JPS6399275A - Undercoating composition - Google Patents
Undercoating compositionInfo
- Publication number
- JPS6399275A JPS6399275A JP24618486A JP24618486A JPS6399275A JP S6399275 A JPS6399275 A JP S6399275A JP 24618486 A JP24618486 A JP 24618486A JP 24618486 A JP24618486 A JP 24618486A JP S6399275 A JPS6399275 A JP S6399275A
- Authority
- JP
- Japan
- Prior art keywords
- coating film
- water
- coating
- resin
- soluble
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title abstract description 18
- 238000000576 coating method Methods 0.000 claims abstract description 59
- 239000011248 coating agent Substances 0.000 claims abstract description 58
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 12
- 239000000463 material Substances 0.000 claims abstract description 3
- 229920005989 resin Polymers 0.000 abstract description 15
- 239000011347 resin Substances 0.000 abstract description 15
- 239000000853 adhesive Substances 0.000 abstract description 9
- 230000001070 adhesive effect Effects 0.000 abstract description 9
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract description 4
- 229920000180 alkyd Polymers 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 229910021529 ammonia Inorganic materials 0.000 abstract description 2
- 150000007514 bases Chemical class 0.000 abstract description 2
- 239000006185 dispersion Substances 0.000 abstract description 2
- 230000003472 neutralizing effect Effects 0.000 abstract description 2
- 230000001105 regulatory effect Effects 0.000 abstract 2
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 description 25
- 238000012360 testing method Methods 0.000 description 11
- 229910000831 Steel Inorganic materials 0.000 description 8
- 239000008199 coating composition Substances 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- 238000010422 painting Methods 0.000 description 7
- 239000000049 pigment Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- -1 ammonia Chemical class 0.000 description 4
- 238000007591 painting process Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002987 primer (paints) Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000009503 electrostatic coating Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000005028 tinplate Substances 0.000 description 2
- 239000004908 Emulsion polymer Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、工業用塗装ラインなどで被塗物を吊り下げも
しくは載せたりするハンガーや台車など(以下、「ハン
ガーなど」と略称する)の腐食を防止し、しかも該塗装
ラインの塗装工程でハンガーなどに付着した塗料を容易
に剥離することができる下塗塗料組成物に間する。DETAILED DESCRIPTION OF THE INVENTION The present invention prevents corrosion of hangers, carts, etc. (hereinafter abbreviated as "hangers, etc.") on which objects to be coated are hung or placed on industrial painting lines, etc. To provide an undercoat paint composition capable of easily peeling off paint adhering to a hanger or the like during the painting process of a painting line.
工業用塗装ラインなどにおける塗装工程は、通常、被塗
物を、ハンガーなどに吊り下げもしくは載せたりなどし
た状態で表面処理−塗装(例えば電着塗装、静電塗装、
スプレー塗装、浸漬塗装などによる下、中、上塗り塗装
)−乾燥(焼付)の各工程を順次搬送した後、被塗物を
ハンガーなどから取りはずし1次いでこのハンガーなど
に新たな被塗物を取りつけて再び上記の工程を循環する
。したがって、このような塗装ラインでは、ハンガーな
どは繰り返して使用され、塗装−乾燥工程を多数回循環
するので、これらのハンガーなどには塗料が塗着しそれ
が次第に蓄積され、その厚さは3〜4mm以上にも達す
るので、定期的に剥離除去する必要がある。In the painting process in industrial painting lines, etc., the object to be coated is usually suspended or mounted on a hanger, etc., and subjected to surface treatment and painting (e.g. electrodeposition coating, electrostatic coating, etc.).
After sequentially transporting each process of bottom, middle, and top coating (spray painting, dipping, etc.) and drying (baking), the object to be coated is removed from a hanger, etc., and then a new object is attached to this hanger, etc. The above steps are repeated again. Therefore, in such a painting line, hangers and the like are used repeatedly and the painting-drying process is cycled many times, so paint is coated on these hangers and gradually accumulates, and the thickness of the paint increases to 3. Since it can reach up to 4 mm or more, it is necessary to peel and remove it periodically.
従来、ハンガーなどに塗着した肉厚な塗膜は、ハンマー
やヘラなどで削り取ったり、ショツトブラストなどで衝
撃剥離していたが、密着性がすぐれているために容易に
剥離することができない。Traditionally, thick coatings applied to hangers and the like have been scraped off with a hammer or spatula, or removed by shock blasting, but because of their excellent adhesion, they cannot be removed easily.
また、ハンガーなどは、使用前もしくは塗膜剥離してか
ら放置しておくとサビが発生し、腐食が進行して強度な
どを低下させることがある。Additionally, if hangers and the like are left unused before use or after the coating has been peeled off, rust may develop and corrosion may progress, reducing strength.
そこで、本発明者等は、ハンガーなどに塗着した上記の
ごとく肉厚の塗膜を容易に剥離除去することができ、し
かもサビの発生を防止するのに有用な塗膜を形成する下
塗塗料M1成物の開発を目的に研究を行なった結果、特
定範囲の軟化点と数モ均分子量を有する熱可塑性の水溶
性樹脂又は水分n!I性樹脂を主成分とする水性下塗塗
料組成物によって形成される塗膜が上記性能を有するこ
と、加えて有機溶剤を全くもしくは殆ど使用しないので
火災の心配がなく、人体への衛生面にも好ましい無公害
システムであることから本発明を完成するに至った。Therefore, the present inventors have developed an undercoat that can be easily peeled off and removed from the above-mentioned thick coating film applied to hangers, etc., and that also forms a coating film that is useful for preventing the occurrence of rust. As a result of research aimed at developing M1 products, we found that thermoplastic water-soluble resins or water n! The coating film formed by the water-based undercoating paint composition containing I resin as the main component has the above performance, and in addition, since no or almost no organic solvents are used, there is no risk of fire, and it is also hygienic for the human body. The present invention was completed because it is a preferable pollution-free system.
すなわち、本発明は軟化点50〜300°Cで。That is, the present invention has a softening point of 50 to 300°C.
かつ数平均分子量500〜500.000である水溶性
もしくは水分散性の熱可塑性樹脂を主成分とし、しかも
形成塗膜の被塗面に対する付着力を0 、01〜15k
g/cm2.塗膜伸び率を1%(20’Cり以下に調整
してなる下地塗料組成物に関する。The main component is a water-soluble or water-dispersible thermoplastic resin with a number average molecular weight of 500 to 500.000, and the adhesion of the formed coating to the coated surface is 0.01 to 15k.
g/cm2. It relates to a base coating composition whose coating film elongation is adjusted to 1% (20'C) or less.
本発明において、水溶性又は水分散性樹脂を用いること
は、有機溶剤を用いる場合と比べ火災の危険、人体への
衛生上の問題、省資源、大気汚染等の問題点を一気に解
決できるメリットを持っている。In the present invention, the use of a water-soluble or water-dispersible resin has the advantage of solving problems such as fire danger, human hygiene problems, resource conservation, and air pollution at once compared to the use of organic solvents. have.
本発明において、上記熱可塑性樹脂は、軟化点が50〜
300℃、好ましくは80〜250°Cで、かつ数平均
分子量が500〜500,000゜好ましくは10,0
00〜450.000の範囲内であって、しかも加熱な
どによって、三次元に架橋硬化反応しない樹脂である。In the present invention, the thermoplastic resin has a softening point of 50 to
300°C, preferably 80 to 250°C, and a number average molecular weight of 500 to 500,000°, preferably 10.0°C.
00 to 450.000, and is a resin that does not undergo a three-dimensional crosslinking and curing reaction by heating or the like.
したがって、該樹脂は、水酸基、カルボキシル基、エポ
キシ基およびアミ7基などの官能基を全くもしくは殆ど
有さない非官能性樹脂またはこれらの官能基を含有して
も他の樹脂や架橋剤などと硬化反応しなければ熱可塑性
樹脂として使用できる。Therefore, the resin is a non-functional resin that has no or almost no functional groups such as hydroxyl groups, carboxyl groups, epoxy groups, and amide groups, or even if it contains these functional groups, it cannot be mixed with other resins or crosslinking agents. If there is no curing reaction, it can be used as a thermoplastic resin.
熱可塑性樹脂において、軟化点が50’Cより低くなる
と形成塗膜が粘着性を帯び、300″Cより高くなると
塗膜が硬質になり、いずれも塗着塗膜の剥離性が低下す
るので好ましくない。また、数平均分子賃が500より
小さくなると塗膜が著しく脆くなって、特に低温度雰囲
気(10℃以下)においてわずかの振動をゲえただけで
塗膜が自然落下し、さらにサビ防止性も十分でなく。In thermoplastic resins, if the softening point is lower than 50'C, the formed coating film becomes sticky, and if it is higher than 300'C, the coating film becomes hard, which is preferable because the releasability of the applied coating film decreases. In addition, if the number average molecular weight is less than 500, the coating film becomes extremely brittle, and the coating film will naturally fall off even with the slightest vibration, especially in a low-temperature atmosphere (below 10°C), and the rust prevention properties will deteriorate. Not enough.
500.000よりも高くなると塗膜の可撓性および耐
衝撃性が強くなって可剥性塗料として使用出来ず、水溶
化、水分散化が困難となるなどの欠点が生じるので好ま
しくない。If it is higher than 500.000, the flexibility and impact resistance of the coating film will become too strong, making it impossible to use it as a peelable coating material, and disadvantages such as difficulty in water solubilization and water dispersion will occur, which is not preferable.
本発明で用いる軟化点が50〜300℃で、しかも数モ
均分子量が500〜500,000である熱可塑性樹脂
の水溶液もしくは水分散液における該熱可塑性樹脂は、
加熱もしくは反応によって、架橋硬化せず、溶媒である
水が揮発することで塗膜を形成する樹脂で、例えば次に
列挙するものが好ましい。The thermoplastic resin used in the present invention has a softening point of 50 to 300°C and a number average molecular weight of 500 to 500,000.
Preferred are resins that do not undergo cross-linking and hardening upon heating or reaction and form a coating film by volatilization of water as a solvent, such as those listed below.
■ カルボキシル基を導入した樹脂(例えば。■Resins with carboxyl groups introduced (for example.
アルキド樹脂、ポリエステル樹脂、エポキシ樹脂、ウレ
タン樹脂、アクリル樹脂など)を塩基性化合物(例えば
、アンモニア、各種アミン類、カセイカリ、カセイソー
ダなど)で中和して、水溶化もしくは水分散化した熱可
塑性樹脂。Thermoplastic resins made by neutralizing alkyd resins, polyester resins, epoxy resins, urethane resins, acrylic resins, etc.) with basic compounds (e.g., ammonia, various amines, caustic potash, caustic soda, etc.) and making them water-soluble or water-dispersed. .
・′■ フェノールホルムアルデヒド初期縮合物および
メラミンホルムアルデヒド初期縮合物などの水溶性メチ
ルエーテル化物。・′■ Water-soluble methyl etherified products such as phenol formaldehyde initial condensates and melamine formaldehyde initial condensates.
■ 乳化重合体液もしくは適当な界面活性剤や保護コロ
イドの存在下で高分子微粒子(粒径0.1〜5ル)を懸
濁した液で、これらの重合体もしくは高分子微粒子とし
て、ポリ酢酸ビニル、スチレン−ブタジェン共重合体、
塩化ビニル−塩化ビニリデン共重合体、アクリル系重合
体、スチレン−アクリロニトリル共重合体などが好適で
ある。■ An emulsion polymer liquid or a liquid in which fine polymer particles (particle size 0.1 to 5 l) are suspended in the presence of an appropriate surfactant or protective colloid. , styrene-butadiene copolymer,
Suitable examples include vinyl chloride-vinylidene chloride copolymers, acrylic polymers, and styrene-acrylonitrile copolymers.
■ 水溶性のセルロースやデンプン。■ Water-soluble cellulose and starch.
■ 水溶性もしくは水分散性のポリビニルアルコール、
ポリアクリル酸ソーダ、ポリエチレンオキシドなど。■ Water-soluble or water-dispersible polyvinyl alcohol,
Sodium polyacrylate, polyethylene oxide, etc.
これらは、1種もしくは2種以上併用することができる
が、併用することによってそれらが架橋硬化反応する組
合わせは避けるべきである。特に好ましくは上記■、(
少および〆少から選ばれた樹脂である。These can be used alone or in combination, but combinations in which crosslinking and curing reactions occur when used together should be avoided. Particularly preferably, the above ■, (
Resin selected from Sho and Shima Sho.
本発明の下塗塗料組成物は、上記熱可塑性樹脂を木に溶
解もしくは分散せしめることによって得られるが、さら
に、顔料、ハジキ防止剤、沈降防止剤などを必要に応じ
て配合できる。The base coating composition of the present invention is obtained by dissolving or dispersing the thermoplastic resin in wood, and may further contain pigments, anti-cissing agents, anti-settling agents, etc., as required.
顔料としてはタンカル、シリカ、バリタ、クレーシリカ
などの体質顔料、チタン白、カーボンブラックなどの着
色顔料、クロム酸鉛などの防錆顔料などを配合すること
ができ、その配合量は、熱可塑性樹脂100重量部あた
り、500重量部以下、特に100〜350重量部が好
ましい、ハジキ防止剤としては1例えばシリコーン系、
アクリルエステル系など、沈降防止剤として例えば、ア
クリル樹脂、耐化ポリエチレン、アマイド系ワックス、
モンモリナイトアミン誘導体などがあげられる。Pigments that can be blended include extender pigments such as tancal, silica, barita, and clay silica, coloring pigments such as titanium white and carbon black, and rust preventive pigments such as lead chromate. The amount of the anti-cissing agent is preferably 500 parts by weight or less, particularly 100 to 350 parts by weight, such as silicone-based,
Acrylic resins, anti-settling agents such as acrylic esters, anti-settling polyethylene, amide waxes,
Examples include montmorinite amine derivatives.
本発明の下塗塗料組成物は、固形分含有率を約40〜9
0重量%、好ましくは50〜85重量%に調整し、スプ
レー塗装、ハケ塗り、浸漬塗装。The base coating composition of the present invention has a solids content of about 40 to 9
Adjust to 0% by weight, preferably 50 to 85% by weight, and apply spray coating, brush coating, or dip coating.
静電塗装、流し塗りなどによって塗装することが好まし
い、塗装膜厚は、特に制限されないが、乾燥塗膜に基づ
いて、20g以上、特に60〜120pの範囲が好まし
い、塗膜の乾燥は、組成に応じて任意に採択でき、常温
もしくは100℃以下の強制乾燥、または、100℃以
上で加熱溶融してもさしつかえない。It is preferable to apply the coating by electrostatic coating, flow coating, etc. The coating film thickness is not particularly limited, but is preferably 20 g or more, especially in the range of 60 to 120 p, based on the dry coating film. It can be arbitrarily adopted depending on the situation, and forced drying at room temperature or below 100°C, or heating and melting at above 100°C is also acceptable.
本発明の下塗塗料組成物に関し、さらに形成塗膜の被塗
物(ハンガーなど)に対する付着力が0 、01〜15
kg/c+w2.好ましくは0.05〜5kg/Cl1
12で、しかも形成塗膜の伸び率を20°Cにおいて1
%以下にする必要がある。形成塗膜の付着力および伸び
率は上記熱可塑性樹脂の組成と分子量および顔料の組成
と配合量などを組み合わせることによって任意に調整で
きる。そして、本発明において形成塗膜の付着力および
伸び率の測定は次の方法で行なった。Regarding the primer coating composition of the present invention, the adhesive strength of the formed coating film to the coated object (hanger, etc.) is 0, 01 to 15.
kg/c+w2. Preferably 0.05 to 5 kg/Cl1
12, and the elongation rate of the formed coating film is 1 at 20°C.
% or less. The adhesion and elongation rate of the formed coating film can be arbitrarily adjusted by combining the composition and molecular weight of the thermoplastic resin, the composition and blending amount of the pigment, etc. In the present invention, the adhesion and elongation of the formed coating film were measured by the following method.
付着力は、下塗塗料をダル鋼板(大きさ0.8X100
X100mm)に膜厚が形成塗膜に基づいて60μにな
るように塗装し、100℃−1O′以上に加熱して塗膜
を成形させたものを試験板とする0次に、この試験板の
塗膜面に付着力測定用アタッチメントの接着面(広さ4
X4cm)を2液型工ポキシ樹脂系接着剤で接合固着さ
せた後、20℃において、該試験板を固定してから上記
アタッチメントをショツパ一式引張試験機を用いて50
am/分の速さで引張り、上記塗膜がダル鋼板から剥離
させるに要した最小の力を付着力とした。単位はkg/
c+s”である。For adhesion, apply the primer paint to a dull steel plate (size 0.8 x 100
x100mm) to a film thickness of 60μ based on the formed coating film, and heated to 100℃-1O' or more to form a coating film. The adhesive surface of the attachment for adhesion measurement (width 4
After bonding and fixing the test plate (x4cm) with a two-component poxy resin adhesive, the test plate was fixed at 20°C, and then the above attachment was tested at 50°C using a Schoppa complete tensile tester.
The adhesion force was defined as the minimum force required to peel the coating film from the dull steel plate by pulling at a speed of am/min. The unit is kg/
c+s".
伸び率は、ブリキ板に下塗塗料を形成塗膜で501Lに
なるように塗装し加熱した後、長さ60mm、巾5mr
mの長方形にカッターで切り込みを入れ、水銀を用いて
塗膜を剥離し、この塗膜を用いてTENSILON
UTM−11−20(ToYo BALDWINCo、
、 LTD)で20℃における伸び率を測定した。The elongation rate is determined by applying an undercoat to a tin plate, painting it to a coating film of 501L, and heating it to a length of 60mm and a width of 5mm.
Make a cut in the m rectangle with a cutter, peel off the coating using mercury, and use this coating to create TENSILON.
UTM-11-20 (ToYo BALDWINCo,
, LTD) and measured the elongation rate at 20°C.
本発明において、形成塗膜の付着力が0.01kg/c
rrr2より小さくなると、塗膜が臆すごて、わずかの
振動を与えただけで塗膜が自然落下し、−力付着力が1
5 kg/ cm2より、伸び率が1%よりそれぞれ多
くなると、可瀾性が低下するのでいずれも好ましくない
。In the present invention, the adhesive force of the formed coating film is 0.01 kg/c
If it becomes smaller than rrr2, the coating film becomes unstable and falls off by itself even with the slightest vibration, and the -force adhesion force becomes 1.
If the elongation rate exceeds 5 kg/cm2 or 1%, both are unfavorable because the shearability decreases.
本発明の下地塗料組成物をハンガーなどの金属製基体に
塗装しておくと該基体の発錆を防止することができる。When the base coating composition of the present invention is applied to a metal substrate such as a hanger, rusting of the substrate can be prevented.
さらに形成塗膜は伸び率およびたわみ性が小さく、付着
性も上記範囲内に調製しであるので、ハンガーなどに塗
装工程前にあらかじめ塗装しておくと、塗装工程におい
て該ハンガーなどに塗着した塗料はハンマーなどで軽く
衝撃を与えるだけで小片状にボロボロと本発明の塗料組
成物の塗膜と共に剥離除去することができ、この!A1
1lI作業は従来の一時保護塗料(ストリッパブルペイ
ント)に比べて著しく簡素化された。さらに、本発明に
よる下塗塗料組成物の形成塗膜は。Furthermore, the formed coating film has a small elongation rate and flexibility, and the adhesion has to be adjusted within the above range, so if you apply the coating to the hanger, etc. before the painting process, it will be easier to coat the hanger etc. during the painting process. The paint can be peeled off and removed together with the coating film of the paint composition of the present invention in small pieces by simply giving it a light impact with a hammer or the like. A1
The 1lI operation is significantly simplified compared to conventional temporary protective paints (strippable paints). Furthermore, the coating film formed by the base coating composition according to the present invention.
環境温度が10℃よりも低温になってもヒビ、ワレ、ハ
ガレなどの発生が全く認められず、寒冷地域における塗
装ラインなどにも十分に適用できる。Even when the environmental temperature is lower than 10°C, no cracks, cracks, or peeling are observed, making it suitable for painting lines in cold regions.
本発明の塗料組成物は、金属、プラスチック、ガラス、
木、無機材料、ゴム、既塗装面などに塗装することがで
きる。The coating composition of the present invention can be applied to metals, plastics, glass,
It can be applied to wood, inorganic materials, rubber, pre-painted surfaces, etc.
次に、本発明に関する実施例および比較例を説明する。Next, examples and comparative examples related to the present invention will be described.
工 実施例および比較例
第1表に示した成分を混合、分散せしめて木発明が目的
とする塗料組成物を製造した。EXAMPLES EXAMPLES AND COMPARATIVE EXAMPLES The components shown in Table 1 were mixed and dispersed to produce a coating composition aimed at by the Wood Invention.
第 1 表
(11)熱可塑性樹脂
該樹脂の組成および物性値は@2表のとおりである。配
合量はすべて樹脂固形分である。Table 1 (11) Thermoplastic resin The composition and physical properties of the resin are as shown in @Table 2. All amounts are based on resin solid content.
(零2)ハジキ防止剤ニ
アロンS−4002(東亜合成補装)
(13)消泡剤:
アンチホームB−748(旭電化株製)II 性能試
験結果
黒皮鋼板(大きさ100100X300X2を#400
サンドペーパーで研磨し、トルエンで脱脂後、上記第1
表の下塗塗料組成物をハケで乾燥膜厚にもとすいて70
終になるように塗装し、室温で24時間放置して塗膜を
乾燥させた。(02) Anti-cissing agent Nearon S-4002 (Toagosei Hoso) (13) Antifoaming agent: Antiform B-748 (manufactured by Asahi Denka Co., Ltd.) II Performance test results Black skin steel plate (size 100100X300X2 #400
After polishing with sandpaper and degreasing with toluene,
Brush the undercoat paint composition on the surface to a dry film thickness of 70.
The coating film was dried by leaving it at room temperature for 24 hours.
次に、この塗装鋼板に、アミラックTP26(アミン赤
アルキド樹脂系中塗塗料、関西ペイント補装)を硬化塗
膜にもとずいて40pになるようにスプレー塗装し、1
40℃で20分間焼付けた後、アミラック白(アミン・
アルキド樹脂系上塗塗料、関西ペイント■)をスプレー
塗装し、140°Cで30分間焼付けた(膜厚40p)
、そして、さらに、これらのアミラックTP26および
−に塗り塗料を上記のごとく塗装、焼伺けて順次塗り重
ね、合計で30回くり返して塗装した。Next, on this painted steel plate, Amirac TP26 (amine red alkyd resin intermediate coating paint, Kansai Paint Repair) was spray-painted to a thickness of 40p based on the cured coating.
After baking at 40℃ for 20 minutes, Amylac white (Amine・
Spray coated with alkyd resin top coat (Kansai Paint) and baked at 140°C for 30 minutes (film thickness 40p)
, and furthermore, these Amirac TP26 and - were coated with the paint as described above, and after baking, the coating was repeated one after another, and the coating was repeated 30 times in total.
中塗り塗膜および上塗り塗膜の合計塗膜厚は約1600
gであった。The total thickness of the intermediate coat and top coat is approximately 1,600 mm.
It was g.
このように塗装して得た試験板を用いて、下塗塗料組成
物の各種性能を調べた。その結果第3表に示した。Using the test plates thus coated, various performances of the undercoat composition were investigated. The results are shown in Table 3.
上記塗装系は、すでに下塗塗料組成物を塗装した被塗物
を台車に載せ、中塗および上塗りを塗装する工程を想定
したものであり、黒皮鋼板は台車もしくはハンガーに見
立てている。The above coating system assumes a process in which an object to be coated, which has already been coated with an undercoat paint composition, is placed on a trolley and an intermediate coat and a top coat are applied, and the black-skinned steel plate is likened to a trolley or a hanger.
第3表において。In Table 3.
(jl) 付着カニ第1表記載の塗料組成物をダル鋼
板(大きさ0.8X100X100ma)に膜厚が乾燥
塗膜にもとすいてSopになるように塗装し、常温で2
0時間乾燥させて試験板とする6次に、この試験板の塗
膜面に付着力測定用のアタッチメントの接着面(広さ4
X 4 cm)を2液型工ポキシ樹脂系接着剤で接合
固着させた後、20℃において、該試験板を固定してか
ら一ヒ記アタッチメントをショツパ一式引張試験機を用
いて50am/分の速さで引張り、上記塗膜がダル鋼板
から召蕩させるに要した最小の力を付着力とした。単位
はkg/Cm2である。(jl) Adhesive Crab The coating composition listed in Table 1 was applied to a dull steel plate (size: 0.8 x 100 x 100 ma) so that the film thickness was equal to that of the dry coating, and the paint composition was coated with the paint composition listed in Table 1 at room temperature.
Dry for 0 hours to obtain a test plate. 6 Next, attach the adhesive surface of the attachment for adhesion measurement (width 4
x 4 cm) with a two-component poxy resin adhesive, fix the test plate at 20°C, and then test the test plate with the above attachment at 50 am/min using a Schottspa tensile tester. The adhesion force was defined as the minimum force required for the coating film to separate from the dull steel plate. The unit is kg/Cm2.
C第2) 伸び率:ブリキ板に下塗塗料を形成塗膜で
50pになるように塗装し100℃−15分加熱した後
、長さ601℃m、巾5■の長方形にカッターで切り込
みを入れ、水銀を用いて塗膜を剥離し、この塗膜を用い
て丁ENSILON UTM−11−20(ToYo
BALDWIN Co、、 LTD)で20℃における
伸び率を測定した。C2) Elongation rate: Apply an undercoat to a tin plate to a coating film of 50p. After heating at 100℃ for 15 minutes, cut into a rectangle with a length of 601℃m and a width of 5cm using a cutter. , the coating film was peeled off using mercury, and this coating film was used to manufacture Toyo ENSILON UTM-11-20 (ToYo
The elongation rate at 20°C was measured using BALDWIN Co., Ltd.).
(”3) #食性二上記(11)と同様に作成した試
験板に水道水10ccを噴霧し、24時間放置後のサビ
の発生の有無を調べた。(3) #Eating property 2 10 cc of tap water was sprayed on a test plate prepared in the same manner as in (11) above, and the presence or absence of rust was examined after leaving it for 24 hours.
0:サビ発生殆ど認められず。0: Almost no rust observed.
×:サビ発生多く認められる。×: Much rust is observed.
(ヨ4) 塗膜外観二上記(零1)と同様に作成した
試験板を室内(10℃)で10日間放置しその外観を観
察する。(Y4) Paint film appearance 2 A test plate prepared in the same manner as above (01) was left indoors (10°C) for 10 days and its appearance was observed.
O:キレン、ワレ、ハガレなどの塗膜欠陥が認められな
い。O: No coating film defects such as cracks, cracks, or peeling are observed.
Δ:キレツ、ワレ、ハガレなどの塗膜欠陥はないが塗膜
に粘着性がある。Δ: There are no paint film defects such as cracks, cracks, or peeling, but the paint film is sticky.
×:キレツ、ワレ、ハガレなとの塗膜欠陥が認められる
。×: Paint film defects such as cracks, cracks, and peeling are observed.
(ヨ5) 塗着塗料の′A離性:黒皮鋼板に前記のご
とく本発明の下塗塗料組成物および中、上塗り塗料を塗
装した試験板を、塗膜側を上にして水平に置き、20℃
において、eドライバーを塗面に対して45°の角度で
ハンマーでたたき、塗膜の調離状態を観察した。(Y5) 'A releasability of applied paint: A test plate coated with the base coat composition of the present invention and the intermediate and top coat paints as described above was placed on a black steel plate horizontally with the coated side facing up. 20℃
The e-driver was struck with a hammer at an angle of 45° to the coated surface, and the state of separation of the coated film was observed.
O:素地面から小片状にすみやかに剥離した。O: Promptly peeled off into small pieces from the base surface.
Δ:剥離性塗膜自体の剥離が極めて困難。Δ: Peelability It is extremely difficult to peel off the coating film itself.
×:剥離することは殆ど不可能。×: Almost impossible to peel off.
上記試験において2
■ 付着力、伸び率、耐食性および塗膜外観は下塗塗料
組成物の単独塗膜について行なった評価である。In the above test, 2. adhesion, elongation, corrosion resistance, and coating film appearance were evaluated for a single coating film of the undercoat composition.
くの 塗着塗料の剥離性は中塗り、上塗り塗料を前記の
ごとく塗り重ねたものについて試験した。The releasability of the applied paint was tested using the intermediate coat and top coat coated as described above.
■ 比較例1は、本発明の下塗塗料組成物を使用せず、
中塗りおよび上塗り塗料を直接塗り重ねたものである。■ Comparative Example 1 did not use the primer coating composition of the present invention,
This is a direct coating of intermediate and top coats.
以下余白 第 3 表Margin below Table 3
Claims (1)
000の水溶性又は水分散型熱可塑性樹脂を主成分とし
、素材との付着力0.01〜15kg/cm^2、塗膜
伸び率1%以下に調整した水溶性又は水分散性下塗塗料
組成物。Softening point 50~300℃, number average molecular weight 300~500,
000 water-soluble or water-dispersible thermoplastic resin as the main component, and has an adhesion force to the material of 0.01 to 15 kg/cm^2 and a coating film elongation rate of 1% or less. thing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24618486A JPS6399275A (en) | 1986-10-16 | 1986-10-16 | Undercoating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24618486A JPS6399275A (en) | 1986-10-16 | 1986-10-16 | Undercoating composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6399275A true JPS6399275A (en) | 1988-04-30 |
Family
ID=17144760
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24618486A Pending JPS6399275A (en) | 1986-10-16 | 1986-10-16 | Undercoating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6399275A (en) |
-
1986
- 1986-10-16 JP JP24618486A patent/JPS6399275A/en active Pending
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