JP3008373B2 - Bonding method between fiber and rubber compound - Google Patents
Bonding method between fiber and rubber compoundInfo
- Publication number
- JP3008373B2 JP3008373B2 JP2334372A JP33437290A JP3008373B2 JP 3008373 B2 JP3008373 B2 JP 3008373B2 JP 2334372 A JP2334372 A JP 2334372A JP 33437290 A JP33437290 A JP 33437290A JP 3008373 B2 JP3008373 B2 JP 3008373B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- rubber
- weight
- rubber compound
- urethane prepolymer
- 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 - Lifetime
Links
- 239000000835 fiber Substances 0.000 title claims description 54
- 229920001971 elastomer Polymers 0.000 title claims description 30
- 239000005060 rubber Substances 0.000 title claims description 30
- 150000001875 compounds Chemical class 0.000 title claims description 29
- 238000000034 method Methods 0.000 title claims description 19
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000003822 epoxy resin Substances 0.000 claims description 17
- 229920000647 polyepoxide Polymers 0.000 claims description 17
- 229920000768 polyamine Polymers 0.000 claims description 14
- 229920000126 latex Polymers 0.000 claims description 12
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 238000004073 vulcanization Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 description 15
- 230000001070 adhesive effect Effects 0.000 description 15
- 239000002131 composite material Substances 0.000 description 10
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
- -1 tires Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229960001755 resorcinol Drugs 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 229920001084 poly(chloroprene) Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 229920003235 aromatic polyamide Polymers 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 1
- DLYLVPHSKJVGLG-UHFFFAOYSA-N 4-(cyclohexylmethyl)cyclohexane-1,1-diamine Chemical compound C1CC(N)(N)CCC1CC1CCCCC1 DLYLVPHSKJVGLG-UHFFFAOYSA-N 0.000 description 1
- SOKFWRPORPTXSA-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)-2-methylpropyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)CC1=CC=C(O)C=C1 SOKFWRPORPTXSA-UHFFFAOYSA-N 0.000 description 1
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 101710162453 Replication factor A Proteins 0.000 description 1
- 102100035729 Replication protein A 70 kDa DNA-binding subunit Human genes 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- QUEICCDHEFTIQD-UHFFFAOYSA-N buta-1,3-diene;2-ethenylpyridine;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=N1 QUEICCDHEFTIQD-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Tyre Moulding (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Reinforced Plastic Materials (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、繊維とゴム配合物との接着方法に関し、詳
しくは、繊維の強力を保持しつつ、繊維とゴム配合物と
の間に強固な接着を達成することができる繊維とゴム配
合物との接着方法に関する。Description: FIELD OF THE INVENTION The present invention relates to a method of bonding a fiber and a rubber compound, and more particularly, to a method of bonding a fiber and a rubber compound while maintaining the strength of the fiber. And a method of bonding a fiber and a rubber compound to achieve the following.
従来の技術 一般に、タイヤ、ゴム・ホース、伝動ベルト、コンベ
ヤベルト等の工業用ゴム製品は、ゴムに繊維材料を接着
して補強されてなる接着複合体である。従来、このよう
に、繊維とゴム配合物とを接着するには、通常、レゾル
シン・ホルマリン・ゴムラテツクス混合液(以下、RFL
液という。)にて繊維を処理する方法が知られている。
しかし、この方法によれば、多くの場合、繊維とゴム配
合物との間に得られる接着力は不十分である。2. Description of the Related Art In general, industrial rubber products such as tires, rubber hoses, power transmission belts, and conveyor belts are adhesive composites formed by bonding a fiber material to rubber and reinforced. Conventionally, in order to bond the fiber and the rubber compound as described above, usually, a resorcinol-formalin-rubber latex mixture (hereinafter, RFL) is used.
Called liquid. ) Is known.
However, according to this method, the adhesion obtained between the fiber and the rubber compound is often insufficient.
そこで、従来、かかる問題を解決するために、繊維を
RFL処理する前に、エポキシ樹脂で処理する方法が提案
されている。エポキシ樹脂による前処理は、接着性にす
ぐれる接着複合体を与えるものの、耐衝撃性に劣る。そ
こで、例えば、特開昭58−5243号公報には、繊維をエポ
キシ化合物と液状ゴムとを含む溶液にて処理した後、RF
L液にて処理する方法が記載されている。また、特開昭5
8−124631号公報には、ウレタン変性エポキシ樹脂にて
繊維を処理した後、RFL液にて処理する方法が提案され
ている。Therefore, conventionally, in order to solve this problem, fiber
Prior to RFL treatment, a method of treating with an epoxy resin has been proposed. The pretreatment with an epoxy resin gives an adhesive composite having excellent adhesiveness, but is inferior in impact resistance. Therefore, for example, JP-A-58-5243 discloses that after treating a fiber with a solution containing an epoxy compound and a liquid rubber, RF
A method of treating with L solution is described. In addition,
Japanese Patent Application Laid-Open No. 8-124632 proposes a method in which fibers are treated with a urethane-modified epoxy resin and then treated with an RFL solution.
これらの方法によれば、接着力及び可撓性にすぐれる
接着複合体を得ることができるが、繊維の強力が低下す
る傾向がみられる。このような繊維の強力の低下は、接
着複合体の耐久性を低めるので、実用上、重要な問題で
ある。According to these methods, an adhesive composite having excellent adhesive strength and flexibility can be obtained, but the strength of the fiber tends to decrease. Such a decrease in fiber strength is a practically important problem because it reduces the durability of the adhesive composite.
発明が解決しようとする課題 本発明は、従来の繊維とゴム配合物の接着における上
記したような問題を解決するためになされたものであつ
て、繊維の強力を保持しつつ、繊維とゴム配合物との間
に強固な接着を達成することができる繊維とゴム配合物
との接着方法を提供することを目的とする。DISCLOSURE OF THE INVENTION The present invention has been made to solve the above-mentioned problems in the conventional bonding of a fiber and a rubber compound, and it is intended that the fiber and the rubber compound be mixed while maintaining the strength of the fiber. It is an object of the present invention to provide a method of bonding a fiber and a rubber compound, which can achieve a strong bond with a product.
問題点を解決するための手段 本発明による繊維とゴム配合物との接着方法は、エポ
キシ樹脂とブロツク化ウレタンプレポリマーと分子内に
1つ以上のアミノ基を有するポリアミンとを含む処理溶
液で繊維を処理し、次いで、レゾルシン・ホルマリン・
ゴムラテツクスにて処理した後、繊維を未加硫ゴム配合
物と加硫接着することを特徴とする。Means for Solving the Problems A method for bonding a fiber and a rubber compound according to the present invention is a method for bonding a fiber with a treatment solution containing an epoxy resin, a blocked urethane prepolymer, and a polyamine having one or more amino groups in a molecule. And then resorcinol / formalin /
After the treatment with the rubber latex, the fibers are vulcanized and bonded to the unvulcanized rubber compound.
上記エポキシ樹脂は、分子内に少なくとも1つのエポ
キシ基を有する化合物であつて、例えば、エチレングリ
コール、グリセリン、ソルビトール、ペンタエリスリト
ール等の多価アルコールや、ポリエチレングリコール等
のポリアルキレングリコールとエピクロルヒドリンのよ
うなハロゲン含有エポキシ化合物との反応生成物や、レ
ゾルシン、ビス(4−ヒドロキシフエニル)ジメチルエ
タン、フエノール・ホルムアミド樹脂、レゾルシン・ホ
ルムアミド樹脂等の多価フエノール類やフエノール樹脂
とエピクロルヒドリンのようなハロゲン含有エポキシ化
合物との反応生成物が好ましく用いられる。脂肪族又は
脂環族不飽和化合物の有する二重結合を化酢酸等にて酸
化して得られるエポキシ化合物も好ましく用いられる。
また、エポキシ基を有する種々のシランカツプリング剤
も好ましく用いられる。The epoxy resin is a compound having at least one epoxy group in a molecule, for example, a polyhydric alcohol such as ethylene glycol, glycerin, sorbitol, and pentaerythritol, and a polyalkylene glycol such as polyethylene glycol and epichlorohydrin. Reaction products with halogen-containing epoxy compounds, polyphenols such as resorcin, bis (4-hydroxyphenyl) dimethylethane, phenol-formamide resin, resorcin-formamide resin, and halogen-containing epoxy such as phenol resin and epichlorohydrin The reaction product with the compound is preferably used. An epoxy compound obtained by oxidizing a double bond of an aliphatic or alicyclic unsaturated compound with acetic acid or the like is also preferably used.
Various silane coupling agents having an epoxy group are also preferably used.
上記ブロツク化ウレタンプレポリマーは、ウレタンプ
レポリマーの末端イソシアネート基をブロツク化してな
るものであつて、既に知られており、市販品を用いるこ
とができる。ブロツク化ウレタンプレポリマーは、例え
ば、よく知られているように、トリレンジイソシアネー
ト、メタフエニレンジイソシアネート、ジフエニルメタ
ンジイソシアネート、ヘキサメチレンジイソシアネー
ト、ポリメチレンポリフエニルジイソシアネート等のポ
リイソシアネートと種々のポリオール類とを反応させて
ウレタンプレポリマーとし、その末端のイソシアネート
基をトリメチロールプロパン、ペンタエリスリトール等
のように分子内に活性水素を2つ以上有する化合物を反
応させることによつて得ることができる。また、ブロツ
ク化ウレタンプレポリマーは、ウレタンプレポリマーに
ケトオキシム類、フエノール類、アミン類等を反応させ
ることによつても得ることができる。The above-mentioned blocked urethane prepolymer is obtained by blocking the terminal isocyanate group of the urethane prepolymer, and is already known and a commercially available product can be used. Blocked urethane prepolymers are, for example, as well known, polyisocyanates such as tolylene diisocyanate, metaphenylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, polymethylene polyphenyl diisocyanate and various polyols. To give a urethane prepolymer, and the terminal isocyanate group is reacted with a compound having two or more active hydrogens in the molecule, such as trimethylolpropane or pentaerythritol. Further, the blocked urethane prepolymer can also be obtained by reacting a urethane prepolymer with a ketoxime, a phenol, an amine or the like.
本発明の方法において、処理溶液は、その合計量に基
づいて、エポキシ樹脂80〜30重量%、ブロツク化ウレタ
ンプレポリマーを20〜70重量%含有する。また、処理溶
液は、エポキシ樹脂とブロツク化ウレタンプレポリマー
とを合計量にて固形分で1〜20重量%の範囲で含有す
る。In the method of the present invention, the treatment solution contains 80 to 30% by weight of an epoxy resin and 20 to 70% by weight of a blocked urethane prepolymer, based on the total amount. Further, the treatment solution contains the epoxy resin and the blocked urethane prepolymer in a total amount of 1 to 20% by weight in solid content.
更に、本発明による方法においては、処理溶液は、ポ
リアミンを含有する。このポリアミンは分子内にアミノ
基を1つ以上有する単量体化合物であつて、本発明にお
いては、ウレタンプレポリマー及びエポキシ樹脂のため
の硬化剤として用いられる。通常、エポキシ樹脂とポリ
ウレタンとポリアミンを反応させた場合、ポリウレタン
とポリアミンの反応が圧倒的に速いので、生成する重合
体は、可撓性は上がるが接着強さが低下する。そこで、
本発明によれば、ブロツク化ウレタンプレポリマーを用
いることにより、エポキシ樹脂とポリアミンの反応速
度、ブロツク化ウレタンプレポリマーとポリアミンの反
応速度をほぼ同じにし、接着強さを低下させることなく
可撓性を得る。Furthermore, in the method according to the invention, the treatment solution contains a polyamine. This polyamine is a monomer compound having one or more amino groups in the molecule, and is used as a curing agent for urethane prepolymers and epoxy resins in the present invention. Normally, when an epoxy resin is reacted with a polyurethane and a polyamine, the reaction between the polyurethane and the polyamine is overwhelmingly fast, so that the resulting polymer has higher flexibility but lower adhesive strength. Therefore,
According to the present invention, by using the blocked urethane prepolymer, the reaction rate between the epoxy resin and the polyamine and the reaction rate between the blocked urethane prepolymer and the polyamine are substantially the same, and the flexibility is reduced without lowering the adhesive strength. Get.
本発明においては、このようなポリアミンとして、例
えば、ジエチレントリアミン、3,3′−ジクロロ−4,4′
−ジアミノジフエニルメタン、トリエチレンテトラミ
ン、テトラエチレンペンタミン、3,3′−ジメチル−4,
4′−ジアミノジシクロヘキシルメタン、ポリアミドポ
リアミン、メンセンジアミン、イソホロンジアミン、メ
タキシレンジアミン、ジアミノジフエニルメタン、ジア
ミノジフエニルスルホン、ジシアンジアミド等を挙げる
ことができる。In the present invention, as such a polyamine, for example, diethylenetriamine, 3,3'-dichloro-4,4 '
-Diaminodiphenylmethane, triethylenetetramine, tetraethylenepentamine, 3,3'-dimethyl-4,
Examples thereof include 4'-diaminodicyclohexylmethane, polyamide polyamine, mensendiamine, isophoronediamine, metaxylenediamine, diaminodiphenylmethane, diaminodiphenylsulfone, and dicyandiamide.
本発明において、かかるポリアミンは、特に限定され
るものではないが、通常、(エポキシ基+イソシアネー
ト基)/アミンの活性水素当量が0.5〜1.5の範囲となる
ように含まれる。In the present invention, such a polyamine is not particularly limited, but is usually contained such that the active hydrogen equivalent of (epoxy group + isocyanate group) / amine is in the range of 0.5 to 1.5.
このような処理溶液を形成するための溶剤としては、
特に、限定されるものではないが、通常、ベンゼン、キ
シレン、トルエン等の芳香族炭化水素、メチルエチルケ
トン、メチルイソブチルケトン等の脂肪族ケトン、酢酸
エチル、酢酸アミル等のエステル等が好適に用いられ
る。As a solvent for forming such a processing solution,
In particular, although not particularly limited, aromatic hydrocarbons such as benzene, xylene, and toluene, aliphatic ketones such as methyl ethyl ketone and methyl isobutyl ketone, and esters such as ethyl acetate and amyl acetate are preferably used.
このような処理溶液による繊維の処理は、通常、繊維
を処理溶液に浸漬した後、熱処理することによつて行な
われる。この熱処理は、繊維に付着させた処理溶液を反
応定着させるに足る温度にて行なえばよく、通常、160
〜250℃にて数分間処理すればよい。The treatment of the fiber with such a treatment solution is usually performed by immersing the fiber in the treatment solution and then performing a heat treatment. This heat treatment may be performed at a temperature sufficient to cause the treatment solution attached to the fibers to react and fix.
What is necessary is just to process at ~ 250 degreeC for several minutes.
次いで、本発明の方法によれば、繊維をRFL液にて処
理する。RFL液は、前述したように、レゾルシン・ホル
マリンとゴムラテツクスの水性混合物であり、従来よ
り、一般にゴムと繊維との接着において知られているも
のであつて、通常、レゾルシンとホルマリンとをレゾル
シン/ホルマリンモル比1/3〜3/1にて塩基性触媒の存在
下に縮合させて得られる初期縮合物をゴムラテツクスと
混合してなる水性混合物である。レゾルシン/ホルマリ
ンモル比が上記範囲をはずれるときは、接着に必要な分
子量を有する初期縮合物を得ることができない。Then, according to the method of the present invention, the fibers are treated with an RFL solution. As described above, the RFL solution is an aqueous mixture of resorcinol-formalin and rubber latex, and is generally known in the past for bonding rubber and fiber. It is an aqueous mixture obtained by mixing an initial condensate obtained by condensing at a molar ratio of 1/3 to 3/1 in the presence of a basic catalyst with a rubber latex. When the resorcinol / formalin molar ratio is outside the above range, an initial condensate having a molecular weight necessary for adhesion cannot be obtained.
上記ゴムラテツクスとしては、通常、合成ゴムラテツ
クスが用いられる。例えば、クロロプレンゴムラテツク
ス、スチレン−ブタジエン−ビニルピリジンゴムラテツ
クス、アクリロニトリル−ブタジエンゴムラテツクス、
水素化ニトリルゴムラテツクス等が好適に用いられる。As the rubber latex, generally, a synthetic rubber latex is used. For example, chloroprene rubber latex, styrene-butadiene-vinylpyridine rubber latex, acrylonitrile-butadiene rubber latex,
Hydrogenated nitrile rubber latex is preferably used.
繊維のRFL液による処理も、繊維に付着させたRFL液を
繊維に反応定着させるに足る温度にて行なえばよく、通
常、100〜270℃にて数分間処理すればよい。The treatment of the fiber with the RFL solution may be performed at a temperature sufficient to cause the RFL solution attached to the fiber to react and fix the fiber, and may be generally treated at 100 to 270 ° C. for several minutes.
以上のように処理した繊維をゴム配合物と密着され、
そのゴム配合物において知られている通常の処理条件に
て加硫接着することによつて、繊維の強力を保持しつ
つ、繊維とゴム配合物との間に強固な接着を達成するこ
とができる。The fiber treated as described above is adhered to the rubber compound,
By vulcanizing and bonding under the usual processing conditions known for the rubber compound, strong adhesion between the fiber and the rubber compound can be achieved while maintaining the strength of the fiber. .
本発明においては、ゴムとしては、例えば、天然ゴ
ム、ブタジエンゴム、イソプレンゴム、スチレン−ブタ
ジエンゴム、エチレン−プロピレンゴム、ブチルゴム、
クロロプレンゴム、アクリロニトリル−ブタジエンゴ
ム、水素化ニトリルゴム、ウレタンゴム、シリコーンゴ
ム、フツ素ゴム等が用いられる。かかるゴムは、それぞ
れに応じて、通常のゴム配合物として知られてる種々の
補強性充填剤、老化防止剤、可塑剤、加硫助剤、加工助
剤等の適宜量を含有してもよい。In the present invention, as the rubber, for example, natural rubber, butadiene rubber, isoprene rubber, styrene-butadiene rubber, ethylene-propylene rubber, butyl rubber,
Chloroprene rubber, acrylonitrile-butadiene rubber, hydrogenated nitrile rubber, urethane rubber, silicone rubber, fluorine rubber and the like are used. Such rubbers may, depending on each case, contain appropriate amounts of various reinforcing fillers, antioxidants, plasticizers, vulcanization aids, processing aids, etc. known as ordinary rubber compounds. .
また、繊維としては、代表的には、絹、人絹、ポリビ
ニルアルコール繊維、脂肪族及び芳香族ポリアミド繊
維、ポリエステル繊維、炭素繊維、ガラス繊維等を挙げ
ることができるが、これらに限定されるものではない。The fibers typically include silk, human silk, polyvinyl alcohol fibers, aliphatic and aromatic polyamide fibers, polyester fibers, carbon fibers, glass fibers, and the like, but are not limited thereto. is not.
実施例 以下に実施例を挙げて本発明を説明するが、本発明は
これら実施例により何ら限定されるものではない。EXAMPLES Hereinafter, the present invention will be described with reference to examples, but the present invention is not limited to these examples.
実施例1 第1表に示すように、種々の配合組成の処理溶液を調
製し、これにポリエステル繊維コード(1000D/2×5)
を浸漬した後、235℃で1分間熱処理した。Example 1 As shown in Table 1, treatment solutions having various composition were prepared, and polyester fiber cords (1000D / 2 × 5) were prepared.
Was immersed and then heat-treated at 235 ° C. for 1 minute.
レゾルシン17重量部、ホルマリン15重量部、10重量%
水酸化ナトリウム水溶液13重量部及び脱イオン水を用い
てレゾルシン・ホルマリン樹脂液を調製し、このレゾル
シン・ホルマリン樹脂液30重量部をクロロプレンゴムラ
テツクス32重量部及び脱イオン水38重量部と混合して、
RFL液を調製した。17 parts by weight of resorcinol, 15 parts by weight of formalin, 10% by weight
A resorcinol-formalin resin solution is prepared using 13 parts by weight of an aqueous sodium hydroxide solution and deionized water, and 30 parts by weight of the resorcinol-formalin resin solution is mixed with 32 parts by weight of chloroprene rubber latex and 38 parts by weight of deionized water. hand,
An RFL solution was prepared.
前記繊維コードをこのRFL液に浸漬し、200℃で1分間
熱処理した。The fiber cord was immersed in this RFL solution and heat-treated at 200 ° C. for 1 minute.
次いで、クロロプレンゴム100重量部、酸化マグネシ
ウム4重量部、酸化亜鉛15重量部、加硫促進剤2重量
部、イオウ0.5重量部、老化防止剤2重量部、カーボン
ブラツク65重量部及びオイル8重量部なる組成を有する
ゴム配合物の未加硫シート上に上記繊維コードを平行に
配列し、170℃で30分間加硫して、接着複合体を得た。Then, 100 parts by weight of chloroprene rubber, 4 parts by weight of magnesium oxide, 15 parts by weight of zinc oxide, 2 parts by weight of a vulcanization accelerator, 0.5 parts by weight of sulfur, 2 parts by weight of an antioxidant, 65 parts by weight of carbon black and 8 parts by weight of oil The above fiber cords were arranged in parallel on an unvulcanized sheet of a rubber compound having the following composition, and vulcanized at 170 ° C. for 30 minutes to obtain an adhesive composite.
この接着複合体から幅1インチの試料を裁断し、剥離
速度100mm/分にて繊維コードとゴムとの間の180゜剥離
接着力を測定した。結果を第1図に示す。A 1-inch wide sample was cut from the adhesive composite, and the 180 ° peel adhesion between the fiber cord and the rubber was measured at a peel speed of 100 mm / min. The results are shown in FIG.
実施例2 実施例1において、繊維コードとして、芳香族ポリア
ミド繊維コード(デユポン社製ケブラー繊維からなる15
00D/2×3の繊維コード)を 用いた以外は、実施例1と同様にして、接着複合体を
得、180゜剥離接着力を測定した。結果を第2図に示
す。Example 2 In Example 1, the fiber cord was an aromatic polyamide fiber cord (made of Kevlar fiber manufactured by DuPont).
00D / 2 × 3 fiber cord) Except for using, an adhesive composite was obtained in the same manner as in Example 1, and the 180 ° peel adhesion was measured. The results are shown in FIG.
発明の効果 以上のように、本発明の方法によれば、エポキシ樹脂
とポリアミンと共に、ブロツク化ウレタンプレポリマー
を含む処理溶液で繊維を処理し、次いで、レゾルシン・
ホルマリン・ゴムラテツクスにて処理した後、繊維を未
加硫ゴム配合物と加硫接着することによつて、繊維の強
力を保持しつつ、繊維とゴム配合物とが強固に接着され
た接着複合体を得ることができる。As described above, according to the method of the present invention, the fiber is treated with a treatment solution containing a blocked urethane prepolymer together with an epoxy resin and a polyamine, and then treated with resorcinol.
An adhesive composite in which the fiber and the rubber compound are firmly bonded while maintaining the strength of the fiber by vulcanizing and bonding the fiber to the unvulcanized rubber compound after treatment with formalin rubber latex. Can be obtained.
ブロツク化ウレタンプレポリマーに代えて、通常のウ
レタンプレポリマーを用いるときは、ウレタンプレポリ
マーとポリアミンとの反応がエポキシ樹脂とポリアミン
との反応よりも優先して起こるために、得られる接着複
合体において、繊維の強力を避けることができない。When a normal urethane prepolymer is used in place of the blocked urethane prepolymer, the reaction between the urethane prepolymer and the polyamine occurs in preference to the reaction between the epoxy resin and the polyamine. Unavoidable, the strength of fiber.
第1図は、処理溶液におけるブロツク化ウレタンプレポ
リマーとエポキシ樹脂の重量比と、得られる接着複合体
におけるポリエステル繊維コードの接着力との関係を示
すグラフ、第2図は、処理溶液におけるブロツク化ウレ
タンプレポリマーとエポキシ樹脂の重量比と、得られる
接着複合体における芳香族ポリアミド繊維コードの接着
力との関係を示すグラフである。FIG. 1 is a graph showing the relationship between the weight ratio of the blocked urethane prepolymer and the epoxy resin in the treatment solution and the adhesive strength of the polyester fiber cord in the resulting adhesive composite. FIG. 5 is a graph showing a relationship between a weight ratio of a urethane prepolymer and an epoxy resin and an adhesive strength of an aromatic polyamide fiber cord in an obtained adhesive composite.
フロントページの続き (51)Int.Cl.7 識別記号 FI C08J 5/12 CFC C08J 5/12 CFC CFF CFF // C08L 21:00 Continued on the front page (51) Int.Cl. 7 Identification symbol FI C08J 5/12 CFC C08J 5/12 CFC CFF CFF // C08L 21:00
Claims (2)
リマーと分子内に1つ以上のアミノ基を有するポリアミ
ンとを含む処理溶液で繊維を処理し、次いで、レゾルシ
ン・ホルマリン・ゴムラテツクスにて処理した後、繊維
を未加硫ゴム配合物と加硫接着することを特徴とする繊
維とゴム配合物との接着方法。(1) treating fibers with a treatment solution containing an epoxy resin, a blocked urethane prepolymer, and a polyamine having at least one amino group in a molecule, and then treating the fibers with resorcinol-formalin rubber latex; A method of bonding a fiber to a rubber compound, comprising bonding the fiber to an unvulcanized rubber compound by vulcanization.
タンプレポリマーとの合計量に基づいて、エポキシ樹脂
を80〜30重量%、ブロツク化ウレタンプレポリマーを20
〜70重量%含有することを特徴とする請求項第1項記載
の繊維とゴム配合物との接着方法。2. A treatment solution comprising 80-30% by weight of epoxy resin and 20% by weight of blocked urethane prepolymer, based on the total amount of epoxy resin and blocked urethane prepolymer.
The method for bonding a fiber and a rubber compound according to claim 1, characterized in that it is contained in an amount of 70 to 70% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2334372A JP3008373B2 (en) | 1990-11-29 | 1990-11-29 | Bonding method between fiber and rubber compound |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2334372A JP3008373B2 (en) | 1990-11-29 | 1990-11-29 | Bonding method between fiber and rubber compound |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04202332A JPH04202332A (en) | 1992-07-23 |
JP3008373B2 true JP3008373B2 (en) | 2000-02-14 |
Family
ID=18276635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2334372A Expired - Lifetime JP3008373B2 (en) | 1990-11-29 | 1990-11-29 | Bonding method between fiber and rubber compound |
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Country | Link |
---|---|
JP (1) | JP3008373B2 (en) |
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JP6605974B2 (en) * | 2015-01-30 | 2019-11-13 | 三ツ星ベルト株式会社 | Aramid core wire manufacturing method and treatment agent, and transmission belt manufacturing method |
-
1990
- 1990-11-29 JP JP2334372A patent/JP3008373B2/en not_active Expired - Lifetime
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JPH04202332A (en) | 1992-07-23 |
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