JP2662281B2 - Rubber composition for large tire tread - Google Patents

Rubber composition for large tire tread

Info

Publication number
JP2662281B2
JP2662281B2 JP1004621A JP462189A JP2662281B2 JP 2662281 B2 JP2662281 B2 JP 2662281B2 JP 1004621 A JP1004621 A JP 1004621A JP 462189 A JP462189 A JP 462189A JP 2662281 B2 JP2662281 B2 JP 2662281B2
Authority
JP
Japan
Prior art keywords
rubber
parts
weight
rubber composition
value
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 - Lifetime
Application number
JP1004621A
Other languages
Japanese (ja)
Other versions
JPH02185543A (en
Inventor
一郎 中島
真史 大原
佐藤  進
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.)
Bridgestone Corp
Original Assignee
Bridgestone Corp
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 Bridgestone Corp filed Critical Bridgestone Corp
Priority to JP1004621A priority Critical patent/JP2662281B2/en
Publication of JPH02185543A publication Critical patent/JPH02185543A/en
Application granted granted Critical
Publication of JP2662281B2 publication Critical patent/JP2662281B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は大型タイヤトレッド用ゴム組成物に関し、詳
しくはトラックおよびバス用大型タイヤにおいて耐摩耗
性の向上を図りタイヤ寿命を大幅に向上し得るトレッド
用ゴム組成物に関するものである。
Description: TECHNICAL FIELD The present invention relates to a rubber composition for a large tire tread, and more particularly, to an improvement in wear resistance of a large tire for trucks and buses, which can greatly improve the tire life. The present invention relates to a rubber composition for a tread.

(従来の技術) 従来、大型タイヤの耐摩耗性を向上させるための技術
としてカーボンブラックの配合量の増加、ブタジエンゴ
ム(BR)の添加量の増加、プロセスオイル等の軟化剤の
減量等の手法が採られてきた。
(Prior art) Conventionally, techniques for improving the wear resistance of large tires include increasing the amount of carbon black, increasing the amount of butadiene rubber (BR) added, and reducing the amount of softener such as process oil. Has been adopted.

(課題を解決するための手段) しかしながら、従来採られてきた耐摩耗性の向上技術
は必ずしも満足のいくものではなかった。
(Means for Solving the Problems) However, techniques for improving wear resistance which have been conventionally adopted have not always been satisfactory.

すなわち、ゴム中のカーボンブラックの配合量を増加
すると、従来から理解されているようにある配合量範囲
内では耐摩耗性を向上させることができるが、その範囲
を越えて増加すると却って耐摩耗性向上効果の低減を招
く結果となる。更にカーボンブラックの配合量を増加す
るとそれに伴い発熱性の低下、可塑度上昇による作業性
の低下を生じる。
That is, as the amount of carbon black in the rubber is increased, the wear resistance can be improved within a certain compounding range as conventionally understood. As a result, the improvement effect is reduced. Further, when the blending amount of carbon black is increased, heat generation is reduced and workability is lowered due to increase in plasticity.

また、ブタジエンゴムの添加量の増加も耐摩耗性、特
には高入力耐摩耗性を向上させることができるが、大型
タイヤの寿命の向上を企図する場合にこの手法のみでは
十分といえない。
Also, an increase in the amount of butadiene rubber can improve abrasion resistance, especially high input abrasion resistance, but this technique alone cannot be said to be sufficient when the life of a large tire is to be improved.

更に、プロセスオイル等の軟化剤の減量は耐摩耗性の
向上を図ることができるが、練りゴムのまとまりを悪く
したり、可塑度上昇等による作業性の低下を来すことに
なる。
Furthermore, although the reduction in the amount of the softening agent such as process oil can improve the abrasion resistance, it deteriorates the consistency of the kneaded rubber and lowers the workability due to an increase in plasticity.

一方、従来より粒径が小さく、連鎖構造を持った集合
体(ストラクチャー)の割合の高いカーボンブラックは
知られており、例えば特開昭62−277446号公報には窒素
吸着比表面積(N2SA)が130m2/g〜160m2/gでDBP吸油量
が110〜150ml/100gのカーボンブラックを天然ゴム単独
系ゴム組成物に適用する技術が開発されている。しか
し、天然ゴム単独系ではヒステリシスロスが大きくな
り、この系ではかかるカーボンブラックのもつ耐摩耗性
向上効果を得ることはできなかった。
On the other hand, carbon blacks having a smaller particle size and a higher proportion of aggregates (structures) having a chain structure are known. For example, Japanese Patent Application Laid-Open No. 62-277446 discloses a nitrogen black specific surface area (N 2 SA). ) technology that a DBP oil absorption 130m 2 / g~160m 2 / g to apply carbon black 110~150ml / 100g natural rubber alone rubber composition have been developed. However, the hysteresis loss is large in the natural rubber alone system, and in this system, the effect of improving the wear resistance of the carbon black cannot be obtained.

そこで本発明の目的は、トラックおよびバス用大型タ
イヤにおいて従来技術に比し更に一層耐摩耗性の向上が
図れ、タイヤ寿命を大幅に向上することのできるトレッ
ド用ゴム組成物を提供することにある。
Therefore, an object of the present invention is to provide a rubber composition for a tread which can further improve the wear resistance of a large truck and bus tire as compared with the prior art and can greatly improve the tire life. .

(課題を解決するための手段) ゴムの損失係数tanδ値を下げるとヒステリシスロス
を下げることができ、かかるヒステリシスロスの低下は
摩耗係数の低下をもたらす。また、動的貯蔵弾性率E′
を上げると路面からの異物等の侵入を防ぐことができ耐
摩耗性を向上することができる。高ストラクチャー、小
粒子径のカーボンブラックはこれらを両立し耐摩耗性を
改善することができると考えられるが、上述の如く天然
ゴム単独系ではヒステリシスロスが高くなり上記耐摩耗
性の改良効果を十分に発揮できないため、本発明者らは
かかるカーボンブラックでtanδ値を下げることのでき
るゴム系を見い出すべく鋭意検討を行った。その結果、
ブタジエンゴムと天然ゴム/イソプレンゴムとの最適量
のブレンド系を用いると上記カーボンブラックとの相乗
効果で著しく耐摩耗性が向上し得ることを見い出し、本
発明を完成するに至った。
(Means for Solving the Problems) The hysteresis loss can be reduced by lowering the loss coefficient tan δ value of rubber, and such a reduction in the hysteresis loss causes a reduction in the wear coefficient. In addition, the dynamic storage modulus E '
When the height is increased, invasion of foreign matter and the like from the road surface can be prevented, and the wear resistance can be improved. It is thought that carbon black having a high structure and a small particle diameter can balance these properties and improve wear resistance.However, as described above, the natural rubber alone has a high hysteresis loss, and the effect of improving the wear resistance is sufficiently improved. Therefore, the present inventors have conducted intensive studies to find a rubber system capable of reducing the tan δ value with such carbon black. as a result,
It has been found that when an optimum amount of a butadiene rubber and a natural rubber / isoprene rubber is used in a blend system, the abrasion resistance can be remarkably improved by the synergistic effect of the carbon black, and the present invention has been completed.

すなわち本発明はブタジエンゴム(BR)15〜70重量部
と、天然ゴム(NR)および/またはイソプレンゴム(I
R)30〜85重量部とから成るゴム成分100重量部に対し、
セシルトリメチルアンモニウムブロマイド(CTAB)吸着
比表面積140〜150m2/gおよびジブチルフタレート(DB
P)吸油量130〜150ml/100gのカーボンブラック30〜75重
量部を配合してなることを特徴とする大型タイヤトレッ
ド用ゴム組成物に関するものである。
That is, the present invention relates to 15 to 70 parts by weight of butadiene rubber (BR) and natural rubber (NR) and / or isoprene rubber (I).
R) For 100 parts by weight of the rubber component consisting of 30 to 85 parts by weight,
Cecil bromide (CTAB) adsorption specific surface area 140~150m 2 / g and dibutyl phthalate (DB
P) A rubber composition for a large tire tread, comprising 30 to 75 parts by weight of carbon black having an oil absorption of 130 to 150 ml / 100 g.

本発明のゴム組成物は、動的貯蔵弾性率E′値が1.00
×108〜1.35×108kg/cm2で損失係数tanδ値が0.23〜0.2
8であるのが好ましい。
The rubber composition of the present invention has a dynamic storage modulus E ′ of 1.00.
× 10 8 to 1.35 × 10 8 kg / cm 2 and loss factor tanδ value is 0.23 to 0.2
Preferably it is 8.

また、ブタジエンゴムの配合量は好ましくは35〜70重
量部とする。
The amount of butadiene rubber is preferably 35 to 70 parts by weight.

尚、本発明のゴム組成物においては、ゴム工業で通常
使用される配合剤、例えば軟化剤、老化防止剤、加硫促
進剤、加硫促進助剤、加硫剤、補強性充填剤等を必要に
応じて通常の配合量の範囲で適宜配合することができる
のは勿論のことである。
In the rubber composition of the present invention, compounding agents usually used in the rubber industry, for example, a softening agent, an antioxidant, a vulcanization accelerator, a vulcanization accelerator, a vulcanizing agent, a reinforcing filler and the like. Needless to say, it can be appropriately compounded within the usual range of the compounding amount as required.

(作 用) 本発明におけるBRとNR/IRとのブレンド系では、本発
明に係るカーボンブラックは小粒子化によりE′値を上
昇させ、かつ高ストラクチャー化によって発熱性の向上
によるtanδ値の低下を生ぜしめるものと考えられる。
すなわち、上記ブレンドゴム系ではカーボンブラックの
小粒子化および高ストラクチャー化はE′値の上昇とta
nδ値の低下の二点を両立する効果があるといえる。こ
の効果は摩擦係数の中でもヒステリシスロス(μ)の
要因に大きく関係し、このことはE′値を上昇させtan
δ値を低下させると摩擦係数の低下を引き起こし、結果
として摩耗量の減少につながることを意味するものであ
る。
(Operation) In the blend system of BR and NR / IR in the present invention, the carbon black according to the present invention increases the E ′ value by reducing the particle size and decreases the tan δ value due to the improvement in heat generation due to the high structure. It is thought to cause.
In other words, in the above-mentioned blended rubber system, the reduction of the particle size and the structure of the carbon black are caused by the increase in the E ′ value and the ta value.
It can be said that there is an effect of balancing the two points of the decrease of the nδ value. This effect is largely related to the factor of hysteresis loss (μ H ) among the friction coefficients, which increases the E ′ value and increases tan.
Decreasing the value of δ causes a decrease in the coefficient of friction, which means that the amount of wear is reduced.

本発明においてはブタジエンゴム(BR)15〜70重量部
を配合するブレンドゴム系とすることを要するが、この
理由はBRがゴム成分100重量部に対し15重量未満である
とBRブレンド効果を奏せずに耐摩耗性向上効果が不足
し、一方70重量部を越えると外観不良が発生し使用不可
能となるからである。
In the present invention, it is necessary to use a blend rubber system in which 15 to 70 parts by weight of butadiene rubber (BR) is blended. The reason for this is that if BR is less than 15 parts by weight per 100 parts by weight of the rubber component, a BR blending effect is exhibited. This is because the effect of improving the wear resistance is insufficient without using it, and when it exceeds 70 parts by weight, the appearance is poor and it cannot be used.

尚、Co触媒を用いて重合したBRは、Li,Nb触媒を用い
て重合したBRに比し、本発明に係るカーボンブラックと
組み合わせた際の耐摩耗性改良効果はより大きくなり、
好ましい。
Incidentally, the BR polymerized using the Co catalyst is Li, compared to the BR polymerized using the Nb catalyst, the abrasion resistance improving effect when combined with the carbon black according to the present invention is larger,
preferable.

また、使用するカーボンブラックはCTAB吸着比表面積
およびDBP吸油量が所定の範囲内にあることを要する
が、これは以下の理由による。
The carbon black used must have a CTAB adsorption specific surface area and a DBP oil absorption within a predetermined range for the following reason.

先ず、CTAB吸着比表面積について、これが140m2/g未
満であると粒子径が大きくなり過ぎ耐摩耗性が不足し、
一方150m2/gを越えると硬くなり過ぎて作業不可能とな
る。
First, regarding the CTAB adsorption specific surface area, if this is less than 140 m 2 / g, the particle size becomes too large and the wear resistance is insufficient,
On the other hand, if it exceeds 150 m 2 / g, it becomes too hard to work.

次にDBP吸油量について、この値が130ml/100g未満で
はストラクチャーの割合が小さくなり過ぎ耐摩耗性が不
足し、一方150ml/100gを越えると耐疲労性が悪くなりし
かも外観不良を起こし使用不可能となる。
Next, as for DBP oil absorption, if this value is less than 130 ml / 100 g, the proportion of the structure becomes too small and the wear resistance is insufficient, while if it exceeds 150 ml / 100 g, the fatigue resistance deteriorates and the appearance deteriorates and it can not be used Becomes

かかるカーボンブラックの配合量はゴム成分100重量
部に対し30〜75重量部の範囲内であることを要するが、
この理由は30重量部未満ではカーボンブラックの補強性
がとれず耐摩耗性は良好ではなく、一方75重量部を越え
るとカーボンブラックの分散不良を起こしタイヤ製造時
の加工が不可能となるからである。
Although the compounding amount of such carbon black is required to be in the range of 30 to 75 parts by weight based on 100 parts by weight of the rubber component,
The reason for this is that if the amount is less than 30 parts by weight, the carbon black cannot be reinforced and the wear resistance is not good, whereas if it exceeds 75 parts by weight, the carbon black disperses poorly and processing during tire production becomes impossible. is there.

本発明のゴム組成物は損失係数tanδ値が0.230〜0.28
0範囲で動的貯蔵弾性率E′値が1.00×108〜1.35×108k
g/cm2の範囲内となるのが好ましいが、この理由はこれ
らの値はヒステリシスロス(μ)に効くため、かかる
所定の範囲内とすることにより耐摩耗性の改良効果が大
となるからである。
The rubber composition of the present invention has a loss factor tan δ value of 0.230 to 0.28.
In the 0 range, the dynamic storage modulus E ′ value is 1.00 × 10 8 to 1.35 × 10 8 k
g / cm 2 is preferred. This is because these values have an effect on hysteresis loss (μ H ). By setting the content within such a predetermined range, the effect of improving the wear resistance is increased. Because.

(実施例) 次に本発明を実施例により具体的に説明する。(Examples) Next, the present invention will be specifically described with reference to examples.

以下の第1表に示す配合割合(ゴム成分100重量部に
対する重量部)から成る各ゴム組成物に対し以下の物性
値を測定した。
The following physical properties were measured for each rubber composition having the mixing ratio (parts by weight based on 100 parts by weight of the rubber component) shown in Table 1 below.

CTAB吸着比表面積 ASTM D−3765−85に準拠して実施した。CTAB adsorption specific surface area It carried out based on ASTM D-3765-85.

DBP吸油量 JIS K6221−1982A法に準拠して実施した。DBP oil absorption This was carried out in accordance with the JIS K6221-1982A method.

E′およびtanδ 岩本製作所(株)製粘弾性スペクトロメータを用い、
室温にて初期歪5%、動歪2%および周波数50Hzの条件
下で測定を行った。
E 'and tan δ Using a viscoelastic spectrometer manufactured by Iwamoto Manufacturing Co., Ltd.
The measurement was performed at room temperature under the conditions of an initial strain of 5%, a dynamic strain of 2%, and a frequency of 50 Hz.

次にこれらゴム組成物をトレッドに用いてTBR1000R20
14 PR R210 Zの供試タイヤを製造し、これらタイヤに
ついて耐摩耗性の評価を行った。評価方法は、約10万Km
走行後の溝深さの平均より摩耗1mmあたり走行距離を求
め、次式、 に従い比較例1を100として指数で表示した。数値が大
きい程結果は良好である。
Next, using these rubber compositions for the tread, TBR1000R20
Test tires of 14 PR R210 Z were manufactured, and the wear resistance of these tires was evaluated. Evaluation method is about 100,000km
The running distance per 1 mm of wear is calculated from the average of the groove depth after running. In accordance with the above, Comparative Example 1 was set to 100 and indicated by an index. The higher the value, the better the result.

得られた結果を第1表に併記する。 The results obtained are shown in Table 1.

(発明の効果) 第1表の測定結果からも分かるように、本発明の要件
を満すゴム組成物においてはいずれも作業性および外観
を損うことなく耐摩耗性が大幅に改良された。従って、
本発明のゴム組成物は大型タイヤの寿命を大幅に向上さ
せることができる。
(Effects of the Invention) As can be seen from the measurement results in Table 1, in each of the rubber compositions satisfying the requirements of the present invention, the abrasion resistance was significantly improved without impairing workability and appearance. Therefore,
The rubber composition of the present invention can greatly improve the life of large tires.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ブタジエンゴム15〜70重量部と、天然ゴム
および/またはイソプレンゴム30〜85重量部とから成る
ゴム成分100重量部に対し、セシルトリメチルアンモニ
ウムブロマイド(CTAB)吸着比表面積140〜150m2/gおよ
びジブチルフタレート(DBP)吸油量130〜150ml/100gの
カーボンブラック30〜75重量部を配合してなることを特
徴とする大型タイヤトレッド用ゴム組成物。
1. A rubber component consisting of 15 to 70 parts by weight of butadiene rubber and 30 to 85 parts by weight of natural rubber and / or isoprene rubber, 100 parts by weight of cesyltrimethylammonium bromide (CTAB) adsorption specific surface area of 140 to 150 m A rubber composition for a large tire tread, comprising 30 to 75 parts by weight of carbon black having a 2 / g and dibutyl phthalate (DBP) oil absorption of 130 to 150 ml / 100 g.
【請求項2】動的貯蔵弾性率E′値が1.00×108〜1.35
×108kg/cm2で損失係数tanδ値が0.23〜0.28である請求
項1記載のゴム組成物。
2. A dynamic storage modulus E 'value is 1.00 × 10 8 ~1.35
The rubber composition according to claim 1, wherein the rubber composition has a loss coefficient tan δ value of 0.23 to 0.28 at × 10 8 kg / cm 2 .
【請求項3】ブタジエンゴムが35〜70重量部配合されて
いる請求項1記載のゴム組成物。
3. The rubber composition according to claim 1, wherein 35 to 70 parts by weight of butadiene rubber is compounded.
JP1004621A 1989-01-13 1989-01-13 Rubber composition for large tire tread Expired - Lifetime JP2662281B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1004621A JP2662281B2 (en) 1989-01-13 1989-01-13 Rubber composition for large tire tread

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1004621A JP2662281B2 (en) 1989-01-13 1989-01-13 Rubber composition for large tire tread

Publications (2)

Publication Number Publication Date
JPH02185543A JPH02185543A (en) 1990-07-19
JP2662281B2 true JP2662281B2 (en) 1997-10-08

Family

ID=11589127

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1004621A Expired - Lifetime JP2662281B2 (en) 1989-01-13 1989-01-13 Rubber composition for large tire tread

Country Status (1)

Country Link
JP (1) JP2662281B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0723435B2 (en) * 1990-11-26 1995-03-15 株式会社ブリヂストン Tread rubber composition for heavy duty tires

Also Published As

Publication number Publication date
JPH02185543A (en) 1990-07-19

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