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JPH08302239A - Transparent coating - Google Patents

Transparent coating

Info

Publication number
JPH08302239A
JPH08302239A JP7105215A JP10521595A JPH08302239A JP H08302239 A JPH08302239 A JP H08302239A JP 7105215 A JP7105215 A JP 7105215A JP 10521595 A JP10521595 A JP 10521595A JP H08302239 A JPH08302239 A JP H08302239A
Authority
JP
Japan
Prior art keywords
coating
test
agent
matting agent
particle diameter
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
Application number
JP7105215A
Other languages
Japanese (ja)
Inventor
Mitsuo Hamasaka
光雄 浜坂
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.)
Artience Co Ltd
Original Assignee
Toyo Ink Mfg 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 Toyo Ink Mfg Co Ltd filed Critical Toyo Ink Mfg Co Ltd
Priority to JP7105215A priority Critical patent/JPH08302239A/en
Publication of JPH08302239A publication Critical patent/JPH08302239A/en
Pending legal-status Critical Current

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  • Paints Or Removers (AREA)

Abstract

PURPOSE: To form an effective transparent protecting film having durability without changing the original hue such as of a mortar, a concrete, a stone or a brick by coating with a composition containing a flatting agent added to a transparent resin coating material. CONSTITUTION: (B) A flatting agent comprising an inorganic precipitated barium sulfate, calcium carbonate, talc, alumina, diatomaceous earth, silica, etc., or glass, a polymeric bead or a hollow bead having preferably 2-10μm particle diameter in an amount of 5-30wt.% is added to (A) a transparent resin coating material comprising a polymeric aqueous emulsion of an acrylic resin having preferably <=100nm average particle diameter.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業の利用分野】本発明は、モルタル、コンクリー
ト、石材、レンガ等の多孔質無機建材等の透明仕上げ塗
装方法に関するものであり、コンクリート、モルタル等
の本来の色相を変えることなく有効な耐久性のある保護
皮膜を与えることのできる透明塗装方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a transparent finish coating method for porous inorganic building materials such as mortar, concrete, stone, brick, etc., and has an effective durability without changing the original hue of concrete, mortar, etc. The present invention relates to a transparent coating method capable of providing a protective coating having a color.

【0002】[0002]

【従来の技術】従来、モルタル、コンクリート、石材、
レンガ、セラミック等に保護皮膜等を施さずにそのまま
仕上材として用いた建築物等では、雨水による変色や大
気中の汚染物質により汚れたりして、外観が損なわれ問
題となっている。それらの建築物等の保護を目的とし、
材料の外観を損なわせない種々の透明塗装方法が開発さ
れてきたが、溶剤型のクリヤー塗料を用いて塗装する技
術では、塗料により下地が本来の色相より濃く(以下濡
れ色と称す)仕上がり、外観が損なわれて設計当初の本
来の思考を満たすことは困難であった。
2. Description of the Related Art Conventionally, mortar, concrete, stone materials,
In a building or the like, which is used as a finishing material as it is without applying a protective film or the like on bricks, ceramics, etc., its appearance is impaired due to discoloration caused by rainwater and contamination by pollutants in the atmosphere, which is a problem. For the purpose of protecting those buildings,
Various transparent coating methods have been developed that do not impair the appearance of the material, but in the technique of coating with a solvent-based clear coating, the base finish is darker than the original hue (hereinafter referred to as wet color) with the paint, It was difficult to satisfy the original thought of the original design because the appearance was damaged.

【0003】また、従来の粒子径の比較的大きな水性合
成樹脂エマルジョンを用いた場合には、溶剤型の塗料と
比べて濡れ色の発生は回避されるものの、エマルジョン
粒子の粒子径が大きいために下地への密着性が乏しく、
水分の影響により塗膜の膨れや剥がれを生じ必要な塗膜
物性を満たすことは困難であった。
Further, when an aqueous synthetic resin emulsion having a relatively large particle diameter is used, the occurrence of wet color is avoided as compared with a solvent type paint, but the emulsion particles have a large particle diameter. Poor adhesion to the base,
Due to the influence of water, the coating film swells or peels off, making it difficult to satisfy the required physical properties of the coating film.

【0004】[0004]

【発明が解決しようとする課題】本発明は、前記の問題
点を解決すべく、鋭意研究を重ねた結果、建築物等の保
護を目的として、合成樹脂を使用した塗料を用いる事が
でき、モルタル、コンクリート、石材、レンガ、セラミ
ック等の外観を損なわず、濡れ色を発生させることなく
仕上げる透明塗装方法を提供するものである。
DISCLOSURE OF THE INVENTION In the present invention, as a result of intensive studies to solve the above-mentioned problems, a paint using a synthetic resin can be used for the purpose of protecting buildings and the like. The present invention provides a transparent coating method for finishing mortar, concrete, stone materials, bricks, ceramics, etc. without impairing the appearance and producing no wet color.

【0005】[0005]

【課題を解決するための手段】すなわち、本発明は、一
般的な塗膜材料の艶消し材として用いられている艶消し
剤を合成樹脂中に添加して、従来の問題点を克服した塗
装方法を提供する。艶消し剤としては、特に制限はな
く、無機系の沈降性硫酸バリウム、炭酸カルシウム、ク
レー、タルク、アルミナ、ケイソウ土、シリカ等や、ガ
ラス、高分子系のビーズ、中空ビーズ等が艶消し剤とし
て挙げられるが、本発明はこれらの艶消し剤に限定され
るものではない。また、塗布される基材の風合いを損な
わせないために、艶消し剤単独の屈折率が2.0以下で
あることが好ましい。
[Means for Solving the Problems] That is, according to the present invention, a matting agent used as a matting material for general coating materials is added to a synthetic resin to overcome the conventional problems. Provide a way. There is no particular limitation on the matting agent, and inorganic matting agents such as barium sulfate, calcium carbonate, clay, talc, alumina, diatomaceous earth, silica, etc., glass, polymer beads, hollow beads, etc. However, the present invention is not limited to these matting agents. Further, the refractive index of the matting agent alone is preferably 2.0 or less so as not to impair the texture of the coated substrate.

【0006】一般的に用いられる艶消し剤において、そ
の粒子径が2.0μmより小さいと、比表面積が大きく
なり樹脂中への分散安定性が低下するおそれがあるため
に、艶消し剤の添加量を少なくせざるをえない。しか
し、本発明に於ける塗膜材料を提供するためには、一定
量の艶消し剤量が必要であり、十分な効果を発揮させる
にはある特定量以上の艶消し剤を必要とする。また、艶
消し剤の粒子径が大きくなると艶消し剤の沈降等の問題
が発生するおそれがある。これらのことより艶消し剤の
粒子径が2〜10μmの範囲にある事が好ましい。又、
下地の外観を損なわないためには隠蔽力の低いものが適
している。
In a commonly used matting agent, if the particle size is smaller than 2.0 μm, the specific surface area becomes large and the dispersion stability in the resin may be deteriorated. There is no choice but to reduce the amount. However, in order to provide the coating material of the present invention, a certain amount of the matting agent is required, and a certain amount or more of the matting agent is required to exert a sufficient effect. Further, if the particle size of the matting agent becomes large, problems such as sedimentation of the matting agent may occur. From these facts, it is preferable that the particle size of the matting agent is in the range of 2 to 10 μm. or,
A material with low hiding power is suitable so as not to impair the appearance of the base.

【0007】艶消し剤の添加量としては、個々の艶消し
剤の隠蔽力や屈折率にもよるが、入射光の乱反射を起こ
させる為に添加量は重要な要素であり、合成樹脂固形分
に対して5.0%以上は必要で、好ましくは10〜30
%である。
The amount of the matting agent added depends on the hiding power and refractive index of each matting agent, but the amount added is an important factor for causing diffuse reflection of incident light. 5.0% or more is necessary, and preferably 10 to 30
%.

【0008】合成樹脂としては、水性の高分子系エマル
ジョンで、従来の水性エマルジョンの欠点であった下地
への密着性を改善するため、すなわち下地の細孔中への
浸透を向上させるために、エマルジョンの粒子径は10
0nm以下、さらにより好ましくは80nm以下であ
る。水性の高分子系エマルジョンとしては、アクリル、
シリコン、ポリエステル、ウレタン、フッ素、合成ゴ
ム、オレフィン系などが上げられるが、分散性や粘度調
整の扱いやすさ等、塗料としての適性等を考えると、ア
クリル系のエマルジョンが望ましい。
As the synthetic resin, an aqueous polymer emulsion is used, in order to improve the adhesion to the substrate, which is a drawback of conventional aqueous emulsions, that is, to improve the penetration into the pores of the substrate, Emulsion particle size is 10
It is 0 nm or less, and even more preferably 80 nm or less. Aqueous polymer emulsion, acrylic,
Silicon, polyester, urethane, fluorine, synthetic rubber, olefins, and the like can be used, but acrylic emulsions are preferable in consideration of dispersibility, ease of handling viscosity adjustment, and suitability as a paint.

【0009】塗装方法としては、本開発品の単独塗装方
法以外に、本開発品のクリヤー塗料や、他の微粒子エマ
ルジョンを下塗り剤として使用する方法や、現行の下塗
り剤を用いることも可能であるが、下塗り剤として濡れ
色を発生させないためには、水性の下塗り剤をもちいる
ことが好ましい。その他下塗り剤としては、シラン系の
浸透性吸水防止剤等を用いることも可能である。
As the coating method, in addition to the single coating method of the developed product, a clear coating of the developed product, a method of using another fine particle emulsion as an undercoating agent, or a current undercoating agent can be used. However, in order to prevent a wet color from being generated as the undercoat, it is preferable to use an aqueous undercoat. In addition, it is also possible to use a silane-based penetrating water absorption inhibitor or the like as the undercoating agent.

【0010】また、塗装材としての表面保護の観点か
ら、屋外使用の場合、耐候性、耐汚染性等の耐性をより
向上させるため、本開発品の塗装後に、一般的なトップ
・コート剤を用いて二層に重塗りすることも可能であ
る。トップコート剤としてはアクリル、シリコン、ポリ
エステル、ウレタン、フッ素、合成ゴム、オレフィン系
等が挙げられる。但し、塗料としては、クリヤー、若し
くは艶消し用塗料でなければならない。その他、下塗り
剤との組み合わせにより、下塗り剤、本発明品、上塗り
剤の重ね塗りによる三層コート方法等も可能である。
Further, from the viewpoint of surface protection as a coating material, in order to further improve resistance such as weather resistance and stain resistance in the case of outdoor use, a general top coat agent is applied after coating the developed product. It is also possible to use and to coat two layers. Examples of the top coat agent include acrylics, silicones, polyesters, urethanes, fluorine, synthetic rubbers and olefins. However, the paint must be clear or matting paint. In addition, by combining with an undercoating agent, a three-layer coating method by overcoating the undercoating agent, the product of the present invention, and the overcoating agent is also possible.

【0011】[0011]

【実施例】【Example】

実施例1〜6 本発明品の単独塗装で、ベース樹脂としてアクリル系エ
マルジョン、艶消し剤としてケイ酸微粉末を用いた例。 実施例7 本発明品の単独塗装で、ベース樹脂としてアクリル系エ
マルジョン、艶消し剤として高分子系ポリマービーズを
用いた例。 実施例8〜9 本発明品を上塗り剤として用いた塗装で、ベース樹脂と
してアクリル系エマルジョン、艶消し剤としてケイ酸微
粉末を使用し、下塗り剤にアクリル系エマルジョンを用
いた例(実施例8)、シラン系浸透性吸水防止剤を用い
た例(実施例9)。 実施例10〜11 本発明品を下塗り剤として用いた塗装で、ベース樹脂と
してアクリル系エマルジョン、艶消し剤としてケイ酸微
粉末を使用し、上塗り剤に市販のポリエステル系二液タ
イプの溶剤型塗料(艶消しタイプ)を用いた例(実施例
10)、市販のフッ素系二液タイプの溶剤型塗料(艶消
しタイプ)を用いた例(実施例11)。 実施例12〜13 本発明品を中塗り剤として用いた塗装で、ベース樹脂と
してアクリル系エマルジョン、艶消し剤としてケイ酸微
粉末を使用し、下塗り剤にアクリル系エマルジョンを用
い、上塗り剤に市販のポリエステル系二液タイプの溶剤
型塗料(艶消しタイプ)を用いた例(実施例12)、市
販のフッ素系二液タイプの溶剤型塗料(艶消しタイプ)
を用いた例(実施例13)。
Examples 1 to 6 Examples in which an acrylic emulsion is used as the base resin and fine silicic acid powder is used as the matting agent in the single coating of the product of the present invention. Example 7 An example in which an acrylic emulsion is used as the base resin and high-molecular-weight polymer beads are used as the matting agent in the single coating of the product of the present invention. Examples 8 to 9 Coatings using the product of the present invention as an overcoating agent, using an acrylic emulsion as a base resin, fine silicic acid powder as a matting agent, and an acrylic emulsion as an undercoating agent (Example 8) ), An example using a silane-based penetrating water absorption inhibitor (Example 9). Examples 10 to 11 A coating using the product of the present invention as an undercoating agent, using an acrylic emulsion as a base resin and fine powder of silicic acid as a matting agent, and a commercially available polyester-based two-component type solvent-based coating material as an overcoating agent. An example using (matte type) (Example 10), an example using a commercially available fluorine-based two-component type solvent-based paint (matt type) (Example 11). Examples 12 to 13 Coating using the product of the present invention as an intermediate coating agent, using acrylic emulsion as a base resin, fine powder of silicic acid as a matting agent, acrylic emulsion as a base coating agent, and commercially available as a top coating agent. Example (Example 12) using the polyester-based two-component type solvent-based paint (matte type), commercially available fluorine-based two-component type solvent-based paint (matte type)
Example using (Example 13).

【0012】以下実施例により本発明を説明する、特に
断りのないかぎり、部及び%は重量による。
The invention is illustrated by the following examples, in which all parts and percentages are by weight, unless stated otherwise.

【0013】[0013]

【実施例1】 屈折率1.46、平均粒子径2.0μmのケイ酸系微粒
子艶消し剤を樹脂固形分に対し10%のケイ酸系微粒子
艶消し剤を用いた例。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ケイ酸系微粉末) 3.0部 (屈折率1.46 平均粒子径2μm) 分散剤 (ポイズ520 花王(株)製) 1.0部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 45.9部 合 計 110.0部 上記配合でホモ・ミキサーでの撹拌により得られた塗料
をハケにてJIS A−6910に規定されるモルタル
に200g/平方メートルとなるように塗布したものを
7日間室温にて乾燥させ、試験に用いた。
Example 1 An example in which a silicic acid-based fine particle matting agent having a refractive index of 1.46 and an average particle diameter of 2.0 μm was used in an amount of 10% based on the resin solid content. Blending composition Acrylic emulsion 60.0 parts (solid content 50% average particle diameter 52 nm) Matting agent (silicic acid type fine powder) 3.0 parts (refractive index 1.46 average particle diameter 2 μm) Dispersant (Poise 520 Kao) (Manufactured by Co., Ltd.) 1.0 part Antifoaming agent (manufactured by Nopco 8034 San Nopco Co., Ltd.) 0.1 part Water 45.9 parts Total 110.0 parts Paint obtained by stirring with a homo mixer with the above composition A mortar prescribed by JIS A-6910 was applied with a brush at 200 g / square meter, dried at room temperature for 7 days, and used for the test.

【0014】[0014]

【実施例2】艶消し剤として屈折率1.46、平均粒子
径4.9μのケイ酸系微粒子を樹脂固形分に対して10
%使用した例。実施例1と同様の方法にて塗料液、試験
片を作成した。
Example 2 As a matting agent, silicic acid-based fine particles having a refractive index of 1.46 and an average particle size of 4.9 μ were used with respect to the resin solid content.
% Used example. A coating liquid and a test piece were prepared in the same manner as in Example 1.

【0015】[0015]

【実施例3】艶消し剤として屈折率1.46、平均粒子
径4.9μmのケイ酸系微粒子を樹脂固形分に対し15
%用いた例。実施例1と同様の方法で塗料液、試験片を
作成した。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ケイ酸系微粉末) 4.5部 (屈折率1.46 平均粒子径4.9μm) 分散剤 (ポイズ520 花王(株)製) 1.5部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 48.9部 合 計 110.0部
Example 3 As a matting agent, silica particles having a refractive index of 1.46 and an average particle diameter of 4.9 μm were used in an amount of 15 relative to the resin solid content.
% Used example. A coating liquid and a test piece were prepared in the same manner as in Example 1. Blending composition Acrylic emulsion 60.0 parts (solid content 50% average particle diameter 52 nm) Matting agent (silica fine powder) 4.5 parts (refractive index 1.46 average particle diameter 4.9 μm) Dispersant (poise) 520 Kao Co., Ltd. 1.5 parts Defoamer (Nopco 8034 San Nopco Co., Ltd.) 0.1 parts Water 48.9 parts Total 110.0 parts

【0016】[0016]

【実施例4】艶消し剤として屈折率1.46、平均粒子
径4.9μmのケイ酸系微粒子を樹脂固形分に対し20
%用いた例。実施例1と同様の方法で塗料液、試験片を
作成した。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ケイ酸系微粉末) 6.0部 (屈折率1.46 平均粒子径4.9μm) 分散剤 (ポイズ520 花王(株)製) 2.0部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 51.9部 合 計 120.0部
Example 4 Silicic acid fine particles having a refractive index of 1.46 and an average particle diameter of 4.9 μm were used as a matting agent with respect to the resin solid content.
% Used example. A coating liquid and a test piece were prepared in the same manner as in Example 1. Blending composition Acrylic emulsion 60.0 parts (solid content 50% average particle size 52 nm) Matting agent (silica fine powder) 6.0 parts (refractive index 1.46 average particle size 4.9 μm) Dispersant (poise) 520 Kao Co., Ltd. 2.0 parts Antifoam (Nopco 8034 San Nopco Co., Ltd.) 0.1 parts Water 51.9 parts Total 120.0 parts

【0017】[0017]

【実施例5】艶消し剤として屈折率1.46、平均粒子
径4.9μmのケイ酸系微粒子を樹脂固形分に対し25
%用いた例。実施例1と同様の方法で塗料液、試験片を
作成した。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ケイ酸系微粉末) 7.5部 (屈折率1.46 平均粒子径4.9μm) 分散剤 (ポイズ520 花王(株)製) 2.5部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 54.9部 合 計 125.0部
[Example 5] As a matting agent, fine particles of silicic acid particles having a refractive index of 1.46 and an average particle diameter of 4.9 µm were added to 25% of the resin solid content.
% Used example. A coating liquid and a test piece were prepared in the same manner as in Example 1. Blending composition Acrylic emulsion 60.0 parts (solid content 50% average particle diameter 52 nm) Matting agent (silica fine powder) 7.5 parts (refractive index 1.46 average particle diameter 4.9 μm) Dispersant (poise) 520 Kao Co., Ltd. 2.5 parts Defoamer (Nopco 8034 San Nopco Co., Ltd.) 0.1 parts Water 54.9 parts Total 125.0 parts

【0018】[0018]

【実施例6】艶消し剤として屈折率1.46、平均粒子
径8.0μmのケイ酸系微粒子を樹脂固形分に対し10
%用いた例。実施例1と同様の方法で塗料液、試験片を
作成した。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ケイ酸系微粉末) 3.0部 (屈折率1.46 平均粒子径8.0μm) 分散剤 (ポイズ520 花王(株)製) 1.0部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 45.9部 合 計 110.0部
[Example 6] As a matting agent, silica particles having a refractive index of 1.46 and an average particle diameter of 8.0 µm were used in an amount of 10 relative to the resin solid content.
% Used example. A coating liquid and a test piece were prepared in the same manner as in Example 1. Blending composition Acrylic emulsion 60.0 parts (solid content 50% average particle diameter 52 nm) Matting agent (silica fine powder) 3.0 parts (refractive index 1.46 average particle diameter 8.0 μm) Dispersant (poise) 520 Kao Co., Ltd. 1.0 part Antifoam (Nopco 8034 San Nopco Co., Ltd.) 0.1 part Water 45.9 parts Total 110.0 parts

【0019】[0019]

【実施例7】艶消し剤として屈折率1.49、平均粒子
径8.0μmのポリマービーズ系微粒子を樹脂固形分に
対し10%用いた例。実施例1と同様の方法で塗料液、
試験片を作成した。 配合組成 アクリル系エマルジョン 60.0部 (固形分50% 平均粒子径52nm) 艶消し剤 (ポリマービーズ) 3.0部 (屈折率1.49 平均粒子径8.0μm) 分散剤 (ポイズ520 花王(株)製) 1.0部 消泡剤 (ノプコ8034 サンノプコ(株)製) 0.1部 水 45.9部 合 計 110.0部
Example 7 An example of using 10% of polymer bead type fine particles having a refractive index of 1.49 and an average particle diameter of 8.0 μm as a matting agent with respect to the resin solid content. In the same manner as in Example 1, the coating liquid,
A test piece was prepared. Blend composition Acrylic emulsion 60.0 parts (solid content 50% average particle diameter 52 nm) Matting agent (polymer beads) 3.0 parts (refractive index 1.49 average particle diameter 8.0 μm) Dispersant (Poise 520 Kao ( Co., Ltd.) 1.0 part Defoamer (Nopco 8034 San Nopco Co., Ltd.) 0.1 part Water 45.9 parts Total 110.0 parts

【0020】[0020]

【実施例8】 下塗り剤にアクリル系水性エマルジョンを用いた例。 市販のアクリル系水性エマルジョン下塗り剤を100g
/平方メートルとなるようにモルタル基材に塗布し、室
温にて1日乾燥後に実施例4で得られた塗料を上塗り塗
料とし実施例1と同条件で塗布した。
Example 8 An example in which an acrylic aqueous emulsion is used as a primer. 100g of commercially available acrylic water-based emulsion primer
The coating composition obtained in Example 4 was applied as a top coating composition under the same conditions as in Example 1 after being coated on a mortar substrate so that the coating composition would have a thickness of 1 / square meter and dried at room temperature for 1 day.

【0021】[0021]

【実施例9】 下塗り剤に水性シラン系浸透性吸水防止剤を用いた例。 市販の水性シラン系浸透性吸水防止剤を、200g/平
方メートルとなるように基材に塗布し、直後に実施例4
で作成した塗料を上塗り塗料とし、実施例1と同条件で
試験片を作成した。
Example 9 An example in which an aqueous silane-based penetrating water absorption inhibitor was used as the undercoating agent. A commercially available water-based silane-based water-absorption inhibitor was applied to the base material so that the amount was 200 g / square meter, and immediately after Example 4
A test piece was prepared under the same conditions as in Example 1, using the paint prepared in 1 above as the topcoat paint.

【0022】[0022]

【実施例10】 上塗り剤を併用した例。 実施例4で得られた試料を室温にて1日乾燥させた後
に、市販の溶剤型艶消し塗料(ポリエステル系二液型)
を上塗り塗料として用い、200g/平方メートルとな
るように塗布し、再度室温にて7日間乾燥させ試験片を
作成した。
Example 10 Example in which a topcoat agent was used in combination. After drying the sample obtained in Example 4 at room temperature for 1 day, a commercially available solvent-type matte coating (polyester two-component type)
Was used as an overcoating material to apply 200 g / square meter, and dried again at room temperature for 7 days to prepare a test piece.

【0023】[0023]

【実施例11】 上塗り剤を併用した例。 実施例4で得られた試料を室温にて1日乾燥させた後
に、市販の溶剤型艶消し塗料(フッ素系二液型)を上塗
り塗料として用い、150g/平方メートルとなるよう
に塗布し、再度室温にて7日間乾燥させ試験片を作成し
た。
Example 11 Example in which a topcoat agent was used in combination. The sample obtained in Example 4 was dried at room temperature for 1 day, and then a commercially available solvent-type matting paint (fluorine-based two-component type) was used as the topcoat paint, and the coating was applied at 150 g / sq. A test piece was prepared by drying at room temperature for 7 days.

【0024】[0024]

【実施例12】 上塗り剤、下塗り剤を併用した三層塗装の中間層に使用
した例。 実施例8で得られた試料を室温にて1日乾燥させた後
に、実施例10で使用した市販の溶剤型艶消し塗料(ポ
リエステル系二液型)を塗布量が200g/平方メート
ルとなるように三層の最上層の上塗り塗料として用い、
再度室温にて7日間乾燥させ試験片を作成した。
Example 12 Example of use as an intermediate layer in a three-layer coating in which a top coating agent and a base coating agent were used in combination. The sample obtained in Example 8 was dried at room temperature for 1 day, and then the commercially available solvent-type matte coating (polyester two-component type) used in Example 10 was applied so that the coating amount was 200 g / square meter. Used as the top coating of the top three layers,
It was dried again at room temperature for 7 days to prepare a test piece.

【0025】[0025]

【実施例13】 上塗り剤、下塗り剤を併用した三層塗装の中間層に使用
した例。 実施例8で得られた試料を室温にて1日乾燥させた後
に、実施例11で使用した市販の溶剤型艶消し塗料(フ
ッ素系二液型)を塗布量が150g/平方メートルとな
るように三層の最上層の上塗り塗料として用い、再度室
温にて7日間乾燥させ試験片を作成した。
Example 13 Example of use as an intermediate layer in a three-layer coating in which a top coating agent and a base coating agent were used in combination. The sample obtained in Example 8 was dried at room temperature for 1 day, and then the commercially available solvent-type matting paint (fluorine-based two-component type) used in Example 11 was applied so that the coating amount was 150 g / square meter. The test piece was prepared by using it as the top coating material of the uppermost three layers and drying it again at room temperature for 7 days.

【0026】[0026]

【比較例】[Comparative example]

艶消し剤を使用しない例(比較例1) 以下比較例により説明する、特に断りのないかぎり、部
及び%は重量による。
Example in which no matting agent is used (Comparative Example 1) Explained in Comparative Examples below, parts and% are by weight unless otherwise specified.

【0027】[0027]

【比較例1】 艶消し剤を使用しない例。 実施例1に用いた水性アクリルエマルジョンのみを用い
て実施例1と同様の方法にて塗料液、試験片を作成し
た。
Comparative Example 1 An example in which no matting agent is used. A coating liquid and a test piece were prepared in the same manner as in Example 1 using only the aqueous acrylic emulsion used in Example 1.

【0028】 試験方法 実施例および比較例より得られた塗料および試験片の試
験方法、評価基準は以下の通りである。 1.濡れ色発生の防止性 試験方法:実施例、比較例より得られた各塗装片を、未
塗装片と目視にて比較する。 評価基準 ○:塗装面がモルタル本来の外観をしており、黒っぽく
なる等の色相の変化が見られない。
Test Method The test methods and evaluation criteria for the paints and test pieces obtained from the examples and comparative examples are as follows. 1. Prevention of wet color generation Test method: Each coated piece obtained from the examples and comparative examples is visually compared with an uncoated piece. Evaluation Criteria O: The coated surface has the original appearance of the mortar, and no change in hue such as darkening is observed.

【0029】△:塗装面がモルタル本来の外観と比較
し、やや黒味を帯びており、色相の変化が若干認められ
る。 ×:塗装面が黒味を帯びており、モルタル本来の色相と
異なる。 2.隠蔽性 試験方法:濡れ色発生防止性での試験方法と同じく、各
塗装片を、未塗装片と目視にて比較する。 評価基準 ○:塗膜の隠ペイ性が低く、モルタル表面の自然な濃淡
の状態が得られる。
Δ: The coated surface is slightly blackish compared to the original appearance of the mortar, and a slight change in hue is observed. X: The painted surface has a black tint, which is different from the original hue of the mortar. 2. Concealment test method: Similar to the test method for preventing the occurrence of wet color, each coated piece is visually compared with an uncoated piece. Evaluation Criteria ◯: The hiding payability of the coating film is low, and a natural shading state of the mortar surface is obtained.

【0030】△:塗膜の隠ペイ性がやや高く、モタル表
面の自然な濃淡の状態が得難い。 ×:塗膜の隠ペイ性が高く、モタル表面の自然な濃淡の
状態が見られない。 3.密着性 試験方法:実施例、比較例より得られる各塗装片を室温
状態で放置したものについて、JIS−K5400に規
定される碁盤目試験の試験方法にもとずき塗膜を2mm
角に切り、セロテープにて剥離試験を行った。 評価基準 ○:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全く認められない。
Δ: The hidden pay property of the coating film is slightly high, and it is difficult to obtain a natural shading state of the mortar surface. X: The coating film has high concealing payability, and no natural shading of the mortar surface is observed. 3. Adhesion test method: For each of the coated pieces obtained in Examples and Comparative Examples, which were left at room temperature, a coating film of 2 mm was formed based on the test method of the cross cut test specified in JIS-K5400.
It was cut into a corner and a peeling test was performed using a cellophane tape. Evaluation Criteria ◯: No peeling of the coating film is observed in the cellophane peeling test of the cross cut portion of 2 mm square.

【0031】△:2mm角の碁盤目カット部分のセロテ
ープ剥離試験で、塗膜の剥離が全体の5%以下である。 ×:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全体の50%以上である。 4.耐温水性 試験方法:実施例、比較例より得られる各塗装片を室温
状態で放置したものについて、50℃の温水中に24時
間浸漬。フクレ・剥がれについては、温水浸漬終了直後
の状態を目視にて比較。密着については、温水浸漬終了
直後の塗装片について、常態密着性試験の試験方法と同
様にJIS−K5400に規定される碁盤目試験の試験
方法にもとずき塗膜を2mm角に切り、セロテープにて
剥離試験を行った。
Δ: In a cellotape peeling test of a cross cut portion of 2 mm square, the peeling of the coating film was 5% or less of the whole. X: In a cellotape peeling test of a cross cut portion of 2 mm square, peeling of the coating film was 50% or more of the whole. 4. Hot water resistance test method: Each of the coated pieces obtained in Examples and Comparative Examples was left at room temperature and immersed in warm water at 50 ° C for 24 hours. For blistering and peeling, visually compare the state immediately after the completion of warm water immersion. Regarding adhesion, for the coated piece immediately after completion of hot water immersion, the coating film was cut into 2 mm squares based on the test method of the cross-cut test specified in JIS-K5400, similarly to the test method of the normal adhesion test, and then the tape was cut. A peeling test was performed.

【0032】評価基準: フクレ・剥がれ ○:温水試験後の試料表面に、フクレや剥がれ現象が全
く観られない。 △:温水試験後の試料表面全体の50%以下にフクレや
剥がれ現象が観られる。 ×:温水試験後の試料表面全体の全体にフクレや剥がれ
現象が観られる。 密着性 ○:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全く認められない。
Evaluation Criteria: Blistering / Peeling A: No blistering or peeling phenomenon is observed on the surface of the sample after the hot water test. Δ: Puffing or peeling phenomenon is observed on 50% or less of the entire sample surface after the hot water test. Poor: Puffing or peeling phenomenon is observed on the entire surface of the sample after the hot water test. Adhesion ∘: No peeling of the coating film was observed in the cellotape peeling test of the cross cut portion of 2 mm square.

【0033】△:2mm角の碁盤目カット部分のセロテ
ープ剥離試験で、塗膜の剥離が全体の5%以下である。 ×:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全体の50%以上である。 常態密着性試験の評価方法と同様塗料一般 5.耐候促進後の密着性 試験方法:前記にて作製した各塗装片をデューサイクル
・ウエザオメーターにて、サンシャイン・カーボンアー
ク1灯を使用し、フィルターを使用せず、60分点灯−
60分消灯のサイクルで500時間露試験を行なったも
のについて、常態密着性試験の試験方法と同様塗料一般
試験方法のJIS−K5400、碁盤目試験の試験方法
にもとずき塗膜を2mm角に切り、セロテープにて剥離
試験を行った。
Δ: In a cellotape peeling test of a cross cut portion of 2 mm square, peeling of the coating film was 5% or less of the whole. X: In a cellotape peeling test of a cross cut portion of 2 mm square, peeling of the coating film was 50% or more of the whole. Similar to the evaluation method of the normal adhesion test, general paints 5. Adhesion after weather resistance test method: Each coated piece prepared above was lit for 60 minutes with a Ducycle Cycle Weatherometer using one sunshine carbon arc lamp and no filter.
Regarding the one that was subjected to a dew test for 500 hours in a 60-minute light-off cycle, the coating film was 2 mm square based on JIS-K5400, which is a general paint test method, and the cross-cut test method, similar to the test method for the normal adhesion test It was cut into pieces and subjected to a peeling test with cellophane tape.

【0034】評価基準 ○:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全く認められない。 △:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全体の5%以下である。 ×:2mm角の碁盤目カット部分のセロテープ剥離試験
で、塗膜の剥離が全体の50%以上である。 常態密着性試験の評価方法と同様塗料一般 6.塗料の安定性 試験方法:前記にて作製した各塗料の直後の状態と、経
時による状態(室温30日後)とを比較。
Evaluation Criteria ◯: No peeling of the coating film was observed in the cellotape peeling test of the cross-cut portion of 2 mm square. (Triangle | delta): The peeling of a coating film is 5% or less of the whole in the cellophane tape peeling test of the cross-cut cut part of 2 mm square. X: In a cellotape peeling test of a cross cut portion of 2 mm square, peeling of the coating film was 50% or more of the whole. Similar to the evaluation method of the normal adhesion test, general paint 6. Paint stability test method: The state immediately after each of the above-prepared paints was compared with the state over time (after 30 days at room temperature).

【0035】評価基準 ○:塗料化後の粘度上昇や、塗料の分離、沈降等が見ら
れず安定である。 △:塗料化後の粘度上昇や、塗料の分離、沈降等の傾向
がやや見られる。 ×:塗料化後の粘度上昇や、ゲル化現象が見られたり塗
料の分離や沈降等が発生する。
Evaluation Criteria ◯: Stable with no increase in viscosity after coating and no separation or sedimentation of the coating. Δ: A slight increase in viscosity after conversion into a paint and a tendency toward separation and sedimentation of the paint are observed. X: Viscosity increase after coating, gelation phenomenon is observed, and coating separation or sedimentation occurs.

【0036】実施例および比較例より得られた試料の試
験結果を表1および表2に示した。
The test results of the samples obtained from the examples and comparative examples are shown in Tables 1 and 2.

【0037】[0037]

【表1】 [Table 1]

【0038】[0038]

【発明の効果】合成樹脂中へ艶消し剤を添加した塗膜材
料を用い、モルタル、コンクリート、石材、レンガ、セ
ラミック等をそのまま仕上げた建築物等へ塗布を行う
と、濡れ色を発生させず、さらに下地の外観を変えるこ
となく、保護塗膜を形成させることができた。上記の発
明では、艶消し剤を添加した合成樹脂単独でも塗膜材料
として用いることができるが、一般の建築塗膜材料の施
工方法と同様に、下塗り剤, 上塗り剤を用いても効果は
確認出来る。特に、上塗り剤に溶液( 油性 )の塗料を用
いた場合にも濡れの発生もなく、十分な効果が確認出来
た。屋外を想定した場合にはむしろ耐候性、耐汚染性の
点から下塗り剤、上塗り剤の併用が好ましい。
[Effects of the Invention] When a coating material containing a matting agent added to a synthetic resin is applied to a building or the like in which mortar, concrete, stone, brick, ceramic, etc. are finished as they are, no wet color is generated. Further, the protective coating film could be formed without changing the appearance of the base. In the above invention, the synthetic resin alone with the addition of the matting agent can be used as the coating material, but the effect is confirmed by using the undercoating agent and the topcoating agent as in the general construction coating material construction method. I can. In particular, when a solution (oil-based) paint was used as the topcoat, wetting did not occur and a sufficient effect was confirmed. Considering outdoors, it is preferable to use an undercoating agent and a topcoating agent together from the viewpoints of weather resistance and stain resistance.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C09D 133/00 PGA C09D 133/00 PGA ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location C09D 133/00 PGA C09D 133/00 PGA

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 透明樹脂塗料中に艶消し剤を入れてなる
組成物を塗布することを特徴とする透明塗装方法。
1. A transparent coating method comprising applying a composition comprising a transparent resin coating material and a matting agent.
【請求項2】 透明樹脂塗料がアクリル樹脂の高分子水
性エマルジョンであることを特徴とする請求項1記載の
透明塗装方法。
2. The transparent coating method according to claim 1, wherein the transparent resin coating material is a polymer aqueous emulsion of acrylic resin.
【請求項3】 アクリル樹脂の高分子水性エマルジョン
の平均粒子径が100nm以下であることを特徴とする
請求項2記載の透明塗装方法。
3. The transparent coating method according to claim 2, wherein the average particle diameter of the polymer aqueous emulsion of acrylic resin is 100 nm or less.
【請求項4】 艶消し剤の粒子径が2〜10μmである
ことを特徴とする請求項1ないし3いずれか記載の透明
塗装方法。
4. The transparent coating method according to claim 1, wherein the matting agent has a particle size of 2 to 10 μm.
【請求項5】 艶消し剤の添加量がその透明樹脂塗料に
用いられる樹脂の固形分に対して5〜30重量%である
ことを特徴とする請求項1ないし4いずれか記載の透明
塗装方法。
5. The transparent coating method according to claim 1, wherein the amount of the matting agent added is 5 to 30% by weight based on the solid content of the resin used in the transparent resin coating material. .
JP7105215A 1995-04-28 1995-04-28 Transparent coating Pending JPH08302239A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7105215A JPH08302239A (en) 1995-04-28 1995-04-28 Transparent coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7105215A JPH08302239A (en) 1995-04-28 1995-04-28 Transparent coating

Publications (1)

Publication Number Publication Date
JPH08302239A true JPH08302239A (en) 1996-11-19

Family

ID=14401455

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7105215A Pending JPH08302239A (en) 1995-04-28 1995-04-28 Transparent coating

Country Status (1)

Country Link
JP (1) JPH08302239A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100333247B1 (en) * 1999-09-16 2002-04-25 우만곤 Rock-coating composition and camouflage method using the same
JP2002338896A (en) * 2001-05-21 2002-11-27 Maruo Calcium Co Ltd Matting agent for coating material and coating material composition containing the same
WO2004067657A1 (en) * 2003-01-31 2004-08-12 Sk Kaken Co., Ltd. Multicolor coating compositions and method of forming patterned surface
JP2007137692A (en) * 2005-11-15 2007-06-07 Matsushita Electric Works Ltd Method of surface-treating artificial marble
CN100365089C (en) * 2003-01-31 2008-01-30 Sk化研株式会社 Multicolor coating compositions and method of forming patterned surface
JP2011162665A (en) * 2010-02-10 2011-08-25 Kikusui Chemical Industries Co Ltd Aqueous coating composition
CN103333559A (en) * 2013-06-28 2013-10-02 中国建筑股份有限公司 Water-based transparent concrete water-proof carbonization-preventing coating and preparation method thereof
WO2017038802A1 (en) * 2015-08-31 2017-03-09 日本ペイント株式会社 Multi-layer coating

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62288668A (en) * 1986-06-06 1987-12-15 Hoechst Gosei Kk Aqueous primer conditioner
JPS6363760A (en) * 1986-09-04 1988-03-22 Nippon Paint Co Ltd Matte electrodeposition paint composition
JPH02248471A (en) * 1989-03-23 1990-10-04 Nippon Paint Co Ltd Method for forming transparent coating film
JPH03174401A (en) * 1989-12-04 1991-07-29 Mitsubishi Yuka Badische Co Ltd Aqueous acrylic resin emulsion composition
JPH051240A (en) * 1991-06-25 1993-01-08 Nippon Oil & Fats Co Ltd Matte coating composition
JPH059409A (en) * 1991-06-28 1993-01-19 Toray Dow Corning Silicone Co Ltd Water-based coating composition
JPH05214194A (en) * 1991-12-13 1993-08-24 Japan Synthetic Rubber Co Ltd Aqueous emulsion of polymer fine particle

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62288668A (en) * 1986-06-06 1987-12-15 Hoechst Gosei Kk Aqueous primer conditioner
JPS6363760A (en) * 1986-09-04 1988-03-22 Nippon Paint Co Ltd Matte electrodeposition paint composition
JPH02248471A (en) * 1989-03-23 1990-10-04 Nippon Paint Co Ltd Method for forming transparent coating film
JPH03174401A (en) * 1989-12-04 1991-07-29 Mitsubishi Yuka Badische Co Ltd Aqueous acrylic resin emulsion composition
JPH051240A (en) * 1991-06-25 1993-01-08 Nippon Oil & Fats Co Ltd Matte coating composition
JPH059409A (en) * 1991-06-28 1993-01-19 Toray Dow Corning Silicone Co Ltd Water-based coating composition
JPH05214194A (en) * 1991-12-13 1993-08-24 Japan Synthetic Rubber Co Ltd Aqueous emulsion of polymer fine particle

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WO2004067657A1 (en) * 2003-01-31 2004-08-12 Sk Kaken Co., Ltd. Multicolor coating compositions and method of forming patterned surface
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JP2007137692A (en) * 2005-11-15 2007-06-07 Matsushita Electric Works Ltd Method of surface-treating artificial marble
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