JPS62205177A - Nbr based vulcanizable adhesive and bonding using said adhesive - Google Patents
Nbr based vulcanizable adhesive and bonding using said adhesiveInfo
- Publication number
- JPS62205177A JPS62205177A JP4754386A JP4754386A JPS62205177A JP S62205177 A JPS62205177 A JP S62205177A JP 4754386 A JP4754386 A JP 4754386A JP 4754386 A JP4754386 A JP 4754386A JP S62205177 A JPS62205177 A JP S62205177A
- Authority
- JP
- Japan
- Prior art keywords
- nbr
- adhesive
- nitrile content
- bonding
- solvent
- 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.)
- Granted
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 30
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 30
- 150000002825 nitriles Chemical class 0.000 claims abstract description 28
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims abstract description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 16
- 239000002184 metal Substances 0.000 claims abstract description 16
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 10
- 239000005011 phenolic resin Substances 0.000 claims abstract description 10
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 8
- 150000002576 ketones Chemical class 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 5
- 239000012046 mixed solvent Substances 0.000 claims abstract description 5
- 238000009472 formulation Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 238000013329 compounding Methods 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- 238000004073 vulcanization Methods 0.000 description 6
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 4
- 230000003712 anti-aging effect Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000007788 roughening Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- GQVCNZBQZKXBMX-UHFFFAOYSA-N butan-2-one;toluene Chemical compound CCC(C)=O.CC1=CC=CC=C1 GQVCNZBQZKXBMX-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 etc. are used Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、 NBR系加硫接着剤およびそれを用いる接
着方法に関する。更に詳しくは、金属と低乃至中ニトリ
ル含量NBRとの接着用NBR系加硫接着剤およびそれ
を用いる接着方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an NBR-based vulcanized adhesive and an adhesion method using the same. More specifically, the present invention relates to an NBR-based vulcanized adhesive for adhering metal and low to medium nitrile content NBR, and an adhesion method using the same.
〔従来の技術〕および〔発明が解決しようとする問題点
〕従来、金属とNBRとの接着剤としては、一般にフェ
ノール系樹脂を用いたものが使用されているが、低乃至
中ニトリル含量NBR(アクリロニトリル含量19〜3
2%)に対しては殆んど接着性がみられなかった。[Prior Art] and [Problems to be Solved by the Invention] Conventionally, phenolic resins have been generally used as adhesives between metals and NBR, but low to medium nitrile content NBR ( Acrylonitrile content 19-3
2%), almost no adhesion was observed.
本発明者は、かかる現状に鑑み、低乃至中ニトリル含量
NBRに対しても良好な接着性を示す加硫接着剤を求め
゛C種々検討の結果、高ニトリル含量NBR(アクリロ
ニトリル含量34〜46%)の有機溶剤溶液が好適に使
用されることおよび接着に際しては金属のプライマーと
してフェノール系樹脂溶液を用いることが好ましいこと
を見出した。In view of the current situation, the present inventor sought a vulcanized adhesive that exhibits good adhesion even to NBR with a low to medium nitrile content. ) was found to be suitable for use, and that it was preferable to use a phenolic resin solution as a metal primer for adhesion.
〔問題点を解決するための手段〕および〔作用〕従って
、本発明は金属と低乃至中ニトリル含量NBRとの接着
用NBR系加硫接着剤に係り、このNBR系加硫接着剤
は、加硫剤その他の配合剤を配合した高ニトリル含量N
BR配合物をケトン、芳香族炭化水素またはこれらの混
合物よりなる溶剤中に溶解せしめてなる。[Means for Solving the Problems] and [Operation] Accordingly, the present invention relates to an NBR-based vulcanizable adhesive for bonding metals with low to medium nitrile content NBR, and this NBR-based vulcanizable adhesive High nitrile content N containing sulfur agents and other additives
The BR formulation is dissolved in a solvent consisting of a ketone, an aromatic hydrocarbon, or a mixture thereof.
本発明はまた、かかるNBR系加硫接着剤を用いる接着
方法に係り、接着は、金属にプライマーとしてフェノー
ル系樹脂溶液を下塗りした後、加硫剤その他の配合剤を
配合した高ニトリル含量NBR配合物をケトン、芳香族
炭化水素またはこれらの混合物よりなる溶剤中に溶解せ
しめたNBR系加硫接着剤を用い、低乃至中ニトリル含
量NBRを金属に接着させることにより行われる。The present invention also relates to an adhesion method using such an NBR-based vulcanizable adhesive, in which the adhesion is performed by undercoating a metal with a phenolic resin solution as a primer, and then applying a high nitrile content NBR compound containing a vulcanizing agent and other compounding agents. This is done by adhering low to medium nitrile content NBR to metal using an NBR-based vulcanizing adhesive in which the material is dissolved in a solvent consisting of ketones, aromatic hydrocarbons or mixtures thereof.
NBR系加硫接着剤の接着性成分となる高ニトリル含量
NBR配合物は、加硫剤を始めとして一般にNBRに配
合されている各種の配合剤1例えばカーボンブラック、
ホワイトカーボンなどの充填剤、亜鉛華、可塑剤、老化
防止剤、加硫促進剤などを適宜必要に応じて配合したも
のであり、かかる配合物を溶解させるケトン、芳香族炭
化水素またはこれらの混合物よりなる溶剤中に、固型分
濃度が約5〜15%になるように溶解せしめた溶液とし
て用いられる。The high nitrile content NBR compound, which is the adhesive component of the NBR-based vulcanizable adhesive, contains various compounding agents that are generally added to NBR, including a vulcanizing agent, such as carbon black,
Fillers such as white carbon, zinc white, plasticizers, anti-aging agents, vulcanization accelerators, etc. are blended as necessary, and ketones, aromatic hydrocarbons, or mixtures thereof are used to dissolve such blends. It is used as a solution dissolved in a solvent such that the solid content concentration is about 5 to 15%.
ケトンとしてはメチルエチルケトンなどが、また芳香族
炭化水素としてはトルエン、ベンゼンなどが用いられる
が、好ましくはメチルエチルケトンとそれに対して重量
比1以上のトルエンとの混合溶剤が用いられる。メチル
エチルケトンがこれより多い割合で用いられると、調製
された加硫接着剤溶液がゲル化し易い傾向がみられ、ま
たメチルエチルケトンの沸点が比較的低いため、気泡を
生じ易いという傾向がみられる。一方、トルエンのみを
用いた場合には、高ニトリル含量NBR配合物が完全に
溶解しきれないことがある。このような観点から、メチ
ルエチルケトンは約5〜50重量%、好ましくは約10
重量%の割合で、またトルエンは約95〜50重量%、
好ましくは約90重量%の割合で用いられる。Methyl ethyl ketone and the like are used as the ketone, and toluene, benzene and the like are used as the aromatic hydrocarbon, but preferably a mixed solvent of methyl ethyl ketone and toluene in a weight ratio of 1 or more is used. If methyl ethyl ketone is used in a larger proportion than this, the prepared vulcanized adhesive solution tends to gel, and since methyl ethyl ketone has a relatively low boiling point, it tends to generate bubbles. On the other hand, if toluene alone is used, the high nitrile content NBR formulation may not be completely dissolved. From this point of view, methyl ethyl ketone is about 5 to 50% by weight, preferably about 10% by weight.
% by weight, and toluene is about 95-50% by weight;
Preferably, it is used in a proportion of about 90% by weight.
このようにして調製された加硫接着剤溶液を用いての接
着に際しては、まず金属にプライマーとしてのフェノー
ル系樹脂溶液の下塗りが行われる。When adhering using the vulcanized adhesive solution prepared in this way, the metal is first coated with a phenolic resin solution as a primer.
金属としては、軟鋼、ステンレススチール、アルミニウ
ム、アルミニウムダイキャスト、黄銅、亜鉛などが用い
られ、そこに従来NBRとの接着に用いられていたフェ
ノール系樹脂がプライマー溶液として塗布される。As the metal, mild steel, stainless steel, aluminum, aluminum die-cast, brass, zinc, etc. are used, and a phenolic resin conventionally used for bonding with NBR is applied thereto as a primer solution.
プライマー塗布後、室温乃至約180℃で約5〜30分
間溶剤乾燥を行なった後、加硫金型を用いてやはり配合
物の形で一般に用いられる低乃至中ニトリル含量NBR
と同時に接触させ、約140〜180℃で約3〜30分
間加熱することにより、金属と低乃至中ニトリル含量N
BRとの加硫接着を行なう。After application of the primer, and after solvent drying for about 5 to 30 minutes at room temperature to about 180°C, a low to medium nitrile content NBR, also commonly used in the form of a formulation, is prepared using a vulcanization mold.
Metal and low to medium nitrile content N
Perform vulcanization adhesion with BR.
本発明に係るNBR系加硫接着剤は、金属にプライマー
としてのフェノール系樹脂溶液を塗布し。The NBR-based vulcanized adhesive according to the present invention is produced by applying a phenolic resin solution as a primer to metal.
このフェノール系樹脂に対して良好な接着性を有する高
ニトリル含量NBHの配合物として、それの溶液の形で
用いることにより、低乃至中ニトリル含量NBRとの良
好な接着性を確保させる。As a formulation of high nitrile content NBH with good adhesion to this phenolic resin, its use in solution form ensures good adhesion with low to medium nitrile content NBR.
更に、従来低乃至中ニトリル含量NBRの接着剤として
用いられてきた塩化ゴム系接着剤のように。Furthermore, such as chlorinated rubber adhesives that have conventionally been used as adhesives with low to medium nitrile content NBR.
含ハロゲン物質特有の金属腐食や耐水接着性の低下など
といった問題もあまりみられない。Problems such as metal corrosion and decreased water-resistant adhesion that are typical of halogen-containing substances are not observed.
従って、本発明に係るNBR系加硫接着剤は、各種工業
用ゴム部品、例えばオイルシール、ガスケット、パツキ
ンなど、特に低温雰囲気中でも使用されるものを製造す
る際に、金属材料と低温性のよい低乃至中ニトリル含量
NBRとを接着させる加硫接着剤として有効に使用する
ことができる。Therefore, the NBR-based vulcanized adhesive according to the present invention is suitable for manufacturing various industrial rubber parts such as oil seals, gaskets, packings, etc., especially those used even in low-temperature atmospheres. It can be effectively used as a vulcanized adhesive for bonding NBR with a low to medium nitrile content.
次に、実施例について本発明を説明する。なお。 Next, the present invention will be explained with reference to examples. In addition.
部は1重量部である。part is 1 part by weight.
実施例
高ニトリ/4II種(日本ゼオン製品ハイカー1供の
1ω部タデカーボンブラック
60亜鉛華
10ステアリン酸
1可塑
卯J(II)OP)
5加硫促進弁1(テトラメチルチウラ
ムジスルフィド同(N−シクロヘキシB)−2−ベンゾ
チアジルスルフェンアミド)1.5老化防止剤[ポリ(
2,2.4−1−リメチノI/−1.2−ジヒドロキノ
リン) 1イオウ
0.5以上の各配合成分よりなる高ニ
トリル含量NBR配合物10部およびメチルエチルケト
ン−トルエン(10重虚部:90重量%)混合溶剤90
部よりなるNBR系加硫接着剤を調製した。Example High Nitori/4II type (Nippon Zeon product Hiker 1 child)
1ω part Tade carbon black
60 zinc white
10 stearic acid
1 plastic rabbit J (II) OP)
5 Vulcanization accelerator valve 1 (tetramethylthiuram disulfide (N-cyclohexyB)-2-benzothiazyl sulfenamide) 1.5 Anti-aging agent [poly(
2,2.4-1-rimethino I/-1,2-dihydroquinoline) 1 sulfur
10 parts of a high nitrile content NBR blend consisting of each compounding component of 0.5 or more and 90 parts of a mixed solvent of methyl ethyl ketone-toluene (10 parts: 90% by weight)
An NBR-based vulcanized adhesive was prepared.
溶剤による脱脂処理およびショツトブラスト処理による
表面粗化処理した軟鋼板上に、フェノール樹脂系プライ
マー(アンカーケミカル社製品タイブライBN)を塗布
した。このプライマ一層の上に.上記NBR系加硫接着
剤を塗布し,150℃で10分間乾燥させた。A phenolic resin primer (Tybrie BN, manufactured by Anchor Chemical Co., Ltd.) was applied onto a mild steel plate that had been subjected to surface roughening treatment by degreasing with a solvent and roughening by shot blasting. On top of this primer layer. The above NBR-based vulcanized adhesive was applied and dried at 150°C for 10 minutes.
次に、低二1ーリル含量NBR配合物〔前記高ニトリル
含量NBR配合物において. NBRとしてアクリロニ
トリル含量1部の日本ゼオン製品二ボールDN401を
、また老化防止剤としてポリ(2,2.4−シクロヘキ
シル−2−ベンゾチアジルスルフェンアミド)をそれぞ
れ同量用いた配合物〕または中ニトリル含ffiNBR
配合物〔前記高ニトリル含量NBR配合物において、N
BRとしてアタリロ,二(−リル含景28気の日本ゼオ
ン製品二ボールDN302を、また老化防止剤としてポ
リ(2。Next, a low nitrile content NBR blend [in the above-mentioned high nitrile content NBR blend]. A formulation using the Nippon Zeon product Niball DN401 containing 1 part of acrylonitrile as NBR and the same amount of poly(2,2.4-cyclohexyl-2-benzothiazylsulfenamide) as an anti-aging agent] or medium Nitrile-containing ffiNBR
Blend [In the high nitrile content NBR blend, N
Nippon Zeon's Nippon Zeon product Ni-Ball DN302 of Atariro, Ni(-Ril Contains 28 Ki) was used as a BR, and Poly(2) was used as an anti-aging agent.
2、4−シクロへキシル−2−ベンゾチアジルスルフェ
ンアミド)をそれぞれ同量用いた配合物〕を用い、JI
S K−6301 8.3項90°剥離接着試験法に従
って、前記NBR系加硫接着剤塗布軟鋼板への加硫接着
を。JI
Vulcanization adhesion to the mild steel plate coated with the NBR-based vulcanization adhesive was performed according to the 90° peel adhesion test method in Section 8.3 of S K-6301.
180℃、60kg/a7. 4分間の条件下で行なっ
た。180℃, 60kg/a7. The test was carried out for 4 minutes.
比較例
実施例において、NBR系加硫接着剤の塗布が行われな
かった。Comparative Example In the example, no NBR-based vulcanizable adhesive was applied.
以」二の実施例および比較例でそれぞれ得られた軟鋼板
および低または中ニトリル含.tNBRとの接着物につ
いて、オートグラフを用い.90”方向,200Ill
1分の速度で剥離試験を行なった。得られた結果は、次
の表に示される。The mild steel sheets and low or medium nitrile content obtained in the following Examples and Comparative Examples, respectively. For adhesives with tNBR, autograph was used. 90” direction, 200Ill
Peel tests were conducted at a speed of 1 minute. The results obtained are shown in the following table.
Claims (1)
BR配合物をケトン、芳香族炭化水素またはこれらの混
合物よりなる溶剤中に溶解せしめた、金属と低乃至中ニ
トリル含量NBRとの接着用NBR系加硫接着剤。 2、用いられた溶剤がメチルエチルケトンとそれに対し
て重量比1以上のトルエンとの混合溶剤である特許請求
の範囲第1項記載のNBR系加硫接着剤。 3、金属にプライマーとしてフェノール系樹脂溶液を下
塗りした後、加硫剤その他の配合剤を配合した高ニトリ
ル含量NBR配合物をケトン、芳香族炭化水素またはこ
れらの混合物よりなる溶剤中に溶解せしめたNBR系加
硫接着剤を用い、低乃至中ニトリル含量NBRを金属に
接着させることを特徴とする接着方法。 4、用いられた溶剤がメチルエチルケトンとそれに対し
て重量比で1以上のトルエンとの混合溶剤である特許請
求の範囲第3項記載の接着方法。[Claims] 1. High nitrile content N containing a vulcanizing agent and other compounding agents
An NBR-based vulcanizable adhesive for bonding metals with low to medium nitrile content NBR, in which a BR compound is dissolved in a solvent consisting of a ketone, an aromatic hydrocarbon or a mixture thereof. 2. The NBR-based vulcanized adhesive according to claim 1, wherein the solvent used is a mixed solvent of methyl ethyl ketone and toluene in a weight ratio of 1 or more. 3. After undercoating the metal with a phenolic resin solution as a primer, a high nitrile content NBR formulation containing a vulcanizing agent and other additives was dissolved in a solvent consisting of ketones, aromatic hydrocarbons, or mixtures thereof. An adhesion method characterized by adhering low to medium nitrile content NBR to metal using an NBR-based vulcanized adhesive. 4. The bonding method according to claim 3, wherein the solvent used is a mixed solvent of methyl ethyl ketone and toluene in a weight ratio of 1 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61047543A JPH0717880B2 (en) | 1986-03-05 | 1986-03-05 | NBR-based vulcanizing adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61047543A JPH0717880B2 (en) | 1986-03-05 | 1986-03-05 | NBR-based vulcanizing adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62205177A true JPS62205177A (en) | 1987-09-09 |
JPH0717880B2 JPH0717880B2 (en) | 1995-03-01 |
Family
ID=12778059
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61047543A Expired - Lifetime JPH0717880B2 (en) | 1986-03-05 | 1986-03-05 | NBR-based vulcanizing adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0717880B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0973838A4 (en) * | 1997-04-11 | 2000-07-05 | Hi Shear Corp | Strongly adherent film forming compositions with low coefficient of friction |
US6345775B1 (en) | 1998-07-30 | 2002-02-12 | Wilsoart International, Inc. | Very high solid content aerosol delivery system |
US6635703B1 (en) | 1998-07-30 | 2003-10-21 | Premark Rwp Holdings, Inc. | Very high solids adhesive |
JP2013256618A (en) * | 2012-06-14 | 2013-12-26 | Yokohama Rubber Co Ltd:The | Cement composition and method for adhering rubber |
JP2018150441A (en) * | 2017-03-10 | 2018-09-27 | 日本ゼオン株式会社 | Adhesive composition, and complex |
CN110982454A (en) * | 2019-12-18 | 2020-04-10 | 湖南省和祥润新材料有限公司 | Environment-friendly waterproof sealant and preparation method thereof |
-
1986
- 1986-03-05 JP JP61047543A patent/JPH0717880B2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0973838A4 (en) * | 1997-04-11 | 2000-07-05 | Hi Shear Corp | Strongly adherent film forming compositions with low coefficient of friction |
US6345775B1 (en) | 1998-07-30 | 2002-02-12 | Wilsoart International, Inc. | Very high solid content aerosol delivery system |
US6635703B1 (en) | 1998-07-30 | 2003-10-21 | Premark Rwp Holdings, Inc. | Very high solids adhesive |
JP2013256618A (en) * | 2012-06-14 | 2013-12-26 | Yokohama Rubber Co Ltd:The | Cement composition and method for adhering rubber |
JP2018150441A (en) * | 2017-03-10 | 2018-09-27 | 日本ゼオン株式会社 | Adhesive composition, and complex |
CN110982454A (en) * | 2019-12-18 | 2020-04-10 | 湖南省和祥润新材料有限公司 | Environment-friendly waterproof sealant and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0717880B2 (en) | 1995-03-01 |
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