JP2002173642A - Stainproof painting agent composition for surface of structure and method for manufacturing the same - Google Patents

Stainproof painting agent composition for surface of structure and method for manufacturing the same

Info

Publication number
JP2002173642A
JP2002173642A JP2001295535A JP2001295535A JP2002173642A JP 2002173642 A JP2002173642 A JP 2002173642A JP 2001295535 A JP2001295535 A JP 2001295535A JP 2001295535 A JP2001295535 A JP 2001295535A JP 2002173642 A JP2002173642 A JP 2002173642A
Authority
JP
Japan
Prior art keywords
weight
parts
water
organosilicate
coating
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
JP2001295535A
Other languages
Japanese (ja)
Inventor
Yasushi Matsuyoshi
靖 松吉
Hideo Sekiguchi
日出夫 関口
Katsuyuki Miyasato
勝之 宮里
Hideo Tateno
英雄 舘野
Ichiro Ishikawa
一郎 石川
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.)
Tama Kagaku Kogyo Co Ltd
Atomix Corp
Original Assignee
Tama Kagaku Kogyo Co Ltd
Atomix Corp
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 Tama Kagaku Kogyo Co Ltd, Atomix Corp filed Critical Tama Kagaku Kogyo Co Ltd
Priority to JP2001295535A priority Critical patent/JP2002173642A/en
Publication of JP2002173642A publication Critical patent/JP2002173642A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a stainproof painting agent composition capable of exhibiting hydrophilicity and stainproof property directly after the painting on the surface of a structure without needing an acid treatment or the like, excellent in storage stability, drying property and handleability, and capable of forming paint film excellent in adhesivity and transparency, and having good appearance, and to provide a method for manufacturing the composition. SOLUTION: An organo silicate of the general formula 1 (wherein, R is a 1-10C hydrocarbon group; and n is an integer of >=1) is hydrolyzed in the presence of an acid catalyst so that the amount of hydrolyzing water is 60-600 pts.wt. based on 100 pts.wt. of the Si in the organo silicate in terms of SiO2, and a water-containing diluent is added to the obtained hydrolyzate so that the water content after the adjustment is 600-4,000 pts.wt. based on 100 pts.wt. of the Si in the organo silicate in terms of SiO2.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】この発明は、構造物の表面が
汚染されるのを防止するために用いられる汚染防止用塗
装剤組成物に係り、特に限定するものではないが、屋外
の構造物表面に塗布されて、この構造物表面が煤煙や排
気ガス等の汚染原因により汚染されるのを可及的に防止
する構造物表面の汚染防止用塗装剤組成物及びその製造
方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coating composition for preventing contamination of a surface of a structure used for preventing the surface of the structure from being stained. The present invention relates to a coating composition for preventing contamination of a surface of a structure, which is applied to a surface of the structure to prevent the surface of the structure from being contaminated as much as possible by soot and exhaust gas, and a method for producing the same.

【0002】[0002]

【従来の技術】建築物等の構造物の表面、特に常時屋外
で煤煙や排気ガス等の汚染原因に曝されている建築物の
塗装面には、煤煙や排気ガス等の汚染原因物質が付着し
易く、また、これら汚染原因物質が建築物の塗装面に付
着すると、降雨時に流れ出して塗装面上に黒い筋状の汚
れとなって現れ、建築物の塗装面の美観を著しく損ねる
という問題がある。
2. Description of the Related Art Pollutants such as smoke and exhaust gas adhere to the surface of structures such as buildings, especially painted surfaces of buildings that are constantly exposed to pollution sources such as smoke and exhaust gas outdoors. Also, if these pollutants adhere to the painted surface of the building, they will flow out during rainfall and appear as black streaks on the painted surface, significantly impairing the appearance of the painted surface of the building. is there.

【0003】そこで、従来においては、このような建築
物の塗装面の汚染をできるだけ防止するための方法とし
て、疎水性のフッ素樹脂塗料にアルキルシリケート又は
その縮合物が添加されたフッ素系コーティング剤が提案
されている(特開平8-120,211号、特開平8-120,212号、
特開平8-176,304号の各公報)。
Therefore, conventionally, as a method for preventing such contamination of the painted surface of a building as much as possible, a fluorine-based coating agent obtained by adding an alkyl silicate or a condensate thereof to a hydrophobic fluororesin paint is used. It has been proposed (JP-A-8-120211, JP-A-8-120212,
JP-A-8-176,304).

【0004】しかしながら、これらのフッ素系コーティ
ング剤は、アルキルシリケート又はその縮合物が添加さ
れてある程度の汚染は改善されるが、疎水性の強いフッ
素樹脂塗料に起因して、表面が親水性を呈するまでに長
期間を要し、塗膜形成後の初期における耐防汚性が低
く、極初期において雨筋汚れが付着し易く、建築物の塗
装面の汚染を完全には防止することができない。このた
め、本来の汚染防止の期待を一時的にも裏切るものであ
るといわざるを得ない。
[0004] However, these fluorine-based coating agents can improve the contamination to some extent by adding an alkyl silicate or a condensate thereof, but the surface exhibits hydrophilicity due to the highly hydrophobic fluororesin paint. It takes a long time to complete the process, the antifouling resistance in the initial stage after the formation of the coating film is low, rain streaks easily adhere in the very early stage, and the contamination of the painted surface of the building cannot be completely prevented. For this reason, it must be said that the expectation of pollution prevention is temporarily disappointed.

【0005】また、最近では、低汚染、非汚染を目的と
する場合には、むしろ水になじみやすく(親水性)する
方が有効であることが分かってきた(1995年2月10日発
行「月刊建築材ニュース」第18−19頁)。それは、親
水性塗膜の方が電気抵抗が低く帯電し難いので、ゴミや
汚れが付着し難い、ゴミや汚れが付着しても塗膜との
なじみが悪いので塗膜の中に入り込み難い、雨水が当
たったとき、汚れは雨水に置換されて流れ落ちる、とい
うことに起因している。
[0005] Recently, it has been found that it is more effective to make the material more water-friendly (hydrophilic) for the purpose of low-contamination and non-contamination (published on February 10, 1995). Monthly Building Materials News, pp. 18-19). The reason is that the hydrophilic coating has a lower electric resistance and is harder to be charged, so it is difficult for dirt and dirt to adhere, and even if dirt or dirt adheres, it does not easily fit into the coating, so it is difficult to enter the coating, When rainwater hits, dirt is replaced by rainwater and flows down.

【0006】そして、このような親水性塗膜を得る方法
として、下塗り塗料を塗装し、その上に、有機珪素硬化
型溶剤系塗料にオルガノシリケート及び/又はその縮合
物を配合してなり、酸処理後の硬化塗膜表面の水に対す
る接触角が70度以下である上塗り塗料を塗装し、続い
て硬化させる方法が提案されている(特開平7-136,584
号公報及び特許第2,869,443号掲載公報)。しかしなが
ら、この方法では、上塗り塗料に親水性を付与するため
に、塗布後の硬化塗膜の表面を酸処理しなければなら
ず、それだけ処理工程が増加して費用も嵩むという問題
がある。
[0006] As a method for obtaining such a hydrophilic coating film, an undercoat is applied, and an organosilicate and / or a condensate thereof is blended with an organic silicon-curable solvent-based coating on the undercoat. A method has been proposed in which an overcoating material having a contact angle of water of 70 ° or less on the surface of a cured coating film after treatment is applied and then cured (JP-A-7-136,584).
And Japanese Patent No. 2,869,443). However, in this method, in order to impart hydrophilicity to the top coat, the surface of the cured coating film after application must be subjected to an acid treatment, which causes a problem that the number of treatment steps increases and the cost increases.

【0007】また、上塗り塗膜表面に生じる塵埃や油性
成分等に起因する汚れを防止する方法として、構造物表
面に、オルガノシリケートを酸触媒の存在下にオルガノ
シリケート中Si原子のSiO2換算100重量部に対
して3〜70重量部の水で加水分解して得られた加水分
解反応物を塗布することも提案されている(特開平7-13
6,583号公報)。しかしながら、この方法においては、
加水分解に使用する水が少ないため、得られた加水分解
物中にアルコキシ基が残留し、塗装後時間の経過と共に
空気中の水分で加水分解して親水性が得られることはあ
っても、塗装直後には親水性が得られず、結果として十
分な汚染防止効果が得られない場合がある。
Further, as a method for preventing contamination caused by dust and oily components on the surface of the overcoat film, an organosilicate is coated on the surface of the structure in the presence of an acid catalyst in terms of the conversion of Si atoms in the organosilicate to SiO 2 in terms of SiO 2. It has also been proposed to apply a hydrolysis reaction product obtained by hydrolysis with 3 to 70 parts by weight of water with respect to parts by weight (JP-A-7-13).
No. 6,583). However, in this method,
Due to the small amount of water used for hydrolysis, the alkoxy group remains in the obtained hydrolyzate, and even if it is hydrolyzed with moisture in the air with the passage of time after coating, hydrophilicity may be obtained, Immediately after coating, hydrophilicity cannot be obtained, and as a result, a sufficient effect of preventing contamination may not be obtained.

【0008】[0008]

【発明が解決しようとする課題】そこで、本発明者ら
は、このような酸処理を必要とすることなく硬化塗膜の
表面に親水性を付与し、構造物表面に優れた耐汚染性を
発揮せしめることができる構造物表面の汚染防止用塗装
剤組成物について鋭意検討した結果、オルガノシリケー
トを加水分解触媒の存在下にゲル化しない程度の水で加
水分解し、次いで得られた加水分解反応物を水含有希釈
剤で希釈して所定の水分量に調整した水分調整組成物が
塗装直後から親水性を発揮して優れた耐汚染性を発揮す
るだけでなく、貯蔵安定性や乾燥性を有して取扱性に優
れており、しかも、硬化塗膜に対する密着性や透明性に
も優れていて外観のよい塗膜を形成することができるこ
とを見出し、本発明を完成した。
Accordingly, the present inventors have provided hydrophilicity to the surface of a cured coating film without the need for such acid treatment, and provided excellent stain resistance to the surface of the structure. As a result of intensive studies on a coating composition for preventing contamination of the surface of the structure that can be exerted, the organosilicate is hydrolyzed with water that does not gel in the presence of a hydrolysis catalyst, and then the obtained hydrolysis reaction is performed. The moisture control composition, which is obtained by diluting the product with a water-containing diluent and adjusting the water content to a predetermined level, exhibits hydrophilicity immediately after painting and exhibits excellent stain resistance, as well as storage stability and drying properties. They have found that they have excellent handleability and that they can form a coating film with good appearance as well as excellent adhesion and transparency to the cured coating film, and completed the present invention.

【0009】従って、本発明の目的は、酸処理等の特別
な処理を必要とすることなく構造物表面に塗装直後から
親水性を付与することができ、これによって構造物表面
に優れた耐汚染性を発揮せしめることができると共に、
同時に優れた貯蔵安定性や乾燥性を有して取扱性に優れ
ており、しかも、密着性や透明性にも優れていて外観の
よい塗膜を形成することができる構造物表面の汚染防止
用塗装剤組成物を提供することにある。
It is therefore an object of the present invention, immediately after the coating on the structure surface without the need for special processing of the acid treatment or the like can be rendered hydrophilic, thereby stain with excellent structural surface While being able to demonstrate the nature,
At the same time, it has excellent storage stability and drying properties, is excellent in handling, and has excellent adhesion and transparency, and can form a good-looking coating film. An object of the present invention is to provide a coating composition.

【0010】また、本発明の他の目的は、酸処理等の特
別な処理を必要とすることなく構造物表面に塗装直後か
ら親水性を付与することができ、耐汚染性、貯蔵安定
性、取扱性、密着性、及び透明性に優れていて外観のよ
い塗膜を形成することができる構造物表面の汚染防止用
塗装剤組成物の製造方法を提供することにある。
Another object of the present invention is to impart hydrophilicity to a surface of a structure immediately after coating without requiring special treatment such as acid treatment, and to provide stain resistance, storage stability, and the like. handling, and to provide a manufacturing method of adhesion, and infection preventive coating composition of the structure surface is excellent in transparency can be formed a good coating film appearance.

【0011】[0011]

【課題を解決するための手段】すなわち、本発明は、下
記一般式(1)
That is, the present invention provides a compound represented by the following general formula (1):

【化3】 (但し、式中、Rは炭素数1〜10の炭化水素基を示
し、互いに同じであっても異なっていてもよく、また、
nは1以上の整数を示す。)で表わされるオルガノシリ
ケートを加水分解触媒の存在下にオルガノシリケート中
Si原子のSiO2換算100重量部に対して60〜6
00重量部の加水分解水分量の水で加水分解し、得られ
た加水分解反応物に水含有希釈剤を添加して調整後水分
量がオルガノシリケート中Si原子のSiO2換算10
0重量部に対して600〜4000重量部の範囲となる
ように水分調整し、得られた水分調整組成物を主成分と
して含有する、構造物表面の汚染防止用塗装剤組成物で
ある。また、本発明は、このような構造物表面の汚染防
止用塗装剤組成物の製造方法である。
Embedded image (Wherein, R represents a hydrocarbon group having 1 to 10 carbon atoms, and may be the same or different from each other;
n shows the integer of 1 or more. The organosilicate represented by) in the presence of a hydrolysis catalyst relative terms of SiO 2 to 100 parts by weight of the organosilicate in Si atom 60-6
After hydrolyzing with water having a hydrolysis water content of 00 parts by weight and adding a water-containing diluent to the obtained hydrolysis reaction product, the water content is adjusted to 10% of SiO 2 in terms of Si atoms in the organosilicate.
It is a coating agent composition for preventing contamination of the surface of a structure, wherein the water content is adjusted to be in a range of 600 to 4000 parts by weight with respect to 0 parts by weight, and the obtained water adjusting composition is contained as a main component. The present invention is also a method for producing such a coating composition for preventing contamination of the surface of a structure.

【0012】本発明において、一般式(1)で表される
オルガノシリケートとしては、その炭化水素基Rとして
アルキル基、アリル基、アリール基等が例示され、より
具体的には、例えば、アルキル基としてメチル基、エチ
ル基、n-プロピル基、iso-プロピル基、n-ブチル基、is
o-ブチル基、tert-ブチル基、n-ペンチル基、iso-ペン
チル基、neo-ペンチル基、n-ヘキシル基、iso-ヘキシル
基等や、アリル基としてフェニル基、トルイル基、キシ
リル基、ナフチル基等や、アリール基としてビニル基等
をそれぞれ挙げることができる。これらの中で、加水分
解し易いという観点から特に好ましくは炭素数1〜4の
アルキル基である。
In the present invention, examples of the organosilicate represented by the general formula (1) include an alkyl group, an allyl group, and an aryl group as the hydrocarbon group R. More specifically, for example, an alkyl group As methyl, ethyl, n-propyl, iso-propyl, n-butyl, is
o-butyl group, tert-butyl group, n-pentyl group, iso-pentyl group, neo-pentyl group, n-hexyl group, iso-hexyl group, etc., and allyl groups such as phenyl group, toluyl group, xylyl group, and naphthyl And a vinyl group as the aryl group. Among them, an alkyl group having 1 to 4 carbon atoms is particularly preferable from the viewpoint of easy hydrolysis.

【0013】また、上記オルガノシリケートについて
は、それがn=1の単量体であっても、また、n=2〜
10の縮合体であっても、更には、これらの混合物であ
ってもよい。
In the above organosilicate, even if it is a monomer of n = 1, n = 2 to 2
Even condensate 10, further it may be a mixture thereof.

【0014】本発明の汚染防止用塗装剤組成物は、上記
オルガノシリケートを加水分解触媒の存在下にオルガノ
シリケート中Si原子のSiO2換算100重量部に対
して60〜600重量部の加水分解水分量の水で加水分
解し、得られた加水分解反応物に水含有希釈剤を添加し
て調整後水分量がオルガノシリケート中Si原子のSi
2換算100重量部に対して600〜4000重量部
の範囲となるように水分調整し、得られた水分調整組成
物を主成分とするものである。
The coating composition for preventing contamination according to the present invention is characterized in that the organosilicate is hydrolyzed in the presence of a hydrolysis catalyst in an amount of from 60 to 600 parts by weight of hydrolyzed water based on 100 parts by weight of Si atoms in terms of SiO 2 in the organosilicate. After the addition of a water-containing diluent to the resulting hydrolysis reaction product, the water content is adjusted to the Si content of the Si atoms in the organosilicate.
Moisture is adjusted to be in the range of 600 to 4000 parts by weight with respect to 100 parts by weight in terms of O 2 , and the obtained water adjusting composition is the main component.

【0015】ここで、このオルガノシリケートを加水分
解するのに用いる加水分解水分量の「オルガノシリケー
ト中Si原子のSiO2換算100重量部に対して60
〜600重量部」は、このオルガノシリケートを完全に
加水分解できる理論量以上であって、得られた加水分解
反応物がゲル化しない程度の量であり、好ましくは12
0重量部以上400重量部以下であるのがよい。この加
水分解水分量が60重量部より少ないと加水分解が十分
に進まず、所望の親水性が得られないという問題が生
じ、反対に、600重量部より多くなると加水分解反応
物がゲル化し易くなるので好ましくない。なお、この加
水分解水分量とは、オルガノシリケートを加水分解する
際にその反応系に存在する全水分の量をいい、加水分解
反応系に反応剤として添加される水に限らず、この加水
分解反応系に加水分解触媒と共に、あるいは、反応溶剤
と共に導入される水も含む全ての水分量をいう。
Here, the amount of hydrolyzed water used to hydrolyze this organosilicate is 60 parts per 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2.
"-600 parts by weight" is not less than the theoretical amount at which the organosilicate can be completely hydrolyzed, and is such an amount that the obtained hydrolysis reaction product does not gel, preferably 12 parts by weight.
The amount is preferably from 0 to 400 parts by weight. If the amount of the hydrolyzed water is less than 60 parts by weight, the hydrolysis does not proceed sufficiently, and a problem that desired hydrophilicity cannot be obtained occurs. Conversely, if the amount of the hydrolyzed water is more than 600 parts by weight, the hydrolyzate tends to gel. Is not preferred. The amount of hydrolyzed water refers to the total amount of water present in the reaction system when hydrolyzing the organosilicate, and is not limited to water added as a reactant to the hydrolysis reaction system. It refers to the total amount of water including water introduced into the reaction system together with the hydrolysis catalyst or together with the reaction solvent.

【0016】また、オルガノシリケートの加水分解反応
に用いる加水分解触媒としては、特に制限はないが、好
ましくは硝酸、硫酸、塩酸、燐酸等の鉱酸類や、蟻酸、
酢酸等の有機酸類等の酸触媒である。この加水分解触媒
の使用量は、例えば酸触媒の場合、反応系中に、通常
0.01〜5重量%、好ましくは0.05〜2重量%で
あり、0.01重量%より少ないと加水分解速度が遅く
なるという問題が生じ、反対に、5重量%より多くなる
と加水分解反応物がゲル化し易くなるほか、反応のコン
トロールが難しくなるという問題が生じる。
The hydrolysis catalyst used in the hydrolysis reaction of the organosilicate is not particularly limited, but is preferably a mineral acid such as nitric acid, sulfuric acid, hydrochloric acid or phosphoric acid, or a formic acid,
Acid catalysts such as organic acids such as acetic acid. The amount of the hydrolysis catalyst used is, for example, in the case of an acid catalyst, usually 0.01 to 5% by weight, preferably 0.05 to 2% by weight in the reaction system. On the contrary, when the amount exceeds 5% by weight, the hydrolysis reaction product is liable to gel, and the control of the reaction becomes difficult.

【0017】更に、オルガノシリケートの加水分解反応
に際しては、好ましくは反応系のオルガノシリケートと
水とを互いに溶解せしめる反応溶剤を用いるのがよく、
この反応溶剤としてはこれら両者を互いに溶解せしめる
ものであれば特に制限はないが、塗装時の取扱性等を考
慮すると、好ましくはアルコール類がよく、具体的に
は、エチルアルコール、iso-プロピルアルコール、ブチ
ルアルコール等が好ましい。この反応溶剤の使用量は、
オルガノシリケート中Si原子のSiO2換算100重
量部に対して通常100〜3000重量部、好ましくは
200〜2000重量部であり、100重量部より少な
いとゲル化し易いという問題が生じ、反対に、3000
重量部より多くなると反応が不充分になるほか、反応速
度が遅くなるという問題が生じる。
Further, in the hydrolysis reaction of the organosilicate, it is preferable to use a reaction solvent which can dissolve the organosilicate and water in the reaction system with each other.
The reaction solvent is not particularly limited as long as it can dissolve both of them. However, in view of handling properties at the time of coating, alcohols are preferable, and specific examples thereof include ethyl alcohol and iso-propyl alcohol. And butyl alcohol. The amount of this reaction solvent used is
The amount is usually 100 to 3000 parts by weight, preferably 200 to 2000 parts by weight, based on 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2.
If the amount is more than 10 parts by weight, the reaction will be insufficient and the reaction rate will be slow.

【0018】この加水分解反応により得られた加水分解
反応物は、水含有希釈剤を添加してその調整後水分量が
オルガノシリケート中Si原子のSiO2換算100重
量部に対して600〜4000重量部、好ましくは10
00〜3500重量部、より好ましくは1500〜30
00重量部の範囲となるように水分調整され、得られた
水分調整組成物が本発明の構造物表面の汚染防止用塗装
剤組成物の主成分とされる。ここで、この調整後水分量
が600重量部より少ないと最終的にアルコキシ基が残
存して所望の親水性が得られないという問題があり、反
対に、4000重量部より多くなると貯蔵安定性が低下
して製品ライフが短くなるという問題が生じる。
After the hydrolysis reaction product obtained by this hydrolysis reaction is added with a water-containing diluent and adjusted to have a water content of 600 to 4000 parts by weight based on 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2. Parts, preferably 10
00-3500 parts by weight, more preferably 1500-30
The water content is adjusted so as to be within the range of 00 parts by weight, and the obtained water content adjusting composition is used as the main component of the coating composition for preventing contamination of the structure surface of the present invention. Here, if the water content after the adjustment is less than 600 parts by weight, there is a problem that the alkoxy group is finally left and desired hydrophilicity cannot be obtained, and if it is more than 4000 parts by weight, the storage stability becomes poor. There is a problem that the product life is shortened and the product life is shortened.

【0019】この水分調整に用いる水含有希釈剤は、加
水分解反応物と水とを互いに溶かし合うものであれば特
に制限はないが、有機溶剤−水系のものを使用するのが
よく、この有機溶剤としては、塗装後の塗膜の乾燥状態
を考慮に入れると反応溶剤の場合と同様に、アルコール
類、特にエチルアルコール、iso-プロピルアルコール、
ブチルアルコール等が好ましい。また、本発明の塗装剤
組成物には、必要により粘度調整用あるいは塗膜の乾燥
速度を調整する目的で、エチルアルコール、iso-プロピ
ルアルコール、ブチルアルコール等のアルコール類や、
粘度の高い溶剤、沸点の高い溶剤等の他の溶剤を添加し
てもよい。
The water-containing diluent used for the water content adjustment is not particularly limited as long as it can dissolve the hydrolysis reaction product and water with each other, but an organic solvent-water system is preferably used. As the solvent, alcohols, especially ethyl alcohol, iso-propyl alcohol,
Butyl alcohol and the like are preferred. Further, the coating composition of the present invention, for the purpose of adjusting the viscosity or drying speed of the coating film as necessary, ethyl alcohol, isopropyl alcohol, alcohols such as butyl alcohol,
Other solvents such as a solvent having a high viscosity and a solvent having a high boiling point may be added.

【0020】本発明の汚染防止用塗装剤組成物が適用さ
れる構造物表面としては、例えば、コンクリート、繊維
強化コンクリート、スレート、ガラス等の無機材表面
や、アクリル樹脂、フッ素樹脂、ポリウレタン樹脂、ポ
リエステル樹脂、ポリカーボネイト樹脂、塩化ビニル樹
脂、ポリエチレン樹脂等の樹脂で成形されたフィルム、
シート等の樹脂成形品、ゴム製品等の有機材表面や、ア
ルミニウム、鉄、ステンレス、亜鉛鋼板、鋼板等の金属
材表面や、更に繊維強化樹脂等の有機無機複合材等の有
機無機複合材表面を始め、これら無機材、有機材、及び
有機無機複合材の表面に、予め、フッ素樹脂塗料、ポリ
ウレタン樹脂塗料、アクリル系樹脂塗料、ポリエステル
樹脂塗料及び水性樹脂塗料から選ばれた塗膜層を設けた
塗装面等を挙げることができる。これらの構造物表面に
は、本発明の塗装剤組成物を直接塗装してもよく、ま
た、プライマー等の表面処理をした後に、又は、下塗り
した後に塗装してもよい。
The surface of a structure to which the coating composition for preventing contamination of the present invention is applied includes, for example, surfaces of inorganic materials such as concrete, fiber reinforced concrete, slate and glass, acrylic resins, fluororesins, polyurethane resins, and the like. A film molded from a resin such as polyester resin, polycarbonate resin, vinyl chloride resin, polyethylene resin,
Surface of organic materials such as resin molded products such as sheets and rubber products, surface of metal materials such as aluminum, iron, stainless steel, zinc steel plate and steel plate, and surface of organic-inorganic composite materials such as organic-inorganic composite materials such as fiber-reinforced resin In addition, on the surface of these inorganic materials, organic materials, and organic-inorganic composite materials, a coating layer selected from a fluororesin paint, a polyurethane resin paint, an acrylic resin paint, a polyester resin paint, and an aqueous resin paint is provided in advance. Painted surface and the like. The surface of these structures may be directly coated with the coating composition of the present invention, or may be coated after being subjected to a surface treatment such as a primer or after undercoating.

【0021】本発明の汚染防止用塗装剤組成物を、例え
ば建築用外板パネル、テント、防水シート、風防シー
ト、建築用シート、屋根材、天窓、コンクリート壁、貯
水タンク、タンク、シャッター、サッシュ等の建築用部
材、建築物外壁、ガードレール、歩道橋、外装板、透光
板、防音壁、標識、高速道路側壁、トンネル壁面、鉄道
高架橋、橋梁等の道路部材等の種々の屋外物品の汚れが
発生し易い箇所に塗装することにより、極めて長期間に
亘って汚れの発生を防止することができる。
The coating composition for preventing pollution of the present invention is used, for example, for building exterior panels, tents, waterproof sheets, windshield sheets, building sheets, roofing materials, skylights, concrete walls, water storage tanks, tanks, shutters, and sashes. Dirt on various outdoor goods such as building members such as building exterior walls, guard rails, pedestrian bridges, exterior panels, translucent boards, soundproof walls, signs, side walls of expressways, tunnel walls, railway viaducts, bridges, and other road members. By coating on a place where the occurrence is easy, it is possible to prevent the occurrence of dirt for an extremely long time.

【0022】本発明の汚染防止用塗装剤組成物は、通常
の塗装方法、例えば、刷毛塗り、ローラー塗り、スプレ
ー塗り、フローコーター、グラビアコーター、スピンコ
ートによる塗装等により容易に塗装することができる。
また、乾燥方法は、常温でもよいし加熱してもよいが、
加熱した方が短期間で乾燥塗膜が得られる。
The coating composition for preventing contamination of the present invention can be easily applied by a usual coating method, for example, by brush coating, roller coating, spray coating, flow coater, gravure coater, or spin coating. .
Also, the drying method may be room temperature or may be heated,
A dried film can be obtained in a shorter time by heating.

【0023】本発明の汚染防止用塗装剤組成物におい
て、多量の水が含まれているにもかかわらず、加水分解
反応物がゲル化することなく安定に存在する理由は必ず
しも明確ではないが、オルガノシリケートを完全に加水
分解し、また、加水分解反応物がゲル化しない程度の反
応水で予めオルガノシリケートを加水分解し、重縮合さ
せると、加水分解反応物において反応により生成した加
水分解生成物は球状のコロイド状態となって水含有溶剤
中に分散し、ここに多量の水を加えた場合、このコロイ
ド状態の加水分解反応物は、初めは重合反応が進んで重
合物を形成するが、この重合物は多量に存在する水との
平衡反応により加水分解され、結果として多量の水が存
在するにも係わらず、比較的安定に存在するものと考え
られる。
Although the coating composition for preventing contamination of the present invention contains a large amount of water, the reason why the hydrolysis reaction product stably exists without gelling is not necessarily clear, When the organosilicate is completely hydrolyzed, and the organosilicate is previously hydrolyzed with reaction water to such an extent that the hydrolysis reaction product does not gel, and polycondensed, the hydrolysis product formed by the reaction in the hydrolysis reaction product Is dispersed in a water-containing solvent in a spherical colloidal state, and when a large amount of water is added thereto, the hydrolysis reaction product in the colloidal state initially undergoes a polymerization reaction to form a polymer, It is considered that this polymer is hydrolyzed by an equilibrium reaction with a large amount of water, and as a result, it is present relatively stably despite the presence of a large amount of water.

【0024】[0024]

【実施例】以下、実施例及び比較例に基づいて、本発明
を具体的に説明する。 実施例1 500ml三口フラスコ内に、エチルシリケートのオリ
ゴマー体(多摩化学工業株式会社製商品名:ES−4
0、平均重合度4〜5)40gと、エタノール88gとを
仕込んで均一に混合し、ここに純水21.6gと触媒と
しての6wt%-硝酸28gとを加え、加熱還流下に4時間反
応させ、冷却して加水分解反応物(第1反応物)を得
た。
The present invention will be specifically described below based on examples and comparative examples. Example 1 In a 500 ml three-necked flask, an oligomer of ethyl silicate (trade name: ES-4, manufactured by Tama Chemical Industry Co., Ltd.)
0, average polymerization degree 4-5) 40 g and ethanol 88 g were charged and uniformly mixed, and 21.6 g of pure water and 28 g of 6 wt% -nitric acid as a catalyst were added thereto, and the mixture was reacted under heating and reflux for 4 hours. After cooling, a hydrolysis reaction product (first reaction product) was obtained.

【0025】次に、得られた第1反応物中に、イソプロ
ピルアルコール190gと純水430gとを十分に撹拌混
合して得られた水含有希釈剤を加え、更に撹拌混合して
実施例1の塗装剤組成物とした。
Next, a water-containing diluent obtained by sufficiently stirring and mixing 190 g of isopropyl alcohol and 430 g of pure water was added to the obtained first reaction product, and further mixed by stirring. A coating composition was obtained.

【0026】実施例2 第1反応液中のES−40に代えて、メチルシリケート
のオリゴマー体(多摩化学工業株式会社製商品名:MS
−51、平均重合度3〜4)を31.4g加えた以外
は、実施例1と同様にして実施例2の塗装剤組成物を調
製した。
Example 2 Methyl silicate oligomer (trade name: MS, manufactured by Tama Chemical Industry Co., Ltd.) was used instead of ES-40 in the first reaction solution.
A coating composition of Example 2 was prepared in the same manner as in Example 1, except that 31.4 g of -51, average degree of polymerization 3 to 4) was added.

【0027】実施例3 水含有希釈剤中の純水を272gとした以外は、実施例
1と同様にして実施例3の塗装剤組成物を調製した。
Example 3 A coating composition of Example 3 was prepared in the same manner as in Example 1 except that 272 g of pure water in the water-containing diluent was used.

【0028】実施例4 水含有希釈剤中の純水を112gとした以外は、実施例
1と同様にして実施例4の塗装剤組成物を調製した。
Example 4 A coating composition of Example 4 was prepared in the same manner as in Example 1 except that the amount of pure water in the water-containing diluent was changed to 112 g.

【0029】実施例5 水含有希釈剤中の純水を48gとした以外は、実施例1
と同様にして実施例5の塗装剤組成物を調製した。
Example 5 Example 1 was repeated except that the amount of pure water in the water-containing diluent was changed to 48 g.
In the same manner as in the above, a coating composition of Example 5 was prepared.

【0030】比較例1 1500ml三口フラスコ内に、ES−40を40g、
エタノール88g、イソプロピルアルコール190g、及
び純水650gを仕込んで均一に混合し、次いで6wt%-硝
酸28gを加え、加熱還流下に4時間反応させたが、反
応液は途中でゲル化した。
Comparative Example 1 40 g of ES-40 was placed in a 1500 ml three-necked flask.
88 g of ethanol, 190 g of isopropyl alcohol, and 650 g of pure water were charged and uniformly mixed, and then 28 g of 6 wt% -nitric acid was added. The mixture was reacted under heating and reflux for 4 hours, but the reaction solution gelled on the way.

【0031】比較例2 実施例1で用いた水含有希釈剤とは異なり、イソプロピ
ルアルコール19gのみを希釈剤として用いた以外は、
実施例1と同様にして比較例2の塗装剤組成物を調製し
た。
Comparative Example 2 Unlike the water-containing diluent used in Example 1, except that only 19 g of isopropyl alcohol was used as the diluent.
A coating composition of Comparative Example 2 was prepared in the same manner as in Example 1.

【0032】[試験結果/実施例の検証]上記実施例1
〜5及び比較例2の各塗装剤組成物について検証した。
貯蔵安定性は、塗装剤組成物を容器に入れて密封し、温
度40℃で3ヶ月間保持した後室温に戻し、容器の中の
状態を観察し、◎:まったく変化が認められない、○:
やや白味を呈す、△:白色に濁る、及び×:ゲル化し
た、の4段階で評価した。また、塗装剤組成物をガラス
板上に塗装して乾燥性、透明性、及び外観を目視で観察
した。乾燥性については◎:1時間後に完全に乾燥・成
膜した、及び×:1時間後に乾燥・成膜せず、の2段階
で評価し、また、透明性については、◎:1時間後に透
明になる、△:1時間後にやや白味を帯びる、×:1時
間後に白味を帯びる、の3段階で評価し、塗膜外観につ
いては◎:1時間後に完全に成膜した、及び×:1時間
後に乾燥・成膜せずに粉化した、の2段階で評価した。
以上の結果を表1に示す。
[Test Results / Verification of Example] Example 1 above
Each coating composition of Comparative Examples 2 to 5 and Comparative Example 2 was verified.
The storage stability was as follows: the coating composition was sealed in a container, kept at a temperature of 40 ° C. for 3 months, returned to room temperature, and observed in the container. ◎: No change was observed. :
It was evaluated in four stages: slightly white, Δ: turbid white, and ×: gelled. Further, the coating composition was applied on a glass plate, and the drying property, the transparency, and the appearance were visually observed. Drying properties ◎: 1 hour after completely dry-deposited, and ×: 1 hour after without drying and film forming was evaluated in two stages, also the transparency, ◎: clear after 1 hour △: Slightly whitish after 1 hour, ×: Whitish after 1 hour, and evaluated as 3 grades. Coating appearance: 外 観: Completely formed after 1 hour, and ×: One hour later, the powder was evaluated without drying or film formation.
Table 1 shows the above results.

【0033】[0033]

【表1】 [Table 1]

【0034】更に、表2に示すように、溶剤フッ素樹脂
塗料、溶剤ポリウレタン樹脂塗料、焼付フッ素樹脂塗
料、及び焼付ポリエステル樹脂塗料がそれぞれ塗布され
た基板、アルミ板、塩ビ板、あるいはポリカーボネート
板上に、上記各実施例1〜6及び比較例2の塗装剤組成
物を0.03kg/m2の割合で塗装し、実施例1〜5及び
比較例2の試験片を調製した。
Further, as shown in Table 2, on a substrate, an aluminum plate, a PVC plate, or a polycarbonate plate to which a solvent fluororesin paint, a solvent polyurethane resin paint, a baked fluororesin paint, and a baked polyester resin paint were applied, respectively. The coating compositions of Examples 1 to 6 and Comparative Example 2 were applied at a rate of 0.03 kg / m 2 to prepare test pieces of Examples 1 to 5 and Comparative Example 2.

【0035】得られた各実施例1〜5及び比較例2の試
験片について、その塗装面を屋外に暴露し、屋外暴露試
験を行なつた。この屋外暴露試験による汚れの評価は、
6ヶ月後の暴露前と暴露後の明度の差を△L*とした。
この明度差の測定は色彩色差計(ミノルタ株式会社製C
R−300)で行い、◎:−2以上、○:−2〜−5、
△:−5〜−8、及び×:−8以下の基準で評価した。
なお、明度差△L*は、大きな数値ほど汚れが少ないこ
とを示す。
With respect to the test pieces obtained in Examples 1 to 5 and Comparative Example 2, the painted surfaces were exposed outdoors, and an outdoor exposure test was performed. Evaluation of dirt by this outdoor exposure test
The difference in brightness after exposure and before exposure after 6 months △ was L *.
The measurement of this lightness difference is performed by a colorimeter (C
R-300), ◎: -2 or more, :: -2 to -5,
Δ: -5 to -8 and ×: -8 were evaluated based on the following criteria.
It should be noted that the brightness difference ΔL * indicates that the larger the numerical value, the less the stain.

【0036】また、親水性の度合いとして屋外暴露前の
初期接触角の測定を行なった。この接触角の測定は、上
記塗装面上に0.02ccの脱イオン水を滴下し、接触角
測定装置(協和化学株式会社製商品名:CONTACT−ANGLE
METER CA-A型)を用いて20℃で水滴の接触角を測定
した。これらの3点測定平均値の結果を表2に示す。
The initial contact angle before outdoor exposure was measured as the degree of hydrophilicity. The contact angle was measured by dropping 0.02 cc of deionized water onto the painted surface and using a contact angle measuring device (trade name: CONTACT-ANGLE manufactured by Kyowa Chemical Co., Ltd.).
The contact angle of a water droplet was measured at 20 ° C. using a METER CA-A type). Table 2 shows the results of these three-point average values.

【0037】[0037]

【表2】 [Table 2]

【0038】上記表1及び表2の結果から明らかなよう
に、各実施例1〜5の塗装剤組成物は、これを用いて得
られた塗膜が親水性であるため、雨水が当たっときに汚
れはこの雨水と置換されて流れ落ちることになり、耐汚
染性が長期に亘って発揮され、構造物表面の汚染を効果
的に防止することができる。
As is clear from the results in Tables 1 and 2, the coating compositions obtained in Examples 1 to 5 were coated with the coating composition obtained by using the coating composition. The dirt is replaced by the rainwater and flows down, and the contamination resistance is exhibited for a long period of time, so that the contamination of the structure surface can be effectively prevented.

【0039】比較例3 2000ml三口フラスコ内に、実施例1で用いたと同
じエチルシリケートのオリゴマー体40gと、エタノー
ル88g及びイソプロピルアルコール190gとを仕込ん
で均一に混合し、ここに純水453gと触媒としての6wt
%-硝酸28gとを加え、加熱還流下に4時間反応させ、
冷却してオルガノシリケート中Si原子のSiO2換算
100重量部に対して最終的に水分量が3000重量部
である加水分解反応物(塗装剤組成物)を得た。
Comparative Example 3 In a 2000 ml three-necked flask, 40 g of the same ethyl silicate oligomer as used in Example 1, 88 g of ethanol and 190 g of isopropyl alcohol were charged and uniformly mixed. 6wt
%-Nitric acid 28g was added and reacted under heating and reflux for 4 hours.
After cooling, a hydrolysis reaction product (coating agent composition) having a water content of 3,000 parts by weight based on 100 parts by weight of SiO 2 in terms of Si atoms in the organosilicate was finally obtained.

【0040】比較例4 エチルシリケートのオリゴマー体に代えて、実施例2で
用いたと同じメチルシリケートのオリゴマー体を31.
4g使用した以外は、比較例3と同様にして、オルガノ
シリケート中Si原子のSiO2換算100重量部に対
して最終的に水分量が3000重量部である比較例4の
塗装剤組成物を調製した。
Comparative Example 4 The same methyl silicate oligomer used in Example 2 was used in place of the ethyl silicate oligomer.
A coating composition of Comparative Example 4 was prepared in the same manner as in Comparative Example 3 except that 4 g of the coating composition was used. Finally, the water content was 3000 parts by weight based on 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2. did.

【0041】比較例5 純水の使用量を293gとした以外は、比較例3と同様
にして、オルガノシリケート中Si原子のSiO2換算
100重量部に対して最終的に水分量が2000重量部
である比較例5の塗装剤組成物を調製した。
Comparative Example 5 In the same manner as in Comparative Example 3, except that the amount of pure water used was changed to 293 g, the final water content was 2,000 parts by weight based on 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2. Was prepared.

【0042】[試験結果/実施例の検証]上記実施例1
〜3及び比較例3〜5の各塗装剤組成物について、その
密着性と、初期親水性(接触角)と、3ヶ月屋外暴露前
後の塗膜の外観、親水性(接触角)を評価し、更に、6
ヶ月屋外暴露前後の塗膜の外観、汚れの評価(明度差△
*)、親水性(接触角)を検証した。結果を表3に示
す。
[Test Results / Verification of Example] Example 1 above
Each of the coating agent compositions of Comparative Examples 3 to 5 and Comparative Examples 3 to 5
Adhesion, initial hydrophilicity (contact angle), 3 months before outdoor exposure
Coating appearance, hydrophilicity (contact angle) was evaluated after further 6
Evaluation of appearance and stain of coating film before and after outdoor exposure for one month (brightness difference
L *), Hydrophilicity (contact angle) was verified. The results are shown in Table 3.
You.

【0043】この際、屋外暴露、接触角及び明度差△L
*の測定、及び塗膜外観の評価は、基板上に溶剤フッ素
樹脂塗料(塗料A;アトミクス社製商品名:アトムセフ
ロンH)又は溶剤ポリウレタン樹脂塗料(塗料B;アト
ミクス社製商品名:ライフテックス#70)をそれぞれ3
0μm1回塗りの条件で塗布して塗装面を形成し、この
塗装面上に上記各実施例1〜3及び比較例3〜5の塗装
剤組成物を0.03g/m2の割合で塗装し、各実施例1〜
3及び比較例3〜5の試験片を調製して行った。
At this time, outdoor exposure, contact angle and lightness difference ΔL
The measurement of * and the evaluation of the appearance of the coating film were carried out by coating a solvent fluororesin paint (paint A; trade name: Atomseflon H) or solvent polyurethane resin paint (paint B; trade name: Atomix product name: Lifetex #) on the substrate. 70) is 3
The composition was applied under the condition of a single coating of 0 μm to form a coated surface, and the coating composition of each of Examples 1 to 3 and Comparative Examples 3 to 5 was applied on the coated surface at a rate of 0.03 g / m 2. each example 1
3 and Comparative Examples 3 to 5 were prepared and performed.

【0044】なお、密着性については、上記各実施例1
〜3及び比較例3〜5の試験片について、JIS K5400 8.
5.3に準じてXカットテープ法で測定し、10:剥れが
全く認められない、8:交点に剥れがなく、Xカット部
に僅かに剥れが認められる、6:Xカット部の交点から
いずれかの方向に1.5mm以下の剥れが認められる、
4:Xカット部の交点からいずれかの方向に1.5mm超
え3.0mm以下の剥れが認められる、2:Xカット部の
大部分に剥れが認められる、0:Xカット部よりも大き
く剥れる、という観点で評価した。
As for the adhesion, each of the above Examples 1 to 5 was used.
JIS K5400 for the test pieces of Comparative Examples 3 to 5 and Comparative Examples 3 to 5.
Measured by the X-cut tape method according to 5.3, 10: No peeling was observed, 8: No peeling was observed at the intersection, and slight peeling was observed at the X-cut part, 6: Intersection of the X-cut part From 1.5mm or less in any direction is recognized,
4: Peeling of 1.5 mm or more and 3.0 mm or less is observed in any direction from the intersection of the X cuts. 2: Peeling is observed in most of the X cuts, 0: Compared with the X cuts The evaluation was made from the viewpoint of large peeling.

【0045】また、屋外暴露試験は、図1に示すよう
に、上部に45°の傾斜面を有すると共に下部に垂直面
を有する試験片(垂直面と傾斜面との間の角度:135
°)を調製し、垂直面で塗膜の外観を、また、傾斜面で
塗膜の汚れの評価をそれぞれ行った。この屋外暴露後の
塗膜の外観は、目視観察により、◎:全く雨筋が認めら
れない、○:一部に薄い雨筋が認められる、△:一部に
はっきりした雨筋が認められる、×:全面に雨筋が認め
られる、の4段階で評価した。
In the outdoor exposure test, as shown in FIG. 1, a test piece having an inclined surface of 45 ° at the top and a vertical surface at the bottom (the angle between the vertical surface and the inclined surface: 135)
°) was prepared, and the appearance of the coating film was evaluated on a vertical surface, and the contamination of the coating film was evaluated on an inclined surface. The appearance of the coating film after this outdoor exposure was visually observed, ◎: no rain streaks were observed at all, ○: thin rain streaks were partially observed, Δ: clear rain streaks were partially observed, X: Evaluation was made in four steps: rain streaks were observed on the entire surface.

【0046】[0046]

【表3】 [Table 3]

【0047】[0047]

【発明の効果】本発明の汚染防止用塗装剤組成物は、酸
処理等の特別な処理を必要とすることなく構造物表面に
塗装直後から親水性を付与することができ、これによっ
て構造物表面に優れた耐汚染性を発揮せしめると共に、
同時に優れた貯蔵安定性や乾燥性を有して取扱性に優れ
ており、しかも、密着性や透明性にも優れていて外観の
よい塗膜を形成することができる。
Industrial Applicability The coating composition for preventing contamination of the present invention can impart hydrophilicity to the surface of a structure immediately after coating without requiring special treatment such as acid treatment. While exhibiting excellent contamination resistance on the surface,
At the same time, it has excellent storage stability and drying properties, is excellent in handleability, and is excellent in adhesion and transparency, and can form a coating film with good appearance.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 図1は、屋外暴露試験において、塗膜の外観
と塗膜の汚れの評価を行なう際に用いた試験片の形状を
示す説明図である。
FIG. 1 is an explanatory view showing the shape of a test piece used for evaluating the appearance of a coating film and stains on the coating film in an outdoor exposure test.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 関口 日出夫 神奈川県川崎市川崎区駅前本町12番1、川 崎駅前タワー・リバーク17階、多摩化学工 業株式会社内 (72)発明者 宮里 勝之 東京都板橋区舟渡3−9−6、アトミクス 株式会社内 (72)発明者 舘野 英雄 東京都板橋区舟渡3−9−6、アトミクス 株式会社内 (72)発明者 石川 一郎 東京都板橋区舟渡3−9−6、アトミクス 株式会社内 Fターム(参考) 4J038 DL021 KA06 LA02 NA01 NA05 NA12 PB05 PC02 PC03 PC04 PC08  ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Hideo Sekiguchi 12-1, Ekimae Honcho, Kawasaki-ku, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture, 17th floor of Tower Reverk, Kawasaki Station, inside Tama Chemical Industry Co., Ltd. (72) Katsuyuki Miyazato Tokyo 3-9-6 Funato, Itabashi-ku, Atomics Inc. (72) Inventor Hideo Tateno 3-9-6, Funato, Itabashi-ku, Tokyo, Atomics Inc. (72) Inventor Ichiro Ishikawa 3-, Funato, Itabashi-ku, Tokyo 9-6, Atomics Inc. F term (reference) 4J038 DL021 KA06 LA02 NA01 NA05 NA12 PB05 PC02 PC03 PC04 PC08

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 下記一般式(1) 【化1】 (但し、式中、Rは炭素数1〜10の炭化水素基を示
し、互いに同じであっても異なっていてもよく、また、
nは1以上の整数を示す。)で表わされるオルガノシリ
ケートを加水分解触媒の存在下にオルガノシリケート中
Si原子のSiO2換算100重量部に対して60〜6
00重量部の加水分解水分量の水で加水分解し、得られ
た加水分解反応物に水含有希釈剤を添加して調整後水分
量がオルガノシリケート中Si原子のSiO2換算10
0重量部に対して600〜4000重量部の範囲となる
ように水分調整し、得られた水分調整組成物を主成分と
して含有することを特徴とする構造物表面の汚染防止用
塗装剤組成物。
[Claim 1] The following general formula (1) (Wherein, R represents a hydrocarbon group having 1 to 10 carbon atoms, and may be the same or different from each other;
n shows the integer of 1 or more. The organosilicate represented by) in the presence of a hydrolysis catalyst relative terms of SiO 2 to 100 parts by weight of the organosilicate in Si atom 60-6
After hydrolyzing with water having a hydrolysis water content of 00 parts by weight and adding a water-containing diluent to the obtained hydrolysis reaction product, the water content is adjusted to 10% of SiO 2 in terms of Si atoms in the organosilicate.
A coating composition for preventing contamination of the surface of a structure, wherein the water content is adjusted to be in a range of 600 to 4000 parts by weight with respect to 0 parts by weight, and the obtained water adjusting composition is contained as a main component. .
【請求項2】 加水分解反応系に導入される加水分解水
分量がオルガノシリケート中Si原子のSiO2換算1
00重量部に対して120〜400重量部である請求項
1に記載の構造物表面の汚染防止用塗装剤組成物。
2. The amount of hydrolyzed water introduced into the hydrolysis reaction system is 1 in terms of SiO 2 in terms of Si atoms in the organosilicate.
The coating composition according to claim 1, wherein the amount is 120 to 400 parts by weight based on 00 parts by weight.
【請求項3】 調整後水分量がオルガノシリケート中S
i原子のSiO2換算100重量部に対して1000〜
3500重量部である請求項1又は2に記載の構造物表
面の汚染防止用塗装剤組成物。
3. The water content after the adjustment is S in the organosilicate.
1000 to 100 parts by weight of i-atom in terms of SiO 2
The coating composition for preventing surface contamination of a structure according to claim 1 or 2, which is 3500 parts by weight.
【請求項4】 構造物表面がフッ素樹脂塗料、ポリウレ
タン樹脂塗料、アクリル系樹脂塗料、ポリエステル樹脂
塗料及び水性樹脂塗料から選ばれた塗膜層を有する請求
項1〜3のいずれかに記載の構造物表面の汚染防止用塗
装剤組成物。
4. The structure according to claim 1, wherein the surface of the structure has a coating layer selected from a fluororesin coating, a polyurethane resin coating, an acrylic resin coating, a polyester resin coating and an aqueous resin coating. A coating composition for preventing contamination of an object surface.
【請求項5】 構造物の基材が金属、ガラス、ホーロ
ー、セラミックス、コンクリート、木材、プラスチック
から選ばれたいずれかの材質で形成されている請求項1
〜4のいずれかに記載の構造物表面の汚染防止用塗装剤
組成物。
5. The structure according to claim 1, wherein the base material is formed of any material selected from metal, glass, enamel, ceramics, concrete, wood, and plastic.
5. The coating composition for preventing contamination of a surface of a structure according to any one of items 4 to 4.
【請求項6】 下記一般式(1) 【化2】 (但し、式中、Rは炭素数1〜10の炭化水素基を示
し、互いに同じであっても異なっていてもよく、また、
nは1以上の整数を示す。)で表わされるオルガノシリ
ケートを加水分解触媒の存在下にオルガノシリケート中
Si原子のSiO2換算100重量部に対して60〜6
00重量部の加水分解水分量の水で加水分解し、次いで
得られた加水分解反応物に水含有希釈剤を添加して調整
後水分量がオルガノシリケート中Si原子のSiO2
算100重量部に対して600〜4000重量部の範囲
となるように水分調整し、得られた水分調整組成物を主
成分として含有せしめることを特徴とする構造物表面の
汚染防止用塗装剤組成物の製造方法。
6. The following general formula (1): (Wherein, R represents a hydrocarbon group having 1 to 10 carbon atoms, and may be the same or different from each other;
n shows the integer of 1 or more. The organosilicate represented by) in the presence of a hydrolysis catalyst relative terms of SiO 2 to 100 parts by weight of the organosilicate in Si atom 60-6
After hydrolyzing with water having a hydrolysis water content of 00 parts by weight and then adding a water-containing diluent to the obtained hydrolysis reaction product, the water content is adjusted to 100 parts by weight of Si atoms in the organosilicate in terms of SiO 2. A method for producing a coating composition for preventing surface structure contamination, comprising adjusting the water content to be in the range of 600 to 4000 parts by weight with respect to the water content, and incorporating the obtained water content adjusting composition as a main component.
JP2001295535A 2000-09-28 2001-09-27 Stainproof painting agent composition for surface of structure and method for manufacturing the same Pending JP2002173642A (en)

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JP2000-296792 2000-09-28
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003103712A (en) * 2001-09-28 2003-04-09 Atomix Co Ltd Surface treated synthetic resin sheet
JP2005015572A (en) * 2003-06-24 2005-01-20 Chugoku Marine Paints Ltd Epoxy resin composition, anticorrosive coating film formed therefrom, substrate covered with the anticorrosive coating film and corrosion protection method of the substrate
WO2005083006A1 (en) * 2004-02-27 2005-09-09 Mitsubishi Chemical Corporation Silicon-containing liquid composition
JP2008500208A (en) * 2004-05-28 2008-01-10 ピーピージー インダストリーズ オハイオ, インコーポレイテッド Multilayer coatings and related methods

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0812922A (en) * 1993-07-14 1996-01-16 Asahi Glass Co Ltd Method for treating surface of outdoor article
JPH08157771A (en) * 1994-12-01 1996-06-18 Mitsubishi Chem Corp Coated inorganic powder, its preparation coating agent for inorganic powder and its preparation

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0812922A (en) * 1993-07-14 1996-01-16 Asahi Glass Co Ltd Method for treating surface of outdoor article
JPH08157771A (en) * 1994-12-01 1996-06-18 Mitsubishi Chem Corp Coated inorganic powder, its preparation coating agent for inorganic powder and its preparation

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003103712A (en) * 2001-09-28 2003-04-09 Atomix Co Ltd Surface treated synthetic resin sheet
JP2005015572A (en) * 2003-06-24 2005-01-20 Chugoku Marine Paints Ltd Epoxy resin composition, anticorrosive coating film formed therefrom, substrate covered with the anticorrosive coating film and corrosion protection method of the substrate
WO2005083006A1 (en) * 2004-02-27 2005-09-09 Mitsubishi Chemical Corporation Silicon-containing liquid composition
EP1719805A1 (en) * 2004-02-27 2006-11-08 Mitsubishi Chemical Corporation Silicon-containing liquid composition
EP1719805A4 (en) * 2004-02-27 2012-05-02 Mitsubishi Chem Corp Silicon-containing liquid composition
JP2008500208A (en) * 2004-05-28 2008-01-10 ピーピージー インダストリーズ オハイオ, インコーポレイテッド Multilayer coatings and related methods

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