JP2510067B2 - Disassembly method of waste rubber tires - Google Patents

Disassembly method of waste rubber tires

Info

Publication number
JP2510067B2
JP2510067B2 JP5244693A JP5244693A JP2510067B2 JP 2510067 B2 JP2510067 B2 JP 2510067B2 JP 5244693 A JP5244693 A JP 5244693A JP 5244693 A JP5244693 A JP 5244693A JP 2510067 B2 JP2510067 B2 JP 2510067B2
Authority
JP
Japan
Prior art keywords
rubber
product
gas
waste rubber
oil
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 - Lifetime
Application number
JP5244693A
Other languages
Japanese (ja)
Other versions
JPH0797578A (en
Inventor
黄 傳 陳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP5244693A priority Critical patent/JP2510067B2/en
Publication of JPH0797578A publication Critical patent/JPH0797578A/en
Application granted granted Critical
Publication of JP2510067B2 publication Critical patent/JP2510067B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/52Mechanical processing of waste for the recovery of materials, e.g. crushing, shredding, separation or disassembly
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

Landscapes

  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Processing Of Solid Wastes (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ゴムタイヤの分解方法
に関する。さらに、詳細には、廃却用のゴムタイヤの分
解方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for disassembling a rubber tire. More specifically, it relates to a method for disassembling a rubber tire for disposal.

【0002】[0002]

【従来の技術およびその課題】従来、使用済みまたは廃
却用のゴムタイヤは、粉砕、再生して限られた割合でゴ
ム製品に再生されている。また、再生されたゴムタイヤ
の粉体は、ゴム製品の加工過程において押し出し、圧延
などの加工特性の助けとなるが添加物の比率は極少量で
あり、米国では新たなゴム原料中に僅か約10%の再生
ゴムが消耗されているのが実情である。
2. Description of the Related Art Conventionally, used or discarded rubber tires have been crushed and recycled to be recycled as rubber products at a limited rate. Further, the regenerated rubber tire powder assists processing characteristics such as extrusion and rolling in the process of processing rubber products, but the ratio of additives is extremely small, and in the United States, it is only about 10% in new rubber raw materials. The actual situation is that% of the recycled rubber is exhausted.

【0003】しかしながら、環境保護問題は益々増加し
つつあり、古ゴムタイヤは処理しなくてはならないのも
現実である。
However, environmental protection problems are increasing more and more, and it is a reality that old rubber tires must be treated.

【0004】今まで応用されている廃却ゴムタイヤの分
解方法(cracking process)として
は、燃料油と気体を発生させる方法、その他1000℃
以上、3〜30Kg/cmの高温高圧の下で反応を進
行させる方法等がある。
[0004] As a cracking process of a waste rubber tire that has been applied so far, a method of generating fuel oil and a gas, and other 1000 ° C
As mentioned above, there is a method of advancing the reaction under high temperature and high pressure of 3 to 30 Kg / cm 2 .

【0005】しかし、高温高圧におけるゴムの分解方法
は下記の如き難点が見受けられる。 1.高温高圧を発生させるための分解反応器(crac
king reactor)の製造投資が莫大であるこ
と。
However, the following problems are found in the method of decomposing rubber at high temperature and high pressure. 1. A cracking reactor (crac) for generating high temperature and high pressure.
King reactor) manufacturing investment is enormous.

【0006】2.分解過程において可燃性気体、例えば
水素;メタン、エタン、プロパン、ブタン、イソブタ
ン、ブチレン等を含む低炭化水素化合物気体が多量発生
する。高温高圧の反応器より生ずる可燃性気体は、工業
的安全の観点から見れば非常に危険な代物で、例えば水
素の着火点は585℃でメタンが537℃、エタン51
5℃等凡そ1000℃より低く、かりに反応温度が10
00℃を越える反応器からこれらの気体が漏れると容易
に自然に火災や爆発などの事故が発生し、仕事現場環境
の弊害となる。それゆえ、反応器の稼働操作と共に十分
気をつけなければならないばかりか操作が一層困難とな
り、原価がかさむこと。
2. In the decomposition process, a large amount of combustible gas such as hydrogen; a low hydrocarbon compound gas containing methane, ethane, propane, butane, isobutane, butylene, etc. is generated. Combustible gas generated from a high temperature and high pressure reactor is a very dangerous substitute from the viewpoint of industrial safety. For example, the ignition point of hydrogen is 585 ° C, methane is 537 ° C, and ethane is 51 ° C.
5 ℃, etc. is lower than about 1000 ℃, and the reaction temperature is 10
Leakage of these gases from a reactor that exceeds 00 ° C easily causes spontaneous accidents such as fires and explosions, which is a detriment to the workplace environment. Therefore, not only must careful attention be paid to the operation of the reactor, but also the operation becomes more difficult and costly.

【0007】3.高温で分解反応をさせるため貴重なエ
ネルギーの浪費となること。
3. Wastes valuable energy because the decomposition reaction occurs at high temperatures.

【0008】以上の観点から、低温低圧の下でのゴムを
分解する方法の出現が待たれる。
From the above viewpoint, the appearance of a method of decomposing rubber under low temperature and low pressure is awaited.

【0009】本発明の目的は、新規な廃却ゴムタイヤの
分解方法を提供することにある。
An object of the present invention is to provide a novel method for disassembling a waste rubber tire.

【0010】さらに本発明の他の目的は、雲母(マイ
カ)を触媒とし、230〜400℃の温度と1〜2.5
の大気圧の下でゴムタイヤまたはゴム製品を分解反応さ
せ、油やカーボン、ブラック、気体、その他の残留物を
得て、安全でかつ経済的な廃却ゴムタイヤまたはその他
のゴム製品を分解する方法を提供することにある。
Still another object of the present invention is to use mica (mica) as a catalyst at a temperature of 230 to 400 ° C. and 1 to 2.5.
A method of decomposing rubber tires or rubber products under atmospheric pressure to obtain oil, carbon, black, gas, and other residues, and decomposing waste rubber tires or other rubber products safely and economically. To provide.

【0011】[0011]

【課題を解決するための手段】本発明は、a)廃却ゴム
タイヤを洗浄および粉砕してゴム粉砕物とし、b)該ゴ
ム粉砕物と絹雲母(SERICITE)、白雲母(MU
SCOVITE)および黒雲母(BIOTITE)から
なる群より選ばれた少なくと1種の雲母触媒とを210
℃に加熱して混合し、c)加熱して1時間、1〜2.5
気圧(Atm)で230〜400℃の温度を保持して気
体製品と混合油とを含む気相製品(Vapo−phas
e−product)およびカーボンブラックと残留物
とを含む固形製品とを含む分解物を得るように分解反応
に供給される廃却ゴムタイヤ全量(100%)に対して
触媒量2〜3%の該雲母触媒の存在下に該ゴム粉砕物を
乾留して分解し、さらにd)該分解物を気体製品、混合
油、カーボンブラックおよび残留物に分離することを特
徴とする廃却ゴムタイヤの分解方法に関する。本発明に
おいて、該雲母触媒が絹雲母粉末であることが好まし
い。
According to the present invention, a) washed and crushed waste rubber tires are crushed into rubber, and b) the crushed rubber, sericite and muscovite (MU).
210 at least one mica catalyst selected from the group consisting of SCOVITE) and biotite (BIOTITE).
Heat to ℃ to mix, c) Heat for 1 hour, 1-2.5
A gas phase product (Vapo-phas) containing a gas product and a mixed oil while maintaining a temperature of 230 to 400 ° C. at atmospheric pressure (Atm).
e-product) and the mica having a catalytic amount of 2 to 3% with respect to the total amount (100%) of a waste rubber tire supplied to a decomposition reaction so as to obtain a decomposed product containing a carbon black and a solid product containing a residue. The present invention relates to a method for decomposing a waste rubber tire, which comprises dry-distilling the rubber pulverized product in the presence of a catalyst to decompose it, and further d) separating the decomposed product into a gas product, a mixed oil, carbon black and a residue. In the present invention, the mica catalyst is preferably sericite powder.

【0012】添付図面は、本発明の製造工程を示すフロ
ー、チャートである。以下、添付図面をに基づいて本発
明の内容を説明する。
The attached drawings are a flow chart showing the manufacturing process of the present invention. The contents of the present invention will be described below with reference to the accompanying drawings.

【0013】a)廃却ゴムタイヤの洗浄1:各種のチュ
ーブを含むゴムタイヤ、その他のゴム製品を水等で洗浄
する。
A) Cleaning of waste rubber tires 1: Rubber tires including various tubes and other rubber products are washed with water or the like.

【0014】b)洗浄したゴムタイヤを粉砕する2:ま
たはタイヤを約5cmx5cmに切断または粉砕する。
B) Grind the washed rubber tire 2: Or cut or grind the tire to about 5 cm x 5 cm.

【0015】c)分解されたゴム粒子を粉末状の雲母触
媒とミキサー内で十分混合する3:また210℃に予熱
する。
C) The decomposed rubber particles are thoroughly mixed with powdered mica catalyst in a mixer 3: Preheated to 210 ° C.

【0016】d)得られた混合物を密閉された反応器に
送り、破壊蒸留で分解する4:雲母触媒と混合したゴム
粒子を加熱し、230〜400℃の温度で保持し、1〜
2.5気圧(Atm)で分解反応させる。分解反応は2
30℃で始まり、350℃のときが最も強烈で、最高温
度は400℃で十分である。反応圧力は1〜2.5気圧
の下で行われるから、分解反応で生じた気体は、その他
の不活性気体(Inert)、例えば窒素等を吸入しな
い。
D) The resulting mixture is sent to a closed reactor and decomposed by destructive distillation. 4: Rubber particles mixed with a mica catalyst are heated and kept at a temperature of 230 to 400 ° C.
The decomposition reaction is performed at 2.5 atmospheric pressure (Atm). The decomposition reaction is 2
It starts at 30 ° C and is most intense at 350 ° C with a maximum temperature of 400 ° C being sufficient. Since the reaction pressure is 1 to 2.5 atm, the gas generated by the decomposition reaction does not inhale other inert gas (Inert) such as nitrogen.

【0017】e)冷却および分離作用で気相製品(Va
po−phase−product)5を気体製品51
と混合油52に分解させ、また混合油52は分留(Fr
actional Distillation)7によ
り軽油(Light oil)およびガソリン71、石
油(Kerosene)72、ディーゼルオイル73お
よび重油74に分解する。
E) Gas phase products (Va
Po-phase-product 5 is a gas product 51
And the mixed oil 52 is decomposed into the mixed oil 52.
It is decomposed into light oil (Light oil) and gasoline 71, petroleum (Kerosene) 72, diesel oil 73 and heavy oil 74 by means of the actionable distribution 7.

【0018】f)分解反応4後、反応容器に固形製品6
が残され、カーボンブラック61、鋼線(steel
wire)62、およびその他の残留物63に分離され
る。
F) After the decomposition reaction 4, the solid product 6 is placed in the reaction vessel.
Left behind, carbon black 61, steel wire (steel)
(wire) 62 and other residues 63.

【0019】本発明に用いられる触媒は、白雲母(MU
SCOVITE)、絹雲母(SERICITE)、およ
び黒雲母(BIOTITE)より選ばれる少なくとも1
種であるが、中でも絹雲母(SERICITE)が最も
好ましい。絹雲母(SERICITE)の化学式はKA
(AlSiO10)(OH)で下記の成分重
量比(%)で構成されている。
The catalyst used in the present invention is muscovite (MU).
SCOVITE), sericite (SERICITE), and at least one selected from biotite (BIOTITE)
Among them, sericite is the most preferable. The chemical formula of sericite is KA
1 2 (AlSiO 3 O 10 ) (OH) 2 with the following component weight ratio (%).

【0020】SiO−−−− 47.65% Al−−− 37.03% KO−−−−− 9.02% TiO−−−− 0.10% Fe−−− 0.01% MgO−−−−− 0.04% NaO−−−− 0.76% HO−−−−− 0.73〜4.97% P−−−− 0.02% FeO、MnOおよびCaO−−微量 使用される触媒の量は、廃却ゴム全重量の2〜3%であ
る。
SiO 2 ----- 47.65% Al 2 O 3 --- 37.03% K 2 O --- 9.02% TiO 2 --- 0.10% Fe 2 O 3 --- 0.01% MgO ----- 0.04% Na 2 O ---- 0.76% H 2 O ----- 0.73~4.97% P 2 O 5 - --0.02% FeO, MnO and CaO-- Traces The amount of catalyst used is 2-3% of the total weight of the waste rubber.

【0021】混合油は、軽油(Light oil)、
ガソリン、石油(Kerosene)、ディーゼルオイ
ルおよび重油に再分離する必要なくそのまま混合油であ
る燃料油として使用され、必要により分留を経て各種の
油に分離される。
The mixed oil is light oil,
It is used as a fuel oil which is a mixed oil as it is without having to re-separate into gasoline, petroleum (Kerosene), diesel oil and heavy oil, and is separated into various oils through fractional distillation if necessary.

【0022】気体製品は、水素;メタン、プロパン、ブ
タン、ブチレンを含む低炭化水素化合物、一酸化炭素、
二酸化炭素およびその他の微量の気体製品、例えば硫黄
等を含んでいる。
Gas products are hydrogen; low hydrocarbon compounds including methane, propane, butane, butylene, carbon monoxide,
Contains carbon dioxide and other trace gas products such as sulfur.

【0023】硫黄は、タイヤを製造する際のゴムの硫化
(Vulcanization)過程において硫黄を加
えた為に含まれる。気体製品も燃料に使用されるが、そ
の中に大量のイソブチレン、およびブチレンが含まれて
おり、再分離によって有用な、例えばブチルゴム用の物
質となる。
Sulfur is included due to the addition of sulfur during the vulcanization process of rubber during the production of tires. Gaseous products are also used as fuels, but with large amounts of isobutylene and butylene contained therein, the re-separation makes them useful materials, eg for butyl rubber.

【0024】本発明で処理し得る廃却ゴムタイヤは、鋼
線(Sreel wire)を有するタイヤを主とし、
その他の付属のタイヤ、チューブあるいは天然または合
成ゴム製品を含んでも良い。鋼線を含むゴムタイヤは固
体成分として破壊乾留により鋼線が残る。
The waste rubber tires that can be treated in the present invention are mainly tires having a steel wire (Sreeel wire),
Other included tires, tubes or natural or synthetic rubber products may be included. A rubber tire containing a steel wire has a steel wire left as a solid component by fracture carbonization.

【0025】[0025]

【実施例】次に、本発明を下記の実施例に基づいて詳細
に説明する。
EXAMPLES Next, the present invention will be described in detail based on the following examples.

【0026】実施例 1 間欠攪拌機を有する32リットルのオートクレーブに約
5x5cmに粉砕したタイヤチューブを6680g投入
し、触媒として絹雲母150gを加えた後、オートクレ
ーブを徐々に230℃に加熱して分解反応を行わせた。
分解反応の温度は230〜400℃の間で、圧力は絶対
圧力1〜2.5圧(Atm)に保持して1時間反応させ
た。反応が完了した際に表1に記載の製品得られた。
Example 1 6680 g of a tire tube crushed to a size of about 5 × 5 cm was placed in a 32 liter autoclave equipped with an intermittent stirrer, 150 g of sericite was added as a catalyst, and the autoclave was gradually heated to 230 ° C. for decomposition reaction. Let it be done.
The temperature of the decomposition reaction was between 230 and 400 ° C., the pressure was kept at an absolute pressure of 1 to 2.5 pressure (Atm), and the reaction was performed for 1 hour. The products listed in Table 1 were obtained when the reaction was complete.

【0027】[0027]

【表1】 製品 重量(g) 重量(%) 気体製品 1400 21 混合油 2280 34 カーボンブラック および残留物 2850 43 水分 150 2 混合油はさらに分留され、表2に示す製品が得られた。Table 1 Product Weight (g) Weight (%) Gas product 1400 21 Mixed oil 2280 34 Carbon black and residue 2850 43 Moisture 150 2 The mixed oil was further fractionated to obtain the product shown in Table 2.

【0028】[0028]

【表2】油(蒸留温度範囲) 重量(g) 重量(%) 軽油、50〜186℃ 370 16 (常圧分留) ガソリン 376 16.6 (500mmHg、真空下) 石油(Kerosene) 310 14 (500mmHg、Vac) ディーゼルオイル 810 36 (500mmHg、Vac) 重油 385 17.4 気体製品を分析した結果、表3の結果が得られた。[Table 2] Oil (distillation temperature range) Weight (g) Weight (%) Light oil, 50 to 186 ° C 370 16 (normal pressure fractionation) Gasoline 376 16.6 (500 mmHg, under vacuum) Petroleum (Kerosene) 310 14 ( 500 mmHg, Vac) Diesel oil 810 36 (500 mmHg, Vac) Heavy oil 385 17.4 The gas product was analyzed and the results in Table 3 were obtained.

【0029】[0029]

【表3】 気体 容積(%) 水素 12 メタン 20.59 エタン 4.42 エチレン 1.07 プロパン 2.85 プロピレン 1.66 イソブタン 5.13 イソブチレンおよびブチレン−1 45.3 ブチレン−2 0.04 n−ペンタン 0.15 ペンチレン 0.49 CO 4.54 CO 1.65 表3の気体製品の中でイソブチレンとブチレン−2の容
積が全体の45.3%を占め、これをまた有用な工業製
品に分離できる。
Table 3 Gas Volume (%) Hydrogen 12 Methane 20.59 Ethane 4.42 Ethylene 1.07 Propane 2.85 Propylene 1.66 Isobutane 5.13 Isobutylene and Butylene-1 45.3 Butylene-2 0.04 n -Pentane 0.15 Pentylene 0.49 CO 2 4.54 CO 1.65 Among the gaseous products of Table 3, the volume of isobutylene and butylene-2 account for 45.3% of the total, which is also a useful industrial product. Can be separated into

【0030】実施例 2 実施例1と同じ方法で、タイヤチューブの代りに鋼線
(Steel wire)を含むタイヤを圧力釜に投入
した。その製品の組成を表4に示す。表4では実施例1
のデータが併記され比較に使用される。
Example 2 In the same manner as in Example 1, a tire containing steel wire instead of the tire tube was put into a pressure cooker. The composition of the product is shown in Table 4. In Table 4, Example 1
Data is also shown and used for comparison.

【0031】[0031]

【表4】製品 実施例2 実施例1 気体製品 12% 21% 混合油 50% 34% カーボンブラック 32% 43% および残留物 水分 2% 2% 鋼線 4% − 表4で示した通り鋼線(Steel wire)を含む
ゴムタイヤより分解した製品は、鋼線を含まないタイヤ
チューブより分解したものに比べて混合油が多く、気体
製品が少ないことが分かる。
[Table 4] Product Example 2 Example 1 Gas product 12% 21% Mixed oil 50% 34% Carbon black 32% 43% and residual moisture 2% 2% Steel wire 4% -Steel wire as shown in Table 4 It can be seen that the product decomposed from the rubber tire containing (Steel wire) contained more oil and contained less gas product than the product decomposed from the tire tube containing no steel wire.

【0032】また、実施例1または実施例2を問わず混
合油を分留した後、その組成(重量)比は表5に示した
通りほぼ同等である。
After fractionating the mixed oil regardless of Example 1 or Example 2, the composition (weight) ratio is almost the same as shown in Table 5.

【0033】[0033]

【表5】油類 実施例1 実施例2 軽油/ガソリン 32.6 33 石油 14 15.5 ディーゼルオイル 36 35 重油 17.4 16.5 表5のデータから判るように本発明の処理方法によって
生じた製品は有用で安全性の高い燃料であり、廃却され
たタイヤの放棄や浪費が防止されると共に無用の代物が
価値ある油類、気体およびカーボンブラックに転化で
き、廃物利用により資源の再利用ができる。
Oils Example 1 Example 2 Light oil / gasoline 32.6 33 Petroleum 14 15.5 Diesel oil 36 35 Heavy oil 17.4 16.5 Produced by the process of the invention as can be seen from the data in Table 5. The product is a useful and safe fuel, which prevents waste tires from being abandoned and wasted, and can convert waste products into valuable oils, gases and carbon black, which can be used to recycle resources. Available.

【0034】[0034]

【発明の効果】前記の如く、本発明は新たな処理方法に
より廃却されるゴムタイヤを分解し、有用でかつ価値あ
る製品に転化するもので、従来の分解再生方法に比べて
次のような効果がある。
As described above, the present invention decomposes rubber tires to be discarded by a new treatment method and converts them into useful and valuable products. effective.

【0035】1.分解反応が低温低圧で行われるので、
反応がより安全であること(注:本発明によれば僅か4
00℃で、前記の水素、メタンやエタンの着火点より低
いゆえに従来の方法より安全である)。
1. Since the decomposition reaction is carried out at low temperature and low pressure,
The reaction is safer (note: only 4 according to the invention
At 00 ° C, it is safer than conventional methods because it is lower than the ignition point of hydrogen, methane and ethane mentioned above).

【0036】2.低温低圧の反応条件であるから、製造
原価、稼働、操作、保守等の費用が安く、資源の消耗が
少ないこと。
2. Since the reaction conditions are low temperature and low pressure, the cost of manufacturing, operation, operation, maintenance, etc. are low, and the consumption of resources is small.

【0037】3.反応圧力が低いから反応器または製造
システムからガスが漏れる可能性が低いため空気の汚染
が防止または減少されること。
3. Preventing or reducing air pollution by reducing the possibility of gas leaking from the reactor or manufacturing system due to the low reaction pressure.

【0038】なお、本発明は特許請求の範囲の記載に反
しない限り適宜に修飾または変更することを制限するも
のではない。
It should be noted that the present invention does not limit appropriate modification or alteration unless it contradicts the scope of the claims.

【0039】また、その他の高分子、融合物についても
本発明の方法により分解反応を行なうことができる。
Further, other polymers and fusion products can be decomposed by the method of the present invention.

【図面の簡単な説明】[Brief description of drawings]

【図1】は、本発明の製造方法の一例を示すフローチャ
ートである。
FIG. 1 is a flowchart showing an example of a manufacturing method of the present invention.

【符号の説明】[Explanation of symbols]

1−−−廃却ゴムタイヤの洗浄工程、 2−−−洗浄したゴムタイヤを粉砕する工程、 3−−−分解されたゴムを雲母触媒と共に混合、予熱す
る工程、および 4−−−ゴムを分解する工程。
1 --- Washing process of waste rubber tire, 2 --- Process of crushing washed rubber tire, 3-- Process of mixing decomposed rubber with mica catalyst, preheating, and 4-decomposing rubber Process.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C10J 3/00 B09B 3/00 302B 302A ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location C10J 3/00 B09B 3/00 302B 302A

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 a)廃却ゴムタイヤを洗浄および粉砕し
てゴム粉砕物とし、 b)該ゴム粉砕物と絹雲母、白雲母および黒雲母からな
る群より選ばれた少なくとも1種の雲母触媒とを210
℃に加熱して混合し、 c)加熱して1時間、1〜2.5気圧で230〜400
℃の温度を保持して気体製品と混合油とを含む気相製品
およびカーボンブラックと残留物とを含む固形製品とを
含む分解物を得るように分解反応に供給される廃却ゴム
タイヤ全量(100%)に対して触媒量2〜3%の該雲
母触媒の存在下に該ゴム粉砕物を乾留して分解し、さら
に d)該分解物を気体製品、混合油、カーボンブラックお
よび残留物に分離することを特徴とする廃却ゴムタイヤ
の分解方法。
1. A) washing and crushing a waste rubber tire to obtain a crushed rubber, and b) the crushed rubber and at least one mica catalyst selected from the group consisting of sericite, muscovite and biotite. 210
Heat to ℃ to mix, c) Heat for 1 hour, 230-400 at 1-2.5 atm.
The total amount of the waste rubber tires supplied to the decomposition reaction so as to obtain the gas phase product containing the gas product and the mixed oil and the decomposed product containing the carbon black and the solid product containing the residue while maintaining the temperature of 100 ° C. (100 %) To dry decompose the rubber pulverized product in the presence of the catalyst having a catalytic amount of 2 to 3%, and d) separate the decomposed product into a gas product, a mixed oil, carbon black and a residue. A method for disassembling a waste rubber tire, which comprises:
【請求項2】 該雲母触媒が絹雲母粉末である請求項1
に記載の方法。
2. The mica catalyst is sericite powder.
The method described in.
JP5244693A 1993-03-12 1993-03-12 Disassembly method of waste rubber tires Expired - Lifetime JP2510067B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5244693A JP2510067B2 (en) 1993-03-12 1993-03-12 Disassembly method of waste rubber tires

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5244693A JP2510067B2 (en) 1993-03-12 1993-03-12 Disassembly method of waste rubber tires

Publications (2)

Publication Number Publication Date
JPH0797578A JPH0797578A (en) 1995-04-11
JP2510067B2 true JP2510067B2 (en) 1996-06-26

Family

ID=12914961

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5244693A Expired - Lifetime JP2510067B2 (en) 1993-03-12 1993-03-12 Disassembly method of waste rubber tires

Country Status (1)

Country Link
JP (1) JP2510067B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008024907A (en) * 2006-07-20 2008-02-07 Shinichiro Kojima Extracting reaction assistant for waste rubber, waste tire and oil
WO2023153378A1 (en) * 2022-02-08 2023-08-17 株式会社ブリヂストン Method for decomposing crosslinked rubber
WO2023153377A1 (en) * 2022-02-08 2023-08-17 株式会社ブリヂストン Method for decomposing crosslinked rubber
WO2023153381A1 (en) * 2022-02-08 2023-08-17 株式会社ブリヂストン Method for decomposing crosslinked rubber

Also Published As

Publication number Publication date
JPH0797578A (en) 1995-04-11

Similar Documents

Publication Publication Date Title
US5286374A (en) Process for cracking waste rubber tires
JP3170290B2 (en) Method for producing light oil from waste plastic containing phthalic polyester and / or polyvinyl chloride
CA2061600C (en) Polymer cracking
US4251500A (en) Process for hydrocracking a waste rubber
US20110089081A1 (en) Process for producing fuel from plastic waste material by using dolomite catalyst
JPS6040193A (en) Manufacture of liquid hydrocarbon
Abdul-Raouf et al. Thermochemical recycling of mixture of scrap tyres and waste lubricating oil into high caloric value products
JPS62253689A (en) Improved method for regenerating carbon-containing waste
AU5896299A (en) Catalyst for the low-temperature pyrolysis of hydrocarbon-containing polymer materials
EP1633501A2 (en) Method to recapture energy from organic waste
JP2534461B2 (en) Syngas production method
JP2510067B2 (en) Disassembly method of waste rubber tires
JP2727031B2 (en) Liquefaction and partial oxidation of plastic materials
CN1034739C (en) Pyrolysis process for waste tyre rubber
US4098677A (en) Catalytic cracking process with CO2 -stripped regenerated catalyst
JPH10310778A (en) Purification of oil made from waste plastic and purified fraction
RU2250239C1 (en) Rubber-containing waste processing
US5772777A (en) Method for processing composite materials to enable recycling thereof
JP3430245B2 (en) Method for producing liquid hydrocarbon and carbon black
RU2362795C1 (en) Method of liquation of rubbers and rubber-containing wastes
JPH11140460A (en) Thermal decomposition of plastics, and device and dechlorinating agent used therefor
RU2149885C1 (en) Method of processing petroleum and petroleum derivatives
JP2931968B2 (en) Coal decomposition method
JP2007291290A (en) Method for treating plastic material
JPH07138576A (en) Method of processing waste plastic