JPS58171446A - Thermosetting resin composition - Google Patents

Thermosetting resin composition

Info

Publication number
JPS58171446A
JPS58171446A JP5231982A JP5231982A JPS58171446A JP S58171446 A JPS58171446 A JP S58171446A JP 5231982 A JP5231982 A JP 5231982A JP 5231982 A JP5231982 A JP 5231982A JP S58171446 A JPS58171446 A JP S58171446A
Authority
JP
Japan
Prior art keywords
parts
resin
thermosetting resin
resin composition
polymer additive
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
Application number
JP5231982A
Other languages
Japanese (ja)
Other versions
JPH0587535B2 (en
Inventor
Hirobumi Takeda
竹田 博文
Koji Tokunaga
幸次 徳永
Akio Shoji
東海林 章夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DIC Corp
Original Assignee
Dainippon Ink and Chemicals Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dainippon Ink and Chemicals Co Ltd filed Critical Dainippon Ink and Chemicals Co Ltd
Priority to JP5231982A priority Critical patent/JPS58171446A/en
Publication of JPS58171446A publication Critical patent/JPS58171446A/en
Publication of JPH0587535B2 publication Critical patent/JPH0587535B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To prepare the titled resin composition giving a coating film having excellent smoothness, gloss and brightness, and sufficiently high hiding power and flexibility, and useful as a coating material, especially a powder coating material, by adding a specific amount of a silicon-containing polymer additive to the base resin. CONSTITUTION:100pts.wt. of a thermosetting resin such as polyester resin, vinyl polymer, epoxy resin, etc., is compounded with 0.01-10pts.wt., especially 0.1- 5pts.wt. of a silicon-containing polymer additive having a number-average molecular weight of >=500, preferably 1,000-100,000.

Description

【発明の詳細な説明】 本発明は塗料用、%KI&体塗料用として有用なる熱硬
化性の樹脂組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a thermosetting resin composition useful for paints and %KI & body paints.

粉体塗装によって、金属の表面上にポリエステル、アク
リル樹脂およびエポキシ樹脂系などの熱硬化性樹脂組成
物を被榎することは既に公知であり、特に公害対策上か
らも、自動化に適する処からも、近年、装飾的塗装など
に広く利用されてはいるが、かかる粉体塗料が溶剤を使
用していない処から、得られる塗料は平滑性などの外観
上、溶剤型塗料に劣る傾向にある。
It is already known that powder coating is used to coat metal surfaces with thermosetting resin compositions such as polyester, acrylic resin, and epoxy resin. In recent years, powder coatings have been widely used for decorative coatings, etc., but since such powder coatings do not use solvents, the resulting coatings tend to be inferior to solvent-based coatings in terms of appearance such as smoothness.

とりわけ、耐候性が優れている点では、近年、脚光を浴
びているビニル重合体系塗料にしても、顔料分散性が良
くないために顔料濃度を高くすることができなく、した
がつ【隠蔽力が小さいという欠点を有していた。
In particular, even with vinyl polymer paints, which have been in the spotlight in recent years for their excellent weather resistance, it is not possible to increase the pigment concentration due to poor pigment dispersibility. It had the disadvantage of being small.

その結果、顔料として、たとえば酸化チタンを使用した
場合は、平滑で、かつ、光沢のすぐれた塗膜を得るため
の顔料濃度は25重量嗟が限度であった。
As a result, when titanium oxide, for example, is used as a pigment, the pigment concentration required to obtain a smooth and glossy coating film is limited to 25% by weight.

加えて、かかる粉体塗料の新しい用途として、PCM(
プレ・コート・メソッド)化が現実的な時代の要請とな
ってきて、その早急な解決も望まれている。
In addition, PCM (
Pre-court method) has become a realistic requirement of the times, and an immediate solution is desired.

しかるに、本発明者らは上述の如き現状に鑑みヤ鋭意研
究した結果、ここに特定の高分子添加剤を特定量配合さ
せることにより、熱硬化性樹脂本来のすぐれた塗膜特性
を損うことなしに、著しく平滑性、光沢および鮮映性に
すく2れ、しかも十分な隠蔽力および可撓性を有する塗
料が得られることを、さらに進んで、こうしたすぐれた
効果が単に粉体塗料ばかりではなく、通常の有機溶剤溶
液系、水溶液系および分散液の各塗料に対しても、その
まま保持できることをも見出して、本発明を完成させる
に到った。
However, as a result of intensive research in view of the current situation as described above, the present inventors have found that by incorporating a specific amount of a specific polymer additive here, the excellent coating film properties inherent to the thermosetting resin are impaired. Furthermore, we have demonstrated that it is possible to obtain a coating material that has excellent smoothness, gloss, and sharpness, as well as sufficient hiding power and flexibility, without using powder coatings. The present invention was completed based on the discovery that the present invention can be maintained as is even in ordinary organic solvent solution-based, aqueous solution-based and dispersion-based paints.

すなわち、本発明は熱硬化性樹脂体)と、数平均分子量
が500以上なる珪素含有高分子添加剤(B)とを必須
の成分とし、前者樹脂(4)成分の100重量部に対し
、後者添加剤(B)がα01〜10重量部となる割合で
含んで成る熱硬化性樹脂組成物を提供するものである。
That is, the present invention uses a thermosetting resin (thermosetting resin body) and a silicon-containing polymer additive (B) having a number average molecular weight of 500 or more as essential components, and the latter is added to 100 parts by weight of the former resin (4) component. The present invention provides a thermosetting resin composition comprising an additive (B) in a proportion of α01 to 10 parts by weight.

ここにおいて、前記熱硬化性樹脂(4)としては、公知
のものがそのまま使用できるが、そのうち代表的なもの
とじてはポリエステル系、ビニル重合体系およびエポキ
シ樹脂系などが挙げられる。
Here, as the thermosetting resin (4), known resins can be used as they are, and typical examples include polyester resins, vinyl polymer resins, and epoxy resin resins.

ポリエステル系KM当するものkは多価カルボン酸類と
多価アルコール類とから得られるポリエステルに硬化剤
を配合せしめたものとか、自己架橋硬化性のポリエステ
ルなどがあり、またビニル重合体系に該当するものとし
ては水酸基、カルボキシル基、グリシジル基もしくはオ
キサゾリニル基などの官能基を有するビニル系単量体と
その他のビニル系単量体とから得られるビニル共重合体
に硬化剤を配合せしめたものとか、ブトキシメチルアミ
ド基の如き自己架橋性官能基を有するビニル系共重合体
とか、さらには上記両タイプのビニル系共重合体をエポ
キシ樹脂またはポリエステルなどで変性せしめたものな
どが用いられるし、これら両系の樹脂に用いられる硬化
剤としては、各共重合体の官能基が水酸基である場合に
は、ヘキサメトキシメチルメラミンもしくはテトラブト
キシベンゾグアナミンなどのアミノ樹脂またはブロック
ポリイソシアネートなどが用いられるし、カルボキシル
基の場合にはエポキシ樹脂またはポリオキサゾリンなど
が用いられるし、またグリシジル基の場合には多価カル
ボン酸類や多価アルコール類などが用いられる。
Polyester KM refers to polyesters obtained from polycarboxylic acids and polyhydric alcohols with a curing agent added, self-crosslinking and curing polyesters, and vinyl polymer systems. For example, a vinyl copolymer obtained from a vinyl monomer having a functional group such as a hydroxyl group, a carboxyl group, a glycidyl group, or an oxazolinyl group and another vinyl monomer is blended with a curing agent, or a butoxy resin. Vinyl copolymers having self-crosslinking functional groups such as methylamide groups, and vinyl copolymers of both types mentioned above modified with epoxy resins or polyesters, etc., are used. When the functional group of each copolymer is a hydroxyl group, an amino resin such as hexamethoxymethylmelamine or tetrabutoxybenzoguanamine or a block polyisocyanate is used as a curing agent for the resin. In the case of glycidyl groups, epoxy resins or polyoxazolines are used, and in the case of glycidyl groups, polyhydric carboxylic acids and polyhydric alcohols are used.

さらに、エポキシ樹脂系に該当するものkはビスフェノ
ール型もしくはエステル型などの多価エポキシ化合物と
アミ7類もしくは酸類などの硬化剤とを組み合わせたも
のなどがある。
Further, examples of the epoxy resin type include those that combine a polyhydric epoxy compound such as a bisphenol type or an ester type with a curing agent such as Ami-7 or an acid.

他方、前記した珪素含有高分子添加剤(B)とは、珪素
含有重合性単量体とその他の重合性単量体との共重合に
より得られる数平均分子量が500以上のものを指体す
るものであるが、そのうち該珪素含有重合性単量体とし
て代表的なものには、次に示すようなものがある。
On the other hand, the above-mentioned silicon-containing polymer additive (B) refers to one having a number average molecular weight of 500 or more obtained by copolymerization of a silicon-containing polymerizable monomer and another polymerizable monomer. Among these, typical silicon-containing polymerizable monomers include the following.

また、その他の重合性単量体として代表的なものにはス
チレン、メチル(メタ)アクリレート、エチル(メタ)
アクリレート、プロピル(メタ)アクリレート、ブチル
(メタ)アクリレート、2−エチルヘキシル(メタ)ア
クリレート、ジエチルフマレート、ジブチルフマレート
、アクリルアミド、アクリロニトリル、(メタ)アクリ
ル酸または酢酸ビニルなどがある。
In addition, other typical polymerizable monomers include styrene, methyl (meth)acrylate, and ethyl (meth)acrylate.
Examples include acrylate, propyl (meth)acrylate, butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, diethyl fumarate, dibutyl fumarate, acrylamide, acrylonitrile, (meth)acrylic acid or vinyl acetate.

当である。この分子量が500よりも低いものの場合に
は、本発明の特長の一つである、塗膜の十分な光沢およ
び平滑性を有することのできる顔料濃度を高くすること
が不可能となり、この濃度を著しく低下させる結果とな
る。
That's true. If this molecular weight is lower than 500, it becomes impossible to increase the pigment concentration to provide sufficient gloss and smoothness of the coating film, which is one of the features of the present invention. This results in a significant decrease.

本発明組成物は前記した樹脂(4)の100重量部に対
して前記高分子添加剤(B)が0.01〜10重量部好
ましくは0.1〜5重量部となる割合で、これら(A)
、(B)両成分を必須の成分として配合せしめて得られ
るものである。
The composition of the present invention contains the polymer additive (B) in a ratio of 0.01 to 10 parts by weight, preferably 0.1 to 5 parts by weight, based on 100 parts by weight of the resin (4). A)
, (B) are obtained by blending both components as essential components.

この場合に、高分子添加剤(B)がQ、01重量部未満
となって配合比が小さくなると、どうしても前記したよ
うな効果。
In this case, if the amount of the polymer additive (B) is less than 01 parts by weight and the blending ratio becomes small, the above-mentioned effect will inevitably occur.

特長が十分に発揮され得なく、逆に10重量部を越えて
配合比が大きくなると塗膜の物理的性質とか、耐汚染性
などが低下するので、いずれも好ましくない。
On the other hand, if the blending ratio exceeds 10 parts by weight, the physical properties and stain resistance of the coating film will deteriorate, which is not preferable.

かくして得られる本発明の樹脂組成物は塗料用として、
とくに粉体塗料用として有用なものであり、本発明組成
物から粉体塗料を調製するには、予め溶融混合された該
樹脂組成物に顔料、充填剤、添加剤その他の配合成分を
投入して溶融混合させ、冷却させたのち粉砕せしめる方
法であるとか、前記したそれぞれ樹脂(A)、高分子添
加剤(B)およびその他の配合成分なる各成分の乾式混
合物を溶融混合させ、冷却後粉砕せしめる方法であると
か、さらKは溶剤中で核樹脂組成物と前記その他の配合
成分とを混合させ、スプレー・ドライヤー処理せしめる
方法など、いずれの方法によってもよい。
The thus obtained resin composition of the present invention can be used for paints,
It is particularly useful for powder coatings, and to prepare powder coatings from the composition of the present invention, pigments, fillers, additives, and other ingredients are added to the resin composition that has been melt-mixed in advance. Alternatively, a dry mixture of each of the resin (A), polymer additive (B), and other ingredients described above may be melt-mixed, cooled, and then pulverized. Any method may be used, such as a method in which the core resin composition and the other ingredients mentioned above are mixed in a solvent, and then treated with a spray dryer.

そして、粉体塗料の塗布法としては静電塗装または流動
浸漬塗装などの如き公知慣用の方法が、いずれも採用で
きる。
As a method for applying the powder coating, any known and commonly used method such as electrostatic coating or fluidized dip coating can be employed.

もちろん、本発明組成物は通常の有機溶剤溶液系、水溶
液系および分散液系などの塗料として用いることもでき
る。
Of course, the composition of the present invention can also be used as a coating material such as a conventional organic solvent solution type, aqueous solution type, or dispersion type.

次K、本発明を参考例、実施例および比較例により詳細
に説明するが、以下において部およびチは特に断りのな
い限り、すべて重量基準であるものとする。
Next, the present invention will be explained in detail with reference to Reference Examples, Examples, and Comparative Examples. In the following, all parts and parts are based on weight unless otherwise specified.

参考例1 (珪素含有高分子添加剤(B)の調製例)温
度計、攪拌機および還流冷却器を備えた反応器中に、5
0部のキシレンと50部の酢酸n−ブチルとを加えて1
25℃に加熱し、そこへ40部のスチレン、50部のメ
タクリル酸n−ブチル、10部のγ−メタクリロキシプ
ロピルトリメトキシシランおよび3部のアゾビスイソブ
チロニトリルからなる混合物を4時間に亘って加え、同
温度に10時間保持し【得られた溶液から、減圧(5W
H&)に℃溶剤を除去せしめて数平均分子量が4000
なる目的物添加剤を得た。以下、これを高分子添加剤(
B−1)と略記する。
Reference Example 1 (Preparation example of silicon-containing polymer additive (B)) In a reactor equipped with a thermometer, a stirrer and a reflux condenser, 5
Add 0 parts of xylene and 50 parts of n-butyl acetate to 1
Heating to 25°C, a mixture consisting of 40 parts of styrene, 50 parts of n-butyl methacrylate, 10 parts of γ-methacryloxypropyltrimethoxysilane and 3 parts of azobisisobutyronitrile was added for 4 hours. The resulting solution was heated under reduced pressure (5W) and kept at the same temperature for 10 hours.
The number average molecular weight is 4000 after removing the solvent in H&).
A target additive was obtained. Below, this is referred to as a polymer additive (
It is abbreviated as B-1).

参考例2 (同  上) γ−メタクリロキシグロビルトリメトキシシランの代わ
りK、同量のビニルトリエトキシシランを使用した以外
は、参考例1と同様の操作を繰り返して数平均分子量が
5,500なる目的物添加剤を得た。
Reference Example 2 (Same as above) The same operation as Reference Example 1 was repeated except that K was used instead of γ-methacryloxyglobiltrimethoxysilane and the same amount of vinyltriethoxysilane was used to obtain a number average molecular weight of 5,500. A target additive was obtained.

以下、これを高分子添加剤(B−2)と略記する。Hereinafter, this will be abbreviated as a polymer additive (B-2).

実施例1.2および比較例1.2 参考例1と同様の反応器に、100部のキシレンを加え
て125℃に加熱し、そこへ40部のスチレン、go部
のグリシジルメタクリレート、30部のイソブチルメタ
クリレート、4部のアゾビスイソブチロニトリルおよび
1部のt−ブチルパーベンゾエートからなる混合物を2
時間に亘って加え、同温度VC10時間保持したのち、
溶剤を除去せしめて軟化点が108℃で数平均分子量が
5.000なる樹脂を得た。
Example 1.2 and Comparative Example 1.2 100 parts of xylene was added to the same reactor as in Reference Example 1 and heated to 125°C, and 40 parts of styrene, go part of glycidyl methacrylate, and 30 parts of xylene were added thereto. A mixture of isobutyl methacrylate, 4 parts azobisisobutyronitrile and 1 part t-butyl perbenzoate was added to 2
After adding it over a period of time and maintaining the same temperature VC for 10 hours,
The solvent was removed to obtain a resin having a softening point of 108° C. and a number average molecular weight of 5.000.

次いで、この樹脂の85部に対して15部の1.10−
デカンジカルボン酸、1部の「モダフロー」(米国モン
サ、′、、・ ント社製の流展剤)、および43部の酸化チタンを配合
させただけのものを比較例1とし、さらにこの配合物に
各別k、参考例1または2で得られた高分子添加剤(B
−1)または(B−2)のそれぞれ3部を加えて本発明
組成物を2穫類得た。
Then 15 parts of 1.10- to 85 parts of this resin
Comparative Example 1 was prepared by simply blending decanedicarboxylic acid, 1 part of "Modaflow" (a flow agent manufactured by Monsa, Inc., USA), and 43 parts of titanium oxide. The polymer additive obtained in Reference Example 1 or 2 (B
Two compositions of the present invention were obtained by adding 3 parts each of -1) or (B-2).

なお、酸化チタンの配合量を25部に変更させたものを
比較例2とした。
Comparative Example 2 was prepared by changing the amount of titanium oxide to 25 parts.

しかるのち、得られた都合4穫の樹脂組成物について、
それぞれな押出機にて100℃で混練させ【から、20
0メツシユの金網で分級せしめて同メツシュ以下の粉体
塗料を得た。
After that, regarding the obtained resin composition,
The mixture was kneaded at 100℃ using various extruders.
It was classified using a wire mesh with a mesh size of 0 to obtain a powder coating with a mesh size of less than the same mesh.

次K、これら3樵の塗料を各別に、静電吹付塗装にて燐
酸亜鉛処理鋼板に塗布し、180℃で20分間焼き付け
て、それぞれの塗膜を得た。
Next, each of these three paints was applied to a zinc phosphate-treated steel plate by electrostatic spray coating, and baked at 180°C for 20 minutes to obtain each coating film.

各塗膜についての性能試験の結果は、第1表にまとめて
示す。
The performance test results for each coating film are summarized in Table 1.

Claims (1)

【特許請求の範囲】[Claims] l、必須の成分として、(4)熱硬化性樹脂と、(B)
数平均分子量が500以上である珪素含有高分子添加剤
とを、前者樹脂囚の100重量部に対し、後者添加剤(
B)がQ、01〜10重量部となる割合で含んで成る熱
硬化性樹脂組成物。
l. As essential components, (4) thermosetting resin, and (B)
A silicon-containing polymer additive having a number average molecular weight of 500 or more is added to 100 parts by weight of the former resin, and the latter additive (
A thermosetting resin composition comprising B) in a proportion of Q, 01 to 10 parts by weight.
JP5231982A 1982-04-01 1982-04-01 Thermosetting resin composition Granted JPS58171446A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5231982A JPS58171446A (en) 1982-04-01 1982-04-01 Thermosetting resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5231982A JPS58171446A (en) 1982-04-01 1982-04-01 Thermosetting resin composition

Publications (2)

Publication Number Publication Date
JPS58171446A true JPS58171446A (en) 1983-10-08
JPH0587535B2 JPH0587535B2 (en) 1993-12-17

Family

ID=12911462

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5231982A Granted JPS58171446A (en) 1982-04-01 1982-04-01 Thermosetting resin composition

Country Status (1)

Country Link
JP (1) JPS58171446A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63260964A (en) * 1987-04-20 1988-10-27 Dainippon Ink & Chem Inc Thermosetting resin paint for can
WO1990009412A1 (en) * 1989-02-10 1990-08-23 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Thermosetting composition
JP2002348527A (en) * 2001-05-23 2002-12-04 Kusumoto Kasei Kk Smoothing agent for powder coating
US20170267799A1 (en) * 2014-12-02 2017-09-21 Basf Coatings Gmbh Pigmented coating agent and coatings produced therefrom
CN107207672A (en) * 2014-12-02 2017-09-26 巴斯夫涂料有限公司 Coloured coating agent and coating prepared therefrom
JP2018505237A (en) * 2014-12-02 2018-02-22 ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH Copolymer and pigmented coating agent containing said copolymer

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49107086A (en) * 1973-02-12 1974-10-11
JPS5434405A (en) * 1977-08-17 1979-03-13 Dow Chemical Co High strength nonwoven fiber mateial
JPS5443242A (en) * 1977-09-13 1979-04-05 Kansai Paint Co Ltd Resin composition for rust preventive coating compound
JPS5443940A (en) * 1977-09-14 1979-04-06 Kansai Paint Co Ltd Resin composition for corrosion-resistant coating
JPS5614556A (en) * 1979-07-13 1981-02-12 Hitachi Ltd Curing method of thermosetting resin composition
JPS5730754A (en) * 1980-07-31 1982-02-19 Toray Silicone Co Ltd Vinyl type resin composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49107086A (en) * 1973-02-12 1974-10-11
JPS5434405A (en) * 1977-08-17 1979-03-13 Dow Chemical Co High strength nonwoven fiber mateial
JPS5443242A (en) * 1977-09-13 1979-04-05 Kansai Paint Co Ltd Resin composition for rust preventive coating compound
JPS5443940A (en) * 1977-09-14 1979-04-06 Kansai Paint Co Ltd Resin composition for corrosion-resistant coating
JPS5614556A (en) * 1979-07-13 1981-02-12 Hitachi Ltd Curing method of thermosetting resin composition
JPS5730754A (en) * 1980-07-31 1982-02-19 Toray Silicone Co Ltd Vinyl type resin composition

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63260964A (en) * 1987-04-20 1988-10-27 Dainippon Ink & Chem Inc Thermosetting resin paint for can
JPH0258302B2 (en) * 1987-04-20 1990-12-07 Dainippon Ink & Chemicals
WO1990009412A1 (en) * 1989-02-10 1990-08-23 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Thermosetting composition
JP2002348527A (en) * 2001-05-23 2002-12-04 Kusumoto Kasei Kk Smoothing agent for powder coating
CN107207673A (en) * 2014-12-02 2017-09-26 巴斯夫涂料有限公司 Coloured coating agent and coating prepared therefrom
CN107207672A (en) * 2014-12-02 2017-09-26 巴斯夫涂料有限公司 Coloured coating agent and coating prepared therefrom
US20170267799A1 (en) * 2014-12-02 2017-09-21 Basf Coatings Gmbh Pigmented coating agent and coatings produced therefrom
JP2018501343A (en) * 2014-12-02 2018-01-18 ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH Pigmented coating agent and coating made from the pigmented coating agent
JP2018502944A (en) * 2014-12-02 2018-02-01 ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH Pigmented coating agent and coating made from the pigmented coating agent
JP2018505237A (en) * 2014-12-02 2018-02-22 ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH Copolymer and pigmented coating agent containing said copolymer
US10465088B2 (en) 2014-12-02 2019-11-05 Basf Coatings Gmbh Pigmented coating agent and coatings produced therefrom
US10544250B2 (en) 2014-12-02 2020-01-28 Basf Coatings Gmbh Pigmented coating agent and coatings produced therefrom
CN107207673B (en) * 2014-12-02 2020-07-24 巴斯夫涂料有限公司 Colored coating agent and coating produced therefrom
CN107207672B (en) * 2014-12-02 2020-07-24 巴斯夫涂料有限公司 Colored coating agent and coating produced therefrom

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