JPH028988B2 - - Google Patents

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Publication number
JPH028988B2
JPH028988B2 JP9808686A JP9808686A JPH028988B2 JP H028988 B2 JPH028988 B2 JP H028988B2 JP 9808686 A JP9808686 A JP 9808686A JP 9808686 A JP9808686 A JP 9808686A JP H028988 B2 JPH028988 B2 JP H028988B2
Authority
JP
Japan
Prior art keywords
weight
parts
atactic polypropylene
molecular weight
water
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
JP9808686A
Other languages
Japanese (ja)
Other versions
JPS62256749A (en
Inventor
Kyoji Naruse
Asahi Azuma
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.)
KITSUKOONA KK
Original Assignee
KITSUKOONA KK
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 KITSUKOONA KK filed Critical KITSUKOONA KK
Priority to JP9808686A priority Critical patent/JPS62256749A/en
Publication of JPS62256749A publication Critical patent/JPS62256749A/en
Publication of JPH028988B2 publication Critical patent/JPH028988B2/ja
Granted legal-status Critical Current

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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
    • C04B24/2611Polyalkenes

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)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 この発明は、セメントモルタルの白華(エフロ
レツセンス)現象を防止する方法に関し、より詳
しくは、セメントモルタル中に高分子量アタクチ
ツクポリプロピレン水性エマルジヨン組成物を配
合することによつてセメントモルタルの白華現象
を防止する方法に関する。 〔従来の技術〕 モルタルの白華現象は、モルタルが外部から水
分を吸収すると炭酸カルシユウムが溶解して外部
へ溶け出し、再び白い炭酸カルシユウムの結晶が
析出する現象である。白華現象はモルタル外壁に
タイルやその他化粧材を施こしてある場合、白い
結晶が美観を著しく損う。 白華現象を生じた外壁は希塩酸などを用いて、
炭酸カルシユウムを溶解除去するが、間をおか
ず、再び白色結晶を析出し始めるため、その対策
は非常にやつかいであつて、これまで満足すべき
解決策は見出されていない。 〔発明が解決しようとする問題点〕 本発明の目的はセメントモルタルの白華現象の
発生そのものを有効に防止する方法を提供するに
ある。 〔問題点を解決するための手段〕 本発明のセメントモルタルの白華現象の防止方
法は、セメントモルタルに対し、該セメントモル
タル中のセメント100重量部に基づき、0.5重量部
以上(固型分換算)の高分子量アタクチツクポリ
プロピレン水性エマルジヨン組成物を配合するこ
とを特徴とし、且つ、該高分子量アタクチツクポ
リプロピレン水性エマルジヨン組成物は平均分子
量約3000〜約30000を有し実質的にアタクチツク
なポリプロピレン、該ポリプロピレン1重量部あ
たり0.03〜0.5重量部の部分ケン化ポリビニルア
ルコールおよび該部分ケン化ポリビニルアルコー
ル1重量部あたり約0.05〜2重量部の水からなる
均一混練物を水中に分散してなるものであること
を特徴とする。 上述の方法で用いる高分子量アタクチツクポリ
プロピレン水性エマルジヨン組成物に代えて、平
均分子量約3000〜約30000を有し実質的にアタク
チツクなポリプロピレン、該アタクチツクポリプ
ロピレン1重量部あたり0.03〜0.5重量部の分散
剤および該分散剤1重量部あたり約0.05〜2重量
部の水を剪断力を付与しながら混練し、得られた
均一混練物を水および上記アタクチツクポリプロ
ピレン1重量部あたり0.5〜2.0重量部のアスフア
ルトと混合してなるものを用いてもよい。 本発明方法の主眼は、モルタル自体を水密化し
て、炭酸カルシユウムの溶解を防ぐ点にある。 セメントモルタルとしては、そのまま使用した
ときに白華現象を生じるようなものであればいず
れも本発明の対象となる。 セメントモルタルに配合する高分子量アタクチ
ツクポリプロピレン組成物は、平均分子量約3000
〜約30000を有し実質的にアタクチツクなポリプ
ロピレン、該ポリプロピレン1重量部当り0.03〜
0.5重量部の部分ケン化ポリビニルアルコールお
よび該部分ケン化ポリビニルアルコール1重量部
当り約0.05〜2重量部の水からなる均一混練物を
水中に分散してなるものである。 ここにおいて使用する「実質的にアタクチツク
なポリプロピレン」とは、アタクチツクポリプロ
ピレンを主成分とし、これと少量のアイソタクチ
ツクまたはシンジオタクチツクの如き立体特異性
構造を有するポリプロピレンの低分子量体との混
合物を指し、これは通常、立体特異性触媒による
ポリプロピレンの重合時に重合生成物をn−ヘプ
タンの如き溶剤で抽出することによつて得られ
る。アタクチツクポリプロピレンに対する部分ケ
ン化ポリビニルアルコールの配合量はアタクチツ
クポリプロピレン1重量部に対し0.03〜0.5重量
部、好ましくは0.05〜0.3重量部である。アタク
チツクポリプロピレンに対し乳化剤として作用す
ると考えられる部分ケン化ポリビニルアルコール
はケン化度70〜98%、特に80〜97%のものが好ま
しい。 水の配合量は、主として部分ケン化ポリビニル
アルコールの使用量に依存して変るが、通常部分
ケン化ポリビニルアルコール1重量部あたり約
0.05〜2重量部、好ましくは約0.1〜2重量部の
範囲で使用する。部分ケン化ポリビニルアルコー
ルとほぼ等重量乃至1.5倍量の水を用いて混練す
ると最も良好なエマルジヨンが得られる。 なお、アタクチツクポリプロピレン、部分ケン
化ポリビニルアルコールおよび水の三者に少量の
石油樹脂を併用することによつて生成するエマル
ジヨンの安定性は一層向上する。石油樹脂として
は、シクロペンタジエンを主原料とするもの、高
級オレフイン系炭化水素を主原料とするものいず
れも使用できるが、常温で固体のものが好まし
い。石油樹脂の配合量は高分子量アタクチツクポ
リプロピレン1重量部に対し約0.05〜約0.2重量
部が好ましい。 また、部分ケン化ポリビニルアルコールに加え
て少量の常用される分散剤、例えばオレイン酸ソ
ーダおよびステアリン酸ソーダの如きアニオン活
性剤やポリオキシエチレンアルキルフエノールエ
ーテルの如きノニオン活性剤を併用してもよい。 また、上述の高分子量アタクチツクポリプロピ
レン水性エマルジヨン組成物にアスフアルトを加
えてもよい。 ここで使用するアスフアルトとは、メジウムま
たはペトローレン、マルテンと呼ばれる炭化水素
油状成分を主成分とし、アスフアルト樹脂とよば
れる保護質およびコロイド粒子状ないし超微粒子
状炭素からなるビチユーメンを指し、天然アスフ
アルトであつてもまた石油アスフアルトであつて
もよい。概して、融点が約60℃〜約160℃の範囲
のものである。高分子量アタクチツク重合体に対
するアスフアルトの配合量は前者1重量部あたり
0.5〜2.0重量部、好ましくは0.7〜1.5重量部であ
る。高分子量アタクチツクポリプロピレンに対す
るアスフアルトの割合があまり高くなるとエマル
ジヨンの安定性が損われる。エマルジヨン状組成
物を製造するには、まず高分子量アタクチツクポ
リプロピレン、部分ケン化ポリビニルアルコール
および水、さらに要すれば石油樹脂を充分に均一
混練する。混練手段としては、従来公知のいかな
る方法でもよく、例えばニーダー、バンバリーミ
キサーが好適に採用出来る。混練すべき物質の仕
込順序には特に制限はないが、前記三者または四
者を同時に混練機に投入するか、あるいは水溶性
高分子と水とのペースト状またはパテ状の混合物
をあらかじめ調整しこれをアタクチツクポリプロ
ピレンと混練するのがよい。均一混練をより効果
的に達成するためには、混練を加温下に行うのが
よい。アスフアルトを加える場合は先ず高分子量
アタクチツクポリプロピレンの水性エマルジヨン
を調製しこれを加熱溶融せるアスフアルトおよび
水と混合する。 かくして得られた均一混練物質は、次いで多量
の水と均一混合することにより、直ちに安定なエ
マルジヨン状となり、ここに高分子量アタクチツ
クポリプロピレンのエマルジヨン状組成物が形成
される。なお、該組成物の低温での安定性をよく
するために、温度を低下してほぼ常温で混練物質
と水を均一混合するのが望ましい。得られる水性
エマルジヨンは非常に安定で、温度変化、長期間
の放置および水による希釈によつて殆ど変化しな
い。一般に、水性エマルジヨン中の高分子量アタ
クチツク重合体濃度が30〜60重量%程度とするの
が望ましい。 高分子量アタクチツクポリプロピレン水性エマ
ルジヨン組成物のセメントモルタルへの混入量は
モルタルに使用されるセメント100重量部に対し、
エマルジヨンは0.5重量部以上(固型分換算)で
あれば良く、普通はモルタルの諸性能への効果を
考えて1〜3重量部混入する。 エマルジヨンの混入方法としては、生コンクリ
ート工場のバツチヤーでモルタルを混練する際、
エマルジヨンも同時に混合する方法、或は生モル
タル輸送用トラツクアジテーターにエマルジヨン
を投入し、高速で3分間程度混練する方法、更に
は、建築現場で使用するモルタルミキサーにエマ
ルジヨンを投入して混練する方法のいずれも採用
可能である。 〔発明の効果〕 本発明方法によれば高分子量アタクチツクポリ
プロピレン組成物がモルタルの空隙に充填される
結果、水密となり、モルタルに水分が吸収され難
くなり、炭酸カルシウムの溶出に基づく白華現象
が防止される。また、モルタルの乾燥収縮率が減
少し、モルタルにひび割れが生じ難くなる。 〔実施例〕 以下、実施例について本発明を具体的に説明す
る。 実施例1,2、比較例1 下記の化合物 アタクチツクポリプロピレン(平均分子量約
21000) 1000g 石油樹脂60#(東邦樹脂製) 95g ポリビニルアルコール(ケン化度88%)(日本
合成化学PVA217) 150g 水 150g を加圧されたニーダー中で内部温度90℃にて20分
間混練し、次いで60℃にて水300gを添加混合し、
更に多量の冷水を添加して10分間混合し、固形分
50重量%のエマルジヨン状組成物を得た。 セメントモルタルに上記エマルジヨン状組成物
を下記表1に示す割合(B)で配合し、その硬化
物の吸水比および透水比をテストした(実施例
1)。結果を表1に示す。 比較のために、上記エマルジヨン状組成物を配
合しない普通モルタル(A)について同様にテス
トした(比較例1)。結果を表1に示す。 また、上記エマルジヨン状組成物(60℃)に約
150℃のアスフアルトを徐々に添加し(配合割合
はエマルジヨン中のアタクチツクポリプロピレン
1重量部に対しアスフアルト1.4重量部)、添加終
了後約10分間撹拌して、アスフアルト含有水性エ
マルジヨン組成物を得た。この組成物をセメント
モルタルに配合したもの(C)についても同様に
テストした(実施例2)。結果を表1に示す。
[Industrial Application Field] The present invention relates to a method for preventing the efflorescence phenomenon of cement mortar, and more specifically, to a method for preventing the efflorescence phenomenon in cement mortar. The present invention therefore relates to a method for preventing efflorescence of cement mortar. [Prior Art] Mortar efflorescence is a phenomenon in which when mortar absorbs moisture from the outside, calcium carbonate dissolves and leaks out to the outside, and white calcium carbonate crystals precipitate again. Efflorescence occurs when tiles or other decorative materials are applied to mortar exterior walls, and the white crystals significantly impair the aesthetic appearance. Exterior walls with efflorescence can be cleaned using dilute hydrochloric acid, etc.
Calcium carbonate is dissolved and removed, but white crystals begin to precipitate again soon afterward, and countermeasures to this problem are extremely difficult, and no satisfactory solution has been found to date. [Problems to be Solved by the Invention] An object of the present invention is to provide a method for effectively preventing the occurrence of efflorescence itself in cement mortar. [Means for Solving the Problems] The method for preventing the efflorescence phenomenon of cement mortar of the present invention is to prevent the efflorescence phenomenon of cement mortar by adding 0.5 parts by weight or more (in terms of solid content) to cement mortar based on 100 parts by weight of cement in the cement mortar. ), and the high molecular weight atactic polypropylene aqueous emulsion composition has an average molecular weight of about 3,000 to about 30,000 and contains substantially atactic polypropylene; It is made by dispersing in water a homogeneous kneaded product consisting of 0.03 to 0.5 parts by weight of partially saponified polyvinyl alcohol per 1 part by weight of polypropylene and about 0.05 to 2 parts by weight of water per 1 part by weight of the partially saponified polyvinyl alcohol. It is characterized by In place of the high molecular weight atactic polypropylene aqueous emulsion composition used in the above-described method, a dispersion of substantially atactic polypropylene having an average molecular weight of about 3,000 to about 30,000, 0.03 to 0.5 part by weight per part by weight of the atactic polypropylene. About 0.05 to 2 parts by weight of water per 1 part by weight of the atactic agent and the dispersant are kneaded while applying a shearing force, and the resulting homogeneous kneaded product is mixed with water and about 0.5 to 2.0 parts by weight per 1 part by weight of the above-mentioned atactic polypropylene. A material mixed with asphalt may also be used. The main focus of the method of the present invention is to make the mortar itself watertight and prevent dissolution of calcium carbonate. Any cement mortar that causes efflorescence when used as is is subject to the present invention. The high molecular weight atactic polypropylene composition used in cement mortar has an average molecular weight of approximately 3000.
~30,000 and substantially attic polypropylene, from 0.03 per part by weight of the polypropylene
It is prepared by dispersing in water a homogeneous kneaded product consisting of 0.5 part by weight of partially saponified polyvinyl alcohol and about 0.05 to 2 parts by weight of water per 1 part by weight of the partially saponified polyvinyl alcohol. As used herein, "substantially atactic polypropylene" refers to a mixture containing atactic polypropylene as a main component and a small amount of low molecular weight polypropylene having a stereospecific structure such as isotactic or syndiotactic. , which is usually obtained during stereospecific catalyzed polymerization of polypropylene by extracting the polymerized product with a solvent such as n-heptane. The amount of partially saponified polyvinyl alcohol added to the atactic polypropylene is 0.03 to 0.5 part by weight, preferably 0.05 to 0.3 part by weight, per 1 part by weight of the atactic polypropylene. The partially saponified polyvinyl alcohol which is considered to act as an emulsifier for atactic polypropylene preferably has a degree of saponification of 70 to 98%, particularly 80 to 97%. The amount of water mixed mainly depends on the amount of partially saponified polyvinyl alcohol used, but it is usually about 1 part by weight of partially saponified polyvinyl alcohol.
It is used in a range of 0.05 to 2 parts by weight, preferably about 0.1 to 2 parts by weight. The best emulsion can be obtained by kneading with approximately the same weight to 1.5 times the amount of water as the partially saponified polyvinyl alcohol. Note that the stability of the emulsion produced is further improved by using a small amount of petroleum resin in combination with atactic polypropylene, partially saponified polyvinyl alcohol, and water. As the petroleum resin, either one whose main raw material is cyclopentadiene or one whose main raw material is a higher olefinic hydrocarbon can be used, but one that is solid at room temperature is preferable. The amount of petroleum resin blended is preferably about 0.05 to about 0.2 parts by weight per 1 part by weight of high molecular weight atactic polypropylene. In addition to the partially saponified polyvinyl alcohol, small amounts of commonly used dispersants, such as anionic activators such as sodium oleate and sodium stearate, and nonionic activators such as polyoxyethylene alkyl phenol ether, may also be used. Asphalt may also be added to the above-described high molecular weight atactic polypropylene aqueous emulsion composition. Asphalt as used here refers to a bitumen whose main component is a hydrocarbon oil component called medium, petrolene, or marten, a protective substance called asphalt resin, and colloidal particulate or ultrafine particulate carbon, and is natural asphalt. It may also be petroleum asphalt. Generally, the melting point will be in the range of about 60°C to about 160°C. The amount of asphalt added to the high molecular weight atactic polymer is per 1 part by weight of the former.
It is 0.5 to 2.0 parts by weight, preferably 0.7 to 1.5 parts by weight. If the ratio of asphalt to high molecular weight atactic polypropylene is too high, the stability of the emulsion will be impaired. In order to produce an emulsion-like composition, first, high molecular weight atactic polypropylene, partially saponified polyvinyl alcohol, water, and, if necessary, a petroleum resin are sufficiently and uniformly kneaded. As the kneading means, any conventionally known method may be used, such as a kneader or a Banbury mixer. There is no particular restriction on the order in which the substances to be kneaded are added, but the above three or four substances may be added to the kneader at the same time, or a paste or putty-like mixture of water-soluble polymer and water may be prepared in advance. This is preferably kneaded with atactic polypropylene. In order to achieve uniform kneading more effectively, kneading is preferably carried out under heating. When asphalt is added, an aqueous emulsion of high molecular weight atactic polypropylene is first prepared and mixed with heat-melted asphalt and water. The homogeneously kneaded material thus obtained is then uniformly mixed with a large amount of water to immediately form a stable emulsion, thereby forming an emulsion-like composition of high molecular weight atactic polypropylene. In order to improve the stability of the composition at low temperatures, it is desirable to lower the temperature and uniformly mix the kneaded material and water at approximately room temperature. The resulting aqueous emulsion is very stable and changes little with temperature changes, long-term standing and dilution with water. Generally, it is desirable that the concentration of the high molecular weight atactic polymer in the aqueous emulsion be about 30 to 60% by weight. The amount of high molecular weight atactic polypropylene aqueous emulsion composition mixed into cement mortar is as follows:
It is sufficient that the emulsion is 0.5 part by weight or more (in terms of solid content), and usually 1 to 3 parts by weight is mixed in consideration of the effect on various properties of the mortar. The emulsion is mixed in when mixing mortar in a batcher at a ready-mixed concrete factory.
There are two methods: mixing the emulsion at the same time, or putting the emulsion into a truck agitator for transporting raw mortar and kneading it at high speed for about 3 minutes, or putting the emulsion into a mortar mixer used at construction sites and kneading it. All of them can be adopted. [Effects of the Invention] According to the method of the present invention, the high molecular weight atactic polypropylene composition is filled into the voids of the mortar, making it watertight, making it difficult for the mortar to absorb moisture, and preventing the efflorescence phenomenon caused by the elution of calcium carbonate. Prevented. Furthermore, the drying shrinkage rate of the mortar is reduced, making it difficult for the mortar to crack. [Example] The present invention will be specifically described below with reference to Examples. Examples 1 and 2, Comparative Example 1 The following compounds Atactic polypropylene (average molecular weight approx.
21000) 1000g petroleum resin 60# (manufactured by Toho Plastics) 95g polyvinyl alcohol (degree of saponification 88%) (Nippon Gosei PVA217) 150g water 150g was kneaded for 20 minutes at an internal temperature of 90℃ in a pressurized kneader. Next, add and mix 300g of water at 60℃,
Add more cold water and mix for 10 minutes to reduce the solids content.
A 50% by weight emulsion-like composition was obtained. The above emulsion-like composition was blended into cement mortar in the ratio (B) shown in Table 1 below, and the water absorption ratio and water permeability ratio of the cured product were tested (Example 1). The results are shown in Table 1. For comparison, ordinary mortar (A) without the emulsion-like composition was similarly tested (Comparative Example 1). The results are shown in Table 1. In addition, the above emulsion composition (at 60°C)
Asphalt at 150° C. was gradually added (blending ratio: 1.4 parts by weight of asphalt per 1 part by weight of atactic polypropylene in the emulsion), and after the addition was completed, stirring was carried out for about 10 minutes to obtain an asphalt-containing aqueous emulsion composition. A similar test (C) in which this composition was blended with cement mortar was conducted (Example 2). The results are shown in Table 1.

【表】 透した深さを測定。
上記B配合のモルタルにてコンクリート造の外
壁に塗布し、その上からタイル貼りした。3ケ年
を経過するが、白華現象は全く見られない。
[Table] Measure the depth of penetration.
Mortar of the above blend B was applied to the concrete exterior wall, and tiles were pasted on top. Three years have passed, but no efflorescence has been observed.

Claims (1)

【特許請求の範囲】 1 セメントモルタルに対し、該セメントモルタ
ル中のセメント100重量部に基づき、0.5重量部以
上(固型分換算)の高分子量アタクチツクポリプ
ロピレン水性エマルジヨン組成物を配合すること
を特徴とし、且つ、該高分子量アタクチツクポリ
プロピレン水性エマルジヨン組成物は平均分子量
約3000〜約30000を有し実質的にアタクチツクな
ポリプロピレン、該ポリプロピレン1重量部あた
り0.03〜0.5重量部の部分ケン化ポリビニルアル
コールおよび該部分ケン化ポリビニルアルコール
1重量部あたり約0.05〜2重量部の水からなる均
一混練物を水中に分散してなるものであることを
特徴とするセメントモルタルの白華現象を防止す
る方法。 2 セメントモルタルに対し、該セメントモルタ
ル中のセメント100重量部に基づき、0.5重量部以
上(固型分換算)の高分子量アタクチツクポリプ
ロピレン水性エマルジヨン組成物を配合すること
を特徴とし、且つ、該高分子量アタクチツクポリ
プロピレン水性エマルジヨン組成物は平均分子量
約3000〜約30000を有し実質的にアタクチツクな
ポリプロピレン、該アタクチツクポリプロピレン
1重量部あたり0.03〜0.5重量部の分散剤および
該分散剤1重量部あたり約0.05〜2重量部の水を
剪断力を付与しながら混練し、得られた均一混練
物を水および上記アタクチツクポリプロピレン1
重量部あたり0.5〜2.0重量部のアスフアルトと混
合してなるものであることを特徴とするセメント
モルタルの白華現象を防止する方法。
[Claims] 1. A cement mortar is blended with 0.5 parts by weight or more (in terms of solid content) of a high molecular weight atactic polypropylene aqueous emulsion composition based on 100 parts by weight of cement in the cement mortar. and the high molecular weight atactic polypropylene aqueous emulsion composition comprises substantially atactic polypropylene having an average molecular weight of about 3,000 to about 30,000, 0.03 to 0.5 parts by weight of partially saponified polyvinyl alcohol per 1 part by weight of the polypropylene, and A method for preventing efflorescence in cement mortar, comprising dispersing in water a homogeneous kneaded material consisting of about 0.05 to 2 parts by weight of water per 1 part by weight of the partially saponified polyvinyl alcohol. 2. A high molecular weight atactic polypropylene aqueous emulsion composition of 0.5 parts by weight or more (in terms of solid content) is blended into the cement mortar based on 100 parts by weight of cement in the cement mortar, and The molecular weight atactic polypropylene aqueous emulsion composition comprises a substantially atactic polypropylene having an average molecular weight of from about 3,000 to about 30,000, from 0.03 to 0.5 parts by weight of a dispersant per part by weight of the atactic polypropylene, and per part by weight of the dispersant. Approximately 0.05 to 2 parts by weight of water is kneaded while applying a shearing force, and the resulting homogeneous kneaded product is mixed with water and the above-mentioned atactic polypropylene 1.
A method for preventing efflorescence in cement mortar, characterized in that it is mixed with asphalt in an amount of 0.5 to 2.0 parts by weight.
JP9808686A 1986-04-30 1986-04-30 Prevention of efflorescence of cement mortar Granted JPS62256749A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9808686A JPS62256749A (en) 1986-04-30 1986-04-30 Prevention of efflorescence of cement mortar

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9808686A JPS62256749A (en) 1986-04-30 1986-04-30 Prevention of efflorescence of cement mortar

Publications (2)

Publication Number Publication Date
JPS62256749A JPS62256749A (en) 1987-11-09
JPH028988B2 true JPH028988B2 (en) 1990-02-28

Family

ID=14210531

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9808686A Granted JPS62256749A (en) 1986-04-30 1986-04-30 Prevention of efflorescence of cement mortar

Country Status (1)

Country Link
JP (1) JPS62256749A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5922124A (en) * 1997-09-12 1999-07-13 Supplee; William W. Additive for, method of adding thereof and resulting cured cement-type concreations for improved heat and freeze-thaw durability
JP2011001222A (en) * 2009-06-18 2011-01-06 Ohbayashi Corp Polymer cement mortar and finishing method

Also Published As

Publication number Publication date
JPS62256749A (en) 1987-11-09

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