JPH0469194B2 - - Google Patents
Info
- Publication number
- JPH0469194B2 JPH0469194B2 JP58067622A JP6762283A JPH0469194B2 JP H0469194 B2 JPH0469194 B2 JP H0469194B2 JP 58067622 A JP58067622 A JP 58067622A JP 6762283 A JP6762283 A JP 6762283A JP H0469194 B2 JPH0469194 B2 JP H0469194B2
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- chloride resin
- paint
- parts
- inorganic material
- 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
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- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
本発明は塩化ビニル樹脂デイスパージヨン塗料
に係り、さらに詳しくは特定無機質材料を塩化ビ
ニル樹脂に対し特定量配合してなる暴露汚染性に
優れ、表面硬度の良好な表面塗膜を与えうる塩化
ビニル樹脂デイスパージヨン塗料に関するもので
ある。
合成樹脂被覆鋼板のなかで、塩化ビニル樹脂被
覆鋼板は、折曲げ、打抜き、深絞り等の加工に十
分に耐え、厚膜に塗装できることから耐候性、耐
食性が優れており用途拡大が計られている。
しかし可塑剤を含むため、表面硬度の点で問題
があり、その改良のため例えば塩化ビニル樹脂デ
イスパージヨン塗料の可塑剤量を減じ、溶剤を用
いるとかあるいはアクリル樹脂などの他種樹脂を
ブレンドすることが屡々おこなわれている。
しかしながら外装用途には耐候性、耐食性付与
の目的で厚膜(100〜300μ塗装が必要であり、上
記の如き溶剤の使用、あるいは他種樹脂のブレン
ドでは塗装後の焼付時にワキ(塗膜のフクレ)が
発生し、均一な塗膜が得られないという問題を生
じる。さらに塩化ビニル樹脂の塗膜は屋外暴露時
にチリ、ゴミが付着し易く、汚染され美観がそこ
なわれ易い(暴露汚染性)という欠点もある。そ
こで通常の熱可塑性の塩化ビニル樹脂デイスパー
ジヨン塗料の長所をいかし外装用途にもそのまま
使用でき、塗装作業性、塗膜性能をそこなうこと
なく塗膜の表面硬度を向上させ、且つ暴露汚染性
にも優れた塗装面を与えうるデイスパージヨン型
塗料が得られるなら業界に益するところ極めて大
である。
如上に鑑み種々の検討を進めた結果、上記の様
な、熱可塑性塩化ビニル樹脂デイスパージヨン塗
料に粒径3〜100μ、モース硬度2〜14の粒状無
機質材を塩化ビニル樹脂100部に対して10〜100未
満部(重量部)の割合で含むことを特徴とする塩
化ビニル樹脂デイスパージヨン塗料が、発明目的
に極めてよく合致するものであることを知り本発
明を完成するに至つた。
本発明のデイスパージヨン塗料は通常プレコー
ト鋼板に適用され耐候性、耐食性、加工性、耐薬
品性、耐湿性等にすぐれ、表面硬度が大で傷が付
き難く、また暴露汚染に対する耐性に優れた塗膜
を与えうる。
本発明でベースとして用いられる塩化ビニル樹
脂デイスパージヨン塗料は塩化ビニル樹脂粉末を
可塑剤に分散した通常のプラスチゾルあるいは一
部溶剤に分散した、または多種樹脂を配合したオ
ルガノゾルの何れであつてもかまわない。
しかしながら好ましくは、例ええば塩化ビニル
ペーストレジン100部、可塑剤30〜70部、安定剤
3〜6部、着色顔料5〜30部、添加剤0.5〜1部
(各重量部)から成る一般的なプラスチゾルであ
る。なお、伐機を添加する関係上、配合物の貯蔵
安定性の面から塗料粘度はB型粘度型でV30=
1000〜8000cpsが望ましい。
この塩化ビニル樹脂デイスパージヨン塗料は熱
可塑性であり、硬化剤を配合した熱硬化性塗料と
は区別されるものである。
本発明に於て使用せられる無機質材料はモース
硬度2〜14で平均粒径が3〜100μの粒状無機充
填材である。かかるモース硬度2〜14の無機材料
としては、例えばCaO,CaCO3,MgO,SiO2,
Al2O3,SiC,CaSO4などの単体もしくは混合物
を主成分とする各種材料があげられ、就中モース
硬度6〜13の例えばCaO,CaCO3,MgO,SiO2,
Al2O3,SiCの単体もしくは混合物を主成分とす
る石コウ、重炭、ガラス、石英、ゲイ砂、アルミ
ナ、炭化ケイ素等が特に好ましく使用せられる。
粒状無機質材の粒径は塗膜の膜厚によつても左
左されるが、通常の塗膜厚(100〜300μ)を考慮
する場合、本発明においては平均粒径3〜100μ
であることが必要である。というのは粒径があま
り小さすぎると発明目的が達成されず又100μを
こえて大きすぎると均一塗膜が得られないからで
ある。
またこのもののベース塗料への混合量は、10〜
100PHR未満、(塩化ビニル樹脂100部に対する部
数)に選択せられる。表面硬度をあげる為には充
填材の量をできるだけ多くすることが望ましいが
多量に配合しすぎると連続塗装作業に於て均一な
る塗装が得られなくなり、また塗膜性能面におい
ても外装面としては不適当になる。従つてその上
限は100PHR程度に限定せられる。他方充填材の
量が10PHR以下の場合には充填材の補強効果は
得られなくなるので望ましくない。無機質充填材
と塗料との混合は通常の高速撹拌機を用いて行な
われ、混合物として貯蔵されるし、又塗装直前に
無機質充填材を塗料に混入することも可能であ
る。十分に混合されれば塩化ビニル樹脂デイスパ
ージヨン塗料は粘性をもつているため、短時間に
沈降することはない。(貯蔵する場合には沈降性
に対してベースのゾル塗料の粘度の高いもの、充
填材の比重が3.0以下のものを用いることが特に
好ましい。)
本発明塗料の焼付塗膜は通常のゾル塗膜に比較
した場合粒状無機質材の量が多い時光沢が下る傾
向にあるが塗膜感としては市場性のあるものであ
り何ら弊害とはならない。また塗膜性能は加工性
を損うこともなく通常のゾル塗膜よりも透湿度の
良好なものが得られる。
以下実施例により本発明を説明する。
実施例 1〜16
ビニゾール1000 OX−20ホワイト(日本ペ
イント社製外装用プラスチゾル)に表の各粒状
無機質材を表中の量だけ(塩化ビニル樹脂100
部当りの量)加え高速撹拌機により均一に混合し
て粒状無気質材含有塩ビゾル塗料を得た。
グラノジン46(日本ペイント社製のリン酸亜鉛
処理剤)によつて塗装前処理を施した亜鉛メツキ
鋼板(板厚0.27〓)に塩化ビゾル用下塗塗料(エ
ポキシ変性アクリル樹脂系)を乾燥膜厚3〜5μ
になる様ナチユラルコーターで塗装し、素材の到
達最高温度が200℃になる様60秒間焼付ける。次
に上記の粒状無機質材含有塩ビゾル塗料をリバー
スコーターで乾燥膜厚200μになる様塗装し素材
の到達最高温度が200℃になる様焼付けし、粒状
無機質材入り塩化ビニル樹脂塗料鋼板を得た。
得られた塗装鋼板の塗膜性能は表の通りであ
る。
The present invention relates to a vinyl chloride resin dispersion paint, and more specifically to a vinyl chloride resin dispersion paint which is made by blending a specific amount of a specific inorganic material into a vinyl chloride resin and which has excellent resistance to exposure and staining and can provide a surface coating film with good surface hardness. This invention relates to resin dispersion paints. Among synthetic resin-coated steel sheets, vinyl chloride resin-coated steel sheets can withstand bending, punching, deep drawing, etc., and can be coated with a thick film, so they have excellent weather resistance and corrosion resistance, and are expected to be used in a wide range of applications. There is. However, since it contains a plasticizer, there is a problem in terms of surface hardness, and to improve this, for example, the amount of plasticizer in the vinyl chloride resin dispersion paint can be reduced, a solvent can be used, or other types of resins such as acrylic resin can be blended. This is often done. However, for exterior applications, a thick coating (100 to 300 μm) is required for the purpose of imparting weather resistance and corrosion resistance, and the use of solvents such as those mentioned above, or blending of other resins, causes underarm (paint blistering) during baking after painting. ), which causes the problem that a uniform coating film cannot be obtained.Furthermore, when exposed outdoors, vinyl chloride resin coatings tend to attract dust and dirt, making them easily contaminated and deteriorating their aesthetic appearance (exposure contamination). Therefore, by taking advantage of the advantages of ordinary thermoplastic vinyl chloride resin dispersion paints, it can be used as is for exterior applications, and improves the surface hardness of the paint film without impairing painting workability or film performance. It would be of great benefit to the industry if a dispersion type paint could be obtained that could provide a coated surface with excellent resistance to exposure and contamination. The vinyl chloride resin dispersion paint contains granular inorganic material having a particle size of 3 to 100μ and a Mohs hardness of 2 to 14 at a ratio of 10 to less than 100 parts (parts by weight) per 100 parts of vinyl chloride resin. We have completed the present invention after discovering that a vinyl chloride resin dispersion paint meets the purpose of the invention very well.The dispersion paint of the present invention is usually applied to pre-coated steel sheets and has excellent weather resistance, corrosion resistance, The vinyl chloride resin dispersion used as a base in the present invention has excellent processability, chemical resistance, moisture resistance, etc., has a high surface hardness, is difficult to scratch, and can provide a coating film with excellent resistance to exposure and contamination. The paint may be either a conventional plastisol in which vinyl chloride resin powder is dispersed in a plasticizer or an organosol partially dispersed in a solvent or blended with various resins.However, it is preferable to use vinyl chloride paste resin 100, for example. This is a general plastisol consisting of 30 to 70 parts of plasticizer, 3 to 6 parts of stabilizer, 5 to 30 parts of color pigment, and 0.5 to 1 part of additive (each part by weight). In terms of storage stability of the formulation, the paint viscosity is type B viscosity, and V 30 =
1000~8000cps is desirable. This vinyl chloride resin dispersion paint is thermoplastic and is distinguished from thermosetting paints containing a curing agent. The inorganic material used in the present invention is a granular inorganic filler having a Mohs hardness of 2 to 14 and an average particle size of 3 to 100 microns. Examples of such inorganic materials having a Mohs hardness of 2 to 14 include CaO, CaCO 3 , MgO, SiO 2 ,
There are various materials whose main components are Al 2 O 3 , SiC, CaSO 4 , etc. alone or in mixtures, among them CaO, CaCO 3 , MgO, SiO 2 , and others with a Mohs hardness of 6 to 13.
Gypsum, heavy carbon, glass, quartz, gay sand, alumina, silicon carbide, and the like whose main components are Al 2 O 3 or SiC alone or in a mixture are particularly preferably used. The particle size of the granular inorganic material also depends on the film thickness of the coating film, but when considering the normal coating film thickness (100 to 300μ), the average particle size in the present invention is 3 to 100μ.
It is necessary that This is because if the particle size is too small, the object of the invention will not be achieved, and if the particle size is too large, exceeding 100 μm, a uniform coating will not be obtained. Also, the amount of this substance mixed into the base paint is 10~
Selected to be less than 100 PHR (number of parts per 100 parts of vinyl chloride resin). In order to increase the surface hardness, it is desirable to increase the amount of filler as much as possible, but if too much is added, it will not be possible to obtain a uniform coating during continuous coating work, and it will also be detrimental to the exterior surface in terms of coating film performance. become inappropriate. Therefore, the upper limit is limited to about 100 PHR. On the other hand, if the amount of the filler is less than 10 PHR, it is not desirable because the reinforcing effect of the filler cannot be obtained. The mineral filler and paint can be mixed using a conventional high-speed stirrer and stored as a mixture, or the mineral filler can be mixed into the paint just before painting. If thoroughly mixed, the vinyl chloride resin dispersion paint will not settle in a short period of time since it has viscosity. (When storing, it is particularly preferable to use a base sol paint with a high viscosity relative to sedimentation properties and a filler with a specific gravity of 3.0 or less.) When compared to a film, when the amount of granular inorganic material is large, the gloss tends to decrease, but the feel of the film is marketable and does not pose any problem. In addition, the coating film has better moisture permeability than ordinary sol coatings without impairing processability. The present invention will be explained below with reference to Examples. Examples 1 to 16 Each granular inorganic material listed in the table was added to Vinisol 1000 OX-20 White (exterior plastisol manufactured by Nippon Paint Co., Ltd.) in the amount shown in the table (vinyl chloride resin 100
(amount per part) and mixed uniformly using a high-speed stirrer to obtain a PVC sol paint containing granular aerogenous material. A dry film thickness of 3 ml undercoat for bisol chloride (epoxy-modified acrylic resin) was applied to a galvanized steel plate (thickness 0.27〓) that had been pre-treated with Granozin 46 (a zinc phosphate treatment agent manufactured by Nippon Paint Co., Ltd.). ~5μ
Paint with a natural coater and bake for 60 seconds to reach a maximum temperature of 200℃. Next, the above-mentioned PVC sol paint containing granular inorganic material was applied to a dry film thickness of 200μ using a reverse coater, and baked so that the maximum temperature reached by the material was 200°C to obtain a steel plate coated with PVC resin containing granular inorganic material. . The coating performance of the obtained coated steel sheet is shown in the table.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
Claims (1)
ガノゾルに、塩化ビニル樹脂固形分100重量部当
たり10〜100重量部未満の割合で、平均粒子径3
〜100μ、モース硬度2〜14の粒状無機質材料を
含有せしめてなるプレコート鋼板用熱可塑性の塩
化ビニル樹脂デイスパージヨン塗料。1 Plastisol or organosol of vinyl chloride resin is added with an average particle diameter of 3 at a ratio of 10 to less than 100 parts by weight per 100 parts by weight of vinyl chloride resin solid content.
A thermoplastic vinyl chloride resin dispersion paint for pre-coated steel sheets containing a granular inorganic material with a Mohs hardness of ~100μ and a Mohs hardness of 2 to 14.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6762283A JPS59193967A (en) | 1983-04-15 | 1983-04-15 | Vinyl chloride resin dispersion coating material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6762283A JPS59193967A (en) | 1983-04-15 | 1983-04-15 | Vinyl chloride resin dispersion coating material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59193967A JPS59193967A (en) | 1984-11-02 |
| JPH0469194B2 true JPH0469194B2 (en) | 1992-11-05 |
Family
ID=13350256
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6762283A Granted JPS59193967A (en) | 1983-04-15 | 1983-04-15 | Vinyl chloride resin dispersion coating material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59193967A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6469089B2 (en) * | 1999-10-08 | 2002-10-22 | Cabot Corporation | Elastomeric compounds with improved wet skid resistance and methods to improve wet skid resistance |
| EP1388365B1 (en) * | 2002-08-08 | 2007-01-17 | Kansai Paint Co., Ltd. | Method and apparatus for mixing toned paint |
| JP5339097B2 (en) * | 2011-04-01 | 2013-11-13 | 大日本印刷株式会社 | Decorative material, door using the same, and method for producing decorative material |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52125542A (en) * | 1976-02-14 | 1977-10-21 | Ota Toshuki | Painting method |
| JPS5541664A (en) * | 1978-09-19 | 1980-03-24 | Tokyo Shibaura Electric Co | Filament coil for bulb |
-
1983
- 1983-04-15 JP JP6762283A patent/JPS59193967A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59193967A (en) | 1984-11-02 |
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