JPH044242A - Formed rubber article having anisotropic strength - Google Patents
Formed rubber article having anisotropic strengthInfo
- Publication number
- JPH044242A JPH044242A JP10671590A JP10671590A JPH044242A JP H044242 A JPH044242 A JP H044242A JP 10671590 A JP10671590 A JP 10671590A JP 10671590 A JP10671590 A JP 10671590A JP H044242 A JPH044242 A JP H044242A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- parts
- weight
- fatty acid
- pts
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はある一定方向に強度が高く、それと異なる方向
には強度が高くない強度に異方性を有するゴム成形物に
関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a rubber molded article having anisotropy in strength, having high strength in a certain direction and not having high strength in a different direction.
(従来の技術)
近年、機能性素材への要求は高度となり、ゴムの弾性を
持ちかつ強度に異方性を持ったゴム材料が各種機械部品
、スポーツ用品、各種ホース等の工業用品で要求される
ようになってきている。(Prior art) In recent years, demands for functional materials have become more sophisticated, and rubber materials that have the elasticity of rubber and anisotropy in strength are required for various mechanical parts, sporting goods, and industrial products such as various hoses. It is becoming more and more common.
現在までのところ、ゴム成形物に強度の異方性を持たせ
るには、繊維(例えば短繊維)や充填剤を混合時に一定
方向に配向させることにより行なわれている。このよう
な他の配向性付与剤、特に短繊維を配合する方法は充分
従来の要求を満足してはいるが、より高い強度の異方性
が必要な場合には必ずしも適した方法ではなかった。よ
り高い異方性が必要な場合は短繊維の量を多くすればよ
いが、成形性やその他の性能を大きく害する。Up to now, in order to impart strength anisotropy to rubber molded products, fibers (for example, short fibers) and fillers have been oriented in a certain direction during mixing. Although this method of incorporating other orientation-imparting agents, especially short fibers, satisfies the conventional requirements, it is not necessarily a suitable method when higher strength anisotropy is required. . If higher anisotropy is required, the amount of short fibers may be increased, but this greatly impairs moldability and other properties.
(発明が解決しようとする課題)
本発明は、上記短繊維を用いる技術にゴム組成の点から
改良を加えて、短繊維の量を余り多くしないで従来より
高い強度の異方性を持たせる技術を提供することにある
。(Problems to be Solved by the Invention) The present invention improves the technique using short fibers from the viewpoint of rubber composition, and provides a higher strength anisotropy than before without increasing the amount of short fibers too much. The goal is to provide technology.
(課題を解決するための手段)
本発明は、イソプレンゴム、天然ゴム、ブタジエンゴム
、スチレン−ブタジエンゴム、ニトリルゴム、エチレン
プロピレンゴム、クロロプレンゴムおよびブチルゴムか
ら成る群から選択された基材ゴム100重量部、短繊維
3〜100重量部、σ、β−不飽和脂肪酸の金属塩3〜
100重量部、有機過酸化物0.5〜5.0重量部を含
むゴム組成物を一定方向に剪断力をかけて混練した後、
加硫することにより得られた強度に異方性を有するゴム
成形物を提供する。(Means for Solving the Problems) The present invention provides a base rubber 100% by weight selected from the group consisting of isoprene rubber, natural rubber, butadiene rubber, styrene-butadiene rubber, nitrile rubber, ethylene propylene rubber, chloroprene rubber, and butyl rubber. part, short fiber 3 to 100 parts by weight, σ, β-unsaturated fatty acid metal salt 3 to
After kneading a rubber composition containing 100 parts by weight and 0.5 to 5.0 parts by weight of an organic peroxide by applying shear force in a certain direction,
A rubber molded product having anisotropy in strength obtained by vulcanization is provided.
本発明の基材ゴムは従来ゴム組成物に用いられるすべて
のゴム成分、イソプレンゴム、天然ゴム、ブタジェンゴ
ム、スチレン−ブタジエンゴム、ニトリルゴム、エチレ
ンプロピレンゴム、クロロプレンゴムおよびブチルゴム
から成る群から選択される。特に好ましい基材ゴムはc
is−1,4−ポリブタジェンであって、cis構造が
90%以上のものである。The base rubber of the present invention is selected from the group consisting of all rubber components conventionally used in rubber compositions, isoprene rubber, natural rubber, butadiene rubber, styrene-butadiene rubber, nitrile rubber, ethylene propylene rubber, chloroprene rubber and butyl rubber. . Particularly preferable base rubber is c
is-1,4-polybutadiene with a cis structure of 90% or more.
本発明に用いる短繊維は炭素繊維、アルミナ繊維、芳香
族ポリアミド繊維、炭化ケイ素繊維、シリカ繊維、ポロ
ン繊維、チタン酸カリウム繊維、ポリアミド繊維、ポリ
エステル繊維、ポリヒニルアルコール繊維、ポリアクリ
ル繊維、ポリ塩化ビニル繊維、ポリ塩化ビニリデン繊維
、ポリエチレン繊維、ポリプロピレン繊維、ポリ尿素繊
維等の一般的な合成繊維あるいは天然繊維が挙げられ、
これらの繊維に強度をもたせるためのヒートストレッチ
ング処理、接着処理をおこなうと更によい。The short fibers used in the present invention include carbon fibers, alumina fibers, aromatic polyamide fibers, silicon carbide fibers, silica fibers, poron fibers, potassium titanate fibers, polyamide fibers, polyester fibers, polyhinyl alcohol fibers, polyacrylic fibers, and polyamide fibers. General synthetic fibers or natural fibers such as vinyl chloride fiber, polyvinylidene chloride fiber, polyethylene fiber, polypropylene fiber, polyurea fiber, etc.
It is even better if these fibers are subjected to heat stretching treatment and adhesion treatment to give them strength.
好ましくはポリアミド(特に、ナイロン)繊維である。Preferred are polyamide (especially nylon) fibers.
短繊維の繊維の長さは、l/7111以上であり、好ま
しくは30朋以下、太さはld(デニール)以上である
。特に長さl+nm以上で太さ5d以上のものが好まし
い。短繊維のゴム組成物中への配合量は基材ゴム100
重量部に対して3〜100重量部、好ましくは10〜5
0重量部である。10重量部より少ないと強度の異方性
が不足し、100重量部を越えると成形性等に問題が発
生する。The length of the short fibers is 1/7111 or more, preferably 30 mm or less, and the thickness is ld (denier) or more. In particular, it is preferable to have a length of 1+nm or more and a thickness of 5d or more. The amount of short fibers added to the rubber composition is 100% of the base rubber.
3 to 100 parts by weight, preferably 10 to 5 parts by weight
It is 0 parts by weight. If it is less than 10 parts by weight, the anisotropy of strength will be insufficient, and if it exceeds 100 parts by weight, problems will occur in moldability, etc.
本発明において用いられるa、β−不飽和脂肪酸の金属
塩としては炭素数3〜8を有するσ、β−モノエチレン
性不飽和カルボン酸の金属塩が好適であり、そのような
ものの例としてはメタクリル酸、アクリル酸、イタコン
酸、クロトン酸などの金属塩が挙げられる。金属は二価
の金属、好ましくは亜鉛、マグネシウム等が一般的であ
るが、その他の金属、例えば、ナトリウム、リチウム、
アルミニウム等を用いてもよい。α、β−不飽和脂肪酸
の金属塩の配合量は基材ゴム100重量部に対し、3〜
100重量部、好ましくは10〜70重量部である。3
重量部より少ないと強度に異方性が得られず、所定の効
果が達成されない。100重量部を越えると配合物が硬
くなり、作業性が悪くなる。また成形性も劣る。この成
分は金属塩としてではなく、α、β−不飽和脂肪酸と金
属酸化物、水酸化物または炭酸塩として配合して、ゴム
組成物中で塩を形成してもよい。As the metal salt of the a,β-unsaturated fatty acid used in the present invention, a metal salt of a,β-monoethylenically unsaturated carboxylic acid having 3 to 8 carbon atoms is suitable, and examples of such salts include: Examples include metal salts of methacrylic acid, acrylic acid, itaconic acid, crotonic acid, and the like. The metal is generally a divalent metal, preferably zinc, magnesium, etc., but other metals such as sodium, lithium,
Aluminum or the like may also be used. The blending amount of the metal salt of α,β-unsaturated fatty acid is 3 to 3 to 100 parts by weight of the base rubber.
The amount is 100 parts by weight, preferably 10 to 70 parts by weight. 3
If the amount is less than parts by weight, anisotropy in strength will not be obtained and the desired effect will not be achieved. If it exceeds 100 parts by weight, the compound will become hard and workability will deteriorate. In addition, moldability is also poor. Rather than as a metal salt, this component may be combined with the α,β-unsaturated fatty acid as a metal oxide, hydroxide or carbonate to form a salt in the rubber composition.
本発明のゴム組成物中に配合する有機過酸化物は過安息
香酸、過酸化ベンゾイル、クメンパーオキシド、ジクミ
ルパーオキシド等が挙げられる。Examples of the organic peroxide to be blended into the rubber composition of the present invention include perbenzoic acid, benzoyl peroxide, cumene peroxide, and dicumyl peroxide.
好ましくはジクミルパーオキシドである。有機過酸化物
の配合量は基材ゴム100重量部に対し0゜5〜5.0
重量部である。0.5重量部より少ないとα、β−不飽
和脂肪酸の金属塩の架橋か起こりにくく、5.0重量部
を越えると成形物が脆くなり実用的でない。有機過酸化
物の配合量は基材ゴム100重量部に対し1.0〜3.
0重量部が好ましい。Preferred is dicumyl peroxide. The amount of organic peroxide blended is 0.5 to 5.0 parts per 100 parts by weight of the base rubber.
Parts by weight. If it is less than 0.5 parts by weight, crosslinking of the metal salt of α,β-unsaturated fatty acid is difficult to occur, and if it exceeds 5.0 parts by weight, the molded product becomes brittle and is not practical. The amount of organic peroxide blended is 1.0 to 3.0 parts by weight per 100 parts by weight of the base rubber.
0 parts by weight is preferred.
一般にα、β−不飽和脂肪酸の金属塩はゴムと共架橋し
て高硬度や高耐久性を与えることか知られている。驚く
べきことに本発明ではa、β−不飽和脂肪酸の金属塩の
結晶がゴム組成物を混練加工する際に、その結晶が大き
くゴムの列理方向に配向していることがX線照射するこ
とによりわかった。そこで本発明者らは短繊維とa、β
−不飽和脂肪酸の金属塩を配合して一定方向に剪断力を
かけて混練加工したゴム組成物をそのまま型内で加硫す
ると、多量の短繊維を配合しなくてもゴム列理方向に極
めて強度が強く、それとは異なる方向、特に配向方向に
90°をなす方向には強度がそれほど高くないゴム成形
体が得られることを見い出した。本発明のゴム成形物を
得るための剪断力をかけたゴム組成物の混練方法は特に
限定的ではないが、ロールの場合はロールの周方向にゴ
ムか配列し、押出機を用いる場合にはその押出し方向が
配向方向と同一である。さらに本発明らの研究によれば
、本発明のゴム成形物は強度のみならず伸びについても
高い配向性が見られ、強度の配向性と同様に配向方向に
はあまり伸びず、他の方向には大きく伸びることがわか
った。It is generally known that metal salts of α,β-unsaturated fatty acids co-crosslink with rubber to provide high hardness and high durability. Surprisingly, in the present invention, when the crystals of the metal salt of a, β-unsaturated fatty acid are kneaded into the rubber composition, it is found that the crystals are largely oriented in the grain direction of the rubber when irradiated with X-rays. I realized that. Therefore, the present inventors have developed short fibers and a, β
- If a rubber composition prepared by blending a metal salt of an unsaturated fatty acid and kneading it by applying shearing force in a certain direction is vulcanized in a mold as it is, the rubber composition will move in the grain direction of the rubber even without blending a large amount of short fibers. It has been found that a rubber molded article having high strength but not so high strength can be obtained in a direction different from the above direction, particularly in a direction making 90° to the orientation direction. The method of kneading the rubber composition under shearing force to obtain the rubber molded product of the present invention is not particularly limited. The extrusion direction is the same as the orientation direction. Furthermore, according to the research of the present inventors, the rubber molded product of the present invention shows high orientation not only in strength but also in elongation.Similar to the strength orientation, it does not elongate much in the orientation direction, but has a high degree of orientation in other directions. was found to grow significantly.
本発明のゴム成形物は複数の未加硫ゴム組成物を配向を
一方向に合わせ、あるいは異なる配向方向に組合わせて
一体成形することにより、特性の異なるゴム成形物とな
り得る。成形(加硫)は従来公知の条件で行なわれる。The rubber molded product of the present invention can be made into a rubber molded product with different properties by integrally molding a plurality of unvulcanized rubber compositions oriented in one direction or in combination in different orientation directions. Molding (vulcanization) is performed under conventionally known conditions.
−船釣には型内で140〜170℃の温度で10〜40
分間実施される。-For boat fishing, the temperature is 10-40℃ in the mold.
It is carried out for minutes.
本発明のゴム成形物はスポーツ靴の靴底(横方向に高強
度な靴底を成形することにより、左右に強く、曲げには
弾性を有する靴底が得られる。またゴムホース類として
は周方向に高い強度を有し、曲げに対して柔軟なホース
が得られる。また、タイミングベルト、チェーン、ゴム
バネ等にも好適に用いられる。The rubber molded product of the present invention can be used as a sole for sports shoes (by molding a sole with high strength in the lateral direction, a sole that is strong in the left and right directions and has elasticity in bending can be obtained. A hose that has high strength and is flexible against bending can be obtained.It is also suitably used for timing belts, chains, rubber springs, etc.
(発明の効果)
本発明は従来の短繊維配合方法では得られなかった高い
強度に異方性を有するゴム成形物が得られる。このゴム
成形物は非常に安価であり、しかもその強度は高い。(Effects of the Invention) According to the present invention, a rubber molded article having high strength and anisotropy, which could not be obtained by conventional short fiber blending methods, can be obtained. This rubber molded product is very inexpensive and has high strength.
(実施例)
本発明を実施例により更に詳細に説明する。本発明はこ
れら実施例に限定されるものと解してはならない。(Example) The present invention will be explained in more detail with reference to Examples. The present invention should not be construed as being limited to these examples.
実施例1〜4および比較例1.2
表−1に示す配合成分をロールで周方向に剪断力をかけ
て混練した。得られたゴム組成物を160℃で30分間
板状(厚さ約2 mm)の形態に成形した。Examples 1 to 4 and Comparative Example 1.2 The ingredients shown in Table 1 were kneaded with a roll by applying shearing force in the circumferential direction. The obtained rubber composition was molded into a plate (about 2 mm thick) at 160° C. for 30 minutes.
Claims (1)
レン−ブタジエンゴム、ニトリルゴム、エチレンプロピ
レンゴム、クロロプレンゴムおよびブチルゴムから成る
群から選択された基材ゴム100重量部、短繊維3〜1
00重量部、α,β−不飽和脂肪酸の金属塩3〜100
重量部、有機過酸化物0.5〜5.0重量部を含むゴム
組成物を一定方向に剪断力をかけて混練加工した後、加
硫することにより得られた強度に異方性を有するゴム成
形物。1. 100 parts by weight of base rubber selected from the group consisting of isoprene rubber, natural rubber, butadiene rubber, styrene-butadiene rubber, nitrile rubber, ethylene propylene rubber, chloroprene rubber and butyl rubber, 3 to 1 parts by weight of short fibers
00 parts by weight, metal salt of α,β-unsaturated fatty acid 3-100
A rubber composition containing 0.5 to 5.0 parts by weight of an organic peroxide is kneaded by applying shearing force in a certain direction, and then vulcanized to have anisotropic strength. Rubber moldings.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10671590A JPH044242A (en) | 1990-04-23 | 1990-04-23 | Formed rubber article having anisotropic strength |
| EP19910303620 EP0454411A3 (en) | 1990-04-23 | 1991-04-23 | Production of rubber article |
| US07/943,546 US5288446A (en) | 1990-04-23 | 1992-09-11 | Production of rubber article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10671590A JPH044242A (en) | 1990-04-23 | 1990-04-23 | Formed rubber article having anisotropic strength |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH044242A true JPH044242A (en) | 1992-01-08 |
Family
ID=14440656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10671590A Pending JPH044242A (en) | 1990-04-23 | 1990-04-23 | Formed rubber article having anisotropic strength |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH044242A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5351973A (en) * | 1992-01-31 | 1994-10-04 | Sumitomo Wiring Systems, Ltd. | Rubber seal for waterproof connector |
| US7335807B2 (en) * | 2001-12-21 | 2008-02-26 | Freudenberg-Nok General Partnership | Solventless liquid isoprene compounds |
-
1990
- 1990-04-23 JP JP10671590A patent/JPH044242A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5351973A (en) * | 1992-01-31 | 1994-10-04 | Sumitomo Wiring Systems, Ltd. | Rubber seal for waterproof connector |
| US7335807B2 (en) * | 2001-12-21 | 2008-02-26 | Freudenberg-Nok General Partnership | Solventless liquid isoprene compounds |
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