JP2000080206A - Rubber composition for tire tread - Google Patents
Rubber composition for tire treadInfo
- Publication number
- JP2000080206A JP2000080206A JP10248462A JP24846298A JP2000080206A JP 2000080206 A JP2000080206 A JP 2000080206A JP 10248462 A JP10248462 A JP 10248462A JP 24846298 A JP24846298 A JP 24846298A JP 2000080206 A JP2000080206 A JP 2000080206A
- Authority
- JP
- Japan
- Prior art keywords
- water
- rubber composition
- weight
- tire tread
- 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.)
- Withdrawn
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 39
- 239000005060 rubber Substances 0.000 title claims abstract description 39
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000011347 resin Substances 0.000 claims abstract description 22
- 229920005989 resin Polymers 0.000 claims abstract description 22
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 16
- 239000006229 carbon black Substances 0.000 claims abstract description 12
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 6
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 6
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 6
- 239000011630 iodine Substances 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims abstract description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 6
- 238000001179 sorption measurement Methods 0.000 claims abstract description 6
- 239000002250 absorbent Substances 0.000 claims description 8
- 238000013329 compounding Methods 0.000 claims description 2
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 abstract description 3
- 230000000694 effects Effects 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 6
- 229920002857 polybutadiene Polymers 0.000 description 6
- 238000005096 rolling process Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- 229920003048 styrene butadiene rubber Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- 230000005611 electricity Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 229920003049 isoprene rubber Polymers 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- 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
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol 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
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- ATYBNKYOXTWSBY-UHFFFAOYSA-N ethoxy-[3-(3-ethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[SiH2]CCCSSSSCCC[SiH2]OCC ATYBNKYOXTWSBY-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000012360 testing method Methods 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
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Tires In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、タイヤトレッド用
ゴム組成物に関する。[0001] The present invention relates to a rubber composition for a tire tread.
【0002】[0002]
【従来の技術】従来から、タイヤの転がり抵抗とウェッ
トグリップ性を両立するために、タイヤトレッド用ゴム
組成物にカーボンブラックを配合せず、シリカのみを配
合することが行なわれている。2. Description of the Related Art Conventionally, in order to achieve both rolling resistance and wet grip performance of a tire, it has been practiced to compound only silica without compounding carbon black into a rubber composition for a tire tread.
【0003】しかし、このシリカのみを含むゴム組成物
をタイヤトレッドに適用すると、シリカが導電性に劣る
ことから自動車に静電気を蓄積させ、ラジオノイズや電
気系統への害を発生させるという問題があった。また、
帯電している静電気が一度に放電すると火花が発生し、
給油時には燃料に引火する可能性もあった。However, when a rubber composition containing only silica is applied to a tire tread, there is a problem in that silica has poor conductivity, causing static electricity to accumulate in an automobile, causing radio noise and harm to an electric system. Was. Also,
Sparks occur when the charged static electricity is discharged at once,
At the time of refueling, the fuel could ignite.
【0004】かかる帯電を防止するために、ポリエチレ
ングリコールエステルなどの帯電防止剤をタイヤトレッ
ド用ゴム組成物に配合することが行なわれているが、配
合量が少ないと改善の効果が小さく、配合量が多くても
改善の効果は充分ではなくかつ耐摩耗性などのほかの性
能を低下させるという問題があった。[0004] In order to prevent such electrification, an antistatic agent such as polyethylene glycol ester is blended into a rubber composition for a tire tread. However, there is a problem that the effect of improvement is not sufficient even if the content is large, and that other performances such as abrasion resistance are lowered.
【0005】ところで、静電気は一般に乾燥した状態で
強く帯電し、湿度が高い条件下では空気中の水分を媒介
にして放電される。[0005] Incidentally, static electricity is generally strongly charged in a dry state, and is discharged through moisture in the air under high humidity conditions.
【0006】そこで、本発明者らは、タイヤトレッド用
ゴム組成物に保水性を付与してタイヤトレッドの表面の
放電性を高めれば、帯電しにくく電気抵抗の小さいタイ
ヤを提供し得ることに着目し、本発明を完成するに至っ
た。Accordingly, the present inventors have paid attention to the fact that if the rubber composition for a tire tread is imparted with water retention to enhance the discharge property of the surface of the tire tread, a tire which is hardly charged and has a small electric resistance can be provided. Thus, the present invention has been completed.
【0007】なお、特開昭60−259503号明細書
記載のタイヤを構成するゴム組成物には、スキッド効果
を向上させるために吸水剤が配合されている。しかし、
ここで用いられている吸水剤は水不溶性の親水性物質で
あり、水溶性樹脂に比して保水性に劣るという問題があ
る。The rubber composition constituting the tire described in Japanese Patent Application Laid-Open No. 60-259503 contains a water absorbing agent in order to improve the skid effect. But,
The water-absorbing agent used here is a water-insoluble hydrophilic substance, and has a problem that it is inferior in water retention as compared with a water-soluble resin.
【0008】[0008]
【発明が解決しようとする課題】すなわち、本発明の目
的は、電気抵抗の小さいタイヤトレッドを提供し得る放
電性の高いゴム組成物を得ることにある。That is, an object of the present invention is to provide a rubber composition having a high discharge property capable of providing a tire tread having a small electric resistance.
【0009】[0009]
【課題を解決するための手段】本発明は、ゴム成分10
0重量部に対し、シリカを50〜150重量部、シラン
カップリング剤を4〜15重量部および水溶性吸水性樹
脂を5〜20重量部含んでなるタイヤトレッド用ゴム組
成物に関する。According to the present invention, there is provided a rubber component comprising:
The present invention relates to a rubber composition for a tire tread, comprising 50 to 150 parts by weight of silica, 4 to 15 parts by weight of a silane coupling agent, and 5 to 20 parts by weight of a water-soluble water-absorbent resin with respect to 0 parts by weight.
【0010】この場合、ヨウ素吸着量が80mg/g以
上のカーボンブラックの配合量が10重量部以下である
のが好ましい。In this case, the amount of carbon black having an iodine adsorption of 80 mg / g or more is preferably 10 parts by weight or less.
【0011】また、水溶性吸水性樹脂の形状が粒子状で
あり、その粒径が20〜100μmであるのが好まし
い。It is preferable that the shape of the water-soluble water-absorbent resin is particulate, and the particle size is 20 to 100 μm.
【0012】また、水溶性吸水性樹脂がポリビニルアル
コールであるのが好ましい。Preferably, the water-soluble water-absorbing resin is polyvinyl alcohol.
【0013】[0013]
【発明の実施の形態】冒頭で述べたとおり、本発明の最
大の特徴は、タイヤトレッド用ゴム組成物に水溶性吸水
性樹脂を配合することにより保水性を付与し、得られる
タイヤトレッドの水分を含む大気中への放電性を高め、
電気抵抗の低いタイヤトレッドを提供することにある。
また、水溶性の吸水性樹脂を用いることにより、タイヤ
と路面との間の水膜に溶出し、ウェットグリップ性が向
上するという利点を得ることもできる。BEST MODE FOR CARRYING OUT THE INVENTION As described at the outset, the most significant feature of the present invention is that a rubber composition for a tire tread is blended with a water-soluble water-absorbent resin to impart water retention, and the resulting tire tread has a water content. To increase the discharge to the atmosphere including
It is to provide a tire tread with low electric resistance.
In addition, by using a water-soluble water-absorbing resin, it is possible to obtain an advantage that the water-soluble resin is eluted into a water film between the tire and the road surface, and wet grip properties are improved.
【0014】本発明において用いることのできる水溶性
吸水性樹脂は、得られるゴム組成物に保水性を付与して
放電性を向上させ、徐々に路面との間の水に溶出するも
のが好ましく、具体的にはポリビニルアルコール、メチ
ルセルロース、ヒドロキシエチルセルロースおよびソジ
ウムカルボキシセルロースなどの水溶性セルロース誘導
体などがあげられる。これらのなかでも、価格と効果の
バランスという点から、ポリビニルアルコールを用いる
のが好ましい。The water-soluble water-absorbing resin that can be used in the present invention is preferably one that imparts water retention to the obtained rubber composition to improve dischargeability and gradually elutes into water between the road surface and the resin. Specific examples include water-soluble cellulose derivatives such as polyvinyl alcohol, methyl cellulose, hydroxyethyl cellulose and sodium carboxy cellulose. Among these, it is preferable to use polyvinyl alcohol from the viewpoint of the balance between price and effect.
【0015】また、本発明において用いる水溶性吸水性
樹脂の形状としては、ゴム組成物中で均一に分散し得る
形状であればよく、たとえば粒子状、短繊維状などがあ
げられる。The shape of the water-soluble water-absorbing resin used in the present invention may be any shape as long as it can be uniformly dispersed in the rubber composition, and examples thereof include a particle shape and a short fiber shape.
【0016】水溶性吸水性樹脂の寸法は、得られるゴム
組成物中にける分散性を損なわない範囲であればよく、
特に粒子状の場合、粒径は20〜100μmであるのが
好ましい。100μmを超えると破壊核となってゴム組
成物の強度を低下させ、また20μm未満の場合は分散
性に劣るからである。さらに、強度と分散性のバランス
の点から、20〜60μmであるのが特に好ましい。The size of the water-soluble water-absorbing resin may be within a range that does not impair the dispersibility in the obtained rubber composition.
In particular, in the case of particles, the particle diameter is preferably 20 to 100 μm. If it exceeds 100 μm, it becomes a breaking nucleus to lower the strength of the rubber composition, and if it is less than 20 μm, the dispersibility is poor. Further, from the viewpoint of the balance between the strength and the dispersibility, it is particularly preferred that the thickness is 20 to 60 μm.
【0017】かかる水溶性吸水性樹脂の配合量として
は、後述するゴム成分100重量部に対して5〜20重
量部であればよい。5重量部未満であると、トレッド表
面に存在する水溶性吸水性樹脂の量が少なくなって充分
な保水性および放電性を得ることができず、得られるタ
イヤの電気抵抗の低減を期待できないこととなり、また
20重量部を超えると得られるトレッドの耐摩耗性に劣
るからである。さらに、放電性と耐摩耗性のバランスと
いう点から、5〜10重量部であるのが好ましい。The amount of the water-soluble water-absorbing resin may be 5 to 20 parts by weight based on 100 parts by weight of a rubber component described later. When the amount is less than 5 parts by weight, the amount of the water-soluble water-absorbent resin present on the tread surface is reduced, so that sufficient water retention and discharge properties cannot be obtained, and reduction in electric resistance of the obtained tire cannot be expected. The reason is that if it exceeds 20 parts by weight, the obtained tread has poor abrasion resistance. Further, the amount is preferably 5 to 10 parts by weight from the viewpoint of a balance between discharge performance and wear resistance.
【0018】本発明において用いることのできるゴム成
分としては、従来からタイヤトレッドに適用されていた
ものであれば特に制限はなく、たとえば天然ゴム(N
R)、スチレンブタジエンゴム(SBR)、ブタジエン
ゴム(BR)、イソプレンゴム(IR)、イソブチレン
ゴム(IIR)などがあげられる。また、これらゴム成
分はそれぞれ単独でまたは任意に組み合わせて用いるこ
とができるが、ウェットグリップ性がよいという点か
ら、SBRとBRを用いるのが好ましい。なお、SBR
とBRを用いる場合の両者の比は、本発明の効果を損な
わない範囲で当業者であれば適宜選択することができ
る。The rubber component that can be used in the present invention is not particularly limited as long as it has been conventionally applied to a tire tread.
R), styrene butadiene rubber (SBR), butadiene rubber (BR), isoprene rubber (IR), isobutylene rubber (IIR) and the like. These rubber components can be used alone or in any combination. However, it is preferable to use SBR and BR from the viewpoint of good wet grip properties. In addition, SBR
Those skilled in the art can appropriately select the ratio between the two when BR and BR are used, as long as the effects of the present invention are not impaired.
【0019】つぎに、本発明において用いるシリカとし
ては、従来からタイヤの分野において用いられているも
のであれば特に制限はない。The silica used in the present invention is not particularly limited as long as it has been conventionally used in the field of tires.
【0020】シリカの配合量としては、ゴム成分100
重量部に対して50〜150重量部であればよいが、ウ
ェットグリップと転がり抵抗のバランスという点から、
50〜100重量部であるのが好ましい。The mixing amount of silica is preferably 100 parts by weight of the rubber component.
It is sufficient if it is 50 to 150 parts by weight with respect to parts by weight, but from the viewpoint of the balance between wet grip and rolling resistance,
It is preferably 50 to 100 parts by weight.
【0021】つぎに、本発明のゴム組成物において配合
するシランカップリング剤としては、従来からタイヤの
分野においてシリカと併用されているものであれば特に
制限はないが、たとえばビス(3−トリエトキシシリル
プロピル)テトラスルフィド、γ−メルカプトプロピル
トリメトキシシラン、γ−グリシドキシプロピルトリメ
トキシシランなどがあげられ、これらをそれぞれ単独
で、または任意に組み合わせて用いることができる。な
かでも、シリカとの反応性や効果がよいという点から、
ビス(3−トリエトキシシリルプロピル)テトラスルフ
ィドを用いるのが好ましい。The silane coupling agent blended in the rubber composition of the present invention is not particularly limited as long as it is conventionally used in combination with silica in the field of tires. (Ethoxysilylpropyl) tetrasulfide, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, and the like. These can be used alone or in any combination. Among them, from the viewpoint of good reactivity and effect with silica,
It is preferred to use bis (3-triethoxysilylpropyl) tetrasulfide.
【0022】シランカップリング剤の配合量としては、
シリカに対する量として8〜10重量%が好ましい。ゴ
ム成分100重量部に対しては4〜15重量部であれば
よいが、価格と効果のバランスという点から、4〜12
重量部であるのが好ましい。The amount of the silane coupling agent is as follows:
The amount based on silica is preferably 8 to 10% by weight. The amount may be 4 to 15 parts by weight with respect to 100 parts by weight of the rubber component.
It is preferably in parts by weight.
【0023】また、本発明のトレッド用ゴム組成物は、
カーボンブラックを含んでいなくても放電性に優れる
が、さらに放電性を向上させるために添加する場合は、
ヨウ素吸着量が80mg/g以上のカーボンブラックを
ゴム成分100重量部に対して10重量部以下にするこ
とが好ましい。さらに、シリカの特性を引き出すために
は、2〜6重量部に抑えるのが特に好ましい。The rubber composition for a tread of the present invention comprises:
Even if it does not contain carbon black, it has excellent discharge performance, but when added to further improve discharge performance,
Preferably, carbon black having an iodine adsorption of 80 mg / g or more is used in an amount of 10 parts by weight or less based on 100 parts by weight of the rubber component. Further, in order to bring out the properties of silica, it is particularly preferable to suppress the amount to 2 to 6 parts by weight.
【0024】本発明のゴム組成物には、前記成分のほか
に、たとえばクレーなどの充填材、パラフィン系、アロ
マ系、ナフテン系のプロセスオイルなどの軟化剤、クマ
ロンインデン樹脂、ロジン系樹脂、シクロペンタジエン
系樹脂などの粘着付与剤、イオウ、過酸化物などの加硫
剤、加硫促進剤、ステアリン酸、酸化亜鉛などの加硫助
剤、老化防止剤などを、本発明の効果を損なわない範囲
で必要に応じて適宜配合することができる。また、前記
要件を満たすシリカおよびカーボンブラック以外のシリ
カおよびカーボンブラックなどの充填材も、本発明の効
果を損なわない範囲であれば配合してよい。The rubber composition of the present invention may further contain, in addition to the above components, a filler such as clay, a softening agent such as a paraffinic, aroma or naphthenic process oil, a coumarone indene resin, a rosin resin, Tackifiers such as cyclopentadiene-based resins, vulcanizing agents such as sulfur and peroxides, vulcanization accelerators, vulcanization aids such as stearic acid and zinc oxide, antioxidants, etc., impair the effects of the present invention. It can be appropriately compounded as needed within the range not present. In addition, fillers such as silica and carbon black other than silica and carbon black satisfying the above requirements may be blended as long as the effects of the present invention are not impaired.
【0025】本発明のゴム組成物は、たとえばバンバリ
ーミキサー、ニーダーなどの密閉式の混練り機、および
オープンロールなどを用いて、常法によりうることがで
きる。The rubber composition of the present invention can be obtained by a conventional method using, for example, a closed kneader such as a Banbury mixer or a kneader, and an open roll.
【0026】以上のようにしてえられる本発明のゴム組
成物は、常法によりタイヤトレッドに適用することがで
き、放電性に優れることから、電気抵抗の低いタイヤト
レッドを提供し得る。The rubber composition of the present invention obtained as described above can be applied to a tire tread by a conventional method, and can provide a tire tread having low electric resistance since it has excellent dischargeability.
【0027】以下に、実施例を用いて本発明をさらに詳
細に説明するが、本発明はこれらのみに制限されるもの
ではない。Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited thereto.
【0028】[0028]
【実施例】まず、以下に実施例において用いた材料を示
す。EXAMPLES First, materials used in the examples are shown below.
【0029】・SBR:日本ゼオン(株)製のNipo
l9520(スチレン含量35重量%、37.5重量部
油展) ・BR:宇部興産(株)製のBR150B ・シリカ:日本シリカ工業(株)製のNipsilVN
3 ・シランカップリング剤:デグサジャパン社製のX−5
0−S(ビス(3−トリエトキシシリルプロピル)テト
ラスルフィドとカーボンブラック(N330、ヨウ素吸
着量82g/kg)との100:100(重量比)混合
物)。なお、ここに含まれるカーボンブラックをカーボ
ンブラックBとする。SBR: Nipo manufactured by Zeon Corporation
19520 (35% by weight of styrene content, 37.5 parts by weight of oil) BR: BR150B manufactured by Ube Industries, Ltd. Silica: Nipsil VN manufactured by Nippon Silica Industry Co., Ltd.
3. Silane coupling agent: X-5 manufactured by Degussa Japan
0-S (100: 100 (weight ratio) mixture of bis (3-triethoxysilylpropyl) tetrasulfide and carbon black (N330, iodine adsorption amount 82 g / kg)). The carbon black contained here is referred to as carbon black B.
【0030】・カーボンブラックA:昭和キャボット
(株)製のN220(ヨウ素吸着量121g/kg) ・水溶性吸水性樹脂A:クラレ(株)製のクラロンK−
II(ポリビニルアルコール粉末)を200メッシュ(7
5μm)のふるいにかけたもの。Carbon black A: N220 manufactured by Showa Cabot Corporation (Iodine adsorption amount 121 g / kg) Water-soluble water-absorbent resin A: Kuraron K- manufactured by Kuraray Co., Ltd.
II (polyvinyl alcohol powder) with 200 mesh (7
5 μm).
【0031】実施例1〜2 表1に示す配合割合となるように、バンバリーミキサー
を用いて上述の材料を混練して本発明のタイヤトレッド
用ゴム組成物1〜2を得た。Examples 1 and 2 The above-mentioned materials were kneaded using a Banbury mixer so that the mixing ratios shown in Table 1 were obtained, thereby obtaining tire tread rubber compositions 1 and 2 of the present invention.
【0032】得られたゴム組成物1〜2を押出機を用い
て常法でトレッドの形状で押し出し、225/60R1
6のサイズのタイヤ1〜2を作製し、ついで内圧を2.
2kscとして7−1/2JJのアルミニウム製のリム
に組んだ。かかるタイヤ1〜2を以下の方法で評価し
た。結果を表1に示す。The obtained rubber compositions 1 and 2 are extruded in the form of tread by an ordinary method using an extruder.
6. The tires 1 and 2 of the size 6 were produced, and then the internal pressure was set to 2.
It was assembled on a 7-1 / 2JJ aluminum rim as 2 ksc. The tires 1 and 2 were evaluated by the following methods. Table 1 shows the results.
【0033】[評価方法] タイヤの電気抵抗値の測定 タイヤの帯電性を評価すべく、得られたタイヤ1〜2を
用いて荷重負荷時の電気抵抗値を測定した。測定方法は
1995年10月にドイツにおいて公表された「wdk
110 Blatt 3」に準じ、荷重を450kg
fとした。また、トレッド表面の大気の湿度に対する影
響を評価するために、湿度を28%および62%にし、
タイヤをこれらの湿度の環境に24時間放置した後に測
定を行なった。一般には、電気抵抗値が100MΩ以下
であれば帯電によるタイヤの不都合の発生は少ないとさ
れている。[Evaluation Method] Measurement of Tire Electrical Resistance In order to evaluate the chargeability of the tire, the electrical resistance under load was measured using the obtained tires 1 and 2. The measurement method is “wdk” published in Germany in October 1995.
The load is 450kg according to "110 Blatt 3"
f. To evaluate the effect of the tread surface on atmospheric humidity, the humidity was set to 28% and 62%,
Measurements were taken after the tires were left in these humidity environments for 24 hours. Generally, if the electric resistance value is 100 MΩ or less, it is considered that inconvenience of the tire due to electrification is small.
【0034】転がり抵抗の測定 直径1707.6mmのドラム式転がり抵抗測定機に
て、速度80kmでの転がり抵抗を測定した。結果は、
後述する比較例1の場合を100として指数で示した。
指数が大きいほど転がり抵抗が低く、好ましい。Measurement of Rolling Resistance The rolling resistance at a speed of 80 km was measured by a drum type rolling resistance measuring machine having a diameter of 1707.6 mm. Result is,
The case of Comparative Example 1 to be described later is indicated by an index with 100 being set.
The larger the index, the lower the rolling resistance, which is preferable.
【0035】ウェットブレーキ 3000ccのABS付き乗用車にてABSを作動さ
せ、初速40km/hから20km/hまでの減速度か
ら制動摩擦係数を求め、後述する比較例1の値を100
として指数で示した。指数が大きいほど制動力が高く良
好である。The ABS is operated on a 3000 cc passenger car with an ABS, and the braking friction coefficient is determined from the deceleration from the initial speed of 40 km / h to 20 km / h.
As an index. The larger the index, the higher and better the braking force.
【0036】耐摩耗性 得られたタイヤを3000ccの乗用車に装着し、1
0,000km走行後の摩耗量を測定し、後述する比較
例1の値を100として指数で示した。指数が大きいほ
ど耐摩耗性に優れる。Wear resistance The obtained tire was mounted on a 3000 cc passenger car and
The amount of abrasion after running at 000 km was measured, and was indicated by an index with the value of Comparative Example 1 described later as 100. The larger the index, the better the wear resistance.
【0037】ラジオノイズ 耐摩耗性を評価するための走行の際において、乾燥路面
走行時のラジオノイズ発生の有無を評価した。ラジオノ
イズの発生が認められなかった場合をA、ラジオノイズ
が若干発生した場合をB、ラジオノイズが発生した場合
をCとした。Radio noise When traveling for evaluating abrasion resistance, the occurrence of radio noise when traveling on a dry road surface was evaluated. A indicates that no radio noise was generated, B indicates a case where radio noise was slightly generated, and C indicates a case where radio noise was generated.
【0038】比較例1〜4 表1に示す配合割合にかえたほかは、実施例1と同様に
して比較ゴム組成物1〜4を得、実施例と同様の試験を
行なった。結果を表1に示す。Comparative Examples 1 to 4 Comparative rubber compositions 1 to 4 were obtained in the same manner as in Example 1 except that the mixing ratios shown in Table 1 were changed, and the same tests as those in Examples were performed. Table 1 shows the results.
【0039】[0039]
【表1】 [Table 1]
【0040】表1より、水溶性吸水性樹脂の配合量が5
重量部未満の場合は電気抵抗の低減が不充分で、ノイズ
が発生したことがわかり(比較例2および3)、水溶性
吸水性樹脂の配合量が25重量部を超える場合、電気抵
抗値の低減下を図ることができるが、耐摩耗性に劣るこ
とがわかる。According to Table 1, the amount of the water-soluble water-absorbing resin was 5
When the amount is less than 10 parts by weight, the reduction of the electric resistance is insufficient and it is understood that noise occurs (Comparative Examples 2 and 3). It can be seen that the reduction can be achieved, but the wear resistance is poor.
【0041】また、本発明の実施例1および2より、本
発明の組成範囲であれば他の性能を犠牲にせず電気抵抗
値の低減が可能であることがわかる。Further, it can be seen from Examples 1 and 2 of the present invention that the electric resistance can be reduced without sacrificing other performances within the composition range of the present invention.
【0042】[0042]
【発明の効果】本発明によれば、電気抵抗の小さいタイ
ヤトレッドを提供し得る放電性の高いゴム組成物を得る
ことができる。According to the present invention, it is possible to obtain a highly dischargeable rubber composition capable of providing a tire tread having a small electric resistance.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) //(C08L 21/00 101:14) (C08L 21/00 29:04) ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) // (C08L 21/00 101: 14) (C08L 21/00 29:04)
Claims (4)
50〜150重量部、シランカップリング剤を4〜15
重量部および水溶性吸水性樹脂を5〜20重量部含んで
なるタイヤトレッド用ゴム組成物。1. Silica is 50 to 150 parts by weight, and a silane coupling agent is 4 to 15 parts by weight based on 100 parts by weight of a rubber component.
A rubber composition for a tire tread, comprising 5 parts by weight and 5 to 20 parts by weight of a water-soluble water-absorbent resin.
ボンブラックの配合量が10重量部以下である請求項1
記載のタイヤトレッド用ゴム組成物。2. The compounding amount of carbon black having an iodine adsorption of 80 mg / g or more is 10 parts by weight or less.
The rubber composition for a tire tread according to the above.
り、その粒径が20〜100μmである請求項1または
2記載のタイヤトレッド用ゴム組成物。3. The rubber composition for a tire tread according to claim 1, wherein the shape of the water-soluble water-absorbent resin is particulate, and the particle size is 20 to 100 μm.
ルである請求項1〜3のいずれかに記載のタイヤトレッ
ド用ゴム組成物。4. The rubber composition for a tire tread according to claim 1, wherein the water-soluble water-absorbent resin is polyvinyl alcohol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10248462A JP2000080206A (en) | 1998-09-02 | 1998-09-02 | Rubber composition for tire tread |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10248462A JP2000080206A (en) | 1998-09-02 | 1998-09-02 | Rubber composition for tire tread |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000080206A true JP2000080206A (en) | 2000-03-21 |
Family
ID=17178506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10248462A Withdrawn JP2000080206A (en) | 1998-09-02 | 1998-09-02 | Rubber composition for tire tread |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000080206A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20030043361A (en) * | 2001-11-28 | 2003-06-02 | 한국타이어 주식회사 | Tire tread rubber composition |
| JP2006528253A (en) * | 2003-07-21 | 2006-12-14 | ソシエテ ド テクノロジー ミシュラン | Tire tread |
| EP1900548A1 (en) * | 2006-09-08 | 2008-03-19 | The Goodyear Tire & Rubber Company | Carbon black-rich rubber composition containing particulate hydrophylic water absorbing polymer and tire with tread thereof |
| CN103087367A (en) * | 2013-01-18 | 2013-05-08 | 中国石油天然气股份有限公司 | A kind of high-performance water-absorbing swelling rubber and its preparation method |
-
1998
- 1998-09-02 JP JP10248462A patent/JP2000080206A/en not_active Withdrawn
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20030043361A (en) * | 2001-11-28 | 2003-06-02 | 한국타이어 주식회사 | Tire tread rubber composition |
| JP2006528253A (en) * | 2003-07-21 | 2006-12-14 | ソシエテ ド テクノロジー ミシュラン | Tire tread |
| EP1900548A1 (en) * | 2006-09-08 | 2008-03-19 | The Goodyear Tire & Rubber Company | Carbon black-rich rubber composition containing particulate hydrophylic water absorbing polymer and tire with tread thereof |
| CN103087367A (en) * | 2013-01-18 | 2013-05-08 | 中国石油天然气股份有限公司 | A kind of high-performance water-absorbing swelling rubber and its preparation method |
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