所述之裝置, 其中該熱交換器係由至少60%之垂直管件構成。 54·如申請專利範圍第49項至第53項之其中一項所述之装置, 其中該熱父換器用以輸送具有3%至50%之固體含量且主要由生 物質構成之該固-液混合物,該生物質具有木質 (lignocellulose)及/或含澱粉之材料。 + * μ.如甲堉寻利乾圍第49項至第54項之其中一項所述之 其中該熱父換器係設計為用於60¾至3〇〇°C之溫度,或至^、一 組或一單元為用於2〇〇。(:至3〇〇°C之溫度。 夕 56·如申請專利範圍帛49項至第%項之其中一項所述 、中該熱父換器係設計為用於10巴至丨2〇巴之壓力,或、 模組或一單元為用於60巴至12〇巴之壓力。 ^夕 57·如申請專利範圍第49項至第56項之其中—項所述之 熱交換器或至少—模組或—單元係設計為用於高達250 以第57項之其中-項所述之震置, 防“質接觸,該管件係*耐熱及防飯及 59. 接觸裝置,其中該熱交換器與介質 二述之裝置,其中該熱交換器與介質 97 201118162 6】.如申請專利範圍第49項至第60項之其中一項所 f中熱交換H為具有調和系統之管式反應H、雙細^ ’ $束式(tubular bundle)熱交換器或板式熱交換器或上述、之^且人°。、 62.申請專利範圍第49項至第61項之其中一項裝口 中該熱交換器由數個類似單元構成及/或具有模組結構。裝罝其 L3二訧第62項所述之裝置’其—該熱交換器之該等 6單4元==;:==工第63項所述之*置’其,該模組 如t請專利範圍第49項至第64項之其中一項所述之裝置, 其中該管式反應器的調和系統係由雙層壁構成。 66.如申請專利範圍f65項所述之裝置,其 過該管式反應H之之Μ雜。 讎〃買係通 如申請專利範圍帛66項所述之裝置,其中該熱能 熱油、水蒸汽或是製程水。 Μ ”買為 68.如申請專利範圍第66項或第67項所述之裝置,其埶 換器為了不同的熱能載體介質所設計。 夂、、、 69·如申請專利範圍第66項至第68項之其中一項所述之裝置, 熱交換器是為了熱能載體介質之最終溫度為⑹它及35〇ΐ 70. 如申^專利範圍第66項至第69項之其中一項所述之裝置, 其中該熱父換器係由不同的模組、單元或是區段所構成。 71. 如申請專利範圍第5〇項所述之裝置,其中該水解裝置包含一 反壓栗(counterpressure pump&gt;。 72. —種用於產生燃料、含碳材料或物質、腐殖質、梅納德或類 似反應產物之方法,包含在超過1〇〇°c之溫度及超過5巴之壓力 下處理水及含石反成份之固_液混合物,例如生物質,其特徵在於: 該處理係連續實行。 、、’ 73. 如申凊專利範圍第72項所述之方法,其中該處理至少持續一 小時及/或包含生物質的加工及/或反應產物、中間產物、次級產 98 201118162 物及/或最終產物的調整。 74. ^申請專利範圍第72項或第73項所述之方法,其中談 係調整。超過16G°C,較佳是在16〇。(:及綱之間,尤佳是在 及225 C之間及/或以自動控制的方式進行調整。 75. 如申請專利範圍第72項至第74項之其中一 f中該壓力係調整至少7巴,較佳是在1G巴及34巴之間方^ 疋在10巴及17巴之間、18巴及26巴或27巴及34巴, 瓜如申請專利範圍帛π項至第75項之其中一項所述 其中該處理時間至少2小時’雛是3小啦6(M、時,尤佳 小時至30小時或3卜丨、啦6(M、時’尤妓 13小時至24小時。 J 77. 如申請專利範圍帛72項至第76項之其中一項所述之 其中根據生物f的種類及/或需要的反應產物^擇處理。 78. 如申請專利範圍第72項至第77項之其中之一項所述之 法’其中特別是糊除水、研磨、以添加物預培養、混 熱以預處理該生物質。 4疋預 ,以酸 79.如申請專利範圍第78項所述之方法,其中在處理之前 性pH值培養該生物質。 80.如申請專利範圍第79項所述之方法,其中該pH值係低於6, 較佳是低於5,此外較佳是低於4,尤佳是低於3,特別的是低於 2 ° _ 、 81. 如申請專利範圍第72項至第8〇項之其中一項所述之方法, 其中在處理之前、當中或之後係將該生物f碎磨,較佳是切細 或研磨。 ' 82. 如申請專利範圍第81項所述之方法,其中該碎磨的生物質的 顆粒大小係小於10公分’特別較佳的是小於丨公分,尤其是小於 2毫米。 八 、 83. 如申請專利範圍第72項至第82項之其中一項所述之方法, 其中在處理之前及/或當中加入至少一催化劑於該生物皙,。 84. 如申請專利範圍第83項所述之方法,其中該催化劑由數個不 99 201118162 同成伤構成’該等成份一起形成催化劑混合物。 85·如申請專利範圍第83項或第84項所述之方法,其中該催化 劑係為無機酸,較佳是硫酸,及/或是單體、二元或三元綾酸,較 佳是酒石酸或禪樣酸。 86. 如申請專利範圍第85項所述之方法,其中該酸係作為催化劑 且同時在培養步驟中用以調整酸性pH值。 87. 如申請專利範圍第83項至第86項之其中一項所述之方法, 其中該催化劑包含一或數種金屬及/或金屬化合物。 88. 如申請專利範圍第87項所述之方法,其中該金屬、及/或金 屬化合物包含至少一種在元素週期表中之亞族ia、na、iva、va、 Via及Vila之過渡金屬,較佳是鎳、鈷、鐵、銅、鉻、鎢、鉬 鈦,尤佳的是鐵。 〆 89·如申請專利範圍第83項至第88項之其中一項所述之方法, 其中該催化劑包含至少一生物催化劑,較佳是酵素(enzyme)、微 生物(micro organism)、植物細胞(vegetable cell)、動物細胞(animai cell)及/或細胞萃取物(cell extract) 〇 90. 如申請專利範圍第72項至第89項之其中一項所述之方法, 其中在處理步之前及/或處理期間混合該生物質,較佳是藉由 動、混合、懸浮及/或攪拌。 91. 請專利範圍第90項所述之方法,其中係使用一或數個混合裝 置用於混合,特別是不同混合裝置的組合,較佳的是至少一流體 喷射混合器(fluid jet mixer)、泵或一喷嘴(nozzle)。 92. 如申請專利範圍第72項至第91項之其中一項所述之方法, 其=在處理步骤之後係利用一乾燥器乾燥該反應產物,較佳是一 對流式乾燥器(convection drier)或接觸式乾燥器(contact drier)、尤 其較佳的是流動式(stream)及/或帶式(band drier)及/或流體化 無器(fluidized bed drier)。 93·如申請專利範圍第72項至第92項之其中一項所述之方法, 其中程序進行期間產生的製程水較佳是經由一固_液分離裝置回 收及/或加以清潔並使之返回至該反應混合物。 100 201118162 94·如申請專利範圍第93項所述之方法,其中該固-液分離裝置 係至少是一用於微過濾(micro filtration)、超過濾(ultra flirtation)、 奈米過遽(nanofiltration)及逆渗透法(reverse osmosis)之震置或是 上述各種裝置之組合’特別是具有陶兗過濾元件(ceramic element)及較佳的是旋轉盤(r〇tati〇n disk)及/或是離心式薄臈過濾 器(centrifugal membrane filter)。 95. 如申請專利範圍第72項至第94項之其中一項所述之方法, 其中以機械式、化學式及/或生物式清潔所產生的廢水。 96. 如申請專利範圍第72項至第95項之其中一項所述之方法, 其中利用機械式、化學式、及/或生物式方式清潔在處理、加工及 /或調整中所產生之廢氣。 97. 如申請專利範圍第72項至第96項之其中一項所述之方法, 其中該反應產物、中間產物、次級產物及最終產物包含泥煤(peat) 之燃料’從褐煤(brown coal)到類黑煤類燃料(black c〇aWike fUel)、腐殖質、梅納德或類似反應產物、含碳材料例如有毒物質 (damping substance)、奈米海綿(nano sponge)、奈米丸狀物(咖〇 pellet)、奈米纖維(nano flber)、奈米纜線(nan〇、活性炭MM coal)或吸附炭(sorption coal)、木炭取代材料(charc〇al material)、高度壓縮碳產物及材料,特別的是用於石墨及含石墨 或是近似石墨的產物的起始物質以及碳纖維及用於複合材料或纖 維複合材料(fiber compound material)之起始物質。 … 98. 如申,專利範圍第72項至第97項之其中一項所述之方法, 由水及含碳成份之固-液混合物中產生材料或燃料、腐殖質、梅納 德或類似反應產物,其中在超過1〇〇°c之溫度及超過5巴 六 處理該固-液混合物,其特徵在於: ⑽ 固續方式或以間隔方式在一薄膜反應器中從該 99. 如申請專利範圍第98項所述之方法,其中該薄膜反應器包含 至少一個用於固-液分離之裝置。 100. 如申請專利範圍第98項或第99項所述之方法,其中至少一 101 201118162 ,於固-液分離之裝置包含一粗濾及/或一細濾裝置或兩者之組 口,其可以結合在一過濾裝置内。 如申明,利範圍第98項至第100項之其中一項所述之方法, :=利用該薄膜反應器以選擇性的由反應混合物移除反應產物、 產物、次級產物及最終產物,以受控方式添加或移除析出物, 或疋增強析出物的接觸。 102士如申請專利範圍第98項至第1〇1項之其中一項所述之方法, 離作^連續的方式或是間隔的方式進行該薄膜反應11之固-液分 用Ϊ由水及含碳成份之固液混合物中水解及/或產生材 二痒腐殖質、梅納德或類似產物的方法,其中在超過1〇〇 經tb 超過5巴之壓力下處理該固_液混合物,其特徵在於: 人第一輪送線輸送相對於總體積具有25%至97%的固體 -势始物質並以平行或支線(Gffset)方式經由一第 i 3%&quot; — 果送103項或第104項所述之方法,其中非可 至反^器 製程水之蒸氣壓之壓力下由第—輸送線輸送 Μ法’其中·將非可泵送 應器的輸送裝輸送線加入至反 extruder)、偏心射裝置.雙重紋入式擠壓器(double screw Pump),分別配^ i^泵(eCCentnC Spiral PumP)、一活塞式泵(piston 雙重螺旋式螺严賴(一 _P_r)或是- 果送起始======法嚐中非可 至反應器且塗覆-來自該“;=5二;送線提供 102 201118162 範圍第103項至第107項之其中—項所述之方 法,/、中k供與加入的起始物質的質量產量比&amp; 1:2〇至 1:5 至 1:1 。 * 4 項之其中一項所述之方 109.如申請專利範圍第1〇3項至第1〇8 法’更包含使用其他輸送線。 110.如申請專利範圍第1G3項至第1G9項之其中一項所述之方 法,更包含共同使用其他裝置,例如儲存容器、碎磨裝置、混人 容器、定量給料製置、培養容器、輸送裝置、製程水容器 °、 熱交換器或是反應器。 111·如申請專利範圍第103項至第11〇項之其中一項所述之方 法其中在該第一輸送線中用於輸送固-液混合物之泵係設計以用 於固體含量至少5%至10%或是10〇/〇至25%。 ° 112. 如申請專利範圍第103項至第m項之其中一項所述之方 法’其中在該第二輸送線中用以輸送固-液混合物之泵為一偏心式 螺旋泵、一螺旋式位移(spiral displacement)或是一活塞式栗(pist〇n pump) ° 113. —種用於由水及含碳成份之固·液混合物中水解及/或產生材 料或燃料、梅納德或類似反應產物之方法,其中在超過1〇〇1之 溫度及超過5巴之壓力下處理該固-液混合物,其特徵在於: 該固-液混合物流經一熱交換器以加熱,其管軸相對於水平面 的角度量大於10度。 114. 如申請專利範圍第113項所述之方法,其中當該固_液混合物 通過進料裝置時,該固-液混合物之黏度係降低,且在程序的^點 係至少降低至該起始物質四分之三的黏度。 '‘’ 115 —種用於饋入反應器以由水及含碳成份之固_液混合物產生 材料或燃料、腐殖質、梅納德或類似反應產物的方法,其中在超 過100°c之溫度及超過5巴之壓力下處理該固-液混合物,其特徵 在於: Μ ^ 該固-液混合物流經一熱交換器以加熱’其管軸相對於水平面 的角度量大於10度。 103 201118162 116. 如申請專利範圍第113項至第115項之其中一 軸咖啊,此通過至少 117. 如申請專利範圍第115項或第116項所述之方法,其中去詨 經該熱交換器時係降低黏度’且該固-液ϋΐΐ 黏度在^序鱗點敍少降低至該紗材 二:申,圍第113項至第117項之其中一=之方 ^ ’其中該固·液混合物具有介於3%及35%之間之固體含量 介於35%及60〇/〇之間之固體含量。 〆 專利範圍第113項至第117項之其中一項所述之方 法,其中利用一泵將該固-液混合物導入該埶交換器。 120.如申請專利範圍第119項所述之方法,其中用以輸送該固_ 液混合物之該祕設制於至少5%至職或職至25%之固體 含量。 121.,如申晴專利範圍第η9項或第uo項所述之方法,其中用以 輸送該固-液混合物之栗及/或一反壓泵(c〇unterpressure pump)是 了偏心式螺旋泵(eccentric spiral pump)、一螺旋式位移(spiral displacement)或一活塞式果(piston pump) 〇 122. —種用於在超過100°c之溫度及超過5巴之壓力下處理水及 含碳成份之固•液混合物之裝置,包含一反應器’其特徵在於: 該裝置包含一進料裝置,其具有: a. —栗’用以輸送具有至少至Μ%之固體含量之固-液混 合物;及 b. 熱交換器,其管轴相對於水平面的角度量大於1〇度。 123. 如申請專利範圍第122項所述之裝置,其中該泵是一偏心式 spiral pump)或一活塞式聚(piston pump)。 124. 如申請專利範圍第122項或第123項所述之裝置,其中該泵 係為至少為10巴至130巴之壓力設計。 125. 如申請專利範圍第122項至第124項之其中一項所述之裝 置’其中該熱交換器由至少60%之垂直管件部件構成。 104 201118162 126. 如申請專利範圍第122項至第125項之其中_項所述之裝 置’其中用以傳送固-液混合物之該熱交換器係設計用於具有3% 至50/&gt;之固體3置、主要由包括木質纖維素⑴之生物 質所構成及/或含澱粉之材料。 127. 如申請專利範圍第122項至第126項之其中一項所述之裝 置,其中該熱交換器係設計用於之溫度,或至少_2 模組或一單元係用於2〇〇。(:至300。(:之溫度。 128. 如申請專利範圍第122項至第127項之其中一項所述之裝 置,其中該熱交換器係設計用於1〇巴至12〇巴之壓力,或至少一 模組或一單元係設計用於60巴至120巴之壓力。 129. 如申請專利範圍第122項至第128項之其中一項所述之裝 置,其中該熱父換器或至少一模組或一單元係設計用於高達25〇 °(:之溫度。 130. 如申請專利範圍第122項至第129項之其中一項所述之裝 置,其中該熱父換器與介質接觸之管件係由财熱及耐钮及防水材 成,例如為經塗佈之金屬,尤為責金屬、陶瓷材料或是琺瑯 131. 如申請專利範圍第122項至第130項之其中一項所述之裝 置,其中該熱父換器與介質接觸之管件係由耐餘材料構成。 132. 如申請專利範圍第122項至第131項之其中一項所述之裴 置,其中該熱交換器與介質接觸之管件係由不銹鋼構成,如奥乂 體鋼(austenitic steels)或是增加鉻及鉬含量之6、7及8族之鋼或者 由雙相不銹鋼(duplex steels)、銅-錄合金、高鉬含量之鎳合金/ 2.4610或鈦構成。 133. 如申請專利範圍第122項至第132項之其中一項所述之裴 置,其中該熱交換器為具有調和系統之管式反應器、一雙管件^ 交換器、管束式(tubular bundle)熱交換器或一板式熱交換器或ρ 之組合。 134. 如申請專利範圍第122項至第133項之其中一項所述之 置,其中該熱交換器係由數個類似單元構成及/或具有模組結構: 105 201118162 騎衛,㈣敝換器之該 她触換器之該 Μ如申請專利範圍第137項所述=層 流經該管式反應器之雙層壁的中〃中麻載體介質係 項所述之裝置,其中該熱载體介質為 ====:項所述之裝置,其中該熱 ΓϊΓϊί,圍第138項至第140項之其中-項所述之裝 最終&amp;度二3㈣了該熱載體介質介於_至戰之間之 7:T^tT:m 122 133 其中〜…、父換器由不同的模組、單元或是區段所構成。 143. 了種用於在超過觸^之溫度及超過5巴之壓力下處理水及 含碳成份之固-液混合物之裝置,包含一反應器,其特徵在於: 該裝置包含一水解裝置,其具有: 、 a. —泵’用以輸送具有至少10〇/〇至15%之固體含量之固-液混 合物;及 b. —熱交換器,其管軸相對於水平面的角度量大於1〇度。 144. 如申請專利範圍第143項所述之裝置,其中該水解裝置包含 一反壓系(counterpressure pump)。 145. 如申請專利範圍第143項或第144項所述之裝置,其中用於 輸送固-液混合物之該泵或反壓泵係為一偏心式螺旋泵(eccentric spiral pump)、一螺旋式位移(Spirai displacement)或一活塞式栗 (piston pump)。 146. 如申請專利範圍第143項至第145項之其中一項所述之裳 106 201118162 置’其中用於輸送固_液混合物之該泵或抗壓泵係為至少1〇巴至 130巴之壓力設計。 147·如申請專利範圍第143項至第146項之其中一項所述之裝 置,其中該熱交換器由至少60。/。之垂直管件部件構成。 148·如申請專利範圍第143項至第147項之其中一項所述之裴 置,其^用於輸送固_液混合物之該熱交換器是為了 3%至5〇%之 固體含重、主要由包括木質纖維素(lign〇cellul〇se)之生物質及/ 含澱粉之材料所設計。 — 149. 如申請專利範圍第143項至第148項之其中一項所述之裝 置,其中該熱交換器是為了 60。(:至30(TC之溫度設計,或至少一 模組或一單元係為2〇〇。(:至300X:之溫度所設計。 150. 如申請專利範圍第143項至第149項之其中一項所述之裝 置,其中該熱交換器是為了 10巴至12〇巴之壓力設計,或至少_2 模組或一單元係為60巴至120巴之壓力所設計。 151. 如申請專利範圍第143項至第15〇項之其中一項所述之裝 置,其中該熱交換器或至少一模組或一單元是為了高至25〇。 溫度所設計。 152. 如申請專利範圍第143項至第151項之其中—項所述之裳 置,其中該熱父換器與介質接觸之管件係由耐熱及财钱及防水 料構成,例如經塗佈之金屬,尤其是貴重金屬、陶瓷材料 瑯材質。 153. 如中請專利範圍第143項至第152項之其中—項所述之 置,其中該熱父換器與介質接觸之管件係由耐餘材料構成。 154. 如申請專利範圍第143項至第153項之其中一項所述之 置,其中該熱交換器與介質接觸之管件係由不銹鋼如奥氏二 (austenitic steels)或是增加鉻及鉬含量之6、7及8族之鋼構成,$ 者是由雙相不銹鋼(duplex steels)、銅-鎳合金、高鉬含量 : 金,如2.4610或鈦構成。 # σ 155.如申請專利範圍第143項至第154項之其中—項所 置,其中該熱交換器係具有調和系統之管式反應器、一雙管件^ 107 201118162 父換器、管束式(tubular bundle)熱交換器或一板式熱交換器或上述 之組合。 156.如申請專利範圍第143項至第153項之其中一項所述之裝 置’其中該熱交換器由數個類似單元所構成及/或具有模組結: 項所述之裝置’其中該熱交換器之該 158·=請專利範圍第143項至第157項之其中一項所述之裝 ,其中該熱交換器之該等模組單元以空間鄰近的方式配置。 申,利範圍第143項至第158項之其中—項所述 置,其中該管式反應器的調和系統由雙層壁構成。 16==請專利麵第159項所述之裝置,其中熱能載體 〜經該管狀反應器之該雙層壁之中間空間。 糸 請ΐ利翻第16。項所述之裝置,其中該熱能載體介質 為熱油、水蒸汽或是製程水。 負 162.=請專利麵第143項絲161項之其中—項所述之 置,其中該熱交換器為了不同的熱能載體介質所設計。 衣 1 晉63:ίΓί!,圍第143項至第162項之其中-項所述之! 之最ί溫ί 為了該熱賴體介質介於6(rc至350t之^ 164.如申請專利範圍第143項至第155 置,其中該熱_由不同的模組、單元或是區之袭 腐猪二種^_水及含碳成份之固_液混合物產生_或燃料、 扣、梅納德或類似反應產物之方法,其中在超過1〇〇ί之 度^超過5巴之壓力處理該固-液混合物,其特徵在於1心皿 濃縮(enriched)製程水係部份用於起始物質 t,·液混合物產生可紐性,用於在反應混^= | 口 Ϊ回=免備之反應器中塗佈或附加至既有的起始物質,5 的程序,作為熱載體介質用於例如在設備内 仙 序或是作為一促進劑(fertilizer)成份。 一他 敗如申請專利範圍第⑹項所述之方法,其中利用固-液分離方 108 201118162 式實行濃縮。 專利細第165項所述之方法,其中利用水的蒸發作 圍第165項至第167項之其中-項所述之方 八中在’農縮期間移除至少1%至10%之水。 利範圍第165項至第168項之其中一項所述之方 法八中在濃縮期間移除至少1〇〇/〇之水。 『·ΐί請專利範圍第165項至第169項之其中一項所述之方 L 程水直接由進行的程序移除,或由用於未處理之製 私水且為了祕而設計為—壓力容H之酿贿ϋ中移除。 171. 如申請專利範圍帛165項至第17〇項之其中一項所述之方 法,其中由製程水的蒸發得到的水蒸汽係用於程序之其它部份, 例如在進入熱交換器之前用於加熱起始物質、經由熱交換程序加 熱熱油及/或用於操作乾燥反應產物之裝置,如空氣擾流碾磨機。 172. —種由水及含碳成份之固_液混合物中產生材料或燃料、腐 瘦質、梅納德或類似反應物之方法所產生之濃縮製程水的用途, 其中固-液混合物係超過l〇(TC之溫度以及超過5巴之壓力下處 理’該濃縮製程水係用於: 、預培養、預熱該起始物質,產生可泵送固-液混合物、在反應 混合物中佔有主導地位、在設備之反應器中塗覆既有的起始物質 或與之混合,用於返回該進行程序作為熱載體介質及/或作為促進 劑成份。 173. 如申請專利範圍第172項所述之用途,其中該製程水係在個 別使用之溫度以上1°C至5(TC之溫度下得到。 174. 如申請專利範圍第172項所述之用途,其中額外使用以25。〇 至5(TC、5(TC至70°C或7〇°C至99°C之溫度加熱的製程水。 175. —種用於由水及含碳成份之固-液混合物產生材料或燃料、 腐殖質、梅納德或類似反應產物並將之處理的裝置,其中係在超 過100°C之溫度及超過5巴之壓力下處理該固-液混合物,其特徵 在於: 109 201118162 回至該固 一裝置’用於濃縮回收製程水及用於使濃縮製程水返 -液混合物。 更包含用以固-液分離 176.如申請專利範圍第175項所述之裝置, 之裝置。 177. 如申請專利範圍第175項所述之裝置,更包含一蒸發器。 178. 如申請專利範圍第175項至第177項之其中一‘裝 置’更包含用於未處理之製程水、形成為壓力容器之隔熱貯存器: 179. —種用於由水及含碳成份之固_液混合物中產生材料^燃 料、腐殖質、梅納德或類似反應產物並在超過1〇〇〇c之溫度及&amp; 過5巴之壓力下將之處理的設備,其特徵在於: 又 該設備下列裝置: a. —進料裝置包含: 合物; /或 泵’用以輸送具有至少10%至15〇/〇之固體含量之固_液混 熱父換器,其管軸相對於水平面的角度量大於度;及 少兩個反鮮’其巾之-個反應魏置有-義或混合系 統或具有至少2:1之高度-徑度比。 圍第179項所述之設備,其中該熱交換器包含 第53項至第64項之其中一項所述之特徵。 請專繼Μ Μ縣第⑽韻述之設備 ,更包含一 專利範圍第181項所述之設備,其中該減壓裝置包含 、有調和系統之反應器或-敏換器或兩者的組合。 110201118162 VII. Patent application scope: 1.  A method for producing and treating a material or fuel, humus, Maynard or the like from a solid-liquid mixture of water and a carbonaceous component, wherein the solid-liquid mixed character is at a temperature exceeding 100 ° C and At a pressure of more than 5 bar (bar), the starting material is continuously fed into a first reactor via a heat exchanger at a reaction time of at least six tenths, and the reaction mixture is in batch mode. The reactor is passed to the next reactor, and the reaction product is continuously released from a final reaction at a reaction time of at least six tenths. 2.  The method of claim 1, wherein one batch is at least 10 to 25 mass percent of the individual helium reactor or at least 25 mass percent &amp; ratio reactor capacity.  The method of claim 1 or 2, wherein the batch used to avoid backmixing is retained in a closed reactor for at least one percent of the reaction time 'the closed reactor is flowing The direction is set at least in the first reactor. 4.  The method of claim 3, comprising closing the control reactor via a closed component such as a pressure valve or a shut-off valve. j 5.  The method of any one of the preceding claims, wherein the capacity of the batch is not more than 6%, and the capacity of the batch is fed to the closed reactor. 6.  A method according to any one of claims 1 to 5, wherein the plurality of batches having residual reaction times of similar length are combined from at least two reactors into the next reactor. &quot; 7.  The method of claim 6, wherein the residual of the combined batch is reversed. Time ## Deviation from the longest residual reaction time of the batch being merged  Such as the scope of application for patents! The method of claim 7, wherein the last reactor is another heat exchanger. 9.  The method of claim 11, wherein the heat exchanger can be a tubular reactor with a blending system, a double tube heat exchanger, a tubular bundle, or the method of any one of the claims. A heat exchanger or a plate heat exchanger or a combination of the above. 10.  The method of any one of clauses 1 to 9, wherein the heat exchanger for heating the starting material flows through the starting material at a reaction time of at least six tenths. 11.  The method of claim 8, wherein the other heat exchange means for cooling the reaction mixture flows through the starting material at a reaction time of at least six tenths. The method of any one of clauses 1 to 11, wherein the reaction mixture is guided through the reaction mixture as it is directed from one reactor to the next. - heat exchangers. 13. The method of any one of clauses 1 to 12, wherein the reaction mixture is directed through a heat exchanger for decompression (decompressio, as described in the scope of the patent application, wherein The heat exchanger is separated from the reaction mixture by at least two-sixth of the reaction. The method of any one of the preceding claims, wherein the heat exchange (10) is constituted by a number of side analogous units and/or has a model structure. </ RTI> </ RTI> <RTIgt; </ RTI> <RTIgt; </ RTI> <RTIgt; </ RTI> <RTIgt;  The method of the tubular reactor of the present invention, wherein the method of the tubular reactor of the method of claim 18, wherein the double of the tubular reactor is The middle space of the layer wall. ", war" enamel machine 20 · The method described in claim 19, hot oil, steam or process water (p ss water). ~, 'this carrier The enamel is 21. For example, the scope of the patent application, item 19 or item 2, of the thermal energy carrier medium is combined. The method of rose, which is different 93 201118162 22. The method of any one of clauses 19 to 21, wherein the final temperature of the thermal energy carrier medium flowing through the heat exchanger is between 6 and 350 °C. twenty three.  The method of any one of clauses 15 to 22, wherein the heat exchanger is composed of different modules, units or sections. twenty four.  The method of claim 23, wherein the temperature of the first block or the first module of the heat exchanger is 仞 it to 1〇〇°c or (8): to 12〇, In the second. The temperature of the segment or the second module is between 丨(9) force and 14〇〇c or 120. (: and 16 (between TC, the temperature in the third section is between 14 (rc and 丨 (10). It is between 160 ° C and 200. (: between, and the temperature in the fourth section丨 它 它 it and 220 ° C, 20 (TC and 24 (TC between or between 240 〇 C and 350. (: between. 25.  . The method of claim 22, wherein the heat transfer device is the same. The units, modules or sections are connected in series such that the temperature of the solid-liquid mixture is a lower inlet or outlet temperature after reaching, for example, 2〇 to 26 (the high temperature or peak temperature of the TC.) The method of any one of claims 1 to 25, wherein the heat exchanger is provided with a holding passage so that the temperature can be maintained from 1 C to 8. The uniform level of the crucible. . A method according to any one of the preceding claims, wherein, after the anti-ship compound is passed through a heat exchange crucible, the anti-flight compound is introduced into a stir or The reactor of the mixing system, or a reactor at least twice the height to mix or disperse. The method of any one of claims 1 to 27, wherein the components consist of a starting material and a water-clearing agent. t. The method of claiming one of the scopes of the patent scopes 1 to 28, the batch of the chest coffee system is shouting, anti-knocking, process water or i as described in the scope of the patent application. The method wherein the component, the reaction product, the process water or the catalyst are at least at a percent of time. The method of claim 29 or claim 30, wherein the reaction product, process water or catalyst is added during a residence time of the reactor during a residence time of at least one percent during a residence time of the batch of 94 201118162. 32.  The method of claim 31, wherein the added process water is processed. 33.  The method of claim 32, wherein the processing of the added process water comprises at least one solid-liquid separation or other water conditioning. 34.  The method of any one of clauses 1 to 33, wherein the method is carried out under exclusion of oxygen. 35.  The method of any one of claims 1 to 34, wherein the treatment of the solid-liquid mixture consisting of water and a carbonaceous component is hydrolysis. 36.  - a pumpable secret liquid or a granulated substance prepared according to one of the scopes of the application of the scope of the application of the third to the 35th, wherein the temperature of the towel exceeds 10 ° C and A solid-liquid mixture of treated water and a carbonaceous component at a pressure of more than 5 bar produces the pumpable fuel suspension or dispersion characterized by: a mountain comprising at least 4% solids in the suspension or the dispersion Amount and at least carbon content. 37 An additional float or dispersion made according to one of the methods of claim 5 to 35, wherein the temperature exceeds 1 Torr and the pressure exceeds 5 bar Under the condition of treating water and carbonaceous components, the solids or dispersions and the liquid or dispersion are used to manufacture materials, characterized in that: VIII, the suspension or the dispersion comprises At least 4% by weight of solids and at least 5% by weight of carbon!! Two methods of using a mixture of water and a carbonaceous component as a starting material or a substance to produce a heat insulating material and/or a ceramic material, wherein Treating the solid-liquid mixture under the condition that the temperature exceeds 00 C and the Lili exceeds 5 bar, which is characterized by the fine content of the reduced portion, and the solid-liquid mixed sulfur and/or ash portion is applied for the third day. In the method described, the cap mixture is acidic and the ceramic material is produced by an alkaline sol (sol). Θ文注 95 201118162 40.  For example, in the method described in claim 37, the sol-gel method is used to sneak a fine smear, and the acid suspension (four) is initially recorded. Add to the glue  The method according to claim 39 or 4, wherein the sol comprises the inorganic salt (Silieate), the second meal, the sage, and the water glass, as claimed in claim 41. Or the method according to item 42 is a gel of a carbon compound and a phthalate compound. Ϋ3 === The 43rd 檐 檐 檐 檐 檐 檐 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第 第Porosity model. 47.  The method of claim 46, wherein the smear type comprises graphite. 48.  Such as the scope of patent application! The method according to any one of item 47, wherein the material produced is tantalum carbide, in particular, tantalum carbide or tantalum carbide (SiSicj. = · a type of equipment; The liquid mixture is a solid-liquid mixture of water and a carbonaceous component, the apparatus treating the solid-liquid mixture at a temperature exceeding 1 〇〇〇c and a pressure exceeding 5 bar, the apparatus comprising a reactor characterized in that : The inlet device comprises a pump for conveying a solid-liquid mixture having a solid content of at least 10 mass % or to 15 mass percent, or a heat exchanger wherein the tube axis is at an angle greater than 1 degree to the horizontal plane ' ' A device for treating a solid-liquid mixture, which is a solid-liquid mixture of water and a component, which is treated at a temperature of more than 1 Torr (at a temperature of rc and a pressure of more than 5 bar) a solid-liquid mixture comprising a reactor, characterized in that: a hydrolysis device comprising a pump for delivering a solid-liquid mixture having a solid content of at least 〇 mass percent or at least 15 mass percent, or a heat Switch, 9 6 201118162 The angle of the tube axis to the horizontal plane is greater than 10 degrees.  For example, the device described in claim 49 or 50, wherein the fruit is an eccentric spiral pump or a piston pump (piston pui^: 52.  The apparatus of claim 51, wherein the pump is designed to have a pressure of 1 〇 130 bar. 53.  The apparatus of any one of clauses 49 to 52, wherein the heat exchanger is composed of at least 60% of vertical tubes. 54. The apparatus of any one of clauses 49 to 53 wherein the hot parent exchanger is for conveying the solid-liquid having a solid content of 3% to 50% and consisting mainly of biomass. A mixture of lignocellulose and/or starch-containing material. + * μ. For example, the hot parent converter is designed to be used for a temperature of 603⁄4 to 3 °C, or to a group, or a group, as described in one of items 49 to 54 of the The unit is for 2〇〇. (: to a temperature of 3 ° ° C. 夕 56 · as claimed in one of the 49 to the first item of the patent scope, the hot parent converter is designed for 10 bar to 丨 2 〇 The pressure, or module, or a unit is used for a pressure of 60 to 12 bar. ^57. The heat exchanger according to item 49 to item 56 of the patent application scope or at least - The module or unit is designed to be used for up to 250 parts of item 57, to prevent "quality contact, the tube is * heat resistant and anti-rice and 59.   Contact device, wherein the heat exchanger and the medium are described, wherein the heat exchanger and medium are 97 201118162 6]. For example, in one of the 49th to 60th claims, the heat exchange H is a tubular reaction H with a blending system, a double bundle, a bundle bundle heat exchanger or a plate heat exchanger. Or the above, and the person °. 62. In one of the 49th to 61st applications of the patent application, the heat exchanger is composed of a plurality of similar units and/or has a modular structure. Mounting the device described in item 62 of the L3 ' ' ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ ─ The apparatus of any one of clauses 49 to 64, wherein the blending system of the tubular reactor is composed of a double wall. 66. A device as claimed in claim f65, which is noisy by the tubular reaction H.雠〃 系 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如Μ "Buy for 68. The device of claim 66 or 67 is designed for different thermal energy carrier media.夂,,, 69. As claimed in one of the items 66 to 68 of the patent application, the heat exchanger is for the final temperature of the thermal energy carrier medium (6) and 35 〇ΐ 70.  The device of any one of clauses 66 to 69, wherein the hot parent converter is composed of different modules, units or sections. 71.  The device of claim 5, wherein the hydrolysis device comprises a counterpressure pump (72.  a method for producing a fuel, a carbonaceous material or substance, a humus, a Maynard or a similar reaction product, comprising treating the water and the stone-containing anti-ingredient at a temperature of more than 1 ° C and a pressure of more than 5 bar A solid-liquid mixture, such as biomass, characterized in that the treatment is carried out continuously. ,,’ 73.  The method of claim 72, wherein the treatment lasts for at least one hour and/or includes adjustment of biomass processing and/or reaction products, intermediates, secondary products 98 201118162 and/or final products. . 74.  ^ The method described in Article 72 or Item 73 of the patent application, in which the adjustment is made. More than 16G ° C, preferably at 16 。. (Between and between classes, especially between 225 C and/or with automatic control.)  The pressure is adjusted to at least 7 bar, preferably between 1G and 34 bar, between 10 and 17 bar, 18 bar, in one of the items in the 72nd to 74th paragraphs of the patent application. 26 bar or 27 bar and 34 bar, such as the scope of application for patents 帛 π to 75, wherein the processing time is at least 2 hours 'the chick is 3 small 6 (M, hour, especially good hours to 30 hours or 3 divination, 6 (M, when 'yous 13 hours to 24 hours. J 77.  As described in one of the claims 72 to 76, the treatment product is selected according to the type of the organism f and/or the desired reaction product. 78.  The method of any one of claims 72 to 77, wherein in particular, paste water, grinding, pre-incubation with an additive, and heat mixing to pretreat the biomass. 4 疋 pre-, with acid 79. The method of claim 78, wherein the biomass is cultured at a pre-treatment pH. 80. The method of claim 79, wherein the pH is less than 6, preferably less than 5, more preferably less than 4, particularly preferably less than 3, and especially less than 2 °. _ , 81.  The method of any one of clauses 72 to 8, wherein the organism f is ground, preferably shredded or ground, before, during or after the treatment. ' 82.  The method of claim 81, wherein the milled biomass has a particle size of less than 10 cm', particularly preferably less than 丨 cm, especially less than 2 mm. Eight, 83.  The method of any one of clauses 72 to 82, wherein at least one catalyst is added to the biopterin before and/or during the treatment. 84.  The method of claim 83, wherein the catalyst consists of a plurality of non-99 201118162 identical injuries. The components together form a catalyst mixture. 85. The method of claim 83, wherein the catalyst is a mineral acid, preferably sulfuric acid, and/or a monomer, a binary or a ternary tannic acid, preferably tartaric acid. Or zen sour. 86.  The method of claim 85, wherein the acid is used as a catalyst and simultaneously used to adjust the acidic pH in the culturing step. 87.  The method of any one of claims 83 to 86, wherein the catalyst comprises one or more metals and/or metal compounds. 88.  The method of claim 87, wherein the metal and/or metal compound comprises at least one transition metal of the subgroups ia, na, iva, va, Via, and Vila in the periodic table, preferably Nickel, cobalt, iron, copper, chromium, tungsten, molybdenum and titanium, and especially iron. The method of any one of clauses 83 to 88, wherein the catalyst comprises at least one biocatalyst, preferably an enzyme, a micro organism, or a plant cell (vegetable) Cell), animal cells (animai cell) and / or cell extract (cell extract) 〇 90.  The method of any one of clauses 72 to 89, wherein the biomass is mixed prior to and/or during the treatment step, preferably by moving, mixing, suspending and/or stirring. 91.  The method of claim 90, wherein one or more mixing devices are used for mixing, in particular a combination of different mixing devices, preferably at least one fluid jet mixer, pump or A nozzle (nozzle). 92.  The method of any one of clauses 72 to 91, wherein after the treating step, the reaction product is dried by a dryer, preferably a pair of convection driers or contacts. A contact drier, particularly preferably a stream and/or a band drier and/or a fluidized bed drier. 93. The method of any one of clauses 72 to 92, wherein the process water produced during the process is preferably recovered via a solid-liquid separation device and/or cleaned and returned To the reaction mixture. The method of claim 93, wherein the solid-liquid separation device is at least one for micro filtration, ultra flirtation, nanofiltration. And a combination of reverse osmosis or a combination of the above various devices, in particular having a ceramic element and preferably a rotating disk and/or centrifugation Centrifugal membrane filter. 95.  The method of any one of claims 72 to 94, wherein the wastewater produced by mechanical, chemical and/or biological cleaning is cleaned. 96.  The method of any one of clauses 72 to 95, wherein the waste gas produced in the treatment, processing and/or adjustment is cleaned by mechanical, chemical, and/or biological means. 97.  The method of any one of clauses 72 to 96, wherein the reaction product, intermediate product, secondary product, and final product comprise a peat fuel from a brown coal to a brown coal Black coal-based fuel (black c〇aWike fUel), humus, Maynard or similar reaction product, carbonaceous material such as damping substance, nano sponge, nano pellet (Curry pellet) ), nano flber, nano cable (nan 〇, activated carbon MM coal) or sorption coal, charc〇al material, highly compressed carbon products and materials, especially Starting materials for graphite and graphite or near graphite products as well as carbon fibers and starting materials for composite or fiber compound materials. ... 98.  The method of any one of clauses 72 to 97, wherein the material or fuel, humus, Maynard or the like is produced from a solid-liquid mixture of water and a carbonaceous component, wherein Treating the solid-liquid mixture at a temperature of more than 1 ° C and more than 5 bar, characterized by: (10) in a film reactor from the 99.  The method of claim 98, wherein the thin film reactor comprises at least one device for solid-liquid separation. 100.  The method of claim 98 or claim 99, wherein at least one of 101 201118162, the solid-liquid separation device comprises a coarse filter and/or a fine filter device or a combination of the two, which can be combined In a filter unit. The method of any one of clauses 98 to 100, wherein: the membrane reactor is used to selectively remove reaction products, products, secondary products, and final products from the reaction mixture, Add or remove precipitates in a controlled manner, or enhance the contact of the precipitates. 102. If the method described in one of the items 98 to 1 of the patent application is applied, the solid-liquid separation of the film reaction 11 is carried out in a continuous manner or in a spaced manner. a method of hydrolyzing and/or producing a material of two itch humus, Maynard or the like in a solid-liquid mixture containing a carbon component, wherein the solid-liquid mixture is treated at a pressure of more than 1 bar at a pressure of more than 5 bar; It is: the first round of wire feeding of the person has 25% to 97% of the solid-potential substance relative to the total volume and is sent in a parallel or branch (Gffset) mode via an i 3% &quot; The method according to the item, wherein the pressure of the vapor pressure of the non-reducible process water is sent by the first conveying line method, wherein the conveying line of the non-pumpable feeder is added to the anti-extruder, Eccentric injection device. Double screw pump, equipped with eCCentnC Spiral PumP, piston pump (piston double screw snail) (or _P_r) or - fruit feed start = ===== method to the middle of the reactor and coating - from the "; = 5 two; send line provides 102 201118162 range of items 103 to 107 of the method, /, medium k The mass yield ratio of the starting material to be added is &amp; 1:2 〇 to 1:5 to 1:1. * One of the items mentioned in item 4 109. For example, the application of patent scopes 1 to 3 to 1 〇 8 laws include the use of other conveyor lines. 110. The method according to any one of the claims 1G3 to 1G9, further comprising using other devices together, such as a storage container, a grinding device, a mixing container, a dosing device, a culture container, a conveying device, Process water container °, heat exchanger or reactor. The method of any one of clauses 103 to 11 wherein the pumping system for conveying the solid-liquid mixture in the first conveying line is designed for a solid content of at least 5% to 10% or 10〇/〇 to 25%. ° 112.  The method of claim 103, wherein the pump for conveying the solid-liquid mixture in the second conveying line is an eccentric screw pump, a spiral displacement (spiral) Displacement) or a piston pump (pist〇n pump) ° 113.  a method for the hydrolysis and/or production of materials or fuels, Maynard or similar reaction products from a solid-liquid mixture of water and carbonaceous components, wherein a temperature of more than 1〇〇1 and a pressure of more than 5 bar The solid-liquid mixture is treated underneath, characterized in that the solid-liquid mixture flows through a heat exchanger for heating, the tube axis having an angle of more than 10 degrees with respect to the horizontal plane. 114.  The method of claim 113, wherein when the solid-liquid mixture passes through the feeding device, the viscosity of the solid-liquid mixture is lowered, and at least a point in the program is lowered to the starting material Three points of viscosity. ''' 115 - a method for feeding a reactor to produce a material or fuel, humus, Maynard or similar reaction product from a solid-liquid mixture of water and a carbonaceous component, wherein at a temperature in excess of 100 ° C and The solid-liquid mixture is treated at a pressure of more than 5 bar, characterized in that: Μ ^ The solid-liquid mixture flows through a heat exchanger to heat the amount of its tube axis relative to the horizontal plane by more than 10 degrees. 103 201118162 116.  For example, one of the 113th to 115th patent applications of the patent scope, this pass at least 117.  For example, in the method of claim 115 or 116, wherein the viscosity is lowered when the heat exchanger is removed, and the solid-liquid 黏 viscosity is reduced to the yarn 2 in the order of the scale: Shen, one of the items 113 to 117 = 'where the solid-liquid mixture has a solid content between 3% and 35% with a solid content between 35% and 60〇/〇 content. The method of any one of clauses 113 to 117, wherein the solid-liquid mixture is introduced into the helium exchanger by a pump. 120. The method of claim 119, wherein the secret to deliver the solid mixture is at least 5% to or from 25% solids. 121. For example, the method described in the ninth or uoth of the Shenqing patent range, wherein the pump for transporting the solid-liquid mixture and/or a backpressure pump is an eccentric screw pump (eccentric) Spiral pump), a spiral displacement or a piston pump 〇122.  a device for treating a solid solution of water and a carbonaceous component at a temperature exceeding 100 ° C and a pressure exceeding 5 bar, comprising a reactor characterized in that: the device comprises a feeding device, Has: a.  - a pump for transporting a solid-liquid mixture having a solids content of at least Μ%; and b.  The heat exchanger has an angle of the tube axis with respect to the horizontal plane greater than 1 degree. 123.  The apparatus of claim 122, wherein the pump is an eccentric spiral pump or a piston pump. 124.  The apparatus of claim 122, wherein the pump is designed to have a pressure of at least 10 to 130 bar. 125.  A device as claimed in any one of claims 122 to 124 wherein the heat exchanger is comprised of at least 60% of vertical tubular members. 104 201118162 126.  The apparatus of the invention of claim 122, wherein the heat exchanger for conveying the solid-liquid mixture is designed to have a solid 3 of 3% to 50/&gt; It is mainly composed of biomass including lignocellulose (1) and/or starch-containing material. 127.  The apparatus of any one of claims 122 to 126, wherein the heat exchanger is designed for the temperature, or at least _2 modules or a unit is used for 2 turns. (: to 300. (: temperature. 128.  The apparatus of any one of claims 122 to 127, wherein the heat exchanger is designed for a pressure of from 1 bar to 12 bar, or at least one module or one unit design At a pressure of 60 to 120 bar. 129.  The apparatus of any one of claims 122 to 128, wherein the hot parent or at least one module or unit is designed for a temperature of up to 25 〇 (: 130.  The apparatus of any one of claims 122 to 129, wherein the hot parent exchanger is in contact with the medium by a heat and a button and a waterproof material, such as a coated metal. , especially for metal, ceramic materials or 珐琅131.  A device according to any one of claims 122 to 130, wherein the tubular member in contact with the medium is made of a durable material. 132.  A device as claimed in any one of claims 122 to 131, wherein the heat exchanger is in contact with the medium in the form of stainless steel, such as austenitic steels or chrome and Steels of Groups 6, 7 and 8 with molybdenum content or duplex steels, copper-recorded alloys, nickel alloys with high molybdenum content. 4610 or titanium. 133.  The apparatus of any one of claims 122 to 132, wherein the heat exchanger is a tubular reactor having a blending system, a pair of tubes, an exchanger, and a tube bundle heat. Exchanger or a plate heat exchanger or a combination of ρ. 134.  The method of claim 122, wherein the heat exchanger is composed of a plurality of similar units and/or has a modular structure: 105 201118162 riding a bicycle, (4) a converter The apparatus of the present invention, as described in claim 137 of the patent application, wherein the layer is passed through the double-walled medium-sized medium-sized medium carrier medium of the tubular reactor, wherein the heat carrier medium The device described in the item ====: wherein the heat carrier ,, the end of the items 138 to 140, the final &amp; degree 2 (4) the heat carrier medium is between _ to war 7:T^tT:m 122 133 where ~..., the parent converter consists of different modules, units or sections. 143.  A device for treating a solid-liquid mixture of water and a carbonaceous component at a temperature exceeding a temperature of more than 5 bar, comprising a reactor, characterized in that the device comprises a hydrolysis device having: a.  - a pump for delivering a solid-liquid mixture having a solids content of at least 10 〇 / 〇 to 15%; and b.  - a heat exchanger having an angle of the tube axis relative to the horizontal plane greater than 1 degree. 144.  The apparatus of claim 143, wherein the hydrolysis apparatus comprises a counterpressure pump. 145.  The apparatus of claim 143 or 144, wherein the pump or the back pressure pump for conveying the solid-liquid mixture is an eccentric spiral pump and a spiral displacement (Spirai) Displacement) or a piston pump. 146.  As described in one of claims 143 to 145, the skirt 106 201118162 is in which the pump or the pressure-resistant pump for conveying the solid-liquid mixture is designed to have a pressure of at least 1 bar to 130 bar. . 147. The apparatus of any one of clauses 143 to 146, wherein the heat exchanger is at least 60. /. The vertical pipe part is constructed. 148. The apparatus according to any one of claims 143 to 147, wherein the heat exchanger for transporting the solid-liquid mixture is for 3% to 5% solids weight, It is mainly designed from biomass including lignocellulose (lign〇cellul〇se) and/or starch-containing materials. - 149.  The apparatus of any one of claims 143 to 148, wherein the heat exchanger is for 60. (: to 30 (TC temperature design, or at least one module or one unit is 2 〇〇. (: to 300X: the temperature is designed. 150.  The apparatus of any one of claims 143 to 149, wherein the heat exchanger is designed for a pressure of 10 to 12 bar, or at least _2 modules or a unit of 60 bar Designed to a pressure of 120 bar. 151.  The apparatus of any one of claims 143 to 15, wherein the heat exchanger or at least one module or unit is for up to 25 inches. The temperature is designed. 152.  The skirt according to any one of the items 143 to 151 of the patent application, wherein the hot contactor is in contact with the medium and is composed of heat-resistant and financial materials and a waterproof material, such as coated metal. Especially for precious metals and ceramic materials. 153.  For example, in the item 143 to 152 of the patent scope, wherein the tube in contact with the medium is composed of a durable material. 154.  The apparatus of any one of claims 143 to 153, wherein the heat exchanger is in contact with the medium by a stainless steel such as austenitic steels or an increase in chromium and molybdenum content. , 7 and 8 steel, $ is composed of duplex steels, copper-nickel alloy, high molybdenum content: gold, such as 2. 4610 or titanium. # σ 155. As set forth in paragraphs 143 to 154 of the patent application, wherein the heat exchanger is a tubular reactor having a blending system, a pair of tubes ^ 107 201118162 a parent exchanger, a bundle bundle heat An exchanger or a plate heat exchanger or a combination of the above. 156. A device as claimed in any one of claims 143 to 153, wherein the heat exchanger is composed of a plurality of similar units and/or has a module: the device described in the item wherein the heat exchange The apparatus of any one of clauses 143 to 157, wherein the module units of the heat exchanger are disposed in a spatially adjacent manner. The scope of the item 143 to 158 of the application, wherein the blending system of the tubular reactor is composed of double walls. 16== The device of claim 159, wherein the thermal energy carrier is intermediate to the double wall of the tubular reactor.糸 Please turn 16th. The device of item wherein the thermal energy carrier medium is hot oil, water vapor or process water. Negative 162. = Please refer to item 143 of the 153th item of the patent, wherein the heat exchanger is designed for different thermal energy carrier media. Clothing 1 Jin 63: ίΓί!, around the 143th to 162th of the items mentioned in the item! The most ί warm ί for the thermal latitude medium between 6 (rc to 350t ^ 164. For example, in the scope of application for patents Nos. 143 to 155, the heat is generated by a different module, unit or zone of two kinds of rotted pigs, water and carbon-containing solid-liquid mixture _ or fuel, buckle , Maynard or a similar reaction product method in which the solid-liquid mixture is treated at a pressure of more than 1 ^ ^ more than 5 bar, characterized in that an enriched process water system portion is used for The starting material t, the liquid mixture produces a bondability, which is used for coating or attaching to the existing starting material in the reaction reactor, as a heat carrier. The medium is used, for example, in the device or as a fertilizer component. One defeated the method described in claim 6 (6), in which the concentration was carried out using a solid-liquid separation method. The method of claim 165, wherein the evaporation of water is used to remove at least 1% to 10% of the water during the agricultural shrinkage in the eighth of the items 165 to 167. In the method of any one of items 165 to 168, the water of at least 1 〇〇/〇 is removed during concentration. 『·ΐί Please request one of the methods described in one of the 165th to 169th patents to be removed directly from the process performed, or used for untreated private water and designed for the sake of pressure - pressure Rong H’s bribes were removed. 171.  The method of any one of claims 165 to 17, wherein the water vapor obtained by evaporation of the process water is used in other parts of the process, for example, for heating before entering the heat exchanger. Starting materials, heating of the hot oil via a heat exchange process and/or means for operating the dried reaction product, such as an air turbulence mill. 172.  - the use of concentrated process water produced by a process for producing materials or fuels, succulent lean, Maynard or similar reactants from a solid-liquid mixture of water and carbonaceous components, wherein the solid-liquid mixture is more than 10% (TC temperature and treatment at a pressure exceeding 5 bar. 'The concentrated process water system is used for: pre-cultivating, preheating the starting material, producing a pumpable solid-liquid mixture, predominating in the reaction mixture, The reactor of the apparatus is coated with or mixed with an existing starting material for returning to the process as a heat carrier medium and/or as a promoter component.  For use as described in claim 172, wherein the process water system is obtained at a temperature of from 1 ° C to 5 (TC) at a temperature in which it is used alone.  For the use described in claim 172, the additional use is 25. 〇 to 5 (TC, 5 (TC to 70 ° C or 7 ° ° C to 99 ° C temperature heating process water. 175.  a device for producing and treating a material or fuel, humus, Maynard or similar reaction product from a solid-liquid mixture of water and a carbonaceous component, wherein it is at a temperature exceeding 100 ° C and exceeding 5 bar The solid-liquid mixture is treated under pressure and is characterized by: 109 201118162 Returning to the solid-state device 'for concentration of the process water and for returning the concentrated process water to the liquid mixture. Also included for solid-liquid separation 176. A device as claimed in claim 175. 177.  The apparatus of claim 175, further comprising an evaporator. 178.  For example, one of the 'devices' of items 175 to 177 of the patent application includes an insulated reservoir for unprocessed process water and formed into a pressure vessel: 179.  - used to produce materials, fuel, humus, Maynard or similar reaction products from a solid-liquid mixture of water and carbonaceous components and at a temperature of more than 1 〇〇〇c and at a pressure of 5 bar The device for processing, characterized in that: the device is as follows: a.  - the feeding device comprises: a compound; / or a pump 'for conveying a solid-liquid mixing father having a solid content of at least 10% to 15 〇 / ,, the angle of the tube axis relative to the horizontal plane is greater than the degree; And less than two anti-fresh 'small--a reaction-like-sense or hybrid system or have a height-to-diameter ratio of at least 2:1. The apparatus of item 179, wherein the heat exchanger comprises the feature of any one of items 53 to 64. Please refer to the equipment of the (10) rhyme of the county, and further include the apparatus of claim 181, wherein the pressure reducing device comprises a reactor with a blending system or a sensor or a combination of the two. 110
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TWI447598B (en) * 2012-06-13 2014-08-01 China Steel Corp Method for drying biomass and computer product thereof
CN109156408A (en) * 2018-09-22 2019-01-08 陈蜀乔 A kind of fish pond robot that can intelligently herd fishing
CN111745860A (en) * 2020-06-08 2020-10-09 武汉科技大学 Waste tire smashing and desulfurizing integrated device based on supercritical carbon dioxide jet flow and application method
WO2021215948A1 (en) * 2020-04-23 2021-10-28 Woodchem S. A. Process of catalytic cracking of solid waste from pine derivatives industry
TWI777854B (en) * 2020-11-25 2022-09-11 日商三菱重工環境 化學工程股份有限公司 Hydrothermal treatment apparatus and hydrothermal treatment system

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US20080016770A1 (en) * 2006-07-18 2008-01-24 Norbeck Joseph M Method for high energy density biomass-water slurry

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Publication number Priority date Publication date Assignee Title
TWI447598B (en) * 2012-06-13 2014-08-01 China Steel Corp Method for drying biomass and computer product thereof
CN109156408A (en) * 2018-09-22 2019-01-08 陈蜀乔 A kind of fish pond robot that can intelligently herd fishing
WO2021215948A1 (en) * 2020-04-23 2021-10-28 Woodchem S. A. Process of catalytic cracking of solid waste from pine derivatives industry
CN111745860A (en) * 2020-06-08 2020-10-09 武汉科技大学 Waste tire smashing and desulfurizing integrated device based on supercritical carbon dioxide jet flow and application method
CN111745860B (en) * 2020-06-08 2022-03-04 武汉科技大学 Waste tire smashing and desulfurizing integrated device based on supercritical carbon dioxide jet flow and application method
TWI777854B (en) * 2020-11-25 2022-09-11 日商三菱重工環境 化學工程股份有限公司 Hydrothermal treatment apparatus and hydrothermal treatment system

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