JPS6021879A - Manufacture of carbonate gypsum foamed body board - Google Patents
Manufacture of carbonate gypsum foamed body boardInfo
- Publication number
- JPS6021879A JPS6021879A JP58128541A JP12854183A JPS6021879A JP S6021879 A JPS6021879 A JP S6021879A JP 58128541 A JP58128541 A JP 58128541A JP 12854183 A JP12854183 A JP 12854183A JP S6021879 A JPS6021879 A JP S6021879A
- Authority
- JP
- Japan
- Prior art keywords
- carbonate
- gypsum
- cloth
- aqueous solution
- fiber
- 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
Links
Landscapes
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Laminated Bodies (AREA)
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】
従来,石膏ボードを製造するに際し,気泡助剤として界
面活性剤を使用するが,半分石膏の種類例えば,α型の
半水石膏及びβ型の半水石膏等その他銘柄に応じて個別
に界面活性剤を選択しなければならない。しかしながら
,界面活性剤のみを用いて合成樹脂のエマルジヨン水溶
液と半水石膏及び硬化促進剤等の添加剤を加えてミキシ
ングした場合,膨張したスラリー中の微細な気泡は粗大
化したり,トビ状の気泡が発生したりして不均質な気泡
密度になるのが普通である。従つて,この現象を緩和す
るためには膨張率を高めてスラリーの比重を小さくする
工夫が必要とされるが,その反面石膏の耐圧強度が低下
してしまうという製造上の難点があつた。本発明者はこ
の点に鑑み研究し,従来の製造法上の欠点を排除しよう
とするものである。更に詳述すれば,本発明方法によつ
て製造する発泡石膏体ボードの嵩比重は1,3以下の範
囲内にあり,使用して配合する各種添加物質は次のよう
である。これらは選択的に用いて添加することができる
ものである。[Detailed Description of the Invention] Conventionally, when manufacturing gypsum board, a surfactant is used as a foaming aid, but other types of gypsum such as α-type hemihydrate gypsum, β-type hemihydrate gypsum, etc. The surfactant must be selected individually depending on the However, when mixing a synthetic resin emulsion aqueous solution with additives such as gypsum hemihydrate and a hardening accelerator using only a surfactant, the fine air bubbles in the expanded slurry may become coarser or become spiky. It is normal for this to occur, resulting in a non-uniform bubble density. Therefore, in order to alleviate this phenomenon, it is necessary to increase the expansion coefficient and reduce the specific gravity of the slurry, but this poses a manufacturing problem in that the compressive strength of the gypsum decreases. The present inventor has conducted research in view of this point and has attempted to eliminate the drawbacks of conventional manufacturing methods. More specifically, the bulk specific gravity of the foamed gypsum board produced by the method of the present invention is within the range of 1.3 or less, and the various additives used and blended are as follows. These can be added selectively.
本発明方法による各種添加物質
「半分石膏」:化学式がCaSO4・1/2H2Oで示
されるα型またはβ型の半水石膏の粉末,粒度はなるべ
く100メツシユ以下が望ましい。Various additives according to the method of the present invention, ``half gypsum'': α-type or β-type hemihydrate gypsum powder whose chemical formula is CaSO4.1/2H2O, and the particle size is preferably 100 mesh or less.
「界面活性剤」:リニヤアルキルサルフエート,ラウリ
ル硫酸ソーダ,アルキルアリルスルフオン酸ソーダ,ド
デシルベンゼンスルフオン酸ソーダ,リグニンスルフオ
ン酸ソーダ,脂肪酸のアルカリ金属塩等界面活性剤であ
れば何んでもよい。"Surfactant": Any surfactant such as linear alkyl sulfate, sodium lauryl sulfate, sodium alkylaryl sulfonate, sodium dodecylbenzenesulfonate, sodium lignin sulfonate, alkali metal salts of fatty acids, etc. good.
「炭酸塩または重炭酸塩の炭酸塩」:炭酸亜鉛,炭酸ア
ンモニウム,炭酸カドミウム,炭酸カリウム,炭酸カリ
ウムナトリウム,炭酸カルシウム,炭酸クロム,炭酸コ
バルト,水酸化炭酸コバルト水酸化炭酸銅,水酸化炭酸
鉛,水酸化炭酸ニツケル,水酸化炭酸マグネシウム,炭
酸鉄,炭酸銅,炭酸ナトリウム,炭酸ナトリウムカリウ
ム,炭酸鉛,炭酸ニツケル,炭酸バリウム,炭酸マグネ
シウム,炭酸マグネシウムカルシウム及び炭酸マンガン
等の炭酸塩,三炭酸二水素四アンモニウム,炭酸水素ア
ンモニウム,炭酸水素ナトリウム,炭酸水素カリウム,
炭酸水素マグネシウムカリウム炭酸水素リチウム等の重
炭酸塩の炭酸塩。"Carbonates of carbonates or bicarbonates": zinc carbonate, ammonium carbonate, cadmium carbonate, potassium carbonate, potassium sodium carbonate, calcium carbonate, chromium carbonate, cobalt carbonate, cobalt hydroxide carbonate, copper hydroxide carbonate, lead hydroxide carbonate , nickel hydroxide carbonate, magnesium hydroxide carbonate, iron carbonate, copper carbonate, sodium carbonate, sodium potassium carbonate, lead carbonate, nickel carbonate, barium carbonate, magnesium carbonate, magnesium carbonate calcium carbonate, manganese carbonate, and other carbonates; Tetraammonium hydrogen, ammonium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate,
Carbonates of bicarbonates such as potassium magnesium bicarbonate and lithium bicarbonate.
「酸性の弗化化合物」:珪弗化ナトリウム,珪弗化カル
シウム,珪弗化カリウム,珪弗化亜鉛,珪弗化鉛,珪弗
化アンモニウム及び珪弗化バリウム塩等の珪弗化塩,珪
弗化水素酸水溶液,弗化水素酸水溶液,酸性弗化ナトリ
ウム及び酸性弗化カリウム等の酸性の弗化化合物または
酸性弗化物。"Acidic fluoride compounds": silicofluoride salts such as sodium silicofluoride, calcium silicofluoride, potassium silicofluoride, zinc silicofluoride, lead silicofluoride, ammonium silicofluoride, and barium silicofluoride salts, Acidic fluoride compounds or acidic fluorides, such as hydrosilicic acid aqueous solution, hydrofluoric acid aqueous solution, acidic sodium fluoride, and acidic potassium fluoride.
「合成樹脂のエマルジヨン水溶液」:ポリ酢酸ビニール
エマルジヨン水溶液,アクリル酸エステル共重合体エマ
ルジヨン水溶液,ポリスチレンエマルジヨン水溶液,ス
チレンブタジエン共重合体エマルジヨン水溶液,ポリビ
ニールアルコール塩化ビニール共重合体エマルジヨン水
溶液,その他合成樹脂のエマルジヨン水溶液であれば何
んでもよい。"Synthetic resin emulsion aqueous solution": polyvinyl acetate emulsion aqueous solution, acrylic acid ester copolymer emulsion aqueous solution, polystyrene emulsion aqueous solution, styrene-butadiene copolymer emulsion aqueous solution, polyvinyl alcohol vinyl chloride copolymer emulsion aqueous solution, other synthesis Any aqueous emulsion solution of resin may be used.
「ポリビニールアルコール」:5〜10重量%に調製し
たポリビニールアルコール水溶液を使用するが,粉末状
のポリビニールアルコールも使用することができる。"Polyvinyl alcohol": An aqueous polyvinyl alcohol solution prepared to a concentration of 5 to 10% by weight is used, but powdered polyvinyl alcohol can also be used.
「硬化促進剤」:硫酸アンモニウム,硫酸カリウム明バ
ン,硫酸マグネシウム等の硫酸塩,珪酸質物質及び動物
の膠質物質。"Hardening accelerator": Sulfates such as ammonium sulfate, potassium alum sulfate, magnesium sulfate, silicic substances, and animal colloid substances.
「防水剤」:パラフインのエマルジヨン水溶液またはア
スフアルトのエマルジヨン水溶液等。固形分(乾燥重量
)に換算し,2重量%以下の添加量で防水にすることが
できる。"Waterproofing agent": Paraffin emulsion aqueous solution or asphalt emulsion aqueous solution, etc. Waterproofing can be achieved by adding 2% by weight or less in terms of solid content (dry weight).
「繊維物質」:硝子繊維,シリカ繊維,カーボン繊維,
パルプ繊維,ポリエステル繊維,プロピレン繊維及び金
属繊維等繊維物質であれば何んでもよい。"Fiber materials": glass fibers, silica fibers, carbon fibers,
Any fiber material may be used, such as pulp fiber, polyester fiber, propylene fiber, and metal fiber.
「珪酸塩」:珪酸カルシウム塩(例えば,メタ珪酸カル
シウム及び珪酸二石灰等。),珪酸バリウム塩珪酸鉛塩
,珪酸マグネシウム塩,珪酸マンガン塩及びメタ珪酸マ
グネシウムカルシウム塩等。"Silicate": Calcium silicate salts (for example, calcium metasilicate and dicalcium silicate, etc.), barium silicate salts, lead silicate salts, magnesium silicate salts, manganese silicate salts, magnesium calcium metasilicate salts, etc.
「塩化物」:塩化カルシウム,塩化バリウム,塩化マグ
ネシウム塩,塩化鉛塩及び塩化アンモニウム塩等。"Chloride": Calcium chloride, barium chloride, magnesium chloride salt, lead chloride salt, ammonium chloride salt, etc.
本発明方法に使用する布には木綿繊維布,麻繊維布及び
純毛繊維布等の天然繊維布,レーヨン繊維布等の化学繊
維布,炭素繊維布,アクリロニトリル繊維布,ポリプロ
ピレン繊維布,ポリエステル繊維布,ナイロン繊維布,
アセテート繊維布等の合成繊維布,木棉とポリエステル
の混紡繊維布木綿とナイロンの混紡繊維布,アスベスト
繊維布皮革の布,合成皮革の布等その他繊維または繊維
状の布であれば何んでも使用することができる。Fabrics used in the method of the present invention include natural fiber cloths such as cotton fiber cloth, linen fiber cloth and pure wool fiber cloth, chemical fiber cloth such as rayon fiber cloth, carbon fiber cloth, acrylonitrile fiber cloth, polypropylene fiber cloth, polyester fiber cloth. , nylon fiber cloth,
Synthetic fiber cloth such as acetate fiber cloth, blended fiber cloth of cotton and polyester, blended fiber cloth of cotton and nylon, asbestos fiber cloth, leather cloth, synthetic leather cloth, and any other fiber or fibrous cloth can be used. can do.
発泡石膏体ボードの厚みは,1,6ミリ前後の厚みのも
のは勿論のこと,3ミリ,6ミリ,9ミリ,12ミリ,
15ミリ,20ミリ,60ミリ,100ミリ,120ミ
リ等の発泡石膏体ボードを成型して製造することができ
る。その場合必要に応じて二枚以上の布の間,例えば,
二枚の布の間,三枚の布の間,四枚の布の間,五枚の布
の間,六■の布の間等に発泡石膏スラリーを流し込んで
ボード状に成型して製造することも可能であり,内側ま
たは中心になる布のかわりに石膏ボード原紙(例えば,
硝子繊維布)または紙を使用することもできる。次に本
発明方法を実施例によつて説明する。The thickness of foamed gypsum board is of course around 1.6 mm, but also 3 mm, 6 mm, 9 mm, 12 mm, etc.
It can be manufactured by molding foamed gypsum boards of 15 mm, 20 mm, 60 mm, 100 mm, 120 mm, etc. In that case, if necessary, between two or more pieces of cloth, e.g.
It is manufactured by pouring foamed gypsum slurry between two pieces of cloth, between three pieces of cloth, between four pieces of cloth, between five pieces of cloth, between six pieces of cloth, etc. and molding it into a board shape. It is also possible to use gypsum board paper (e.g.
Glass fiber cloth) or paper can also be used. Next, the method of the present invention will be explained with reference to examples.
実施例1
配 合
β型の半水石膏 100 重量部
リニヤアルキルサルフエート 0.08 〃平均粒子径
0.15ミクロンの炭酸カルシウム0.4 〃
10%の珪弗化カルシウム水溶液
3.6 〃
15%の酢酸ビニールエマルジヨン水溶液10 重量部
硫酸アンモニウム 1.2 〃
水 60 〃
上記からなる配合添加物質をミキサー中において10秒
間以内で均質に撹拌または混合し,無数の微細な炭酸ガ
スの気泡を含有する流動性のよい発泡石膏スラリーを作
成後,これを2枚の木綿の布の型枠内に流し込み8分で
硬化せしめ150℃の温度で乾燥後,12ミリ厚,嵩比
重0.81の発泡石膏体ボードの成型品を製造した。Example 1 Blend β-type gypsum hemihydrate 100 parts by weight Linear alkyl sulfate 0.08 Calcium carbonate with average particle size of 0.15 microns 0.4 10% calcium silicofluoride aqueous solution 3.6 15% A vinyl acetate emulsion aqueous solution of 10 parts by weight ammonium sulfate 1.2 〃 Water 60 〃 The blended additives consisting of the above are homogeneously stirred or mixed within 10 seconds in a mixer to form a fluid containing countless fine carbon dioxide gas bubbles. After creating a foamed gypsum slurry with good properties, it was poured into a mold made of two pieces of cotton cloth and cured in 8 minutes. After drying at a temperature of 150°C, a foamed gypsum body with a thickness of 12 mm and a bulk specific gravity of 0.81 was created. Manufactured board moldings.
実施例2
配 合
β型の半水石膏 100 重量部
リニヤアルキルサルフエート 0.08 〃平均粒子径
0.15ミクロンの炭酸カルシウム0.4 〃
10%の珪弗化カルシウム水溶液
3.6 〃
15%の酢酸ビニールエマルジヨン水溶液10 〃
硫酸アンモニウム 1.3 重量部
ガラス繊維 0.4 〃
水 60 〃
実施例1と同様な作業を行い,2枚の木綿とポリエステ
ルの混紡繊維布の型枠内に流し込み8分で硬化せしめ1
50℃の温度で乾燥後,9ミリ厚嵩比重0.82の発泡
石膏体ボードを製造した。Example 2 Blend β-type gypsum hemihydrate 100 parts by weight Linear alkyl sulfate 0.08 Average particle size 0.15 microns Calcium carbonate 0.4 10% calcium silicofluoride aqueous solution 3.6 15% 10 parts by weight of vinyl acetate emulsion solution Ammonium sulfate 1.3 parts by weight Glass fiber 0.4 parts by weight Water 60 parts The same procedure as in Example 1 was carried out, and the mixture was poured into a mold made of two pieces of cotton and polyester blend fabric. Harden in 1 minute
After drying at a temperature of 50° C., a foamed gypsum board with a thickness of 9 mm and a specific gravity of 0.82 was produced.
実施例3
配 合
β型の半水石膏 100 重量部
リニヤアルキルサルフエート 0.08 〃平均粒子径
0.15ミクロンの炭酸カルシウム1.0 〃
10%の珪弗化ナトリウム水溶液
10.3 〃
10%のメタ珪酸カルシウム水溶液
1.2 〃
塩化カルシウム(CaCl2・2H2O)0.8 〃
15%の酢酸ビニールエマルジヨン水溶液10 重量部
5%のポリビニールアルコール水溶液
20 〃
硫酸アンモニウム 1.4 〃
水 42 〃
実施例1と同様な作業を行い,2枚のポリエステル繊維
布の型枠内に流し込み8分で硬化せしめ,150℃の温
度で乾燥後,60ミリ厚,嵩比重 0.65の発泡石膏
体ボードを製造した。発泡反応は次のようである。発泡
反応は次のようである。Example 3 Blend β-type gypsum hemihydrate 100 parts by weight Linear alkyl sulfate 0.08 Calcium carbonate with average particle size of 0.15 microns 1.0 10% sodium silifluoride aqueous solution 10.3 10% Calcium metasilicate aqueous solution 1.2 Calcium chloride (CaCl2.2H2O) 0.8 15% vinyl acetate emulsion aqueous solution 10 5% by weight aqueous polyvinyl alcohol solution 20 Ammonium sulfate 1.4 Water 42 Examples Perform the same procedure as in step 1, pour into two polyester fiber cloth molds, harden in 8 minutes, and dry at 150°C to produce a foamed gypsum board with a thickness of 60 mm and a bulk specific gravity of 0.65. did. The foaming reaction is as follows. The foaming reaction is as follows.
Na2SiF6+CaSiO3+CaCO3+CaCl
2+2H2O→3CaF2↓+2H2SiO3↓+2N
aCl+CO2↑実施例3はポリビニールアルコール水
溶液を併用して実施できることを示している。以上,詳
述のように本発明によると,布と石膏との接着性のよい
微細な気泡を含有する発泡石膏体ボードを経済的に低廉
に製造することが可能であるために工業的利用価値は広
範である。Na2SiF6+CaSiO3+CaCO3+CaCl
2+2H2O→3CaF2↓+2H2SiO3↓+2N
aCl+CO2↑Example 3 shows that it can be carried out in combination with a polyvinyl alcohol aqueous solution. As described in detail above, according to the present invention, it is possible to economically and inexpensively manufacture a foamed gypsum board containing fine air bubbles that has good adhesiveness between cloth and plaster, and therefore has industrial value. is extensive.
特許出願人 阿部賢一Patent applicant: Kenichi Abe
Claims (1)
面活性剤,炭酸塩または重炭塩の炭酸塩,酸性の弗化化
合物,合成樹脂のエマルジヨン水溶液,硬化促進剤及び
半水石膏の混水量の水を加え,ミキサー中で均質に撹拌
または混合し,無数の炭酸ガスの微細気泡を含有する流
動性のよい発泡石膏スラリーを作成し,これを布の間に
流し込んでボード状に成型後硬化せしめ乾燥することを
特徴とする発泡石膏体ボードの製造方法。1. The main raw material is α-type or β-type gypsum hemihydrate, which contains a surfactant, carbonate or bicarbonate carbonate, an acidic fluoride compound, an aqueous emulsion solution of synthetic resin, a hardening accelerator, and gypsum hemihydrate. A mixed amount of water is added and stirred or mixed homogeneously in a mixer to create a highly fluid foamed gypsum slurry containing countless microscopic carbon dioxide gas bubbles, which is poured between cloth and formed into a board shape. A method for producing a foamed gypsum board, characterized by post-curing and drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58128541A JPS6021879A (en) | 1983-07-14 | 1983-07-14 | Manufacture of carbonate gypsum foamed body board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58128541A JPS6021879A (en) | 1983-07-14 | 1983-07-14 | Manufacture of carbonate gypsum foamed body board |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6021879A true JPS6021879A (en) | 1985-02-04 |
Family
ID=14987304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58128541A Pending JPS6021879A (en) | 1983-07-14 | 1983-07-14 | Manufacture of carbonate gypsum foamed body board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6021879A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58145770U (en) * | 1982-03-25 | 1983-09-30 | 大日本印刷株式会社 | certificate |
-
1983
- 1983-07-14 JP JP58128541A patent/JPS6021879A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58145770U (en) * | 1982-03-25 | 1983-09-30 | 大日本印刷株式会社 | certificate |
JPH0131511Y2 (en) * | 1982-03-25 | 1989-09-27 |
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