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JPS61143458A - High hardness rubber composition - Google Patents

High hardness rubber composition

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Publication number
JPS61143458A
JPS61143458A JP59265134A JP26513484A JPS61143458A JP S61143458 A JPS61143458 A JP S61143458A JP 59265134 A JP59265134 A JP 59265134A JP 26513484 A JP26513484 A JP 26513484A JP S61143458 A JPS61143458 A JP S61143458A
Authority
JP
Japan
Prior art keywords
rubber
ethylene
olefin
hardness
isobutylene
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
JP59265134A
Other languages
Japanese (ja)
Inventor
Yoshio Tanimoto
谷本 嘉雄
Koichi Iketani
池谷 孝一
Yasutaka Hatada
畑田 恭孝
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 Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co 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 Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP59265134A priority Critical patent/JPS61143458A/en
Publication of JPS61143458A publication Critical patent/JPS61143458A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the titled composition of high processability suitable for packings, hydro-extracting rubber, etc., by incorporating each specified amount of specific diene rubber and sulfur in ethylene-alpha-olefin rubber and/or isobutylene- isoprene rubber. CONSTITUTION:The objective composition can be obtained by incorporating (A) 100 pts by wt of isobutylene-isoprene rubber and/or ethylene-alpha-olefin rubber from ethylene, alpha-olefin (e.g., propylene) and at least one sort of nonconjugated diene (e.g., dicyclopentadiene) with (B) 10-60 (pref. 15-60) pts by wt of diene rubber with a Mooney viscosity <=80 and (C) 3-35pts by wt of sulfur. This composition has high processability at kneading, rolling, extrusion, etc. during uncured state, being capable of curing under atmospheric pressure, giving a hardness >=85.

Description

【発明の詳細な説明】 本発明は高硬度ゴム組成物、特にエチレン・d−オレフ
ィン系ゴムおよび/またはイソブチレン・イソプレンゴ
ムをベースとした混線加工性、ロール加工性および押出
加工性にすぐれた高硬度なゴム組成物に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a high-hardness rubber composition, particularly a high-hardness rubber composition based on ethylene/d-olefin rubber and/or isobutylene/isoprene rubber, which has excellent cross-wire processability, roll processability, and extrusion processability. This invention relates to a hard rubber composition.

従来よす、エチレン・d−オレフィン系ゴムオヨび/ま
たはイソブチレン・イソプレンゴムは耐熱性、耐候性等
にすぐれるため、自動車用コ′ム部品、建築材料等に広
く用いられている。
Conventionally, ethylene/d-olefin rubber and/or isobutylene/isoprene rubber have excellent heat resistance, weather resistance, etc., and are therefore widely used in automobile parts, building materials, and the like.

しかし、これらのゴムも使用目的によってはその硬度が
問題となり、そのために、JI8に6301の硬度計A
型による硬度として硬度85以上にその硬度を高くする
ことが揮々検討され、たとえば上記ゴムに■補強剤を多
量に配合し、軟化剤、可塑剤を少量混合するか、■熱硬
化性のアルキルフェノール樹脂を配合する方法などが知
られている。
However, the hardness of these rubbers can be a problem depending on the purpose of use, and for this reason, JI8 has a 6301 hardness tester A.
Many efforts have been made to increase the hardness of the mold to a hardness of 85 or higher. Methods of blending resin are known.

しかしながら、前者の方法による場合には未加流ゴム組
成物C以下、単にコンパウンドという)の粘度が著しく
上昇し、混練加工性、ロール加工性および押出機へのフ
ィード性(押出加工性)などの加工性が著しく劣るとい
う問題があり、一方後者の方法による場合には上記加工
性は良好であるが、常圧加流ができず、また加硫ゴム組
成物のスナッピー性等の物性が劣る等の問題があり、実
用上十分とは言えない。
However, when the former method is used, the viscosity of the unwashed rubber composition C (hereinafter simply referred to as compound) increases significantly, resulting in poor kneading processability, roll processability, feedability to an extruder (extrusion processability), etc. On the other hand, when using the latter method, the above-mentioned processability is good, but normal pressure vulcanization is not possible, and physical properties such as snappy properties of the vulcanized rubber composition are inferior. There is a problem, and it cannot be said that it is practically sufficient.

このようなことから、本発明者らはかかる問題のない高
硬度のゴム組成物を開発すべく鋭意検討の結果、本発明
を完成するに至った。
Under these circumstances, the present inventors conducted intensive studies to develop a high hardness rubber composition free from such problems, and as a result, completed the present invention.

すなわち本発明は、エチレン・α−オレフィン系ゴムお
よび/またはイソブチレン・イソプレンゴムに、該ゴム
100重景部当り10重量部を越えて60重量部以下の
常温で固体状のジエン系ゴムおよび3〜35重量部の硫
黄を配合せしめてなることを特徴とする硬度(曲述と同
じ)85以上の高硬度ゴム組成物を提供するものであり
、かかる高硬度ゴム組成物は未加硫時の混線加工性、ロ
ール加工性、押出加工性などの加工性にすぐれ、常圧加
硫可能であって、しかも高硬度であるというすぐれた性
質を有する。
That is, the present invention provides an ethylene/α-olefin rubber and/or an isobutylene/isoprene rubber, and a diene rubber that is solid at room temperature in an amount of more than 10 parts by weight and 60 parts by weight or less per 100 parts of the rubber, and 3 to 3 parts by weight. The present invention provides a high-hardness rubber composition with a hardness of 85 or higher (same as in the description), which is characterized by containing 35 parts by weight of sulfur, and such a high-hardness rubber composition has no cross-contamination when unvulcanized. It has excellent processability such as processability, roll processability, and extrusion processability, can be vulcanized under normal pressure, and has high hardness.

本発明において、エチレン・d−オレフィン系ゴムとは
、エチレン、α−オレフィンおよび1種以上の非共役ジ
エンからなる共重合体を意味し、α−オレフィンとして
はプロピレン、1−プテン、l−ペンテン、l−ヘキセ
ン等力例示され、また非共役ジエンとしてはジシクロペ
ンタジェン、エチリデンノルボルネン、■、4−へキサ
ジエン、メチルテトラヒドロインデンメチルノルボルネ
ン等が例示される。
In the present invention, the ethylene/d-olefin rubber refers to a copolymer consisting of ethylene, an α-olefin, and one or more nonconjugated dienes, and examples of the α-olefin include propylene, 1-butene, and 1-pentene. , l-hexene, and examples of non-conjugated dienes include dicyclopentadiene, ethylidenenorbornene, 4-hexadiene, methyltetrahydroindenemethylnorbornene, and the like.

また、イソブチレン・イソプレンゴムとはイソブチレン
とイソプレンとの共重合体またはその塩素化物、臭素化
物を意味する。
In addition, isobutylene/isoprene rubber means a copolymer of isobutylene and isoprene, or a chlorinated or brominated product thereof.

かかるエチレン・d−オレフィン系ゴムとイソブチレン
・イソプレンゴムはそれぞれの単独であってもよく、任
意の割合の混合物であってもよい。
The ethylene/d-olefin rubber and the isobutylene/isoprene rubber may be used alone or as a mixture in any proportion.

このようなゴムに配合するジエン系ゴムとしては天然ゴ
ム(NR)、ポリイソプレンゴム(I R)、ポリブタ
ジェンゴム(BR)、スチレンブタジェンゴム(8BK
)、アクリロニトリルブタジェンゴム(NBR)などの
常温で固体状のジエン系ゴムが挙げられ、これらの内、
合成ゴムは乳化重合法、溶液重合法などで製造されてい
るが、この製造法には特に制限されない。
Diene rubbers that can be blended into such rubbers include natural rubber (NR), polyisoprene rubber (IR), polybutadiene rubber (BR), and styrene-butadiene rubber (8BK).
), acrylonitrile butadiene rubber (NBR) and other diene rubbers that are solid at room temperature.
Synthetic rubber is manufactured by emulsion polymerization, solution polymerization, etc., but the manufacturing method is not particularly limited.

尚、8BR,NBRについては、スチレンまたはアクリ
ロニトリルの含有量は特に制限されるものではないが、
含有量の少ないものが加硫ゴム組成物の物理的性質にす
ぐれるため好ましい。
Regarding 8BR and NBR, the content of styrene or acrylonitrile is not particularly limited, but
A small content is preferable because the vulcanized rubber composition has excellent physical properties.

また、BR,IRについても結合様式には何ら制限され
ず、いずれの結合様式であってもよい。
Furthermore, there are no restrictions on the binding mode of BR and IR, and any binding mode may be used.

かかるジエン系ゴムは1種のみでも2種以上を併用して
もよいが、ジエン系ゴムのムーニー粘度は未加硫ゴム組
成物のムーニー粘度の点から80以下であることが望ま
しく、また常温で固体状を維持する範囲内で常温で液状
または水飴状のジエン系ゴムを併用してもよい。
Such diene rubbers may be used alone or in combination of two or more, but the Mooney viscosity of the diene rubber is preferably 80 or less from the viewpoint of the Mooney viscosity of the unvulcanized rubber composition. A diene rubber that is liquid or starch syrup-like at room temperature may be used in combination within a range that maintains the solid state.

本発明において、ジエン系ゴムの配合量ハエチレン・d
−オレフィン系ゴムおよび/またはイソブチレン・イソ
プレンゴムtoot置部に対してio重量部を越えて6
0i1i?を部以下、好ましくは15〜60重量部の範
囲であることが必要であり、10Mgk部以下では目的
とする十分な硬度が得られず、また60重量部を越える
と加硫ゴムの伸び等の物性が低下する。
In the present invention, the compounding amount of diene rubber is ethylene・d
- Exceeding 6 parts by weight of olefin rubber and/or isobutylene/isoprene rubber relative to the toot position
0i1i? If it is less than 10 Mgk parts, the desired hardness cannot be obtained, and if it exceeds 60 parts by weight, the elongation of the vulcanized rubber etc. Physical properties deteriorate.

また、硫黄の配合量はエチレン・α−オレフィン系ゴム
および/またはジエン系ゴム100重量部に対して8〜
35軍量部の範囲であることが好ましく、この範囲より
少ないと十分な硬度が得られず、またこの範囲を越える
と耐熱老化性等の他の特性が低下する。
The amount of sulfur added is 8 to 100 parts by weight of ethylene/α-olefin rubber and/or diene rubber.
The amount is preferably in the range of 35 molar parts; if it is less than this range, sufficient hardness will not be obtained, and if it exceeds this range, other properties such as heat aging resistance will deteriorate.

本発明のゴム組成物は、基本的には上記したエチレン・
d−オレフィン系ゴムおよび/またはイソブチレン・イ
ソプレンゴム、ジエン系ゴムおよび硫黄からなるもので
あるが、必要に応じてゴム業界において周知の各種のM
II資材、たとえば補強剤、充填剤、軟化剤、加工助剤
、消泡剤、亜鉛革、ステアリン酸、加硫促進剤、硫黄以
外の加硫剤、老化防止剤等を配合することができる。
The rubber composition of the present invention basically consists of the above-mentioned ethylene and
It consists of d-olefin rubber and/or isobutylene/isoprene rubber, diene rubber, and sulfur, and if necessary, various types of M well known in the rubber industry may be added.
II materials such as reinforcing agents, fillers, softeners, processing aids, defoamers, zinc leather, stearic acid, vulcanization accelerators, vulcanizing agents other than sulfur, anti-aging agents, etc. can be blended.

かかる本発明のゴム組成物はゴム業界で周知の各種の加
硫法、たとえばプレス加硫、罐加硫、射出成形、UHF
加硫、■人加硫、PCM加硫、LOW加硫等とそれの組
合わせよりなる常圧連続加硫が適用でき、これにより目
的とするJI8に6801の硬度計A型による硬度とし
て硬度85以上の高硬度のゴム組成物が得られる。
The rubber composition of the present invention can be cured by various vulcanization methods well known in the rubber industry, such as press vulcanization, can vulcanization, injection molding, and UHF vulcanization.
Normal pressure continuous vulcanization consisting of vulcanization, manual vulcanization, PCM vulcanization, LOW vulcanization, etc., and a combination thereof can be applied, and by this, the target JI8 can be achieved with a hardness of 85 as measured by a 6801 hardness tester type A. A rubber composition with the above-mentioned high hardness can be obtained.

かかる本発明のゴム組成物はs p、;!E;した如き
すぐれた性質を有するため、パツキン類、水切りゴム、
グラスランラバー、ウェザ−ストリップおよびこれらに
適用される軟質ゴム材との複合体の硬質ゴム材、ドアシ
ール、トう〉クシールに適用されるスポンジゴムとソリ
ッドゴムの複合体のソリッドゴム材、泥除は等の自動車
用部品、ゴムロール、各種シール材、パツキン類等の工
業用部品、セツティングブロック、ゴムタイル、ガスケ
ット等の建築用材料などに好適に使用することができる
Such a rubber composition of the present invention is sp,;! E: Due to its excellent properties, it is used in packings, draining rubber,
Glass run rubber, weather strips, hard rubber materials that are composites of soft rubber materials that are applied to these materials, solid rubber materials that are composites of sponge rubber and solid rubber that are applied to door seals, toke seals, and mudguards. It can be suitably used for automobile parts such as rubber rolls, various sealing materials, industrial parts such as packings, and building materials such as setting blocks, rubber tiles, and gaskets.

以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 表1に示す配合剤(1)の各成分を同表に示す配合量(
重量部)でバンバリーミキサ−にて混合し、これに配合
剤(2)の各成分をロールに添加混合してゴム組成物を
得る。
Example 1 Each component of compounding agent (1) shown in Table 1 was mixed in the amount shown in the same table (
(parts by weight) in a Banbury mixer, and each component of compounding agent (2) is added and mixed on a roll to obtain a rubber composition.

得られたそれぞれのゴム組成物をプレス加硫法で160
°C120分加硫した。
Each of the obtained rubber compositions was vulcanized to 160% by press vulcanization.
Vulcanization was performed at °C for 120 minutes.

得られた加硫ゴムの物性を表2に示す。Table 2 shows the physical properties of the obtained vulcanized rubber.

*1 エチレンやプロピレン・エチリデンノルボルネン
共重合ゴム(住友化学社製) *2 エチレン・l−ブテン・エチリデンノルボルネン
共重合ゴム(三井石油化学社製)*3 乳化重合タイプ
8BR(住友化学工業社製)*4 ポリブタジェン(日
本合成ゴム工業社製)*5  NBR(日本ゼオン社製
) *7 溶液重合タイプのポリブタジェン1.2結合 7
5憾  1.4結合 く、千チML絢100°C60 1す4 *8 液状ポリブタジェン(日本曹達社製)*9 熱硬
性アルキルフェノール樹脂(住友ベークライト社製) *10  FEFブランク(東海カーボン工業社製)*
11  パー7フイン系プロセスオイル(出光興II社
製)
*1 Ethylene or propylene/ethylidene norbornene copolymer rubber (manufactured by Sumitomo Chemical Co., Ltd.) *2 Ethylene/l-butene/ethylidene norbornene copolymer rubber (manufactured by Mitsui Petrochemicals Co., Ltd.) *3 Emulsion polymerization type 8BR (manufactured by Sumitomo Chemical Co., Ltd.) *4 Polybutadiene (manufactured by Nippon Synthetic Rubber Industries, Ltd.) *5 NBR (manufactured by Nippon Zeon Co., Ltd.) *7 Solution polymerization type polybutadiene 1.2 bond 7
5 1.4 Bonds 1,000 ML Aya 100°C60 1su4 *8 Liquid polybutadiene (manufactured by Nippon Soda Co., Ltd.) *9 Thermosetting alkylphenol resin (manufactured by Sumitomo Bakelite Co., Ltd.) *10 FEF blank (manufactured by Tokai Carbon Industries Co., Ltd.) )*
11 Par 7 fine process oil (manufactured by Idemitsu Kou II Co., Ltd.)

Claims (1)

【特許請求の範囲】[Claims] (1)エチレン・α−オレフィン系ゴムおよび/または
イソブチレン・イソプレンゴムに、該ゴム100重量部
当り10重量部を越えて60重量部以下の常温で固体状
のジエン系ゴムおよび3〜35重量部の硫黄を配合せし
めてなることを特徴とする硬度85以上の高硬度ゴム組
成物。
(1) Ethylene/α-olefin rubber and/or isobutylene/isoprene rubber, and more than 10 parts by weight but not more than 60 parts by weight of diene rubber that is solid at room temperature and 3 to 35 parts by weight per 100 parts by weight of the rubber. A high hardness rubber composition having a hardness of 85 or more, characterized in that it contains sulfur.
JP59265134A 1984-12-14 1984-12-14 High hardness rubber composition Pending JPS61143458A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59265134A JPS61143458A (en) 1984-12-14 1984-12-14 High hardness rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59265134A JPS61143458A (en) 1984-12-14 1984-12-14 High hardness rubber composition

Publications (1)

Publication Number Publication Date
JPS61143458A true JPS61143458A (en) 1986-07-01

Family

ID=17413089

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59265134A Pending JPS61143458A (en) 1984-12-14 1984-12-14 High hardness rubber composition

Country Status (1)

Country Link
JP (1) JPS61143458A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6490240A (en) * 1987-09-30 1989-04-06 Sumitomo Chemical Co Rubber composition
US4946888A (en) * 1989-03-09 1990-08-07 Sumitomo Chemical Company Limited High-hardness rubber composition
US5446097A (en) * 1988-05-17 1995-08-29 Mitsui Petrochemical Industries Ltd. Vulcanizable rubber composition and vulcanized rubber
JP2000344979A (en) * 1999-06-01 2000-12-12 Jsr Corp High hardness vulcanized rubber composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6490240A (en) * 1987-09-30 1989-04-06 Sumitomo Chemical Co Rubber composition
US5446097A (en) * 1988-05-17 1995-08-29 Mitsui Petrochemical Industries Ltd. Vulcanizable rubber composition and vulcanized rubber
US4946888A (en) * 1989-03-09 1990-08-07 Sumitomo Chemical Company Limited High-hardness rubber composition
JP2000344979A (en) * 1999-06-01 2000-12-12 Jsr Corp High hardness vulcanized rubber composition

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