JP2000017278A - Preparation of refuse solid fuel - Google Patents
Preparation of refuse solid fuelInfo
- Publication number
- JP2000017278A JP2000017278A JP10184071A JP18407198A JP2000017278A JP 2000017278 A JP2000017278 A JP 2000017278A JP 10184071 A JP10184071 A JP 10184071A JP 18407198 A JP18407198 A JP 18407198A JP 2000017278 A JP2000017278 A JP 2000017278A
- Authority
- JP
- Japan
- Prior art keywords
- water
- solid fuel
- refuse
- waste
- refuse solid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004449 solid propellant Substances 0.000 title claims abstract description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000010849 combustible waste Substances 0.000 claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims description 17
- 239000010813 municipal solid waste Substances 0.000 claims description 14
- 239000000446 fuel Substances 0.000 claims description 11
- 239000002699 waste material Substances 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 21
- 239000000460 chlorine Substances 0.000 abstract description 21
- 229910052801 chlorine Inorganic materials 0.000 abstract description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract description 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract description 4
- 150000001805 chlorine compounds Chemical class 0.000 abstract description 3
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 abstract description 2
- 239000011780 sodium chloride Substances 0.000 abstract description 2
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 11
- 238000001035 drying Methods 0.000 description 10
- 238000000465 moulding Methods 0.000 description 10
- 238000010298 pulverizing process Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 238000010828 elution Methods 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- 150000002013 dioxins Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000002910 solid waste Substances 0.000 description 5
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 238000011033 desalting Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 239000000292 calcium oxide Substances 0.000 description 2
- 235000012255 calcium oxide Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 101100219325 Phaseolus vulgaris BA13 gene Proteins 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000010806 kitchen waste Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000011802 pulverized particle Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000004056 waste incineration Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
- Processing Of Solid Wastes (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、厨芥類や紙類を含
む可燃性廃棄物から塩素含有量の少ないゴミ固形燃料を
製造する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing refuse solid fuel having a low chlorine content from combustible waste including kitchen waste and paper.
【0002】[0002]
【従来の技術】従来より、可燃性廃棄物は減容化を目的
として焼却され、焼却により発生した焼却灰を埋立によ
り処分してきた。しかし、近年、廃棄物の焼却時に猛毒
のダイオキシン類が発生することが明らかになり、ダイ
オキシン類を大量に排出する焼却施設の運転が制限され
ることになり、またダイオキシン類の発生対策として、
焼却温度を850℃以上の高温に維持して連続運転を行
い、さらに排ガス温度を300℃以下まで急冷すること
によってダイオキシン類の発生を抑制することが義務化
された。2. Description of the Related Art Conventionally, combustible waste has been incinerated for the purpose of volume reduction, and incinerated ash generated by incineration has been disposed of by landfill. However, in recent years, it has been clarified that highly toxic dioxins are generated during waste incineration, which limits the operation of incineration facilities that emit large amounts of dioxins.
It has become mandatory to suppress the generation of dioxins by performing continuous operation while maintaining the incineration temperature at a high temperature of 850 ° C. or higher, and rapidly cooling the exhaust gas temperature to 300 ° C. or lower.
【0003】焼却炉を以上のような高温で安定に連続運
転するには、できるだけ成分の均質なゴミを継続的に確
保することが必要であるが、一般に、ゴミの成分は排出
源等によって多種多様であり、また、その輸送や中間の
処理方法によっても大きく異なる。従って、ゴミの輸送
や処理方法を含めたゴミ処理の広域化を検討する必要が
あり、非常に困難な問題を含んでいる。[0003] In order to stably operate the incinerator at such high temperatures as described above, it is necessary to continuously keep dust as homogeneous as possible. They vary widely and vary greatly depending on their transport and intermediate processing methods. Therefore, it is necessary to consider a wider area of garbage disposal including garbage transportation and disposal methods, which involves a very difficult problem.
【0004】このようなゴミ処理の広域化に依存せず、
比較的均質なゴミ燃料を得ることができる方法としてゴ
ミ固形燃料化技術が注目されている。このゴミ固形燃料
は、可燃性廃棄物を原料とし、これを粉砕して金属など
の不燃物を除去し、乾燥、成形等の工程を経て得られ
る。このような処理により可燃性廃棄物が均質化され安
定した燃焼が可能な固形燃料となり、また、ダイオキシ
ン生成時の触媒となる金属類が除かれるのでダイオキシ
ンの生成が抑制される。さらに、必要に応じて添加され
る石灰系添加材が燃焼時に塩素分を固定するので、これ
によっても更にダイオキシン生成を抑制することができ
る。[0004] Without depending on such a wide area of garbage disposal,
As a method for obtaining relatively homogeneous refuse fuel, refuse solid fuel conversion technology has attracted attention. This refuse solid fuel is obtained by using a combustible waste as a raw material, pulverizing the combustible waste to remove incombustible substances such as metal, and drying and molding. By such a treatment, the combustible waste is homogenized to become a solid fuel capable of stable combustion, and since a metal serving as a catalyst at the time of dioxin generation is removed, generation of dioxin is suppressed. Furthermore, since the lime-based additive added as required fixes the chlorine content during combustion, dioxin production can be further suppressed.
【0005】しかし、従来のゴミ固形燃料はダイオキシ
ン類の生成を抑制する点では有効であるが、塩化水素等
の腐食性ガスの発生に対しては十分な抑制効果が得られ
ない問題がある。塩化水素等の腐食性ガスは、焼却設備
に止まらず排ガス集塵設備などをも腐食させるため、ダ
イオキシン類の生成抑制と共に可能な限り排除する必要
がある。そこで、ゴミ固形燃料の製造工程に脱塩工程を
加え、塩素含有量の少ないゴミ固形燃料を製造する方法
が種々提案されている。しかし、いずれの方法も高コス
トであり、また処理条件の最適化が難しい等の問題があ
る。このため効率よく塩素源を除去して塩素量の少ない
ゴミ固形燃料を製造する方法が望まれている。[0005] However, the conventional refuse solid fuel is effective in suppressing the generation of dioxins, but has a problem in that a sufficient effect of suppressing generation of corrosive gas such as hydrogen chloride cannot be obtained. Since corrosive gas such as hydrogen chloride corrodes not only incineration equipment but also exhaust gas dust collection equipment, it is necessary to suppress generation of dioxins and eliminate as much as possible. Therefore, various methods have been proposed for adding a desalting step to the refuse solid fuel production process to produce refuse solid fuel having a low chlorine content. However, both methods have problems such as high cost and difficulty in optimizing processing conditions. Therefore, there is a demand for a method of efficiently removing a chlorine source to produce a refuse solid fuel having a small amount of chlorine.
【0006】[0006]
【発明が解決しようとする課題】本発明は、従来のゴミ
燃料化処理における上記問題を解決するものであり、可
燃性廃棄物を燃料化する際に、塩化水素やダイオキシン
類等の生成の原因となる食塩等の水溶性塩化物を効率よ
く除去して、塩素含有量の少ないゴミ固形燃料を製造す
る方法を提供することを目的とする。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems in the conventional refuse-to-fuel processing, and causes the generation of hydrogen chloride, dioxins, and the like when converting combustible waste into fuel. It is an object of the present invention to provide a method for producing a refuse solid fuel having a low chlorine content by efficiently removing water-soluble chlorides such as salt.
【0007】[0007]
【課題を解決するための手段】すなわち、本発明は、
(1)可燃性廃棄物を30mm以下に粉砕し、その粉砕物
を水温25℃以上で2分以上水洗または水中に分散させ
た後に脱水し、乾燥することを特徴とするゴミ固形燃料
の製造方法に関する。本発明のゴミ燃料製造方法は、
(2)可燃性廃棄物を20mm以下に粉砕した後に、水温
30℃以上で3分以上、水量比30倍以上で水洗または
水中に分散させる製造方法、(3)脱水、乾燥した可燃
性廃棄物の粉砕物をさらに成形する製造方法、および
(4)可燃性廃棄物がすでに成形したゴミ固形燃料であ
る製造方法を含む。That is, the present invention provides:
(1) A method for producing a refuse solid fuel, comprising crushing combustible waste to 30 mm or less, washing or dispersing the crushed material at a water temperature of 25 ° C. or more for 2 minutes or more, and then dehydrating and drying. About. The garbage fuel production method of the present invention comprises:
(2) A manufacturing method in which flammable waste is crushed to 20 mm or less, and then washed or dispersed in water at a water temperature of 30 ° C. or more for 3 minutes or more and a water amount ratio of 30 times or more, (3) Dewatered and dried flammable waste And (4) a method in which the combustible waste is already formed garbage solid fuel.
【0008】[0008]
【発明の実施の形態】以下に本発明を実施例と共に詳し
く説明する。本発明の製造方法は、可燃性廃棄物を30
mm以下、好ましくは20mm以下に粉砕し、その粉砕物を
水温25℃以上、好ましくは30℃以上で、2分以上、
好ましくは3分以上、水洗または水中に分散させること
により、粉砕物に含まれる水溶性塩化物を水中に溶出さ
せて除去し、脱水後、乾燥してゴミ固形燃料を製造する
方法である。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described below in detail with examples. The production method of the present invention reduces the amount of combustible waste to 30.
mm or less, preferably crushed to 20 mm or less, and the crushed product is at a water temperature of 25 ° C. or more, preferably 30 ° C. or more, for 2 minutes or more,
Preferably, the water-soluble chloride contained in the pulverized material is eluted and removed from water by washing or dispersing in water for at least 3 minutes, followed by dehydration and drying to produce a refuse solid fuel.
【0009】本発明において可燃性廃棄物とは、厨芥類
や、木材、紙類ないし繊維類を主成分とする廃棄物を云
い、厨芥類および紙類から不燃物や金属類を除去したも
のであって、一般に可燃ゴミと称される廃棄物である。
ゴミ収集の際に予め可燃ゴミとして分別収集されたもの
でも良く、あるいはゴミ収集後、分別処理により得られ
るものでも良い。In the present invention, the term "combustible waste" refers to waste mainly composed of kitchen garbage, wood, paper or fiber, and is obtained by removing incombustibles and metals from kitchen garbage and paper. Therefore, it is waste generally called combustible waste.
The garbage may be separated and collected in advance as combustible garbage at the time of garbage collection, or may be obtained by separation processing after garbage collection.
【0010】この可燃性廃棄物を、廃棄物に含まれる水
溶性塩化物の除去効率を高めるために粉砕する。可燃性
廃棄物は紙類や繊維類を多く含むために粉砕し難い場合
がある。それらは、一旦加圧成形を行い、その後に粉砕
すると良い。ここで粉砕度と塩素溶出量の関係を図1に
示すと、同図に示すように、粉砕物の粒度が小さいほ
ど、粉砕物と水の接触面積が増大するので水溶性塩化物
が水に溶出し易くなり、脱塩効果が高い。一方、粒径が
小さいほど粉砕コストが上昇するので脱塩効果との兼ね
合いから粉砕の程度を定めるのが好ましい。図1に示す
ように、塩素溶出量は粉砕物の粒径が20mm付近から大
きくなるのに従って次第に低下し、30mm付近を越える
と急激に低下する。一方、1mm以下ではあまり変わらな
い。従って、粉砕の程度は、粒径30mm以下〜1mm前後
が適当であり、粒径20mm以下〜1mm前後が好ましい。The combustible waste is pulverized in order to increase the efficiency of removing water-soluble chloride contained in the waste. Combustible waste may be difficult to pulverize because it contains a large amount of papers and fibers. It is preferable that they are once subjected to pressure molding and then pulverized. FIG. 1 shows the relationship between the degree of pulverization and the amount of chlorine eluted. As shown in FIG. 1, the smaller the particle size of the pulverized material, the larger the contact area between the pulverized material and water. It is easy to elute and has a high desalting effect. On the other hand, the smaller the particle size, the higher the pulverization cost. Therefore, it is preferable to determine the degree of pulverization in consideration of the desalting effect. As shown in FIG. 1, the amount of chlorine eluted gradually decreases as the particle size of the pulverized material increases from around 20 mm, and sharply decreases when it exceeds 30 mm. On the other hand, at 1 mm or less, there is not much change. Therefore, the degree of pulverization is appropriately from 30 mm to 1 mm in particle size, and preferably from 20 mm to 1 mm in particle size.
【0011】次に、粉砕物を水洗し、あるいは水中に分
散させることにより、粉砕物に含まれる塩化ナトリウム
や塩素酸ナトリウムなどの水溶性(水可溶性)塩化物を溶
出させて除去する。この水処理の温度と塩素溶出量の関
係を図2に示した。同図に示すように、水温が20℃以
下では塩素の溶出量が急激に低下する。25℃〜90℃
では温度上昇にほぼ比例して溶出量が増加し、同図の処
理条件下において、水温30℃以上で約45%以上の含
有塩化物が溶出する。なお、90℃を越えると加熱コス
トが嵩む。従って処理水温は25℃以上が適当であり、
30℃〜90℃が好ましい。Next, water-soluble (water-soluble) chlorides such as sodium chloride and sodium chlorate contained in the ground material are eluted and removed by washing the ground material or dispersing it in water. FIG. 2 shows the relationship between the water treatment temperature and the chlorine elution amount. As shown in the figure, when the water temperature is lower than 20 ° C., the amount of chlorine eluted sharply decreases. 25 ° C to 90 ° C
In this case, the elution amount increases almost in proportion to the temperature rise, and under the processing conditions shown in the figure, about 45% or more of the contained chloride elutes at a water temperature of 30 ° C. or more. If the temperature exceeds 90 ° C., the heating cost increases. Therefore, the temperature of the treated water is more than 25 ° C,
30 ° C to 90 ° C is preferred.
【0012】また、水処理時間と塩素溶出量の関係を示
す図3によれば、塩素溶出量は2分未満の処理時間では
大幅に低下し、処理時間が3分を越えると次第に飽和し
15分以上になると殆ど変わらない。従って、脱塩処理
の水処理時間は2分以上が適当であり、3分〜15分が
好ましい。なお、水量は粉砕物重量に対して30〜50
倍が適当であり、撹拌するのが好ましい。処理方法は粉
砕物を水中に分散させるほか、上記水温および処理時間
を確保し、十分な水量を用いて粉砕物全体を均一にシャ
ワー状に洗浄しても良い。According to FIG. 3 showing the relationship between the water treatment time and the chlorine elution amount, the chlorine elution amount is significantly reduced when the treatment time is less than 2 minutes, and is gradually saturated when the treatment time exceeds 3 minutes. When it is more than minutes, it hardly changes. Therefore, the water treatment time of the desalination treatment is suitably 2 minutes or more, and preferably 3 minutes to 15 minutes. The amount of water is 30 to 50 with respect to the weight of the pulverized material.
A factor of 2 is appropriate and stirring is preferred. In the treatment method, in addition to dispersing the pulverized material in water, the above-mentioned water temperature and processing time may be ensured, and the entire pulverized material may be uniformly washed in a shower using a sufficient amount of water.
【0013】上記水処理の後に粉砕物を回収し脱水す
る。回収および脱水操作は特に制限されない。遠心分離
器、フィルタープレス機等を使用すると良い。なお、脱
水して得たケーキは次の乾燥工程を考慮して含水率を約
70重量%以下にすることが好ましい。After the above-mentioned water treatment, the pulverized material is recovered and dehydrated. The recovery and dehydration operations are not particularly limited. It is preferable to use a centrifuge, a filter press or the like. The cake obtained by dehydration preferably has a water content of about 70% by weight or less in consideration of the next drying step.
【0014】次に、脱水ケーキを乾燥する。乾燥手段と
しては、生石灰などの発熱反応を伴う添加材を混合し、
その発熱反応を利用すると良い。また、ボイラー等の外
熱を利用して乾燥しても良い。なお、外熱により乾燥す
る場合には、乾燥の前あるいは後に、生石灰や消石灰な
どの石灰粉末、石炭灰、セメント、あるいは石膏等を混
合し、これらの吸水性を利用して乾燥効率を向上させる
共に成形助剤としての効果を利用することができる。Next, the dehydrated cake is dried. As a drying means, mixing additives with exothermic reaction such as quicklime,
It is good to utilize the exothermic reaction. Further, drying may be performed using external heat of a boiler or the like. In the case of drying by external heat, before or after drying, lime powder such as quicklime or slaked lime, coal ash, cement, or gypsum are mixed, and drying efficiency is improved by using their water absorption. In both cases, the effect as a molding aid can be utilized.
【0015】上記乾燥後、必要に応じて成形する。本発
明の固形燃料は粉末でも良く、成形体でも良い。成形は
輸送や燃焼設備に適した形状とするために行われるが、
燃焼に際して粉粒体の形状が好ましい場合は成形する必
要はない。むしろ必要粒度になるよう粉砕する。成形す
る場合には、使用する成型機に応じて石灰粉末などの添
加物量を調整し、所望の形状、大きさ、硬さ等が得られ
るように成形する。なお、成形機は押出し成型機やロー
ルプレス成型機などの公知の成型機を使用することがで
きる。After the above-mentioned drying, it is formed as required. The solid fuel of the present invention may be a powder or a compact. Molding is performed to make the shape suitable for transportation and combustion equipment,
In the case where the shape of the granular material during combustion is preferable, it is not necessary to mold. Rather, pulverize to the required particle size. In the case of molding, the amount of additives such as lime powder is adjusted according to the molding machine to be used, and molding is performed so as to obtain a desired shape, size, hardness and the like. As the molding machine, a known molding machine such as an extrusion molding machine or a roll press molding machine can be used.
【0016】以上の製造方法は、既存の手段によってゴ
ミ固形燃料としたものを利用することもできる。すなわ
ち、これを可燃性廃棄物として用い、上記方法によって
処理する。例えば、ビニール袋やヒモなどのように粉砕
し難い廃棄物は、これを一度、加圧成形することにより
粉砕し易くなり、微粉化により脱塩効果が向上する。In the above-mentioned production method, a solid fuel made into garbage by existing means can be used. That is, this is used as combustible waste and treated by the above method. For example, waste that is difficult to grind, such as a plastic bag or a string, is easily crushed by pressing once, and the desalting effect is improved by pulverization.
【0017】このようにして得られる本発明のゴミ固形
燃料は、水溶性塩化物の含有量が少ないので、塩化水素
の発生が大幅に抑制され、燃料としての利用分野が広が
り、かつその使用量も増大することができる。従って、
埋立処分地の確保が難しくなっているゴミ処理の問題解
決にも寄与する。The refuse solid fuel of the present invention thus obtained has a low content of water-soluble chloride, so that the generation of hydrogen chloride is greatly suppressed, the field of application as a fuel is widened, and the amount of its use is increased. Can also be increased. Therefore,
It also contributes to solving the problem of garbage disposal, for which it is difficult to secure landfill sites.
【0018】[0018]
【実施例】次に実施例により本発明を具体的に示す。な
お、以下は例示であり本発明の範囲を限定するものでは
ない。Next, the present invention will be specifically described by way of examples. The following is an exemplification and does not limit the scope of the present invention.
【0019】実施例1〜4 表1に示す成分の可燃性廃棄物を用い、この廃棄物10
kgを二軸破砕機によって乾式一次粉砕し、さらに衝撃・
剪断併用の回転式破砕機を用いて乾式二次粉砕して表2
に示す粒径の粉砕物とした。これらの粉砕物を表2に示
す条件で水中に投入して撹拌した。この水処理の後に、
粉砕物を回収し、遠心分離器を用いて脱水し、得られた
ケーキを樹脂製濾布で被覆した濾板上に敷き並べ、10
0kgの水を散布して洗浄した後に濾布付き圧縮プレス機
に移して含水率が70重量%になるまで脱水した。更
に、この脱水ケーキをスラッジドライヤーで含水率5重
量%まで乾燥し、粉体状のゴミ固形燃料約6kgを得
た。これらのゴミ固形燃料の塩素含有量および発熱量を
表2にまとめて示した。 Examples 1 to 4 Combustible waste having the components shown in Table 1 was used.
kg by dry primary crushing using a twin-screw crusher.
Dry secondary pulverization using a rotary crusher combined with shearing
The crushed product having the particle size shown in Table 1 was obtained. These pulverized materials were put into water and stirred under the conditions shown in Table 2. After this water treatment,
The pulverized material was collected, dehydrated using a centrifuge, and the obtained cake was spread on a filter plate covered with a resin filter cloth and arranged.
After washing with 0 kg of water, the mixture was transferred to a compression press equipped with a filter cloth and dehydrated until the water content became 70% by weight. Further, this dehydrated cake was dried to a water content of 5% by weight with a sludge dryer to obtain about 6 kg of powdery refuse solid fuel. Table 2 summarizes the chlorine content and calorific value of these refuse solid fuels.
【0020】実施例5 実施例1で得た粉体状の固形燃料を押し出し成型機を用
いて成形し、円筒状のゴミ固形燃料(直径15mm,長さ30m
m)を製造した。この円筒状固形燃料10kgを表2に示す
処理条件に従って粉砕・水処理し、脱水・乾燥して粉体
状のゴミ固形燃料約6kgを得た。このゴミ固形燃料の塩
素含有量および発熱量を表2に示した。 Example 5 The powdery solid fuel obtained in Example 1 was molded by using an extrusion molding machine, and was formed into a cylindrical solid waste fuel (diameter 15 mm, length 30 m).
m) was prepared. 10 kg of this cylindrical solid fuel was pulverized and water-treated according to the processing conditions shown in Table 2, dehydrated and dried to obtain about 6 kg of powdery solid waste fuel. Table 2 shows the chlorine content and the calorific value of this refuse solid fuel.
【0021】実施例6 実施例1と同様の可燃性廃棄物10kgを二軸破砕機によ
って乾式粉砕によって粒径50mm以下に粉砕した。この
粉砕物をスラッジドライヤーで含水率が5重量%になる
まで乾燥した。次いで、押し出し形成機を用いて上記粉
砕物を成形し、円筒状(直径15mm,長さ30mm)のゴミ固形
燃料約6kgを得た。この円筒状固形燃料6kgを、二軸破
砕機を用いて乾燥一次粉砕、および、衝撃・剪断併用の
回転式破砕機を用いた乾燥二次粉砕により表2に示す粒
径に粉砕した。この粉砕物を表2に示す条件で水中に投
入して撹拌した。この水処理の後に、粉砕物を回収し、
遠心分離器を用いて脱水し、得られたケーキを樹脂製濾
布で被覆した濾板上に敷き並べ、100kgの水を散布し
て洗浄した後に濾布付き圧縮プレス機に移して含水率が
70重量%になるまで脱水した。更に、この脱水ケーキ
をスラッジドライヤーで含水率5重量%まで乾燥し、粉
体状のゴミ固形燃料約6kgを得た。これらのゴミ固形燃
料の塩素含有量および発熱量を表2にまとめて示した。 Example 6 The same combustible waste as in Example 1 (10 kg) was pulverized to a particle size of 50 mm or less by dry pulverization using a twin-screw crusher. The pulverized product was dried with a sludge dryer until the water content became 5% by weight. Next, the above-mentioned pulverized material was molded using an extruder to obtain about 6 kg of a cylindrical (15 mm in diameter, 30 mm in length) refuse solid fuel. 6 kg of this cylindrical solid fuel was pulverized to a particle size shown in Table 2 by primary dry pulverization using a twin-screw crusher and secondary dry pulverization using a rotary crusher combined with impact and shearing. This pulverized product was put into water and stirred under the conditions shown in Table 2. After this water treatment, the crushed material is collected,
The cake was dehydrated using a centrifugal separator, and the obtained cake was laid out on a filter plate covered with a resin filter cloth. It was dehydrated to 70% by weight. Further, this dewatered cake was dried with a sludge dryer to a water content of 5% by weight to obtain about 6 kg of powdery solid waste fuel. Table 2 summarizes the chlorine content and calorific value of these refuse solid fuels.
【0022】比較例 粉砕物の粒径を30mm、処理水温を20℃、処理時間を
1分とした以外は実施例1〜4と同様にして、上記可燃
性廃棄物10kgを粉砕・水処理し、脱水・乾燥して粉体
状のゴミ固形燃料を得た。更に、このゴミ固形燃料を押
出し成形機を用いて成形し、円筒状のゴミ固形燃料(直
径15mm,長さ30mm)約6kgを得た。このゴミ固形燃料の塩
素含有量および発熱量を表2に示した。[0022] 30mm the particle size of Comparative Example grind process water temperature and 20 ° C., except that the processing time was 1 minute in the same manner as in Example 1-4, was ground and water treatment the combustible waste 10kg The powder was dehydrated and dried to obtain a powdery solid fuel. Further, this solid waste fuel was molded using an extruder to obtain about 6 kg of a cylindrical solid waste fuel (diameter 15 mm, length 30 mm). Table 2 shows the chlorine content and the calorific value of this refuse solid fuel.
【0023】[0023]
【表1】 [Table 1]
【0024】[0024]
【表2】 [Table 2]
【0025】表2の実施例1〜6に示すように、粉砕粒
径および水処理条件を最適化して水溶性塩化物を除去し
た本発明のゴミ固形燃料は、いずれも比較例と比べて塩
素含有量が極めて少なく、かつ発熱量が高い。As shown in Examples 1 to 6 in Table 2, the refuse solid fuel of the present invention, from which the water-soluble chloride was removed by optimizing the pulverized particle size and the water treatment conditions, was compared with the comparative example. Extremely low content and high calorific value.
【0026】[0026]
【発明の効果】本発明のゴミ固形燃料の製造方法によれ
ば、可燃性廃棄物から水溶性塩化物を容易に除去でき、
含有塩素量が極めて少なく、しかも発熱量が高いゴミ固
形燃料を得ることができる。According to the method for producing refuse solid fuel of the present invention, water-soluble chloride can be easily removed from combustible waste,
A refuse solid fuel having a very low chlorine content and a high calorific value can be obtained.
【図1】 粉砕物の粒径と塩素溶出量の関係を示すグラ
フFIG. 1 is a graph showing the relationship between the particle size of the pulverized material and the chlorine elution amount.
【図2】 処理水温と塩素溶出量の関係を示すグラフFIG. 2 is a graph showing a relationship between a treatment water temperature and a chlorine elution amount.
【図3】 処理時間と塩素溶出量の関係を示すグラフFIG. 3 is a graph showing the relationship between treatment time and chlorine elution amount.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 和泉 一志 千葉県佐倉市大作二丁目4番2号 秩父小 野田株式会社中央研究所内 Fターム(参考) 4H015 AA01 AA12 BA08 BA09 BA13 BB10 BB13 ────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Kazushi Izumi 2-4-2 Daisaku, Sakura-shi, Chiba F-term in Central Research Laboratory, Noda Co., Ltd. F-term (reference) 4H015 AA01 AA12 BA08 BA09 BA13 BB10 BB13
Claims (4)
の粉砕物を水温25℃以上で2分以上水洗または水中に
分散させた後に脱水し、乾燥することを特徴とするゴミ
固形燃料の製造方法。1. A garbage solid fuel characterized in that flammable waste is crushed to 30 mm or less, and the crushed material is washed or dispersed in water at a water temperature of 25 ° C. or more for 2 minutes or more, and then dewatered and dried. Production method.
に、水温30℃以上で3分以上、水量比30倍以上で水
洗または水中に分散させる請求項1に記載するゴミ固形
燃料の製造方法。2. The method for producing refuse solid fuel according to claim 1, wherein the combustible waste is pulverized to a size of 20 mm or less, and then washed or dispersed in water at a water temperature of 30 ° C. or more for 3 minutes or more and a water amount ratio of 30 times or more. .
さらに成形する請求項1または2に記載するゴミ固形燃
料の製造方法。3. The method for producing a refuse solid fuel according to claim 1, wherein a dewatered and dried pulverized combustible waste is further formed.
燃料である請求項1〜3のいずれかに記載するゴミ燃料
の製造方法。4. The method for producing a refuse fuel according to claim 1, wherein the combustible waste is a previously formed refuse solid fuel.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10184071A JP2000017278A (en) | 1998-06-30 | 1998-06-30 | Preparation of refuse solid fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10184071A JP2000017278A (en) | 1998-06-30 | 1998-06-30 | Preparation of refuse solid fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000017278A true JP2000017278A (en) | 2000-01-18 |
Family
ID=16146881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10184071A Pending JP2000017278A (en) | 1998-06-30 | 1998-06-30 | Preparation of refuse solid fuel |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000017278A (en) |
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---|---|---|---|---|
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JP2008063362A (en) * | 2006-09-04 | 2008-03-21 | Sumitomo Osaka Cement Co Ltd | Method and apparatus for treating chlorine-containing organic waste |
WO2009057713A1 (en) * | 2007-10-31 | 2009-05-07 | Sumitomo Osaka Cement Co., Ltd. | Method of desalting organic waste, process for producing biomass, and biomass fuel |
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JP2010077191A (en) * | 2008-09-24 | 2010-04-08 | Sumitomo Osaka Cement Co Ltd | Method for converting water-containing organic waste into fuel and biomass fuel |
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1998
- 1998-06-30 JP JP10184071A patent/JP2000017278A/en active Pending
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