JPS641428B2 - - Google Patents

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Publication number
JPS641428B2
JPS641428B2 JP10247478A JP10247478A JPS641428B2 JP S641428 B2 JPS641428 B2 JP S641428B2 JP 10247478 A JP10247478 A JP 10247478A JP 10247478 A JP10247478 A JP 10247478A JP S641428 B2 JPS641428 B2 JP S641428B2
Authority
JP
Japan
Prior art keywords
parts
starch
cmc
modified starch
cationic
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
Application number
JP10247478A
Other languages
Japanese (ja)
Other versions
JPS5532711A (en
Inventor
Shungo Hiraoka
Shigeki Kio
Hiroshi Hayakawa
Kyoichi Nagatsuka
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.)
Nippon Starch Chemical Co Ltd
Original Assignee
Nippon Starch Chemical Co Ltd
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 Nippon Starch Chemical Co Ltd filed Critical Nippon Starch Chemical Co Ltd
Priority to JP10247478A priority Critical patent/JPS5532711A/en
Publication of JPS5532711A publication Critical patent/JPS5532711A/en
Publication of JPS641428B2 publication Critical patent/JPS641428B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は建築物の主として壁及び天井の内装仕
上げ、工事に用いる繊維壁塗材用組成物に関す
る。更に詳しくは左官工事の化粧用上塗り材料
で、有機質又は無機質の繊維材料、色土、パーラ
イトなどの混和材料などにカチオン変性澱粉、カ
ルボキシメチルセルロース(以下CMCと略す。)
等の糊材料を主原料とした繊維壁塗材用組成物に
関する。 従来、天然物である澱粉、コンニヤク粉、フノ
リなどが繊維壁塗材用の糊材として用いられてい
たが糊剤自身が極めて腐敗しやすく、壁にカビや
シミが発生したり、糊を蒸煮しなければ粘着性が
出なかつたり多くの欠点を有した。 これらの欠点を除くため近年CMCのような合
成糊料が用いられ始めたがこれとてコテさばき等
の作業性の悪さ、塗工後のケバ伏せなど十分でな
く、また乾燥までの接着力が不足するため塗工面
からの剥離が起きたり不都合な点が多いものであ
る。 本発明者らは、コテさばきが良好でケバ立ちの
目立たなくかつ接着力の大きな糊材について鋭意
研究を重ねた結果、カチオン性を有する澱粉と
CMCの両者を糊材として用いることにより本発
明を完成るに至つた。 すなわち、繊維質上塗材の全固形分重量に対し
てカチオン変性澱粉を0.5〜20重量%、好ましく
は2.0〜10重量%、CMCを1.0〜20重量%、好まし
くは4.0〜10重量%添加することによりコテさば
き等の作業性が良好でかつ塗工後のケバ立ちの目
立たない繊維壁塗材用組成物が得られる。 また本発明よつて得られた塗材組成物はカチオ
ン性の高分子電解質であるカチオン変性澱粉とア
ニオン性の高分子電解質であるCMCとがなんだ
かよくわからないが、両者の間に非常に大きな力
が働きすばらしい凝集力と高い粘着力が見い出さ
れ梅雨時の高温多湿状態で乾燥のおそい時期です
ら塗工面から剥離することなく長時間未乾燥のま
まで安定して接着している。またカチオン変性澱
粉は澱粉でありながら澱粉のように腐敗したり表
面にカビが発生したりしない。 本発明に供すべきカチオン変性澱粉は馬鈴薯、
トウモロコシ、小麦、甘藷、米、タピオカ、サ
ゴ、等の未処理澱粉、又は澱粉含有物、もしくは
これらを酸化、酸処理、デキストリン化、酵素処
理、架橋、エーテル化、エステル化等により得ら
れた変性澱粉のいずれかの澱粉に公知の反応によ
りカチオン化剤を作用させて置換度0.005〜0.2
(無水グルコース残基1モル当り置換基0.005〜
0.2モル)に化工したものが適当である。また本
目的で使用するカチオン変性澱粉は常温水(5℃
〜35℃)で溶解することが好ましいためカチオン
変性後又はカチオン変性と同時にドラムドライヤ
ー等で更にα化処理乾燥したものが好ましい。 カチオン化は2―クロロ―3―ヒドロキシトリ
メチルクロライド、β―ジエチルアミノエチルク
ロライド、等ハロゲン化アルキル4級アルキルア
ンモニウム塩、ハロゲン化アルキル3級(2級又
は1級)アルキルアミン、ハロゲン化アルキルジ
アミン、エポキシ化アルキル4級アルキルアンモ
ニウム塩、エポキシ化アルキル3級(2級又は1
級)アルキルアミン、アミノエチル硫酸、エチレ
ンイミン、スルホニウム、ホスホニウム、シアナ
ミド、アルカリ金属シアナミド、アルカリ土類金
属シアナミド等の一般的なカチオン変性化剤によ
り直接得られるカチオン澱粉のみならず澱粉にエ
ピクロルヒドリンを作用させた後でアルキルアミ
ンを作用させて行うカチオン変性、澱粉にアクリ
ルアミドをエーテル結合させた後で、ホフマン分
解、又はマンニツヒ反応によるカチオン変性、澱
粉に(メタ)アクリロニトリルをエーテル結合さ
せた後で水素化するカチオン変性、など最終的な
澱粉にカチオン性を示す置換基を含むものならば
どのようなものでも良いばかりか、(メタ)アク
リル酸アミノアルキルエステル、或いはそれらの
4級アンモニウム塩、ビニルピリジンおよびその
誘導体等のカチオン性のモノマーによるグラフト
共重合変性澱粉およびアクリルアミド、(メタ)
アクリロニトリル、(メタ)アクリル酸アルキル
エステル、(メタ)アクリル酸グリシジルエステ
ル、アクロレイン等カチオン変性可能なモノマー
をグラフト共重合させた後カチオン変性を行うこ
とも可能である。 本発明で用いるCMCの置換度は0.5〜2.0好まし
くは0.6〜1.5である。 本発明に用いる組成物中の糊剤としてカチオン
変性澱粉、CMCを必須として他にポリビニルア
ルコール、メチルセルロース、天然澱粉、各種化
工澱粉、植物ガム、ポリアクリル酸およびそのア
ルカリ塩、ポリアクリルアミド等を必要により添
加することも本発明に含まれる。 本発明の組成物はあらかじめ混合もしくは使用
時に混合して用いられ、カチオン変性澱粉、
CMC等の糊剤の他にトリコツト、綿粉、マイカ
(雲母)、上白アルミくず、しんちゆうくず、ツ
ゲ、ヒノキ、杉等の木粉、骨材、金箔、銅箔、合
成繊維等の素材と共に用いられる。 次に参考例、実施例および比較例を挙げて本発
明をさらに詳しく説明する。 参考例 1 苛性ソーダ2.5部(重量、以下同じ)、硫酸ソー
ダ50部を水150部に溶解した後、無処理の馬鈴薯
澱粉100部を均一に懸濁させ、撹拌しながらジエ
チルアミノエチルクロライド7.5部を添加し40℃、
6時間反応を行う。 反応終了後中和、水洗し、ドラムドライヤー
(表面温度135℃)でα化乾燥を行ない常温水可溶
性とする。 参考例 2 参考例1のカチオン変性を行なわないで馬鈴薯
澱粉をドラムドライヤー(表面温度135℃)でα
化乾燥を行なつた。 比較例 1 トリコツト繊維90部、CMC10部をよくほぐし
て混合した後、水570部を加えて均等になるよう
混練し、30分後下地板に塗工を行ない各種の試験
を行なつた。 比較例 2 比較例1のCMC10部の替りに参考例2のα化
馬鈴薯澱粉10部を用いて各種試験を行なつた。 比較例 3 比較例1と同様でCMC10部の替りに参考例1
のカチオン変性澱粉10部を加えて各種の試験を行
なつた。 実施例 1 トリコツト繊維90部、CMC7部、参考例1のカ
チオン変性澱粉3部をよくほぐして混合したのち
水570部を加えて均等になるように混練し、30分
後に下地板に塗工を行ない各種の試験を行なつ
た。 実施例 2 実施例1と同様でCMC3部、参考例1のカチオ
ン変性澱粉7部を添加して各種の試験を行なつ
た。 実施例 3 参考例1のカチオン変性澱粉でα乾燥を行なわ
ないで反応後、中和、水洗、乾燥を行なつたもの
5部、CMC5部を水570部に分散させて85℃以上
で30分間糊化を行ない25℃に冷却後よくほぐした
トリコツト繊維90部に加えて均等になるように混
練し30分後下地板に塗工を行ない各種の試験を行
なつた。 実施例 4 比較例1〜3、実施例1〜3、各種の塗工試験
を行ない表に示した。
The present invention relates to a fiber wall coating composition used mainly for interior finishing and construction of walls and ceilings of buildings. More specifically, it is a decorative topcoat material for plastering, which includes organic or inorganic fiber materials, colored clay, mixed materials such as perlite, cationically modified starch, and carboxymethyl cellulose (hereinafter abbreviated as CMC).
The present invention relates to a composition for fiber wall coating materials whose main raw material is a glue material such as. Conventionally, natural products such as starch, konnyaku flour, and funori have been used as glue for fiber wall coatings, but the glue itself is extremely perishable, causing mold and stains on the walls, and the glue being steamed. Otherwise, it would not be sticky and would have many disadvantages. In order to eliminate these drawbacks, synthetic glues such as CMC have recently begun to be used, but they have poor workability such as troweling, are not sufficiently fluffy after coating, and have poor adhesive strength until drying. There are many inconveniences such as peeling from the coated surface due to insufficient amount. The inventors of the present invention have conducted intensive research on glue materials that have good trowel handling, do not cause noticeable fluff, and have strong adhesive strength.
The present invention was completed by using both CMC and CMC as adhesive materials. That is, cationically modified starch is added in an amount of 0.5 to 20% by weight, preferably 2.0 to 10% by weight, and CMC is added in an amount of 1.0 to 20% by weight, preferably 4.0 to 10% by weight based on the total solid weight of the fibrous top coating material. As a result, a composition for a fiber wall coating material that has good workability such as troweling and does not leave noticeable fluff after coating can be obtained. In addition, although it is not clear what the cationic modified starch, which is a cationic polymer electrolyte, and CMC, which is an anionic polymer electrolyte, are in the coating material composition obtained by the present invention, there is a very large force between them. It has been found to have excellent cohesive strength and high adhesive strength, and even in the hot and humid conditions of the rainy season, when drying is slow, it does not peel off from the coated surface and remains undried for a long time and remains stable and adheres. Furthermore, although cationically modified starch is a starch, unlike starch, it does not rot or mold grows on its surface. The cationically modified starch to be used in the present invention is potato,
Untreated starch or starch-containing materials such as corn, wheat, sweet potato, rice, tapioca, sago, etc., or modified products obtained by oxidation, acid treatment, dextrinization, enzyme treatment, crosslinking, etherification, esterification, etc. The degree of substitution is 0.005 to 0.2 by applying a cationizing agent to any of the starches through a known reaction.
(0.005 substituents per mole of anhydroglucose residue
0.2 mol) is suitable. In addition, the cationically modified starch used for this purpose is watered at room temperature (5℃).
Since it is preferable to dissolve at a temperature of 35° C. to 35° C., it is preferable to further gelatinize and dry with a drum dryer or the like after cationic modification or at the same time as cationic modification. Cationization is 2-chloro-3-hydroxytrimethyl chloride, β-diethylaminoethyl chloride, halogenated alkyl quaternary alkyl ammonium salt, halogenated alkyl tertiary (secondary or primary) alkylamine, halogenated alkyldiamine, epoxy epoxidized alkyl quaternary alkylammonium salt, epoxidized alkyl tertiary (secondary or primary)
The action of epichlorohydrin on starch as well as cationic starch directly obtained with general cationic modifiers such as alkylamines, aminoethyl sulfates, ethyleneimines, sulfoniums, phosphoniums, cyanamides, alkali metal cyanamides, alkaline earth metal cyanamides, etc. cationic modification by ether bonding acrylamide to starch and then Hofmann degradation or Mannitz reaction; hydrogenation after ether bonding (meth)acrylonitrile to starch Any substance that contains a substituent that exhibits cationic properties in the final starch, such as cationic modification, may be used, as well as (meth)acrylic acid aminoalkyl esters or their quaternary ammonium salts, vinylpyridine, and Graft copolymerized modified starch and acrylamide with cationic monomers such as its derivatives, (meth)
It is also possible to perform cationic modification after graft copolymerizing a cationically modifiable monomer such as acrylonitrile, (meth)acrylic acid alkyl ester, (meth)acrylic acid glycidyl ester, or acrolein. The degree of substitution of CMC used in the present invention is 0.5 to 2.0, preferably 0.6 to 1.5. As the sizing agent in the composition used in the present invention, cationically modified starch and CMC are essential, and in addition, polyvinyl alcohol, methylcellulose, natural starch, various modified starches, vegetable gums, polyacrylic acid and its alkali salts, polyacrylamide, etc. are optionally used. The present invention also includes the addition of such substances. The composition of the present invention is used by mixing in advance or at the time of use, and includes cationically modified starch,
In addition to adhesives such as CMC, other adhesives such as tricot, cotton powder, mica (mica), white aluminum scraps, shinchi scum, wood powders such as boxwood, cypress, and cedar, aggregates, gold leaf, copper leaf, synthetic fibers, etc. Used with materials. Next, the present invention will be explained in more detail by referring to Reference Examples, Examples, and Comparative Examples. Reference Example 1 After dissolving 2.5 parts of caustic soda (weight, same hereinafter) and 50 parts of sodium sulfate in 150 parts of water, 100 parts of untreated potato starch was uniformly suspended, and 7.5 parts of diethylaminoethyl chloride was added while stirring. 40℃,
The reaction is carried out for 6 hours. After the reaction is complete, neutralize, wash with water, and gelatinize and dry with a drum dryer (surface temperature 135°C) to make it soluble in water at room temperature. Reference Example 2 Potato starch was dried in a drum dryer (surface temperature 135°C) without the cationic modification of Reference Example 1.
It was dried by heat. Comparative Example 1 After thoroughly loosening and mixing 90 parts of tricot fiber and 10 parts of CMC, 570 parts of water was added and kneaded until evenly mixed. After 30 minutes, the mixture was coated on a base plate and various tests were conducted. Comparative Example 2 Various tests were conducted using 10 parts of pregelatinized potato starch of Reference Example 2 instead of 10 parts of CMC of Comparative Example 1. Comparative Example 3 Same as Comparative Example 1, but use Reference Example 1 instead of 10 parts of CMC.
Various tests were carried out by adding 10 parts of cationically modified starch. Example 1 After thoroughly loosening and mixing 90 parts of tricot fiber, 7 parts of CMC, and 3 parts of the cationically modified starch from Reference Example 1, 570 parts of water was added and kneaded until evenly mixed. After 30 minutes, the mixture was coated on the base plate. and conducted various tests. Example 2 In the same manner as in Example 1, various tests were conducted by adding 3 parts of CMC and 7 parts of the cationically modified starch of Reference Example 1. Example 3 After reacting with the cationically modified starch of Reference Example 1 without α-drying, neutralizing, washing with water, and drying, 5 parts of CMC and 5 parts of CMC were dispersed in 570 parts of water and heated at 85°C or higher for 30 minutes. After gelatinization and cooling to 25°C, the mixture was added to 90 parts of well loosened tricot fibers, kneaded evenly, and after 30 minutes was coated on a base plate and various tests were conducted. Example 4 Various coating tests were conducted for Comparative Examples 1 to 3 and Examples 1 to 3, and the results are shown in the table.

【表】【table】

【表】 ○ 優れている × 良くない
[Table] ○ Excellent × Not good

Claims (1)

【特許請求の範囲】[Claims] 1 繊維壁塗材の全固形分重量に対してカチオン
変性澱粉を0.5〜20重量%、カルボキシメチルセ
ルロースを1.0〜20重量%添加することを特徴と
する繊維壁塗材用組成物。
1. A composition for a fiber wall coating material, characterized in that 0.5 to 20% by weight of cation-modified starch and 1.0 to 20% by weight of carboxymethyl cellulose are added to the total solid weight of the fiber wall coating material.
JP10247478A 1978-08-23 1978-08-23 Fibrous wall coating material composition Granted JPS5532711A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10247478A JPS5532711A (en) 1978-08-23 1978-08-23 Fibrous wall coating material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10247478A JPS5532711A (en) 1978-08-23 1978-08-23 Fibrous wall coating material composition

Publications (2)

Publication Number Publication Date
JPS5532711A JPS5532711A (en) 1980-03-07
JPS641428B2 true JPS641428B2 (en) 1989-01-11

Family

ID=14328443

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10247478A Granted JPS5532711A (en) 1978-08-23 1978-08-23 Fibrous wall coating material composition

Country Status (1)

Country Link
JP (1) JPS5532711A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1395548A (en) * 2000-11-10 2003-02-05 三菱商事建材株式会社 Building material composition and building material
EP4001244A1 (en) * 2020-11-23 2022-05-25 Knauf Gips KG Starch as a primer for substrates

Also Published As

Publication number Publication date
JPS5532711A (en) 1980-03-07

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