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JPH01228537A - Dispersion of fine particle - Google Patents

Dispersion of fine particle

Info

Publication number
JPH01228537A
JPH01228537A JP63053135A JP5313588A JPH01228537A JP H01228537 A JPH01228537 A JP H01228537A JP 63053135 A JP63053135 A JP 63053135A JP 5313588 A JP5313588 A JP 5313588A JP H01228537 A JPH01228537 A JP H01228537A
Authority
JP
Japan
Prior art keywords
fine particles
viscosity
organic solvent
oil
room temperature
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.)
Pending
Application number
JP63053135A
Other languages
Japanese (ja)
Inventor
Eigo Tsuchiya
土屋 栄吾
Shizuo Iwai
岩井 静夫
Hideo Hayashi
英雄 林
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP63053135A priority Critical patent/JPH01228537A/en
Publication of JPH01228537A publication Critical patent/JPH01228537A/en
Pending legal-status Critical Current

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  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Colloid Chemistry (AREA)

Abstract

PURPOSE:To increase dispersion stability of fine particles in an organic solvent by adding 12-hydroxystearic acid, polyhydric alcohol and benzaldehyde to an organic solvent of a viscosity not lower than 10cp at room temperature, wherein fine particles are dispersed. CONSTITUTION:A dispersion liquid of fine particles is prepared by adding at least one species of gelling agent selected from a group composed of a mixture of 12-hydroxystearic acid, polyhydric alcohol and benzaldehyde, an amine salt of N-acylamino acid, an amide of N-acylamino acid, an ester of N-acylamino acid, to an organic solvent of a viscosity not lower than 10cp at room temperature, wherein fine particles are dispersed. As for the fine particles, preferably having an average grain size of 10mum or smaller, and silicon dioxide, titanium oxide, talc, etc., are usable. As for the organic solvent of a viscosity not lower than 10cp at room temperature, soybean oil, coconut oil, linseed oil, whale oil, liquid paraffin, etc., are available.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、微粒子に関するものであり、特に有機媒体中
の微粒子の分散剤として油ゲル化剤を必須成分として配
合することにより微粒子を分散させる方法に関する。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to fine particles, and particularly to a method for dispersing fine particles by incorporating an oil gelling agent as an essential component as a dispersant for fine particles in an organic medium. Regarding the method.

〔従来の技術〕[Conventional technology]

従来より、微粒子の分散方法としては、l)微粒子の径
を小さくする。2)有機媒体と微粒子との密度差を小さ
くする。3)有機媒体の粘度を大きくする。4)分散剤
を利用する等があげられる。目的に応じて微粒子と有機
媒体を選択すると微粒子の径、両者の密度差及び有機媒
体の粘度が必然的に決まり、従って、適切な分散剤の選
択が分散の良否を決める大きなポイントとなる。従来よ
り、分散剤としては界面活性剤、表面改質剤、カップリ
ング剤等が用いられるが、微粒子と有機媒体との組合せ
の違いで適切な分散剤も異なり、汎用的なものはなく、
その都度、適切な分散剤を選択するのが実情であり、簡
便で汎用的な分散方法の開発が望まれている。
Conventionally, methods for dispersing fine particles include l) reducing the diameter of the fine particles; 2) Reduce the density difference between the organic medium and the fine particles. 3) Increase the viscosity of the organic medium. 4) Examples include using a dispersant. When the fine particles and organic medium are selected according to the purpose, the diameter of the fine particles, the density difference between the two, and the viscosity of the organic medium are inevitably determined. Therefore, the selection of an appropriate dispersant is a major point in determining the quality of dispersion. Traditionally, surfactants, surface modifiers, coupling agents, etc. have been used as dispersants, but the appropriate dispersant varies depending on the combination of fine particles and organic medium, and there is no universally applicable dispersant.
The reality is that an appropriate dispersant must be selected for each case, and there is a desire to develop a simple and versatile dispersion method.

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

先に述べた界面活性剤、表面改質剤、カップリング剤等
は適切な分散剤で使用方法も簡便であるが、使用する微
粒子と有機媒体の選択により、微粒子の有する形状、粒
子分布、比表面積、表面電位等の物理的性質及び表面の
酸・塩基度、官能基などの化学的性質がそれぞれ異なる
こと、更に有機媒体への溶解性が異なるためその都度、
適切な分散剤を選択する必要があり、汎用性に乏しい欠
点があった。
The above-mentioned surfactants, surface modifiers, coupling agents, etc. are appropriate dispersants and are easy to use, but depending on the selection of the fine particles and organic medium used, the shape, particle distribution, and ratio of the fine particles may vary. Physical properties such as surface area and surface potential, chemical properties such as surface acidity/basicity, and functional groups are different, and solubility in organic media is also different.
It is necessary to select an appropriate dispersant, which has the drawback of poor versatility.

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

本発明者らは、かかる実情を鑑み、鋭意研究を行った結
果、 常温で10センチボイズ(cP)以上の有機媒体中の微
粒子の分散剤として油ゲル化剤を配合することから本発
明を完成した。
In view of the above circumstances, the present inventors conducted intensive research and completed the present invention by blending an oil gelling agent as a dispersant for fine particles in an organic medium with a diameter of 10 centivoise (cP) or more at room temperature. .

本発明に係る微粒子は平均粒径10μm以下が望ましく
、二酸化ケイ素、チタン白、三酸化アンチモン、アルミ
ナ等の酸化物、炭酸カルシウム、炭酸バリウム、炭酸マ
グネシウム等炭酸塩、硫酸バリウム、硫酸カルシウム等
の硫酸塩、リン酸カルシウム、リン酸鉄等のリン酸塩、
タルク、カオリン等のケイ酸塩、水素1ヒアルミニウム
、水素化マグネシウム等の水酸化物、合成石英、窒化ケ
イ素、炭化ケイ素、炭化タングステン、チタン酸バリウ
ム等のニューセラミック等が無機化合物として、ステア
リン酸亜鈴、ステアリン酸カルシウム、オクチル酸アル
ミニウム等の金属石鹸、テトラブロモビスフェノールA
、デカブロモジフェニルエーテル等のブロム化合物、N
a−ラウロイルリジン、N−ラウロイルアスパラギン酸
−β−ラウリルエステル等のアミノ酸系化合物、ナイロ
ンノ(ウダー、ポリスチレンパウダー、セルロース及び
セルロース誘導体パウダー等の高分子化合物等が有機化
合物として用いられる。
The fine particles according to the present invention preferably have an average particle size of 10 μm or less, and include oxides such as silicon dioxide, titanium white, antimony trioxide, and alumina, carbonates such as calcium carbonate, barium carbonate, and magnesium carbonate, and sulfuric acids such as barium sulfate and calcium sulfate. salts, phosphates such as calcium phosphate, iron phosphate,
Silicates such as talc and kaolin, hydroxides such as hydrogen 1 hyaluminum and magnesium hydride, new ceramics such as synthetic quartz, silicon nitride, silicon carbide, tungsten carbide, and barium titanate are inorganic compounds, and stearic acid Metal soaps such as dumbbell, calcium stearate, aluminum octylate, tetrabromobisphenol A
, bromine compounds such as decabromodiphenyl ether, N
Amino acid compounds such as a-lauroyl lysine and N-lauroyl aspartic acid-β-lauryl ester, polymer compounds such as nylon powder, polystyrene powder, cellulose and cellulose derivative powder, etc. are used as the organic compound.

有機媒体としては常温において粘度が10センチボイズ
以上であればよく、大豆油、ヤシ油、アマニ油、鯨油等
の動植物油、ジオクチルフタレート、トリクレジルホス
フェート、塩素化パラフィン等の可塑剤、流動パラフィ
ン、タービン油等の炭化水素、ポリブタジェン、エポキ
シ樹脂、ウレタン樹脂、不飽和ポリエステル、シリコー
ンオイル等の高分子化合物等が用いられる。更に、油ゲ
ル化剤としては12−ヒドロキシステアリン酸、多価ア
ルコールとベンズアルデヒドとの縮合物、例えばジベン
ジリデンソルビトール、ジベンジリデンキシリトール、
N−アシルアミノ酸アミン塩、例えば、N、N’ −シ
カブロイル−し−リジンラウリルアミン塩、 N−アシ
ルアミノ酸アミド、例えばN−ラウロイル−し−グルタ
ミン酸ジブチルアミド、N−N’ −ジラウロイル−し
−リジンラウリルアミド、N−アシルアミノ酸エステル
、例えば、N、N’ −シカブロイル−し−リジンラウ
リルエステル等が有機媒体に対し0.01〜0゜5重量
%用いられる。微粒子の添加量は微粒子を有機媒体に添
加した組成物が流動性を保つ程度が望ましい。
The organic medium may have a viscosity of 10 centiboise or more at room temperature, and may include animal and vegetable oils such as soybean oil, coconut oil, linseed oil, and whale oil, plasticizers such as dioctyl phthalate, tricresyl phosphate, and chlorinated paraffin, liquid paraffin, Hydrocarbons such as turbine oil, polymer compounds such as polybutadiene, epoxy resins, urethane resins, unsaturated polyesters, and silicone oils are used. Further, oil gelling agents include 12-hydroxystearic acid, condensates of polyhydric alcohols and benzaldehyde, such as dibenzylidene sorbitol, dibenzylidene xylitol,
N-acylamino acid amine salts, such as N,N'-cicabroyl-shi-lysine laurylamine salt, N-acylamino acid amides, such as N-lauroyl-shi-glutamic acid dibutylamide, N-N'-dilauroyl-shi-lysine Laurylamide, N-acylamino acid ester, such as N,N'-cicabroyl-d-lysine lauryl ester, is used in an amount of 0.01 to 0.5% by weight based on the organic medium. The amount of fine particles added is preferably such that the composition in which the fine particles are added to the organic medium maintains fluidity.

分散方法は有機媒体を80〜160℃に加熱し、油ゲル
化剤を加え、溶解後冷却し、これに微粒子を加え、混合
することにより達成される。
The dispersion method is achieved by heating an organic medium to 80 to 160°C, adding an oil gelling agent, cooling after dissolution, adding fine particles thereto, and mixing.

本発明の微粒子の分散方法により、微粒子と分散媒であ
る有機媒体とのいずれの組合せにおいても良好な分散状
態を保ち、幅広い用途における分散方法として汎用的な
方法である。
The method for dispersing fine particles of the present invention maintains a good dispersion state in any combination of fine particles and an organic medium as a dispersion medium, and is a versatile method for dispersing in a wide range of applications.

〔発明の効果〕〔Effect of the invention〕

本発明の分散方法は、微粒子と分散媒である有機媒体と
のいずれの組合せにおいても微粒子の分散状態す良好に
保つことにより、これら微粒子と有機媒体とからなる塗
料、複合液状難燃剤及び塩化ビニルプラスチゾル、エポ
キシ樹脂、不飽和ポリエステル樹脂等の液状ブラスツチ
・ンクス配合物等に速用することができ、その効果は非
常に太きい。
The dispersion method of the present invention maintains a well-dispersed state of fine particles in any combination of fine particles and an organic medium as a dispersion medium, thereby dispersing paints, composite liquid flame retardants, and vinyl chloride made of these fine particles and an organic medium. It can be quickly applied to liquid blasting compounds such as plastisol, epoxy resin, and unsaturated polyester resin, and its effects are extremely large.

次に本発明に係る微粒子の分散方法による分散性の評価
結果を実施例に示したが、本発明はこれらの実施例によ
って限定されるものではない。
Next, the results of evaluating the dispersibility by the method for dispersing fine particles according to the present invention are shown in Examples, but the present invention is not limited by these Examples.

〔実施例〕〔Example〕

実施例1 ジオクチルフタレート(粘度10cP以上)100ml
に12−ヒドロキシステアリン酸く以下HRと略す)0
.1gを加え、130”Cに加熱し、溶解させ、室温に
てデカブロモジフェニルエーテル(平均粒径10μm以
下)Igを加え、攪拌混合し、分散させた。
Example 1 Dioctyl phthalate (viscosity 10 cP or more) 100 ml
12-hydroxystearic acid (hereinafter abbreviated as HR) 0
.. 1 g was added and heated to 130''C to dissolve it, and at room temperature Ig of decabromodiphenyl ether (average particle size 10 μm or less) was added and mixed with stirring to disperse.

実施例2 実施例1においてHRo、1gを0.4gに変え、実施
例1と同様にして分散させた。
Example 2 HRo was dispersed in the same manner as in Example 1 except that 1 g of HRo was changed to 0.4 g.

実施例3 実施例1においてHRをN−ラウロイル−し−グルタミ
ン酸ジブチルアミド(油ゲル化剤GP−1味の素■製、
以下GP−1と略す、)に変え、実施例1と同様にして
分散させた。
Example 3 In Example 1, HR was replaced with N-lauroyl-glutamic acid dibutylamide (oil gelling agent GP-1 manufactured by Ajinomoto Co., Ltd.)
(hereinafter abbreviated as GP-1), and was dispersed in the same manner as in Example 1.

実施例4 実施例1においてデカブロモジフェニルエーテルHRを
タルク(平均粒径10μm以下)に変え、実施例1と同
様にして分散させた。
Example 4 In Example 1, decabromodiphenyl ether HR was replaced with talc (average particle size of 10 μm or less), and dispersion was carried out in the same manner as in Example 1.

実施例5 ジオクチルフタレート(粘度10cP以上)100ml
にGP−1領 05gを加え、150’Cに加熱し、溶
解させ、室温にて五酸化アンチモン(平均粒径10μm
以下)0.5gを加え、攪拌混合し、分散させた。
Example 5 Dioctyl phthalate (viscosity 10 cP or more) 100 ml
Add 05g of GP-1 to the solution, heat to 150'C, dissolve, and add antimony pentoxide (average particle size 10μm) at room temperature.
(below) 0.5g was added and stirred and mixed to disperse.

実施例6 トリクレジルホスフェート(粘度10cP以上)100
mlにジベンジリデンソルビトール(ゲルオールD 新
日本理化曲製、以下DBSと略す、)0.1gを加え、
 150”Cに加熱し、溶解させ、40℃にて二酸化ア
ンチモン(平均粒径10μm以下)Igを加え、攪拌混
合し、分散させた。
Example 6 Tricresyl phosphate (viscosity 10 cP or more) 100
ml, add 0.1 g of dibenzylidene sorbitol (Gelol D Shin Nippon Rikaku Co., Ltd., hereinafter abbreviated as DBS),
The mixture was heated to 150''C to dissolve it, and antimony dioxide (average particle size: 10 μm or less) Ig was added at 40°C, mixed with stirring, and dispersed.

実施例7 実施例3においてジオクチルフタレート100m1にを
タービン油(粘度10cP以上)に変え実施例1と同様
にして分散させた。
Example 7 In Example 3, 100 ml of dioctyl phthalate was replaced with turbine oil (viscosity of 10 cP or more) and dispersed in the same manner as in Example 1.

実施例8 大豆油(粘度10cP以上)100mlにDBSo、4
gを加え、 150°Cに加熱し、溶解させ、室温にて
炭酸カルシウム(平均粒径10Jim以下)0.5gを
加え、攪拌混合し、分散させた。
Example 8 DBSo, 4 to 100 ml of soybean oil (viscosity 10 cP or more)
The mixture was heated to 150°C to dissolve it, and at room temperature 0.5 g of calcium carbonate (average particle size: 10 Jim or less) was added, stirred and mixed, and dispersed.

実施例9 実施例8において、DBSをN、N’ −シカブロイル
−し−リジンラウロイルエステルに変え、実施例8と同
様にして分散させた。
Example 9 In Example 8, DBS was changed to N,N'-cicabroyl-d-lysine lauroyl ester, and the dispersion was carried out in the same manner as in Example 8.

比較例1 実施例1においてHRo、1gを添加せずに、実施例1
と同様にして分散させた。
Comparative Example 1 Example 1 without adding 1 g of HRo in Example 1
It was dispersed in the same way.

比較例2 実施例1においてHRo、1gを1gに変え、実施例1
と同様にして分nりさせた。
Comparative Example 2 In Example 1, HRo, 1g was changed to 1g, and Example 1
It was separated in the same manner as above.

比較例3 実施例1においてジオクチルフタレートをトルエン(粘
度10cP以下)に変え、実施例1と同様にして分散さ
せた。
Comparative Example 3 Dioctyl phthalate in Example 1 was replaced with toluene (viscosity of 10 cP or less), and the same procedure as in Example 1 was carried out to disperse the toluene.

比較例4 実施例1においてタルクを平均粒径10μm以下のもの
に変え、実施例1と同様にして分散させた。
Comparative Example 4 Dispersion was carried out in the same manner as in Example 1 except that the talc in Example 1 was changed to one having an average particle size of 10 μm or less.

比較例5 実施例1においてHRをβ−ナフタリンスルホン酸ホル
ムアルデヒド縮金物のナトリウム塩に変え、実施例1と
同様にして分散させた。
Comparative Example 5 In Example 1, HR was changed to the sodium salt of β-naphthalene sulfonic acid formaldehyde condensed metal product, and the same procedure as in Example 1 was carried out to disperse the mixture.

比較例6 実施例1においてHRをビニルトリクロロシランに変え
、実施例1と同様にして分散させた。
Comparative Example 6 In Example 1, HR was changed to vinyltrichlorosilane, and dispersion was carried out in the same manner as in Example 1.

比較例7 実施例8において大豆油をアセトン(粘度10cP以下
)に変え、実施例1と同様にして分散させた。
Comparative Example 7 In Example 8, the soybean oil was replaced with acetone (viscosity: 10 cP or less), and dispersion was carried out in the same manner as in Example 1.

比較例8 実施例8において炭酸カルシウムを平均粒径10μm以
上のものに変え、実施例1と同様にして分散させた。
Comparative Example 8 In Example 8, the calcium carbonate was changed to one with an average particle size of 10 μm or more, and the same procedure as in Example 1 was used to disperse the calcium carbonate.

実施例10 実施例1〜8及び比較例1〜8で得た組成物を試験管に
とり粉体の沈降性を肉眼で観察し、分散性を評価した6
次に、これらの観察結果を表1に示した。
Example 10 The compositions obtained in Examples 1 to 8 and Comparative Examples 1 to 8 were placed in test tubes, and the settling properties of the powders were observed with the naked eye to evaluate the dispersibility6.
Next, these observation results are shown in Table 1.

表1より、明かな様に、本発明の微粒子の分散方法によ
り分散性が良好であることが判る。
From Table 1, it is clearly seen that the method for dispersing fine particles of the present invention provides good dispersibility.

表1 分散性の評価 ○ 分散性良好 × 分散性不良Table 1 Evaluation of dispersibility ○ Good dispersibility × Poor dispersibility

Claims (1)

【特許請求の範囲】[Claims] 常温で粘度10センチポイズ(cP)以上の有機溶媒中
の微粒子の分散剤として、12−ヒドロキシステアリン
酸、多価アルコールとベンズアルデヒドとの縮合物、N
−アシルアミノ酸アミン塩、N−アシルアミノ酸アミド
、N−アシルアミノ酸エステル(以下油ゲル化剤化剤と
いう。)のうち少なくとも1種を用いることを特徴とす
る微粒子の分散方法。
12-hydroxystearic acid, a condensate of polyhydric alcohol and benzaldehyde, N
- A method for dispersing fine particles, which comprises using at least one of an acylamino acid amine salt, an N-acylamino acid amide, and an N-acylamino acid ester (hereinafter referred to as an oil gelling agent).
JP63053135A 1988-03-07 1988-03-07 Dispersion of fine particle Pending JPH01228537A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63053135A JPH01228537A (en) 1988-03-07 1988-03-07 Dispersion of fine particle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63053135A JPH01228537A (en) 1988-03-07 1988-03-07 Dispersion of fine particle

Publications (1)

Publication Number Publication Date
JPH01228537A true JPH01228537A (en) 1989-09-12

Family

ID=12934379

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63053135A Pending JPH01228537A (en) 1988-03-07 1988-03-07 Dispersion of fine particle

Country Status (1)

Country Link
JP (1) JPH01228537A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0766959A1 (en) * 1995-10-04 1997-04-09 L'oreal Cosmetic sunscreening compositions containing TiO2 nanopigments and an acrylaminoacid

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0766959A1 (en) * 1995-10-04 1997-04-09 L'oreal Cosmetic sunscreening compositions containing TiO2 nanopigments and an acrylaminoacid
WO1997012590A1 (en) * 1995-10-04 1997-04-10 L'oreal ULTRAVIOLET-PROTECTING COSMETIC COMPOSITIONS CONTAINING TiO2 NANOPIGMENTS AND AN ACYLAMINOACID
FR2739555A1 (en) * 1995-10-04 1997-04-11 Oreal PHOTOPROTECTIVE COSMETIC COMPOSITIONS CONTAINING TIO2 NANOPIGMENTS AND ACYLAMINOACID

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