JPH0530786B2 - - Google Patents
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- Publication number
- JPH0530786B2 JPH0530786B2 JP1970984A JP1970984A JPH0530786B2 JP H0530786 B2 JPH0530786 B2 JP H0530786B2 JP 1970984 A JP1970984 A JP 1970984A JP 1970984 A JP1970984 A JP 1970984A JP H0530786 B2 JPH0530786 B2 JP H0530786B2
- Authority
- JP
- Japan
- Prior art keywords
- inorganic
- water
- fatty acid
- reacting
- parts
- 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 - Lifetime
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- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は無機質板の耐水化方法に関する。
さらに詳しくは、脂肪酸エステルならびに脂肪
酸金属塩および脂肪酸の少なくとも1種からなる
水溶性耐水化剤および/または脂肪酸にポリアル
キレンポリアミンおよび/またはジアルキルアル
キレンジアミンを反応させて得た水溶性耐水化剤
で無機質板用原料を処理する無機質板の製造方法
に関する。
従来、無機質板の耐水剤として脂肪酸金属塩等
特にそのカルシウム塩が用いられていたが耐水性
の面或は歩留り、抄造時の発泡の面等で、数々の
欠点を有していた。
本発明に使用する水溶性耐水化剤は飽和もしく
は不飽和脂肪酸又はその混合物の誘導体を水溶性
としたものである。
これらの欠点を改善すべく本発明者等は鋭意研
究を重ねた結果、脂肪酸エステル、ならびに脂肪
酸、脂肪酸石ケン又は脂肪酸金属塩の混合系が優
れた効果を発揮する事を見い出した、特に飽和も
しくは不飽和脂肪酸の炭素数が8〜22のものが好
ましく、さらに好ましくは8〜18のもの、最も好
ましくは14〜18のものである。
一方、飽和又は不飽和脂肪酸にポリアルキレン
ポリアミンおよび/またはジアルキルアルキレン
ジアミンを反応した後、無機酸、有機酸又は四級
化剤を反応して得た水溶性耐水化剤又はそれらの
混合物も従来品に比べ優れた効果を有することが
見い出された。ポリアルキレンポリアミン又はジ
アルキルアルキレンジアミンと反応させる脂肪酸
は炭素数12〜22好ましくは16〜18の飽和脂肪酸で
ある。
本発明は無機充填剤ならびに無機酸化物、炭酸
塩、硫酸塩、珪酸塩、塩化物およびそれらの複合
塩からなる群から選ばれた一種又は二種以上の無
機物質、
必要に応じて有機パルプ繊維を加えた原料を抄
造又は成型することにより無機質板を製造する方
法において、
(a) 脂肪酸エステルならびに脂肪酸および脂肪酸
金属塩の少なくとも1種からなる水溶性耐水化
剤および/または
(b) 脂肪酸にポリアルキレンポリアミンおよび/
またはジアルキルアルキレンジアミンを反応さ
せた後、さらに無機酸、有機酸もしくは四級化
剤を反応させて得た水溶性耐水化剤
で一種又は二種以上の前記原料を反応又は吸着処
理した後、さらに前記水溶性耐水化剤で処理して
いない無機物質および/またはパルプ繊維を混合
し、さらに抄造又は成型することを特徴とする無
機質板の製造方法に関する、
耐水化剤(a)の脂肪酸として飽和又は不飽和であ
り、それの炭素数8〜22、炭素数8〜22が好まし
くは8−18そして炭素数14〜18がもつとも好まし
い。脂肪酸金属塩を構成する金属塩としてはカリ
ウム、ナトリウム、カルシウム、マグネシウム、
亜鉛、アルミニウム、ジルコニウム、アンモニウ
ム、アルカノールアミンまたはモルホリン等の塩
が揚げられる。脂肪酸のエステルとしてはメチ
ル、エチル等のアルキルエステル等が使用でき
る。
耐水化剤(b)の原料である脂肪酸は飽和又は不飽
和であり、炭素数は12〜22でありそして炭素数16
〜18が好ましい。
本発明で使用するポリアルキレンポリアミンと
してはジエチレントリアミン、トリエチレンテト
ラアミン等が揚げられる。ジアルキルアルキレン
ジアミンとしてはジメチルプロピレンジアミン等
が使用できる。四級化剤としてはエピクロルヒド
リン、エチレンクロヒドリン等が使用できる。
本発明の原料として使用される無機物質は石
綿、ガラス繊維、石膏、パーライト、セメント、
珪藻土、タルク、アスベスト、パーライト、ゼオ
ライト等である炭酸カルシウム、炭酸マグネシウ
ム、塩化カルシウム等の無機化合物も又使用でき
る。
本発明の耐水化剤の製法に際しては飽和或は不
飽和或はそれらの混合脂肪酸の塩又はその金属塩
又はアルキルエステル等から選ばれた二種以上の
混合物を乳化分散した後高圧乳化機を用い圧力
100Kg/cm2〜300Kg/cm2好ましくは200〜300Kg/cm2
で1回又は数回通過させる事により得られる。一
方好ましくは炭素数12〜22さらに好ましくは16〜
18の飽和脂肪酸にポリアルキレンポリアミン或は
ジアルキルアルキレンジアミンを反応した後無機
酸、有機酸或はエピクロルヒドリン、エチレンク
ロルヒドリン等の四級化剤を反応して水溶性耐水
化剤を得る事も出来る。
本発明の製造方法においては耐水剤で処理した
原料(以下、処理原料という)に耐水剤で処理し
ていない原料(以下、未処理原料という)を混合
することを一つの特徴としている。本発明による
原料の混合方法の態様は次のものが考えられる
が、それらに限定されない。
1 一種の未処理原料を耐水化剤で処理した後、
これに他の未処理原料と混合する。
2 二種の未処理原料を混合し、これを耐水化剤
で処理した後、さらに他の未処理原料を加えて
混合する。
3 二種の未処理原料を別々に耐水化剤で処理
し、これらを混合後、さらに他の未処理原料を
混合する。
4 二種の未処理原料を別々に耐水化剤で処理
し、このうち一方の処理原料と他の未処理原料
とを混合後、さらに他の一方の処理原料をこれ
に混合する。
以下詳細は製造例及び実施例を持つて説明する
がその範囲に限定されない。
製造例 1
撹伴機付反応釜にステアリン酸50部とオレイン
酸30部を仕込み加熱溶融し150℃に昇温した後消
石灰8.44部を徐々に加え3時間反応を行なつた。
反応終了後炭素数14〜18ヨウ素価60の脂肪酸メチ
ルエステル20部加え混合した。次に系内の温度を
90℃に冷却し50%KOH水溶液6.4部を加え反応し
た後70℃の温水4256部を徐々に添加、乳化分散し
たのちピストン型高圧乳化機を用いて250Kg/cm2
の圧力で1回通した後急冷し、有効成分20%の耐
水化剤を得た。
製造例 2
撹伴機付反応釜に炭素数14〜18、ヨウ素価60の
脂肪酸メチルエステル80部にステアリン酸20部を
加え混融した後系内温度を80℃に保持し50%
KOH8.0部徐々に加え反応した。次に70℃の水温
300部を徐々に添加し乳化分散を行なつた。然る
後同温度でピストン型高圧乳化機を用いて300
Kg/cm2の圧力で2回通した後急冷し有効成分25%
の耐水化剤を得た。
製造例 3
撹伴機付反応釜にステアリン酸284部仕込み80
℃で溶融した後ジエチレントリアミン103部加え
た後徐々に昇温し180℃で3時間脱水反応を行な
つた。反応終了後系内の温度を100℃まで冷却し
た後氷酢酸120部を加え続いて70℃の温水を1356
部徐々に加え乳化を行なう。その後ピストン型高
圧乳化機を用いて150Kg/cm2の圧力で1回通し急
冷し有効成分20%の耐水化剤を得た。
実施例 1−3
重質炭酸カルシウム500部を水1000部に分散し
た後撹伴しながら製造例1−3で得られた耐水化
剤を重質炭酸カルシウムに対して固型分で0.5%
相当量加え10分間撹伴を行なう。次に予かじめ用
意したパルプ5部とセメント85部の混合液(濃度
15%)に上記で得た耐水化処理重質炭酸カルシウ
ムスラリーを固型分で10部に相当する量を加え撹
伴混合した後脱水成型した。
次に得られた成型品を80〜90℃−24時間、60℃
−48時間養生した後80℃で10分間、60℃で24時間
乾燥した後水に浸漬し吸水率を測定した。結果を
第1表に示す。
比較例 1
製造例1−3で得られた耐水化剤の代わりにス
テアリン酸カルシウム0.5%添加して実施例1の
操作を繰返した。
得られた無機質板の耐水性の結果を第1表に示
す。
比較例 2
耐水化剤を使用せずに上記実施例の操作を繰返
した。得られた無機質板の耐水性の結果を第1表
に示す。
The present invention relates to a method for making an inorganic board waterproof. More specifically, it is a water-soluble water-resistant agent made of a fatty acid ester, a fatty acid metal salt, and at least one of fatty acids, and/or a water-soluble water-resistant agent obtained by reacting a fatty acid with a polyalkylene polyamine and/or a dialkyl alkylene diamine. The present invention relates to a method for manufacturing an inorganic board by processing raw material for the board. Hitherto, fatty acid metal salts, especially their calcium salts, have been used as water-resistant agents for inorganic boards, but they have had a number of drawbacks in terms of water resistance, yield, foaming during paper-making, etc. The water-soluble waterproofing agent used in the present invention is a water-soluble derivative of a saturated or unsaturated fatty acid or a mixture thereof. In order to improve these drawbacks, the present inventors have conducted extensive research and have found that a mixture system of fatty acid esters, fatty acids, fatty acid soaps, or fatty acid metal salts exhibits excellent effects, especially when saturated or The unsaturated fatty acid preferably has 8 to 22 carbon atoms, more preferably 8 to 18 carbon atoms, and most preferably 14 to 18 carbon atoms. On the other hand, water-soluble waterproofing agents obtained by reacting saturated or unsaturated fatty acids with polyalkylene polyamines and/or dialkyl alkylene diamines and then reacting with inorganic acids, organic acids, or quaternizing agents, or mixtures thereof, are also conventional products. It was found that it has a superior effect compared to. The fatty acid to be reacted with the polyalkylene polyamine or dialkyl alkylene diamine is a saturated fatty acid having 12 to 22 carbon atoms, preferably 16 to 18 carbon atoms. The present invention comprises an inorganic filler, one or more inorganic substances selected from the group consisting of inorganic oxides, carbonates, sulfates, silicates, chlorides, and composite salts thereof, and optionally organic pulp fibers. In a method for manufacturing an inorganic board by papermaking or molding a raw material to which a alkylene polyamine and/or
Or, after reacting a dialkyl alkylene diamine, and then reacting or adsorbing one or more of the above raw materials with a water-soluble waterproofing agent obtained by reacting an inorganic acid, an organic acid, or a quaternizing agent, further A method for producing an inorganic board characterized by mixing an inorganic substance and/or pulp fibers that have not been treated with the water-soluble waterproofing agent and further paper-making or molding. It is unsaturated and has 8 to 22 carbon atoms, preferably 8 to 22 carbon atoms, preferably 8 to 18 carbon atoms, and preferably 14 to 18 carbon atoms. The metal salts that make up fatty acid metal salts include potassium, sodium, calcium, magnesium,
Salts such as zinc, aluminum, zirconium, ammonium, alkanolamines or morpholine are fried. As the fatty acid ester, alkyl esters such as methyl and ethyl can be used. The fatty acid that is the raw material for the water resistant agent (b) is saturated or unsaturated, has 12 to 22 carbon atoms, and has 16 carbon atoms.
~18 is preferred. Examples of polyalkylene polyamines used in the present invention include diethylenetriamine and triethylenetetraamine. Dimethylpropylene diamine and the like can be used as the dialkyl alkylene diamine. As the quaternizing agent, epichlorohydrin, ethylene chlorhydrin, etc. can be used. Inorganic substances used as raw materials in the present invention include asbestos, glass fiber, gypsum, perlite, cement,
Inorganic compounds such as calcium carbonate, magnesium carbonate, calcium chloride, diatomaceous earth, talc, asbestos, perlite, zeolites, etc. can also be used. In the manufacturing method of the water resistant agent of the present invention, a mixture of two or more selected from salts of saturated, unsaturated or mixed fatty acids, metal salts thereof, alkyl esters, etc. is emulsified and dispersed, and then a high-pressure emulsifier is used. pressure
100Kg/cm 2 - 300Kg/cm 2 Preferably 200 - 300Kg/cm 2
can be obtained by passing it through once or several times. On the other hand, preferably 12 to 22 carbon atoms, more preferably 16 to 22 carbon atoms
A water-soluble waterproofing agent can also be obtained by reacting 18 saturated fatty acids with polyalkylene polyamine or dialkyl alkylene diamine and then reacting with an inorganic acid, an organic acid, or a quaternizing agent such as epichlorohydrin or ethylene chlorohydrin. . One feature of the production method of the present invention is that a raw material that has been treated with a waterproofing agent (hereinafter referred to as treated raw material) is mixed with a raw material that has not been treated with a waterproofing agent (hereinafter referred to as untreated raw material). The method of mixing raw materials according to the present invention may include the following, but is not limited thereto. 1. After treating one type of untreated raw material with a waterproofing agent,
This is mixed with other raw materials. 2. Mix two types of untreated raw materials, treat this with a waterproofing agent, and then add and mix other untreated raw materials. 3. Two types of untreated raw materials are treated separately with a waterproofing agent, and after mixing these, another untreated raw material is further mixed. 4. Two types of untreated raw materials are treated separately with a waterproofing agent, one of the treated raw materials is mixed with the other untreated raw material, and then the other treated raw material is further mixed therewith. The details will be explained below with reference to production examples and examples, but the scope is not limited thereto. Production Example 1 50 parts of stearic acid and 30 parts of oleic acid were placed in a reaction vessel equipped with an agitator, heated and melted, and after raising the temperature to 150°C, 8.44 parts of slaked lime was gradually added and the reaction was carried out for 3 hours.
After the reaction was completed, 20 parts of fatty acid methyl ester having 14 to 18 carbon atoms and an iodine value of 60 were added and mixed. Next, the temperature in the system is
Cool to 90℃, add 6.4 parts of 50% KOH aqueous solution and react, then gradually add 4256 parts of 70℃ warm water, emulsify and disperse, and then use a piston type high pressure emulsifier to produce 250Kg/cm 2
After passing through the solution once at a pressure of Production example 2 Add 20 parts of stearic acid to 80 parts of fatty acid methyl ester with 14 to 18 carbon atoms and an iodine value of 60 in a reaction vessel equipped with a stirrer, mix and melt, then maintain the system internal temperature at 80°C to reduce to 50%.
8.0 parts of KOH was gradually added to cause a reaction. Then the water temperature is 70℃
300 parts were gradually added to perform emulsification and dispersion. After that, at the same temperature, using a piston-type high-pressure emulsifier,
Passed twice under pressure of Kg/cm 2 and then rapidly cooled to 25% active ingredient.
A water resistant agent was obtained. Production example 3: Pour 284 parts of stearic acid into a reaction vessel equipped with an agitator 80
After melting at 180°C, 103 parts of diethylenetriamine was added and the temperature was gradually raised to carry out a dehydration reaction at 180°C for 3 hours. After the reaction was completed, the temperature in the system was cooled to 100°C, 120 parts of glacial acetic acid was added, and then 1356 parts of 70°C hot water was added.
Add gradually and emulsify. Thereafter, the mixture was rapidly cooled once at a pressure of 150 kg/cm 2 using a piston-type high-pressure emulsifier to obtain a water-resistant agent containing 20% of the active ingredient. Example 1-3 After dispersing 500 parts of heavy calcium carbonate in 1000 parts of water, and stirring, the water resistance agent obtained in Production Example 1-3 was added to the solid content of 0.5% based on the weight of heavy calcium carbonate.
Add the appropriate amount and stir for 10 minutes. Next, a mixture of 5 parts of pulp and 85 parts of cement prepared in advance (concentration
15%) was added with the above-obtained water-resistant treated heavy calcium carbonate slurry in an amount equivalent to 10 parts solids, stirred and mixed, and then dehydrated and molded. Next, the obtained molded product was heated at 80-90℃ for 24 hours at 60℃.
After curing for -48 hours, the samples were dried at 80°C for 10 minutes and at 60°C for 24 hours, then immersed in water to measure water absorption. The results are shown in Table 1. Comparative Example 1 The operation of Example 1 was repeated with the addition of 0.5% calcium stearate instead of the waterproofing agent obtained in Production Example 1-3. Table 1 shows the results of the water resistance of the obtained inorganic board. Comparative Example 2 The procedure of the above example was repeated without using the waterproofing agent. Table 1 shows the results of the water resistance of the obtained inorganic board.
【表】
試験結果に示したように、本発明により製造し
た無機質板は従来品よりも優れた耐水性を有する
ことが確認された。[Table] As shown in the test results, it was confirmed that the inorganic board manufactured according to the present invention has better water resistance than conventional products.
Claims (1)
酸塩、珪酸塩、塩化物およびそれらの複合塩から
なる群から選ばれた一種又は二種以上の無機物
質、必要に応じて有機パルプ繊維を加えた原料を
抄造又は成型することにより無機質板を製造する
方法において、 (a) 脂肪酸エステルならびに脂肪酸および脂肪酸
金属塩の少なくとも1種からなる水溶性耐水化
剤および/または (b) 脂肪酸にポリアルキレンポリアミンおよび/
またはジアルキルアルキレンジアミンを反応さ
せた後、さらに無機酸、有機酸もしくは四級化
剤を反応させて得た水溶性耐水化剤 で一種又は二種以上の前記原料を反応又は吸着処
理した後、さらに前記水溶性耐水化物で処理して
いない無機物質および/またはパルプ繊維を混合
し、さらに抄造又は成型することを特徴とする無
機質板の製造方法。[Claims] 1. An inorganic filler and one or more inorganic substances selected from the group consisting of inorganic oxides, carbonates, sulfates, silicates, chlorides, and complex salts thereof, as necessary. A method for manufacturing an inorganic board by paper-making or molding a raw material to which organic pulp fibers are added, comprising: (a) a water-soluble waterproofing agent comprising at least one of a fatty acid ester and a fatty acid and a fatty acid metal salt; and/or (b) ) fatty acids with polyalkylene polyamines and/or
Or, after reacting a dialkyl alkylene diamine, and then reacting or adsorbing one or more of the above raw materials with a water-soluble waterproofing agent obtained by reacting an inorganic acid, an organic acid, or a quaternizing agent, further A method for producing an inorganic board, comprising mixing an inorganic substance and/or pulp fibers that have not been treated with the water-soluble waterproofing material, and further paper-making or molding.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1970984A JPS60166255A (en) | 1984-02-06 | 1984-02-06 | Manufacturing method of inorganic board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1970984A JPS60166255A (en) | 1984-02-06 | 1984-02-06 | Manufacturing method of inorganic board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60166255A JPS60166255A (en) | 1985-08-29 |
| JPH0530786B2 true JPH0530786B2 (en) | 1993-05-10 |
Family
ID=12006813
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1970984A Granted JPS60166255A (en) | 1984-02-06 | 1984-02-06 | Manufacturing method of inorganic board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60166255A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6126545A (en) * | 1984-07-11 | 1986-02-05 | 株式会社クボタ | Manufacture of water-repellant inorganic product |
-
1984
- 1984-02-06 JP JP1970984A patent/JPS60166255A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60166255A (en) | 1985-08-29 |
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