JPS62123053A - Calcium silicate and manufacture - Google Patents

Calcium silicate and manufacture

Info

Publication number
JPS62123053A
JPS62123053A JP26131185A JP26131185A JPS62123053A JP S62123053 A JPS62123053 A JP S62123053A JP 26131185 A JP26131185 A JP 26131185A JP 26131185 A JP26131185 A JP 26131185A JP S62123053 A JPS62123053 A JP S62123053A
Authority
JP
Japan
Prior art keywords
calcium silicate
parts
weight
latex
dispersant
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
JP26131185A
Other languages
Japanese (ja)
Inventor
小林 和一
聡 大高
中田 敏宏
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.)
Ube Corp
Original Assignee
Ube Industries 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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP26131185A priority Critical patent/JPS62123053A/en
Publication of JPS62123053A publication Critical patent/JPS62123053A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、ケイ酸カルシウム成形体およびその製造方法
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a calcium silicate molded body and a method for producing the same.

更に詳しくは、本発明は、軽徂かつ強靭で、耐熱性、耐
水性を有し、木材と同様の加工性を具備した建築材料と
して好適に使用することができるケイ酸カルシウム、補
強繊維、ラテックスおよび分散剤からなるケイ酸カルシ
ウム成形体およびその製造方法に関する。
More specifically, the present invention provides calcium silicate, reinforcing fibers, and latex, which are light and strong, have heat resistance, water resistance, and can be suitably used as building materials with workability similar to that of wood. and a calcium silicate molded body comprising a dispersant and a method for producing the same.

[従来の技術] ケイ酸カルシウム成形体については、(1)ケイ酸カル
シウム水和物100重量部、水硬性石膏10〜150重
量部、重合体エマルジョン5〜30重量部、重合体エマ
ルジョン用凝集剤および水、ざらには補強繊維からなる
水性スラリを成形、乾燥してなるケイ酸カルシウム成形
物(特開昭54−160428号公報)、(2)ケイ酸
カルシウムにガラス繊維を分散させたケイ酸カルシウム
成形体(特開昭50−69121号公報)等が提案され
ている。
[Prior Art] Regarding the calcium silicate molded body, (1) 100 parts by weight of calcium silicate hydrate, 10 to 150 parts by weight of hydraulic gypsum, 5 to 30 parts by weight of polymer emulsion, and a flocculant for polymer emulsion. and water, and a calcium silicate molded product obtained by molding and drying an aqueous slurry consisting of reinforcing fibers (Japanese Unexamined Patent Publication No. 160428/1982), (2) Silicic acid in which glass fibers are dispersed in calcium silicate. Calcium molded bodies (JP-A-50-69121) and the like have been proposed.

[発明が解決しようとする問題点] しかしながら、(1)の成形物には水硬性石膏がかなり
の母で添加されているため耐水性に若干の難点があるだ
けでなく、高温にさらされた場合、還元条件下800〜
1000℃で石膏が分解して有毒な硫黄酸化物が発生し
たり、石膏の結晶水が100〜500℃で失われるため
に成形物の体積変化、強度低下が生じ、安全性、耐熱性
、寸法安定性等の面で難点がある。以上より前記(1)
の方法で嵩比重が0.3〜0.79/ CTdと軽量で
、強靭にして耐熱性、耐水性、寸法安定性などが木材と
同様の加工性を具備する安全性の高いケイ酸カルシウム
成形体を得ることは困難である。
[Problems to be solved by the invention] However, since the molded product of (1) contains a considerable amount of hydraulic gypsum, it not only has some difficulty in water resistance, but also has a tendency to be exposed to high temperatures. 800~ under reducing conditions
Gypsum decomposes at 1000°C, producing toxic sulfur oxides, and gypsum crystallization water is lost at 100 to 500°C, resulting in volume changes and strength reductions in molded products, which can lead to problems with safety, heat resistance, and dimensions. There are some drawbacks in terms of stability, etc. From the above, (1)
This method produces highly safe calcium silicate molding that is lightweight with a bulk specific gravity of 0.3 to 0.79/CTd, strong, heat resistant, water resistant, dimensional stability, etc., and has processability similar to that of wood. It is difficult to get the body.

また、前記(2)の成形体も嵩比重0.3〜0゜7g/
CTl1と軽量とすると強度、加工性等に問題が生じる
In addition, the molded product of (2) above also has a bulk specific gravity of 0.3 to 0°7 g/
If it is as light as CTl1, problems will arise in strength, workability, etc.

本発明は、これらの難点が改良された合成木材等の建築
材料、特に耐熱性建築材料として好適なケイ酸カルシウ
ム成形体およびその製造方法を提供することにある。
An object of the present invention is to provide a calcium silicate molded body suitable for use as a building material such as synthetic wood, particularly a heat-resistant building material, which has improved these drawbacks, and a method for producing the same.

[問題点を解決するための手段および作用]本発明は、
ケイ酸カルシウム100重辺部、補強繊維1〜30重社
部、ラテックス1〜40重量部および分散剤0.1〜5
重量部からなるケイ酸カルシウム成形体およびその製造
方法に関する。
[Means and effects for solving the problems] The present invention has the following features:
100 parts of calcium silicate, 1 to 30 parts of reinforcing fiber, 1 to 40 parts by weight of latex, and 0.1 to 5 parts of dispersant.
The present invention relates to a calcium silicate molded body consisting of parts by weight and a method for producing the same.

本発明のケイ酸カルシウム成形体は、ケイ酸カルシウム
スラリ、補強繊維、ラテックスおよび分散剤を、ケイ酸
カルシウム100fflffi部に対して補強1維1〜
30重量部、ラテックス1〜40単口部および分散剤0
.1〜5重量部の割合で混合し、成形した後、乾燥する
ことによって製造することができ、組成割合の特定によ
って、特に分散剤の使用によって従来のケイ酸カルシウ
ム成形体の難点を改良することができる。
In the calcium silicate molded article of the present invention, calcium silicate slurry, reinforcing fibers, latex, and dispersant are added to 100 fflfffi parts of calcium silicate to 1 to 1 reinforcing fibers.
30 parts by weight, 1 to 40 parts of latex and 0 parts of dispersant
.. It can be produced by mixing in a proportion of 1 to 5 parts by weight, molding, and then drying, and by specifying the composition ratio, especially by using a dispersant, the drawbacks of conventional calcium silicate molded bodies can be improved. I can do it.

本発明においてケイ酸カルシウムとしては、生石灰、消
石灰の如き石灰質原料、ケイ石の如きケイ酸質原料およ
び水とから水熱合成反応によって得られた通常トバモラ
イト、ゾノトライトと呼ばれるケイ酸カルシウム水和物
が好適でおり、ケイ酸カルシウム成形体の製造にあたっ
ては、ケイ酸カルシウムスラリ、詳しくはケイ酸カルシ
ウム水和物水スラリとして使用される。
In the present invention, the calcium silicate is a calcium silicate hydrate usually called tobermorite or xonotrite, which is obtained by a hydrothermal synthesis reaction from calcareous raw materials such as quicklime and slaked lime, silicic acid raw materials such as silica stone, and water. It is suitable and used as a calcium silicate slurry, specifically a calcium silicate hydrate aqueous slurry, in the production of calcium silicate molded bodies.

補強繊維としては、ガラス繊維、カーボン繊維等の無U
N 8M m、ナイロン、ポリプロピレン、レーヨン、
ビニロン等の有機繊維が使用可能で、これらを単独また
は2種以上混合してもよい。補強繊維は、成形体の強度
および弾性率を向上させ、製造時のスラリ中でケイ酸カ
ルシウムおよびラテックスの保持性を向上させて加圧脱
水時のろ過分離を良好ならしめる作用があるが、加工性
、耐水性、耐熱性等の面からその使用但は、ケイ酸カル
シウム100重足部に対して1〜30重聞部単口ましく
は3〜15重旦部がよい。
Reinforcing fibers include glass fiber, carbon fiber, etc.
N 8M m, nylon, polypropylene, rayon,
Organic fibers such as vinylon can be used, and these may be used alone or in combination of two or more. Reinforcing fibers have the effect of improving the strength and elastic modulus of the molded product, improving the retention of calcium silicate and latex in the slurry during production, and improving filtration separation during pressurized dehydration. From the viewpoint of properties, water resistance, heat resistance, etc., it is preferable to use 1 to 30 parts per 100 parts of calcium silicate, or 3 to 15 parts per 100 parts of calcium silicate.

補強繊維を混合する時期は、特に制限されないが、混合
による補強繊維の損傷防止、補強繊維の分散性向上効果
の面から、ケイ酸カルシウムスラリ、ラテックスおよび
分散剤を混合した後に補強繊維を混合するのが好ましい
The timing of mixing the reinforcing fibers is not particularly limited, but from the viewpoint of preventing damage to the reinforcing fibers due to mixing and improving the dispersibility of the reinforcing fibers, the reinforcing fibers are mixed after the calcium silicate slurry, latex, and dispersant are mixed. is preferable.

ラテックスとしては、溶液型、エマルジョン型のいずれ
でもよく、具体的にはスチレン−ブタジェン共重合体、
アクリロニトリル−ブタジェン共重合体、ブタジェン重
合体、メタクリル酸メチル−ブタジェン共重合体、イソ
プレン(共)重合体、エチレン−プロピレン共重合体等
のラテックスが挙げられる。
The latex may be either a solution type or an emulsion type, and specifically, styrene-butadiene copolymer,
Latexes such as acrylonitrile-butadiene copolymer, butadiene polymer, methyl methacrylate-butadiene copolymer, isoprene (co)polymer, and ethylene-propylene copolymer are mentioned.

ラテックスは、それ自身でも成形体中でケイ酸カルシウ
ム同志およびケイ酸カルシウムと補強繊維を固着する作
用を有する。それ故成形体は高強度を示し切削加工時に
粉末が飛散せず、釘等の保持力が良い等のすぐれた加工
性を示す。
The latex itself has the effect of fixing the calcium silicate itself and the calcium silicate and reinforcing fibers in the molded article. Therefore, the molded product exhibits high strength, no powder scattering during cutting, and exhibits excellent workability such as good holding power for nails and the like.

なお、ラテックスの固着作用を更に改善するには、クマ
ロン、インデン樹脂等の通常ゴムラテックスの付着強度
を改善する粘着付与剤を使用することが可能である。
In order to further improve the fixing effect of the latex, it is possible to use a tackifier that improves the adhesive strength of ordinary rubber latex, such as coumaron or indene resin.

また使用するラテックスの特性を改善するには、通常使
用されている硫黄系加硫剤、非硫黄系加硫剤(たとえば
、ジェポキシ化合物、ブロックイソシアナートなど)お
よび融着付与剤なども使用することか可能であり、これ
らの添加物の使用により、成形体の表面硬度、弾性、釘
の保持力の向上を図ることができる。
In addition, to improve the properties of the latex used, commonly used sulfur-based vulcanizing agents, non-sulfur vulcanizing agents (e.g., jepoxy compounds, blocked isocyanates, etc.) and fusing agents may also be used. By using these additives, it is possible to improve the surface hardness, elasticity, and nail holding power of the molded product.

ラテックスは、ケイ酸カルシウム100重量部に対して
1〜40重間部、好ましくは5〜25重四部使用される
。ラテックスの使用量が少なすぎると加工性に難がおり
、また過度に多すぎると耐熱性に問題が生じる。
The latex is used in an amount of 1 to 40 parts by weight, preferably 5 to 25 parts by weight, per 100 parts by weight of calcium silicate. If the amount of latex used is too small, processability will be difficult, and if it is too large, problems will arise in heat resistance.

分散剤としては、セメント用分散剤(減水剤を含む)と
して知られているものが好適に使用される。具体的には
、リグニン系、高級多価アルコールのスルホン酸塩系、
オキシ有機酸系、アルキルアリルスルホン酸塩および高
縮合物系、ポリオキシエチレンアルキルエーテル系、メ
ラミン縮合物系、β−ナフタリンスルホン酸ホルマリン
縮合等が挙げられる。またリン酸ナトリウム等の無機塩
も使用することができる。分散剤の使用量は、分散剤の
種類によっても若干異なるが、ケイ酸カルシウムに対し
て0.1〜5重量部、好ましくは0゜5〜4重量部の範
囲で使用される。分散剤の使用によって成形体製造時の
6原1’E+の均一分散が可能となり高分散性ケイ酸カ
ルシウムスラリになるため、補強繊維の損傷も防止され
、軽量、強靭にして耐熱性、耐水性、寸法安定性等がよ
く、木材と同様の加工性を!7!備する安全性の高い従
来にないケイ酸カルシウム成形体を17ることができる
。分散剤の使用量が少なすぎると、成形体の加工性、強
度等に問題があり、多すぎると経湾的でないだけでなく
耐水性に難がおる。
As the dispersant, those known as cement dispersants (including water reducing agents) are preferably used. Specifically, lignin-based, higher polyhydric alcohol sulfonate-based,
Examples include oxyorganic acid systems, alkylaryl sulfonate and high condensate systems, polyoxyethylene alkyl ether systems, melamine condensate systems, β-naphthalene sulfonic acid formalin condensation, and the like. Inorganic salts such as sodium phosphate can also be used. The amount of the dispersant used varies slightly depending on the type of dispersant, but it is used in the range of 0.1 to 5 parts by weight, preferably 0.5 to 4 parts by weight, based on the calcium silicate. By using a dispersant, it is possible to uniformly disperse the 6 elements 1'E+ during the production of molded objects, resulting in a highly dispersed calcium silicate slurry, which prevents damage to reinforcing fibers, making it lightweight, strong, heat resistant, and water resistant. , good dimensional stability, etc., and workability similar to wood! 7! It is possible to create an unprecedented calcium silicate molded body with a high degree of safety. If the amount of dispersant used is too small, there will be problems with the processability, strength, etc. of the molded product, and if it is too large, it will not only not be smooth but also have difficulty in water resistance.

本発明のケイ酸カルシウム成形体の好適な製)方法の1
例を次に示す。
1) Preferred method for producing the calcium silicate molded article of the present invention
For example:

Si 02 /Ca O(モル比)が1になるように石
灰質原料とケイ酸原料を用い、原料に対して水を5〜1
5重口倍加えて水熱合成反応させ、ケイ酸カルシウムス
ラリ、詳しくはケイ酸カルシrクム水和物の水スラリを
得る。水熱合成反応には一般にオートクレーブが採用さ
れる。
Calcareous raw materials and silicic acid raw materials are used so that the Si 02 /Ca O (molar ratio) is 1, and water is added at a ratio of 5 to 1 % to the raw materials.
Add 5 times the amount and carry out a hydrothermal synthesis reaction to obtain a calcium silicate slurry, specifically an aqueous slurry of calcium silicate hydrate. Autoclaves are generally used for hydrothermal synthesis reactions.

ケイ酸カルシウムスラリに所定量のラテックスおよび分
散剤を混合した後、補強繊維を混合し、これらが均一に
分散したスラリを成形する。スラリの成形法としては、
例えば型枠に充填して加圧脱水する方法が挙げられるが
、目的、用途に応じて従来公知の成形法が適宜採用され
る。
After a predetermined amount of latex and a dispersant are mixed into the calcium silicate slurry, reinforcing fibers are mixed thereinto and a slurry in which these are uniformly dispersed is formed. The slurry forming method is as follows:
For example, a method of filling a mold and dehydrating under pressure may be mentioned, but a conventionally known molding method may be adopted as appropriate depending on the purpose and use.

成形物は、これを屹燥すると目的とするケイ酸カルシウ
ム成形体が得られる。屹燥する際の温度は特に結成され
ないが、100〜180’C,通常110〜160°C
の温度が採用される。
When the molded product is dried, the desired calcium silicate molded product can be obtained. The temperature for drying is not particularly determined, but it is 100-180'C, usually 110-160'C.
temperature is adopted.

以下に本発明の実施例を示す。Examples of the present invention are shown below.

(実施例) 実施例にあける試験結果は次の方法に依った。(Example) The test results provided in the examples were based on the following method.

曲げ強度:JISA1408に準じた。Bending strength: According to JISA1408.

加工性:かんながCプ、釘打ち、のこぎり引き等の木材
の加工操作を実施した場合の木材との比較で判定した。
Workability: Judgment was made by comparing with wood that has been subjected to wood processing operations such as planing, nailing, sawing, etc.

耐熱性二成形体を1000’C電気炉内で2時間加熱し
た後の有毒ガス発生の有無、強度および寸法安定性より
判定した。
The heat-resistant two molded bodies were heated in a 1000'C electric furnace for 2 hours and then judged based on the presence or absence of toxic gas generation, strength, and dimensional stability.

耐水性:成形体を24時間、水温20’Cの水中に浸し
た後の強度および寸法安定性より判定した。
Water resistance: Judgment was made from the strength and dimensional stability after the molded body was immersed in water at a water temperature of 20'C for 24 hours.

実施例1 ケイ石粉と消石灰とを5i02:CaOのモル比が1:
1になるように調合し、CaOとSiO2どの合計型ω
に対して10 F mの水を加えてオートクレーブ中で
撹拌しながら温度210°C1圧力19Kg/Cmで5
時間水熱合成反応させた。このようにしてjqられたケ
イ酸カルシウム水m物スラリに、ケイ酸カルシウム10
0重量部に対して、ラテックス(日本ゼオン■装、商品
名LX416)固体型は5重d部、メラミン縮合物系の
分散剤(昭和電工(体製、商品名メルメント「−10)
3小母部を添加、混合した俊、ガラス繊維(日東紡(珠
装、商品名C3−12−GYD)7中足部を添加、混合
した。
Example 1 Silica powder and slaked lime were mixed at a molar ratio of 5i02:CaO of 1:
Mix it so that it becomes 1, and determine which total type ω of CaO and SiO2.
Add 10 Fm of water to the autoclave and heat at 210°C and 19Kg/Cm of pressure in an autoclave with stirring.
The hydrothermal synthesis reaction was carried out for an hour. Calcium silicate 10 is added to the calcium silicate water slurry thus prepared.
0 parts by weight, latex (Nippon Zeon Corporation, trade name LX416) solid type is 5 parts by weight, melamine condensate-based dispersant (Showa Denko Co., Ltd., trade name Melment "-10")
Glass fiber (Nittobo (Tamaso, trade name: C3-12-GYD) 7 midfoot was added and mixed.

次いで、1qられた高分散ケイ酸カルシウムスラリを3
0cm×30cm型枠に充1眞し、25Kyf/C尻の
圧力で加圧脱水し、145°Cで160寺間乾燥し、ケ
イ酸カルシウム成形体を1ゴた。
Next, 1q of highly dispersed calcium silicate slurry was added to 3
The mixture was filled into a 0 cm x 30 cm mold, dehydrated under pressure of 25 Kyf/C, dried at 145°C for 160 minutes, and formed into a calcium silicate molded body.

成形体の試験結果を第1表に示す。The test results of the molded bodies are shown in Table 1.

比較例1 ガラス繊維を無添加とした以外は実施例1と同様にして
成形体を得た。その試験結果を第1表に示す。
Comparative Example 1 A molded article was obtained in the same manner as in Example 1 except that no glass fiber was added. The test results are shown in Table 1.

比較例2 ラテックスを無添加とした以外は実施例1と同様にして
成形体を得た。その試験結果を第1表に示す。
Comparative Example 2 A molded article was obtained in the same manner as in Example 1 except that no latex was added. The test results are shown in Table 1.

比較例3 分散剤を無添加とした以外は実施例1と同様ににして成
形体を1qだ。その試験結果を第1表に示す。
Comparative Example 3 A molded article of 1 q was prepared in the same manner as in Example 1 except that no dispersant was added. The test results are shown in Table 1.

比較例4 特開昭54 160428M公報の実施例1と同様にケ
イ酸カルシウム100@ff1部に対してα型半水石f
J 50重量部およびアクリルアミド系高分子凝集剤1
.2重足を添加し、分散剤無添加とした以外は実施例1
と同様にして成形体を得た。
Comparative Example 4 α-type hemihydrate f for 1 part of calcium silicate 100@ff, similar to Example 1 of JP-A-160428M.
J 50 parts by weight and acrylamide polymer flocculant 1
.. Example 1 except that double foot was added and no dispersant was added.
A molded body was obtained in the same manner as above.

その試験結果を第1表に示す。The test results are shown in Table 1.

実施例2〜5 分散剤に添加割合を第2表に示すように変えた以外は実
施例1と同様にして成形体を得た。その試験結果を第2
表に示す。
Examples 2 to 5 Molded bodies were obtained in the same manner as in Example 1 except that the proportion of the dispersant added was changed as shown in Table 2. The test results are shown in the second
Shown in the table.

実施例6〜8 ガラス繊維の添加割合を第3表に示すように変えた以外
は実施例1と同様にして成形体を得た。
Examples 6 to 8 Molded bodies were obtained in the same manner as in Example 1 except that the proportion of glass fiber added was changed as shown in Table 3.

その試験結果を第3表に示す。The test results are shown in Table 3.

比較例5 ガラス繊維の添加割合をケイ酸カルシウム100重量部
に対して35重量部とした以外は、実施例1と同様にし
て成形体を得た。その試験結果を第3表に示す。
Comparative Example 5 A molded article was obtained in the same manner as in Example 1, except that the proportion of glass fiber added was 35 parts by weight relative to 100 parts by weight of calcium silicate. The test results are shown in Table 3.

実施例9〜11 ラテックスの添加割合を第4表に示すように変えた以外
は実施例1と同様にして成形体を得た。
Examples 9 to 11 Molded bodies were obtained in the same manner as in Example 1, except that the addition ratio of latex was changed as shown in Table 4.

その試験結果を第4表に示す。The test results are shown in Table 4.

比較例6 ラテックスの添加割合をケイ酸カルシウム100単口部
に対して50重量部とした以外は実施例1と同様にして
成形体を得た。その試験結果を第4表に示す。
Comparative Example 6 A molded article was obtained in the same manner as in Example 1, except that the addition ratio of latex was 50 parts by weight per 100 parts of calcium silicate. The test results are shown in Table 4.

実施例12〜14 水熱合成反応時の水の使用Fit 10倍量を第5表に
示すように変えた以外は、実施例1と同様にして成形体
を得た。その試験結果を第5表に示す。
Examples 12 to 14 Molded bodies were obtained in the same manner as in Example 1, except that the Fit 10 amount of water used during the hydrothermal synthesis reaction was changed as shown in Table 5. The test results are shown in Table 5.

実施例15〜18 ラテックスに、粘着付与剤(日本ゼオン(…製、商品名
N707)、硫黄系加硫剤(日本ゼオン■製、商品名N
811)、非硫黄系加硫剤(武田薬品工業■製、商品名
プロミネートB−830)、ゲル化剤(ケイフッ化ソー
ダ)をラテックス100重量部に対し25手量部添加し
た以外は実施例1と同様にして成形体を得た。その試験
結果を第6表に示す。
Examples 15 to 18 Adding a tackifier (manufactured by Nippon Zeon Co., Ltd., product name N707) and a sulfur-based vulcanizing agent (manufactured by Nippon Zeon Corporation, product name N707) to latex.
Example 1 except that 25 parts by weight of a non-sulfur vulcanizing agent (manufactured by Takeda Pharmaceutical Company Ltd., trade name Prominate B-830), and a gelling agent (sodium fluorosilicide) were added to 100 parts by weight of latex. A molded body was obtained in the same manner as above. The test results are shown in Table 6.

実施例19 ラテックスに、実施例15〜18に記載の粘着付与剤、
非硫黄系加硫剤、ゲル化剤をラテックス100重量部に
対して各々5重量部を混合添加した以外は実施例1と同
様にして成形体を得た。その試験結果第6表に示す。
Example 19 The tackifier described in Examples 15 to 18 was added to the latex,
A molded article was obtained in the same manner as in Example 1, except that 5 parts by weight of each of the non-sulfur vulcanizing agent and gelling agent were mixed and added to 100 parts by weight of latex. The test results are shown in Table 6.

〔発明の効果〕〔Effect of the invention〕

本発明のケイ酸カルシウム成形体は、嵩比重が0.3〜
0.7g/C−rIiと小ざいにもかかわらず強度が大
きく、耐熱性、耐水性、寸法安定性等に優れ、木材と同
等の加工性を有し、かつ高温に加熱したときに、S02
等の有毒ガスを発生しないので、優れた建築材料として
好適に使用される。
The calcium silicate molded article of the present invention has a bulk specific gravity of 0.3 to
Although it is small at 0.7 g/C-rIi, it has high strength, excellent heat resistance, water resistance, dimensional stability, etc., and has workability equivalent to wood, and when heated to high temperatures, it has a S02
Since it does not emit toxic gases such as, it is suitable for use as an excellent building material.

Claims (4)

【特許請求の範囲】[Claims] (1)ケイ酸カルシウム100重量部、補強繊維1〜3
0重量部、ラテックス1〜40重量部および分散剤0.
1〜5重量部からなるケイ酸カルシウム成形体。
(1) 100 parts by weight of calcium silicate, 1 to 3 reinforcing fibers
0 parts by weight, 1 to 40 parts by weight of latex and 0.0 parts by weight of dispersant.
A calcium silicate molded article consisting of 1 to 5 parts by weight.
(2)分散剤がセメント用分散剤である特許請求の範囲
第1項記載のケイ酸カルシウム成形体。
(2) The calcium silicate molded article according to claim 1, wherein the dispersant is a cement dispersant.
(3)ラテックスが、ラテックス100重量部に対して
粘着付与剤、硫黄系加硫剤または非硫黄系加硫剤、ゲル
化剤の少なくとも1種が0.01〜20重量部添加され
たものからなる特許請求の範囲第1項記載のケイ酸カル
シウム成形体。
(3) The latex is one in which 0.01 to 20 parts by weight of at least one of a tackifier, a sulfur-based vulcanizing agent, a non-sulfur vulcanizing agent, and a gelling agent are added to 100 parts by weight of the latex. A calcium silicate molded article according to claim 1.
(4)ケイ酸カルシウムスラリ、補強繊維、ラテックス
および分散剤を、ケイ酸カルシウム100重量部に対し
て補強繊維1〜30重量部、ラテックス1〜40重量部
および分散剤0.1〜5重量部の割合で混合し、成形し
た後、乾燥することを特徴とするケイ酸カルシウム成形
体の製造方法。
(4) Calcium silicate slurry, reinforcing fibers, latex, and dispersant are added to 100 parts by weight of calcium silicate, 1 to 30 parts by weight of reinforcing fibers, 1 to 40 parts by weight of latex, and 0.1 to 5 parts by weight of dispersant. 1. A method for producing a calcium silicate molded body, which comprises mixing the calcium silicate molded body at a ratio of 1 to 3, molding it, and then drying it.
JP26131185A 1985-11-22 1985-11-22 Calcium silicate and manufacture Pending JPS62123053A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26131185A JPS62123053A (en) 1985-11-22 1985-11-22 Calcium silicate and manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26131185A JPS62123053A (en) 1985-11-22 1985-11-22 Calcium silicate and manufacture

Publications (1)

Publication Number Publication Date
JPS62123053A true JPS62123053A (en) 1987-06-04

Family

ID=17360028

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26131185A Pending JPS62123053A (en) 1985-11-22 1985-11-22 Calcium silicate and manufacture

Country Status (1)

Country Link
JP (1) JPS62123053A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988010338A1 (en) * 1987-06-26 1988-12-29 Kabushiki Kaisha Osaka Packing Seizosho Formed calcium silicate plate and process for its production
JPH01270551A (en) * 1988-04-19 1989-10-27 Mitsubishi Kasei Corp Calcium silicate compact
JPH0363107A (en) * 1989-08-02 1991-03-19 Denki Kagaku Kogyo Kk Form material and buried form using same and manufacture thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988010338A1 (en) * 1987-06-26 1988-12-29 Kabushiki Kaisha Osaka Packing Seizosho Formed calcium silicate plate and process for its production
JPH01270551A (en) * 1988-04-19 1989-10-27 Mitsubishi Kasei Corp Calcium silicate compact
JPH0363107A (en) * 1989-08-02 1991-03-19 Denki Kagaku Kogyo Kk Form material and buried form using same and manufacture thereof

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