JPH0515686B2 - - Google Patents
Info
- Publication number
- JPH0515686B2 JPH0515686B2 JP62057207A JP5720787A JPH0515686B2 JP H0515686 B2 JPH0515686 B2 JP H0515686B2 JP 62057207 A JP62057207 A JP 62057207A JP 5720787 A JP5720787 A JP 5720787A JP H0515686 B2 JPH0515686 B2 JP H0515686B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- plate
- porous
- shaped
- kaolin
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0254—Platelets; Flakes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0279—Porous; Hollow
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/08—Preparations containing skin colorants, e.g. pigments for cheeks, e.g. rouge
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q3/00—Manicure or pedicure preparations
- A61Q3/02—Nail coatings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
Description
〈産業上の利用分野〉
本発明は、板状であるため平滑性、密着性に優
れ、多孔性であるため通気性に優れた粉体を配合
した化粧料に関する。
〈従来の技術〉
従来、化粧料に使用される多孔性の粉体とし
て、金属炭酸化合物、燃焼性物質等を珪酸化合物
で被覆したもの(特開昭53−15433)、セルロース
粉末(特開昭61−189210)などが知られており、
保香性、保湿性、通気性に優れている。
一方、板状の粉体としては、平滑性、密着性に
優れるマイカが広く使用されている。
〈発明が解決しようとする問題点〉
従来の多孔性粉体は球状であるため、平滑性、
密着性に劣るという欠点があつた。多孔性粉体を
板状とする試みもなされているが、十分な物理的
強度が得られず、実用化には至つていなかつた。
また、マイカ等の板状粉体は、平滑性、密着性
に優れるものの、通気性に欠けるため皮膚に悪影
響を及ぼし、また化粧崩れもしやすかつた。
〈問題点を解決するための手段〉
本発明者らは、上記問題点を解決するため、鋭
意検討を行い、珪藻土と板状結晶のカオリンと長
石との分散混合物を焼成して、板状多孔性粉体を
開発した(特許出願中、昭和62年2月26日出願、
出願人:株式会社ノエビア、三郷陶器株式会社)。
この粉体は、平滑性・密着性と通気性を兼ね備え
ており、これを化粧料に配合することにより、上
記問題点を解決することができた。
〈作用〉
すなわち、本発明は、珪藻土と板状結晶のカオ
リンと長石との分散混合物を焼成して調製した板
状多孔性粉体を配合してなる化粧料に関する。
本発明の目的には、板状多孔性粉体の原料であ
る珪藻土は、あらかじめ800〜1200℃で焼成し、
水を加えて粉砕した後分級する水簸分級により選
択した5〜20μの粒子が好ましい。また、上記混
合物を900〜1000℃で焼成したものを用いる。
出発原料である珪藻土の焼成、粉砕、分級とい
う処理により、希望の粒径を有する粒子を得るこ
とが容易となり、また次の工程におけるカオリン
と長石との混合性及び焼結性を良くし、さらに不
純物を揮発、除去させることができる。
次の珪藻土、カオリン、長石の分散混合物を焼
成する工程において、カオリンの微細粒子が多孔
性の珪藻土粒子の表面に被膜となつて付着し、焼
結する。この際、長石が焼結を促進するため、粉
体の強度が向上する。これを再び解砕分級して、
希望の粒径範囲の粉体粒子を得ることができる。
以上のようにして得た粉体は、板状で且つ多孔
性であり、粒度及び空孔径も均一で、物理的強度
にも優れている。従つて、平滑性、密着性及び通
気性のすべてにおいて優れており、化粧料に配合
する際の混合、粉砕、充填、圧縮成型等の処理に
よつて、多孔性構造が破壊されたり、粒径が変化
したりするようなこともない。
上記板状多孔性粉体の配合量は、一般に化粧料
に粉末原料として用いられる範囲で選択できる
が、通常1〜70重量%、好ましくは5〜30重量%
程度である。
本発明に係る化粧料の剤形としては、乳液状、
ローシヨン状、クリーム状、軟膏状、ステイツク
状、粉体状、プレス状等、通常化粧料として用い
られる形態のものであればいずれでも良く、用途
もフエイシヤル用、メイクアツプ用、頭髪用、ボ
デイ用、芳香剤等、どのようなものにでも使用で
きるが、当然のことながら、フアンデーシヨン、
チークカラー、アイシヤドウ、白粉、口紅、ネイ
ルエナメル等のメイクアツプ化粧料に最も好適で
ある。
次に、本発明の化粧料に配合する板状多孔性粉
体について、製造例を挙げ、比較製造例とともに
説明する。
(製造例 1)
珪藻土をシヤトルキルンにて1000℃で5時間焼
成する。次にボールミル中に移し、重量比にして
70%の水を加えて粉砕処理を3時間行い、水簸分
級して最大粒径15〜20μの粒子とする。次いで得
られた粒子に重量比にしてカオリン10%、微粉砕
長石0.2%を混合し、水を60%となるように加え、
過粉砕を防止するため粘度調整剤としてカルボキ
シメチルセルロースを0.5%添加し、ボールミル
にて1時間混合する。この後、この混合物を90℃
で6時間乾燥した後、1000℃で5時間焼成する。
これを再び解砕分級して最大粒径20μ以下の粒子
を得た。走査型電子顕微鏡(明石製走査型電子顕
微鏡ALPHA−10型)にて観察したところ、板状
で多孔性の粒子構造を有する粉体であることが確
認された。また、当該粉体の対破砕強度試験とし
て、製造例1に係る粉体をワセリンに分散せしめ
てスラリー状とした後ライカイ機にて15分間処理
した。試験後の粉体の粒子構造を前記の走査型電
子顕微鏡で観察したところ、上記処理により当該
粉体がほとんど破砕されていないことが認められ
た。
製造例1に係る粉体の化学組成、粒度分布、
Lab系白色度、PH、見かけ比重を表1に示した。
(製造例 2)
珪藻土をシヤトルキルンにて1100℃で5時間焼
成する。次いでボールミル中に移し、重量比にし
て70%となるように水を加え、3時間粉砕後、水
簸分級して最大粒径15〜20μの粒子とする。この
粒子に、重量比にしてカオリン30%、微粉砕長石
0.4%を混合し、水を60%となるまで添加して、
過粉砕を防止するため、粘度調整剤としてカルボ
キシビニルポリマーを0.5%加えてボールミル中
で1時間混合する。この混合物を90℃で6時間乾
燥し、1000℃で6時間焼成する。これを再び解砕
分級して、最大粒径20μ以下の粉体を得た。この
粉体を前記走査型電子顕微鏡にて観察した結果、
板状で多孔性の粒子構造が認められた。また、製
造例2に係る粉体を15分間ライカイ機にて処理
し、粒子構造を前記走査型電子顕微鏡にて観察し
たところ、上記処理を行つても、粉体の板状多孔
性の粒子構造はほとんど破砕されていなかつた。
製造例2に係る粉体の化学組成、粒度分布、
Lab系白色度、PH、見かけ比重を表1に示した。
(比較製造例)
珪藻土をシヤトルキルンで1000℃で5時間焼成
する。得られた粉体を前記走査型電子顕微鏡で観
察した結果多孔質であつた。しかし、これを最大
粒径20μ以下になるように解砕分級したところ、
前記走査型電子顕微鏡下で全く多孔性構造が失わ
れていた。
<Industrial Application Field> The present invention relates to a cosmetic containing a powder that is plate-shaped and has excellent smoothness and adhesion, and is porous and has excellent air permeability. <Prior art> Conventionally, porous powders used in cosmetics include metal carbonate compounds, combustible substances, etc. coated with silicic acid compounds (Japanese Patent Laid-Open No. 53-15433), and cellulose powder (Japanese Patent Laid-Open No. 15433-1989). 61-189210) are known,
Excellent fragrance retention, moisture retention, and breathability. On the other hand, as the plate-shaped powder, mica is widely used because of its excellent smoothness and adhesion. <Problems to be solved by the invention> Since conventional porous powders are spherical, smoothness,
It had the disadvantage of poor adhesion. Attempts have been made to make porous powder into a plate shape, but sufficient physical strength was not obtained and it was not put to practical use. Furthermore, although plate-shaped powders such as mica have excellent smoothness and adhesion, they lack air permeability, which adversely affects the skin, and also tends to cause makeup to come off. <Means for Solving the Problems> In order to solve the above-mentioned problems, the present inventors conducted intensive studies, fired a dispersed mixture of diatomaceous earth, plate-shaped kaolin, and feldspar, and produced plate-shaped porous (Patent pending, filed on February 26, 1988,
Applicant: Noevir Co., Ltd., Misato Pottery Co., Ltd.).
This powder has both smoothness, adhesion, and breathability, and by incorporating it into cosmetics, the above problems could be solved. <Function> That is, the present invention relates to a cosmetic containing a plate-shaped porous powder prepared by firing a dispersed mixture of diatomaceous earth, plate-shaped kaolin, and feldspar. For the purpose of the present invention, diatomaceous earth, which is a raw material for plate-shaped porous powder, is calcined in advance at 800 to 1200 °C,
Particles of 5 to 20 microns are preferred, which are selected by elutriation classification, which is performed by adding water and pulverizing the particles, followed by classification. Further, the above mixture fired at 900 to 1000°C is used. By processing the starting material, diatomaceous earth, by firing, crushing, and classifying, it becomes easy to obtain particles with the desired particle size, and it also improves the mixing and sinterability of kaolin and feldspar in the next step, and Impurities can be volatilized and removed. In the next step of firing the dispersed mixture of diatomaceous earth, kaolin, and feldspar, fine particles of kaolin adhere as a film to the surface of the porous diatomaceous earth particles and are sintered. At this time, since the feldspar promotes sintering, the strength of the powder is improved. This is crushed and classified again,
Powder particles with a desired particle size range can be obtained. The powder obtained as described above is plate-shaped and porous, has uniform particle size and pore size, and has excellent physical strength. Therefore, it has excellent smoothness, adhesion, and air permeability, and processing such as mixing, crushing, filling, and compression molding when blending into cosmetics does not destroy the porous structure or reduce the particle size. There is no such thing as changing. The amount of the above-mentioned plate-like porous powder can be selected within the range generally used as a powder raw material for cosmetics, but it is usually 1 to 70% by weight, preferably 5 to 30% by weight.
That's about it. The dosage form of the cosmetic according to the present invention includes emulsion, emulsion,
It can be in any form that is normally used as a cosmetic, such as lotion, cream, ointment, stick, powder, press, etc., and can be used for facial, makeup, hair, body, etc. It can be used for anything such as fragrance, but of course foundation,
It is most suitable for make-up cosmetics such as cheek color, eye shadow, white powder, lipstick, and nail enamel. Next, the plate-shaped porous powder to be blended into the cosmetic of the present invention will be described with reference to production examples and comparative production examples. (Production Example 1) Diatomaceous earth is fired at 1000°C for 5 hours in a shuttle kiln. Next, transfer it to a ball mill and convert it into a weight ratio.
Add 70% water, grind for 3 hours, and elutriate to obtain particles with a maximum particle size of 15-20μ. Next, the obtained particles were mixed with 10% kaolin and 0.2% finely ground feldspar by weight, and water was added to make the weight 60%.
To prevent over-grinding, 0.5% carboxymethylcellulose is added as a viscosity modifier, and the mixture is mixed in a ball mill for 1 hour. After this, mix this mixture at 90℃
After drying for 6 hours at 1000℃, it is fired for 5 hours.
This was crushed and classified again to obtain particles with a maximum particle size of 20μ or less. When observed with a scanning electron microscope (Akashi scanning electron microscope ALPHA-10 model), it was confirmed that the powder had a plate-like porous particle structure. Further, as a crush strength test of the powder, the powder according to Production Example 1 was dispersed in Vaseline to form a slurry, and then processed in a Raikai machine for 15 minutes. When the particle structure of the powder after the test was observed using the scanning electron microscope, it was found that the powder was hardly crushed by the above treatment. Chemical composition and particle size distribution of the powder according to Production Example 1,
Lab whiteness, pH, and apparent specific gravity are shown in Table 1. (Production Example 2) Diatomaceous earth is fired at 1100°C for 5 hours in a shuttle kiln. Next, the mixture is transferred to a ball mill, water is added to give a weight ratio of 70%, and after pulverization for 3 hours, the mixture is classified by elutriation to obtain particles with a maximum particle size of 15 to 20 μm. This particle contains 30% kaolin and finely ground feldspar by weight.
Mix 0.4% and add water until 60%.
To prevent over-grinding, 0.5% carboxyvinyl polymer is added as a viscosity modifier and mixed in a ball mill for 1 hour. This mixture is dried at 90°C for 6 hours and calcined at 1000°C for 6 hours. This was crushed and classified again to obtain a powder with a maximum particle size of 20μ or less. As a result of observing this powder with the scanning electron microscope,
A plate-like and porous particle structure was observed. In addition, when the powder according to Production Example 2 was treated with a Raikai machine for 15 minutes and the particle structure was observed using the scanning electron microscope, it was found that even after the above treatment, the powder had a plate-like porous particle structure. was hardly crushed. Chemical composition and particle size distribution of powder according to Production Example 2,
Lab whiteness, pH, and apparent specific gravity are shown in Table 1. (Comparative production example) Diatomaceous earth is fired at 1000°C for 5 hours in a shuttle kiln. When the obtained powder was observed using the scanning electron microscope, it was found to be porous. However, when this was crushed and classified to a maximum particle size of 20μ or less,
No porous structure was lost under the scanning electron microscope.
【表】
〈効果〉
さらに本発明の効果について、実施例により詳
細に説明する。
(実施例1) 固型フアンデーシヨン
実施例1 比較例1
(重量%)
(1) 酸化チタン 10.0 10.0
(2) セリサイト 15.0 30.0
(3) タルク 23.3 33.3
(4) 製造例1に係る粉体 25.0 −
(5) ベンガラ 1.0 1.0
(6) 黄酸化鉄 2.0 2.0
(7) 黒酸化鉄 0.3 0.3
(8) 流動パラフイン 15.0 15.0
(9) シリコン油 8.0 8.0
(10) 防腐剤 0.2 0.2(11)香料 0.2 0.2
100.0 100.0
製造方法
(1)〜(7)の成分を混合粉砕後均一化し、これに(8)
〜(11)を添加して混合均一化する。その後、これを
金皿に充填し、圧縮成型機にてプレス成型する。
(実施例2) 流し込み型フアンデーシヨン
実施例2 比較例2
(重量%)
(1) 酸化チタン 12.0 12.0
(2) セリサイト 14.1 32.1
(3) 製造例1に係る粉体 18.0 −
(4) ベンガラ 1.1 1.1
(5) 黄酸化鉄 2.1 2.1
(6) 黒酸化鉄 0.3 0.3
(7) 流動パラフイン 30.0 30.0
(8) ワセリン 10.0 10.0
(9) シリコン油 5.0 5.0
(10) マイクロクリスタ
リンワツクス 7.0 7.0
(11)防腐剤 0.2 0.2(12)香料 0.2 0.2
100.0 100.0
製造方法
(1)〜(6)を混合粉砕後均一化し、これをあらかじ
め混合し加熱溶解した(7)〜(11)に添加して攪拌均一
化した後(12)を加え、所定の容器に流し込む。
(実施例3) 乳化型フアンデーシヨン
実施例3 比較例3
(重量%)
(1) 酸化チタン 1.90 1.90
(2) タルク 1.12 6.12
(3) 製造例2に係る粉体 9.00 −
(4) ベンガラ 0.15 0.15
(5) 黄酸化鉄 0.27 0.27
(6) 黒酸化鉄 0.06 0.06
(7) カオリン 6.00 10.00
(8) セレシン 3.50 3.50
(9) パラフインワツクス 1.50 1.50
(10) 液状ラノリン 1.50 1.50
(11)流動パラフイン 13.50 13.50
(12)P.O.E.(20) 1.00 1.00
ソルビタンモノオレエート
(13)ソルビタンモノオレエート 1.00 1.00
(14)モノステアリン酸グリセリン
0.70 0.70
(15)精製水 55.20 55.20
(16)カルボキシメチルセルロース
0.40 0.40
(17)プロピレングリコール 3.00 3.00
(18)防腐剤 0.10 0.10(19)香料 0.10 0.10
100.00 100.00
製造方法
(1)〜(7)を混合粉砕後均一化し、これをあらかじ
め混合し加熱した(12)〜(18)に添加し、ホモミキサー
で均一化する。その後、これにあらかじめ混合し
加熱均一化した(8)〜(11)を徐々に添加し、ホモミキ
サーで攪拌乳化させる。冷却後、(18)を添加する。
(実施例4) 固型粉末アイシヤドウ
実施例4 比較例4
(重量%)
(1) 酸化チタン 3.00 3.00
(2) マイカ 15.00 35.00
(3) 製造例2に係る粉体 30.00−
(4) タルク 18.00 28.00
(5) カオリン 6.00 6.00
(6) 黄酸化鉄 3.60 3.60
(7) 黒酸化鉄 4.00 4.00
(8) グンジヨウ 14.30 14.30
(9) スクワラン 6.00 6.00
(10) 防腐剤 0.05 0.05(11)香料 0.05 0.05
100.00 100.00
製造方法
(1)〜(8)を混合粉砕後均一化し、これに(9)〜(11)を
添加して混合均一化する。その後、これを金皿に
充填し、圧縮成型機にてプレス成型する。
上記実施例及び比較例について、官能評価試験
及びガス透過性試験を行つた。
官能評価試験は、女子30名のパネルを被験者と
して、のび、密着感、化粧持ちの3項目を5段階
評価法にて実施した。その結果を表2に示した。[Table] <Effects> Further, the effects of the present invention will be explained in detail with reference to Examples. (Example 1) Solid foundation Example 1 Comparative example 1 (% by weight) (1) Titanium oxide 10.0 10.0 (2) Sericite 15.0 30.0 (3) Talc 23.3 33.3 (4) Powder according to Production example 1 25.0 − (5) Red iron oxide 1.0 1.0 (6) Yellow iron oxide 2.0 2.0 (7) Black iron oxide 0.3 0.3 (8) Liquid paraffin 15.0 15.0 (9) Silicone oil 8.0 8.0 (10) Preservative 0.2 0.2 (11) Fragrance 0.2 0.2 100.0 100.0 Manufacturing method The ingredients (1) to (7) are mixed and pulverized, then homogenized, and (8)
Add ~(11) and mix to make it homogeneous. Thereafter, this is filled into a metal plate and press-molded using a compression molding machine. (Example 2) Pour-in type foundation Example 2 Comparative example 2 (% by weight) (1) Titanium oxide 12.0 12.0 (2) Sericite 14.1 32.1 (3) Powder according to Production Example 1 18.0 - (4) Red iron oxide 1.1 1.1 (5) Yellow iron oxide 2.1 2.1 (6) Black iron oxide 0.3 0.3 (7) Liquid paraffin 30.0 30.0 (8) Vaseline 10.0 10.0 (9) Silicone oil 5.0 5.0 (10) Microcrystalline wax 7.0 7.0 (11) Preservative Agent 0.2 0.2 (12) Fragrance 0.2 0.2 100.0 100.0 Production method (1) to (6) were mixed and pulverized and homogenized, and this was added to (7) to (11) that had been mixed in advance and dissolved by heating, and the mixture was stirred and homogenized. Add the remainder (12) and pour into the designated container. (Example 3) Emulsified foundation Example 3 Comparative example 3 (% by weight) (1) Titanium oxide 1.90 1.90 (2) Talc 1.12 6.12 (3) Powder according to Production Example 2 9.00 - (4) Red iron 0.15 0.15 (5) Yellow iron oxide 0.27 0.27 (6) Black iron oxide 0.06 0.06 (7) Kaolin 6.00 10.00 (8) Ceresin 3.50 3.50 (9) Paraffin wax 1.50 1.50 (10) Liquid lanolin 1.50 1.50 (11) Liquid paraffin 13.5 0 13.50 (12)POE(20) 1.00 1.00 Sorbitan monooleate (13) Sorbitan monooleate 1.00 1.00 (14) Glyceryl monostearate
0.70 0.70 (15) Purified water 55.20 55.20 (16) Carboxymethylcellulose
0.40 0.40 (17) Propylene glycol 3.00 3.00 (18) Preservative 0.10 0.10 (19) Fragrance 0.10 0.10 100.00 100.00 Production method (1) to (7) were mixed and ground, homogenized, and this was mixed in advance and heated (12) Add to (18) and homogenize with a homomixer. Thereafter, (8) to (11), which have been mixed in advance and homogenized by heating, are gradually added thereto, and the mixture is stirred and emulsified using a homomixer. After cooling, (18) is added. (Example 4) Solid powder eyeshadow Example 4 Comparative example 4 (% by weight) (1) Titanium oxide 3.00 3.00 (2) Mica 15.00 35.00 (3) Powder according to Production Example 2 30.00− (4) Talc 18.00 28.00 (5) Kaolin 6.00 6.00 (6) Yellow iron oxide 3.60 3.60 (7) Black iron oxide 4.00 4.00 (8) Gunjiyo 14.30 14.30 (9) Squalane 6.00 6.00 (10) Preservative 0.05 0.05 (11) Fragrance 0.05 0.05 100 .00 100.00 Manufacturing Methods (1) to (8) are mixed and pulverized and homogenized, and (9) to (11) are added thereto and mixed and homogenized. Thereafter, this is filled into a metal plate and press-molded using a compression molding machine. A sensory evaluation test and a gas permeability test were conducted on the above Examples and Comparative Examples. The sensory evaluation test was conducted on a panel of 30 women using a five-point evaluation method on three items: spreadability, adhesion, and makeup durability. The results are shown in Table 2.
【表】
上表に示されるように、本発明の実施例の方
が、のび、密着感、化粧持ちのいずれにおいても
比較例よりも高い評価を得ていた。
次に、ガス透過性試験は以下のように行つた。
ヒト前腕部に16cm2の広さに試料を塗布し、ガス採
集器を密着させ、内部を窒素ガスで置換した後、
圧力を0.5Kg/cm2とし、そのまま2時間静置する。
その後採集したガスをガスクロマトグラフイーに
て分析し、炭酸ガス濃度を測定した。試料未塗布
部のガス濃度を100として、各実施例及び各比較
例のガス透過率を計算した。この測定を10名のパ
ネルについて行い、その平均値を表3に示した。[Table] As shown in the table above, the examples of the present invention were rated higher than the comparative examples in terms of spreadability, adhesion, and makeup durability. Next, a gas permeability test was conducted as follows.
The sample was applied to a 16 cm 2 area on the human forearm, a gas collector was placed in close contact with the sample, and the inside was replaced with nitrogen gas.
The pressure was set to 0.5 Kg/cm 2 and the mixture was allowed to stand for 2 hours.
Thereafter, the collected gas was analyzed by gas chromatography to measure the carbon dioxide concentration. The gas permeability of each Example and each Comparative Example was calculated by setting the gas concentration of the sample-unapplied area to 100. This measurement was performed on a panel of 10 people, and the average values are shown in Table 3.
【表】【table】
【表】
上表より明らかなように、本発明の実施例の方
が比較例よりもガス透過率が大きく、通気性に優
れていた。
以上のように、本発明においては、板状で且つ
多孔性である粉体を用いることにより、従来のよ
うに多孔性粉体と板状粉体を併用することなく、
平滑性、密着性及び通気性のいずれにおいても優
れた化粧料を提供することができた。
また、本発明で使用する板状多孔性粉体は、ラ
イカイ機等による粉砕、混合処理等を行つても、
多孔性構造が損なわれることがないため、化粧料
に配合したとき、十分な通気性を与えることがで
きるものであつた。[Table] As is clear from the above table, the examples of the present invention had higher gas permeability and superior air permeability than the comparative examples. As described above, in the present invention, by using a plate-shaped and porous powder, there is no need to use porous powder and plate-shaped powder together as in the past.
It was possible to provide a cosmetic with excellent smoothness, adhesion, and breathability. In addition, the plate-shaped porous powder used in the present invention can be crushed and mixed using a Raikai machine, etc.
Since the porous structure is not impaired, when it is blended into cosmetics, it can provide sufficient air permeability.
Claims (1)
して成る板状多孔性粉体を配合することを特徴と
する、化粧料。 2 珪藻土に板状結晶のカオリンと長石とを焼結
して成る板状多孔性粉体の配合量が、1〜70重量
%であることを特徴とする、特許請求の範囲第1
項に記載の化粧料。[Scope of Claims] 1. A cosmetic comprising diatomaceous earth mixed with a plate-shaped porous powder obtained by sintering plate-shaped crystals of kaolin and feldspar. 2. Claim 1, characterized in that the amount of the plate-shaped porous powder made by sintering diatomaceous earth with plate-shaped crystals of kaolin and feldspar is 1 to 70% by weight.
Cosmetics listed in section.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5720787A JPS63222108A (en) | 1987-03-11 | 1987-03-11 | Cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5720787A JPS63222108A (en) | 1987-03-11 | 1987-03-11 | Cosmetic |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63222108A JPS63222108A (en) | 1988-09-16 |
| JPH0515686B2 true JPH0515686B2 (en) | 1993-03-02 |
Family
ID=13049062
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5720787A Granted JPS63222108A (en) | 1987-03-11 | 1987-03-11 | Cosmetic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63222108A (en) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6019281B2 (en) * | 1976-07-28 | 1985-05-15 | ポ−ラ化成工業株式会社 | cosmetics |
| JPS55160711A (en) * | 1979-05-31 | 1980-12-13 | Pola Chem Ind Inc | Powder cosmetic composition |
| DE3237264A1 (en) * | 1982-10-08 | 1984-04-12 | Basf Ag, 6700 Ludwigshafen | METHOD FOR PRODUCING EFFECT PIGMENTS COATED WITH METAL OXIDE |
| JPS61176513A (en) * | 1985-01-30 | 1986-08-08 | Pentel Kk | Solid cosmetic |
-
1987
- 1987-03-11 JP JP5720787A patent/JPS63222108A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63222108A (en) | 1988-09-16 |
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