JPS60186509A - Acrylic rubber composition for sealing material - Google Patents
Acrylic rubber composition for sealing materialInfo
- Publication number
- JPS60186509A JPS60186509A JP4463384A JP4463384A JPS60186509A JP S60186509 A JPS60186509 A JP S60186509A JP 4463384 A JP4463384 A JP 4463384A JP 4463384 A JP4463384 A JP 4463384A JP S60186509 A JPS60186509 A JP S60186509A
- Authority
- JP
- Japan
- Prior art keywords
- acrylic
- acrylic rubber
- rubber composition
- component
- vulcanization
- 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
Links
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、容易に硬度をあげることが可能であり、かつ
、加硫速度の調整が容易であり、後加硫を省略すること
のできる密封材用アクリルゴム組吸物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides an acrylic rubber composition for sealing materials that can easily increase the hardness, easily adjust the vulcanization rate, and omit post-vulcanization. Regarding.
従来、アクリルゴムは、耐熱性、耐油性、耐候性、耐オ
ゾン性などに優れ、各種の密封材(ガスケット、パツキ
ン類、Oリング類、ベアリングシール、オイルシールな
ど)、ボース類や被11[すどに広く用いられている。Conventionally, acrylic rubber has excellent heat resistance, oil resistance, weather resistance, ozone resistance, etc., and is used in various sealing materials (gaskets, packings, O-rings, bearing seals, oil seals, etc.), bosses, and sealing materials. It is widely used in sudo.
しかし、たとえば、ミニチュアベアリング等、従来のア
クリルゴムで成型した密封材は、硬度が低いため強度的
な問題から芯金を入れる必要性があった。この問題を解
決するために、充填剤を増量する方法、フェノール樹脂
を添加する方法、加硫剤を増量して架橋密度をあげる方
法などが実施されたが、常態物性、耐熱老化性、低温ゼ
イ化などの物性面で満足した値が得られない欠点があっ
た0
本発明は、これらの欠点を除去し、理想的密封利用アク
リルゴムを提供するものである0本発明はアクリル酸エ
ステル0単量体に対して、架橋サイト成分を15〜50
重t%、好ましくは25〜40重量%含有することを特
長としたアクリルエラストマーである密封材用アクリル
ゴム組成物である。However, for example, conventional sealing materials molded from acrylic rubber, such as miniature bearings, have low hardness and therefore require the insertion of a core metal due to strength issues. In order to solve this problem, methods such as increasing the amount of filler, adding phenolic resin, and increasing the crosslinking density by increasing the amount of vulcanizing agent have been implemented, but these methods The present invention eliminates these drawbacks and provides an ideal sealing acrylic rubber. The crosslinking site component is 15 to 50
This is an acrylic rubber composition for a sealing material, which is an acrylic elastomer and is characterized by containing t% by weight, preferably 25 to 40% by weight.
該密封材用アクリルゴム組吸物は、諸物性を低下させな
いで容易に硬度をあげることが出来るので芯金を必要と
しないシールを成型することが出来る。また、架橋サイ
ト成分飯が多いので、加fi&速度の調整が容易に行な
え、短時間成型が可能であり、従来しばしば問題にされ
ている後加硫を省略することが出来るなど、非常に優れ
たアクリルゴム組成物である。The hardness of the acrylic rubber composition for sealing materials can be easily increased without deteriorating various physical properties, so it is possible to mold seals that do not require a core metal. In addition, since there are many crosslinking site components, it is easy to adjust the vulcanization and speed, and it is possible to mold in a short time, and it is possible to omit post-vulcanization, which has often been a problem in the past. It is an acrylic rubber composition.
本発明のアクリルゴム組成物中の架橋サイト成分である
エポキシ基含有単敞体としては、グリシジルアクリレー
ト、グリシジルメタクリレート、アリルグリシジルエー
テルなどが用いられる◇まり、ハロゲン含有単量体とし
ては、2−クロロエチルビニルエーテル、ビニルクロル
アセテート、ビニルベンジルクロライドなどが月Jいら
れる。また、アクリルエラストマーの主成分であるアク
リル酸エステルとしては、メチルアクリレート、エチル
アクリレート、n−ブチルアクリレートなどの低級アル
キルアクリレートやメトキシエチルアクリレート、エト
キシメチルアクリレート、2−メトキシエチルアクリレ
ート、2−エトキシエチルアクリレートなどのアルコキ
シアルキルアクリレートが使用される。As the epoxy group-containing monomer that is the crosslinking site component in the acrylic rubber composition of the present invention, glycidyl acrylate, glycidyl methacrylate, allyl glycidyl ether, etc. are used. Ethyl vinyl ether, vinyl chloroacetate, vinyl benzyl chloride, etc. are included. In addition, acrylic acid esters that are the main components of acrylic elastomers include lower alkyl acrylates such as methyl acrylate, ethyl acrylate, and n-butyl acrylate, methoxyethyl acrylate, ethoxymethyl acrylate, 2-methoxyethyl acrylate, and 2-ethoxyethyl acrylate. Alkoxyalkyl acrylates such as are used.
以Fの実施例によって本発明を実に具体的に説明する。The present invention will be explained in detail with reference to the following examples.
なお、部数は全て重量部である。Note that all parts are parts by weight.
実施例
次の単量体混合物A〜0を共重合させ、それぞれアクリ
ルエラストマーANC(0は比較例)を合成した。Examples The following monomer mixtures A to 0 were copolymerized to synthesize acrylic elastomers ANC (0 is a comparative example).
〈表1〉
共重合反応は、次のようにして行った。まず、単量体混
合物100部、水200部及び乳化剤として、ラウリル
スルホン酸ソーダ0.8部、ポリオキシエチレンラウリ
ルエーテル2部を反応容器に仕込み、液温を50°Cに
保持しながら窒素置換を行なう。次いで、過硫酸アンモ
ニウム0.2部及び亜硫酸水素す) IJウム0.2部
を添加すると温度が上昇し始めるが、この温度を60°
Cに保持しながら、1.5時間攪拌し、重合反応を完結
させた。得られた共重合体ラテックスを約80℃の15
%食塩水中に投入し、凝析物を水洗した後、乾燥させて
アクリルエラストマーを得た。重合率は98%以上であ
った。<Table 1> The copolymerization reaction was performed as follows. First, 100 parts of the monomer mixture, 200 parts of water, 0.8 parts of sodium lauryl sulfonate as an emulsifier, and 2 parts of polyoxyethylene lauryl ether were charged into a reaction vessel, and the mixture was replaced with nitrogen while maintaining the liquid temperature at 50°C. Do this. Next, when 0.2 parts of ammonium persulfate and 0.2 parts of hydrogen sulfite are added, the temperature begins to rise, but this temperature is kept at 60°C.
The mixture was stirred for 1.5 hours while maintaining the temperature at C. to complete the polymerization reaction. The obtained copolymer latex was heated at about 80°C for 15 minutes.
% saline solution, the coagulated product was washed with water, and then dried to obtain an acrylic elastomer. The polymerization rate was 98% or more.
〈表2〉
(1) Pz;大向新興化学工業、ジメチルジチオカル
バミン酸亜鉛(2)ノンサール5x−1: 日本油脂株
式会社製、カリ石鹸(3)゛ノンザール5N−i: 日
本油脂株式会社製、ソーダ石鹸得られたそれぞれのアク
リルエラストマーについて、〈表2〉よりなる配合処方
に従って8インチロールで混練し、アクリルエラストマ
ーA、B及びCからそれぞれ対応する配合物11■及び
■(Nは比較例)を調製した0
各配合物の加硫温度、加硫時間及びそれぞれの加硫物の
諸物性値を〈表6〉に示す。<Table 2> (1) Pz: Ohmukai Shinko Kagaku Kogyo, zinc dimethyldithiocarbamate (2) Nonsal 5x-1: manufactured by Nippon Oil & Fats Co., Ltd., potash soap (3) Nonsal 5N-i: manufactured by Nippon Oil & Fats Co., Ltd. Each of the obtained acrylic elastomers for soda soap was kneaded with an 8-inch roll according to the formulation shown in Table 2, and the corresponding formulations 11 and 11 were obtained from acrylic elastomers A, B, and C (N is a comparative example). The vulcanization temperature, vulcanization time, and physical property values of each vulcanizate are shown in Table 6.
〈表6〉
また、本発明のアクリルゴムと従来のアクリルゴムの加
硫状態をグラフにすると図面のごとくになった。図面か
ら判るように、配合物Aでは、短時間でトルク値が最大
に達し、その後、加硫平担性を示し、一定加硫時間での
トルク値は、配合物Bと比較すれば大幅に上回っている
ことが明らかである。<Table 6> In addition, when the vulcanization states of the acrylic rubber of the present invention and the conventional acrylic rubber are plotted as a graph, the results are as shown in the drawing. As can be seen from the drawing, in compound A, the torque value reaches the maximum in a short period of time, and thereafter exhibits flat vulcanization, and the torque value at a constant vulcanization time is significantly greater than that of compound B. It is clear that it is superior.
以上の結果から、架橋サイト成分を15〜50重景%含
重重るアクリルエラストマーを用いることにより、容易
に硬度(JA、9Q度以上、J0.7Q度以上)をあげ
ることが出来、従来のアクリルゴムの欠点である引張強
度を大幅に向上することが出来る。しかも、従来のアク
リルゴムは、常態物性、耐熱老化性、耐油性等の諸物性
値を満足させるために長時間にわたる後加硫が必要であ
ったが、本発明のアクリルエラストマーでは、短時間の
プレス加硫によるだけでも良好な諸物性値を示すことが
判る。From the above results, it is possible to easily increase the hardness (JA, 9Q degrees or more, J0.7Q degrees or more) by using an acrylic elastomer with a crosslinking site component content of 15 to 50% by weight, and compared to conventional acrylic elastomers. The tensile strength, which is a drawback of rubber, can be significantly improved. In addition, conventional acrylic rubber required long post-vulcanization to satisfy various physical properties such as normal physical properties, heat aging resistance, oil resistance, etc., but the acrylic elastomer of the present invention can be cured in a short time. It can be seen that even press vulcanization alone shows good physical property values.
この様に本発明の密封材用アクリルゴム組吸物によれば
容易に硬度をあげることが可能で、かつ加硫速度を調整
し、加硫速度を向上せしめ、後加硫を省略でき、諸物性
もすぐれた数値を示すなどすぐれた特長を有している。As described above, according to the acrylic rubber composition for sealing materials of the present invention, the hardness can be easily increased, the vulcanization rate can be adjusted and the vulcanization rate can be improved, post-vulcanization can be omitted, and various physical properties can be improved. It has excellent features such as showing excellent numerical values.
図面は本発明のアクリルゴムと従来のアクリルゴムの加
硫状態を示すグラフである。
A・・・配合物l
B・・・配合物]
特許出願人 内山工業株式会社The drawing is a graph showing the vulcanization states of the acrylic rubber of the present invention and conventional acrylic rubber. A...Blend B...Blend] Patent applicant Uchiyama Kogyo Co., Ltd.
Claims (1)
15〜50重量%含有するアクリルエラストマーである
密封材用アクリルゴム組成物。An acrylic rubber composition for a sealing material, which is an acrylic elastomer containing 15 to 50% by weight of a crosslinking site component, which is applied to a single acrylic acid ester body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4463384A JPS60186509A (en) | 1984-03-07 | 1984-03-07 | Acrylic rubber composition for sealing material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4463384A JPS60186509A (en) | 1984-03-07 | 1984-03-07 | Acrylic rubber composition for sealing material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60186509A true JPS60186509A (en) | 1985-09-24 |
Family
ID=12696825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4463384A Pending JPS60186509A (en) | 1984-03-07 | 1984-03-07 | Acrylic rubber composition for sealing material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60186509A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5518456A (en) * | 1978-07-26 | 1980-02-08 | Nitto Electric Ind Co Ltd | Elastic sealant |
JPS5518453A (en) * | 1978-07-26 | 1980-02-08 | Nitto Electric Ind Co Ltd | Elastic sealant |
JPS56114943A (en) * | 1980-02-15 | 1981-09-09 | Oki Electric Ind Co Ltd | Negative type resist material for electron beam |
JPS58185604A (en) * | 1982-04-26 | 1983-10-29 | Tokuyama Soda Co Ltd | Production of polyglycidyl methacrylate latex |
-
1984
- 1984-03-07 JP JP4463384A patent/JPS60186509A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5518456A (en) * | 1978-07-26 | 1980-02-08 | Nitto Electric Ind Co Ltd | Elastic sealant |
JPS5518453A (en) * | 1978-07-26 | 1980-02-08 | Nitto Electric Ind Co Ltd | Elastic sealant |
JPS56114943A (en) * | 1980-02-15 | 1981-09-09 | Oki Electric Ind Co Ltd | Negative type resist material for electron beam |
JPS58185604A (en) * | 1982-04-26 | 1983-10-29 | Tokuyama Soda Co Ltd | Production of polyglycidyl methacrylate latex |
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