JPS5935856B2 - Curing composition - Google Patents

Curing composition

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Publication number
JPS5935856B2
JPS5935856B2 JP11274781A JP11274781A JPS5935856B2 JP S5935856 B2 JPS5935856 B2 JP S5935856B2 JP 11274781 A JP11274781 A JP 11274781A JP 11274781 A JP11274781 A JP 11274781A JP S5935856 B2 JPS5935856 B2 JP S5935856B2
Authority
JP
Japan
Prior art keywords
silica sol
powder
weight
present
suspension
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
JP11274781A
Other languages
Japanese (ja)
Other versions
JPS5815059A (en
Inventor
正恒 菊地
能彦 岡田
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.)
Onoda Cement Co Ltd
Original Assignee
Onoda Cement 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 Onoda Cement Co Ltd filed Critical Onoda Cement Co Ltd
Priority to JP11274781A priority Critical patent/JPS5935856B2/en
Publication of JPS5815059A publication Critical patent/JPS5815059A/en
Publication of JPS5935856B2 publication Critical patent/JPS5935856B2/en
Expired legal-status Critical Current

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  • Aftertreatments Of Artificial And Natural Stones (AREA)
  • Silicon Compounds (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】 本発明はシリカゾルを主原料としコーチング材料、接着
材、充填材として好適な硬化組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cured composition containing silica sol as a main raw material and suitable as a coating material, adhesive, or filler.

コーチング材は従来、主として有機系のエマルジョンが
使用されてきた。
Conventionally, organic emulsions have been mainly used as coating materials.

ところが最近公害防止の観点から無機系材料が望まれて
おり、これに応するものとしてシリカゾルを用いたもの
が提案されている。
However, recently, inorganic materials have been desired from the viewpoint of pollution prevention, and in response to this demand, materials using silica sol have been proposed.

その一例としてシリカゾル等の可溶シリカ化合物に鉛、
亜鉛、クロム、ニッケル等の金属化合物および雲母等の
増量材を混合した無機系エマルジョンのコーチング材が
知られているが、これらのものも鉛、クロム等の有害重
金属を含むため結局公害防止の点からは不充分である。
As an example, lead is added to soluble silica compounds such as silica sol.
Inorganic emulsion coating materials are known, which are made by mixing metal compounds such as zinc, chromium, and nickel, and extenders such as mica, but these also contain harmful heavy metals such as lead and chromium, so they end up being a problem in preventing pollution. It is insufficient.

本発明は鉛、クロム等の有害重金属を含まず、しかも硬
化強度の大きい無機系硬化組成物を提供するものであっ
て、その構成は、シリカゾルを主成分としこれに明パン
石粉末を混合してなることを特徴とする。
The present invention provides an inorganic curing composition that does not contain harmful heavy metals such as lead and chromium and has a high curing strength, and its composition is composed of silica sol as a main component and aarkanite powder mixed therein. It is characterized by being

以下に本発明を実施例と共に詳細に説明する。The present invention will be explained in detail below along with examples.

本発明の硬化組成物はシリカゾルを主成分とし、これに
明パン石粉末を混合してなるものである。
The cured composition of the present invention has silica sol as its main component, and is made by mixing amaranthite powder therein.

ここでシリカゾルとは微細なSiO2粒子が水に懸濁し
たコロイド溶液であり、例えば10〜20mμ粒度のS
iO□粒子が水に懸濁した2、0〜0.05%のアルカ
リ(Na20+に20)を含む溶液を云う。
Here, silica sol is a colloidal solution in which fine SiO2 particles are suspended in water, for example, S with a particle size of 10 to 20 mμ.
It refers to a solution containing 2.0 to 0.05% alkali (20 to Na20+) in which iO□ particles are suspended in water.

一般にはカタロイド(商品名)、コロイダルシリカ(商
品名)等を用いることかできる。
In general, Cataloid (trade name), Colloidal Silica (trade name), etc. can be used.

又、明パン石とはAlとKないしNaとの塩基性硫酸塩
鉱物でありNaAl 3(SO4)2(OH)aおよび
KAI a (SO4) 2 (OH) csあるいは
これらの無水物の化学成分を含むものである。
Alcanite is a basic sulfate mineral of Al and K or Na, and its chemical components are NaAl 3 (SO4) 2 (OH) a and KAI a (SO4) 2 (OH) cs or anhydrides thereof. This includes:

次に上記シリカゾルと明パン石粉末との配合比は用途、
シリカゾルの種類、明パン石の粒度等によっても種々異
なるが、一般的には通常の7リカゾルの場合にシリカゾ
ル中のシリカ含有量に対し明ばん石粉末を0.5〜85
0重量%用いるが、コーチング材料、充填材として用い
る場合は明ばん石粉末を0.5〜200重量%用いるの
が好ましく、5〜100重量%用いるのがより好ましい
Next, the blending ratio of the silica sol and Akpanite powder is determined based on the application.
Although it varies depending on the type of silica sol and the particle size of the alumite, generally, in the case of a normal 7-lika sol, the amount of alumite powder is 0.5 to 85% of the silica content in the silica sol.
When used as a coating material or filler, the alumite powder is preferably used in an amount of 0.5 to 200 weight %, more preferably 5 to 100 weight %.

また接着材として用いる場合は明ばん石粉末を300〜
850重量%用いるのが好ましく、500〜800重量
%用いるのがより好ましい。
Also, when using it as an adhesive, use alumite powder of 300~
It is preferable to use 850% by weight, and more preferably 500 to 800% by weight.

同様に明パン石粉末の粒度も硬化組成物の用途等によっ
てその最適範囲が異なる。
Similarly, the optimum range of the particle size of the acanthrite powder differs depending on the use of the curing composition.

更にシリカゾルと明パン石粉末との懸濁液についてその
懸濁状態の安定性は明パン石の粉末度に依存する。
Furthermore, the stability of the suspension of silica sol and Alarkite powder depends on the fineness of Alarkite.

例えば10μ以下に粉砕した明パン石を適量懸濁させた
ものは約1日間安定である。
For example, a suspension of an appropriate amount of alumite crushed to a size of 10 μm or less is stable for about one day.

このように明パン石の粒度は種々の条件によってその最
適範囲が異なるが一般的には50μ以下であればよい。
As described above, the optimum particle size of Alpanite varies depending on various conditions, but generally it is sufficient that it is 50 μm or less.

上記硬化組成物において、シリカゾルと明パン石粉末は
充分な水の存在状態下では互いに反応しないが、水の蒸
発によりこれらの反応が進みガラス状の強固で安定な硬
化体が得られる。
In the above-mentioned cured composition, the silica sol and the light starch powder do not react with each other in the presence of sufficient water, but the evaporation of water promotes these reactions, resulting in a glass-like, strong and stable cured product.

従って本硬化組成物を懸濁状にしたものを多孔質物質の
表面に塗布した場合、該硬化組成物は表面の微細な孔隙
に侵透し、水が蒸発、吸収される結果上記反応が進行し
、強固な硬化被膜が形成される。
Therefore, when a suspension of this cured composition is applied to the surface of a porous material, the cured composition penetrates into the fine pores on the surface, and as a result of water evaporation and absorption, the above reaction progresses. A strong cured film is formed.

該被膜はシリカゾル単独のものに比べて強固であり、し
かも耐候性、耐薬品性に優れた安定な性質を有する。
The coating is stronger than silica sol alone and has stable properties with excellent weather resistance and chemical resistance.

更に可溶性アルカリ含有量の少ないシリカゾルであるた
めアルカリ公害を発生することもない。
Furthermore, since the silica sol has a low soluble alkali content, it does not cause alkali pollution.

本発明の硬化組成物はモルタル、コンクリート等のセメ
ント系材料およびセラコラ等のCaを主体とする材料に
塗布するとより一層強固な被膜を得ることができる。
When the cured composition of the present invention is applied to cement materials such as mortar and concrete, and materials mainly composed of Ca such as Ceracola, an even stronger film can be obtained.

上記セメント系材料およびCa主体の材料は毛細間隙お
よび表面が消石灰、硫酸カルシウムで覆われており、こ
の間隙に本発明の硬化組成物が浸透すると、消石灰、硫
酸カルシウムと硬化組成物中のシリカゾル、明パン石粉
末とが効果的に反応し、強固で安定な被膜を生成する。
The capillary gaps and surfaces of the above cementitious materials and Ca-based materials are covered with slaked lime and calcium sulfate, and when the hardening composition of the present invention penetrates into these gaps, the slaked lime, calcium sulfate and the silica sol in the hardening composition, It reacts effectively with Akpanite powder to form a strong and stable coating.

以上のように上記材料に本発明の硬化組成物を用いる場
合には単にシリカゾルと明パン石との反応だけではな(
、消石灰、硫酸カルシウムとシリカゾルとの反応あるい
は消石灰、硫酸カルシウムと明パン石との反応が副次的
に進むのでより一層強固安定な被膜を形成できる利点が
ある。
As described above, when the cured composition of the present invention is used in the above materials, it is not only the reaction between the silica sol and the alarkite (
Since the reaction between slaked lime, calcium sulfate and silica sol, or the reaction between slaked lime, calcium sulfate and alumite proceeds as a secondary reaction, it has the advantage of forming a stronger and more stable coating.

本発明の硬化組成物はこのような性質を有するために大
谷石、軽量気泡コンクリート等の多孔質材料、モルタル
、コンクリート等のセメント系材料、セラコラ等のCa
主体材料のような基材に対してコーチング材、接着材、
充填材、補修材として用(冑ることかできる。
Because the cured composition of the present invention has such properties, it can be used in porous materials such as Oya stone and lightweight cellular concrete, cement materials such as mortar and concrete, and calcium carbonate materials such as Ceracola.
Coating materials, adhesives,
Used as a filler or repair material.

本発明の硬化組成物はシリカゾル中に明パン石粉末を懸
濁させた状態で用いるが、水が存在すればシリカゾルと
明パン石とは反応しないので、明パン石粉末が沈澱した
場合でも再度これを攪拌して懸濁状にすることができ、
使用が容易である。
The curing composition of the present invention is used in a state in which the silica sol is suspended with the aarkanite powder, but if water is present, the silica sol and the aarkanite do not react, so even if the aarkanite powder precipitates, it will be reused. This can be stirred to form a suspension,
Easy to use.

尚使用時においては液を充分に攪拌して懸濁状態とし、
明パン石粉末とシリカゾルとを充分に馴染せるのがよい
When using, stir the liquid thoroughly to make it into a suspended state.
It is best to thoroughly blend the acanthrite powder and silica sol.

更にシリカゾルと明パン石粉末とを安定に懸濁させるに
はアルキルアリルスルホン酸塩等の分散性に優れた界面
活性剤を添加すればよい。
Furthermore, in order to stably suspend the silica sol and the acanthite powder, a surfactant with excellent dispersibility such as an alkylaryl sulfonate may be added.

本発明の硬化組成物を塗装材として用いる場合には、必
要に応じて少量の硝酸ニッケル、硝酸鉄、重クロム酸カ
リ、クロム酸カリ等の化合物を添加して着色させること
も可能である。
When the cured composition of the present invention is used as a coating material, it is also possible to add a small amount of a compound such as nickel nitrate, iron nitrate, potassium dichromate, potassium chromate, etc. for coloring, if necessary.

又、本発明の硬化組成物を多孔質体の充填材として使用
する場合には、スルホコハク酸ジオクチルエステル(商
品名: Aerasoi OT )等の浸透性に優
れた界面活性剤を併用すれば多孔質体への浸透が一層良
好となる。
In addition, when the cured composition of the present invention is used as a filler for a porous body, if a surfactant with excellent permeability such as sulfosuccinic acid dioctyl ester (trade name: Aerasoi OT) is used in combination, the porous body can be filled. Penetration becomes even better.

次に本発明の実施例を示す。Next, examples of the present invention will be shown.

実施例 l 5i02濃度30重量%のシリカゾルに対し、40μ以
下に粉砕した明パン石粉末を混合して本発明に係る硬化
組成物の懸濁液を造った。
Example 1 A suspension of a cured composition according to the present invention was prepared by mixing a silica sol with a 5i02 concentration of 30% by weight with an acanthrite powder crushed to a size of 40 μm or less.

ここでシリカゾルおよび明パン石粉末の性質を第1表に
、その配合割合を第2表に示す。
Here, the properties of the silica sol and the acanthrite powder are shown in Table 1, and their blending ratios are shown in Table 2.

乾燥した豊浦標準砂100重量部に対して上記硬化組成
物の懸濁液を20重量部混合し、3CrrLφX3cr
rLhの型枠に5に9/c4の圧力でこれら混合物を充
填し、その後直ちに脱型したものを金網の棚に置き室温
下で乾燥させ明パン石とシリカゾルの配合比が異なる各
試料ごとにその一軸圧縮強さを測定した。
20 parts by weight of the suspension of the above cured composition was mixed with 100 parts by weight of dried Toyoura standard sand, and 3CrLφX3cr
Fill the rLh mold with these mixtures at a pressure of 5 to 9/c4, then immediately remove the mold, place it on a wire mesh shelf, and dry at room temperature. Its unconfined compressive strength was measured.

この結果を第2表に示す。第2表から明らかなように明
パン石粉末を配合した本発明の硬化組成物を用いるもの
はいずれも単なるシリカゾルのものに比べて格段に大き
な圧縮強度を有することがわかる。
The results are shown in Table 2. As is clear from Table 2, all the compositions using the cured composition of the present invention containing Akpanite powder have significantly higher compressive strength than those using simple silica sol.

実施例 2 実施例1と同様のシリカゾルと明パン石粉末とを用いシ
リカゾル100重量部に明パン石粉末を5重量部混合し
て懸濁させ50m1のビーカーに30mmの高さまで入
れ、20℃の温度下で10日間放置したところ本発明に
係る硬化組成物の懸濁液は水の蒸発、飛散により表面か
ら25mmの厚さまで半透明なガラス状に硬化した。
Example 2 Using the same silica sol and Akpanite powder as in Example 1, 5 parts by weight of Akpanite powder was mixed and suspended in 100 parts by weight of silica sol, placed in a 50 ml beaker to a height of 30 mm, and heated at 20°C. When the suspension was left at a temperature for 10 days, the suspension of the cured composition according to the present invention was cured into a translucent glass-like form up to a thickness of 25 mm from the surface due to water evaporation and scattering.

一方、比較のためシリカゾル単味のものを同様の条件下
で10日間放置したところ、本発明に係る硬化組成物の
懸濁液より硬化が遅(、しかもガラス状になったのは表
面より2mm程度であった。
On the other hand, for comparison, when a single silica sol was left for 10 days under the same conditions, it cured more slowly than the suspension of the curing composition of the present invention (and it became glassy only 2 mm below the surface). It was about.

次に、本発明のシリカゾルと明パン石との懸濁液、シリ
カゾル単味が硬化した半透明ガラス状物質を粉末X線回
折したところ、シリカゾル単味の場合378人に最大値
を持つ5.54人〜2.64人の幅広Q正規分布図状の
回折図が得られ、又−志木発明の懸濁液の場合、3.1
9人に最大値を持つ5.54λ〜2,30人の幅広の正
規分布状の回折図が得られた。
Next, when powder X-ray diffraction was performed on the suspension of the silica sol and alarkite of the present invention, a translucent glass-like substance obtained by hardening the silica sol alone, the maximum value of 5. A diffraction pattern with a wide Q normal distribution pattern of 54 to 2.64 people was obtained, and in the case of the suspension of Shiki's invention, 3.1
A wide normally distributed diffractogram of 5.54λ to 2,30 individuals with a maximum value in 9 individuals was obtained.

この結果シリカゾール単味の場合は乾燥により得られた
物質はシリカゲルが大部分であるのに対し、本発明の懸
濁液の場合乾燥により得られた物質はピーク位置が異な
ること、明パン鉱物の回折図がみられないことから、シ
リカゾルと明パン石粉末とは、水の蒸発、飛散により反
応していることが推定される。
As a result, in the case of silicasol alone, the substance obtained by drying is mostly silica gel, whereas in the case of the suspension of the present invention, the substance obtained by drying has a different peak position, and it is found that the substance obtained by drying the suspension of the present invention has different peak positions. Since no diffraction pattern was observed, it is presumed that the silica sol and the Akpanite powder reacted through evaporation and scattering of water.

実施例 3 SiO2含有量30重量%のシリカゾル100重量部に
対して、40μ以下に粉砕したカリ含有量70重量%の
明パン石粉末10重量部を充分攪拌して懸濁させた懸濁
液を造り、この液を市販の軽量気泡コンクリート板の表
面に刷毛を用い10分間隔で3回塗布し、表面と塗装膜
が肉眼でみとめられない程度まで薄(均一に塗布した。
Example 3 A suspension of 10 parts by weight of silica sol with a SiO2 content of 30% by weight and 10 parts by weight of Akpanite powder with a potash content of 70% by weight, which has been ground to 40μ or less, is sufficiently stirred and suspended. This solution was applied to the surface of a commercially available lightweight aerated concrete board using a brush three times at 10-minute intervals, so that the surface and coating film were applied thinly (uniformly) to such an extent that they could not be seen with the naked eye.

この塗装面は時間が経過するに従って光沢を示し、強固
で均一な塗装面を形成し、疎水性を有するものであった
This coated surface became glossy over time, formed a strong and uniform coated surface, and had hydrophobic properties.

一方、同様な方法で5i02含有量30重量%のシリカ
ゾル溶液のみを塗装したところ、上記の場合はど光沢を
持たず、また塗装面は10日経過後のものでも爪で軽く
ひつかくと傷がついた。
On the other hand, when applying only a silica sol solution with a 5i02 content of 30% by weight using the same method, the above case did not have any gloss, and the painted surface was scratched when lightly scratched with a fingernail even after 10 days. Ta.

実施例 4 普通ポルトランドセメントに粗粒率3.0の砂を1:5
の重量比に配合したものを水/セメント比90%の条件
下で4X4X16cfrLのモルタルを造った。
Example 4 1:5 of sand with a coarse grain ratio of 3.0 to ordinary Portland cement
A mortar of 4X4X16cfrL was prepared by mixing the mixture in a weight ratio of 4X4X16cfrL under conditions of a water/cement ratio of 90%.

このモルタルを1日間温度20℃、湿度90%の湿空箱
内で養生抜脱型し、20℃湿度40%で3日間乾燥養生
した後、020℃の水、@SiO2含有量25%のシリ
カゾル、08iO2含有量25%のシリカゾルにに20
6.0%含む明ばん石を40μ以下に粉砕したものを0
.055重量部混懸濁した液に、それぞれ1日間浸漬し
た後、更に7日間温度20℃、湿度90%で養生したも
のにつき、それぞれ曲げ強さ、−軸圧縮強さを測定した
ところ第3表の結果を得た。
This mortar was cured in a humid air box at a temperature of 20°C and humidity of 90% for one day, then removed from the mold, and dried and cured for three days at a humidity of 40% at 20°C. , 20 to silica sol with 25% iO2 content.
Alumite containing 6.0% is crushed to 40μ or less.
.. Table 3 shows the results of measuring the bending strength and -axial compressive strength of each sample after immersing it in a mixed suspension of 055 parts by weight for 1 day and curing it for another 7 days at a temperature of 20°C and a humidity of 90%. I got the result.

第3表から明らかなように本発明の硬化組成物を用いる
Oのものは曲げ強さ、圧縮強さのいずれも他の■@に比
べて大きな値を示した。
As is clear from Table 3, the specimen O using the cured composition of the present invention showed larger values in both bending strength and compressive strength than the other specimens ■@.

実施例 5 幅約0.5〜1mrnの放射上にヒビ割れを生じた雨漏
りのする屋上コンクリートスラブに、SiO□含有量3
0重量%のシリカゾルと30μ以下に粉砕したに20含
有量5.8%の明パン石粉末を、シリカゾルに対して1
5重量%を懸濁させた液を注入し、7日間養生した。
Example 5 A leaky rooftop concrete slab with a radial crack of approximately 0.5 to 1 mrn in width was treated with SiO□ content of 3
0% by weight of silica sol and 5.8% of Akpanite powder crushed to 30μ or less, 1% by weight per silica sol.
A suspension of 5% by weight was injected and cured for 7 days.

尚この際、降雨の時は注入箇所にシートをかげて雨水の
浸入を防いだ。
At this time, when it rained, a sheet was covered over the injection site to prevent rainwater from entering.

一方、比較のため同様にしてシリカゾル単味を注入した
On the other hand, for comparison, silica sol alone was injected in the same manner.

養生終了後約1ケ月間にわたって降雨の際の雨漏りの様
子を観察したところ、本発明のシリカゾルと明パン石と
の懸濁液を注入した箇所は完全に雨漏りが防止できたが
、シリカゾル単味の注入箇所のところは若干の雨漏りが
みられた。
When we observed leakage during rain for about one month after curing, we found that the areas where the suspension of silica sol and Akpanite of the present invention were injected were completely prevented from leaking, but when the silica sol alone Some rain leakage was observed at the injection point.

JIS R5201により、普通ポルトランドセメン
ト:豊浦標準砂:水−1:2:0.65(重量比)のモ
ルタルを混練して、4×4×16CrfLのモルタル供
試体を造り、これを28日間20℃の水中で養生後ミバ
エリス曲げ試験機で半分に切断した。
According to JIS R5201, mortar of ordinary Portland cement: Toyoura standard sand: water - 1:2:0.65 (weight ratio) was kneaded to make a mortar specimen of 4 x 4 x 16 CrfL, and this was heated at 20°C for 28 days. After curing in water, the specimens were cut in half using a Miberris bending tester.

切断した供試体を1日間温度30℃、湿度65%で乾燥
後、■5i02含有量30重量%のシリカゾル040μ
以下に粉砕したに20含有量9.8重量%の明ばん石粉
末200重量部とSiO2含有量30重量%のシリカゾ
ル100重量部との混合懸濁液、Oエポキシ系接着剤(
商品名:ボンドクイックヤンダー)を、それぞれ切断面
に塗付し密実に接着させた。
After drying the cut specimen for one day at a temperature of 30°C and a humidity of 65%, ■ Silica sol 040μ with a 5i02 content of 30% by weight was applied.
A mixed suspension of 200 parts by weight of pulverized alumite powder with a content of 9.8% by weight and 100 parts by weight of silica sol with a SiO2 content of 30% by weight, O epoxy adhesive (
Product name: BOND QUICK YANDER) was applied to each cut surface and adhered tightly.

接着1時間後供試体の両端を手でもち曲げたところ、■
を塗付した供試体は簡単に2つに割れたが、@またはθ
を塗付した供試体は手で割ることができなかった。
After 1 hour of adhesion, both ends of the specimen were bent by hand, and ■
The specimen coated with
It was not possible to break the specimen coated with it by hand.

そこで@またはOを塗付した供試体を1日間室内に放置
した後ミハエリエス曲げ試験機で曲げ強さを測定したと
ころ@を塗付した供試体の曲げ強さは30.7 kg/
crti、 Oを塗付した供試体の曲げ強さは32.1
に9/caであり、本発明硬化組成物は接着材として市
販のエポキシ系接着剤とほぼ同様の接着性を発揮するこ
とがわかる。
Therefore, after leaving the specimen coated with @ or O indoors for one day, the bending strength of the specimen coated with @ was measured using a Michaelis bending tester.The bending strength of the specimen coated with @ was 30.7 kg/
The bending strength of the specimen coated with crti, O is 32.1
9/ca, indicating that the cured composition of the present invention exhibits almost the same adhesive properties as commercially available epoxy adhesives as adhesives.

以上、実施例と共に詳細に説明したように本発明の硬化
組成物は格別に強固なかつ安定な硬化体を得ることがで
き、更に有害組成物を含まないので公害を招(こともな
いなど実用上の利点を具える。
As explained above in detail together with Examples, the cured composition of the present invention can provide an exceptionally strong and stable cured product, and furthermore, since it does not contain harmful compositions, it does not cause any pollution. It has the advantages of

Claims (1)

【特許請求の範囲】[Claims] 1 シリカゾルを主成分としこれに明パン石粉末を混合
してなることを特徴とする硬化組成物。
1. A hardening composition comprising silica sol as a main component and mixed with Akpanite powder.
JP11274781A 1981-07-18 1981-07-18 Curing composition Expired JPS5935856B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11274781A JPS5935856B2 (en) 1981-07-18 1981-07-18 Curing composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11274781A JPS5935856B2 (en) 1981-07-18 1981-07-18 Curing composition

Publications (2)

Publication Number Publication Date
JPS5815059A JPS5815059A (en) 1983-01-28
JPS5935856B2 true JPS5935856B2 (en) 1984-08-31

Family

ID=14594535

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11274781A Expired JPS5935856B2 (en) 1981-07-18 1981-07-18 Curing composition

Country Status (1)

Country Link
JP (1) JPS5935856B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6147659U (en) * 1984-08-31 1986-03-31 シチズン時計株式会社 ribbon cartridge
CZ352796A3 (en) * 1995-04-07 1997-04-16 Holderchem Holding Ag The use of salt brines for treating surface of unsolidified and solidified binding suspensions

Also Published As

Publication number Publication date
JPS5815059A (en) 1983-01-28

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