JP3534329B2 - Rubber composition - Google Patents

Rubber composition

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Publication number
JP3534329B2
JP3534329B2 JP14689095A JP14689095A JP3534329B2 JP 3534329 B2 JP3534329 B2 JP 3534329B2 JP 14689095 A JP14689095 A JP 14689095A JP 14689095 A JP14689095 A JP 14689095A JP 3534329 B2 JP3534329 B2 JP 3534329B2
Authority
JP
Japan
Prior art keywords
rubber
styrene
rubber composition
weight
butadiene
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
JP14689095A
Other languages
Japanese (ja)
Other versions
JPH08311244A (en
Inventor
護 滝村
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 JP14689095A priority Critical patent/JP3534329B2/en
Publication of JPH08311244A publication Critical patent/JPH08311244A/en
Application granted granted Critical
Publication of JP3534329B2 publication Critical patent/JP3534329B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明はゴム組成物に関し、詳し
くは、航空機用タイヤのスティフナーに使用されるゴム
組成物に関するものである。 【0002】 【従来の技術】従来、航空機用タイヤでは、ビード周辺
部材の一つである硬スティフナー用ゴム組成物の配合ポ
リマー組成は天然ゴムのみであった。 【0003】タイヤの耐久性を確保するためには、ゴム
部材として硬さ(弾性率)と発熱性を考慮しなければな
らないが、その点で天然ゴムは高弾性率、低発熱であ
り、発熱性の面で優れている。また、航空機用タイヤと
しては、飛行中上空での気温低下も考慮しなければなら
ないが、天然ゴムはガラス転移温度も低く、その点でも
有利である。 【0004】 【発明が解決しようとする課題】近年、タイヤの軽量化
が進む一方で高耐久化も求められており、更なる発熱
性、耐熱性の改良が必要となってきている。天然ゴムは
前述の通り発熱性の面で優れているものの、耐熱性の面
ではなお改良の余地を残している。また、天然ゴムは、
加工性(工場作業性)の面でも改善の余地がある。 【0005】そこで、本発明の目的は、低発熱を維持し
つつ耐熱性および工場作業性を改良して、航空機用タイ
ヤのスティフナーに使用することのできるゴム組成物を
提供することにある。 【0006】 【課題を解決するための手段】本発明者は、上記課題を
解決するために鋭意検討した結果、ゴム組成物の原料ゴ
ムを天然ゴム一種ではなく、天然ゴムと特定のスチレン
−ブタジエンゴムとのブレンド系とすることにより上記
目的を達成し得ることを見出し、本発明を完成するに至
った。 【0007】すなわち、本発明のゴム組成物は、原料ゴ
ムが5〜30重量部のスチレン−ブタジエンゴムと、9
5〜70重量部の天然ゴムとからなるゴム組成物であっ
て、前記スチレン−ブタジエンゴムが溶液重合による重
合体ゴムであり、該重合体ゴムのビニル構成比が20〜
40%であり、かつそのガラス転移温度が−60℃以下
であることを特徴とするものである。 【0008】前記ゴム組成物は、航空機用タイヤのステ
ィフナーへ適用することが好ましい。 【0009】本発明のゴム組成物には、補強性充填剤、
軟化剤、老化防止剤、加硫剤、加硫促進剤、加硫促進助
剤等、通常ゴム工業で使用される配合剤を適宜配合する
ことができるのは勿論のことである。 【0010】 【作用】本発明のゴム組成物において、天然ゴムとブレ
ンド系を構成するスチレン−ブタジエンゴムの重合形態
を溶液重合に限定するのは、加工性(工場作業性)およ
び低温特性が乳化重合に比べ優れているためである。 【0011】また、前記スチレン−ブタジエンゴムのビ
ニル構成比を20〜40%の範囲内としたのは、20%
未満であると耐熱性の改良効果が小さく、一方40%を
超えるとガラス転移点(Tg)が高くなり過ぎ、好まし
くないためである。好ましくは30〜40%の範囲内で
ある。ここで、本発明では、かかるガラス転移点を−6
0℃以下に制限するが、これは−60℃を超えると、低
温特性について他のスチレン−ブタジエンゴムに対して
の優位性がなくなるためである。すなわち、本発明に係
るスチレン−ブタジエンゴムは天然ゴム並みのガラス転
移点を持つことが特徴である。ガラス転移点は−60℃
以下で、低ければ低い程よい。 【0012】上述のスチレン−ブタジエンゴムの原料ゴ
ムに対する割合は、原料ゴム100重量部に対して5〜
30重量部であり、残りは全て天然ゴムである。スチレ
ン−ブタジエンゴムが5重量部未満では工場作業性(未
加硫ゴム粘度)の改善効果が小さ過ぎ、一方、30重量
部を超えるとゴムの高温での伸びおよび破壊強力が低下
し、好ましくない。 【0013】本発明のゴム組成物は、航空機用タイヤの
スティフナーへの適用に適している。なお、現在使用さ
れている航空機用タイヤの内圧下限値は約12.0kg
f/cm2 であることから、換言すれば、内圧が12.
0kgf/cm2 以上の航空機用タイヤのスティフナー
への適用に適しているといえる。 【0014】 【実施例】次に本発明を実施例および比較例により具体
的に説明する。下記の表2に示す配合処方(重量部)の
各種試験用ゴム組成物を調製した。なお、表2に示すS
BR−A,B,Cとは、下記の表1に示す重合法により
合成し、また同表に示すビニル構成比(%)およびガラ
ス転移点(Tg)を有するスチレン−ブタジエンゴムの
ことである。 【0015】 【表1】 【0016】表1中のビニル構成比(%)は、以下よう
にして求めたものである。13C−NMR測定装置(GX
400,日本電子社(株)製を使用して、スチレン−ブ
タジエンゴム中の結合ビニル含量(%)を測定した。測
定条件は以下の通りである。 溶媒:重クロロホルム 測定温度:室温 パルス繰り返し時間:3秒 パルス幅:45° 【0017】得られた各種ゴム組成物について下記の試
験を行った。 (1)発熱性(レジリエンス) ブリティッシュ・スタンダード903:Part A
8:1963に準じて行った反発弾性試験から、下記式
により算出した。 発熱性指数=供試試験片の反発弾性率/天然ゴムのみの
比較例1の試験片の反発弾性率 発熱性指数が大きいほど、発熱性の面で優れているこ
と、すなわち発熱量が小さいことを示す。 【0018】(2)耐熱性 荷重68kg(150LB)、回転数300rpm(1
0分毎に100rpmづつ増加)、測定開始温度160
℃の状況下において、動的剪断試験を実施し、ブローア
ウトするまでの時間を測り、これを耐熱性の指標とし
た。評価は、比較例1を100として指数にて行った。
指数値が大きいほど耐熱性が良好であることを示す。 【0019】(3)工場作業性 ここでいう工場作業性とは、未加硫ゴムが工場内を流動
するときの粘度に関する事項であり、評価は、比較例1
を100として指数にて行った。指数値が大きいほど工
場作業性が良好であることを示す。得られた結果を下記
の表2に示す。 【0020】 【表2】 【0021】 【発明の効果】以上説明してきたように、本発明のゴム
組成物においては、発熱が天然ゴム並みに低く維持され
つつ、耐熱性および工場作業性が大幅に向上する。よっ
て、本発明のゴム組成物は、内圧が12.0kgf/c
2 以上の航空機用タイヤのスティフナーへの適用に適
している。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rubber composition, and more particularly to a rubber composition used for a stiffener of an aircraft tire. 2. Description of the Related Art Conventionally, in an aircraft tire, a rubber composition for a hard stiffener, which is one of the peripheral parts of a bead, is composed of only natural rubber. In order to ensure the durability of a tire, it is necessary to consider hardness (elastic modulus) and heat generation as a rubber member. In that respect, natural rubber has a high elastic modulus, low heat generation, and heat generation. Excellent in terms of sex. In addition, for an aircraft tire, it is necessary to consider a decrease in air temperature during the flight, but natural rubber is also advantageous in that it has a low glass transition temperature. [0004] In recent years, while the weight of tires has been reduced, high durability has also been required, and further improvements in heat generation and heat resistance have been required. Although natural rubber is excellent in terms of heat generation as described above, there is still room for improvement in heat resistance. Also, natural rubber is
There is also room for improvement in terms of workability (factory workability). Accordingly, an object of the present invention is to provide a rubber composition which can be used for a stiffener of an aircraft tire while improving heat resistance and factory workability while maintaining low heat generation. The present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, the raw material rubber of the rubber composition is not a natural rubber but a natural rubber and a specific styrene-butadiene. It has been found that the above object can be achieved by using a blend system with rubber, and the present invention has been completed. That is, the rubber composition of the present invention comprises a styrene-butadiene rubber containing 5 to 30 parts by weight of a raw rubber;
A rubber composition comprising 5 to 70 parts by weight of natural rubber, wherein the styrene-butadiene rubber is a polymer rubber obtained by solution polymerization, and the vinyl composition ratio of the polymer rubber is 20 to
40% and a glass transition temperature of −60 ° C. or less. Preferably, the rubber composition is applied to a stiffener of an aircraft tire. The rubber composition of the present invention comprises a reinforcing filler,
Needless to say, compounding agents usually used in the rubber industry, such as a softening agent, an antioxidant, a vulcanizing agent, a vulcanization accelerator, and a vulcanization accelerator, can be appropriately compounded. In the rubber composition of the present invention, the polymerization mode of the styrene-butadiene rubber constituting the blend system with the natural rubber is limited to the solution polymerization because the processability (factory workability) and the low-temperature characteristics are emulsified. This is because it is superior to polymerization. The reason why the vinyl composition ratio of the styrene-butadiene rubber is in the range of 20 to 40% is that 20% or less.
If it is less than 40%, the effect of improving heat resistance is small, while if it exceeds 40%, the glass transition point (Tg) becomes too high, which is not preferable. Preferably it is in the range of 30 to 40%. Here, in the present invention, such a glass transition point is -6.
The temperature is limited to 0 ° C. or less, because if the temperature exceeds −60 ° C., the low-temperature properties lose their advantage over other styrene-butadiene rubbers. That is, the styrene-butadiene rubber according to the present invention is characterized by having a glass transition point comparable to that of natural rubber. Glass transition point is -60 ° C
Below, the lower the better. The ratio of the styrene-butadiene rubber to the raw rubber is 5 to 100 parts by weight of the raw rubber.
30 parts by weight, the rest being all natural rubber. If the styrene-butadiene rubber is less than 5 parts by weight, the effect of improving factory workability (unvulcanized rubber viscosity) is too small, while if it exceeds 30 parts by weight, elongation and breaking strength of the rubber at high temperatures are reduced, which is not preferable. . [0013] The rubber composition of the present invention is suitable for application to a stiffener of an aircraft tire. The lower limit of the internal pressure of currently used aircraft tires is about 12.0 kg.
f / cm 2 , in other words, the internal pressure is 12.
It can be said that it is suitable for application to aircraft stiffeners of 0 kgf / cm 2 or more. Next, the present invention will be described in detail with reference to examples and comparative examples. Various test rubber compositions having the formulation (parts by weight) shown in Table 2 below were prepared. In addition, S shown in Table 2
BR-A, B, and C are styrene-butadiene rubbers synthesized by a polymerization method shown in Table 1 below and having a vinyl composition ratio (%) and a glass transition point (Tg) shown in the table. . [Table 1] The vinyl composition ratio (%) in Table 1 is determined as follows. 13 C-NMR measurement device (GX
400, manufactured by JEOL Ltd., the bound vinyl content (%) in the styrene-butadiene rubber was measured. The measurement conditions are as follows. Solvent: deuterated chloroform Measurement temperature: room temperature Pulse repetition time: 3 seconds Pulse width: 45 ° The following tests were performed on the obtained various rubber compositions. (1) Exothermicity (resilience) British Standard 903: Part A
8: It was calculated from the following equation from a rebound resilience test performed according to 1963. Exothermic index = rebound resilience of test specimen / rebound resilience of test piece of Comparative Example 1 using only natural rubber The larger the exothermic index, the better the exothermic property, that is, the smaller the calorific value. Is shown. (2) Heat resistance load 68 kg (150 LB), rotation speed 300 rpm (1
100 rpm increments every 0 minutes), measurement start temperature 160
Under a condition of ° C., a dynamic shear test was carried out, a time until blow-out was measured, and this was used as an index of heat resistance. The evaluation was performed using an index with Comparative Example 1 being 100.
The larger the index value, the better the heat resistance. (3) Factory workability The factory workability as referred to herein is a matter relating to the viscosity when unvulcanized rubber flows in a factory.
And the index was set as 100. The larger the index value, the better the factory workability. The results obtained are shown in Table 2 below. [Table 2] As described above, in the rubber composition of the present invention, heat generation and factory workability are greatly improved while heat generation is maintained as low as natural rubber. Therefore, the rubber composition of the present invention has an internal pressure of 12.0 kgf / c.
m 2 or more is suitable for application to the stiffener of aircraft tires.

Claims (1)

(57)【特許請求の範囲】 【請求項1】 原料ゴムが5〜30重量部のスチレン−
ブタジエンゴムと、95〜70重量部の天然ゴムとから
なるゴム組成物であって、前記スチレン−ブタジエンゴ
ムが溶液重合による重合体ゴムであり、該重合体ゴムの
ビニル構成比が20〜40%であり、かつそのガラス転
移温度が−60℃以下であることを特徴とする航空機用
タイヤのスティフナーに使用されるゴム組成物。
(57) [Claims 1] The raw rubber is 5 to 30 parts by weight of styrene.
A rubber composition comprising butadiene rubber and 95 to 70 parts by weight of a natural rubber, wherein the styrene-butadiene rubber is a polymer rubber obtained by solution polymerization, and the vinyl constituent ratio of the polymer rubber is 20 to 40%. Characterized by having a glass transition temperature of -60 ° C or lower .
A rubber composition used for tire stiffeners .
JP14689095A 1995-05-23 1995-05-23 Rubber composition Expired - Lifetime JP3534329B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14689095A JP3534329B2 (en) 1995-05-23 1995-05-23 Rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14689095A JP3534329B2 (en) 1995-05-23 1995-05-23 Rubber composition

Publications (2)

Publication Number Publication Date
JPH08311244A JPH08311244A (en) 1996-11-26
JP3534329B2 true JP3534329B2 (en) 2004-06-07

Family

ID=15417896

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14689095A Expired - Lifetime JP3534329B2 (en) 1995-05-23 1995-05-23 Rubber composition

Country Status (1)

Country Link
JP (1) JP3534329B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4810145B2 (en) * 2005-07-12 2011-11-09 株式会社ブリヂストン Pneumatic radial tire for high speed and high load
JP5101865B2 (en) * 2006-04-11 2012-12-19 住友ゴム工業株式会社 Rubber composition for bead apex and tire having bead apex using the same
JP5475032B2 (en) * 2006-04-11 2014-04-16 住友ゴム工業株式会社 Rubber composition for bead apex and tire having bead apex using the same

Also Published As

Publication number Publication date
JPH08311244A (en) 1996-11-26

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