JPS6067542A - Primer composition for fluororubber coating - Google Patents

Primer composition for fluororubber coating

Info

Publication number
JPS6067542A
JPS6067542A JP58176763A JP17676383A JPS6067542A JP S6067542 A JPS6067542 A JP S6067542A JP 58176763 A JP58176763 A JP 58176763A JP 17676383 A JP17676383 A JP 17676383A JP S6067542 A JPS6067542 A JP S6067542A
Authority
JP
Japan
Prior art keywords
fluororubber
epoxy
composition
silicone resin
resin
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
Application number
JP58176763A
Other languages
Japanese (ja)
Other versions
JPH051313B2 (en
Inventor
Takeshi Suzuki
武 鈴木
Tsutomu Terada
寺田 勉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daikin Industries Ltd
Original Assignee
Daikin Industries Ltd
Daikin Kogyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daikin Industries Ltd, Daikin Kogyo Co Ltd filed Critical Daikin Industries Ltd
Priority to JP58176763A priority Critical patent/JPS6067542A/en
Publication of JPS6067542A publication Critical patent/JPS6067542A/en
Publication of JPH051313B2 publication Critical patent/JPH051313B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide titled composition capable of affording fluororubber coating with firm bonding to base material esp. silicone rubber without impairing the excellent characteristics inherent in the fluororubber, containing at least one sort of epoxy-modified silicone resin. CONSTITUTION:An epoxy-modified silicone resin derived from the condensation between the hydroxyl group of epoxy resin and the silanol group of silicone resin is incorporated in a liquid carrier such as toluene, xylene, acetone, methyl cellosolve so as to be 1-90 (pref. 5-60)wt% in concentration, thats obtaining the objective composition. This composition is coated (by brushing, dipping, spray coating, etc.) on the surface of e.g. silicone rubber, being dried followed by applying to the coated surface a fluororesin-contg. fluororubber coating. Said composition may be modified with fatty acid, also being preferably incorporated with drying promotor such as lead, manganese, cobalt and/or curing agent such as organic amine, acid anhydride, phenolic resin.

Description

【発明の詳細な説明】 本発明は、フッ素ゴム塗料用下塗り組成物に関し、更に
詳しくは、フッ素ゴムの卓越した耐熱性、耐油性、耐薬
品性、耐溶剤性などの特性を損うことなく、基材、特に
シリコーンゴムに対し強固な接着性を付与するためのフ
ッ素ゴム塗料用下塗り組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an undercoat composition for fluororubber paints, and more specifically, the present invention relates to an undercoat composition for fluororubber paints, and more specifically, an undercoat composition that can be used without impairing the outstanding properties of fluororubber such as heat resistance, oil resistance, chemical resistance, and solvent resistance. , relates to an undercoat composition for fluororubber paints for imparting strong adhesion to substrates, particularly silicone rubber.

フッ素ゴムは、接着性に乏しいため、金属、ゴム、プラ
スチック等の基材表面に被覆する場合、通常基材表面を
粗面化したり、溶剤脱脂による前処理を行い、さらに下
塗り組成物を塗布し、その上にフッ素ゴムが被覆される
Fluororubber has poor adhesive properties, so when coating it on the surface of a base material such as metal, rubber, or plastic, the base material surface is usually roughened or pretreated with solvent degreasing, and then an undercoat composition is applied. , on which fluororubber is coated.

フッ素ゴム塗料用下塗り組成物としては、一般【二、エ
ポキシ樹脂系またはシランカップリング剤系のものが使
用されている。これらは、基材が金属の場合は概ね良好
な接着性を示すが、基材がフッ素ゴム以外のゴムの場合
、満足される接着効果が発揮されない。
As undercoat compositions for fluororubber paints, those based on general epoxy resins or silane coupling agents are used. These generally exhibit good adhesion when the base material is metal, but do not exhibit a satisfactory adhesive effect when the base material is a rubber other than fluororubber.

フッ素ゴムは不活性であり、また、池の一般のゴム、プ
ラスチックとは相溶性が悪く、特に基材がシリコーンゴ
ムである場合、実用に耐えうるような接着を行うことが
非常に困難である。例えば、電子複写機において、被印
刷物上に形成されたトナー画像は、最終的に定着および
バックアップロールにより融着されるが、これらロール
として、シリコーンゴム層を設けた弾性体ロールが最も
多く使用されている。けれども、融着トナーがこれらロ
ールに付着しやすく、印刷物の画像が不鮮明になるため
、融着トナーに対して非粘着性の定着およびバックアッ
プロールが要求されている。
Fluororubber is inert and has poor compatibility with common rubbers and plastics, making it extremely difficult to achieve practical adhesion, especially when the base material is silicone rubber. . For example, in an electronic copying machine, the toner image formed on the printing material is finally fused by a fixing and backup roll, but elastic rolls with a silicone rubber layer are most often used as these rolls. ing. However, non-tacky fusing and back-up rolls are required for fusing toner because fusing toner tends to adhere to these rolls, resulting in blurred printed images.

かかる要求を満たすためにロール本体外周表面にフッ素
樹脂を含むフッ素ゴム塗料層を設けた非粘着性弾性体ロ
ール(vf開昭58−5770号公報)が提案されてい
る。これらの定着およびバックアップロールは、融着ト
ナーとの非粘着性については十分満足で外るものである
が、とくに基材がシリコーンゴムの場合、つまりロール
本体にシリコーンゴム層を介して前記フッ素樹脂を含む
フッ素ゴム塗料層を設けたものの接着性が充分でない。
In order to meet such requirements, a non-adhesive elastic roll (VF Publication No. 58-5770) has been proposed in which a fluororubber paint layer containing a fluororesin is provided on the outer peripheral surface of the roll body. These fixing and backup rolls are quite satisfactory in terms of non-adhesion with the fused toner, but this is especially true when the base material is silicone rubber, that is, when the fluororesin is applied to the roll body through a silicone rubber layer. Although a fluororubber coating layer containing

本発明者等は、上記従来法の欠点を排除すべく検討を加
えた結果、とくに基材としてのシリコーンゴムとフッ素
ゴムとの接着性を大巾に改良したフッ素ゴム塗料用下塗
り組成物を見い出し、本発明を完成するに至った。
As a result of conducting studies to eliminate the drawbacks of the above-mentioned conventional methods, the present inventors have discovered an undercoat composition for fluororubber paints that has greatly improved the adhesion between silicone rubber and fluororubber as base materials. , we have completed the present invention.

本発明の要旨は、エポキシ変性シリコーン樹脂の少くと
も1種を含んで成るフッ素ゴム塗料用下塗り組成物に存
する。
The gist of the present invention resides in an undercoat composition for fluororubber paints comprising at least one epoxy-modified silicone resin.

エポキシ変性シリコーン樹脂はエポキシ樹脂の水酸基と
シリコーン樹脂のシラノール基の縮合反応によって得ら
れる。さらに、得られたエポキシ変性シリコーン樹脂を
脂肪酸で変性してもよい。
Epoxy-modified silicone resins are obtained by a condensation reaction between hydroxyl groups of epoxy resins and silanol groups of silicone resins. Furthermore, the obtained epoxy-modified silicone resin may be modified with a fatty acid.

本発明の下塗り組成物には、エポキシ変性シリコーン樹
脂の乾燥促進剤である鉛、マンガン、コバルト、亜鉛、
カルシウムなどの有機塩、および/または硬化剤である
有機アミン、酸無水物、7エ/−ル樹脂、アミノ樹脂、
ポリアミドなどを添加するのが好ましい。
The undercoat composition of the present invention contains lead, manganese, cobalt, zinc, which is a drying accelerator for epoxy-modified silicone resin,
Organic salts such as calcium, and/or organic amines as curing agents, acid anhydrides, 7-ether resins, amino resins,
It is preferable to add polyamide or the like.

通常用いられる液状担体は、トルエン、キシレンなどの
芳香族系溶剤、アセトン、メチルエチルケトン、メチル
イソブチルケトンなどのケトン系溶剤、メチルセロソル
ブ、ブチルセロソルブなどのセロソルブ系溶剤、低級ア
ルコール類、カルピトール類、水などである。
Commonly used liquid carriers include aromatic solvents such as toluene and xylene, ketone solvents such as acetone, methyl ethyl ketone, and methyl isobutyl ketone, cellosolve solvents such as methyl cellosolve and butyl cellosolve, lower alcohols, calpitols, and water. be.

エポキシ変性シリコーン樹脂の濃度は、通常1〜90重
量%、好ましくは5〜60重量%で・ある。
The concentration of the epoxy-modified silicone resin is usually 1 to 90% by weight, preferably 5 to 60% by weight.

本発明のフッ素ゴム塗料用下塗り組成物は、通常の方法
により、液状担体にエポキシ変性シリコーン樹脂を添加
することにより調製される。
The undercoat composition for fluororubber paints of the present invention is prepared by adding an epoxy-modified silicone resin to a liquid carrier by a conventional method.

調製された組成物は、通常の塗装方法(たとえ3− ばハケ塗り、浸漬、噴霧塗装など)により、基材、特に
シリコーンゴム表面に塗布され、乾燥される。
The prepared composition is applied to a substrate, especially a silicone rubber surface, by conventional coating methods (eg, 3-brushing, dipping, spraying, etc.) and dried.

乾燥した下塗り表面上には、フッ素ゴム塗料が、通常の
方法により塗布、硬化される。
On the dried undercoat surface, a fluororubber paint is applied and cured by a conventional method.

次に実施例および比較例を示し、本発明を具体的に説明
する。
Next, examples and comparative examples will be shown to specifically explain the present invention.

実施例1〜2および比較例1〜3 シリコーンゴム加硫板に、次表に示す下塗り組成物をハ
ケ塗りし、60’Cで5分間乾燥した。さらにその上に
下記組成(ただし、実施例2ではA液のフッ素樹脂ティ
スパーンョンを用いない。)のフッ素ゴム塗料をスプレ
ー塗装し、60℃で10分間乾燥後、300℃で硬化さ
せて、上記シリコーンゴム加硫板上に厚さ約30μのフ
ッ素ゴム塗膜層を設けた。
Examples 1 to 2 and Comparative Examples 1 to 3 The undercoat composition shown in the following table was brushed onto a silicone rubber vulcanized plate and dried at 60'C for 5 minutes. Furthermore, a fluororubber paint having the following composition (however, the fluororesin paint of liquid A was not used in Example 2) was spray-coated on top of the coating, dried at 60°C for 10 minutes, and then cured at 300°C to coat the silicone. A fluororubber coating layer with a thickness of about 30 μm was provided on a rubber vulcanized plate.

このようにして得られた試料について、シリコーンゴム
加硫板とフッ素ゴム塗膜層との剥離強度を万能引張り試
験機により測定した。結果を次表に示す。
Regarding the sample thus obtained, the peel strength between the silicone rubber vulcanized plate and the fluororubber coating layer was measured using a universal tensile tester. The results are shown in the table below.

なお、比較のため、下塗り組成物を使用しない4− 場合(比較例1)および従来公知のフッ素ゴム塗料用下
塗り組成物を用いた場合(比較例2および3)について
も同様に試験した。その結果を次表に併記する。
For comparison, the same tests were conducted for the case where no undercoat composition was used (Comparative Example 1) and the case where a conventionally known undercoat composition for fluororubber paint was used (Comparative Examples 2 and 3). The results are also listed in the table below.

フッ素ゴム塗料(次のA液100重量部に対し、次のB
液3重量部を配合) A液 フッ素ゴム1)水性ディスバージタン (フッ素ゴム含有量60重量%) ・・・・・・・・・100重量部 フッ素樹脂2)水性ディスパージョン (フッ素樹脂含有量50重量%) ・・・・・・・・・100 〃 酸化マグネシウム ・・・・・・・・・ 3 //ノニ
オンH8−210 (日本油脂(株)製) ・・・・・・・・・ 2 〃水
 ・・・・・・・・・ 50 〃 B液 γ−アミノプロピルトリエトキシシラン・・・・・・・
・・ 40 〃 8.9−ビス(8−7ミノプロビル)−2,4,8,1
0−テトラオキサスピロ(5,5]ウンデカン ・・・
・・・・・・ 20 〃水 ・・・・・・・・・ 40
 〃 注1)ビニリデンフルオライド/テトラフルオロエチレ
ン/ヘキサフルオロプロピレン弾性状共重合体 2)テトラフルオロエチレン/ヘキサフルオロプロピレ
ン共重合体 7− 注1)エポキシ変性シリコーン樹脂 (トーレ・シリコーン(株)製) 2)エポキシ変性シリコーン樹脂硬化剤(トーレ・シリ
コーン(株)製) 3)シリコーン樹脂 (信越化学工業(株)製)4)エ
ポキシ樹脂 (シェル化学(株)製)5)ポリアミン系
硬化剤 (三菱油化(株)製)特許出願人 ダイキン工
業株式会社 代 理 人 弁理士 青用 葆(外2名)8−
Fluororubber paint (for 100 parts by weight of the following liquid A, the following B)
3 parts by weight of liquid) Liquid A fluororubber 1) Aqueous disvergitane (fluororubber content 60% by weight) ......100 parts by weight fluororesin 2) Aqueous dispersion (fluororesin content 50% by weight) ・・・・・・・・・100 〃 Magnesium oxide ・・・・・・・・・ 3 //Nonion H8-210 (manufactured by NOF Corporation) ・・・・・・・・・2 〃 Water ・・・・・・・・・ 50 〃 B liquid γ-aminopropyltriethoxysilane ・・・・・・・・・
・・ 40 〃 8.9-bis(8-7minoprovir)-2,4,8,1
0-tetraoxaspiro(5,5]undecane...
・・・・・・ 20 〃Water ・・・・・・・・・ 40
〃 Note 1) Vinylidene fluoride/tetrafluoroethylene/hexafluoropropylene elastic copolymer 2) Tetrafluoroethylene/hexafluoropropylene copolymer 7- Note 1) Epoxy-modified silicone resin (manufactured by Toray Silicone Co., Ltd.) 2) Epoxy-modified silicone resin curing agent (manufactured by Toray Silicone Co., Ltd.) 3) Silicone resin (manufactured by Shin-Etsu Chemical Co., Ltd.) 4) Epoxy resin (manufactured by Shell Chemical Co., Ltd.) 5) Polyamine-based curing agent (Mitsubishi Manufactured by Yuka Co., Ltd.) Patent applicant Daikin Industries Co., Ltd. Agent Patent attorney Aoyou Ao (2 others) 8-

Claims (3)

【特許請求の範囲】[Claims] (1)エポキシ変性シリコーン樹脂の少くとも1種を含
んで成るフッ素ゴム塗料用下塗り組成物。
(1) An undercoat composition for a fluororubber paint comprising at least one epoxy-modified silicone resin.
(2) シリコーンゴム基材に用いる特許請求の範囲第
1項記載の組成物。
(2) A composition according to claim 1 for use in a silicone rubber base material.
(3)フッ素ゴム塗料がフッ素樹脂を含んだものである
特許請求の範囲第1項記載の組成物。
(3) The composition according to claim 1, wherein the fluororubber paint contains a fluororesin.
JP58176763A 1983-09-24 1983-09-24 Primer composition for fluororubber coating Granted JPS6067542A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58176763A JPS6067542A (en) 1983-09-24 1983-09-24 Primer composition for fluororubber coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58176763A JPS6067542A (en) 1983-09-24 1983-09-24 Primer composition for fluororubber coating

Publications (2)

Publication Number Publication Date
JPS6067542A true JPS6067542A (en) 1985-04-17
JPH051313B2 JPH051313B2 (en) 1993-01-07

Family

ID=16019383

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58176763A Granted JPS6067542A (en) 1983-09-24 1983-09-24 Primer composition for fluororubber coating

Country Status (1)

Country Link
JP (1) JPS6067542A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6383177A (en) * 1986-09-29 1988-04-13 Kouseinou Jushi Shinseizou Gijutsu Kenkyu Kumiai Primer composition
JPH03258876A (en) * 1990-03-07 1991-11-19 Nippon Paint Co Ltd Coating compound composition of middle coating for covering silicone rubber
US5525673A (en) * 1989-03-03 1996-06-11 Kansai Paint Company, Limited Hydroxyl and epoxy polymer, hydrolyzable silicone polymer, either containing flourine monomer
US6525160B1 (en) * 1999-06-17 2003-02-25 Arakawa Chemical Industries Ltd. Epoxy resin composition and process for producing silane-modified epoxy resin
WO2007034866A1 (en) * 2005-09-22 2007-03-29 Daikin Industries, Ltd. Coating composition and coated article
JP2009522414A (en) * 2005-12-30 2009-06-11 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Fluoropolymer coated films useful for photovoltaic modules

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6383177A (en) * 1986-09-29 1988-04-13 Kouseinou Jushi Shinseizou Gijutsu Kenkyu Kumiai Primer composition
US5525673A (en) * 1989-03-03 1996-06-11 Kansai Paint Company, Limited Hydroxyl and epoxy polymer, hydrolyzable silicone polymer, either containing flourine monomer
JPH03258876A (en) * 1990-03-07 1991-11-19 Nippon Paint Co Ltd Coating compound composition of middle coating for covering silicone rubber
US6525160B1 (en) * 1999-06-17 2003-02-25 Arakawa Chemical Industries Ltd. Epoxy resin composition and process for producing silane-modified epoxy resin
WO2007034866A1 (en) * 2005-09-22 2007-03-29 Daikin Industries, Ltd. Coating composition and coated article
JP2009522414A (en) * 2005-12-30 2009-06-11 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー Fluoropolymer coated films useful for photovoltaic modules

Also Published As

Publication number Publication date
JPH051313B2 (en) 1993-01-07

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