[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

JPH04224839A - Rubber composition for tire tread - Google Patents

Rubber composition for tire tread

Info

Publication number
JPH04224839A
JPH04224839A JP2414704A JP41470490A JPH04224839A JP H04224839 A JPH04224839 A JP H04224839A JP 2414704 A JP2414704 A JP 2414704A JP 41470490 A JP41470490 A JP 41470490A JP H04224839 A JPH04224839 A JP H04224839A
Authority
JP
Japan
Prior art keywords
rubber
weight
calcium oxide
styrene
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2414704A
Other languages
Japanese (ja)
Inventor
Toru Fukumoto
徹 福本
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.)
Sumitomo Rubber Industries Ltd
Original Assignee
Sumitomo Rubber Industries Ltd
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 Sumitomo Rubber Industries Ltd filed Critical Sumitomo Rubber Industries Ltd
Priority to JP2414704A priority Critical patent/JPH04224839A/en
Publication of JPH04224839A publication Critical patent/JPH04224839A/en
Pending legal-status Critical Current

Links

Landscapes

  • Tires In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the title compsn. which prevents the degradation of durability of a tire caused by heat buildup during high-speed running without detriment to the grip of the tire. CONSTITUTION:100 pts.wt. rubber component comprising at least one styrene- butadiene copolymer rubber having a combined styrene content of 30 % or higher, 70 pts.wt. or higher carbon black having an iodine adsorption capacity of 90 mg/g or higher, and 1-15 pts.wt. calcium oxide are compounded to give the title compsn., which has an improved heat resistance without detriment to the grip.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】この発明は主として空気入りタイ
ヤ例えば、乗用車用、二輪車用、レーシング用などのタ
イヤのトレッドに使用するゴム組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates primarily to rubber compositions used in the treads of pneumatic tires, such as tires for passenger cars, motorcycles, and racing tires.

【0002】0002

【従来の技術】車両の性能向上につれ、レーシング用は
もとより、一般車両にも高速性能の優れたタイヤに対す
る要求が高まっている。そこで、特に重要なグリップ性
能についても種々、改良が図られている。例えば、タイ
ヤのトレッドゴム組成物としてスチレン含有率の高いス
チレン─ブタジエン共重合体ゴムにプロセスオイルや、
カーボンブラックを多く配合してグリップ性能を確保し
ている。
2. Description of the Related Art As the performance of vehicles improves, there is an increasing demand for tires with excellent high-speed performance not only for racing but also for general vehicles. Therefore, various improvements have been made regarding particularly important grip performance. For example, process oil is added to styrene-butadiene copolymer rubber with a high styrene content as a tire tread rubber composition.
A large amount of carbon black is blended to ensure grip performance.

【0003】しかし、高いグリップ性能を得るために、
スチレン─ブタジエン共重合体ゴムのスチレン含有量を
多くしたり、プロセスオイルや、カーボンブラックを多
く配合するとグリップ性能を高くすることは可能である
が、反面そのためにゴム組成物の発熱が大きくなる。す
なわち、ゴム組成物の発熱量の指標である損失係数、い
わゆるtanδ値の大きい配合系となる。このようなト
レッドのタイヤをつけて高速走行するとトレッド部分が
高温になり、ゴムの内部に発泡が生じる、いわゆるブロ
ー現象といわれる現象が発生し、ひどいときには、トレ
ッドゴムが飛散してタイヤの破壊をもたらす。この発熱
に耐えるように耐熱性老化防止剤の添加などが行われて
いるが、問題の解決には到っていないのが実情である。
However, in order to obtain high grip performance,
It is possible to improve the grip performance by increasing the styrene content of the styrene-butadiene copolymer rubber or by adding a large amount of process oil or carbon black, but on the other hand, this increases the heat generation of the rubber composition. That is, the compound system has a large loss coefficient, so-called tan δ value, which is an index of the calorific value of the rubber composition. When a tire with such a tread is worn and driven at high speeds, the tread becomes hot, causing foam to form inside the rubber, a phenomenon known as the blow phenomenon. In severe cases, the tread rubber can fly off and destroy the tire. bring. In order to withstand this heat generation, heat-resistant anti-aging agents have been added, but the reality is that the problem has not been solved.

【0004】特開昭47─29471にポリエステルゴ
ム積層物中のポリエステルの熱加水分解防止のため酸化
カルシウムを添加することの記載があるが、タイヤ補強
層に関するもので、グリップ性能と耐熱性のバランスが
重要であるトレッド部分の問題に関するものではない。 特開昭57─195760には、空気タイヤの空気を保
持するためのインナーライナーもしくはチューブに使用
するブチルゴムにつき、混練り中または走行中の気泡を
抑えて空気透過性を小さくするため、酸化カルシウムを
配合することが記載されている。また、特開昭60─1
90440には酸化カルシウムを含むゴム充填剤に関す
る発明が開示されているが、これもゴムの一般加硫物性
に関するものである。
[0004] JP-A No. 47-29471 describes the addition of calcium oxide to prevent thermal hydrolysis of polyester in polyester rubber laminates, but this relates to a tire reinforcing layer, and the balance between grip performance and heat resistance is described. It's not about the tread part issue, which is important. JP-A-57-195760 discloses that calcium oxide is added to butyl rubber used for inner liners or tubes for retaining air in pneumatic tires in order to suppress air bubbles and reduce air permeability during kneading or running. It is described that it is mixed. Also, JP-A-60-1
No. 90440 discloses an invention relating to a rubber filler containing calcium oxide, which also relates to general vulcanized physical properties of rubber.

【0005】[0005]

【発明が解決しようとする課題】車両の走行によりトレ
ッドゴムは急激な温度の上昇下降が繰り返されタイヤの
破壊の原因となるブロー現象を生じるが、この発明は高
いグリップ性能を保ちながら、ブロー現象を防止するた
め耐熱性を向上させたゴム組成物を提供するものである
[Problems to be Solved by the Invention] When a vehicle runs, the temperature of the tread rubber repeatedly rises and falls rapidly, causing a blow phenomenon that can cause tire destruction.This invention eliminates the blow phenomenon while maintaining high grip performance. The object of the present invention is to provide a rubber composition with improved heat resistance in order to prevent this.

【0006】[0006]

【課題を解決するための手段】この発明の発明者はこの
ような従来の欠点を解決するためにトレッドゴムに対す
るゴムおよび充填剤等の配合に鋭意検討を重ねてきた。 その結果、結合スチレンの割合が30重量%以上の量に
なる、スチレン─ブタジエン共重合体ゴムを1種以上含
むジエン系ゴムの100重量部に対し、ヨウ素吸着量(
IA)が90mg/g以上である、粒子の小さいカーボ
ンブラックを70〜250重量部と酸化カルシウムまた
は、高級脂肪酸ないし混合脂肪酸あるいはプロセスオイ
ルで処理した酸化カルシウムを1〜15重量部配合する
ことを特徴としたゴム組成物がきわめて有効であること
をつきとめ、この発明に到達した。
[Means for Solving the Problems] In order to solve these conventional drawbacks, the inventors of the present invention have made intensive studies on the blending of rubber, fillers, etc. in tread rubber. As a result, the amount of iodine adsorbed (
It is characterized by blending 70 to 250 parts by weight of small-particle carbon black with IA) of 90 mg/g or more and 1 to 15 parts by weight of calcium oxide or calcium oxide treated with higher fatty acid or mixed fatty acid or process oil. The inventors have discovered that the rubber compositions described above are extremely effective, and have thus arrived at the present invention.

【0007】高いグリップ性能を得るためには、結合ス
チレンの合計量が全スチレン─ブタジエン共重合体ゴム
の30重量%以上であるスチレン─ブタジエン共重合体
ゴムとヨウ素吸着量(IA)が90mg/g以上のカー
ボンブラックをこのジエン系ゴム100重量部に対し、
70以上配合することを要する。これにより、70°C
で測定したtanδの値を大きくすることができ、高グ
リップ性能のトレッドゴムが得られる。カーボンブラッ
ク量は250重量部以上配合しようとすると、混練りが
困難となるため250重量部以下とした。
In order to obtain high grip performance, a styrene-butadiene copolymer rubber in which the total amount of bound styrene is 30% by weight or more of the total styrene-butadiene copolymer rubber and an iodine adsorption amount (IA) of 90 mg/ g or more of carbon black per 100 parts by weight of this diene rubber,
It is necessary to mix 70 or more. As a result, 70°C
The value of tan δ measured in can be increased, and a tread rubber with high grip performance can be obtained. The amount of carbon black was set to be 250 parts by weight or less since kneading becomes difficult if more than 250 parts by weight is blended.

【0008】酸化カルシウムまたは、脂肪酸あるいはプ
ロセスオイルで処理した酸化カルシウムを1〜15重量
部と制限したのは、1重量部より少なければ走行時のゴ
ムの耐発熱発泡性の向上が認められず、また、15重量
部より多ければ車両走行テストにおいて従来のトレッド
ゴムをつけたタイヤと比較して、グリップ性能において
大幅な低下が認められることによる。
[0008] Calcium oxide or calcium oxide treated with fatty acid or process oil is limited to 1 to 15 parts by weight because if it is less than 1 part by weight, no improvement in the exothermic foaming resistance of the rubber during running is observed. Further, if the amount is more than 15 parts by weight, a significant decrease in grip performance is observed in vehicle running tests compared to tires with conventional tread rubber.

【0009】ここで、酸化カルシウムをオレイン酸、ス
テアリン酸等の高級脂肪酸ないしはこれらの混合脂肪酸
あるいはナフテン系、パラフィン系、アロマテイ ック
系等のプロセスオイルで処理したものを使うと、未処理
の酸化カルシウムの場合よりも配合時の計量作業性がよ
く、また酸化カルシウムのゴム中の分散性がよい。
[0009] Here, if calcium oxide is treated with higher fatty acids such as oleic acid and stearic acid, or mixed fatty acids thereof, or process oils such as naphthenic, paraffinic, and aromatic oils, the untreated oxidized Calcium oxide is easier to measure during blending than calcium, and calcium oxide has better dispersibility in rubber.

【0010】なおこの発明において、ゴムとしてはスチ
レン─ブタジエン共重合体ゴムを単独で用い得ることは
もちろんのこと、その他のゴム成分、例えば天然ゴム、
合成イソプレンゴム、1,4ブタジエンゴム、スチレン
含有量の異なる各種のスチレン─ブタジエン共重合体ゴ
ム等と混合して用いることができる。さらに、この発明
のゴム組成物は前記の配合剤の他に、ゴム工業、なかで
もトレッドゴムの配合で通常使用される配合剤、例えば
充填剤、軟化剤、老化防止剤、加硫剤、加硫促進剤、加
硫促進助剤などを必要に応じて組合せにより適当とされ
る配合量配合することができる。
In the present invention, as the rubber, styrene-butadiene copolymer rubber can of course be used alone, but other rubber components such as natural rubber,
It can be used in combination with synthetic isoprene rubber, 1,4-butadiene rubber, various styrene-butadiene copolymer rubbers having different styrene contents, and the like. Furthermore, in addition to the above-mentioned compounding agents, the rubber composition of the present invention may also contain compounding agents commonly used in the rubber industry, especially in the compounding of tread rubber, such as fillers, softeners, anti-aging agents, vulcanizing agents, vulcanizing agents, etc. Sulfur accelerators, vulcanization accelerating aids, and the like can be added in suitable amounts by combining them as necessary.

【0011】以下実施例によりこの発明を説明する。ゴ
ムとしては、スチレン含有率40%のスチレン─ブタジ
エン共重合体ゴムを用い、カーボンブラックはヨウ素吸
着量(IA)が140mg/gのものをゴム100に対
して90重量部使用した。酸化カルシウムとしては表1
に示すように粉体状の商品名VESTA−PP(井上石
灰社製)を変量して配合した。脂肪酸処理を施した酸化
カルシウムとして粒状のVESTA−BS、プロセスオ
イル処理した酸化カルシウムとしてペースト状の商品名
CML21(近江化学社製)を使用した。加硫剤、充填
剤等を加えたこの配合物を常法にしたがって、バンバリ
ーミキサーにて混練りし、押出機を経て、成型、加硫し
てタイヤにした。
The present invention will be explained below with reference to Examples. As the rubber, styrene-butadiene copolymer rubber with a styrene content of 40% was used, and carbon black with an iodine adsorption amount (IA) of 140 mg/g was used at 90 parts by weight based on 100 parts of the rubber. Table 1 for calcium oxide
Powdered product VESTA-PP (manufactured by Inoue Lime Co., Ltd.) was mixed in varying amounts as shown in FIG. Granular VESTA-BS was used as calcium oxide treated with fatty acid, and CML21 (manufactured by Ohmi Kagaku Co., Ltd.) in paste form was used as calcium oxide treated with process oil. This mixture, to which a vulcanizing agent, filler, etc. were added, was kneaded in a Banbury mixer according to a conventional method, passed through an extruder, molded, and vulcanized to form a tire.

【0012】表1に示した配合のゴム組成物につき加硫
した後、動的粘弾性試験、加熱ブロー現象テスト、およ
び車両走行テストを行って評価した。粘弾性試験:粘弾
性は岩本製作所製の粘弾性測定機を用い、動的歪み5%
、周波数10HZ、温度70°Cの条件でtanδを測
定した。加熱ブロー現象テスト:10×10×4mmの
加硫ゴム試験片を温度を変えて設定した各テスト温度の
熱風循環式オーブン中に30分間放置後、試験片の切断
断面の気泡を観察して、気泡が発生し始めた温度をブロ
ーアウト温度とする方法で行った。したがって、ブロー
アウト温度が高いほど耐熱性が良いことになる。
[0012] After the rubber compositions having the formulations shown in Table 1 were vulcanized, they were evaluated by performing a dynamic viscoelasticity test, a heat blow phenomenon test, and a vehicle running test. Viscoelasticity test: Viscoelasticity was measured using a viscoelasticity measuring machine manufactured by Iwamoto Seisakusho at a dynamic strain of 5%.
, the tan δ was measured under the conditions of a frequency of 10 Hz and a temperature of 70°C. Heating blow phenomenon test: After leaving a 10 x 10 x 4 mm vulcanized rubber test piece in a hot air circulation oven set at various test temperatures for 30 minutes, observe the air bubbles on the cut section of the test piece. The blowout temperature was the temperature at which bubbles started to form. Therefore, the higher the blowout temperature, the better the heat resistance.

【0013】車両走行テスト:各配合のトレッドゴムを
用いた二輪車用タイヤであるサイズ380/600R1
7を二輪車の後輪に取付けて、1周が4.4kmのサー
キットの乾燥路面をできるだけ高速で、約時速270k
mになるよう走行し、フィーリング採点を行い、各タイ
ヤでグリップレベルがもっとも良いときの点数をグリッ
プ性能とした。また、このような高速で走り続けると走
行中ブローアウトにより急激にグリップ性能が低下する
が、そのときに至までの走行距離を耐ブローアウト性と
した。このグリップ性能、耐ブローアウト性は従来のト
レッドを付けたタイヤに対し、指数で表している。これ
らの両指数とも値が大きい方が性能が良いことを示すも
のである。
Vehicle running test: Size 380/600R1 motorcycle tires using tread rubber of various compositions
7 attached to the rear wheel of a motorcycle and run as fast as possible on the dry road surface of a circuit with one lap of 4.4km, at approximately 270km/h.
The tires were driven to achieve a maximum grip of m, and the feeling was scored, and the score when the grip level was the best for each tire was taken as the grip performance. Furthermore, if the vehicle continues to run at such high speeds, the grip performance will rapidly deteriorate due to blowouts during the run, but the distance traveled up to that point was defined as the blowout resistance. This grip performance and blowout resistance are expressed as an index compared to tires with conventional treads. The larger the value of both of these indexes, the better the performance.

【0014】[0014]

【表1】[Table 1]

【0015】表1に示した試験結果からも分かるように
、スチレン含有率の高いスチレン─ブタジエン共重合体
ゴムを用い、ヨウ素吸着量の大きいカーボンブラックを
適量使用したゴムに酸化カルシウムを1〜15重量部配
合したトレッドゴムは、グリップ性能を損なわず、ゴム
の温度が従来のゴム組成物では発泡を生じるまで上昇し
ても発泡せず、より高温にたえる。いわゆる、耐ブロー
アウト性が向上している。酸化カルシウムの配合量とし
て、より好ましくは5〜10重量部付近である。また、
酸化カルシウムを脂肪酸処理、またはプロセスオイル処
理を施したものでも同様な効果が得られることが分かっ
た。
As can be seen from the test results shown in Table 1, styrene-butadiene copolymer rubber with a high styrene content was used, and an appropriate amount of carbon black with a high iodine adsorption amount was used, and calcium oxide was added to the rubber by 1 to 15%. The tread rubber compounded in parts by weight does not impair grip performance, does not foam even when the temperature of the rubber rises to the point where conventional rubber compositions would foam, and can withstand higher temperatures. The so-called blowout resistance is improved. The amount of calcium oxide to be blended is more preferably around 5 to 10 parts by weight. Also,
It has been found that similar effects can be obtained by treating calcium oxide with fatty acids or process oil.

【0016】[0016]

【発明の効果】以上説明したようにこの発明のタイヤの
トレッド用ゴム組成物はタイヤにとって最も重要である
グリップ性能を保ち、しかも高速走行などにおける耐熱
性のきわめて良好なタイヤを提供することができる。そ
れによって、従来のタイヤにみられたような、連続走行
中にトレッドゴムの発熱からゴム内部に発生する気泡に
起因する、グリップ性能の低下、さらにはトレッド部の
破壊飛散といった大事故につながる危険を防止すること
ができる。
[Effects of the Invention] As explained above, the rubber composition for tire tread of the present invention maintains grip performance, which is most important for a tire, and can provide a tire that has extremely good heat resistance during high-speed running. . As a result, as with conventional tires, the tread rubber generates heat during continuous driving, causing air bubbles to be generated inside the rubber, resulting in a reduction in grip performance and even the risk of serious accidents such as the tread being broken and flying off. can be prevented.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】結合スチレンの合計量がスチレン─ブタジ
エン共重合体ゴムの30重量%以上である少なくとも1
種のスチレン─ブタジエン共重合体ゴムを含むジエン系
ゴム100重量部に対して、ヨウ素吸着量が1グラム当
たり90ミリグラム以上のカーボンブラック70重量部
以上250重量部以下および酸化カルシュウム単体また
は酸化カルシュウムを脂肪酸もしくはプロセスオイルで
処理した酸化カルシュウム1重量部以上15重量部以下
を配合することを特徴とするタイヤのトレッド用ゴム組
成物。
Claim 1: At least one compound in which the total amount of bound styrene is 30% by weight or more of the styrene-butadiene copolymer rubber.
70 parts by weight or more and 250 parts by weight or less of carbon black with an iodine adsorption amount of 90 mg or more per gram and calcium oxide alone or calcium oxide for 100 parts by weight of diene rubber containing styrene-butadiene copolymer rubber. A rubber composition for a tire tread, characterized in that it contains 1 part by weight or more and 15 parts by weight or less of calcium oxide treated with fatty acid or process oil.
JP2414704A 1990-12-26 1990-12-26 Rubber composition for tire tread Pending JPH04224839A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2414704A JPH04224839A (en) 1990-12-26 1990-12-26 Rubber composition for tire tread

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2414704A JPH04224839A (en) 1990-12-26 1990-12-26 Rubber composition for tire tread

Publications (1)

Publication Number Publication Date
JPH04224839A true JPH04224839A (en) 1992-08-14

Family

ID=18523154

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2414704A Pending JPH04224839A (en) 1990-12-26 1990-12-26 Rubber composition for tire tread

Country Status (1)

Country Link
JP (1) JPH04224839A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0770370A (en) * 1993-09-01 1995-03-14 Bridgestone Corp Rubber composition for tire tread
JPH0790124A (en) * 1993-09-24 1995-04-04 Bridgestone Corp Tire tread rubber composition
KR100411013B1 (en) * 2001-01-05 2003-12-18 금호타이어 주식회사 Carcass Rubber composition
EP1367092A3 (en) * 1994-08-19 2004-01-07 Bridgestone Corporation Rubber composition for tire treads
JP2006176579A (en) * 2004-12-21 2006-07-06 Bridgestone Corp Rubber composition and pneumatic tire using the same
US7432318B2 (en) 2004-01-30 2008-10-07 Sumitomo Rubber Industries, Ltd. Rubber composition for a tire and pneumatic tire using the same
KR101314554B1 (en) * 2010-11-26 2013-10-07 한국타이어 주식회사 Rubber composition for tire cord topping and tire manufactured by using the same
JP6209649B1 (en) * 2016-06-10 2017-10-04 南国興産株式会社 Filler for rubber compound

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0770370A (en) * 1993-09-01 1995-03-14 Bridgestone Corp Rubber composition for tire tread
JPH0790124A (en) * 1993-09-24 1995-04-04 Bridgestone Corp Tire tread rubber composition
EP1367092A3 (en) * 1994-08-19 2004-01-07 Bridgestone Corporation Rubber composition for tire treads
KR100411013B1 (en) * 2001-01-05 2003-12-18 금호타이어 주식회사 Carcass Rubber composition
US7432318B2 (en) 2004-01-30 2008-10-07 Sumitomo Rubber Industries, Ltd. Rubber composition for a tire and pneumatic tire using the same
JP2006176579A (en) * 2004-12-21 2006-07-06 Bridgestone Corp Rubber composition and pneumatic tire using the same
KR101314554B1 (en) * 2010-11-26 2013-10-07 한국타이어 주식회사 Rubber composition for tire cord topping and tire manufactured by using the same
JP6209649B1 (en) * 2016-06-10 2017-10-04 南国興産株式会社 Filler for rubber compound
JP2017218549A (en) * 2016-06-10 2017-12-14 南国興産株式会社 Filler for rubber compound

Similar Documents

Publication Publication Date Title
JP2005075856A (en) Rubber composition for tire
JP2011174027A (en) Rubber composition for tire tread and pneumatic tire using the same
JP2008184545A (en) Rubber composition and pneumatic tire using it
JPH04224839A (en) Rubber composition for tire tread
JP2010126671A (en) Rubber composition for tire tread
JP2930525B2 (en) Rubber composition for tire tread
EP0831123B1 (en) Racing tyre tread rubber composition
JP2004307749A (en) Sidewall rubber composition and pneumatic tire using the same
JP2004315746A (en) Rubber composition for tire and pneumatic tire using the composition
US5717016A (en) Caoutchouc mixture, tire tread manufactured therefrom and tire having this tread
JP2004196944A (en) Rubber composition for tyre tread
JPH07133377A (en) Rubber composition and tire made therefrom
JP4074164B2 (en) tire
JP4015844B2 (en) Additive for rubber composition, additive composition for rubber composition, rubber composition using the same, and tire
JP2944906B2 (en) Rubber composition, tire tread manufactured from the rubber composition, and tire having the tread
JP3240770B2 (en) Method for producing rubber composition
JPH01215838A (en) Rubber composition for tire tread
JPS58152030A (en) Rubber composition
JPH0790124A (en) Tire tread rubber composition
JPS6099144A (en) Rubber composition
JPS581734A (en) Rubber composition for tire cap tread
JP2006265400A (en) Method of manufacturing rubber composition and pneumatic tire using the same
JP2001335664A (en) Rubber composition for tire tread and pnewmatic tire using it
JP7534681B1 (en) Rubber composition for tires
JPH1060175A (en) Tire tread rubber composition