JPS609977B2 - Binder for plaster moldings - Google Patents
Binder for plaster moldingsInfo
- Publication number
- JPS609977B2 JPS609977B2 JP7825677A JP7825677A JPS609977B2 JP S609977 B2 JPS609977 B2 JP S609977B2 JP 7825677 A JP7825677 A JP 7825677A JP 7825677 A JP7825677 A JP 7825677A JP S609977 B2 JPS609977 B2 JP S609977B2
- Authority
- JP
- Japan
- Prior art keywords
- binder
- gypsum
- acrylamide
- hydrophobic monomer
- mol
- 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
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
【発明の詳細な説明】 本発明は石膏成形体用バインダーに関する。[Detailed description of the invention] The present invention relates to a binder for gypsum molded bodies.
従来より石膏成形体用バインダーとしては、ポリアクリ
ルアミドやポリアクリル酸が知られているが、これらを
用いる時には半水石膏の水和反応が著しく阻害されその
硬化に長時間を要するという重大な欠点がある。たとえ
ばポリアクリルアミドを半水石膏に対して5重量%用い
た場合石膏の硬化には6時間以上を要する。またポリア
クリル酸の場合には24時間でも硬化しない。本発明は
上記公知の石膏成形体用バインダーに代り、石膏の硬化
を実質的に遅延させることなく、しかも得られる石膏成
形体に充分な強度を付与し得る新しい石膏成形体用バイ
ンダーを提供するものである。Conventionally, polyacrylamide and polyacrylic acid have been known as binders for gypsum moldings, but when these are used, the hydration reaction of gypsum hemihydrate is significantly inhibited and it takes a long time to harden, which is a serious drawback. be. For example, when polyacrylamide is used in an amount of 5% by weight based on gypsum hemihydrate, it takes more than 6 hours for the gypsum to harden. Moreover, in the case of polyacrylic acid, it does not harden even after 24 hours. The present invention provides a new binder for gypsum moldings that does not substantially retard the curing of gypsum and can impart sufficient strength to the obtained gypsum moldings, in place of the above-mentioned known binders for gypsum moldings. It is.
即ち本発明は45〜95モル%のアクリルアミド類と5
〜55モル%の疎水性モノマーを構成モノマーとする共
重合体を有効成分とする石膏成形体用バインダーに関す
る。That is, in the present invention, 45 to 95 mol% of acrylamide and 5
The present invention relates to a binder for gypsum molded bodies whose active ingredient is a copolymer containing ~55 mol% of a hydrophobic monomer as a constituent monomer.
本発明の石膏成形体用バインダーは、アクリルアミド類
と疎水性モノマ−とを所定割合で共重合させて得られる
共重合体を有効成分とすることにより、従来のこの種バ
インダーの重大な欠点であった石膏の硬化時間を大中に
遅延させるという弊害が完全に解消できると共に、石膏
成形体製品に優れた強度を付与し得る。The binder for gypsum moldings of the present invention uses as an active ingredient a copolymer obtained by copolymerizing acrylamide and a hydrophobic monomer in a predetermined ratio, thereby overcoming the serious drawbacks of conventional binders of this type. The disadvantage of slowing down the hardening time of plaster can be completely eliminated, and excellent strength can be imparted to the plaster molded product.
殊にこの製品強度の増進効果は、この種バインダーとし
て汎用されるポリアクリルアミドのそれをも凌ぐもので
ある。本発明の石膏成形体用バインダーに使用されるア
クリルアミド類には、アクリルァミド及びメタクリルア
ミドが包含される。また疎水性モノマーとしては上記ア
クリルァミド類と共重合しうる各種の疎水性のモノマ−
がいずれも使用できる。その例としてはアクリロニトリ
ル、メタクリロニトリルなどのアクリロニトリル類:ア
クリル酸メチル、アクリル酸エチル、アクリル酸ブチル
、アクリル酸2−エチルヘキシル、アクリル酸2−ヒド
ロキシェチル、アクリル酸ジメチルアミノェチル、アク
リル酸ジェチルアミノェチルなどのアクリル酸ェステル
並びに之等に対応するメタクリル酸ェステル等のアクリ
ル酸ェステル類;酢酸ビニル、プロピオン酸ビニルなど
のビニルヱステル類;スチレン、Qーメチルスチレン、
ビニルトルェンなどのスチレン類が挙げられる。これら
は単独であるいは混合して使用することができる。上記
アクリルアミド類と疎水性モノマ−との使用割合はアク
リルアミド類が45〜95モル%好ましくは70〜90
モル%及び疎水性モノマ−が5〜55モル%好ましくは
10〜30モル%の範囲とする必要がある。アクリルア
ミド類が45モル%に満たない場合は得られるバインダ
ーを用いた石膏成形体の物理強度が低下するので好し〈
ない。またアクリルァミド類が95モル%を越える場合
則ち疎水性モノマーが5モル%に満たない場合は石膏の
硬化を遅延するので好ましくない。本発明の石膏成形体
用バインダーは、上記アクリルアミド類と疎水性モノマ
ーとを所定割合で共重合することにより収得できる。In particular, this effect of increasing product strength even exceeds that of polyacrylamide, which is commonly used as this type of binder. Acrylamides used in the binder for gypsum molded bodies of the present invention include acrylamide and methacrylamide. In addition, as the hydrophobic monomer, various hydrophobic monomers that can be copolymerized with the above acrylamides are used.
can be used. Examples include acrylonitriles such as acrylonitrile and methacrylonitrile: methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, dimethylaminoethyl acrylate, Acrylic acid esters such as tylaminoethyl and corresponding methacrylic acid esters; vinyl esters such as vinyl acetate and vinyl propionate; styrene, Q-methylstyrene,
Examples include styrenes such as vinyltoluene. These can be used alone or in combination. The ratio of the acrylamide and the hydrophobic monomer used is 45 to 95 mol% of the acrylamide, preferably 70 to 90 mol%.
The mole % and hydrophobic monomer should be in the range of 5 to 55 mole %, preferably 10 to 30 mole %. If the acrylamide content is less than 45 mol%, the physical strength of the resulting gypsum molded product using the binder will decrease, so it is preferable.
do not have. Furthermore, if the acrylamide content exceeds 95 mol %, that is, if the hydrophobic monomer content is less than 5 mol %, this is not preferable because the curing of the gypsum will be delayed. The binder for gypsum molded bodies of the present invention can be obtained by copolymerizing the above-mentioned acrylamide and a hydrophobic monomer in a predetermined ratio.
共重合方法は特に制限はなく、従来より公知の各種方法
が広く適用できる。例えば水性媒体中で上記特定割合の
アクリルアミド類及び疎水性モノマ−を重合開始剤の存
在下に10〜9000程度の温度で共重合させればよい
。その際界面活性剤や保護コロイドを使用して乳化重合
させる方法を採用することもできる。か)る保護コロイ
ドとしては公知のものをいずれも使用できるが、ノニオ
ン性のものが好ましくたとえばヒドロキシエチルスター
チ、ポリビニルアルコールなどを好適な例として挙げる
ことができる。本発明の石膏成形体用バインダーは、之
を使用するに当っては、通常半水石膏及び適当量の水と
3混合後、成形・乾燥すればよい。The copolymerization method is not particularly limited, and various conventionally known methods can be widely applied. For example, acrylamide and a hydrophobic monomer in the above specified proportions may be copolymerized in an aqueous medium in the presence of a polymerization initiator at a temperature of about 10 to 9,000 ℃. At this time, a method of emulsion polymerization using a surfactant or a protective colloid can also be adopted. Any known protective colloid can be used, but nonionic ones are preferred, such as hydroxyethyl starch, polyvinyl alcohol, and the like. When using the binder for gypsum molded bodies of the present invention, it is generally necessary to mix it with hemihydrate gypsum and an appropriate amount of water, then mold and dry it.
この際混合物には、必要に応じて石綿、岩線、ガラス繊
維、鋼線などの無機質や木綿、麻、合成繊維、木材パル
プなどの有機質繊維を補強剤として添加することができ
る。また所望成形体製品が石膏ボードの場合3には、更
に通学のボード原紙等を補強剤として用いることができ
る。上記において本発明バインダーの使用量は通常半水
石膏に対して固形分基準で0.01〜1の重量%程度の
範囲とすればよい。また得ようとする成形体が石膏ボー
ドである場合には、4半水石膏に対して0.1〜1重量
%程度とするのが好ましい。かくして本発明によれば、
石膏の硬化を実質的に遅延させることなく、比較的短時
間に、大きな強度と小さな吸水率とを有する本発明所期
の効果を奏する石膏成形体製品が収得できる。At this time, inorganic materials such as asbestos, rock wire, glass fiber, and steel wire, and organic fibers such as cotton, hemp, synthetic fibers, and wood pulp may be added to the mixture as reinforcing agents, if necessary. Further, when the desired molded product is a gypsum board (3), base paper for school board or the like can be used as a reinforcing agent. In the above, the amount of the binder of the present invention to be used is usually in the range of about 0.01 to 1% by weight based on solid content based on hemihydrate gypsum. Further, when the molded product to be obtained is a gypsum board, the amount is preferably about 0.1 to 1% by weight based on 4-hemihydrate gypsum. Thus, according to the invention:
A gypsum molded product having high strength and low water absorption and exhibiting the desired effects of the present invention can be obtained in a relatively short time without substantially delaying the hardening of the gypsum.
以下に実施例及び比較例を挙げて本発明の特徴とすると
ころを明らかにする。Examples and comparative examples will be given below to clarify the characteristics of the present invention.
実施例 1
2その四ツロフラスコにアクリルアミドの50%水溶液
353.6夕、アクリロニトリル23.2夕、インプロ
ピルアルコール10夕、ポリビニルアルコール(重合度
500)の10%水溶液60夕及び水460夕を仕込み
、窒素気流下に昇温し、65qoに達した時点で2夕の
過硫酸カリを100夕の水に溶解した溶液を添加した。Example 1 2 353.6 times of a 50% aqueous solution of acrylamide, 23.2 times of acrylonitrile, 10 times of inpropyl alcohol, 60 times of a 10% aqueous solution of polyvinyl alcohol (degree of polymerization 500) and 460 times of water were charged into the four-way flask. The temperature was raised under a nitrogen stream, and when the temperature reached 65 qo, a solution of 2 quarts of potassium persulfate dissolved in 100 quarts of water was added.
その後70〜75午0の温度で3時間保温した。重合終
了後冷却して固形分20.1%、pH3.2、粘度(B
型粘度計2000以下同じ)370比psの共重合体の
水性分散液を得た。これをバインダー1とする。実施例
2
2その四ツロフラスコにアクリルアミドの50%水溶液
303夕、アクリロニトリル48.5夕、インプロピル
アルコール10夕「ポリビニルアルコール(重合度50
0)の10%水溶液100夕及び水436夕を仕込み、
以後実施例1と同様にして固形分22.8%、pH4.
8 粘度2800比psの水性分散液を得た。Thereafter, it was kept warm for 3 hours at a temperature of 70 to 75 pm. After the polymerization is completed, it is cooled to obtain a solid content of 20.1%, pH 3.2, and viscosity (B
An aqueous dispersion of a copolymer with a specific ps of 370 (as measured by a type viscometer of 2000 or less) was obtained. This will be referred to as binder 1. Example 2 2 Into the four-way flask, 303 g of a 50% aqueous solution of acrylamide, 48.5 g of acrylonitrile, and 10 g of inpropyl alcohol were added.
Prepare 100 units of a 10% aqueous solution of 0) and 436 units of water,
Thereafter, in the same manner as in Example 1, the solid content was 22.8% and the pH was 4.
8 An aqueous dispersion having a viscosity of 2800 ps was obtained.
これをバインダー0とする。実施例 3
2その四ツロフラスコにアクリルアミドの50%水溶液
229夕、アクリロニトリル85.5夕、インプロピル
アルコール10夕、ボリビニルアルコール(重合度50
0)の10%水溶液100夕及び水473夕を仕込み、
以後実施例1と同様にして固形分22.9%、pH3.
0、粘度10比psの水性分散液を得た。This is referred to as binder 0. Example 3 2 Into the four-piece flask, 229 g of a 50% aqueous solution of acrylamide, 85.5 g of acrylonitrile, 10 g of inpropyl alcohol, and vorivinyl alcohol (degree of polymerization 50
Prepare 100 units of a 10% aqueous solution of 0) and 473 units of water,
Thereafter, in the same manner as in Example 1, the solid content was 22.9% and the pH was 3.
An aqueous dispersion having a viscosity of 0 and a viscosity of 10 ps was obtained.
これをバインダーmとする。実施例 4
2その四ッロフラスコに酢酸ビニル46.5夕、ポリエ
チレングリコールアリルエーテル1.2夕、インプロピ
ルアルコール10夕及び水343夕を仕込み、窒素気流
下に昇温し7000に達した時点でアクリルアミドの5
0%水溶液307夕、過硫酸カリ1夕及び水292夕の
混合液を3時間を要して滴下し、滴下終了後8000で
1時間保温した。This is referred to as binder m. Example 4 2 46.5 tons of vinyl acetate, 1.2 tons of polyethylene glycol allyl ether, 10 tons of inpropyl alcohol, and 343 tons of water were charged into the 2-four-meter flask, and the temperature was raised under a nitrogen stream until it reached 7,000, and then acrylamide was added. 5
A mixture of 307 g of 0% aqueous solution, 1 g of potassium persulfate, and 292 g of water was added dropwise over a period of 3 hours, and after the dropwise addition was completed, the temperature was kept at 8,000 ℃ for 1 hour.
重合終了後冷却して固形分20.1%、pH4、粘度2
40比psの水性分散液を得た。これをバインダーWと
する。実施例 52その四ツロフラスコにアクリルアミ
ドの50%水溶液296夕、メタクリル酸メチル52夕
、インプロピルアルコール5夕、ボリビニルアルコール
(重合度500)の10%水溶液50夕及び水490夕
を仕込み以後実施例1と同様にして固形分21.5%、
粘度175比ps、pH3.0の水性分散液を得た。After polymerization is completed, it is cooled to a solid content of 20.1%, pH 4, and viscosity 2.
An aqueous dispersion of 40 ps was obtained. This will be referred to as binder W. Example 52 296 times of a 50% aqueous solution of acrylamide, 52 times of methyl methacrylate, 5 times of inpropyl alcohol, 50 times of a 10% aqueous solution of vorivinyl alcohol (degree of polymerization 500) and 490 times of water were placed in the four-way flask. Same as 1, solid content 21.5%,
An aqueous dispersion having a viscosity of 175 ps and a pH of 3.0 was obtained.
これをバインダーVとする。実施例 6
2その四ツロフラスコにアクリルアミドの50%水溶液
292.8夕、スチレン53.6夕、インプロピルアル
コール10夕、ドデシルベンゼンスルホン酸ソーダ(合
水率40%)3.3夕及び水520夕を仕込み、以後実
施例1と同様にして固形分22.7%、PH3.1、粘
度8500比psの水性分散体を得た。This will be referred to as binder V. Example 6 2 Into the four-piece flask, 292.8 hours of a 50% aqueous solution of acrylamide, 53.6 hours of styrene, 10 hours of inpropyl alcohol, 3.3 hours of sodium dodecylbenzenesulfonate (water ratio 40%), and 520 minutes of water were added. Thereafter, in the same manner as in Example 1, an aqueous dispersion having a solid content of 22.7%, a pH of 3.1, and a viscosity of 8500 ps was obtained.
これをバインダーのとする。実施例 7
2その四ツロフラスコにアクリルアミドの50%水溶液
128.8夕、メタクリル酸ジメチルアミノェチル35
.6夕、62.5%硫酸17.3夕及び水805夕を仕
込み、窒素気流下に昇溢し、65q0に達した時点で2
夕の過硫酸カリを100夕の水に溶解した溶液10夕を
添加した。This will be used as a binder. Example 7 2 Into the four-piece flask, add 128.8% of a 50% aqueous solution of acrylamide and 35% of dimethylaminoethyl methacrylate.
.. 6 days, 17.3 times of 62.5% sulfuric acid and 805 times of water were charged, and the mixture was heated up and overflowed under a nitrogen stream, and when it reached 65q0, 2
10 parts of a solution of 10 parts of potassium persulfate dissolved in 10 parts of water was added.
その後70〜80℃で4時間保温した。重合終了後冷却
して固形分9.9%、pH4.7、粘度260比psの
水性分散液を得た。これをバインダー皿とする。比較例
1
2その四ツロフラスコにアクリルアミドの50%水溶液
400夕、インプロピルアルコール10夕及び水480
夕を仕込み、以後実施例1と同様にして固形分20.ん
pH3.4、粘度420比psの水性分散液を得た。Thereafter, the temperature was kept at 70 to 80°C for 4 hours. After the polymerization was completed, it was cooled to obtain an aqueous dispersion having a solid content of 9.9%, a pH of 4.7, and a viscosity of 260 ps. This will be used as a binder plate. Comparative Example 1 2 In a four-way flask, 400 g of a 50% aqueous solution of acrylamide, 10 g of inpropyl alcohol, and 480 g of water were added.
After that, the solid content was reduced to 20% in the same manner as in Example 1. An aqueous dispersion having a pH of 3.4 and a viscosity of 420 ps was obtained.
これを比較バインダーとする。<応用試験>
上記実施例1〜7で得たバインダー1〜肌及び比較例で
得たバインダー(ポリァクリルァミド)を使用して石膏
成形体を作成した。This will be used as a comparison binder. <Application Test> Gypsum molded bodies were created using the binder 1 to skin obtained in Examples 1 to 7 above and the binder (polyacrylamide) obtained in Comparative Example.
i)硬化時間
バインダーを固形分として0.5タ含有する水溶液67
夕を200のとビーカーにとり、ついで鷹梓下に半水石
膏100夕を添加し5分間混合し石膏組成物を得た。i) Curing time Aqueous solution containing 0.5 ta of binder as solid content 67
200 g of gypsum was taken in a beaker, and then 100 g of gypsum was added to the takaazusa and mixed for 5 minutes to obtain a gypsum composition.
たゞちにその中心部に温度計を挿入し最高温度に達する
迄の時間を測定した。(JISR 9112)ii)曲
げ強度
前記二i)と同様にして得た組成物を内容10cの×1
0肌×1.5伽の型枠に流込み成形後これを60℃に調
整された循風乾燥機中に2加持間静層して乾燥した。Immediately a thermometer was inserted into the center and the time until the maximum temperature was reached was measured. (JISR 9112) ii) Bending strength The composition obtained in the same manner as above 2i) was
After casting into a mold of 0.0 mm x 1.5 mm, the mold was placed in a circulating dryer adjusted to 60° C. for 2 hours to dry.
ついで20oo、65%R.日の条件で一昼夜調湿した
試料につき測定した。結果を各バインダーにつき夫々1
川固の試料の平均値で第1表に示す。Then 20oo, 65%R. Measurements were made on samples that were conditioned all day and night under the same conditions. 1 result for each binder
Table 1 shows the average values of the Kawago samples.
第1表Table 1
Claims (1)
ル%の疎水性モノマーを構成モノマーとする共重合体を
有効成分とする石膏成形体用バインダー。 2 疎水性モノマーがアクリロニトリル類である特許請
求の範囲第1項記載のバインダー。 3 疎水性モノマーがアクリル酸エステル類である特許
請求の範囲第1項記載のバインダー。 4 疎水性モノマーがビニルエステルである特許請求の
範囲第1項記載のバインダー。 5 疎水性モノマーがスチレン類である特許請求の範囲
第1項記載のバインダー。 6 構成モノマーが70〜90モル%のアクリルアミド
類と10〜30モル%の疎水性モノマーである特許請求
の範囲第1項記載のバインダー。[Scope of Claims] 1. A binder for gypsum moldings, the active ingredient of which is a copolymer comprising 45 to 95 mol% of acrylamide and 5 to 55 mol% of a hydrophobic monomer. 2. The binder according to claim 1, wherein the hydrophobic monomer is an acrylonitrile. 3. The binder according to claim 1, wherein the hydrophobic monomer is an acrylic ester. 4. The binder according to claim 1, wherein the hydrophobic monomer is a vinyl ester. 5. The binder according to claim 1, wherein the hydrophobic monomer is a styrene. 6. The binder according to claim 1, wherein the constituent monomers are 70 to 90 mol% of acrylamide and 10 to 30 mol% of a hydrophobic monomer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7825677A JPS609977B2 (en) | 1977-06-29 | 1977-06-29 | Binder for plaster moldings |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7825677A JPS609977B2 (en) | 1977-06-29 | 1977-06-29 | Binder for plaster moldings |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5411930A JPS5411930A (en) | 1979-01-29 |
JPS609977B2 true JPS609977B2 (en) | 1985-03-14 |
Family
ID=13656904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7825677A Expired JPS609977B2 (en) | 1977-06-29 | 1977-06-29 | Binder for plaster moldings |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS609977B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02127227A (en) * | 1988-10-21 | 1990-05-15 | Taisei Kikai:Kk | Pack filling method and apparatus |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6139889Y2 (en) * | 1981-06-16 | 1986-11-14 | ||
US5461737A (en) * | 1993-02-16 | 1995-10-31 | France Bed Co., Ltd. | Mattress apparatus and method for manufacturing the same |
-
1977
- 1977-06-29 JP JP7825677A patent/JPS609977B2/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02127227A (en) * | 1988-10-21 | 1990-05-15 | Taisei Kikai:Kk | Pack filling method and apparatus |
Also Published As
Publication number | Publication date |
---|---|
JPS5411930A (en) | 1979-01-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2666082C (en) | Hydrophobically modified cationic copolymers | |
KR102221189B1 (en) | Block copolymer | |
JP2507280B2 (en) | Dispersant for cement | |
CN111925489B (en) | High-water-reduction slump-retaining type polycarboxylate superplasticizer and preparation method and application thereof | |
CN109134784B (en) | Coagulation-accelerating early-strength polycarboxylic acid superplasticizer and preparation method thereof | |
CN107987224A (en) | A kind of short-chain branch crosslinking water conservation solvent layer control release type polycarboxylic acid slump retaining agent and preparation method | |
DK163586B (en) | Aqueous synthetic dispersion on the basis of a copolymer of olefinically unsaturated compounds, its preparation and use | |
EP0145685B1 (en) | A cement mortar and concrete with a reduced water absorption and a method for manufacture thereof | |
JP4089838B2 (en) | Cement composition and cement paste and cement mortar | |
JPS5945949A (en) | Cement composition and manufacture | |
JPS609977B2 (en) | Binder for plaster moldings | |
JPS641426B2 (en) | ||
JPS6225622B2 (en) | ||
JPH08113613A (en) | Cement additive | |
US3950295A (en) | Method of preparing a composition containing gypsum, a vinyl monomer and sulfite ion | |
JPH0545539B2 (en) | ||
US4293344A (en) | Setting retardatives for compositions with a gypsum plaster base or anhydrite | |
JP2886662B2 (en) | Polymer cement mortar composition | |
JP2882623B2 (en) | Method for promoting hardening of hydraulic cement composition and method for improving strength of the hardened product | |
JPH04209737A (en) | Self-leveling cement water base composition | |
JPS59203745A (en) | Self levelling cement aqueous composition | |
JPH01172250A (en) | Retardant for cement | |
JPS62212252A (en) | Dispersant for cement | |
JPS6337059B2 (en) | ||
JP2647839B2 (en) | Concrete curing method |