JP2012031283A - Method of manufacturing fuel - Google Patents

Method of manufacturing fuel Download PDF

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JP2012031283A
JP2012031283A JP2010172040A JP2010172040A JP2012031283A JP 2012031283 A JP2012031283 A JP 2012031283A JP 2010172040 A JP2010172040 A JP 2010172040A JP 2010172040 A JP2010172040 A JP 2010172040A JP 2012031283 A JP2012031283 A JP 2012031283A
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waste plastic
vinyl chloride
fuel
treatment apparatus
water vapor
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Hirofumi Mori
浩文 森
Hiroyuki Takano
博幸 高野
Yasuyuki Ishida
泰之 石田
Tomofumi Kikuzaki
智文 菊崎
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Taiheiyo Cement Corp
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Taiheiyo Cement Corp
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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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

Abstract

PROBLEM TO BE SOLVED: To provide a method of efficiently manufacturing solid fuel which is easily pulverized and used by hardly causing thermal degradation of waste plastics containing vinyl chloride and separating only chlorine at low temperature for facilitating waste heat.SOLUTION: In the method, waste plastics containing vinyl chloride are processed at 220-300°C in an external treatment apparatus with agitation which is filled with water vapor. The external treatment apparatus is selected from a kiln, a two axes paddle mixer and a multistage dryer.

Description

本発明は、塩ビ含有廃プラスチックから、燃料を製造する方法に関する。   The present invention relates to a method for producing fuel from PVC-containing waste plastic.

廃プラスチックは、ボイラーやセメントキルン等の炉で代替燃料として利用されているが、塩ビを含む廃プラスチックは、ボイラーの腐食、セメント品質への悪影響などから、使用量が制限されてきた。このため、自動車シュレッダーダスト(ASR)や、建設系廃プラスチック等、大量の廃プラスチックが埋め立てられたり、焼却されたりしている。
しかしながら、埋立地の確保は年々難しくなっている。また、温暖化ガス排出量制限のためには、廃プラスチックは、焼却せず、燃料として利用し、化石燃料の使用量を削減するのが望ましい。
Waste plastics are used as alternative fuels in furnaces such as boilers and cement kilns, but the amount of waste plastics containing PVC has been limited due to corrosion of boilers and adverse effects on cement quality. For this reason, a large amount of waste plastic such as automobile shredder dust (ASR) and construction waste plastic is buried or incinerated.
However, securing landfills has become more difficult every year. In order to limit greenhouse gas emissions, it is desirable that waste plastic be used as fuel without being incinerated to reduce the amount of fossil fuel used.

従来、このような塩素含有量の高い廃プラスチックのサーマルリサイクルを推進するため、過熱脱塩やガス化プロセスの適用が検討されている。しかし、これらの技術は、事業化された例はあるが、どれも普及していないのが実情である。また、過熱脱塩やガス化プロセスでは、350℃以上の高い温度で運転するため、化石燃料などを熱源として利用するのが一般的である。   Conventionally, in order to promote the thermal recycling of waste plastics having a high chlorine content, application of superheated desalination and gasification processes has been studied. However, although these technologies have been commercialized, none of them are widely used. Further, in the overheated desalination and gasification process, since it operates at a high temperature of 350 ° C. or higher, it is common to use fossil fuel or the like as a heat source.

例えば、特許文献1には、塩ビ含有廃プラスチック等の高分子材料を、過飽和水蒸気雰囲気内において、150〜350℃の温度範囲で加熱して炭化する方法が記載され、乾留ガスを燃やさずに回収除去できることが記載されている。
しかしながら、高分子材料を炭化するには、この温度範囲では時間がかかりすぎるため、高分子材料を遠赤外線によって直接加熱する必要があり、遠赤外線の効果を前処理として5cm以下に破砕したり、発泡体を予め加熱減容処理しておく必要があった。
また、一般に、高分子材料を炭化すると、乾留ガスが炭化装置の排ガスダクト内で凝縮したり、重合したりして、タール状に付着してトラブルとなることが多い。
さらには、炭化するため、乾留ガス、炭化物、熱分解油、タール状物、廃液等、多くの種類の産物が発生するため、それらを有効利用するためには多額の設備や費用が必要となるという問題点がある。
For example, Patent Document 1 describes a method of heating and carbonizing a polymer material such as vinyl chloride-containing waste plastic in a supersaturated steam atmosphere at a temperature range of 150 to 350 ° C., and recovering dry distillation gas without burning it. It is described that it can be removed.
However, carbonization of the polymer material takes too much time in this temperature range, so it is necessary to directly heat the polymer material with far infrared rays, and the effect of the far infrared rays is crushed to 5 cm or less as a pretreatment, It was necessary to heat and reduce the volume of the foam beforehand.
In general, when a polymer material is carbonized, the dry distillation gas often condenses or polymerizes in the exhaust gas duct of the carbonization apparatus and adheres in a tar-like shape, often causing trouble.
Furthermore, carbonization generates many types of products such as carbonized gas, carbides, pyrolysis oil, tar-like products, waste liquids, etc., and a large amount of equipment and costs are required to use them effectively. There is a problem.

特許文献2には、塩ビを含む廃プラスチックを脱塩した炭化燃料の内部に、揮発分の少ない微粉燃料が分散して一体化した固体燃料が記載され、当該固体燃料は、塩ビを含む廃プラスチックと微粉燃料を掻き上げて落下させることで混合しながら300〜380℃に加熱して製造されることが記載されている。
この方法は、一般に加熱脱塩で脱塩反応が生じる300℃以上において、溶融した廃プラスチックと粉体を混合して、粉砕しやすい固体を回収し、燃料化するものである。混合する微粉燃料については、熱分解によってガス化する量が少ないことが必要とされている。これは、300〜380℃ではガス化が少なからず起こるためであり、材料や温度によっては、固体燃料の回収率が低下するとともに、発生したガスの処理のための設備が大きくなるという問題がある。
Patent Document 2 describes a solid fuel in which a finely pulverized fuel is dispersed and integrated inside a carbonized fuel obtained by desalting waste plastic containing vinyl chloride. The solid fuel is waste plastic containing vinyl chloride. It is described that it is manufactured by heating to 300 to 380 ° C. while mixing by scraping and dropping the pulverized fuel.
In this method, generally, at 300 ° C. or higher at which a desalting reaction occurs by heat desalting, molten waste plastic and powder are mixed, and a solid that is easily pulverized is recovered and converted into fuel. The pulverized fuel to be mixed is required to have a small amount of gasified by pyrolysis. This is because gasification occurs at a temperature of 300 to 380 ° C., and depending on the material and temperature, there is a problem that the recovery rate of the solid fuel decreases and the equipment for processing the generated gas becomes large. .

特許文献3には、融着防止剤として、有機物を燃焼した後の燃焼ガスに同伴するダスト又は微粉炭を、廃プラスチックとともに加熱炉に供給し、大気圧より低い圧力下で及び/又は酸素含有ガスを供給しながら加熱・熱分解を行う固体原燃料の製造方法が記載されている。
しかしながら、この方法においては、圧力調整や酸素ガスの供給などの設備や、高温での加熱処理が必要であるという問題があった。
In Patent Document 3, as an anti-fusing agent, dust or pulverized coal accompanying the combustion gas after burning an organic substance is supplied to a heating furnace together with waste plastic, and at a pressure lower than atmospheric pressure and / or containing oxygen. A method for producing a solid raw fuel that is heated and pyrolyzed while supplying a gas is described.
However, this method has a problem that it requires equipment such as pressure adjustment and supply of oxygen gas, and heat treatment at a high temperature.

特開2005−15555号公報JP 2005-15555 A 特開2009−235215号公報JP 2009-235215 A 特開2009−269965号公報JP 2009-269965 A

従って、本発明の目的は、塩ビ含有廃プラスチックを熱分解させず、塩素だけを分離し、且つ、粉砕しやすく、利用しやすい固形燃料を、廃熱を利用しやすい低温で、効率良く製造する方法を提供することにある。   Accordingly, an object of the present invention is to efficiently produce a solid fuel that is easy to use and separate waste fuel, at a low temperature that makes it easy to use waste heat, without pyrolyzing the waste plastic containing vinyl chloride, separating only chlorine, and easily crushing. It is to provide a method.

本発明者らは、斯かる実情に鑑み、種々検討した結果、水蒸気を充満させた熱処理装置内で、220〜300℃で被処理物を処理することにより、塩素を効率良く除去し、燃料を製造できることを見出し、本発明を完成した。   As a result of various investigations in view of such circumstances, the present inventors have efficiently removed chlorine by treating an object to be treated at 220 to 300 ° C. in a heat treatment apparatus filled with water vapor, The present invention was completed by finding that it can be produced.

すなわち、本発明は、塩ビ含有廃プラスチックを、攪拌しながら水蒸気を充満させた熱処理装置内で、220〜300℃で処理することを特徴とする燃料の製造方法を提供するものである。   That is, this invention provides the manufacturing method of the fuel characterized by processing vinyl chloride containing waste plastic at 220-300 degreeC in the heat processing apparatus filled with water vapor | steam, stirring.

本発明によれば、少ないエネルギーで塩ビ含有廃プラスチックを分解し、塩素を効率良く除去することができ、常圧で連続処理して、燃料を効率良く製造することができる。また、得られる燃料は、総発熱量が高く、粉砕性も良好である。   According to the present invention, vinyl chloride-containing waste plastic can be decomposed with less energy, chlorine can be efficiently removed, and fuel can be efficiently produced by continuous treatment at normal pressure. Further, the obtained fuel has a high total calorific value and good grindability.

本発明で用いる塩ビ含有廃プラスチックとしては、例えば、ASR、建設系廃プラスチック、パルパーかす、容器包装廃プラ選別残渣等が挙げられる。   Examples of the vinyl chloride-containing waste plastic used in the present invention include ASR, construction waste plastic, pulper residue, container packaging waste plastic sorting residue, and the like.

本発明においては、前記のような塩ビ含有廃プラスチックを、水蒸気が充満した220〜300℃のほぼ大気圧の熱処理装置に連続的に投入し、攪拌しながら処理を行う。
熱処理装置としては、例えば、キルン、二軸パドルミキサー、多段式乾燥機等の外熱式処理装置を用いることができる。
In the present invention, the vinyl chloride-containing waste plastic as described above is continuously charged into a heat treatment apparatus at 220 to 300 ° C. and almost atmospheric pressure filled with water vapor, and the treatment is performed while stirring.
As the heat treatment apparatus, for example, an external heat processing apparatus such as a kiln, a twin-screw paddle mixer, a multistage dryer, or the like can be used.

また、これらの装置に水蒸気を導入する方法としては、(a)原料の水分として処理装置に導入する、(b)直接処理装置に飽和水蒸気を導入する、(c)処理装置の摺動部シールガスとして導入する、(d)過熱水蒸気を導入する方法が挙げられる。
更に、220〜300℃の過熱水蒸気雰囲気とするには、(a)〜(c)の場合、処理装置を外熱式として水蒸気と原料を過熱する方式をとることができる。また、(d)の場合、過熱水蒸気のみで原料を熱処理することが可能であるが、外熱式加熱との併用によって原料を熱処理することもできる。
導入される水蒸気の量は、熱処理装置の形状、充填率、処理する廃プラスチックの塩素含有量、含水率、性状等によって異なり、特に限定されない。例えば、流通させる水蒸気量が少ないと、熱処理装置の加熱されていない部分において水蒸気が凝縮し、濃い塩酸となって処理物に混じる可能性があるため、注意が必要である。一方、水蒸気量が多いと、水蒸気を製造するためのエネルギーが膨大となり、エネルギー効率が低下するので、好ましくない。
In addition, as a method of introducing water vapor into these apparatuses, (a) introducing water vapor into the processing apparatus as raw material moisture, (b) introducing saturated water vapor directly into the processing apparatus, (c) sliding part seal of the processing apparatus Examples thereof include (d) a method of introducing superheated steam that is introduced as a gas.
Furthermore, in order to obtain a superheated steam atmosphere at 220 to 300 ° C., in the case of (a) to (c), a method of superheating steam and raw materials by using an external heating type processing apparatus can be adopted. In the case of (d), the raw material can be heat-treated only with superheated steam, but the raw material can also be heat-treated in combination with external heating.
The amount of water vapor to be introduced varies depending on the shape of the heat treatment apparatus, the filling rate, the chlorine content of the waste plastic to be treated, the moisture content, the properties, etc., and is not particularly limited. For example, if the amount of water vapor to be circulated is small, the water vapor may condense in an unheated portion of the heat treatment apparatus and become concentrated hydrochloric acid, which must be mixed with the processed material. On the other hand, if the amount of water vapor is large, the energy for producing water vapor becomes enormous and energy efficiency is lowered, which is not preferable.

処理温度は、220〜300℃であるが、特に250〜280℃が好ましく、30〜60分程度処理するのが好ましい。
熱処理装置の熱源としては、セメントキルン、廃棄物焼却炉等の低温の廃熱を効率的に使用することができ、安価に処理できるほか、爆発等の心配がなく、安全に処理することができる。
The treatment temperature is 220 to 300 ° C, but 250 to 280 ° C is particularly preferable, and the treatment is preferably performed for about 30 to 60 minutes.
As a heat source for heat treatment equipment, low-temperature waste heat such as cement kilns, waste incinerators, etc. can be used efficiently and can be processed at low cost, and can be processed safely without worrying about explosions. .

本発明においては、塩ビ含有廃プラスチックを処理する際、有機物含有粉粒体を混合して処理することができる。
上記のような処理により、廃プラスチック中の塩ビから塩素が分離し、HClとして水蒸気といっしょに排気される。しかし、廃プラスチックの種類等によっては、処理中に溶融し、処理装置に付着してトラブルを起こしやすい場合があり、また、一度溶融した廃プラスチックは、排出されるときには塊となってしまい、粉砕されにくくなる場合もある。
そのような場合に、有機物含有粉粒体を混合して処理すると、粉粒体が廃プラスチックの融着防止効果を発揮して、安定した処理が可能になるとともに、被粉砕性の良い処理物を得ることができる。
In this invention, when processing a vinyl chloride containing waste plastic, an organic substance containing granular material can be mixed and processed.
Through the treatment as described above, chlorine is separated from the vinyl chloride in the waste plastic and is exhausted together with water vapor as HCl. However, depending on the type of waste plastic, etc., it may melt during processing and adhere to the processing equipment and cause troubles. It may be difficult to be done.
In such a case, when the organic substance-containing powder is mixed and processed, the powder exhibits the effect of preventing the waste plastic from fusing, enabling stable processing and processing with good pulverizability. Can be obtained.

かかる有機物含有粉粒体としては、例えば、乾燥下水汚泥、下水汚泥炭化物、コークスダスト、木くず等が挙げられる。
有機物含有粉粒体は、廃プラスチック由来の灰分と有機物含有粉体との合計で、全処理物中に20〜60質量%、特に30〜50質量%となるよう、混合されるのが好ましい。
なお、特許文献2には、溶融したプラスチックと混合する粉体として、揮発分の少ない微粉燃料を用いるとしている。これは、300〜380℃では、プラスチックの熱分解・ガス化が多くなることから、固体燃料の回収率低下防止と発生するガス量の抑制およびガス・廃水処理設備費用の抑制のために規定されているものである。
本発明においては、熱分解が殆ど起こらない低い温度で処理するため、溶融したプラスチックに混合する粉体について、揮発分を制限する必要がない。
Examples of the organic substance-containing granular material include dry sewage sludge, sewage sludge carbide, coke dust, wood waste and the like.
It is preferable that the organic substance-containing granular material is mixed so that the total amount of the ash derived from the waste plastic and the organic substance-containing powder is 20 to 60% by mass, particularly 30 to 50% by mass in the entire processed product.
In Patent Document 2, a pulverized fuel with a small volatile content is used as a powder to be mixed with molten plastic. This is stipulated in order to reduce the recovery rate of solid fuel, to reduce the amount of gas generated, and to reduce the cost of gas / waste water treatment equipment, because the plastic is frequently decomposed and gasified at 300 to 380 ° C. It is what.
In the present invention, since the treatment is performed at a low temperature at which thermal decomposition hardly occurs, it is not necessary to limit the volatile content of the powder mixed with the molten plastic.

熱処理装置内で分解・気化した塩素は、水蒸気とともに装置外に導出される。
排出された塩素を含む水蒸気は、アルカリ成分を含む水を用いたスクラバー等で塩素を除去したり、塩酸回収設備で塩酸を回収後、残留した少量のガスはセメントキルン燃焼用空気として利用したり、脱塩設備の熱源において燃焼脱臭したりして、利用することが可能である。
Chlorine decomposed and vaporized in the heat treatment apparatus is led out of the apparatus together with water vapor.
Steam discharged from chlorine containing chlorine can be removed with a scrubber using water containing alkali components, or after a hydrochloric acid recovery facility recovers hydrochloric acid, a small amount of residual gas can be used as cement kiln combustion air. It is possible to use by deodorizing by combustion in the heat source of the desalination facility.

一方、処理後に得られる固形分は、再生固形燃料として使用される。
この固形分は、塩素濃度が0.5質量%程度まで低減され、そのまま、燃料として利用可能なものである。
また、廃プラスチックに含まれていた塩素は十分に除去されつつ、燃料となり得る他の化学成分(炭素、水素等)は、ほとんど除去されていないので、固形燃料として用いた際の総発熱量も高いものである。
On the other hand, the solid content obtained after the treatment is used as a regenerated solid fuel.
This solid content has a chlorine concentration reduced to about 0.5% by mass and can be used as a fuel as it is.
In addition, the chlorine contained in the waste plastic is sufficiently removed, but other chemical components that can be used as fuel (carbon, hydrogen, etc.) are hardly removed, so the total calorific value when used as a solid fuel is also low. It is expensive.

また、本発明により得られる燃料は、被粉砕性も良好なものである。
例えば、固形燃料をセメントキルンで好適に使用できる条件として、粒度が1.5mm以下の割合を90%以上とするのが好ましいが、本発明の燃料は、このような粒度に粉砕することが可能である。
In addition, the fuel obtained by the present invention also has good pulverizability.
For example, it is preferable that the ratio of the particle size of 1.5 mm or less is 90% or more as a condition that the solid fuel can be suitably used in the cement kiln, but the fuel of the present invention can be pulverized to such a particle size. It is.

実施例1
原料の温度が所定の処理温度になるよう、外熱式キルン(プロパンガスを熱源とした外熱式ロータリーキルン(内径500mm×長さ4950mm(加熱部分長3000mm))を加熱し、外熱式キルンのフードから水蒸気を送入した。滞留時間は、キルンの回転数により調整した。自動車シュレッダーダスト、建設系混合廃プラスチックを処理したときの処理温度と滞留時間、塩素残量を、表1に示す。
Example 1
An external heating kiln (an external heating rotary kiln (inner diameter 500 mm × length 4950 mm (heating part length 3000 mm)) using propane gas as a heat source) is heated so that the temperature of the raw material becomes a predetermined processing temperature. Steam was fed from the hood, and the residence time was adjusted by the number of revolutions of the kiln Table 1 shows the treatment temperature, residence time, and residual chlorine amount when automobile shredder dust and construction mixed waste plastic were treated.

なお、塩素濃度は、エシュカ法により測定した値を用い、脱塩率は、次式により算出した。   In addition, the chlorine concentration used the value measured by the Eshka method, and the desalination rate was computed by following Formula.

Figure 2012031283
Figure 2012031283

また、歩留まりは、次式のより算出した。   The yield was calculated from the following equation.

Figure 2012031283
Figure 2012031283

Figure 2012031283
Figure 2012031283

処理温度が220〜300℃では、十分な脱塩効果が得られるとともに、歩留まりも良好である。
これに対し、200℃では、十分な脱塩効果が得られず、350℃では、歩留まりが低下する。
歩留まりは、原料が本来有する水分の蒸発による低下の他、粉塵の散逸、有機物の揮発・熱分解ガス化によっても低下する。300℃では、有機物の揮発・熱分解ガス化が始まるものと考えられ、熱量の損失に繋がるほか、排ガスの処理に負荷をかけるため、300℃を超える加熱は好ましくない。
When the treatment temperature is 220 to 300 ° C., a sufficient desalting effect is obtained and the yield is also good.
On the other hand, at 200 ° C., a sufficient desalting effect cannot be obtained, and at 350 ° C., the yield decreases.
Yield decreases due to evaporation of moisture inherent in the raw material, dust dissipation, and volatilization / pyrolysis gasification of organic substances. At 300 ° C., volatilization / pyrolysis gasification of organic substances is considered to start, which leads to loss of heat and places a load on the treatment of exhaust gas, so heating above 300 ° C. is not preferable.

実施例2
原料の温度が所定の処理温度になるよう、外熱式キルン(プロパンガスを熱源とした外熱式ロータリーキルン(内径500mm×長さ4950mm(加熱部分長3000mm))を加熱し、外熱式キルンのフードから水蒸気を送入した。滞留時間は、キルンの回転数により調整した。容器包装胚プラスチック再商品化残渣(以下、容リ残渣という)及び乾燥下水汚泥を、以下の条件で処理し、歩留まり、塩素残量及び脱塩率を、実施例1と同様にして求めた。結果を表2に示す。
Example 2
An external heating kiln (an external heating rotary kiln (inner diameter 500 mm × length 4950 mm (heating part length 3000 mm)) using propane gas as a heat source) is heated so that the temperature of the raw material becomes a predetermined processing temperature. Steam was fed from the hood, and the residence time was adjusted by the number of rotations of the kiln. The remaining amount of chlorine and the desalting rate were determined in the same manner as in Example 1. The results are shown in Table 2.

(1)処理条件:
処理温度:250℃
滞留時間:60分
(2)材料:
容リ残渣:比重分離残渣(重質残渣) 塩素=3.2%、水分8%
粉粒体:乾燥下水汚泥 塩素0.06%、水分1.2%
(1) Processing conditions:
Processing temperature: 250 ° C
Residence time: 60 minutes (2) Materials:
Volume residue: Specific gravity separation residue (heavy residue) Chlorine = 3.2%, moisture 8%
Powder: Dry sewage sludge 0.06% chlorine, 1.2% moisture

Figure 2012031283
Figure 2012031283

容リ残渣は、主に塩ビ、あるいはオレフィン系樹脂にアルミが付着したもので構成されており、容リ残渣のみを処理すると、溶融した樹脂がキルンに付着し、排出不良となる傾向があった。
これに対し、容リ残渣80質量部に乾燥下水汚泥を20〜60質量部の割合で配合した場合、キルンへの付着は解消された。
Residue residue is mainly composed of vinyl chloride or olefinic resin with aluminum attached, and when only the residue is treated, the molten resin tends to adhere to the kiln, resulting in poor discharge. .
On the other hand, when dry sewage sludge was blended at a ratio of 20 to 60 parts by mass with 80 parts by mass of the residue, adhesion to the kiln was eliminated.

Claims (5)

塩ビ含有廃プラスチックを、攪拌しながら水蒸気を充満させた熱処理装置内で、220〜300℃で処理することを特徴とする燃料の製造方法。   A method for producing a fuel, characterized in that a vinyl chloride-containing waste plastic is treated at 220 to 300 ° C in a heat treatment apparatus filled with water vapor while stirring. 塩ビ含有廃プラスチックと有機物含有粉粒体を、混合して処理する請求項1記載の製造方法。   The manufacturing method according to claim 1, wherein the vinyl chloride-containing waste plastic and the organic matter-containing granular material are mixed and processed. 全処理物における有機物含有粉粒体の質量割合が、20〜60質量%である請求項2記載の製造方法。   The manufacturing method of Claim 2 whose mass ratio of the organic substance containing granular material in all the processed materials is 20-60 mass%. 熱処理装置が、キルン、二軸パドルミキサー及び多段式乾燥機から選ばれる外熱式処理装置である請求項1〜3のいずれか1項記載の製造方法。   The manufacturing method according to any one of claims 1 to 3, wherein the heat treatment apparatus is an external heat treatment apparatus selected from a kiln, a twin-screw paddle mixer, and a multistage dryer. 水蒸気を、(a)原料の水分として処理装置に導入、(b)直接処理装置に飽和水蒸気を導入、(c)処理装置の摺動部シールガスとして導入、(d)過熱水蒸気を導入のいずれかにより処理装置に導入する請求項1〜4のいずれか1項記載の製造方法。   Water vapor is introduced into the processing equipment as (a) raw material moisture, (b) saturated steam is introduced directly into the processing equipment, (c) is introduced as a sliding part seal gas of the processing equipment, or (d) superheated steam is introduced. The manufacturing method of any one of Claims 1-4 introduce | transduced into a processing apparatus by this.
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JP2013202497A (en) * 2012-03-28 2013-10-07 Taiheiyo Cement Corp System and method for treating waste

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JPH10259273A (en) * 1997-01-20 1998-09-29 Nkk Corp Chlorine removal from chlorine-containing polymeric resin
JPH1119622A (en) * 1997-06-30 1999-01-26 Nkk Corp Treatment of chlorine-containing synthetic resin by pyrolysis and apparatus therefor
JPH1128441A (en) * 1997-07-08 1999-02-02 Toyota Motor Corp Treatment of waste material containing chlorine-containing resin
JPH11263871A (en) * 1998-03-18 1999-09-28 Toshiba Corp Method for treating organic waste containing nitrogen atom or halogen atom
JP2003253037A (en) * 2002-02-28 2003-09-10 Jfe Steel Kk Method for dechlorinating chlorine-containing synthetic resin
JP2005255933A (en) * 2004-03-15 2005-09-22 Nakamichi Yamazaki Method for treating chlorine-containing polymer
JP2010106133A (en) * 2008-10-30 2010-05-13 Kubota Kankyo Service Kk Process and apparatus for making waste into fuel

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Publication number Priority date Publication date Assignee Title
JPH10101841A (en) * 1996-09-27 1998-04-21 Mitsubishi Heavy Ind Ltd Thermal treatment of waste
JPH10259273A (en) * 1997-01-20 1998-09-29 Nkk Corp Chlorine removal from chlorine-containing polymeric resin
JPH1119622A (en) * 1997-06-30 1999-01-26 Nkk Corp Treatment of chlorine-containing synthetic resin by pyrolysis and apparatus therefor
JPH1128441A (en) * 1997-07-08 1999-02-02 Toyota Motor Corp Treatment of waste material containing chlorine-containing resin
JPH11263871A (en) * 1998-03-18 1999-09-28 Toshiba Corp Method for treating organic waste containing nitrogen atom or halogen atom
JP2003253037A (en) * 2002-02-28 2003-09-10 Jfe Steel Kk Method for dechlorinating chlorine-containing synthetic resin
JP2005255933A (en) * 2004-03-15 2005-09-22 Nakamichi Yamazaki Method for treating chlorine-containing polymer
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Publication number Priority date Publication date Assignee Title
JP2013202497A (en) * 2012-03-28 2013-10-07 Taiheiyo Cement Corp System and method for treating waste

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