JP2001247718A - Rubber composition - Google Patents
Rubber compositionInfo
- Publication number
- JP2001247718A JP2001247718A JP2000058876A JP2000058876A JP2001247718A JP 2001247718 A JP2001247718 A JP 2001247718A JP 2000058876 A JP2000058876 A JP 2000058876A JP 2000058876 A JP2000058876 A JP 2000058876A JP 2001247718 A JP2001247718 A JP 2001247718A
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- Japan
- Prior art keywords
- weight
- silica
- rubber
- rubber composition
- salt
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、シリカとシランカ
ップリング剤を含むゴム組成物に関し、加工性を低下さ
せることなく、転がり摩擦抵抗性(燃費特性)および耐
摩耗性に特に優れたゴム組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rubber composition containing silica and a silane coupling agent, and more particularly to a rubber composition excellent in rolling friction resistance (fuel consumption characteristics) and abrasion resistance without lowering workability. About things.
【0002】[0002]
【従来の技術】近年、自動車に対する安全性および低燃
費性への要求にもとなって、タイヤ用ゴム材料において
ウエットスキッド特性、燃費特性、耐摩耗性の同時改良
が望まれているがお互いに二律背反の関係にあることは
よく知られている。2. Description of the Related Art In recent years, there has been a demand for safety and low fuel consumption of automobiles, and it has been desired to simultaneously improve wet skid characteristics, fuel consumption characteristics and wear resistance of rubber materials for tires. It is well known that there is a trade-off.
【0003】従来から、このような問題を解決する方法
としては、低発熱化充填材としてシリカを使用する方法
などが知られている。シリカはその表面官能基であるシ
ラノール基が水素結合するために、シリカ粒子同士が凝
集する傾向にあり、シランカップリング剤はこれらのシ
ラノール基と結合してシリカ同士の凝集を防ぎ、加工性
を改善すると考えられている。一方、性能面においては
シリカとポリマーがシランカップリング剤と化学的に結
合することにより、転がり抵抗の低減や摩耗性が改善さ
れると考えられている。しかし、これらの目的を達成す
るためにはシリカとシランカップリング剤を混練り、加
工中に化学的に反応させる必要があり、シリカとシラン
カップリング剤を充分に反応させるためには高温でよく
練る方がよいとされている。ところが、シランカップリ
ング剤中のゴムと反応をする官能基部分が混練りなどの
加工中にかかる温度によって一部ゴムとの反応を起こし
てしまうため、ゲル化といわれるゴム焼けの現象が起こ
る。しかしながら、ゴム焼けが起こらないような低温で
混練りするとシリカとシランカップリング剤の反応が不
充分となるという矛盾点が生じる。Conventionally, as a method of solving such a problem, a method of using silica as a low heat generation filler has been known. Silica tends to agglomerate with each other because the silanol groups that are its surface functional groups are hydrogen-bonded, and the silane coupling agent binds with these silanol groups to prevent agglomeration of the silicas and improve processability. It is thought to improve. On the other hand, in terms of performance, it is considered that the silica and the polymer are chemically bonded to the silane coupling agent, so that the rolling resistance is reduced and the abrasion is improved. However, in order to achieve these objects, it is necessary to knead the silica and the silane coupling agent and chemically react them during processing. It is better to knead it. However, a part of the functional group that reacts with the rubber in the silane coupling agent partially reacts with the rubber due to the temperature applied during processing such as kneading, so that a rubber burning phenomenon called gelation occurs. However, if kneading is performed at such a low temperature that rubber scorching does not occur, there occurs a contradiction that the reaction between the silica and the silane coupling agent becomes insufficient.
【0004】[0004]
【発明が解決しようとする課題】本発明は、天然ゴムお
よび/またはジエン系合成ゴムに対して特定量のシリカ
およびシランカップリング剤を含むゴム組成物の加工特
性を低下させることなく転がり摩擦抵抗性(燃費特性)
および耐磨耗性を改善したゴム組成物を提供することを
目的とする。SUMMARY OF THE INVENTION The present invention provides a rubber composition containing a specific amount of silica and a silane coupling agent with respect to natural rubber and / or diene-based synthetic rubber without reducing the processing characteristics of the rubber composition. Performance (fuel efficiency characteristics)
Another object of the present invention is to provide a rubber composition having improved abrasion resistance.
【0005】[0005]
【課題を解決するための手段】本発明者らは、前記の諸
問題を改善すべく鋭意検討した結果、ゴム焼けを起こさ
ず、シリカとシランカップリング剤の反応を効率よく促
進(補助)し得るような特定の化合物を用いることによ
り、加工性を低下させることなく、転がり抵抗特性およ
び耐摩耗性を満足させる方法を見出し、本発明を完成す
るに至ったのである。Means for Solving the Problems The present inventors have conducted intensive studies to improve the above-mentioned problems, and as a result, have efficiently promoted (assisted) the reaction between silica and a silane coupling agent without causing rubber scorch. By using a specific compound as obtained, a method for satisfying the rolling resistance characteristics and the wear resistance without lowering the workability was found, and the present invention was completed.
【0006】すなわち、本発明は、天然ゴムおよび/ま
たはジエン系合成ゴム100重量部に対して、シリカを
5〜100重量部、シランカップリング剤をシリカ重量
に対して2〜20重量%およびナトリウム塩をシリカ重
量に対して1〜20重量%含むことを特徴とするゴム組
成物(請求項1)である。That is, according to the present invention, 5 to 100 parts by weight of silica, 2 to 20% by weight of silane coupling agent and 2 to 20% by weight of sodium based on 100 parts by weight of natural rubber and / or diene synthetic rubber are used. A rubber composition (claim 1) comprising a salt in an amount of 1 to 20% by weight based on the weight of silica.
【0007】また、本発明は、ナトリウム塩が酸素酸塩
または有機酸塩である請求項1記載のゴム組成物(請求
項2)である。Further, the present invention is the rubber composition according to claim 1, wherein the sodium salt is an oxyacid salt or an organic acid salt (claim 2).
【0008】また、本発明は、ナトリウム塩が結晶水を
有する含水塩である請求項1または2記載のゴム組成物
(請求項3)である。Further, the present invention is the rubber composition according to claim 1 or 2, wherein the sodium salt is a hydrous salt having water of crystallization.
【0009】また、本発明は、ナトリウム塩がリン酸塩
である請求項1、2または3記載のゴム組成物(請求項
4)である。The present invention also provides the rubber composition according to any one of claims 1, 2 and 3, wherein the sodium salt is a phosphate.
【0010】[0010]
【発明の実施の形態】以下本発明を詳細に説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail.
【0011】本発明のゴム組成物はゴム成分として天然
ゴム(NR)および/またはジエン系合成ゴムを含む。
本発明において用いるジエン系合成ゴムとしては、スチ
レン−ブタジエンゴム(SBR)、ポリブタジエンゴム
(BR)、ポリイソプレンゴム(IR)、エチレン−プ
ロピレン−ジエンゴム(EPDM)、クロロプレンゴム
(CR)、アクリロニトリル−ブタジエンゴム(NB
R)などがあげられ、本発明に使用されるゴム成分中に
1種類または2種類以上含まれていてもよい。The rubber composition of the present invention contains a natural rubber (NR) and / or a diene-based synthetic rubber as a rubber component.
Examples of the diene synthetic rubber used in the present invention include styrene-butadiene rubber (SBR), polybutadiene rubber (BR), polyisoprene rubber (IR), ethylene-propylene-diene rubber (EPDM), chloroprene rubber (CR), and acrylonitrile-butadiene. Rubber (NB
R) and the like, and one or more kinds may be contained in the rubber component used in the present invention.
【0012】本発明のゴム組成物は充填材としてシリカ
を含む。シリカとしては、特に制限はないが、乾式法シ
リカ(無水ケイ酸)、湿式法シリカ(含水ケイ酸)など
があげられ、湿式法シリカが好ましい。湿式法シリカの
好適例としては、デグサ製Ultrasil VN3
(商品名)、日本シリカ(株)製ニップシールVN3A
Q(商品名)などがあげられる。シリカとしては、たと
えば、窒素吸着比表面積が100〜300m2/gのシ
リカを用いることができる。窒素吸着比表面積が小さい
シリカでは充分な弾性率が得られず耐磨耗性が悪化する
傾向があり、大きいシリカではグリップ力向上が望めな
いわりに混練り作業性が低下する傾向がある。[0012] The rubber composition of the present invention contains silica as a filler. The silica is not particularly limited, and examples thereof include dry silica (silicic anhydride) and wet silica (hydrous silicic acid), with wet silica being preferred. Preferred examples of wet-process silica include Ultrasil VN3 manufactured by Degussa.
(Trade name), Nippon Silica Co., Ltd. Nip Seal VN3A
Q (product name) and the like. As the silica, for example, silica having a nitrogen adsorption specific surface area of 100 to 300 m 2 / g can be used. With silica having a small nitrogen adsorption specific surface area, a sufficient elastic modulus cannot be obtained, and abrasion resistance tends to be deteriorated. With silica having a large nitrogen adsorption specific surface area, kneading workability tends to be reduced without improving grip power.
【0013】シリカの配合量は、ゴム成分100重量部
に対して5〜100重量部、好ましくは10〜85重量
部、さらに好ましくは20〜65重量部である。シリカ
の配合が5重量部未満では、補強効果が小さく、100
重量部を超えると発熱性が増大し、作業性が悪化するた
め好ましくない。低発熱性および作業性の両面から、シ
リカの配合量は20〜65重量部が好ましい。The amount of silica is 5 to 100 parts by weight, preferably 10 to 85 parts by weight, more preferably 20 to 65 parts by weight, based on 100 parts by weight of the rubber component. If the silica content is less than 5 parts by weight, the reinforcing effect is small, and
Exceeding the weight part is not preferable because heat generation increases and workability deteriorates. From the viewpoint of both low heat generation and workability, the amount of silica is preferably 20 to 65 parts by weight.
【0014】本発明のゴム組成物は、充填材とゴム成分
の結合を強め、耐磨耗性を向上させるために、シランカ
ップリング剤を含む。シランカップリング剤としては、
従来からシリカ充填材と併用される任意のシランカップ
リング剤を使用することができる。The rubber composition of the present invention contains a silane coupling agent in order to strengthen the bond between the filler and the rubber component and to improve abrasion resistance. As a silane coupling agent,
Any silane coupling agent conventionally used in combination with the silica filler can be used.
【0015】シランカップリング剤としては、具体的に
は、ビス(3−トリエトキシシリルプロピル)テトラス
ルフィド、ビス(2−トリエトキシシリルエチル)テト
ラスルフィド、ビス(3−トリメトキシシリルプロピ
ル)テトラスルフィド、ビス(2−トリメトキシシリル
エチル)テトラスルフィド、3−メルカプトプロピルト
リメトキシシラン、3−メルカプトプロピルトリエトキ
シシラン、2−メルカプトエチルトリメトキシシラン、
2−メルカプトエチルトリエトキシシラン、3−ニトロ
プロピルトリメトキシシラン、3−ニトロプロピルトリ
エトキシシラン、3−クロロプロピルトリメトキシシラ
ン、3−クロロプロピルトリエトキシシラン、2−クロ
ロエチルトリメトキシシラン、2−クロロエチルトリエ
トキシシラン、3−トリメトキシシリルプロピル−N,
N−ジメチルチオカルバモイルテトラスルフィド、3−
トリエトキシシリルプロピル−N,N−ジメチルチオカ
ルバモイルテトラスルフィド、2−トリエトキシシリル
エチル−N,N−ジメチルチオカルバモイルテトラスル
フィド、3−トリメトキシシリルプロピルベンゾチアゾ
ールテトラスルフィド、3−トリエトキシシリルプロピ
ルベンゾチアゾールテトラスルフィド、3−トリエトキ
シシリルプロピルメタクリレートモノスルフィド、3−
トリメトキシシリルプロピルメタクリレートモノスルフ
ィドなどがあげられ、カップリング剤添加効果とコスト
の両立から、ビス(3−トリエトキシシリルプロピル)
テトラスルフィドなどが好ましい。Examples of the silane coupling agent include bis (3-triethoxysilylpropyl) tetrasulfide, bis (2-triethoxysilylethyl) tetrasulfide, and bis (3-trimethoxysilylpropyl) tetrasulfide. , Bis (2-trimethoxysilylethyl) tetrasulfide, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltrimethoxysilane,
2-mercaptoethyltriethoxysilane, 3-nitropropyltrimethoxysilane, 3-nitropropyltriethoxysilane, 3-chloropropyltrimethoxysilane, 3-chloropropyltriethoxysilane, 2-chloroethyltrimethoxysilane, 2-chloropropyltrimethoxysilane Chloroethyltriethoxysilane, 3-trimethoxysilylpropyl-N,
N-dimethylthiocarbamoyl tetrasulfide, 3-
Triethoxysilylpropyl-N, N-dimethylthiocarbamoyltetrasulfide, 2-triethoxysilylethyl-N, N-dimethylthiocarbamoyltetrasulfide, 3-trimethoxysilylpropylbenzothiazole tetrasulfide, 3-triethoxysilylpropylbenzo Thiazole tetrasulfide, 3-triethoxysilylpropyl methacrylate monosulfide, 3-
Trimethoxysilylpropyl methacrylate monosulfide; and bis (3-triethoxysilylpropyl)
Tetrasulfide is preferred.
【0016】シランカップリング剤の配合量は前記シリ
カ重量に対して2〜20重量%である。シランカップリ
ング剤の配合量が2重量%未満では、カップリング効果
が小さく、20重量%を超えると、コストが上がる割に
カップリング効果が得られないため好ましくない。カッ
プリング効果と分散効果の両面からシランカップリング
剤の配合量は4〜15重量%であることが好ましい。The amount of the silane coupling agent is 2 to 20% by weight based on the weight of the silica. If the amount of the silane coupling agent is less than 2% by weight, the coupling effect is small, and if it exceeds 20% by weight, the coupling effect is not obtained although the cost is increased. The amount of the silane coupling agent is preferably 4 to 15% by weight from the viewpoint of both the coupling effect and the dispersion effect.
【0017】本発明のゴム組成物はナトリウム塩を含
む。本発明で使用できるナトリウム塩は、たとえば、酸
素酸塩もしくは有機酸塩、好ましくはリン酸塩であり、
または、結晶水を有する含水塩であり、より好ましくは
酸素酸塩または有機酸塩の結晶水を有する含水塩、さら
に好ましくは結晶水を有するリン酸塩である。[0017] The rubber composition of the present invention contains a sodium salt. The sodium salt that can be used in the present invention is, for example, an oxyacid salt or an organic acid salt, preferably a phosphate,
Alternatively, a hydrate salt having water of crystallization, more preferably a hydrate salt having water of crystallization of an oxyacid salt or an organic acid salt, still more preferably a phosphate salt having water of crystallization.
【0018】ナトリウム塩としては、具体的には、リン
酸水素二ナトリウム、リン酸二水素ナトリウム、リン酸
三ナトリウム、亜リン酸水素二ナトリウム、二リン酸二
水素二ナトリウム、ホスフィン酸ナトリウム、炭酸ナト
リウム、炭酸水素ナトリウム、硫酸ナトリウム、亜硫酸
ナトリウム、二硫酸ナトリウム、二亜硫酸ナトリウム、
酢酸ナトリウム、クエン酸三ナトリウム、シュウ酸ナト
リウム、コハク酸二ナトリウムなどがあげられる。ま
た、含水塩としては、リン酸水素二ナトリウム・7水和
物、リン酸水素二ナトリウム・12水和物、リン酸二水
素ナトリウム・2水和物、リン酸三ナトリウム・12水
和物、亜リン酸水素二ナトリウム・5水和物、炭酸ナト
リウム・10水和物、硫酸ナトリウム・10水和物、亜
硫酸ナトリウム・7水和物、酢酸ナトリウム・3水和
物、クエン酸三ナトリウム・2水和物、コハク酸二ナト
リウム・6水和物などがあげられる。Specific examples of the sodium salt include disodium hydrogen phosphate, sodium dihydrogen phosphate, trisodium phosphate, disodium hydrogen phosphite, disodium dihydrogen diphosphate, sodium phosphinate, carbonate Sodium, sodium bicarbonate, sodium sulfate, sodium sulfite, sodium disulfate, sodium disulfite,
Examples include sodium acetate, trisodium citrate, sodium oxalate, disodium succinate and the like. Examples of the hydrated salt include disodium hydrogen phosphate heptahydrate, disodium hydrogen phosphate dodecahydrate, sodium dihydrogen phosphate dodecahydrate, trisodium phosphate dodecahydrate, Disodium hydrogen phosphite pentahydrate, sodium carbonate decahydrate, sodium sulfate decahydrate, sodium sulfite hemihydrate, sodium acetate trihydrate, trisodium citrate dihydrate Hydrate, disodium succinate hexahydrate and the like.
【0019】ナトリウム塩の配合量は、シリカ重量に対
して1〜20重量%、好ましくは2〜15重量%であ
る。ナトリウム塩の配合量が1重量%未満であるとシリ
カとシランカップリング剤の反応促進効果が小さく、2
0重量%を超えると補強性の悪化が生じるために好まし
くない。ナトリウム塩の配合量はカップリング反応促進
効果の面から2〜15重量%が好ましい。The amount of the sodium salt is from 1 to 20% by weight, preferably from 2 to 15% by weight, based on the weight of the silica. If the amount of the sodium salt is less than 1% by weight, the reaction promoting effect between silica and the silane coupling agent is small,
If it exceeds 0% by weight, the reinforcing property is deteriorated, which is not preferable. The amount of the sodium salt is preferably 2 to 15% by weight from the viewpoint of the effect of promoting the coupling reaction.
【0020】本発明のゴム組成物は、上記シリカ以外に
も充填材として、カーボンブラックを含むことができ
る。カーボンブラックとしては、たとえば、HAF、I
SAF、SAFなどがあげられるが、特に限定されるも
のではない。カーボンブラックの配合量は、上記ゴム成
分100重量部に対して80重量部以下であることが好
ましい。カーボンブラックの配合量が80重量部を超え
ると、発熱性が増大する傾向がある。カーボンブラック
の配合量は、補強性および低発熱性の面から25〜65
重量部が好ましい。The rubber composition of the present invention can contain carbon black as a filler in addition to the above silica. Examples of the carbon black include HAF, I
Examples include SAF and SAF, but are not particularly limited. The compounding amount of carbon black is preferably 80 parts by weight or less based on 100 parts by weight of the rubber component. If the amount of carbon black exceeds 80 parts by weight, the heat buildup tends to increase. The amount of the carbon black is 25 to 65 from the viewpoint of reinforcing properties and low heat generation.
Parts by weight are preferred.
【0021】本発明のゴム組成物は、シリカおよびカー
ボンブラック以外の無機充填材を含むことができる。シ
リカおよびカーボンブラック以外の無機充填材として
は、たとえば、クレー、水酸化アルミニウム、炭酸カル
シウム、アルミナなどがあげられる。The rubber composition of the present invention may contain an inorganic filler other than silica and carbon black. Examples of the inorganic filler other than silica and carbon black include clay, aluminum hydroxide, calcium carbonate, and alumina.
【0022】なお、本発明のゴム組成物は、上記のゴム
成分、充填材(シリカ、カーボンブラックなどの無機充
填材)、シランカップリング剤、ナトリウム塩以外に、
必要に応じて、軟化剤、老化防止剤、加硫剤、加硫促進
剤、加硫促進助剤などの通常のゴム工業で使用される配
合剤を適宜含むことができる。The rubber composition of the present invention comprises, in addition to the above rubber component, filler (inorganic filler such as silica and carbon black), a silane coupling agent and a sodium salt,
If necessary, compounding agents used in the ordinary rubber industry, such as a softening agent, an antioxidant, a vulcanizing agent, a vulcanization accelerator, and a vulcanization accelerator, can be appropriately contained.
【0023】本発明のゴム組成物は、タイヤ、ホース、
ベルトその他の各種工業用品などの機械的特性および耐
摩耗性が要求されるゴム組成物として使用することがで
きる。[0023] The rubber composition of the present invention comprises a tire, a hose,
It can be used as a rubber composition requiring mechanical properties and abrasion resistance of belts and other various industrial products.
【0024】[0024]
【実施例】以下、本発明を実施例に基づいて具体的に説
明するが、これは本発明の目的を制限するものではな
い。EXAMPLES The present invention will be described below in detail with reference to examples, but this does not limit the purpose of the present invention.
【0025】実施例1〜6および比較例1 ジエン系合成ゴム100重量部、シリカ55重量部、シ
ランカップリング剤4.4重量部(シリカ重量に対して
8重量%)、ナトリウム塩2重量部または4重量部(シ
リカ重量に対して3.64重量%または7.27重量
%)、ステアリン酸2重量部、酸化亜鉛3重量部、老化
防止剤1重量部、硫黄1.5重量部、TBBS(加硫促
進剤)1重量部およびDPG(加硫促進剤)0.5重量
部を混練り配合して、各ゴム組成物を得た。Examples 1 to 6 and Comparative Example 1 100 parts by weight of a diene-based synthetic rubber, 55 parts by weight of silica, 4.4 parts by weight of a silane coupling agent (8% by weight based on the weight of silica), 2 parts by weight of a sodium salt Or 4 parts by weight (3.64% by weight or 7.27% by weight based on the weight of silica), 2 parts by weight of stearic acid, 3 parts by weight of zinc oxide, 1 part by weight of an antioxidant, 1.5 parts by weight of sulfur, TBBS (Vulcanization accelerator) 1 part by weight and DPG (vulcanization accelerator) 0.5 part by weight were kneaded and blended to obtain each rubber composition.
【0026】得られた各ゴム組成物を170℃で20分
間プレス加硫して加硫物を得た。得られた各加硫物につ
いて以下に示す各特性の試験を行なった。各ゴム組成物
について、配合したナトリウム塩の種類および配合量な
らびに各特性の試験結果を表1に示す。ナトリウム塩を
配合しない場合を比較例1とした。Each of the obtained rubber compositions was press-vulcanized at 170 ° C. for 20 minutes to obtain a vulcanized product. Each of the obtained vulcanizates was tested for the following properties. Table 1 shows the type and amount of sodium salt compounded and the test results of each characteristic for each rubber composition. Comparative Example 1 was a case where no sodium salt was added.
【0027】表1中、ナトリウム塩(1)はリン酸水素
二ナトリウム・12水和物、ナトリウム塩(2)はリン
酸三ナトリウム・12水和物、ナトリウム塩(3)はリ
ン酸二水素ナトリウム・2水和物、ナトリウム塩(4)
は硫酸ナトリウム・10水和物、ナトリウム塩(5)は
酢酸ナトリウム・3水和物を示す。In Table 1, sodium salt (1) is disodium hydrogen phosphate dodecahydrate, sodium salt (2) is trisodium phosphate dodecahydrate, and sodium salt (3) is dihydrogen phosphate. Sodium dihydrate, sodium salt (4)
Represents sodium sulfate decahydrate, and sodium salt (5) represents sodium acetate trihydrate.
【0028】各種薬品の説明 各種薬品としては以下の市販品を用いた。 ジエン系合成ゴム:ジェイエスアール(株)製のSBR
1502(スチレン−ブタジエン共重合体) シリカ:デグッサ製のUltrasil VN3 シランカップリング剤:デグッサ製のSi69(ビス
(3−トリエトキシシリルプロピル)テトラスルフィ
ド) 老化防止剤:大内新興化学(株)製のノクラック6C
(N−(1,3−ジメチルブチル)−N′−フェニル−
p−フェニレンジアミン) 加硫促進剤(TBBS):大内新興化学(株)製のノク
セラーNS(N−t−ブチル−2−ベンゾチアジル・ス
ルフェンアミド) 加硫促進剤(DPG):大内新興化学(株)製のノクセ
ラーD(N,N′−ジフェニル・グアニジン)Description of Various Chemicals The following commercial products were used as various chemicals. Diene-based synthetic rubber: SBR manufactured by JSR Corporation
1502 (styrene-butadiene copolymer) Silica: Ultrasil VN3 manufactured by Degussa Silane coupling agent: Si69 (bis (3-triethoxysilylpropyl) tetrasulfide manufactured by Degussa) Anti-aging agent: manufactured by Ouchi Shinko Chemical Co., Ltd. No crack 6C
(N- (1,3-dimethylbutyl) -N′-phenyl-
(p-phenylenediamine) Vulcanization accelerator (TBBS): Noxeller NS (Nt-butyl-2-benzothiazyl sulfenamide) manufactured by Ouchi Shinko Chemical Co., Ltd. Vulcanization accelerator (DPG): Ouchi Emerging Noxeller D (N, N'-diphenylguanidine) manufactured by Chemical Co., Ltd.
【0029】試験方法の説明 (ムーニー粘度)JIS K6300に定められたムー
ニー粘度の測定法に従い、温度130℃で予熱1分間お
よび測定4分間の条件で各加硫物のムーニー粘度(ML
1+4)を測定した。ムーニー粘度が低いほど、加工性が
優れる。Description of Test Method (Mooney Viscosity) According to the Mooney viscosity measurement method specified in JIS K6300, the Mooney viscosity (ML) of each vulcanizate was measured at a temperature of 130 ° C. for 1 minute and a measurement of 4 minutes.
1 + 4 ) was measured. The lower the Mooney viscosity, the better the processability.
【0030】(T90)キュラストメーターを用いて評
価した。すなわち、キュラストメーターによるねじりト
ルクの最大値と最小値との差の90%+最小値に達する
までの時間をT90とした。測定温度は170℃で測定
した。T90の値が短いほど加硫速度が速いことを示
す。(T90) Evaluation was made using a curastometer. That is, the time required to reach 90% of the difference between the maximum value and the minimum value of the torsion torque measured by the curast meter + the minimum value was defined as T90. The measurement temperature was measured at 170 ° C. The shorter the value of T90, the faster the vulcanization rate.
【0031】(引張応力)JIS K6301に準拠し
て、各加硫物の伸び300%時の引張応力(300%モ
ジュラス)を測定した。数値が大きいほど、引張応力に
優れている。(Tensile Stress) The tensile stress (300% modulus) at 300% elongation of each vulcanizate was measured according to JIS K6301. The higher the value, the better the tensile stress.
【0032】(磨耗指数)ランボーン摩耗試験機を用い
て、温度20℃、スリップ率20%および試験時間5分
間の条件で各加硫物の容積損失量を測定した。比較例1
の磨耗指数を100とし、各実施例の磨耗指数は下記計
算式で算出した。磨耗指数が大きいほど耐摩耗性が優れ
る。 各実施例の摩耗指数 =比較例1の容積損失量÷各実施
例の容積損失量 × 100(Abrasion Index) The volume loss of each vulcanizate was measured using a Lambourn abrasion tester at a temperature of 20 ° C., a slip ratio of 20% and a test time of 5 minutes. Comparative Example 1
Was set to 100, and the wear index of each example was calculated by the following formula. The higher the wear index, the better the wear resistance. Wear index of each example = volume loss of comparative example 1 例 volume loss of each example × 100
【0033】(転がり抵抗指数)粘弾性スペクトロメー
ター VES(岩本製作所製)を用いて、温度70℃、
初期歪み10%および動歪み2%の条件下で各加硫物の
tanδを測定した。比較例1の転がり抵抗指数を10
0とし、各実施例の転がり抵抗指数は下記計算式で算出
した。指数が大きいほど転がり抵抗特性が優れる。 各実施例の転がり抵抗指数 =比較例1のtanδ÷各
実施例のtanδ × 100(Rolling Resistance Index) Using a viscoelastic spectrometer VES (manufactured by Iwamoto Seisakusho), a temperature of 70 ° C.
The tan δ of each vulcanizate was measured under the conditions of an initial strain of 10% and a dynamic strain of 2%. The rolling resistance index of Comparative Example 1 was 10
The rolling resistance index of each example was calculated by the following formula. The higher the index, the better the rolling resistance characteristics. Rolling resistance index of each example = tan δ of comparative example 1 tan δ of each example × 100
【0034】(ウエットスキッド指数)スタンレー社製
のポータブルスキッドテスターを用いてASTM E3
03−83の方法に従って各硫化物についてウエットス
キッド試験を行なった。比較例1のウエットスキッド指
数を100とし、各実施例のウエットスキッド指数は以
下の計算式で算出した。ウエットスキッド指数が大きい
ほどウエットスキッド性能が優れる。 各実施例のウエットスキッド指数 =各実施例の測定結
果(数値)÷比較例1の測定結果(数値) × 100(Wet skid index) ASTM E3 using a portable skid tester manufactured by Stanley.
Each sulfide was subjected to a wet skid test according to the method of 03-83. The wet skid index of Comparative Example 1 was set to 100, and the wet skid index of each example was calculated by the following formula. The greater the wet skid index, the better the wet skid performance. Wet skid index of each example = measurement result of each example (numerical value) ÷ measurement result of comparative example 1 (numerical value) × 100
【0035】[0035]
【表1】 [Table 1]
【0036】[0036]
【発明の効果】本発明によれば、加工性が高く、しか
も、転がり摩擦抵抗性(燃費特性)および耐磨耗性に優
れたゴム組成物を提供することができる。According to the present invention, it is possible to provide a rubber composition having high workability, and excellent in rolling friction resistance (fuel consumption characteristics) and abrasion 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) C08K 5/098 C08K 5/098 5/544 5/544 5/548 5/548 C08L 7/00 C08L 7/00 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C08K 5/098 C08K 5/098 5/544 5/544 5/548 5/548 C08L 7/00 C08L 7 / 00
Claims (4)
ム100重量部に対して、シリカを5〜100重量部、
シランカップリング剤をシリカ重量に対して2〜20重
量%およびナトリウム塩をシリカ重量に対して1〜20
重量%含むことを特徴とするゴム組成物。1 to 100 parts by weight of natural rubber and / or a diene-based synthetic rubber, 5 to 100 parts by weight of silica;
The silane coupling agent is 2 to 20% by weight based on the weight of silica, and the sodium salt is 1 to 20% based on the weight of silica.
A rubber composition characterized by containing by weight.
である請求項1記載のゴム組成物。2. The rubber composition according to claim 1, wherein the sodium salt is an oxyacid salt or an organic acid salt.
ある請求項1または2記載のゴム組成物。3. The rubber composition according to claim 1, wherein the sodium salt is a hydrated salt having water of crystallization.
1、2または3記載のゴム組成物。4. The rubber composition according to claim 1, wherein the sodium salt is a phosphate.
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EP1566404A1 (en) * | 2004-02-19 | 2005-08-24 | Sumitomo Rubber Industries Ltd. | Rubber composition |
WO2006057143A1 (en) * | 2004-11-25 | 2006-06-01 | Bridgestone Corporation | Rubber composition and pneumatic tire using the same |
EP1743919A1 (en) * | 2005-07-15 | 2007-01-17 | Sumitomo Rubber Industries Limited | Rubber composition and process for preparing the same |
JP2007154058A (en) * | 2005-12-06 | 2007-06-21 | Sumitomo Rubber Ind Ltd | Production method for rubber composition |
JP2008115220A (en) * | 2006-11-01 | 2008-05-22 | Yokohama Rubber Co Ltd:The | Rubber composition |
US7893146B2 (en) | 2005-09-15 | 2011-02-22 | Sumitomo Rubber Industries, Ltd. | Tire having a tire tread |
WO2011062099A1 (en) | 2009-11-19 | 2011-05-26 | 住友ゴム工業株式会社 | Rubber composition for tires and pneumatic tire |
WO2011132461A1 (en) | 2010-04-19 | 2011-10-27 | 住友ゴム工業株式会社 | Rubber composition for tire, and pneumatic tire |
JP2014070131A (en) * | 2012-09-28 | 2014-04-21 | Yokohama Rubber Co Ltd:The | Rubber composition and pneumatic tire using the same |
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JP4733968B2 (en) * | 2004-11-25 | 2011-07-27 | 株式会社ブリヂストン | Rubber composition for tire and pneumatic tire using the same |
WO2006057143A1 (en) * | 2004-11-25 | 2006-06-01 | Bridgestone Corporation | Rubber composition and pneumatic tire using the same |
JP2006152022A (en) * | 2004-11-25 | 2006-06-15 | Bridgestone Corp | Rubber composition and pneumatic tire obtained using the same |
EP1743919A1 (en) * | 2005-07-15 | 2007-01-17 | Sumitomo Rubber Industries Limited | Rubber composition and process for preparing the same |
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JP2007154058A (en) * | 2005-12-06 | 2007-06-21 | Sumitomo Rubber Ind Ltd | Production method for rubber composition |
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WO2011062099A1 (en) | 2009-11-19 | 2011-05-26 | 住友ゴム工業株式会社 | Rubber composition for tires and pneumatic tire |
US8859657B2 (en) | 2009-11-19 | 2014-10-14 | Sumitomo Rubber Industries, Ltd. | Rubber composition for tires and pneumatic tire |
WO2011132461A1 (en) | 2010-04-19 | 2011-10-27 | 住友ゴム工業株式会社 | Rubber composition for tire, and pneumatic tire |
JPWO2011132461A1 (en) * | 2010-04-19 | 2013-07-18 | 住友ゴム工業株式会社 | Rubber composition for tire and pneumatic tire |
JP5552158B2 (en) * | 2010-04-19 | 2014-07-16 | 住友ゴム工業株式会社 | Rubber composition for tire and pneumatic tire |
US10005893B2 (en) | 2010-04-19 | 2018-06-26 | Sumitomo Rubber Industries, Ltd. | Rubber composition for tire, and pneumatic tire |
JP2014070131A (en) * | 2012-09-28 | 2014-04-21 | Yokohama Rubber Co Ltd:The | Rubber composition and pneumatic tire using the same |
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