JPS6383176A - Primer composition - Google Patents
Primer compositionInfo
- Publication number
- JPS6383176A JPS6383176A JP23079286A JP23079286A JPS6383176A JP S6383176 A JPS6383176 A JP S6383176A JP 23079286 A JP23079286 A JP 23079286A JP 23079286 A JP23079286 A JP 23079286A JP S6383176 A JPS6383176 A JP S6383176A
- Authority
- JP
- Japan
- Prior art keywords
- binder
- resin
- metal
- cast iron
- undercoat composition
- 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
- 239000000203 mixture Substances 0.000 title claims description 38
- 229910052751 metal Inorganic materials 0.000 claims abstract description 61
- 239000002184 metal Substances 0.000 claims abstract description 61
- 239000011347 resin Substances 0.000 claims abstract description 48
- 229920005989 resin Polymers 0.000 claims abstract description 48
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910001018 Cast iron Inorganic materials 0.000 claims abstract description 22
- 239000011230 binding agent Substances 0.000 claims abstract description 22
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 21
- 239000010703 silicon Substances 0.000 claims abstract description 21
- 239000011248 coating agent Substances 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 11
- -1 amine silicate Chemical class 0.000 claims abstract description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004677 Nylon Substances 0.000 claims abstract description 4
- 239000004962 Polyamide-imide Substances 0.000 claims abstract description 4
- 239000004695 Polyether sulfone Substances 0.000 claims abstract description 4
- 239000004697 Polyetherimide Substances 0.000 claims abstract description 4
- 239000003822 epoxy resin Substances 0.000 claims abstract description 4
- 229920001778 nylon Polymers 0.000 claims abstract description 4
- 229920002492 poly(sulfone) Polymers 0.000 claims abstract description 4
- 229920002312 polyamide-imide Polymers 0.000 claims abstract description 4
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 4
- 229920006393 polyether sulfone Polymers 0.000 claims abstract description 4
- 229920001601 polyetherimide Polymers 0.000 claims abstract description 4
- 229920001721 polyimide Polymers 0.000 claims abstract description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000004642 Polyimide Substances 0.000 claims abstract description 3
- 239000000084 colloidal system Substances 0.000 claims abstract description 3
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 3
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 3
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 5
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 5
- 239000004696 Poly ether ether ketone Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 229920002530 polyetherether ketone Polymers 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 4
- 150000002739 metals Chemical class 0.000 abstract description 4
- 238000004132 cross linking Methods 0.000 abstract 1
- 239000011247 coating layer Substances 0.000 description 22
- 239000010410 layer Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000000126 substance Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005007 epoxy-phenolic resin Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011521 glass Substances 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
- 238000010438 heat treatment 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
- 230000001771 impaired effect Effects 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- GALOTNBSUVEISR-UHFFFAOYSA-N molybdenum;silicon Chemical compound [Mo]#[Si] GALOTNBSUVEISR-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 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、金属との密着性に優れた樹脂被覆層が得られ
る下塗り組成物に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an undercoat composition that provides a resin coating layer with excellent adhesion to metal.
(従来の技術)
金属に樹脂を被覆する場合、樹脂の金属に対する密着性
を改良するために1例えば、金属に化成処理を施す方法
がある。(Prior Art) When coating a metal with a resin, there is, for example, a method of subjecting the metal to a chemical conversion treatment in order to improve the adhesion of the resin to the metal.
化成処理には、リン酸亜鉛などが用いられる。Zinc phosphate or the like is used for chemical conversion treatment.
しかし、化成処理により形成された処理層は耐熱性に欠
ける。そのために、化成処理を施した金属表面に樹脂を
被覆した後、焼付は時の加熱により処理層が劣化して、
樹脂と金属との密着性が損なわれる。However, a treated layer formed by chemical conversion treatment lacks heat resistance. For this reason, after coating the metal surface with a chemical conversion treatment with a resin, the treatment layer deteriorates due to the heating during baking.
Adhesion between resin and metal is impaired.
このような欠点を解決するために、下塗り剤を用いて金
属に下塗りを施す方法が提案されている。In order to solve these drawbacks, a method has been proposed in which the metal is undercoated using an undercoat.
特公昭59〜44912号公報には、基材にフッ素樹脂
を被覆するための下塗り組成物として、ポリアミドイミ
ド樹脂やポリイミド樹脂などの有機質プライマーが開示
されている。しかし、これら有機質プライマーは、有機
質のみで構成されるため、金属との線膨張率の差が大き
い。それゆえ、この有機質プライマーで下塗り処理した
後、樹脂を被覆すれば、樹脂と金属との長期間にわたる
密着性が得られない。下塗り組成物として、亜鉛の微粉
化粒子とポリアルキルシリケートのような熱安定性結合
剤との混合物(特開昭49−128836号公報に開示
)や粒状アルミニウム粉末9粒状亜鉛粉末とアルキルシ
リケート縮金物とを含む組成物(特開昭54−2934
0号公報に開示)も知られている。ポリアルキルシリケ
ートなどに金属粉末、特にアルミニウム粉末を添加した
下値り組成物は、フッ素樹脂やポリフェニレンサルファ
イド樹脂と金属との密着性を向上させる。しかし、アル
ミニウムや亜鉛は耐食性、耐水性に欠けるため、樹脂と
金属との持続的な密着性が得られない。金属に代えて、
酸化鉄や酸化チタンなどの金属酸化物を用いても、被覆
層の耐食性は得られるものの、金属との密着性が不充分
である。Japanese Patent Publication No. 59-44912 discloses an organic primer such as a polyamide-imide resin or a polyimide resin as an undercoat composition for coating a substrate with a fluororesin. However, since these organic primers are composed only of organic materials, there is a large difference in coefficient of linear expansion from that of metals. Therefore, if the resin is coated after undercoating with this organic primer, long-term adhesion between the resin and the metal cannot be obtained. As an undercoat composition, a mixture of finely divided particles of zinc and a heat-stable binder such as a polyalkyl silicate (disclosed in JP-A-49-128836), a granular aluminum powder, a 9-granular zinc powder, and an alkyl silicate condensate are used. A composition containing (JP-A-54-2934)
(disclosed in Publication No. 0) is also known. A low price composition in which metal powder, especially aluminum powder, is added to polyalkyl silicate or the like improves the adhesion between fluororesin or polyphenylene sulfide resin and metal. However, since aluminum and zinc lack corrosion resistance and water resistance, lasting adhesion between resin and metal cannot be obtained. Instead of metal,
Even if metal oxides such as iron oxide and titanium oxide are used, the corrosion resistance of the coating layer can be obtained, but the adhesion to the metal is insufficient.
(発明が解決しようとする問題点)
本発明は上記従来の問題点を解決するものであり、その
目的とするところは、金属との密着性に優れた樹脂被覆
が得られる下塗り組成物を提供することにある。(Problems to be Solved by the Invention) The present invention solves the above conventional problems, and its purpose is to provide an undercoat composition that provides a resin coating with excellent adhesion to metal. It's about doing.
(問題点を解決するための手段)
本発明は、従来の下塗り組成物に含有される金属や金属
酸化物に代えて、高ケイ素鋳鉄粉を用いることにより、
金属との密着性に優れ、耐食性。(Means for Solving the Problems) The present invention uses high-silicon cast iron powder in place of the metals and metal oxides contained in conventional undercoating compositions.
Excellent adhesion to metal and corrosion resistance.
耐水性を有する下塗り層が得られ、それにより。A subbing layer with water resistance is thereby obtained.
樹脂と金属との密着性が向上する。との発明者の知見に
もとづいて完成された。Adhesion between resin and metal is improved. It was completed based on the inventor's knowledge.
本発明の下塗り組成物は、金属に樹脂を被覆するための
下塗り組成物であって、高ケイ素鋳鉄粉および結合剤を
含有し、そのことにより上記目的が達成される。The undercoat composition of the present invention is an undercoat composition for coating metal with resin, and contains high silicon cast iron powder and a binder, thereby achieving the above object.
高ケイ素鋳鉄とは、ケイ素を約14〜17%含む鋳鉄で
あり、耐熱性、 Et食性、耐化学薬品性に優れている
。これにモリブデンを約3%含む高ケイ素−モリブテン
鋳鉄も用いられる。高ケイ素鋳鉄の組成は9例えば、下
表に示される。High-silicon cast iron is cast iron containing about 14 to 17% silicon, and has excellent heat resistance, Et corrosion resistance, and chemical resistance. High silicon-molybdenum cast iron containing about 3% molybdenum is also used. The composition of high-silicon cast iron is shown in the table below, for example.
(以下余白) 高ケイ素鋳鉄粉の平均粒径は、0.1〜100μm。(Margin below) The average particle size of the high-silicon cast iron powder is 0.1 to 100 μm.
好ましくは0.5〜20μmの範囲とされる。100μ
mを上まわると、高ケイ素鋳鉄粉の下塗り組成物中での
分散性が低下する。0.1μmを下まわってもかまわな
いが、このような粒径の高ケイ素鋳鉄は。Preferably it is in the range of 0.5 to 20 μm. 100μ
If it exceeds m, the dispersibility of the high-silicon cast iron powder in the undercoat composition decreases. High-silicon cast iron with such a grain size may be less than 0.1 μm.
通常得られない。Usually not available.
結合剤には5例えば、有機系結合剤として、ポリイミド
、ポリアミドイミド、エポキシ樹脂、フェノール樹脂、
ポリエステルなどの架橋性オリゴマー;ポリエーテルサ
ルフォン、ポリサルフォン。The binder may include 5, for example, organic binders such as polyimide, polyamideimide, epoxy resin, phenol resin,
Crosslinkable oligomers such as polyester; polyether sulfone, polysulfone.
ポリパラバン酸、ポリエーテルイミド、ポリエーテルエ
ーテルケトン、ポリフェニレンサルファイド、ナイロン
などの線状高分子;およびフン素樹脂がある。無機系結
合剤には、リチウムポリシリケート、アミンシリケート
、アルキルシリケート。Linear polymers such as polyparabanic acid, polyetherimide, polyetheretherketone, polyphenylene sulfide, and nylon; and fluorine resins. Inorganic binders include lithium polysilicate, amine silicate, and alkyl silicate.
二酸化ケイ素コロイドなどが挙げられる。結合剤には、
金属に被覆される樹脂と同種の樹脂を含むのが好ましい
。例えば、被覆樹脂がフッ素樹脂であれば、結合剤とし
てフッ素樹脂が用いられる。Examples include silicon dioxide colloid. The binder includes
It is preferable that the resin contains the same type of resin as the resin coated on the metal. For example, if the coating resin is a fluororesin, the fluororesin is used as the binder.
高ケイ素鋳鉄粉100重量部に対し、結合剤は15〜9
00重量部、好ましくは25〜400重量部の範囲で含
有される。15重量部を下まわると、下塗り組成物の金
属に対する密着性が低下する。900重1部を上まわる
と、持続的な密着性が得られない。For 100 parts by weight of high-silicon cast iron powder, the amount of binder is 15 to 9
00 parts by weight, preferably in the range of 25 to 400 parts by weight. If the amount is less than 15 parts by weight, the adhesion of the undercoat composition to metal will decrease. If it exceeds 900 parts by weight, lasting adhesion cannot be obtained.
本発明の下塗り組成物は、金属(例えば、鉄。The basecoat composition of the present invention is suitable for use on metals (e.g. iron).
アルミニウム、ステンレス鋼、各種合金)に樹脂を被覆
するための下塗り剤として用いられる。樹脂には2例え
ば、フッ素樹脂、エンプラ、特殊エンプラ、エポキシ樹
脂、フェノール樹脂など上記有機系結合剤に用いられる
樹脂が挙げられる。Used as an undercoat to coat resin on materials (aluminum, stainless steel, various alloys). Examples of the resin include resins used in the above organic binders, such as fluororesins, engineering plastics, special engineering plastics, epoxy resins, and phenolic resins.
この下塗り組成物を用いて1例えば2次のようにして金
属に樹脂が被覆され、被覆金属体が形成される。Using this undercoat composition, a metal is coated with a resin in one, for example, two steps, to form a coated metal body.
金属表面に本発明の下塗り組成物が塗布される。A metal surface is coated with an undercoat composition of the present invention.
塗布面には9次いで焼付けが施され、下塗り層が形成さ
れる。焼付は温度は100〜250℃が好ましい。下塗
り層の層厚は、5〜100μm、好ましくは10〜30
μmの範囲とされる。5μmを下まわると、下塗り層が
均一に形成されず、ピンホールやクラックが発生しやす
い。100μmを上まわると。The coated surface is then baked to form an undercoat layer. The baking temperature is preferably 100 to 250°C. The layer thickness of the undercoat layer is 5 to 100 μm, preferably 10 to 30 μm.
It is assumed to be in the μm range. If it is less than 5 μm, the undercoat layer will not be formed uniformly, and pinholes and cracks will likely occur. When it exceeds 100 μm.
下塗り層と金属との密着性が低下する。下塗り層には、
さらに樹脂が塗布される。塗布面には焼付けが施され、
樹脂被覆層が形成される。被覆層の層厚は50〜200
0μm、好ましくは250〜750 μmの範囲とされ
る。50μmを下まわると、被覆層が均一に形成されず
、ピンホールやクランクが発生しやすい。2000μm
を上まわると、焼付けなどに時間がかかり1発泡などが
生じて緻密な樹脂被覆層が得られない。Adhesion between the undercoat layer and metal decreases. In the undercoat layer,
Further resin is applied. The painted surface is baked,
A resin coating layer is formed. The thickness of the coating layer is 50 to 200
0 μm, preferably in the range of 250 to 750 μm. If it is less than 50 μm, the coating layer will not be formed uniformly and pinholes and cranks will likely occur. 2000μm
If it exceeds this value, it takes time for baking, etc., and foaming occurs, making it impossible to obtain a dense resin coating layer.
このようにして得られた被覆金属体は、化学プラントの
パイプ、容器など耐薬品性を要する材料として、好適に
用いられる。The coated metal body thus obtained is suitably used as a material requiring chemical resistance, such as pipes and containers for chemical plants.
(実施例) 以下に本発明を実施例について述べる。(Example) The present invention will be described below with reference to examples.
尖立尉工
高ケイ素鋳鉄粉(平均粒径40μm以下)20重量部
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(凍結粉砕により平均粒径10μm以下に微粉化
した) 5重量部アミノビスマレイ
ミド樹脂 51!量部N−メチルー2−ピロリ
ドン 10重量部上記処方を配合し、均一に混合
して下塗り組成物を調製した。20 parts by weight Tetrafluoroethylene-hexafluoropropylene copolymer (pulverized to an average particle size of 10 μm or less by freeze-pulverization) 5 parts by weight Amino bismaleimide resin 51 ! Amount N-Methyl-2-pyrrolidone 10 parts by weight The above formulation was blended and mixed uniformly to prepare an undercoat composition.
100龍×100璽臘×31曹の鉄板をグリ・ントフ′
ラスト処理した後、圧縮空気を吹付けて清浄化した。100 dragons x 100 tablets x 31 pieces of iron plate
After the last treatment, compressed air was blown to clean it.
この鉄板に、上記下塗り組成物をハケで塗布し。The above-mentioned undercoat composition was applied to this iron plate with a brush.
塗布面を200℃で1時間、380℃で30分間乾燥。Dry the coated surface at 200°C for 1 hour and at 380°C for 30 minutes.
焼付けした。得られた下塗り層の層厚は平均20μmで
あった。この下塗り層に上記テトラフルオロエチレン−
ヘキサフルオロプロピレンを静電圧60KVで粉体塗装
し、340℃で1時間脱泡した後、水冷して樹脂被覆層
を形成した。被覆層の層厚は平均500μmであった。Baked. The average layer thickness of the obtained undercoat layer was 20 μm. This undercoat layer is coated with the above tetrafluoroethylene.
Hexafluoropropylene was powder coated at an electrostatic voltage of 60 KV, defoamed at 340° C. for 1 hour, and then cooled with water to form a resin coating layer. The average thickness of the coating layer was 500 μm.
得られた被覆金属体の樹脂被覆層と金属との密着性を1
次のようにして評価した。The adhesion between the resin coating layer of the obtained coated metal body and the metal was 1
Evaluation was made as follows.
(11剥離試験
塗膜剥離試験(90°ビ一ル強度試験、 JIS K−
6555)により、常温にて被覆金属体のfJ+離強度
を測定した。その結果、90°剥離強度は1.6kg/
cmであった。(11 Peeling test Paint film peeling test (90° building strength test, JIS K-
6555), the fJ+separation strength of the coated metal body was measured at room temperature. As a result, the 90° peel strength was 1.6 kg/
It was cm.
(2)熱水試験
被覆金属体を95°Cの熱水中に100時間浸漬した後
、被覆層の状態を観察したところ、異状は認められなか
った。(2) Hot water test After the coated metal body was immersed in hot water at 95°C for 100 hours, the state of the coating layer was observed, and no abnormality was observed.
災ル皿l
エチルシリケート”40 (エチルシリケートモノマー
5分子の縮合物、 SiO□として計算される含量は4
0重■%) 100ffl1部およびエチルアルコー
ル40重量部をガラス製反応器に入れ、混合し攪拌しな
がら、 IN塩11121重量部および水9重量部を2
時間かけて連続的に滴下した。滴下終了後、さらに3時
間攪拌した後、20時間放置してエチルシリケート縮合
物溶液を得た。このエチルシリケート縮合物溶液には、
エチルシリケート縮合物が50重量%含有されていた。Disaster dish l Ethyl silicate 40 (Condensation product of 5 molecules of ethyl silicate monomer, content calculated as SiO□ is 4
1 part by weight of IN salt and 40 parts by weight of ethyl alcohol were placed in a glass reactor, and while stirring, 11121 parts by weight of IN salt and 9 parts by weight of water were added.
It was dripped continuously over time. After the dropwise addition was completed, the mixture was stirred for an additional 3 hours and left to stand for 20 hours to obtain an ethylsilicate condensate solution. This ethylsilicate condensate solution contains
It contained 50% by weight of ethylsilicate condensate.
エチルシリケート縮合物溶液 15重量部高ケイ
素鋳鉄粉 40重量部ブチルセルソ
ルブ 5重世部上記処方を配合し混合
して下塗り組成物を得た。Ethyl silicate condensate solution 15 parts by weight High silicon cast iron powder 40 parts by weight Butyl cellosolve 5 parts The above formulations were blended and mixed to obtain an undercoat composition.
この下塗り組成物を用いて、実施例1と同様にして鉄板
上に下塗り層を形成した。ただし、200℃での焼付は
時間は30分間とした。この下塗り層にポリフェニレン
サルファイド樹脂を粉体塗装し。Using this undercoat composition, an undercoat layer was formed on an iron plate in the same manner as in Example 1. However, the baking time at 200°C was 30 minutes. This undercoat layer is powder coated with polyphenylene sulfide resin.
380℃で40分間焼成した後、水冷して樹脂波ri層
を形成した。被覆層の層厚は500μmであった。After baking at 380° C. for 40 minutes, it was cooled with water to form a resin corrugated layer. The layer thickness of the coating layer was 500 μm.
得られた被覆金属体の樹脂被覆層と金属との密着性を、
実施例1と同様の方法により評価したところ、剥離強度
は3.5kg/cmであり、熱水試験では異状は認めら
れなかった。The adhesion between the resin coating layer of the obtained coated metal body and the metal was determined by
When evaluated using the same method as in Example 1, the peel strength was 3.5 kg/cm, and no abnormalities were observed in the hot water test.
止較更土
下塗り組成物に高ケイ素鋳鉄粉を用いなかったこと以外
は、実施例1と同様の方法により被覆金属体を形成した
。A coated metal body was formed in the same manner as in Example 1, except that high-silicon cast iron powder was not used in the undercoating composition.
得られた被覆金属体の樹脂被覆層と金属との密着性を、
実施例1と同様の方法により評価したところ、剥離強度
は1.3kg/cn+であり、熱水試験では一部ブリス
ターが発生した。The adhesion between the resin coating layer of the obtained coated metal body and the metal was determined by
When evaluated by the same method as in Example 1, the peel strength was 1.3 kg/cn+, and some blisters occurred in the hot water test.
土較貫主
下塗り組成物に、高ケイ素鋳鉄粉に代えて酸化チタンを
5重量部配合したこと以外は、実施例1と同様の方法に
より被覆金属体を形成した。A coated metal body was formed in the same manner as in Example 1, except that 5 parts by weight of titanium oxide was added to the base coating composition in place of the high-silicon cast iron powder.
得られた被覆金属体の樹脂被覆層と金属との密着性を、
実施例1と同様の方法により評価したところ、剥離強度
は1.2kg/cmであり、熱水試験では一部ブリスタ
ーが発生した。The adhesion between the resin coating layer of the obtained coated metal body and the metal was determined by
When evaluated by the same method as in Example 1, the peel strength was 1.2 kg/cm, and some blisters occurred in the hot water test.
ル較±1
下塗り組成物に、高ケイ素鋳鉄粉に代えてアルミニウム
粉末(平均粒径10〜20μm)を10ififf1部
を配合したこと以外は、実施例1と同様の方法により被
覆金属体を形成した。Comparison ±1 A coated metal body was formed in the same manner as in Example 1, except that 10ififf 1 part of aluminum powder (average particle size 10 to 20 μm) was added to the undercoat composition in place of the high-silicon cast iron powder. .
得られた被覆金属体の樹脂被覆層と金属との密着性を、
実施例1と同様の方法により評価したところ、剥離強度
は1 、6 kg / anであり、熱水試験では一部
ブリスターが発生した。The adhesion between the resin coating layer of the obtained coated metal body and the metal was determined by
When evaluated by the same method as in Example 1, the peel strength was 1.6 kg/an, and some blisters occurred in the hot water test.
ル較■↓
下塗り組成物を用いず、鉄板をリン酸溶液により処理し
たこと以外は、実施例2と同様の方法により被IW金属
体を形成した。Comparison ■↓ An IW metal body was formed in the same manner as in Example 2, except that the iron plate was treated with a phosphoric acid solution without using an undercoat composition.
得られた被覆金属体の樹脂被覆層と金属との密着性を、
実施例1と同様の方法により評価したところ、剥離強度
は2 、 Okg / amであり、熱水試験では一部
に被覆層の剥離が生じた。The adhesion between the resin coating layer of the obtained coated metal body and the metal was determined by
When evaluated by the same method as in Example 1, the peel strength was 2.0 kg/am, and peeling of the coating layer occurred in some parts in the hot water test.
実施例および比較例から明らかなように1本発明の下塗
り組成物によれば、樹脂被覆層と金属との密着性に優れ
た被覆金属体が得られる。この被覆金属体は、剥離試験
や熱水試験でも、被覆層の剥離やブリスターの発生がな
い。高ケイ素鋳鉄粉を含有しない下塗り組成物や高ケイ
素鋳鉄粉に代えて金属粉末や金属酸化物を含有する下塗
り組成物を用いて形成された被覆金属体は、樹脂被覆層
の剥離強度に欠け、熱水試験ではブリスターが発生する
。リン酸塩処理により得られた従来の被覆金属体も樹脂
被覆層の剥離強度が低く、熱水試験では被覆層が一部剥
離する。As is clear from the Examples and Comparative Examples, according to the undercoat composition of the present invention, a coated metal body with excellent adhesion between the resin coating layer and the metal can be obtained. This coated metal body does not peel off the coating layer or generate blisters even in peel tests and hot water tests. A coated metal body formed using an undercoat composition that does not contain high-silicon cast iron powder or an undercoat composition that contains metal powder or metal oxide instead of high-silicon cast iron powder lacks the peel strength of the resin coating layer. Blisters occur during hot water tests. Conventional coated metal bodies obtained by phosphate treatment also have low peel strength of the resin coating layer, and part of the coating layer peels off in a hot water test.
(発明の効果)
本発明の下塗り組成物は、このように、高ケイ素鋳鉄粉
を含有するため、金属との密着性が良好である。それゆ
え、この下塗り組成物を下塗り剤とてして、金属表面に
樹脂を被覆すれば、樹脂と金属との密着性に優れた被覆
金属体が得られる。(Effects of the Invention) Since the undercoat composition of the present invention contains high-silicon cast iron powder as described above, it has good adhesion to metal. Therefore, by coating a metal surface with a resin using this undercoat composition as an undercoat, a coated metal body with excellent adhesion between the resin and the metal can be obtained.
この被覆金属体は化学プラントのパイプ、容器など耐薬
品性を要する材料として、好適に用いられる。This coated metal body is suitably used as a material that requires chemical resistance, such as pipes and containers for chemical plants.
以上
出願人 高性能樹脂新製造技術研究組合理事長 安井
昭夫Applicant: Akio Yasui, Chairman of the High Performance Resin New Manufacturing Technology Research Association
Claims (1)
、 高ケイ素鋳鉄粉および結合剤を含有する下塗り組成物。 2、前記結合剤が、ポリイミド、ポリアミドイミド、エ
ポキシ樹脂、フェノール樹脂、ポリエステルなどの架橋
性オリゴマー;ポリエーテルサルフォン、ポリサルフォ
ン、ポリパラバン酸、ポリエーテルイミド、ポリエーテ
ルエーテルケトン、ポリフェニレンサルファイド、ナイ
ロンなどの線状高分子;およびフッ素樹脂のうちの少な
くとも一種の有機系結合剤および/またはリチウムポリ
シリケート、アミンシリケート、アルキルシリケートお
よび二酸化ケイ素コロイドのうちの少なくとも一種の無
機系結合剤である特許請求の範囲第1項に記載の下塗り
組成物。 3、前記高ケイ素鋳鉄粉100重量部に対し、前記結合
剤が15〜900重量部の範囲で含有された特許請求の
範囲第1項に記載の下塗り組成物。 4、前記樹脂がポリエーテルサルフォン、ポリサルフォ
ン、ポリパラバン酸、ポリエーテルイミド、ポリエーテ
ルエーテルケトン、ポリフェニレンサルファイド、ナイ
ロンなどの線状高分子;およびフッ素樹脂のうちの少な
くとも一種の樹脂であって結合剤に含まれるものと同一
の樹脂である特許請求の範囲第1項に記載の下塗り組成
物。[Scope of Claims] 1. An undercoat composition for coating metal with a resin, the undercoat composition containing high-silicon cast iron powder and a binder. 2. The binder is a crosslinkable oligomer such as polyimide, polyamideimide, epoxy resin, phenol resin, polyester; polyethersulfone, polysulfone, polyparabanic acid, polyetherimide, polyetheretherketone, polyphenylene sulfide, nylon, etc. A linear polymer; and at least one organic binder selected from fluororesin and/or at least one inorganic binder selected from lithium polysilicate, amine silicate, alkyl silicate, and silicon dioxide colloid. The undercoat composition according to item 1. 3. The undercoat composition according to claim 1, wherein the binder is contained in an amount of 15 to 900 parts by weight based on 100 parts by weight of the high-silicon cast iron powder. 4. The resin is at least one of linear polymers such as polyethersulfone, polysulfone, polyparabanic acid, polyetherimide, polyetheretherketone, polyphenylene sulfide, and nylon; and a fluororesin, and is a binder. The undercoat composition according to claim 1, which is the same resin as that contained in the undercoat composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23079286A JPH0625316B2 (en) | 1986-09-29 | 1986-09-29 | Undercoat composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23079286A JPH0625316B2 (en) | 1986-09-29 | 1986-09-29 | Undercoat composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6383176A true JPS6383176A (en) | 1988-04-13 |
JPH0625316B2 JPH0625316B2 (en) | 1994-04-06 |
Family
ID=16913338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23079286A Expired - Lifetime JPH0625316B2 (en) | 1986-09-29 | 1986-09-29 | Undercoat composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0625316B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005007756A1 (en) * | 2003-05-21 | 2005-01-27 | Hitachi Chemical Co., Ltd. | Primer, conductor foil with resin, laminate and process for producing the laminate |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100896913B1 (en) * | 2007-06-15 | 2009-05-12 | 그린닉스주식회사 | A composition of painting and varnishing for metal coating and forming method for coating layer |
-
1986
- 1986-09-29 JP JP23079286A patent/JPH0625316B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005007756A1 (en) * | 2003-05-21 | 2005-01-27 | Hitachi Chemical Co., Ltd. | Primer, conductor foil with resin, laminate and process for producing the laminate |
US7648770B2 (en) | 2003-05-21 | 2010-01-19 | Hitachi Chemical Company, Ltd. | Primer, conductor foil with resin, laminated sheet and method of manufacturing laminated sheet |
US8507100B2 (en) | 2003-05-21 | 2013-08-13 | Hitachi Chemical Company, Ltd. | Primer, conductor foil with resin, laminated sheet and method of manufacturing laminated sheet |
Also Published As
Publication number | Publication date |
---|---|
JPH0625316B2 (en) | 1994-04-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4177320A (en) | Article coated with fluorocarbon polymer | |
US4179542A (en) | Synergistic primer for fluoropolymer coatings | |
US4143204A (en) | Articles coated with fluorocarbon resins | |
US5626907A (en) | Process for coating metal surfaces with a fluororesin using a primer | |
JPS6035379B2 (en) | coating composition | |
JPS6011756B2 (en) | Fluoropolymer coating composition | |
JPS6035381B2 (en) | Fluorocarbon primer composition | |
EP0343282B1 (en) | An undercoat composition and a metal substrate coated with a resin composition | |
CN113604114A (en) | Fluororesin powder coating composition with high corrosion resistance | |
EP0043862B1 (en) | Composition for coating fluoroplastics | |
US5670010A (en) | Process for adhering a fluororesin film to a metal surface using a primer | |
JPH11510544A (en) | Permeation resistant ETFE composition and coating | |
JPS6383176A (en) | Primer composition | |
JPS63304068A (en) | Undercoating composition | |
US4965102A (en) | Method for coating a metal substrate by the use of a resin composition | |
JPS6010547B2 (en) | Polyphenylene sulfide composition | |
JPS63251477A (en) | Primer composition | |
JPS6383177A (en) | Primer composition | |
JPH01278556A (en) | Primer composition | |
JPH0292536A (en) | Coated metallic sheet | |
JPH01278580A (en) | Under-coating composition | |
JPH01280547A (en) | Resin coated metallic body | |
JPH05295300A (en) | Powder-coating composition composed of polyphenylene sulfide resin | |
JPS5944912B2 (en) | Fluorine resin coating method | |
JPH0684059B2 (en) | Resin coated metal body |