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JPH0621266B2 - Undercoat paint - Google Patents
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JPH0621266B2 - Undercoat paint - Google Patents

Undercoat paint

Info

Publication number
JPH0621266B2
JPH0621266B2 JP61187880A JP18788086A JPH0621266B2 JP H0621266 B2 JPH0621266 B2 JP H0621266B2 JP 61187880 A JP61187880 A JP 61187880A JP 18788086 A JP18788086 A JP 18788086A JP H0621266 B2 JPH0621266 B2 JP H0621266B2
Authority
JP
Japan
Prior art keywords
copolymer
weight
undercoat paint
vinylidene chloride
vinyl chloride
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 - Fee Related
Application number
JP61187880A
Other languages
Japanese (ja)
Other versions
JPS6343970A (en
Inventor
安司 磯部
正伸 小山
伸 谷川
嵩 小栗
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.)
Toagosei Co Ltd
Original Assignee
Toagosei 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 Toagosei Co Ltd filed Critical Toagosei Co Ltd
Priority to JP61187880A priority Critical patent/JPH0621266B2/en
Publication of JPS6343970A publication Critical patent/JPS6343970A/en
Publication of JPH0621266B2 publication Critical patent/JPH0621266B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 (イ) 発明の目的 「産業上の利用分野」 本発明は建築物や構造物の表面を塗装する際特には建築
物の防水のために施工される塗膜防水工法において使用
される下塗り塗料に関するものであり、冷熱の差の大き
い条件下あるいは耐アルカリ性を要求される条件下で高
度の耐久性を求められる塗膜防水工法において格別に有
用な下塗り塗料に関するものであり、土木建築業界にお
いて広く利用されうるものである。
DETAILED DESCRIPTION OF THE INVENTION (a) Purpose of the invention "Industrial field of application" The present invention is a coating film waterproofing method for coating the surface of a building or structure, particularly for waterproofing the building. The present invention relates to the undercoat paint used in, and particularly to the undercoat paint that is particularly useful in a waterproof coating method requiring a high degree of durability under conditions where there is a large difference in cold and heat conditions or conditions where alkali resistance is required. , Which can be widely used in the civil engineering and construction industry.

「従来の技術」 合成ゴム系エマルジョン、アクリル系エマルジョンある
いはウレタンゴム等を用いた塗膜防止工法において、従
来より塗膜と下地との密着性を高めるために下塗り塗料
すなわちプライマーが広く用いられている。それ等の下
塗り塗料の構成成分としては塩素化ポリプロピレンが主
として用いられ、塩化ビニル−酢酸ビニル共重合体、塩
化ゴム等も使用されている。
"Prior art" Undercoating paints, or primers, have been widely used to improve the adhesion between the coating and the substrate in the coating prevention method using synthetic rubber emulsion, acrylic emulsion or urethane rubber. . Chlorinated polypropylene is mainly used as a constituent of such undercoat paint, and vinyl chloride-vinyl acetate copolymer, chlorinated rubber and the like are also used.

「発明が解決しようとする問題点」 しかしながら、上記の下塗り塗料は、それによって形成
された皮膜強度が非常に小さく且つ低温脆性破壊が容易
に起こるため、伸縮の大きいゴム系塗膜への密着が不良
であったり、冷熱の差の大きい気候の条件下では熱分解
するという問題点を有しているものである。そのような
問題点のないものでも、耐アルカリ性が、特に80℃前
後に加温された条件下では著しく不良であり、アルカリ
性の高いコンクリート壁面では経時的に密着性が低下す
るという問題点を有するものである。
[Problems to be Solved by the Invention] However, the above-mentioned undercoat paint has a very small film strength formed thereby and easily undergoes brittle fracture at low temperature, so that adhesion to a rubber-based paint film with large expansion and contraction It has a problem of thermal decomposition under bad or climatic conditions with a large difference in cold heat. Even if it does not have such a problem, it has a problem that the alkali resistance is remarkably poor especially under the condition of being heated to about 80 ° C., and the adhesion property is deteriorated with time on a highly alkaline concrete wall surface. It is a thing.

本発明者等は上記問題点のない下塗り塗料を求めるべく
種々検討を続け、本発明を完成したものである。
The inventors of the present invention have conducted various studies to find an undercoat paint which does not have the above-mentioned problems, and completed the present invention.

(ロ) 発明の構成 「問題点を解決するための手段」 本発明者等は前記問題点が2種の化合物を併用すること
により解決され得ることを見出して本発明を完成した。
(B) Structure of the Invention "Means for Solving Problems" The present inventors have completed the present invention by finding that the above problems can be solved by using two kinds of compounds in combination.

すなわち、本発明は、塩化ビニル50〜90重量%と塩
化ビニリデン50〜10重量%との共重合体と塩素化パ
ラフィンからなり、両者の割合は共重合体が50〜95
重量%で塩素化パラフィンが50〜5重量%であること
を特徴とする土木建築用下塗り塗料に関するものであ
る。
That is, the present invention comprises a copolymer of vinyl chloride 50 to 90% by weight and vinylidene chloride 50 to 10% by weight and chlorinated paraffin, and the ratio of both is 50 to 95%.
The present invention relates to an undercoat paint for civil engineering, which is characterized by containing 50 to 5% by weight of chlorinated paraffin.

塩化ビニルと塩化ビニリデンとの共重合体 塩化ビニルと塩化ビニリデンとの共重合体は、塩化ビニ
ルと塩化ビニリデンを通常の重合方法すなわち懸濁重合
法、乳化重合法又は溶液重合法方等の方法でラジカル共
重合することにより得られるものである。
Copolymer of vinyl chloride and vinylidene chloride A copolymer of vinyl chloride and vinylidene chloride can be prepared by a conventional polymerization method of vinyl chloride and vinylidene chloride, that is, a suspension polymerization method, an emulsion polymerization method or a solution polymerization method. It is obtained by radical copolymerization.

共重合の例を本発明にとり好ましい懸濁重合法による場
合について説明すれば、懸濁剤として部分ケン化PV
A、メチルセルロース、エチレンオキサイドとプロピレ
ンオキサイドとの共重合体或いは酢酸ビニルとマレイン
酸との共重合体などを用い、ラジカル発生型触媒として
ベンゾイルパーオキサイド、ラウロイルパーオキサイ
ド、ジ2−エチルヘキシルパーオキシジカーボネート、
α,α′−ジメチルパレロニトリルなどを用い水を媒体
として、重合温度40〜70℃で7〜20Hr撹拌下に重合
することによって得られる。塩化ビニルと塩化ビニリデ
ンとの共重合体中における両者の割合は、塩化ビニルが
50〜90重量%で、塩化ビニリデン50〜10重量%
であり、これにより本発明の目的が達成される。
An example of the copolymerization in the case of the preferred suspension polymerization method according to the present invention will be described. As a suspending agent, partially saponified PV
A, methyl cellulose, a copolymer of ethylene oxide and propylene oxide, a copolymer of vinyl acetate and maleic acid, or the like is used, and benzoyl peroxide, lauroyl peroxide, di2-ethylhexyl peroxydicarbonate as a radical-generating catalyst. ,
It can be obtained by polymerization using α, α′-dimethylpareronitrile or the like in water as a medium at a polymerization temperature of 40 to 70 ° C. with stirring for 7 to 20 hours. In the copolymer of vinyl chloride and vinylidene chloride, the ratio of both is 50 to 90% by weight of vinyl chloride and 50 to 10% by weight of vinylidene chloride.
Which achieves the object of the invention.

なお該共重合体として塩化ビニルと塩化ビニリデン以外
のラジカル重合性単量体を第三成分として共重合させた
ものも本発明に適用できる。
As the copolymer, a copolymer obtained by copolymerizing vinyl chloride and a radical-polymerizable monomer other than vinylidene chloride as a third component is also applicable to the present invention.

その際の第三成分の単量体の量は全単量体中の20重量
%以下であることが本発明の目的の達成を阻害しないた
めに好ましい。
At that time, the amount of the monomer of the third component is preferably 20% by weight or less based on the total amount of monomers so as not to impair the achievement of the object of the present invention.

第三成分の単量体の例としては、酢酸ビニル、ブチルビ
ニルエーテル、ヒドロキシエチルアクリレート、無水マ
レイン酸、グリシジルメタアクリレート等を挙げること
ができる。
Examples of the third component monomer include vinyl acetate, butyl vinyl ether, hydroxyethyl acrylate, maleic anhydride, glycidyl methacrylate and the like.

本発明にとり好ましい塩化ビニルと塩化ビニリデンとの
共重合体はトルエンに可溶な共重合体である。トルエン
に可溶な共重合体は、塩素可パラフィンとの相溶性が著
しく良好になるため、これを用いた下塗り塗料は下地に
対する密着性が良好で且つ柔軟性の高い皮膜を与えるこ
とができる。
The copolymer of vinyl chloride and vinylidene chloride preferred for the present invention is a toluene-soluble copolymer. Since a copolymer soluble in toluene has a remarkably good compatibility with a chlorine-compatible paraffin, an undercoat paint using the copolymer can give a film having good adhesion to a base and high flexibility.

共重合体をトルエンに可溶性にするためには、易重合性
単量体である塩化ビニリデンの重合反応器への分割添
加、すなわち重合反応開始後に塩化ビニリデンの1部又
は全部を逐次添加していく重合方法を採用するか、連鎖
移動剤を併用した重合方法あるいは両者を併用した重合
方法を採用することが必要で、その様な重合方法により
トルエンに可溶な共重合体が得られる。
In order to make the copolymer soluble in toluene, vinylidene chloride, which is an easily polymerizable monomer, is dividedly added to the polymerization reactor, that is, one part or all of vinylidene chloride is sequentially added after the initiation of the polymerization reaction. It is necessary to adopt a polymerization method, a polymerization method in which a chain transfer agent is used in combination, or a polymerization method in which both of them are used in combination, and a copolymer soluble in toluene can be obtained by such a polymerization method.

連鎖移動剤としてはメチル基あるいはクロルメチル基を
含有する連鎖移動型単量体、特にメタアリルクロライド
又はγ,γ′−ジクロロイソブチレンを使用するのが好
ましい。
As the chain transfer agent, it is preferable to use a chain transfer type monomer containing a methyl group or a chloromethyl group, particularly methallyl chloride or γ, γ'-dichloroisobutylene.

メタアリルクロライド又はγ,γ′−ジクロロイソブチ
レンを使用した本発明にとり特に好ましい共重合体は各
単量体の構成比として塩化ビニル80〜55重量%、塩
化ビニリデン19〜40重量%、メタアリルクロライド
又はγ,γ′−ジクロロイソブチレン1〜5重量%の単
量体を共重合させて得られたものである。
Particularly preferred copolymers of the present invention using methallyl chloride or γ, γ'-dichloroisobutylene are vinyl chloride 80 to 55% by weight, vinylidene chloride 19 to 40% by weight, and methallyl chloride as a constituent ratio of each monomer. Alternatively, it is obtained by copolymerizing 1 to 5% by weight of γ, γ'-dichloroisobutylene.

共重合体のトルエンへの溶解性は目視によって十分に判
断し得るが、例えば共重合体20重量部をトルエン80
重量部に添加混合し1時間撹拌後1昼夜静置し不溶解物
を過し乾燥後得られた不溶解物が最初の共重合体の5
0重量%以下であるものが好ましく、より好ましくは2
0重量%以下、特に好ましくは0.5重量%以下のもの
が本発明にとり好ましい。
Although the solubility of the copolymer in toluene can be sufficiently judged by visual observation, for example, 20 parts by weight of the copolymer is mixed with 80 parts of toluene.
The mixture was added to 1 part by weight, stirred for 1 hour, and allowed to stand for 1 day to pass through the insoluble matter. After drying, the insoluble matter was 5% of the first copolymer.
It is preferably 0% by weight or less, more preferably 2
It is preferably 0% by weight or less, particularly preferably 0.5% by weight or less for the present invention.

塩素化パラフィン 本発明に用いられる塩素化パラフィンとしては、普通に
入手し得る市販品を挙げることができ、そのなかでは塩
素含有量が30〜70重量%であるものが好ましく、よ
り好ましくは40〜60重量%のものである。又分子量
としては400〜600のものが好ましい。上記の範囲
を外れるようになると、コンクリート或いはスレート壁
等との接着性が不良になったり、柔軟性が低下し低温脆
性破壊を示すようになる恐れが生じる。
Chlorinated Paraffin Examples of the chlorinated paraffin used in the present invention include commercially available products that are commonly available, among which those having a chlorine content of 30 to 70% by weight are preferable, and more preferably 40 to 60% by weight. The molecular weight is preferably 400 to 600. If the amount is out of the above range, there is a possibility that the adhesiveness to concrete or a slate wall or the like will be poor, or the flexibility will be deteriorated to exhibit low temperature brittle fracture.

併用割合 塩化ビニルと塩化ビニリデンとの共重合体と塩素化パラ
フィンの併用割合としては、両者の総和のうち該共重合
体が50〜95重量%であり、塩素化パラフィンが50
〜5重量%である必要があり、好ましくは該共重合体が
60〜80重量%で、塩素化パラフィンが40〜20重
量%である。共重合体の量が50重量%より少ない場合
は、耐熱性及び下地への密着性が不良となり、95重量
%を越えるようになると、皮膜の柔軟性が低下し、低温
脆性破壊する恐れが生じ、下地との密着性も低下する。
Ratio of combined use The ratio of combined use of the copolymer of vinyl chloride and vinylidene chloride and the chlorinated paraffin is 50 to 95% by weight of the total amount of both and 50% of the chlorinated paraffin.
It is necessary to be 5 to 5% by weight, preferably 60 to 80% by weight of the copolymer and 40 to 20% by weight of chlorinated paraffin. When the amount of the copolymer is less than 50% by weight, the heat resistance and the adhesion to the base become poor, and when it exceeds 95% by weight, the flexibility of the film is lowered and there is a risk of brittle fracture at low temperature. Also, the adhesiveness with the base is reduced.

下塗り塗料 塩化ビニルと塩化ビニリデンとの共重合体と塩素化パラ
フィンは水に分散させたエマルジョンとするか有機溶剤
に溶解した溶液とすることによって下塗り塗料として適
用され得るようになる。
Undercoat paint A copolymer of vinyl chloride and vinylidene chloride and chlorinated paraffin can be applied as an undercoat paint by forming an emulsion dispersed in water or a solution dissolved in an organic solvent.

下塗り塗料としては溶液の方が製造面及び取扱面から本
発明にとり好ましく、溶液にする際の溶剤としては一般
的に塗料において用いられているものが使用し得るが、
好ましくはトルエン又はトルエンを30重量%以上含有
する混合溶剤が好ましい。
As the undercoat paint, a solution is preferable in the present invention from the viewpoint of production and handling, and as the solvent for forming the solution, those generally used in paints can be used,
Toluene or a mixed solvent containing 30% by weight or more of toluene is preferable.

用いられる溶剤の具体例としては、ベンゼン、キシレ
ン、ソルベントナフサ、モノクロルベンゼン、ニトロベ
ンゼン、テトラリンなどの芳香族系化合物、メチレンク
ロライド、クロロホルム、四塩化炭素、ジクロルエタ
ン、トリクロロエチレン、パークロルエチレン、メチル
クロロホルムなどの塩素化炭化水素、エチルアセテー
ト、ブチルアセテート、セロソルブアセテートなどのエ
ステル、メチルエチルケトン、メチルイソブチルケトン
などのケトン等を挙げることができる。
Specific examples of the solvent used include aromatic compounds such as benzene, xylene, solvent naphtha, monochlorobenzene, nitrobenzene, and tetralin, methylene chloride, chloroform, carbon tetrachloride, dichloroethane, trichloroethylene, perchlorethylene, methylchloroform, and the like. Examples thereof include chlorinated hydrocarbons, esters such as ethyl acetate, butyl acetate and cellosolve acetate, and ketones such as methyl ethyl ketone and methyl isobutyl ketone.

下塗り塗料中における塩化ビニルと塩化ビニリデンとの
共重合体と塩素化パラフィンの量は下塗り塗料に求めら
れる流動性に基いて決められるもので、例えばスプレー
ガンを用いる塗装方法に適用されるものは下塗り塗料中
に10〜20重量%含有させたものが好ましい。
The amount of vinyl chloride and vinylidene chloride copolymer and chlorinated paraffin in the undercoating material is determined based on the fluidity required for the undercoating material.For example, the one applied to the coating method using a spray gun is the undercoating material. It is preferable that the coating composition contains 10 to 20% by weight.

「作 用」 本発明は、下塗り塗料の成分として、特定の共重合割合
の塩化ビニルと塩化ビニリデンとの共重合体と塩素化パ
ラフィンの両者を特定量併用することを特徴とするもの
で、それによって、従来の下塗り塗料では認められなか
った下地との密着性が良く、ゴムのように伸縮の大きさ
塗膜への密着性も良好で、耐寒性、耐熱性及び耐アルカ
リ性という基本的な耐久性能等のすべてを満足させ得る
という優れた作用を見出してなされたものである。本発
明は従来のものよりも一段と優れた下塗り塗料を提供し
得るものである。
"Working" The present invention is characterized in that, as a component of an undercoat paint, a specific amount of both a copolymer of vinyl chloride and vinylidene chloride in a specific copolymerization ratio and a chlorinated paraffin are used in combination. Adhesion to the base, which was not observed with conventional undercoating, is excellent, and adhesion to a coating film that has elasticity such as rubber is also good. Basic durability such as cold resistance, heat resistance and alkali resistance It was made by finding an excellent action of satisfying all of the performance and the like. INDUSTRIAL APPLICABILITY The present invention can provide a base coating material which is far superior to the conventional one.

「実施例」 以下、実施例及び比較例を挙げて、本発明をさらに具体
的に説明する。尚、各例の下塗り塗料の各特性は、スラ
ブコンクリート片に固形分として20gr/m2下塗り塗
料を塗布した試験片につき次の方法により評価した。
[Examples] Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples. Each property of the undercoat paint of each example was evaluated by the following method with respect to a test piece obtained by applying a 20 gr / m 2 undercoat paint as a solid content to a slab concrete piece.

1)温冷繰り返し試験 −40℃で5HR維持し、次いで80℃で5HR維持す
る繰り返し試験を2000HR行い、外観を目視で観察
した。
1) Warm-cooling repeated test A repeated test was carried out at -40 ° C for 5 HR and then at 80 ° C for 5 HR for 2000 HR, and the appearance was visually observed.

2)脱塩酸による分解性 1)の試験の前后で下塗り塗料の皮膜をとり塩素含有量
の低下を試験前の塩素含有量を100として求めた。
2) Degradability due to dehydrochlorination 1) Before and after the test of 1), a film of the undercoat paint was taken and the decrease in chlorine content was determined with the chlorine content before the test being 100.

3)接着力 1)の試験の前后の接着力を、垂直吸引型試験により測
定した。
3) Adhesive force The adhesive force before and after the test of 1) was measured by a vertical suction type test.

実施例1 (1) 共重合体の製法 5オートクレーブに塩化ビニル990gr、塩化ビニ
リデン255gr、懸濁剤としてOKS−7514(ケン
化度40モル%の部分ケン化PVA、日本合成化学(株)
製)7.5gr及びエパン485(酸化エチレンと酸化
プロピレンとのブロック共重合体、第一工業製薬(株)
製)15grを使用し、ラジカル発生型触媒として2−
エチルヘキシルパーオキシジカーボネート5gr及び純
水3000grを仕込み、500rpmの撹拌下にて6
0℃で重合反応させた。途中2HR毎に塩化ビニリデン5
1grを5回(合計量255gr)にわたって圧入添加
し、12時間重合反応を行った。遠心脱水分離后、乾燥
し、粉末状共重合体を得た。
Example 1 (1) Method for producing copolymer 5 Vinyl chloride 990 gr, vinylidene chloride 255 gr in an autoclave, OKS-7514 as a suspending agent (partially saponified PVA with a saponification degree of 40 mol%, Nippon Synthetic Chemical Co., Ltd.)
7.5 gr and Epan 485 (block copolymer of ethylene oxide and propylene oxide, Daiichi Kogyo Seiyaku Co., Ltd.)
15 gr, and used as a radical-generating catalyst
Ethylhexyl peroxydicarbonate (5 gr) and pure water (3,000 gr) were charged, and the mixture was stirred at 500 rpm to give 6
A polymerization reaction was performed at 0 ° C. Vinylidene chloride 5 every 2 HR on the way
1 gr was added under pressure 5 times (total amount 255 gr), and a polymerization reaction was carried out for 12 hours. After centrifugal separation and dehydration, it was dried to obtain a powdery copolymer.

(2) 下塗り塗料の調整 上記の(1)で得た共重合体80gr、エンパラ40(塩
素含有量41%、分子量560の塩素化パラフィン、味
の素(株)製)20gr、トルエン400grを混合し均
一に溶解させ下塗り塗料を得た。
(2) Preparation of undercoat paint 80 g of the copolymer obtained in (1) above, 20 g of Empara 40 (chlorine content 41%, chlorinated paraffin having a molecular weight of 560, manufactured by Ajinomoto Co., Inc.), and 400 g of toluene were mixed to homogeneity. To obtain an undercoat paint.

この下塗り塗料の物性を評価した結果を表1に示す。The results of evaluating the physical properties of this undercoat paint are shown in Table 1.

実施例2〜8、比較例1 実施例1の(1)共重合体の製法と同様に表1に従って単
量体の仕込組成を変化させ(塩化ビニリデン単量体の仕
込は実施例1と同じ比率で1/2量を逐次添加する。)共
重合体を得てさらに塩素化パラフィンの種類及び使用量
を表1の如くして得た下塗り塗料につき物性を評価した
結果を表1に示す。
Examples 2 to 8 and Comparative Example 1 The composition of the charged monomers was changed according to Table 1 in the same manner as in the production method of the copolymer (1) of Example 1 (the vinylidene chloride monomer was charged in the same manner as in Example 1). The results are shown in Table 1 in which the physical properties of the undercoating paint obtained by obtaining copolymers and the types and amounts of chlorinated paraffins used are shown in Table 1.

比較例2 塩化ビニルのみを1245gr使用した以外は、実施例
1の(1)共重合体の製法と同様にして重合体を製造し、
これと塩素化パラフィンの種類及び使用量を表2の如く
して得た下塗り塗料につき、物性を評価した結果を表2
に示す。
Comparative Example 2 A polymer was produced in the same manner as in the production method of the copolymer (1) of Example 1, except that only 1245 gr of vinyl chloride was used.
Table 2 shows the results of the evaluation of the physical properties of the undercoating paint obtained as shown in Table 2 along with the type and amount of chlorinated paraffin used.
Shown in.

比較例3 塩化ビニルの代わりに塩化ビニリデンのみを1245g
r使用した以外は、比較例2と同様にして得た下塗り塗
料につき、物性を評価した結果を表2に示す。
Comparative Example 3 1245 g of vinylidene chloride alone instead of vinyl chloride
Table 2 shows the results of evaluating the physical properties of the undercoat paint obtained in the same manner as in Comparative Example 2 except that r was used.

比較例4 比較例2及び3で得た塩化ビニル単独重合体と塩化ビニ
リデン単独重合体を66対34の重量比で混合したもの
を使用した以外は、比較例2と同様にして得た下塗り塗
料につき、物性を評価した結果を表2に示す。
Comparative Example 4 Undercoat paint obtained in the same manner as in Comparative Example 2 except that the vinyl chloride homopolymers obtained in Comparative Examples 2 and 3 and the vinylidene chloride homopolymer were mixed in a weight ratio of 66:34. Table 2 shows the results of the evaluation of the physical properties.

(ハ) 発明の効果 本発明の下塗り塗料は下地および塗膜への密着性が良
く、耐寒性、耐熱性及び耐アルカリ性等の性能に優れて
いるため塗料を用いる土木建築業界に及ぼす塗料の有効
活用という面で大きな効果を有するものであり、特にゴ
ム系エマルジョン等を用いる伸縮の大きい塗膜を用いる
防水塗膜工法に適した下塗り塗料であるため、防水塗膜
における防水効果をより顕著に向上させるという優れた
効果を持たらすものである。
(C) Effect of the invention The undercoat paint of the present invention has good adhesion to the base and coating film, and is excellent in performance such as cold resistance, heat resistance, and alkali resistance. It has a great effect in terms of utilization, and since it is an undercoat paint suitable for a waterproof coating method that uses a highly elastic coating film such as a rubber emulsion, the waterproof effect of the waterproof coating is significantly improved. It has the excellent effect of

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭49−29332(JP,A) ─────────────────────────────────────────────────── ─── Continuation of front page (56) References JP-A-49-29332 (JP, A)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】塩化ビニル50〜90重量%と塩化ビニリ
デン50〜10重量%との共重合体と塩素化パラフィン
からなり、両者の割合は共重合体が50〜95重量%で
塩素化パラフィンが50〜5重量%であることを特徴と
する土木建築用下塗り塗料。
1. A copolymer of 50 to 90% by weight of vinyl chloride and 50 to 10% by weight of vinylidene chloride and a chlorinated paraffin, wherein the proportion of both is 50 to 95% by weight of the copolymer and chlorinated paraffin. An undercoat paint for civil engineering, which is characterized by being 50 to 5% by weight.
JP61187880A 1986-08-12 1986-08-12 Undercoat paint Expired - Fee Related JPH0621266B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61187880A JPH0621266B2 (en) 1986-08-12 1986-08-12 Undercoat paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61187880A JPH0621266B2 (en) 1986-08-12 1986-08-12 Undercoat paint

Publications (2)

Publication Number Publication Date
JPS6343970A JPS6343970A (en) 1988-02-25
JPH0621266B2 true JPH0621266B2 (en) 1994-03-23

Family

ID=16213817

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61187880A Expired - Fee Related JPH0621266B2 (en) 1986-08-12 1986-08-12 Undercoat paint

Country Status (1)

Country Link
JP (1) JPH0621266B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4929332A (en) * 1972-07-15 1974-03-15
JPS6039478A (en) * 1983-08-13 1985-03-01 松本油脂製薬株式会社 Fiber processing agent

Also Published As

Publication number Publication date
JPS6343970A (en) 1988-02-25

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