JPS6013992B2 - Alkali silicate and curing agent compounds for architectural coatings such as wall materials - Google Patents
Alkali silicate and curing agent compounds for architectural coatings such as wall materialsInfo
- Publication number
- JPS6013992B2 JPS6013992B2 JP3269082A JP3269082A JPS6013992B2 JP S6013992 B2 JPS6013992 B2 JP S6013992B2 JP 3269082 A JP3269082 A JP 3269082A JP 3269082 A JP3269082 A JP 3269082A JP S6013992 B2 JPS6013992 B2 JP S6013992B2
- Authority
- JP
- Japan
- Prior art keywords
- alkali silicate
- curing agent
- wall materials
- architectural coatings
- parts
- 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
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
【発明の詳細な説明】
本発明は、壁材等の建築塗料用達酸アルカリ、硬化剤配
合物の改良に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in alkali acid and curing agent formulations for architectural coatings such as wall materials.
珪酸アルカリ、特に蓮酸ソーダは安価であり、多くの材
料、例えば木、紙、コンクリート、金属等に強力な接着
力を有し、且つ、不燃性、耐熱性であることから、接着
剤及び塗料等の原料として有用視されて来ている。Alkali silicates, especially sodium silicates, are inexpensive, have strong adhesion to many materials such as wood, paper, concrete, metal, etc., and are nonflammable and heat resistant, so they are used as adhesives and paints. It is being considered useful as a raw material for etc.
而して、珪酸アルカリは水溶性であるため、これを接着
剤や塗料として用いる場合に、珪酸アルカリ水溶液に、
所謂「硬化剤」を添加しておき、接着、塗料等の工程を
経た後に、室温放置又は加熱することにより、添加した
硬化剤によって該接着剤層、塗料層を硬化させ、水に不
溶化させて所期の目的を達成するものである。Since alkali silicate is water-soluble, when using it as an adhesive or paint, it is added to an aqueous alkali silicate solution.
A so-called "curing agent" is added, and after the adhesion, coating, etc. processes are left at room temperature or heated, the adhesive layer and paint layer are cured by the added curing agent and made insoluble in water. It accomplishes the intended purpose.
この目的のために、従来より蓬酸アルカリ用硬化剤とし
て、著しく多数の物質が研究界発され、特許出願等もな
されてきたのであるが、それらの硬化剤によっては珪酸
アルカリの硬化後に、必要にして十分な耐水性を備えた
接着剤層及び塗料層を未だ形成付与し得ていないのが現
状である。For this purpose, an extremely large number of substances have been developed in research circles and patent applications have been filed as hardening agents for alkali silicate. At present, adhesive layers and paint layers with sufficient water resistance have not yet been formed or applied.
本発明者等は上記の問題に対処し、これを解決するため
に種々研求、検討を重ねた結果、適当な硬化速度をもち
、而も室温で完全に硬化し、且つ硬化後の珪酸アルカ川
こ十分満足できる耐水性を付与し得る硬化剤を見出し、
本発明を完成したのである。即ち、珪酸アルカリ100
重量部(固形分換算)に対し、塩基性炭酸マグネシウム
(M雛C03(OH)2・傘q.)を0.5〜100部
と、必要に応じて、酸化亜鉛(Z対0)及び/又は蓮酸
カルシウム(CaSi03)の0.5〜100部を添加
することにより、硬化後の珪酸アルカリは、必要且つ十
分な耐水性を有する接着剤層及び塗料層を形成できるこ
とを確認したものである。The present inventors have dealt with the above problem, and as a result of various research and studies to solve this problem, the present inventors have developed an alkali silicate material that has an appropriate curing speed, is completely cured at room temperature, and has an alkali silicate material after curing. Kawako discovered a hardening agent that could provide satisfactory water resistance.
The present invention was completed. That is, alkali silicate 100
0.5 to 100 parts of basic magnesium carbonate (M chick C03(OH)2・umbrella q.) per part by weight (solid content) and, if necessary, zinc oxide (Z: 0) and/or It has been confirmed that by adding 0.5 to 100 parts of calcium lotus acid (CaSi03), the alkali silicate after curing can form an adhesive layer and a paint layer that have the necessary and sufficient water resistance. .
従来、蓮酸アルカリ硬化剤としては、例えば珪弗イQ塩
、縮合燐酸アルミニウム、棚酸塩、亜硫酸塩、アルミン
酸塩等の無機物や、アミン棚酸塩、酸ァミド等の有機物
等極めて多数の物質が研究開発され、特許出願等もされ
ているが、これらのうち、あるものは硬化速度が早過ぎ
たり、又は遅過ぎたりして、所謂「可便時間」が適当で
なく、そのため接着、塗装操作が困難である等の欠点が
あり、或はまた、硬化速度は適当であっても、硬化物の
耐水性が不十分なため、硬化後の接着剤層や塗料層が髪
水した際に、溶出して仕舞って実用価値を全く失うとい
う重大な欠点があった。Conventionally, as alkali curing agents for lotus acid, a large number of compounds have been used, such as inorganic substances such as silifluoride Q salts, condensed aluminum phosphates, shelf salts, sulfites, and aluminates, and organic substances such as amine shelf salts and acid amides. Substances have been researched and developed, and patent applications have been filed, but some of these have curing speeds that are too fast or too slow, and the so-called "convenient time" is inappropriate, so adhesives, There are drawbacks such as difficulty in painting operations, or even if the curing speed is appropriate, the water resistance of the cured product is insufficient, so when the adhesive layer or paint layer gets wet after curing, However, it had the serious drawback that it elutes and is stored away, completely losing its practical value.
本発明は、斯かる欠点を完全に解消して、接着、塗装等
の作業を支障なく行い得る「可便時間」を有し、且つ硬
化後も十分に満足できる耐水性、耐候‘性を付与し得る
肇材等の建築塗料用蓮酸アルカリ、硬化剤配合物を提供
することを目的とするものである。The present invention completely eliminates these drawbacks, has a "handy time" that allows work such as gluing and painting to be performed without any trouble, and provides satisfactorily water resistance and weather resistance even after curing. The object of the present invention is to provide an alkali lotus acid and curing agent formulation for architectural coatings such as sillage materials.
以下に実施例を示し、本発明を具体的に詳述する。EXAMPLES The present invention will be specifically explained in detail with reference to Examples below.
なお、実施例では、酸化亜鉛及び/又は葦酸カルシウム
を添加した事例を示したが、これらの二物質は本発明に
おける必須不可欠の成分ではなく、該二物質を添加併用
することにより、硬化物に一層万全の耐水性を付与でき
ることを確認できたものである。In addition, in the examples, examples were shown in which zinc oxide and/or calcium reedate were added, but these two substances are not essential components in the present invention, and by adding and using these two substances together, the cured product can be improved. It was confirmed that even more complete water resistance could be imparted to the product.
〔実施例 1〕
珪酸アルカリ(X20・nSi02)〔Xはアルカリ金
属、nは1〜4.2〕、例えばJIS蓬酸ソーダ2号1
00重量部、塩基性炭酸マグネシウム(M&C03(O
H)2・傘q.)3の重量部、酸化亜鉛(Zn0)10
重量部、蓮砂(豊浦標準砂)30広重量部から成る壁材
等の建築塗料用珪酸アルカリ、硬化剤配合物に、水12
の重量部を加え、室温にて数分間混練したものを木、ス
レート板、コンクリート(ボルトランドセメント:砂=
1:3)等の面上に2側厚に吹付け、こてぬり等により
塗装した。[Example 1] Alkali silicate (X20・nSi02) [X is an alkali metal, n is 1 to 4.2], for example, JIS sodium oxalate No. 2 1
00 parts by weight, basic magnesium carbonate (M&C03(O
H) 2. Umbrella q. ) 3 parts by weight, zinc oxide (Zn0) 10
Add 12 parts by weight of water to an alkali silicate and curing agent compound for architectural paints such as wall materials, which consists of 30 parts by weight of lotus sand (Toyoura standard sand).
of wood, slate, concrete (Boltland cement: sand =
1:3), etc., by spraying two sides thick and painting with a trowel.
該混線物の可便時間は、温度23℃、R.日.60%で
約3時間であり、塗装作業に適する可便時間であった。
上記塗装面を室温(230)で2独時間放置した結果、
完全に硬化したが、この試料を更に室温で3日間放置し
たものについて、建築用無機塗料材としてJIS一A一
6910によって性能試験を行った結果は次表に示すと
おりである。〔実施例 2〕
珪酸ソーダ、例えばJIS3号粉末瑳酸ソーダ100部
、塩基性炭酸マグネシウム10の邦、珪酸カルシウム(
CaSiQ)粉末20部、蓬砂(豊浦標準砂)30庇部
、合成樹脂粉末(例えばへキスト社「モビニールDM一
300」粉末アクリル系樹脂)5部、から成る壁材等で
建築塗料用珪酸アルカリ、硬化剤配合物に、水25の部
をよく濃練し、これをスレ−ト板、A.L.C.板等の
面上に吹付塗装し、2肋厚に施工した。The contaminant's availability time is at a temperature of 23°C and an R. Day. It took about 3 hours at 60%, which was a convenient time suitable for painting work.
As a result of leaving the above painted surface at room temperature (230) for 2 hours,
After being completely cured, this sample was further left at room temperature for 3 days and was subjected to a performance test as an architectural inorganic paint material according to JIS-A-6910.The results are shown in the following table. [Example 2] Sodium silicate, for example, 100 parts of JIS No. 3 powdered sodium silicate, 10 parts of basic magnesium carbonate, calcium silicate (
An alkali silicate for architectural paint for wall materials, etc., consisting of 20 parts of CaSiQ) powder, 30 parts of Japanese sand (Toyoura standard sand), and 5 parts of synthetic resin powder (for example, Hoechst's "Movinyl DM-300" powdered acrylic resin). , 25 parts of water was thoroughly stirred into the curing agent formulation, and the mixture was mixed onto a slate plate. L. C. It was spray-painted on the surface of the board, etc., and was applied to a thickness of 2 ribs.
該混糠物の可便時間は室温(23℃)で約2時間であり
、塗装したものを室温で3日間放置した後、前記JIS
一A一6910によって品質を検当した結果、実施例1
の場合と同様に全試験項目に合格した。なお、合成樹脂
を添加したことによって、透水性は更に改良されていた
。The potability time of the bran mixture is about 2 hours at room temperature (23°C), and after leaving the coated material at room temperature for 3 days, the above-mentioned JIS
As a result of quality inspection using 1A-6910, Example 1
As in the case of , all test items were passed. Note that water permeability was further improved by adding synthetic resin.
Claims (1)
ルカリ金属、即ち、Li,K,Na等。 nは1〜4.2〕100重量部(固形分として)に対し
、塩基性炭酸マグネシウム(Mg_2CO_3(OH)
_2・4aq.)〔固形分換算〕0.5〜100部を添
加してなることを特徴とする壁材等の建築塗料用珪酸ア
ルカリ、硬化剤配合物。[Claims] 1 Alkali silicate (X_2O·nSiO_2) [X is an alkali metal, ie, Li, K, Na, etc. n is 1 to 4.2] Basic magnesium carbonate (Mg_2CO_3(OH)
_2・4aq. ) An alkali silicate and curing agent compound for architectural coatings such as wall materials, characterized in that it contains 0.5 to 100 parts (in terms of solid content).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3269082A JPS6013992B2 (en) | 1982-03-01 | 1982-03-01 | Alkali silicate and curing agent compounds for architectural coatings such as wall materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3269082A JPS6013992B2 (en) | 1982-03-01 | 1982-03-01 | Alkali silicate and curing agent compounds for architectural coatings such as wall materials |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58151357A JPS58151357A (en) | 1983-09-08 |
JPS6013992B2 true JPS6013992B2 (en) | 1985-04-10 |
Family
ID=12365853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3269082A Expired JPS6013992B2 (en) | 1982-03-01 | 1982-03-01 | Alkali silicate and curing agent compounds for architectural coatings such as wall materials |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6013992B2 (en) |
-
1982
- 1982-03-01 JP JP3269082A patent/JPS6013992B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS58151357A (en) | 1983-09-08 |
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