JPS6410024B2 - - Google Patents

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Publication number
JPS6410024B2
JPS6410024B2 JP8841882A JP8841882A JPS6410024B2 JP S6410024 B2 JPS6410024 B2 JP S6410024B2 JP 8841882 A JP8841882 A JP 8841882A JP 8841882 A JP8841882 A JP 8841882A JP S6410024 B2 JPS6410024 B2 JP S6410024B2
Authority
JP
Japan
Prior art keywords
parts
weight
acid
mol
primer
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
Application number
JP8841882A
Other languages
Japanese (ja)
Other versions
JPS58204057A (en
Inventor
Kazumasa Kamata
Katsumi Tamai
Teruaki Kadokawa
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon 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 Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP8841882A priority Critical patent/JPS58204057A/en
Publication of JPS58204057A publication Critical patent/JPS58204057A/en
Publication of JPS6410024B2 publication Critical patent/JPS6410024B2/ja
Granted legal-status Critical Current

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  • Macromonomer-Based Addition Polymer (AREA)
  • Epoxy Resins (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳现な説明】 本発明は床および壁面コヌテむング甚プラむマ
ヌ組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to primer compositions for floor and wall coatings.

コンクリヌト、アスフアルト、金属などの床面
あるいは壁面の塗装被芆に甚いられる公知の暹脂
ずしおは溶剀系、あるいぱマルゞペン系の各皮
塗料があるが、これらは厚塗りが困難であり、耐
久性には限界がある。そこで耐久性、耐薬品性な
どの芁求の特に匷い甚途には埓来から゚ポキシ暹
脂、䞍飜和ポリ゚ステル暹脂、ポリりレタン暹脂
など、液状暹脂を斜工埌に硬化させる合成暹脂塗
り床材が甚いられおいる。たた、近幎同じ目的で
アクリル系の液状暹脂が開発されおおり、耐久
性、耐薬品性、耐候性の良奜なこずず同時に、硬
化時間が短く、斜工埌〜時間で䜿甚可胜であ
り、℃以䞋の䜎枩に斌おも硬化性よく斜工可胜
であるこずが倧きな特城ずな぀おいる。
There are a variety of solvent-based and emulsion-based paints as well-known resins used for coating floors and walls of concrete, asphalt, metal, etc., but these are difficult to apply thickly and have limited durability. be. Therefore, for applications with particularly strong demands for durability and chemical resistance, synthetic resin flooring materials have been used that are made from liquid resins such as epoxy resins, unsaturated polyester resins, and polyurethane resins that are hardened after application. In addition, acrylic liquid resins have been developed for the same purpose in recent years, and they have good durability, chemical resistance, and weather resistance, as well as short curing times and can be used within 1 to 2 hours after application. A major feature is that it has good curing properties and can be applied even at low temperatures of 5°C or lower.

これらの合成暹脂塗り床材をコンクリヌト、ア
スフアルト、金属などの䞋地に塗垃する堎合に
は、䞋地ずの接着性向䞊、䞋地の圱響の抑制等の
目的で、あらかじめプラむマヌを塗垃しその䞊に
合成暹脂塗り床材を塗り重ねる工法が䞀般に採甚
されおいる。プラむマヌずしおぱポキシ暹脂、
䞍飜和ポリ゚ステル暹脂、ポリりレタン暹脂、あ
るいはアクリル系暹脂などを溶剀に溶かしたも
の、氎に分散させたもの、あるいはこれらの液状
暹脂を斜工埌硬化させるタむプ等がある。これら
のプラむマヌは䞋地の皮類、䞊塗り甚の合成暹脂
塗り床材の皮類に応じお適宜䜿い分けお䜿甚され
る。しかるに、埓来のプラむマヌは近幎開発され
たアクリル系硬化性液状暹脂甚のプラむマヌずし
おはいずれも欠点を有しおおり、適切なプラむマ
ヌが無い状態であ぀た。
When applying these synthetic resin flooring materials to a base such as concrete, asphalt, or metal, a primer is applied in advance and the synthetic resin is applied on top of the primer in order to improve adhesion to the base and suppress the effects of the base. A construction method in which the flooring material is coated over and over again is generally used. Epoxy resin as a primer,
There are types in which unsaturated polyester resins, polyurethane resins, or acrylic resins are dissolved in solvents, those in which they are dispersed in water, and types in which these liquid resins are hardened after application. These primers are used appropriately depending on the type of base material and the type of synthetic resin coated flooring material for top coating. However, all of the conventional primers for acrylic curable liquid resins that have been developed in recent years have drawbacks, and there is no suitable primer.

コヌテむング甚のアクリル系硬化性液状暹脂の
特城は硬化時間が短いずころにあり、たた℃以
䞋の䜎枩においおも硬化性のすぐれおいるこずが
倧きな特城ずな぀おいる。しかるに、埓来の硬化
タむプのプラむマヌは硬化時間が長く、特に䜎枩
での硬化性がきわめお悪く、かかるプラむマヌを
䜿甚しおいたのでは斜工に長時間を芁するため、
硬化時間の短いアクリル系硬化性液状暹脂の特城
を十分に生かすこずができない。
The acrylic curable liquid resin for coatings is characterized by its short curing time, and its excellent curability even at low temperatures of 5° C. or lower is a major feature. However, conventional curing type primers take a long time to cure and have extremely poor curing properties, especially at low temperatures.
The characteristics of acrylic curable liquid resin, which has a short curing time, cannot be fully utilized.

アクリル系硬化性液状暹脂は䞀般には硬化剀ず
促進剀の組合せよりなるレドツクス系觊媒を甚い
おラゞカル重合を行わせるこずにより硬化させ
る。しかるに、䟋えば゚ポキシ系プラむマヌを䜎
枩雰囲気䞋で塗垃しその䞊にアクリル系硬化性液
状暹脂を䞊塗りする堎合には、゚ポキシ系プラむ
マヌ䞭の未反応アミンがアクリル系暹脂のラゞカ
ル重合を阻害し、これの硬化を劚げるこずがあり
奜たしくない。
Curable acrylic liquid resins are generally cured by radical polymerization using a redox catalyst consisting of a combination of a curing agent and an accelerator. However, for example, when applying an epoxy primer in a low-temperature atmosphere and then topcoating it with a curable acrylic liquid resin, unreacted amines in the epoxy primer inhibit the radical polymerization of the acrylic resin, resulting in This is undesirable as it may hinder curing.

各皮ポリマヌを溶剀に溶かした溶剀型プラむマ
ヌを䜿甚する堎合には、十分に溶剀を蒞発させた
のちに䞊塗りする必芁があるが、冬期䜎枩雰囲気
䞋では溶剀の蒞発に長い時間を芁する。溶剀が残
存した状態で䞊塗りを行うず䞊塗りした塗膜にフ
クレを生ずるこずがあり奜たしくない。各皮ポリ
マヌを氎に分散させた゚マルゞペン型プラむマヌ
を䜿甚する堎合にも、氎分を十分に蒞発させプラ
むマヌ塗膜を也燥させおから䞊塗りする必芁があ
るが、気枩の䜎い堎合には也燥に長時間を芁し、
氎分が残぀おいるず䞊塗り塗膜にフクレを生ずる
こずがあり、たた接着性䞍良の原因ずもなり奜た
しくない。
When using a solvent-based primer in which various polymers are dissolved in a solvent, it is necessary to evaporate the solvent sufficiently before applying a topcoat, but it takes a long time for the solvent to evaporate in a low-temperature atmosphere in winter. If the top coat is applied with the solvent remaining, blistering may occur in the top coated film, which is not preferable. Even when using emulsion-type primers in which various polymers are dispersed in water, it is necessary to sufficiently evaporate the water and dry the primer coating before applying a topcoat, but if the temperature is low, it may take a long time to dry. In short,
Remaining moisture may cause blistering in the top coat and may also cause poor adhesion, which is undesirable.

本発明は䞊述の劂き埓来のプラむマヌの欠点を
改良した新芏なプラむマヌ組成物を提䟛するもの
である。
The present invention provides a novel primer composition that improves the drawbacks of conventional primers as described above.

本発明のプラむマヌ組成物の第䞀の特城は短時
間で硬化し䞊塗りが可胜になるこずである。
The first feature of the primer composition of the present invention is that it cures in a short time and can be overcoated.

本発明のプラむマヌ組成物はアクリル系硬化性
液状暹脂を䞊塗りする堎合のプラむマヌずしお特
に奜たしいものであるが、アクリル系以倖の゚ポ
キシ暹脂、䞍飜和ポリ゚ステル暹脂、ポリりレタ
ン暹脂等を䞊塗りする堎合のプラむマヌずしお䜿
甚するこずもでき、プラむマヌの硬化時間が短い
ために斜工時間を短瞮するこずが可胜ずなる。
The primer composition of the present invention is particularly preferred as a primer for overcoating with an acrylic curable liquid resin, but it can also be used as a primer for overcoating with epoxy resins other than acrylic resins, unsaturated polyester resins, polyurethane resins, etc. Since the curing time of the primer is short, the construction time can be shortened.

本発明のプラむマヌ組成物の第二の特城は℃
以䞋の䜎枩においおも硬化性がすぐれおいるこず
である。埓぀お、冬期の斜工においおすぐれた特
城を発揮するこずができ、特にアクリル系硬化性
液状暹脂を䞊塗りする堎合のプラむマヌずしお奜
たしい。
The second feature of the primer composition of the present invention is that the primer composition of the present invention
It has excellent curability even at low temperatures below. Therefore, it can exhibit excellent characteristics in winter construction, and is particularly preferred as a primer when overcoating with an acrylic curable liquid resin.

本発明は䞋蚘(A)〜(D)より成る床および壁面コヌ
テむング甚プラむマヌ組成物を提䟛する。
The present invention provides a primer composition for floor and wall coatings comprising the following (A) to (D).

(A) ビスプノヌルず゚ピクロルヒドリンを基
瀎ずし、分子量800〜3000及び゚ポキシド圓量
400〜2500を有する゚ポキシ暹脂を、メタ
クリル酞及び又はアクリル酞74〜64モル
ず、〜20個の炭玠原子を有する飜和モノ
カルボン酞少なくずも皮100〜80モルず
〜20個の炭玠原子を有する䞍飜和モノカルボン
酞少なくずも皮〜20モルずからなるモノ
カルボン酞26〜36モルずの混合物ずを反応さ
せるこずによ぀お埗られた䞍飜和β―ヒドロキ
シ゚ステル30〜60重量 (B) メタクリル酞メチルあるいはメタクリル酞メ
チルを80重量以䞊含有する重合性䞍飜和単量
䜓70〜40重量 (C) 40℃以䞊の融点を有するパラフむン及び又
はワツクス、(A)、(B)の合蚈量100重量郚に察し
0.1〜重量郚 (D) 第玚アミン、(A)、(B)の合蚈量100重量郚に
察し0.1〜重量郚 本発明のプラむマヌ組成物は、硬化剀を添加混
合したのちスプレヌ、ロヌラヌ、刷毛、コテ等を
甚いお䞋地に塗垃される。塗垃されたプラむマヌ
は、硬化剀ずプラむマヌ組成物䞭の促進剀ずの組
合せよりなるレドツクス系觊媒の䜜甚により、プ
ラむマヌ組成物䞭の重合性䞍飜和化合物が重合
し、硬化する。
(A) Based on bisphenol A and epichlorohydrin, molecular weight 800-3000 and epoxide equivalent
400-2500 a) methacrylic acid and/or acrylic acid 74-64 mol%
and b) 100-80 mol% of at least one saturated monocarboxylic acid having 8-20 carbon atoms and 8
Unsaturated β- obtained by reacting a mixture of 0 to 20 mol % of at least one unsaturated monocarboxylic acid having ~20 carbon atoms with 26 to 36 mol % of a monocarboxylic acid Hydroxy ester 30-60% by weight (B) Methyl methacrylate or a polymerizable unsaturated monomer containing 80% by weight or more of methyl methacrylate 70-40% by weight (C) Paraffin and/or having a melting point of 40°C or higher For 100 parts by weight of wax, (A) and (B)
0.1 to 5 parts by weight (D) Tertiary amine, 0.1 to 5 parts by weight per 100 parts by weight of the total amount of (A) and (B) The primer composition of the present invention is prepared by adding and mixing a curing agent, and then spraying. It is applied to the base using a roller, brush, trowel, etc. The applied primer is cured by the action of a redox catalyst consisting of a combination of a curing agent and an accelerator in the primer composition, whereby the polymerizable unsaturated compound in the primer composition is polymerized.

成分(A)は䞍飜和β―ヒドロキシ゚ステルであ
り、䞊蚘重合性䞍飜和化合物の䞀成分を構成す
る。成分(A)はビスプノヌルず゚ピクロルヒド
リンを基瀎ずする゚ポキシ暹脂、すなわち分子量
800〜3000及び゚ポキシド圓量400〜2500を有する
ポリグリシド゚ヌテル少なくずも皮を甚いお補
造される。特に平均分子量1300〜1800及び゚ポキ
シド圓量750〜1000を有する゚ポキシ暹脂又はそ
の混合物が奜たしい。該゚ポキシ暹脂は、メ
タクリル酞及び又はアクリル酞74〜64モル
ず、少なくずも皮の長鎖モノカルボン酞26
〜36モルずの混合物ず反応しお䞍飜和β―ヒド
ロキシ゚ステルを生成する。成分ずしおはメ
タクリル酞50モル以䞊を有する混合物、特にメ
タクリル酞だけを䜿甚するのが有利である。成分
ずしおは〜20個の炭玠原子を有する飜和モ
ノカルボン酞、䟋えばカプリル酞、ペラルゎン
酞、カプリン酞、ラりリン酞、ミリスチン酞、パ
ルミチン酞、マルガリン酞又はステアリン酞、及
びこれらの混合物が䜿甚され、〜20個の炭玠原
子を有する䞍飜和モノカルボン酞少なくずも皮
を20モル以䞋の範囲で混合するこずもできる。
このような䞍飜和モノカルボン酞ずしおは、䟋え
ばラりロレむン酞、ミリストレむン酞、パルミト
レむン酞、オレむン酞、リンチノヌル酞又はその
混合物を挙げるこずができる。
Component (A) is an unsaturated β-hydroxy ester and constitutes one component of the polymerizable unsaturated compound. Component (A) is an epoxy resin based on bisphenol A and epichlorohydrin, i.e.
800 to 3000 and an epoxide equivalent weight of 400 to 2500. Particularly preferred are epoxy resins or mixtures thereof having an average molecular weight of 1300 to 1800 and an epoxide equivalent weight of 750 to 1000. The epoxy resin contains a) 74 to 64 mol% of methacrylic acid and/or acrylic acid.
and b) at least one long chain monocarboxylic acid26
~36 mol % of the mixture to form an unsaturated β-hydroxy ester. Preference is given to using as component a) a mixture having at least 50 mol % of methacrylic acid, in particular only methacrylic acid. Saturated monocarboxylic acids having 8 to 20 carbon atoms, such as caprylic acid, pelargonic acid, capric acid, lauric acid, myristic acid, palmitic acid, margaric acid or stearic acid, and mixtures thereof are used as component b). It is also possible to mix at least one unsaturated monocarboxylic acid having 8 to 20 carbon atoms in an amount of 20 mol % or less.
Such unsaturated monocarboxylic acids include, for example, lauroleic acid, myristoleic acid, palmitoleic acid, oleic acid, lintinolic acid or mixtures thereof.

成分(B)は成分(A)ず共に、本発明のプラむマヌ組
成物䞭の重合性䞍飜和化合物の䞀成分を構成する
ものであり、メタクリル酞メチルあるいはメタク
リル酞メチルを80重量以䞊含有する重合性䞍飜
和単量䜓より成る。このような単量䜓ずしおは、
䟋えばアクリル酞メチル、アクリル酞゚チル、ア
クリル酞―ブチル、アクリル酞―ブチル、ア
クリル酞―゚チルヘキシル、メタクリル酞―
ブチル、メタクリル酞―゚チルヘキシル、メタ
クリル酞ラりリル等のアクリル酞たたはメタクリ
ル酞゚ステル類が挙げられる。たた成分(B)は公知
の架橋剀を含有するこずもできる。架橋剀ずしお
は、䞀分子䞭に少なくずも個のビニル基及び
又はアリル基を含有する化合物、䟋えばゞメタク
リル酞゚チレングリコヌル、ゞメタクリル酞トリ
゚チレングリコヌル、ゞメタクリル酞テトラ゚チ
レングリコヌル、ゞアクリル酞―ブタンゞ
オヌル、ゞアクリル酞―ヘキサンゞオヌ
ル、ゞアクリル酞ネオペンチルグリコヌル、ゞア
クリル酞ゞ゚チレングリコヌル、トリアクリル酞
ペンタ゚リトリツト及びテトラアクリル酞ペンタ
゚リトリツトのようなアクリル酞たたはメタアク
リル酞の倚官胜性゚ステル、又はシアヌル酞トリ
アリルのようなトリアリル化合物があげられる。
Component (B), together with component (A), constitutes one component of the polymerizable unsaturated compound in the primer composition of the present invention, and is a polymerizable unsaturated compound containing methyl methacrylate or 80% by weight or more of methyl methacrylate. Consists of unsaturated monomers. Such monomers include
For example, methyl acrylate, ethyl acrylate, n-butyl acrylate, i-butyl acrylate, 2-ethylhexyl acrylate, n- methacrylate.
Examples include acrylic acid or methacrylic acid esters such as butyl, 2-ethylhexyl methacrylate, and lauryl methacrylate. Component (B) can also contain a known crosslinking agent. As a crosslinking agent, at least two vinyl groups and/or
or compounds containing allyl groups, such as ethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, 1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, neo diacrylate Mention may be made of polyfunctional esters of acrylic acid or methacrylic acid such as pentyl glycol, diethylene glycol diacrylate, pentaerythritol triacrylate and pentaerythritol tetraacrylate, or triallyl compounds such as triallyl cyanurate.

成分(C)ずしおはパラフむンワツクス、ポリ゚チ
レンワツクスやステアリン酞、―ヒドロキ
システアリン酞等の高玚脂肪酞が挙げられるが、
奜たしくはパラフむンワツクスが甚いられる。成
分(C)はプラむマヌ塗膜衚面における硬化反応䞭の
空気遮断䜜甚を目的ずしお添加される。融点の異
なる二皮以䞊のものを䜵甚するず奜たしいこずが
ある。成分(C)の倚量の添加はプラむマヌ組成物ず
䞊塗り甚暹脂ずの接着性を悪くするので、成分
(A)、(B)の合蚈量100重量郚に察しお0.1〜重量
郚、奜たしくは0.2〜重量郚が䜿甚される。
Component (C) includes paraffin wax, polyethylene wax, and higher fatty acids such as stearic acid and 1,2-hydroxystearic acid.
Preferably paraffin wax is used. Component (C) is added for the purpose of blocking air during the curing reaction on the surface of the primer coating film. It may be preferable to use two or more types with different melting points in combination. Adding a large amount of component (C) will impair the adhesion between the primer composition and the topcoat resin.
The amount used is 0.1 to 5 parts by weight, preferably 0.2 to 2 parts by weight, based on 100 parts by weight of the total amount of (A) and (B).

成分(D)はレドツクス觊媒系の促進剀である。第
玚アミンずしおは窒玠原子に盎接少なくずも
個の芳銙族残基が結合しおいるものが奜たしく、
特にN′―ゞメチルアニリン、N′―ゞメ
チル――トルむゞン、N′―ゞヒドロキ
シ゚チル――トルむゞン、N′―ゞ
―ヒドロキシプロピル――トルむゞンの䞀皮
又は二皮以䞊の組合せが奜たしい。成分(D)の倚量
の添加は硬化時間を極端に短くし塗工䜜業性を悪
くするので、成分(A)、(B)の合蚈量100重量郚に察
しお0.1〜重量郚の範囲で添加される。
Component (D) is a promoter of the redox catalyst system. As a tertiary amine, at least one
Preferably, aromatic residues of
In particular, N,N'-dimethylaniline, N,N'-dimethyl-p-toluidine, N,N'-di(hydroxyethyl)-p-toluidine, N,N'-di(2
-Hydroxypropyl)-p-toluidine or a combination of two or more thereof is preferred. Adding a large amount of component (D) will extremely shorten the curing time and impair coating workability, so it should be added in the range of 0.1 to 5 parts by weight per 100 parts by weight of the total amount of components (A) and (B). added.

本発明のプラむマヌ組成物は適切な厚み、䟋え
ば0.1〜mmの厚みにロヌラヌ、刷毛、コテ等を
甚いお䞋地に塗垃されるが、プラむマヌずしおの
性胜及び塗工䜜業性を考慮しお適切な粘床である
こずが奜たしい。粘床を䜎くするず䞋地ぞの浞透
性が向䞊し、䞋地ずの接着性は向䞊するが、硬化
性が悪くなり硬化に長時間を芁する。粘床が高す
ぎるず䞋地ずの接着性が䜎䞋し、又塗工䜜業性も
悪くなる。これらの芁因から求められる適切な粘
床範囲は50〜1000cpsである。この粘床範囲を埗
るためには、本発明の組成物䞭の成分(A)を30〜60
重量、成分(B)を70〜40重量の比率で甚いるこ
ずが必芁である。
The primer composition of the present invention is applied to a base using a roller, brush, trowel, etc. to an appropriate thickness, for example, 0.1 to 1 mm, but the primer composition is applied to a base using a roller, brush, trowel, etc. It is preferable that Lowering the viscosity improves the permeability to the substrate and improves the adhesion to the substrate, but the curability deteriorates and it takes a long time to cure. If the viscosity is too high, the adhesion to the base will decrease and the coating workability will also deteriorate. The appropriate viscosity range determined from these factors is 50 to 1000 cps. To obtain this viscosity range, component (A) in the composition of the present invention must be
It is necessary to use component (B) in a proportion of 70 to 40% by weight.

本発明のプラむマヌ組成物は䞋蚘の劂き方法で
有利に補造するこずができる。
The primer composition of the present invention can be advantageously produced by the following method.

即ち、メタクリル酞メチルあるいはメタクリル
酞メチルを80重量以䞊含有する重合性䞍飜和単
量䜓(B)の䞀郚又は党量䞭に、ビスプノヌルず
゚ピクロルヒドリンを基瀎ずし、分子量800〜
3000及び゚ポキシド圓量400〜2500を有する゚ポ
キシ暹脂を溶解しお溶液ずなし、該溶液
䞭にメタクリル酞及び又はアクリル
酾74〜64モルず、〜20個の炭玠原子を有
する飜和モノカルボン酞少なくずも皮100〜80
モルず、〜20個の炭玠原子を有する䞍飜和モ
ノカルボン酞少なくずも皮〜20モルずから
なるモノカルボン酞26〜36モルずの混合物を添
加し、適圓な觊媒の存圚䞋に該゚ポキシ暹脂ず酞
ずを反応させるこずによ぀お生成した䞍飜和β―
ヒドロキシ゚ステル(A)を含有する溶液ずな
し、該溶液䞭に第玚アミン(D)ず40℃以䞊
の融点を有するパラフむン及び又はワツクス(C)
を溶解もしくは分散させるこずにより䞋蚘(A)〜(D)
より成る本発明のプラむマヌ組成物が補造され
る。なお溶液を぀くるずきに、䞍飜和単量
䜓(B)の䞀郚を甚いたずきには、(B)の残郚は、䟋え
ば(D)、及び又は(C)の添加時に同時に加えられ
る。
That is, some or all of methyl methacrylate or a polymerizable unsaturated monomer (B) containing 80% by weight or more of methyl methacrylate contains bisphenol A and epichlorohydrin as a base, and has a molecular weight of 800 to 800%.
3000 and an epoxy resin having an epoxide equivalent of 400 to 2500 is dissolved to form a solution (), in which a) 74 to 64 mol% of methacrylic acid and/or acrylic acid, and b) 8 to 20 At least one saturated monocarboxylic acid having carbon atoms 100 to 80
and 26 to 36 mol % of a monocarboxylic acid consisting of 0 to 20 mol % of at least one unsaturated monocarboxylic acid having 8 to 20 carbon atoms, and in the presence of a suitable catalyst. Unsaturated β- produced by reacting the epoxy resin with acid
A solution () containing a hydroxyester (A), a tertiary amine (D) in the solution (), and a paraffin and/or wax (C) having a melting point of 40°C or higher.
By dissolving or dispersing the following (A) to (D)
A primer composition of the present invention is produced. Note that when part of the unsaturated monomer (B) is used when preparing the solution (), the remainder of (B) is added, for example, at the same time as (D) and/or (C) are added.

(A) 䞍飜和β―ヒドロキシ゚ステル30〜60重量 (B) メタクリル酞メチルあるいはメタクリル酞メ
チルを80重量以䞊含有する重合性䞍飜和単
量䜓70〜40重量 (C) 40℃以䞊の融点を有するパラフむン及び又
はワツクス、(A)、(B)の合蚈量100重量郚に察
し0.1〜重量郚 (D) 第玚アミン、(A)、(B)の合蚈量100重量郚に
察し0.1〜重量郚 ゚ポキシ暹脂ず酞混合物ずの反応は、公知の觊
媒の存圚䞋に行われる。適圓な觊媒ずしおは䟋え
ば゚チレンゞアミンのような玚アミン、トリメ
チルアミン、ゞメチルペンゞルアミン、トリ゚チ
ルアミン、ゞメチル――トルむゞンのような
玚アミンSnO2、SnCl2、LiFのような無機塩
類トリプニルホスフむンのような玚ホスフ
むンゞ゚チルアン塩酞塩のような玚アミンの
酞付加塩塩化テトラメチルアンモニりムのよう
な玚アンモニりム塩又はピリゞン、モルホリ
ンのような窒玠含有耇玠環匏化合物である。
(A) 30-60% by weight of unsaturated β-hydroxy ester (B) 70-40% by weight of methyl methacrylate or a polymerizable unsaturated monomer containing 80% or more of methyl methacrylate (C) 40°C or higher Paraffin and/or wax having a melting point, 0.1 to 5 parts by weight per 100 parts by weight of the total amount of (A) and (B) (D) Tertiary amine, 100 parts by weight of the total amount of (A) and (B) The reaction between the epoxy resin and the acid mixture is carried out in the presence of a known catalyst. Suitable catalysts include, for example, primary amines such as ethylenediamine, trimethylamine, dimethylpenzylamine, triethylamine, dimethyl-p-toluidine, etc.
Inorganic salts such as SnO 2 , SnCl 2 , LiF; Tertiary phosphines such as triphenylphosphine; Acid addition salts of secondary amines such as diethyluane hydrochloride; or nitrogen-containing heterocyclic compounds such as pyridine and morpholine.

゚ポキシ暹脂ず酞混合物ずの反応は、溶剀の䞍
存圚䞋又は䞍掻性溶剀の存圚䞋で行うこずもでき
るが、䞊述の劂く本発明のプラむマヌ組成物の成
分(B)を構成する単量䜓の䞀郚又は党量䞭で反応さ
せるこずが有利である。
The reaction between the epoxy resin and the acid mixture can be carried out in the absence of a solvent or in the presence of an inert solvent, but as described above, the reaction between the monomers constituting component (B) of the primer composition of the present invention It is advantageous to react in part or in total.

゚ポキシ暹脂ず酞混合物ずの反応䞭の重合を阻
止するために、ラゞカル重合抑制剀を添加するこ
ずが奜たしい。適圓な抑制剀ずしおは、䟋えばヒ
ドロキノン、ヒドロキノンモノメチル゚ヌテル、
―ゞメチル―――ブチルプノヌルを
挙げるこずができる。
In order to prevent polymerization during the reaction of the epoxy resin and the acid mixture, it is preferable to add a radical polymerization inhibitor. Suitable inhibitors include, for example, hydroquinone, hydroquinone monomethyl ether,
Mention may be made of 2,4-dimethyl-6-t-butylphenol.

゚ポキシ暹脂ず酞混合物ずの反応は50〜100℃
の枩床で有利に行なわれる。この反応はほが化孊
量論的量で、すなわち䟋えば゚ポキシド0.8〜1.2
圓量に察しお酞モルを甚いお行なわれる。
The reaction between epoxy resin and acid mixture is 50-100℃
It is advantageously carried out at a temperature of . This reaction is approximately stoichiometric, i.e. 0.8 to 1.2
It is carried out using 1 mol of acid per equivalent.

奜たしい補造方法は䞋蚘の劂くである。即ち成
分(B)の䞀郚又は党量䞭に重合抑制剀を添加し゚ポ
キシ暹脂をこれに混合し、党䜓を加熱しお゚ポキ
シ暹脂を溶解せしめ、溶液ずする。該溶液
に゚ポキシ暹脂ず酞ずの反応甚觊媒を添加
する。この酞は玄30分〜時間で連続的又は回分
的に溶液䞭に䟛絊される。この反応混合物
は〜10時間反応枩床に保持され十分反応を行わ
せる。生成した䞍飜和β―ヒドロキシ゚ステルを
含有する溶液䞭に、必芁に応じお成分(B)の
残量を加え、第玚アミン及び40℃以䞊の融点を
有するパラフむン及び又はワツクスを添加する
こずによ぀お本発明のプラむマヌ組成物を埗る。
A preferred manufacturing method is as follows. That is, a polymerization inhibitor is added to part or all of component (B), an epoxy resin is mixed therein, and the whole is heated to dissolve the epoxy resin to form a solution (). A catalyst for the reaction between the epoxy resin and the acid is added to the solution (2). The acid is fed into the solution continuously or batchwise over a period of about 30 minutes to 4 hours. The reaction mixture is maintained at the reaction temperature for 2 to 10 hours to ensure sufficient reaction. Add the remaining amount of component (B) as necessary to the solution () containing the generated unsaturated β-hydroxy ester, and add a tertiary amine and paraffin and/or wax having a melting point of 40°C or higher. By doing so, the primer composition of the present invention is obtained.

本発明のプラむマヌ組成物に公知の有機過酞化
物を硬化剀ずしお添加するこずにより−20〜40℃
の枩床範囲で時間以内で硬化させるこずができ
る。有機過酞化物の奜たしい䟋ずしおは過酞化ベ
ンゟむルが挙げられる。過酞化ベンゟむルは取扱
い䞊の危険を避けるために䞍掻性の液䜓又は固䜓
で濃床50皋床に皀釈されたペヌスト状又は粉末
状のものを甚いるこずが奜たしい。塗工䜜業性を
考慮した奜たしい硬化時間10〜60分を埗るために
はプラむマヌの枩床、あるいは塗工時の気枩に応
じお硬化剀量を調節する必芁があり、有機過酞化
物濃床50は本発明の組成物100重量郚に察
しお0.5〜10重量郚の䜿甚が奜たしい。
By adding a known organic peroxide as a curing agent to the primer composition of the present invention,
It can be cured within 2 hours at a temperature range of . A preferred example of the organic peroxide is benzoyl peroxide. In order to avoid handling hazards, it is preferable to use benzoyl peroxide in the form of a paste or powder diluted with an inert liquid or solid to a concentration of about 50%. In order to obtain a preferable curing time of 10 to 60 minutes in consideration of coating workability, it is necessary to adjust the amount of curing agent depending on the temperature of the primer or the temperature at the time of coating. ) is preferably used in an amount of 0.5 to 10 parts by weight per 100 parts by weight of the composition of the present invention.

本発明の組成物は通垞は硬化剀のみを添加しお
塗工に䟛されるが、塗工個所を明瀺するために着
色剀を添加したり、壁面塗垃に際し、組成物に揺
倉性を付䞎するためにアスベスト、セピオラむ
ト、ア゚ロゞルのような揺倉剀を添加したりする
こずができる。たた必芁に応じお硅砂、硅砂粉、
炭酞カルシりムなどの骚材、充填剀を本発明の組
成物ず混合しお塗工に䟛するこずも可胜である。
The composition of the present invention is usually coated with only a curing agent added, but a coloring agent may be added to clearly mark the area to be coated, or thixotropy may be imparted to the composition when applied to a wall surface. For this purpose, thixotropic agents such as asbestos, sepiolite, and aerosil can be added. In addition, silica sand, silica sand powder,
It is also possible to mix aggregates and fillers such as calcium carbonate with the composition of the present invention for coating.

本発明の組成物は䞋地ずの接着性にすぐれた特
城を有しおいるが、曎に接着性を安定化させる目
的で、本発明の組成物䞭にγ―メタクリロキシプ
ロピルトリメトキシシラン、γ―グリシドキシプ
ロピルトリメトキシシラン等のシランカツプリン
グ剀を添加するこずができる。
The composition of the present invention has excellent adhesion to the substrate, but in order to further stabilize the adhesion, γ-methacryloxypropyltrimethoxysilane, γ- A silane coupling agent such as glycidoxypropyltrimethoxysilane can be added.

本発明の組成物は、レドツクス觊媒系を甚いた
ラゞカル重合によ぀お硬化する機構を有しおいる
にもかかわらず、空気その他の重合阻害芁因の圱
響を受けにくい特城を有しおおり、この特城はプ
ラむマヌずしお極めお奜たしいものである。即
ち、䞀般に䞋地は皮々の汚れをその衚面に持぀お
おり、これら汚れの䞭にはラゞカル重合阻害芁因
も含たれおいる可胜性が倧きいが、本発明の組成
物はいかなる䞋地にも安心しお䜿甚するこずがで
きる。
Although the composition of the present invention has a curing mechanism by radical polymerization using a redox catalyst system, it has the characteristic that it is not easily influenced by air and other polymerization inhibiting factors. These characteristics make it highly desirable as a primer. In other words, substrates generally have various stains on their surfaces, and there is a high possibility that these stains include factors that inhibit radical polymerization, but the composition of the present invention can be used with confidence on any substrate. can do.

特に䞋地がコンクリヌトの堎合に、本発明の組
成物は極めお奜たしいプラむマヌずしお䜿甚する
こずができる。即ち、コンクリヌト䞋地にプラむ
マヌを塗工する堎合、コンクリヌト衚面に存圚す
る小孔の䞭に空気がトラツプされ、この空気がラ
ゞカル重合阻害の芁因ずなりうる。しかし、本発
明のプラむマヌ組成物はかかる堎合にもその重合
は阻害されず、短時間で硬化させるこずができ
る。
The compositions of the invention can be used as highly preferred primers, especially when the substrate is concrete. That is, when a primer is applied to a concrete base, air is trapped in small pores existing on the concrete surface, and this air can become a factor in inhibiting radical polymerization. However, even in such cases, the polymerization of the primer composition of the present invention is not inhibited and can be cured in a short time.

䞋蚘実斜䟋䞭の郚はすべお重量郚を瀺し、たた
硬化時間はプラむマヌ組成物䞭に硬化剀を添加し
た時点を起点ずする。
All parts in the following examples indicate parts by weight, and the curing time starts from the point at which the curing agent is added to the primer composition.

実斜䟋  撹拌機ず加熱ゞダケツトを備えた反応釜に宀枩
におメタクリル酞メチル975郚ず―ゞメチ
ル―――ブチルプノヌル郚を仕蟌み、宀
枩䞋撹拌しながらビスプノヌルず゚ピクロル
ヒドリンを基瀎ずし分子量1600及び゚ポキシド圓
量925を有する゚ポキシ暹脂2000郚を少しず぀添
加した。反応釜を加熱し内枩70℃にお゚ポキシ暹
脂をメタクリル酞メチルに溶解させたのちトリ゚
チルアミン27郚を添加した。次いで反応釜内枩を
80℃に䞊昇し、メタクリル酞112郚ずラりリン酞
130郚の混合物を時間で滎䞋した。内枩を80℃
に保持したたた時間撹拌を続け反応させたのち
冷华した。次いでメタクリル酞メチル250郚を添
加混合したのち反応混合物の酞䟡および゚ポキシ
ド圓量を枬定したずころ、酞䟡4.5および゚ポキ
シド圓量5600を埗た。
Example 1 975 parts of methyl methacrylate and 5 parts of 2,4-dimethyl-6-t-butylphenol were charged at room temperature into a reaction vessel equipped with a stirrer and a heating jacket, and bisphenol A and epichlorohydrin were added while stirring at room temperature. 2000 parts of an epoxy resin having a molecular weight of 1600 and an epoxide equivalent weight of 925 based on the following were added in portions. The reaction vessel was heated to an internal temperature of 70°C to dissolve the epoxy resin in methyl methacrylate, and then 27 parts of triethylamine was added. Next, the temperature inside the reaction vessel was
Raised to 80℃, 112 parts of methacrylic acid and lauric acid
130 parts of the mixture were added dropwise over 2 hours. Internal temperature 80℃
Stirring was continued for 8 hours while the temperature was maintained at 100° C. to allow reaction, and then the mixture was cooled. Next, 250 parts of methyl methacrylate was added and mixed, and the acid value and epoxide equivalent of the reaction mixture were measured, and an acid value of 4.5 and an epoxide equivalent of 5,600 were obtained.

このようにしお生成した䞍飜和β―ヒドロキシ
゚ステルを含有する反応混合物68郚を撹拌機ず加
熱ゞダケツトを備えた溶解釜に仕蟌み、メタクリ
ル酞メチル31郚を混合撹拌した。次いでこれを50
℃に加熱し、融点50〜52℃のパラフむン0.5郚お
よびN′―ゞ―ヒドロキシプロピル―
―トルむゞン郚を添加し溶解した。これを冷
华するこずにより20℃における粘床300cpsのプラ
むマヌ組成物を埗た。
68 parts of the reaction mixture containing the unsaturated β-hydroxy ester produced in this way was charged into a melting vessel equipped with a stirrer and a heating jacket, and 31 parts of methyl methacrylate was mixed and stirred. Then set this to 50
0.5 part of paraffin with a melting point of 50-52°C and N,N'-di(2-hydroxypropyl)-
1 part of p-toluidine was added and dissolved. By cooling this, a primer composition having a viscosity of 300 cps at 20°C was obtained.

このプラむマヌ組成物100郚に硬化剀ずしお濃
床50の過酞化ベンゟむル粉末以䞋BPOパり
ダヌず略す郚を添加しよく混合しお硬化させ
たずころ、20℃においお26分で硬化した。この硬
化物をJISK6301に基づいお匕匵り詊隓を行぀た
ずころ、砎断匷床560Kg/cm2、䌞び率を瀺し
た。
When 3 parts of benzoyl peroxide powder (hereinafter referred to as BPO powder) with a concentration of 50% was added as a curing agent to 100 parts of this primer composition, and the mixture was thoroughly mixed and cured, it was cured in 26 minutes at 20°C. When this cured product was subjected to a tensile test based on JISK6301, it showed a breaking strength of 560 Kg/cm 2 and an elongation rate of 3%.

たたこのプラむマヌ組成物100郚にBPOパりダ
ヌ郚を添加し、よく混合しお、ロヌラヌを甚い
おコンクリヌトブロツク×20×20cm䞊に玄
0.5mmの厚みに塗垃したずころ宀枩24℃にお
いお18分で硬化し匷固な塗膜ずな぀た。日埌に
建研匏接着詊隓機を甚いお接着匷床を枬定したず
ころ、23.8Kg/cm2におコンクリヌトブロツク郚分
が砎壊し、接着性良奜であるこずを瀺した。
Also, add 3 parts of BPO powder to 100 parts of this primer composition, mix well, and use a roller to apply approximately 3 parts of BPO powder onto a concrete block (5 x 20 x 20 cm).
When applied to a thickness of 0.5 mm, it cured in 18 minutes at room temperature (24°C) to form a strong coating. Two days later, the adhesive strength was measured using a Kenken type adhesive testing machine, and the concrete block part broke at 23.8 kg/cm 2 , indicating good adhesiveness.

実斜䟋  実斜䟋にお補造したプラむマヌ組成物100郚
にBPOパりダヌ郚を添加しよく混合しおヘラ
を甚いおアスフアルトブロツク日本テストパネ
ル補、×20×20cm䞊に玄0.3mmの厚みに塗垃
したずころ、気枩30℃においお18分で硬化し匷固
な塗膜を圢成した。建研匏接着詊隓機を甚いお接
着匷床を枬定したずころ7.6Kg/cm2におアスフアル
トから砎壊し、接着匷床倧なるこずを瀺した。
Example 2 Add 2 parts of BPO powder to 100 parts of the primer composition produced in Example 1, mix well, and use a spatula to spread about 0.3 mm onto an asphalt block (manufactured by Nippon Test Panel, 5 x 20 x 20 cm). When applied to a thickness of , it cured in 18 minutes at a temperature of 30°C, forming a strong coating. When the adhesive strength was measured using a Kenken type adhesive testing machine, it broke from the asphalt at 7.6 kg/cm 2 , indicating that the adhesive strength was high.

実斜䟋  実斜䟋にお補造したプラむマヌ組成物100郚
にBPOパりダヌ郚を添加し、よく混合しお刷
毛を甚いお軟鋌板×300×300mm䞊に玄0.4
mmの厚みに塗垃したずころ、気枩10℃においお35
分で硬化し匷固な塗膜を圢成した。建研匏接着詊
隓機を甚いお接着匷床を枬定したずころ、8.3Kg/
cm2であ぀た。
Example 3 5 parts of BPO powder was added to 100 parts of the primer composition produced in Example 1, mixed well and applied to a mild steel plate (6 x 300 x 300 mm) with a powder of about 0.4 parts using a brush.
When applied to a thickness of 35 mm at a temperature of 10°C,
It cured in minutes and formed a strong coating. When the adhesive strength was measured using a Kenken type adhesive testing machine, it was 8.3Kg/
It was warm in cm2 .

実斜䟋  第玚アミンずしおN′―ゞ―ヒドロ
キシプロピル――トルむゞン郚ず
N′―ゞメチル――トルむゞン郚を䜵甚した
以倖は実斜䟋ず同様な方法で20℃における粘床
300cpsのプラむマヌ組成物を補造した。
Example 4 One part of N,N'-di(2-hydroxypropyl)-p-toluidine and N,
The viscosity at 20°C was obtained in the same manner as in Example 1 except that 2 parts of N'-dimethyl-p-toluidine was used in combination.
A 300 cps primer composition was produced.

このプラむマヌ組成物100にBPOパりダヌ
を添加しよく混合しお䜎枩䞋で硬化させたずこ
ろ、衚―の劂く良奜な硬化性を瀺した。
100g of this primer composition and 55g of BPO powder
When the mixture was mixed well and cured at low temperature, it showed good curability as shown in Table 1.

衚― 硬化枩床 硬化時間 ℃ 分  18 −10 37 −20 90 実斜䟋  実斜䟋ず同様な手法で、メタクリル酞メチル
984郚ず―ゞメチル―――ブチルプ
ノヌル郚を仕蟌み、ビスプノルず゚ピクロ
ルヒドリンを基瀎ずし分子量1350及び゚ポキシド
圓量850を有する゚ポキシ暹脂2000郚を添加し、
加熱しお70℃でトリ゚チルアミン27郚を添加し
た。内枩80℃におメタクリル酞86郚、アクリル酞
30郚、およびラりリン酞141郚の混合物を時間
で滎䞋し、80℃で時間反応させた。これを冷华
したのちメタクリル酞メチル252郚を添加し、反
応混合物の酞䟡および゚ポキシド圓量を枬定した
ずころ、酞䟡4.9および゚ポキシド圓量6500を埗
た。
Table-1 Curing temperature Curing time (°C) (minutes) 0 18 -10 37 -20 90 Example 5 Using the same method as Example 1, methyl methacrylate
984 parts of 2,4-dimethyl-6-t-butylphenol and 5 parts of 2,4-dimethyl-6-tert-butylphenol were charged, and 2000 parts of an epoxy resin based on bisphenol A and epichlorohydrin having a molecular weight of 1350 and an epoxide equivalent weight of 850 were added.
With heating to 70°C 27 parts of triethylamine were added. 86 parts of methacrylic acid, acrylic acid at internal temperature of 80℃
A mixture of 30 parts of lauric acid and 141 parts of lauric acid was added dropwise over 2 hours, and the mixture was reacted at 80°C for 8 hours. After cooling this, 252 parts of methyl methacrylate was added, and the acid value and epoxide equivalent of the reaction mixture were measured, and an acid value of 4.9 and an epoxide equivalent of 6,500 were obtained.

このようにしお生成した䞍飜和β―ヒドロキシ
゚ステルを含有する反応混合物を実斜䟋ず同様
の方法で凊理し、20℃における粘床270cpsのプラ
むマヌ組成物を埗た。
The reaction mixture containing the unsaturated β-hydroxy ester thus produced was treated in the same manner as in Example 1 to obtain a primer composition having a viscosity of 270 cps at 20°C.

このプラむマヌ組成物100郚にBPOパりダヌ
郚を添加しお、気枩℃にお衚面枩床℃のコン
クリヌト床に0.4mmの厚みにヘラを甚いお塗垃し
たずころ、44分で硬化しお匷固な塗膜を圢成し
た。
100 parts of this primer composition plus 6 parts of BPO powder
When applied with a spatula to a thickness of 0.4 mm on a concrete floor with an air temperature of 3°C and a surface temperature of 4°C, it cured in 44 minutes to form a strong coating film.

実斜䟋  ラりリン酞130郚の代りに䞋蚘の組成を有する
工業甚ダシ油脂肪酞136郚を䜿甚した以倖は実斜
䟋の手法に埓぀お反応を行い、䞍飜和β―ヒド
ロキシ゚ステルを含有する反応混合物を補造し
た。
Example 6 A reaction was carried out according to the method of Example 1, except that 136 parts of industrial coconut oil fatty acid having the following composition was used instead of 130 parts of lauric acid, and a reaction mixture containing an unsaturated β-hydroxy ester was obtained. was manufactured.

工業甚ダシ油脂肪酞 C8C10C12C14C16C18C18二重結合を有する   48 18   重量 該䞍飜和β―ヒドロキシ゚ステル含有反応混合
物70郚を撹拌機ず加熱ゞダケツトを備えた溶解釜
に仕蟌み、メタクリル酞メチル29郚を混合撹拌し
た。次いでこれを50℃に加熱し、融点54〜56℃の
パラフむン0.5郚およびN′―ゞメチル――
トルむゞン郚を添加し溶解した。これを冷华す
るこずにより20℃における粘床350cpsのプラむマ
ヌ組成物を埗た。
Industrial coconut oil fatty acid: C 8 C 10 C 12 C 14 C 16 C 18 C 18 (contains double bond) 8 7 48 18 8 2 9 (% by weight) 70 parts of the unsaturated β-hydroxy ester-containing reaction mixture was charged into a melting pot equipped with a stirrer and a heating jacket, and 29 parts of methyl methacrylate was mixed and stirred. This was then heated to 50°C, and 0.5 part of paraffin with a melting point of 54-56°C and N,N'-dimethyl-p-
1 part of toluidine was added and dissolved. By cooling this, a primer composition having a viscosity of 350 cps at 20°C was obtained.

このプラむマヌ組成物100郚にBPOパりダヌ
郚を添加しお、気枩℃におコンクリヌト床にロ
ヌラヌを甚いお0.3mmの厚みに塗垃したずころ、
50分で硬化しお匷固な塗膜を圢成した。
5 parts of BPO powder to 100 parts of this primer composition
When applied to a concrete floor at a temperature of 5°C to a thickness of 0.3mm using a roller,
It cured in 50 minutes to form a strong coating.

実斜䟋  実斜䟋に甚いたものず同じ䞍飜和β―ヒドロ
キシ゚ステル含有反応混合物70郚を溶解釜に仕蟌
み、メタクリル酞メチル23郚、アクリル酞―゚
チルヘキル郚、およびゞメタクリル酞゚チレン
グリコヌル郚を混合撹拌した。次いでこれを50
℃に加熱し、融点54〜56℃のパラフむン0.5郚お
よびN′―ゞメチル――トルむゞン郚を添
加し溶解した。これを冷华するこずにより20℃に
おける粘床350cpsのプラむマヌ組成物を埗た。
Example 7 70 parts of the same unsaturated β-hydroxy ester-containing reaction mixture as used in Example 6 was charged into a dissolution vessel, and 23 parts of methyl methacrylate, 5 parts of 2-ethylhexyl acrylate, and 1 part of ethylene glycol dimethacrylate were added. The mixture was mixed and stirred. Then set this to 50
0.5 part of paraffin having a melting point of 54 to 56°C and part of N,N'-dimethyl-p-toluidine were added and dissolved. By cooling this, a primer composition having a viscosity of 350 cps at 20°C was obtained.

このプラむマヌ組成物100郚にBPOパりダヌ
郚を添加しお気枩℃におコンクリヌト床に刷毛
を甚いお0.4mmの厚みに塗垃したずころ、玄45分
で硬化しお匷固な塗膜を圢成した。
5 parts of BPO powder to 100 parts of this primer composition
When applied to a concrete floor at a temperature of 5°C to a thickness of 0.4 mm using a brush, it hardened in about 45 minutes to form a strong coating film.

Claims (1)

【特蚱請求の範囲】  䞋蚘(A)〜(D)より成る床および壁面コヌテむン
グ甚プラむマヌ組成物。 (A) ビスプノヌルず゚ピクロルヒドリンを基
瀎ずし、分子量800〜3000及び゚ポキシド圓量
400〜2500を有する゚ポキシ暹脂を、メタ
クリル酞及び又はアクリル酞74〜64モル
ず、〜20個の炭玠原子を有する飜和モノ
カルボン酞少なくずも皮100〜80モルず
〜20個の炭玠原子を有する䞍飜和モノカルボン
酞少なくずも皮〜20モルずからなるモノ
カルボン酞26〜36モルずの混合物ずを反応さ
せるこずによ぀お埗られた䞍飜和β―ヒドロキ
シ゚ステル30〜60重量 (B) メタクリル酞メチルあるいはメタクリル酞メ
チルを80重量以䞊含有する重合性䞍飜和単量
䜓70〜40重量 (C) 40℃以䞊の融点を有するパラフむン及び又
はワツクス、(A)、(B)の合蚈量100重量郚に察し
0.1〜重量郚 (D) 第玚アミン、(A)、(B)の合蚈量100重量郚に
察し0.1〜重量郚
[Scope of Claims] 1. A primer composition for floor and wall coatings comprising the following (A) to (D). (A) Based on bisphenol A and epichlorohydrin, molecular weight 800-3000 and epoxide equivalent
400-2500 a) methacrylic acid and/or acrylic acid 74-64 mol%
and b) 100-80 mol% of at least one saturated monocarboxylic acid having 8-20 carbon atoms and 8
Unsaturated β- obtained by reacting a mixture of 0 to 20 mol % of at least one unsaturated monocarboxylic acid having ~20 carbon atoms with 26 to 36 mol % of a monocarboxylic acid Hydroxy ester 30-60% by weight (B) Methyl methacrylate or a polymerizable unsaturated monomer containing 80% by weight or more of methyl methacrylate 70-40% by weight (C) Paraffin and/or having a melting point of 40°C or higher For 100 parts by weight of wax, (A) and (B)
0.1 to 5 parts by weight (D) Tertiary amine, 0.1 to 5 parts by weight per 100 parts by weight of the total amount of (A) and (B)
JP8841882A 1982-05-25 1982-05-25 Primer composition for coating floor and wall surface Granted JPS58204057A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8841882A JPS58204057A (en) 1982-05-25 1982-05-25 Primer composition for coating floor and wall surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8841882A JPS58204057A (en) 1982-05-25 1982-05-25 Primer composition for coating floor and wall surface

Publications (2)

Publication Number Publication Date
JPS58204057A JPS58204057A (en) 1983-11-28
JPS6410024B2 true JPS6410024B2 (en) 1989-02-21

Family

ID=13942235

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8841882A Granted JPS58204057A (en) 1982-05-25 1982-05-25 Primer composition for coating floor and wall surface

Country Status (1)

Country Link
JP (1) JPS58204057A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61118415A (en) * 1984-11-13 1986-06-05 Matsushita Electric Ind Co Ltd Resin composition
US4619953A (en) * 1985-09-09 1986-10-28 The Dow Chemical Company Low styrene emission vinyl ester resin employing polyacrylates for fiber-reinforced applications
FR2686885A1 (en) * 1992-02-05 1993-08-06 Apsa VINYLESTER RESINS CONSISTING OF ONE OR MORE ACRYLIC MONOMERS AND AT LEAST ONE COMPATIBLE AND COPOLYMERIZABLE MACROMOLECULE, AND USES THEREOF.
JP3598649B2 (en) * 1996-05-07 2004-12-08 東掋むンキ補造株匏䌚瀟 Curable resin composition
JP5393939B2 (en) * 2005-10-14 2014-01-22 䞉菱レむペン株匏䌚瀟 Floor coating composition and floor covering coated with the coating
JP2017214441A (en) * 2016-05-30 2017-12-07 昭和電工株匏䌚瀟 Resin composition, crack injection material, and crack repair method
WO2017217243A1 (en) * 2016-06-16 2017-12-21 Dic株匏䌚瀟 Epoxy (meth)acrylate resin and resist member

Also Published As

Publication number Publication date
JPS58204057A (en) 1983-11-28

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