JPH04339839A - Surface treatment of rubber product - Google Patents
Surface treatment of rubber productInfo
- Publication number
- JPH04339839A JPH04339839A JP11347191A JP11347191A JPH04339839A JP H04339839 A JPH04339839 A JP H04339839A JP 11347191 A JP11347191 A JP 11347191A JP 11347191 A JP11347191 A JP 11347191A JP H04339839 A JPH04339839 A JP H04339839A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- rubber product
- surface treatment
- parts
- weight
- 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
- 229920001971 elastomer Polymers 0.000 title claims abstract description 34
- 239000005060 rubber Substances 0.000 title claims abstract description 34
- 238000004381 surface treatment Methods 0.000 title claims description 3
- 239000004530 micro-emulsion Substances 0.000 claims abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 4
- 238000000576 coating method Methods 0.000 abstract description 4
- 238000001035 drying Methods 0.000 abstract description 2
- 239000004925 Acrylic resin Substances 0.000 abstract 1
- 229920000178 Acrylic resin Polymers 0.000 abstract 1
- 239000000178 monomer Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000012756 surface treatment agent Substances 0.000 description 6
- 229920003052 natural elastomer Polymers 0.000 description 5
- 229920001194 natural rubber Polymers 0.000 description 5
- 244000043261 Hevea brasiliensis Species 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 229920003051 synthetic elastomer Polymers 0.000 description 4
- 239000005061 synthetic rubber Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 229920006173 natural rubber latex Polymers 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 210000002445 nipple Anatomy 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
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 238000010058 rubber compounding Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は天然ゴム及びジェン系ラ
バーを含む合成ゴムよりなるゴム製品の表面処理方法、
詳しくは非粘着及び滑性を付与されたゴム製品を得る方
法に関するものである。[Industrial Application Field] The present invention relates to a method for surface treatment of rubber products made of natural rubber and synthetic rubber including gene-based rubber;
More specifically, the present invention relates to a method for obtaining a rubber product that is non-adhesive and has slipperiness.
【0002】0002
【従来の技術】従来、天然ゴム及びジェン系ラバーを含
む合成ゴムからなるゴム製品の表面を処理する方法とし
ては、(1) 塩素を表面に付加する(塩素化)、(2
) 溶剤処理による表面脱脂、(3) 強酸処理、プラ
ズマ処理、コロナ処理などの表面酸化、(4)ブラスト
処理による表面粗面化、(5) シリカ、タルク、スタ
ーチ類の粉体付着、(6) シリコーン、フッ素樹脂な
どの樹脂付着等があった。[Prior Art] Conventionally, methods for treating the surface of rubber products made of synthetic rubber including natural rubber and gene-based rubber include (1) adding chlorine to the surface (chlorination);
) Surface degreasing by solvent treatment, (3) Surface oxidation by strong acid treatment, plasma treatment, corona treatment, etc., (4) Surface roughening by blasting, (5) Powder adhesion of silica, talc, and starch, (6) ) There was adhesion of resins such as silicone and fluororesin.
【0003】0003
【発明が解決しようとする問題点】しかしながら、これ
らの方法は作業に手間が掛るとともに、有害物質や強酸
化剤の使用による作業環境の低下や高エネルギーの使用
による設備コストの増大など、多くの問題があった。[Problems to be solved by the invention] However, these methods are time-consuming and have many problems, such as deterioration of the working environment due to the use of harmful substances and strong oxidizing agents, and increased equipment costs due to the use of high energy. There was a problem.
【0004】更に、塩素化をしたものについては、洗浄
後の乾燥条件によりゴム製品上に水跡が残ることがあり
、かつ塩素化されるためゴムの表面が硬化して微小な亀
裂を生じると云う問題もあった。Furthermore, with regard to chlorinated products, water marks may remain on the rubber product depending on the drying conditions after washing, and due to chlorination, the surface of the rubber may harden and cause micro-cracks. There was also a problem.
【0005】また表面への樹脂付着については、これら
ゴム製品の素材である天然及び合成ゴム類は、その組成
から、官能基が少いため、表面に樹脂類が付着すること
は出来るが、付着力が弱いと云う欠点があったRegarding the adhesion of resin to the surface, the natural and synthetic rubbers that are the raw materials for these rubber products have few functional groups due to their composition, so resins can adhere to the surface, but the adhesion strength is low. It had the disadvantage of being weak
【000
6】また、シリコンオイルや粉体などは短時間の使用で
ゴム表面から除去され、粘着感が出ると云う欠点があり
、かつ他の合成樹脂類も、そのエマルジョンの粉径が0
.05〜0.2 μのためゴム製品の静置状態では付着
しているものの、ゴム表面がミクロ的に凹凸面であるた
めゴム製品を伸ばした場合には、クラックが入り部分的
に簡単に剥離、除去されるため長時間の使用が困難であ
った。000
6] In addition, silicone oil and powder have the disadvantage that they are removed from the rubber surface after a short time of use, resulting in a sticky feeling, and other synthetic resins also have the disadvantage that the emulsion powder diameter is 0.
.. 05 to 0.2μ, so it sticks to the rubber product when it is standing still, but because the rubber surface is microscopically uneven, when the rubber product is stretched, it cracks and easily peels off in parts. , it was difficult to use it for a long time because it was removed.
【0007】[0007]
【問題点を解決するための手段】本発明は、このような
事情に鑑みてなされたものであり、その手段はゴム製本
体の表面に、ハイドロゾル型水溶性樹脂のアクリルマイ
クロエマルジョンを塗布し、乾燥皮膜を設けることであ
る。[Means for Solving the Problems] The present invention has been made in view of the above circumstances, and its means include applying an acrylic microemulsion of a hydrosol-type water-soluble resin to the surface of a rubber body, It is to provide a dry film.
【0008】[0008]
【実施例】本発明の実施例について説明するに、ゴム製
本体は此種の技術分野において周知な天然ゴム及びジェ
ン系ラバーを含む合成ゴムよりなる各種のゴム製品、例
えばゴムフィルム、指サック、乳首、ドライスーツ、長
靴、自動車のゴム枠、ワイパーブレード、医療用具(ド
レージバック、カテーテルバルーン、尿道カテーテル、
コンドーム)、チューブ、パッキングゴム、輪ゴム、手
袋等であり、これらは浸漬方法、押出し方法など周知の
製造方法によって得られたもので、その外表面又は内表
面或いは内外表面に、ハイドロゾル型水溶性樹脂のアク
リルマイクロエマルジョンをコーティング、吹付け、浸
漬など任意な方法で塗布し、乾燥して表面に皮膜を設け
る。[Embodiments] To explain the embodiments of the present invention, the rubber body can be used for various rubber products made of natural rubber and synthetic rubber including gene-based rubber, which are well known in this technical field, such as rubber films, finger cots, etc. Nipples, dry suits, boots, automobile rubber frames, wiper blades, medical equipment (drayage bags, catheter balloons, urinary catheters,
condoms), tubes, packing rubber, rubber bands, gloves, etc., which are obtained by well-known manufacturing methods such as dipping and extrusion methods, and are coated with a hydrosol-type water-soluble resin on their outer or inner surfaces. The acrylic microemulsion is applied by any method such as coating, spraying, or dipping, and then dried to form a film on the surface.
【0009】ハイドロゾル型水溶性樹脂のアクリルマイ
クロエマルジョンの組成は、メタアクリル酸エステルモ
ノマー及びアクリル酸エステルモノマー類の共重合体よ
りなるものであって、モノマーとして選定される要因と
しては、親水性、高反応性、密着性、摩擦係数が低い等
を考慮し、性能の良いモノマー類としては、メタアクリ
ル酸、2−ヒドロキシエチルメタクリレート、2−ヒド
ロキシプロピルメタアクリレート、ジメチルアミノエチ
ルメタクリレート、ジェチルアミノエチルメタクリレー
ト、エチレングリコールジメタクリレート、トリエチレ
ングリコールジメタクリレート、トリメチロールプロパ
ントリメタクリレート、メチルメタアクリレート、2−
エチルヘキシルメタクリレート等であり、特に性能の高
いモノマー類はメタアクリル酸、2−ヒドロキシエチル
メタクリレート、2−エチルヘキシルメタアクリレート
等である。又これらを共重合体の基本モノマーとして他
のモノマーとの併用を行うことは可能である。The composition of the acrylic microemulsion of the hydrosol type water-soluble resin consists of a copolymer of a methacrylic acid ester monomer and an acrylic acid ester monomer, and the factors for selecting the monomer include hydrophilicity, Considering high reactivity, adhesion, and low coefficient of friction, monomers with good performance include methacrylic acid, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, dimethylaminoethyl methacrylate, and jetylaminoethyl. Methacrylate, ethylene glycol dimethacrylate, triethylene glycol dimethacrylate, trimethylolpropane trimethacrylate, methyl methacrylate, 2-
Monomers with particularly high performance include methacrylic acid, 2-hydroxyethyl methacrylate, and 2-ethylhexyl methacrylate. Moreover, it is possible to use these in combination with other monomers as the basic monomer of the copolymer.
【0010】又、本発明ではこのアクリル系マイクロエ
マルジョンの溶液濃度を各ゴム製本体に合う様に調整す
る必要があり、0.1 〜20%の範囲が適当であって
、通常のゴム製品では0.5 〜10%がより効果を発
揮し得るものである。[0010] Furthermore, in the present invention, it is necessary to adjust the solution concentration of this acrylic microemulsion to suit each rubber body, and a range of 0.1 to 20% is appropriate; A content of 0.5 to 10% is more effective.
【0011】上記ハイドロゾル型水溶性樹脂のアクリル
マイクロエマルジョンは粒径が0.05μ以下であり、
粒径の中心値が0.02μ以下と云う微小粒径のため、
ゴム製本体の表面におけるミクロ的凹凸に対しても充分
そのエマルジョン粒子が入り込み得るものである。[0011] The acrylic microemulsion of the hydrosol type water-soluble resin has a particle size of 0.05μ or less,
Due to the small particle size with a median particle size of 0.02μ or less,
The emulsion particles can sufficiently penetrate into microscopic irregularities on the surface of the rubber body.
【0012】このようなエマルジョンに対して耐溶剤性
、耐熱性、耐水性の向上を計るために、水溶性メラミン
やエポキシ樹脂等を架橋剤として、有機アミン類もしく
はアンモニュウム塩類を触媒としてそれぞれ添加して表
面処理剤となし、ゴム製本体をこの表面処理剤中に浸漬
するか或いは表面処理剤を吹きつけ又はコーティングで
表面に塗布する。In order to improve the solvent resistance, heat resistance, and water resistance of such emulsions, water-soluble melamine, epoxy resin, etc. are added as crosslinking agents, and organic amines or ammonium salts are added as catalysts. The rubber body is immersed in the surface treatment agent, or the surface treatment agent is applied to the surface by spraying or coating.
【0013】この表面処理剤の配合処方例を示すと、ア
クリル系マイクロエマルジョン(40%)100 重量
部に対して、水100 〜40000 部、水溶性メラ
ミン1〜4部、有機アミン系触媒0.1 〜0.4 部
である。この塗布量は、乾燥して皮膜となった際、その
厚みを考慮しなければならないが、できるだけ薄膜に形
成しゴム製品の風合いを変えることがないようにする。An example of the formulation of this surface treatment agent is as follows: 100 parts by weight of acrylic microemulsion (40%), 100 to 40,000 parts of water, 1 to 4 parts of water-soluble melamine, and 0.0 parts of organic amine catalyst. 1 to 0.4 parts. The amount of coating must be determined by taking into consideration the thickness of the film when it dries, but it should be formed as thin as possible so as not to change the texture of the rubber product.
【0014】次に具体的な実施の態様及び比較例(従来
の方法)について詳述する。
実施例1及び比較例1
表1の天然ドライラバー配合を押出法によって、ゴムチ
ューブを形成し、表2に示す工程により加工を施す。実
施例1における表面処理剤の配合例はアクリル系マイク
ロエマルジョン(固形分40%)100 重量部に対し
て、水300 部、水溶性メラミン2部、有機アミン系
触媒0.2 部を添加したものである。Next, specific embodiments and comparative examples (conventional methods) will be described in detail. Example 1 and Comparative Example 1 Rubber tubes are formed by extruding the natural dry rubber formulations shown in Table 1 and processed according to the steps shown in Table 2. The blending example of the surface treatment agent in Example 1 was as follows: 300 parts of water, 2 parts of water-soluble melamine, and 0.2 parts of an organic amine catalyst were added to 100 parts by weight of an acrylic microemulsion (solid content 40%). It is.
【0015】
天然ゴム 100 重量部S
2 重量部ZnO
3 重量部TET
1 重量部TMT
0.5 重量部ステアリン
酸 1 重量部老化防止剤
1 重量部Natural rubber 100 parts by weight S
2 parts by weight ZnO
3 Part by weight TET
1 Part by weight TMT
0.5 parts by weight stearic acid 1 part by weight anti-aging agent
1 part by weight
【0016】[0016]
【表1】[Table 1]
【0017】実施例2及び比較例2
表3の天然ゴムラテックス配合に浸漬法によってバルー
ンカテーテルを成形し、表4に示す工程により加工を施
す。実施例2における表面処理剤は実施例1と同じ配合
である。Example 2 and Comparative Example 2 Balloon catheters were formed using the natural rubber latex formulation shown in Table 3 by the dipping method, and processed according to the steps shown in Table 4. The surface treatment agent in Example 2 has the same formulation as in Example 1.
【0018】
天然ゴムラテックス(DRY)100 重量
部S
1 重量部ZnO
1
重量部ジチオカーバメイト系加硫促進剤 0.8
重量部老化防止剤
1 重量部安定剤
適
量Natural rubber latex (DRY) 100 parts by weight S
1 part by weight ZnO
1
Part by weight dithiocarbamate vulcanization accelerator 0.8
Part by weight anti-aging agent
1 parts by weight stabilizer
Appropriate amount
【0019】[0019]
【表2】
次に表3に示す天然ゴムラテックス配合によるフィルム
を造り、実施例1における表面処理剤を施したフィルム
と未処理のフィルムとの物性及び性能表を表5に示す。[Table 2] Next, films were prepared using the natural rubber latex formulation shown in Table 3, and Table 5 shows the physical properties and performance of the film treated with the surface treatment agent in Example 1 and the untreated film.
【0020】[0020]
【表3】[Table 3]
【0021】[0021]
【発明の効果】本発明はゴム製本体の表面に、ハイドロ
ゾル型水溶性樹脂のアクリルマイクロエマルジョンを塗
布し乾燥皮膜を設けるから、非粘着性及び滑性を付与さ
れることはもちろん、これらが向上したものが得られ、
しかも従来の方法に比して前処理加工を要することなく
極めて簡単であり、使用に際し及び伸長に対しても剥離
のないものである。[Effects of the Invention] In the present invention, an acrylic microemulsion of a hydrosol-type water-soluble resin is applied to the surface of the rubber body to form a dry film, which not only imparts non-adhesion and lubricity but also improves these properties. you get what you want,
Moreover, compared to conventional methods, it is extremely simple without requiring any pretreatment, and there is no peeling during use or during elongation.
【0022】すなわちハイドロゾル型水溶性のアクリル
マイクロエマルジョンは粒径が0.05μ以下であり、
ゴム表面のミクロ的な凹凸に対しても充分にエマルジョ
ン粒子が入り込み固着することにより強固な皮膜となっ
てゴム製品の表面に恒久的に形成することが出来ると共
に粉体等を使用しないから汚染されることなく使用時に
除去されることがない。[0022] That is, the hydrosol type water-soluble acrylic microemulsion has a particle size of 0.05μ or less,
The emulsion particles sufficiently penetrate and adhere to the microscopic irregularities on the rubber surface, forming a strong film that can be permanently formed on the surface of the rubber product, and since no powder is used, there is no contamination. without being removed during use.
Claims (1)
ル型水溶性樹脂のアクリルマイクロエマルジョンを塗布
し、乾燥皮膜を設けることを特徴とするゴム製品の表面
処理方法。1. A method for surface treatment of rubber products, which comprises applying an acrylic microemulsion of a hydrosol-type water-soluble resin to the surface of a rubber body to form a dry film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3113471A JPH0753808B2 (en) | 1991-05-17 | 1991-05-17 | Surface treatment method for rubber products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3113471A JPH0753808B2 (en) | 1991-05-17 | 1991-05-17 | Surface treatment method for rubber products |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04339839A true JPH04339839A (en) | 1992-11-26 |
JPH0753808B2 JPH0753808B2 (en) | 1995-06-07 |
Family
ID=14613098
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3113471A Expired - Fee Related JPH0753808B2 (en) | 1991-05-17 | 1991-05-17 | Surface treatment method for rubber products |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0753808B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113810519A (en) * | 2020-06-15 | 2021-12-17 | Oppo(重庆)智能科技有限公司 | Shell of electronic equipment and processing method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6232127A (en) * | 1985-08-05 | 1987-02-12 | Kao Corp | Antitack composition for unvulcanized rubber |
JPS62132939A (en) * | 1985-12-06 | 1987-06-16 | Kao Corp | Antiblocking agent for rubber |
-
1991
- 1991-05-17 JP JP3113471A patent/JPH0753808B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6232127A (en) * | 1985-08-05 | 1987-02-12 | Kao Corp | Antitack composition for unvulcanized rubber |
JPS62132939A (en) * | 1985-12-06 | 1987-06-16 | Kao Corp | Antiblocking agent for rubber |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113810519A (en) * | 2020-06-15 | 2021-12-17 | Oppo(重庆)智能科技有限公司 | Shell of electronic equipment and processing method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0753808B2 (en) | 1995-06-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0199318B1 (en) | Dipped rubber article | |
US3856561A (en) | Rubber articles having improved slip coating | |
EP0594410B1 (en) | Treatment of rubber articles | |
EP1569702B1 (en) | Crosslinking agent for coated elastomeric article | |
CA2485746C (en) | Double-donnable glove | |
JPH11506627A (en) | Surgeon gloves made of neoprene copolymer | |
US3967014A (en) | Rubber articles having improved slip coating | |
JPH11507085A (en) | Acrylic emulsion coating for rubber articles | |
JP2016536395A (en) | Hydrophilic / hydrophobic polymer aqueous emulsions and related products and methods | |
JP2017503032A (en) | Hydrophilic / hydrophobic polymer aqueous emulsions and related products and methods | |
JPH04339839A (en) | Surface treatment of rubber product | |
JP3643912B2 (en) | Rubber product surface treatment method | |
JPH0638084Y2 (en) | Rubber gloves | |
JPH0613734Y2 (en) | Medical rubber products | |
JPH0546765Y2 (en) | ||
JPH061868A (en) | Method for treating surface of rubber article | |
JP3523757B2 (en) | Method for preventing adhesion of natural rubber latex film | |
JPH0719819Y2 (en) | Finger sack | |
JPH061700Y2 (en) | condom | |
AU747769B2 (en) | Acrylic emulsion compositions and process for the production of rubber articles | |
KR100433993B1 (en) | Acrylic emulsion coatings for rubber products | |
JPH064014U (en) | Rubber gloves | |
JPH0738967B2 (en) | Surface treatment method for rubber products | |
DE10329669A1 (en) | PVC soft film, coating or molded body used in the production of tubes, rods and profiles has a barrier-like surface modified by fluorination and having long-term stability with a specified surface tension and adhesive strength | |
JPH0521916U (en) | Drainage back |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |