JPS5974136A - Rubber composition - Google Patents
Rubber compositionInfo
- Publication number
- JPS5974136A JPS5974136A JP18286282A JP18286282A JPS5974136A JP S5974136 A JPS5974136 A JP S5974136A JP 18286282 A JP18286282 A JP 18286282A JP 18286282 A JP18286282 A JP 18286282A JP S5974136 A JPS5974136 A JP S5974136A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- weight
- parts
- specific gravity
- kinematic viscosity
- 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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Links
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は硬度の経時変化の少ないコム組成物に関し、さ
らに詳しくはロジン酸01〜10重量係を含有するスチ
レン−ブタジェンゴムおよび/寸/コバブタ7エンゴム
(以下ジエンゴムと略称することがある)100重量部
に対し比重(15/4℃)1015以」−1動粘度(9
8,89℃) 4 Q cst以上の芳香、疾系炭化水
素軟化剤10〜100重量部を含むコム組成物に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a comb composition with little change in hardness over time, and more specifically to a styrene-butadiene rubber containing 01 to 10 weight percent rosin acids and a comb composition containing 01 to 10 weight percent of rosin acid and a comb composition containing 01 to 10 weight percent of rosin acid. Specific gravity (15/4°C) 1015 or more per 100 parts by weight (sometimes) -1 kinematic viscosity (9
8,89° C.) 4 Q cst or higher, the present invention relates to a comb composition containing 10 to 100 parts by weight of an aromatic, aggressive hydrocarbon softener.
一般にジエンゴムは/凡用ゴムとしてタイヤ、ベルト、
はきものその他の工業用品、日用品等に幅広く使用され
ており、その要求される性能は多種多様にわたっている
。その中で製品の加工性改良、コストダウンを目的とし
てジエンゴムに多−計の1次化剤が添加されるケースが
多い。軟化剤(は石/llI系伸展油が主で、その組成
によって芳香族系、ナフテン系、パラフィン系に分類さ
れる。しかしこれら軟化剤を多量に添加したゴム製品は
従来から使用中に硬度が著しく上昇する傾向が見られた
。Generally, diene rubber is used for general purpose rubber such as tires, belts, etc.
It is widely used in footwear, other industrial goods, daily necessities, etc., and the required performance is wide-ranging. Among these, many primary forming agents are often added to diene rubber for the purpose of improving product processability and reducing costs. Softeners (mainly stone/III-based extender oils are classified into aromatic, naphthenic, and paraffinic types depending on their composition. However, rubber products to which large amounts of these softeners have been added have traditionally experienced hardness during use. A marked upward trend was observed.
ゴム製品の硬度上昇の原因については通常熱、光等の化
学的、物理的要因冗よる製品の劣化が主であるが、本発
明者らの研究によると上記以外の原因としてゴム製品中
の軟化剤が熱履歴により飛散あるいは水等の接触で抽出
され、減少していくためであることが判明した。The main cause of increase in the hardness of rubber products is usually product deterioration due to chemical and physical factors such as heat and light, but according to research by the present inventors, softening in the rubber product is also a cause other than the above. It turns out that this is because the agent is scattered due to thermal history or extracted by contact with water, etc., and decreases.
従って製品の硬度上昇を抑え、耐用年数を伸ばすために
は、この製品中の軟化剤の飛散および油出を防止、もし
くは少なくすることが必要となり、本発明者らはこれら
の点について鋭意研究した結果、ジエンゴム中に含捷れ
る有機酸としてロジン酸を必須とし、軟[ヒ剤として作
業性上の問題から一般的には使われていない高粘度高比
重のものを選択することによってはじめて硬度の経時変
化の少ないゴム組成物が得られることを見出し本発明に
到達した。すなわち本発明はロジン酸0.1〜10重5
i係を含有するスチレンーブタジエンコ゛ムおよび/丑
/コはブタジェンゴム100重量部に対し、比重(15
部4℃)1.015以上、動粘度(98,89℃) 4
Q cs1以上の芳香族系炭化水素軟化剤10〜10
0重量部を含むゴム組成物を提供する。Therefore, in order to suppress the increase in hardness of the product and extend its service life, it is necessary to prevent or reduce the scattering and oil leakage of the softener in this product, and the inventors have conducted extensive research on these points. As a result, rosin acid is essential as an organic acid to be included in diene rubber, and hardness can only be improved by selecting a high viscosity and high specific gravity that is not generally used as a softening agent due to workability problems. The present invention was achieved by discovering that a rubber composition with little change over time can be obtained. That is, the present invention uses 0.1 to 10% rosin acid.
The styrene-butadiene rubber and /ox/co containing group i have a specific gravity (15 parts by weight) per 100 parts by weight of butadiene rubber.
Part 4℃) 1.015 or more, kinematic viscosity (98,89℃) 4
Q Aromatic hydrocarbon softener with cs1 or higher 10 to 10
A rubber composition containing 0 parts by weight is provided.
本発明で使用されるジエンゴムは乳化重合せたにJ、浴
液重合に」:り製造することができる。ジェノゴムのス
チレン含有量は0〜45重量%、さらには10〜35重
肝係が好ましい。45重重量部超えると樹脂状となり、
硬度が上昇し弾性が損われるので好捷しくない。The diene rubber used in the present invention can be produced by emulsion polymerization or bath liquid polymerization. The styrene content of Geno rubber is preferably 0 to 45% by weight, more preferably 10 to 35% by weight. If it exceeds 45 parts by weight, it becomes resinous,
This is not desirable because the hardness increases and the elasticity is impaired.
ジエンゴムのロジン酸含有量は0.1〜10重量%、好
捷しくけ1〜7重量%である。0.1重i%未満では硬
度変化を減少させる効果がなく、10@ 41%を超え
ると粘性が増しすき、寸だ弾性が損われるので好捷しく
ない。The rosin acid content of the diene rubber is 0.1 to 10% by weight, preferably 1 to 7% by weight. If it is less than 0.1% by weight, there is no effect of reducing hardness change, and if it exceeds 10@41%, the viscosity increases and the elasticity is significantly impaired, which is not preferable.
本発明で使用する軟化剤は芳香族系炭化水素であり、し
かも比重および動粘度の高いものを使用することが本発
明の効果を得るために必要であり、従来広く使用されて
いるナンテン系、パラフィン系および比重1015未満
、動粘”(4Q cst未満の芳香族系軟化剤では本発
明の効果は見出せない3、本発明の軟化剤の比重(15
×4℃)は1015以上、好ましくは1017以上であ
る。丑た」二限は105以下であることが実用上好捷し
い。The softening agent used in the present invention is an aromatic hydrocarbon, and it is necessary to use one with high specific gravity and kinematic viscosity in order to obtain the effects of the present invention. The effects of the present invention cannot be found with paraffinic and aromatic softeners with a specific gravity of less than 1015 and a kinematic viscosity of less than 4Q cst3.
×4°C) is 1015 or more, preferably 1017 or more. Practically speaking, it is preferable that the second limit of "Ushita" is 105 or less.
軟化剤の動粘度(98,89℃)は4 Q cst以上
、好ましくは5 Q cs1以上である。丑だ上限は1
00以下であることが実用」二好ましい。The kinematic viscosity (98.89° C.) of the softener is 4 Q cst or more, preferably 5 Q cs1 or more. The upper limit is 1
00 or less is preferred for practical use.
ジエンゴム100重量部に対する軟化剤の配合量は10
〜100重量部、好丑しくは10〜70重量部である。The amount of softener added to 100 parts by weight of diene rubber is 10
~100 parts by weight, preferably 10 to 70 parts by weight.
10重量部未満ではジエンゴムの加工性改良効果はでず
、100重量部を超えると特注が損われるので上記範囲
に限定される。If it is less than 10 parts by weight, no improvement in the processability of the diene rubber will be achieved, and if it exceeds 100 parts by weight, customization will be impaired, so it is limited to the above range.
本発明のゴム組成物はその特性を生かしてタイヤ、ベル
ト製品、はきもの等に広く使用でき、しかも硬度が経時
的に変化しないので耐用年数が長い。The rubber composition of the present invention can be widely used in tires, belt products, footwear, etc. by taking advantage of its characteristics, and has a long service life because its hardness does not change over time.
次に実施例をあげて本発明をさらに詳細に説明するが、
本発明はこれらに限定されるものではない。Next, the present invention will be explained in more detail with reference to Examples.
The present invention is not limited to these.
実施例においてジエンゴムのロジン酸含有量およびスチ
レン含有量はJI8K 6383に準じて測定した。In the examples, the rosin acid content and styrene content of the diene rubber were measured according to JI8K 6383.
軟化剤の比重はJTSK2249、動粘度はJl8に2
283に準じて6A1)定した。The specific gravity of the softener is JTSK2249, and the kinematic viscosity is Jl8.
6A1) was determined according to 283.
ジエンゴム組成物の経時変化試験は次の方法により行な
った。すなわちテストチューブ老化試験機を用い、これ
に活性炭を入れ、その中に20×30 X 2 mm
犬の加硫ゴム試験片を浸漬し100℃に保ち、2週間毎
に試験片をとり出し、コ゛ム組成物の硬度、電歇および
アセトン抽出量変化を求めた。なお硬度についてはJI
S K、6301、アセトン抽出量についてはJl、S
K6350に準じ、重量変イしについては次式により
求めた。The aging test of the diene rubber composition was conducted by the following method. That is, using a test tube aging tester, put activated carbon in it and measure 20 x 30 x 2 mm.
A dog vulcanized rubber test piece was immersed and kept at 100°C, and the test piece was taken out every two weeks to determine changes in the hardness, electrical resistance, and amount of acetone extracted from the comb composition. Regarding hardness, JI
S K, 6301, Jl, S for acetone extraction amount.
According to K6350, weight change was determined by the following formula.
実施例1〜4、比較例1
乳化剤の種類、量を変えてえた表1のスチレン含i 、
23 %のスチレンーンリジエンゴム(5r31t )
に芳香族系炭化水素軟化剤として比重(15×4℃)1
016、動粘度(98,89℃) 57,6 cstの
もの(商品名三菱38ヘビープロセス油)を使用した。Examples 1 to 4, Comparative Example 1 Styrene-containing i in Table 1 obtained by changing the type and amount of emulsifier,
23% styrene lysine rubber (5r31t)
Specific gravity (15 x 4℃) 1 as an aromatic hydrocarbon softener
016, kinematic viscosity (98.89°C) 57.6 cst (trade name: Mitsubishi 38 Heavy Process Oil) was used.
混練りはBI(、型バンバリーミキサ−と2本ロールで
行ない、SBR,100部に対してI IAFブラック
100部、軟化剤50部、亜鉛華5部、ステアリン酸1
部、a 黄1.2部、N−シクロヘキシルベンゾチアゾ
ールスルフェンアミド15部(いずれも重量部)を添加
し混練りした。加硫は160°×30分プレス加硫した
。Kneading was carried out using a BI (type Banbury mixer) and two rolls, and 100 parts of SBR was mixed with 100 parts of IIAF black, 50 parts of softener, 5 parts of zinc white, and 1 part of stearic acid.
1.2 parts of yellow and 15 parts of N-cyclohexylbenzothiazolesulfenamide (all parts by weight) were added and kneaded. Vulcanization was performed by press vulcanization at 160° for 30 minutes.
評価結果を表1に示したつ
実施例5 シンタックHA−25(神戸油化単基)・
6 AR’oMAx亜5(富士興衆製)比較例2
叫3(に )I 3 :ll
:1(〃 )−4JSRAROMA(日本合成ゴム製
)# 5 ソニックプロセス油r(、−1000(共同
石油基ナンテン系伸展油)
・ 6 三菱10ライトプロセス油(三菱石油製 パラ
フィン系伸展油)
# 7 コウモレソクス700(日本石油製)以北の結
果から本発明のゴム組成物・は硬度の経時変化が少ない
優れた特注を示すことが明らかであり問題点を解決した
ゴム組成物であることがわかる。The evaluation results are shown in Table 1. Example 5 Syntac HA-25 (Kobe Oil Chemical Single Unit)
6 AR'oMAX A5 (manufactured by Fuji Koshu) Comparative Example 2
Shout 3 (ni) I 3 :ll
:1 (〃 )-4JSRAROMA (made by Japan Synthetic Rubber) #5 Sonic process oil r (, -1000 (Kyodo Oil Base Nandene-based extender oil) ・6 Mitsubishi 10 light process oil (Mitsubishi Oil made paraffin-based extender oil) #7 From the results of Komoresox 700 (manufactured by Nippon Oil Co., Ltd.), it is clear that the rubber composition of the present invention exhibits excellent customization properties with little change in hardness over time, and is a rubber composition that has solved the problems.
代理人 弁理士伊東 彰Agent: Patent attorney Akira Ito
Claims (1)
ジェンゴムおよび/またはブタジェンゴム100重量部
に対し、比重(15/4℃)]、、015以上、動粘度
(98,89℃) 40 cst以上の)′J香族系炭
化水素軟化剤10〜100重危部を含むことを特徴とす
るゴム組成物For 100 parts by weight of styrene-butadiene rubber and/or butadiene rubber having a weight coefficient of 0.1 to 10 rosin acid, specific gravity (15/4°C)], 015 or higher, kinematic viscosity (98, 89°C) 40 cst or higher) A rubber composition characterized by containing 10 to 100 critical parts of an aromatic hydrocarbon softener
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18286282A JPS5974136A (en) | 1982-10-20 | 1982-10-20 | Rubber composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18286282A JPS5974136A (en) | 1982-10-20 | 1982-10-20 | Rubber composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5974136A true JPS5974136A (en) | 1984-04-26 |
JPH0240096B2 JPH0240096B2 (en) | 1990-09-10 |
Family
ID=16125743
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18286282A Granted JPS5974136A (en) | 1982-10-20 | 1982-10-20 | Rubber composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5974136A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2252978A (en) * | 1991-02-21 | 1992-08-26 | Exxon Research Engineering Co | Rubber processing oil |
-
1982
- 1982-10-20 JP JP18286282A patent/JPS5974136A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2252978A (en) * | 1991-02-21 | 1992-08-26 | Exxon Research Engineering Co | Rubber processing oil |
US5504135A (en) * | 1991-02-21 | 1996-04-02 | Exxon Research And Engineering Company | Rubber processing oil and rubber products containing it |
Also Published As
Publication number | Publication date |
---|---|
JPH0240096B2 (en) | 1990-09-10 |
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