JPS5996189A - Polymer substance pyrolysis and apparatus - Google Patents
Polymer substance pyrolysis and apparatusInfo
- Publication number
- JPS5996189A JPS5996189A JP359583A JP359583A JPS5996189A JP S5996189 A JPS5996189 A JP S5996189A JP 359583 A JP359583 A JP 359583A JP 359583 A JP359583 A JP 359583A JP S5996189 A JPS5996189 A JP S5996189A
- Authority
- JP
- Japan
- Prior art keywords
- reactor tube
- polymeric material
- reactor
- fluidized bed
- oxygen
- 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
- 239000000126 substance Substances 0.000 title claims description 10
- 238000000197 pyrolysis Methods 0.000 title claims description 9
- 229920000642 polymer Polymers 0.000 title 1
- 239000000463 material Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 23
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 239000003575 carbonaceous material Substances 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 239000007789 gas Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 238000002485 combustion reaction Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000011261 inert gas Substances 0.000 claims description 6
- 238000000746 purification Methods 0.000 claims description 6
- 238000010926 purge Methods 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 5
- 238000007701 flash-distillation Methods 0.000 claims description 4
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 4
- 238000013021 overheating Methods 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 2
- 239000002861 polymer material Substances 0.000 claims description 2
- 238000003287 bathing Methods 0.000 claims 1
- 238000007599 discharging Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 12
- 239000004743 Polypropylene Substances 0.000 description 11
- -1 polypropylene Polymers 0.000 description 11
- 229920001155 polypropylene Polymers 0.000 description 11
- 238000003860 storage Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 5
- 239000000446 fuel Substances 0.000 description 5
- 239000000295 fuel oil Substances 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 238000009825 accumulation Methods 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000002679 ablation Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000013459 approach Methods 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000010954 commercial manufacturing process Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/02—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by distillation
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G9/14—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
- C10G9/16—Preventing or removing incrustation
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は熱分解による重合体物質の分解、詳しくはアク
クチツクのポリプロピレンから燃料油及び他の有用な生
産物を製造する方法及び装置に関する。DETAILED DESCRIPTION OF THE INVENTION This invention relates to the cracking of polymeric materials by pyrolysis, and more particularly to a method and apparatus for producing fuel oil and other useful products from thermal polypropylene.
これまで、産業上の工程における副産物としての不用の
重合体物質は産出が増加しつつあり、それらの物質の処
置の為にそれらを経済的且つ商業的に使用する方策が必
要であると−良く認識されてきている。It has long been recognized that the production of unwanted polymeric substances as by-products in industrial processes is increasing and that there is a need for strategies to use them economically and commercially for the treatment of these substances. It is becoming recognized.
はとんどの不用な重合体物質の熱の内容はそれら全燃料
として潜在的に利用可能にしている。しかしながら、多
くの高い、また中間の分子量の重合体物質、例えばアタ
クチックのポリプロピレンは室温において半固体であり
、供給したり粉砕するのが困難であり、この為また従来
のシステムに於て直接燃焼させるには適当でない。これ
らの不用の重合体物質を低分子量砕片に熱的に分解して
扱い易くシ、燃料油及び産業上の原料物質等経済的に価
値ある種々の方法が先行技術として例えばアメリカ合衆
国特許第3,829,558号、第3,832゜151
号又は第4,151,216号に記載されている。The heat content of most waste polymeric materials makes them all potentially usable as fuel. However, many high and intermediate molecular weight polymeric materials, such as atactic polypropylene, are semisolid at room temperature and difficult to feed and grind, which also makes them difficult to combust directly in conventional systems. It is not suitable for Various methods of thermally decomposing these waste polymeric materials into low molecular weight fragments to make them easier to handle and economically valuable for fuel oil and industrial feedstock materials are known in the prior art, such as in U.S. Pat. No. 3,829. , No. 558, No. 3,832゜151
No. 4,151,216.
既知の工程での主要な問題は、熱反応装置の熱移転面に
おける副産物、特に炭素質の物質の蓄積である。熱移転
面上でこれらの物質が蓄積するとそれらの能力を制限し
てしまい、このためバッチ型即ち−かまど毎の操作又は
洗浄の為に定期的操業休止が要請される。従来の炉の均
一でない加熱特性は、炭素質の物質の蓄積を促進する、
熱分解をされるべき不用物質の行路に沿った熱移転面上
にホット・スポラトラ増加させる一因になる。低反応温
度、蓄積した炭素の分散、及び反応物質の炭素を豊富に
含んだ部分の排出等この問題を扱う先行技術は、商業的
に実行可能な連続的工程を創出するためこの問題を十分
に解決、除去していない。A major problem with the known process is the accumulation of by-products, especially carbonaceous materials, on the heat transfer surfaces of the thermal reactor. The accumulation of these substances on the heat transfer surfaces limits their capacity and requires periodic shutdowns for batch-type, ie, furnace-by-furnace, operation or cleaning. The non-uniform heating characteristics of conventional furnaces promote the accumulation of carbonaceous materials,
This contributes to the increase of hot sporatra on the heat transfer surface along the path of the waste material to be pyrolyzed. Prior art approaches to this problem, such as low reaction temperatures, dispersion of accumulated carbon, and evacuation of the carbon-rich portion of the reactants, have sufficiently addressed this problem to create a commercially viable continuous process. Not resolved or removed.
本発明に於て、アタクチックのポリプロピレン等不用の
重合体物質は、望ましくは5oないし250 ps i
gの圧力でポンプにより汲上げれるように加熱タンク内
で溶解される。この溶解した原料は熱的に絶縁したパイ
プを通して反応器導管、望ましくは2又はそれ以上の独
立した反応器チューブ、そしてより一層望捷しくは所定
の寸法のらせん形に巻いたチューブにポンプで送られ、
そこで熱即ち熱分解によって、所定時間酸素の不存在下
で、重合体物質上の親分子の分子量と比較して低い分子
量の物質に熱分解するものである。反応時間は反応器チ
ューブの寸法とそこを通る原料物質の流量の割合によっ
て大定される。この反応器チューブ及びその中の原料は
流動床により均一に正確な温度に加熱される。熱分解さ
れた生成物は反応器チューブから分離装置内例えばフラ
ッシュ蒸留装置に排出され、そこで生成物の重合体物質
はその分子量に従って実質的に各グループに分離される
。In the present invention, the unnecessary polymeric material such as atactic polypropylene is preferably used at a temperature of 50 to 250 psi.
It is melted in a heated tank so that it can be pumped up at a pressure of g. This molten feedstock is pumped through a thermally insulated pipe into a reactor conduit, preferably two or more separate reactor tubes, and even more preferably a helically wound tube of predetermined dimensions. is,
Therefore, by heat or thermal decomposition, the polymer material is thermally decomposed in the absence of oxygen for a predetermined period of time to a substance having a lower molecular weight compared to the molecular weight of the parent molecule on the polymeric material. The reaction time is determined by the dimensions of the reactor tube and the rate of flow of feed material therethrough. The reactor tube and the feedstock therein are heated uniformly to a precise temperature by means of a fluidized bed. The pyrolyzed products are discharged from the reactor tube into a separation device, such as a flash distillation device, where the product polymeric materials are separated into groups substantially according to their molecular weights.
アタクチックのポリプロピレンの場合約427℃(80
0下)の温度で約10分間で反応し、主な生成物は扁6
及び扁2の燃料油といくらかの軽いガス状の燃料であり
、これは望ましくは溶解タンク及び流動床用の加熱装置
の燃料として用いることができる。Approximately 427°C (80°C) for atactic polypropylene
The reaction takes about 10 minutes at a temperature of
and 2-grade fuel oil and some light gaseous fuel, which can desirably be used as fuel for melting tanks and heating equipment for fluidized beds.
本発明の目的は、重合体物質を低分子量物質に熱分解し
、反応器チューブ内で均一な温度とレベルを精密に制御
することによって均一な生成物全生産する方法及び装置
を提供することである。It is an object of the present invention to provide a method and apparatus for the pyrolysis of polymeric materials into low molecular weight materials and the production of uniform products by precisely controlling uniform temperatures and levels within the reactor tubes. be.
本発明の他の目的は、重合体物質から燃料油を生産する
能率的で経済的な方法及び装置k提供することである。Another object of the present invention is to provide an efficient and economical method and apparatus for producing fuel oil from polymeric materials.
本発明の別の目的は、実質的に連続操作をするのに適し
ており、−又はそれ以上の反応器チューブを他のチュー
ブの操作に影響を与えないで下記の通り洗浄することが
できる方法及び装置を提供することである。Another object of the invention is a method which is suitable for substantially continuous operation and in which one or more reactor tubes can be cleaned without affecting the operation of other tubes as described below. and equipment.
上記及び他の付随する目的をふまえて、特許による保護
を目差す、構広上の特徴、部分、それらの組合せ、及び
下記又は添附図面に図示した操作の形態、又はその均等
物を含む発明はここに、より一層詳細且つ十分に説明す
る。In view of the foregoing and other incidental purposes, the invention which is intended for patent protection and which includes the structural features, parts, combinations thereof, and modes of operation illustrated below or in the accompanying drawings, or equivalents thereof, is hereby disclosed. will be explained in more detail and more fully below.
添附図面には本発明に従って構成されたアタクチックの
ポリプロピレンの熱分解の為のシステムで、本発明の主
要部分の概略工程系統図を図示している。この図面では
、一定の付属器具類、バルブ装置、計器、加熱器、攪拌
器、ポンプ等は発明を明瞭にするために省略しているが
、それらは必要に応じて又は所望により適合しつる従来
からの方法で備えることができる。The accompanying drawings are a system for pyrolyzing atactic polypropylene constructed in accordance with the present invention, and a schematic process flow diagram of the main parts of the present invention. Certain appurtenances, valve equipment, gauges, heaters, agitators, pumps, etc. have been omitted from this drawing for clarity of the invention; It can be prepared using the following methods.
図示した辿り、本発明の装置は導管12によりポンプに
接続した加熱溶解タンク10を含んでいる。該ポンプ1
4は導管16に吐出し、該導管16は、該当する反応器
チューブ20及び20′の各々に連通するだめの分離供
給管18及び18′に分けられており、該各供給管には
各々バルブ19及び19′が設けられている。該反応器
導管即ちチューブ20及び20′は下記の通ジ、望1し
くはらせん状のコイルで流動床炉22内に配置されてい
る。該流動床は、下部に分配板26を有する囲繞装置2
4を含んでおり、該分配板によって該囲繞装#を下方充
満室28と上方法区域30に分けている。該下方充満室
28には該分配板26を介して流動床区域30へ加熱空
気を上方へ通すためバーナー装置32が設けられている
。固体粒子の流動床媒体は該床区域3oに配置されてお
り、該分配板26を通して上方へ来る熱いガス流内で浮
動状態になり流動化物質33になり、この流動化物質3
0はその内部に巻き込まれている反応器チューブ20及
び20′に熱を伝える。流動化した空気は囲繞装置24
から導管34を辿って分離器36、望捷しくはサイクロ
ン内に排出され、該分離器36は排出ガス即ち空気と共
に流れて来た流動化された固体を分離し、分離したガス
を大気中に排出する。上記反応器チューブ20及び20
′は分離器38、例えばフラッシュ蒸留装置に導管37
及び37′を通して生成物を排出する。導管42は該分
離器;38の下部から冷却器44に接続しており、高い
分子量の生成物を第1貯蔵タンク46に送る。As shown, the apparatus of the invention includes a heated melt tank 10 connected to a pump by a conduit 12. The pump 1
4 discharges into a conduit 16, which is divided into separate tank feed tubes 18 and 18' communicating with each of the respective reactor tubes 20 and 20', each feed tube having a respective valve. 19 and 19' are provided. The reactor conduits or tubes 20 and 20' are arranged in a fluidized bed furnace 22 with the following passages, preferably helical coils. The fluidized bed is placed in an enclosing device 2 with a distribution plate 26 at the bottom.
4, and the distribution plate divides the enclosure # into a lower filling chamber 28 and an upper fill area 30. A burner device 32 is provided in the lower plenum 28 for passing heated air upwardly through the distribution plate 26 into the fluidized bed section 30 . A fluidized bed medium of solid particles is placed in the bed area 3o and becomes suspended in the hot gas stream coming upwardly through the distribution plate 26 into a fluidized material 33, which fluidized material 3
0 transfers heat to the reactor tubes 20 and 20' wrapped inside it. The fluidized air is sent to the surrounding device 24.
from the conduit 34 into a separator 36, preferably a cyclone, which separates the fluidized solids flowing with the exhaust gas or air and discharges the separated gas into the atmosphere. Discharge. The above reactor tubes 20 and 20
' is a conduit 37 to a separator 38, e.g. a flash distillation device.
and 37' to discharge the product. A conduit 42 connects from the bottom of the separator 38 to a cooler 44 and delivers the high molecular weight product to a first storage tank 46 .
導管48は該分離器38をコンデンサー装置5゜に接続
している。該コンデンサー装置5oは、低い分子量のガ
ス状の生成物用の第1排出導管52と、中程度の分子量
の液状生成物用の第2排出導管54を備えており、該導
管は各々適当な貯蔵設備、例えば第2貯蔵タンク56、
第3貯蔵タンク57に接続している。A conduit 48 connects the separator 38 to the condenser arrangement 5°. The condenser device 5o comprises a first discharge conduit 52 for gaseous products of low molecular weight and a second discharge conduit 54 for liquid products of medium molecular weight, each conduit being connected to a suitable storage. equipment, such as a second storage tank 56;
It is connected to a third storage tank 57.
本発明の好ましい実施例において、アタクチックのポリ
プロピレン、即ち室温で固体又は半固体であり、ポリプ
ロピレンの商業上の製造工程で不用の副産物の混合物を
構成する部分的に結晶体から厄る物質は熱分解によす扁
6及び茄2の燃料油及び他の有用の物質に変化する。典
型的には、商業的ポリプロピレン設備からの不用のアタ
クチックのポリプロピレンは溶解タンク10に集められ
、50ないし250psigの圧力で反応器チューブ2
0及び20′にポンプで供給できるよう十分液体になる
まで約204℃(約400”F )に通常加熱される。In a preferred embodiment of the invention, atactic polypropylene, i.e., a solid or semi-solid at room temperature and a partially crystalline material that constitutes a mixture of unwanted by-products in the commercial manufacturing process of polypropylene, is thermally decomposed. It is converted into fuel oil and other useful substances. Typically, waste atactic polypropylene from a commercial polypropylene facility is collected in a dissolution tank 10 and transferred to a reactor tube 2 at a pressure of 50 to 250 psig.
It is typically heated to about 204°C (about 400"F) until it is sufficiently liquid to be pumped to 0 and 20'.
該反応器チューブでは該不用の物質中の炭素−炭素結合
を破壊し所望の生成物を生産するよう十分な温度(おお
よそ約427℃(800下)で十分な時間)加熱する。The reactor tube is heated to a sufficient temperature (approximately 427°C (below 800°C) for a sufficient time) to break the carbon-carbon bonds in the waste material and produce the desired product.
該生成物は約25℃で液体で通常90重重量及びガス状
燃料で10重重量であり、該反応器チューブから分離器
38に排出され、該分離器38で該液体は重い(高い粘
度の)部分と軽い(低い粘度の)部分と残りのガスの混
合物に分離され、該混合物はコンデンサー装置に送られ
軽い(低い粘度の)部分は凝縮され、残りのガスは適当
な貯蔵容器に排出される。このガスは望ましくは上記溶
解タンクと流動床用の加熱装置の燃料として用いられる
。The product, typically 90 gw as a liquid and 10 gw as a gaseous fuel at about 25° C., is discharged from the reactor tube to a separator 38 where the liquid is a heavy (high viscosity) ) part, light (low viscosity) part and remaining gas mixture, the mixture is sent to a condenser device where the light (low viscosity) part is condensed and the remaining gas is discharged into a suitable storage container. Ru. This gas is preferably used as fuel for the melting tank and heating equipment for the fluidized bed.
流動床による極めて精密で均一な加熱は、長期間の操作
により反応器チューブ内に形成される炭素質の堆積物の
量を少なくするが、これらの副産物である堆積物は反応
器チューブの内面に集まりその機能を妨げ且つ流動床か
ら該チューブ内の物質への熱伝導率を低下させる。The extremely precise and uniform heating provided by the fluidized bed reduces the amount of carbonaceous deposits that form within the reactor tubes over long periods of operation; Collecting impedes its function and reduces the thermal conductivity from the fluidized bed to the material within the tube.
反応器チューブ20及び20’には重合体物質とは別に
、窒素と空包を別々に供給し、それらは他の反応器チュ
ーブ内の工程に影響を与え、ることなく焼灼され、即ち
きれいにされ、連続操作を行うことができる。Reactor tubes 20 and 20' are supplied with nitrogen and blanks separately, apart from the polymeric material, so that they can be cauterized, ie, cleaned, without affecting the processes in the other reactor tubes. , continuous operations can be performed.
この例を詳しく説明すると、炉灼操作は操作装置内の選
ばれた反応器チューブ20へのアタクチックのポリプロ
ピレンの流れを中断することによって上記の装置内で行
われ、この操作は供給バルブ19を閉じ、調節可能な浄
化バルブ00を開き不活性ガス、望甘しくけ窒素を流入
させ、該チューブ20内の供給されているいかなる物質
及び/又は熱分解物質をも押しやり該装置のその部分を
きれいにする。その後址もなく生成物排出バルブ(52
を閉じて生成物や浄化ガスが分離器38に流れるのを中
断させ、且つ浄化排出バルブ64を開けて該窒素浄化ガ
スが大気中に排出し、又は太り中への排出の前に熱分解
物質を燃焼させるために流動床炉の充満室内に流入させ
る。調節可能な空気流入バルブ(56はその後開かれガ
スを含んでいる酸素を該反応器チューブ20に流入させ
、窒素による浄化の後膣チューブ内に残っている全ての
炭素質の堆積、付着物を自然に燃焼させる。窒素流入の
為の浄化バルブ60はこの時点で閉じて、利用できる酸
素を増加することによって該燃焼を促進させる。この燃
焼による熱は、従来のシステムでは反応器チューブを過
熱温度により損傷させ又は破壊するのが常であった。し
かし本発明においては、反応器チューブの温度は流動床
により安全レベルで制御されており、該流動床は、炭素
質堆積物の燃燐熱によって生ずる過剰の熱を効果的に取
り去り、過熱による損傷を防止する。To elaborate on this example, the ablation operation is carried out in the apparatus described above by interrupting the flow of atactic polypropylene to selected reactor tubes 20 in the operating apparatus, which operation is carried out by closing the supply valve 19. , open the adjustable purge valve 00 and allow inert gas, preferably nitrogen, to flow in to displace any feed material and/or pyrolysis material in the tube 20 and clean that portion of the apparatus. do. Thereafter, the product discharge valve (52
is closed to interrupt the flow of product or purified gas to the separator 38, and the purification discharge valve 64 is opened to allow the nitrogen purification gas to be discharged to the atmosphere or to the pyrolyzed material prior to discharge into the feedstock. into the filling chamber of the fluidized bed furnace for combustion. An adjustable air inlet valve (56) is then opened to allow gaseous oxygen to flow into the reactor tube 20 to remove any carbonaceous deposits remaining in the vaginal tube after purging with nitrogen. The purge valve 60 for nitrogen inflow is closed at this point to enhance the combustion by increasing the available oxygen.The heat from this combustion brings the reactor tubes to a superheat temperature in conventional systems. However, in the present invention, the temperature of the reactor tubes is controlled at a safe level by a fluidized bed, which is heated by the heat of combustion of the carbonaceous deposits. Effectively removes excess heat generated and prevents damage due to overheating.
上記チューブ20の全ての炭素質の物質が上記の辿9焼
灼すると、空気流入バルブ66を閉じ全ての酸素が排出
されるまで窒素で反応器チューブ20に浄化する。浄化
排出バルブ64及び窒素流入バルブ60をその後閉じ且
つ、供給バルブ19を再ひ開いて該チューブ内に重合体
物質を流入させる。最後に生成物排出バルブ62を開き
該チューブ20を全操作に復帰させる。Once all of the carbonaceous material in the tube 20 has been cauterized as described above, the air inlet valve 66 is closed and the reactor tube 20 is flushed with nitrogen until all oxygen has been exhausted. The purge exhaust valve 64 and nitrogen inlet valve 60 are then closed and the supply valve 19 is reopened to allow polymeric material to flow into the tube. Finally, the product discharge valve 62 is opened to return the tube 20 to full operation.
上記の辿り、他の反応器チューブ20′は、チューブ2
0の焼灼操作によっては影響を受け々いて本来の操作を
行う状態にある。反応器チューブ20が熱分解操作に戻
ると、次は上記他の反応器チューブ20′が反応器チュ
ーブ2oに影響を与えないで、該チューブ20′へのバ
ルブ操作を行い同様の方法で焼灼操作を行う。本発明で
は該装置は望ましくは2から6の複数の反応器チューブ
を備えるのが望ましく、これらのチューブの1以上のチ
ューブが同時に、上記方法を修正した方法によって焼灼
浄化操作を行うことができる。Following the above, the other reactor tube 20' is tube 2
0 is affected by the cauterization operation and is in a state where it can perform its original operation. When the reactor tube 20 returns to the pyrolysis operation, next, the other reactor tube 20' operates the valve to the reactor tube 20' without affecting the reactor tube 2o, and performs the cauterization operation in the same manner. I do. According to the invention, the apparatus preferably comprises a plurality of reactor tubes, preferably from 2 to 6, of which one or more tubes can be simultaneously subjected to an ablation purification operation by a modification of the above method.
上記説明から、前記した辿り、利点についての各々の特
徴を有する上記装置を提供するものであり、その有して
いる本質を逸脱せず、またその利点を失うことなく、そ
の形態の変更、割合、詳細な構成及び部分の配置を変え
ることは可能である。From the above description, it can be seen that the above device is provided having each of the features of the above-mentioned sequence and advantages, and that changes in its form and proportions can be made without departing from its essence or losing its advantages. , it is possible to vary the detailed construction and arrangement of parts.
本発明は法律の規定に従うよう、構成上の特徴についで
ある部分は詳細に、またある部分は概略的に説明したが
、本発明は上記の特徴的部分に限定されるものでは々く
、ここに開示した装置及び構成は発明を実際に実施する
上で種々の態様を含むものであり、特許請求の範囲にお
いて開示した正当且つ有効な権利範囲内で本発明はその
態様及び修正、変更例の全てについて権利が請求されて
いることが理解されなければならない。In order to comply with the provisions of the law, some of the structural features of the present invention have been described in detail and some parts have been described in outline, but the present invention is not limited to the above-mentioned characteristic parts. The device and structure disclosed in the above include various aspects for actually carrying out the invention, and the present invention covers such aspects, modifications, and variations within the scope of legitimate and valid rights disclosed in the claims. It must be understood that rights are claimed for all.
図面は本発明に従って構成されたアタクチックのポリプ
ロピレンの熱分解の為の装置で本発明の主要部分の概略
工程系統図である。
主要部分の符号の説明
10・・・加熱溶解タンク 12・・・導管14・・・
ポンプ 16・・・導管18.18’・・・分
離供給管 19.19’・・・バルブ20 、2
0’・・反応器チューブ 22・・流動床炉24・・
囲繞装置 26・・・分配板28・・・下方充満
室 30・・・上方流動床区域32・・バーナー装
置 33・・・流動化物質34・・導管
36・・・分離器44・・冷却器 46・
・第1貯蔵タンク50・・・コンデンサー装置 56・
・・第2貯蔵タンク57 ・・第3貯蔵タンク 6
0.l’・・・浄化ノ幻しブ62・・・排出バルブ
64・・・浄化排出ノクルブ66.66’・・・流
入バルブ
手続補正内
昭和58年4月4日
特許庁長官 若 杉 和 夫 殿
1、事例の表示 特願昭58−3595号2、発明の
名称 重合体物質の熱分解の方法及びその装置
3、補正をする者
事イ′4との関係 ’B+ i’i’l出願人住 所
アメリカ合衆国 ニュージャーシイ州ニュー ブランズ
ウィック 4ノマーレッ1〜ス1〜リ−1〜 221
名 称 プロ廿タイン コーボレイション代表者 ハー
バ−1−ケニス スタッフイン11.1 籍 アメリ
カ会衆[i、14、代理人
東京都港]ス新橋1 ’T−[’j 18ffl 19
号キムラA)人垣ヒル6階手続補正書
昭和58年4月21日
特許庁長官 若 杉 和 夫 殿
1、事件の表示 特願昭58−3595号2、発明の
名称 重合体物質の熱分解の方法及びその装置
3、補正をする者
事イ9どの関係 特¥[出願人
住 所 アメリカ合衆国 ニュージA7−ジイ州ニュー
ブランズウィック サマーセラ1〜ス1〜リ−1〜
221
名 称 プロ廿タイン コーボレイション代表者 ハー
バ−1−ケニス スタッフイン国 籍 アメリカ合衆国
4、代理人The drawing is a schematic process diagram of the main parts of an apparatus for pyrolysis of atactic polypropylene constructed according to the present invention. Explanation of symbols of main parts 10... Heating melting tank 12... Conduit 14...
Pump 16...Conduit 18.18'...Separation supply pipe 19.19'...Valve 20, 2
0'...Reactor tube 22...Fluidized bed furnace 24...
Surrounding device 26...Distribution plate 28...Lower filling chamber 30...Upper fluidized bed area 32...Burner device 33...Fluidized substance 34...Conduit
36...Separator 44...Cooler 46.
・First storage tank 50... Condenser device 56.
...Second storage tank 57 ...Third storage tank 6
0. l'...Purification illusion 62...Discharge valve
64... Purification and discharge valve 66. 66'... Inflow valve procedure amendment April 4, 1980 Kazuo Wakasugi, Commissioner of the Patent Office 1, Indication of examples, Patent Application No. 1983-3595 2, Invention Name: Method and apparatus for thermal decomposition of polymeric substances 3; Relationship with person making the amendment A'4 'B+ i'i'l Applicant's address
New Brunswick, New Jersey, United States of America 4Nomares 1-1-221 Name Pro-Tyne Coalition Representative Harbor 1-Kenneth Staffin 11.1 Register American Congregation [I, 14, Agent Tokyo] Port] Shinbashi 1 'T-['j 18ffl 19
No. Kimura A) Hitogaki Hill 6th floor procedural amendment April 21, 1980 Kazuo Wakasugi, Commissioner of the Patent Office 1. Indication of the case: Japanese Patent Application No. 58-3595 2. Title of the invention: Thermal decomposition of polymeric substances. Method and apparatus 3, person making the correction, a9 relationship Special ¥ [Applicant address: New Brunswick, New Jersey, United States of America, Summersella 1~S1~Lee 1~
221 Name Pro Tyne Cooperation Representative Harbor 1-Kenneth Staffin Nationality United States 4, Agent
Claims (1)
質を通過させ、これにょシ該重合体物質を低分子量物質
に熱分解を生じさせる熱分解温度に該重合体物質をさら
す工程から成ることを特徴とする重合体物質の熱分解の
方法3゜ 2、上記重合体物質を上記反応器チューブを通過させる
に先立って、該重合体物質を溶解する工程を含む特許請
求の範囲第1項に記載の方法。 3 上記反応器チューブで処理された重合体物質が該反
応器チューブから出るときに、該重合体物質をサイズに
より分離する工程を含む特許請求の範囲第1項又は第2
項に記載の方法。 4 上記反応器チューブ内に句着した炭素質物質の堆積
物を、該物質が燃焼するに十分な温度下で酸素にさらし
該反応器チューブから該物質の堆積物を浄化し且つ、該
反応器チューンの過熱を防止するために上記流動床内に
該燃焼熱の少なくとも一部を伝導する工程を含む特許請
求の範囲第1項に記載の方法。 5 上記反応器チューブは複数設けられており且つ上記
浄化工程は、少なくとも1つの反応器チューブで重合体
物質の熱分解を行っている間に、少なくとも他の1つの
反応器チューブ内で行い、低分子物質を連続的に装置で
生成する特許請求の範囲第4項に記載の方法。 6 上記反応器チューブ内で炭素質物質の堆積物を酸素
にさらす前に該反応器チューブ内全不活性ガスで浄化す
る工程を含む特許請求の範囲第5項に記載の方法。 7 上記反応器チューブ内で炭素質物質の堆積物を燃焼
した後に該反応器チューフ内を不活性ガスで浄化する工
程を含む特許請求の範囲第6項に記載の方法。 8 上記不活性ガスが窒素である特許請求の範囲第6項
に記載の方法。 9 上記不活性ガスが窒素である特許請求の範囲第7項
に記載の方法5゜ 10 上記酸素は上記反応器チューブに導入する空気
に含まれている特許請求の範囲第4項、第5項、第6項
、第7項、第8項又は第9項に記載の方法。 11 酸素にさらしたときに炭素質物質の堆積物が燃
焼する温度に反応器チューブ内の炭素質物質を加熱し; 該炭素質物質の燃焼を生ぜしめるよう該炭素質物質の堆
積物に酸素を浴びせ: 該反応器チューブの一表面の過熱を防ぐために流動床内
に該燃焼による温度の一部を伝導する工程から成る流動
床と熱交換をする装置の表面から炭素質物質の堆積物を
浄化する方法。 12 人口開口部及び出口開口部を有する少々くとも
1以上の反応器チューブを備え、熱分解温度で用られる
流動床と、 該反応器チューブの入口開口部から出口開口部に該チュ
ーブを介して重合体物質を移動させて、該重合体物質を
熱分解状態に置き、該重合体物質を低分子量物質に熱分
解する装置とから成る重合体物質を熱分解するだめの装
置。 13、上記重合体物質を溶解し上記反応器チューブに排
出する加熱タンクを含む特許請求の範囲第12項に記載
の装置。 14 上記重合体物質を移動させる装置はポンプ装置
である特許請求の範囲第13項に記載の装置。 15、上記反応器チューブは複数設置されており、該反
応器の各々は互に独立して重合体物質を上記入口開口部
に調節可能に供給する装置を含んでいる特許請求の範囲
第12項、第13項又は第14項に記載の装置。 16 上記各反応器チューブの入口開口部に不活性ガ
スを調節可能に供給する装置と、 該谷反応器チューブの入口開口部に酸素を含むガスを調
節可能に供給する装置とを含む特許請求の範囲第15項
に記載の装置。 17 上記反応器チューブの出口開口部から排出され
る熱分解された重合体物質を受は取り且つ留分ごとに分
離する分離装置を含んでいる特許請求の範囲第12項、
第13項又は第14項に記載の装置。 18 上記分離装置はフラッシュ蒸留装置である特許
請求の範囲第17項に記載の装置。 19、上記反応器チューブの開口部から排出される熱分
解された重合体物質を受は取り且つ留分ごとに分離する
分離装置を含んでいる特許請求の範囲第15項に記載の
装置。 20、上記分離装置はフラッシュ蒸留装置である特許請
求の範囲第19項に記載の装置。[Claims]] Passing a polymeric material through a reactor tube placed in a fluidized bed, which exposes the polymeric material to a pyrolysis temperature that causes thermal decomposition of the polymeric material to lower molecular weight materials. A method of pyrolysis of a polymeric material comprising the steps 3.2, comprising the step of dissolving said polymeric material prior to passing said polymeric material through said reactor tube. The method described in paragraph 1. 3. Claims 1 or 2 further comprising the step of separating by size the polymeric material treated in the reactor tube as it exits the reactor tube.
The method described in section. 4. exposing the deposits of carbonaceous material trapped in the reactor tubes to oxygen at a temperature sufficient to cause the materials to burn; 2. The method of claim 1, including the step of conducting at least a portion of the heat of combustion into the fluidized bed to prevent overheating of the tune. 5. A plurality of the reactor tubes are provided, and the purification step is performed in at least one reactor tube while the polymer material is being thermally decomposed in at least one reactor tube, and the purification step is performed in at least one other reactor tube to reduce the 5. A method according to claim 4, wherein the molecular substance is produced continuously in an apparatus. 6. The method of claim 5, including the step of purging the reactor tube with all inert gas before exposing the carbonaceous material deposit to oxygen in the reactor tube. 7. The method of claim 6, further comprising the step of purifying the reactor tube with an inert gas after burning the carbonaceous material deposit within the reactor tube. 8. The method of claim 6, wherein the inert gas is nitrogen. 9. The method according to claim 7, wherein the inert gas is nitrogen. 10. Claims 4 and 5, wherein the oxygen is contained in the air introduced into the reactor tube. , 6, 7, 8 or 9. 11 heating the carbonaceous material in the reactor tube to a temperature at which the carbonaceous material deposit burns when exposed to oxygen; introducing oxygen to the carbonaceous material deposit to cause combustion of the carbonaceous material; Bathing: Cleaning deposits of carbonaceous material from the surface of a device that exchanges heat with a fluidized bed, consisting of the step of conducting a portion of the temperature from the combustion into the fluidized bed to prevent overheating of one surface of the reactor tube. how to. 12 a fluidized bed used at a pyrolysis temperature, comprising at least one or more reactor tubes having an artificial opening and an outlet opening; 1. An apparatus for pyrolyzing a polymeric material, comprising: moving the polymeric material, subjecting the polymeric material to a pyrolytic condition, and pyrolyzing the polymeric material to lower molecular weight materials. 13. The apparatus of claim 12 including a heated tank for dissolving and discharging said polymeric material into said reactor tube. 14. The device of claim 13, wherein the device for moving the polymeric material is a pump device. 15. A plurality of said reactor tubes are provided, each of said reactors including a device for adjustably supplying polymeric material to said inlet opening independently of one another. , 13 or 14. 16. Apparatus for adjustably supplying an inert gas to the inlet opening of each of said reactor tubes; and apparatus for adjustably supplying an oxygen-containing gas to the inlet opening of said valley reactor tube. Apparatus according to scope 15. 17. Claim 12, further comprising a separation device for receiving and separating the pyrolyzed polymeric material discharged from the outlet opening of the reactor tube into fractions.
The device according to item 13 or 14. 18. The apparatus of claim 17, wherein the separation apparatus is a flash distillation apparatus. 19. The apparatus of claim 15 including a separator for receiving and separating the pyrolyzed polymeric material discharged from the opening of the reactor tube into fractions. 20. The apparatus according to claim 19, wherein the separation apparatus is a flash distillation apparatus.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US44323582A | 1982-11-22 | 1982-11-22 | |
| US443235 | 1982-11-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5996189A true JPS5996189A (en) | 1984-06-02 |
Family
ID=23759962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP359583A Pending JPS5996189A (en) | 1982-11-22 | 1983-01-14 | Polymer substance pyrolysis and apparatus |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS5996189A (en) |
| DE (1) | DE3300673A1 (en) |
| FR (1) | FR2536330A1 (en) |
| GB (1) | GB2131044B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06136368A (en) * | 1992-10-26 | 1994-05-17 | Houjiyou:Kk | Oil treatment method for waste |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2158089A (en) * | 1984-05-16 | 1985-11-06 | Jen Szu Jen | Treatment of waste plastics |
| DE69914385T2 (en) * | 1998-03-06 | 2004-11-04 | Matsushita Electric Industrial Co., Ltd., Kadoma | Reuse of cross-linked phenolic resin |
| EP2486178B1 (en) | 2009-10-09 | 2018-08-22 | Starlinger & Co Gesellschaft m.b.H. | Bags made of open mesh material |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5160269A (en) * | 1974-11-25 | 1976-05-26 | Hitachi Shipbuilding Eng Co | Haipurasuchitsukushorihoho oyobi sochi |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4914721B1 (en) * | 1970-08-11 | 1974-04-10 | ||
| GB1501729A (en) * | 1974-05-06 | 1978-02-22 | Redker Young Processes Inc | Conversion of organic waste material |
| DE2448354C3 (en) * | 1974-10-10 | 1978-12-21 | Bergwerksverband Gmbh, 4300 Essen | Fluidized bed reactor for the generation of steam, combustible gases and liquid by-products from coal |
| DE2520754A1 (en) * | 1975-05-09 | 1976-11-18 | Lampl Helma | METHOD AND DEVICE FOR PYROLYSIS OF WASTE PRODUCTS |
| JPS5236918A (en) * | 1975-09-18 | 1977-03-22 | Nippon C Ee T Bui Kk | Receiving set for subscription television broadcasting |
| DE2651302C3 (en) * | 1976-05-12 | 1981-07-09 | PLS Gesellschaft für Pyrolyse-Müllverwertungsverfahren mbH, 8000 München | Device for generating distillation gas from waste |
| US4210491A (en) * | 1976-11-01 | 1980-07-01 | Tosco Corporation | Method and apparatus for retorting a substance containing organic matter |
| GB1564151A (en) * | 1976-11-19 | 1980-04-02 | Procedyne Corp | Cleaning of piece parts by the use of a fluidized-solids bed |
| GB1569152A (en) * | 1976-11-19 | 1980-06-11 | Procedyne Co | Use of neutralizing solids or gases in the fluidise bed cleaning of contaminated piece parts |
| NZ194405A (en) * | 1979-08-02 | 1982-05-25 | Dut Pty Ltd | Producing liquid hydrocarbon streams by hydrogenation of fossil-based feedstock |
| JPS5665084A (en) * | 1979-08-30 | 1981-06-02 | Jensen Frank C | Thermal decomposition and device |
-
1983
- 1983-01-11 DE DE19833300673 patent/DE3300673A1/en not_active Withdrawn
- 1983-01-14 JP JP359583A patent/JPS5996189A/en active Pending
- 1983-01-14 FR FR8300581A patent/FR2536330A1/en not_active Withdrawn
- 1983-01-14 GB GB08301064A patent/GB2131044B/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5160269A (en) * | 1974-11-25 | 1976-05-26 | Hitachi Shipbuilding Eng Co | Haipurasuchitsukushorihoho oyobi sochi |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06136368A (en) * | 1992-10-26 | 1994-05-17 | Houjiyou:Kk | Oil treatment method for waste |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2536330A1 (en) | 1984-05-25 |
| GB8301064D0 (en) | 1983-02-16 |
| DE3300673A1 (en) | 1984-05-24 |
| GB2131044A (en) | 1984-06-13 |
| GB2131044B (en) | 1987-04-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4613713A (en) | Method and apparatus for pyrolysis of atactic polypropylene | |
| JPH0819420B2 (en) | Degradation method for low-grade raw materials | |
| US20020048545A1 (en) | Synthesis gas production and power generation with zero emissions | |
| JPH03505601A (en) | Heavy oil catalytic cracking method and equipment | |
| CA2654535A1 (en) | Carbon nano-fibre production | |
| CN217368415U (en) | Material thermal decomposition device without contacting oxygen | |
| JP2000503336A (en) | Method and apparatus for waste oil treatment | |
| CN106513423A (en) | Waste circuit board recycling system and method | |
| CN105542854A (en) | Device and method for recovering paraffin from Fischer-Tropsch paraffin residues | |
| JPH08253773A (en) | Method for thermal decomposition of plastics and plastic thermal decomposition catalyst used therefor | |
| CN113316608A (en) | Method and apparatus for dry distillation of polyethylene and polypropylene waste | |
| JP7021234B2 (en) | Dihydrogen production equipment, dihydrogen production method using such equipment and usage of such equipment | |
| GB2131044A (en) | Method and apparatus for pyrolysis of atactic polypropylene | |
| CN107177365A (en) | Automatic reallocation, heating, cooling and negative pressure gas gathering system and its application method | |
| JP2008094694A (en) | Nanocarbon generator | |
| EA011643B1 (en) | Pyrolysis of residual hydrocarbons | |
| USRE22957E (en) | Residual hydrocarbon treatment | |
| WO2022166242A1 (en) | Cracked carbon black secondary treatment process and device | |
| JP2000234714A (en) | Flue tube thermal cracking furnace and recycling facility for wasted rubber product | |
| JPH07500808A (en) | Carbonization of materials | |
| CN116478718B (en) | Heating furnace and online decoking method | |
| CN114907868B (en) | Thermal decomposition method and thermal decomposition device | |
| JPH02212592A (en) | Device for thermal decomposition of waste material | |
| JP2005120211A (en) | Waste gasification processing system | |
| JPH02212591A (en) | Method for thermal decomposition of waste material |