JPS61200138A - Rubber composition - Google Patents

Rubber composition

Info

Publication number
JPS61200138A
JPS61200138A JP4151785A JP4151785A JPS61200138A JP S61200138 A JPS61200138 A JP S61200138A JP 4151785 A JP4151785 A JP 4151785A JP 4151785 A JP4151785 A JP 4151785A JP S61200138 A JPS61200138 A JP S61200138A
Authority
JP
Japan
Prior art keywords
rubber
weight
parts
diene
blended
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
JP4151785A
Other languages
Japanese (ja)
Inventor
Shinichi Miyazaki
真一 宮崎
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 JP4151785A priority Critical patent/JPS61200138A/en
Priority to AU54207/86A priority patent/AU574267B2/en
Priority to NZ21535386A priority patent/NZ215353A/en
Publication of JPS61200138A publication Critical patent/JPS61200138A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a rubber composition having excellent processability in unvulcanized state and giving a vulcanized product having high hardness, by compounding a liquid phenolic compound having double bond on a side chain. CONSTITUTION:100pts.(wt.) of natural rubber, diene rubber, diene copolymer rubber,or their blended rubber is compounded with 1-50pts. of a liquid phenolic compound having double bond on a side chain. A phenolic compound existing in cashew oil is most effective. Preferably, the composition is further compounded with <=30pts. of a novolac phenolic resin and <=8pts. of morpholine disulfide.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、タイヤのトレッド、ビードフィラー等に使
用される高硬度のゴム組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a high hardness rubber composition used for tire treads, bead fillers, etc.

(従来技術とその問題点) 加硫ゴムの状態で高い硬度を有するゴム配合物では、加
硫ゴムの硬度と動的弾性率が高くなるにつれて未加硫ゴ
ムの状態での硬度と引張応力も大きくなる傾向がある。
(Prior art and its problems) In a rubber compound that has high hardness in the vulcanized rubber state, as the hardness and dynamic modulus of the vulcanized rubber increase, the hardness and tensile stress in the unvulcanized rubber state also increase. It tends to get bigger.

第1図はこの様子をあられすもので、加硫ゴムの硬度お
よび動的弾性率と、未加硫ゴムの状態における硬度およ
び引張応力が直線関係にあり、加硫後に高い硬度を有す
るゴム配合物(例えばDで示す範囲のもの)は未加硫ゴ
ムの状態における硬度と引張応力も非常に高くなること
がわかる。このため、高硬度が必要なゴム配合物では、
未加硫ゴムの段階での押出し、折曲げ加工等における加
工性が著しく低下し、加工が困骸になるという問題があ
った。
Figure 1 shows this situation, and shows that the hardness and dynamic modulus of vulcanized rubber are in a linear relationship with the hardness and tensile stress in the unvulcanized rubber state, and rubber compounds that have high hardness after vulcanization. It can be seen that the hardness and tensile stress in the unvulcanized rubber state of the products (for example, those in the range indicated by D) are also very high. For this reason, in rubber compounds that require high hardness,
There was a problem in that the processability in extrusion, bending, etc. at the stage of unvulcanized rubber was significantly reduced, making processing difficult.

(発明の目的) この発明は、未加硫ゴムの段階での加工性が良好で、加
硫後に高硬度の得られるゴム組成物を提供することを目
的としている。
(Objective of the Invention) An object of the present invention is to provide a rubber composition which has good processability in the unvulcanized rubber stage and which provides high hardness after vulcanization.

(発明の開示) 本発明にかかるゴム組成物は、天然ゴム、ジエン系ゴム
もしくはジエン系共重合ゴムまたはこれらの2N以−ヒ
をブレンドしたブレンドゴム(以下、これらを総称して
ゴムと呼ぶ)100重量部に対し、側鎖に二重結合を持
つ液状のフェノール類1〜50重量部を配合したことを
特徴としている。
(Disclosure of the Invention) The rubber composition according to the present invention is a natural rubber, a diene rubber, a diene copolymer rubber, or a blend rubber obtained by blending 2N or more of these rubbers (hereinafter, these are collectively referred to as rubber). It is characterized in that 1 to 50 parts by weight of a liquid phenol having a double bond in the side chain is blended per 100 parts by weight.

このように、側鎖に二重結合を有する液状のフェノール
類を一定の範囲内でゴムに添加しておくことにより、未
加硫の状態で加工性がよく、加硫後に所望の高硬度を有
するゴム組成物が得られるのである。この場合において
、側鎖に二重結合を持つ液状のフェノール類の配合量が
ゴム100重量部に対し1重量部以下では期待されるよ
うな未加硫持における硬度低下効果が得られず、加工性
も悪いものとなる。逆に上記フェノール類の配合j−゛
が50重賃部を越える場合は、未加硫ゴムの粘度が低下
しすぎて、加工性に支障をきたすようになるので、いず
れも好ましくない。なお、実験の結果では、上記側鎖に
二重結合を持つ液状フェノール類としてカシューオイル
中に主成分として含まれるフェノール類を使用するのが
最も効果的であった。
By adding liquid phenols having double bonds in their side chains to rubber within a certain range, it is possible to improve processability in the unvulcanized state and achieve the desired high hardness after vulcanization. A rubber composition having the following characteristics is obtained. In this case, if the amount of liquid phenols having a double bond in the side chain is less than 1 part by weight per 100 parts by weight of rubber, the expected effect of reducing hardness in the uncured state cannot be obtained, and processing Sexuality also becomes bad. On the other hand, if the proportion of the phenols exceeds 50 parts by weight, the viscosity of the unvulcanized rubber decreases too much, impeding processability, which is undesirable. According to the results of the experiment, it was most effective to use the phenols contained in cashew oil as a main component as the liquid phenols having double bonds in their side chains.

また、これらゴムとフェノール類に加えて、従来主とし
て硬化剤として使用されているノボラック型フェノール
樹脂をゴム100重績部に対し30咀量部以下の範囲で
添加しておいても良好な結果が得られた。さらに、加硫
剤として、硫黄の他にモルホリンジスルフィドをゴム1
00重量部に対し8重醍部以下の範囲で添加しておいて
も同様に良好な結果が得られた。
In addition to these rubbers and phenols, good results can also be obtained by adding novolac type phenolic resin, which has conventionally been mainly used as a curing agent, in an amount of 30 parts by weight or less per 100 parts by weight of rubber. Obtained. Furthermore, as a vulcanizing agent, in addition to sulfur, morpholine disulfide was added to the rubber.
Similarly good results were obtained even when the amount was added in an amount of 8 parts by weight or less per 00 parts by weight.

(実施例および比較例) 以下、本発明の実施例と比較例について説明すれば、第
1表は種々の配合における加硫ゴムと未加硫ゴムの性質
をあられすもので、実施例1では比較例1と較べてカー
ボンブラック配合量が少ないにもかかわらず、加硫ゴム
での硬度と動的弾性率が比較例1と同等である。また、
未加硫ゴムでの硬度と引張応力が低く、加工性にすぐれ
ていることがわかる。
(Examples and Comparative Examples) Below, the Examples and Comparative Examples of the present invention will be explained. Table 1 shows the properties of vulcanized rubber and unvulcanized rubber in various formulations. Although the amount of carbon black blended is smaller than that of Comparative Example 1, the hardness and dynamic elastic modulus of the vulcanized rubber are the same as those of Comparative Example 1. Also,
It can be seen that the hardness and tensile stress of unvulcanized rubber are low, and it has excellent workability.

実施例2は、従来主として硬化剤として使用されている
ノボラック型フェノール樹脂および硬化剤に代えて、側
鎖に二重結合を有する液状のフェノール類および硬化剤
を用いた例であり、加硫ゴムの硬度と動的弾性率は比較
例2とほぼ同等であり、未加硫ゴムの加工性は比較例2
よりも大幅に改良されていることがわかる。
Example 2 is an example in which a liquid phenol having a double bond in the side chain and a curing agent were used in place of the novolak type phenolic resin and curing agent that have been conventionally mainly used as a curing agent. The hardness and dynamic modulus of elasticity are almost the same as those of Comparative Example 2, and the processability of the unvulcanized rubber is that of Comparative Example 2.
It can be seen that it is significantly improved.

実施例3は上記液状のフェノール類と7ポラツク型フエ
ノールレジンとを併用した例をあられし、実施例4は加
硫剤としてモリホリンジスルフィドを硫黄と併用した例
をあられす、実施例3.4のいずれにおいても、実施例
1.2の場合と同様に加硫ゴム物性を損なうことなく未
加硫ゴムにおける加工性が改善されている。
Example 3 shows an example in which the above-mentioned liquid phenols and 7-Pollack type phenol resin were used in combination, and Example 4 shows an example in which morpholine disulfide was used in combination with sulfur as a vulcanizing agent. Example 3.4 In both cases, the processability of the unvulcanized rubber is improved without impairing the physical properties of the vulcanized rubber, as in the case of Example 1.2.

(発明の効果) 以Hに説明した如く本発明にかかるゴム組成物は・未加
硫ゴムの状態における加工性が良好で、加硫後に高硬度
のゴム組成物を得ることのできるすぐれたものとなった
。このゴム組成物は、タイヤのトレッドやビードフィラ
ーその他高硬度が必要とされるゴム製品の原料として好
適に使用することができるものである。
(Effects of the Invention) As explained in H below, the rubber composition according to the present invention has excellent processability in the unvulcanized rubber state and is capable of obtaining a rubber composition with high hardness after vulcanization. It became. This rubber composition can be suitably used as a raw material for tire treads, bead fillers, and other rubber products that require high hardness.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、未加硫ゴムと加硫ゴムの物性の相関性をあら
れすグラフである。 (以下余白)
FIG. 1 is a graph showing the correlation between the physical properties of unvulcanized rubber and vulcanized rubber. (Margin below)

Claims (4)

【特許請求の範囲】[Claims] (1)天然ゴム、ジエン系ゴムもしくはジエン系共重合
ゴムまたはこれらの2種以上をブレンドしたブレンドゴ
ム100重量部に対し、側鎖に二重結合を持つ液状のフ
ェノール類1〜50重量部を配合したことを特徴とする
ゴム組成物。
(1) 1 to 50 parts by weight of a liquid phenol having a double bond in the side chain is added to 100 parts by weight of natural rubber, diene rubber, diene copolymer rubber, or a blended rubber of two or more of these. A rubber composition comprising:
(2)側鎖に二重結合を持つ液状のフェノール類が、カ
シューオイル中に主成分として含まれるフェノール類で
あるゴム組成物。
(2) A rubber composition in which liquid phenols having double bonds in side chains are phenols contained as a main component in cashew oil.
(3)天然ゴム、ジエン系ゴムもしくはジエン系共重合
ゴムまたはこれらの2種以上をブレンドしたブレンドゴ
ム100重量部に対し、30重量部以下のノボラック型
フェノール樹脂を配合してなる特許請求の範囲第1項記
載のゴム組成物。
(3) Claims comprising 30 parts by weight or less of a novolac-type phenolic resin mixed with 100 parts by weight of natural rubber, diene rubber, diene copolymer rubber, or a blended rubber of two or more of these. The rubber composition according to item 1.
(4)天然ゴム、ジエン系ゴムもしくはジエン系共重合
ゴムまたはこれらの2種以上をブレンドしたブレンドゴ
ム100重量部に対し、8重量部以下のモルホリンジス
ルフィドを配合してなる特許請求の範囲第1項記載のゴ
ム組成物。
(4) 8 parts by weight or less of morpholine disulfide is blended with 100 parts by weight of natural rubber, diene rubber, diene copolymer rubber, or a blended rubber of two or more of these. The rubber composition described in .
JP4151785A 1985-03-01 1985-03-01 Rubber composition Pending JPS61200138A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP4151785A JPS61200138A (en) 1985-03-01 1985-03-01 Rubber composition
AU54207/86A AU574267B2 (en) 1985-03-01 1986-03-03 Rubber-phenol compound
NZ21535386A NZ215353A (en) 1985-03-01 1986-03-03 Rubber compositions containing phenol derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4151785A JPS61200138A (en) 1985-03-01 1985-03-01 Rubber composition

Publications (1)

Publication Number Publication Date
JPS61200138A true JPS61200138A (en) 1986-09-04

Family

ID=12610565

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4151785A Pending JPS61200138A (en) 1985-03-01 1985-03-01 Rubber composition

Country Status (3)

Country Link
JP (1) JPS61200138A (en)
AU (1) AU574267B2 (en)
NZ (1) NZ215353A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100237253B1 (en) * 1997-07-29 2000-01-15 홍건희 A rubber composition for tread of tire

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8710171D0 (en) * 1987-04-29 1987-06-03 Shell Int Research Copolymer composition

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4238470A (en) * 1979-07-30 1980-12-09 Stauffer Chemical Company Method for oil-treating insoluble sulfur
US4644988A (en) * 1984-01-31 1987-02-24 The B.F. Goodrich Company High performance tire and tread compound for it
JPS61200137A (en) * 1985-03-01 1986-09-04 Sumitomo Rubber Ind Ltd Dispersion-improving agent for rubber composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100237253B1 (en) * 1997-07-29 2000-01-15 홍건희 A rubber composition for tread of tire

Also Published As

Publication number Publication date
AU5420786A (en) 1986-09-04
AU574267B2 (en) 1988-06-30
NZ215353A (en) 1989-02-24

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