JPS5843348B2 - Method for producing inorganic cured body - Google Patents
Method for producing inorganic cured bodyInfo
- Publication number
- JPS5843348B2 JPS5843348B2 JP51092583A JP9258376A JPS5843348B2 JP S5843348 B2 JPS5843348 B2 JP S5843348B2 JP 51092583 A JP51092583 A JP 51092583A JP 9258376 A JP9258376 A JP 9258376A JP S5843348 B2 JPS5843348 B2 JP S5843348B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- inorganic cured
- reaction rate
- cured body
- aluminate
- 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
Landscapes
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- 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.
石灰成分原料とアルミナ成分原料を所定の割合で配合し
て焼成し3力ルシウムアルミネート固溶体(3CaO−
A1203)を製造味 これに所要量の水を加えて3力
ルシウムアルミネート6ハイドレート固溶体(3CaO
−A1203・6H20)を製造し、これらの固溶体の
いずれかと石こう成分原料とを混合してカルシウムアル
ミネートトリサルフェートハイドレート(3CaO−A
1203・3CaSO4・31〜32H20、以下TS
Hという)を合成し、これを所望の形状に賦形したのち
養生してTSH無機硬化体を製造する無機硬化体の製造
方法は、反応速度が遅いために生産量を高めることがで
きないという問題があった。A lime component raw material and an alumina component raw material are mixed in a predetermined ratio and fired to form a tri-lucium aluminate solid solution (3CaO-
A1203) was added to this and the required amount of water was added to produce a 3-force lucium aluminate 6 hydrate solid solution (3CaO
Calcium aluminate trisulfate hydrate (3CaO-A
1203・3CaSO4・31~32H20, hereinafter TS
The method for producing an inorganic cured body in which TSH is synthesized, shaped into a desired shape, and then cured to produce an inorganic cured TSH body has the problem that the production volume cannot be increased due to the slow reaction rate. was there.
したがって、この発明の目的は、生産量を高めることが
できる無機硬化体の製造方法を提供することである。Therefore, an object of the present invention is to provide a method for producing an inorganic cured product that can increase the production amount.
要約すれば、この発明は、3力ルシウムアルミネート固
溶体(3CaO−A1203、以下C3Aと略す)また
は3力ルシウムアミネート6ハイトレート固溶体(3C
aO−A1203・6H20、以下C3AH6と略す)
に石こうとエタノールアミンを加えて混合し、所望の形
状に賦形したのち養生して無機硬化体を製造するもので
ある。In summary, the present invention provides a trivalent lucium aluminate solid solution (3CaO-A1203, hereinafter abbreviated as C3A) or a trivalent lucium aluminate 6 hydrate solid solution (3C
aO-A1203・6H20, hereinafter abbreviated as C3AH6)
Gypsum and ethanolamine are added and mixed, shaped into a desired shape, and then cured to produce an inorganic hardened product.
C3AまたはC3AH6と石こうの混合モル比は、C3
AまたはC3AH61モルに対して石こう(CaSO4
・2H20,CaSO4・1/2H20,Ca5O4)
が2.1〜3.3モルになるように選ぶことが好ましい
。The mixing molar ratio of C3A or C3AH6 and gypsum is C3
Gypsum (CaSO4
・2H20, CaSO4 ・1/2H20, Ca5O4)
It is preferable to select it so that it is 2.1 to 3.3 moles.
エタノールアミンの添加量は、C3AまたはC3AH6
と石こう水を加えてスラリ状混合物にしたものに対して
1〜7%になるように選ぶことが好ましい。The amount of ethanolamine added is C3A or C3AH6
It is preferable to select the amount from 1 to 7% based on the slurry mixture obtained by adding gypsum and gypsum water.
以上の原料のほかに、補強材、充填材などその他の添加
物を加えてもよい。In addition to the above raw materials, other additives such as reinforcing materials and fillers may be added.
つぎに無機硬化体の製造方法について説明する。Next, a method for producing an inorganic cured body will be explained.
この発明に用いるC3Aは、どのようにして得られたも
のでもよいが例えばCaOとAl2O3をほぼ3:1の
モル比で混合し、これを900〜1400°Cの高温で
焼成することにより得ることができる。The C3A used in this invention may be obtained in any way, but for example, it can be obtained by mixing CaO and Al2O3 at a molar ratio of approximately 3:1 and firing this at a high temperature of 900 to 1400°C. I can do it.
C3AH6は、例えばC3Aを微粉状にして水和するか
、CaOとAl2O3をほぼ3:1のモル比で混合し、
この固形分全量に対して0.5〜6倍量になるよ・)に
水を加えて混合し、これをオートクレーブ中で湿熱反応
させることにより得ることができる。C3AH6 can be obtained by, for example, hydrating C3A in the form of fine powder, or mixing CaO and Al2O3 in a molar ratio of approximately 3:1.
It can be obtained by adding water to and mixing the mixture, which is 0.5 to 6 times the amount of the solid content, and subjecting the mixture to a wet heat reaction in an autoclave.
エタノールアミンは、モノエタノールアミン(HOCH
2CH2NH2)、ジェタノールアミン(HOCH2C
H2)2NH、トリエタノールアミン(HOCH2CH
2) s Nをいう。Ethanolamine is monoethanolamine (HOCH
2CH2NH2), jetanolamine (HOCH2C
H2)2NH, triethanolamine (HOCH2CH
2) s N.
以上の原料と石こうを所望の配合比率となるように配合
する。The above raw materials and gypsum are blended in a desired blending ratio.
この際混水比率を適当に調節する。そして得られた混合
物を賦形し、これを養生して無機硬化体を製造する。At this time, adjust the water mixing ratio appropriately. Then, the obtained mixture is shaped and cured to produce an inorganic cured body.
つぎに実施例について説明する。Next, examples will be described.
実施例 1
200メツシュ通過のCaO561部(重量基準以下同
じ)と100メツシュ通過のAl(OH)3780部を
混合し、電気炉中に入れ1,100℃で2時間加熱して
塊状C3Aを得た。Example 1 561 parts of CaO that had passed through 200 meshes (same weight basis and below) and 3780 parts of Al(OH) that had passed through 100 meshes were mixed and placed in an electric furnace and heated at 1,100°C for 2 hours to obtain lumpy C3A. .
この塊状C3Aを粉砕して300メツシュ通過分をC3
A原料とした。This lumpy C3A is crushed and the amount passing through 300 meshes is converted into C3.
It was used as raw material A.
つぎに、アスベスト(カナダ産クリソタイル6D)40
部を水2000部を用い高速ミキサ中で解繊し、これに
ガラス繊維(1部2インチチョップストランド)25部
を加えてさらに解繊して繊維溶液をつくる。Next, asbestos (Canadian chrysotile 6D) 40
1 part is defibrated in a high-speed mixer using 2000 parts of water, and 25 parts of glass fiber (1 part 2-inch chopped strand) is added thereto and further defibrated to prepare a fiber solution.
一方、前述のC3A270.3部と2水石こう516.
3部と水1,000部とを高速ミキサで混合して混合物
をつくる。On the other hand, the aforementioned C3A270.3 parts and dihydrate gypsum 516.
A mixture is made by mixing 3 parts and 1,000 parts water in a high speed mixer.
これらの繊維溶液と混合物をプロペラ式撹拌機に移し、
トリエタノールアミン240部および水5,000部を
追加して均一に混合する。Transfer these fiber solutions and mixture to a propeller type stirrer,
Add 240 parts of triethanolamine and 5,000 parts of water and mix uniformly.
ついでこれを抄造機で抄造したのち型枠に入れ、プレス
により加圧成形して板状賦形体を製造し、これを温度2
5℃、湿度100%RHで2日間養生して無機硬化体を
得た。Next, this is made into paper using a paper making machine, placed in a mold, and pressure-molded using a press to produce a plate-shaped extruded body, which is heated at a temperature of 2.
After curing for 2 days at 5° C. and 100% RH, an inorganic cured product was obtained.
この硬化体の各かさ比重における曲げ強度はつぎの通り
である。The bending strength of this cured product at each bulk specific gravity is as follows.
実施例 2
Ca (OH) 2741部、Al(OH)3780部
、水3000部を撹拌機付きのオートクレーブに仕込み
これを、約45分で190℃にまで昇温させ、190℃
で2時間反応させたのち100℃以下に冷却し、C3A
H6スラリーを得た。Example 2 2741 parts of Ca(OH), 3780 parts of Al(OH), and 3000 parts of water were placed in an autoclave equipped with a stirrer, and the temperature was raised to 190°C in about 45 minutes.
After reacting for 2 hours at
A H6 slurry was obtained.
このC3AH6スラリを378.3部用いた以外は実施
例1と同一配合で同一操作をして無機硬化体を得た。An inorganic cured body was obtained using the same formulation and operation as in Example 1, except that 378.3 parts of this C3AH6 slurry was used.
得られた硬化体の各かさ比重における曲げ強度はつぎの
通りである。The bending strength of the obtained cured product at each bulk specific gravity is as follows.
比較例1,2:実施例1,2のトリエタノールアミンを
除いた以外は実施例1,2と同様にして無機硬化体を得
た。Comparative Examples 1 and 2: Inorganic cured products were obtained in the same manner as in Examples 1 and 2, except that triethanolamine in Examples 1 and 2 was omitted.
以上の実施例、比較例における反応速度をX線回折によ
り求めて第1図に示す。The reaction rates in the above Examples and Comparative Examples were determined by X-ray diffraction and are shown in FIG.
図において、Aは実施例1.Bは実施例2.Cは比較例
1.Dは比較例2の反応速度曲線である。In the figure, A is Example 1. B is Example 2. C is Comparative Example 1. D is the reaction rate curve of Comparative Example 2.
図から明らかなように、トリエタノールアミンを添加す
ると反応速度が極めて速くなる。As is clear from the figure, addition of triethanolamine greatly increases the reaction rate.
つぎに、エタノールアミンの種類による反応速度向上度
を第2図に示す。Next, FIG. 2 shows the degree of improvement in reaction rate depending on the type of ethanolamine.
すなわち、第2図は、C3A27部と石こう51.6部
と水47部に各エタノールアミン3.77部を加えたと
きの反応速度向上度を示すもので、Fはトリエタノール
アミンを用いた場合、Gはジェタノールアミンを用いた
場合、Hはモノエタノールアミンを用いた場合、■はエ
タノールアミンを除いた場合の反応速度曲線を示す。That is, Figure 2 shows the degree of reaction rate improvement when 3.77 parts of each ethanolamine was added to 27 parts of C3A, 51.6 parts of gypsum, and 47 parts of water, and F is the increase in reaction rate when triethanolamine is used. , G shows the reaction rate curve when jetanolamine is used, H shows the reaction rate curve when monoethanolamine is used, and ■ shows the reaction rate curve when ethanolamine is excluded.
図から明らかなように、トリエタノールアミンが最も反
応速晩を向上しジェタノールアミン、モノエタノールア
ミンの順となる。As is clear from the figure, triethanolamine improves the reaction rate the most, followed by jetanolamine and then monoethanolamine.
以上のように、この発明の無機硬化体の製造方法は、3
力ルシウムアルミネート固溶体または3力ルシウムアル
ミネート6ハイドレート固溶体に石こうとエタノールア
ミンを加えて混合し、所望の形状に賦形したのち養生す
るため、反応速度が速くなる。As described above, the method for producing an inorganic cured body of the present invention comprises three steps.
Gypsum and ethanolamine are added to and mixed with a lucium aluminate solid solution or a 3-lucium aluminate hexahydrate solid solution, shaped into a desired shape, and then cured, resulting in a faster reaction rate.
その結果、無機硬化体の生産量を高めることができる。As a result, the production amount of the inorganic cured product can be increased.
第1図は反応速度曲線図、第2図はエタノールアミンの
種類による反応速度向上変曲線図である。FIG. 1 is a reaction rate curve diagram, and FIG. 2 is a reaction rate improvement curve diagram depending on the type of ethanolamine.
Claims (1)
アルミネート6ハイドレート固溶体に石こうとエタノー
ルアミンを加えて混合し、所望の形状に賦形したのち養
生することを特徴とする無機硬化体の製造方法。A method for producing an inorganic hardened body, which comprises adding gypsum and ethanolamine to a 13-force lucium aluminate solid solution or a 3-force lucium aluminate 6-hydrate solid solution, mixing the mixture, shaping it into a desired shape, and then curing it.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP51092583A JPS5843348B2 (en) | 1976-07-31 | 1976-07-31 | Method for producing inorganic cured body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP51092583A JPS5843348B2 (en) | 1976-07-31 | 1976-07-31 | Method for producing inorganic cured body |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5317619A JPS5317619A (en) | 1978-02-17 |
JPS5843348B2 true JPS5843348B2 (en) | 1983-09-26 |
Family
ID=14058446
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51092583A Expired JPS5843348B2 (en) | 1976-07-31 | 1976-07-31 | Method for producing inorganic cured body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5843348B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3122244A1 (en) * | 1981-06-04 | 1982-12-23 | Henkel KGaA, 4000 Düsseldorf | Binder based on alkali metal silicate solutions and their use |
-
1976
- 1976-07-31 JP JP51092583A patent/JPS5843348B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5317619A (en) | 1978-02-17 |
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