JPS628787B2 - - Google Patents
Info
- Publication number
- JPS628787B2 JPS628787B2 JP3554381A JP3554381A JPS628787B2 JP S628787 B2 JPS628787 B2 JP S628787B2 JP 3554381 A JP3554381 A JP 3554381A JP 3554381 A JP3554381 A JP 3554381A JP S628787 B2 JPS628787 B2 JP S628787B2
- Authority
- JP
- Japan
- Prior art keywords
- glass beads
- beads
- paint
- coating
- small
- 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
Links
- 239000011324 bead Substances 0.000 claims description 57
- 239000011521 glass Substances 0.000 claims description 34
- 239000003973 paint Substances 0.000 claims description 26
- 239000002245 particle Substances 0.000 claims description 18
- 238000000576 coating method Methods 0.000 claims description 13
- 239000011248 coating agent Substances 0.000 claims description 12
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical group [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 6
- 235000019353 potassium silicate Nutrition 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 2
- 238000005507 spraying Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000005871 repellent Substances 0.000 description 4
- 230000002940 repellent Effects 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000000378 calcium silicate Substances 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 2
- 235000010261 calcium sulphite Nutrition 0.000 description 2
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- FAYYUXPSKDFLEC-UHFFFAOYSA-L calcium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Ca+2].[O-]S([O-])(=O)=S FAYYUXPSKDFLEC-UHFFFAOYSA-L 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Description
【発明の詳細な説明】
本発明は貼紙防止用被覆体に関する。
従来、広告宣伝用の貼紙は電柱に多く見られた
が交通事情の変化により道路軌道等が立体化さ
れ、それによつて橋脚、高架壁さらに地下道壁面
等の対象物が増加し、いたる所に貼紙が見られ
る。これらは周囲の美観を損なうばかりでなくそ
の除去のために多くの人手と費用を要している。
これらの貼紙を防止するためには電柱等に多数の
突起物を有するゴムまたは樹脂板等が施され、ま
た橋脚等にシリコン系塗料が施されている。しか
しながらこれらはいづれも有機性物質よりできて
いるためその表面の耐久性、耐候性等の面で不充
分であり長期間の貼紙防止効果は期待できない。
また他の方法として常温乾燥性塗料あるいは熱硬
化性塗料中にガラスビーズ等の骨材と潤滑剤を含
有させた貼紙防止用塗料組成物も提案されている
(特開昭53−31739号公報)。
この方法は突起物に変えてガラスビーズ等によ
り形成される凹凸面を利用したものであるがこの
ような塗料組成物を吹き付けるとガラスビーズ等
が部分的に塗膜内に埋没しまた主体となる塗料が
ポリウレタン、アルキツド等の有機質塗料でガラ
スビーズに馴染み難く必ずしも充分な効果の得ら
れない面があつた。本発明者らはこのようなガラ
スビーズを利用した貼紙防止用被覆体につき種々
検討を行つた結果、異なつた粒径を有するガラス
ビーズを使用すれば極めて効果的に貼紙防止を行
いうるという知見を得て本発明を完成したもので
ある。
本発明はすなわち基材表面に施された塗料の塗
膜上に少くとも大小2種のガラスビーズを分散付
着せしめたことを特徴とする貼紙防止用被覆体で
ある。
本発明に使用される塗料は特に制限なく常温硬
化性または熱硬化性の各種の有機質塗料または無
機質塗料が適用可能であるが常温硬化性の水ガラ
ス系無機質塗料が有利である。このような水ガラ
ス系塗料は一般式M2OnSiO2(MはLi、K、Na、
NH4等でありnは0.5〜10である)で表わされる
ケイ酸アルカリ、ケイ酸アンモニウムの水溶液に
無機質の硬化剤を加え、骨材、充填剤等を適宜配
合したものである。硬化剤として好ましいのは亜
硫酸カルシウム、チオ硫酸カルシウムおよびケイ
酸カルシウムを含むものであり、これらにさらに
酸化亜鉛、水酸化アルミニウム、アルミナ、水和
アルミナ等を加えてもよい。骨材としては炭酸カ
ルシウム、ケイ砂、パーライト、充填材としては
タルク等が一般的に使用される。このように配合
された塗料は基体上に好ましくは約1〜3Kg/m2
の割合で吹付け、その他の方法で塗布される。
本発明の特色はガラスビーズとして少くとも大
小2種の粒径の異なる粒体を分散付着させること
であるが、好ましい範囲は大なるガラスビーズ
(以下大ビーズという)の粒径が800〜2500μ、さ
らに好ましくは800〜1200μであり、小なるビー
ズ(以下小ビーズという)の粒径が10〜150μさ
らに好ましくは10〜100μである。上記の粒径以
外では後述する本発明の貼紙防止効果が充分でな
い。
このようなガラスビーズを基体に塗布された塗
膜が充分に乾燥せず未硬化の間に吹き付け等の方
法により分散付着せしめる。適当な圧力によつて
吹付けられたガラスビーズは塗料中に完全に埋没
することなくその表面が露出された状態にある。
ガラスビーズの塗料表面への付着状態は粒径の約
4〜6割が露出しているのが好ましい。また水ガ
ラス系塗料の場合、下吹きおよび上吹きの2回に
より仕上げられるが上吹き塗料に所定量のビーズ
を練り込みそれを吹き付けた後、塗料硬化後その
表面を研磨する事によりガラスビーズを露出させ
ることもできる。
本発明を実施する場合このように粒径の異なつ
たガラスビーズを塗膜面に均等に分散付着させる
には大ビーズおよび小ビーズを相互によく混合し
て吹き付けることが必要である。いづれか一方の
ガラスビーズを先に吹き付ける場合またはよく混
合せずに吹き付ける場合は一方の先に付着したガ
ラスビーズに阻害されて後で吹き付けるガラスビ
ーズの付着が不完全になり大ビーズおよび小ビー
ズが相互によく分散された塗面を得ることができ
ない。また大ビーズ、小ビーズは各1種類づつあ
つてもよいが上記粒径の範囲内でそれぞれ複数種
類使用しても差支えない。本発明による貼紙防止
効果を図面により説明すると第1図のように基体
1表面に塗層2を設けほぼ同一粒径のガラスビー
ズ3を分散付着させると、その上に接着された貼
紙4はガラスビーズ3がほとんど同一平面を形成
するため全体に接着された状態になる。いま第2
図のように大ビーズ5と小ビーズ6とを分散付着
させると大ビーズ5群の間隙に多数の小ビーズ6
群が分散された状態となり凹凸面を形成するた
め、貼紙4は大ビーズ5のみに接着され小ビーズ
6にはほとんど接着されない。それ故第1図に比
較して同一面積の塗面に対しガラスビーズと貼紙
との接着面積はきわめて小となる。また貼紙を接
着させるため多量の糊を用いるとか手で全体を強
く圧着させても大ビーズ群の間隙に小ビーズ群が
分散しているためその部分の接着力は非常に弱め
られる。本発明者らの実験によると大ビーズ100
重量部に対し小ビーズ20〜100重量部特に20〜70
重量部の割合が最も良好な結果が得られる。
また本発明の貼紙防止効果を高めるためにはガ
ラスビーズが付着された表面にシリコン系撥水剤
を塗布してもよい。この撥水剤はメチルシリコ
ン、アクリル変性シリコン等水性油性いづれでも
よいが屋外塗装の場合は油性系の撥水剤が好まし
い。
以上のごとく本発明被覆体は粒径の小さいビー
ズが粒径の大きいビーズの間隙に分散されている
ため、従来のごとく多少の粒径差はあつても略均
一粒径であるガラスビーズを分散させた被覆体に
比較して紙貼着の際の有効面積が減少され貼紙し
難いのみならず一旦貼り着けてもきわめて剥がし
易いという効果を生ずる。またガラスビーズの粒
径が相異なるため光線の反射が複雑で単味でない
独特の美観を呈する。
特に常温硬化性の水ガラス系塗料を使用する場
合はセメント等の無機塗料または有機塗料に比べ
てガラスビーズとの接着力が非常に優れており長
期間屋外曝露しても紫外線、オゾン等による塗料
の酸化劣化がなく、またガラスビーズが離脱する
ことはない。
また常温硬化性であるため加熱硬化が不便であ
る表面積の大なる建造物に施すのに有利であり特
に貼紙の多い架橋下壁面、脚柱、地下道壁面の塗
装用として好適である。以下示す実施例、比較例
において組成はいづれも重量基準である。
実施例、比較例
ケイ酸ソーダ水溶液(固形分34%)28部に炭酸
カルシウム56部、亜硫酸カルシウム7部、ケイ酸
カルシウム2部、水酸化アルミニウム1部、無機
顔料等6部を加え組成が均一になるまでよく撹拌
する。得られた常温硬化性塗料組成物をスプレー
ガンにて厚さ3mmの石綿板に塗膜厚み約1mmに吹
き付け塗料が湿潤状態にある間に第1表に示す粒
径のガラスビーズ100部を塗料表面に均一に吹き
付け供試板とした。
また油性のシリコン系撥水剤はガラスビーズ吹
付後24時間養生して塗布した。
このようにして得られた供試板に澱粉のりを略
一定量塗布しこれに巾5cm、長さ15cmの紙を貼り
120時間養生接着した後、第3図7に示すような
目盛付ぜんまい秤を紙4の先端に設け同一速度で
引張り貼紙4が剥離する力を測定し剥離の難易度
を求めた。結果を第1表に示す。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a covering for preventing pasting. Traditionally, advertising posters were often seen on utility poles, but due to changes in traffic conditions, road tracks have become three-dimensional, and as a result, the number of objects such as bridge piers, elevated walls, and underpass walls has increased, and advertising posters are now being posted everywhere. can be seen. These not only spoil the beauty of the surrounding area, but also require a lot of manpower and expense to remove them.
In order to prevent these stickers from appearing, rubber or resin plates having numerous protrusions are applied to telephone poles and the like, and silicone paint is applied to bridge piers and the like. However, since these are all made of organic substances, their surface durability and weather resistance are insufficient, and they cannot be expected to have a long-term sticker-preventing effect.
As another method, a coating composition for preventing pasting has been proposed in which aggregates such as glass beads and a lubricant are contained in a room temperature drying coating or a thermosetting coating (Japanese Patent Laid-Open No. 53-31739). . This method uses an uneven surface formed by glass beads, etc. instead of protrusions, but when such a paint composition is sprayed, the glass beads, etc. are partially buried in the paint film and become the main body. Since the paint is an organic paint such as polyurethane or alkyd, it is difficult to get acquainted with the glass beads and a sufficient effect may not always be obtained. The present inventors have conducted various studies on coatings for preventing stickers using glass beads, and as a result, have found that it is possible to prevent stickers extremely effectively by using glass beads with different particle sizes. As a result, the present invention has been completed. The present invention is a coating for preventing pasting, characterized in that at least two types of glass beads, large and small, are dispersed and adhered to a paint film applied to the surface of a base material. The paint used in the present invention is not particularly limited, and various organic or inorganic paints that are curable at room temperature or thermosetting can be used, but water glass-based inorganic paints that are curable at room temperature are advantageous. Such water glass-based paints have the general formula M 2 OnSiO 2 (M is Li, K, Na,
An inorganic curing agent is added to an aqueous solution of an alkali silicate or ammonium silicate represented by NH4 , etc., where n is 0.5 to 10, and aggregates, fillers, etc. are appropriately blended. Preferred hardening agents include calcium sulfite, calcium thiosulfate and calcium silicate, to which zinc oxide, aluminum hydroxide, alumina, hydrated alumina, etc. may be added. Calcium carbonate, silica sand, perlite is generally used as the aggregate, and talc is generally used as the filler. The paint thus formulated is preferably applied on the substrate from about 1 to 3 kg/m 2
applied by spraying or other methods. The feature of the present invention is to disperse and adhere at least two types of particles with different particle sizes as glass beads, and the preferable range is that the particle size of the large glass beads (hereinafter referred to as large beads) is 800 to 2500 μm, More preferably, the particle size is 800 to 1200μ, and the particle size of small beads (hereinafter referred to as small beads) is 10 to 150μ, and more preferably 10 to 100μ. If the particle size is other than the above, the sticker prevention effect of the present invention, which will be described later, will not be sufficient. Such glass beads are dispersed and adhered by a method such as spraying while the coating film applied to the substrate is not sufficiently dried and cured. The glass beads sprayed with appropriate pressure are not completely submerged in the paint, but their surfaces are exposed.
Regarding the state of adhesion of the glass beads to the paint surface, it is preferable that about 40 to 60% of the particle size is exposed. In addition, in the case of water glass paint, finishing is done twice by under-spraying and top-spraying, but after kneading a predetermined amount of beads into the top-spraying paint and spraying it, the glass beads are removed by polishing the surface after the paint has hardened. It can also be exposed. In carrying out the present invention, in order to uniformly disperse and adhere glass beads of different particle sizes onto the coating surface, it is necessary to mix the large beads and small beads well with each other before spraying. If one of the glass beads is sprayed first, or if the glass beads are sprayed without mixing well, the glass beads adhering to one end will interfere with the adhesion of the glass beads to be sprayed later, and the large beads and small beads will not be able to interact with each other. It is not possible to obtain a well-dispersed coating surface. Further, one type each of large beads and small beads may be used, but there is no problem in using multiple types of each type within the above particle size range. The effect of preventing stickers according to the present invention will be explained with reference to the drawings. As shown in FIG. Since the beads 3 form almost the same plane, they are completely glued together. Now the second
As shown in the figure, when large beads 5 and small beads 6 are dispersed and attached, a large number of small beads 6 are placed in the gaps between the groups of 5 large beads.
Since the group is dispersed and forms an uneven surface, the sticker 4 is adhered only to the large beads 5 and hardly adhered to the small beads 6. Therefore, compared to FIG. 1, the adhesive area between the glass beads and the sticker is extremely small for the same area of the painted surface. Furthermore, even if a large amount of glue is used to adhere the paper, or if the whole is pressed firmly by hand, the adhesive force in that area will be extremely weakened because the small beads are dispersed between the large beads. According to experiments by the inventors, large beads 100
Small beads 20-100 parts by weight, especially 20-70 parts by weight
The ratio of parts by weight gives the best results. Further, in order to enhance the sticker prevention effect of the present invention, a silicone water repellent may be applied to the surface to which the glass beads are attached. This water repellent may be either water-based or oil-based such as methyl silicone or acrylic modified silicon, but in the case of outdoor painting, oil-based water repellents are preferred. As described above, in the coated body of the present invention, beads with a small particle size are dispersed in the gaps between beads with a large particle size, so glass beads with a substantially uniform particle size are dispersed even though there is some difference in particle size as in the conventional case. The effective area for pasting paper is reduced compared to a covered body made of paper, which not only makes it difficult to paste, but also makes it extremely easy to peel off once pasted. In addition, because the glass beads have different particle sizes, the reflection of light is complex, creating a unique and beautiful appearance. In particular, when using water glass-based paints that harden at room temperature, they have a much better adhesion to glass beads than inorganic paints such as cement or organic paints, and even if exposed outdoors for long periods of time, the paints will not be exposed to ultraviolet rays, ozone, etc. There is no oxidative deterioration of the glass beads, and the glass beads do not come off. In addition, since it cures at room temperature, it is advantageous for coating buildings with large surface areas where heat curing is inconvenient, and is particularly suitable for coating lower bridge walls, pedestals, and underground passage walls where there are many pasted papers. In the Examples and Comparative Examples shown below, the compositions are all based on weight. Examples and Comparative Examples 56 parts of calcium carbonate, 7 parts of calcium sulfite, 2 parts of calcium silicate, 1 part of aluminum hydroxide, and 6 parts of inorganic pigments were added to 28 parts of aqueous sodium silicate solution (solid content 34%) to obtain a uniform composition. Stir well until. The obtained room-temperature curable paint composition was sprayed onto a 3 mm thick asbestos board with a spray gun to a coating thickness of about 1 mm, and while the paint was still wet, 100 parts of glass beads having the particle size shown in Table 1 was applied to the paint. It was sprayed uniformly on the surface to prepare a test plate. The oil-based silicone water repellent was applied after being cured for 24 hours after spraying the glass beads. Approximately a certain amount of starch glue was applied to the test board obtained in this way, and paper 5 cm wide and 15 cm long was pasted on it.
After curing for 120 hours, a clockwork scale with a scale as shown in FIG. 3 was placed at the tip of the paper 4, and the force with which the paper 4 was peeled off at the same speed was measured to determine the degree of difficulty in peeling. The results are shown in Table 1. 【table】
第1図、第2図はそれぞれガラスビーズを塗層
に分散付着させた従来品および本発明品を説明す
るための略断面図であり、第3図は本発明品の貼
紙剥離試験方法を説明するための略断面図であ
る。
1……基体、2……塗層、3,5,6……ガラ
スビーズ、4……貼紙、7……目盛付ぜんまい
秤。
Figures 1 and 2 are schematic cross-sectional views for explaining a conventional product and a product of the present invention in which glass beads are dispersed and adhered to the coating layer, respectively, and Figure 3 is a diagram illustrating a method for testing the peeling of paper stickers for the product of the present invention. FIG. 1...Substrate, 2...Coating layer, 3, 5, 6...Glass beads, 4...Paper, 7...Spring scale with scale.
Claims (1)
大小2種のガラスビーズを分散付着せしめたこと
を特徴とする貼紙防止用被覆体。 2 大なる種のガラスビーズの粒径が800μ以上
であり、小なる種のガラスビーズの粒径が150μ
以下である特許請求の範囲第1項記載の貼紙防止
用被覆体。 3 大なる種のガラスビーズ100重量部に対し小
なる種のガラスビーズが20〜100重量部である特
許請求の範囲第1項もしくは第2項記載の貼紙防
止用被覆体。 4 塗料が常温硬化性の水ガラス系無機質塗料で
ある特許請求の範囲第1項より第3項いづれかに
記載の貼紙防止用被覆体。[Scope of Claims] 1. A coating for preventing pasting, characterized in that at least two types of glass beads, large and small, are dispersed and adhered to a paint film applied to the surface of a base material. 2 The particle size of the large seed glass beads is 800μ or more, and the particle size of the small seed glass beads is 150μ.
A covering for preventing pasting according to claim 1, which is as follows. 3. The coating for preventing pasting according to claim 1 or 2, wherein the amount of small seed glass beads is 20 to 100 parts by weight per 100 parts by weight of large seed glass beads. 4. The coating for preventing pasting according to any one of claims 1 to 3, wherein the paint is a water glass-based inorganic paint that cures at room temperature.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3554381A JPS57148783A (en) | 1981-03-11 | 1981-03-11 | Coating body for preventing billing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3554381A JPS57148783A (en) | 1981-03-11 | 1981-03-11 | Coating body for preventing billing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57148783A JPS57148783A (en) | 1982-09-14 |
JPS628787B2 true JPS628787B2 (en) | 1987-02-24 |
Family
ID=12444636
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3554381A Granted JPS57148783A (en) | 1981-03-11 | 1981-03-11 | Coating body for preventing billing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57148783A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59134255A (en) * | 1983-01-24 | 1984-08-01 | 菊水化学工業株式会社 | Paper patch preventing method |
JP5019911B2 (en) * | 2007-03-01 | 2012-09-05 | 大林道路株式会社 | Short-term forming method for display surface |
KR101331669B1 (en) * | 2012-03-08 | 2013-11-20 | 삼성전기주식회사 | Substrate for power module |
-
1981
- 1981-03-11 JP JP3554381A patent/JPS57148783A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS57148783A (en) | 1982-09-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2756272B2 (en) | Primer composition for surface containing inorganic oxide | |
US5851618A (en) | Peelable floor coating systems | |
ES8301520A1 (en) | Anti-graffiti facing of walls or similar surfaces. | |
KR101177349B1 (en) | Paint composition concrete | |
US6620464B2 (en) | Coated construction substrates | |
JPS628787B2 (en) | ||
JPS61242252A (en) | Building exterior finishing method, exterior sheet adhesive and exterior sheet | |
JP5069634B2 (en) | Coating liquid for coloring calcium-based inorganic base materials | |
JPS5849581B2 (en) | How to prevent pasting | |
JPS6035389B2 (en) | Paint to prevent pasting marks | |
JPS6132076B2 (en) | ||
JPS6219906B2 (en) | ||
JP2514511B2 (en) | Adhesive composition for patterned floor | |
JPS59170160A (en) | Coating compound composition for preventing traces of patch of paper | |
KR20020089664A (en) | Adhesion preventive matter | |
JPS615149A (en) | Water-proof construction method | |
JPH0323230B2 (en) | ||
JPS60222175A (en) | Treatment for painting of structure surface | |
JPS6132075B2 (en) | ||
JPH11290769A (en) | Formation of decorative coating film, its repairing method and pattern transfer sheet | |
JPS59233063A (en) | Anti-staining of elastic spray material and anti-stain building | |
KR820002344B1 (en) | The method of preparing a black board | |
JP2549483B2 (en) | Surface smoothing method for cellular concrete building materials | |
JPS62107167A (en) | Repairing of reinforced concrete | |
JPS5845260A (en) | Surface treatment for caulking material |