JPS6011993B2 - Liquid fuel production equipment using wood pyrolysis - Google Patents
Liquid fuel production equipment using wood pyrolysisInfo
- Publication number
- JPS6011993B2 JPS6011993B2 JP56031545A JP3154581A JPS6011993B2 JP S6011993 B2 JPS6011993 B2 JP S6011993B2 JP 56031545 A JP56031545 A JP 56031545A JP 3154581 A JP3154581 A JP 3154581A JP S6011993 B2 JPS6011993 B2 JP S6011993B2
- Authority
- JP
- Japan
- Prior art keywords
- wood
- water
- liquid
- reactor
- temperature
- 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.)
- Expired
Links
- 239000007788 liquid Substances 0.000 title claims description 29
- 239000002023 wood Substances 0.000 title claims description 21
- 239000000446 fuel Substances 0.000 title claims description 9
- 238000000197 pyrolysis Methods 0.000 title description 12
- 238000004519 manufacturing process Methods 0.000 title description 2
- 239000012530 fluid Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 238000009833 condensation Methods 0.000 description 11
- 230000005494 condensation Effects 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 238000005979 thermal decomposition reaction Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 241001251054 Formica truncorum Species 0.000 description 3
- 239000013064 chemical raw material Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- 210000000416 exudates and transudate Anatomy 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011269 tar Substances 0.000 description 2
- CYJRNFFLTBEQSQ-UHFFFAOYSA-N 8-(3-methyl-1-benzothiophen-5-yl)-N-(4-methylsulfonylpyridin-3-yl)quinoxalin-6-amine Chemical compound CS(=O)(=O)C1=C(C=NC=C1)NC=1C=C2N=CC=NC2=C(C=1)C=1C=CC2=C(C(=CS2)C)C=1 CYJRNFFLTBEQSQ-UHFFFAOYSA-N 0.000 description 1
- 244000274847 Betula papyrifera Species 0.000 description 1
- 235000009113 Betula papyrifera Nutrition 0.000 description 1
- 235000009109 Betula pendula Nutrition 0.000 description 1
- 235000010928 Betula populifolia Nutrition 0.000 description 1
- 235000002992 Betula pubescens Nutrition 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000011276 wood tar 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
Landscapes
- Coke Industry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
【発明の詳細な説明】
本発明は、木材等の熱分解による液体燃料の製造装置に
関し、原木、廃材、チップ、おがくず、木皮、植物など
を、325qo〜600℃の条件下で熱分解して分解生
成物を得る際、分解生成物中の可燃分を熱分解液の凝縮
過程で粗分離し、直接燃焼可能な液体燃料を製造装置に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an apparatus for producing liquid fuel by pyrolyzing wood, etc., which pyrolyzes raw wood, waste wood, chips, sawdust, bark, plants, etc. under conditions of 325 qo to 600°C. The present invention relates to an apparatus for producing a directly combustible liquid fuel by roughly separating combustible components in the decomposition product during the condensation process of the thermal decomposition liquid when obtaining the decomposition product.
従来、木材の炭化を目的とした木材の乾留工程において
、その際の副産物として生成する留出液を回収する方法
としては、分解して蒸気化した液体を単純に空冷あるい
は水袷式の熱交換器で冷却し、凝縮して回収する方法が
とられている。Conventionally, the method of recovering the distillate produced as a byproduct during the carbonization process of wood for the purpose of carbonizing the wood has been to simply air-cool the decomposed and vaporized liquid or use a water tank type heat exchange method. The method used is to cool it in a container, condense it, and recover it.
この従来の回収方法では、木材や他の植物の熱分解液を
回収しようとした場合、分解して生成する揮発性物質中
に含まれている多量の水分の影響をうけて、ガス温度は
急激に低下し、容易に水の沸点以下となってしまい、水
の沸点以上の液体と水とが同時に凝縮して、これらを分
離することができない。したがって、このようにして得
られた蟹出液中には、原料の含湿分によっても異なるが
、水分量が40〜80%と多いため、発熱量が低く、直
接燃焼に適さないものもあり、またこれを化学原料とし
て使用するとしても、多量の含水分の分離が必要であり
、しかも水の分離は非常に困難であるため、蟹出液の用
途は限られ、価値は低いものとなつている。In this conventional recovery method, when attempting to recover the pyrolyzed liquid of wood or other plants, the gas temperature rapidly increases due to the large amount of water contained in the volatile substances produced by decomposition. The temperature drops to below the boiling point of water, and the liquid above the boiling point of water and water condense at the same time, making it impossible to separate them. Therefore, the crab exudate obtained in this way has a high moisture content of 40 to 80%, depending on the moisture content of the raw material, so it has a low calorific value and is not suitable for direct combustion. Furthermore, even if it were to be used as a chemical raw material, it would be necessary to separate a large amount of water, and separating water is extremely difficult, so the uses of crab exudate are limited and its value is low. ing.
例えば、蒸留作用によって木材や植物の熱分解によって
得られたセルロース油の脱水を行う場合初留点は約60
ooであるが、その後水の沸点である100ooとなり
、この蒸留の最中に釜残液の方に溶解タールが折出して
黒色のペースト状になり、さらに温度が高くなるにつれ
て固型化や二次分解を起こす。For example, when dehydrating cellulose oil obtained by pyrolysis of wood or plants by distillation, the initial boiling point is approximately 60
oo, but then it reaches 100oo, which is the boiling point of water, and during this distillation, dissolved tar precipitates into the bottom of the pot and becomes a black paste, and as the temperature further increases, it solidifies and doubles. The next decomposition occurs.
このように、常圧蒸留によって水を分離した後の熱分解
液は、軍縮合等により高分子化して、全く異なる物質に
変化して釜から取出すことも困難となる。本発明は上述
のような木材の乾留における生成液の回収技術の欠点を
解消しようとするものであり、本発明は水分を多く含む
木材や植物を熱分解する際、生成経路に加熱手段や、冷
却手段を設けることにより、熱分解装置側の温度が高く
なるような温度勾配をつけ、この温度勾配のある部分に
留出液の取出し口を設置し、可燃物の木タールや木酢液
と大部分の水分を凝縮過程において粗分離して取出すよ
うにした点を特長とするものである。In this way, the thermal decomposition liquid after water has been separated by atmospheric distillation is polymerized by military condensation, etc., and turns into a completely different substance, making it difficult to remove it from the pot. The present invention aims to solve the above-mentioned drawbacks of the technology for recovering the product liquid in the carbonization of wood, and the present invention provides a heating means in the production path when pyrolyzing wood or plants containing a large amount of water. By providing a cooling means, we create a temperature gradient that increases the temperature on the pyrolysis equipment side, and install a distillate outlet in the area where this temperature gradient exists, so that it can be separated from combustible wood tar and pyroligneous vinegar. The feature is that the moisture in the portion is roughly separated and taken out during the condensation process.
なおここで、最初の凝縮液の取出し口の温度は水の沸点
以上の温度とし、水分を多く含んだガス状物質が通過す
る場合にも水の凝縮を避ける必要がある。例えば110
qo〜200q○の温度とすることによって、多量に含
まれる水分の凝縮をさげ沸点の高い油分などを初めの取
出し口で凝縮させ、水分は後方の取出し口から別に回収
する。したがって本発明により得られた木材の熱分解液
はそのまま燃焼させることも可能であり、また化学原料
とする場合にも有利となる。Note that the temperature at the outlet of the first condensate should be set to a temperature higher than the boiling point of water to avoid condensation of water even when a gaseous substance containing a large amount of water passes through. For example 110
By setting the temperature to qo~200q○, condensation of a large amount of water contained is reduced, and oils with a high boiling point are condensed at the first outlet, and water is separately recovered from the rear outlet. Therefore, the wood pyrolysis liquid obtained by the present invention can be burned as it is, and is also advantageous when used as a chemical raw material.
第1図は本発明の装置の一例の概略図であり、第1図に
おいて、7は反応器である。FIG. 1 is a schematic diagram of an example of the apparatus of the present invention, and in FIG. 1, 7 is a reactor.
反応器7内に入れられた試料8は流動熱媒体9によって
熱分解され、生成された熱分解生成物は反応器7から上
方に延出する取出し径路管2川こ流出する。径路管20
は互いに蓮適する複数個の室に分割されている。径路管
2川こは、加熱ヒーター10、冷却器12,13により
反応器7側が高温の温度勾配がつけられている。1〜6
は各温度勾配の個所ならびに径路管20の適所に設けた
受器で、各受器には、その設置場所の温度により凝縮し
た成分が液状で回収される。The sample 8 placed in the reactor 7 is thermally decomposed by the fluid heat medium 9, and the generated thermal decomposition products flow out of the reactor 7 through two take-out path pipes extending upward. Route pipe 20
It is divided into several chambers that fit each other. The two route pipes have a temperature gradient where the reactor 7 side is at a high temperature due to the heating heater 10 and the coolers 12 and 13. 1-6
is a receiver provided at each temperature gradient point and at an appropriate location in the route pipe 20, and components condensed due to the temperature at the location are collected in liquid form in each receiver.
11は保温材で反応器7の上方および加熱ヒーター10
のまわりに捲回されておりTo〜T6は要所に設けた温
度計1 4,1 5は冷却器12,13に流通する温水
、冷水を示す。11 is a heat insulating material that is placed above the reactor 7 and the heating heater 10
Thermometers 14, 15, which are wound around the water coolers 14 and 15, are provided at key points To to T6, indicating hot water and cold water flowing to the coolers 12 and 13, respectively.
そして最後まで液化されなかった生成物はガス16とな
って装置外へ導出される。このガスは一酸化炭素、メタ
ン、ェタン、プロパン、エチレン、水素、炭酸ガスなど
が含まれており、不燃ガスの除去により燃料として使用
できる。熱分解液の凝縮過程において、水の粗分離を行
い燃料として使える留出液を得る本発明の装置を用いれ
ば、従来、木材や植物の熱分解液は脱水が困難で厄介も
の扱いされていたが、このような再生産が可能な植物か
ら液体燃料を有利に製造することができる。The product that has not been liquefied to the end becomes gas 16 and is led out of the apparatus. This gas contains carbon monoxide, methane, ethane, propane, ethylene, hydrogen, carbon dioxide, etc., and can be used as fuel by removing nonflammable gases. In the condensation process of pyrolysis liquid, if the device of the present invention is used to roughly separate water and obtain a distillate that can be used as fuel, the pyrolysis liquid of wood and plants, which was conventionally difficult to dehydrate and was treated as a nuisance, can be used. However, liquid fuels can advantageously be produced from such reproducible plants.
たとえば、従釆の方法によって、約10%の水分を含む
比較的乾燥した木材を450℃で回収されたセルロース
油の発熱量は約1800cal/夕であり、このまま単
独で燃料として用いることはできず、他の高カロリー燃
料と混合しなければ利用できない。これに対し、本発明
の装置を用いれば約5000〜600比al/夕のター
ル液が熱分解の凝縮過程において容易に水と分離して得
られ、このままで燃焼可能なセルロース油が得られる。
さらに凝縮温度別に粗分離された熱分解液を化学原料に
利用する場合、従来方法に較べ水の含有量が極めて少な
く有機質濃度が高く、非常に有利である。以下実施例を
あげて本発明を具体的に説明する。For example, the calorific value of cellulose oil recovered from relatively dry wood containing approximately 10% water at 450°C using the conventional method is approximately 1,800 cal/night, and it cannot be used alone as a fuel. , which can only be used by mixing with other high-calorie fuels. On the other hand, if the apparatus of the present invention is used, a tar liquid having a ratio of about 5,000 to 600 al/l can be easily separated from water in the condensation process of thermal decomposition, and a cellulose oil that can be combusted as it is can be obtained.
Furthermore, when the thermal decomposition liquid roughly separated according to the condensation temperature is used as a chemical raw material, the water content is extremely low compared to the conventional method, and the organic concentration is high, which is very advantageous. The present invention will be specifically explained below with reference to Examples.
実施例 1
第1図の装置を用い、反応器7に木材チップ(白樺)1
00夕を充填し、受器1,2,3,4の上部位置の温度
計T3,T4,T5,T6がそれぞれ160℃、120
qC、10び○、70qoになるように加熱ヒータ10
および冷却器12,13を制御し(冷却器12には50
qoの温水を、同13には5℃の冷水を流通)、各凝縮
液取出し口の温度が設定温度に安定した後、500oo
’の流動熱媒体9に反応器7を浸し、熱分解を行った。Example 1 Using the apparatus shown in Fig. 1, 1 wood chip (white birch) was placed in the reactor 7.
00℃ is filled, and the thermometers T3, T4, T5, and T6 at the upper positions of receivers 1, 2, 3, and 4 are 160℃ and 120℃, respectively.
Heater 10 so that qC, 10 bi○, 70 qo
and controls coolers 12 and 13 (cooler 12 has a
After the temperature of each condensate outlet stabilized at the set temperature, 500oo
The reactor 7 was immersed in the fluid heat medium 9 of ', and thermal decomposition was performed.
生成した熱分解ガスおよび蒸気は温度制御された径路管
20を通過し、受器1〜6の部分において凝縮現象が認
められ、それぞれの受器に生成液が蓄積された。目視に
よる凝縮液の性状は、受器1には黒かつ色のタール状物
質、受器2には1部淡黄色の透明液を含む柔いタール状
物質、受器3には1部タール物質を含む淡黄色の透明液
、受器4には、若干白濁した淡黄色透明液、受器5は液
量が最も多く淡黄色の白濁液、受器6は量が最少で香り
の良好な透明な淡黄色の液体がそれぞれ確認された。The generated pyrolysis gas and steam passed through the temperature-controlled path pipe 20, and a condensation phenomenon was observed in the receivers 1 to 6, and the product liquid was accumulated in each receiver. Visually, the properties of the condensate were as follows: Receiver 1 contained a black and colored tar-like substance, Receiver 2 contained a soft tar-like substance containing part of a pale yellow transparent liquid, and Receiver 3 contained part of a tar-like substance. Receiver 4 contains a slightly cloudy pale yellow transparent liquid, Receiver 5 contains the largest volume of pale yellow white turbid liquid, Receiver 6 contains the smallest volume and is clear with a good aroma. A pale yellow liquid was confirmed.
各凝縮液のポンプ熱量計による発熱量の測定結果は、受
器1について560比al/タ同2については460比
al/夕、同3については380比al/夕、同4につ
いては2800cal/夕、同5については100ca
l/夕、同6については200比al′夕であった。第
2図は流動熱媒体の温度が325qo〜530q0の範
囲で木材を熱分解して得られた留出液の発熱量と流動熱
媒体の温度との関係をあらわすグラフで、図中1〜6は
凝縮液の取出し口の番号である。このグラフより木材の
熱分解液に含まれる水の大部分が受器5に集中し、本発
明により熱分解の凝縮過程において、400比al/タ
以上の可燃性液体が容易に分離できることが明らかであ
る。また、木材る400qo以上で熱分解した場合、受
器1〜3で得られる凝縮液はいずれも3000cal′
好以上の発熱量を示し、受器5は発熱量が殆んどない液
体であることから、その大部分は水と考えられる。The measurement results of the calorific value of each condensate using a pump calorimeter are as follows: 560 cal/al/night for Receiver 1, 460 cal/night for Receiver 2, 380 cal/night for Receiver 3, and 2800 cal/night for Receiver 4. In the evening, 100ca for the same 5
1/evening, and 6 was 200 ratio al'evening. Figure 2 is a graph showing the relationship between the calorific value of the distillate obtained by thermally decomposing wood and the temperature of the fluid heat carrier when the temperature of the fluid heat carrier is in the range of 325qo to 530q0. is the number of the condensate outlet. From this graph, it is clear that most of the water contained in the wood pyrolysis liquid concentrates in the receiver 5, and that the present invention can easily separate a flammable liquid of 400 specific al/ta or more in the condensation process of pyrolysis. It is. In addition, when wood is thermally decomposed at 400 qo or more, the condensate obtained in receivers 1 to 3 is 3000 cal'
Since the receiver 5 is a liquid with almost no calorific value, most of it is considered to be water.
受器4,6での発熱量は1500〜2800cal′夕
であり、水の混入が推測されるが従来法による回収液の
発熱量に比べて同じくらいか、あるいは若干高い懐向に
ある。第3図は、第2図で示した凝縮液1〜5の密度と
熱分解温度との関係をあらわし、1の密度が最高で1.
23夕/めで5は水に最も近く1.02〜1.05夕/
地である。The calorific value in the receivers 4 and 6 is 1,500 to 2,800 cal, and although it is assumed that water is mixed in, the calorific value is about the same or slightly higher than the calorific value of the recovered liquid by the conventional method. FIG. 3 shows the relationship between the density of condensates 1 to 5 shown in FIG. 2 and the thermal decomposition temperature, with the density of 1 being the highest and the density of 1.
23 evening/Mede 5 is closest to the water 1.02~1.05 evening/
It is the earth.
水分を粗分離した他の凝縮液は、従来の木材の熱分解液
と比べ発熱量が高く、そのままで燃焼可能なセルロース
系の熱分解液が得られた。The other condensate from which water was roughly separated had a higher calorific value than conventional wood pyrolysis liquid, and a cellulose-based pyrolysis liquid that could be combusted as it was was obtained.
また、従来の方法によるセルロース系物質の熱分解液は
水分が多く、除去が困難なことと多くの有機物が混入し
て不安定なことから、一部で邪魔もの扱いにされてきた
が、本発明により得られた凝縮温度別留分は従来の方法
によるセルロース系熱分解液の蒸留では得られないもの
であり、化学薬品の原料としても有利であることは明ら
かであろう。In addition, the thermal decomposition solution of cellulose materials produced by conventional methods has a high water content, making it difficult to remove, and is unstable due to the contamination of many organic substances. It is clear that the condensation temperature separate fraction obtained by the present invention cannot be obtained by distillation of cellulosic pyrolysis liquid by conventional methods, and is also advantageous as a raw material for chemicals.
第1図は本発明の一例の縦型分留装置の側断面図、第2
図は本発明における木材の熱分解温度と得られた各凝縮
液の発熱量との関係を表すグラフを示した説明図、第3
図は同各流出液の密度を表すグラフを示した説明図であ
る。
1〜6・・・・・・受器。
7・・・・・・反応器。
9・・・・・・試料。
10…・・・加熱ヒータ。
12,13・・・・・・冷却器。
20・・・・・・径路管。
L〜T6・…・・温度計。第1図第2図
第3図FIG. 1 is a side sectional view of a vertical fractionator as an example of the present invention, and FIG.
Figure 3 is an explanatory diagram showing a graph showing the relationship between the thermal decomposition temperature of wood and the calorific value of each condensate obtained in the present invention.
The figure is an explanatory diagram showing a graph representing the density of each effluent. 1-6... Receiver. 7...Reactor. 9... Sample. 10... Heater. 12,13...Cooler. 20...Route pipe. L~T6...Thermometer. Figure 1 Figure 2 Figure 3
Claims (1)
入れる反応器を浸漬し、該反応器には該反応器内で生成
した生成物を導出するための径路管を互いに連通する複
数個の室に分割すると共に前記径路管の外側には加熱ヒ
ーター及び冷却器を反応器側から順序的に配設し、径路
管内の前記室には凝縮した液体を取出すための取出し口
を設けてなる木材の熱分解による液体燃料の製造装置。1 A fluid heat transfer medium is accommodated in a container, a reactor containing wood is immersed in the fluid heat transfer medium, and the reactor has a plurality of path pipes communicating with each other for extracting the products produced in the reactor. At the same time, a heating heater and a cooler are arranged in order from the reactor side on the outside of the route pipe, and an outlet for taking out the condensed liquid is provided in the chamber in the route pipe. A device for producing liquid fuel by pyrolyzing wood.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56031545A JPS6011993B2 (en) | 1981-03-04 | 1981-03-04 | Liquid fuel production equipment using wood pyrolysis |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56031545A JPS6011993B2 (en) | 1981-03-04 | 1981-03-04 | Liquid fuel production equipment using wood pyrolysis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57145177A JPS57145177A (en) | 1982-09-08 |
| JPS6011993B2 true JPS6011993B2 (en) | 1985-03-29 |
Family
ID=12334154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56031545A Expired JPS6011993B2 (en) | 1981-03-04 | 1981-03-04 | Liquid fuel production equipment using wood pyrolysis |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6011993B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60133187A (en) * | 1983-12-19 | 1985-07-16 | メタコ企業株式会社 | Film body of roll screen apparatus |
| JP2021055026A (en) * | 2019-10-02 | 2021-04-08 | エムラボ株式会社 | Apparatus and method for converting organic matter into oil |
| JP2021095498A (en) * | 2019-12-17 | 2021-06-24 | 株式会社ジャパンErcm | Fuel, method for producing fuel, apparatus for treating organic matter-containing waste, and method for treating organic matter-containing waste |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10619113B2 (en) * | 2017-05-19 | 2020-04-14 | Sam Su | Method and system for coal purification and complete burning for clean fossil fuel |
-
1981
- 1981-03-04 JP JP56031545A patent/JPS6011993B2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60133187A (en) * | 1983-12-19 | 1985-07-16 | メタコ企業株式会社 | Film body of roll screen apparatus |
| JP2021055026A (en) * | 2019-10-02 | 2021-04-08 | エムラボ株式会社 | Apparatus and method for converting organic matter into oil |
| JP2021095498A (en) * | 2019-12-17 | 2021-06-24 | 株式会社ジャパンErcm | Fuel, method for producing fuel, apparatus for treating organic matter-containing waste, and method for treating organic matter-containing waste |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57145177A (en) | 1982-09-08 |
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