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JPH058048B2 - - Google Patents
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JPH058048B2 - - Google Patents

Info

Publication number
JPH058048B2
JPH058048B2 JP59259579A JP25957984A JPH058048B2 JP H058048 B2 JPH058048 B2 JP H058048B2 JP 59259579 A JP59259579 A JP 59259579A JP 25957984 A JP25957984 A JP 25957984A JP H058048 B2 JPH058048 B2 JP H058048B2
Authority
JP
Japan
Prior art keywords
powder
emulsion
weight
parts
microencapsulated
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
Application number
JP59259579A
Other languages
Japanese (ja)
Other versions
JPS61136433A (en
Inventor
Kosuke Sugimoto
Masumi Koishi
Kazuo Watanabe
Masao Tooyama
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.)
Kikusui Chemical Industries Co Ltd
Original Assignee
Kikusui Chemical Industries 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 Kikusui Chemical Industries Co Ltd filed Critical Kikusui Chemical Industries Co Ltd
Priority to JP25957984A priority Critical patent/JPS61136433A/en
Publication of JPS61136433A publication Critical patent/JPS61136433A/en
Publication of JPH058048B2 publication Critical patent/JPH058048B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)

Description

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

(産業上の利用分野) 本発明は、粉末エマルシヨンに防カビ剤、セメ
ント用混和剤等を、自動混和機、攪拌機その他粉
末混合機を利用した粉体混合法により表面改質さ
れたマイクロカプセル化粉末エマルシヨンに関す
る。 (従来の技術) 合成樹脂エマルシヨンを、凍結粉砕或はスプレ
ードライにて、粉末状とした通称粉末エマルシヨ
ンは、塗料、接着剤、インスタントセメント、湿
式系仕上げ材に広く利用されている。粉末化エマ
ルシヨンは、液状の合成樹脂エマルシヨンに比較
して、前記の塗料、接着剤、インスタントセメン
ト、湿式系仕上げ材等の使用者の施工性を向上す
ることに役立つているし、製造者にとつては製品
製造上の加工性や輸送上のメリツトや、製品の安
定性に役立つている。 しかしながら、粉末エマルシヨンは液状エマル
シヨンに比較して、顔料、防カビ剤、セメント用
混和剤の混合をする場合においてそれらの分散が
むずかしく、例えば顔料の分散系に於いてしばし
ば色むらの発生を見る。又セメント混和剤に於い
てもセメントの凝固等にばらつきを生じ、強度等
の物性に悪影響をする場合がある。又防カビ剤等
に於いても塗料の表面に均一に分散することは、
顔料同様に困難であり、防カビ剤の効果を十分に
発揮できないこともしばしば起こる。 (発明の目的) 本発明は、粉末エマルシヨンに顔料、防カビ
剤、セメント用混和剤を、マイクロカプセル化す
ることにより上記の問題を解決することを目的と
する。 (発明の構成) 本発明は、マイクロカプセル化技法により、顔
料、防カビ剤、セメント用混和剤等を粉末エマル
シヨンと一体化させ粉体エマルシヨン表面に薄膜
を連続的又は不連続的に、形成させることにより
両者の界面に電気的又は化学的な結合により各分
子が極めて安定な状態になる。 粉末エマルシヨンが被媒体の中に分散する時、
粉末エマルシヨンはこれら顔料、防カビ剤或はセ
メント用混和剤と界面に於いて一体化した状態で
再乳化する。この事は従来の分散した場合と全く
異なつた安定した性状となる。 マイクロカプセルは、医薬、農薬、香料等に広
く利用されている。特に感圧被写紙への応用は、
極めて高く評価されている。 マイクロカプセル化法には、界面重合法、
insitu法、コアセルベーシヨン法、液中乾燥
法、オリフイス法、融解分散冷却法、気中
懸濁法、スプレイドライング法、無機質壁カ
プセル法等に分類される。 本発明に於いて利用されるマイクロカプセル化
法は無機質壁カプセル法等に分類される。このメ
カノケミカルな表面改質法は、粉体とのカプセル
化技法として多く利用されている。 本発明によるメカノケミカル技法は混合による
摩擦熱と帯電を利用したもので、粉末化されたビ
ニル系合成樹脂エマルシヨンを核物質として表面
に顔料、防カビ剤、セメント用混和剤等のそれぞ
れを被覆形成せしめる。混合には、当然外部より
の圧力によつて熱エネルギーが生じ、界面の帯電
又は融解等が起こり、両者の安定した結合が出来
る。 又この結合は、化学反応によらないので両者の
特性が失われる事はない。 発明の詳細を実施例に従つて述べる。 (実施例 1) ビニル系合成樹脂粉末エマルシヨン[モビニー
ルDM200:粒子径20μ〜150μm、ヘキスト合成(株)
製]100重量部に対して、防カビ剤コートサイド
N[武田薬品工業(株)製]5重量部を加えマイクロ
カプセル化粉末エマルシヨンを作成した。次に下
記に示す処方により水系白色塗料を調合した。 マイクロカプセル化粉末エマルシヨン
105(重量部) 炭酸カルシウム 400 酸化チタン 100 メチルセルローズ 4 水 300 エチレングルコール 10 テキサノール 10 次にJIS Z 2911に準じて試験を行ないカビの
発生状況を観察した。(但し、カビの発生を促進
する為、溶出滲出を確認する為、一週間毎に一度
滅菌水で表面の洗浄を行ない、菌株溶液として5
%デキストローズの液を再度添加した。)結果は
表1で示されるようにカビの発生を遅らせること
ができた。 (実施例 2) 実施例1に於いて作成した防カビ剤マイクロカ
プセル化粉末エマルシヨン100重量部に対してモ
ンタン酸エステルワツクス50重量部を添加し自動
混合攪拌機で混合し、一次マイクロカプセル化粉
末エマルシヨンの表面に二次マイクロカプセル化
を行なつた。カビの発生については、実施例1の
方法で観察を行なつたところ、カビの発生を著し
く遅らせることが出来た。結果は表2に示す。 (実施例 3) 実施例1と同様の混合機を使用し、実施例1に
使用した粉末エマルシヨン100重量部に対して、
セメント用混和剤としてのメチルセルロース2重
量部を加えマイクロカプセル化粉末エマルシヨン
を作成した。次にマイクロカプセル化した粉体
10.2重量部と白色ポルトランドセメント100重量
部を加え、水40重量部を添加しJIS A6916に規定
する付着強さを測定した。結果は標準状態におい
て20Kg/cm2であつた。 (参考例 1) ビニル系合成樹脂粉末エマルシヨン[モビニー
ルDM200:粒子径20μ〜150μm、ヘキスト合成(株)
製]100重量部に対して、着色顔料として酸化第
2鉄、顔料(粒子径0.1〜0.8μm)50重量部を自動
混合攪拌機にて5時間混合した。混合直後の粉末
温度は、混合前の20℃から約5℃上昇し、粉体の
状態は目視によつて均一であつた。次にこのマイ
クロカプセル化した粉体15重量部と白色ポルトラ
ンドセメント100重量部を加え、水40重量部を添
加しJIS R5201に規定する練り混ぜ用はち及びさ
じを用いて混合し、高さ20mm×長さ100mm×巾100
mmの直方体を成形し、室内にて7日間養生をし試
験体を作成した。養生を終了した後に、発色性や
表面のち密度の観察をし、さらにこの試験体を4
週間屋外に曝露し、その表面の色調について観察
したところ、発色性、表面ち密度、曝露後の色調
については、非常に優れていた。 結果は表3に示す。 (比較例 1) 参考例1で成形した試験体と同じ成分すなわち 白色ポルトランドセメント 100(重量部) ビニル系粉末エマルシヨン 10 酸化第2鉄系顔料 5 水 40 を参考例1に示す方法と同様な方法で成形し養生
をし、発色性、表面ち密度、曝露後の色調につい
て評価した。結果は表3に示す。 (比較例 2) 実施例1に示す水系塗料の処方のうち、マイク
ロカプセル化粉末エマルシヨン(モビニール
DM200)100重量部と防カビ剤(コートサイド
N)を5重量部にかえて水系塗料を作成し実施例
1に示す方法、実施例2に示す方法で評価した。
結果は表1、表2に示す。 (比較例 3) 実施例3で作成したモルタルと同じ成分すなわ
ち 白色ポルトランドセメント 100(重量部) ビニル系粉末エマルシヨン 10 メチルセルロース 0.2 水 40 を実施例3と同様な方法で試験体を作成し、付着
強さ試験を同様な方法で評価した。結果は標準状
態において13Kg/cm2であつた。 実施例、比較例の評価を示す記号において、発
色性については、+記号が多いほど発色性が良い
ことを示している。また、表1、表2の防カビ性
を示す評価記号については、−はカビの発生が認
められない。±はカビの発生が認められるか認め
られないか識別が困難な状態である。+記号は1
つのばあいは、かすかにカビの発生が認められ、
その数が多くなるほに従つてカビが多量に発生し
たことを示している。
(Industrial Application Field) The present invention is a powder emulsion containing a fungicide, a cement admixture, etc., into microcapsules that have been surface-modified by a powder mixing method using an automatic mixer, stirrer, or other powder mixer. Concerning powder emulsions. (Prior Art) Synthetic resin emulsions are freeze-pulverized or spray-dried into a powder form, commonly known as powder emulsions, which are widely used in paints, adhesives, instant cements, and wet finishing materials. Compared to liquid synthetic resin emulsions, powdered emulsions are useful for improving the ease of application for the aforementioned paints, adhesives, instant cement, wet finishing materials, etc., and they are also useful for manufacturers. This is useful for product manufacturing processability, transportation benefits, and product stability. However, powder emulsions are more difficult to disperse than liquid emulsions when pigments, fungicides, and cement admixtures are mixed, and, for example, color irregularities often occur in pigment dispersions. Also, cement admixtures may cause variations in solidification of cement, which may adversely affect physical properties such as strength. Also, when it comes to antifungal agents, it is important to ensure that they are uniformly dispersed on the surface of the paint.
Similar to pigments, this is difficult, and the effects of antifungal agents are often not fully demonstrated. (Objective of the Invention) The object of the present invention is to solve the above problems by microencapsulating a pigment, a fungicide, and a cement admixture in a powder emulsion. (Structure of the Invention) The present invention integrates pigments, fungicides, cement admixtures, etc. with a powder emulsion using microencapsulation techniques, and forms a thin film continuously or discontinuously on the surface of the powder emulsion. As a result, each molecule becomes extremely stable due to electrical or chemical bonding at the interface between the two. When the powder emulsion is dispersed into the medium,
The powder emulsion is re-emulsified with these pigments, fungicides, or cement admixtures at the interface. This results in stable properties that are completely different from the conventional dispersed case. Microcapsules are widely used in medicines, agricultural chemicals, fragrances, and the like. Especially when applied to pressure-sensitive paper,
It is highly rated. Microencapsulation methods include interfacial polymerization method,
It is classified into in situ method, coacervation method, submerged drying method, orifice method, melt dispersion cooling method, air suspension method, spray drying method, inorganic wall capsule method, etc. The microencapsulation method used in the present invention is classified as an inorganic wall encapsulation method. This mechanochemical surface modification method is often used as an encapsulation technique with powder. The mechanochemical technique of the present invention utilizes frictional heat and electrification caused by mixing, and uses a powdered vinyl synthetic resin emulsion as a core material to coat the surface with pigments, fungicides, cement admixtures, etc. urge Naturally, during mixing, thermal energy is generated due to external pressure, which causes charging or melting of the interface, resulting in a stable bond between the two. Moreover, since this bond is not based on a chemical reaction, the properties of both will not be lost. The details of the invention will be described based on examples. (Example 1) Vinyl synthetic resin powder emulsion [Movinyl DM200: particle size 20 μm to 150 μm, Hoechst Synthetic Co., Ltd.
A microencapsulated powder emulsion was prepared by adding 5 parts by weight of the antifungal agent Coatside N (manufactured by Takeda Pharmaceutical Co., Ltd.) to 100 parts by weight (manufactured by Takeda Pharmaceutical Co., Ltd.). Next, a water-based white paint was prepared according to the recipe shown below. Microencapsulated powder emulsion
105 (parts by weight) Calcium carbonate 400 Titanium oxide 100 Methyl cellulose 4 Water 300 Ethylene glycol 10 Texanol 10 Next, a test was conducted according to JIS Z 2911 to observe the growth of mold. (However, in order to promote the growth of mold and to check for elution and exudation, wash the surface with sterile water once every week, and use 50% as a bacterial strain solution.
% dextrose solution was added again. ) As shown in Table 1, the growth of mold could be delayed. (Example 2) 50 parts by weight of montanic acid ester wax was added to 100 parts by weight of the fungicidal microencapsulated powder emulsion prepared in Example 1 and mixed with an automatic mixer to obtain the primary microencapsulated powder. Secondary microencapsulation was performed on the surface of the emulsion. Regarding the growth of mold, observation was carried out using the method of Example 1, and it was found that the growth of mold could be significantly delayed. The results are shown in Table 2. (Example 3) Using the same mixer as in Example 1, for 100 parts by weight of the powder emulsion used in Example 1,
A microencapsulated powder emulsion was prepared by adding 2 parts by weight of methyl cellulose as an admixture for cement. Next, the microencapsulated powder
10.2 parts by weight and 100 parts by weight of white Portland cement were added, 40 parts by weight of water was added, and the adhesion strength specified in JIS A6916 was measured. The result was 20Kg/cm 2 under standard conditions. (Reference example 1) Vinyl synthetic resin powder emulsion [Movinyl DM200: particle size 20 μm to 150 μm, Hoechst Synthetic Co., Ltd.
50 parts by weight of ferric oxide as a colored pigment and a pigment (particle size 0.1 to 0.8 μm) were mixed for 5 hours with an automatic mixer. Immediately after mixing, the powder temperature rose by about 5°C from 20°C before mixing, and the state of the powder was visually uniform. Next, add 15 parts by weight of this microencapsulated powder and 100 parts by weight of white Portland cement, add 40 parts by weight of water, and mix using a mixing tip and spoon specified in JIS R5201. Length 100mm x width 100
A rectangular parallelepiped of mm in size was molded and cured indoors for 7 days to prepare a test specimen. After curing, the color development and surface density were observed, and the specimen was further tested for 4
When exposed outdoors for a week and observed for its surface color tone, it was found to be very excellent in terms of color development, surface density, and color tone after exposure. The results are shown in Table 3. (Comparative Example 1) The same ingredients as the test specimen molded in Reference Example 1, namely, white Portland cement 100 (parts by weight) vinyl powder emulsion 10 ferric oxide pigment 5 water 40 were prepared in the same manner as in Reference Example 1. After molding and curing, color development, surface density, and color tone after exposure were evaluated. The results are shown in Table 3. (Comparative Example 2) Among the water-based paint formulations shown in Example 1, microencapsulated powder emulsion (Movinyl
A water-based paint was prepared by changing 100 parts by weight of DM200) and 5 parts by weight of the antifungal agent (Courtside N), and evaluated by the method shown in Example 1 and the method shown in Example 2.
The results are shown in Tables 1 and 2. (Comparative Example 3) A test specimen was prepared in the same manner as in Example 3 using the same ingredients as the mortar prepared in Example 3, namely, white Portland cement 100 (parts by weight), vinyl powder emulsion 10, methyl cellulose 0.2 and water 40. The test was evaluated in a similar manner. The result was 13Kg/cm 2 under standard conditions. In the symbols indicating the evaluation of Examples and Comparative Examples, regarding color development, the more + symbols there are, the better the color development is. Furthermore, regarding the evaluation symbols indicating mold resistance in Tables 1 and 2, - means no mold growth is observed. ± is a state in which it is difficult to distinguish whether mold growth is observed or not. + sign is 1
In some cases, slight mold growth is observed,
The larger the number, the more mold has grown.

【表】【table】

【表】【table】

【表】 「発明の効果」 本発明では、上記の実施例、比較例からも解せ
られるように、マイクロカプセル化したエマルシ
ヨンの種類により様々な効果が得られる。 例えば、参考例1のように顔料をマイクロカプ
セル化に利用した場合、安定した発色性、耐候性
に於いて優れた製品が得られる。又、実施例1の
ように防カビ剤をマイクロカプセル化し利用した
場合は防カビ性に於いても、従来の防カビ剤を直
接塗料に添加した場合に比べ長期に安定した効果
が得られる。そして更に、実施例2のようにマイ
クロカプセル化について二次加工を行なえば、防
カビ剤についてのみの結果についても、更にその
効果の延長を認めることが出来る。実施例3のよ
うにセメント混和剤について用いた場合は安定し
た凝集力が得られる。 このように、マイクロカプセル化したエマルシ
ヨンと顔料、防カビ剤の相乗効果によりそれぞれ
の物質の持つ特性を初期、長期に恒つて発揮する
効果をもつものである。
[Table] "Effects of the Invention" In the present invention, as can be understood from the above Examples and Comparative Examples, various effects can be obtained depending on the type of microencapsulated emulsion. For example, when a pigment is used for microencapsulation as in Reference Example 1, a product with stable color development and excellent weather resistance can be obtained. In addition, when the antifungal agent is microencapsulated and used as in Example 1, a stable effect can be obtained over a long period of time compared to when a conventional antifungal agent is directly added to the paint. Furthermore, if secondary processing is performed for microencapsulation as in Example 2, the effect can be further extended even with respect to the results for the antifungal agent alone. When used as a cement admixture as in Example 3, stable cohesive force can be obtained. In this way, the synergistic effect of the microencapsulated emulsion, pigment, and antifungal agent has the effect of consistently exhibiting the characteristics of each substance both initially and over a long period of time.

Claims (1)

【特許請求の範囲】 1 粉末エマルシヨンの表面に常温で粉状の防カ
ビ剤ないしセメント用混和剤の粉末を粉体混合の
方法によつて粉末エマルシヨンの表面に連続的又
は不連続的に粉状の薄膜を形成してマイクロカプ
セル化を行なうことを特徴とするマイクロカプセ
ル化粉末エマルシヨン。 2 粉末エマルシヨンの表面に常温で粉状の防カ
ビ剤ないしセメント用混和剤と顔料の粉末を粉体
混合の方法によつて粉末エマルシヨンの表面に連
続的又は不連続的に粉状の薄膜を形成してマイク
ロカプセル化を行なうことを特徴とするマイクロ
カプセル化粉末エマルシヨン。
[Claims] 1. Powdered fungicide or cement admixture powder is continuously or discontinuously applied to the surface of the powder emulsion at room temperature by a powder mixing method. A microencapsulated powder emulsion characterized by forming a thin film to perform microencapsulation. 2 Form a powdery thin film continuously or discontinuously on the surface of the powder emulsion by mixing powdered fungicide or cement admixture and pigment powder at room temperature on the surface of the powdered emulsion. A microencapsulated powder emulsion characterized by microencapsulation.
JP25957984A 1984-12-07 1984-12-07 Microencapsulated powder emulsion Granted JPS61136433A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25957984A JPS61136433A (en) 1984-12-07 1984-12-07 Microencapsulated powder emulsion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25957984A JPS61136433A (en) 1984-12-07 1984-12-07 Microencapsulated powder emulsion

Publications (2)

Publication Number Publication Date
JPS61136433A JPS61136433A (en) 1986-06-24
JPH058048B2 true JPH058048B2 (en) 1993-02-01

Family

ID=17336074

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25957984A Granted JPS61136433A (en) 1984-12-07 1984-12-07 Microencapsulated powder emulsion

Country Status (1)

Country Link
JP (1) JPS61136433A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0775665B2 (en) * 1986-10-27 1995-08-16 日本合成ゴム株式会社 Method for producing microencapsulated fine particles

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58136049A (en) * 1982-02-08 1983-08-12 Canon Inc Microcapsule toner
JPS5946125A (en) * 1982-09-07 1984-03-15 Nippon Sanso Kk Preparation of microcapsule
JPS59137356A (en) * 1983-01-25 1984-08-07 ヘキスト合成株式会社 Water separation defect preventing agent upon cement composition setting and prevention of defect

Also Published As

Publication number Publication date
JPS61136433A (en) 1986-06-24

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