JPH09221350A - Cement composition - Google Patents

Cement composition

Info

Publication number
JPH09221350A
JPH09221350A JP2879496A JP2879496A JPH09221350A JP H09221350 A JPH09221350 A JP H09221350A JP 2879496 A JP2879496 A JP 2879496A JP 2879496 A JP2879496 A JP 2879496A JP H09221350 A JPH09221350 A JP H09221350A
Authority
JP
Japan
Prior art keywords
component
cement
weight
composition
surfactant
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
JP2879496A
Other languages
Japanese (ja)
Inventor
Katsuaki Endo
克秋 遠藤
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 Chemical BASF Co Ltd
Original Assignee
Mitsubishi Chemical BASF 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 Chemical BASF Co Ltd filed Critical Mitsubishi Chemical BASF Co Ltd
Priority to JP2879496A priority Critical patent/JPH09221350A/en
Publication of JPH09221350A publication Critical patent/JPH09221350A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24Macromolecular compounds
    • C04B24/26Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/2688Copolymers containing at least three different monomers
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/40Surface-active agents, dispersants
    • C04B2103/408Dispersants
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/44Thickening, gelling or viscosity increasing agents
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/60Flooring materials
    • C04B2111/62Self-levelling compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a cement compsn. excellent in self-levelability and work efficiency. SOLUTION: This cement compsn. contains cement, a resin-contg. aq. dispersion liq., 0.01-10wt.% associable thickener and 0.01-10wt.% surfactant having two or more sulfonic acid groups in one, molecule or cationic surfactant. The ratio of the thickener to the (cationic) surfactant is 0.1-15.

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】本発明は、セメント組成物に
関し、特にセルフレベリング性、及び、作業性に優れた
セメント組成物に関する。
TECHNICAL FIELD The present invention relates to a cement composition, and more particularly to a cement composition having excellent self-leveling properties and workability.

【0002】[0002]

【従来の技術】従来、建造物、水槽その他の防水材、仕
上げ材、下地調整材として、セメントに樹脂水性分散液
を配合したものや、更に骨材を配合した組成物が、シー
ムレス状の塗膜が得られること、小面積部分や入り組ん
だ複雑な個所への施工が簡単であること、加熱及び火気
を必要とせずに硬化すること、溶剤を使用しないこと等
の利点を生かして用いられている。
2. Description of the Related Art Conventionally, as a waterproofing material for buildings, aquariums, etc., a finishing material, and a ground control material, a mixture of cement with an aqueous resin dispersion, and a composition of further aggregate have been used as a seamless coating. It is used by taking advantage of the fact that a film can be obtained, that it can be easily applied to small areas and complicated complicated places, that it cures without the need for heating and fire, and that it does not use solvents. There is.

【0003】[0003]

【発明が解決しようとする課題】これらセメント組成物
によれば、弾力性及び耐水性を有する塗膜を形成しうる
が、コンクリートスラブ等の上に吹付け、鏝塗り、ロー
ラー塗工等で塗布した場合に表面が均一になりにくい、
特に施工してから経時した後で表面を手直しした場合に
は表面がむらになり均一になりにくい等、いわゆるセル
フレベリング性が十分でないため作業性が悪く、これら
の改良が望まれている。本発明は、上記のような従来の
問題を解決し、セルフレベリング性に優れたセメント組
成物を提供することを目的とするものである。
According to these cement compositions, a coating film having elasticity and water resistance can be formed, but it can be applied by spraying, trowel coating, roller coating, etc. onto a concrete slab or the like. If you do, the surface will not be uniform,
In particular, when the surface is reworked after a lapse of time after construction, the surface becomes uneven and it is difficult to make it uniform, so that the so-called self-leveling property is not sufficient and the workability is poor, and these improvements are desired. It is an object of the present invention to solve the above conventional problems and provide a cement composition having excellent self-leveling properties.

【0004】[0004]

【課題を解決するための手段】本発明者らは鋭意検討の
結果、セメントに、樹脂水性分散液、会合性増粘剤及び
1分子中に2個以上のスルホン酸基を有する界面活性剤
又はカチオン性界面活性剤とを配合することにより上記
目的を達成することができた。即ち、本発明の第1は、 (A)成分:セメント (B)成分:樹脂水性分散液 (C)成分:会合性増粘剤 (D)成分:1分子中に2個以上のスルホン酸基を有す
る界面活性剤又はカチオン性界面活性剤 を含有する組成物であって、該組成物中(C)成分を
0.01〜10重量%、及び(D)成分を0.01〜1
0重量%含有し、かつ(C)成分と(D)成分の割合
(C/D)が0.1〜15であることを特徴とするセメ
ント組成物である。また、該組成物が更に(E)成分と
して骨材を含有するのが好ましい。更にまた、該組成物
が、(A)成分100重量部に対して、(B)成分0.
01〜300重量部を含有するのが好ましい。
Means for Solving the Problems As a result of intensive investigations by the present inventors, an aqueous resin dispersion, an associative thickener, and a surfactant having two or more sulfonic acid groups in one molecule have been added to cement. The above object could be achieved by blending with a cationic surfactant. That is, the first aspect of the present invention is: (A) component: cement (B) component: resin aqueous dispersion (C) component: associative thickener (D) component: 2 or more sulfonic acid groups in one molecule A composition containing a surfactant or a cationic surfactant having a content of 0.01 to 10% by weight of the component (C) and 0.01 to 1% of the component (D) in the composition.
A cement composition containing 0% by weight and having a ratio (C / D) of component (C) to component (D) of 0.1 to 15. Further, it is preferable that the composition further contains an aggregate as the component (E). Furthermore, the composition contains 100 parts by weight of the component (A) and 0.
It is preferable to contain 01 to 300 parts by weight.

【発明の実施の形態】BEST MODE FOR CARRYING OUT THE INVENTION

【0005】本発明における(A)成分のセメントとし
ては、水硬性石灰;ローマンセメント;天然セメント;
普通ポルトランドセメント、早強ポルトランドセメン
ト、超早強ポルトランドセメント、中庸熱ポルトランド
セメント、白色ポルトランドセメント等のポルトランド
セメント;アルミナセメント;高炉セメント;シリカセ
メント;ポゾランセメント;フライアッシュセメント;
特殊セメント等の水硬性セメントや消石灰・ドロマイト
プラスター;焼き石膏;無水石膏;半水石膏;マグネシ
アセメント等の気硬性セメント等が挙げられる。これら
のセメントは単独で、もしくは2種以上を混合して用い
ることができる。
As the cement of the component (A) in the present invention, hydraulic lime; roman cement; natural cement;
Normal Portland cement, early strength Portland cement, super early strength Portland cement, moderate heat Portland cement, white Portland cement, etc. Portland cement; Alumina cement; Blast furnace cement; Silica cement; Pozzolan cement; Fly ash cement;
Specific examples include hydraulic cements such as special cements, slaked lime and dolomite plaster, calcined gypsum, anhydrous gypsum, hemihydrate gypsum, and hydraulic cements such as magnesia cement. These cements can be used alone or in combination of two or more.

【0006】本発明における(B)成分の樹脂水性分散
液は、アクリル系、酢酸ビニル系、エチレン・酢酸ビニ
ル系、塩化ビニル系等の各種樹脂水性分散液やスチレン
・ブタジエン共重合体、天然ゴム等の各種ゴムラテック
ス等が使用できるが、特に耐アルカリ性や耐候性及び耐
久性を考慮するとアクリル系樹脂水性分散液が好まし
い。好ましいアクリル系樹脂水性分散液は、各種単量体
を重合して調整されるが、得られるセメントの塗膜の強
度や伸び等の点から、下記(a)〜(c)の単量体の組
み合わせが好ましい。
The aqueous resin dispersion of component (B) in the present invention is an aqueous dispersion of various resins such as acrylic, vinyl acetate, ethylene / vinyl acetate, vinyl chloride, styrene / butadiene copolymer, natural rubber. Although various rubber latexes such as the above can be used, an acrylic resin aqueous dispersion is preferable especially in consideration of alkali resistance, weather resistance and durability. A preferred acrylic resin aqueous dispersion is prepared by polymerizing various monomers, but from the viewpoint of strength and elongation of the coating film of the resulting cement, the following (a) to (c) monomers are used. Combinations are preferred.

【0007】(a)アクリル酸エチル、アクリル酸nー
プロピル、アクリル酸nーブチル、アクリル酸イソブチ
ル、アクリル酸2ーエチルヘキシル、アクリル酸オクチ
ル、アクリル酸ラウリル、アクリル酸トリデシル、アク
リル酸ヒドロキシエチル、アクリル酸ヒドロキシプロピ
ル等の、単独重合体のガラス転移点が、0℃未満である
アクリル酸アルキルエステル;メタクリル酸ラウリル、
メタクリル酸トリデシル等の、単独重合体のガラス転移
点が0℃以下であるメタクリル酸アルキルエステル;エ
チレン、イソブチレン、塩化ビニリデン、ブタジエン等
の、単独重合体のガラス転移点が0℃未満であるその他
の単量体 10〜95重量%
(A) Ethyl acrylate, n-propyl acrylate, n-butyl acrylate, isobutyl acrylate, 2-ethylhexyl acrylate, octyl acrylate, lauryl acrylate, tridecyl acrylate, hydroxyethyl acrylate, hydroxy acrylate Homopolymers such as propyl have a glass transition point of less than 0 ° C. alkyl acrylate; lauryl methacrylate
Homopolymers such as tridecyl methacrylate, which have a glass transition temperature of 0 ° C. or lower; methacrylic acid alkyl esters; ethylene, isobutylene, vinylidene chloride, butadiene, etc., which have a glass transition temperature of less than 0 ° C. Monomer 10-95% by weight

【0008】(b)アクリル酸メチル、アクリル酸tー
ブチル等の、単独重合体のガラス転移点が0℃以上であ
るアクリル酸アルキルエステル;メタクリル酸メチル、
メタクリル酸エチル、メタクリル酸プロピル、メタクリ
ル酸ブチル、メタクリル酸ヒドロキシエチル等の、単独
重合体のガラス転移点が0℃以上であるメタクリル酸ア
ルキルエステル;スチレン、α−メチルスチレン、塩化
ビニル、酢酸ビニル、プロピオン酸ビニル、分岐脂肪酸
ビニル(バーサチック酸ビニル)、アクリロニトリル、
メタクリロニトリル、アクリルアミド、メタクリルアミ
ド等の、単独重合体のガラス転移点が0℃以上であるそ
の他の単量体 0〜90重量%
(B) Alkyl acrylates such as methyl acrylate, t-butyl acrylate, etc., whose homopolymer has a glass transition point of 0 ° C. or higher; methyl methacrylate,
Alkyl methacrylates such as ethyl methacrylate, propyl methacrylate, butyl methacrylate, hydroxyethyl methacrylate, etc., whose homopolymer has a glass transition point of 0 ° C. or higher; styrene, α-methylstyrene, vinyl chloride, vinyl acetate, Vinyl propionate, branched fatty acid vinyl (vinyl versatate), acrylonitrile,
0 to 90% by weight of other monomers such as methacrylonitrile, acrylamide and methacrylamide whose homopolymer has a glass transition point of 0 ° C or higher.

【0009】(c)アクリル酸、メタクリル酸、イタコ
ン酸等の不飽和カルボン酸、無水マレイン酸等の不飽和
カルボン酸の無水物 0〜0.7重
量%
(C) Unsaturated carboxylic acids such as acrylic acid, methacrylic acid and itaconic acid, and anhydrides of unsaturated carboxylic acids such as maleic anhydride 0-0.7% by weight

【0010】(d)N−メチロールアクリルアミド、N
−メチロールメタクリルアミド、N−フェニルマレイミ
ド、N−(メチル)フェニルマレイミド、N−(ヒドロ
キシ)フェニルマレイミド、N−(メトキシ)フェニル
マレイミド、N−安息香酸マレイミド、N−メチルマレ
イミド、N−エチルマレイミド、N−n−プロピルマレ
イミド、N−イソプロピルマレイミド、N−n−ブチル
マレイミド、N−イソブチルマレイミド、N−t−ブチ
ルマレイミド等の特殊な官能基を有するその他の単量体

0〜20重量%
(D) N-methylol acrylamide, N
-Methylol methacrylamide, N-phenylmaleimide, N- (methyl) phenylmaleimide, N- (hydroxy) phenylmaleimide, N- (methoxy) phenylmaleimide, N-benzoic acid maleimide, N-methylmaleimide, N-ethylmaleimide, Other monomers having a special functional group such as N-n-propylmaleimide, N-isopropylmaleimide, Nn-butylmaleimide, N-isobutylmaleimide and Nt-butylmaleimide.

0-20% by weight

【0011】本発明においては、上記単量体の一種また
は二種以上を適宜組み合わせて使用すればよいが、硬化
後のセメント組成物の物性を考慮すれば、重合体のガラ
ス転移点を−50℃〜50℃に調整することが好まし
い。ガラス転移点が50℃を越えると、塗膜の剛性は高
くなるものの、常温で造膜しにくくなり、造膜不足によ
る物性の低下が発生しやすくなる傾向があり、また、ガ
ラス転移点が余りに低く過ぎても、柔軟性、伸展性は向
上するものの塗膜強度が弱くなる傾向があるので好まし
くない。また使用する目的に合わせて多官能性化合物に
より分子間を架橋することもできる。
In the present invention, one kind or two or more kinds of the above-mentioned monomers may be used in an appropriate combination, but in consideration of the physical properties of the cement composition after curing, the glass transition point of the polymer is -50. It is preferable to adjust the temperature to 50 ° C. If the glass transition temperature exceeds 50 ° C, the rigidity of the coating film increases, but it becomes difficult to form a film at room temperature, and the physical properties tend to deteriorate due to insufficient film formation, and the glass transition point is too high. If it is too low, the flexibility and extensibility are improved, but the coating film strength tends to be weak, which is not preferable. Further, it is possible to crosslink between the molecules with a polyfunctional compound according to the purpose of use.

【0012】本発明における樹脂水性分散液は、以上の
単量体又は各種単量体混合物を用いて、懸濁重合、乳化
重合、分散重合のような周知の多様な方法によって製造
することもできるが、好ましくは乳化重合によって製造
される。即ち、乳化剤または保護コロイド剤を含む水中
に不飽和単量体及び各種単量体混合物を加え、過硫酸カ
リウムなどの重合開始剤の存在下に50〜95℃に加熱
することにより(共)重合させ、固形分40〜60重量
%の樹脂水性分散液とする。
The aqueous resin dispersion according to the present invention can be prepared from the above monomers or various monomer mixtures by various well-known methods such as suspension polymerization, emulsion polymerization and dispersion polymerization. Are preferably produced by emulsion polymerization. That is, (co) polymerization by adding an unsaturated monomer and various monomer mixtures into water containing an emulsifier or a protective colloid agent, and heating at 50 to 95 ° C. in the presence of a polymerization initiator such as potassium persulfate. To obtain a resin aqueous dispersion having a solid content of 40 to 60% by weight.

【0013】乳化剤としては、ジアルキルスルホコハク
酸ナトリウム、アルキルスルホン酸のアルカリ塩、オキ
シアルキル化されたアルコールまたはアルキルフェノー
ルのアルカリ金属塩、脂肪酸のアルカリ塩などアニオン
性界面活性剤、ノニオン性界面活性剤の各種のものが使
用できる。その使用量は、通常樹脂分に対し0.1〜5
重量%の割合である。又、目的によっては、カチオン性
界面活性剤を単独で、あるいはノニオン性界面活性剤と
併用して使用することもできる。
As the emulsifier, various kinds of anionic surfactants and nonionic surfactants such as sodium dialkyl sulfosuccinate, alkali salts of alkyl sulfonic acids, alkali metal salts of oxyalkylated alcohols or alkylphenols, alkali salts of fatty acids, etc. Can be used. The amount used is usually 0.1 to 5 with respect to the resin content.
% By weight. In addition, depending on the purpose, a cationic surfactant may be used alone or in combination with a nonionic surfactant.

【0014】また、前記した保護コロイドとしては、た
とえばヒドロキシエチルセルロースやポリエチレンオキ
サイド・プロピレンオキサイドブロックポリマー、不飽
和カルボン酸共重合体のアルカリ可溶物等がある。乳化
重合において用いる重合開始剤は、過硫酸カリウム、過
硫酸アンモニウム、過酸化水素などの無機過酸化物が好
ましいが、その他ベンゾビスイソブチロニトリル、アゾ
ビスバレロニトリルなどのアゾ系開始剤;ベンゾイルパ
ーオキサイド、ラウロイルパーオキサイド、tーブチル
パーオキサイドなどの有機過酸化物系開始剤も使用でき
る。また、これらの開始剤に、ロンガリット、Lーアス
コルビン酸、有機アミンなどの還元剤を併用してレドッ
クス開始剤として用いてもよい。
Examples of the above-mentioned protective colloid include hydroxyethyl cellulose, polyethylene oxide / propylene oxide block polymer, and alkali soluble products of unsaturated carboxylic acid copolymers. The polymerization initiator used in emulsion polymerization is preferably an inorganic peroxide such as potassium persulfate, ammonium persulfate or hydrogen peroxide, but other azo initiators such as benzobisisobutyronitrile and azobisvaleronitrile; benzoylper Organic peroxide type initiators such as oxide, lauroyl peroxide and t-butyl peroxide can also be used. Further, reducing agents such as Rongalit, L-ascorbic acid and organic amines may be used in combination with these initiators as a redox initiator.

【0015】乳化重合における単量体の供給方法は、種
々の方法を用いることができる。たとえば一括仕込法、
モノマー添加法、エマルジョン添加法等の種々の方法を
用いることができる。また、添加する単量体の組成を逐
次に変化させるシード重合法、又はパワーフィード重合
法等も用いることができる。
Various methods can be used as the method of supplying the monomers in the emulsion polymerization. For example, the batch charging method,
Various methods such as a monomer addition method and an emulsion addition method can be used. Further, a seed polymerization method or a power feed polymerization method in which the composition of the added monomer is sequentially changed can also be used.

【0016】本発明における(C)成分の会合性増粘剤
は、2以上の疎水性末端基を有する親水性基を有する活
性剤である。親水性基が水と作用し、一方の疎水性末端
基が粒子に吸着し、更に他方の疎水性末端基が他の粒子
又は疎水性末端基と吸着することにより増粘作用を発現
するものと考えられる。会合性増粘剤としては、ポリエ
ーテル系、ウレタン変性ポリエーテル系、ポリエーテル
変性アクリル系があるが、特にウレタン変性ポリエーテ
ル系であるポリウレタン増粘剤が好ましい。
The associative thickener as the component (C) in the present invention is an activator having a hydrophilic group having two or more hydrophobic end groups. The hydrophilic group acts on water, one hydrophobic end group is adsorbed on the particles, and the other hydrophobic end group is adsorbed on another particle or the hydrophobic end group to exert a thickening effect. Conceivable. Examples of the associative thickener include polyether-based, urethane-modified polyether-based, and polyether-modified acrylic-based, and urethane-modified polyether-based polyurethane thickeners are particularly preferable.

【0017】このポリウレタン増粘剤は、通常は3個以
上の疎水性基を有し、その2個以上が末端基であり、そ
れらの疎水性基は親水性ポリエーテル基を通して連結さ
れ、更にポリウレタン基を有することを特徴とする活性
剤である。これらのものはCollacral PU
85(独BASF社製)、アデカノールUH−420、
UH−438(旭電化工業社製)、SN シックナー
612(サンノプコ社製)等の市販品がある。また、特
開昭48−97783、特公昭52−25840、特開
昭54−80349及び特公平1−55292等にその
製造方法が記載されている。(C)成分の含有量は0.
01〜10重量%、好ましくは0.03〜6重量%であ
り、少なすぎるとセルフレベリング性の改良効果が小さ
く、多すぎると粘度が高くなり塗布が困難になるだけで
なく、耐水性等の物性の低下が著しい。
This polyurethane thickener usually has three or more hydrophobic groups, two or more of which are terminal groups, and these hydrophobic groups are linked through a hydrophilic polyether group. It is an activator characterized by having a group. These are Collacral PU
85 (manufactured by BASF Germany), ADEKA NOL UH-420,
UH-438 (Made by Asahi Denka Co., Ltd.), SN thickener
There are commercially available products such as 612 (manufactured by San Nopco). Further, its manufacturing method is described in JP-A-48-97783, JP-B-52-25840, JP-A-54-80349, JP-B-1-55292, and the like. The content of the component (C) is 0.
It is from 0 to 10% by weight, preferably from 0.03 to 6% by weight. If it is too small, the effect of improving the self-leveling property is small, and if it is too large, not only the viscosity becomes high and coating becomes difficult, but also the water resistance and the like. The deterioration of physical properties is remarkable.

【0018】本発明における(D)成分の1分子中に2
個以上のスルホン酸基を有する界面活性剤としては、ペ
レックスSS−H、SS−L(花王社製)、Dowfa
x2A−1(米ダウケミカル社製)等のアルキルジフェ
ニルエーテルジスルホン酸塩系界面活性剤やデモール
N、マイテイ100(花王社製)等のナフタレンスルホ
ン酸ホルマリン縮合物のアルカリ塩、等が使用できる。
2 in one molecule of the component (D) in the present invention
As the surfactant having one or more sulfonic acid groups, Perex SS-H, SS-L (manufactured by Kao Corporation), Dowfa
For example, an alkyl diphenyl ether disulfonate-based surfactant such as x2A-1 (manufactured by Dow Chemical Co., Ltd.), an alkali salt of a naphthalene sulfonic acid formalin condensate such as DEMOL N and Mighty 100 (manufactured by Kao) can be used.

【0019】又カチオン性界面活性剤としては、ラウリ
ルトリメチルアンモニウムクロライド、ステアリルトリ
メチルアンモニウムクロライド等の第四級アンモニウム
塩、ステアリルアミン塩酸塩等のアルキルアミン塩、ラ
ウリルベタイン等のアルキルベタイン型、等が使用でき
る。又、ポリオキシエチレンアルキルアミン等の弱いカ
チオン性界面活性剤としての性質を持っているアルキル
アミン類も使用できる。このアルキルアミン類は酸化エ
チレンの低モル付加物を有する方が高モル付加物を有す
る方より好ましい。本発明においては上記の界面活性剤
が使用できるが、カチオン性界面活性剤の方が効果が大
きく好ましく、特に、第四級アンモニウム塩型カチオン
性界面活性剤が好ましい。
As the cationic surfactant, quaternary ammonium salts such as lauryltrimethylammonium chloride and stearyltrimethylammonium chloride, alkylamine salts such as stearylamine hydrochloride and alkylbetaine type such as laurylbetaine are used. it can. Also, alkylamines such as polyoxyethylene alkylamine, which have the property as a weak cationic surfactant, can be used. It is preferred that these alkylamines have low molar adducts of ethylene oxide over high molar adducts. Although the above-mentioned surfactants can be used in the present invention, cationic surfactants are more effective and preferred, and quaternary ammonium salt type cationic surfactants are particularly preferred.

【0020】(D)成分の含有量は0.01〜10重量
%、好ましくは0.05〜6重量%であり、少なすぎる
と初期の粘度が高過ぎ、塗布が困難になり、多すぎると
耐水性等の物性が低下するだけでなく、セルフレベリン
グ性の低下も著しい。尚、(B)成分の樹脂水性分散液
を1分子中に2個以上のスルホン酸基を有する界面活性
剤又はカチオン性界面活性剤を用いて、乳化重合によっ
て製造した場合、使用され、該系内に存在するこれら1
分子中に2個以上のスルホン酸基を有する界面活性剤又
はカチオン性界面活性剤も本発明の(D)成分とする。
The content of the component (D) is 0.01 to 10% by weight, preferably 0.05 to 6% by weight. If it is too small, the initial viscosity will be too high and coating will be difficult, and if it is too large. Not only the physical properties such as water resistance are deteriorated, but also the self-leveling property is significantly deteriorated. It is used when the aqueous resin dispersion of component (B) is produced by emulsion polymerization using a surfactant or a cationic surfactant having two or more sulfonic acid groups in one molecule. These 1 that exist in
A surfactant or a cationic surfactant having two or more sulfonic acid groups in the molecule is also the component (D) of the present invention.

【0021】本発明における(C)成分と(D)成分の
割合(C/D)は0.1〜15、好ましくは0.1〜1
3であり、小さすぎるとセルフレベリング性の改良効果
が小さく、大きすぎると粘度が高くなり過ぎ塗布が困難
になる。
The ratio (C / D) of the components (C) and (D) in the present invention is 0.1 to 15, preferably 0.1 to 1.
When it is too small, the effect of improving the self-leveling property is small, and when it is too large, the viscosity becomes too high and coating becomes difficult.

【0022】本発明において更に含有し得る(E)成分
の骨材としては、珪砂、タルク、マイカ、ケイ藻土、二
水石膏、アモルファスシリカ、カオリン、石英、鉄粉、
フライアッシュ、ウルトラホワイト、酸化チタン、炭酸
カルシウム、石綿粉、ホワイトカーボン、ジルコニア、
カーボンブラック、パーライト、酸化亜鉛、発砲樹脂粒
子、パーライト粒子、ガラス球粒子などが挙げられる。
As the aggregate of the component (E) which can be further contained in the present invention, silica sand, talc, mica, diatomaceous earth, gypsum dihydrate, amorphous silica, kaolin, quartz, iron powder,
Fly ash, ultra white, titanium oxide, calcium carbonate, asbestos powder, white carbon, zirconia,
Examples thereof include carbon black, perlite, zinc oxide, foamed resin particles, perlite particles, glass sphere particles and the like.

【0023】該骨材の使用量は、セメント100重量部
に対し0〜600重量部、好ましくは0〜300重量部
の割合で配合されるものであり、600重量部を越える
とセメントの効果が低下する。
The amount of the aggregate used is 0 to 600 parts by weight, preferably 0 to 300 parts by weight, based on 100 parts by weight of cement. descend.

【0024】また、本発明のセメント組成物は、その塗
工性、乾燥性、硬化性等を考慮して、適宜水を添加する
ことができ、その系中の固形分が50〜90重量%にな
るように調節するのが好ましい。尚、(B)成分の樹脂
水性分散液からの水で使用可能な濃度になっている場合
には言うまでもなく、更に水を添加する必要はない。
Water can be added to the cement composition of the present invention in consideration of its coating property, drying property, curability, etc., and the solid content in the system is 50 to 90% by weight. It is preferable to adjust so that Needless to say, it is not necessary to add further water when the concentration is such that it can be used with water from the resin aqueous dispersion of the component (B).

【0025】本発明のセメント組成物は、得られる塗膜
の性能を損なわない範囲で、更に分散剤、減水剤、遅延
剤、硬化促進剤、湿潤剤、消泡剤、溶剤、可塑剤、造膜
助剤、凍結防止剤、他の増粘剤等の各種添加剤を配合す
ることもできる。
The cement composition of the present invention further contains a dispersant, a water-reducing agent, a retarder, a curing accelerator, a wetting agent, a defoaming agent, a solvent, a plasticizer, and a composition within a range that does not impair the performance of the resulting coating film. Various additives such as a film auxiliary agent, an antifreezing agent, and other thickening agents can also be blended.

【0026】本発明のセメント組成物は、コンクリー
ト、モルタル、スレート、アスファルト、鉄、アルミ、
ファイバー、ガラス、木、布および塩化ビニル、ポリエ
チレンなどのプラスチック類にハケ塗り、鏝塗り、ロー
ラー塗装、吹付けなどの方法で、数十ミクロンオーダー
から数cmの膜厚の塗膜を形成することができる。
The cement composition of the present invention comprises concrete, mortar, slate, asphalt, iron, aluminum,
To form a coating film with a thickness of several tens of microns to several cm by brushing, trowel coating, roller coating, spraying, etc. on fibers, glass, wood, cloth and plastics such as vinyl chloride and polyethylene. You can

【0027】[0027]

【実施例】次に本発明を実施例および比較例を挙げて詳
細に説明する。例中の部および%は特に例記しない限り
重量部および重量%である。 樹脂水性分散液製造例1〜3 いかり型攪拌機温度計および還流冷却機を装着した3L
の4つ口丸底フラスコに水200部を投入して90℃に
加熱し、表1に示す不飽和単量体混合物300部、アニ
オン性界面活性剤としてドデシルベンゼンスルホン酸ナ
トリウムを3部、ノニオン性界面活性剤としてポリオキ
シエチレンノニルフェニルエーテルを1.5部、過硫酸
カリウム2.5部およびイオン交換水100部の混合物
を90℃で4.5時間乳化重合させて、固形分濃度が5
0%、平均粒径0.3ミクロンの樹脂水性分散液を得
た。また、ガラス転移点を示差走査熱量計(DSC)
(デュポン社製装置名:デュポン910)より求めた。
EXAMPLES Next, the present invention will be described in detail with reference to Examples and Comparative Examples. Parts and% in the examples are parts by weight and% by weight, unless otherwise specified. Aqueous Resin Dispersion Production Examples 1 to 3 L equipped with anchor type stirrer thermometer and reflux condenser
200 parts of water was charged into a four-necked round bottom flask and heated to 90 ° C., 300 parts of the unsaturated monomer mixture shown in Table 1, 3 parts of sodium dodecylbenzenesulfonate as an anionic surfactant, and nonion. As a surface active agent, a mixture of 1.5 parts of polyoxyethylene nonylphenyl ether, 2.5 parts of potassium persulfate and 100 parts of ion-exchanged water was emulsion polymerized at 90 ° C. for 4.5 hours to give a solid content concentration of 5
An aqueous resin dispersion with 0% and an average particle size of 0.3 micron was obtained. In addition, the glass transition point is measured by a differential scanning calorimeter (DSC)
(DuPont device name: DuPont 910).

【0028】[0028]

【表1】 [Table 1]

【0029】セメント組成物1の調整 ポルトランドセメント100部に、樹脂水性分散液製造
例1で得られた樹脂水性分散液100部(固形分)、
(C)成分の会合性増粘剤として、ウレタン変性ポリエ
ーテル系高分子(旭電化工業社製 商品名アデカノール
UH−438(有効成分30%))を2.0部、(D)
成分として1分子中に2個以上のスルホン酸基を有する
界面活性剤であるアルキルジフェニルエーテルジスルホ
ン酸ナトリウム(花王社製 商品名ペレックスSS−H
(有効成分50%))を2.0部、ケイ砂100部及び
消泡剤1部を配合してセメント組成物を調整した。
Preparation of Cement Composition 1 100 parts of Portland cement was mixed with 100 parts of resin aqueous dispersion obtained in Production Example 1 of resin aqueous dispersion (solid content),
As the associative thickener for the component (C), 2.0 parts of a urethane-modified polyether polymer (Adekanol UH-438 (Asahi Denka Kogyo Co., Ltd., trade name: 30% active ingredient)), (D)
Sodium alkyldiphenyl ether disulfonate, which is a surfactant having two or more sulfonic acid groups in one molecule as a component (trade name Perex SS-H manufactured by Kao Corporation)
2.0 parts (active ingredient 50%), 100 parts silica sand and 1 part antifoaming agent were mixed to prepare a cement composition.

【0030】得られた組成物の初期および1時間後の粘
度を、B型粘度計(東京計器製)を使用し、ローター回
転数6rpm、60rpmの時の粘度を測定して求め、
この比(6rpm時の粘度÷60rpm時の粘度)より
セルフレベリング性の指標であるTI値を求めた。な
お、TI値は小さい程セルフレベリング性が良いことを
示す。また得られた組成物200gを水平に置いたガラ
ス板上に厚み2mmで表面が均一になるように流し、2
0分経過後にJIS A 5548に規定する標準くし
目ごてを用いて表面を前後左右に荒らし、その後の表面
の回復状態を以下基準で評価して、セルフレベリング性
を確認した。
The viscosity of the obtained composition at the initial stage and after 1 hour was determined by measuring the viscosity at a rotor rotation speed of 6 rpm and 60 rpm using a B type viscometer (manufactured by Tokyo Keiki).
From this ratio (viscosity at 6 rpm / viscosity at 60 rpm), the TI value which is an index of self-leveling property was determined. The smaller the TI value, the better the self-leveling property. In addition, 200 g of the obtained composition was poured on a glass plate placed horizontally so as to have a uniform surface with a thickness of 2 mm.
After the lapse of 0 minutes, the surface was roughened front and back and to the left and right using a standard comb iron specified in JIS A 5548, and the recovery state of the surface was evaluated according to the following criteria to confirm the self-leveling property.

【0031】 結果を表2に示す。なお、表中の(C)成分、(D)成
分の重量(%)は、それぞれの有効成分の重量(%)で
ある。
[0031] Table 2 shows the results. The weight (%) of the components (C) and (D) in the table is the weight (%) of each active ingredient.

【0032】実施例2〜22及び比較例1〜8 樹脂水性分散液の種類、会合性増粘剤の種類及び量、
(D)成分の種類及び量、並びに、骨材の量を表2〜7
に示すように変更した以外は、実施例1と同様にしてセ
メント組成物を調整し、実施例1と同様に評価した。
Examples 2 to 22 and Comparative Examples 1 to 8 Type of aqueous resin dispersion, type and amount of associative thickener,
The types and amounts of component (D) and the amount of aggregate are shown in Tables 2 to 7
A cement composition was prepared in the same manner as in Example 1 except that the cement composition was changed as shown in, and evaluated in the same manner as in Example 1.

【0033】[0033]

【表2】 (注)A*1:ウレタン変性ポリエーテル系高分子(旭電
化工業社製 商品名アデカノールUH−438製) B*2:アルキルジフェニルエーテルジスルホン酸ナトリ
ウム(花王社製商品名ペレックスSS−H)
[Table 2] (Note) A * 1 : Urethane-modified polyether polymer (made by Asahi Denka Co., Ltd., trade name: ADEKANOL UH-438) B * 2 : Sodium alkyldiphenyl ether disulfonate (Kao Corporation, trade name Perex SS-H)

【0034】[0034]

【表3】 [Table 3]

【0035】[0035]

【表4】 (注)C*3:ラウリルトリメチルアンモニウムクロライ
ド(花王社製 商品名コータミン24P)
[Table 4] (Note) C * 3 : Lauryl trimethyl ammonium chloride (trade name Kotamine 24P manufactured by Kao Corporation)

【0036】[0036]

【表5】 [Table 5]

【0037】[0037]

【表6】 [Table 6]

【0038】[0038]

【表7】 [Table 7]

【0039】[0039]

【発明の効果】本発明のセメント組成物は、セルフレベ
リング性及び作業性に優れる。
The cement composition of the present invention is excellent in self-leveling property and workability.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C04B 103:44 111:62 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location C04B 103: 44 111: 62

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】(A)成分:セメント (B)成分:樹脂水性分散液 (C)成分:会合性増粘剤 (D)成分:1分子中に2個以上のスルホン酸基を有す
る界面活性剤又はカチオン性界面活性剤 を含有する組成物であって、該組成物中(C)成分を
0.01〜10重量%、及び(D)成分を0.01〜1
0重量%含有し、かつ(C)成分と(D)成分の割合
(C/D)が0.1〜15であることを特徴とするセメ
ント組成物。
1. Component (A): cement (B) component: aqueous resin dispersion (C) component: associative thickener (D) component: surface active agent having two or more sulfonic acid groups in one molecule. A composition containing an agent or a cationic surfactant, wherein the component (C) is 0.01 to 10% by weight, and the component (D) is 0.01 to 1 by weight.
A cement composition containing 0% by weight and a ratio (C / D) of the component (C) to the component (D) of 0.1 to 15.
【請求項2】 該組成物が更に(E)成分として骨材を
含有することを特徴とするセメント組成物。
2. A cement composition, wherein the composition further contains an aggregate as a component (E).
【請求項3】 該組成物が、(A)成分100重量部に
対して、(B)成分1〜300重量部を含有することを
特徴とするセメント組成物。
3. A cement composition, wherein the composition contains 1 to 300 parts by weight of the component (B) with respect to 100 parts by weight of the component (A).
JP2879496A 1996-02-16 1996-02-16 Cement composition Pending JPH09221350A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2879496A JPH09221350A (en) 1996-02-16 1996-02-16 Cement composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2879496A JPH09221350A (en) 1996-02-16 1996-02-16 Cement composition

Publications (1)

Publication Number Publication Date
JPH09221350A true JPH09221350A (en) 1997-08-26

Family

ID=12258338

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2879496A Pending JPH09221350A (en) 1996-02-16 1996-02-16 Cement composition

Country Status (1)

Country Link
JP (1) JPH09221350A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000086311A (en) * 1998-09-09 2000-03-28 Taiheiyo Cement Corp Cement admixture and cement composition containing the same
JP2003192412A (en) * 2001-12-25 2003-07-09 Asahi Kasei Corp Reforming material for lime based plaster and composition
JP2004067453A (en) * 2002-08-07 2004-03-04 Kao Corp Void filling material and void filling work
JP2005289719A (en) * 2004-03-31 2005-10-20 Ube Ind Ltd High-strength hydraulic composition
JP2014133663A (en) * 2013-01-08 2014-07-24 Matsumoto Yushi Seiyaku Co Ltd Admixture for cement extrusion molding and its use
KR101873488B1 (en) * 2018-02-06 2018-07-02 정태지 Eco-Friendly Mortar Composite for Repair Comprising Function of Preventing Neutralization and Saltdamage and Constructing Methods Using Thereof
KR101974081B1 (en) 2018-08-31 2019-04-30 동진산업개발 주식회사 Construction method using curing for carbonation and chloride prevention of concrete and steel structures
JPWO2020196102A1 (en) * 2019-03-25 2021-10-28 株式会社日本触媒 Additives for hydraulic materials

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000086311A (en) * 1998-09-09 2000-03-28 Taiheiyo Cement Corp Cement admixture and cement composition containing the same
JP2003192412A (en) * 2001-12-25 2003-07-09 Asahi Kasei Corp Reforming material for lime based plaster and composition
JP2004067453A (en) * 2002-08-07 2004-03-04 Kao Corp Void filling material and void filling work
JP2005289719A (en) * 2004-03-31 2005-10-20 Ube Ind Ltd High-strength hydraulic composition
JP2014133663A (en) * 2013-01-08 2014-07-24 Matsumoto Yushi Seiyaku Co Ltd Admixture for cement extrusion molding and its use
KR101873488B1 (en) * 2018-02-06 2018-07-02 정태지 Eco-Friendly Mortar Composite for Repair Comprising Function of Preventing Neutralization and Saltdamage and Constructing Methods Using Thereof
KR101974081B1 (en) 2018-08-31 2019-04-30 동진산업개발 주식회사 Construction method using curing for carbonation and chloride prevention of concrete and steel structures
JPWO2020196102A1 (en) * 2019-03-25 2021-10-28 株式会社日本触媒 Additives for hydraulic materials

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