JPH028991B2 - - Google Patents
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- Publication number
- JPH028991B2 JPH028991B2 JP56049725A JP4972581A JPH028991B2 JP H028991 B2 JPH028991 B2 JP H028991B2 JP 56049725 A JP56049725 A JP 56049725A JP 4972581 A JP4972581 A JP 4972581A JP H028991 B2 JPH028991 B2 JP H028991B2
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- weight
- gypsum
- slurry
- added
- hemihydrate
- Prior art date
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- Expired - Lifetime
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- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は、高炉水砕スラグと半水石膏を主材料
としこれに必要に応じてガラス繊維等の補強繊維
を添加して、靭性を高め、さらに調合材料、即ち
反応刺激剤を添加することにより、早硬性、高強
度、耐水性を有する繊維強化スラグ石膏系複合材
の製造方法に関するもので、特にその早硬性によ
り従来のバツチ式製造法に代わり、連続成形法に
よる生産を可能としたことを大きな特徴とする。
近年、建築物の高層化とともに壁材の工法も湿
式から乾式に変わりつつあり、それに伴つて安価
で施工性のよい壁装材の出現が望まれている。従
来の壁製材は石膏系の場合吸水量が大きいこと
や、吸水時の物性が極端に低下するという欠点を
もつており、セメント系のものは衝撃強度に劣る
などの欠点があつた。
本発明は高炉水砕スラグと半水石膏を主材料と
してこれらを重量比で2:8〜8:2の割合に混
合したものに無機質繊維を前記主材料の全重量に
対して0.3〜20重量%添加し、さらにポルトラン
ドセメントを0.5〜20重量%、硫酸アルミニウム
含有物質を硫酸アルミニウム換算で0.1〜2.0重量
%、弗化塩類を0.1〜2.0重量%の割合で単独、あ
るいは、複合添加して調合材料とし、これに適量
の水を加えてスラリーとしたものをベルト上で連
続的に成型し、10〜30分で凝結させ、これを50℃
〜200℃の温度で加熱養成乾燥することにより連
続的に壁装材を生産するものである。
本発明の複合材、即ち硬化体を構成する主材料
は高炉水砕スラグと半水石膏であるが、高炉水砕
スラグは潜在水硬性のある反応性高炉スラグを指
し、この粉末度は大きいほど凝結が早くなり高強
度の硬化体が得られて好ましいが、その比表面積
は3000cm2/g以上有すればよい。高炉水砕のスラ
グの化学組成の一例を第一表に示す。
The present invention uses granulated blast furnace slag and gypsum hemihydrate as the main materials, and if necessary, reinforcing fibers such as glass fibers are added thereto to increase toughness, and furthermore, by adding a compounding material, that is, a reaction stimulant. , relates to a method for manufacturing fiber-reinforced slag gypsum composites that have quick hardening, high strength, and water resistance.In particular, the quick hardening properties enable production by continuous molding instead of the conventional batch manufacturing method. Make it a major feature. In recent years, as buildings have become taller, the method of constructing wall materials has been changing from a wet method to a dry method, and along with this, there has been a desire for a wall covering material that is inexpensive and easy to construct. Conventional wall lumber has the disadvantages that gypsum-based materials absorb a large amount of water and have extremely poor physical properties when water is absorbed, while cement-based materials have drawbacks such as poor impact strength. The present invention mainly consists of granulated blast furnace slag and gypsum hemihydrate, which are mixed in a weight ratio of 2:8 to 8:2, and inorganic fibers are added in an amount of 0.3 to 20% by weight based on the total weight of the main materials. %, and further add 0.5 to 20% by weight of Portland cement, 0.1 to 2.0% by weight of aluminum sulfate-containing substances, and 0.1 to 2.0% by weight of fluoride salts either singly or in combination. A suitable amount of water is added to make a slurry, which is continuously formed on a belt, solidified in 10 to 30 minutes, and heated to 50°C.
Wall covering material is continuously produced by heating, curing and drying at a temperature of ~200°C. The main materials constituting the composite material of the present invention, that is, the hardened material, are granulated blast furnace slag and gypsum hemihydrate. This is preferable because it allows for rapid setting and a cured product with high strength, but it is sufficient that the specific surface area is 3000 cm 2 /g or more. An example of the chemical composition of slag from granulated blast furnaces is shown in Table 1.
【表】
半水石膏にはα型と一般に焼石膏であるβ型の
2種類があるが、これらはどちらでも適用でき
る。但し本発明はスラリーの凝結時間を10〜30分
にすることが必要であつて、初期強度は半水石膏
の二水化に一部依存しているために半水石膏でな
くてはならない。α−半水石膏は、β−半水石膏
に比べて混水量が小さくても混練が可能なため、
初期強度はβ−半水石膏を使用したものに比べて
大きくなるが、本発明によつて得られた硬化体が
高強度を示すのは、本質的にスラグの水和物
(CaO−SiO2−Al2O3−nH2Oなど)と、一部にス
ラグの主成分であるCaO−Al2O3−MgO−SiO2
系のガラス質が石膏と反応して生成されたカルシ
ウムサルホアルミネート水和物(3CaO・
Al2O3・3CaSO4・32H2O)によるものである。
それ故、α−半水石膏を使用することは本発明の
硬化体の本質的な強度に何ら関与しない。壁装材
に汎用するためには、それに使用される原材料は
安価で安定供給が可能なものである必要があり、
本発明の複合材の原材料としてはβ−半水石膏と
して排煙脱硫石膏、リン酸石膏などの副産石膏の
ほか、天然石膏でも一般に焼石膏と称する材料を
使用して何ら支障はない。
必要に応じて主材料中に配合される補強繊維と
しては、本発明の複合材を不燃材料とする必要性
から無機質繊維や炭素繊維を使用することが好ま
しい。無機質繊維としてはガラス繊維、スラグウ
ール、あるいは、アスベスト等を使用することが
できる。本発明の複合材は主材料にアルカリ性の
高炉水砕スラグを使用しているが、後で述べる調
合材料によつてその反応時においてもPHを10以下
にすることが可能であるので、ガラス繊維として
は、無アルカリガラス、または、低アルカリガラ
スの一般にEガラスと呼ばれるものが使用でき
る。補強繊維を添加すると、硬化体の曲げ強度が
増加すると共に、靭性が著しく改良されて耐衝撃
性に優れた材料となる。補強繊維にガラス繊維を
使用する場合、その繊維長や添加量、またはスト
ランドの収束性の大小によつて物性は変化する。
繊維長は、長くなるほど補強効果が優れている
が、成型時の難易度や加工性を考慮して13〜50mm
が適当である。添加量は主材料に対して0.3〜7.0
重量%が適当であるが、、これはストランドの収
束性と大いに関係があつて収束性が小さい場合、
即ち解繊度の高い場合には0.3〜3.0重量%が適当
でこれ以上の添加量ではむしろ曲げ強度、圧縮強
度ともに低下する。調合材料にはポルトランドセ
メント、硫酸アルミニウム含有物質、および、弗
化塩類物質を使用するが、これらは高炉水砕スラ
グの凝結を促進させる反応刺激剤とすることを主
目的としており、調合に際してはこれら三種類の
うち一種類、あるいは、二種類を組み合わせて使
用する。
ポルトランドセメントは、一般市販の普通ポル
トランドセメントで比表面積が3000cm2/g程度の
ものでよい。その添加量は主材料に対して0.5〜
20重量%である。
硫酸アルミニウム含有物質としては、硫酸アル
ミニウム、ナトリウム明ばん、カリウム明ばんの
いずれでもよく、その添加量は主材料に対して
0.1〜20重量%である。
弗化塩類物質としてはケイ弗化ナトリウム、ケ
イ弗化カリウム、弗化ナトリウム、弗化カリウム
のいずれでもよく、その添加量は主材料に対して
0.1〜20重量%である。
次に、本発明の硬化体はその早硬性の故に連続
押出し成型方法が採用できる。これにより版材の
大きさはベルトの幅によつて自在に変えられ、連
続的な生産によつて得られた未硬化体を50℃〜
200℃の温度の熱風乾燥炉によつて15〜48時間乾
燥する。
このように本発明方法によれば、スラリーは添
加したポルトランドセメント、硫酸アルミニウム
及び弗化塩類などの制御により、混練後、ベルト
上で数分間流動性を維持しつつ、成形され、次工
程へベルトから剥離し、かつ、担送出来る程度の
強度に凝結し、爾後の加熱養成乾燥でエトリンガ
イトにより更に硬化するため高強度、耐水性、お
よび、加工法に優れていることや、安価な主材料
を用い連続的に生産できることなど、建築材料と
しての価値はきわめて大きい。
以下に実施例について示す。但し本発明は、以
下の実施例に限定されるものではない。
実施例 1
高炉水砕スラグ60重量部、β−半水石膏40重量
部からなる主材料に対し、補強繊維として25mmの
チヨツプドストランイドガラス繊維1.0重量%と、
調合材料、即ち、反応刺激剤としてポルトランド
セメント2.0重量%、硫酸アルミニウム0.2又は0.6
又は1.0重量%をそれぞれ添加し、水を60重量%
加え、第2表に示す3種の試料No.1〜No.3を作
り、混練後スラリーを鋼製型枠に流し込んで成型
し、60℃で48時間乾燥した後、これら硬化体No.1
〜No.3の物性値を求め、これらを第3表に示す。
実施例 2
高炉水砕スラグ60重量部、β−半水石膏40重量
部からなる主材料に対し、補強繊維として25mmの
チヨツプドストランドガラス繊維1.0重量%と、
反応刺激剤としてポルトランドセメント2.0重量
%、ケイ弗化ナトリウム0.2又は0.6又は1.0重量%
をそれぞれ添加し、水を60重量%加え、第2表に
示す3種の試料No.4〜No.6を作り、混練後、スラ
リーを鋼製型枠に流し込んで成型し、60℃で48時
間乾燥した後、これら硬化体No.4〜No.6の物性値
を求めこれらを第3表に示す。[Table] There are two types of gypsum hemihydrate: α type and β type, which is generally calcined gypsum, and either of these can be applied. However, in the present invention, it is necessary to set the slurry for 10 to 30 minutes, and since the initial strength depends in part on the dihydration of gypsum hemihydrate, it must be made of gypsum hemihydrate. Compared to β-hemihydrate gypsum, α-hemihydrate gypsum can be mixed even with a smaller amount of water, so
The initial strength is higher than that using β-hemihydrate gypsum, but the reason why the hardened product obtained by the present invention shows high strength is that it is essentially a slag hydrate (CaO-SiO 2 −Al 2 O 3 −nH 2 O, etc.) and CaO−Al 2 O 3 −MgO−SiO 2 which is the main component of slag.
Calcium sulfoaluminate hydrate (3CaO・
Al2O3・3CaSO4・32H2O ) .
Therefore, the use of α-hemihydrate gypsum has no effect on the essential strength of the cured product of the present invention. In order to be used as a general-purpose wall covering material, the raw materials used must be inexpensive and have a stable supply.
As raw materials for the composite material of the present invention, in addition to by-product gypsum such as flue gas desulfurization gypsum and phosphate gypsum as β-hemihydrate gypsum, there is no problem in using natural gypsum, a material generally called calcined gypsum. It is preferable to use inorganic fibers or carbon fibers as the reinforcing fibers that may be mixed into the main material if necessary, since it is necessary to make the composite material of the present invention a noncombustible material. Glass fiber, slag wool, asbestos, or the like can be used as the inorganic fiber. The composite material of the present invention uses alkaline granulated blast furnace slag as the main material, but it is possible to reduce the pH to 10 or less even during the reaction by using the blended materials described later. As the glass, alkali-free glass or low-alkali glass, generally called E glass, can be used. Addition of reinforcing fibers increases the bending strength of the cured product and significantly improves toughness, resulting in a material with excellent impact resistance. When glass fibers are used as reinforcing fibers, the physical properties vary depending on the length of the fibers, the amount added, or the degree of convergence of the strands.
The longer the fiber length, the better the reinforcing effect, but considering the difficulty and processability during molding, the fiber length should be 13 to 50 mm.
is appropriate. Addition amount is 0.3 to 7.0 to the main material
The weight percentage is appropriate, but this has a lot to do with the convergence of the strand, and if the convergence is small,
That is, when the degree of defibration is high, 0.3 to 3.0% by weight is appropriate; if the amount added is more than this, both the bending strength and the compressive strength will decrease. Portland cement, aluminum sulfate-containing substances, and fluoride salt substances are used as compounding materials, but their main purpose is to act as a reaction stimulant to promote the coagulation of granulated blast furnace slag, so these materials are used in the compounding process. Use one of the three types or a combination of two types. The Portland cement may be a commercially available ordinary Portland cement with a specific surface area of about 3000 cm 2 /g. The amount added is 0.5 to the main material.
It is 20% by weight. The aluminum sulfate-containing substance may be aluminum sulfate, sodium alum, or potassium alum, and the amount added should be determined based on the main material.
It is 0.1-20% by weight. The fluoride salt substance may be sodium silicofluoride, potassium silicofluoride, sodium fluoride, or potassium fluoride, and the amount added should be determined based on the main material.
It is 0.1-20% by weight. Next, the cured product of the present invention can be molded by continuous extrusion because of its quick hardening properties. As a result, the size of the plate material can be freely changed depending on the width of the belt, and the uncured material obtained through continuous production can be
Dry for 15-48 hours in a hot air drying oven at a temperature of 200°C. According to the method of the present invention, the slurry is kneaded by controlling the added Portland cement, aluminum sulfate, fluoride salts, etc., and then shaped while maintaining fluidity on the belt for several minutes before being transferred to the belt for the next process. It condenses to a strength that allows it to be peeled off and carried, and is then further hardened by ettringite during heating and drying, so it has high strength, water resistance, and excellent processing methods, and uses inexpensive main materials. Its value as a building material is extremely large, as it can be used and produced continuously. Examples are shown below. However, the present invention is not limited to the following examples. Example 1 Main material consisting of 60 parts by weight of granulated blast furnace slag and 40 parts by weight of β-hemihydrate gypsum, 1.0% by weight of 25 mm chopped stranded glass fiber as reinforcing fiber,
Preparation materials: Portland cement 2.0% by weight as reaction stimulant, aluminum sulfate 0.2 or 0.6
Or add 1.0% by weight each and 60% by weight of water.
In addition, three types of samples No. 1 to No. 3 shown in Table 2 were prepared, and after kneading, the slurry was poured into a steel mold, molded, and dried at 60°C for 48 hours.
~The physical property values of No. 3 were determined, and these are shown in Table 3. Example 2 Main material consisting of 60 parts by weight of granulated blast furnace slag and 40 parts by weight of β-hemihydrate gypsum, 1.0% by weight of 25 mm chopped strand glass fiber as reinforcing fiber,
Portland cement 2.0% by weight, sodium silicofluoride 0.2 or 0.6 or 1.0% by weight as reaction stimulants
and 60% by weight of water to make the three types of samples No. 4 to No. 6 shown in Table 2. After kneading, the slurry was poured into a steel form and molded, and heated to 48°C at 60°C. After drying for a period of time, the physical properties of these cured products No. 4 to No. 6 were determined and are shown in Table 3.
【表】【table】
【表】
試験を行つた圧縮強度を示す。
実施例 3
高炉水砕スラグ50重量部、β−半水石膏50重量
部からなる主材料に対し反応刺激剤として、硫酸
ナトリウム0又は0.4又は0.8重量%を添加し、水
を60重量%加え、第4表に示す試料No.1〜No.3を
作り、混練後ビカー針装置凝結時間測定器によつ
て見掛けの凝結時間を測定し、これを第5表に示
す。
実施例 4
高炉水砕スラグ70重量部、β−半水石膏30重量
部からなる主材料に対し反応刺激剤として硫酸ア
ルミニウム0又は0.4又は0.8又は1.2又は1.6又は
2.0重量%を添加し、水を50重量%加え、第4表
に示す試料No.4〜No.9を作り、混練後ビカー針装
置凝結時間測定器によつて見掛けの凝結時間を測
定し、これを第5表に示す。これは第1図に明ら
かなように、硫酸アルミニウム等の反応刺激剤を
使用することにより高炉水砕スラグ石膏複合剤の
凝結時間を20分以内とすることができ、連続押出
し成型による製造法が可能であることを示すもの
である。[Table] Shows the compressive strength tested.
Example 3 To the main material consisting of 50 parts by weight of granulated blast furnace slag and 50 parts by weight of β-hemihydrate gypsum, 0, 0.4 or 0.8% by weight of sodium sulfate was added as a reaction stimulant, and 60% by weight of water was added. Samples No. 1 to No. 3 shown in Table 4 were prepared, and after kneading, the apparent setting time was measured using a Vicat needle device setting time measuring device, and the results are shown in Table 5. Example 4 Aluminum sulfate 0 or 0.4 or 0.8 or 1.2 or 1.6 or
2.0% by weight and 50% by weight of water to prepare samples No. 4 to No. 9 shown in Table 4, and after kneading, measure the apparent setting time with a Vicat needle setting time measuring device, This is shown in Table 5. As is clear from Figure 1, by using a reaction stimulant such as aluminum sulfate, the setting time of the blast furnace granulated slag gypsum composite can be reduced to within 20 minutes, and the production method using continuous extrusion molding is This shows that it is possible.
【表】【table】
【表】【table】
【表】
スラリーに徐々に始発用針を落下させ、針の先
端が上面より約1mmのところに止まるときを始発
とし、終結は終結用針を同じく落下させて、針の
跡はとどめるが環の跡は残さないときを終結とす
る。即ち凝結の所要時間は終結時間となる。
実施例 5
高炉水砕スラグ20乃至80重量部と、β−半水石
膏80乃至20重量部からなる7種類の主材料に対
し、補強繊維として25mmのチヨツプドストランド
ガラス繊維2.0重量%と、反応刺激剤としてポル
トランドセメント2.0重量%、硫酸アルミニウム
0.4重量%をそれぞれ添加しこれらを第6表に示
す7種の試料No.1〜No.7とし、これらに第6表の
末尾に示す所定量の水を添加し、混練後、スラリ
ーを鋼製型枠に流し込んで成型し、60℃で48時間
乾燥した後、これら硬化体No.1〜No.7の物性値を
求め、これらを第7表に示す。[Table] Gradually drop the starting needle into the slurry, and the starting point is when the tip of the needle stops approximately 1 mm from the top surface.To finish, drop the ending needle in the same way. It ends when it leaves no trace. That is, the time required for coagulation is the final time. Example 5 Seven main materials consisting of 20 to 80 parts by weight of granulated blast furnace slag and 80 to 20 parts by weight of β-hemihydrate gypsum were combined with 2.0% by weight of 25 mm chopped strand glass fiber as reinforcing fibers. , Portland cement 2.0% by weight as reaction stimulant, aluminum sulfate
0.4% by weight was added to each of the seven types of samples No. 1 to No. 7 shown in Table 6. To these, a predetermined amount of water shown at the end of Table 6 was added, and after kneading, the slurry was made into steel. After pouring into a mold and molding and drying at 60° C. for 48 hours, the physical properties of these cured products No. 1 to No. 7 were determined and are shown in Table 7.
【表】【table】
【表】
試験を行つた圧縮強度を示す。
[Table] Shows the compressive strength tested.
第1図は高炉水砕スラグ50又は70重量部、β−
半水石膏50又は30重量部のそれぞれからなる主材
料に対し、水を前者の場合60重量%、後者は50重
量%入れ反応刺激剤として硫酸アルミニウムを0
〜2.0重量%の範囲に添加して混練した場合の硫
酸アルミニウムの添加量とスラリーの凝結時間
(見掛けの終結時間)との関係を示すものである。
Figure 1 shows 50 or 70 parts by weight of granulated blast furnace slag, β-
The main material consists of 50 or 30 parts by weight of gypsum hemihydrate, 60% by weight for the former and 50% by weight for the latter, and 0% aluminum sulfate as a reaction stimulant.
This figure shows the relationship between the amount of aluminum sulfate added and the coagulation time (apparent completion time) of the slurry when the aluminum sulfate is added in the range of ~2.0% by weight and kneaded.
Claims (1)
れらを重量比で2:8〜8:2の割合に混合した
ものに無機質繊維を前記主材料の全重量に対して
0.3〜20重量%添加し、さらにポルトランドセメ
ントを0.5〜20重量%、硫酸アルミニウム含有物
質を硫酸アルミニウム換算で0.1〜2.0重量%、弗
化塩類を0.1〜2.0重量%の割合で単独あるいは複
合添加して調合材料とし、これに適量の水を加え
てスラリーとしたものをベルト上で連続的に成型
し、10〜30分で凝結させ、これを50℃〜200℃の
温度で加熱養成乾燥することを特徴とする繊維強
化スラグ石膏系複合材の製造方法。1 The main materials are granulated blast furnace slag and gypsum hemihydrate, which are mixed in a weight ratio of 2:8 to 8:2, and inorganic fibers are added to the total weight of the main materials.
Add 0.3 to 20% by weight, and further add 0.5 to 20% by weight of Portland cement, 0.1 to 2.0% by weight of aluminum sulfate-containing substances, and 0.1 to 2.0% by weight of fluoride salts, singly or in combination. A slurry is formed by adding an appropriate amount of water to the slurry, which is continuously molded on a belt, solidified in 10 to 30 minutes, and heated and cured at a temperature of 50 to 200 degrees Celsius to dry it. A method for producing a fiber-reinforced slag gypsum composite material characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4972581A JPS57166357A (en) | 1981-04-01 | 1981-04-01 | Manufacture of fiber reinforced slag gypsum composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4972581A JPS57166357A (en) | 1981-04-01 | 1981-04-01 | Manufacture of fiber reinforced slag gypsum composite material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57166357A JPS57166357A (en) | 1982-10-13 |
| JPH028991B2 true JPH028991B2 (en) | 1990-02-28 |
Family
ID=12839158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4972581A Granted JPS57166357A (en) | 1981-04-01 | 1981-04-01 | Manufacture of fiber reinforced slag gypsum composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57166357A (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59217662A (en) * | 1983-05-26 | 1984-12-07 | 株式会社ノダ | Inorganic construction material and manufacture |
| JPS59223264A (en) * | 1983-05-27 | 1984-12-15 | 株式会社 ノダ | Manufacture of inorganic construction material |
| JPS6389447A (en) * | 1986-10-01 | 1988-04-20 | 三菱マテリアル株式会社 | Manufacture of fiber reinforced gypsum base hardened body |
| JPH06102331B2 (en) * | 1990-07-27 | 1994-12-14 | 東京都 | Method for manufacturing multi-layer block |
| JPH07101767A (en) * | 1991-03-29 | 1995-04-18 | Noda Corp | Lightweight inorganic building material |
| JP4897530B2 (en) * | 2007-03-23 | 2012-03-14 | ルネサスエレクトロニクス株式会社 | Photocoupler and its assembly method |
| JP4802255B2 (en) * | 2009-03-06 | 2011-10-26 | 吉野石膏株式会社 | Gypsum-based solidifying material mainly composed of a gypsum composition capable of suppressing hydrogen sulfide |
| JP5632768B2 (en) * | 2011-02-10 | 2014-11-26 | 吉野石膏株式会社 | Method for suppressing hydrogen sulfide generation |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53130723A (en) * | 1977-03-23 | 1978-11-15 | Mitsubishi Mining & Cement Co | Method of producing hardened body of gypsum reinforced with fiber |
| JPS5843345B2 (en) * | 1977-11-10 | 1983-09-26 | 三菱鉱業セメント株式会社 | Method for producing plaster-based cured product |
-
1981
- 1981-04-01 JP JP4972581A patent/JPS57166357A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57166357A (en) | 1982-10-13 |
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