JPH0137737B2 - - Google Patents
Info
- Publication number
- JPH0137737B2 JPH0137737B2 JP17676283A JP17676283A JPH0137737B2 JP H0137737 B2 JPH0137737 B2 JP H0137737B2 JP 17676283 A JP17676283 A JP 17676283A JP 17676283 A JP17676283 A JP 17676283A JP H0137737 B2 JPH0137737 B2 JP H0137737B2
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- fluororubber
- silicone rubber
- roll
- undercoat
- 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
Links
- 229920001973 fluoroelastomer Polymers 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 19
- 239000003973 paint Substances 0.000 claims description 17
- 229920002379 silicone rubber Polymers 0.000 claims description 16
- 239000004945 silicone rubber Substances 0.000 claims description 15
- 239000004925 Acrylic resin Substances 0.000 claims description 6
- 229920000178 Acrylic resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- -1 acrylic ester Chemical class 0.000 claims description 2
- 239000000463 material Substances 0.000 description 10
- 239000010410 layer Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 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
- 241000047703 Nonion Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 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
- 238000013007 heat curing Methods 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Fixing For Electrophotography (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Description
本発明は、フツ素ゴム塗料用下塗り組成物に関
し、更に詳しくは、フツ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ツ素ゴム塗料用下
塗り組成物に関する。
フツ素ゴムは、接着性に乏しいため、金属、ゴ
ム、プラスチツ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
上にフツ素ゴムが被覆される。
フツ素ゴム塗料用下塗り組成物としては、一般
に、エポキシ樹脂系またはシランカツプリング剤
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
ツ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。
フツ素ゴムは不活性であり、また、他の一般の
ゴム、プラスチツ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ツクアツ
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
定着およびバツクアツプロールが要求されてい
る。
かかる要求を満たすためにロール本体外周表面
にフツ素樹脂を含むフツ素ゴム塗料層を設けた非
粘着性弾性体ロール(特開昭58−5770号公報)が
提案されている。これらの定着およびバツクアツ
プロールは、融着トナーとの非粘着性については
十分満足できるものであるが、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ツ素樹脂を含むフツ素塗
料層を設けたものの接着性が充分でない。
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
ンゴムとフツ素ゴムとの接着性を大巾に改良した
フツ素ゴム塗料用下塗り組成物を見い出し、本発
明を完成するに至つた。
本発明の要旨は、アクリル樹脂の少くとも1種
を含んで成る、電子複写機の定着ロールまたはバ
ツクアツプロール用フツ素ゴム塗料用下塗り組成
物に存する。
アクリル樹脂は、アクリル酸またはそのエステ
ル、もしくはメタクリル酸またはそのエステルの
重合体、または共重合体である。エステルとして
は、メチル、エチル、プロピル、ブチル、2−エ
チルヘキシル、グリシジルの各エステル、多価ア
ルコールとのエステルなどが挙げられ、また、共
重合体としては酢酸ビニル、塩化ビニル、スチレ
ンなどとの共重合体が挙げられる。
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、カルビ
トール類、水などである。
アクリル樹脂の濃度は、通常1〜90重量%、好
ましくは5〜50重量%である。
さらにシランカツプリング剤または有機チタネ
ートを配合することにより、シリコーンゴム基材
または充填材(たとえば、ホワイトカーボン、ベ
ンガラなど)配合のシリコーンゴムにも本発明の
下塗り組成物は有用である。
本発明のフツ素ゴム塗料用下塗り組成物は、通
常の方法により、液状担体にアクリル樹脂を溶解
するか、または溶液重合することにより調製され
る。
調製された組成物は、通常の塗装方法(たとえ
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。乾燥した下塗り表面上には、フツ素ゴム塗
料が、通常の方法により塗布、硬化される。
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。
実施例1〜4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℃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4ではA液
のフツ素樹脂デイスパージヨンを用いない。)の
フツ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のフツ素ゴム塗膜層を設
けた。
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ツ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。
なお、比較のため、下塗り組成物を使用しない
場合(比較例1)および従来公知のフツ素ゴム塗
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。
フツ素ゴム塗料(次のA液100重量部に対し、
次のB液3重量部を配合)
A液
フツ素ゴム(1)水性デイスパージヨン(フツ素ゴ
ム含有量60重量%) ……100重量部
フツ素樹脂(2)水性デイスパージヨン(フツ素樹
脂含有量50重量%) ……100 〃
酸化マグネシウム ……3 〃
ノニオンHS−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−アミノプロピル)−2,4,
8,10−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
(注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
The present invention relates to an undercoat composition for fluoro-rubber paints, and more specifically, the present invention relates to an undercoat composition for fluoro-rubber paints, and more specifically, it can be applied to base materials, especially without impairing the excellent properties of fluoro-rubber, such as heat resistance, oil resistance, chemical resistance, and solvent resistance. The present invention relates to an undercoat composition for fluororubber paints for imparting strong adhesion to silicone rubber. Fluoro rubber has poor adhesive properties, so when coating it on the surface of a base material such as metal, rubber, or plastic,
Usually, the surface of the base material is roughened or pretreated by solvent degreasing, and then an undercoat composition is applied, and the fluororubber is coated thereon. As undercoat compositions for fluoro rubber paints, those based on epoxy resins or silane coupling agents are generally 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 fluoro rubber. Fluorine rubber is inert and has poor compatibility with other general rubbers and plastics, making it extremely difficult to achieve practical adhesion, especially when the base material is silicone rubber. be. For example, in an electronic copying machine, the toner image formed on the printing material is finally fused by fixing and back-up rolls, but elastic rolls with a silicone rubber layer are most often used as these rolls. has been done. However, non-tacky fusing and back-up rolls are required for the fusing toner because the fusing toner tends to adhere to these rolls, resulting in blurred printed images. In order to meet such requirements, a non-adhesive elastic roll (Japanese Patent Application Laid-Open No. 58-5770) has been proposed in which a fluorocarbon rubber paint layer containing a fluorocarbon resin is provided on the outer peripheral surface of the roll body. These fixing and back-up rolls are sufficiently satisfactory in terms of non-adhesion with the fused toner, but especially when the base material is silicone rubber, in other words, the fluororesin is attached to the roll body through a silicone rubber layer. Although a fluorine paint layer containing fluorine paint is provided, the adhesion is not sufficient. As a result of studies to eliminate the drawbacks of the above-mentioned conventional methods, the present inventors have developed an undercoat composition for fluoro-rubber paints that has greatly improved the adhesion between silicone rubber and fluoro-rubber as base materials. They discovered this and completed the present invention. The gist of the present invention resides in an undercoat composition for a fluororubber paint for a fixing roll or a backup roll of an electronic copying machine, which comprises at least one kind of acrylic resin. The acrylic resin is a polymer or copolymer of acrylic acid or its ester, or methacrylic acid or its ester. Examples of esters include methyl, ethyl, propyl, butyl, 2-ethylhexyl, and glycidyl esters, and esters with polyhydric alcohols. Copolymers include copolymers with vinyl acetate, vinyl chloride, styrene, etc. Examples include polymers. 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, carbitols, and water. It is. The concentration of the acrylic resin is usually 1 to 90% by weight, preferably 5 to 50% by weight. Furthermore, by incorporating a silane coupling agent or an organic titanate, the undercoat composition of the present invention is also useful for silicone rubbers containing silicone rubber base materials or fillers (eg, white carbon, red iron, etc.). The undercoat composition for fluororubber paints of the present invention is prepared by dissolving an acrylic resin in a liquid carrier or by solution polymerization by a conventional method. The prepared composition is applied to a substrate, especially a silicone rubber surface, by conventional coating methods (eg brushing, dipping, spraying, etc.) and dried. A fluororubber paint is applied and cured on the dried undercoat surface by a conventional method. Next, examples and comparative examples will be shown to specifically explain the present invention. Examples 1 to 4 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 with the following composition (however, the fluororesin dispersion of liquid A was not used in Example 4) was spray-coated on top of the coating, dried at 60°C for 10 minutes, and then cured at 300°C. Then, a fluororubber coating layer with a thickness of about 30 μm was provided on the silicone rubber vulcanized plate. For 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. For comparison, the same tests were conducted in the case where no undercoat composition was used (Comparative Example 1) and in the case where conventionally known undercoat compositions for fluororubber paints were used (Comparative Examples 2 and 3). The results are also listed in the table below. Fluoro rubber paint (for 100 parts by weight of the following liquid A,
Blend 3 parts by weight of the following B liquid) A liquid fluororubber (1) Aqueous dispersion (fluororubber content 60% by weight) ......100 parts by weight Fluororesin (2) Aqueous dispersion (fluororubber) Resin content 50% by weight) ...100 Magnesium oxide ...3 Nonion HS-210 (manufactured by NOF Corporation)
...2〃 Water ...50〃 B liquid γ-Aminopropyltriethoxysilane
...40 〃 8,9-bis(8-aminopropyl)-2,4,
8,10-tetraoxaspiro[5.5]undecane ...20 〃 Water ...40 〃 (Note 1) Vinylidene fluoride/tetrafluoroethylene/hexafluoropropylene elastic copolymer (Note 2) Tetrafluoroethylene/hexafluoro propylene copolymer
【表】
実施例 5
アルミニウム製芯金の表面をサンドブラストに
より粗面化し、アセトンで洗浄し、乾燥した後、
HTV(加熱硬化型)シリコーンゴムを巻き付け、
170℃で15分間加硫成型し、更に200℃で2時間2
次加硫を行つた。次いで、加硫シリコーンゴムの
表面を研摩してロールを作製した。
このロール表面に、ノズル径1.0mmのスプレー
ガンを用い、2Kg/cm2Gのエアー圧でプライマー
Dをスプレー塗装し、60℃で10分間乾燥した。さ
らに、その上に、実施例1と同様のフツ素ゴム塗
料を同じ条件でスプレー塗装し、60℃で10分間乾
燥し、次いで300℃で30分間硬化させた。なお、
下塗り層の厚さは約10μmであり、フツ素ゴム塗
膜層の厚さは約30μmであつた。
このようにして得られた定着ロールを組み込ん
だ定着装置を有する乾式複写機でA4紙30万枚の
通紙を行つた。この時、定着ロールの表面温度は
160〜170℃であつた。放冷後、定着ロールを取り
外し、外観を観察したところ、シリコーンゴム層
とフツ素ゴム層との剥離、しわの発生などの異常
は全く見られなかつた。[Table] Example 5 After roughening the surface of an aluminum core metal by sandblasting, washing with acetone, and drying,
Wrapped with HTV (heat curing type) silicone rubber,
Vulcanization molding at 170℃ for 15 minutes, then 2 hours at 200℃
Next vulcanization was performed. Next, the surface of the vulcanized silicone rubber was polished to produce a roll. The surface of this roll was spray-coated with Primer D using a spray gun with a nozzle diameter of 1.0 mm at an air pressure of 2 kg/cm 2 G, and dried at 60° C. for 10 minutes. Furthermore, the same fluororubber paint as in Example 1 was spray-painted thereon under the same conditions, dried at 60°C for 10 minutes, and then cured at 300°C for 30 minutes. In addition,
The thickness of the undercoat layer was about 10 μm, and the thickness of the fluororubber coating layer was about 30 μm. A dry copying machine equipped with a fixing device incorporating the fixing roll thus obtained was used to pass 300,000 sheets of A4 paper. At this time, the surface temperature of the fixing roll is
The temperature was 160-170℃. After cooling, the fixing roll was removed and the appearance was observed. No abnormalities such as peeling between the silicone rubber layer and the fluorine rubber layer or wrinkles were observed.
Claims (1)
電子複写機の定着ロールまたはバツクアツプロー
ル用フツ素ゴム塗料用下塗り組成物。 2 定着ロールまたはバツクアツプロールの少く
とも表面がシリコーンゴムから成る特許請求の範
囲第1項記載の組成物。 3 アクリル樹脂がアクリル酸エステル系樹脂で
ある特許請求の範囲第1項記載の組成物。 4 フツ素ゴム塗料がフツ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。[Claims] 1. Comprising at least one type of acrylic resin,
An undercoat composition for fluoro rubber paints for fixing rolls or backup rolls of electronic copying machines. 2. The composition according to claim 1, wherein at least the surface of the fixing roll or backup roll is made of silicone rubber. 3. The composition according to claim 1, wherein the acrylic resin is an acrylic ester resin. 4. The composition according to claim 1, wherein the fluororubber paint contains a fluororesin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17676283A JPS6067541A (en) | 1983-09-24 | 1983-09-24 | Undercoat composition for fluororubber paints |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17676283A JPS6067541A (en) | 1983-09-24 | 1983-09-24 | Undercoat composition for fluororubber paints |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6067541A JPS6067541A (en) | 1985-04-17 |
| JPH0137737B2 true JPH0137737B2 (en) | 1989-08-09 |
Family
ID=16019363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17676283A Granted JPS6067541A (en) | 1983-09-24 | 1983-09-24 | Undercoat composition for fluororubber paints |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6067541A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000060016A1 (en) * | 1999-04-01 | 2000-10-12 | Daikin Industries, Ltd. | Primer composition for fluororubber composition and article coated with primer |
-
1983
- 1983-09-24 JP JP17676283A patent/JPS6067541A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6067541A (en) | 1985-04-17 |
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