JPH05213657A - Production of calcium silicate formed body - Google Patents
Production of calcium silicate formed bodyInfo
- Publication number
- JPH05213657A JPH05213657A JP1661892A JP1661892A JPH05213657A JP H05213657 A JPH05213657 A JP H05213657A JP 1661892 A JP1661892 A JP 1661892A JP 1661892 A JP1661892 A JP 1661892A JP H05213657 A JPH05213657 A JP H05213657A
- Authority
- JP
- Japan
- Prior art keywords
- slurry
- raw material
- molar ratio
- range
- calcium silicate
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/18—Compositions 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 mixtures of the silica-lime type
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、珪酸カルシウム成形体
の製造方法に関するものである。FIELD OF THE INVENTION The present invention relates to a method for producing a calcium silicate compact.
【0002】[0002]
【従来の技術・課題】建築材料として使用されている珪
酸カルシウム成形体の多くは、石灰質原料、珪酸質原
料、補強繊維及び軽量骨材等の充填材を成形後に水熱反
応を行うことにより製造されている。しかし、この方法
では、嵩比重を0.45〜0.55と軽量化するために
は、相当量の軽量充填材を必要とするため、曲げ強度が
低下するという問題があった。また、気孔量が多くなる
ので、吸水による寸法変化率が大きくなり、防水処理を
行わない限り、建築材料としての使用は困難であった。2. Description of the Related Art Most of the calcium silicate compacts used as building materials are manufactured by hydrothermal reaction after molding filler such as calcareous raw material, siliceous raw material, reinforcing fiber and lightweight aggregate. Has been done. However, in this method, in order to reduce the bulk specific gravity to 0.45 to 0.55, a considerable amount of a lightweight filler is required, so that there is a problem that the bending strength is lowered. Further, since the amount of pores is large, the rate of dimensional change due to water absorption is large, and it is difficult to use it as a building material unless waterproof treatment is performed.
【0003】従って、本発明の目的は、軽量充填材によ
る上述の問題点を解決し、軽量、高強度で寸法安定性に
優れた珪酸カルシウム成形体の製造方法を提供するもの
である。Therefore, an object of the present invention is to solve the above-mentioned problems caused by a lightweight filler, and to provide a method for producing a calcium silicate compact which is lightweight, has high strength and is excellent in dimensional stability.
【0004】[0004]
【課題を解決するための手段】即ち、本発明に係る珪酸
カルシウム成形体の製造方法は、Ca/(Si+Al)モ
ル比1.0〜5.0の範囲内にある石灰質原料、非晶質珪
酸原料及び水よりなるスラリーを常圧下で加熱処理し、
更に、珪酸質原料を加えてCa/(Si+Al)モル比を
0.6〜1.1の範囲内としたスラリー(A)と、Ca/
(Si+Al)モル比0.8〜1.1の範囲内にある石灰質
原料、珪酸質原料及び水よりなるスラリーを水熱合成す
ることにより得られるスラリー(B)を、図1に示す座標
a、b、c及びdで囲まれる範囲内の割合で混合し、更
に、スラリー中の固形分の重量を基準として1〜10%
の補強繊維を添加し、成形し、140〜220℃の範囲
内の温度で水熱反応を行うことを特徴とする。That is, the method for producing a calcium silicate compact according to the present invention comprises a calcareous raw material and an amorphous silicic acid having a Ca / (Si + Al) molar ratio of 1.0 to 5.0. A slurry consisting of raw materials and water is heat-treated under normal pressure,
Further, a slurry (A) having a Ca / (Si + Al) molar ratio within the range of 0.6 to 1.1 by adding a siliceous raw material, and Ca /
A slurry (B) obtained by hydrothermally synthesizing a slurry composed of a calcareous raw material, a siliceous raw material, and water having a (Si + Al) molar ratio in the range of 0.8 to 1.1 is represented by coordinates a, shown in FIG. Mix in a ratio within the range surrounded by b, c and d, and further 1 to 10% based on the weight of the solid content in the slurry.
Is added and molded, and the hydrothermal reaction is performed at a temperature in the range of 140 to 220 ° C.
【0005】更に、本発明に係る珪酸カルシウム成形体
の製造方法は、Ca/(Si+Al)モル比1.0〜5.0
の範囲内にある石灰質原料、非晶質珪酸原料及び水より
なるスラリーを常圧下で加熱処理し、更に、珪酸質原料
を加えてCa/(Si+Al)モル比を0.6〜1.1の範
囲内としたスラリー(A)と、Ca/(Si+Al)モル比
0.8〜1.1の範囲内にある石灰質原料、珪酸質原料及
び水よりなるスラリーを水熱合成することにより得られ
るスラリー(B)を、図1に示す座標a、b、c及びdで
囲まれる範囲内の割合で混合し、更に、スラリー中の固
形分の重量を基準として1〜10%の補強繊維と10%
以下の粘土鉱物を添加し、成形し、140〜220℃の
範囲内の温度で水熱反応を行うことを特徴とする。Further, in the method for producing a calcium silicate compact according to the present invention, the Ca / (Si + Al) molar ratio is 1.0 to 5.0.
The slurry consisting of the calcareous raw material, the amorphous silicic acid raw material and the water within the range of is heat treated under normal pressure, and the siliceous raw material is further added to adjust the Ca / (Si + Al) molar ratio to 0.6 to 1.1. Slurry obtained by hydrothermally synthesizing the slurry (A) within the range and a slurry consisting of a calcareous raw material, a siliceous raw material and water within a Ca / (Si + Al) molar ratio of 0.8 to 1.1. (B) is mixed at a ratio within a range surrounded by coordinates a, b, c and d shown in FIG. 1, and further, 1 to 10% of reinforcing fiber and 10% based on the weight of solid content in the slurry.
It is characterized in that the following clay minerals are added, molded, and hydrothermally reacted at a temperature within the range of 140 to 220 ° C.
【0006】[0006]
【作用】本発明方法において使用する石灰質原料として
は消石灰、生石灰等が挙げられ、また、珪酸質原料とし
ては珪砂、焼成珪藻土等、非晶質原料としては珪藻土、
シリカフューム、ニップシール等が挙げられる。The calcareous raw material used in the method of the present invention includes slaked lime, quick lime, etc., the siliceous raw material is silica sand, calcined diatomaceous earth, etc., and the amorphous raw material is diatomaceous earth,
Examples thereof include silica fume and nip seal.
【0007】本発明方法において使用するスラリー(A)
は、石灰質原料と非晶質珪酸原料をCa/(Si+Al)
モル比1.0〜5.0の割合で配合し、更に水を加えたも
のを常圧下で加熱処理し、更に、珪酸質原料を加えてC
a/(Si+Al)モル比を0.6〜1.1としたものであ
る。ここで、スラリー(A)のCa/(Si+Al)モル比
が0.6未満であったり、1.1を超えると、得られる珪
酸カルシウム成形体の強度及び寸法安定性が低下する。
なお、該モル比は好適には0.8〜1.0の範囲内であ
る。なお、上記加熱処理は70〜95℃、好ましくは8
0〜90℃の温度範囲で行われる。Slurry (A) used in the method of the present invention
Is Ca / (Si + Al) for calcareous raw material and amorphous silicic acid raw material.
The mixture was added at a molar ratio of 1.0 to 5.0, and water was added to the mixture, which was then heat-treated under normal pressure.
The a / (Si + Al) molar ratio was set to 0.6 to 1.1. Here, if the Ca / (Si + Al) molar ratio of the slurry (A) is less than 0.6 or exceeds 1.1, the strength and dimensional stability of the obtained calcium silicate compact will be reduced.
The molar ratio is preferably in the range of 0.8 to 1.0. The heat treatment is performed at 70 to 95 ° C., preferably 8
It is performed in a temperature range of 0 to 90 ° C.
【0008】本発明方法において使用するスラリー(B)
は、石灰質原料と珪酸質原料をCa/(Si+Al)モル
比0.8〜1.1の割合で配合し、更に水を加えたものを
慣用の操作にて水熱合成したものである。なお、スラリ
ー(B)中の未反応石灰量は5%以下であることが好まし
い。ここで、スラリー(B)のCa/(Si+Al)モル比
が0.8未満では未反応珪酸質原料が多くなり、珪酸カ
ルシウム成形体の軽量化すなわち低比重化には不適であ
り、また、該モル比が1.1を超えると未反応石灰量が
5%を超えるために好ましくない。なお、スラリー(B)
を使用することにより、珪酸カルシウム成形体の低比重
化、高強度化及び寸法安定性の向上に寄与する。Slurry (B) used in the method of the present invention
Is a mixture of a calcareous raw material and a siliceous raw material at a Ca / (Si + Al) molar ratio of 0.8 to 1.1, and water added thereto, which is hydrothermally synthesized by a conventional operation. The amount of unreacted lime in the slurry (B) is preferably 5% or less. Here, if the Ca / (Si + Al) molar ratio of the slurry (B) is less than 0.8, the amount of unreacted siliceous raw material increases, which is unsuitable for reducing the weight of the calcium silicate compact, that is, reducing the specific gravity. If the molar ratio exceeds 1.1, the amount of unreacted lime exceeds 5%, which is not preferable. In addition, slurry (B)
By using, it contributes to the low specific gravity, high strength, and improvement in dimensional stability of the calcium silicate compact.
【0009】上記スラリー(A)とスラリー(B)の配合割
合は、スラリー(A)の石灰質原料と非晶質珪酸原料のC
a/(Si+Al)モル比とスラリー(B)の割合(%)の関
係を示す図1の座標a、b、c及びdで囲まれる範囲内
である。The mixing ratio of the slurry (A) and the slurry (B) is such that the calcareous raw material of the slurry (A) and the amorphous silicic acid raw material of C are mixed.
It is within the range surrounded by the coordinates a, b, c and d in FIG. 1, which shows the relationship between the a / (Si + Al) molar ratio and the ratio (%) of the slurry (B).
【0010】ここで、図1の座標aとbを結ぶ線よりも
左側では、スラリー(A)の常圧下での加熱処理におい
て、嵩高となり過ぎるため、低比重となり過ぎ、スラリ
ー(B)の割合を少なくする必要があるため高強度及び寸
法安定性が得られない。また、図1の座標cとdを結ぶ
線よりも右側では、スラリー(A)の常圧下で加熱処理し
てもゲル化が少なく、低比重化にはスラリー(B)を多く
加える必要があり、濾水性が低下し、生産性が悪くなる
と共にコスト的に問題がある。Here, on the left side of the line connecting the coordinates a and b in FIG. 1, since the slurry (A) becomes too bulky in the heat treatment under normal pressure, the specific gravity becomes too low, and the ratio of the slurry (B) is high. Therefore, high strength and dimensional stability cannot be obtained. Further, on the right side of the line connecting the coordinates c and d in FIG. 1, gelation is small even if the slurry (A) is heat-treated under normal pressure, and it is necessary to add a large amount of the slurry (B) to reduce the specific gravity. However, drainage is lowered, productivity is deteriorated, and there is a problem in cost.
【0011】上述のような配合割合でスラリー(A)とス
ラリー(B)を混合した後、スラリーの固形分の重量を基
準として1〜10%の補強繊維を添加する。補強繊維と
してはセルロース、ビニロン、PAN、カーボン繊維及
びガラス繊維等を使用することができる。After mixing the slurry (A) and the slurry (B) in the above mixing ratio, 1 to 10% of reinforcing fibers are added based on the weight of the solid content of the slurry. As the reinforcing fiber, cellulose, vinylon, PAN, carbon fiber, glass fiber or the like can be used.
【0012】また、本発明方法においては、上記スラリ
ーに粘土鉱物をスラリーの固形分の重量を基準として1
0%以下、好ましくは5〜10%の量で添加することも
できる。粘土鉱物の添加量が10%を超えると得られる
珪酸カルシウム成形体の軽量性と強度が低下する。粘土
鉱物としてはセピオライトやタルクを使用することが好
ましい。なお、セピオライトは吸放湿特性に優れ、調湿
効果を向上させる。これはセピオライトが低比重で気孔
率が高く、吸放湿による寸法安定性が良好であるためで
ある。また、タルクは切削加工性を向上させるものであ
り、珪酸カルシウム成形体を軽量化すると共に加工性を
特に優れたものにする。In the method of the present invention, clay mineral is added to the above slurry based on the weight of the solid content of the slurry.
It can also be added in an amount of 0% or less, preferably 5 to 10%. If the amount of the clay mineral added exceeds 10%, the lightness and strength of the obtained calcium silicate compact will decrease. It is preferable to use sepiolite or talc as the clay mineral. In addition, sepiolite has an excellent moisture absorbing / releasing property and improves the humidity control effect. This is because sepiolite has a low specific gravity, high porosity, and good dimensional stability due to moisture absorption and desorption. In addition, talc improves the machinability, reduces the weight of the calcium silicate compact and makes the machinability particularly excellent.
【0013】スラリーに補強繊維と所望により粘土鉱物
を添加した後、所定の形状に成形し、140〜220℃
の温度範囲で水熱反応を行う。水熱反応の際に、温度が
140℃未満であると、未反応ものが多くなるために好
ましくなく、また、220℃を超えると得られる珪酸カ
ルシウム成形体の強度が低下するために好ましくない。After adding reinforcing fibers and, if desired, clay mineral to the slurry, the slurry is molded into a predetermined shape, and the temperature is 140 to 220 ° C.
The hydrothermal reaction is carried out in the temperature range. In the hydrothermal reaction, if the temperature is lower than 140 ° C., unreacted substances increase, which is not preferable, and if the temperature exceeds 220 ° C., the strength of the obtained calcium silicate compact decreases, which is not preferable.
【0014】[0014]
【実施例】以下に実施例を挙げて本発明方法を更に説明
する。 実施例 スラリー(A)の調製 下記の表1に示すCa/(Si+Al)モル比で原料を配
合し、表1に示す加熱条件で処理した後、珪酸質原料の
2次添加を行ってCa/(Si+Al)モル比を調整する
ことによりスラリー(A)を得た。EXAMPLES The method of the present invention will be further described below with reference to examples. Example Preparation of Slurry (A) Raw materials were mixed at a Ca / (Si + Al) molar ratio shown in Table 1 below, treated under the heating conditions shown in Table 1, and then a siliceous raw material was added secondarily to give Ca / A slurry (A) was obtained by adjusting the (Si + Al) molar ratio.
【0015】[0015]
【表1】 [Table 1]
【0016】スラリー(B)の調製 下記の表2に示すCa/(Si+Al)モル比及び条件に
てスラリーを水熱合成することによりスラリー(B)を調
製した。Preparation of Slurry (B) Slurry (B) was prepared by hydrothermally synthesizing the slurry at the Ca / (Si + Al) molar ratio and conditions shown in Table 2 below.
【0017】[0017]
【表2】 [Table 2]
【0018】下記の表3には、本発明方法による珪酸カ
ルシウム成形体の製造条件、配合並びに得られた珪酸カ
ルシウム成形体の諸特性を記載する。なお、スラリーの
成形には、プレスを使用し、150×80×10mmの
寸法とした。また、図2には、実施例1〜7におけるス
ラリー(A)の石灰質原料と非晶質珪酸原料のCa/(S
i+Al)モル比とスラリー(B)の割合の関係を示し
た。Table 3 below shows the production conditions and formulation of the calcium silicate compact according to the method of the present invention, and various characteristics of the obtained calcium silicate compact. A press was used to form the slurry, and the dimensions were 150 × 80 × 10 mm. In addition, in FIG. 2, Ca / (S of the calcareous raw materials and the amorphous silicic acid raw materials of the slurries (A) in Examples 1 to 7 are shown.
The relationship between the (i + Al) molar ratio and the slurry (B) ratio is shown.
【0019】[0019]
【表3】 [Table 3]
【0020】下記の表4には、本発明方法による珪酸カ
ルシウム成形体の製造条件、配合並びに得られた珪酸カ
ルシウム成形体の諸特性を記載する。なお、スラリーの
成形には、プレスを使用し、150×80×10mmの
寸法とした。また、図3には、比較例1〜10における
スラリー(A)の石灰質原料と非晶質珪酸原料のCa/
(Si+Al)モル比とスラリー(B)の割合の関係を示し
た。In Table 4 below, the production conditions and formulation of the calcium silicate compact according to the method of the present invention and various characteristics of the obtained calcium silicate compact are described. A press was used to form the slurry, and the dimensions were 150 × 80 × 10 mm. In addition, in FIG. 3, Ca / of the calcareous raw materials and the amorphous silicic acid raw materials of the slurries (A) in Comparative Examples 1 to 10 is shown.
The relationship between the (Si + Al) molar ratio and the slurry (B) ratio is shown.
【0021】[0021]
【表4】 [Table 4]
【0022】[0022]
【発明の効果】本発明方法によれば、上述のように2種
のスラリーを併用することにより、軽量、高強度で寸法
安定性に優れた珪酸カルシウム成形体を提供することが
できる。According to the method of the present invention, by using two kinds of slurries together as described above, it is possible to provide a calcium silicate compact which is lightweight, has high strength and is excellent in dimensional stability.
【図1】スラリー(A)の石灰質原料と非晶質珪酸原料の
Ca/(Si+Al)モル比とスラリー(B)の割合(%)の
関係を示す図である。FIG. 1 is a diagram showing a relationship between a Ca / (Si + Al) molar ratio of a calcareous raw material of a slurry (A) and an amorphous silicic acid raw material and a ratio (%) of a slurry (B).
【図2】実施例1〜7におけるスラリー(A)の石灰質原
料と非晶質珪酸原料のCa/(Si+Al)モル比とスラ
リー(B)の割合の関係を示す図である。FIG. 2 is a diagram showing a relationship between a Ca / (Si + Al) molar ratio of a calcareous raw material of a slurry (A) and an amorphous silicic acid raw material and a ratio of a slurry (B) in Examples 1 to 7.
【図3】比較例1〜10におけるスラリー(A)の石灰質
原料と非晶質珪酸原料のCa/(Si+Al)モル比とス
ラリー(B)の割合の関係を示す図である。FIG. 3 is a diagram showing the relationship between the Ca / (Si + Al) molar ratio of the calcareous raw material of the slurry (A) and the amorphous silicic acid raw material and the ratio of the slurry (B) in Comparative Examples 1 to 10.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 古賀 憲明 茨城県石岡市大字柏原6番1号 株式会社 アスク中央研究所内 (72)発明者 陶山 優 茨城県石岡市大字柏原6番1号 株式会社 アスク中央研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Noriaki Koga 6-1 Kashiwara, Ishioka-shi, Ibaraki Asuka Central Research Institute Co., Ltd. (72) Yutaka Suyama 6-1 Kashiwara, Ishioka-shi, Ibaraki Ask Central research institute
Claims (2)
の範囲内にある石灰質原料、非晶質珪酸原料及び水より
なるスラリーを常圧下で加熱処理し、更に、珪酸質原料
を加えてCa/(Si+Al)モル比を0.6〜1.1の範
囲内としたスラリー(A)と、Ca/(Si+Al)モル比
0.8〜1.1の範囲内にある石灰質原料、珪酸質原料及
び水よりなるスラリーを水熱合成することにより得られ
るスラリー(B)を、図1に示す座標a、b、c及びdで
囲まれる範囲内の割合で混合し、更に、スラリー中の固
形分の重量を基準として1〜10%の補強繊維を添加
し、成形し、140〜220℃の範囲内の温度で水熱反
応を行うことを特徴とする珪酸カルシウム成形体の製造
方法。1. A Ca / (Si + Al) molar ratio of 1.0 to 5.0.
The slurry consisting of the calcareous raw material, the amorphous silicic acid raw material and the water within the range of is heat-treated under normal pressure, and the silicic raw material is further added to adjust the Ca / (Si + Al) molar ratio to 0.6 to 1.1. Slurry obtained by hydrothermally synthesizing the slurry (A) within the range and a slurry composed of a calcareous raw material, a siliceous raw material and water having a Ca / (Si + Al) molar ratio within the range of 0.8 to 1.1. (B) is mixed in a ratio within a range surrounded by coordinates a, b, c and d shown in FIG. 1, and 1 to 10% of reinforcing fiber is added based on the weight of the solid content in the slurry. , And performing a hydrothermal reaction at a temperature in the range of 140 to 220 ° C., a method for producing a calcium silicate compact.
の範囲内にある石灰質原料、非晶質珪酸原料及び水より
なるスラリーを常圧下で加熱処理し、更に、珪酸質原料
を加えてCa/(Si+Al)モル比を0.6〜1.1の範
囲内としたスラリー(A)と、Ca/(Si+Al)モル比
0.8〜1.1の範囲内にある石灰質原料、珪酸質原料及
び水よりなるスラリーを水熱合成することにより得られ
るスラリー(B)を、図1に示す座標a、b、c及びdで
囲まれる範囲内の割合で混合し、更に、スラリー中の固
形分の重量を基準として1〜10%の補強繊維と10%
以下の粘土鉱物を添加し、成形し、140〜220℃の
範囲内の温度で水熱反応を行うことを特徴とする珪酸カ
ルシウム成形体の製造方法。2. A Ca / (Si + Al) molar ratio of 1.0 to 5.0.
The slurry consisting of the calcareous raw material, the amorphous silicic acid raw material and the water within the range of is heat treated under normal pressure, and the siliceous raw material is further added to adjust the Ca / (Si + Al) molar ratio to 0.6 to 1.1. Slurry obtained by hydrothermally synthesizing the slurry (A) within the range and a slurry consisting of a calcareous raw material, a siliceous raw material and water within a Ca / (Si + Al) molar ratio of 0.8 to 1.1. (B) is mixed at a ratio within a range surrounded by coordinates a, b, c and d shown in FIG. 1, and further, 1 to 10% of reinforcing fiber and 10% based on the weight of solid content in the slurry.
A method for producing a calcium silicate compact, which comprises adding and molding the following clay mineral and performing a hydrothermal reaction at a temperature within a range of 140 to 220 ° C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1661892A JP3273801B2 (en) | 1992-01-31 | 1992-01-31 | Method for producing calcium silicate molded body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1661892A JP3273801B2 (en) | 1992-01-31 | 1992-01-31 | Method for producing calcium silicate molded body |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05213657A true JPH05213657A (en) | 1993-08-24 |
JP3273801B2 JP3273801B2 (en) | 2002-04-15 |
Family
ID=11921328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1661892A Expired - Lifetime JP3273801B2 (en) | 1992-01-31 | 1992-01-31 | Method for producing calcium silicate molded body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3273801B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999042418A1 (en) * | 1998-02-23 | 1999-08-26 | Asahi Kasei Kogyo Kabushiki Kaisha | Cured calcium silicate object with high strength |
JP2002284564A (en) * | 2001-03-26 | 2002-10-03 | Kenzai Gijutsu Kenkyusho:Kk | Calcium silicate molded product and method of manufacture |
-
1992
- 1992-01-31 JP JP1661892A patent/JP3273801B2/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999042418A1 (en) * | 1998-02-23 | 1999-08-26 | Asahi Kasei Kogyo Kabushiki Kaisha | Cured calcium silicate object with high strength |
GB2349879A (en) * | 1998-02-23 | 2000-11-15 | Asahi Chemical Ind | Cured calcium silicate object with high strength |
GB2349879B (en) * | 1998-02-23 | 2001-09-05 | Asahi Chemical Ind | Cured calcium silicate object with high strength |
US6464771B1 (en) | 1998-02-23 | 2002-10-15 | Asahi Kasei Kabushiki Kaisha | Cured calcium silicate object with high strength |
CN100351201C (en) * | 1998-02-23 | 2007-11-28 | 旭化成株式会社 | Cured calcium silicate object with high strength |
JP2002284564A (en) * | 2001-03-26 | 2002-10-03 | Kenzai Gijutsu Kenkyusho:Kk | Calcium silicate molded product and method of manufacture |
JP4694708B2 (en) * | 2001-03-26 | 2011-06-08 | 株式会社エーアンドエーマテリアル | Method for producing calcium silicate molded body |
Also Published As
Publication number | Publication date |
---|---|
JP3273801B2 (en) | 2002-04-15 |
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