JPS5837345B2 - Fast-curing composition for forming coatings - Google Patents
Fast-curing composition for forming coatingsInfo
- Publication number
- JPS5837345B2 JPS5837345B2 JP2200178A JP2200178A JPS5837345B2 JP S5837345 B2 JPS5837345 B2 JP S5837345B2 JP 2200178 A JP2200178 A JP 2200178A JP 2200178 A JP2200178 A JP 2200178A JP S5837345 B2 JPS5837345 B2 JP S5837345B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- water
- emulsion
- composition
- coating film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Landscapes
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明は、速硬性の塗膜形戒用組或物に関するものであ
り、その目的とするところは、塗膜の厚みや自然条件の
如何にかSわらず、諸種の性質、特に耐水性に優れた塗
膜を形成する速硬性の組成物を提供せんとするにある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fast-curing coating film type composition, and its purpose is to cure various types of compositions regardless of the thickness of the coating film or natural conditions. The object of the present invention is to provide a fast-curing composition that forms a coating film with excellent properties, especially water resistance.
合或樹脂エマルジョンの成膜の原理は、水分の蒸発にあ
り、従って水分が充分に蒸発しない間は、実用に耐えう
るような諸種の性質、例えば特に耐水性に優れた塗膜は
得られない。The principle of forming a resin emulsion film is the evaporation of water; therefore, unless water evaporates sufficiently, a coating film with various properties that can withstand practical use, such as particularly excellent water resistance, cannot be obtained. .
例えば建造物表面に防水塗膜を形或させる処理を行う場
合に、合成樹脂エマルジョンを含む組或物を建造物の表
面に厚塗りする方法があるが、この場合、水分が蒸発し
て防水塗膜を形成するのに塗膜の厚みや、自然の気象条
件に大きく左右され、普通は耐水性の良い塗膜を得るま
でにはきわめて長時間を要する。For example, when forming a waterproof coating on the surface of a building, there is a method of coating the building surface with a thick composition containing a synthetic resin emulsion, but in this case, the water evaporates and the waterproof coating is removed. Formation of a coating depends largely on the thickness of the coating and natural weather conditions, and normally it takes an extremely long time to obtain a coating with good water resistance.
例えば気象条件にもよるが、通常数十μの膜厚の塗膜を
得る場合は数時間から数十時間、又膜厚が数百μ、数千
μと厚くなると1日以上の時間を要する。For example, depending on weather conditions, it usually takes several hours to several tens of hours to obtain a coating film with a thickness of several tens of microns, and more than one day if the film thickness is several hundreds or thousands of microns. .
従って、多湿時や低温時には使用しがたいとか、せっか
く塗布施工した後でも充分な成膜以前に降雨などがあれ
が塗布物が流出してしまうなどの欠点をまぬがれ得ない
。Therefore, it cannot avoid disadvantages such as being difficult to use in high humidity or low temperature conditions, and even after coating, if rain occurs before sufficient film formation, the coated material may wash out.
かかる欠点を解消し、前記目的を達或せしめんために、
本発明者らは長年研究を続けた結果、合成樹脂エマルジ
ョンを含む組或物を用いて塗膜を形成させる場合、単に
自然乾燥にゆだねるめではなく、伺らかの添加物を利用
することにより、例えば特に耐水性の良い塗膜を得るま
での時間を人為的に調節すると共に速やかに塗膜を形戒
しうる組或物を見い出し本発明を完或した。In order to eliminate such drawbacks and achieve the above objectives,
As a result of many years of research, the present inventors have found that when forming a coating film using a composition containing a synthetic resin emulsion, it is possible to form a coating film by using additives rather than simply leaving it to dry naturally. For example, the present invention has been completed by discovering a composition that can artificially control the time required to obtain a coating film with particularly good water resistance and can quickly control the shape of the coating film.
即ち、本発明は、(4)アクリル樹脂またはエチレンー
酢酸ビニル共重合樹脂を分散してなり、かつノニオン性
界面活性剤を含有するエマルジョンと(B)セメントな
らびにカルシウム、マグネシウム、亜鉛及びアルミニウ
ムの水難溶性の酸化物又は水酸化物から選ばれる化合物
の一種又は二種以上と(Qカルシウム、マグネシウム、
亜鉛、ストロンチウム及びアルミニウムの水溶性塩の一
種又は二種以上とからなり、
且つ囚の樹脂分100重量部に対して、(B)及び(Q
がそれぞれ0.1〜20重量部であることを特徴とする
速硬性の塗膜形或用組或物に関するものである。That is, the present invention provides (4) an emulsion formed by dispersing an acrylic resin or an ethylene-vinyl acetate copolymer resin and containing a nonionic surfactant, and (B) an emulsion containing cement and poorly water-soluble calcium, magnesium, zinc, and aluminum. one or more compounds selected from the oxides or hydroxides of (Q calcium, magnesium,
It consists of one or more water-soluble salts of zinc, strontium and aluminum, and (B) and (Q) per 100 parts by weight of the resin content.
The present invention relates to a fast-curing coating film type composition or composition, characterized in that the amount of each component is from 0.1 to 20 parts by weight.
本発明の速硬性の塗膜形成用組或物に於いて、(4)成
分のエマルジョン中のノニオン界面活性剤は、本発明組
戊物を安定化させると共に、作業性の向上に寄与するも
のであり、又(B)成分のセメントならびにカルシウム
、マグネシウム、亜鉛及びアルミニウムの水難溶性の酸
化物又は水酸化物は生成塗膜の耐水性の向上に寄与する
ものである。In the composition for forming a fast-curing coating film of the present invention, the nonionic surfactant in the emulsion of component (4) stabilizes the composition of the present invention and contributes to improving workability. Component (B), cement, and poorly water-soluble oxides or hydroxides of calcium, magnesium, zinc, and aluminum contribute to improving the water resistance of the resulting coating film.
又(Q或分のカルシウム、マグネシウム、亜鉛、ストロ
ンチウム及びアルミニウムの水溶性塩は、成膜性能を向
上させるもので、上記(B)戒分と相まって速硬性に寄
与するものである。In addition, (Q) a certain amount of water-soluble salts of calcium, magnesium, zinc, strontium, and aluminum improves film forming performance, and together with the above-mentioned component (B) contributes to rapid hardening.
かかる本発明の速硬性の塗膜形成用組或物は、塗膜の厚
みや、自然条件にかかわらず、水分が分離することなく
迅速に耐水性のよい塗膜を形成し得るので、例えば塗料
、特に外部用塗料、構造物の防水用組成物、コーティン
グ材、その他の表面処理剤等に適用される。The fast-curing composition for forming a coating film of the present invention can quickly form a coating film with good water resistance without moisture separation, regardless of the thickness of the coating film or natural conditions. It is particularly applicable to external paints, waterproofing compositions for structures, coating materials, and other surface treatment agents.
本発明の速硬性の塗膜形成用組或物の構戒成分の具体例
をあげると、(4)戒分のエマルジョンは、アクリル樹
脂またはエチレンー酢酸ビニル共重合樹脂を分散してな
る合成樹脂エマルジョンであり、又そのエマルジョンは
ノニオン性界面活性剤を含有しているものである。To give specific examples of the constituent components of the composition for forming a fast-curing coating film of the present invention, (4) the emulsion of a preservative is a synthetic resin emulsion formed by dispersing an acrylic resin or an ethylene-vinyl acetate copolymer resin. and the emulsion contains a nonionic surfactant.
ここで用いられるアクリル樹脂とはアクリル酸およびそ
のエステル、メタクリル酸およびそのエステルなどの重
合体および共重合体ならびにそれらと酢酸ビニル、スチ
レン、塩化ビニル、塩化ビニリデン、エチレン、プロピ
オン酸ビニル等の一種もしくは二種以上との共重合体か
らなる樹脂である。The acrylic resins used here are polymers and copolymers such as acrylic acid and its esters, methacrylic acid and its esters, and one or more of them and vinyl acetate, styrene, vinyl chloride, vinylidene chloride, ethylene, vinyl propionate, etc. It is a resin consisting of a copolymer with two or more types.
ノニオン性界面活性剤としては、例えばポリオキシエチ
レンのアルキルまたはアルキルフエニールエーテル、ポ
リオキシエチレンのソルビタン脂肪酸またはアシルエス
テル、オキシエチレンオキシプロピレンブロツクポリマ
ーなどがある。Examples of nonionic surfactants include alkyl or alkyl phenyl ethers of polyoxyethylene, sorbitan fatty acids or acyl esters of polyoxyethylene, and oxyethylene oxypropylene block polymers.
(B)成分のセメントとしては、普通ボルトランドセメ
ント、中庸熱ボルトランドセメント、早強ポルトランド
セメント、アルミナセメント、高炉セメントなどであり
、カルシウム、マグネシウム、亜鉛及びアルミニウムの
水難溶性の酸化物または水酸化物としては、たとえば酸
化亜鉛、酸化マグネシウム、水酸化カルシウム、水酸化
マグネシウムなどであり、本発明においてはセメントが
本発明の特徴をより良く具現化するため好ましく用いら
れる。The cement of component (B) includes ordinary boltland cement, moderate heat boltland cement, early-strength portland cement, alumina cement, blast furnace cement, etc., and includes poorly water-soluble oxides or hydroxides of calcium, magnesium, zinc, and aluminum. Examples of the material include zinc oxide, magnesium oxide, calcium hydroxide, magnesium hydroxide, etc. In the present invention, cement is preferably used because it better embodies the characteristics of the present invention.
(C)戒分のカルシウム、マグネシウム、亜鉛、ストロ
ンチウム及びアルミニウムの水溶性塩として一例をあげ
れば、塩化カルシウム、塩化マグネシウム、塩化アルミ
ニウム、塩化ストロンチウム、硫酸アルミニウム、硫酸
マグネシウム、硝酸カルシウム、硝酸ストロンチウムな
どの無機酸の塩であり、酢酸カルシウム、酢酸亜鉛等の
飽和有機酸の塩であり、アクリル酸カルシウム、アクリ
ル酸マグネシウム、アクリル酸アルミニウム、アクリル
酸亜鉛、アクリル酸ストロンチウム、クエン酸カルシウ
ム、クエン酸マグネシウム、マレイン酸カルシウム、マ
レイン酸マグネシウム、グルコン酸カルシウム、ブロピ
オン酸カルシウムなどの不飽和有機酸の塩であるが、特
に本発明の特徴を具現化するためには不飽和有機酸の塩
が好ましく用いられる。(C) Examples of water-soluble salts of calcium, magnesium, zinc, strontium and aluminum in the precepts include calcium chloride, magnesium chloride, aluminum chloride, strontium chloride, aluminum sulfate, magnesium sulfate, calcium nitrate, strontium nitrate, etc. Salts of inorganic acids, salts of saturated organic acids such as calcium acetate, zinc acetate, calcium acrylate, magnesium acrylate, aluminum acrylate, zinc acrylate, strontium acrylate, calcium citrate, magnesium citrate, Salts of unsaturated organic acids such as calcium maleate, magnesium maleate, calcium gluconate, and calcium propionate are used, and salts of unsaturated organic acids are particularly preferably used in order to embody the features of the present invention.
本発明は、上記或分を必須成分とするが、そのほかに可
塑剤、或膜助剤、消泡剤、凍結安定剤、増粘剤、充填剤
、分散剤、架橋剤などを添加することも可能であり、使
用目的に応じて良好な効果が得られる。The present invention has the above-mentioned components as essential components, but in addition, plasticizers, membrane auxiliaries, antifoaming agents, freeze stabilizers, thickeners, fillers, dispersants, crosslinking agents, etc. may also be added. It is possible, and good effects can be obtained depending on the purpose of use.
次に本発明の速硬性の塗膜形或組戒物の戒分割合につい
て述べる。Next, the proportions of the fast-curing coating or composition of the present invention will be described.
(4)成分のエマルジョンの樹脂分濃度は通常40〜6
5%程度であり、含有されるノニオン性界面活性剤の量
は、当該エマルジョンの樹脂分100重量部(以下部と
略す)に対して好ましくは0.1〜10部、さらに好ま
しくは0.5〜5部であり、エマルジョンの製造の際に
既に存在している場合は、あらためて添加する必要はな
い。(4) The resin concentration of the component emulsion is usually 40 to 6
The amount of nonionic surfactant contained is preferably 0.1 to 10 parts, more preferably 0.5 parts, based on 100 parts by weight (hereinafter referred to as "parts") of the resin content of the emulsion. ~5 parts, and if it is already present during the production of the emulsion, there is no need to add it again.
(B)或分のセメントおよび水難溶性の酸化物又は水酸
化物の量は(4)成分のエマルジョンの樹脂分100重
量部に対して0.1〜20部、好ましくは1〜10部で
あり、(C)戒分の水溶性塩は同じく0.1〜20部、
好ましくは0.5〜10部である。(B) The amount of a certain amount of cement and poorly water-soluble oxide or hydroxide is 0.1 to 20 parts, preferably 1 to 10 parts, based on 100 parts by weight of the resin content of the emulsion of component (4). , (C) the water-soluble salt of the precepts is also 0.1 to 20 parts,
Preferably it is 0.5 to 10 parts.
(4)成分のエマルジョン中のノニオン性界面活性剤の
含有量が0.1部未満のときは、組戒物の安定性が悪く
なり、又可使時間が短かくなるため、作業が困難になる
傾向にある。(4) If the content of nonionic surfactant in the emulsion of ingredients is less than 0.1 part, the stability of the composite material will deteriorate and the pot life will be shortened, making work difficult. There is a tendency to
又10部をこえるときは、塗膜の耐水性が低下する傾向
にある。Moreover, when it exceeds 10 parts, the water resistance of the coating film tends to decrease.
(B)戒分のセメントおよび水難溶性の酸化物又は水酸
化物が0.1部未満であったり、(Q成分の水溶性塩が
0.1部未満であったりするときは、速やかに耐水性塗
膜を得ることがむずかしく、又耐水性のある塗膜が得ら
れない。(B) If the amount of cement and poorly water-soluble oxides or hydroxides in the prefecture is less than 0.1 part, or if the water-soluble salt of component Q is less than 0.1 part, immediately It is difficult to obtain a water-resistant coating film, and a water-resistant coating film cannot be obtained.
一方それらが20部をこえて用いられるときは可使時間
が極端に短かくなって作業しがたくなる。On the other hand, if more than 20 parts of them are used, the pot life becomes extremely short and it becomes difficult to work with them.
本発明に於ける組成物の粘度は塗布手段に応じて設定す
ればよいが、通常300cps以上のものが使用され、
その上限は10万cps程度である。The viscosity of the composition in the present invention may be set depending on the application method, but a viscosity of 300 cps or more is usually used.
The upper limit is about 100,000 cps.
本発明の速硬性の塗膜形成組成物は、適用すべき面に刷
毛塗り、こて塗り、吹付等の手段により塗布され、数十
μから数百、数千μの膜厚の塗膜が形成される。The fast-curing film-forming composition of the present invention is applied to the surface to be applied by brushing, troweling, spraying, etc., to form a coating film with a thickness of several tens of microns to several hundred to several thousand microns. It is formed.
本発明の組或物を建造物表面等に塗布する場合、本発明
の組成物は、速硬性を有することから、該組或物のうち
(B)或分のセメントならびに水難溶性の酸化物又は水
酸化物及び(Q成分の水溶性塩は塗布作業直前に囚成分
のエマルジョンに配合してから塗布することが好ましい
が、あらかじめ組成物を調整してこれを施工場所に搬送
し使用することも勿論可能である。When the composition of the present invention is applied to the surface of a building, etc., since the composition of the present invention has quick hardening properties, a certain amount of cement and a poorly water-soluble oxide or It is preferable to mix the hydroxide and the water-soluble salt (component Q) into the emulsion of the active ingredient immediately before application, but it is also possible to prepare the composition in advance and transport it to the construction site for use. Of course it is possible.
配合法としては、例えば
(1)前記(4)成分と(B)成分の混合物に(C)成
分を配合する方法、
(2) (A)成分と(Q或分の混合物に(8)成分
を配合する方法、
(3)cA)成分に(B)戒分と(Q成分の混合物を配
合する方法などがよい。Examples of blending methods include (1) blending component (C) into a mixture of component (4) and component (B), (2) blending component (8) into a mixture of component (A) and (Q). (3) A method of blending a mixture of (B) precepts and (Q component) with component (3) cA).
この場合時期は、或分の種類や配合割合により一既に云
い得ないが、通常は塗装前数時間以内、具体的には5時
間以内であることが好ましい。In this case, the timing cannot be determined depending on the type and proportion of the ingredients, but it is usually within several hours, specifically within 5 hours, before painting.
配合後あまり長時間保存するとゲル化し、塗装が困難と
なる傾向にある。If it is stored for too long after being blended, it tends to gel and become difficult to paint.
父上記各混合物を二液混合型スプレーを用いて実施する
ことも可能である。It is also possible to carry out each of the above mixtures using a two-component mixing type spray.
かくして例等気象条件に左右されることなく所望の時間
、特に短時間、例えばO、2時間〜数時間で耐水性のあ
る塗膜を得ることができる。In this way, a water-resistant coating film can be obtained in a desired period of time, particularly in a short period of time, for example from 2 hours to several hours, regardless of weather conditions.
なお、本発明に係わる組或物を建造物表面などに適用す
るに当って、あらかじめ下地処理剤などで該表面を処理
しておくとか、或は本発明組戒物によって得られた塗膜
の表面にさらに表面保護層を設けるなどの使い方は勿論
可能であるばかりでなく、かかる処理を行うことによっ
て本発明の組或物より得られる塗膜の性能効果を助長し
、良い効果を発揮する。In addition, before applying the composition according to the present invention to the surface of a building, etc., the surface may be treated with a base treatment agent or the like, or the coating film obtained by the composition according to the present invention may be coated. Of course, it is not only possible to further provide a surface protective layer on the surface, but such treatment also enhances the performance effects of the coating film obtained from the composition of the present invention and exhibits good effects.
次に本発明の詳細を実施例を用いて説明する。Next, details of the present invention will be explained using examples.
実施例中の部および%はすべて重量部および重量%であ
る。All parts and percentages in the examples are by weight.
試験法は次に示す通りである。The test method is as follows.
(1)ゲル化時間(水分を含んだままで塑性状態に達す
るまでの時間):
(B)成分と(C)成分の双方を施工前に同時に、又は
各一方をあらかじめ添加しておいて、しかる後施工前に
残り一方を添加した後、混合物の粘度が10万cpsを
越える時間で示した(20’C)。(1) Gelation time (time required to reach a plastic state while still containing water): Both (B) and (C) components may be added at the same time before construction, or each may be added in advance. After adding the remaining portion before post-application, the viscosity of the mixture exceeded 100,000 cps (20'C).
(2)初期耐水性:
組成物を吹きつけた後、3時間経過後に塗膜表面から下
地まで達するようにカッターナイフで十字カットを入れ
、このサンプルを水中下に30分含浸させて塗膜の耐水
性を観察した。(2) Initial water resistance: After 3 hours have passed after spraying the composition, make a cross cut with a utility knife so that it reaches from the surface of the paint film to the base, and soak this sample in water for 30 minutes to test the paint film. Water resistance was observed.
(3)膜物性:
1)水浸後
JIS A 6021に示されている型ワタに吹きつ
けて3時間経過後に水中下に30分含浸させた後、JI
S A 6021に従って皮膜の養生及び物性測定を
行った(測定温度20℃)。(3) Membrane physical properties: 1) After soaking in water, spray it on the mold shown in JIS A 6021, and after 3 hours have passed, soak it under water for 30 minutes, and then
The coating was cured and the physical properties were measured in accordance with SA 6021 (measurement temperature: 20°C).
1[)無処理品
JIS A 6021に準じた(測定温度20’C)
。1 [) Untreated product According to JIS A 6021 (measured temperature 20'C)
.
(4)湿潤面での成膜性:
厚さ20山のコンクリート板を水中下に24時間含浸さ
せてから取り出し、これに組成物を吹きつけて指触によ
り成膜性をみた。(4) Film-forming property on a wet surface: A concrete plate with a thickness of 20 mounds was soaked in water for 24 hours, then taken out, the composition was sprayed on it, and the film-forming property was checked by touch with the fingers.
(5)透水性:
JIS A 6910 「複層模様吹付材」に準じて透
水試験を行った。(5) Water permeability: A water permeability test was conducted according to JIS A 6910 "Multilayer pattern sprayed material".
(6)ウエザオ試験: JIS A 6910に準じた(250Hr)。(6) Uezao test: According to JIS A 6910 (250 hours).
実施例 1
アクリル酸ブチル60部、スチレン30部、酢酸ビニル
6部、アクリル酸4部より或る七ノマー組戒にドデシル
ベンゼンスルホン酸ソーダ2部、過硫酸アンモン0.3
部、水100部を混合し、70℃で4時間通常の方法で
重合し、樹脂分濃度49%の重合体エマルジョンを製造
した後、アンモニア水でpH 6. 5に調節した。Example 1 60 parts of butyl acrylate, 30 parts of styrene, 6 parts of vinyl acetate, 4 parts of acrylic acid were added to a certain heptanomer combination, 2 parts of sodium dodecylbenzenesulfonate, and 0.3 parts of ammonium persulfate.
100 parts of water were mixed and polymerized in a conventional manner at 70°C for 4 hours to produce a polymer emulsion with a resin concentration of 49%, and then adjusted to pH 6.0 with aqueous ammonia. Adjusted to 5.
(これをエマルジョンAと称する)
上記エマルジョンAの樹脂分100部に花王ア1−ラス
■製のノニオン性界面活性剤、エマルケンPP−250
(オキシエチレンオキシプロピレンブロックコポリマー
)、0.2部、消泡剤としてFoamas ter (
サンノプコ■製)0.1部を添加し、さらに(B)の成
分としてボルトランドセメントを5部、増粘剤としてサ
ンノプコ■製のModicolVDO、2部を加えた。(This will be referred to as Emulsion A) 100 parts of the resin content of the above Emulsion A is added to a nonionic surfactant manufactured by Kao Allus ■, and Emulken PP-250.
(oxyethylene oxypropylene block copolymer), 0.2 parts, Foamaster (oxyethylene oxypropylene block copolymer) as an antifoaming agent (
0.1 part (manufactured by San Nopco ■) was added, and further 5 parts of Boltland cement as component (B) and 2 parts of Modicol VDO (manufactured by San Nopco ■) were added as a thickener.
上記配合物を1ケ月室温で放置したものにエアースプレ
ーを用いての吹付作業を行う直前に(Qの成分として塩
化カルシウムを3部加えた。The above formulation was left at room temperature for one month, and immediately before spraying using an air spray, 3 parts of calcium chloride was added as a component of Q.
〔吹付時の粘度は2000cps(B型粘度計、30r
pm,ローター/lf;.2、2 0 ’C )であっ
た〕この組成物の可使時間は約1時間で、それ以後は粘
度が上昇し、エアースプレーでの吹付が不可能であった
。[Viscosity during spraying is 2000 cps (B type viscometer, 30r
pm, rotor/lf;. 2.20'C)] The pot life of this composition was about 1 hour, after which time the viscosity increased and it was impossible to spray it with an air spray.
この組戒物をJIS A 6021 「屋根防水用塗膜
材」に示されている型わく、或は縦15C77L.横3
0crrL1厚さ1crILのスレート板等にエアース
プレーガンを用いて吹きつけ、膜厚が1.2間の防水層
を得、前記試験を行った。This assembly is made into a frame shown in JIS A 6021 "Roof waterproofing coating material" or a vertical 15C77L. horizontal 3
A slate board having a thickness of 0 crrL1 and 1 crIL was sprayed with an air spray gun to obtain a waterproof layer having a film thickness of 1.2 mm, and the above test was conducted.
試験結果を表−1に示す。The test results are shown in Table-1.
実施例 2
メタクリル酸メチル60部、アクリル酸エチル30部、
アクリ口ニトリル8部、メタクリル酸2部より成る七ノ
マー組或にドデシルベンゼンスルホン酸ソーダ2部、過
硫酸アンモン0.2部、水100部を混合し、72℃で
5時間通常の方法で重合し、樹脂分濃度47%の重合体
エマルジョンを製造した後、アンモニア水でpH 7.
0に調節した(これをエマルジョンBと称する)。Example 2 60 parts of methyl methacrylate, 30 parts of ethyl acrylate,
A heptanomer set consisting of 8 parts of acrylic nitrile and 2 parts of methacrylic acid, 2 parts of sodium dodecylbenzenesulfonate, 0.2 parts of ammonium persulfate, and 100 parts of water were mixed and polymerized in a conventional manner at 72°C for 5 hours. After producing a polymer emulsion with a resin concentration of 47%, the pH was adjusted to 7.0 with aqueous ammonia.
(This is referred to as emulsion B).
他の戒分の配合処方は表−1に示す通りで、ボルトラン
ドセメント2部、酸化マグネシウム1部を吹付作業直前
に加えた以外は実施例1と同様の方法で試験した(吹付
時の粘度1200cps)。The formulation of the other precepts is as shown in Table 1, and the test was conducted in the same manner as in Example 1, except that 2 parts of Bortland cement and 1 part of magnesium oxide were added immediately before the spraying operation (viscosity at the time of spraying). 1200cps).
試験結果を表−1に示す。The test results are shown in Table-1.
実施例 3
エチレン70部、酢酸ビニル30部のモノマー組或で界
面活性剤としてポリオキシエチレンアルキルフェノール
サルフエートソーダ塩2部、保護コロイドとして、ポリ
ビニルアルコール3部を用いて常法によりエチレンー酢
酸ビニル系エマルジョンを得た(樹脂分濃度は48%で
ある)。Example 3 An ethylene-vinyl acetate emulsion was prepared by a conventional method using a monomer composition of 70 parts of ethylene and 30 parts of vinyl acetate, 2 parts of polyoxyethylene alkylphenol sulfate sodium salt as a surfactant, and 3 parts of polyvinyl alcohol as a protective colloid. was obtained (resin concentration was 48%).
配合処方を表−1に示す通りで水酸化カルシウム1部及
びアクリル酸アルミニウム4部を吹付作業直前に加えた
以外は実施例1と同様の方法で試験した。The test was conducted in the same manner as in Example 1 except that the formulation was as shown in Table 1 and 1 part of calcium hydroxide and 4 parts of aluminum acrylate were added immediately before the spraying operation.
吹け時の粘度は4000cpsである。The viscosity when blowing is 4000 cps.
試験結果を表−1に示す。The test results are shown in Table-1.
実施例 4
実施例1で説明したエマルジョンAの樹脂分100部に
エマルゲン910(花王アトラス■製のノニオン性界面
活性剤、ポリオキシエチレンノニルフェノールエーテル
)、0.5部、ボルトランドセメンl−20部を添加し
た組或物に、アクリル酸アルミニウム1部を吹け作業直
前に加えた組戒物を用いて実施例1と同様の方法で試験
した。Example 4 To 100 parts of the resin content of emulsion A described in Example 1, 0.5 part of Emulgen 910 (nonionic surfactant, polyoxyethylene nonylphenol ether manufactured by Kao Atlas ■), and 20 parts of Bortland cement. A test was conducted in the same manner as in Example 1 using a composite material to which 1 part of aluminum acrylate was added immediately before blowing.
吹け時の粘度は1500cpsである。The viscosity when blown is 1500 cps.
試験結果を表−1に示す。The test results are shown in Table-1.
実施例 5
実施例1で説明したエマルジョンAの樹脂分100部に
エマルゲン910、2部、炭酸カルシウム30部、カオ
リン30部、FoamasterO.2部及び白セメン
トを10部添加してよく混練した。Example 5 To 100 parts of the resin component of emulsion A described in Example 1, 2 parts of Emulgen 910, 30 parts of calcium carbonate, 30 parts of kaolin, Foamaster O. 2 parts and 10 parts of white cement were added and kneaded well.
一週間後にこの組戒物を現場で施工するに際し、吹け作
業直前にアクリル酸マグネシウム8部を加えてよく攪拌
した。One week later, when constructing this kumikaimono on site, 8 parts of magnesium acrylate was added and thoroughly stirred just before the blowing work.
吹付時の粘度は7500cpsであった。The viscosity during spraying was 7500 cps.
このものを2階建での屋上にあるベントハウスの屋根(
下地モルタルで縦10m1横5m)上に膜厚が1.4間
となるように吹きつけた。This is the roof of the vent house on the roof of the two-story building (
The base mortar was sprayed onto a surface (10 m long x 5 m wide) to a film thickness of 1.4 m.
30分後には著しく増粘してゲル化状態を示し、4時間
後に耐水テストとして水道よりホースを用いて10分間
程皮膜に水をかけた結果、再乳化して合或樹脂エマルジ
ョン等が流れることもなく、初期耐水性は良好であった
。After 30 minutes, the viscosity increased significantly and showed a gelatinous state, and after 4 hours, as a water resistance test, water was poured onto the film for about 10 minutes using a hose from a tap, and as a result, it re-emulsified and a resin emulsion etc. flowed. The initial water resistance was good.
尚、1週間を経て塗膜を観察した結果、亀裂、ヒビ割れ
、ピンホール等がなく、均一で弾性のある防水膜を形或
していた。Furthermore, as a result of observing the coating film after one week, it was found that there were no cracks, cracks, pinholes, etc., and a uniform and elastic waterproof film had been formed.
比較例 1
実施例1で説明したエマルジョンAにセメントまたは水
難溶性の酸化物および水酸化物ならびに水溶性塩を加え
ずに表−2に示す配合より或る組成物を実施例1と同じ
方法で試験した。Comparative Example 1 A certain composition was prepared from the formulation shown in Table 2 in the same manner as in Example 1 without adding cement or poorly water-soluble oxides and hydroxides and water-soluble salts to Emulsion A described in Example 1. Tested.
結果は表−2に示すように初期耐水性試験で十字カット
面から塗膜が完全に溶出してしまい不良であった。As shown in Table 2, the coating film was completely eluted from the cross-cut surface in the initial water resistance test, resulting in a poor result.
比較例 2
実施例2で説明したエマルジョンBに水溶性塩を添加せ
ずに、表−2に示す組或物を用いて実施例1と同じ方法
で試験した。Comparative Example 2 Emulsion B described in Example 2 was tested in the same manner as in Example 1 using the composition shown in Table 2 without adding a water-soluble salt.
尚本例の塗装は刷毛塗りで行った。The coating in this example was done with a brush.
結果は表−2に示すように初期耐水性、水浸後の膜物性
等、何れも戒膜過程で水に遭うと流されてしまって不良
であった。As shown in Table 2, the results were poor in both the initial water resistance and the physical properties of the membrane after immersion in water, as the membrane was washed away when exposed to water during the membrane process.
比較例 3
実施例3で説明したエチレン酢酸ビニル系エマルジョン
にセメントまたは水難溶性の酸化物および水酸化物を添
加せずに表−2に示す組成物を用いて実施例1と同じ方
法で行った。Comparative Example 3 The same method as in Example 1 was carried out using the composition shown in Table 2 without adding cement or poorly water-soluble oxides and hydroxides to the ethylene vinyl acetate emulsion described in Example 3. .
尚本例の塗装は刷毛塗りで行った。The coating in this example was done with a brush.
結果は表−2に示すようにゲルタイムが1分と短かく、
吹付作業が不可能であり、また完全に凝固せずに半凝固
状態である為、初期耐水性試験で塗膜は完全には流され
ないか、固形分が溶出して再乳化した。As shown in Table 2, the gel time was as short as 1 minute.
Since it is impossible to spray and is not completely solidified but in a semi-solidified state, during the initial water resistance test, the coating film was either not completely washed away or the solid content was eluted and re-emulsified.
その結果、水浸漬後の膜物性は伸び、強さ共極端に低下
し不良であった。As a result, the physical properties of the film after immersion in water were poor, with both elongation and strength extremely reduced.
比較例 4〜6
エマルジョンAまたはエマルジョンBを用いて表−2に
示す配合より成る組成物を実施例1と同じ方法で試験し
た。Comparative Examples 4 to 6 Compositions having the formulations shown in Table 2 using Emulsion A or Emulsion B were tested in the same manner as in Example 1.
結果は表−2に示される様にいずれも満足できるもので
はなかった。As shown in Table 2, none of the results were satisfactory.
Claims (1)
共重合樹脂を分散してなり、かつノニオン性界面活性剤
を含有するエマルジョンと (B) セメントならびにカルシウム、マグネシウム
、亜鉛及びアルミニウムの水難溶性の酸化物又は水酸化
物から選ばれる化合物の一種又は二種以上と (q カルシウム、マグネシウム、亜鉛、ストロンチウ
ム及びアルミニウムの水溶性塩の一種又は二種以上とか
らなり、 且つ(4)の樹脂分100重量部に対して、(B)及び
(C)がそれぞれ0.1〜20重量部であることを特徴
とする速硬性の塗膜形戒用紐成物。[Claims] ICA) an emulsion formed by dispersing an acrylic resin or an ethylene-vinyl acetate copolymer resin and containing a nonionic surfactant; and (B) an emulsion containing cement and poorly water-soluble calcium, magnesium, zinc and aluminum. consisting of one or more compounds selected from oxides or hydroxides and one or more water-soluble salts of calcium, magnesium, zinc, strontium, and aluminum, and the resin content of (4) 100 1. A fast-curing coating film-type composition for precepts, characterized in that (B) and (C) are each contained in an amount of 0.1 to 20 parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2200178A JPS5837345B2 (en) | 1978-03-01 | 1978-03-01 | Fast-curing composition for forming coatings |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2200178A JPS5837345B2 (en) | 1978-03-01 | 1978-03-01 | Fast-curing composition for forming coatings |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54116036A JPS54116036A (en) | 1979-09-10 |
| JPS5837345B2 true JPS5837345B2 (en) | 1983-08-16 |
Family
ID=12070761
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2200178A Expired JPS5837345B2 (en) | 1978-03-01 | 1978-03-01 | Fast-curing composition for forming coatings |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5837345B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5655441A (en) * | 1979-10-09 | 1981-05-16 | Nippon Synthetic Chem Ind Co Ltd:The | Curable emulsion composition |
| JPS59199730A (en) * | 1983-04-28 | 1984-11-12 | Badische Yuka Co Ltd | Resin composition for forming coating film |
| JPS61159464A (en) * | 1984-12-29 | 1986-07-19 | Umehiko:Kk | Topcoating composition |
| JPS61159465A (en) * | 1984-12-29 | 1986-07-19 | Umehiko:Kk | Topcoating composition |
| JP2017057348A (en) * | 2015-09-18 | 2017-03-23 | 旭化成アドバンス株式会社 | Aqueous lining material for waterworks |
-
1978
- 1978-03-01 JP JP2200178A patent/JPS5837345B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54116036A (en) | 1979-09-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR0159894B1 (en) | Waterproofing method of plaster | |
| JPS634883A (en) | Method for applying finishing material layer to concrete structure | |
| CZ184893A3 (en) | Sealing acrylic compound, and process for preparing thereof | |
| JP2008162279A (en) | Concrete processing method | |
| EP0594321B1 (en) | Aqueous composition | |
| JPS5837345B2 (en) | Fast-curing composition for forming coatings | |
| JPS6147178B2 (en) | ||
| US4363836A (en) | Priming compositions for a base of cement mortar or concrete | |
| JPS6038424B2 (en) | Elastic paint composition | |
| JP2005015330A (en) | Polymer cement composition | |
| JPS603353B2 (en) | Waterproofing composition | |
| JP4664711B2 (en) | Cement-based material coating curing agent and method for applying the coating curing agent | |
| JPH07102241A (en) | Sealer for inorganic porous substrates | |
| JPH0140065B2 (en) | ||
| US7015273B2 (en) | Polymer complex coating agents, method for the production and use thereof | |
| JPS6123816B2 (en) | ||
| JPH0419187B2 (en) | ||
| JP6171060B1 (en) | Polymer cement composition | |
| JPS5913686A (en) | Rubber-like high resiliency inorganic finishing material | |
| JP2003510401A (en) | Use of water-soluble zirconium compounds as drying accelerators for aqueous coatings | |
| JPS6243954B2 (en) | ||
| JPS638253A (en) | Cement composition | |
| JPS61197458A (en) | Mortar composition | |
| JPS6251223B2 (en) | ||
| JPS5934670B2 (en) | mortar composition |