JPS61127656A - Gypsum hardened body - Google Patents

Gypsum hardened body

Info

Publication number
JPS61127656A
JPS61127656A JP24457384A JP24457384A JPS61127656A JP S61127656 A JPS61127656 A JP S61127656A JP 24457384 A JP24457384 A JP 24457384A JP 24457384 A JP24457384 A JP 24457384A JP S61127656 A JPS61127656 A JP S61127656A
Authority
JP
Japan
Prior art keywords
gypsum
weight
parts
sulfuric acid
kneaded
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
Application number
JP24457384A
Other languages
Japanese (ja)
Other versions
JPH0520376B2 (en
Inventor
恵一 村上
荒井 康夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FUJI FUNEN KENZAI KOGYO KK
Original Assignee
FUJI FUNEN KENZAI KOGYO KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by FUJI FUNEN KENZAI KOGYO KK filed Critical FUJI FUNEN KENZAI KOGYO KK
Priority to JP24457384A priority Critical patent/JPS61127656A/en
Publication of JPS61127656A publication Critical patent/JPS61127656A/en
Publication of JPH0520376B2 publication Critical patent/JPH0520376B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/14Compositions 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 calcium sulfate cements

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (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】 〔産業上の利用分野〕 本発明は、石膏ボードや石膏ブロック等として用いられ
る石膏硬化体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a hardened gypsum body used as a gypsum board, a gypsum block, or the like.

〔従来の技術〕[Conventional technology]

現在、石膏ボード用原料としては、主にリン酸工場や火
力発電所等から副産される化学石膏が使用されている。
Currently, chemical gypsum, which is a by-product from phosphoric acid factories, thermal power plants, etc., is mainly used as a raw material for gypsum board.

そして2、石膏ボードは、上記の化学石膏等の石膏を力
焼し、一旦焼石膏とし、これを水と混合し、水和、硬化
、脱型後、乾燥させて製造されており、これらの工程は
流れ作業で行われている。
2. Gypsum board is manufactured by power-calcining plaster, such as the chemical plaster mentioned above, to make calcined plaster, mixing this with water, hydrating, curing, demolding, and drying. The process is carried out on an assembly line.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

石膏ボード用原料である化学石膏は、現在、リン酸の減
産、低硫黄油の使用等により年々減産され、その不足分
を韓国等からの輸入石膏に依存しており、石膏ボード工
場においては原料安定確保に苦慮しているのが実状であ
る。
Currently, production of chemical gypsum, which is the raw material for gypsum board, is decreasing year by year due to reduced production of phosphoric acid, use of low-sulfur oil, etc., and to make up for the shortage, we rely on gypsum imported from countries such as South Korea. The reality is that Japan is struggling to ensure stability.

また、従来の石膏ボードの製造法においては、余剰水分
の乾燥費に生産コストの約40%を要する問題がある。
Furthermore, in the conventional method of manufacturing gypsum board, there is a problem in that approximately 40% of the production cost is required for drying excess water.

従って、本発明の目的は、安定的に確保できる原料を用
い、生産コストの低減を図って従来品と同等の石膏硬化
体を提供することにある。
Therefore, an object of the present invention is to provide a hardened gypsum product equivalent to conventional products by using stably available raw materials and reducing production costs.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者等は、出発原料として、製鉄、金属工場から多
量に副産される硫酸と我国で資源的に最も安定している
石灰とを用いると共に、それらに特定の化合物を添加し
て反応させると、反応生成物が短時間で脱型可能な迄硬
化し、従来法と同様の流れ作業により石膏ボードを得る
ことができ、且つ得られる石膏ボードは従来品と同程度
の強度を有する上、実質−ヒ乾燥工程を要しないもので
あることを知見した。
The present inventors used sulfuric acid, which is a by-product in large quantities from iron and metal factories, and lime, which is the most stable resource in Japan, as starting materials, and added a specific compound to them to cause a reaction. Then, the reaction product hardens to the point where it can be demolded in a short time, and a gypsum board can be obtained by the same assembly process as the conventional method, and the obtained gypsum board has the same strength as the conventional product. It has been found that virtually no drying step is required.

即ち、本発明は、上記知見に基づきなされたもので、石
灰化合物、硫酸、並びにミョウバン、硫酸アルミニウム
及びシュウ酸ナトリウムからなる群から選択した少なく
とも1種の化合物の混練物を流し込み成形し、硬化させ
てなる、石膏硬化体を提供するものである。
That is, the present invention was made based on the above-mentioned findings, and involves casting a kneaded mixture of a lime compound, sulfuric acid, and at least one compound selected from the group consisting of alum, aluminum sulfate, and sodium oxalate, and hardening the mixture. The purpose is to provide a hardened gypsum body made of

以下に本発明の石膏硬化体について詳述する。The hardened gypsum body of the present invention will be explained in detail below.

本発明の石膏硬化体を製造するのに用いられる石灰化合
物としては、炭酸カルシウム、水酸化カルシウム、酸化
カルシウム、スラグ等が挙げられ、これらは単独又は二
種以上組合せて用いられる。
Examples of the lime compound used to produce the hardened gypsum body of the present invention include calcium carbonate, calcium hydroxide, calcium oxide, and slag, which may be used alone or in combination of two or more.

而して、本発明の石膏硬化体は、次のようにして製造さ
れる。
The hardened gypsum body of the present invention is manufactured as follows.

先ず、上記石灰化合物、硫酸並びにミョウバン、硫酸ア
ルミニウム及びシュウ酸ナトリウムからなる鮮から選択
した少なくとも1種の化合物を混練して混練物を得る。
First, the lime compound, sulfuric acid, and at least one compound selected from the group consisting of alum, aluminum sulfate, and sodium oxalate are kneaded to obtain a kneaded product.

上記硫酸としては、濃度40〜70%のものが好ましく
、またその好ましい使用量は、濃度1゜0%換算で石灰
化合物100重量部に対し略等量である。
The above-mentioned sulfuric acid preferably has a concentration of 40 to 70%, and the preferred amount used is approximately equivalent to 100 parts by weight of the lime compound when converted to a concentration of 1.0%.

また、ミョウバンは、予め上記硫酸に溶解した形で添加
混練されるのが好ましく、またその好ましい使用量は、
石灰化合物100重量部に対し1〜30重量部、特に1
〜10重量部である。
Further, it is preferable that alum is added and kneaded in the form of being dissolved in the above sulfuric acid in advance, and the preferable amount used is as follows:
1 to 30 parts by weight, especially 1 to 100 parts by weight of lime compound
~10 parts by weight.

また、硫酸アルミニウムは、予め上記硫酸に溶解した形
で添加混練されるのが好ましく、またその好ましい使用
量は、石灰化合物100重量部に対し1〜30重量部、
特に1〜10重量部である。
Further, it is preferable that aluminum sulfate is added and kneaded in the form of being dissolved in the sulfuric acid in advance, and the preferable amount used is 1 to 30 parts by weight per 100 parts by weight of the lime compound.
In particular, it is 1 to 10 parts by weight.

また、シュウ酸ナトリウムは、石灰化合物と硫酸を混練
した後、これに添加するのが好ましく、またその好まし
い使用量は、石灰化合物100重量部に対し0.1〜5
.0重量部、特に0.5〜1.0重量部である。
In addition, sodium oxalate is preferably added to the lime compound and sulfuric acid after kneading, and the preferred amount used is 0.1 to 5 parts by weight per 100 parts by weight of the lime compound.
.. 0 parts by weight, especially 0.5 to 1.0 parts by weight.

また、ミβウバン、硫酸アルミニウム及びシュウ酸ナト
リウムの三者を添加する場合には、先ずミョウバン及び
硫酸アルミニウムを添加した、石灰化合物と硫酸との混
練物に、シュウ酸ナトリウムを添加するのが好ましく、
それらの総使用量を石灰化合物100重量部に対して0
.1〜5.0重量部とするのが好ましい。
In addition, when adding three of alum, aluminum sulfate, and sodium oxalate, it is preferable to first add sodium oxalate to a mixture of lime compound and sulfuric acid to which alum and aluminum sulfate have been added. ,
The total amount used is 0 per 100 parts by weight of lime compound.
.. The amount is preferably 1 to 5.0 parts by weight.

次いで、上記混練物を、直ちに(反応開始1〜5分後)
、型枠に流し込み、平板(ボード)状やブロック状等の
所望の形状に成形し、硬化させ、脱型して本発明の石膏
硬化体を得る。
Next, the above kneaded material was immediately added (1 to 5 minutes after the start of the reaction).
, poured into a mold, formed into a desired shape such as a flat plate (board) shape, block shape, etc., hardened, and demolded to obtain a hardened gypsum body of the present invention.

混練物の成形は、焼石膏を原料とする従来法の場合と同
様に行えば良く、成形品として石膏ボードを得る場合に
は成形時にボードの両面に紙を接着させる。
The kneaded product may be shaped in the same manner as in the conventional method using calcined gypsum as a raw material, and when a gypsum board is obtained as a molded product, paper is adhered to both sides of the board during shaping.

成形した混練物の硬化は、常温で60%RH前後の雰囲
気中で行うことが好ましく、硬化時間は、例えばミョウ
バンを石灰化合物100重量部に対し1〜6重量部添加
した混練物の場合には流し込み成形後1〜10分である
The molded kneaded product is preferably cured in an atmosphere of around 60% RH at room temperature, and the curing time is, for example, in the case of a kneaded product in which 1 to 6 parts by weight of alum is added to 100 parts by weight of the lime compound 1 to 10 minutes after casting.

上述の如くして得られる本発明の石膏硬化体は、脱型時
において含水率が2〜5%位であるため乾燥不要であり
、また、焼石膏を原料とする従来法、で得られる石膏硬
化体と略同等の物理特性を有するものである。
The hardened gypsum body of the present invention obtained as described above does not require drying because it has a moisture content of about 2 to 5% at the time of demolding, and is similar to gypsum obtained by the conventional method using calcined gypsum as a raw material. It has approximately the same physical properties as the cured product.

尚、石灰化合物として炭酸カルシウムを用いた場合は、
炭酸カルシウムと硫酸との反応により生成するco2が
発泡して微細な空孔を作るため、石膏硬化体の断熱軽量
化を図れる。
In addition, when calcium carbonate is used as the lime compound,
Since the CO2 generated by the reaction between calcium carbonate and sulfuric acid foams and creates fine pores, it is possible to reduce the weight and heat insulation of the hardened gypsum body.

また、本発明においては、石灰化合物、硫酸、並びにミ
ョウバン、硫酸アルミニウム及び/又はシュウ酸ナトリ
ウムを混練する際に、更に可溶性シリカ、スラグ、フラ
イアッシュ等の反応性珪酸塩を石灰化合物100重量部
に対し1〜50重量部添加することができ、この反応性
珪酸塩の添加によって、石膏硬化体の短所である耐水性
を著しく改善することができる。
In addition, in the present invention, when kneading the lime compound, sulfuric acid, alum, aluminum sulfate and/or sodium oxalate, a reactive silicate such as soluble silica, slag, fly ash, etc. is added to 100 parts by weight of the lime compound. The reactive silicate can be added in an amount of 1 to 50 parts by weight, and the water resistance, which is a disadvantage of hardened gypsum, can be significantly improved.

次に、本発明の石膏硬化体の製造における反応機構を、
石灰化合物として炭酸カルシウムを用いた場合について
説明すると、石灰化合物、硫酸並びにミョウバン、硫酸
アルミニウム及び/又はシュウ酸ナトリウムを混練する
ことにより、石灰化合物と硫酸が反応して石膏を生成し
、その際、発生する反応熱により混練物の温度は70〜
100℃に達し、この反応熱を利用して半水石膏及び■
型無水石膏が生成する。次いで、この反応生成物は、硫
酸中の水分及び上記反応の生成水によって水和され、直
ちに硬化する。この際、ミョウバン、硫酸アルミニウム
及びシュウ酸ナトリウムは、硬化速度の促進及び硬化体
の強度発現に寄与するものと推察される。また、反応性
珪酸塩の添加による耐水性の改善は、石灰化合物と硫酸
との反応熱を利用して、耐水性珪酸カルシウム水和物(
例えば、トバモライト)が生成されるためと推察される
Next, the reaction mechanism in producing the hardened gypsum body of the present invention is as follows.
To explain the case where calcium carbonate is used as the lime compound, by kneading the lime compound, sulfuric acid, and alum, aluminum sulfate and/or sodium oxalate, the lime compound and sulfuric acid react to produce gypsum, and at that time, Due to the reaction heat generated, the temperature of the kneaded material is 70~
The temperature reaches 100℃, and using this reaction heat, hemihydrate gypsum and ■
Type anhydrite is produced. This reaction product is then hydrated by the water in the sulfuric acid and the water produced from the reaction and immediately cures. At this time, it is presumed that alum, aluminum sulfate, and sodium oxalate contribute to accelerating the curing rate and developing strength of the cured product. In addition, water resistance can be improved by adding reactive silicates by utilizing the heat of reaction between lime compounds and sulfuric acid.
For example, it is assumed that this is because tobermorite) is produced.

以下に実施例及び参考例を示し、本発明を更に詳しく説
明する。
The present invention will be explained in more detail by showing Examples and Reference Examples below.

実施例1 炭酸カルシウム100重量部に消石灰50重量部を加え
混合物とする。この混合物に、ミョウバン6重量部を熔
解した硫酸(濃度60%)240ュウ酸ナトリウム1w
量部を加え1分間混合攪拌して混練物を得る。次いでこ
の混練物を直ちに型枠に流し込み、20℃、60%R1
1の雰囲気中に5分間養生硬化抜脱型し、9aunX 
910mmX 1820mmの本発明の石膏ボードを得
た。
Example 1 50 parts by weight of slaked lime was added to 100 parts by weight of calcium carbonate to form a mixture. To this mixture, add 240 sulfuric acid (concentration 60%) and 1 w of sodium oxalate dissolved in 6 parts by weight of alum.
Add a certain amount and mix and stir for 1 minute to obtain a kneaded product. Next, this kneaded product was immediately poured into a mold, and heated at 20°C and 60% R1.
Cured and cured in the atmosphere of 1 for 5 minutes, removed from the mold, and
A gypsum board of the present invention measuring 910 mm x 1820 mm was obtained.

実施例2 実施例1で得たものと同じ混練物を型枠に流し込み、そ
の際、その両面に石膏ボード用紙を接着させ、20℃、
60%R11の雰囲気中に5分間養生硬化抜脱型し、実
施例1で得たものと同じ大きさの本発明の石膏ボードを
得た。
Example 2 The same kneaded material obtained in Example 1 was poured into a mold, with gypsum board paper adhered to both sides of the mold, and heated at 20°C.
The gypsum board of the present invention having the same size as that obtained in Example 1 was obtained by curing, hardening and demolding in an atmosphere of 60% R11 for 5 minutes.

実施例3 炭酸カルシウム100重量部に消石灰50重量部を加え
混合物とする。この混合物に、ミョウバン6重量部を溶
解した硫酸(濃度60%)240重量部を加え3分間混
合攪拌して混練物を得る。
Example 3 50 parts by weight of slaked lime was added to 100 parts by weight of calcium carbonate to form a mixture. To this mixture, 240 parts by weight of sulfuric acid (concentration 60%) in which 6 parts by weight of alum was dissolved were added and mixed and stirred for 3 minutes to obtain a kneaded product.

次いでこの混練物を直ちに型枠に流し込み、20℃、6
0%RHの雰囲気中に5分間養生硬化抜脱型し、実施例
1で得たものと同じ大きさの本発明の石膏ボードを得た
Next, this kneaded material was immediately poured into a mold and heated at 20°C for 6
The gypsum board of the present invention having the same size as that obtained in Example 1 was obtained by curing, hardening, and demolding in an atmosphere of 0% RH for 5 minutes.

参考例1 炭酸カルシウム100重量部に消石灰50重量部を加え
混合物とする。この混合物に硫酸(濃度60%)240
重量部を加え1分間混合攪拌後、混練物を直ちに型枠に
流し込み、20℃、60%RHの雰囲気中に30分間養
生硬化後脱型し、実施例1で得たものと同じ大きさの石
膏ボードを得た。
Reference Example 1 50 parts by weight of slaked lime was added to 100 parts by weight of calcium carbonate to form a mixture. Add 240 sulfuric acid (concentration 60%) to this mixture.
After adding parts by weight and mixing and stirring for 1 minute, the kneaded mixture was immediately poured into a mold, cured in an atmosphere of 20°C and 60% RH for 30 minutes, and then removed from the mold. Got plasterboard.

参考例2 参考例1で得たものと同じ混練物を直ちに型枠に流し込
み、その際、その両面に石膏ボード用紙を接着させ、2
0℃、60%RHの雰囲気中に30分間養生硬化後脱型
し、実施例1で得たものと同じ大きさの本発明の石膏ボ
ードを得た。
Reference Example 2 Immediately pour the same kneaded material as that obtained in Reference Example 1 into a mold, and at that time, adhere gypsum board paper to both sides of the mold.
After curing and curing in an atmosphere of 0° C. and 60% RH for 30 minutes, the mold was removed to obtain a gypsum board of the present invention having the same size as that obtained in Example 1.

尚、参考例1及び2においては養生5分後では硬化が不
充分で脱型不能であった。
In addition, in Reference Examples 1 and 2, curing was insufficient after 5 minutes of curing and demolding was impossible.

上記実施例1,2.3及び参考例1.2で得られた石膏
ボードについて、種々の物性測定を行った。その結果は
下表の通りであった。
Various physical property measurements were performed on the gypsum boards obtained in Examples 1 and 2.3 and Reference Example 1.2. The results were as shown in the table below.

〔発明の効果〕〔Effect of the invention〕

本発明の石膏硬化体は、石灰化合物及び硫酸を用い、こ
れらにミョウバン、硫酸アルミニウム及びシュウ酸ナト
リウムからなる群から選択した少なくとも1種の化合物
を添加混練し、この混練物を成形し硬化させてなるもの
で、焼石膏を原料とする従来法で得られる石膏硬化体と
略同等の物理特性を有するものである。まな、本発明の
石膏硬化体の原料は、容易に安定確保できるもので、そ
の製造に際しては、混練物を流し込み後1〜10分で脱
型可能に硬化できるため流れ作業に支障をきたすことが
なく、従来法で用いられる石膏ボード製造装置等をその
まま転用でき、しかも乾燥工程は不要であるので生産コ
ストを著しく低下させることができ、上記混練物は石膏
ボード用紙との接着も極めて良好である。更に、本発明
においては、石灰化合物として炭酸カルシウムを用いれ
ば、炭酸カルシウムと硫酸との反応を制御することによ
り、得られる石膏硬化体のかさ比重を任意に調節し軽量
化することも可能である。
The hardened gypsum of the present invention is produced by using a lime compound and sulfuric acid, adding and kneading at least one compound selected from the group consisting of alum, aluminum sulfate, and sodium oxalate, and molding and hardening the kneaded product. This material has approximately the same physical properties as a hardened gypsum obtained by a conventional method using calcined gypsum as a raw material. Furthermore, the raw material for the hardened gypsum body of the present invention can be easily and stably secured, and during its production, the kneaded material can be hardened in a manner that allows it to be removed from the mold within 1 to 10 minutes after pouring, so there is no problem with assembly work. The gypsum board manufacturing equipment used in the conventional method can be used as is, and since no drying process is required, production costs can be significantly reduced.The kneaded product also has extremely good adhesion to gypsum board paper. . Furthermore, in the present invention, if calcium carbonate is used as the lime compound, it is also possible to arbitrarily adjust the bulk specific gravity of the resulting hardened gypsum product to reduce its weight by controlling the reaction between calcium carbonate and sulfuric acid. .

Claims (2)

【特許請求の範囲】[Claims] (1)石灰化合物、硫酸、並びにミョウバン、硫酸アル
ミニウム及びシュウ酸ナトリウムからなる群から選択し
た少なくとも1種の化合物の混練物を流し込み成形し、
硬化させてなる、石膏硬化体。
(1) pouring and molding a kneaded product of a lime compound, sulfuric acid, and at least one compound selected from the group consisting of alum, aluminum sulfate, and sodium oxalate;
A hardened gypsum body made by hardening.
(2)上記混練物が平板に成形され、その両面に紙が接
着されている、特許請求の範囲第(1)項記載の石膏硬
化体。
(2) The hardened gypsum body according to claim (1), wherein the kneaded material is formed into a flat plate, and paper is adhered to both sides of the flat plate.
JP24457384A 1984-11-21 1984-11-21 Gypsum hardened body Granted JPS61127656A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24457384A JPS61127656A (en) 1984-11-21 1984-11-21 Gypsum hardened body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24457384A JPS61127656A (en) 1984-11-21 1984-11-21 Gypsum hardened body

Publications (2)

Publication Number Publication Date
JPS61127656A true JPS61127656A (en) 1986-06-14
JPH0520376B2 JPH0520376B2 (en) 1993-03-19

Family

ID=17120726

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24457384A Granted JPS61127656A (en) 1984-11-21 1984-11-21 Gypsum hardened body

Country Status (1)

Country Link
JP (1) JPS61127656A (en)

Cited By (9)

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DE4443761A1 (en) * 1994-12-08 1996-06-13 Schueco Int Kg Heat-binding component for indoor and outdoor construction in fire protection design
JP2013518795A (en) * 2010-02-04 2013-05-23 ユナイテッド・ステイツ・ジプサム・カンパニー Snap-cured compound joint material
WO2014027613A1 (en) * 2012-08-15 2014-02-20 吉野石膏株式会社 Method for selectively inhibiting sulfate-reducing bacterium, gypsum composition capable of inhibiting proliferation of sulfate-reducing bacterium by said method, gypsum-type solidifying material, and gypsum-type building material
JP2014037364A (en) * 2012-08-15 2014-02-27 Yoshino Gypsum Co Ltd Selective fungistatic method of sulfate-reducing bacterium
JP2014037330A (en) * 2012-08-15 2014-02-27 Yoshino Gypsum Co Ltd Gypsum compositions, gypsum-based solidification materials and gypsum-based construction materials
JP2015083537A (en) * 2014-11-13 2015-04-30 ユナイテッド・ステイツ・ジプサム・カンパニー Snap cure-prepared joint filler
JP2019531251A (en) * 2016-10-12 2019-10-31 ユナイテッド・ステイツ・ジプサム・カンパニー Method for making lightweight gypsum compositions using internally generated foam and products made therefrom
US10669215B2 (en) 2009-01-14 2020-06-02 United States Gypsum Company Snap-set, ready-mix joint compound
US11453613B2 (en) 2017-11-07 2022-09-27 United States Gypsum Company Joint compounds, activators and methods for setting a joint compound and preventing seed setting

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CN110128045A (en) * 2019-04-30 2019-08-16 江苏一夫科技股份有限公司 II type anhydrous gypsum fast hydration exciting agent of one kind and fast hydration method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5571654A (en) * 1978-11-21 1980-05-29 Tohoku Hiryo Kk Curing material based on 2 type anhydrous gypsum
JPS56164046A (en) * 1980-05-15 1981-12-16 Daikin Ind Ltd Anhydrous gypsum composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5571654A (en) * 1978-11-21 1980-05-29 Tohoku Hiryo Kk Curing material based on 2 type anhydrous gypsum
JPS56164046A (en) * 1980-05-15 1981-12-16 Daikin Ind Ltd Anhydrous gypsum composition

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4443761A1 (en) * 1994-12-08 1996-06-13 Schueco Int Kg Heat-binding component for indoor and outdoor construction in fire protection design
US10669215B2 (en) 2009-01-14 2020-06-02 United States Gypsum Company Snap-set, ready-mix joint compound
US11560338B2 (en) 2009-01-14 2023-01-24 United States Gypsum Company Snap-set, ready-mix joint compound
JP2013518795A (en) * 2010-02-04 2013-05-23 ユナイテッド・ステイツ・ジプサム・カンパニー Snap-cured compound joint material
WO2014027613A1 (en) * 2012-08-15 2014-02-20 吉野石膏株式会社 Method for selectively inhibiting sulfate-reducing bacterium, gypsum composition capable of inhibiting proliferation of sulfate-reducing bacterium by said method, gypsum-type solidifying material, and gypsum-type building material
JP2014037364A (en) * 2012-08-15 2014-02-27 Yoshino Gypsum Co Ltd Selective fungistatic method of sulfate-reducing bacterium
JP2014037330A (en) * 2012-08-15 2014-02-27 Yoshino Gypsum Co Ltd Gypsum compositions, gypsum-based solidification materials and gypsum-based construction materials
US9901101B2 (en) 2012-08-15 2018-02-27 Yoshino Gypsum Co., Ltd. Method for selectively inhibiting sulfate-reducing bacterium, gypsum composition capable of inhibiting proliferation of sulfate-reducing bacterium by said method, gypsum-type solidifying material, and gypsum-type building material
JP2015083537A (en) * 2014-11-13 2015-04-30 ユナイテッド・ステイツ・ジプサム・カンパニー Snap cure-prepared joint filler
JP2019531251A (en) * 2016-10-12 2019-10-31 ユナイテッド・ステイツ・ジプサム・カンパニー Method for making lightweight gypsum compositions using internally generated foam and products made therefrom
US11453613B2 (en) 2017-11-07 2022-09-27 United States Gypsum Company Joint compounds, activators and methods for setting a joint compound and preventing seed setting

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