JP2890328B2 - Rubber composition for tire tread - Google Patents
Rubber composition for tire treadInfo
- Publication number
- JP2890328B2 JP2890328B2 JP31765390A JP31765390A JP2890328B2 JP 2890328 B2 JP2890328 B2 JP 2890328B2 JP 31765390 A JP31765390 A JP 31765390A JP 31765390 A JP31765390 A JP 31765390A JP 2890328 B2 JP2890328 B2 JP 2890328B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- parts
- rubber
- cut resistance
- 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 - Fee Related
Links
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、耐カット性を向上させたタイヤトレッド用
ゴム組成物、特に建設車両、トラック、バス、ライトト
ラックなどの大型タイヤのトレッド用ゴム組成物に関す
る。The present invention relates to a rubber composition for a tire tread having improved cut resistance, particularly a rubber for a tread of a large tire such as a construction vehicle, a truck, a bus, and a light truck. Composition.
従来、耐カット性が特に要求される場合のタイヤトレ
ッド用ゴム組成物の配合設計としては、硬度および弾性
率の増大、破断伸び大、ヒステリシスロス大とする方向
にあり、具体的には例えば主成分ゴムに対しスチレン−
ブタジエン共重合体ゴムおよび各種の樹脂を配合する等
を行っている。また、さらなる耐カット性の向上をはか
るために、例えば、特開昭57−102933号公報に開示され
ているように、スチレン含量が30〜70重量%である高ス
チレン含有スチレン−ブタジエン共重合体ゴムを配合す
ることが提案されている。このようにスチレン−ブタジ
エン共重合体ゴムを配合することにより得られるゴム組
成物の常温での弾性率および硬度は大幅に上昇し、常温
での耐カット性が著しく向上する。しかしながら、高温
(60℃以上)の場合には、スチレン−ブタジエン共重合
体ゴムは熱可塑性が大きいため、弾性率および硬度の上
昇率が常温に比べて小さく、耐カット性が充分に向上し
ないという欠点があった。Conventionally, as a compounding design of a rubber composition for a tire tread when cut resistance is particularly required, there is a tendency to increase hardness and elastic modulus, increase breaking elongation, and increase hysteresis loss. Styrene to component rubber
Butadiene copolymer rubber and various resins are blended. Further, in order to further improve the cut resistance, for example, as disclosed in JP-A-57-102933, a high styrene-containing styrene-butadiene copolymer having a styrene content of 30 to 70% by weight. It has been proposed to compound rubber. As described above, the rubber composition obtained by blending the styrene-butadiene copolymer rubber significantly increases the modulus of elasticity and hardness at room temperature, and significantly improves the cut resistance at room temperature. However, at a high temperature (60 ° C. or higher), the styrene-butadiene copolymer rubber has a large thermoplasticity, so that the rate of increase in elastic modulus and hardness is smaller than that at normal temperature, and the cut resistance is not sufficiently improved. There were drawbacks.
本発明は、常温から高温まで広い温度域に亘って耐カ
ット性を向上させたタイヤトレッド用ゴム組成物を提供
することを目的とする。An object of the present invention is to provide a rubber composition for a tire tread having improved cut resistance over a wide temperature range from normal temperature to high temperature.
ここで、耐カット性とは、タイヤの走行に際してトレ
ッド部が路上の石等によるカット傷を受けにくい性質を
いう。Here, the cut resistance refers to a property in which the tread portion is less likely to be cut by a stone or the like on the road when the tire runs.
本発明のタイヤトレッド用ゴム組成物は、スチレン−
ブタジエン共重合体ゴム20重量部以上と天然ゴムおよび
/又はポリイソプレンゴム80重量部以下からなる原料ゴ
ム100重量部に対し、クレゾール−ホルムアルデヒド重
縮合樹脂、フェノール−ホルムアルデヒド重縮合樹脂、
およびレゾルシン−ホルムアルデヒド重縮合樹脂から選
ばれた1種以上の樹脂aと、ロジン系樹脂および石油系
樹脂から選ばれた1種以上の樹脂bとを、aのbとの合
計量が3〜15重量部およびa/bの配合量比が1/9〜9/1の
条件下に配合してなり、20℃で貯蔵弾性率が8.5MPa以上
であって100℃での貯蔵弾性率が4.0MPa以上であること
を特徴とする。The rubber composition for a tire tread of the present invention comprises styrene-
A cresol-formaldehyde polycondensation resin, a phenol-formaldehyde polycondensation resin, based on 100 parts by weight of a raw rubber consisting of not less than 20 parts by weight of butadiene copolymer rubber and not more than 80 parts by weight of natural rubber and / or polyisoprene rubber
And at least one resin a selected from a resorcin-formaldehyde polycondensation resin and at least one resin b selected from a rosin-based resin and a petroleum-based resin, the total amount of b of a being 3 to 15 The blending ratio of parts by weight and a / b is 1/9 to 9/1, and the storage elastic modulus at 20 ° C. is 8.5 MPa or more and the storage elastic modulus at 100 ° C. is 4.0 MPa. It is characterized by the above.
以下、本発明の構成につき詳しく説明する。 Hereinafter, the configuration of the present invention will be described in detail.
(1) 原料ゴム。(1) Raw rubber.
スチレン−ブタジエン共重合体ゴム(SBR)20重量部
以上と天然ゴム(NR)および/又はポリイソプレンゴム
(IR)80重量部以下からなる。It comprises at least 20 parts by weight of styrene-butadiene copolymer rubber (SBR) and at most 80 parts by weight of natural rubber (NR) and / or polyisoprene rubber (IR).
このようにSBRとNRおよび/又はIRとからなるとした
のは、大型車両用タイヤに要求されるゴム強度の確保に
加えて、耐カット性と大型車両として求められる外部応
力による発熱性との二律背反特性のバランスのためであ
る。SBRが20重量部未満では、充分な耐カット性向上が
みられない。As described above, SBR and NR and / or IR are the reasons for the trade-off between cut resistance and heat generation due to external stress required for heavy-duty vehicles, in addition to securing the rubber strength required for heavy-duty tires. This is for balance of characteristics. If the SBR is less than 20 parts by weight, sufficient improvement in cut resistance is not observed.
(2) 本発明のゴム組成物は、この原料ゴム100重量
部に対し、樹脂aと樹脂bとを、aとbとの合計量が3
〜15重量部およびa/bの配合量比が1/9〜9/1の条件下に
配合してなる。さらに、カーボンブラック等の他の配合
剤を必要に応じて配合してもよい。(2) In the rubber composition of the present invention, the resin a and the resin b are mixed with 100 parts by weight of the raw rubber so that the total amount of the resins a and b is 3
1515 parts by weight and a / b in a ratio of 1/9 to 9/1. Further, other compounding agents such as carbon black may be compounded as needed.
樹脂aは、クレゾール−ホルムアルデヒド重縮合樹
脂、フェノール−ホルムアルデヒド重縮合樹脂、および
レゾルシン−ホルムアルデヒド重縮合樹脂から選ばれた
1種以上のものである。また、樹脂bは、ロジン系樹脂
および石油系樹脂から選ばれた1種以上のものである。
ロジン系樹脂は、例えば、ガムロジンWW、トール油ロジ
ン、ウッドロジン、ハリタックAQシリーズのロジン変性
樹脂、マレイン化ロジン等のロジン誘導体などである。
石油系樹脂は、具体的には例えば、エスコレッツ1102等
の脂肪族系石油樹脂やペトロジン等の芳香族系石油樹脂
などである。The resin a is at least one selected from a cresol-formaldehyde polycondensation resin, a phenol-formaldehyde polycondensation resin, and a resorcin-formaldehyde polycondensation resin. The resin b is at least one selected from a rosin resin and a petroleum resin.
The rosin-based resin includes, for example, gum rosin WW, tall oil rosin, wood rosin, rosin-modified resin of the Haritac AQ series, and rosin derivatives such as maleated rosin.
The petroleum resin is, for example, an aliphatic petroleum resin such as Escolets 1102 or an aromatic petroleum resin such as petrozine.
aとbとの合計量が3重量部未満では耐カット性の向
上効果が充分でなく、一方、15重量部超では耐カット性
の改善効果が飽和し、且つ発熱性の増加が顕著であるた
め好ましくない。また、a/bの配合比率が1/9未満では弾
性率・硬度の上昇が小さいため耐カット性の改善効果が
小さく、一方、9/1超では老化による物性変化が顕著と
なるので好ましくない。If the total amount of a and b is less than 3 parts by weight, the effect of improving the cut resistance is not sufficient, while if it exceeds 15 parts by weight, the effect of improving the cut resistance is saturated, and the increase in heat generation is remarkable. Therefore, it is not preferable. In addition, when the mixing ratio of a / b is less than 1/9, the effect of improving cut resistance is small because the increase in elastic modulus and hardness is small.On the other hand, when the mixing ratio is more than 9/1, physical property changes due to aging become remarkable, which is not preferable. .
(3) また、本発明のゴム組成物は、20℃での貯蔵弾
性率が8.5以上であって100℃での貯蔵弾性率が4.0PMa以
上でなければならない(20℃/100℃での貯蔵弾性率がそ
れぞれ8.5/4.0以上)。20℃/100℃の貯蔵弾性率が8.5/
4.0MPa未満では、常温〜高温の温度域の耐カット性が不
足するためである。(3) The rubber composition of the present invention must have a storage modulus at 20 ° C of 8.5 or more and a storage modulus at 100 ° C of 4.0 PMa or more (storage at 20 ° C / 100 ° C). The elastic modulus is 8.5 / 4.0 or more respectively). 8.5 ° C storage elasticity at 20 ° C / 100 ° C
If the pressure is less than 4.0 MPa, the cut resistance in the temperature range from normal temperature to high temperature is insufficient.
以下に実施例および比較例を示す。 Examples and comparative examples are shown below.
実施例、比較例 第1表にゴム組成物(実施例1〜2、比較例1〜5)
の配合内容(重量部)および物性(指数)を示す。Examples and Comparative Examples Table 1 shows the rubber compositions (Examples 1 and 2 and Comparative Examples 1 to 5).
Shows the blending content (parts by weight) and physical properties (index).
実施例1、2は、本発明の範囲内のものであって、貯
蔵弾性率が20℃/100℃共に大となり、耐カット性も向上
する。 Examples 1 and 2 are within the scope of the present invention, and the storage elastic modulus is increased at both 20 ° C / 100 ° C, and the cut resistance is also improved.
比較例1は、スチレン−ブタジエン共重合体ゴム/天
然ゴムの比率が10重量部/90重量部の場合であり、100℃
の貯蔵弾性率はむしろ向上するものの、ヒステリシスロ
スの減少により耐カット性の向上は小さい。Comparative Example 1 was a case where the ratio of styrene-butadiene copolymer rubber / natural rubber was 10 parts by weight / 90 parts by weight,
Although the storage elastic modulus of R.I. increases, the improvement in cut resistance is small due to the decrease in hysteresis loss.
比較例2は、ポリブタジエン/天然ゴムのブレンドと
した場合であり、耐カット性が大幅に低下し、不味であ
る。Comparative Example 2 is a case where a blend of polybutadiene / natural rubber was used, and cut resistance was significantly reduced and taste was not good.
比較例3は、樹脂配合量が3重量部未満の場合であ
り、耐カット性の改善効果が小さい。Comparative Example 3 is a case where the amount of the resin is less than 3 parts by weight, and the effect of improving the cut resistance is small.
比較例4は、樹脂配合量が20重量部超の場合であり、
発熱性が顕著となり好ましくない。Comparative Example 4 is a case where the resin compounding amount is more than 20 parts by weight,
Exothermicity becomes remarkable, which is not preferable.
比較例5は、配合的には本発明の範囲内であるが、貯
蔵弾性率が20℃/100℃でいずれも8.5/4.0MPa未満であ
り、耐カット性が発揮されない。Comparative Example 5 is blended within the range of the present invention, but has a storage elastic modulus of less than 8.5 / 4.0 MPa at 20 ° C./100° C., and does not exhibit cut resistance.
以上説明したように本発明によれば、常温から高温ま
での広い温度域に亘って耐カット性を向上させることが
可能となる。As described above, according to the present invention, it is possible to improve cut resistance over a wide temperature range from room temperature to high temperature.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 93:04 57:02) (C08L 9/00 9:06 61:06 93:04 57:02) (56)参考文献 特開 昭56−47470(JP,A) 特開 昭61−225231(JP,A) 特開 昭60−99703(JP,A) 特開 昭59−204637(JP,A) 特開 昭58−120650(JP,A) 特開 昭58−117235(JP,A) 特開 平2−185543(JP,A) 特開 昭64−43544(JP,A) (58)調査した分野(Int.Cl.6,DB名) C08L 7/00 - 21/02 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C08L 93:04 57:02) (C08L 9/00 9:06 61:06 93:04 57:02) (56) References JP-A-56-47470 (JP, A) JP-A-61-225231 (JP, A) JP-A-60-99703 (JP, A) JP-A-59-204637 (JP, A) JP-A-58-120650 (JP, A) JP, A) JP-A-58-117235 (JP, A) JP-A-2-185543 (JP, A) JP-A-64-43544 (JP, A) (58) Fields investigated (Int. Cl. 6 , (DB name) C08L 7/00-21/02
Claims (1)
部以上と天然ゴムおよび/又はポリイソプレンゴム80重
量部以下からなる原料ゴム100重量部に対し、クレゾー
ル−ホルムアルデヒド重縮合樹脂、フェノール−ホルム
アルデヒド重縮合樹脂、およびレゾルシン−ホルムアル
デヒド重縮合樹脂から選ばれた1種以上の樹脂aと、ロ
ジン系樹脂および石油系樹脂から選ばれた1種以上の樹
脂bとを、aとbとの合計量が3〜15重量部およびa/b
の配合量比が1/9〜9/1の条件下に配合してなり、20℃で
貯蔵弾性率が8.5MPa以上であって100℃での貯蔵弾性率
が4.0MPa以上であるタイヤトレッド用ゴム組成物。1. A cresol-formaldehyde polycondensation resin, a phenol-formaldehyde polycondensate, and a styrene-butadiene copolymer rubber (20 parts by weight or more) and a natural rubber and / or polyisoprene rubber (80 parts by weight or less) raw material 100 parts by weight Condensed resin, and at least one resin a selected from resorcin-formaldehyde polycondensation resin and at least one resin b selected from rosin-based resin and petroleum-based resin, the total amount of a and b 3 to 15 parts by weight and a / b
The compounding ratio of 1/9 to 9/1 is used for tire treads whose storage modulus at 20 ° C is 8.5MPa or more and whose storage modulus at 100 ° C is 4.0MPa or more. Rubber composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31765390A JP2890328B2 (en) | 1990-11-26 | 1990-11-26 | Rubber composition for tire tread |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31765390A JP2890328B2 (en) | 1990-11-26 | 1990-11-26 | Rubber composition for tire tread |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04189844A JPH04189844A (en) | 1992-07-08 |
JP2890328B2 true JP2890328B2 (en) | 1999-05-10 |
Family
ID=18090545
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31765390A Expired - Fee Related JP2890328B2 (en) | 1990-11-26 | 1990-11-26 | Rubber composition for tire tread |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2890328B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20020044257A (en) * | 2000-12-05 | 2002-06-15 | 신형인 | Tread rubber composition for light truck radial tire |
JP2007161900A (en) * | 2005-12-14 | 2007-06-28 | Sumitomo Rubber Ind Ltd | Rubber composition for tread of motocross tire for two-wheeled vehicle |
PL1902864T3 (en) | 2006-09-20 | 2010-04-30 | Arizona Chem | Rubber compositions with building tack |
JP5665475B2 (en) * | 2010-10-25 | 2015-02-04 | 株式会社ブリヂストン | Rubber composition and pneumatic tire using the same |
JP5772227B2 (en) * | 2011-05-30 | 2015-09-02 | 横浜ゴム株式会社 | Rubber composition for tire tread for heavy load and pneumatic tire using the same |
-
1990
- 1990-11-26 JP JP31765390A patent/JP2890328B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH04189844A (en) | 1992-07-08 |
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