JPS586722B2 - How to recycle waste rubber - Google Patents
How to recycle waste rubberInfo
- Publication number
- JPS586722B2 JPS586722B2 JP52006787A JP678777A JPS586722B2 JP S586722 B2 JPS586722 B2 JP S586722B2 JP 52006787 A JP52006787 A JP 52006787A JP 678777 A JP678777 A JP 678777A JP S586722 B2 JPS586722 B2 JP S586722B2
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- waste rubber
- parts
- weight
- recycling
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920001971 elastomer Polymers 0.000 title claims description 52
- 239000005060 rubber Substances 0.000 title claims description 52
- 239000002699 waste material Substances 0.000 title claims description 32
- 238000000034 method Methods 0.000 claims description 22
- 238000004064 recycling Methods 0.000 claims description 16
- JEHKKBHWRAXMCH-UHFFFAOYSA-N benzenesulfinic acid Chemical class O[S@@](=O)C1=CC=CC=C1 JEHKKBHWRAXMCH-UHFFFAOYSA-N 0.000 claims description 15
- 238000004898 kneading Methods 0.000 claims description 12
- 239000003921 oil Substances 0.000 claims description 11
- DILXLMRYFWFBGR-UHFFFAOYSA-N 2-formylbenzene-1,4-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(S(O)(=O)=O)C(C=O)=C1 DILXLMRYFWFBGR-UHFFFAOYSA-N 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 2
- 239000010495 camellia oil Substances 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 9
- 238000011069 regeneration method Methods 0.000 description 8
- 230000008929 regeneration Effects 0.000 description 7
- 244000043261 Hevea brasiliensis Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229920003052 natural elastomer Polymers 0.000 description 5
- 229920001194 natural rubber Polymers 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000010734 process oil Substances 0.000 description 4
- 229920003051 synthetic elastomer Polymers 0.000 description 4
- 239000005061 synthetic rubber Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- 239000010920 waste tyre Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- FLIBMGVZWTZQOM-UHFFFAOYSA-N benzene;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CC=CC=C1 FLIBMGVZWTZQOM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- JEJKYBWZGPZXAF-UHFFFAOYSA-N ethyl benzenesulfinate Chemical compound CCOS(=O)C1=CC=CC=C1 JEJKYBWZGPZXAF-UHFFFAOYSA-N 0.000 description 1
- 238000010169 landfilling Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011297 pine tar Substances 0.000 description 1
- 229940068124 pine tar Drugs 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- 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
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
【発明の詳細な説明】
本発明は廃タイヤ等の廃ゴムを効果的に再生する方法に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for effectively recycling waste rubber such as waste tires.
近年、モータリゼーションの著しい発展とともに、使用
済み古タイヤの廃棄量も急激に増大し、それの処理が問
題になりつつある。In recent years, with the remarkable development of motorization, the amount of discarded used tires has also increased rapidly, and the disposal of them has become a problem.
これまで廃タイヤの処理方法としては、原形利用、埋立
、焼却等が主として行なわれてきたが、環境汚染防止、
資源の有効利用等の社会的要請に合致したものとはいえ
ない。Up until now, the main methods of disposing of waste tires have been reusing them in their original form, landfilling, and incineration.
It cannot be said that it meets social demands such as effective use of resources.
かくの如き要請を満たすものの一つとして、古くから廃
ゴムの再生が行なわれており、これは今後、積極的に発
展させるべきものと思われる。One way to meet these demands is to recycle waste rubber, which has been practiced for a long time, and this seems to be something that should be actively developed in the future.
従来、廃ゴムの再生法として、種々多様な方法が提案さ
れてきたが、その殆んどが、150℃以上の高温を必要
とし、その為の特別の装置を有する者でなければ容易に
実施することができなかった。In the past, various methods have been proposed for recycling waste rubber, but most of them require high temperatures of 150°C or higher and are difficult to implement unless someone has special equipment for that purpose. I couldn't.
又、従来の再生法の多くは、天然ゴムを対象として開発
されたものであり、合成ゴムを多量に含有するゴムを有
効に再生することはできなかった。Furthermore, most of the conventional recycling methods were developed for natural rubber, and rubber containing a large amount of synthetic rubber could not be effectively recycled.
本発明はこれらの欠点を克服する新規な廃ゴムの再生方
法を提供することを目的とする。The object of the present invention is to provide a new method for recycling waste rubber that overcomes these drawbacks.
本発明は廃ゴムを油およびアルキル置換ベンゼンスルフ
イン酸と共に混練りすることを特徴とする廃ゴムの再生
方法を要旨とする。The gist of the present invention is a method for recycling waste rubber, which comprises kneading waste rubber with oil and alkyl-substituted benzenesulfinic acid.
本発明の方法は他の再生方法に比べて処理温度が低く、
またロール等通常ゴム工業に従事する者が現有の設備を
そのまま利用することができる。The method of the present invention has a lower processing temperature than other regeneration methods,
In addition, those who normally work in the rubber industry, such as rolls, can use the existing equipment as is.
また本発明によれば天然ゴムのみならず従来の方法では
困難とされていた合成ゴムを多量に含む廃ゴムをも効果
的に再生することができる。Furthermore, according to the present invention, not only natural rubber but also waste rubber containing a large amount of synthetic rubber, which has been difficult to regenerate using conventional methods, can be effectively recycled.
更に本発明の方法で得られた再生ゴムは従来の方法によ
る再生ゴムよりも優れた性能を示す。Furthermore, the recycled rubber obtained by the method of the present invention exhibits superior performance than recycled rubber obtained by conventional methods.
以下本発明を詳細に説明する。The present invention will be explained in detail below.
本発明で再生しうる廃ゴムは、天然ゴムが主として用い
られるトラックバス用タイヤ、合成ゴムが好んで用いら
れる乗用車用タイヤ、及びベルトホース、シート、パッ
キング等の廃ゴムである。The waste rubber that can be recycled in the present invention includes truck and bus tires in which natural rubber is mainly used, passenger car tires in which synthetic rubber is preferably used, and waste rubber such as belt hoses, sheets, and packing.
勿論上記物品成型の際に生じる屑ゴムもこれに含まれる
。Of course, this also includes waste rubber generated during the molding of the above-mentioned articles.
これらの廃ゴムは、必ずしも再生処理前に粉末化される
ことを要せず、ロールを通過しうる大きさの切片あるい
はシートであれば良い。These waste rubbers do not necessarily need to be powdered before being recycled, and any piece or sheet that is large enough to pass through the rolls may be used.
再生剤として用いるアルキル置換ベンゼンスルフイン酸
とはP−トルエンスルフィン酸、O−トルエンスルフイ
ン酸、P一エチルベンゼンスルフイン酸、O−エチルベ
ンゼンスルフイン酸等ベンゼンスルフイン酸に炭素数1
〜4程度のアルキル基を1ないし2置換したものを含む
。What are the alkyl-substituted benzenesulfinic acids used as regenerants? P-toluenesulfinic acid, O-toluenesulfinic acid, P-ethylbenzenesulfinic acid, O-ethylbenzenesulfinic acid, etc. benzenesulfinic acid with 1 carbon number
It includes those having 1 to 2 substitutions with about 4 to 4 alkyl groups.
ベンゼンスルフイン酸も同程度の効果がある。Benzene sulfuric acid is equally effective.
この中でもP−トルエンスルフイン酸が好ましい。Among these, P-toluenesulfinic acid is preferred.
アルキル置換ベンゼンスルフイン酸は再生を効果的に行
ない、かつ再生ゴムの再加硫反応を阻害しない程度の量
を使用することが好ましい。It is preferable to use the alkyl-substituted benzenesulfuric acid in an amount that allows effective regeneration and does not inhibit the revulcanization reaction of the recycled rubber.
このような見地から廃ゴム100重量部肖り0.1〜1
0重量部程度が用いられる。From this point of view, the ratio of 100 parts by weight of waste rubber is 0.1 to 1.
About 0 parts by weight is used.
この中でも0,3〜5重量部の範囲で効果的な再生と、
再加硫反応が行われる。Among these, effective regeneration is achieved within the range of 0.3 to 5 parts by weight.
A revulcanization reaction takes place.
本発明において、アルキル置換ベンゼンスルフイン酸は
必ず油とともに使用しなければならない。In the present invention, the alkyl-substituted benzenesulfuric acid must be used together with oil.
ゴムとの混練りに際しアルキル置換ベンゼンスルフイン
酸単独あるいは油単独でも可塑化しないことはないが極
めて不充分であり、両者を併用した時のみ著しい効果が
認められる。When kneading with rubber, alkyl-substituted benzenesulfinic acid alone or oil alone does not cause plasticization, but it is extremely insufficient, and a significant effect is observed only when both are used together.
本発明で用いうる油は、ゴム工業において用いられる軟
化油、再生油なら何でも良い。The oil that can be used in the present invention may be any softening oil or recycled oil used in the rubber industry.
例えば、パラフィン系、ナフテン系、芳香族系のプロセ
スオイル、石油アスファルト、コールタール等の高沸点
油、トール油、ロジン、パインタール、ジペンテン等の
植物油等を用いることができる。For example, paraffinic, naphthenic, or aromatic process oils, high-boiling oils such as petroleum asphalt and coal tar, and vegetable oils such as tall oil, rosin, pine tar, and dipentene can be used.
油の使用量は、多い程再生に効果がある。The larger the amount of oil used, the more effective it is for regeneration.
しかし、過多の使用は再生ゴムの性能を低下させるので
、通常、廃ゴム100重量部当り1〜40重量部、好ま
しくは5〜20重量部が用いられる。However, since excessive use deteriorates the performance of the recycled rubber, it is usually used in an amount of 1 to 40 parts by weight, preferably 5 to 20 parts by weight, per 100 parts by weight of waste rubber.
廃ゴムの再生は、廃ゴムをアルキルベンゼンスルフィン
酸及び油とともに、ロール上で混練りすることによって
行なわれる。Recycling of waste rubber is carried out by kneading the waste rubber with alkylbenzenesulfinic acid and oil on rolls.
混練りは150℃以下の温度で行なうことができるが、
100℃以下で行なう方が作業性が良く、効果も大きい
。Kneading can be carried out at a temperature of 150°C or lower,
It is better to work at a temperature of 100°C or lower, and the effect is greater.
混練り時間は、要求する可塑度により異なるが、通常、
5〜60分の時間で、充分可塑化することができる。The kneading time varies depending on the degree of plasticity required, but is usually
Sufficient plasticization can be achieved in 5 to 60 minutes.
又、ロール間隙を狭めることにより一層再生効果を上げ
ることができる。Furthermore, by narrowing the gap between the rolls, the regeneration effect can be further improved.
本発明の方法により再生されたゴムは、単独で、あるい
は新ゴムと混合して、タイヤ、ベルト、ホース、シート
、パッキング等の原料として再利用することができる。Rubber recycled by the method of the present invention can be reused as a raw material for tires, belts, hoses, sheets, packing, etc., either alone or in combination with new rubber.
以下に実施例を挙げて、本発明を更に具体的に説明する
。The present invention will be explained in more detail with reference to Examples below.
なお、実施例中、再生度の指標として採用した可塑度は
、ワレス(Wallace)社のラピツド プラステイ
メーターにより、温度100℃、荷重12.7kg/c
r2の条件下で測定した。In the examples, the plasticity used as an index of the degree of regeneration was measured using a Rapid Plastymeter manufactured by Wallace at a temperature of 100°C and a load of 12.7 kg/cm.
Measured under r2 conditions.
この値が小さい程可塑度が大きく、実用的には70以下
の値であることが望まれる。The smaller this value is, the greater the plasticity is, and a value of 70 or less is practically desired.
配合割合の部は重量部である。The parts in the blending ratio are parts by weight.
実施例 1
乗用車用廃タイヤから得た30メッシュの粉末ゴム(天
然ゴム約70%、スチレンプタジエンゴム約20%、ブ
タジエンゴム約10%)100重量部を適轟な容器中で
、1重量部のP−トルエンスルフイン酸及び10重量部
のプロセスオイルと混合した。Example 1 100 parts by weight of 30 mesh powder rubber (about 70% natural rubber, about 20% styrene-ptadiene rubber, about 10% butadiene rubber) obtained from waste passenger car tires was added to 1 part by weight in a suitable container. of P-toluenesulfinic acid and 10 parts by weight of process oil.
この混合物を間隙を狭くしたロール上に移し、薄通しを
繰り返し行なった所、粉末ゴムは直ちにシート状になっ
た。This mixture was transferred onto a roll with a narrow gap and passed through repeatedly, and the powdered rubber immediately became a sheet.
このシートは初期は可塑性に乏しく、依然として弾性を
保持するものであったが、ひき続き混練りする間に、急
速に可塑性が増大した。Although this sheet initially had poor plasticity and still retained elasticity, its plasticity rapidly increased during continued kneading.
30分後、ゴムシートをロールから回収した。After 30 minutes, the rubber sheet was collected from the roll.
この間のロール温度は、40〜60℃に保たれた。During this time, the roll temperature was maintained at 40 to 60°C.
この様にして得られたゴムシートの可塑度は53であり
、効果的に再生が行なわれたことを示す。The plasticity of the rubber sheet thus obtained was 53, indicating that the regeneration was effective.
実施例 2
P−}ルエンスルフィン酸を3部使用したこと以外は、
実施例1と同様の処理を行なった。Example 2 Except that 3 parts of P-}luenesulfinic acid were used.
The same treatment as in Example 1 was performed.
この場合の可塑度は45であり、更に大きな効果が得ら
れた。The plasticity in this case was 45, and an even greater effect was obtained.
比較例 1および2
実施例1で用いた粉末ゴム100部とP−トルエンスル
フイン酸3部及び当該粉末ゴム100部とプロセスオイ
ル10部を用いて、それぞれ実施例1と同様の処理を行
なった。Comparative Examples 1 and 2 The same treatments as in Example 1 were carried out using 100 parts of the powdered rubber used in Example 1 and 3 parts of P-toluenesulfinic acid, and 100 parts of the powdered rubber and 10 parts of process oil. .
この場合の可塑度は、夫々、93及び73であり、単独
で使用した場合はいずれも、両者を併用した時の値45
に及ばないことが解る。The plasticity in this case is 93 and 73, respectively, and when used alone, the value when both are used together is 45.
I understand that it is not as good as .
実施例 3および4
トラックバス用廃タイヤからのゴム屑(天然ゴム主体)
で1〜2mm%の大きさのもの及びスチレンブタジエン
ゴムからなる加硫ゴム2mm角のものを用いて、それぞ
れ実施例1と同様に処理を行なった。Examples 3 and 4 Rubber scraps from waste truck and bus tires (mainly natural rubber)
The same treatment as in Example 1 was carried out using a vulcanized rubber having a size of 1 to 2 mm% and a 2 mm square vulcanized rubber made of styrene-butadiene rubber.
但し、スチレンブタジエンゴムのみからなるゴムでは、
プロセスオイルを15部使用し、混練り時間も60分と
した。However, for rubber made only of styrene-butadiene rubber,
15 parts of process oil was used, and the kneading time was also 60 minutes.
次に、これらの再生ゴムをJIS K6313の処法で
配合、加硫し、厚さ2mmのスラプシートを作成し、硬
度(JIS)、破断時強度、破断時伸長度を測定した。Next, these recycled rubbers were compounded and vulcanized according to the method of JIS K6313 to prepare a slap sheet with a thickness of 2 mm, and the hardness (JIS), strength at break, and elongation at break were measured.
これらの物性値及び再生時の可塑度を整理し、下記の表
1に記載した。These physical property values and plasticity upon regeneration are summarized and listed in Table 1 below.
比較例 3
比較のため、トラックバス用廃タイヤからの市販の再生
ゴムについても、JIS K6313の処法で配合・加
硫し、その物性値を表1に記載した。Comparative Example 3 For comparison, commercially available recycled rubber from waste truck and bus tires was also compounded and vulcanized according to the JIS K6313 process, and its physical properties are listed in Table 1.
表1において、トラックバス用廃タイヤのゴムを、本発
明の方法により再生したゴムの加硫物性は、同種タイヤ
からの市販再生ゴムの加硫物性より優れていることは明
らかである。In Table 1, it is clear that the vulcanized physical properties of rubber recycled from waste truck and bus tires by the method of the present invention are superior to the vulcanized physical properties of commercially available recycled rubber from tires of the same type.
更に実施例4は本発明の方法が合成ゴムのみからなるゴ
ムの再生にも有効であることを示している。Furthermore, Example 4 shows that the method of the present invention is also effective for recycling rubber made only of synthetic rubber.
Claims (1)
酸と共に混練りすることを特徴とする廃ゴムの再生方法
。 2 前記アルキル置換ベンゼンスルフイン酸の配合量が
前記廃ゴム100重量部当り0.1〜10重量部である
特許請求の範囲第1項記載の廃ゴムの再生方法。 3 前記アルキル置換ベンゼンスルフイン酸の配合量が
0.3〜5重量部である特許請求の範囲第2項記載の廃
ゴムの再生方法。 4 前記アルキル置換ベンゼンスルフイン酸がP−トル
エンスルフイン酸である特許請求の範囲第1項記載の廃
ゴムの再生方法。 5 前記油の配合量が前記廃ゴム100重量部当り1〜
40重量部である特許請求の範囲第1項記載m廃ゴムの
再生方法。 6 前記油の配合量が5〜20重量部である特許請求の
範囲第5項記載の廃ゴムの再生方法。 7 前記混練り方法がロール練りである特許請求の範囲
第1項記載の廃ゴムの再生方法。 8 前記混練りの温度が150℃以下である特許請求の
範囲第1項記載の廃ゴムの再生方法。 9 前記混練りの温度が100℃以下である特許請求の
範囲第8項記載の廃ゴムの再生方法。[Scope of Claims] 1. A method for recycling waste rubber, which comprises kneading waste rubber with tea oil and alkyl-substituted benzenesulfinic acid. 2. The method for recycling waste rubber according to claim 1, wherein the amount of the alkyl-substituted benzenesulfinic acid is 0.1 to 10 parts by weight per 100 parts by weight of the waste rubber. 3. The method for recycling waste rubber according to claim 2, wherein the amount of the alkyl-substituted benzenesulfinic acid is 0.3 to 5 parts by weight. 4. The method for recycling waste rubber according to claim 1, wherein the alkyl-substituted benzenesulfinic acid is P-toluenesulfinic acid. 5 The blending amount of the oil is 1 to 1 per 100 parts by weight of the waste rubber.
40 parts by weight of the method for recycling waste rubber according to claim 1. 6. The method for recycling waste rubber according to claim 5, wherein the amount of the oil is 5 to 20 parts by weight. 7. The waste rubber recycling method according to claim 1, wherein the kneading method is roll kneading. 8. The method for recycling waste rubber according to claim 1, wherein the kneading temperature is 150° C. or lower. 9. The method for recycling waste rubber according to claim 8, wherein the kneading temperature is 100°C or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52006787A JPS586722B2 (en) | 1977-01-26 | 1977-01-26 | How to recycle waste rubber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52006787A JPS586722B2 (en) | 1977-01-26 | 1977-01-26 | How to recycle waste rubber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5392883A JPS5392883A (en) | 1978-08-15 |
| JPS586722B2 true JPS586722B2 (en) | 1983-02-05 |
Family
ID=11647877
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52006787A Expired JPS586722B2 (en) | 1977-01-26 | 1977-01-26 | How to recycle waste rubber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS586722B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5164384B2 (en) * | 2007-01-12 | 2013-03-21 | 株式会社ブリヂストン | Processed powder rubber, rubber composition and pneumatic tire using the same |
-
1977
- 1977-01-26 JP JP52006787A patent/JPS586722B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5392883A (en) | 1978-08-15 |
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