JPS592293B2 - Rubber fittings - Google Patents

Rubber fittings

Info

Publication number
JPS592293B2
JPS592293B2 JP50103066A JP10306675A JPS592293B2 JP S592293 B2 JPS592293 B2 JP S592293B2 JP 50103066 A JP50103066 A JP 50103066A JP 10306675 A JP10306675 A JP 10306675A JP S592293 B2 JPS592293 B2 JP S592293B2
Authority
JP
Japan
Prior art keywords
rubber
present
vulcanization
rubber composition
cut resistance
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.)
Expired
Application number
JP50103066A
Other languages
Japanese (ja)
Other versions
JPS5226544A (en
Inventor
和弘 山田
正明 小原
恒雄 小山
裕一 杉浦
義夫 田島
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.)
Yokohama Rubber Co Ltd
Original Assignee
Yokohama Rubber 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 Yokohama Rubber Co Ltd filed Critical Yokohama Rubber Co Ltd
Priority to JP50103066A priority Critical patent/JPS592293B2/en
Publication of JPS5226544A publication Critical patent/JPS5226544A/en
Publication of JPS592293B2 publication Critical patent/JPS592293B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳細な説明】 本発明は、ゴムに芳香族線状ポリエステル樹脂を配合す
ることを特徴とする、加硫後、金属材料および繊維材料
との接着性が良好でかつ耐カット性が良好なゴム組成物
に関する。
Detailed Description of the Invention The present invention is characterized in that an aromatic linear polyester resin is blended into rubber, and after vulcanization, it has good adhesion to metal materials and fiber materials and good cut resistance. The present invention relates to a rubber composition.

従来、ゴムとスチールコード等の金属材料又はゴムとナ
イロンコード等の繊維材料とを接着させる場合、前者は
スチール又はスチールコードの表面に黄銅、青銅等の銅
合金を鍍金する方法が一般に知られており、又後者はナ
イロンコードの表面をRFL液(レゾルシン−ホルムア
ルデヒド−ラテックス)で処理する方法が一般に知られ
ている。
Conventionally, when bonding rubber and a metal material such as a steel cord, or rubber and a fiber material such as a nylon cord, the former method is generally known by plating the surface of the steel or steel cord with a copper alloy such as brass or bronze. The latter method is generally known in which the surface of the nylon cord is treated with RFL liquid (resorcinol-formaldehyde-latex).

しかしながら、特に車輛用タイヤにおいて、自動車の高
速化に伴つて、更に高い接着力が要求される様になつた
。近年、金属材料及ひ繊維材料との接着力をさらに向上
させるために、ゴムにホワイトカーボン、レゾルシン並
びにヘキサメチレンテトラミンを配合する、いわゆるH
RH系が利用されるようになつてきた。
However, as automobile tires become faster, even higher adhesion strength is required, especially in vehicle tires. In recent years, in order to further improve the adhesive strength with metal materials and fiber materials, so-called H
RH systems have come into use.

所が、該HRH系ゴム組成物は、レゾルシンの著しい昇
華性のために、バンバリー混合時、又はロール混合時に
おいて、発煙及び臭気を発生し、環境汚染、作業性悪化
の欠陥があつた。最近ではレゾルシンの上記の欠点を改
善する目的で、HRH系ゴム組成物においてレゾルシン
の代りにレゾルシンとホルマリンの初期縮合物(米国ユ
ニロイヤル社製BondingAgentR−6等)を
使用する方法も知られている(例えば特公昭44−11
066)oしかしながら、この場合、ゴム組成物の加硫
物性及び金属材料、繊維材料との接着性を低下させる難
点があつた。又、土木建築用のOTR(オフ・ザ・ロー
ドOffTheRoad)タイヤおよび高荷重条件下で
使用されるトラックやバスのタイヤにおいて、タイヤト
レツドの耐カット性は最も重要な特性である。
However, due to the remarkable sublimation property of resorcinol, the HRH rubber composition generated smoke and odor during Banbury mixing or roll mixing, resulting in environmental pollution and poor workability. Recently, in order to improve the above-mentioned drawbacks of resorcin, a method of using an initial condensate of resorcin and formalin (such as BondingAgent R-6 manufactured by Uniroyal, Inc. in the United States) in place of resorcin in HRH rubber compositions has been known. (For example, special public relations
066) o However, in this case, there was a problem that the vulcanized physical properties of the rubber composition and the adhesiveness with metal materials and fiber materials were reduced. In addition, cut resistance of the tire tread is the most important characteristic in OTR (Off The Road) tires for civil engineering and construction and tires for trucks and buses used under high load conditions.

これらの耐カット性を改善するために従来では、ジエン
系重合体、例えば天然ゴムおよびスチレン−ブタジエン
共重合体を適当に選択する事、およびカーボンブラック
や無機補強剤を配合する事等が試みられて来た。
In the past, attempts have been made to improve these cut resistances by appropriately selecting diene polymers such as natural rubber and styrene-butadiene copolymers, and by incorporating carbon black and inorganic reinforcing agents. I came.

しかしながら、これらの方法により、耐カット性はある
程度は改善されるが満足すべきものではなく、又カーボ
ンブラツクや無機補強剤の配合量が増加するとゴム組成
物の配合時の加工性は低下し、さらに製品の使用時にお
ける発熱が大きくなるという欠点があつた。
However, although cut resistance is improved to some extent by these methods, it is not satisfactory, and when the amount of carbon black or inorganic reinforcing agent is increased, the processability during compounding of the rubber composition decreases. The drawback was that the product generated a lot of heat during use.

特公昭48−38615号公報は、スチレンーブメジエ
ン共重合体にシクロペンタジエン系樹脂を添加してタイ
アトレットの耐カツト性を改良する事を開示しているが
、この改良はまだ満足すべきものではない。本発明の目
的は、未加硫ゴム組成物の安全、衛生性を改善し、加硫
後、ゴムと金属材料またはゴムと繊維材料との接着性を
向上させ、更には耐カツト性を改良する事を目的とし、
特にタイヤのオーバーヘツド、カーカス以外にタイアト
レットや他の一般ゴム製品にも使用されるゴム組成物を
提供することである。
Japanese Patent Publication No. 48-38615 discloses that a cyclopentadiene resin is added to a styrene-bumediene copolymer to improve the cut resistance of tielets, but this improvement is still unsatisfactory. isn't it. The purpose of the present invention is to improve the safety and hygiene of unvulcanized rubber compositions, improve the adhesion between rubber and metal materials or rubber and fiber materials after vulcanization, and further improve cut resistance. with the aim of
In particular, it is an object of the present invention to provide a rubber composition that can be used not only for tire overheads and carcass but also for tire inlets and other general rubber products.

本発明のゴム組成物は、ゴム物質100重量部に、1〜
30重量部の芳香族線状ポリエステル樹脂を配合するこ
とを特徴とする。
The rubber composition of the present invention contains 1 to 100 parts by weight of the rubber substance.
It is characterized by blending 30 parts by weight of aromatic linear polyester resin.

本発明に用いられるゴム物質は天然ゴム、合成ゴムある
いは天然ゴムと合成ゴムとの混合物であり、加硫可能な
ものである。
The rubber material used in the present invention is natural rubber, synthetic rubber, or a mixture of natural rubber and synthetic rubber, and is vulcanizable.

本発明に用いられる芳香族線状ポリエステル樹脂とは、
2ケのカルボキシル基を有する芳香族化合物をグリコー
ル類でポリエステル化して得られるポリエステル樹脂で
あり、例えばテレフタル酸を、5一般式HO(CH2)
NOH(n−3〜20)のポリメチレングリコール類、
8一般式HO(CH2CH2O)NH(n−2〜200
)のポリエチレングリコール類、のアルキレングリコー
ル類、8二つの−0H間に芳香族グループを有するグリ
コール類、等のグリコール類でポリエステル化して得ら
れるポリエステル樹脂である。
The aromatic linear polyester resin used in the present invention is
It is a polyester resin obtained by polyesterifying an aromatic compound having two carboxyl groups with glycols.
NOH (n-3 to 20) polymethylene glycols,
8 General formula HO(CH2CH2O)NH(n-2~200
It is a polyester resin obtained by polyesterification with glycols such as polyethylene glycols (), alkylene glycols (8), glycols having an aromatic group between two -0H groups, and the like.

また、本発明に用いられる芳香族線状ポリエステル樹脂
はゴム物質100重量部あたり1〜30重量部、好まし
くは5〜20重量部加えることが望ましい。30重量部
を超えて加えると加硫後の硬さが増加し、弾性が低下し
、かつ発熱性が増大し、実用に供し得なくなり、1重量
部未満では本発明の目的を達成し得ない。
Further, it is desirable to add 1 to 30 parts by weight, preferably 5 to 20 parts by weight, of the aromatic linear polyester resin used in the present invention per 100 parts by weight of the rubber material. If more than 30 parts by weight is added, the hardness after vulcanization will increase, elasticity will be reduced, and heat generation will increase, making it impossible to put it into practical use. If it is less than 1 part by weight, the purpose of the present invention cannot be achieved. .

本発明を下記の実施例によりさらに具体的に説明するが
、本発明はこれらの実施例により限定されるものではな
い。
The present invention will be explained in more detail with reference to the following examples, but the present invention is not limited to these examples.

0実施例1〜7および標準例1、比較例1〜2配合処方
を後記第1表に、試験結果を第2表に示す。
The formulations of Examples 1 to 7, Standard Example 1, and Comparative Examples 1 to 2 are shown in Table 1 below, and the test results are shown in Table 2.

(ゴム配合物の作成及び加硫) マスターバツチをバンバリーミキサ一で配合し、これに
加硫系をロールで混合して、ゴム配合物を作成した。
(Preparation and vulcanization of rubber compound) A masterbatch was compounded in a Banbury mixer, and a vulcanization system was mixed therein with a roll to prepare a rubber compound.

物性試験用の加硫は145℃で30分行なつた。(スチ
ールコードとの接着テスト) ゴム配合物を、12.5mm間隔に平行に並べた黄銅鍍
金スチールコードの両面からコーテイングしたフアブリ
ツク(2インチ埋め込み)を、145℃で45分加硫し
、スチールコード引抜テストをASTMD2229に準
拠して行なつた。
Vulcanization for physical property testing was carried out at 145°C for 30 minutes. (Adhesion test with steel cord) A fabric (2 inches embedded) coated with a rubber compound on both sides of brass-plated steel cords arranged in parallel at 12.5 mm intervals was vulcanized at 145°C for 45 minutes, and then the steel cords were coated with a rubber compound. A pull test was conducted in accordance with ASTM D2229.

1実施例8〜12、標準例2、比較例3〜4〔1〕と同
様の方法で配合し、下記の条件で加硫、測定を行つた。
1 Examples 8 to 12, Standard Example 2, and Comparative Examples 3 to 4 were blended in the same manner as [1], and vulcanization and measurement were performed under the following conditions.

配合処方を第3表に、結果を第4表に示す。物性測定用
の条件は148℃×30分である。(ナイロンコードと
の接着テスト) ASTMD2l38によるHテストに準拠して行つた。
The combination recipe is shown in Table 3, and the results are shown in Table 4. The conditions for measuring physical properties were 148°C x 30 minutes. (Adhesion test with nylon cord) This was conducted in accordance with the H test according to ASTM D2138.

加硫系は148℃×30分、その他は〔Dと同様である
。w実施例13〜15、標準例3、比較例5〔1〕と同
様の方法で配合し、下記の条件で加硫、測定を行つた。
The vulcanization system was 148°C for 30 minutes, and the other conditions were the same as [D]. w Examples 13 to 15, standard example 3, and comparative example 5 [1] were blended in the same manner as in Example 13 to 15, standard example 3, and comparative example 5 [1], and vulcanization and measurement were performed under the following conditions.

配合処方を第5表に、結果を第6表に示す。物性測定用
の条件は150℃X3O分である。(耐カツト性テスト
:衝撃落下試験) 12.98k9の鋼鉄刃を、加硫ゴム試験片上に、25
?の高さから落下させる事によつて生ずる切傷(カツト
)の深さで評価する。
The combination recipe is shown in Table 5, and the results are shown in Table 6. The conditions for measuring physical properties were 150°C x 30 minutes. (Cut resistance test: impact drop test) A 12.98k9 steel blade was placed on a vulcanized rubber test piece,
? Evaluation is based on the depth of the cut caused by dropping from a height of

ただし、標準例を100とする指数(インデツクス)で
表示した。数値の大なるほど、改善効果が大きい。第2
表から、本発明の配合によるゴム組成物は、従来のレゾ
ルシン等配合のゴム組成物とくらべて加硫物性はほとん
ど変化ないが、黄銅鍍金スチールコード接着力は同等以
上であり、かつ混合作業時の発煙および臭気がなく、配
合後ブルームする事もない事が明らかである。第4表か
ら、本発明のゴム組成物は、物性は従来のレゾルシン等
配合ゴムと同等であり、またナイロンコードとの接着力
は、そのナイロンコードが無処理ナイロンコードまたは
RFL処理ナイロンのいずれであつてもレゾルシン等配
合ゴムとほぼ同等であり、かつ標準例2(レゾルシン無
添加)にくらべれば大巾に接着力が向上している事が明
らかである。
However, the standard example was expressed as an index of 100. The larger the number, the greater the improvement effect. Second
From the table, it can be seen that the rubber composition according to the present invention has almost no change in vulcanized properties compared to conventional rubber compositions containing resorcinol, etc., but the adhesion strength to brass-plated steel cords is equal to or higher than that during mixing work. It is clear that there is no smoke or odor, and there is no blooming after blending. From Table 4, the physical properties of the rubber composition of the present invention are equivalent to conventional rubbers compounded with resorcinol, etc., and the adhesion strength to nylon cords is determined regardless of whether the nylon cords are untreated nylon cords or RFL-treated nylon cords. It is clear that the adhesive strength is almost the same as that of rubber compounded with resorcin, etc., and the adhesive strength is greatly improved compared to Standard Example 2 (no resorcin added).

又、配合時の発煙性、配合物のブルーム性も著るしく改
善されている。第6表より、本発明のゴム組成物は、加
硫後、従来のものよりも耐カツト性を大巾に改善してい
る事が明らかである。
Furthermore, the smoke generation properties during blending and the blooming properties of the blends are also significantly improved. From Table 6, it is clear that the rubber composition of the present invention has significantly improved cut resistance after vulcanization compared to the conventional rubber composition.

以上説明したように、本発明のゴム組成物は、スチール
コード又はナイロンコードとの接着力及び耐カツト性に
優れている事から、新しいゴム用練り込み接着剤として
、並びに耐カツト性改良剤として利用出来る。
As explained above, the rubber composition of the present invention has excellent adhesion to steel cords or nylon cords and cut resistance, so it can be used as a new rubber kneading adhesive and as a cut resistance improver. Available.

Claims (1)

【特許請求の範囲】[Claims] 1 ゴム物質に、ゴム物質100重量部あたり1〜30
重量部の芳香族線状ポリエステル樹脂を配合したことを
特徴とする、加硫後、金属材料または繊維材料との接着
性が良好でかつ耐カット性が良好なゴム組成物。
1 to the rubber substance, 1 to 30 per 100 parts by weight of the rubber substance
A rubber composition having good adhesion to metal materials or fiber materials and good cut resistance after vulcanization, characterized in that it contains a weight part of aromatic linear polyester resin.
JP50103066A 1975-08-27 1975-08-27 Rubber fittings Expired JPS592293B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50103066A JPS592293B2 (en) 1975-08-27 1975-08-27 Rubber fittings

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50103066A JPS592293B2 (en) 1975-08-27 1975-08-27 Rubber fittings

Publications (2)

Publication Number Publication Date
JPS5226544A JPS5226544A (en) 1977-02-28
JPS592293B2 true JPS592293B2 (en) 1984-01-18

Family

ID=14344283

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50103066A Expired JPS592293B2 (en) 1975-08-27 1975-08-27 Rubber fittings

Country Status (1)

Country Link
JP (1) JPS592293B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH037127A (en) * 1989-06-04 1991-01-14 Takagi Ind Co Ltd Hot/cold water mixed spouting device
JPH037128A (en) * 1989-06-04 1991-01-14 Takagi Ind Co Ltd Hot/cold water mixed spouting device
JPH0328208B2 (en) * 1984-03-19 1991-04-18 Matsushita Electric Ind Co Ltd
JPH0439882Y2 (en) * 1987-11-16 1992-09-18
JPH052777B2 (en) * 1989-09-25 1993-01-13 Takagi Sangyo Kk

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5265542A (en) * 1975-11-27 1977-05-31 Toray Ind Inc Improved rubber composition
JPS52138546A (en) * 1975-11-27 1977-11-18 Toray Ind Inc Elastomer compositions
JPH04193506A (en) * 1990-11-26 1992-07-13 Neste Oy Method and device for impregnating fiber bundle with molten resin

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4999648A (en) * 1973-01-02 1974-09-20

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4999648A (en) * 1973-01-02 1974-09-20

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0328208B2 (en) * 1984-03-19 1991-04-18 Matsushita Electric Ind Co Ltd
JPH0439882Y2 (en) * 1987-11-16 1992-09-18
JPH037127A (en) * 1989-06-04 1991-01-14 Takagi Ind Co Ltd Hot/cold water mixed spouting device
JPH037128A (en) * 1989-06-04 1991-01-14 Takagi Ind Co Ltd Hot/cold water mixed spouting device
JPH052777B2 (en) * 1989-09-25 1993-01-13 Takagi Sangyo Kk

Also Published As

Publication number Publication date
JPS5226544A (en) 1977-02-28

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