JP2000191839A - Rubber composition for tire tread - Google Patents

Rubber composition for tire tread

Info

Publication number
JP2000191839A
JP2000191839A JP10373066A JP37306698A JP2000191839A JP 2000191839 A JP2000191839 A JP 2000191839A JP 10373066 A JP10373066 A JP 10373066A JP 37306698 A JP37306698 A JP 37306698A JP 2000191839 A JP2000191839 A JP 2000191839A
Authority
JP
Japan
Prior art keywords
rubber
rubber composition
alkenylamide
tire tread
compound
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
JP10373066A
Other languages
Japanese (ja)
Inventor
Takeshi Ota
武 太田
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 JP10373066A priority Critical patent/JP2000191839A/en
Publication of JP2000191839A publication Critical patent/JP2000191839A/en
Pending 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
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/80Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86Optimisation of rolling resistance, e.g. weight reduction 

Landscapes

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

Abstract

PROBLEM TO BE SOLVED: To attain both decrease of rolling resistance and improvement of wet grip properties by admixing an N-alkenylamide compound with a rubber component. SOLUTION: With 100 pts.wt. of a rubber component such as a styrene- butadiene copolymer rubber(SBR) alone, a blend of the SBR with a natural rubber, a butadiene rubber or an isoprene rubber, and the like is admixed 1-10 pts.wt. of an alkenylamide compound represented by the formula (wherein R1 and R2 are each H or alkenyl and at least one of them is alkenyl) to obtain a rubber composition for a tire tread. As the alkenylamide compound can be exemplified N-allylbenzamide, N,N-diallylbenzamide, N-octadecenylbenzamide, N,N-dioctadecenylbenzamide, N-oleylbenzamide and the like. Into this rubber composition can be incorporated carbon black as a reinforcing agent, inorganic fillers such as silica, clay and the like, and other ingredients as required.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、転がり抵抗の低減
とウェットグリップ性の向上とを両立させたタイヤトレ
ッド用ゴム組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rubber composition for a tire tread which achieves both a reduction in rolling resistance and an improvement in wet grip.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】近
年、タイヤの性能に対する要求が高まってきており、と
くに安全性に関するグリップ性能の向上と低燃費性に関
する転がり抵抗の低減とは、最も注目されている課題で
ある。
2. Description of the Related Art In recent years, there has been an increasing demand for performance of tires. In particular, improvement in grip performance related to safety and reduction in rolling resistance related to low fuel consumption have received the most attention. Is an issue.

【0003】しかし、グリップ性能の向上と転がり抵抗
の低減とは、相反する性能であり、一方の性能を損わず
に残るもう一方の性能を、あるいは両方の性能を向上さ
せることは困難である。
[0003] However, improvement in grip performance and reduction in rolling resistance are contradictory performances, and it is difficult to improve one or the other remaining without deteriorating the performance. .

【0004】グリップ性能の向上に対しては、N−アル
キルアミド類、N−フェニルアミド類をゴム組成物に配
合することが提案されているが(特開平4−24955
1号公報)、高温でのtanδが高くなるため、低燃費
性能がわるく、グリップ性能の向上と転がり抵抗の低減
との両立という面で満足のいくものではない。
In order to improve grip performance, it has been proposed to incorporate N-alkylamides and N-phenylamides into a rubber composition (JP-A-4-24955).
No. 1), the tan δ at high temperatures is increased, so that the fuel efficiency is poor, and it is not satisfactory in terms of both improving the grip performance and reducing the rolling resistance.

【0005】[0005]

【課題を解決するための手段】本発明は、タイヤトレッ
ド用ゴム組成物にN−アルキルアミド類、N−フェニル
アミド類ではなく、N−アルケニルアミド化合物を配合
することにより、転がり抵抗の低減とグリップ性能、と
くにウェット路面でのグリップ性能の向上とを両立させ
たものである。
DISCLOSURE OF THE INVENTION The present invention provides a rubber composition for a tire tread, in which an N-alkenyl amide compound is added to the rubber composition instead of an N-alkyl amide or N-phenyl amide to reduce rolling resistance. It achieves both improved grip performance, especially on wet road surfaces.

【0006】すなわち、本発明は、ゴム成分100重量
部(以下、部という)に対し、一般式(1):
That is, the present invention relates to 100 parts by weight (hereinafter referred to as "parts") of a rubber component, and the general formula (1):

【0007】[0007]

【化2】 Embedded image

【0008】(R1、R2は、水素原子またはアルケニル
基であり、R1とR2とは同じでも異なっていてもよい
が、少なくともどちらか一方はアルケニル基)で表わさ
れるアルケニルアミド化合物1〜10部を配合したタイ
ヤトレッド用ゴム組成物に関する。
The alkenylamide compound 1 represented by the formula (R 1 and R 2 are hydrogen atoms or alkenyl groups, and R 1 and R 2 may be the same or different, but at least one of them is an alkenyl group) The present invention relates to a rubber composition for a tire tread, which contains 10 to 10 parts.

【0009】[0009]

【発明の実施の形態】本発明のタイヤトレッド用ゴム組
成物のゴム成分には、従来からタイヤトレッドに用いら
れている公知の原料ゴムを、とくに限定なく使用するこ
とができる。
BEST MODE FOR CARRYING OUT THE INVENTION As the rubber component of the rubber composition for a tire tread of the present invention, a known raw rubber conventionally used for a tire tread can be used without any particular limitation.

【0010】前記原料ゴムとしては、たとえば天然ゴム
(NR)やスチレン−ブタジエン共重合体ゴム(SB
R)、ブタジエンゴム(BR)、エチレン−プロピレン
−ジエン共重合体ゴム(EPDM)、イソプレンゴム
(IR)、アクリロニトリル−ブタジエン共重合体ゴム
(NBR)、クロロプレンゴム(CR)、ブチルゴム
(IIR)、ハロゲン化ブチルゴム(X−IIR)など
の合成ゴムなどがあげられる。これらは単独で用いても
よく、2種以上を組み合わせて用いてもよい。これらの
うちでは、耐摩耗性、グリップ性能、転がり抵抗などタ
イヤ性能のバランスが良い点から、SBR単独、SBR
とNR、BR、IRとのブレンドが好ましい。
Examples of the raw rubber include natural rubber (NR) and styrene-butadiene copolymer rubber (SB).
R), butadiene rubber (BR), ethylene-propylene-diene copolymer rubber (EPDM), isoprene rubber (IR), acrylonitrile-butadiene copolymer rubber (NBR), chloroprene rubber (CR), butyl rubber (IIR), And synthetic rubbers such as halogenated butyl rubber (X-IIR). These may be used alone or in combination of two or more. Among these, SBR alone, SBR alone, because of good balance of tire performance such as abrasion resistance, grip performance, and rolling resistance
And NR, BR, and IR are preferred.

【0011】なお、タイヤのグリップ性能の向上のため
に最近では、とくにスチレン含有量の高いSBRが好ま
しく用いられているが、本発明においてもこのようなス
チレン含有量の高いSBRを用いることができる。本発
明は、たとえばスチレン含有量20〜50%のSBRに
対しても効果的である。前記SBRは、溶液重合型であ
っても乳化重合型であっても差し支えない。
In recent years, in particular, SBR having a high styrene content has been preferably used in order to improve the grip performance of a tire. In the present invention, such an SBR having a high styrene content can be used. . The present invention is also effective for SBR having a styrene content of 20 to 50%, for example. The SBR may be of a solution polymerization type or an emulsion polymerization type.

【0012】本発明のタイヤトレッド用ゴム組成物に
は、転がり抵抗の低減とグリップ性能、とくにウェット
路面でのグリップ性能の向上とを両立させるために、一
般式(1):
The rubber composition for a tire tread of the present invention has a general formula (1) for achieving both a reduction in rolling resistance and an improvement in grip performance, particularly, an improvement in grip performance on wet road surfaces.

【0013】[0013]

【化3】 Embedded image

【0014】(R1、R2は、水素原子またはアルケニル
基であり、R1とR2とは同じでも異なっていてもよい
が、少なくともどちらか一方はアルケニル基)で表わさ
れるアルケニルアミド化合物が配合される。アルケニル
アミド化合物がアルケニル基を有するため、転がり抵抗
の低減とウェットグリップ性能の向上とを両立させるこ
とができる。
The alkenylamide compound represented by (R 1 and R 2 are hydrogen atoms or alkenyl groups, and R 1 and R 2 may be the same or different, but at least one of them is an alkenyl group) Be blended. Since the alkenylamide compound has an alkenyl group, it is possible to achieve both a reduction in rolling resistance and an improvement in wet grip performance.

【0015】前記アルケニル基としては、直鎖状であっ
ても分枝状であってもよいが、化合物としての入手のし
易さの点から、炭素数3〜22のものが好ましい。
The alkenyl group may be linear or branched, but preferably has 3 to 22 carbon atoms from the viewpoint of availability as a compound.

【0016】前記アルケニル基の具体例としては、たと
えばアリル基、イソプロペニル基、ブテニル基、ペンテ
ニル基、ヘキセニル基、ヘプテニル基、オクテニル基、
ノネニル基、デセニル基、ウンデセニル基、ドデセニル
基、トリデセニル基、テトラデセニル基、ペンタデセニ
ル基、ヘキサデセニル基、ヘプタデセニル基、オクタデ
セニル基、ノナデセニル基、エイコセニル基、ドコセニ
ル基、オレイル基などがあげられる。これらのうちでは
アルケニルアミド化合物の原料となるアルケニルアミン
の入手のし易さから、アリル基、オクタデセニル基、オ
レイル基などが好ましい。
Specific examples of the alkenyl group include, for example, allyl, isopropenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl,
Nonenyl, decenyl, undecenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl, heptadecenyl, octadecenyl, nonadecenyl, eicosenyl, docosenyl, oleyl and the like. Among these, an allyl group, an octadecenyl group, an oleyl group, and the like are preferable because alkenylamine serving as a raw material of the alkenylamide compound is easily available.

【0017】前記アルケニルアミド化合物の代表例とし
ては、たとえばN−アリルベンズアミド、N,N−ジア
リルベンズアミド、N−オクタデセニルベンズアミド、
N,N−ジオクタデセニルベンズアミド、N−オレイル
ベンズアミドなどがあげられる。
Representative examples of the alkenylamide compound include, for example, N-allylbenzamide, N, N-diallylbenzamide, N-octadecenylbenzamide,
N, N-dioctadecenylbenzamide, N-oleylbenzamide and the like can be mentioned.

【0018】前記アルケニルアミド化合物の使用量とし
ては、添加による効果と性能とのバランスの点から、前
記ゴム成分100部に対し、1〜10部、好ましくは3
〜8部である。1部より少ないと、アルケニルアミド化
合物の添加効果が充分に得られず、10部より多く添加
しても、グリップ性能の向上効果は小さくなり、未加硫
ゴム組成物の焼け(スコーチ)時間が短くなるため、成
形加工が困難となり、また配合のコストが上昇するた
め、実用的ではない。
The amount of the alkenylamide compound to be used is 1 to 10 parts, preferably 3 parts, per 100 parts of the rubber component from the viewpoint of the balance between the effect of the addition and the performance.
~ 8 parts. If the amount is less than 1 part, the effect of adding the alkenylamide compound is not sufficiently obtained, and if the amount is more than 10 parts, the effect of improving the grip performance is reduced, and the burning (scorch) time of the unvulcanized rubber composition is reduced. Since the length is short, molding is difficult, and the cost of compounding increases, which is not practical.

【0019】本発明のタイヤトレッド用ゴム組成物に
は、補強剤としてゴム工業で通常使用されているカーボ
ンブラックや、シリカ、クレーなどの無機充填剤を単独
で、またはブレンドして使用してもよい。
The rubber composition for a tire tread of the present invention may be used alone or as a blend of inorganic fillers such as carbon black, silica and clay commonly used in the rubber industry as reinforcing agents. Good.

【0020】前記カーボンブラックの具体例としては、
たとえばHAF、ISAF、SAFなどがあげられる
が、これらに限定されるものではない。
Specific examples of the carbon black include:
Examples include, but are not limited to, HAF, ISAF, SAF, and the like.

【0021】前記シリカとしては、たとえば乾式法シリ
カ(無水ケイ酸)、湿式法シリカ(含水ケイ酸)などが
あげられ、とくに制限はないが、湿式法シリカが好まし
い。湿式法シリカの好ましい例としては、デグッサ社製
Ultrasil VN3(商品名)、日本シリカ
(株)製ニップシールVN3 AQ(商品名)などがあ
げられる。
Examples of the silica include dry-process silica (silicic anhydride) and wet-process silica (hydrous silicic acid). There is no particular limitation, but wet-process silica is preferred. Preferred examples of the wet process silica include Ultrasil VN3 (trade name) manufactured by Degussa Corporation and Nip Seal VN3 AQ (trade name) manufactured by Nippon Silica Co., Ltd.

【0022】前記クレーとしては、たとえばカオリン質
クレー、パイロフィライト質クレー、セリサイト質クレ
ー、焼成クレーなどがあげられる。
Examples of the clay include kaolin clay, pyrophyllite clay, sericite clay and calcined clay.

【0023】また、本発明のタイヤトレッド用ゴム組成
物には、その他ゴム工業で通常使用されている老化防止
剤、加硫剤、加硫促進剤、加硫遅延剤、しゃっ解剤、加
工助剤、ワックス、プロセスオイル、ステアリン酸、粘
着付与剤などの1種以上を必要に応じて併用してもよ
い。また、シリカなどを補強剤として使用する場合、シ
リカの分散性向上のために、ビス(3−トリエトキシシ
リルプロピル)テトラスルフィドのようなシランカップ
リング剤を用いることもできる。
The rubber composition for a tire tread of the present invention may further contain an antioxidant, a vulcanizing agent, a vulcanization accelerator, a vulcanization retarder, a peptizing agent, One or more of auxiliaries, waxes, process oils, stearic acid, tackifiers and the like may be used in combination as needed. When silica is used as a reinforcing agent, a silane coupling agent such as bis (3-triethoxysilylpropyl) tetrasulfide can be used to improve the dispersibility of silica.

【0024】前記ゴム成分、アルケニルアミド化合物、
一般には無機充填剤および必要に応じてその他の成分を
配合し、バンバリーミキサーやオープンロールなどを用
いて常法により得られるゴム組成物は、タイヤトレッド
用ゴム組成物として好適に使用することができる。ま
た、前記組成物をタイヤトレッドに用いることにより、
転がり抵抗の低減とウェットグリップ性とを両立させた
タイヤを得ることができる。
The rubber component, an alkenylamide compound,
In general, a rubber composition obtained by blending an inorganic filler and other components as necessary, and using a Banbury mixer, an open roll, or the like, can be suitably used as a rubber composition for a tire tread. . Further, by using the composition for a tire tread,
A tire having both reduced rolling resistance and wet grip properties can be obtained.

【0025】[0025]

【実施例】つぎに、本発明のタイヤトレッド用ゴム組成
物を、具体例に基づいてさらに詳細に説明するが、本発
明は、これらに限定されるものではない。
EXAMPLES Next, the rubber composition for a tire tread of the present invention will be described in more detail with reference to specific examples, but the present invention is not limited thereto.

【0026】なお、実施例および比較例で用いた組成物
の原料および評価方法を、以下にまとめて示す。
The raw materials and evaluation methods of the compositions used in the examples and comparative examples are summarized below.

【0027】SBR:住友化学(株)製のSBR150
2 BR:宇部興産(株)製のBR150B NR:一般的なRSS#3グレード N220:三菱化学(株)製のN220 N351:昭和キャボット社製のN351 酸化亜鉛:三井金属鉱業(株)製の酸化亜鉛2種 WAX:日本精蝋(株)製のオゾエース0355 老化防止剤:住友化学(株)製のアンチゲン6C プロセスオイル:ジャパンエナジー社製のプロセスX1
40 硫黄:軽井沢硫黄(株)製の粉末硫黄 加硫促進剤:大内新興化学(株)製のノクセラーNS
SBR: SBR150 manufactured by Sumitomo Chemical Co., Ltd.
2 BR: BR150B manufactured by Ube Industries, Ltd. NR: General RSS # 3 grade N220: N220 manufactured by Mitsubishi Chemical Corporation N351: N351 manufactured by Showa Cabot Co., Ltd. Zinc oxide: oxidation manufactured by Mitsui Mining & Smelting Co., Ltd. Two kinds of zinc WAX: Ozoace 0355 manufactured by Nippon Seiro Co., Ltd. Antioxidant: Antigen 6C manufactured by Sumitomo Chemical Co., Ltd. Process oil: Process X1 manufactured by Japan Energy
40 Sulfur: Powder sulfur manufactured by Karuizawa Sulfur Co., Ltd. Vulcanization accelerator: Noxeller NS manufactured by Ouchi Shinko Chemical Co., Ltd.

【0028】(硬さ(Hs))JIS K6253に準
じて、タイプAデュロメーターで試作したタイヤのトレ
ッドの硬度を測定した。
(Hardness (Hs)) According to JIS K6253, the tread hardness of a prototype tire was measured with a type A durometer.

【0029】N−アルケニル類を配合する場合、単に添
加するとゴム硬度がさがるため、プロセスオイルや加硫
剤を変量させ、各実施例および比較例のトレッドの硬度
が大きくかわらないように調整した。
When N-alkenyls are blended, the rubber hardness is reduced by simply adding them, so that the process oil and the vulcanizing agent are varied to adjust the tread hardness of each of the examples and comparative examples so as not to vary greatly.

【0030】(ウェットグリップ性能(実車操縦安定
性))試作したタイヤを実車に装着し、テストコースに
おいて、アスファルト路面上、ならびに水を散布した路
面上にて、テストドライバーによる官能評価により、操
縦安定性の評価を行なった。評価は、性能を指数で示し
た。指数の大きい方が、性能が良いことを示す。
(Wet grip performance (actual vehicle operation stability)) The prototype tire was mounted on an actual vehicle, and on a test course, on a asphalt road surface and on a road surface sprayed with water, the steering stability was evaluated by a sensory evaluation by a test driver. The sex was evaluated. The evaluation indicated the performance by an index. A larger index indicates better performance.

【0031】(転がり抵抗(低燃費性能))(株)神戸
製鋼所製の試験機を用い、荷重345kg、内圧200
kPa、速度80km/hで試作したタイヤを走行させ
て、転がり抵抗を測定し、低燃費性能を指数で示した。
指数が大きいほど、転がり抵抗が低く良好なことを示
す。
(Rolling resistance (low fuel consumption performance)) Using a testing machine manufactured by Kobe Steel, Ltd., load 345 kg, internal pressure 200
Rolling resistance was measured by running a prototype tire at kPa and a speed of 80 km / h, and the fuel economy performance was indicated by an index.
The higher the index, the lower the rolling resistance and the better.

【0032】実施例1〜3および比較例1〜2 表1に記載の原料を、表1に記載の組成になるように配
合し、バンバリーミキサーおよびオープンロールを用い
て、常法により、すなわち、硫黄および加硫促進剤以外
の原料をバンバリーミキサーで100〜150℃で4分
間混練りしたのち、90℃で硫黄と加硫促進剤を加えて
オープンロールで3分間混練りしてタイヤトレッド用グ
リーンゴム組成物を得た。なお、N−オレイルベンズア
ミドとプロセスオイルとの総量を、各配合とも同じにし
たのは、トレッドの硬さ(Hs)を統一して硬さの違い
が他の評価に与える影響をのぞくためである。得られた
組成物をタイヤトレッドに適用し、加硫して、195/
65R15 91H D8Hのタイヤを常法により試作
した。
Examples 1 to 3 and Comparative Examples 1 to 2 The raw materials shown in Table 1 were blended so as to have the composition shown in Table 1, and were prepared by a conventional method using a Banbury mixer and an open roll, that is, Raw materials other than sulfur and the vulcanization accelerator are kneaded with a Banbury mixer at 100 to 150 ° C. for 4 minutes, and then sulfur and the vulcanization accelerator are added at 90 ° C. and kneaded with an open roll for 3 minutes to obtain a green tire tread. A rubber composition was obtained. The reason why the total amount of N-oleylbenzamide and process oil was the same for each blend was to unify the hardness (Hs) of the tread and to exclude the influence of the difference in hardness on other evaluations. . The resulting composition is applied to a tire tread and vulcanized to give 195 /
A tire of 65R15 91H D8H was prototyped by a conventional method.

【0033】前記タイヤを用いて、硬さ、ウェットグリ
ップ性能および転がり抵抗の評価を行なった。結果を表
1に示す。
Using the tires described above, hardness, wet grip performance and rolling resistance were evaluated. Table 1 shows the results.

【0034】[0034]

【表1】 [Table 1]

【0035】表1の結果から、N−オレイルベンズアミ
ドを添加した実施例1〜3では、いずれもグリップ性能
や低燃費性能が、N−オレイルベンズアミドを添加して
いない比較例1の場合に比べて、向上していることがわ
かる。また、1〜10部程度の添加が両性能とそのバラ
ンスが良好で、N−オレイルベンズアミドを5部添加し
た実施例2が最もすぐれていることがわかる。添加量が
10部をこえる比較例2では、低燃費性能、ウェットグ
リップ性能が実施例3より低下している。
From the results in Table 1, it can be seen that in Examples 1 to 3 in which N-oleylbenzamide was added, the grip performance and fuel efficiency were all lower than those in Comparative Example 1 in which N-oleylbenzamide was not added. It can be seen that it has improved. In addition, it can be seen that the addition of about 1 to 10 parts has a good balance between the two performances, and that Example 2 in which 5 parts of N-oleylbenzamide is added is most excellent. In Comparative Example 2 in which the addition amount exceeds 10 parts, the fuel economy performance and the wet grip performance are lower than in Example 3.

【0036】実施例4、5および比較例3、4 表2に記載の原料を、表2に記載の組成になるように配
合した以外は、実施例1と同様にしてタイヤトレッド用
グリーンゴム組成物を得、同様に評価した。なお、プロ
セスオイルと加硫促進剤の配合量を各配合で変化させた
のは、トレッドの硬さ(Hs)を統一するためである。
Examples 4 and 5 and Comparative Examples 3 and 4 A green rubber composition for a tire tread was prepared in the same manner as in Example 1 except that the raw materials shown in Table 2 were blended so as to have the composition shown in Table 2. Was obtained and evaluated in the same manner. The reason why the blending amounts of the process oil and the vulcanization accelerator were changed in each blending is to unify the hardness (Hs) of the tread.

【0037】[0037]

【表2】 [Table 2]

【0038】表1の場合と同様に、N−オレイルベンズ
アミドを添加した実施例4、5は、比較例3よりもウェ
ットグリップ性能ならびに低燃費性能が向上しており、
添加量が多すぎる比較例4の場合には、ウェットグリッ
プ性能、低燃費性能の向上が見られないことがわかる。
As in the case of Table 1, Examples 4 and 5 to which N-oleylbenzamide was added had improved wet grip performance and low fuel consumption performance as compared with Comparative Example 3.
In the case of Comparative Example 4 where the addition amount is too large, it can be seen that the wet grip performance and the fuel economy performance are not improved.

【0039】[0039]

【発明の効果】本発明のタイヤトレッド用ゴム組成物に
よれば、転がり抵抗の低減とウェットグリップ性とを両
立させたタイヤを得ることができる。
According to the rubber composition for a tire tread of the present invention, a tire having both reduced rolling resistance and wet grip properties can be obtained.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ゴム成分100重量部に対し、一般式
(1): 【化1】 (R1、R2は、水素原子またはアルケニル基であり、R
1とR2とは同じでも異なっていてもよいが、少なくとも
どちらか一方はアルケニル基)で表わされるアルケニル
アミド化合物1〜10重量部を配合したタイヤトレッド
用ゴム組成物。
1. A rubber composition of the general formula (1): (R 1 and R 2 are a hydrogen atom or an alkenyl group;
1 and R 2 may be the same or different, but at least one of them is an alkenyl group) and a rubber composition for a tire tread containing 1 to 10 parts by weight of an alkenylamide compound represented by the formula (1).
JP10373066A 1998-12-28 1998-12-28 Rubber composition for tire tread Pending JP2000191839A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10373066A JP2000191839A (en) 1998-12-28 1998-12-28 Rubber composition for tire tread

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10373066A JP2000191839A (en) 1998-12-28 1998-12-28 Rubber composition for tire tread

Publications (1)

Publication Number Publication Date
JP2000191839A true JP2000191839A (en) 2000-07-11

Family

ID=18501522

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10373066A Pending JP2000191839A (en) 1998-12-28 1998-12-28 Rubber composition for tire tread

Country Status (1)

Country Link
JP (1) JP2000191839A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100505735B1 (en) * 2002-12-09 2005-08-03 한국타이어 주식회사 Rubber composition for tire tread
KR100527305B1 (en) * 2002-12-24 2005-11-09 금호타이어 주식회사 Insulation rubber composition for bias tire of truck or bus having improved properties in heat resistance
EP1682335A1 (en) * 2003-10-27 2006-07-26 TreadFx, LLC Apparatus and method for reducing the likelihood of vehicle rollover
JPWO2005012365A1 (en) * 2003-08-04 2006-09-14 田中 康之 Natural rubber from which protein has been removed, its composition and use
CN103205028A (en) * 2013-04-24 2013-07-17 衡水中铁建工程橡胶有限责任公司 Organic clay rubber composite material for laminated rubber supporting seat and preparation process thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0477536A (en) * 1990-07-13 1992-03-11 Bridgestone Corp Rubber composition
JPH04249551A (en) * 1991-01-07 1992-09-04 Sumitomo Chem Co Ltd Rubber composition
JPH0539382A (en) * 1991-08-06 1993-02-19 Sumitomo Chem Co Ltd Rubber composition
WO1997035918A2 (en) * 1996-06-26 1997-10-02 Bridgestone Corporation Rubber compositions
JP2000017113A (en) * 1998-06-30 2000-01-18 Sumitomo Chem Co Ltd Rubber composition and improvement of temperature dependency of rubber dynamic modulus

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0477536A (en) * 1990-07-13 1992-03-11 Bridgestone Corp Rubber composition
JPH04249551A (en) * 1991-01-07 1992-09-04 Sumitomo Chem Co Ltd Rubber composition
JPH0539382A (en) * 1991-08-06 1993-02-19 Sumitomo Chem Co Ltd Rubber composition
WO1997035918A2 (en) * 1996-06-26 1997-10-02 Bridgestone Corporation Rubber compositions
JP2000017113A (en) * 1998-06-30 2000-01-18 Sumitomo Chem Co Ltd Rubber composition and improvement of temperature dependency of rubber dynamic modulus

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100505735B1 (en) * 2002-12-09 2005-08-03 한국타이어 주식회사 Rubber composition for tire tread
KR100527305B1 (en) * 2002-12-24 2005-11-09 금호타이어 주식회사 Insulation rubber composition for bias tire of truck or bus having improved properties in heat resistance
JPWO2005012365A1 (en) * 2003-08-04 2006-09-14 田中 康之 Natural rubber from which protein has been removed, its composition and use
JP4662848B2 (en) * 2003-08-04 2011-03-30 住友ゴム工業株式会社 Natural rubber from which protein has been removed, rubber composition for tire and tire
EP1682335A1 (en) * 2003-10-27 2006-07-26 TreadFx, LLC Apparatus and method for reducing the likelihood of vehicle rollover
EP1682335A4 (en) * 2003-10-27 2007-12-12 Treadfx Llc Apparatus and method for reducing the likelihood of vehicle rollover
CN103205028A (en) * 2013-04-24 2013-07-17 衡水中铁建工程橡胶有限责任公司 Organic clay rubber composite material for laminated rubber supporting seat and preparation process thereof

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