JPH049319A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPH049319A
JPH049319A JP11230490A JP11230490A JPH049319A JP H049319 A JPH049319 A JP H049319A JP 11230490 A JP11230490 A JP 11230490A JP 11230490 A JP11230490 A JP 11230490A JP H049319 A JPH049319 A JP H049319A
Authority
JP
Japan
Prior art keywords
particle size
powder
average particle
particles
composite hollow
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.)
Granted
Application number
JP11230490A
Other languages
Japanese (ja)
Other versions
JPH0699273B2 (en
Inventor
Koshi Tanaka
田中 耕嗣
Seiji Kyuno
及能 清治
Sueo Kida
木田 末男
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.)
Matsumoto Yushi Seiyaku Co Ltd
Original Assignee
Matsumoto Yushi Seiyaku 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 Matsumoto Yushi Seiyaku Co Ltd filed Critical Matsumoto Yushi Seiyaku Co Ltd
Priority to JP11230490A priority Critical patent/JPH0699273B2/en
Publication of JPH049319A publication Critical patent/JPH049319A/en
Publication of JPH0699273B2 publication Critical patent/JPH0699273B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

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

従来技術 米国特許第4,722,943号明細書には中空球状重
合体の表面に無機微粒子が付着してなる複合中空粒子を
開示している。しかしながらこの米国特許は発泡性のマ
イクロスフェアを発泡させる際に粒子どうしが凝集する
のを防止するため、無機微粒子の存在下にマイクロスフ
ェアを発泡させる技術を提供するものであり、上お複合
中空粒子を得ること自体を目的とするものではなく、ま
た、その複合中空粒子自体に固有の有用性を開示するも
のでもない。
Prior art US Pat. No. 4,722,943 discloses composite hollow particles in which fine inorganic particles are attached to the surface of a hollow spherical polymer. However, this U.S. patent provides a technology for foaming microspheres in the presence of inorganic fine particles in order to prevent the particles from agglomerating when foaming microspheres. The present invention is not aimed at obtaining composite hollow particles per se, nor does it disclose any inherent usefulness of the composite hollow particles themselves.

一方、化粧料の滑り性、触感、伸び、付着性、被覆性、
汗等の吸収性、机上での伸び、効果の持続性等を目的と
して、化粧料に微粉末を配合する技術が書くから提案さ
れている。例えば無機微粉末を用いる新しい技術として
特公昭61−39349号公報には多孔性粉体の表面に
多価金属水酸化物を含浸させた着色多孔性粉末を化粧料
に配合する方法、有機微粉末を用いる方法としては特開
昭59−181205号公報には酢酸綿からなる球状微
粉末、特開昭60184004号公報には中空球状重合
体を用いる方法がそれぞれ開示されている。
On the other hand, the slipperiness, feel, spreadability, adhesion, covering properties of cosmetics,
Techniques for incorporating fine powder into cosmetics have been proposed for the purpose of absorbing sweat, etc., spreading on the desk, and sustaining effects. For example, as a new technology using inorganic fine powder, Japanese Patent Publication No. 61-39349 describes a method of blending colored porous powder into cosmetics in which the surface of porous powder is impregnated with polyvalent metal hydroxide, and an organic fine powder. JP-A-59-181205 discloses a method using a spherical fine powder made of acetic acid cotton, and JP-A-60184004 discloses a method using a hollow spherical polymer.

しかしながら、有機微粉末の場合は被覆性に問題のある
場合が多く、逆に無機微粉末の場合は重く弾力性に乏し
いため触感が悪いと云った傾向があり、より満足すべき
特性を有する化粧料の開発が望まれている。
However, organic fine powders often have problems with coverage, while inorganic fine powders tend to be heavy and lack elasticity, giving them a poor feel to the touch. There is a need for the development of new materials.

発明が解決しようとする課題 本発明は軽く、弾力性があり、隠蔽性、被覆性、触感等
において優れた化粧料を提供することを目的とする。
Problems to be Solved by the Invention An object of the present invention is to provide a cosmetic that is lightweight, elastic, and has excellent concealing properties, covering properties, texture, etc.

課題を解決するための手段 本発明は中空球状重合体の表面に無機微粉末が付着して
なる複合中空粒子を含有する化粧料用配合材およびこの
配合材を含む化粧料に関する。
Means for Solving the Problems The present invention relates to a cosmetic compounding material containing composite hollow particles formed by adhering inorganic fine powder to the surface of a hollow spherical polymer, and a cosmetic material containing this compounding material.

本発明に用いられる中空球状重合体とは、例えば特公昭
42−26524号公報、特公昭60−21770号公
報等に開示されている方法で得られる熱膨張性マイクロ
カプセルを熱膨張させることにより得ることができる。
The hollow spherical polymer used in the present invention is obtained by thermally expanding thermally expandable microcapsules obtained by the method disclosed in, for example, Japanese Patent Publication No. 42-26524, Japanese Patent Publication No. 60-21770, etc. be able to.

即ち、重合性不飽和結合を有する七ツマ−を揮発性膨張
剤および重合開始剤と混合し、これを適当な乳化分散剤
等を含む水性媒体中で重合させて熱膨張性マイクロカプ
セルを得、これを加熱することにより熱膨張させて得る
ことができる。熱膨張性マイクロカプセルを前述の米国
特許第4,722,943号明細書に記載のごとく無機
微粉末と共に加熱するとマイクロカプセルが微粉末がそ
の表面に付着した状態で膨張するため一工程で複合中空
粒子を得ることができる。
That is, a hexamer having a polymerizable unsaturated bond is mixed with a volatile swelling agent and a polymerization initiator, and this is polymerized in an aqueous medium containing a suitable emulsifying and dispersing agent to obtain thermally expandable microcapsules. It can be obtained by thermally expanding it by heating it. When thermally expandable microcapsules are heated together with inorganic fine powder as described in the above-mentioned U.S. Pat. particles can be obtained.

揮発性膨張剤としてはエタン、エチレン、プロパン、ブ
タン、イソブタン、ブテン、イソブチン、ネオペンタン
、アセチレン、ヘキサン、ヘプタン等の脂肪族炭化水素
、トリクロロフロロメタン、ジクロロシフ0ロメタン等
のハロゲン化炭化水素、テトラアルキルシラン等の低沸
点化合物が例示される。
Volatile expansion agents include aliphatic hydrocarbons such as ethane, ethylene, propane, butane, isobutane, butene, isobutyne, neopentane, acetylene, hexane, heptane, halogenated hydrocarbons such as trichlorofluoromethane, dichlorofluoromethane, and tetraalkyl. Examples include low boiling point compounds such as silane.

マイクロカプセルを構成する熱可塑性重合体としてはア
クリル酸、メタクリル酸、イタコン酸、シトラコン酸、
マレイン酸、フマル酸、ビニル安息香酸あるいはそれら
のエステル、アクリロニトリル、メタクリロニトリル、
スチレン、塩化ビニル、塩化ビニリデン、酢酸ビニル、
酪酸ビニル等のモノマーの単独または共重合体が例示さ
れる。
Thermoplastic polymers constituting microcapsules include acrylic acid, methacrylic acid, itaconic acid, citraconic acid,
Maleic acid, fumaric acid, vinylbenzoic acid or their esters, acrylonitrile, methacrylonitrile,
Styrene, vinyl chloride, vinylidene chloride, vinyl acetate,
Examples include monopolymers or copolymers of monomers such as vinyl butyrate.

特に好ましい重合体はアクリル酸、メタクリル酸あるい
はそれらのエステル類、アクリロニトリル、塩化ビニリ
デン、メタクリロニトリル等から選ばれる七ツマ−の二
種以上からなる共重合体である。
Particularly preferred polymers are copolymers of two or more heptamers selected from acrylic acid, methacrylic acid or their esters, acrylonitrile, vinylidene chloride, methacrylonitrile, and the like.

これらの電合体はジビニルベンゼン、エチレングリコー
ルジメタクリレート、トリアクリルフォルマール等で架
橋されていてもよい。
These electrolyte compounds may be crosslinked with divinylbenzene, ethylene glycol dimethacrylate, triacryl formal, or the like.

熱膨張性マイクロカプセルは上述の発泡剤の存在下、上
記七ツマー類を必要ならば架橋性上ツマー類と共に水性
媒体中で乳化重合させる等の方法により得ることができ
る。この方法については特公昭42−26524号公報
等に詳述されている。
Thermally expandable microcapsules can be obtained by a method such as emulsion polymerization of the above-mentioned heptamers in an aqueous medium in the presence of the above-mentioned blowing agent, together with a crosslinkable supertumer if necessary. This method is described in detail in Japanese Patent Publication No. 42-26524.

熱膨張性微小球は平均粒径1−100μm、好ましくは
1〜50μmのものが好ましく、これを加熱膨張するこ
とにより、平均粒径2〜500μm1 より好ましくは
2〜300μmの中空球状重合体とすればよい。ここに
平均粒径とはレーザ回折式粒度分布測定装置(例、日本
電子株式会社HERO5& RODO3)で測定した粒
度分布のうち、累積分布の50%点の粒径を云う。
The thermally expandable microspheres preferably have an average particle size of 1 to 100 μm, preferably 1 to 50 μm, and are heated and expanded to form hollow spherical polymers with an average particle size of 2 to 500 μm, more preferably 2 to 300 μm. Bye. The average particle size herein refers to the particle size at the 50% point of the cumulative distribution of the particle size distribution measured with a laser diffraction particle size distribution analyzer (eg, JEOL Ltd. HERO5 & RODO3).

本発明において複合中空粒子を得るには、熱膨張性微小
球を加熱膨張させるに際し、これを無機粉末の存在下に
行なう等の方法により製造することができる。この様な
方法は例えば米国特許第4722.94.3号明細書に
記載されている。具体的には例えば熱膨張性マイクロカ
プセルの含水ケーキまたは乾燥品と無機粉末を任意の割
合に混合し、これを適当な方法により加熱することによ
り得ることができる。加熱は一般的な接触伝熱型または
直接加熱型の混合式乾燥装置を用いればよい。
In the present invention, composite hollow particles can be produced by a method such as heating and expanding thermally expandable microspheres in the presence of an inorganic powder. Such a method is described, for example, in US Pat. No. 4,722.94.3. Specifically, it can be obtained, for example, by mixing a water-containing cake or dried product of thermally expandable microcapsules and an inorganic powder in an arbitrary ratio, and heating the mixture by an appropriate method. For heating, a general contact heat transfer type or direct heating type mixing dryer may be used.

その機能として温度調節可能で原料を分散混合する能力
、場合により乾燥を早めるため減圧装置や冷却装置を備
えたものが好ましい。
As for its functions, it is preferable to have the ability to adjust the temperature, disperse and mix raw materials, and optionally have a pressure reducing device or a cooling device to speed up drying.

加熱温度は熱膨張カプセルの最適膨張温度とするのが好
ましく約60〜200°C1より好ましくは、熱膨張カ
プセルの種類にもよるが、90〜150°C程度である
The heating temperature is preferably about 60 to 200°C, more preferably about 90 to 150°C, depending on the type of the thermally expandable capsule.

無機微粉末としては化粧品用に用い得る無機粉末であれ
ば、何でもよい。具体的には例えばタルク、セリサイト
、カオリン、酸化チタン、マイカ、シリカ等が例示され
る。無機微粉末の好ましい粒径は平均粒径で0.01〜
500μm、より好ましくは0.01〜300μmであ
り、特に中空球状重合体の平均粒径を100としたとき
01〜100、より好ましくは1〜70の粒径を有する
ものである。
Any inorganic fine powder may be used as long as it can be used for cosmetics. Specific examples include talc, sericite, kaolin, titanium oxide, mica, and silica. The preferred particle size of the inorganic fine powder is 0.01 to 0.01 in average particle size.
The particle size is 500 μm, more preferably 0.01 to 300 μm, and particularly, when the average particle size of the hollow spherical polymer is 100, the particle size is 01 to 100, more preferably 1 to 70.

無機微粉末の形状は特に限定的でなく、所望の物性、特
に化粧品に複合中空粒子を配合したときの触感、伸び、
滑り性、被覆性等を考慮して選択すればよい。一般には
実質上球形の無機粒子を用いればよい。微粉末表面に鋭
角の突起や稜線を有する場合であっても、これを単独で
用いる場合に比べ柔軟性のある中空球状重合体により皮
膚への刺激が抑制される。
The shape of the inorganic fine powder is not particularly limited, and the desired physical properties, especially the feel, elongation, and elongation when compounded with composite hollow particles in cosmetics.
The material may be selected in consideration of slipperiness, covering properties, etc. Generally, substantially spherical inorganic particles may be used. Even if the surface of the fine powder has sharp protrusions or ridgelines, irritation to the skin is suppressed by the flexible hollow spherical polymer compared to when the fine powder is used alone.

中空球状重合体と無機微粒子の配合比は重量比で5対9
5〜50対50が好ましく、特に10対90〜40対6
0が好適である。
The blending ratio of hollow spherical polymer and inorganic fine particles is 5:9 by weight.
5 to 50:50 is preferred, especially 10:90 to 40:6
0 is preferred.

本発明複合中空微粉末は、これを従来の無機微粉末や有
機微粒子に代えて化粧品に配合すればよい。
The composite hollow fine powder of the present invention may be blended into cosmetics in place of conventional inorganic fine powders or organic fine particles.

以下、実施例を挙げて本発明の詳細な説明する。Hereinafter, the present invention will be explained in detail with reference to Examples.

参考例1(複合中空粒子(1)の製造)検板貿易(株)
レーディゲミキサーにマツモトマイクロスフェア−F−
30D(注1)と酸化チタン(注2)、重量比15/8
5の比率で投入し、3分間混合後、ジャケット温度14
0℃で10分間加熱品温90°Cで冷却して複合中空粒
子(1)を得た。
Reference example 1 (manufacture of composite hollow particles (1)) Kenpan Boeki Co., Ltd.
Matsumoto Microsphere-F- for Loedige Mixer
30D (Note 1) and titanium oxide (Note 2), weight ratio 15/8
After mixing for 3 minutes, the jacket temperature was increased to 14.
The mixture was heated at 0°C for 10 minutes and then cooled at a temperature of 90°C to obtain composite hollow particles (1).

得られた複合中空粒子(1)は真比重0.3、見掛比重
0.15、粒径は20〜40μ川であった。この粒子は
酸化チタンの隠蔽性、中空粒子の弾力性を兼ねそなえた
粒子であった。得られた複合中空粒子を用い、酸化チタ
ン水性ペイントを作成したところ20VO1%の酸化チ
タンと代替しても隠蔽性は低下しなかった。
The obtained composite hollow particles (1) had a true specific gravity of 0.3, an apparent specific gravity of 0.15, and a particle size of 20 to 40 μm. These particles had both the concealing properties of titanium oxide and the elasticity of hollow particles. When a titanium oxide aqueous paint was prepared using the obtained composite hollow particles, the hiding power did not decrease even when the paint was replaced with 20VO1% titanium oxide.

注1=塩化ビニリデン/アクリロニトリル共重合体を殻
成分とする平均粒径15μm1真比重d=1.1の熱膨
張性微小球。
Note 1 = thermally expandable microspheres with an average particle size of 15 μm and true specific gravity d = 1.1, whose shell component is vinylidene chloride/acrylonitrile copolymer.

注2= 平均粒径的0.2.um、真比重d=4.2゜
参考例2(複合中空粒子(2)の製造)レーディゲミキ
サー(連続式)に、マツモトマイクロスフェアF−30
(注3)/タルク(注4)を重量比15/85の比率で
連続的に供給し、シャケ・7ト温度140°C1滞留時
間20分、出!側品温90°Cで連続的に熱膨張させた
。得られた複合中空粒子(2)は真比重0.2、見掛比
重0.11平均粒径20μmであった。
Note 2 = Average particle size 0.2. um, true specific gravity d = 4.2° Reference Example 2 (Production of composite hollow particles (2)) Matsumoto Microsphere F-30 was added to a Loedige mixer (continuous type).
(Note 3) / Talc (Note 4) were continuously supplied at a weight ratio of 15/85, and the temperature of the salmon was 140°C, the residence time was 20 minutes, and the water was released! Thermal expansion was carried out continuously at a temperature of 90°C. The obtained composite hollow particles (2) had a true specific gravity of 0.2, an apparent specific gravity of 0.11, and an average particle diameter of 20 μm.

タルクのなめらかさをそなえた圧縮性の粉体で耐荷重性
は300kg/Cm2であった。
It was a compressible powder with the smoothness of talc and had a load capacity of 300 kg/cm2.

注3:塩化ビニリデン/アクリロニトリル共重合体を殻
成分とする平均粒径的15μm、 d= l 。
Note 3: Average particle diameter of 15 μm with vinylidene chloride/acrylonitrile copolymer as the shell component, d=l.

■の熱膨張性微小球。■Thermally expandable microspheres.

注4= 平均粒径約4μm1真比重d=2.8゜実施例
1(フェイスパウダー) 処方A(粉末処方)     重量部(%)複合中空粒
子1      20(54)ナイロンパウダ    
   3 (8,1)セリサイト          
  5(13,5)タルク            4
.4(11,9)弁柄           0.2(
0,5)黄酸化鉄          0.1(0,3
)処方B (流体処方)     重量部(%)流動パ
ラフィン       0.5(1,4)グリセリン−
2−エチル   1.0(2,7)へキシレート イソプロピルミリステート  2.5(6,8)処方C
(香料)      重量部(%)調合香料     
     0.3(0,8)Aをヘンシェルミキサーで
混合した後、粉砕機で粉砕した。これを再度ヘンシェル
ミキサーで攪拌しながら、Bを加え、lO分間攪拌混合
し、更にCを加え3分間混合した。ブロワ−シフターで
均質化し、フェイスパウダーとしたところ、ソフトで滑
らかな使用感、軽快で肌へのつきの均一性が良好な結果
が得られた。
Note 4 = Average particle size approximately 4 μm 1 True specific gravity d = 2.8° Example 1 (Face powder) Prescription A (Powder formulation) Part by weight (%) Composite hollow particles 1 20 (54) Nylon powder
3 (8,1) Sericite
5 (13,5) Talc 4
.. 4(11,9) Bengara 0.2(
0,5) Yellow iron oxide 0.1(0,3
) Prescription B (Fluid formulation) Part by weight (%) Liquid paraffin 0.5 (1,4) Glycerin
2-ethyl 1.0 (2,7) hexylate isopropyl myristate 2.5 (6,8) Formulation C
(Fragrance) Part by weight (%) Mixed fragrance
0.3(0,8)A was mixed in a Henschel mixer and then ground in a grinder. While stirring this again with the Henschel mixer, B was added thereto, and the mixture was stirred and mixed for 10 minutes, and then C was added and mixed for 3 minutes. When the powder was homogenized using a blower sifter and used as a face powder, it had a soft and smooth feel, was lightweight, and applied well to the skin evenly.

実施例2 (プレストパウダー) 処方A (粉末処方)     重量部 %複合中空粒
子(2)        3 (3,7)タルク   
          50(61,7)セリサイト  
         l 5  (18,5)アルミニウ
ムステアレート  3.5(4,3)カオリン    
      3.7(4,6)弁柄         
   0.3(0,4)星互旦 (液体処方)    
重量部 %スフフラン         2.0(2,
5)グリセリン−2−3,0(3,7) エチル−ヘキシレート 処方C(香料)       重量部 %調合香料  
        0.5(0,6)Aをリボンブレンダ
ーで30分間攪拌混合したのち粉砕機で粉砕した。その
粉砕物をヘンシェルミキサーで攪拌しつつ、これにBを
加え12分間混合した。更にCを加え4分間攪拌混合し
た。ブロワ−シフターで均質化しプレストパウダーとし
た。ソフトで軽快な使用感が得られた。
Example 2 (Pressed Powder) Formulation A (Powder Formulation) Weight Parts % Composite Hollow Particles (2) 3 (3,7) Talc
50 (61,7) Sericite
l 5 (18,5) aluminum stearate 3.5 (4,3) kaolin
3.7 (4,6) Bengara
0.3 (0,4) Hoshigoutan (Liquid prescription)
Part by weight % Suffuran 2.0 (2,
5) Glycerin-2-3,0(3,7) Ethyl-hexylate formulation C (fragrance) Part by weight % Mixed fragrance
0.5(0,6)A was stirred and mixed using a ribbon blender for 30 minutes, and then ground using a grinder. While stirring the pulverized product using a Henschel mixer, B was added thereto and mixed for 12 minutes. Furthermore, C was added and mixed with stirring for 4 minutes. It was homogenized using a blower sifter to obtain pressed powder. It felt soft and light to use.

実施例3 (乳化型ファンデーション)処方A (粉末
処方)     重量部 %複合中空粒子(1)   
    1.0(1,0)ステアリン酸       
  2.0(2,1)スフフラン         1
.5(1,6)ステアリルアルコール    2.0(
2,1)2−オクチルドデシル    4.0(4,2
)ミリステート 活性剤           5.0(5,3)着色顔
料ペースト     18.0(18,7)ブチルパラ
ベン       0.1(0,1)BHT     
      O,05(0,05)処方B (液体処方
)     重量部 %プロピレングリコール    
5.0(5,2)メチルパラベン       0.2
(0,2)トリエタノールアミン    O’、7(0
,7)精製水         55.95(58,2
5)処方C(香料)       重量部 %調合香料
          0.5(0,5)Aを75℃で攪
拌しながら加熱溶解、均一に分散させて保温しておく。
Example 3 (Emulsified foundation) Formulation A (Powder formulation) Part by weight % Composite hollow particles (1)
1.0 (1,0) stearic acid
2.0(2,1) Soufuran 1
.. 5(1,6)stearyl alcohol 2.0(
2,1) 2-octyldodecyl 4.0(4,2
) Myristate Activator 5.0 (5,3) Colored Pigment Paste 18.0 (18,7) Butylparaben 0.1 (0,1) BHT
O,05 (0,05) Formulation B (Liquid Formulation) Part by Weight % Propylene Glycol
5.0 (5,2) Methylparaben 0.2
(0,2) Triethanolamine O',7(0
,7) Purified water 55.95 (58,2
5) Prescription C (fragrance) Weight part % Mixed fragrance 0.5 (0,5) Dissolve A by heating while stirring at 75°C, disperse uniformly, and keep warm.

Bは80°Cに加温し保温しておく。加温したBをAに
徐々に加えながら乳化し、温度を10分間保持して攪拌
した後、攪拌冷却して45℃とする。この時にCを加え
、35°Cまで攪拌冷却を続け、取り出し乳化をファン
デーションとした。ソフトで滑らかな使用感が得られt
こ。
Heat B to 80°C and keep warm. The heated B is gradually added to A to emulsify it, the temperature is maintained for 10 minutes and stirred, and then the mixture is cooled to 45° C. with stirring. At this time, C was added, stirring and cooling was continued to 35°C, and the emulsification was taken out and used as a foundation. Provides a soft and smooth feeling of use.
child.

発明の効果 本発明に用いる複合中空粒子は中に空気を含み、粒子の
軽量化が可能であり、かつ所望の比重に調節できるため
、種々の化粧品用粒子としての利用が可能である。また
、この複合中空粒子は弾力性があり圧縮回復機能を有し
、かつ無機粒子の有する特性を備えているため、触感に
刺激性がなく、滑り性、伸び、付着性、被覆性に優れて
いる。また効果の持続性および汗等の吸収性にも優れた
化粧料を得ることができる。
Effects of the Invention The composite hollow particles used in the present invention contain air, can be made lightweight, and can be adjusted to a desired specific gravity, so they can be used as particles for various cosmetics. In addition, these composite hollow particles are elastic and have a compression recovery function, as well as the characteristics of inorganic particles, so they are non-irritating to the touch and have excellent slipperiness, stretchability, adhesion, and covering properties. There is. Furthermore, it is possible to obtain a cosmetic that has excellent long-lasting effects and excellent absorption of sweat and the like.

特許出願人 松本油脂製薬株式会社Patent applicant: Matsumoto Yushi Pharmaceutical Co., Ltd.

Claims (1)

【特許請求の範囲】 1、中空球状重合体の表面に無機微粉末が付着してなる
複合中空粒子を含有する化粧料用配合材。 2、中空球状重合体の平均粒径が2〜500μmであり
、無機微粉末の平均粒径が0.01〜500μmであり
、前者の平均粒径を100としたときの後者の平均粒径
が0.1〜100の範囲にある請求項1に記載の化粧料
用配合材。 3、請求項1または2の配合材を含有する化粧料。
[Claims] 1. A compounding material for cosmetics containing composite hollow particles formed by adhering inorganic fine powder to the surface of a hollow spherical polymer. 2. The average particle size of the hollow spherical polymer is 2 to 500 μm, the average particle size of the inorganic fine powder is 0.01 to 500 μm, and the average particle size of the latter is 100. The cosmetic compounding material according to claim 1, which has a molecular weight in the range of 0.1 to 100. 3. A cosmetic containing the compounding material according to claim 1 or 2.
JP11230490A 1990-04-27 1990-04-27 Cosmetics Expired - Fee Related JPH0699273B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11230490A JPH0699273B2 (en) 1990-04-27 1990-04-27 Cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11230490A JPH0699273B2 (en) 1990-04-27 1990-04-27 Cosmetics

Publications (2)

Publication Number Publication Date
JPH049319A true JPH049319A (en) 1992-01-14
JPH0699273B2 JPH0699273B2 (en) 1994-12-07

Family

ID=14583327

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11230490A Expired - Fee Related JPH0699273B2 (en) 1990-04-27 1990-04-27 Cosmetics

Country Status (1)

Country Link
JP (1) JPH0699273B2 (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0840870A (en) * 1994-07-11 1996-02-13 L'oreal Sa Cosmetic and / or dermatological composition using deformable hollow particles containing fatty substances
US5663213A (en) * 1994-02-28 1997-09-02 Rohm And Haas Company Method of improving ultraviolet radiation absorption of a composition
US6403070B1 (en) 1999-11-25 2002-06-11 L'oreal S.A. Anhydrous deodorant composition
WO2004087078A1 (en) 2003-03-31 2004-10-14 Shiseido Co., Ltd. Cosmetic for cilia
US6849584B2 (en) 2001-11-02 2005-02-01 The Procter & Gamble Company Composition containing a cationic polymer and water insoluble solid material
KR100537952B1 (en) * 2001-04-13 2005-12-21 주식회사 태평양 Hollow type microcapsule made of hydrophobic polymer and preparation method thereof, and cosmetic compositions containing the microcapsule
EP1642619A1 (en) * 2004-10-04 2006-04-05 L'oreal Hair cosmetic composition comprising hollow particles and non-silicone fixing polymer
EP1642620A1 (en) * 2004-10-04 2006-04-05 L'oreal, S.A. Hair cosmetic composition comprising hollow particles and silicone fixing polyurethane
JP2006151918A (en) * 2004-12-01 2006-06-15 Pola Chem Ind Inc Cosmetic for infrared protection
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5663213A (en) * 1994-02-28 1997-09-02 Rohm And Haas Company Method of improving ultraviolet radiation absorption of a composition
JPH0840870A (en) * 1994-07-11 1996-02-13 L'oreal Sa Cosmetic and / or dermatological composition using deformable hollow particles containing fatty substances
US6403070B1 (en) 1999-11-25 2002-06-11 L'oreal S.A. Anhydrous deodorant composition
KR100537952B1 (en) * 2001-04-13 2005-12-21 주식회사 태평양 Hollow type microcapsule made of hydrophobic polymer and preparation method thereof, and cosmetic compositions containing the microcapsule
US6849584B2 (en) 2001-11-02 2005-02-01 The Procter & Gamble Company Composition containing a cationic polymer and water insoluble solid material
WO2004087078A1 (en) 2003-03-31 2004-10-14 Shiseido Co., Ltd. Cosmetic for cilia
FR2876026A1 (en) * 2004-10-04 2006-04-07 Oreal HAIR-BASED COSMETIC COMPOSITION BASED ON HOLLOW PARTICLES AND NON-SILICONE FIXING POLYMER
EP1642620A1 (en) * 2004-10-04 2006-04-05 L'oreal, S.A. Hair cosmetic composition comprising hollow particles and silicone fixing polyurethane
EP1642619A1 (en) * 2004-10-04 2006-04-05 L'oreal Hair cosmetic composition comprising hollow particles and non-silicone fixing polymer
FR2876025A1 (en) * 2004-10-04 2006-04-07 Oreal HAIR COSMETIC COMPOSITION BASED ON HOLLOW PARTICLES AND SILICONE FIXING POLYURETHANE
JP2006151918A (en) * 2004-12-01 2006-06-15 Pola Chem Ind Inc Cosmetic for infrared protection
WO2018221406A1 (en) * 2017-05-31 2018-12-06 日揮触媒化成株式会社 Hollow particles and cosmetic
CN110603223A (en) * 2017-05-31 2019-12-20 日挥触媒化成株式会社 Hollow particle and cosmetic
KR20200014744A (en) * 2017-05-31 2020-02-11 닛키 쇼쿠바이카세이 가부시키가이샤 Hollow particles and cosmetics
JPWO2018221406A1 (en) * 2017-05-31 2020-05-21 日揮触媒化成株式会社 Hollow particles and cosmetics
US11020326B2 (en) 2017-05-31 2021-06-01 Jgc Catalysts And Chemicals Ltd. Hollow particles and cosmetic
WO2019181987A1 (en) * 2018-03-23 2019-09-26 富士フイルム株式会社 Hollow particles and method for producing same, pore-making material, particles for cosmetics, and weight-reducing material
JPWO2019181987A1 (en) * 2018-03-23 2021-01-07 富士フイルム株式会社 Hollow particles and their manufacturing methods, as well as pore-forming materials, cosmetic particles and weight-reducing materials
US11607659B2 (en) 2018-03-23 2023-03-21 Fujifilm Corporation Hollow particles and manufacturing method thereof, pore forming material, particles for cosmetics, and weight reducing material

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