JP3372509B2 - Oil recovery device for waste plastic - Google Patents
Oil recovery device for waste plasticInfo
- Publication number
- JP3372509B2 JP3372509B2 JP20992899A JP20992899A JP3372509B2 JP 3372509 B2 JP3372509 B2 JP 3372509B2 JP 20992899 A JP20992899 A JP 20992899A JP 20992899 A JP20992899 A JP 20992899A JP 3372509 B2 JP3372509 B2 JP 3372509B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- boiling point
- gas
- liquid
- high boiling
- 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 - Fee Related
Links
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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/141—Feedstock
- Y02P20/143—Feedstock the feedstock being recycled material, e.g. plastics
-
- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Coke Industry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、都市ごみから分別
収集された廃プラスチック、又は産業廃棄物として回収
された廃プラスチックから高品質の燃料用の油を効率よ
く回収する廃プラスチックの油回収装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a waste plastic oil recovery apparatus for efficiently recovering high-quality fuel oil from waste plastics separately collected from municipal waste or waste plastics recovered as industrial wastes. Regarding
【0002】[0002]
【従来の技術】従来より廃プラスチックを熱分解により
油を回収する方法として、400℃前後の温度で廃プラ
スチックの炭素骨格を切断して低分子化・液化させるこ
とよりなるものが知られている。さらに廃プラスチック
の熱分解に必要な約500〜1、000kcal/kg
(プラスチック)の熱を与える手段として、溶融したプ
ラスチックをポンプで循環させ、その途中に設けられた
加熱炉でエネルギを与えることを含むものの他に、本出
願人によって特開平9−71684号に開示されている
発明が提案されている。2. Description of the Related Art Conventionally, as a method of recovering oil by thermally decomposing waste plastics, a method is known in which the carbon skeleton of the waste plastics is cut at a temperature of about 400.degree. . Approximately 500 to 1,000 kcal / kg required for thermal decomposition of waste plastic
As a means for applying heat of (plastic), in addition to a method in which a molten plastic is circulated by a pump and energy is applied by a heating furnace provided on the way, disclosed by JP-A-9-71684 by the applicant of the present invention. The proposed invention has been proposed.
【0003】すなわち、かかる基本技術は図3に示すよ
うに、廃プラスチックを200mm前後の粒径に粗粉砕
した後、廃プラスチック供給ライン110を経て、ロー
タリーキルン等の脱塩素手段1において、廃プラスチッ
クPは砂循環ライン7より高温の砂Sと混合され、温度
250〜350℃に加熱されることにより塩素分は除去
される。それ自体の組成により実質的に塩素分を含まな
い廃プラスチックP及び/または前記脱塩素手段1によ
って実質的に塩素分が除去された廃プラスチックPは抜
き出しライン9より流動層若しくは撹拌槽からなる熱分
解手段2に送給される。That is, according to such a basic technique, as shown in FIG. 3, waste plastic P is roughly crushed to a particle size of about 200 mm, and then, through a waste plastic supply line 110, in a dechlorination means 1 such as a rotary kiln, waste plastic P is used. Is mixed with high temperature sand S from the sand circulation line 7 and heated to a temperature of 250 to 350 ° C. to remove chlorine. The waste plastic P containing substantially no chlorine content due to its own composition and / or the waste plastic P from which the chlorine content has been substantially removed by the dechlorination means 1 is discharged from the extraction line 9 as heat generated by a fluidized bed or a stirring tank. It is sent to the disassembling means 2.
【0004】熱分解手段2では、砂取り出しライン20
より高温の砂S及び/又は添加剤供給ライン10より添
加剤T等が添加され、比表面の大きい砂Sにより直接廃
プラスチックPを加熱して、温度略350〜500℃、
好ましくは400〜480℃に加熱されることにより、
ガス状熱分解生成物(ガス状の高沸点油、低沸点油、低
分子ガス)に熱分解されると共に熱分解残渣を副生す
る。熱分解残渣は、ライン17を通って流動床型燃焼炉
3に送られる。In the thermal decomposition means 2, the sand removal line 20
An additive T or the like is added from the higher temperature sand S and / or the additive supply line 10, and the waste plastic P is directly heated by the sand S having a large specific surface, and the temperature is about 350 to 500 ° C.
Preferably by heating to 400-480 ° C,
It is thermally decomposed into a gaseous thermal decomposition product (gaseous high boiling point oil, low boiling point oil, low molecular gas) and a thermal decomposition residue is produced as a by-product. The pyrolysis residue is sent to the fluidized bed type combustion furnace 3 through the line 17.
【0005】そして前記熱分解手段2の上方には還流塔
からなる第1の気液分離手段4が接続されている。第1
の気液分離手段4では下方の熱分解手段2から供給さ
れ、上昇するガス状熱分解生成物と、上方からスプレー
ノズル等の液分散器42により供給され下降する前記熱
分解ガス状生成物の温度以下に冷却・調整された低沸点
油と、向流接触させ、ガス状熱分解生成物は液状の高沸
点油(沸点250℃以上)と低沸点成分(沸点250℃
以下のガス状の低沸点油、低分子ガス)とに分離され
る。そのうち、高沸点油は前記熱分解手段2に還流され
る。尚、この250℃という境界温度は必要に応じて2
00〜400℃の範囲に自由に設定することができる。
そして前記第1の気液分離手段4で高沸点油と分離され
たガス状の低沸点油、低分子ガスは未凝縮ガス抜き出し
ライン13より分留塔若しくは放散塔からなる第2の気
液分離手段5に導入される。A first gas-liquid separation means 4 consisting of a reflux tower is connected above the thermal decomposition means 2. First
In the gas-liquid separation means 4, the gaseous pyrolysis products supplied from the lower pyrolysis means 2 and rising, and the pyrolysis gaseous products supplied from above by the liquid disperser 42 such as a spray nozzle and descending. The low boiling point oil cooled or adjusted to a temperature lower than the temperature is brought into countercurrent contact, and the gaseous thermal decomposition product is a liquid high boiling point oil (boiling point 250 ° C. or higher) and low boiling point component (boiling point 250 ° C.).
It is separated into the following gaseous low boiling point oil and low molecular gas). The high boiling point oil is returned to the thermal decomposition means 2. Note that this boundary temperature of 250 ° C. can be set to 2 if necessary.
It can be freely set in the range of 00 to 400 ° C.
The gaseous low boiling point oil and low molecular weight gas separated from the high boiling point oil by the first gas / liquid separating means 4 are the second gas / liquid separation consisting of a fractionating tower or a stripping tower from the uncondensed gas extraction line 13. Introduced into means 5.
【0006】前記第1の気液分離手段4に直列に接続さ
れた第2の気液分離手段5は上側充填部の上方にクーラ
5aが配置され、該クーラ5aにより前記ガスを常温に
冷却することにより、常温で液体の低沸点油は下方底部
に貯留され、常温で気体の低分子ガスはライン16を介
して流動床燃焼炉3に送られ、該燃焼炉3の燃料に供さ
れる。なお、その第2の気液分離手段5で分離された低
沸点油の一部は循環ライン23を介して第1の気液分離
手段4の液分散器42に戻され、高沸点油の洗浄・捕集
に使用される。また、上記各気液分離手段としては、例
えば充填塔や塔内に上下に配列された複数段の棚段より
段塔等が使用される。In the second gas-liquid separating means 5 connected in series to the first gas-liquid separating means 4, a cooler 5a is arranged above the upper filling part, and the gas is cooled to room temperature by the cooler 5a. Thus, the low boiling point oil that is liquid at room temperature is stored in the lower bottom portion, and the low molecular gas that is gaseous at room temperature is sent to the fluidized bed combustion furnace 3 through the line 16 and is used as fuel for the combustion furnace 3. A part of the low boiling point oil separated by the second gas-liquid separating means 5 is returned to the liquid disperser 42 of the first gas-liquid separating means 4 through the circulation line 23 to wash the high boiling point oil. -Used for collection. Further, as each of the gas-liquid separating means, for example, a packed tower or a tower having a plurality of trays vertically arranged in the tower is used.
【0007】さらに前記熱分解手段2で生成した固体状
の熱分解残渣(炭素質)・固型異物・液化しなかった熱
硬化性樹脂等の有機物は、スクリューフィーダ等で取り
出され、前記した燃焼炉3に導入される。その燃焼炉3
は、空気が吹き込まれることよって砂Sを媒体とする流
動床が形成されており、前記有機物や砂Sに付着した有
機物は完全燃焼し、砂Sは500〜950℃に加熱され
る。砂Sは灰分と分離され、脱塩素手段1と熱分解手段
2とにライン20、11及び7を介して再循環使用され
る。Further, organic matter such as solid pyrolysis residue (carbonaceous matter), solid foreign matter, and non-liquefied thermosetting resin produced by the pyrolysis means 2 is taken out by a screw feeder or the like, and burned as described above. It is introduced into the furnace 3. The combustion furnace 3
, A fluidized bed using sand S as a medium is formed by blowing air, the organic substances and the organic substances attached to the sand S are completely burned, and the sand S is heated to 500 to 950 ° C. The sand S is separated from the ash and recycled to the dechlorination means 1 and the thermal decomposition means 2 via lines 20, 11 and 7.
【0008】以上のように構成されることにより、本従
来技術では、次のような作用を奏する。即ち、熱分解手
段2では、比表面積の大きい高温の砂Sにより直接廃プ
ラスチックPが加熱されるため、従来の間接熱交換器の
ように伝熱面でのコーキングトラブルが回避され、運転
が安定し、長期連続運転が可能となる。副生した熱分解
残渣は砂Sに付着・成長するが、砂Sは絶えず流動し、
流動床型燃焼炉3との間を循環しており、該燃焼炉3で
熱分解残渣が燃焼消失することによって容易に加熱再生
される。With the above-mentioned structure, the conventional technique has the following effects. That is, in the thermal decomposition means 2, since the waste plastic P is directly heated by the high temperature sand S having a large specific surface area, the caulking trouble on the heat transfer surface as in the conventional indirect heat exchanger is avoided, and the operation is stable. However, long-term continuous operation becomes possible. The pyrolysis residue produced as a by-product adheres to and grows on the sand S, but the sand S constantly flows,
It circulates between the fluidized bed type combustion furnace 3 and the thermal decomposition residue is burnt and disappears in the combustion furnace 3 to be easily heated and regenerated.
【0009】次に高沸点油が第1の気液分離手段4によ
って低沸点成分と分離され、熱分解手段2に戻され、さ
らに再加熱・熱分解されることによって低沸点油を生成
するため、低沸点油の収率が増大し、油の品質・貯蔵安
定性が向上する。Next, the high-boiling point oil is separated from the low-boiling point component by the first gas-liquid separating means 4, returned to the thermal decomposition means 2, and further reheated and thermally decomposed to produce a low-boiling point oil. The yield of low boiling point oil is increased, and the quality and storage stability of oil are improved.
【0010】更に第2の気液分離手段5によって低分子
ガスと分離された低沸点油の一部が第1の気液分離手段
4に戻されるため、高沸点油がその第1の気液分離手段
4を誤って通過しようとしても、低沸点油と接触し、そ
れに捕捉され、その中に分散され、熱分解手段2側に確
実に還流される。従って、ワックス分(高沸点油)が低
沸点油側に移行・混入することがなく、高品質の低沸点
油が得られる。Furthermore, since a part of the low boiling point oil separated from the low molecular gas by the second gas-liquid separating means 5 is returned to the first gas-liquid separating means 4, the high boiling point oil is converted into the first gas-liquid. Even if it tries to pass through the separating means 4 by mistake, it comes into contact with the low boiling point oil, is trapped therein, is dispersed therein, and is surely refluxed to the thermal decomposition means 2 side. Therefore, the wax component (high boiling point oil) does not migrate or mix into the low boiling point oil side, and a high quality low boiling point oil can be obtained.
【0011】更に又、前記熱分解手段2で生成した熱分
解残渣等の有機物は、砂Sと共に残渣焼却手段(流動床
型燃焼炉)3に導入され、吹き込まれた空気によって完
全燃焼すると共に、その発生する熱によって砂Sを50
0〜950℃に加熱する。砂Sの一部は、脱塩素手段1
と熱分解手段2とに再循環され、それぞれ熱媒体として
繰り返し使用されるため、廃プラスチックP中の固形分
は100〜200mm以下に破砕されていれば、閉塞な
どのトラブルはなく、前処理は破砕のみでよく、格別の
分別は不要となる。Furthermore, the organic matter such as the thermal decomposition residue produced by the thermal decomposition means 2 is introduced into the residue incineration means (fluidized bed type combustion furnace) 3 together with the sand S and completely combusted by the blown air, 50 S of sand S is generated by the generated heat
Heat to 0-950 ° C. Part of the sand S is dechlorination means 1
Since the solid content in the waste plastic P is crushed to 100 to 200 mm or less, there is no trouble such as clogging, and the pretreatment is carried out. Only crushing is required and no special sorting is required.
【0012】[0012]
【発明が解決しようとする課題】従って本出願人による
前記基本技術によって、熱分解手段2におけるコーキン
グトラブルの回避、長期連続運転の達成、熱分解残渣の
有効利用、高品質の低沸点油の収率向上、ごみの分別の
簡略化が可能となったが、なお、次のような問題があ
る。Therefore, according to the basic technique of the present applicant, the coking trouble in the thermal cracking means 2 can be avoided, long-term continuous operation can be achieved, the thermal cracking residue can be effectively used, and the high-quality low boiling point oil can be collected. Although it has become possible to improve the rate and simplify the separation of garbage, there are still the following problems.
【0013】即ち、都市ゴミから排出されるプラスチッ
クには、PETやPVC等があり、これらのガス状熱分
解生成物が、第1の気液分離手段4では200〜250
℃の温度の低沸点油と向流接触させると200〜250
℃以上の温度に昇華点を有するテレフタール酸(昇華点
300℃)や結晶化しやすい物質があわせて析出し、こ
れらの析出物や熱分解残渣・砂の破砕片等の平均粒径約
10ミクロンの微小固形分(ダスト)が、第1の気液分
離手段4の内の充填層を通って繰り返し熱分解手段2に
戻るが、前記サイクルは無限に繰り返されるために、順
次前記充填層を形成する充填物等に捕捉され、蓄積し、
最悪の場合には前記充填層が閉塞するという問題が発生
する。That is, the plastics discharged from the municipal waste include PET, PVC, etc., and the gaseous thermal decomposition products thereof are 200 to 250 in the first gas-liquid separation means 4.
200 to 250 when countercurrently contacted with a low boiling point oil at a temperature of ℃
Terephthalic acid having a sublimation point at a temperature of ℃ or more (sublimation point of 300 ℃) and substances that are easily crystallized are also precipitated, and these precipitates, pyrolysis residue, crushed fragments of sand, etc. having an average particle size of about 10 microns The fine solids (dust) repeatedly return to the thermal decomposition means 2 through the packed bed in the first gas-liquid separation means 4, but the cycle is repeated indefinitely, so that the packed bed is sequentially formed. Captured and accumulated in filling materials,
In the worst case, there is a problem that the packed bed is clogged.
【0014】かかる技術課題を解決するために、特開平
9−20892号において、図4に示すように、気液接
触槽125底部を垂直仕切板126により2つに分離す
るとともに、炉頂部に液ノズル128を設け、前記垂直
仕切板126により分離された軽質油貯留室135より
クーラ130を介して前記軽質油分を250〜300℃
に冷却しつつ炉頂部の液ノズル128より噴霧可能に構
成されている。又液ノズル128の下方には、傾斜板1
27が配置されており、気液接触された油は先ず重質油
貯留室132に流入可能に構成されている。In order to solve such a technical problem, in Japanese Unexamined Patent Publication No. 9-20892, as shown in FIG. 4, the bottom part of the gas-liquid contact tank 125 is separated into two parts by a vertical partition plate 126, and the liquid is added to the top part of the furnace. A nozzle 128 is provided, and the light oil content is separated from the light oil storage chamber 135 separated by the vertical partition plate 126 via a cooler 130 to 250 to 300 ° C.
It is configured to be sprayed from a liquid nozzle 128 at the top of the furnace while being cooled. Below the liquid nozzle 128, the inclined plate 1
No. 27 is arranged, and the oil that has been brought into gas-liquid contact can first flow into the heavy oil storage chamber 132.
【0015】かかる従来技術によれば、熱分解槽より送
給された例えば400〜450℃前後の温度を有するガ
ス状熱分解生成物をライン131より気液接触槽の重質
油貯留室132に導かれる。重質油貯留室132では前
記400〜450℃前後の温度ガスの流入により低沸点
油等が蒸発するが、炉頂部の液ノズル128より250
〜300℃の温度に冷却された軽質油分と気液接触し、
250℃以上の温度に昇華点を有するテレフタール酸等
が結晶化し、その析出物や250〜400℃に沸点を有
する油が重質油貯留室132に戻される。そして前記重
質油貯留室132の上層の軽質油成分は仕切壁126を
オーバフローして軽質油貯留室135に貯留される。以
下前記操作を繰り返す。According to such a conventional technique, the gaseous thermal decomposition product having a temperature of, for example, about 400 to 450 ° C., which is fed from the thermal decomposition tank, is fed from the line 131 to the heavy oil storage chamber 132 of the gas-liquid contact tank. Be guided. In the heavy oil storage chamber 132, the low boiling point oil and the like evaporate due to the inflow of the temperature gas of about 400 to 450 ° C., but 250 from the liquid nozzle 128 at the furnace top.
Gas-liquid contact with light oil content cooled to a temperature of ~ 300 ° C,
Terephthalic acid or the like having a sublimation point at a temperature of 250 ° C. or higher is crystallized, and its precipitate or oil having a boiling point at 250 to 400 ° C. is returned to the heavy oil storage chamber 132. The light oil component in the upper layer of the heavy oil storage chamber 132 overflows the partition wall 126 and is stored in the light oil storage chamber 135. The above operation is repeated thereafter.
【0016】[0016]
【発明が解決しようとする課題】かかる従来技術におい
ては、熱分解槽より重質油貯留室に常に400〜450
℃前後のガス状熱分解生成物が供給されるために、該貯
留室内が必然的にバブリング状態になり、対流現象によ
り前記析出分が上層まで対流し、垂直仕切壁よりのオー
バフローにより軽質油貯留室側に移行してしまうという
欠点を有する。In the prior art as described above, 400 to 450 is always provided in the heavy oil storage chamber from the thermal decomposition tank.
Since the gaseous pyrolysis products at around ℃ are supplied, the storage chamber inevitably becomes in a bubbling state, the convection phenomenon causes the precipitates to convection to the upper layer, and the light oil storage due to the overflow from the vertical partition wall. It has the drawback of moving to the room side.
【0017】又、400〜450℃前後のガス状熱分解
生成物が供給されるために、該重質油貯留室が常に40
0〜450℃前後で加熱されるために重質油成分が貯留
室壁面に粘着し、保守劣化が生じやすい。Further, since the gaseous thermal decomposition product at about 400 to 450 ° C. is supplied, the heavy oil storage chamber is always kept at 40 ° C.
Since it is heated at around 0 to 450 ° C., the heavy oil component adheres to the wall surface of the storage chamber, and maintenance deterioration easily occurs.
【0018】本発明は、かかる技術的課題に鑑み、テレ
フタール酸類等の析出物・微小固形分(ダスト)の効果
的除去を図るとともに、低沸点油の質的及び収率向上を
図った廃プラスチックの油回収装置を提供することを目
的とする。In view of the above technical problems, the present invention aims to effectively remove precipitates and minute solids (dust) such as terephthalic acids, and to improve the quality and yield of low boiling point oil. It aims at providing the oil recovery device of.
【0019】[0019]
【課題を解決するための手段】本発明はかかる課題を解
決するために、 破砕された廃プラスチックを温度略3
50〜500℃の温度で熱分解して熱分解ガス状生成物
を得る熱分解手段と、前記熱分解ガス状生成物を気液接
触空間に導入し、気液接触空間上方より噴出される油に
接触させて高沸点油を下方の分離手段に流下させる第1
の気液接触手段と、前記第1の気液接触手段をガス状に
通過した低沸点油を含む低沸点成分を冷却して低沸点油
を回収する低沸点油回収手段と、前記分離手段内に貯留
された高沸点油を熱分解手段に戻す廃プラスチックの油
回収装置において、 前記第1の気液接触手段を途中位置
に充填層を有し、底部を前記分離手段内に挿設した直接
析出用充填塔で構成し、該充填層の下方より前記熱分解
ガス状生成物を導入し、前記充填層の上部より冷却調整
された油を散布させて、前記充填層で該油との接触によ
り高沸点油とともにテレフタール酸を含む結晶化物質が
析出し、前記分離手段の底部で高沸点油と結晶化物質が
比重分離可能に構成した廃プラスチックの油回収装置を
提案する。そして好ましくは、前記分離手段の底部を底
側に向けて縮径させて先細のコーン状に形成するととも
に、前記第1の気液接触手段を途中位置に充填層を有す
る直接析出用充填塔で構成し、該充填塔の下側に位置す
る延設筒下端を前記コーン状部途中位置まで上方より垂
下させるとともに、前記充填層の下方より前記熱分解ガ
ス状生成物を導入し、充填層の上部より冷却調整された
油を散布させて、充填層で該油との接触により高沸点油
とともにテレフタール酸を含む結晶化物質が析出して延
設筒より分離手段下方のコーン状部に流下し、該コーン
状部の底部で高沸点油と結晶化物質が比重分離可能に構
成され、具体的には前記冷却調整された油が300℃以
下であり、前記高沸点油が略250〜350℃以上の油
であり、前記結晶化物質が、250℃以上の温度に昇華
点を有するテレフタール酸を含む結晶化物質であるのが
よい。 In order to solve such a problem, the present invention treats crushed waste plastic at a temperature of about 3 ° C.
Pyrolysis means for thermally decomposing at a temperature of 50 to 500 ° C. to obtain a pyrolysis gaseous product, and oil which is introduced into the gas-liquid contact space and jetted from above the gas-liquid contact space. To
By contacting the first to flow down the high-boiling oil separation means below
A gas-liquid contact means, the low-boiling oil recovery means for recovering low-boiling oil to cool the low boiling point component containing a low boiling point oil to said first gas-liquid contact means passing through the gaseous, the separating means in Of waste plastic that returns high boiling point oil stored in the tank to pyrolysis means
In the recovery device, the first gas-liquid contact means is placed at an intermediate position.
Has a packed bed in the bottom, and the bottom is directly inserted into the separating means.
It is composed of a packed column for precipitation, and the thermal decomposition is performed from below the packed bed.
Introduce a gaseous product and adjust cooling from the top of the packed bed
The oil that has been sprayed is sprayed, and by contact with the oil in the packed bed,
Crystallized substances containing terephthalic acid with high boiling point oil
The high boiling point oil and the crystallized substance are deposited at the bottom of the separating means.
We propose a waste plastic oil recovery device that can be separated by specific gravity . And preferably, the bottom of the separating means is
The diameter is reduced toward the side to form a tapered cone shape.
In addition, a packing layer is provided at an intermediate position of the first gas-liquid contacting means.
It is composed of a packed column for direct precipitation and is located below the packed column.
The lower end of the extended cylinder from above to the middle of the cone.
The thermal decomposition gas from below the packed bed.
A soot-like product was introduced, and cooling was adjusted from the top of the packed bed.
High-boiling oil is sprayed with oil, and the high boiling point oil is contacted with the oil in the packed bed.
At the same time, a crystallized substance containing terephthalic acid precipitates and spreads.
It flows down from the installation cylinder to the cone-shaped portion below the separating means,
High-boiling point oil and crystallized substance can be separated at the bottom of
Specifically, the cooling-adjusted oil is 300 ° C or higher.
Below, the high-boiling oil is an oil of approximately 250 to 350 ° C. or higher.
And the crystallized substance sublimates to a temperature of 250 ° C. or higher.
The crystallized substance containing terephthalic acid having points is
Good.
【0020】ガス状熱分解生成物は、前記従来技術のよ
うに、固液分離装置の貯留室内に直接導くのではなく、
その上方に位置する気液接触空間内に導入されるため
に、固液分離装置の貯油室内でバブリング等が生じるこ
となく、析出物と高沸点油との比重差に基づく沈降分離
を精度良く行なうことが出来る。又、固液分離装置で
は、前記気液接触により(300℃以下に)十分冷却さ
れた重質分が落下するために、言い換えれば前記従来技
術で示す400〜450℃前後のガス状熱分解生成物で
加熱されることがないために重質油成分が固液分離装置
としての沈降槽壁面に粘着したり、保守劣化が生じるこ
となく、容易に排出できる。The gaseous thermal decomposition product is not directly introduced into the storage chamber of the solid-liquid separator as in the prior art, but
Since it is introduced into the gas-liquid contact space located above it, bubbling does not occur in the oil storage chamber of the solid-liquid separation device, and sedimentation separation based on the specific gravity difference between the precipitate and the high boiling point oil is performed accurately. You can Further, in the solid-liquid separation device, the heavy component sufficiently cooled (below 300 ° C.) drops due to the gas-liquid contact, in other words, the gaseous thermal decomposition production at about 400 to 450 ° C. shown in the above-mentioned prior art. Since it is not heated by the material, the heavy oil component can be easily discharged without adhering to the wall surface of the settling tank as the solid-liquid separation device or causing maintenance deterioration.
【0021】本発明は、前記熱分解手段と第1の気液接
触手段との間に、前記熱分解ガス状生成物の温度以下に
冷却・調整された油で熱分解ガス状生成物と気液接触さ
せ、前記生成物中のタールやピッチ等の重質分を凝縮さ
せ熱分解手段側に戻す還流手段を設けるのがよい。According to the present invention, between the thermal decomposition means and the first gas-liquid contacting means, the oil is cooled and adjusted to a temperature equal to or lower than the temperature of the thermal decomposition gaseous product, and the gas is decomposed with the thermal decomposition gaseous product. It is preferable to provide a reflux means for bringing into contact with the liquid and condensing heavy components such as tar and pitch in the product and returning them to the thermal decomposition means side.
【0022】かかる発明によれば、熱分解ガス状生成物
中のタールやピッチ等の重質分は前もって除去された
後、第1気液分離手段でテレフタール酸類の析出を行な
うために、該第1気液分離手段や固液分離手段に、これ
らのタールやピッチ等等が壁面に付着する恐れがなく、
一層保守劣化が生じることなく、容易に運転管理が出来
る。According to this invention, since the heavy components such as tar and pitch in the pyrolyzed gaseous product are removed in advance, the first gas-liquid separation means is used to deposit the terephthalic acids. (1) There is no risk of these tars, pitches, etc. adhering to the wall surface in the gas-liquid separation means or the solid-liquid separation means,
Operation management can be performed easily without further maintenance deterioration.
【0023】更に本発明は、前記固液分離手段で生成さ
れた高沸点油を第1の気液接触手段若しくは還流手段の
気液接触油として使用することを特徴とする。この場
合、前記循環経路中に還流クーラ等を用いて温度制御を
図るのがよい。Further, the present invention is characterized in that the high boiling point oil produced by the solid-liquid separation means is used as the gas-liquid contact oil of the first gas-liquid contact means or the reflux means. In this case, it is preferable to control the temperature by using a reflux cooler or the like in the circulation path.
【0024】特に還流手段の気液接触油として使用する
ことにより、その油分は常に熱分解手段側に戻すことが
出来、高沸点油の低沸点油化が一層促進される。しか
も、テレフタール酸類が分離低減された高沸点油がガス
状熱分解生成物の冷却剤として循環使用されるため、冷
却剤中のテレフタール酸の蓄積・増加が起らず、その増
大によってガス状熱分解生成物と接触する気液接触手段
(充填塔等)での閉塞トラブルも解消される。Especially by using as the gas-liquid contact oil of the reflux means, the oil content can be always returned to the pyrolysis means side, and the conversion of the high-boiling oil to the low-boiling oil is further promoted. Moreover, since the high boiling point oil from which terephthalic acids have been separated and reduced is circulated and used as a coolant for the gaseous thermal decomposition products, accumulation and increase of terephthalic acid in the coolant does not occur, and the increase in the gaseous heat causes The clogging trouble in the gas-liquid contact means (packing tower etc.) that comes into contact with the decomposition products is also eliminated.
【0025】又本発明は、前記固液分離手段で生成され
た高沸点油を蒸留手段にて低沸点成分を除去した後、熱
分解手段、第1の気液接触手段若しくは還流手段に戻す
のがよい。Further, according to the present invention, the high boiling point oil produced by the solid-liquid separation means is removed by distillation means to remove low boiling point components, and then returned to the thermal decomposition means, the first gas-liquid contact means or the reflux means. Is good.
【0026】即ち、ガス状熱分解生成物の前記気液接触
手段での接触時の温度が低い場合、落下する高沸点油中
の低沸点油の含量が増大し、そのままそれが熱分解手段
に送られ、再加熱されると、低沸点油がさらに熱分解さ
れ、ガス成分が増大し、低沸点油の収量が低下するおそ
れがある。その対策として、本発明では、得られた高沸
点油のうち、熱分解手段に送られるものは、蒸留され、
低沸点油が回収されるよう構成されているため、それが
再熱分解されることはなく、ガス状熱分解生成物の接触
時の温度が低くても、低沸点油の収量は高い。That is, when the temperature at which the gaseous thermal decomposition product is contacted by the gas-liquid contacting means is low, the content of the low boiling point oil in the falling high boiling point oil increases, and it is directly used in the thermal decomposition means. When sent and reheated, the low boiling point oil is further thermally decomposed, the gas component increases, and the yield of the low boiling point oil may decrease. As a countermeasure, in the present invention, among the high boiling point oils obtained, those sent to the thermal decomposition means are distilled,
Since the low boiling point oil is configured to be recovered, it is not re-pyrolyzed, and the yield of the low boiling point oil is high even if the temperature at the time of contact with the gaseous pyrolysis products is low.
【0027】更に本発明において、前記固液手段を比重
差により固液分離を行なう沈降槽で形成するとともに、
前記第1の気液接触手段の液流出開口を前記沈降槽の貯
留液中に侵入させるのがよい。かかる発明は、前記第1
の気液接触手段の液流出時の重力エネルギが減少し、静
かに液流出が行なわれるために、円滑に比重差により固
液分離を行なうことができる。特に第1気液分離手段に
分離された微小固形物を含む高沸点油は、固液分離手段
によって例えば沈降槽に靜置されるだけで、液体の高沸
点油とテレフタール酸類・微小固形物とに沈降分離され
る。なお、テレフタール酸類・微小固形物は抜き出さ
れ、例えば燃焼炉によって焼却処理される。Further, in the present invention, the solid-liquid means is formed of a settling tank for performing solid-liquid separation by the difference in specific gravity, and
It is preferable that the liquid outflow opening of the first gas-liquid contacting device is made to enter the stored liquid in the settling tank. In the invention, the first
Since the gravitational energy at the time of liquid outflow of the gas-liquid contact means is reduced and the liquid outflow is performed gently, solid-liquid separation can be smoothly performed by the difference in specific gravity. In particular, the high-boiling point oil containing the fine solids separated by the first gas-liquid separation means is simply placed in, for example, a settling tank by the solid-liquid separation means, and the high-boiling point oil of liquid and terephthalic acid / fine solids Is separated by sedimentation. The terephthalic acids and minute solids are extracted and incinerated by, for example, a combustion furnace.
【0028】又本発明は、前記熱分解手段の前に脱塩素
手段を設けるとともに、該脱塩素工程で発生したHCl
リッチガス、前記固液分離手段の底部に貯留した結晶化
物質、及び低沸点油回収手段で発生した低沸点ガスのい
ずれもが、前記熱分解手段と脱塩素手段に熱エネルギを
供給する燃焼炉に供給され、熱エネルギの循環利用を図
る。Further, in the present invention, a dechlorination means is provided in front of the thermal decomposition means, and HCl generated in the dechlorination step is used.
Both the rich gas, the crystallization substance stored in the bottom of the solid-liquid separation means, and the low boiling point gas generated by the low boiling point oil recovery means are supplied to the combustion furnace for supplying thermal energy to the thermal decomposition means and the dechlorination means. It is supplied and aims to circulate and utilize heat energy.
【0029】かかる発明によれば熱エネルギを閉回路に
て効率よく利用でき、無駄に熱エネルギを捨てることが
ない。According to this invention, the heat energy can be efficiently used in the closed circuit, and the heat energy is not wasted.
【0030】従って本発明によれば、高温の熱分解ガス
状生成物を低温の高沸点油と接触させることによって、
析出物及び微小固形分を含む高沸点油を凝縮させ、低沸
点油を含む低沸点成分と分離すること、得られた高沸点
油から析出物及び微小固形分を分離すること、及びその
析出物及び微小固形分を分離した高沸点油のうち、増加
分は加熱し、低沸点成分を留出させたうえ、熱分解手段
に戻し、廃プラスチックと共に熱分解するが、一部は冷
却し、上記高温の熱分解ガス状生成物と低温の高沸点油
との接触に循環再使用することが出来る。Thus, according to the present invention, by contacting a hot pyrolysis gaseous product with a cold high boiling oil,
Condensing a high boiling point oil containing a precipitate and a fine solid content and separating it from a low boiling point component containing a low boiling point oil, separating a precipitate and a fine solid content from the obtained high boiling point oil, and a precipitate thereof And of the high boiling point oil from which the fine solids have been separated, the increased amount is heated to distill out the low boiling point component and then returned to the thermal decomposition means and thermally decomposed together with the waste plastic, but partly cooled, It can be recycled and reused for contacting hot pyrolysis gaseous products with cold high boiling oils.
【0031】[0031]
【発明の実施の形態】以下、本発明を図に示した実施例
を用いて詳細に説明する。但し、この実施例に記載され
るユニット等の種類、温度、そのユニットの配置順序等
の相対配置などは特に特定的な記載がない限り、この発
明の範囲をそれのみに限定する趣旨ではなく単なる説明
例に過ぎない。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below with reference to the embodiments shown in the drawings. However, types of units and the like described in this embodiment, temperature, relative arrangement such as the arrangement order of the units, etc., are not intended to limit the scope of the present invention thereto only unless otherwise specified. It is only an example.
【0032】図1は本発明の基本構成にかかる廃プラ油
化装置の全体システム構成図である。次に本発明の実施
の態様を詳細に説明する。先ず本発明でいう廃プラスチ
ックとは、都市ごみから分別された、主としてプラスチ
ックを含むごみで、ポリエチレン、ポリプロピレン、ポ
リスチレンなど熱可塑性樹脂を主成分として、ポリ塩化
ビニル(PVC)、PET類等を含むものを言い、熱硬
化性樹脂や紙、ちゅう芥類の夾雑雑が混入していても良
い。また、産業廃棄物の中でも、プラスチックダイキャ
スト製品の残渣プラスチック等のポリ塩化ビニル(PV
C)、PET類等を含むものも包含される。要は略20
0〜300℃の気液接触により油より比重の大きい固形
物が析出されるプラスチックを含むものを指す。FIG. 1 is an overall system configuration diagram of a waste plastic oiling apparatus according to the basic configuration of the present invention. Next, embodiments of the present invention will be described in detail. First, the term “waste plastic” as used in the present invention refers to waste that is separated from municipal solid waste and mainly contains plastic, and mainly contains thermoplastic resins such as polyethylene, polypropylene, and polystyrene, and contains polyvinyl chloride (PVC), PETs, and the like. It means a thing, and may be mixed with a thermosetting resin, paper, and miscellaneous substances such as porridge. In addition, among industrial waste, polyvinyl chloride (PV
Those including C) and PETs are also included. The point is about 20
It refers to a material containing a plastic in which a solid substance having a specific gravity larger than that of oil is deposited by gas-liquid contact at 0 to 300 ° C.
【0033】以下、図1を参照して本発明の基本構成に
ついて説明する。30は破砕機で、廃プラスチックP中
の固型分は100〜200mmに破砕した後、脱塩素を
行なうロータリーキルン1に投入される。ロータリーキ
ルン1では、前記廃プラスチックPと400〜950℃
に高温加熱した循環砂Sを押し出し混合させながら、前
記廃プラスチックPを温度250〜350℃に加熱す
る。The basic configuration of the present invention will be described below with reference to FIG. A crusher 30 crushes the solid content of the waste plastic P to 100 to 200 mm, and then throws it into the rotary kiln 1 for dechlorination. In the rotary kiln 1, the waste plastic P and 400 to 950 ° C.
The waste plastic P is heated to a temperature of 250 to 350 ° C. while the circulating sand S heated at a high temperature is extruded and mixed.
【0034】この結果、廃プラスチックP中の塩素は約
95%以上を分離してキルン1上部に設けたHClリッ
チガス抜出しライン53よりHCl主成分のガスが取り
出され、流動床炉3、熱回収器60、バグフィルタ61
を介してHCl吸収塔62により水又はアルカリ吸収液
で回収する。そして、循環砂Sと脱塩素されたプラスチ
ックPとの混合物はスクリューコンベア等からなる抜出
しライン9を介して熱分解槽2に供給される。As a result, about 95% or more of the chlorine in the waste plastic P is separated, and the gas containing HCl as the main component is taken out from the HCl-rich gas extraction line 53 provided in the upper part of the kiln 1, and the fluidized bed furnace 3 and the heat recovery unit are taken out. 60, bag filter 61
The water is recovered as water or an alkali absorption liquid by the HCl absorption tower 62 via the. Then, the mixture of the circulating sand S and the dechlorinated plastic P is supplied to the thermal decomposition tank 2 through an extraction line 9 composed of a screw conveyor or the like.
【0035】かかるロータリーキルン1によれば、高温
の砂Sで直接加熱する為、伝熱面積は砂Sの表面積と大
きく、容易に廃プラスチックPを加熱することができ
る。According to the rotary kiln 1, since the high temperature sand S is directly heated, the heat transfer area is large as the surface area of the sand S and the waste plastic P can be easily heated.
【0036】熱分解槽2は砂S、添加剤T、廃プラスチ
ックPを均一に混合できる撹拌槽からなり、添加剤供給
ライン10より供給された添加剤Tと、循環砂供給ライ
ン11より供給された500〜950℃の高温の循環砂
Sを、抜出しライン9より供給されたプラスチックP混
合物とともに混合し、温度400〜480℃に保持しな
がら加熱分解を行なう。尚、前記添加剤Tには、合成ゼ
オライト又は天然ゼオライト、好ましくは天然のモルデ
ナイトを用いる。The thermal decomposition tank 2 is composed of a stirring tank capable of uniformly mixing the sand S, the additive T, and the waste plastic P. The additive T supplied from the additive supply line 10 and the circulating sand supply line 11 are supplied. Further, the high-temperature circulating sand S of 500 to 950 ° C. is mixed with the plastic P mixture supplied from the extraction line 9, and the thermal decomposition is performed while maintaining the temperature at 400 to 480 ° C. As the additive T, synthetic zeolite or natural zeolite, preferably natural mordenite is used.
【0037】そして、熱分解槽2で生成した固体状の熱
分解残渣(炭素質)、固型異物、液化しなかった熱硬化
性樹脂は熱分解残渣混合物抜出しライン17より、スク
リューフィーダ等で取り出し、流動床燃焼炉3に導入す
る。Then, the solid thermal decomposition residue (carbonaceous material) generated in the thermal decomposition tank 2, solid foreign matter, and the non-liquefied thermosetting resin are taken out from the thermal decomposition residue mixture extraction line 17 with a screw feeder or the like. , The fluidized bed combustion furnace 3.
【0038】前記熱分解槽2の上方には還流塔4が接続
されており、該還流塔4内で前記熱分解槽2より生成し
た熱分解生成ガスと、炉頂に設けたノズル42より噴出
される、前記熱分解ガス状生成物の温度以下に冷却・調
整された油との気液若しくは気気接触接触にて、タール
やワックス等の重質分を重力で熱分解槽2に戻す。尚、
前記ノズル42より噴出される油は、分留塔5で生成し
た回収油を温度調節してノズル42に供給するように構
成してるが、これのみに限定されず、後記沈降槽6の上
澄み油を前記ノズル42に供給しても良い。A reflux tower 4 is connected above the pyrolysis tank 2, and the pyrolysis product gas produced from the pyrolysis tank 2 in the reflux tower 4 and a nozzle 42 provided at the top of the furnace are jetted. The heavy components such as tar and wax are returned to the thermal decomposition tank 2 by gravity by gas-liquid contact or gas-air contact with oil cooled and adjusted to a temperature lower than the temperature of the thermal decomposition gaseous product. still,
The oil ejected from the nozzle 42 is configured so that the recovered oil produced in the fractionating tower 5 is temperature-controlled and supplied to the nozzle 42, but the present invention is not limited to this, and the supernatant oil of the sedimentation tank 6 described later is used. May be supplied to the nozzle 42.
【0039】そして前記重質分が除去された熱分解生成
ガスは析出用充填塔50の気液接触空間59に送給され
る(図2参照)。析出用充填塔50は充填層58の上方
に液ノズル部57を設けるとともに、下方開口を筒状に
下方に延設し、その延設筒40下端開口を沈降槽6の液
中に浸入させる。熱分解生成ガスの導入口49は、図1
に示すように前記充填層58の途中でも、又、前記充填
層58の下方に導入口49を設定してもよく、いずれも
気液接触空間となる。Then, the pyrolysis product gas from which the heavy components have been removed is fed to the gas-liquid contact space 59 of the deposition tower 50 (see FIG. 2). The deposition packed tower 50 is provided with a liquid nozzle portion 57 above the packed bed 58, has a lower opening extending cylindrically downward, and allows the lower end opening of the extending cylinder 40 to penetrate into the liquid of the settling tank 6. The inlet 49 for the pyrolysis product gas is shown in FIG.
As shown in FIG. 5, the inlet 49 may be set in the middle of the filling layer 58 or below the filling layer 58, both of which serve as a gas-liquid contact space.
【0040】又、前記液ノズル部57より噴出される油
は、分溜塔5で生成した回収油で、これをクーラ45で
200〜300℃、好ましくは250〜300℃に冷却
して、ノズル部57に供給するように構成しているが、
これのみに限定されず、図2に示すように沈降槽6の上
澄み油を前記ノズル部57に供給しても良い。この結
果、前記液ノズル部57より250〜300℃の温度に
冷却された回収油と重質分が除去された熱分解ガスと気
液接触し、250℃以上の温度に昇華点を有するテレフ
タール酸等が結晶化し、その析出物とともに250〜4
00℃に沸点を有する高沸点油が延設筒40内に落下
し、該延設筒40下端開口より沈降槽6の液中に侵入す
る。The oil ejected from the liquid nozzle portion 57 is recovered oil produced in the fractionating tower 5, which is cooled by a cooler 45 to 200 to 300 ° C., preferably 250 to 300 ° C. Although it is configured to be supplied to the section 57,
The present invention is not limited to this, and the supernatant oil of the settling tank 6 may be supplied to the nozzle portion 57 as shown in FIG. As a result, terephthalic acid having a sublimation point at a temperature of 250 ° C. or higher comes into gas-liquid contact with the recovered oil cooled to a temperature of 250 to 300 ° C. from the liquid nozzle portion 57 and the pyrolysis gas from which heavy components have been removed. Etc. are crystallized and, together with the precipitate, 250 to 4
The high boiling point oil having a boiling point at 00 ° C. falls into the extension cylinder 40 and enters the liquid in the settling tank 6 through the lower end opening of the extension cylinder 40.
【0041】そして250〜400℃に沸点を有する高
沸点油と結晶化したテレフタール酸は、前記沈降槽6内
で比重分離され、テレフタール酸(比重約1.5)が底
部に、高沸点油(比重0.85前後)が上澄み油として
上部に貯留される。そして前記沈降槽6底部に貯まった
テレフタール酸等は燃料として流動床型燃焼炉3に供給
される。そして上澄み油としての高沸点油はライン47
を介して分溜塔5の底部に導かれた後、ヒータからなる
蒸留器52で低沸点分を蒸発させた後、残余の高沸点油
をノズル部42より還流塔4内に噴出された後、気液接
触された重質分とともに熱分解槽2に戻入循環させる。
このように高沸点油をライン及び還流塔4を介して熱分
解槽2に戻入することにより、高沸点油及び重質分は熱
分解槽2で繰り返し加熱されるので、これらは更に分解
されて低沸点油になり、低沸点油の収率が増大し、油の
品質・貯蔵安定性が向上する。又前記高沸点油の一部
は、析出用充填塔50の液ノズル部57に導かれる。The high-boiling point oil having a boiling point of 250 to 400 ° C. and the crystallized terephthalic acid are separated by specific gravity in the settling tank 6, and the terephthalic acid (specific gravity of about 1.5) is at the bottom of the high-boiling point oil ( (Specific gravity around 0.85) is stored in the upper part as a supernatant oil. The terephthalic acid or the like stored in the bottom of the settling tank 6 is supplied to the fluidized bed combustion furnace 3 as a fuel. And the high boiling point oil as the supernatant oil is line 47
After being led to the bottom of the fractionating tower 5 via a condenser, after evaporating the low boiling point component by a distiller 52 consisting of a heater, the residual high boiling point oil is jetted from the nozzle section 42 into the reflux tower 4 , And returns to the thermal decomposition tank 2 for circulation along with the heavy components that have come into gas-liquid contact.
By returning the high boiling point oil to the thermal decomposition tank 2 through the line and the reflux tower 4 in this manner, the high boiling point oil and the heavy component are repeatedly heated in the thermal decomposition tank 2 and are further decomposed. It becomes a low boiling point oil, the yield of low boiling point oil increases, and the quality and storage stability of oil are improved. Further, a part of the high boiling point oil is guided to the liquid nozzle portion 57 of the precipitation packed tower 50.
【0042】一方、前記析出用充填塔50で液化されな
い、低分子ガス、ガス状の低沸点油(略沸点250℃以
下)は分溜塔5に導かれた後、クーラ51で約30℃に
冷却して低沸点油Oを得、前記分溜塔5の分留部より回
収されるとともに、更に未凝縮の低分子ガスは、低分子
ガス抜出しライン16より燃焼炉3に送出される。On the other hand, the low molecular gas and gaseous low boiling point oil (about boiling point 250 ° C. or less) which is not liquefied in the deposition packed tower 50 is introduced into the fractionating tower 5 and then heated to about 30 ° C. by the cooler 51. The low-boiling oil O is cooled to obtain the low-boiling oil O, which is recovered from the fractionating section of the fractionating tower 5 and the uncondensed low-molecular gas is sent to the combustion furnace 3 through the low-molecular gas extraction line 16.
【0043】燃焼炉3は高速循環流動床若しくは気泡流
動床で構成され、燃焼用空気供給ライン18より空気を
導入し、砂Sを媒体とする流動床を形成せしめ、温度を
500〜950℃、好ましくは750〜950℃に保持
し、ライン17中の有機物を完全燃焼させ、更に二次空
気Aの導入によりその排ガスを850〜950℃に昇温
させてダイオキシン等の発生を抑制させつつ、燃焼排ガ
ス取出しライン21からは燃焼排ガスGを取り出し、熱
交換器による熱回収60、バグフィルタによる灰除去6
1、酸若しくはアルカリ吸収による塩化水素除去62等
の排ガス処理を行なう。The combustion furnace 3 is composed of a high-speed circulating fluidized bed or a bubbling fluidized bed. Air is introduced from the combustion air supply line 18 to form a fluidized bed using sand S as a medium, and the temperature is 500 to 950 ° C. Preferably, the temperature is maintained at 750 to 950 ° C., the organic substances in the line 17 are completely combusted, and the exhaust gas is further heated to 850 to 950 ° C. by introducing the secondary air A to suppress the generation of dioxins and the like, while burning. Combustion exhaust gas G is taken out from the exhaust gas extraction line 21, heat is recovered by a heat exchanger 60, and ash is removed by a bag filter 6
1. Exhaust gas treatment such as hydrogen chloride removal 62 by acid or alkali absorption is performed.
【0044】一方、燃焼炉3で焼却しきれなかった金属
やガラス等の不燃物Fは不燃物抜出しライン19より取
り出す。又、750〜950℃に加熱された流動床中の
砂Sの一部は砂取出しライン20、11、7より脱塩素
用のキルン1及び熱分解炉2に再循環使用する。廃プラ
スチック供給ライン110より供給された廃プラスチッ
クPと400〜950℃に高温加熱された砂Sとが脱塩
素手段1(例えばロータリキルン)内で混合されながら
一端から他端へ向かって送られる間に、廃プラスチック
Pは砂Sからの熱を受けて、温度250〜350℃に加
熱される。On the other hand, the incombustible material F such as metal or glass which has not been completely incinerated in the combustion furnace 3 is taken out from the incombustible material extraction line 19. A part of the sand S in the fluidized bed heated to 750 to 950 ° C. is recycled from the sand removal lines 20, 11 and 7 to the dechlorination kiln 1 and the pyrolysis furnace 2. While the waste plastic P supplied from the waste plastic supply line 110 and the sand S heated to a high temperature of 400 to 950 ° C. are mixed in the dechlorination means 1 (for example, a rotary kiln) and sent from one end to the other end. Then, the waste plastic P receives heat from the sand S and is heated to a temperature of 250 to 350 ° C.
【0045】図2は本発明の実施形態で、熱分解槽2で
生成された熱分解ガス状生成ガスは還流塔4を介するこ
となく直接析出用充填塔50の気液接触空間59に導入
させている。詳細に説明すると、先ず析出用充填塔50
では、充填層58下方の気液接触空間59内に供給さ
れ、上昇する高温(450℃前後)の熱分解ガス状生成
ガスが、上方から液分散ノズル57によって沈降槽6の
上澄み油である高沸点油がクーラ45により300℃以
下、例えば250〜300℃に冷却後散布される。即
ち、前記散布により450℃前後の熱分解ガス状生成物
が、下降する低温の高沸点油と向流接触して冷却され、
熱分解ガス状生成物に含まれる、例えば沸点250℃以
上の中重質油が凝縮するとともに、テレフタール酸類が
析出し、微小固形物と共にいずれも、流下する低温の高
沸点油によって洗浄・捕捉され、ガス状熱分解生成ガス
の250℃以下の低沸点成分と分離される。FIG. 2 shows an embodiment of the present invention. The pyrolysis gaseous product gas produced in the pyrolysis tank 2 is directly introduced into the gas-liquid contact space 59 of the deposition tower 50 without passing through the reflux tower 4. ing. Explaining in detail, first, the packed column for precipitation 50
Then, the pyrolysis gaseous product gas of high temperature (around 450 ° C.), which is supplied into the gas-liquid contact space 59 below the packed bed 58 and rises, is the supernatant oil of the sedimentation tank 6 from above by the liquid dispersion nozzle 57. The boiling point oil is sprayed after being cooled by the cooler 45 to 300 ° C. or lower, for example, 250 to 300 ° C. That is, by the spraying, the pyrolysis gaseous product around 450 ° C. is countercurrently contacted with the descending low temperature high boiling point oil to be cooled,
For example, medium-heavy oil having a boiling point of 250 ° C. or higher, which is contained in the pyrolysis gaseous product, is condensed, and terephthalic acids are precipitated, and both are washed and captured by the low-temperature high-boiling oil that flows down together with the fine solids. , Is separated from the low boiling point component of the gaseous pyrolysis product gas at 250 ° C or lower.
【0046】沈降槽6は、下部がコーン状に形成されて
おり、上記充填塔50より落下する凝縮油とテレフター
ル酸類を受け入れ可能に配置されている。前記析出用充
填塔50の延設筒40下端より沈降槽6内に流下した高
沸点油からは、テレフタール酸類析出物・微小固形物が
沈降し、コーン状の底部に集められ、ドレン43により
抜き出され、例えば前記燃焼炉3の燃料として処理され
る。なお、沈降分離方法として、重力によらず遠心力に
よるものが採用されれば、固形分の分離速度・分離度は
より増大する。The lower part of the settling tank 6 is formed in a cone shape, and is arranged so as to be able to receive the condensed oil and the terephthalic acid falling from the packed tower 50. The terephthalic acid precipitates / fine solids are precipitated from the high boiling point oil that has flowed into the settling tank 6 from the lower end of the extension cylinder 40 of the precipitation column 50, collected at the cone-shaped bottom, and drained by the drain 43. It is discharged and processed as fuel for the combustion furnace 3, for example. If a sedimentation separation method that uses centrifugal force rather than gravity is adopted, the separation speed and degree of separation of solids will increase.
【0047】沈降槽6の上澄み液貯留部と析出充填塔5
0頂部の液ノズル部57との間を接続するライン44に
はポンプ44aとともにクーラ45が設けられており、
該クーラ45によって冷却された、テレフタール酸類析
出物等の固形分の低減された高沸点油が析出充填塔50
の頂部の液分散ノズル部57に供給され、該液分散ノズ
ル57によって散布される。Supernatant liquid storage section of settling tank 6 and deposition packed tower 5
A cooler 45 is provided along with a pump 44a in a line 44 that connects the liquid nozzle portion 57 at the 0 top.
The high boiling point oil having a reduced solid content such as terephthalic acid precipitates cooled by the cooler 45 is deposited and packed in the tower 50.
It is supplied to the liquid dispersion nozzle portion 57 at the top of and is sprayed by the liquid dispersion nozzle 57.
【0048】さらに沈降槽6内の上澄み液は、ライン4
7及びポンプ47aを介して分溜塔5底部に給送され、
更に分溜塔5底部と熱分解槽2との間には、ライン24
及びポンプ24aによる油循環ラインが設けられてお
り、分溜塔5底部に付設された蒸留器(ヒータ)52に
よって低沸点油Oが留出した後、高温の高沸点油が熱分
解槽2に戻され、再熱分解を受ける。Further, the supernatant liquid in the settling tank 6 is stored in the line 4
7 and the pump 47a to the bottom of the fractionating tower 5,
Further, a line 24 is provided between the bottom of the fractionating tower 5 and the thermal decomposition tank 2.
And an oil circulation line by the pump 24a is provided, and after the low boiling point oil O is distilled out by a distiller (heater) 52 attached to the bottom of the fractionating tower 5, the high boiling point oil at high temperature enters the thermal decomposition tank 2. It is returned and undergoes re-pyrolysis.
【0049】かかる実施形態の作用について纏めると、
先ず、析出用充填塔50において、ガス状熱分解生成ガ
スは、冷却剤である300℃以下の高沸点油と接触し、
冷却され、前記生成ガス中の、高沸点油が凝縮し、テレ
フタール酸類が(300℃以下になれば)析出し、微小
固形物と共にいずれも、流下する低温の高沸点油によっ
て洗浄・捕捉され、低沸点成分と分離され、落下する。Summarizing the operation of this embodiment,
First, in the packed column 50 for precipitation, the gaseous pyrolysis product gas comes into contact with a high boiling point oil having a temperature of 300 ° C. or lower, which is a coolant,
When cooled, the high boiling point oil in the produced gas is condensed, terephthalic acids are precipitated (when the temperature is 300 ° C. or less), and both are washed and captured by the low temperature high boiling point oil flowing down together with the fine solid matter. It is separated from low-boiling components and falls.
【0050】上記落下したテレフタール酸類・微小固形
物を含む高沸点油は、例えば沈降槽6に靜置されるだけ
で、その比重差により液体の高沸点油とテレフタール酸
類・微小固形物とに(沈降)分離される。なお、テレフ
タール酸類・微小固形物は抜き出され、例えば燃焼炉3
によって焼却処理される。The high boiling point oil containing the dropped terephthalic acids / fine solids is simply placed in, for example, the settling tank 6, and due to the difference in specific gravity, it becomes liquid high boiling point oil and terephthalic acids / fine solids ( Sedimentation) separated. In addition, terephthalic acids and minute solids are extracted, for example, in the combustion furnace 3
Is incinerated by.
【0051】ガス状熱分解生成物の析出充填塔50での
接触時の温度が低い場合、テレフタール酸類は完全に析
出、下降液によって洗浄・捕捉されるため、低沸点成分
から完全に除かれ、以降の管路等内面に析出し、閉塞ト
ラブルを起こすようなことはない。しかも、テレフター
ル酸類が低減された高沸点油はガス状熱分解生成ガスの
冷却剤として循環使用されるため、冷却剤中のテレフタ
ール酸の蓄積・増加が起らず、その増大によって、ガス
状熱分解生成物と接触する充填塔50等の第1の気液接
触手段での閉塞トラブルも解消される。When the temperature at the time of contacting the gaseous pyrolysis product in the deposition packed tower 50 is low, terephthalic acids are completely precipitated and are washed and captured by the descending liquid, so that they are completely removed from the low boiling point components, It will not be deposited on the inner surface of the subsequent pipeline, etc., and will not cause a blocking trouble. Moreover, since the high boiling point oil with reduced terephthalic acids is circulated and used as a coolant for the gaseous pyrolysis product gas, accumulation and increase of terephthalic acid in the coolant does not occur, and the increase causes a gaseous heat release. The clogging trouble in the first gas-liquid contacting means such as the packed tower 50 that comes into contact with the decomposition products is also eliminated.
【0052】しかしながら、ガス状熱分解生成物の充填
塔50での接触時の温度が低い場合、落下する高沸点油
中の低沸点油の含量が増大し、そのままそれが熱分解手
段2に送られ、再加熱されると、低沸点油がさらに熱分
解され、ガス成分が増大し、低沸点油の収量が低下する
おそれがある。しかし、本発明では、得られた高沸点油
のうち、熱分解槽2に送られるものは、一旦分留塔5内
の蒸留器52で蒸留され、低沸点油Oが回収されるよう
構成されているため、それが再熱分解されることはな
く、ガス状熱分解生成物の接触時の温度が低くても、低
沸点油の収量は高い。However, when the temperature at the time of contacting the gaseous pyrolysis product in the packed tower 50 is low, the content of the low boiling point oil in the falling high boiling point oil increases, and it is sent to the pyrolysis means 2 as it is. When reheated, the low boiling point oil is further thermally decomposed, the gas component increases, and the yield of the low boiling point oil may decrease. However, in the present invention, among the obtained high boiling point oils, the ones sent to the thermal decomposition tank 2 are once distilled in the distiller 52 in the fractionation tower 5 to recover the low boiling point oil O. Therefore, it is not re-pyrolyzed, and the yield of low boiling point oil is high even when the temperature at the time of contacting the gaseous pyrolysis product is low.
【0053】その他、析出充填塔50のガス出口側に
は、未凝縮ガス抜き出しライン48を介して第2の気液
分離手段5が直列に接続されており、析出充填塔50か
ら分溜塔5に送られ、その内部の冷却器51により約3
0℃に冷却された低沸点油Oが排出され、さらに低分子
ガスが低分子ガス抜き出しライン16を経て燃焼炉3に
送出される。又、前記蒸留器52は分溜塔5と一体化す
ることは好ましいことであるが、両者を独立設置させて
も良い。In addition, on the gas outlet side of the precipitation packed tower 50, a second gas-liquid separating means 5 is connected in series via an uncondensed gas extraction line 48, and the precipitation packed tower 50 to the fractionating tower 5 are connected in series. To about 3 by the cooler 51 inside.
The low boiling point oil O cooled to 0 ° C. is discharged, and further the low molecular gas is sent to the combustion furnace 3 through the low molecular gas extraction line 16. Further, it is preferable that the distiller 52 is integrated with the fractionating tower 5, but both may be installed independently.
【0054】[0054]
【発明の効果】以上記載のごとく請求項1記載の発明に
よれば、固液分離装置の貯留室内に直接導くのではな
く、その上方に位置する気液接触空間内に導入されるた
めに、固液分離装置の貯油室内でバブリング等が生じる
ことなく、析出物と高沸点油との比重差に基づく沈降分
離を精度良く行なうことが出来る。又、重質油成分が固
液分離装置としての沈降槽壁面に粘着したり、保守劣化
が生じることなく、容易に排出できる。As described above, according to the invention of claim 1, the gas is introduced not into the storage chamber of the solid-liquid separation device but into the gas-liquid contact space located above the storage chamber. Bubbling does not occur in the oil storage chamber of the solid-liquid separation device, and sedimentation separation based on the difference in specific gravity between the precipitate and the high boiling point oil can be performed accurately. Further, the heavy oil component can be easily discharged without adhering to the wall surface of the settling tank as a solid-liquid separation device or causing maintenance deterioration.
【0055】本発明によれば、熱分解ガス状生成物中の
タールやピッチ等の重質分は前もって除去された後、第
1気液分離手段でテレフタール酸類の析出を行なうため
に、該第1気液分離手段や固液分離手段にこれらのター
ルやピッチ等等が壁面に付着する恐れがなく、一層保守
劣化が生じることなく、容易に運転管理が出来る。According to the present invention, the heavy components such as tar and pitch in the pyrolyzed gaseous product are removed in advance, and then the first gas-liquid separation means is used to deposit terephthalic acids. (1) There is no fear that these tars, pitches, etc. will adhere to the wall surface in the gas-liquid separation means or the solid-liquid separation means, and the operation and management can be easily performed without further deterioration of maintenance.
【0056】又本発明は、前記固液分離手段で生成され
た高沸点油を還流手段の気液接触油として使用すること
により、その油分は常に熱分解手段側に戻す事が出来、
高沸点油の低沸点油化が一層促進される。しかも、テレ
フタール酸類が分離低減された高沸点油がガス状熱分解
生成物の冷却剤として循環使用されるため、冷却剤中の
テレフタール酸の蓄積・増加が起らず、その増大によっ
てガス状熱分解生成物と接触する気液接触手段(充填塔
等)での閉塞トラブルも解消される。Further, in the present invention, by using the high boiling point oil produced by the solid-liquid separation means as the gas-liquid contact oil of the reflux means, the oil content can be always returned to the pyrolysis means side,
The conversion of high boiling oil to low boiling oil is further promoted. Moreover, since the high boiling point oil from which terephthalic acids have been separated and reduced is circulated and used as a coolant for the gaseous thermal decomposition products, accumulation and increase of terephthalic acid in the coolant does not occur, and the increase in the gaseous heat causes The clogging trouble in the gas-liquid contact means (packing tower etc.) that comes into contact with the decomposition products is also eliminated.
【0057】更に本発明では、得られた高沸点油のう
ち、熱分解手段に送られるものは、蒸留され、低沸点油
が回収されるよう構成されているため、それが再熱分解
されることはなく、ガス状熱分解生成物の接触時の温度
が低くても、低沸点油の収量は高い。Further, in the present invention, among the obtained high boiling point oils, the ones sent to the thermal decomposition means are distilled and the low boiling point oils are recovered, so that they are re-thermally decomposed. Nonetheless, the yield of low boiling point oil is high even when the temperature at the time of contacting the gaseous pyrolysis products is low.
【0058】又本発明は、前記第1の気液接触手段の液
流出時の重力エネルギが減少し、静かに液流出が行なわ
れるために、円滑に比重差により固液分離を行なうこと
ができる。Further, according to the present invention, the gravity energy at the time of liquid outflow of the first gas-liquid contact means is reduced, and the liquid outflow is performed gently, so that the solid-liquid separation can be smoothly performed by the difference in specific gravity. .
【0059】更に本発明によれば熱エネルギを閉回路に
て効率よく利用でき、無駄に熱エネルギを捨てることが
ない。Further, according to the present invention, the heat energy can be efficiently used in the closed circuit, and the heat energy is not wasted.
【図1】 本発明の基本構成が組み込まれた、廃プラス
チックからの油回収装置を示す機器全体構成図である。FIG. 1 is an overall device configuration diagram showing an oil recovery device from waste plastic in which the basic configuration of the present invention is incorporated.
【図2】 本発明の実施形態例が組み込まれた、廃プラ
スチックからの油回収装置を示す機器要部構成図であ
る。FIG. 2 is a configuration diagram of a main part of a device showing an oil recovery device from waste plastic, in which an embodiment of the present invention is incorporated.
【図3】 従来技術にかかる廃プラスチックの油回収装
置を示す機器全体構成図である。FIG. 3 is an overall device configuration diagram showing a waste plastic oil recovery device according to a conventional technique.
【図4】 従来技術にかかる熱分解ガス状生成物のテレ
フタル酸等を既出するための要部機器構成図である。FIG. 4 is a configuration diagram of a main part of the related art for producing terephthalic acid or the like which is a thermally decomposed gaseous product.
1 脱塩素手段(ロータリキルン) 2 熱分解手段 3 流動床燃焼炉 4 還流塔 5 分溜塔 50 析出充填塔 40 延設筒 6 固液分離手段 45、51 クーラ 52 蒸留器 23 低温高沸点油循環手段 24 高温高沸点油循環手段 42、57 液分散器 C クーラ F 不燃物 O 低沸点油 P 廃プラスチック S 砂 1 Dechlorination means (rotary kiln) 2 Pyrolysis means 3 fluidized bed combustion furnace 4 reflux tower 5 fractionation tower 50 Precipitation packed tower 40 extended cylinder 6 Solid-liquid separation means 45, 51 cooler 52 Distiller 23 Low temperature and high boiling point oil circulation means 24 High temperature and high boiling point oil circulation means 42,57 Liquid Disperser C cooler F incombustibles O low boiling point oil P Waste plastic S sand
───────────────────────────────────────────────────── フロントページの続き (72)発明者 貝原 裕二 横浜市中区錦町12番地 三菱重工業株式 会社横浜製作所内 (72)発明者 米田 健一 横浜市中区錦町12番地 三菱重工業株式 会社横浜製作所内 (72)発明者 佐藤 繁博 横浜市中区錦町12番地 三菱重工業株式 会社横浜製作所内 (56)参考文献 特開 平9−20892(JP,A) 特開 平7−216364(JP,A) 特開 平9−235562(JP,A) 実開 昭58−140155(JP,U) (58)調査した分野(Int.Cl.7,DB名) C10G 1/10 C10B 53/00 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yuji Kaihara 12 Nishiki-cho, Naka-ku, Yokohama-shi In Mitsubishi Heavy Industries, Ltd. Yokohama Works (72) Kenichi Yoneda 12 Nishiki-machi, Naka-ku, Yokohama-shi In Mitsubishi Heavy Industries, Ltd. 72) Inventor Shigehiro Sato 12 Nishiki-cho, Naka-ku, Yokohama City Mitsubishi Heavy Industries, Ltd. Yokohama Works (56) Reference JP-A-9-20892 (JP, A) JP-A-7-216364 (JP, A) JP Flat 9-235562 (JP, A) Actual development Sho 58-140155 (JP, U) (58) Fields investigated (Int.Cl. 7 , DB name) C10G 1/10 C10B 53/00
Claims (4)
0〜500℃の温度で熱分解して熱分解ガス状生成物を
得る熱分解手段と、 前記熱分解ガス状生成物を気液接触空間に導入し、気液
接触空間上方より噴出される油に接触させて高沸点油を
下方の分離手段に流下させる第1の気液接触手段と、 前記第1の気液接触手段をガス状に通過した低沸点油を
含む低沸点成分を冷却して低沸点油を回収する低沸点油
回収手段と、前記分離 手段内に貯留された高沸点油を熱分解手段に戻
す廃プラスチックの油回収装置において、 前記第1の気液接触手段を途中位置に充填層を有し、底
部を前記分離 手段内に挿設した直接析出用充填塔で構成
し、該充填層の下方より前記熱分解ガス状生成物を導入
し、前記充填層の上部より冷却調整された油を散布させ
て、前記充填層で該油との接触により高沸点油とともに
テレフタール酸を含む結晶化物質が析出し、前記分離手
段の底部で高沸点油と結晶化物質が比重分離可能に構成
した廃プラスチックの油回収装置。 1.Crushed waste plasticThe temperature is about 35
Pyrolysis at a temperature of 0 to 500 ° C produces a pyrolyzed gaseous product.
Thermal decomposition means to obtain, Introduce the pyrolyzed gaseous product into the gas-liquid contact spaceGas-liquid
The high boiling point oil is brought into contact with the oil jetted from above the contact space.
DownwardMinutes ofFirst gas-liquid contacting means for flowing down to the separating means, The low boiling point oil which has passed through the first gas-liquid contact means in a gaseous state is
A low boiling point oil that recovers a low boiling point oil by cooling the low boiling point component that contains
Collection means,Said separation The high boiling point oil stored in the means is returned to the pyrolysis means.
YouIn a waste plastic oil recovery device, The first gas-liquid contact means has a packing layer at an intermediate position, and the bottom
The part Inserted in the meansConsists of a packed column for direct precipitation
Then, the pyrolysis gaseous product is introduced from below the packed bed.
Spray the conditioned oil from the top of the packed bed.
The high boiling point oil by contact with the oil in the packed bed
The crystallization substance containing terephthalic acid precipitates,
High-boiling oil and crystallized substance can be separated by specific gravity at the bottom of the stage
Oil recovery equipment for used plastic waste.
装置において、 前記分離手段の底部を底側に向けて縮径させて先細のコ
ーン状に形成するとともに、前記第1の気液接触手段を
途中位置に充填層を有する直接析出用充填塔で構成し、
該充填塔の下側に位置する延設筒下端を前記コーン状部
途中位置まで上方より垂下させるとともに、前記充填層
の下方より前記熱分解ガス状生成物を導入し、充填層の
上部より冷却調整された油を散布させて、充填層で該油
との接触により高沸点油とともにテレフタール酸を含む
結晶化物質が析出して延設筒より分離手段下方のコーン
状部に流下し、該コーン状部の底部で高沸点油と結晶化
物質が比重分離可能に構成した廃プラスチックの油回収
装置。 2. The method according to claim 1.Oil recovery from waste plastic
In the device, The bottom portion of the separating means is reduced in diameter toward the bottom side to form a tapered core.
And the first gas-liquid contacting means
It is composed of a packed column for direct precipitation having a packed bed at an intermediate position,
The lower end of the extending cylinder located below the packed tower is provided with the cone-shaped portion.
In addition to hanging from the upper part to the middle position, the filling layer
The pyrolysis gaseous product was introduced from below the
Disperse the chilled oil from the upper part,
Includes terephthalic acid with high boiling oil upon contact with
Cone below the separating means from the extension cylinder where the crystallized substance precipitates
And then crystallized with high boiling oil at the bottom of the cone
Oil recovery from waste plastics whose substances can be separated by specific gravity
apparatus.
あり、前記高沸点油が略250〜350℃以上の油であ
り、前記結晶化物質が、250℃以上の温度 に昇華点を
有するテレフタール酸を含む結晶化物質である請求項1
若しくは2記載の廃プラスチックの油回収装置。 3. The cooled conditioned oil is below 300.degree.
Yes, the high boiling point oil is an oil having a temperature of approximately 250 to 350 ° C. or higher.
The crystallization substance has a sublimation point above 250 ° C.
2. A crystallization substance containing terephthalic acid having
Alternatively, the waste plastic oil recovery device described in 2 .
をクーラにより冷却して直接第1の気液接触手段の気液
接触油として使用することを特徴とする請求項1、2若
しくは3記載の廃プラスチックの油回収装置。4. The method of claim 1, 2 young, characterized in that for use as a gas-liquid contact fluid in the first gas-liquid contact means directly cooled by the cooler high boiling oil is gravity separated by the separating means
The waste plastic oil recovery device described in item 3 .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20992899A JP3372509B2 (en) | 1999-07-23 | 1999-07-23 | Oil recovery device for waste plastic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20992899A JP3372509B2 (en) | 1999-07-23 | 1999-07-23 | Oil recovery device for waste plastic |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2001031978A JP2001031978A (en) | 2001-02-06 |
| JP3372509B2 true JP3372509B2 (en) | 2003-02-04 |
Family
ID=16580988
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20992899A Expired - Fee Related JP3372509B2 (en) | 1999-07-23 | 1999-07-23 | Oil recovery device for waste plastic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3372509B2 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3525385B2 (en) * | 2002-01-08 | 2004-05-10 | 優之 松井 | Carbonization furnace |
| JP3836112B2 (en) * | 2004-03-23 | 2006-10-18 | 株式会社御池鐵工所 | Waste plastic oil production facility |
| JP5772419B2 (en) * | 2011-09-09 | 2015-09-02 | 富士通株式会社 | Oil making apparatus and oil making method |
| JP5772503B2 (en) * | 2011-10-26 | 2015-09-02 | 富士通株式会社 | Oil making apparatus and oil making method |
| JP2014240460A (en) * | 2013-06-11 | 2014-12-25 | 株式会社トップ | System for treating waste tire, waste plastic, etc. for conversion into pyrolysis oil |
| JP2015067834A (en) * | 2013-09-30 | 2015-04-13 | エコ燃料製造販売株式会社 | Removal method of crystal objects generated in thermolysis of pet |
| KR20220141319A (en) * | 2020-02-10 | 2022-10-19 | 이스트만 케미칼 컴파니 | Chemical recycling of solvolysis terephthalyl column bottoms by-product stream |
| CA3167350A1 (en) * | 2020-02-10 | 2021-08-19 | Bruce Roger Debruin | Chemical recycling of solvolysis reactor purge coproduct streams |
| KR20220141323A (en) | 2020-02-10 | 2022-10-19 | 이스트만 케미칼 컴파니 | Chemical recycling of solvolysis by-product streams |
| CN115052732A (en) | 2020-02-10 | 2022-09-13 | 伊士曼化工公司 | Chemical recovery of a solvolytic glycol bottoms by-product stream |
| JP7814857B2 (en) * | 2021-08-05 | 2026-02-17 | 荏原環境プラント株式会社 | Treatment device and treatment method for recovering cracked oil from pyrolysis gas |
| WO2023188380A1 (en) * | 2022-03-31 | 2023-10-05 | 日揮グローバル株式会社 | Method for producing pyrolysis oil from waste plastics, and plant for conversion of waste plastics into oil |
| CN119193186A (en) * | 2024-11-13 | 2024-12-27 | 哈尔滨工业大学 | A mixed plastic segmented thermal cracking method |
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1999
- 1999-07-23 JP JP20992899A patent/JP3372509B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001031978A (en) | 2001-02-06 |
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