JPH0475068B2 - - Google Patents
Info
- Publication number
- JPH0475068B2 JPH0475068B2 JP59114818A JP11481884A JPH0475068B2 JP H0475068 B2 JPH0475068 B2 JP H0475068B2 JP 59114818 A JP59114818 A JP 59114818A JP 11481884 A JP11481884 A JP 11481884A JP H0475068 B2 JPH0475068 B2 JP H0475068B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- coating
- seconds
- baking
- coating film
- 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 - Lifetime
Links
- 238000000576 coating method Methods 0.000 claims description 47
- 239000011248 coating agent Substances 0.000 claims description 37
- 239000000843 powder Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 239000003973 paint Substances 0.000 description 6
- 238000011109 contamination Methods 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 239000003822 epoxy resin Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 229910001316 Ag alloy Inorganic materials 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- -1 Generally Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 210000000720 eyelash Anatomy 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
〔産業上の利用分野〕
本発明はプレコート用粉体塗料の塗膜を高温短
時間の焼付けで形成する方法に関する。
〔従来の技術〕
近年、粉体塗料のプレコート方式の実用化が盛
んになつてきたが、その塗膜形成のための焼付け
が230℃で5分間程度の時間をかけて行なわれて
いるため、これを従来の溶剤型塗料なみに20〜80
秒程度の高温短時間焼付で塗膜形成することが要
望されている。
これは焼付装置などの設備のスペース上の制約
に対処し、かつ設備費およびランニングコストの
低減を図るため、できるだけ少ないスペースで、
かつエネルギーコストもできるだけ少なくして、
製品を量産化しようという意図によるものであ
る。
ところで、プレコート用の粉体塗料としては、
一般にエポキシ樹脂系粉体塗料、ポリエステル樹
脂系粉体塗料、アクリル樹脂系粉体塗料などが用
いられているが、これらは加熱により100〜130℃
程度で溶融し、180〜270℃程度で架橋して硬化す
るタイプのものであつて、上述のようにできるだ
け少ないスペースでかつエネルギーコストもでき
るだけ少なく製品を量産化しようとすれば、この
溶融−架橋を前記のような短時間内に終らなけれ
ばならない。
そのため、当初はできるだけ早く高温短時間焼
付に適する架橋温度にまで昇温しようという考え
から、20秒程度で250〜260℃まで昇温することを
検討したが、このように超短時間で架橋温度にま
で昇温したものは、架橋反応が急激に行なわれる
ため、後に詳述するように分子量分布が広く、そ
れによつて塗膜表面にレベリング性不良(波打ち
現象)が現われ塗面の平滑性を欠き、外観が悪
く、また性能面でも高度の加工性や加工部の耐食
性が要求される場合には、それらの要求に応じる
ことができず、外観、性能のいずれの面において
も従来法により焼付けた塗膜に比べて劣つてい
た。そして、上記のように20秒程度で250〜260℃
まで昇温したものをさらに加熱を継続しても上述
のような欠点を解消することができなかつた。
〔発明が解決しようとする問題点〕
本発明は前述のようにできるだけ少ないスペー
スでかつエネルギーコストもできるだけ少なく製
品を量産化しようという目的に合致する80秒以内
の高温短時間焼付で、レベリング性不良の発生を
防止し、外観が良好で、かつ高度の加工性や加工
部の耐食性を有するなど性能面においても優れた
プレコート用粉体塗料の塗膜を形成することを目
的とする。
〔問題点を解決するための手段〕
本発明者らは省スペース、省エネルギーを図る
観点からプレコート用粉体塗料の高温短時間焼付
による塗膜形成について種々研究を重ねた結果、
良好な外観と十分な性能を有する塗膜を得るに
は、短時間焼付とはいえ前述のように昇温を急激
に行なうことは好ましくなく、昇温に比較的時間
をかけ、被塗物の昇温条件を20秒までの昇温を
100〜180℃とし、40秒までの昇温を180℃を超え
る温度で270℃以下とすることが適切であること
を見出した。
すなわち、前述のように急激に架橋温度まで昇
温すると、十分な分子間の接触が得られないまま
に急激な架橋反応が進行し、その結果、低分子量
部分が多く生じ、分子量分布が広くなることによ
る品質の不均一さが生じ、それが塗膜の外観、物
性に悪影響を及ぼすことになるが、本発明のよう
に最初の20秒間は粉体塗料の溶融を主体にし、高
温での初期反応をおさえ、初期溶融期間を長くす
ることによつて流動性を大きくして分子間の接触
を十分に行なわせた上で、次の40秒までの昇温で
粉体塗料の架橋温度である180℃を超える温度で
270℃以下に昇温して粉体塗料を架橋させて高分
子化するときは、得られる塗膜の分子量分布が均
一になり、その結果、塗面の平滑性が向上し、か
つ耐衝撃性、折り曲げ性、抗張力など塗膜の後加
工に重要な影響を与える因子に好結果がもたらさ
れ、外観に優れ、かつ性能面でも優れた塗膜が得
られるようになるのである。
本発明において使用しうる粉体塗料としては、
たとえばポリエステル樹脂系粉体塗料、エポキシ
樹脂系粉体塗料、アクリル樹脂系扮体塗料などが
あげられる。そして、ポリエステル樹脂系粉体塗
料としてはブロツクイソシアネート硬化タイプの
ものやN−メチロールエーテル化メラミン樹脂硬
化タイプのもの、さらにはグリシジル化合物を硬
化剤として用いるものなどがあげられる。エポキ
シ樹脂系粉体塗料としてはBF3コンプレツクスを
硬化剤とするもの、酸無水物アダクト、ジシアン
ジアミド、変性ジシアンジアミドなどを硬化剤と
するものなどがあげられる。またアクリル樹脂系
粉体塗料としてはメラミン樹脂、ブロツクイソシ
アネート、エポキシ樹脂、多価カルボン酸を硬化
剤とするものや自己架橋型のものなどがあげられ
る。
焼付装置としては、高風速熱風炉、超遠赤外線
炉、高周波誘導加熱炉、近赤外線炉などが単独で
または2〜3種組み合わせて使用され、これらは
連続作業に適するように通常コンベアー炉にされ
ている。そして、その熱源としては電気、都市ガ
ス、天然ガス、液化石油ガスなどが使用される。
〔実施例〕
つぎに実施例をあげて本発明をさらに詳細に説
明する。
実施例1〜6および比較例1〜4
まず、試験に供すべき粉体塗料の組成、素材お
よび設備について説明する。なお、配合部数は重
量部によるものである。
粉体塗料の組成
ポリエステル樹脂(OH基価40mg/g) 80部
ブロツクドイソシアネート硬化剤(イソシアネー
ト含有量15%) 17部
エポキシ樹脂(エポキシ当量950) 3部
ベンゾイン(発泡防止剤) 0.5部
チタン白(R−930)(石原産業(株)製) 43部
アクロナール4F(バイエル社製)(レベリング剤)
0.5部
ジブチルチンジラウレート(硬化促進剤) 0.2部
素材:新日本製鉄(株)製合金化処理溶融亜鉛メツキ
鋼板(シルバーアロイ)、厚さ0.45mm
前処理:リン酸亜鉛皮膜処理
塗装機:ゲマ手吹静電ガン
焼付炉:電気熱風循環式コンベアー炉
上記組成の粉体塗料をゲマ手吹ガンを用いてリ
ン酸亜鉛処理済みのシルバーアロイ上に塗装し電
気熱風循環式コンベアー炉を用いて第1表に示す
焼付条件で焼付けて塗板を得た。なお平均塗装膜
厚は35μmである。
[Industrial Field of Application] The present invention relates to a method for forming a coating film of a powder coating material for pre-coating by baking at high temperature for a short time. [Prior art] In recent years, the practical application of pre-coating powder coatings has become popular, but since the baking process to form the coating film is carried out at 230°C for about 5 minutes, This is 20 to 80%, similar to conventional solvent-based paints.
It is desired to form a coating film by baking at a high temperature and for a short time on the order of seconds. This is done in as little space as possible in order to deal with the space constraints of equipment such as printing equipment, and to reduce equipment costs and running costs.
And keep energy costs as low as possible,
This is due to the intention of mass producing the product. By the way, as a powder coating for pre-coating,
Generally, epoxy resin powder coatings, polyester resin powder coatings, acrylic resin powder coatings, etc. are used, but these can be heated to temperatures of 100 to 130℃.
It is a type that melts at a temperature of 180 to 270℃ and crosslinks and hardens at a temperature of 180 to 270℃.As mentioned above, if you want to mass-produce products in as little space as possible and with as little energy cost as possible, this melting-crosslinking method is must be completed within a short period of time as mentioned above. Therefore, we initially considered raising the temperature to 250-260℃ in about 20 seconds with the idea of raising the temperature as quickly as possible to a crosslinking temperature suitable for high-temperature, short-time baking. When heated to a temperature of In cases where there are chips, the appearance is poor, and high workability and corrosion resistance of the machined parts are required in terms of performance, it is impossible to meet these demands, and the conventional baking method is used to improve both appearance and performance. It was inferior to other coatings. Then, as above, heat the temperature to 250-260℃ for about 20 seconds.
Even if the heating was continued after the temperature was raised to 100%, the above-mentioned drawbacks could not be solved. [Problems to be Solved by the Invention] As mentioned above, the present invention solves the problem of poor leveling property by high-temperature, short-time baking within 80 seconds, which meets the purpose of mass-producing products in as little space as possible and with as little energy cost as possible. The purpose of the present invention is to form a pre-coat powder coating film that prevents the occurrence of oxidation, has a good appearance, and has excellent performance such as high workability and corrosion resistance in processed parts. [Means for Solving the Problems] The present inventors have conducted various studies on coating film formation by high-temperature, short-time baking of powder coatings for pre-coat from the viewpoint of saving space and energy.
In order to obtain a coating film with good appearance and sufficient performance, it is not preferable to raise the temperature rapidly as mentioned above, even though it is baked for a short time. Increase temperature for up to 20 seconds
It has been found that it is appropriate to set the temperature to 100 to 180°C and to raise the temperature for up to 40 seconds to a temperature exceeding 180°C and not more than 270°C. In other words, when the temperature is rapidly raised to the crosslinking temperature as described above, the crosslinking reaction proceeds rapidly without sufficient intermolecular contact, resulting in the formation of many low molecular weight parts and a wide molecular weight distribution. However, as in the present invention, the powder coating is mainly melted for the first 20 seconds, and the initial stage at high temperature is After suppressing the reaction and increasing the initial melting period to increase fluidity and ensure sufficient contact between molecules, the temperature is increased over the next 40 seconds to reach the crosslinking temperature of the powder coating. At temperatures above 180℃
When the powder coating is crosslinked and polymerized by raising the temperature to below 270℃, the resulting coating film has a uniform molecular weight distribution, which improves the smoothness of the coating surface and improves impact resistance. Good results are achieved in factors that have an important influence on the post-processing of coating films, such as bendability and tensile strength, and coating films with excellent appearance and performance can be obtained. Powder coatings that can be used in the present invention include:
Examples include polyester resin powder paints, epoxy resin powder paints, acrylic resin disguise paints, and the like. Examples of polyester resin powder coatings include those of the blocked isocyanate curing type, those of the N-methylol etherified melamine resin curing type, and those using a glycidyl compound as a curing agent. Examples of epoxy resin powder coatings include those using BF 3 complex as a curing agent, and those using acid anhydride adducts, dicyandiamide, modified dicyandiamide, etc. as a curing agent. Examples of acrylic resin powder coatings include those using melamine resin, blocked isocyanate, epoxy resin, and polycarboxylic acid as a curing agent, and self-crosslinking types. As a baking device, a high-velocity hot air furnace, an ultra-far infrared furnace, a high-frequency induction heating furnace, a near-infrared furnace, etc. are used singly or in combination of two or three types, and these are usually converted into a conveyor furnace to be suitable for continuous operation. ing. Electricity, city gas, natural gas, liquefied petroleum gas, etc. are used as the heat source. [Example] Next, the present invention will be explained in more detail by giving examples. Examples 1 to 6 and Comparative Examples 1 to 4 First, the composition, material, and equipment of the powder coating to be tested will be explained. Note that the number of parts is based on parts by weight. Composition of powder coating Polyester resin (OH value 40mg/g) 80 parts Blocked isocyanate curing agent (Isocyanate content 15%) 17 parts Epoxy resin (epoxy equivalent 950) 3 parts Benzoin (foaming inhibitor) 0.5 part Titanium white (R-930) (manufactured by Ishihara Sangyo Co., Ltd.) 43 parts Acronal 4F (manufactured by Bayer) (leveling agent)
0.5 parts dibutyltin dilaurate (hardening accelerator) 0.2 parts Material: Alloyed hot-dip galvanized steel sheet (silver alloy) manufactured by Nippon Steel Corporation, thickness 0.45 mm Pretreatment: Zinc phosphate coating coating machine: Gemate Blowing electrostatic gun baking furnace: Electric hot air circulation type conveyor furnace The powder coating of the above composition was applied onto zinc phosphate treated silver alloy using a Gema hand blowing gun, and then the powder coating was applied using an electric hot air circulation type conveyor furnace. A coated plate was obtained by baking under the baking conditions shown in the table. The average coating film thickness was 35 μm.
【表】
さらに、あらかじめ250℃に設定した固定炉を
用い、前記コンベアー炉より取り出した直後の塗
板をさらに固定炉内で保温して塗板を作製した。
その際の焼付温度条件を第2表に示す。なお実施
例5および6におけるコンベアー炉の炉内20秒通
過時の板表面温度は実施例1と同様に156℃であ
る。[Table] Further, using a fixed furnace preset at 250°C, the coated plate immediately after being taken out from the conveyor furnace was further kept warm in the fixed furnace to produce a coated plate.
The baking temperature conditions at that time are shown in Table 2. In addition, the plate surface temperature in Examples 5 and 6 when passing through the conveyor furnace for 20 seconds was 156° C. as in Example 1.
【表】
上記のようにして作製された塗板の塗膜性能試
験結果を第3表に示す。試験方法および評価基準
は下記の通りである。
光沢度:村上色彩研究所製光沢計を使用し、
60゜/60゜鏡面光沢度を測定した。
塗面の平滑性:同じ粉体塗料をシルバーアロイ上
に従来法により230℃、5分間で焼付けて形成
した塗膜と目視により比較した。
評価基準はつぎのとおりである。
◎:従来法による塗膜と同等以上の外観(優)
○:従来法による塗膜とほぼ同等の外観(良)
□:従来法による塗膜に比べて若干劣るが実用
上問題なし(可)
△:従来法による塗膜に比べて非常に劣る(不
可)
20℃折り曲げ加工性:50mm×150mmのテストピー
スのほぼ中央部を180゜折り曲げ(折り曲げ部の
長さ50mm)、折り曲げ後、折り曲げ部に同種テ
ストピースを2枚はさみ万力で締め付け
(2T)、1枚はさみ万力で締め付け(1T)、0
枚すなわちまつたく何もはさむことなく万力で
締め付け(0T)、各折り曲げ部のクラツク発生
度合を目視により観察した。
評価基準をつぎの通りである。
◎:まつたく異状なし(優)
○:1〜2点クラツク発生、他は異状なし
(良)
□:数点微小クラツク発生(可)
◇:かなりのクラツク発生(不可)
耐マジツク汚染性:マジツクインク塗布後20℃で
24時間放置した後、石油ベンジン/エチルアル
コール=50/50混合溶剤にて拭き取り、汚染度
合を目視により観察した。
評価基準はつぎの通りである。
◎:汚染まつたくなし(優)
○:ほとんど汚染なし(良)
□:若干汚染有り(可)
◇:かなり汚染有り(不可)
加工部の耐食性:フランジ曲げ部(曲げ部長さ
300mm)の塩水噴霧テスト500時間後のフクレ度
合いを観察した。
評価基準はつぎの通りである。
◎:フクレまつたくなし
○:1点フクレ発生
□:2〜3点フクレ発生
◇:4〜5点フクレ発生
△:6点以上フクレ発生
また、同じ粉体塗料をシルバーアロイ上に230
℃、5分間で焼付けて形成した塗膜の光沢度、塗
面の平滑性、20℃折り曲げ加工性、耐マジツク汚
染性、加工部の耐食性についても第3表に対照例
として示した。[Table] Table 3 shows the results of the coating film performance test of the coated plate prepared as described above. The test method and evaluation criteria are as follows. Glossiness: Using a gloss meter manufactured by Murakami Color Research Institute,
60°/60° specular gloss was measured. Smoothness of coated surface: Visual comparison was made with a coat formed by baking the same powder coating on a silver alloy using a conventional method at 230°C for 5 minutes. The evaluation criteria are as follows. ◎: Appearance equivalent to or better than the coating film made by the conventional method (Excellent) ○: Appearance almost the same as the coating film made by the conventional method (Good) □: Slightly inferior to the coating film made by the conventional method, but no problem in practical use (Acceptable) △: Very inferior to the coating film made by the conventional method (not possible) 20℃ bending workability: Bend the approximately center part of a 50 mm x 150 mm test piece by 180 degrees (length of the bent part 50 mm), and after bending, the bent part Tighten two test pieces of the same type in a vise with scissors (2T), tighten one test piece with a scissor vise (1T), 0
The sheets were tightened in a vise (0T) without pinching anything, and the degree of crack occurrence at each bend was visually observed. The evaluation criteria are as follows. ◎: No abnormalities (excellent) ○: 1 to 2 cracks, no other abnormalities (good) □: Several small cracks (acceptable) ◇: Significant cracks (unacceptable) Magick stain resistance: Magick ink At 20℃ after application
After leaving it for 24 hours, it was wiped off with a 50/50 mixed solvent of petroleum benzene/ethyl alcohol, and the degree of contamination was visually observed. The evaluation criteria are as follows. ◎: No contamination (excellent) ○: Almost no contamination (good) □: Slight contamination (acceptable) ◇: Considerable contamination (unacceptable) Corrosion resistance of processed parts: Flange bent part (bending length
The degree of blistering was observed after 500 hours of salt water spray test (300 mm). The evaluation criteria are as follows. ◎: No eyelash bulges ○: 1 point of blister occurrence □: 2 to 3 points of blister occurrence ◇: 4 to 5 points of blister occurrence △: 6 or more points of blister occurrence In addition, the same powder paint was applied to silver alloy with 230
Table 3 also shows the glossiness of the coating film formed by baking at 50°C for 5 minutes, the smoothness of the coated surface, the bending workability at 20°C, the stain resistance with magic, and the corrosion resistance of the processed part as a control example.
本発明によれば、省スペース、省エネルギーに
合致する80秒以内の高温短時間焼付で、外観が良
好で、かつ高度の後加工性や加工部の耐食性を有
するなど性能面においても優れたプレコート用粉
体塗料の塗膜が形成された。
According to the present invention, the pre-coating material can be baked at a high temperature for a short period of time within 80 seconds to save space and energy, has a good appearance, and has excellent post-processability and corrosion resistance of the processed parts. A coat of powder paint was formed.
Claims (1)
成するにあたつて80秒以内の高温短時間条件で焼
付けする場合において、その塗装被塗物の昇温条
件を20秒ま超の昇温を100〜180℃、40秒までの昇
温を180℃を超える温度で270℃以下とすることを
特徴とするプレコート用粉体塗料の塗膜形成方
法。1. When forming a pre-coat powder coating film on the object to be coated by baking it under high temperature and short time conditions of 80 seconds or less, the heating condition of the object to be coated shall not be increased for more than 20 seconds. A method for forming a coating film for a powder coating for pre-coating, characterized in that the temperature is increased from 100 to 180°C, and the temperature is increased over 180°C to 270°C or less for up to 40 seconds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11481884A JPS60257878A (en) | 1984-06-04 | 1984-06-04 | Formation of paint film from pre-coat grade powdery paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11481884A JPS60257878A (en) | 1984-06-04 | 1984-06-04 | Formation of paint film from pre-coat grade powdery paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60257878A JPS60257878A (en) | 1985-12-19 |
JPH0475068B2 true JPH0475068B2 (en) | 1992-11-27 |
Family
ID=14647450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11481884A Granted JPS60257878A (en) | 1984-06-04 | 1984-06-04 | Formation of paint film from pre-coat grade powdery paint |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60257878A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2598509B2 (en) * | 1989-02-28 | 1997-04-09 | 川崎製鉄株式会社 | Continuous drying and baking method for strip coating film |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58101768A (en) * | 1981-12-10 | 1983-06-17 | Kawasaki Steel Corp | Production of painted steel plate for working |
-
1984
- 1984-06-04 JP JP11481884A patent/JPS60257878A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58101768A (en) * | 1981-12-10 | 1983-06-17 | Kawasaki Steel Corp | Production of painted steel plate for working |
Also Published As
Publication number | Publication date |
---|---|
JPS60257878A (en) | 1985-12-19 |
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