JP3201330B2 - Rubber reinforcing cord and its treating agent - Google Patents

Rubber reinforcing cord and its treating agent

Info

Publication number
JP3201330B2
JP3201330B2 JP04204798A JP4204798A JP3201330B2 JP 3201330 B2 JP3201330 B2 JP 3201330B2 JP 04204798 A JP04204798 A JP 04204798A JP 4204798 A JP4204798 A JP 4204798A JP 3201330 B2 JP3201330 B2 JP 3201330B2
Authority
JP
Japan
Prior art keywords
rubber
coating layer
nbr
treating agent
cord
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.)
Ceased
Application number
JP04204798A
Other languages
Japanese (ja)
Other versions
JPH11241275A (en
Inventor
光晴 秋山
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.)
Nippon Sheet Glass Co Ltd
Original Assignee
Nippon Sheet Glass 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=12625217&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JP3201330(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Nippon Sheet Glass Co Ltd filed Critical Nippon Sheet Glass Co Ltd
Priority to JP04204798A priority Critical patent/JP3201330B2/en
Priority to CA002262103A priority patent/CA2262103C/en
Priority to US09/251,398 priority patent/US6106943A/en
Priority to EP99102769A priority patent/EP0937740B1/en
Priority to DE69908208T priority patent/DE69908208T2/en
Publication of JPH11241275A publication Critical patent/JPH11241275A/en
Application granted granted Critical
Publication of JP3201330B2 publication Critical patent/JP3201330B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • Y02T10/862

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Tires In General (AREA)
  • Reinforced Plastic Materials (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、耐屈曲性と耐熱性
に優れた水素化ニトリルゴム(以後H−NBRとする)
とメタクリル酸亜鉛を分散させた水素化ニトリルゴム
(以後H−NBR/ZDMAとする)とからなる混合ゴ
ムの補強用に使用されるゴム補強用コードに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hydrogenated nitrile rubber (hereinafter referred to as "H-NBR") having excellent bending resistance and heat resistance.
The present invention relates to a rubber reinforcing cord used for reinforcing a mixed rubber comprising: a hydrogenated nitrile rubber in which zinc methacrylate is dispersed (hereinafter referred to as H-NBR / ZDMA).

【0002】[0002]

【従来の技術】ゴムベルト、ゴムタイヤ等のゴム製品の
耐強度性、耐久性を向上させるために、ガラス繊維、化
学繊維等を補強用繊維としてゴム内に埋め込むことが広
く一般に行われている。
2. Description of the Related Art In order to improve the strength and durability of rubber products such as rubber belts and rubber tires, it is widely practiced to embed glass fibers, chemical fibers and the like as reinforcing fibers in rubber.

【0003】しかし、一般に補強用繊維自体はゴムと馴
染みが悪く接着性が悪いため、補強用繊維の表面を加工
処理せずにゴム内に埋め込んだ場合、補強用繊維とゴム
とは接着しないまたは接着力が弱く使用中に簡単に剥離
してしまう。このような状態では、補強用繊維はゴム製
品の補強材として求められる性能を満たすことが出来な
い。
However, since the reinforcing fibers themselves generally have poor affinity with rubber and have poor adhesiveness, when the surface of the reinforcing fibers is embedded in rubber without processing, the reinforcing fibers do not adhere to the rubber. Adhesion is weak and easily peels off during use. In such a state, the reinforcing fiber cannot satisfy the performance required as a reinforcing material for rubber products.

【0004】そのため、各種補強用繊維をゴム製品に使
用する場合には、使用するゴムとの馴染みを改善し接着
性を向上させる被覆層を、補強用繊維表面に形成させる
ことが広く一般に行われている。
For this reason, when various reinforcing fibers are used in rubber products, it is common practice to form a coating layer on the surface of the reinforcing fibers to improve the familiarity with the rubber used and to improve the adhesiveness. ing.

【0005】例えば、レゾルシン・ホルマリン縮合物と
H−NBRラテックスの混合処理剤をガラス繊維に塗布
し、乾燥硬化させ形成させた被膜を有するガラス繊維コ
ード(特開昭63−270877号)が挙げられる。ま
た、第2層をハロゲン含有ポリマー、イソシアネートで
塗布し、さらにマトリックスゴムと同一のゴムを含む第
3層を形成させたゴム補強用繊維が提案されている(特
公平5−71710号)。しかし、前者はH−NBRお
よびH−NBR/ZDMAを混合したゴムと十分な接着
強度が得られず、後者は3層の塗布が必要であるため製
造工程が煩雑となりコストも高くなる。
For example, a glass fiber cord having a coating formed by applying a mixed treatment of a resorcinol-formalin condensate and H-NBR latex to a glass fiber and drying and curing the glass fiber (JP-A-63-270877) can be mentioned. . Further, there has been proposed a rubber reinforcing fiber in which a second layer is coated with a halogen-containing polymer and isocyanate, and a third layer containing the same rubber as the matrix rubber is formed (Japanese Patent Publication No. 5-71710). However, the former cannot obtain a sufficient adhesive strength with rubber mixed with H-NBR and H-NBR / ZDMA, and the latter requires three layers of coating, which complicates the production process and increases the cost.

【0006】[0006]

【発明が解決しようとする課題】以上述べたように、使
用するゴムと補強用繊維の接着性向上のために補強用繊
維表面に被覆層を形成させることが広く一般に行われて
いる。しかし、現在使用されているゴムと補強用繊維と
の種類は多岐に渡り、ゴムと補強用繊維との種類が異な
れば、当然に接着性を向上させる被覆層の種類も異な
る。
As described above, it is widely and generally practiced to form a coating layer on the surface of the reinforcing fiber in order to improve the adhesion between the rubber used and the reinforcing fiber. However, there are a wide variety of types of rubber and reinforcing fibers currently used, and if the types of rubber and reinforcing fibers are different, the types of coating layers for improving the adhesiveness are naturally different.

【0007】近年、H−NBR/ZDMAゴムが、様々
な方面で注目されている。H−NBR/ZDMAゴムを
H−NBRゴムと混合したゴムは、従来から使用されて
いたH−NBRゴムに比べてさらに耐熱性が高く、従来
使用できなかった分野に、または従来品と比べてより高
性能な代替品として使用可能である。
[0007] In recent years, H-NBR / ZDMA rubber has been receiving attention in various fields. The rubber obtained by mixing H-NBR / ZDMA rubber with H-NBR rubber has higher heat resistance than the conventionally used H-NBR rubber, and is used in a field where it could not be used conventionally, or compared with a conventional product. Can be used as a higher performance alternative.

【0008】本発明は、H−NBRおよびH−NBR/
ZDMAを主成分とするゴムに補強用繊維を使用する場
合において、上記ゴムとの接着性を高めた補強用コード
および当該補強用コードの被覆層(補強用繊維上の第2
層の表面処理膜)を形成する処理剤を得ることを目的と
する。
[0008] The present invention relates to H-NBR and H-NBR /
When a reinforcing fiber is used for rubber containing ZDMA as a main component, a reinforcing cord having improved adhesion to the rubber and a coating layer of the reinforcing cord (the second layer on the reinforcing fiber) may be used.
The purpose of the present invention is to obtain a treating agent for forming a layer (surface treatment film).

【0009】[0009]

【課題を解決するための手段】上記の目的を達成するた
めに、請求項1に記載の発明のゴム補強用コードは、ゴ
ム補強用繊維に、レゾルシン・ホルマリン縮合物とゴム
ラテックスとを含む処理剤を塗布し乾燥硬化させ第1被
覆層とし、当該第1被覆層上にさらに異なる処理剤を塗
布し乾燥硬化させ第2被覆層を形成させたものであっ
て、当該第2被覆層用の処理剤が、ゴム配合物、加硫剤
およびマレイミド系加硫助剤を主成分とするものであ
る。
According to a first aspect of the present invention, there is provided a rubber reinforcing cord comprising a rubber reinforcing fiber comprising a resorcinol-formalin condensate and a rubber latex. A second coating layer formed by applying an agent and drying and curing to form a first coating layer, further applying a different treatment agent on the first coating layer, drying and curing to form a second coating layer, The treating agent contains a rubber compound, a vulcanizing agent and a maleimide-based vulcanizing aid as main components.

【0010】請求項2に記載の発明のゴム補強用コード
は、請求項1記載の発明において、第2被覆層用処理剤
に含まれる加硫助剤がN,N-m-フェニレンジマレイミドで
あるものである。
[0010] A rubber reinforcing cord according to a second aspect of the present invention is the cord according to the first aspect, wherein the vulcanization aid contained in the treating agent for the second coating layer is N, Nm-phenylenedimaleimide. It is.

【0011】請求項3に記載の発明のゴム補強用コード
は、請求項1または2に記載の発明において、第2被覆
層用処理剤に含まれるゴム配合物が水素化ニトリルゴム
とメタクリル酸亜鉛を分散させた水素化ニトリルゴムと
からなる混合ゴムの溶解物であるものである。
According to a third aspect of the present invention, there is provided the rubber reinforcing cord according to the first or second aspect, wherein the rubber compound contained in the treating agent for the second coating layer comprises a hydrogenated nitrile rubber and zinc methacrylate. And a hydrogenated nitrile rubber in which is dispersed a mixed rubber.

【0012】請求項4に記載の発明の処理剤は、請求項
1〜3のいずれか一項に記載された第2被覆層用処理剤
である。
[0012] The treatment agent of the invention according to claim 4 is the treatment agent for the second coating layer according to any one of claims 1 to 3.

【0013】[0013]

【発明の実施の形態】本発明者は、上述の課題を解決す
るために鋭意研究を行った結果、補強用コードの最外被
覆層すなわち本発明でいう第2被覆層に、ゴム配合物、
加硫剤およびマレイミド系加硫助剤を含む被覆層用処理
剤を用いることによって、H−NBRおよびH−NBR
/ZDMAを主成分とするゴムと補強用コードとの接着
性を劇的に改善できることを見出した。以下、本発明の
実施形態について詳細に説明する。
BEST MODE FOR CARRYING OUT THE INVENTION The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and as a result, a rubber compound, a rubber coating,
By using a coating layer treating agent containing a vulcanizing agent and a maleimide-based vulcanizing aid, H-NBR and H-NBR can be obtained.
It has been found that the adhesion between the rubber containing / ZDMA as a main component and the reinforcing cord can be dramatically improved. Hereinafter, embodiments of the present invention will be described in detail.

【0014】本発明で用いられるゴム補強用繊維に制限
はなく、その具体例としてはガラス繊維、ビニロン繊維
に代表されるポリビニルアルコール繊維、ポリエステル
繊維、ナイロン、アラミド(芳香族ポリアミド)などの
ポリアミド繊維、カーボン繊維、ポリパラフェニレンベ
ンゾオキサゾール繊維等を例示することができる。これ
らの中でガラス繊維およびアラミド繊維が好適に用いら
れる。ガラス繊維の種類は、特に限定されるものではな
く、無アルカリガラス、高強度ガラス等が使用できる。
またガラス繊維のフィラメント直径も特に限定されるも
のではないが、5〜1.3μmのものが一般的に使用さ
れる。またアラミド繊維としては、500〜5,000
デニールのものが一般的に使用される。これらの繊維の
形態としては、ステーブル、フィラメント、コード状、
ロープ状もしくは帆布等を具体例として上げることがで
きる。
The rubber reinforcing fiber used in the present invention is not limited, and specific examples thereof include glass fiber, polyvinyl alcohol fiber represented by vinylon fiber, polyester fiber, nylon fiber and polyamide fiber such as aramid (aromatic polyamide). , Carbon fiber, polyparaphenylene benzoxazole fiber and the like. Among these, glass fibers and aramid fibers are preferably used. The type of glass fiber is not particularly limited, and non-alkali glass, high-strength glass, and the like can be used.
The filament diameter of the glass fibers is not particularly limited, but those having a diameter of 5 to 1.3 μm are generally used. Also, as aramid fiber, 500 to 5,000
Denier ones are commonly used. The form of these fibers includes stable, filament, cord,
As a specific example, a rope shape or a canvas can be used.

【0015】請求項1に記載された第1被覆層を形成す
るゴムラテックスは、具体的にはブタジエン・スチレン
共重合体ラテックス、ジカルボキシル化ブタジエン・ス
チレン共重合体ラテックス、ビニルピリジン・ブタジエ
ン・スチレンターポリマーラテックス、クロロプレンラ
テックス、ブタジエンゴムラテックス、クロロスルホン
化ポリエチレンラテックス、アクリロニトリル・ブタジ
エン共重合ラテックス、ニトリル基含有高飽和共重合体
ゴムラテックスなどが好ましい。
The rubber latex forming the first coating layer according to claim 1 is specifically a butadiene / styrene copolymer latex, a dicarboxylated butadiene / styrene copolymer latex, a vinylpyridine / butadiene / styrene. Terpolymer latex, chloroprene latex, butadiene rubber latex, chlorosulfonated polyethylene latex, acrylonitrile / butadiene copolymer latex, and nitrile group-containing highly saturated copolymer rubber latex are preferred.

【0016】第2被覆層用処理剤に含まれるゴム配合物
としては、マトリックスゴムの種類により種々の単独、
あるいは複数の混合ゴムが使用できる。ゴムの種類およ
びその溶媒は限定されるものではないが、ゴムとしては
クロロプレンゴム、クロロスルホン化ポリエチレン、H
−NBRもしくはH−NBR/ZDMA等が用いられ
る。これらのゴムは、マトリックスゴムの種類によりそ
の相溶性等が考慮されて選択されるが、特にマトリック
スゴムがH−NBRとH−NBR/ZDMAとの混合ゴ
ムの場合、第2被覆層用処理剤のゴム配合物も同じゴム
を溶解したものが好適に使用される。
The rubber compound contained in the treating agent for the second coating layer may be any one of various types depending on the type of the matrix rubber.
Alternatively, a plurality of mixed rubbers can be used. The type of rubber and its solvent are not limited. Examples of rubber include chloroprene rubber, chlorosulfonated polyethylene, H
-NBR or H-NBR / ZDMA or the like is used. These rubbers are selected in consideration of the compatibility and the like depending on the type of the matrix rubber. In particular, when the matrix rubber is a mixed rubber of H-NBR and H-NBR / ZDMA, the treating agent for the second coating layer is used. The same rubber compound dissolved in the same rubber is preferably used.

【0017】溶解されるH−NBRとH−NBR/ZD
MAとの重量比は、H−NBR/(H−NBR/ZDM
A)=45〜80/55〜20が好ましく、H−NBR
/ZDMAの割合が小さいと十分な接着強度が得られ
ず、割合が大きくなるとコードが硬くなり屈曲疲労性が
悪くなる。
H-NBR and H-NBR / ZD to be dissolved
The weight ratio to MA is H-NBR / (H-NBR / ZDM).
A) = 45 to 80/55 to 20, preferably H-NBR
If the ratio of / ZDMA is small, sufficient adhesive strength cannot be obtained, and if the ratio is large, the cord becomes hard and the bending fatigue property deteriorates.

【0018】H−NBRとしては、ヨウ素価が120以
下であることがゴムのフィルム強度およびマトリックス
ゴムとの接着性の観点から必要であり、好ましくはヨウ
素価が0〜100である。このゴムとしてゼットポール
(商品名 日本ゼオン社製)が好適に使用できる。な
お、ヨウ素価はJIS K0070にしたがって決めた
値である。
The H-NBR must have an iodine value of 120 or less from the viewpoints of rubber film strength and adhesion to the matrix rubber, and preferably has an iodine value of 0 to 100. Zetpol (trade name, manufactured by Zeon Corporation) can be suitably used as this rubber. The iodine value is a value determined according to JIS K0070.

【0019】本発明でいうH−NBR/ZDMAは、上
記のゼットポールにポリメタクリル酸亜鉛を分散させた
ZSC(商品名 日本ゼオン社製)が好適に使用でき
る。
As the H-NBR / ZDMA used in the present invention, ZSC (trade name, manufactured by Zeon Corporation) in which polyzinc methacrylate is dispersed in the above-mentioned zetpol can be suitably used.

【0020】ゴムを溶解するための溶媒は、ベンゼン、
トルエンもしくはキシレンのような芳香族炭化水素、ト
リクロロエチレンのようなハロゲン化炭化水素、メチル
エチルケトン(以下MEKという)あるいは酢酸エチル
などが使用される。前記のH−NBRの様な配合ゴムの
場合はMEKが通常用いられる。
The solvent for dissolving the rubber is benzene,
An aromatic hydrocarbon such as toluene or xylene, a halogenated hydrocarbon such as trichloroethylene, methyl ethyl ketone (hereinafter referred to as MEK), ethyl acetate, or the like is used. In the case of a compounded rubber such as the aforementioned H-NBR, MEK is usually used.

【0021】第2被覆層用処理剤に含まれる加硫剤は、
硫黄、ジクミルペルオキシド、1,3-ビス(t-ブチルパー
オキシ-イソプロピル)ベンゼン等の有機過酸化物、p-
ジニトロソナフタレン、p-ジニトロソベンゼンなどの芳
香族ニトロソ化合物等があげられる。これらの多くはゴ
ム配合物中にあらかじめ配合されている場合があるた
め、特に必要な場合添加される。
The vulcanizing agent contained in the treatment agent for the second coating layer includes:
Organic peroxides such as sulfur, dicumyl peroxide, 1,3-bis (t-butylperoxy-isopropyl) benzene, p-
Aromatic nitroso compounds such as dinitrosonaphthalene and p-dinitrosobenzene are exemplified. Many of these may be preliminarily compounded in the rubber compound, and are added when necessary.

【0022】第1項記載のマレイミド系加硫助剤は、具
体的にはマレイミド、フェニールマレイミド、N,N-m-フ
ェニレンジマレイミド等が使用できる。特に請求項2に
記載のN,N-m-フェニレンジマレイミドは、接着性向上の
手段として好適に使用できる。
As the maleimide-based vulcanization aid described in item 1, specifically, maleimide, phenylmaleimide, N, Nm-phenylenedimaleimide and the like can be used. In particular, N, Nm-phenylenedimaleimide according to claim 2 can be suitably used as a means for improving the adhesiveness.

【0023】その被覆層用処理剤の配合率は、ゴム配合
物/加硫剤/マレイミド系加硫助剤=100/0〜10
/1〜150重量部であり、100/0〜6/30〜8
0重量部の範囲で好適に使用できる。
The compounding ratio of the coating layer treating agent is as follows: rubber compound / vulcanizing agent / maleimide vulcanizing aid = 100 / 0-10
/ 1 to 150 parts by weight, and 100/0 to 6/30 to 8
It can be suitably used in the range of 0 parts by weight.

【0024】本発明の第2被覆層用処理剤は、カーボン
ブラック等の無機充填剤や可塑剤、老化防止剤、その他
の架橋助剤を含んでもかまわない。
The treating agent for the second coating layer of the present invention may contain an inorganic filler such as carbon black, a plasticizer, an antioxidant, and other crosslinking aids.

【0025】本発明のガラス繊維の第2被覆層用処理剤
は、通常は固形分含量3〜25重量%、より好ましくは
5〜15重量%の溶液または分散液として調整される。
The treating agent for the second coating layer of the glass fiber of the present invention is usually prepared as a solution or dispersion having a solid content of 3 to 25% by weight, more preferably 5 to 15% by weight.

【0026】第2被覆層を形成させる方法は、特に限定
されないが、通常は1次被覆層を備えているゴム補強用
繊維を処理剤の入った溶剤漕に浸し、その後乾燥炉を潜
らせて、被覆層を形成させる。乾燥条件も限定されない
が一般に80〜160℃で0.1〜1分間行われる。付
着量は1〜10%、好ましくは3〜7%である。
The method of forming the second coating layer is not particularly limited, but usually, the rubber reinforcing fiber provided with the primary coating layer is immersed in a solvent tank containing a treating agent, and then dipped in a drying oven. , Forming a coating layer. Although the drying conditions are not limited, the drying is generally performed at 80 to 160 ° C. for 0.1 to 1 minute. The adhesion amount is 1 to 10%, preferably 3 to 7%.

【0027】[0027]

【実施例】[実施例1]ガラス繊維(E-ガラス:9μm
径のガラスフィラメント200本集束)は、3本引き揃
えられて、公知の方法により、下記組成の第1被覆層用
処理剤を塗布された。
[Example 1] Glass fiber (E-glass: 9 μm)
Three glass filaments having a diameter of 200 were bundled, and a treating agent for a first coating layer having the following composition was applied by a known method.

【0028】[0028]

【表1】 -------------------------------------------------------------------- 組成 配合率(重量部) −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− ビニルピリジンラテックス(固形分40%) 45 クロロスルホン化ポリエチレンラテックス(固形分40%) 20 レゾルシン・ホルマリン縮合物(固形分8%) 30 (レゾルシン/ホルマリン=1/1.3 モル比) 25%アンモニア水 1 水 4 --------------------------------------------------------------------[Table 1] ---------------------------------------------- ---------------------- Composition Blending ratio (parts by weight) -------------- −−−−−−−−−−− Vinylpyridine latex (solid content 40%) 45 Chlorosulfonated polyethylene latex (solid content 40%) 20 Resorcin / formalin condensate (solid content 8%) 30 (resorcin / 25% ammonia water 1 water 4 ------------------------------------ -----------------------------------

【0029】第1被覆層が形成されたガラス繊維は、8
回/10cmの下撚後、11本引き揃えられて、さらに
8回/10cmの上撚を掛けられた後、下記に記載の第
2被覆層用処理剤を上記と同様の方法で塗布および乾燥
硬化され、ガラス繊維コードとされた。
The glass fiber on which the first coating layer is formed is 8
After the twist / 10 cm priming, 11 strands are aligned and further 8 times / 10 cm twisted, then the second coating layer treating agent described below is applied and dried in the same manner as described above. It was cured and made into a glass fiber cord.

【0030】[0030]

【表2】 ---------------------------------------------- 被覆層用処理剤の組成 配合率(重量部) −−−−−−−−−−−−−−−−−−−−−−− ゴム組成物 100 トルエン 416 メチルエチルケトン 180 N,N-m-フェニレンジマレイミド 50 ----------------------------------------------[Table 2] ---------------------------------------------- Composition of treatment agent for coating layer Compounding ratio (parts by weight) Rubber composition 100 Toluene 416 Methyl ethyl ketone 180 N, Nm-phenylene Maleimide 50 ----------------------------------------------

【0031】第2被覆層は、ガラス繊維コードの重量に
対して、5重量%であった。上記表2中のゴム組成物を
下記表3に示す。
The second coating layer was 5% by weight based on the weight of the glass fiber cord. Table 3 below shows the rubber compositions in Table 2 above.

【0032】[0032]

【表3】 -------------------------------------------------------------- ゴム組成物の組成 配合率(重量部) −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− ZETPOL2020(*1) 70 ZSC2000L(*2) 30 ZnO 10 ステアリン酸 1 カーボンブラック 30 TOTM(Trioctyl Trimellitate) 5 硫黄 0.1 1,3-Bis-(t-butylperoxy-isopropyl)-benzene 6 -------------------------------------------------------------- (*1)商品名 H−NBR:日本ゼオン社製 (*2)商品名 H−NBR/ZDMA:日本ゼオン社製[Table 3] ---------------------------------------------- ---------------- Composition of rubber composition Compounding ratio (parts by weight) ---------------------------------------------------------------------- −−−−−−−− ZETPOL2020 (* 1) 70 ZSC2000L (* 2) 30 ZnO 10 Stearic acid 1 Carbon black 30 TOTM (Trioctyl Trimellitate) 5 Sulfur 0.1 1,3-Bis- (t-butylperoxy-isopropyl) ) -benzene 6 ---------------------------------------------- ---------------- (* 1) Trade name H-NBR: manufactured by Zeon Corporation (* 2) Trade name H-NBR / ZDMA: manufactured by Zeon Corporation

【0033】当該ガラス繊維コードとH−NBRおよび
H−NBR/ZDMAからなる混合ゴムとの接着性をテ
ストするために、表3の組成の試験片(幅25mm×長さ
50mm×厚さ5mm)上に当該ガラス繊維コードを長辺沿
いに並べて、160℃で30分加熱し接着した。
In order to test the adhesion between the glass fiber cord and the mixed rubber composed of H-NBR and H-NBR / ZDMA, a test piece having a composition shown in Table 3 (width 25 mm × length 50 mm × thickness 5 mm) The glass fiber cords were arranged on the upper side along the long side, and bonded by heating at 160 ° C. for 30 minutes.

【0034】加熱接着後の当該試験片を、引張り試験器
にかけ、繊維方向に引張ってその強度数値を測定した。
その結果を下記表5に示す。
The test piece after the heat bonding was applied to a tensile tester and pulled in the fiber direction to measure the strength value.
The results are shown in Table 5 below.

【0035】[実施例2]実施例1で使用されたガラス
繊維の代わりにアラミド繊維(テクノーラT202:帝
人社製 1500d)を使用し、実施例1と同じ第1被
覆層用処理剤を塗布した後、固形物付着率が12%とな
るよう調整し、250℃で1分間熱処理を行った。これ
を2本合糸して1インチあたり3.1回の下撚を施して
アラミド繊維コードを得た。このようにして得られたア
ラミド繊維コードを用いて実施例1と同じ第2被覆層用
処理剤を用いて処理を行った。第2被覆層は、アラミド
繊維コードの重量に対して、10重量%であった。接着
性の評価方法は、実施例1と同様にした。
[Example 2] Instead of the glass fiber used in Example 1, aramid fiber (Technola T202: 1500d, manufactured by Teijin Limited) was used, and the same treating agent for the first coating layer as in Example 1 was applied. Thereafter, the solid adhered rate was adjusted to 12%, and heat treatment was performed at 250 ° C. for 1 minute. This was plied twice and subjected to 3.1 times of twist per inch to obtain an aramid fiber cord. Using the aramid fiber cord thus obtained, a treatment was performed using the same treating agent for the second coating layer as in Example 1. The second coating layer was 10% by weight based on the weight of the aramid fiber cord. The method of evaluating the adhesion was the same as in Example 1.

【0036】[比較例1]上記実施例1で使用した第2
被覆層を形成する処理剤(表2に記載)の代わりに、下
記表4に記載の処理剤を用いて第2被覆層を形成させ
た。その他は、実施例と同じ条件で試験を行った。
Comparative Example 1 The second example used in Example 1 was used.
The second coating layer was formed using the processing agents shown in Table 4 below instead of the processing agents for forming the coating layer (described in Table 2). Other than that, the test was performed under the same conditions as in the example.

【0037】[0037]

【表4】 ---------------------------------------- 組成 配合率(重量部) −−−−−−−−−−−−−−−−−−−− ゴム組成物 100 トルエン 416 メチルエチルケトン 180 ----------------------------------------[Table 4] ---------------------------------------- Composition Composition ratio (parts by weight) ) ------------------- Rubber composition 100 Toluene 416 Methyl ethyl ketone 180 --------------------- -------------------

【0038】[比較例2]実施例2において、使用した
第2被覆層用処理剤の代わりに、比較例1で使用した表
4に記載の処理剤を用いて第2被覆層を形成させた。そ
の他は、実施例2と同じ条件で試験を行った。
Comparative Example 2 A second coating layer was formed in Example 2 by using the treating agent shown in Table 4 used in Comparative Example 1 instead of the treating agent for the second coating layer used. . Otherwise, the test was performed under the same conditions as in Example 2.

【0039】[0039]

【表5】 [Table 5]

【0040】[0040]

【発明の効果】本発明は、耐屈強性、耐熱性に優れたH
−NBRおよびH−NBR/ZDMAからなる配合ゴム
とガラス繊維との接着性を劇的に改善し、本発明による
ガラス繊維コードを使用することによって、結果として
高温環境下での使用が可能となり、かつ耐久性が大幅に
向上したH−NBR系ゴム製品を得ることが出来る。
According to the present invention, H is excellent in bending resistance and heat resistance.
Dramatically improving the adhesion between the compounded rubber comprising -NBR and H-NBR / ZDMA and the glass fiber, and using the glass fiber cord according to the present invention makes it possible to use it in a high temperature environment, In addition, it is possible to obtain an H-NBR rubber product having significantly improved durability.

フロントページの続き (58)調査した分野(Int.Cl.7,DB名) D06M 13/00 - 15/715 Continuation of front page (58) Field surveyed (Int.Cl. 7 , DB name) D06M 13/00-15/715

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ゴム補強用繊維に、レゾルシン・ホルマ
リン縮合物とゴムラテックスを含む処理剤を塗布し乾燥
硬化させ第1被覆層とし、当該第1被覆層上にさらに異
なる処理剤を塗布し乾燥硬化させ形成させた第2被覆層
を有するゴム補強用繊維コードにおいて、 当該第2被覆層用の処理剤が、ゴム配合物、加硫剤およ
びマレイミド系加硫助剤を主成分とすることを特徴とす
るゴム補強用コード。
1. A treatment agent containing a resorcinol-formalin condensate and rubber latex is applied to a rubber reinforcing fiber, dried and cured to form a first coating layer, and a different treatment agent is further applied on the first coating layer and dried. In a rubber reinforcing fiber cord having a second coating layer formed by curing, a treatment agent for the second coating layer contains a rubber compound, a vulcanizing agent, and a maleimide vulcanization aid as main components. Characteristic cord for rubber reinforcement.
【請求項2】 上記第2被覆層用処理剤に含まれる加硫
助剤が、N,N-m-フェニレンジマレイミドである請求項1
に記載のゴム補強用コード。
2. The vulcanization aid contained in the second coating layer treatment agent is N, Nm-phenylenedimaleimide.
A rubber reinforcing cord according to the item.
【請求項3】 第2被覆層用処理剤に含まれるゴム配合
物が、水素化ニトリルゴムとメタクリル酸亜鉛を分散さ
せた水素化ニトリルゴムとからなる混合ゴムの溶解物で
ある請求項1または2に記載のゴム補強用コード。
3. The rubber compound contained in the second coating layer treating agent is a melt of a mixed rubber comprising a hydrogenated nitrile rubber and a hydrogenated nitrile rubber in which zinc methacrylate is dispersed. 3. The rubber reinforcing cord according to 2.
【請求項4】 請求項1〜3のいずれか1項に記載の第
2被覆層用処理剤。
4. The treatment agent for a second coating layer according to claim 1, wherein
JP04204798A 1998-02-24 1998-02-24 Rubber reinforcing cord and its treating agent Ceased JP3201330B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP04204798A JP3201330B2 (en) 1998-02-24 1998-02-24 Rubber reinforcing cord and its treating agent
CA002262103A CA2262103C (en) 1998-02-24 1999-02-17 Cord for reinforcing a rubber and treating material thereof
US09/251,398 US6106943A (en) 1998-02-24 1999-02-17 Cord for reinforcing a rubber and treating material thereof
EP99102769A EP0937740B1 (en) 1998-02-24 1999-02-23 Cord for reinforcing a rubber and treating material thereof
DE69908208T DE69908208T2 (en) 1998-02-24 1999-02-23 Rope for rubber reinforcement and materials which are used for it

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04204798A JP3201330B2 (en) 1998-02-24 1998-02-24 Rubber reinforcing cord and its treating agent

Publications (2)

Publication Number Publication Date
JPH11241275A JPH11241275A (en) 1999-09-07
JP3201330B2 true JP3201330B2 (en) 2001-08-20

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JP4520069B2 (en) * 2001-04-18 2010-08-04 日本板硝子株式会社 Treatment agent, rubber reinforcing cord and rubber product
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