JP3255501B2 - Composition for surface treatment and method for surface treatment of rubber - Google Patents
Composition for surface treatment and method for surface treatment of rubberInfo
- Publication number
- JP3255501B2 JP3255501B2 JP19567293A JP19567293A JP3255501B2 JP 3255501 B2 JP3255501 B2 JP 3255501B2 JP 19567293 A JP19567293 A JP 19567293A JP 19567293 A JP19567293 A JP 19567293A JP 3255501 B2 JP3255501 B2 JP 3255501B2
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- JP
- Japan
- Prior art keywords
- surface treatment
- composition
- rubber
- groups
- present
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
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Description
【０００１】[0001]
【発明の技術分野】本発明は、各種基材、特にゴム表面
に非粘着性を付与し、均一に表面を仕上げ得る表面処理
用組成物、並びにゴムの表面処理方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition for surface treatment which imparts non-adhesiveness to various substrates, particularly rubber surfaces, and can finish the surface uniformly, and a method for surface treatment of rubber.
【０００２】[0002]
【発明の技術的背景とその問題点】従来、紙、プラスチ
ック、ゴム等の基材表面に非粘着性を付与する処理方法
として、各種ポリオルガノシロキサン組成物が用いられ
ている。これらは、主に末端に水酸基をもつポリオルガ
ノシロキサンにSi-H結合含有ポリオルガノシロキサンを
加えさらに有機スズ化合物を加えたものを有機溶媒で希
釈し、配合液とするものであった。この有機溶媒として
は、不燃性・揮発性の高さから 1,1,1−トリクロロエタ
ンが広く用いられていたが、1,1,1 −トリクロロエタン
がオゾン層破壊物質であるため、この溶媒の使用が1995
年以降できなくなることになっている。このため、その
代替溶剤が検討されているが、十分な性能を示すものは
未だ提供されていない。例えば、一般に塗料用溶剤とし
て用いられているトルエン、キシレンなどを用いた場
合、揮発性が低いため、ゴム表面で溶液が凝集したり流
れ過ぎたりして均一な膜が出来ず、均一な膜を作るため
には溶媒が十分揮発するよう一回の塗布量を少なくする
ことが必要となり、作業効率を著しく低下させる。ま
た、揮発性の高い、ｎ−ヘキサン、ｎ−ヘプタン、ｎ−
オクタンなどではこれらの問題は幾分改善されるとはい
え、塗布効果や塗布皮膜の均一性には未だ問題があり、
さらに改善が要求されている。BACKGROUND OF THE INVENTION Conventionally, various polyorganosiloxane compositions have been used as a treatment method for imparting non-adhesion to the surface of a base material such as paper, plastic, rubber and the like. These compounds were prepared by diluting a polyorganosiloxane having a hydroxyl group at a terminal with a polyorganosiloxane containing a Si—H bond and further adding an organotin compound with an organic solvent to obtain a compounded liquid. As this organic solvent, 1,1,1-trichloroethane was widely used because of its high incombustibility and volatility.However, because 1,1,1-trichloroethane is an ozone depleting substance, Is 1995
It will not be possible after the year. For this reason, alternative solvents have been studied, but none of them exhibiting sufficient performance has yet been provided. For example, when toluene, xylene, or the like, which is generally used as a coating solvent, is used, since the volatility is low, the solution is agglomerated or flows too much on the rubber surface to form a uniform film. In order to make it, it is necessary to reduce the amount of one application so that the solvent is sufficiently volatilized, which significantly lowers the working efficiency. In addition, n-hexane, n-heptane, n-
With octane etc., although these problems are somewhat improved, there are still problems with the coating effect and the uniformity of the coating film.
Further improvements are required.
【０００３】[0003]
【発明の目的】本発明は、上記問題点を解消するために
なされたものであって、各種基材、特にゴム表面に非粘
着性を付与し、均一に表面を仕上げ得る表面処理用組成
物、並びにゴムの表面処理方法を提供することを目的と
する。SUMMARY OF THE INVENTION The present invention has been made in order to solve the above-mentioned problems, and it is an object of the present invention to provide a surface treatment composition capable of imparting a non-adhesive property to various substrates, particularly rubber surfaces, and uniformly finishing the surface. And a method for surface treatment of rubber.
【０００４】[0004]
【発明の構成】本発明者らは、上記目的を達成すべく鋭
意検討した結果、有機溶媒として特定のものを用いるこ
とが有効であることを見出し、本発明を完成するに到っ
た。即ち、本発明は、 (A) 25℃における粘度が50〜10,000,000 cStの両末端が
水酸基閉塞のポリジオルガノシロキサン (B) ケイ素原子に結合した水素原子が１分子中に少なく
とも３個存在するポリオルガノハイドロジェンシロキサ
ン (C) 硬化触媒 (D) 炭素数７〜10の分岐状アルキル系飽和炭化水素を50
重量％以上含む有機溶媒 とを含有する表面処理用組成物、並びに上記表面処理用
組成物をゴム表面に塗布し、室温又は加熱下で硬化させ
ることを特徴とするゴムの表面処理方法である。The present inventors have conducted intensive studies in order to achieve the above object, and as a result, have found that it is effective to use a specific organic solvent, and have completed the present invention. That is, the present invention relates to (A) a polydiorganosiloxane having a viscosity of 50 to 10,000,000 cSt at 25 ° C., both ends of which are hydroxyl-blocked; and (B) a polyorganosiloxane having at least three hydrogen atoms bonded to silicon atoms per molecule. Hydrogensiloxane (C) Curing catalyst (D) 50 to 70 branched alkyl saturated hydrocarbons having 7 to 10 carbon atoms
A composition for surface treatment comprising: an organic solvent containing at least 1% by weight; and a surface treatment composition comprising applying the composition for surface treatment to a rubber surface and curing at room temperature or under heating.
【０００５】本発明で用いられる(A) 成分の両末端水酸
基閉塞ポリジオルガノシロキサンは、ケイ素原子に結合
した水酸基を分子の両末端に持ち、その反応性によって
硬化反応にあずかるものである。分子中のケイ素原子に
結合した有機基は、メチル基、エチル基、プロピル基、
ブチル基、ヘキシル基のようなアルキル基、ビニル基、
プロペニル基のようなアルケニル基、フェニル基のよう
なアリール基、スチレニル基のようなアラルキル基、お
よびこれらの炭化水素基の水素原子の一部がハロゲン原
子、ニトリル基などで置換されたものが例示されるが、
合成の容易さ、硬化前の組成物の粘度と硬化後の皮膜の
物性とのかね合いなどから、メチル基が一般に用いられ
る。このような両末端水酸基閉塞ポリジオルガノシロキ
サンの粘度は、25℃において50〜10,000,000cSt 、好ま
しくは 1,000〜2,000,000cStである。50cSt 未満では硬
化後の皮膜が脆くなり、また10,000,000cSt を越えると
硬化前の組成物の粘度が大きくなって、取扱いに不便で
ある。The polydiorganosiloxane having hydroxyl groups at both ends of the component (A) used in the present invention has hydroxyl groups bonded to silicon atoms at both ends of the molecule and participates in a curing reaction by its reactivity. Organic groups bonded to silicon atoms in the molecule include methyl, ethyl, propyl,
Butyl group, alkyl group such as hexyl group, vinyl group,
Examples include alkenyl groups such as propenyl groups, aryl groups such as phenyl groups, aralkyl groups such as styrenyl groups, and those in which some of the hydrogen atoms of these hydrocarbon groups have been substituted with halogen atoms, nitrile groups, etc. But
A methyl group is generally used because of ease of synthesis, balance between the viscosity of the composition before curing and the physical properties of the film after curing, and the like. The viscosity of such a polydiorganosiloxane having hydroxyl groups terminated at both ends is 50 to 10,000,000 cSt at 25 ° C, preferably 1,000 to 2,000,000 cSt. If it is less than 50 cSt, the film after curing becomes brittle, and if it exceeds 10,000,000 cSt, the viscosity of the composition before curing increases, which is inconvenient to handle.
【０００６】本発明で用いられる(B) 成分のポリオルガ
ノハイドロジェンシロキサンは、(A) 成分の両末端水酸
基閉塞ポリジオルガノシロキサンと脱水素縮合反応して
網状構造を与えるために、ケイ素原子に結合した水素原
子を少なくとも３個有するもので、分子中のケイ素原子
に結合した有機基は、メチル基、エチル基、プロピル
基、ブチル基、ヘキシル基のようなアルキル基、ビニル
基、プロペニル基のようなアルケニル基、フェニル基の
ようなアリール基、スチレニル基のようなアラルキル
基、およびこれらの炭化水素基の水素原子の一部がハロ
ゲン原子、ニトリル基などで置換されたものが例示され
るが、合成の容易さから、特にメチル基が一般的であ
る。このようなポリオルガノハイドロジェンシロキサン
のシロキサン鎖は、直鎖状、分岐状、および環状のいず
れでもよい。(B) 成分の配合量は、一般に(A) 成分100
重量部に対し、0.1 〜20重量部である。[0006] The polyorganohydrogensiloxane of the component (B) used in the present invention is bonded to a silicon atom in order to give a network structure by a dehydrocondensation reaction with the polydiorganosiloxane capped at both terminal hydroxyl groups of the component (A). Organic groups bonded to silicon atoms in the molecule include alkyl groups such as methyl, ethyl, propyl, butyl, and hexyl, vinyl groups, and propenyl groups. Alkenyl groups, aryl groups such as phenyl groups, aralkyl groups such as styrenyl groups, and those in which some of the hydrogen atoms of these hydrocarbon groups are substituted with halogen atoms, nitrile groups, and the like, Particularly, a methyl group is generally used because of ease of synthesis. The siloxane chain of such a polyorganohydrogensiloxane may be linear, branched, or cyclic. In general, the amount of the component (B) is 100
It is 0.1 to 20 parts by weight based on parts by weight.
【０００７】本発明で用いられる(C) 成分の硬化触媒
は、(A) 成分の両末端水酸基閉鎖ポリジオルガノシロキ
サンの水酸基と(B) 成分のポリオルガノハイドロジェン
シロキサンのSi-H結合との間の脱水素縮合を促進する触
媒である。この硬化触媒としては、金属脂肪酸塩、アミ
ン類、アンモニウム類、およびこれらのものを併用して
もよい。金属脂肪酸塩としては、ジブチルスズジアセテ
ート、ジブチルスズジオクトエート、ジブチルスズジラ
ウレート、ジブチルスズジオレエート、ジブチルスズジ
ステアレート、トリブチルスズアセテート、トリブチル
スズオクトエート、トリブチルスズラウレート、ジオク
チルスズジアセテート、ジオクチルスズジラウレート、
ジエチルスズジオレエート、モノメチルスズジオレエー
トのように金属原子に直接結合した有機基を持つもの、
およびオクテン酸亜鉛、オクテン酸鉄、オクテン酸スズ
のように、金属原子に直接結合した有機基を持たないも
のが例示される。またアミン類としては、モノメチルア
ミン、ジメチルアミン、モノエチルアミン、ジエチルア
ミン、エチレンジアミン、ヘキサメチルテトラアミンの
ような有機アミン；α−アミノプロピルトリエトキシシ
ランのようなアミノ基を有するシラン化合物やそれらの
塩が、アンモニウム類としてはテトラメチルアンモニウ
ム、ジメチルベンジルアンモニウムおよびそれらの塩が
例示される。この硬化触媒の量は、(A) 成分と(B) 成分
の合計量 100重量部に対し、 0.5〜10重量部である。
0.5重量部未満では硬化が遅く、基材に組成物を塗布し
て熱処理したのちブロッキングを起こすおそれがあり、
また、これより多いと処理液中で反応が進み、可使時間
が短くなってしまうからである。[0007] The curing catalyst of the component (C) used in the present invention is a polymer which is used between the hydroxyl group of the polydiorganosiloxane having both terminal hydroxyl groups of the component (A) and the Si-H bond of the polyorganohydrogensiloxane of the component (B). Is a catalyst that promotes the dehydrocondensation of As the curing catalyst, metal fatty acid salts, amines, ammoniums, and these may be used in combination. As the metal fatty acid salt, dibutyltin diacetate, dibutyltin dioctoate, dibutyltin dilaurate, dibutyltin dioleate, dibutyltin distearate, tributyltin acetate, tributyltin octoate, tributyltin laurate, dioctyltin diacetate, dioctyltin dilaurate,
Those having an organic group directly bonded to a metal atom, such as diethyltin dioleate and monomethyltin dioleate,
Examples thereof include those having no organic group directly bonded to a metal atom, such as zinc octenoate, iron octenoate, and tin octenoate. Examples of the amines include organic amines such as monomethylamine, dimethylamine, monoethylamine, diethylamine, ethylenediamine, and hexamethyltetraamine; silane compounds having an amino group such as α-aminopropyltriethoxysilane, and salts thereof. Examples of ammoniums include tetramethylammonium, dimethylbenzylammonium and salts thereof. The amount of the curing catalyst is 0.5 to 10 parts by weight based on 100 parts by weight of the total of the components (A) and (B).
If it is less than 0.5 parts by weight, the curing is slow, and there is a possibility that blocking may occur after applying the composition to the substrate and performing heat treatment.
On the other hand, if the amount is larger than this, the reaction proceeds in the processing solution, and the pot life is shortened.
【０００８】本発明で用いられる(D) 成分の有機溶媒
は、炭素数７〜10の分岐状アルキル系飽和炭化水素の単
体及び混合物を40重量％以上含むもので、かかる飽和炭
化水素としてはイソペンタン、イソオクタン、イソノナ
ン、イソデカンが例示される。上記炭素数７〜10の分岐
状アルキル系飽和炭化水素に必要により併用添加される
有機溶媒としては、ｎ−ヘキサン、ｎ−ヘプタン、石油
系炭化水素、トルエン、キシレン、イソプロピルアルコ
ール、ブチルアルコールなどが例示される。このような
有機溶媒の使用量は、処理に用いる組成物に望まれる粘
度により、適宜選択することができる。(D) 成分の有機
溶媒において、炭素数７〜10の分岐状アルキル系飽和炭
化水素の含有率は40重量％以上、好ましくは60〜100 重
量％であるが、それは、この範囲が均一塗布性という効
果をよく発揮させるからである。The organic solvent of component (D) used in the present invention contains at least 40% by weight of a simple substance and a mixture of a branched alkyl-based saturated hydrocarbon having 7 to 10 carbon atoms. , Isooctane, isononane, and isodecane. Examples of the organic solvent which is optionally used in combination with the branched alkyl-based saturated hydrocarbon having 7 to 10 carbon atoms include n-hexane, n-heptane, petroleum hydrocarbon, toluene, xylene, isopropyl alcohol, and butyl alcohol. Is exemplified. The amount of such an organic solvent used can be appropriately selected depending on the viscosity desired for the composition used for the treatment. In the organic solvent (D), the content of the branched alkyl-based saturated hydrocarbon having 7 to 10 carbon atoms is 40% by weight or more, preferably 60 to 100% by weight. This is because the effect of this is exhibited well.
【０００９】また、用途によっては、基材表面の光沢の
抑制が求められる場合があり、そのような場合には艶消
しの目的で、(E) 成分として平均粒径0.01〜100 μm の
フィラーが配合される。このようなフィラーは、有機フ
ィラーとしては、アクリル樹脂粉、ナイロン樹脂粉、ポ
リスチレン樹脂粉、ポリカーボネート樹脂粉、ポリエチ
レン樹脂粉、塩化ビニル樹脂粉、ポリフッ化エチレン樹
脂粉、ポリメチルシルセスキオキサンや粉砕されたシリ
コーン硬化物のようなシリコーン樹脂粉等が挙げられ、
無機フィラーとしては、シリカ粉、カーボン粉、グラフ
ァイト粉、酸化チタン粉、酸化マグネシウム粉、酸化亜
鉛粉等が挙げられる。これらフィラーは、平均粒径が0.
01〜100 μm 、好ましくは0.01〜20μm であることが必
要である。平均粒径が0.01μm 未満のものは必要以上に
配合がしにくいという欠点があり、100 μm を越えると
塗膜の強靱性や柔軟性が失われ、本発明に必要な機能が
得られなくなる。(E) 成分の使用量は特に限定されない
が、(A) 成分と(B) 成分の合計100 重量部に対して0.5
〜200 重量部が一般的である。又、本発明の表面処理用
組成物には、滑り性を更に向上させるために、不活性の
シリコーンオイル、特に高粘度のポリジメチルシロキサ
ンオイルを配合することができる。尚、上記(E) 成分の
平均粒径0.01〜100 μm のフィラーは、光沢抑制効果と
共に滑り性向上効果をも有する。本発明において、(D)
成分と(E) 成分とを併用することにより、均一な表面仕
上げ性と共に、滑り性、耐磨耗性、耐候性、艶消し性に
も優れたものとなる。In some applications, it is required to suppress the gloss of the substrate surface. In such a case, for the purpose of matting, a filler having an average particle diameter of 0.01 to 100 μm is used as the component (E). Be blended. Such fillers include, as organic fillers, acrylic resin powder, nylon resin powder, polystyrene resin powder, polycarbonate resin powder, polyethylene resin powder, vinyl chloride resin powder, polyfluoroethylene resin powder, polymethylsilsesquioxane, and pulverized powder. Silicone resin powder such as cured silicone,
Examples of the inorganic filler include silica powder, carbon powder, graphite powder, titanium oxide powder, magnesium oxide powder, and zinc oxide powder. These fillers have an average particle size of 0.
It is necessary that the thickness be from 01 to 100 μm, preferably from 0.01 to 20 μm. If the average particle size is less than 0.01 μm, there is a disadvantage that it is difficult to mix more than necessary. If it exceeds 100 μm, the toughness and flexibility of the coating film are lost, and the functions required for the present invention cannot be obtained. The amount of the component (E) is not particularly limited, but may be 0.5 to 100 parts by weight of the total of the components (A) and (B).
~ 200 parts by weight are common. The composition for surface treatment of the present invention may further contain an inert silicone oil, particularly a high-viscosity polydimethylsiloxane oil, in order to further improve the slipperiness. The filler (E) having an average particle size of 0.01 to 100 μm has a gloss suppressing effect and a slipperiness improving effect. In the present invention, (D)
When the component and the component (E) are used in combination, uniform slippage, abrasion resistance, weather resistance, and matting properties are obtained as well as uniform surface finish.
【００１０】また本発明において、ゴムとの密着性を向
上させるために、各種シランカップリング剤をゴムの種
類に応じて単体あるいは混合物をそのまま或いは部分縮
合させて添加したり、或いは、アミノ基含有シランとエ
ポキシ基含有オイルや、樹脂の混合物或いは部分縮合物
を添加したり、エポキシ基含有シランとアミノ基含有オ
イルや樹脂の混合物あるいは部分縮合物を添加してもよ
い。特に(F) 成分として、(1) エポキシ基含有ポリオル
ガノシロキサンと(2) 少なくとも１個の炭素原子を介し
てケイ素原子に結合した置換又は非置換アミノ基とケイ
素原子に結合したアルコキシ基を有するシラン及び／又
はシロキサンとの混合物、又は(1) と(2) の反応生成物
を添加するのは好ましい態様である。(F) 成分の詳細は
特開昭54−45361 号公報に記載されている。一般に、本
発明の如き表面処理剤は、そのまま或いは各種シランカ
ップリング剤を配合して用いることにより、シリコーン
ゴム、天然ゴム、アクリルゴム等には良く密着するが、
ＥＰＤＭ、ＮＢＲ、アクリルゴム等の比較的接着・密着
性の乏しい基材の場合は、(F) 成分を配合することが好
ましい。In the present invention, in order to improve the adhesion to the rubber, various silane coupling agents may be added alone or in the form of a mixture depending on the kind of the rubber, either as a single substance or as a mixture. A mixture or partial condensate of silane and epoxy group-containing oil or resin, or a mixture or partial condensate of epoxy group-containing silane and amino group-containing oil or resin may be added. In particular, as the component (F), (1) having an epoxy group-containing polyorganosiloxane, (2) a substituted or unsubstituted amino group bonded to a silicon atom via at least one carbon atom, and an alkoxy group bonded to the silicon atom. It is a preferred embodiment to add a mixture of silane and / or siloxane or the reaction product of (1) and (2). Details of the component (F) are described in JP-A-54-45361. In general, the surface treatment agent of the present invention is used as it is or by blending various silane coupling agents, so that it adheres well to silicone rubber, natural rubber, acrylic rubber, etc.
In the case of a substrate having relatively poor adhesion / adhesion, such as EPDM, NBR, acrylic rubber, etc., it is preferable to blend the component (F).
【００１１】本発明の表面処理用組成物の対象とする基
材は、紙、各種プラスチック、ゴム類であるが、前述の
通り、今まで好ましい処理剤のなかったゴム類に適用し
た場合に本発明の効果が顕著である。本発明に用いられ
るゴムは、天然ゴム、合成ゴム及び再生ゴムのいずれで
もよく、合成ゴムとしては、ＳＢＲ、ＮＢＲ、クロロプ
レン、ＩＩＲ、ＥＰＤＭ、ウレタンゴム、クロロスルホ
ン化ポリエチレン、アクリルゴムなどが例示される。本
発明の組成物は上記各種基材にディプコート、スプレー
コート、刷毛ぬり、ナイフコート、ロールコートなどの
方法によって塗布し、塗布後溶媒を乾燥除去する。つい
で、室温で数時間放置するか、基材に応じて若干の加熱
を行って硬化せしめる。加熱条件は、基材が紙の場合、
温度 120〜180 ℃で10〜30秒間、ゴムの場合、温度 150
〜180 ℃で１〜５分間、プラスチックの場合、温度70〜
150 ℃で30秒〜２分間が推奨される。The substrate to which the composition for surface treatment of the present invention is applicable is paper, various plastics, and rubbers. The effects of the invention are remarkable. The rubber used in the present invention may be any of natural rubber, synthetic rubber and recycled rubber, and examples of the synthetic rubber include SBR, NBR, chloroprene, IIR, EPDM, urethane rubber, chlorosulfonated polyethylene, and acrylic rubber. You. The composition of the present invention is applied to the above-mentioned various substrates by a method such as dip coating, spray coating, brush coloring, knife coating, roll coating and the like, and the solvent is dried and removed after the application. Then, it is left to stand at room temperature for several hours, or is cured by slightly heating according to the base material. The heating conditions are as follows:
10 ~ 30 seconds at a temperature of 120 ~ 180 ℃, 150 for rubber
1 to 5 minutes at ~ 180 ° C, 70 ~ for plastic
30 seconds to 2 minutes at 150 ° C is recommended.
【００１２】[0012]
【発明の効果】本発明の組成物は、炭素数７〜10の分岐
状アルキル系飽和炭化水素を50重量％以上含む有機溶媒
を用いることにより、従来の有機溶媒ではなし得なかっ
た、均一で効率的なゴム表面処理を行うことのできる。According to the composition of the present invention, the use of an organic solvent containing 50% by weight or more of a branched alkyl-based saturated hydrocarbon having 7 to 10 carbon atoms makes it possible to obtain a uniform, unattainable organic solvent. Efficient rubber surface treatment can be performed.
【００１３】[0013]
【実施例】以下、本発明を実施例によって説明する。実
施例において、部はいずれも重量部を示す。 実施例１〜２、比較例１〜３ 表１に示される組成の本発明の処理用組成物（実施例１
〜２）及び比較組成物（比較例１〜３）を調製した。こ
れらの組成物を天然ゴムシートにディプコートにて塗布
し、温度 180℃で３分間加熱処理を施し、天然ゴム表面
に非粘着性のシリコーン皮膜を形成せしめた。これらの
シリコーン皮膜の状態は表１の通りであった。これよ
り、イソオクタンを用いるとディプコートで均一に薄膜
を塗布することができ、さらに濃度や塗り回数を変える
ことにより任意の膜厚を均一にコート可能であることが
明らかである。The present invention will be described below with reference to examples. In Examples, all parts are parts by weight. Examples 1 and 2, Comparative Examples 1 to 3 The treatment compositions of the present invention having the compositions shown in Table 1 (Example 1)
To 2) and comparative compositions (Comparative Examples 1 to 3) were prepared. These compositions were applied to a natural rubber sheet by dip coating, and heat-treated at a temperature of 180 ° C. for 3 minutes to form a non-adhesive silicone film on the surface of the natural rubber. The states of these silicone films were as shown in Table 1. From this, it is clear that when isooctane is used, a thin film can be uniformly applied by dip coating, and that an arbitrary film thickness can be uniformly applied by changing the concentration and the number of coatings.
【００１４】[0014]
【表１】 [Table 1]
【００１５】実施例３〜５、比較例４〜６ 表２に示される組成の本発明の処理用組成物（実施例３
〜５）及び比較組成物（比較例４〜６）を調製した。こ
れらの組成物を天然ゴムシートにスプレーコートにて塗
布し、温度 180℃で３分間加熱処理を施し、天然ゴム表
面に約３μm の非粘着性のシリコーン皮膜を形成せしめ
た。これらのシリコーン皮膜の状態は表２の通りであっ
た。又、同様に、アクリルゴム、ＥＰＤＭの表面にシリ
コーン皮膜を形成せしめ、外観、密着性を目視観察し、
○、△、×の３段階で総合評価し、併せて表２に示し
た。Examples 3 and 5, Comparative Examples 4 and 6 The treatment compositions of the present invention having the compositions shown in Table 2 (Example 3)
To 5) and Comparative Compositions (Comparative Examples 4 to 6). These compositions were applied to a natural rubber sheet by spray coating, and heat-treated at 180 ° C. for 3 minutes to form a non-adhesive silicone film of about 3 μm on the surface of the natural rubber. Table 2 shows the states of these silicone films. Similarly, a silicone film was formed on the surface of acrylic rubber and EPDM, and the appearance and adhesion were visually observed.
The results were comprehensively evaluated in three stages of ○, Δ, and ×, and also shown in Table 2.
【００１６】[0016]
【表２】 [Table 2]
【００１７】実施例６〜７、比較例７〜９ 表３に示される組成の本発明の処理用組成物（実施例６
〜７）及び比較組成物（比較例７〜９）を調製した。こ
れらの組成物を天然ゴムシートにスプレーコートにて塗
布し、温度 180℃で３分間加熱処理を施し、天然ゴム表
面に約３μm の非粘着性のシリコーン皮膜を形成せしめ
た。これらのシリコーン皮膜の状態は表３の通りであっ
た。Examples 6-7, Comparative Examples 7-9 Treatment compositions of the present invention having the compositions shown in Table 3 (Example 6)
To 7) and comparative compositions (Comparative Examples 7 to 9) were prepared. These compositions were applied to a natural rubber sheet by spray coating, and heat-treated at 180 ° C. for 3 minutes to form a non-adhesive silicone film of about 3 μm on the surface of the natural rubber. Table 3 shows the states of these silicone films.
【００１８】[0018]
【表３】 [Table 3]
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭56−78960（ＪＰ，Ａ) 特開 昭62−215667（ＪＰ，Ａ) 特開 平１−313564（ＪＰ，Ａ) 特開 昭63−295646（ＪＰ，Ａ) 特表 昭59−500420（ＪＰ，Ａ) (58)調査した分野(Int.Cl.7，ＤＢ名) C09D 183/00 - 183/16 C08J 7/04 - 7/06 C08L 83/04 - 83/16 ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-56-78960 (JP, A) JP-A-62-215667 (JP, A) JP-A-1-313564 (JP, A) JP-A 63-78 295646 (JP, A) Special table 1979-500420 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C09D 183/00-183/16 C08J 7 /04-7/06 C08L 83/04-83/16
Claims (4)
Stの両末端が水酸基閉塞のポリジオルガノシロキサン (B) ケイ素原子に結合した水素原子が１分子中に少なく
とも３個存在するポリオルガノハイドロジェンシロキサ
ン (C) 硬化触媒 (D) 炭素数７〜10の分岐状アルキル系飽和炭化水素を40
重量％以上含む有機溶媒 とを含有する表面処理用組成物。(A) a viscosity at 25 ° C. of 50 to 10,000,000 c
A hydroxyl-blocked polydiorganosiloxane at both ends of St (B) a polyorganohydrogensiloxane having at least three silicon-bonded hydrogen atoms in one molecule (C) a curing catalyst (D) having 7 to 10 carbon atoms 40 branched alkyl-based saturated hydrocarbons
A composition for surface treatment comprising: an organic solvent containing at least 1% by weight.
ラーを含有する請求項１記載の表面処理用組成物。2. The composition for surface treatment according to claim 1, further comprising (E) a filler having an average particle diameter of 0.01 to 100 μm.
ノシロキサンと(2) 少なくとも１個の炭素原子を介して
ケイ素原子に結合した置換又は非置換アミノ基とケイ素
原子に結合したアルコキシ基を有するシラン及び／又は
シロキサンとの混合物、又は(1) と(2) の反応生成物を
含有する請求項１又は２記載の表面処理用組成物。(F) (1) an epoxy group-containing polyorganosiloxane; and (2) a substituted or unsubstituted amino group bonded to a silicon atom via at least one carbon atom and an alkoxy group bonded to the silicon atom. The surface treatment composition according to claim 1 or 2, which comprises a mixture of a silane and / or a siloxane having a group, or a reaction product of (1) and (2).
用組成物をゴム表面に塗布し、室温又は加熱下で硬化さ
せることを特徴とするゴムの表面処理方法。4. A method for surface treatment of rubber, comprising applying the composition for surface treatment according to claim 1 to a rubber surface and curing the composition at room temperature or under heating.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19567293A JP3255501B2 (en) | 1993-08-06 | 1993-08-06 | Composition for surface treatment and method for surface treatment of rubber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19567293A JP3255501B2 (en) | 1993-08-06 | 1993-08-06 | Composition for surface treatment and method for surface treatment of rubber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0748544A JPH0748544A (en) | 1995-02-21 |
| JP3255501B2 true JP3255501B2 (en) | 2002-02-12 |
Family
ID=16345081
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19567293A Expired - Lifetime JP3255501B2 (en) | 1993-08-06 | 1993-08-06 | Composition for surface treatment and method for surface treatment of rubber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3255501B2 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3476368B2 (en) * | 1998-07-10 | 2003-12-10 | 信越化学工業株式会社 | Room temperature curable organopolysiloxane composition |
| JP4808338B2 (en) * | 2001-07-05 | 2011-11-02 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | Coating agent composition |
| FR2881748B1 (en) * | 2005-02-07 | 2007-03-09 | Rhodia Chimie Sa | AQUEOUS SILICONE DISPERSIONS, IN PARTICULAR FORMULATIONS OF PAINTS COMPRISING SAME AND ONE OF THEIR PREPARATION METHODS |
| JP4493022B2 (en) * | 2005-03-24 | 2010-06-30 | 藤倉ゴム工業株式会社 | Umbrella valve, check valve device for air pump and air pump |
| JP2007070606A (en) * | 2005-08-08 | 2007-03-22 | Soft99 Corporation | Vehicular anti-staining coating agent |
| JP4754445B2 (en) * | 2005-11-17 | 2011-08-24 | 株式会社ソフト９９コーポレーション | Antifouling coating agent for outdoor installations |
| WO2009119841A1 (en) * | 2008-03-28 | 2009-10-01 | 三菱化学株式会社 | Curable polysiloxane composition, and polysiloxane cured product, optical member, member for aerospace industry, semiconductor light emitting device, lighting system, and image display device using the curable polysiloxane composition |
| JP5339804B2 (en) * | 2008-07-16 | 2013-11-13 | 藤倉ゴム工業株式会社 | Surface treatment agent, rubber surface treatment method and rubber product |
| JP5287116B2 (en) * | 2008-10-09 | 2013-09-11 | 三菱化学株式会社 | Hardened polyorganosiloxane and method for producing light emitting device |
| BR112014012596A2 (en) * | 2011-12-02 | 2017-06-06 | Cpfilms Inc | methods for forming a silicone release liner and for storing a roll film |
| KR102348370B1 (en) * | 2020-01-05 | 2022-01-06 | 황영민 | Coating Composition With Good Chemical Resistance And Coating Film Using The Same |
-
1993
- 1993-08-06 JP JP19567293A patent/JP3255501B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0748544A (en) | 1995-02-21 |
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