JPS6015674B2 - Pyrolysis method and equipment for polyolefin plastic waste - Google Patents
Pyrolysis method and equipment for polyolefin plastic wasteInfo
- Publication number
- JPS6015674B2 JPS6015674B2 JP4892983A JP4892983A JPS6015674B2 JP S6015674 B2 JPS6015674 B2 JP S6015674B2 JP 4892983 A JP4892983 A JP 4892983A JP 4892983 A JP4892983 A JP 4892983A JP S6015674 B2 JPS6015674 B2 JP S6015674B2
- Authority
- JP
- Japan
- Prior art keywords
- plastic waste
- thermal decomposition
- polyolefin plastic
- catalyst layer
- reaction section
- 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
- 229920000098 polyolefin Polymers 0.000 title claims description 20
- 239000013502 plastic waste Substances 0.000 title claims description 17
- 238000000197 pyrolysis Methods 0.000 title claims description 10
- 238000000034 method Methods 0.000 title claims description 8
- 239000003054 catalyst Substances 0.000 claims description 29
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 28
- 239000002994 raw material Substances 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000006555 catalytic reaction Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 12
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 239000004033 plastic Substances 0.000 description 9
- 229920003023 plastic Polymers 0.000 description 9
- 238000009826 distribution Methods 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000000446 fuel Substances 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012773 agricultural material Substances 0.000 description 1
- 239000002154 agricultural waste Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229920001870 copolymer plastic Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004184 polymer manufacturing process Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
【発明の詳細な説明】
本発明はポリオレフィン系プラスチック廃棄物を熱分解
して燃料が素原料として有用な液状炭化水素油を得るた
めの方法とその装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method and apparatus for thermally decomposing polyolefin plastic waste to obtain liquid hydrocarbon oil useful as a raw material for fuel.
我国で熱可塑性プラスチック生産量のうち、約50%ほ
ど占めているポリオレフイン系プラスチックは日常用品
、農業用材料から工業用部品まで広い用途をもっており
、生活に密接な関係を持っている。Polyolefin plastics, which account for approximately 50% of the total thermoplastic plastic production in Japan, have a wide range of uses, from daily necessities and agricultural materials to industrial parts, and are closely related to our daily lives.
しかし、使用済の廃プラスチックは焼却されたり、再生
形されて利用されているとはいえ、大部分はそのまま廃
棄されている。However, although used waste plastics are incinerated or recycled, the majority of them are simply discarded.
次第に蓄積量が増大しており、その処理は社会的に重要
な問題になている。このような廃プラスチックをなんら
かの手段で燃料や工業用素材として再生することができ
れば資源やエネルギーの節約につながり、資源の乏しい
我国において重要な意義を有することになる。The amount accumulated is gradually increasing, and its disposal has become a socially important issue. If such waste plastics can be recycled as fuel or industrial materials by some means, it will lead to resource and energy conservation, which will be of great significance in our resource-poor country.
これまで、簾プラスチックを熱分解して炭化水素油を回
収する方法について報告があるが、ポリマーを製造する
過程で副生される重合度が低いポリマーや熱分解によっ
て簡単に生成油になりやすいポリスチレン系プラスチッ
クに限られていた。しかしながら、ポリオレフィン系プ
ラスチックを単に熱分解した場合、即ち触媒を全く用い
ないで熱分解した場合、炭素数分布ら〜C班という広夕
い分子量分布範囲の生成物が得られ、これは室温でワッ
クス状を呈するため、その利用法に限界があり、また単
に熱分解した場合にはカーボンの発生による熱分解装置
のトラブルや配管類の閉鎖等の問題があり、したがって
現状での熱分解技術で0はポリオレフイン系プラスチッ
クの熱分解は非常に困難である。そのため、簡単な方法
と装置によってポIJオレフィン系プラスチックの熱分
解ができ、しかも室温で液状生成物が得られるような技
術が強く要望夕されている。So far, there have been reports on the method of recovering hydrocarbon oil by thermally decomposing bamboo blind plastic, but there are polymers with a low degree of polymerization that are produced as by-products during the polymer manufacturing process, and polystyrene that easily becomes oil by thermal decomposition. Limited to plastics. However, when polyolefin plastics are simply thermally decomposed, that is, when they are thermally decomposed without using any catalyst, a product with a wide molecular weight distribution range from carbon number distribution to group C is obtained, and this product is a wax at room temperature. Because of this, there are limits to how it can be used, and if it is simply pyrolyzed, there are problems with the pyrolysis equipment due to the generation of carbon and the closure of piping. Therefore, the current pyrolysis technology is It is extremely difficult to thermally decompose polyolefin plastics. Therefore, there is a strong demand for a technology that can thermally decompose POIJ olefin plastics using a simple method and equipment, and that can yield a liquid product at room temperature.
この発明は燃料や素原料として有用な液状炭化水素油が
得られるようなポリオレフィン系プラスチック廃棄物の
熱分解法とその装置を開発するために検討を重ねた結果
、熱分解温度の選択やその蒸気状の生成物を特定の温度
に制御されたアルミナ・酸化鉄系、アルミナ・蓮酸系、
珪酸・酸化鉄系等の触媒層に通して再熱分解することに
より、良質な炭化水素油を得ることができることを見出
し、この発明をなすに至ったものである。This invention was developed as a result of repeated studies to develop a method and apparatus for thermally decomposing polyolefin plastic waste that can yield liquid hydrocarbon oil useful as fuel and raw materials. Alumina/iron oxide type, alumina/lotus acid type,
The inventors have discovered that high-quality hydrocarbon oil can be obtained by passing it through a silicic acid/iron oxide catalyst layer and re-thermal decomposition, leading to the creation of this invention.
この発明にしたがえば、ポリオレフィン系プラスチック
廃棄物は熱溶融した後、440〜500℃の範囲で加熱
して熱分解し、熱分解により発生した蒸気状生成物を3
50〜470qoに加熱した粒径1〜15欄の触媒層に
通して二次熱分解処理を行う。According to this invention, polyolefin plastic waste is thermally melted and then thermally decomposed by heating in the range of 440 to 500°C, and the vaporized products generated by the thermal decomposition are
A secondary thermal decomposition treatment is carried out by passing through a catalyst bed of particle sizes 1 to 15 heated to 50 to 470 qo.
この発明方法において、ポリオレフイン系プラスチック
廃棄物の熱分解を440〜50ぴ0の範囲内の温度で行
なうのは、この温度範囲外で行なうと生成油速度が遅く
なったり、生成油の収率が低下するためである。In the method of this invention, the thermal decomposition of polyolefin plastic waste is carried out at a temperature within the range of 440 to 50 psi, because if it is carried out outside this temperature range, the rate of oil production will be slow and the yield of the oil produced will be low. This is because it decreases.
またこの発明に使用する触媒としてはアルミナ・酸化鉄
系触媒、例えばアルミナ・酸化鉄の500qo焼成物、
アルミナ・珪酸系触媒、珪酸・酸化鉄系触媒、例えばゼ
オライト等であり、その粒径は1〜15肋、好ましくは
1&吻程度のものを使用する。Further, the catalyst used in this invention is an alumina/iron oxide based catalyst, such as a 500qo calcined product of alumina/iron oxide,
The catalyst used is an alumina/silicic acid based catalyst, a silicic acid/iron oxide based catalyst, such as zeolite, and has a particle size of 1 to 15 ribs, preferably about 1 mm.
粒径15肋以下としたのは、蒸気状生成物と触媒との触
媒を高めるためであり、また粒径を1肋以上としたのは
、触媒層に気体の通過できる空隙を形成するためである
。The reason why the particle size is set to 15 cells or less is to increase the catalysis between the vaporized product and the catalyst, and the reason why the particle size is set to 1 cell or more is to form voids in the catalyst layer through which gas can pass. be.
更に触媒層の温度が350℃以下であると、熱分解が不
十分でワックスが付着し、470qo以上であると、熱
分解が進み過ぎ、カーボンが付着する。Further, if the temperature of the catalyst layer is 350° C. or lower, thermal decomposition is insufficient and wax adheres to the catalyst layer, and if the temperature is 470 qo or higher, thermal decomposition proceeds too much and carbon adheres to the catalyst layer.
これに対して350〜470qoの温度範囲では分子量
分布範囲が狭く、室温で高品位炭化水素油を得ることが
できる。例えば、熱分解により得られた炭素数分布C5
〜C42の広い分子量分布範囲の生成物は350〜47
0℃の触媒層内を通過させることにより炭素数分布C5
〜C24、C5〜C29の分子量分布範囲の生成油とな
る。On the other hand, in the temperature range of 350 to 470 qo, the molecular weight distribution range is narrow, and high-grade hydrocarbon oil can be obtained at room temperature. For example, carbon number distribution C5 obtained by pyrolysis
~C42 wide molecular weight distribution products are 350-47
Carbon number distribution C5 by passing through the catalyst layer at 0°C
The produced oil has a molecular weight distribution range of ~C24, C5 to C29.
これは熱分解によって蒸気状生成物が触媒層を通過する
ことにより、異性化を起して組成割合が変化するためで
ある。これを平均分子量について比較すると、触媒層の
ない熱分解が245〜285の範囲にあるのに対して触
媒層内を通過させて再分解すると、135〜190の範
囲となり、それぞれ分子量分布範囲が狭く、低分子側に
片寄るので燃料や工業用素原料として好適なものとなる
。This is because the vaporized products of thermal decomposition pass through the catalyst layer, causing isomerization and changing the composition ratio. Comparing this in terms of average molecular weight, thermal decomposition without a catalyst layer has a range of 245 to 285, while re-decomposition through a catalyst layer results in a range of 135 to 190, which means that the molecular weight distribution range is narrower. Since it is biased toward low molecular weight, it is suitable as a fuel or an industrial raw material.
この発明で供V給源料として用いるポリオレフィン系プ
ラスチック廃棄物は、ポリエチレン、ポリプロピレン、
ポリブチレンのようなオレフイン系の単独重合体のほか
、オレフィン系共重合体プラスチックあるいは姿節喬ポ
リエチレンなども包含される。The polyolefin plastic waste used as the V supply material in this invention includes polyethylene, polypropylene,
In addition to olefin-based homopolymers such as polybutylene, olefin-based copolymer plastics and low-profile polyethylene are also included.
この発明によれば、これまで廃棄され放置しているボリ
オレフィン系プラスチック廃棄物を原料として、燃料や
工業用素原料を製造しうるので資源の有効利用及び公害
防止となり、非常に有益な技術となる。According to this invention, it is possible to produce fuel and industrial raw materials using polyolefin plastic waste that has been discarded and left as raw material, resulting in effective use of resources and prevention of pollution, making it a very useful technology. Become.
以下、この発明の装置を図示の実施例に基いて説明する
。Hereinafter, the apparatus of the present invention will be explained based on the illustrated embodiments.
1は、ポリオレフィン系プラスチック廃棄物の熱分解反
応装置であって、熱分解反応装置1は原料供給部2、熱
分解反応部3及びその上部に設けられた触媒層反応部4
からなり、原料供給部2の底部にはその端部を熱分解反
応部3内上部に臨ませたスクリューフィーダ等の原料移
送手段5が設けられ、触媒層反応部4には粒径1仇吻程
度のアルミナ・酸化鉄系触媒を充填し、更に触媒層内に
は熱電対等から構成される温度計6が挿入され、また熱
分解反応部3内にはその先端が溶融原料の適当な位置に
あるようにレベル計7を挿入し、その先端が気相内にあ
るように熱電対等から構成される温度計8が挿入されて
いる。1 is a thermal decomposition reaction apparatus for polyolefin plastic waste, and the thermal decomposition reaction apparatus 1 includes a raw material supply section 2, a thermal decomposition reaction section 3, and a catalyst layer reaction section 4 provided above it.
A raw material transfer means 5 such as a screw feeder is provided at the bottom of the raw material supply section 2 with its end facing the upper part of the pyrolysis reaction section 3. Furthermore, a thermometer 6 consisting of a thermocouple, etc. is inserted into the catalyst layer, and its tip is placed at an appropriate position in the molten raw material inside the thermal decomposition reaction section 3. A level meter 7 is inserted as shown in the figure, and a thermometer 8 composed of a thermocouple or the like is inserted so that its tip is in the gas phase.
熱分解反応装置1の外周にはヒータが設けられ、このヒ
ータによりポリオレフイン系プラスチック廃棄物の投入
された原料供給部2内は例えば360q Cに加熱され
、スクリューフイーダ5により溶融状のポリオレフィン
系プラスチックの供給される熱分解反応部3内は440
〜500℃の温度範囲に、触媒層反応部4内は下部から
供給される蒸気状生成物の熱容量と補助的な外部ヒータ
により350〜470qoの温度範囲に設定される。A heater is provided around the outer periphery of the pyrolysis reactor 1, and this heater heats the inside of the raw material supply section 2 into which the polyolefin plastic waste is fed to, for example, 360qC, and the screw feeder 5 turns the molten polyolefin plastic into The inside of the thermal decomposition reaction section 3 to which is supplied is 440
The inside of the catalyst layer reaction section 4 is set in a temperature range of 350 to 470 qo by the heat capacity of the vaporized product supplied from the lower part and an auxiliary external heater.
そして原料供給部2では投入されたポリオレフイン系プ
ラスチック廃棄物が上記設定温度により溶融され、溶融
された原料はスクリューフィーダ5により熱分解反応部
3内に供給され、ここで上記設定温度によりその一部は
熱分解を受ける。熱分解により生成した蒸気状生成物は
触媒層反応部4を通過する過程で、上述のように再分解
されて低分子量化される。一方触媒層反応部4の上側に
は外部にコンデンサー9を有する冷却管10が接続され
、冷却管10の先端には貯油槽11が設けられている。Then, in the raw material supply section 2, the input polyolefin plastic waste is melted at the above-mentioned set temperature, and the molten raw material is fed into the pyrolysis reaction section 3 by the screw feeder 5, where a part of it is heated at the above-mentioned set temperature. undergoes thermal decomposition. The vaporous product generated by thermal decomposition is re-decomposed and reduced in molecular weight as described above while passing through the catalyst layer reaction section 4. On the other hand, a cooling pipe 10 having an external condenser 9 is connected to the upper side of the catalyst layer reaction section 4, and an oil storage tank 11 is provided at the tip of the cooling pipe 10.
したがって触媒層反応部4内で再分解されて低分子量化
された生成物は冷却管10を通過する過程で冷却され、
液化されて貯油槽11に捕集される。なお貯油槽11の
上部にはコンデンサー12が位遣しているため、貯油槽
11内の生成油はこれにより再度冷却され、殆んど狩油
槽11内に浦集される。捕集された生成油はバルブ13
を開くことにより、外部に取出すことができる。なお触
媒層反応部4の温度制御は温度計6を観察することによ
り行い、熱分解反応部3の温度制御及び液相のレベル制
御は温度計8及びレベル計7を観察することにより行う
。Therefore, the product re-decomposed in the catalyst layer reaction section 4 and reduced in molecular weight is cooled in the process of passing through the cooling pipe 10.
It is liquefied and collected in the oil storage tank 11. Since a condenser 12 is placed above the oil storage tank 11, the produced oil in the oil storage tank 11 is cooled again and most of it is collected in the oil tank 11. The collected oil is transferred to valve 13.
It can be taken out by opening it. Note that the temperature control of the catalyst layer reaction section 4 is performed by observing the thermometer 6, and the temperature control of the thermal decomposition reaction section 3 and the level control of the liquid phase are performed by observing the thermometer 8 and the level meter 7.
次に、この発明に係る熱分解反応装置を用いたポリオレ
フィン系プラスチック廃棄物の熱分解処理の実験結果を
示す。Next, experimental results of pyrolysis treatment of polyolefin plastic waste using the pyrolysis reaction apparatus according to the present invention will be shown.
【1’熱分解反応装置
図示の実施例と同様な構造の鉄制熱分解反応装置で、熱
分解反応部は高さ20仇吻、内径140側、触媒層反応
部は高さ12仇舷、内径65伽。[1' Thermal decomposition reactor This is an iron controlled thermal decomposition reactor having the same structure as the illustrated embodiment, the thermal decomposition reaction part has a height of 20 m, the inner diameter side is 140 m, the catalyst layer reaction part has a height of 12 m, Inner diameter 65.
■ 使用原料ポリエチレン容器廃棄物、農業用廃ポリエ
チレンフイルム70夕。■ Raw materials used Polyethylene container waste, agricultural waste polyethylene film 70 yen.
上記使用原料は原料供給部2内に投入され、360こC
に加熱して溶融し、スクリューフィーダ5により熱分解
反応部3に供繋合され、次に触媒層反応部4に供給され
、それぞれ下表に示す温度で熱分解処理を行った。The raw materials used above are put into the raw material supply section 2 and heated to 360 °C.
The mixture was heated to melt and connected to the thermal decomposition reaction section 3 by the screw feeder 5, and then supplied to the catalyst layer reaction section 4, where it was subjected to thermal decomposition treatment at the temperatures shown in the table below.
得られた炭化水素油の分析結果を次に示す。The analysis results of the obtained hydrocarbon oil are shown below.
図面は、この発明の一実施例を示す熱分解反応装置概略
図。
図中、1は熱分解反応装置、2は原料供給部、3は熱分
解反応部、4は触媒層反応部。The drawing is a schematic diagram of a thermal decomposition reactor showing an embodiment of the present invention. In the figure, 1 is a thermal decomposition reaction device, 2 is a raw material supply section, 3 is a thermal decomposition reaction section, and 4 is a catalyst layer reaction section.
Claims (1)
後、440〜500℃の範囲で加熱して熱分解し、熱分
解により発生した蒸気状生成物を350〜470℃に加
熱した粒径1〜15mmの触媒層に通して二次熱分解処
理することを特徴とするポリオレフイン系プラスチツク
廃棄物の熱分解法。 2 ポリオレフイン系プラスチツク廃棄物を熱溶融する
原料供給部と、溶融状のプラスチツク廃棄物の熱分解反
応部と、粒径1〜15mmの触媒層からなる触媒反応部
とから構成されるポリオレフイン系プラスチツク廃棄物
の熱分解装置。[Claims] 1. Particles obtained by heat-melting polyolefin plastic waste, then heating it in a range of 440 to 500°C to thermally decompose it, and heating the vaporized product generated by the thermal decomposition to 350 to 470°C. A method for pyrolyzing polyolefin plastic waste, which is characterized by subjecting polyolefin plastic waste to secondary pyrolysis treatment by passing it through a catalyst layer having a diameter of 1 to 15 mm. 2. Polyolefin plastic waste consisting of a raw material supply section that thermally melts polyolefin plastic waste, a thermal decomposition reaction section for molten plastic waste, and a catalytic reaction section consisting of a catalyst layer with a particle size of 1 to 15 mm. Equipment for thermal decomposition of materials.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4892983A JPS6015674B2 (en) | 1983-03-25 | 1983-03-25 | Pyrolysis method and equipment for polyolefin plastic waste |
| US06/593,369 US4584421A (en) | 1983-03-25 | 1984-03-26 | Method for thermal decomposition of plastic scraps and apparatus for disposal of plastic scraps |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4892983A JPS6015674B2 (en) | 1983-03-25 | 1983-03-25 | Pyrolysis method and equipment for polyolefin plastic waste |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59174691A JPS59174691A (en) | 1984-10-03 |
| JPS6015674B2 true JPS6015674B2 (en) | 1985-04-20 |
Family
ID=12816952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4892983A Expired JPS6015674B2 (en) | 1983-03-25 | 1983-03-25 | Pyrolysis method and equipment for polyolefin plastic waste |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6015674B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07100795B2 (en) * | 1990-11-14 | 1995-11-01 | フジリサイクル株式会社 | Method for producing aromatic hydrocarbon oil from pyrolytic polyolefin plastic |
-
1983
- 1983-03-25 JP JP4892983A patent/JPS6015674B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59174691A (en) | 1984-10-03 |
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