JPS6011989B2 - High film thickness paint - Google Patents
High film thickness paintInfo
- Publication number
- JPS6011989B2 JPS6011989B2 JP55072216A JP7221680A JPS6011989B2 JP S6011989 B2 JPS6011989 B2 JP S6011989B2 JP 55072216 A JP55072216 A JP 55072216A JP 7221680 A JP7221680 A JP 7221680A JP S6011989 B2 JPS6011989 B2 JP S6011989B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- film thickness
- paint
- high 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
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- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
この発明は車輪、化学プラント及び建材料用に好適な暁
付タイプの高膜厚型塗料に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a high-film thickness type paint suitable for wheels, chemical plants, and building materials.
従来、この種の高膜厚型塗料で塗膜性能、作業性及び仕
上がり外観性を兼ね備えたものは提供されていない。Hitherto, no high film thickness type paint of this type has been provided that combines film performance, workability, and finished appearance.
この主たる原因の一つは、鱗付け時に溶剤の揮発等の影
響を受けて、ワキ(発泡)が発生し仕上がり外観を薯る
しく損うからである。したがって、現在高膜厚型塗料の
使用量の多い建材業界では殆んどの場合、固形分の割合
が高い常温乾燥タイプの塗料が建築現場にて使用されて
いる。しかも少なくとも一回塗布にて確保できる仕上が
り外観が良好な可能塗膜厚も100ム程度である。暁付
タイプの車軸に使用する従来の高膜厚型塗料は、例えば
大量の需要がある自動車用中塗塗料を例にとると、現在
一回塗布にて確保できる可能塗膜厚は70〃以下だとさ
れている。したがって塗料業界に於て、高膜厚型塗料の
市場拡大の為の一要因として、暁付け時のワキの発生を
防止することが急務とされている。そこでこの発明の目
的は、競付け時のワキの発生を防止した、極めて実用性
に富む高膜厚型塗料を提供することである。One of the main reasons for this is that foaming (foaming) occurs under the influence of solvent volatilization during scaling, which severely impairs the finished appearance. Therefore, in the building materials industry, which currently uses a large amount of high film thickness type paints, in most cases, room temperature drying type paints with a high solids content are used at construction sites. Furthermore, the possible coating thickness that can be ensured with at least one coating and with a good finished appearance is about 100 µm. Conventional high-film-thickness paints used on Akatsuki type axles, for example, car intermediate paints for which there is a large demand, currently have a film thickness of 70 mm or less that can be secured in one application. It is said that Therefore, in the paint industry, there is an urgent need to prevent the formation of wrinkles during application, as one of the factors for expanding the market for high film thickness paints. Therefore, an object of the present invention is to provide a highly practical high-film-thickness paint that prevents the occurrence of wrinkles during competition.
この発明の目的は高膜厚型塗料に、ベンゾィソを塗料1
0の重量部に対して0.1〜2重量部使用することによ
って達成される。The purpose of this invention is to add benzoiso to a high film thickness type paint.
This is achieved by using 0.1 to 2 parts by weight relative to 0 parts by weight.
以下、この発明を詳述する。This invention will be explained in detail below.
まずこの発明の要部をなすペンゾィンとは、国際名命法
ではQーオキシベンジルフェニルケトンとして知られて
おり、慣用名ペンジルフェニルカルビノールとしても知
られている化合物である。またこの化学構造式はにて示
される。First, penzoin, which forms the essential part of this invention, is a compound known as Q-oxybenzylphenylketone in the International Nomenclature System, and also known by its common name penzylphenylcarbinol. Moreover, this chemical structural formula is shown by.
そしてこのペンゾインの作用は、暁付け硬化時に溶剤の
揮発により塗料が増粘する際、そのペンゾィンの有する
作用により塗膜を一時的に低粘度化し、ワキを抑制する
ことであり、樹脂及び溶剤との相容により、相乗効果を
もたらし、少量の添加で一層の効果が期待できる。The action of this penzoin is that when the paint thickens due to the volatilization of the solvent during dawn curing, the action of penzoin temporarily lowers the viscosity of the paint film and suppresses the formation of wrinkles. Due to their compatibility, a synergistic effect is produced, and even greater effects can be expected with addition of small amounts.
次にこの発明でいう高膜厚型塗料とは、塗装作業粘度が
1000センチポィズ(C.P.C)以上で、少くとも
被塗物に1回塗布して得られる塗膜厚が70〜600〃
であるものを指す。Next, the high film thickness type paint referred to in this invention has a coating work viscosity of 1000 centipoise (C.P.C.) or more, and a coating thickness of at least 70 to 600 centipoise (C.P.C.) obtained by applying it once to the object to be coated. 〃
Refers to something that is.
この高腰厚型塗料は樹脂、溶剤、ベンゾィン及び2種以
上の顔料と、必要に応じて沈降防止剤等の各種配合剤を
ディスパー等の公知嬢梓器にて配合し、損浮浪合した後
、ボールミルサンドグラィンダ一及びロールミル等の公
知分散機にて均一に分散し、必要ならば、減圧等にて脱
泡して製品とする。前記顔料とは体質顔料と着色顔料を
総称したものであり、具体的には、炭酸カルシウム、シ
リカ、アルミナ、酸化鉄(ベンガラを含む)、ケイ酸ア
ルミニウム(クレー、カオリン等)、アスベスト、含水
ケイ酸マグネシウム(タルクを含む)、硫酸バリウム、
ガラスビーズ、亜鉛華及び酸化チタンであり、この際好
ましくはワキ以外の他の特性、例えば塗布時のタレやス
プレー作業性及び耐チッピング性を向上させる為に顔料
の粒度分布を調整することである。This thick, thick paint is made by blending resin, solvent, benzoin, two or more types of pigments, and various compounding agents such as anti-settling agents as necessary in a known mixing device such as a disper, and then combining them. The mixture is uniformly dispersed using a known dispersing machine such as a ball mill, sand grinder, or roll mill, and if necessary, defoamed under reduced pressure to obtain a product. The above pigment is a general term for extender pigments and color pigments, and specifically includes calcium carbonate, silica, alumina, iron oxide (including red iron oxide), aluminum silicate (clay, kaolin, etc.), asbestos, and hydrated silica. magnesium acid (including talc), barium sulfate,
Glass beads, zinc white, and titanium oxide, and in this case, it is preferable to adjust the particle size distribution of the pigment in order to improve other properties other than the pigment, such as sagging during application, spray workability, and chipping resistance. .
この粒度分布は、0.001〜70仏のいずれかの範囲
内に分布していれば良く、尚好ましくは、全顔料100
重量部中に0.001〜5ムの範囲内に分布する顔料が
3の重量部以下であり、5〜70一の範囲内に分布する
顔料が、70重量部以上に調整して使用することであ*
り、最も好ましくは0.001〜5払の範囲内に分布す
る顔料が3の重量部以下であり、5〜30仏の範囲内に
分布する顔料が35重量部以上であり、30〜70りの
範囲内に分布する顔料が25重量部以下である。小さい
粒径の顔料と大きな粒径のものを同時に使用することに
より平滑な塗膜を得ることができる。この粒度に顔料の
分布中を調整する手法としては、ロールミルやサンドグ
ライダー等で分散する工程にて軟質の顔料は紐粒化する
傾向にあるので、細い粒度を有する領域の調整は問題な
いが5〆以上の粒度は、前記分散工程に於て、紬粒化し
1こくいシリカ、アルミナ、アスベスト等の硬質顔料か
ら少なくとも1種選択して使用し、大きな粒径を高膜厚
型塗料に含有させる方法が有効である。また高膜厚型塗
料中に占める顔料の配合割合は樹脂10匹重量部に対し
て100〜500重量部であり、尚好ましくは150〜
40の重量部である。以上顔料については概略前述の如
くであるが、この発明に使用する顔料について個々に外
観、その粒度分布範囲、及び配合割合を以下に掲げる表
1に示す。表 1
次にこの発明に使用する樹脂は周知の塗料用樹脂がいず
れも使用でき特に制限を設けないが、好ましくはポリエ
ステル樹脂、特にウレタン変性ポリエステル樹脂、オイ
ルフリーアルキッド樹脂、ウレタン樹脂、フェノール変
性樹脂、アクリル樹脂等であり、その配合割合は全高膜
厚型塗料100重量部中に5〜7の重量部であり好まし
くは10〜50重量部である。The particle size distribution may be within the range of 0.001 to 70 mm, more preferably 100 mm of total pigment.
Pigments distributed within the range of 0.001 to 5 mm in weight parts are adjusted to 3 parts by weight or less, and pigments distributed within the range of 5 to 70 mm are adjusted to 70 parts by weight or more. De*
Most preferably, the amount of pigments distributed within the range of 0.001 to 5 degrees is 3 parts by weight or less, the amount of pigments distributed within the range of 5 to 30 degrees is 35 parts by weight or more, and the amount of pigments distributed within the range of 0.001 to 5 degrees is 30 to 70 degrees. The pigment distributed within the range of 25 parts by weight or less. A smooth coating film can be obtained by simultaneously using a pigment with a small particle size and a pigment with a large particle size. As a method of adjusting the pigment distribution to this particle size, since soft pigments tend to become string particles during the dispersion process using a roll mill or sand glider, adjusting the area with a fine particle size is not a problem. In the above-mentioned dispersion process, at least one type of hard pigment such as silica, alumina, asbestos, etc., is selected and used, and the large particle size is included in the high film thickness type paint. The method is valid. The proportion of pigment in the high film thickness paint is 100 to 500 parts by weight, preferably 150 to 500 parts by weight, based on 10 parts by weight of resin.
40 parts by weight. Although the pigments are generally as described above, the appearance, particle size distribution range, and blending ratio of each pigment used in the present invention are shown in Table 1 below. Table 1 Next, as the resin used in this invention, any well-known paint resin can be used without any particular limitation, but polyester resins, particularly urethane-modified polyester resins, oil-free alkyd resins, urethane resins, and phenol-modified resins are preferable. , acrylic resin, etc., and the blending ratio thereof is 5 to 7 parts by weight, preferably 10 to 50 parts by weight, in 100 parts by weight of the total high film thickness type paint.
次に溶剤について述べると、この溶剤についても公知の
ものはいずれも使用できるが好ましくは12000以下
の低沸点溶剤と120午0以上の高沸点溶剤よりなる群
から選ばれた少なくとも2種以上を使用することであり
、最も好ましくは高沸点溶剤を全溶剤10の重量部中に
5の重量部以上使用することである。Next, regarding the solvent, any known solvent can be used, but preferably at least two or more selected from the group consisting of a low boiling point solvent of 12000 or less and a high boiling point solvent of 12000 or more are used. Most preferably, the high boiling point solvent is used in an amount of 5 parts by weight or more per 10 parts by weight of the total solvent.
前記低沸点溶剤の具体的な例はメタノール、エタノール
、ノルマルブタノール及びイソブタノール等の低分子量
のアルコール系溶剤であり、高沸点溶剤の具体的な例は
エチレングリコールモノエーテル、エチレングリコ一ル
モノブチルェーテル等のグリコールェーテルと、シクロ
ヘキサノン、ィソホロン等のケトン系溶剤と、芳香族炭
化水素である。これら溶剤の配合割合は樹脂10の重量
部に対して20〜10の重量部であり、好ましくは30
〜8の重量部である。以上前述した如くこの発明に不可
欠の配合剤としては樹脂、ベンゾィン、顔料及び溶剤の
4成分であるか、これら成分以外にも必要に応じて、レ
ベリング剤及び沈降防止剤等を併用すると尚一層好まし
い高膜厚型塗料を得ることができる。Specific examples of the low boiling point solvent are low molecular weight alcohol solvents such as methanol, ethanol, normal butanol and isobutanol, and specific examples of the high boiling point solvent are ethylene glycol monoether, ethylene glycol monobutyl ether, etc. These are glycol ethers such as ether, ketone solvents such as cyclohexanone and isophorone, and aromatic hydrocarbons. The blending ratio of these solvents is 20 to 10 parts by weight, preferably 30 parts by weight, based on 10 parts by weight of the resin.
~8 parts by weight. As mentioned above, the essential ingredients for this invention are the four components of resin, benzoin, pigment, and solvent, and it is even more preferable to use a leveling agent, an anti-settling agent, etc. in addition to these components, if necessary. A high film thickness type paint can be obtained.
使用するしべリング剤としてはシリコーン系、非シリコ
ーン系及びフッソ系、アクリル系等の共重合体等のしべ
リング剤である。沈降防止剤としては脂肪酸ェステル重
合体、合成ワックス及びシリカ系沈降防止剤等である。
これらの配合剤はあまり多量に使用すると他の物性を損
うので樹脂10の重量部に対して0.01〜5重量部の
範囲にとどめる方が良い。次にこの発明でいう高膜厚型
塗料の好適な塗装作業粘度は1000〜400に.P.
Sであり好ましくは2500〜3500.P.Sである
。The staining agents used include silicone type, non-silicone type, fluorine type, acrylic type and other copolymers. Examples of anti-settling agents include fatty acid ester polymers, synthetic waxes, and silica-based anti-settling agents.
If these compounding agents are used in too large a quantity, other physical properties will be impaired, so it is better to limit the amount to 0.01 to 5 parts by weight based on 10 parts by weight of the resin. Next, the preferred coating work viscosity of the high film thickness type paint in this invention is 1000 to 400. P.
S, preferably 2500 to 3500. P. It is S.
またその固形分としては全高膜厚型塗料10の重量部中
に60〜90重量部であり、最も好ましくは65〜75
重量部である。また塗装の際には好ましくはホットヱア
レススプレーにて作業することである。次にこの発明品
の用途は建築、化学プラント及び自動車等の高膜厚を要
求される分野にはいずれも使用できるが、自動車の中塗
り用の如き実用性の面で仕上がり外観、作業性及び塗膜
性能特に耐チッピング性等の高度の諸条件を兼ね備えな
ければ実用できない分野には特に有効である。The solid content thereof is 60 to 90 parts by weight, most preferably 65 to 75 parts by weight in the total high film thickness type paint 10.
Parts by weight. Also, when painting, it is preferable to work with hot Ares spray. Next, this invention can be used in any field that requires high film thickness, such as architecture, chemical plants, and automobiles, but it is difficult to improve the finished appearance, workability, and practicality, such as as an inner coating for automobiles. It is particularly effective in fields where it cannot be put to practical use unless high-level conditions such as coating film performance, especially chipping resistance, are met.
以上前述した如く、顔料の粒度分布を調整し、好ましい
溶剤や樹脂を選定し、その配合割合も満足したものであ
ればペンゾインを使用しなくても、燐付け条件たとえば
セッティング時間を長く設けたり、二段焼付けにしてプ
レキュア−の温度を低温にして比較的長い時間設ければ
、ワキの問題は解消する。As mentioned above, if the particle size distribution of the pigment is adjusted, the preferred solvent and resin are selected, and the blending ratio is satisfied, then penzoin can be omitted and the phosphorization conditions, such as a longer setting time, can be adjusted. If you perform two-stage baking and keep the precure temperature low and leave it for a relatively long time, the problem of armpits will be solved.
しかしペンゾィンを添加しないと自動車の中塗り塗装の
場合は、ライン化されている為にきびしい作業条件を強
いられるので、高膜厚型塗料の商品価値を損う結果とな
る。ペンゾィンを高膜厚型塗料に配合することによって
きびしい作業条件を克服し、商品価層を高めた実用性の
高い高膜厚型塗料となるのである。実施例 1
不揮発分60%のポリエステル(オイルフリーアルキツ
ド)樹脂25重量部と、不揮発分70%のメラミン樹脂
(硬化剤)9.0重量部と0.01〜3仏の粒度分布を
もつ炭酸カルシウム6.丸重量部と0.2〜1.0仏の
粒度分布をもつ酸化チタン2重量部と、1〜50仏の粒
度分布をもつシリカ3.0重量部と、ベンゾィン0.0
重量部と、ドデシルベンゼンスルホン酸(触媒)0.亀
重量部と、アクリル系消泡剤0.2重量部と、シクロヘ
キサノン5重量部と、キシロール6重量部と、セロソル
ブアセテート1.5重量部をデイスパーに配合して、1
5分間燈杵混合し、サンドグライダー2回通過させて分
散した後、脱泡タンクに移し約70狐Hgの減圧度で脱
泡して高膜厚型塗料を得た。However, if Penzoin is not added, the interior coating of automobiles will require harsh working conditions due to the line-based process, which will result in a loss of commercial value of the high film thickness type paint. By blending Penzoin into a high film thickness type paint, it becomes a highly practical high film thickness type paint that overcomes harsh working conditions and increases its commercial value. Example 1 25 parts by weight of a polyester (oil-free alkyd) resin with a non-volatile content of 60%, 9.0 parts by weight of a melamine resin (hardening agent) with a non-volatile content of 70%, and carbonic acid with a particle size distribution of 0.01 to 3 French. Calcium6. 2 parts by weight of titanium oxide with a particle size distribution of 0.2 to 1.0 degrees, 3.0 parts by weight of silica with a particle size distribution of 1 to 50 degrees, and 0.0 parts by weight of benzoin.
parts by weight, and 0.0 parts by weight of dodecylbenzenesulfonic acid (catalyst). 1 part by weight, 0.2 parts by weight of an acrylic antifoaming agent, 5 parts by weight of cyclohexanone, 6 parts by weight of xylol, and 1.5 parts by weight of cellosolve acetate were mixed into a disper.
After mixing with a pestle for 5 minutes and dispersing by passing through a sand glider twice, the mixture was transferred to a defoaming tank and defoamed at a reduced pressure of about 70 Hg to obtain a high film thickness paint.
実施例 2及び3
ペンゾィンの配合割合を1.0及び2重量部さらにキシ
ロールの配合割合を5.7及び4.0重量部とした以外
は実施例1と同様な配合割合で、且つ同様な製法で高騰
厚型塗料を得た。Examples 2 and 3 The same blending ratio as in Example 1 was used, and the same manufacturing method was used, except that the blending ratio of penzoin was 1.0 and 2 parts by weight, and the blending ratio of xylene was 5.7 and 4.0 parts by weight. Soaring prices were obtained for thick-type paint.
比較例
ペンゾインを配合せず、キシロールの配合割合を6.0
重量部とした以外は実施例1と同様な配合割合で、且つ
同様な製法で高膜厚型塗料を得た。Comparative example Penzoin was not blended, and the xylol blend ratio was 6.0.
A high film thickness type paint was obtained using the same compounding ratio as in Example 1 and using the same manufacturing method except that the parts by weight were changed.
以上、実施例1〜3及び比較例で得られた高騰厚型塗料
についてその仕上がり外観及び塗膜性能をみる為に種々
の試験を行い、その結果を以下に掲げる表2に示した。
表 2
尚、上表2に於ける試験方法は、夕し膜厚とは垂直に直
立した鉄板上にェアレススプレーにて実施例1〜3及び
比較例にて得られた高膜厚型塗料を個々に塗布し、目視
にて鉄板上の塗料が最初に流れ始めた乾燥膜厚を記録し
、その数値をタレ膜厚とした。As mentioned above, various tests were conducted to examine the finished appearance and coating performance of the high-rise thick paints obtained in Examples 1 to 3 and Comparative Examples, and the results are shown in Table 2 below.
Table 2 In addition, the test method in Table 2 above is that the high film thickness type paints obtained in Examples 1 to 3 and Comparative Examples were airless sprayed onto a vertically upright iron plate. were applied individually, and the dry film thickness at which the paint first began to flow on the iron plate was recorded by visual observation, and this value was taken as the sagging film thickness.
またワキ膜厚とは鉄板上に高騰厚型塗料をェアレススプ
レーにて塗布し、5分間室温に放置した後、11000
で7分間焼付けさらに140午0で30分間焼付け放袷
後の外観を目視にてワキ(発泡)が生じた最低の乾燥膜
厚を記録しその数値をワキ膜厚とした。またェアレスス
プレー性(作業性)とは高膜厚型塗料をェアレススプレ
ーにかけて吹き付けた際の作業の困難さにて判断し、容
易に均一に塗布できたものを○とし、困難であったもの
を×とする。平滑性とは鉄板上にワキ膜厚に示された膜
厚から約20仏を減じた膜厚にて個々に高膜厚型塗料を
塗布し、凝付け、乾燥後の表面にて判断し、50肌離れ
た位置から目視で塗膜面の凹凸が識別できないものは○
とし、識別できるものは×とする。耐チッピング性はグ
ラベロメーター試験方法(飛び石試験方法)にて測定し
た。0はlk9の小石を空気圧4.0〜4.5k9′の
にて25肌離れた位置から塗膜に90度角にて3回たた
きつけた際に異常なきものであり、×は異常が発生した
ものである。In addition, the underarm film thickness is 11,000 yen after applying a high-rise thick type paint on an iron plate with an airless sprayer and leaving it at room temperature for 5 minutes.
After baking for 7 minutes at 140:00 pm, the appearance was visually observed, and the lowest dry film thickness at which blisters (foaming) occurred was recorded, and this value was taken as the brink film thickness. In addition, airless sprayability (workability) is determined by the difficulty of the work when spraying a high film thickness type paint using an airless sprayer. Let something be x. Smoothness is determined by applying a high film thickness type paint on an iron plate individually at a film thickness that is approximately 20 degrees less than the film thickness shown in the armpit film thickness, and judging the surface after setting and drying. ○ If the unevenness of the coating surface cannot be visually discerned from a distance of 50 skin.
Those that can be identified are marked with an ×. Chipping resistance was measured using the gravelometer test method (stepping stone test method). 0 indicates that there was no abnormality when a pebble of lk9 was struck against the paint film three times at a 90 degree angle from a position 25 skin away at an air pressure of 4.0 to 4.5k9', and x indicates that an abnormality occurred. It is something.
以上、上表2から明らかな如く、この発明は他の物性を
損うことなくワキの発生をきびしい条件下にても防止し
うる高膜厚型塗料を提供している。As is clear from Table 2 above, the present invention provides a high film thickness type paint that can prevent the formation of wrinkles even under severe conditions without impairing other physical properties.
Claims (1)
厚型塗料に於て、該添加剤にはベンゾインが前記塗料1
00重量部に対して0.1〜2重量部含まれており、か
つ該ベンゾインは前記樹脂及び溶剤と相溶して、均一に
分散していることを特徴とする焼付タイプの前記高膜厚
型塗料。1 In a high film thickness type paint containing at least a resin, a solvent, a pigment, and an additive, the additive includes benzoin.
0.1 to 2 parts by weight per 00 parts by weight, and the benzoin is compatible with the resin and solvent and is uniformly dispersed. mold paint.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55072216A JPS6011989B2 (en) | 1980-05-29 | 1980-05-29 | High film thickness paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55072216A JPS6011989B2 (en) | 1980-05-29 | 1980-05-29 | High film thickness paint |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56167766A JPS56167766A (en) | 1981-12-23 |
| JPS6011989B2 true JPS6011989B2 (en) | 1985-03-29 |
Family
ID=13482819
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55072216A Expired JPS6011989B2 (en) | 1980-05-29 | 1980-05-29 | High film thickness paint |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6011989B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6252686U (en) * | 1985-09-19 | 1987-04-01 | ||
| JPS6325791U (en) * | 1986-07-31 | 1988-02-19 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4568606A (en) * | 1984-12-14 | 1986-02-04 | Morton Thiokol, Inc. | Powder coatable epoxy/polyester composition and electrical conductors coated therewith |
| JPH06336569A (en) * | 1993-04-02 | 1994-12-06 | Kubokou Paint Kk | Baking finish composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS585945B2 (en) * | 1975-07-24 | 1983-02-02 | 日立化成工業株式会社 | Fun Taiyoyouji Yushisoseibutsu |
| JPS5488941A (en) * | 1977-12-27 | 1979-07-14 | Nippon Paint Co Ltd | Coating method |
-
1980
- 1980-05-29 JP JP55072216A patent/JPS6011989B2/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6252686U (en) * | 1985-09-19 | 1987-04-01 | ||
| JPS6325791U (en) * | 1986-07-31 | 1988-02-19 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56167766A (en) | 1981-12-23 |
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