JPS6012986B2 - Method for producing inorganic cured body - Google Patents
Method for producing inorganic cured bodyInfo
- Publication number
- JPS6012986B2 JPS6012986B2 JP9178377A JP9178377A JPS6012986B2 JP S6012986 B2 JPS6012986 B2 JP S6012986B2 JP 9178377 A JP9178377 A JP 9178377A JP 9178377 A JP9178377 A JP 9178377A JP S6012986 B2 JPS6012986 B2 JP S6012986B2
- Authority
- JP
- Japan
- Prior art keywords
- gypsum
- diffraction
- tsh
- reaction rate
- cured body
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 239000010440 gypsum Substances 0.000 claims description 24
- 229910052602 gypsum Inorganic materials 0.000 claims description 24
- 239000013078 crystal Substances 0.000 claims description 21
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- CJONZFZTOGYADY-UHFFFAOYSA-N O.OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O Chemical compound O.OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O CJONZFZTOGYADY-UHFFFAOYSA-N 0.000 claims description 3
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000002245 particle Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 229910052925 anhydrite Inorganic materials 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000282376 Panthera tigris Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- -1 dihydrate salt Chemical class 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
【発明の詳細な説明】 この発明は無機硬化体の製造方法に関するものである。[Detailed description of the invention] This invention relates to a method for producing an inorganic cured body.
一般に、カルシウムアルミネートトリサルフエートハィ
ドレート(*a0・針203・丈aS04・31〜32
日20、以下TSHと略す)からなる無機硬化体はつぎ
のようにして製造される。すなわち、カルシウムアルミ
ネートモノサルフエートハイドレート($ao・AI2
03・CaS04・12日20、以下MSHと略す)を
石灰成分原料とアルミナ成分原料と石こう成分原料と水
とから合成し、これに石こう(CaS04・2日20)
と水とを加えてさらに反応させることによりTSHが製
造される。この場合、MSHのTSH化反応の反応速度
を速めることができれば量産化の要望に応えることがで
きる。したがって、この発明の目的は、TSH化反応の
反応速度を速めることができる無機硬化体の製造方法を
提供することである。この発明の特徴は、カルシウムア
ルミネートモノサルフェートハィドレートと石こうと水
とを反応させてカルシウムアルミネートトリサルフェー
トハィドレートからなる無機硬化体を製造する製造方法
において、石こうとして(020)結晶面に対する(0
02)結晶面の回折X線強度比が大きいものを用いるこ
とにある。Generally, calcium aluminate trisulfate hydrate (*a0, needle 203, length aS04, 31-32
An inorganic cured body made of TSH (hereinafter abbreviated as TSH) is produced as follows. That is, calcium aluminate monosulfate hydrate ($ao・AI2
03・CaS04・12th 20, hereinafter abbreviated as MSH) is synthesized from lime component raw material, alumina component raw material, gypsum component raw material and water, and gypsum (CaS04・2nd 20) is synthesized from this.
TSH is produced by adding and further reacting with water. In this case, if the reaction rate of MSH to TSH reaction can be increased, the demand for mass production can be met. Therefore, an object of the present invention is to provide a method for producing an inorganic cured product that can increase the reaction rate of the TSH conversion reaction. A feature of the present invention is that in a manufacturing method for producing an inorganic hardened body made of calcium aluminate trisulfate hydrate by reacting calcium aluminate monosulfate hydrate, gypsum, and water, the (020) crystal face is 0
02) The purpose is to use a crystal whose crystal plane has a large diffraction X-ray intensity ratio.
つぎに、この発明を詳しく説明する。Next, this invention will be explained in detail.
従は、TSH化反応において、使用する石こうの種類に
より反応速度が異なるということは明らかにされておら
ず、石こうであればどのような種類の石こうを用いても
全て反応速度は同じであると考えられていた。However, it has not been clarified that the reaction rate differs depending on the type of gypsum used in the TSH conversion reaction, and it is believed that the reaction rate is the same regardless of the type of gypsum used. It was considered.
ところが、この発明者等は、さらに研究を進め、一定の
MSHに各種の石こうを反応させてTSH化反応の反応
速度を調べた結果、(020)結晶面に対する(002
)結晶面の回折X線強度比の大きい石こうを使用すると
反応速度が速くなることを見いだした。すなわち、各種
副生物として得られる石こう(2水塩)のX線回折図は
第1図のとおりであり、各回折面の位置は全ての石こう
に共通であるが、回折X線強度が石こうの種類によりそ
れぞれ異なることを見いだした。However, the inventors conducted further research and investigated the reaction rate of the TSH conversion reaction by reacting various types of gypsum with a certain amount of MSH.
) It has been found that the reaction rate becomes faster when gypsum with a large diffraction X-ray intensity ratio of crystal planes is used. In other words, the X-ray diffraction diagram of gypsum (dihydrate) obtained as various by-products is as shown in Figure 1, and the position of each diffraction plane is common to all gypsums, but the diffraction X-ray intensity differs from that of gypsum. We found that it differs depending on the type.
特に強度変化の著しい結晶面は、(020)、(002
)、(022、051)等である。このうち、(020
)、(002)結晶面はそれぞれ回折X線強度の絶対値
が大きいため、強度変化の絶対値も大きくなる。このよ
うな結晶面の回折X線強度のそれぞれ異なる各種の石こ
うと、一定のMSHとを反応させてTSH化反応の反応
速度を調べた。その際、対象とする結晶面としては回折
X線強度の大きい(020)、(002)面を選んだ。
そして、それらの回折X線強度比および石こう中の不純
物ならびに平均粒子径が反応速度に及ぼす影響を調べた
。その結果を第1表に示す。第1表
なお、第1表において、再結晶物とは試料を110q0
、6時間加熱して半水塩にしたのち、水を加えて2水塩
にしたものである。Crystal planes with particularly remarkable changes in intensity are (020), (002)
), (022, 051), etc. Of these, (020
) and (002) crystal planes each have a large absolute value of the diffraction X-ray intensity, so the absolute value of the intensity change also becomes large. The reaction rate of the TSH conversion reaction was investigated by reacting various kinds of gypsum having different diffraction X-ray intensities on crystal planes with a certain amount of MSH. At this time, the (020) and (002) planes with high diffraction X-ray intensity were selected as the target crystal planes.
Then, the effects of their diffraction X-ray intensity ratio, impurities in the gypsum, and average particle diameter on the reaction rate were investigated. The results are shown in Table 1. Table 1 In Table 1, the recrystallized product refers to a sample of 110q0
After heating for 6 hours to make hemihydrate salt, water was added to make dihydrate salt.
また粉砕物とは、試料をコロイドミルで微粉砕したもの
である。また、(002面)/(020面)回折X線強
度比とTSH化反応速度定数の関係を第2図に示した。Moreover, the pulverized product is obtained by finely pulverizing the sample using a colloid mill. Furthermore, the relationship between the (002 plane)/(020 plane) diffraction X-ray intensity ratio and the TSH formation reaction rate constant is shown in FIG.
第1表および第2図からつぎのことがわかる。すなわち
、‘1’TSH化反応速度は、(002副/(02の寅
)回折X線強度比と相関があり、その回折X線強度比が
0.1以上の石こうを用いるとTSH化反応の反応速度
が大きくなる。The following can be seen from Table 1 and Figure 2. In other words, the '1' TSH conversion reaction rate is correlated with the (002 sub/(02 tiger) diffraction X-ray intensity ratio, and if gypsum with a diffraction The reaction rate increases.
【2’(002面)/(020面)回折X線強度比の小
さい石こうでも再結晶によりそれを大きくでき、それが
大きなものはTSH化反応速度が大きい。[2' Even gypsum with a small (002 plane)/(020 plane) diffraction X-ray intensity ratio can be increased by recrystallization, and those with a large ratio have a high TSH conversion reaction rate.
【31 石こうの粒子の大きさはTSH化反応速度とは
関係ないo‘4} 石こう中の不純物によってはTSH
化反応速度は影響されない。[31 The size of gypsum particles has no relation to the TSH conversion reaction rate o'4} Depending on the impurities in gypsum, TSH
The oxidation reaction rate is not affected.
以上のようにMSHと石こうからのTSH反応は、石こ
うの(002)結晶面が成長してその回折X線強度が大
きくなっているものほど反応性は大きく、逆に(020
)結晶面が成長してその回折×線強度が大きくなったい
るほど小さいといえる。As mentioned above, in the TSH reaction between MSH and gypsum, the more the (002) crystal plane of gypsum grows and the diffraction X-ray intensity increases, the higher the reactivity becomes;
) It can be said that the larger the crystal plane grows and its diffraction x-ray intensity becomes smaller, the smaller it becomes.
これはつぎのように考えられる。すなわち、(002)
結晶面は、(020)結晶面に対して溶解速度が大きい
ため、(002)結晶面が成長した石こうはMSHとの
反応性が大になる。そのため、(002)結晶面が成長
した石こうを用いるとTSH化反応の反応速度が遠くな
ると考えられる。なお、(020)結晶面には、(00
2)結晶面と異なり日20分子が多く配位されており、
この面がへき関面となっている。そのため、(020)
結晶面の成長した石こう(第1表試料A、B、C等)で
は、粉砕により粒子蚤を小さくしてもへき開面から分割
されるため、粒子径の大小が反応速度に関係しないこと
が明らかである。以上のように、この発明の製造方法に
よれば、石こうとして(020)結晶面に対する(00
2)結晶面の回折X線強度が大きいものを用いるため、
TSH化反応の反応速度を速めることができる。This can be considered as follows. That is, (002)
Since the crystal plane has a higher dissolution rate than the (020) crystal plane, gypsum on which the (002) crystal plane has grown has a high reactivity with MSH. Therefore, it is thought that when gypsum with grown (002) crystal planes is used, the reaction rate of the TSH formation reaction becomes slower. Note that (020) crystal plane has (00
2) Unlike the crystal plane, many molecules are coordinated,
This surface is the barrier surface. Therefore, (020)
Gypsum with grown crystal planes (Samples A, B, C, etc. in Table 1) is divided from the cleavage plane even if the particle size is reduced by crushing, so it is clear that the size of the particle size does not affect the reaction rate. It is. As described above, according to the manufacturing method of the present invention, as gypsum, the (00
2) Because the crystal plane uses a material with a high diffraction X-ray intensity,
The reaction rate of the TSH conversion reaction can be increased.
第1図は石こうのX線回折図、第2図はTSH化反応速
度定数の回折X線強度比曲線図である。
籍1図第2図FIG. 1 is an X-ray diffraction diagram of gypsum, and FIG. 2 is a diffraction X-ray intensity ratio curve diagram of the TSH conversion reaction rate constant. Figure 1 Figure 2
Claims (1)
ートと石こうと水とを反応させてカルシウムアルミネー
トトリサルフエートハイドレートからなる無機硬化体を
製造する製造方法において、石こうとして(020)結
晶面に対する(002)結晶面の回折X線強度比が大き
いものを用いることを特徴とする無機硬化体の製造方法
。 2 前記回折X線強度比が0.1以上に選ばれているこ
とを特徴とする特許請求の範囲第1項記載の無機硬化体
の製造方法。[Scope of Claims] 1. In a manufacturing method for producing an inorganic hardened body made of calcium aluminate trisulfate hydrate by reacting calcium aluminate monosulfate hydrate, gypsum, and water, (020) crystals as gypsum A method for producing an inorganic cured body, characterized in that an inorganic cured body is used that has a large diffraction X-ray intensity ratio of the (002) crystal plane to the (002) crystal plane. 2. The method for producing an inorganic cured body according to claim 1, wherein the diffraction X-ray intensity ratio is selected to be 0.1 or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9178377A JPS6012986B2 (en) | 1977-07-30 | 1977-07-30 | Method for producing inorganic cured body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9178377A JPS6012986B2 (en) | 1977-07-30 | 1977-07-30 | Method for producing inorganic cured body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5426817A JPS5426817A (en) | 1979-02-28 |
| JPS6012986B2 true JPS6012986B2 (en) | 1985-04-04 |
Family
ID=14036183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9178377A Expired JPS6012986B2 (en) | 1977-07-30 | 1977-07-30 | Method for producing inorganic cured body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6012986B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58174514U (en) * | 1982-05-17 | 1983-11-22 | 株式会社巴コーポレーション | Water-stop structure for exterior wall panel joints |
| JPH0626645Y2 (en) * | 1984-09-27 | 1994-07-20 | 株式会社アスク | Plate-shaped connection jig |
-
1977
- 1977-07-30 JP JP9178377A patent/JPS6012986B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5426817A (en) | 1979-02-28 |
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