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JPS6141322B2 - - Google Patents
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JPS6141322B2 - - Google Patents

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Publication number
JPS6141322B2
JPS6141322B2 JP52154208A JP15420877A JPS6141322B2 JP S6141322 B2 JPS6141322 B2 JP S6141322B2 JP 52154208 A JP52154208 A JP 52154208A JP 15420877 A JP15420877 A JP 15420877A JP S6141322 B2 JPS6141322 B2 JP S6141322B2
Authority
JP
Japan
Prior art keywords
powder
colored
water
inorganic
colored metal
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
Application number
JP52154208A
Other languages
Japanese (ja)
Other versions
JPS5486633A (en
Inventor
Masaaki Horino
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.)
Pola Orbis Holdings Inc
Original Assignee
Pola Chemical Industries 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 Pola Chemical Industries Inc filed Critical Pola Chemical Industries Inc
Priority to JP15420877A priority Critical patent/JPS5486633A/en
Publication of JPS5486633A publication Critical patent/JPS5486633A/en
Publication of JPS6141322B2 publication Critical patent/JPS6141322B2/ja
Granted legal-status Critical Current

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  • Cosmetics (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Description

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

本発明は無機粉末の表面特性を維持し、且つ従
来にない着色効果を有した着色加工粉末を配合し
てなるメークアツプ用の化粧料に関するものであ
る。 従来一般に使用されている化粧料用の無機ある
いは有機の粉体には、タルク、カオリン、二酸化
チタン、酸化亜鉛、セリサイト、合成雲母、白雲
母、炭酸マグネシウム、炭酸カルシウム、ベント
ナイト、珪酸マグネシウム等の無機粉体、有機粉
体では微結晶セルロース、シルクパウダー、ナイ
ロンパウダー、ポリエチレンパウダー、ステアリ
ン酸マグネシウム、ミリスチン酸亜鉛等があるが
白色から白灰色のものが殆どである。これらの粉
体は通常、赤色226号、赤色202号、赤色206部、
橙色203号、黄色4号アルミニウムレーキ、カー
ボンブラツク等の有機顔料あるいは黄酸化鉄、赤
色酸化鉄、紫色酸化鉄、黒色酸化鉄、群青、マン
ゴバイオレツト、酸化クロム、水酸化クロム等の
無機顔料との混合による調色により化粧料の望む
べき色の選択を可能にする。しかしながら、数種
の原料が組合せられた混合系化粧料においては、
粉体と顔料との結晶形、親和性、比重、粒度分
布、表面活性等の相違により、製造時、保管時、
輸送時に色分れ、偏析、色斑等が生じ製品の品質
を著しく低下されるのが通例である。また実際に
化粧料を皮膚に塗布した場合においても、皮膚表
面に分泌される油分、水分、塩分等により、経時
で各顔料が濡れの現象を進行するため色味が濃く
なる一方、粉体は濡れて若干透明性が上つても依
然として白色ないしは白灰色を呈するので、皮膚
表面上での色分れ現象を生じ、その結果、肌への
なじみが悪く浮いた感じとなり密着性の乏しい仕
上りとなつてしまう欠点があり、望ましいもので
はなかつた。 本発明者は上記の欠点を解決すべく種々実験研
究の結果、このような欠点のない化粧料を見出す
に到つた。 本発明は、無機粉末を、水溶性珪酸塩及び/又
は水溶性活性剤を加えた精製水に酸を用いずある
いは用いて分散せしめ、これに酸あるいは精製水
にて予め溶解させておいた有色金属化合物の溶液
を加え、次いでこれを撹拌しながらアルカリを添
加しPH7.5〜13.0として有色金属水酸化物を無機
粉末の表面に沈着せしめ、これを取り出し、水
洗、乾燥させて得られた着色加工粉末を0.5〜98
%配合してなるメークアツプ用の化粧料に関する
もである。 本発明に適用される上記着色加工粉末において
無機粉末と有色金属化合物との構成割合は、1:
0.01〜1:0.6の範囲が適当であり、これより前
者の多いものを配合した化粧料の場合は経時変化
を頗る受けやすく、また化粧効果としても“浮
き”のある仕上り感となり本発明の目的に適わな
い。また後者の多い場合は有色金属化合物特有の
“くすみ”が強張され、これまた望ましい化粧効
果を付与することはできない。 本発明の着色加工粉末に適用される無機粉末と
しては耐酸性、耐アルカリ性で且つ不溶性のもの
が選択されるが、例えばカオリン、カオリオナイ
ト、ナクライト、デツカイト、ハロイサイト、メ
タハロイサイト、ヘクトライト、モンモリロナイ
ト、ハイデライト、ノントロナイト、サポナイ
ト、ゼオライト、ベントナイト、セリサイト、バ
イロフイライト、バーミキユライト、ブラベサイ
ト、バーライト、ロウ石、ソーダ長石、硬玉、ネ
フエライト、葉長石、鱗雲母、ベタライト、マン
グリゴン石、白雲母、金雲母、黒雲母、タルク、
石英、酸化ケイ素、ケイソウ土、ケイ酸カルシウ
ム、ケイ酸マグネシウム、硫酸バリウム、酸化ア
ルミニウム等の透明性無機顔料が挙げられ、平均
粒子径が0.2μ〜50μのものが好ましい。その
他、酸化チタン、酸化亜鉛、酸化チタンコーテイ
ツドマイカ、オキシ塩化ビスマス、ビスマスコー
テイツドマイカ、酸化チタンコーテイツドタル
ク、硫酸バリウムコーテイツド酸化チタン等があ
る。ただ、透明性無機顔料の方が、着色加工粉末
として化粧料に配合した場合、「塗布色と外観色
の一致性」「肌へのなじみ具合(密着性)」等の化
粧効果で著しく優れているものが提供される。本
発明に用いる着色加工粉末においては、これらの
無機粉末と、特願昭52−154947号の着色加工粉末
を得るときに適用される有機粉末とをを組合せて
用いることができる。このように無機粉末と有機
粉末とを組合せた場合には、後述される着色加工
粉末の製造方法により、結果として無機粉末と有
機粉末とのそれぞれの表面に有色金属水酸化物が
沈着されたものが得られる。 また本発明の着色加工粉末に適用される有色金
属化合物としては有色金属炭酸化合物、有色金属
硫酸化合物、有色金属硝酸化合物、有色金属水酸
化々合物、有色金属塩化物等の水溶性のものが選
択され、更に具体的に述べれば、有色金属炭酸化
合物としては炭酸コバルト、炭酸鉄、炭酸クロ
ム、炭酸ニツケル、炭酸マンガン等であり、有色
金属硫酸化合物としては硫酸クロム、硫酸コバル
ト、硫酸第二鉄、硫酸銅、硫酸マンガン等であ
り、有色金属硝酸化合物としては硝酸コバルト、
硝酸クロム、硝酸ニツケル等であり、有色金属水
酸化化合物としては水酸化鉄、水酸化クロム、水
酸化ニツケル、水酸化コバルト、水酸化マンガン
等であり、有色金属塩化物としては塩化第一鉄、
塩化第二鉄、塩化コバルト、塩化マンガン等であ
る。 次に本発明に適用される着色加工粉末の製造方
法の詳細を説明する。 方法 5゜〜80℃の精製水100〜1000部に0.1〜10重量
%の水溶性珪酸塩及び/又は水溶性活性剤を用い
て無機粉末の一種又は二種以上を10〜100部撹拌
しながら徐々に加え、更に15分〜3時間撹拌を続
けて分散せしめ、次いで5゜〜80℃にて硫酸、硝
酸、塩酸等の無機酸(0.01〜5N)あるいは精製
水100〜1000部に予め溶解させておいた有色金属
化合物の溶液を無機粉末と有色金属化合物との割
合が1:0.01〜1:0.6となるように撹拌しなが
ら徐々に加える。更に10分〜3時間撹拌しながら
(必要ならばここで空気導入してもよい)0.01〜
1Nのアンモニア水、水酸化ナトリウム、水酸化
カリウム等のアルカリを用いてPH7.5〜13.0のア
ルカリ領域に移行させると粉末の表面に有色金属
水酸化物が沈着(含浸吸着)する。 その後、これを取出し、水洗し、風乾或いは40
〜100℃の熱風乾燥等により着色加工粉末を得る
ものである。 方法 5゜〜80℃の精製水100〜1000部に0.1〜10重量
%の水溶性珪酸塩及び/又は水溶性活性剤を用い
て無機粉末の一種又は二種以上を10〜500部撹拌
しながら徐々に加え、更に10分〜5時間撹拌を続
けて分散せしめ、この分散溶液に5゜〜80℃にて
硫酸、硝酸、塩酸等の無機酸(0.01〜3N)を用
いてPH2.5〜6.5の酸性領域になるように調整し、
充分に撹拌しながら、次いで硫酸、硝酸、塩酸等
の無機酸(0.01〜3N)又は精製水30〜1000部に
予め溶解させておいた有色金属化合物の溶液を無
機粉末と有色金属化合物との割合が1:0.01〜
1:0.6となるように撹拌しながら徐々にこれに
加え、更に撹拌を続けながら(必要ならばここで
空気導入してもよい)0.1〜5Nのアンモニア水、
水酸化ナトリウム、水酸化カリウム等のアルカリ
を用いてPH7.5〜13.0のアルカリ領域に移向させ
ると粉末の表面に有色金属水酸化物が沈着する。
その後、これを取出し、水洗し風乾或いは40゜〜
100℃の熱風乾燥等により着色加工粉末を得るも
のである。 上記の着色加工粉末の製造過程中に用いられる
水溶性珪酸塩には珪酸ナトリウム、オルト珪酸ナ
トリウム、セスキ珪酸ナトリウム水和物、メタ珪
酸ナトリウム、トリ珪酸ナトリウム、テトラ珪酸
ナトリウム、メタ珪酸カリウム、メタ珪酸カリウ
ム水和物、ジ珪酸カリウム、ジ珪酸水和物、テト
ラ珪酸水和物、オルト珪酸カリウム、オルト珪酸
リチウム、ジ珪酸水リチウム、テトラ珪酸リチウ
ム、オルト珪酸アンモニウム、メタ珪酸アンモニ
ウムが挙げられ、また水溶性活性剤としてはP.
O.E.ソルビタン脂肪酸エステル、P.O.E.ソルビ
トール脂肪酸エステル、P.O.E.脂肪酸エステ
ル、P.O.E.高級アルコールエーテル、P.O.E.ア
ルキルアリルエーテル、P.O.E.ラノリン誘導
体、P.O.E.ヒマシ油誘導体、P.O.E.プロピレ
ン、P.O.E.セチルアルコールエーテル、P.O.E.
アルキルアミンアマイドのようなHLBが約10以
上の非イオン界面活性剤、高級脂肪酸のアルカリ
金属塩や有機アミン塩(例えばトリエタノールア
ミン)のようなアニオン活性剤、第一級アミン
塩、第4級アンモニウム塩、イミダゾール誘導体
のようなカチオン界面活性剤、アルキルグリシン
型・ベタイン型・イミダゾリン型、ポリグリコー
ルアミン硫酸エステル型・アルキルアミンスルホ
ン酸型の両性活性剤が用いられる。 これら水溶性珪酸塩や水溶性活性剤の使用は、
本発明に用いる着色加工粉末を得る上で、有色金
属化合物の分散性を高めるため、粉体としての凝
集をすることが殆どなく、単一粒子の有色金属水
酸化物が無機粉末の表面に均一に沈着し、結果的
に着色効果の向上をはかることができる。無機粉
末において、その表面の濡れの問題から水とのな
じみが悪いものは、上記水溶性珪酸塩や水溶性活
性剤を使用することが濡れの改善に望ましいもの
である。 また本発明においては方法及び方法にて得
られた着色加工粉末を500゜〜1200℃で1〜24時
間程度焼成処理を施すことにより、より安定な色
調及び色調幅の拡大化を図ることも可能である。
この際の焼成雰囲気としては700〜760Hgの減圧
下、酸化、還元等あるいは不活性雰囲気より適宜
選択されるものである。 上記の方法により得られた着色加工粉末は単に
無機粉末の表面に有色金属水酸化物が付着したも
のではなく有色金属水酸化物を含浸したもので、
これらが一体となつて挙動するものであり、分散
性に優れ且つ脆弱であるので特に複雑な粉砕工程
を要しないもである。しかも酸、アルカリに対し
て安定で優れているものである。 次に本発明に適用される着色加工粉末の製造例
を示す。 製造例 1 70℃の精製水1000mlにP.O.E.ソルビタンモノ
ラウレート10gを加え5分間ジエツトアジターで
充分に撹拌し均一な活性剤水溶液とする。この液
にタルク100gを徐々に加えて30分間ジエツトア
ジターで撹拌、分散せしめ、次いで予め塩化第二
鉄13gを100mlの精製水に溶解せしめておいた溶
液を徐々に加える。更に20分間撹拌した後、1N
水酸化ナトリウム溶液を加えPH9.5にし、1時間
撹拌し後遠心沈降させ、1000mlの水でデカンテー
シヨンをPH7.8になるまで繰返し、100℃で熱風乾
燥させるとくちなし色のタルクの着色加工粉末92
gが得られた。 前記製造例1の着色加工粉末を酸化雰囲気800
℃で24時間焼成するとトノコ色のタルクの着色加
工粉末が得られた。 製造例 2 50℃の精製水1000mlにメタケイ酸ナトリウム8
gを加え20分間ジエツトアジターで撹拌し均一な
溶液とする。この液にベントナイト100gを徐々
に加え1時間ジエツトアジターで撹拌し、充分に
分散せしめる。この分散液に23℃の0.01Nの塩酸
を加えPH6.3として充分に撹拌しながら次いで炭
酸コバルト13gを0.1N塩酸50mlに溶解せしめて
おいた溶液を除々に加え30分間撹拌する。ついで
コンプレツサーからノズルを通し強力に空気を吹
きこみ濃アンモニア水を加えて1時間撹拌し、取
出し、遠心分離機で遠心沈澱せしめ、更にデカン
テーシヨンをくり返しPH7.6になるまで水洗し40
℃で乾燥するとパステルブルーのベントナイトの
着色加工粉末96gが得られた。 前記製造例2の着色加工粉末を弱還元雰囲気で
700℃9時間の条件で焼成処理したところケンブ
リツチブルーの着色加工粉末が得られた。 製造例 3 70℃の精製水1000mlにメタケイ酸ナトリウム5
g、P.O.E.ソルビタンモノラウレート3gを加
え5分間ジエツトアジターで充分に撹拌し均一な
溶液とする。 この液にケイ酸カルシウム100gを徐々に加え
て30分間ジエツトアジターで撹拌、分散せしめ、
次いで予め塩化第二鉄13gを100mlの精製水に溶
解せしめておいた溶液を徐々に加える。更に20分
間撹拌した後、1N水酸化ナトリウム溶液を加え
PH9.5にし、1時間撹拌した後遠心沈降させ、
1000mlの水でデカンテーシヨンをPH7.8になるま
で繰返し、100℃で熱風乾燥させるとブルーのケ
イ酸カルシウムの着色加工粉末92gが得られた。 上記の如くして得られた着色加工粉末は、従来
になく無機粉末の表面特性を維持することが可能
であり、更に着色効果が極めて優れているので化
粧料、特にプレストパウダー、ダステイングパウ
ダー、フアンデーシヨン等のメイクアツプ化粧料
に配合せしめた場合、経時にても変色せず、化粧
効果的には皮膚へのなじみ密着性に優れたものが
提供し得るものであり、更に加えるならば、化粧
の浮きを防止すると共に外観色と塗布色とが一致
しやすく、しかも着色力に富んでいるので肌色を
中心とした幅広い色種の選択ができるものであ
る。 次に後記実施例1に示すプレストパウダー
()と従来のプレストパウダー()※につい
て、女性100名に3週間使用させた結果の官能評
価を示す。
The present invention relates to a make-up cosmetic containing a colored processed powder that maintains the surface characteristics of an inorganic powder and has an unprecedented coloring effect. Conventionally used inorganic or organic powders for cosmetics include talc, kaolin, titanium dioxide, zinc oxide, sericite, synthetic mica, muscovite, magnesium carbonate, calcium carbonate, bentonite, magnesium silicate, etc. Inorganic powders and organic powders include microcrystalline cellulose, silk powder, nylon powder, polyethylene powder, magnesium stearate, zinc myristate, etc., but most are white to whitish-gray in color. These powders are usually Red No. 226, Red No. 202, Red No. 206,
Organic pigments such as orange No. 203, yellow No. 4 aluminum lake, carbon black, etc. or inorganic pigments such as yellow iron oxide, red iron oxide, purple iron oxide, black iron oxide, ultramarine blue, mango violet, chromium oxide, chromium hydroxide, etc. It is possible to select the desired color of cosmetics by toning by mixing. However, in mixed cosmetics that combine several types of raw materials,
Due to differences in crystal form, affinity, specific gravity, particle size distribution, surface activity, etc. between the powder and pigment, during manufacturing, storage,
It is common for color separation, segregation, color spots, etc. to occur during transportation, which significantly deteriorates the quality of the product. Furthermore, even when cosmetics are actually applied to the skin, the pigments become wet over time due to the oil, water, salt, etc. secreted on the skin surface, so the color becomes darker. Even if it becomes slightly transparent when wet, it still appears white or whitish-gray, which causes color separation on the skin surface, resulting in poor adhesion and a floating feeling on the skin. It was not desirable because it had the disadvantage of As a result of various experimental studies aimed at solving the above-mentioned drawbacks, the present inventors have discovered a cosmetic that does not have these drawbacks. In the present invention, an inorganic powder is dispersed in purified water to which a water-soluble silicate and/or a water-soluble activator has been added, without or using an acid, and a colored powder that has been dissolved in advance with an acid or purified water is dispersed. A solution of a metal compound is added, and then an alkali is added while stirring to adjust the pH to 7.5 to 13.0, and a colored metal hydroxide is deposited on the surface of the inorganic powder.The colored metal hydroxide is then taken out, washed with water, and dried. Processed powder 0.5~98
This article relates to a make-up cosmetic containing %. In the colored processed powder applied to the present invention, the composition ratio of the inorganic powder and the colored metal compound is 1:
A range of 0.01 to 1:0.6 is appropriate, and cosmetics containing more of the former are more susceptible to changes over time, and also have a "lifting" finish, which is the object of the present invention. Not suitable for Furthermore, if the latter is present in large quantities, the "dullness" characteristic of colored metal compounds will be intensified, making it impossible to impart desirable cosmetic effects. The inorganic powder to be applied to the colored processed powder of the present invention is selected from acid-resistant, alkali-resistant, and insoluble powders, such as kaolin, kaolionite, nacrite, detsuite, halloysite, metahalloysite, hectorite, montmorillonite, and hyde. Light, nontronite, saponite, zeolite, bentonite, sericite, birophyllite, vermiculite, brabesite, barlite, waxite, soda feldspar, jadeite, nephelite, foliolite, lepidolite, betalite, mangligonite, Muscovite, phlogopite, biotite, talc,
Examples include transparent inorganic pigments such as quartz, silicon oxide, diatomaceous earth, calcium silicate, magnesium silicate, barium sulfate, and aluminum oxide, and those having an average particle size of 0.2 μ to 50 μ are preferable. Other examples include titanium oxide, zinc oxide, titanium oxide coated mica, bismuth oxychloride, bismuth coated mica, titanium oxide coated talc, and barium sulfate coated titanium oxide. However, when transparent inorganic pigments are blended into cosmetics as colored processed powders, they are significantly superior in terms of cosmetic effects such as consistency between applied color and external color, and how well they blend into the skin (adhesion). What you have is provided. In the colored processed powder used in the present invention, these inorganic powders can be used in combination with the organic powder used when obtaining the colored processed powder described in Japanese Patent Application No. 154947/1983. When an inorganic powder and an organic powder are combined in this way, colored metal hydroxides are deposited on the surfaces of each of the inorganic powder and organic powder as a result of the colored processed powder manufacturing method described below. is obtained. The colored metal compounds that can be applied to the colored processed powder of the present invention include water-soluble ones such as colored metal carbonate compounds, colored metal sulfate compounds, colored metal nitrate compounds, colored metal hydroxide compounds, and colored metal chlorides. More specifically, colored metal carbonate compounds include cobalt carbonate, iron carbonate, chromium carbonate, nickel carbonate, manganese carbonate, etc., and colored metal sulfate compounds include chromium sulfate, cobalt sulfate, and ferric sulfate. , copper sulfate, manganese sulfate, etc. Colored metal nitrate compounds include cobalt nitrate,
Chromium nitrate, nickel nitrate, etc. Colored metal hydroxide compounds include iron hydroxide, chromium hydroxide, nickel hydroxide, cobalt hydroxide, manganese hydroxide, etc. Colored metal chlorides include ferrous chloride,
These include ferric chloride, cobalt chloride, manganese chloride, etc. Next, details of the method for producing colored processed powder applied to the present invention will be explained. Method: Add 10 to 100 parts of one or more inorganic powders to 100 to 1000 parts of purified water at 5° to 80°C using 0.1 to 10% by weight of a water-soluble silicate and/or water-soluble activator while stirring. Gradually add it and continue stirring for another 15 minutes to 3 hours to disperse it, then pre-dissolve it in 100 to 1000 parts of an inorganic acid such as sulfuric acid, nitric acid, or hydrochloric acid (0.01 to 5N) or purified water at 5° to 80°C. The prepared colored metal compound solution is gradually added while stirring so that the ratio of inorganic powder to colored metal compound is 1:0.01 to 1:0.6. While stirring for another 10 minutes to 3 hours (air may be introduced here if necessary) 0.01~
When the powder is moved to an alkaline range of PH7.5 to 13.0 using an alkali such as 1N ammonia water, sodium hydroxide, or potassium hydroxide, colored metal hydroxides are deposited on the surface of the powder (impregnation adsorption). After that, take it out, wash it with water, air dry it or leave it for 40 minutes.
A colored processed powder is obtained by drying with hot air at ~100°C. Method: Add 10 to 500 parts of one or more inorganic powders to 100 to 1000 parts of purified water at 5° to 80°C using 0.1 to 10% by weight of a water-soluble silicate and/or water-soluble activator while stirring. Gradually add the mixture and continue stirring for another 10 minutes to 5 hours to disperse the solution. Add inorganic acid (0.01 to 3N) such as sulfuric acid, nitric acid, or hydrochloric acid to the dispersion solution at 5° to 80°C to adjust the pH to 2.5 to 6.5. Adjust to be in the acidic region of
While thoroughly stirring, a solution of a colored metal compound previously dissolved in 30 to 1000 parts of an inorganic acid (0.01 to 3N) such as sulfuric acid, nitric acid, or hydrochloric acid or purified water is added to the ratio of the inorganic powder to the colored metal compound. 1:0.01~
Gradually add this while stirring so that the ratio is 1:0.6, and then add 0.1 to 5N ammonia water while continuing to stir (air may be introduced here if necessary).
When the powder is brought to an alkaline range of 7.5 to 13.0 using an alkali such as sodium hydroxide or potassium hydroxide, colored metal hydroxides are deposited on the surface of the powder.
After that, take it out, wash it with water and air dry it or dry it at 40°~
A colored processed powder is obtained by drying with hot air at 100°C. The water-soluble silicates used during the manufacturing process of the colored processed powders mentioned above include sodium silicate, sodium orthosilicate, sodium sesquisilicate hydrate, sodium metasilicate, sodium trisilicate, sodium tetrasilicate, potassium metasilicate, metasilicate. Potassium hydrate, potassium disilicate, disilicate hydrate, tetrasilicate hydrate, potassium orthosilicate, lithium orthosilicate, lithium disilicate water, lithium tetrasilicate, ammonium orthosilicate, ammonium metasilicate, and As a water-soluble active agent, P.
OE sorbitan fatty acid ester, POE sorbitol fatty acid ester, POE fatty acid ester, POE higher alcohol ether, POE alkyl allyl ether, POE lanolin derivative, POE castor oil derivative, POE propylene, POE cetyl alcohol ether, POE
Nonionic surfactants with an HLB of about 10 or more such as alkylamine amides, anionic surfactants such as alkali metal salts of higher fatty acids and organic amine salts (e.g. triethanolamine), primary amine salts, quaternary Cationic surfactants such as ammonium salts and imidazole derivatives, amphoteric surfactants of alkylglycine type, betaine type, imidazoline type, polyglycolamine sulfate type and alkylamine sulfonic acid type are used. The use of these water-soluble silicates and water-soluble active agents
In obtaining the colored processed powder used in the present invention, in order to improve the dispersibility of the colored metal compound, there is almost no aggregation as a powder, and a single particle of the colored metal hydroxide is uniformly distributed on the surface of the inorganic powder. As a result, the coloring effect can be improved. For inorganic powders that are poorly compatible with water due to surface wetting problems, it is desirable to use the water-soluble silicate or water-soluble activator described above to improve wetting. In addition, in the present invention, it is also possible to achieve more stable color tone and expand the color tone range by firing the colored processed powder obtained by the method and method at 500° to 1200°C for about 1 to 24 hours. It is.
The firing atmosphere at this time is appropriately selected from a reduced pressure of 700 to 760 Hg, an oxidizing atmosphere, a reducing atmosphere, or an inert atmosphere. The colored processed powder obtained by the above method is not simply an inorganic powder with colored metal hydroxide attached to the surface, but is impregnated with colored metal hydroxide.
These components behave as one, have excellent dispersibility, and are brittle, so a particularly complicated pulverization process is not required. Moreover, it is stable and excellent against acids and alkalis. Next, an example of manufacturing colored processed powder applied to the present invention will be shown. Production Example 1 Add 10 g of POE sorbitan monolaurate to 1000 ml of purified water at 70°C and stir thoroughly for 5 minutes using a jet stirrer to obtain a uniform aqueous activator solution. 100 g of talc is gradually added to this solution and stirred for 30 minutes using a jet stirrer to disperse it, and then a solution prepared by dissolving 13 g of ferric chloride in 100 ml of purified water is gradually added. After stirring for another 20 minutes, 1N
Add sodium hydroxide solution to bring the pH to 9.5, stir for 1 hour, centrifuge sediment, repeat decantation with 1000 ml of water until the pH reaches 7.8, and dry with hot air at 100°C to create a beadless talc color. powder 92
g was obtained. The colored processed powder of Production Example 1 was placed in an oxidizing atmosphere of 800%
When baked at ℃ for 24 hours, a turquoise colored processed powder of talc was obtained. Production example 2 8 ounces of sodium metasilicate in 1000 ml of purified water at 50℃
Add g and stir with a jet stirrer for 20 minutes to make a homogeneous solution. 100 g of bentonite was gradually added to this solution and stirred for 1 hour using a jet stirrer to thoroughly disperse it. To this dispersion, 0.01N hydrochloric acid at 23°C was added to adjust the pH to 6.3. While thoroughly stirring, a solution of 13 g of cobalt carbonate dissolved in 50 ml of 0.1N hydrochloric acid was gradually added and stirred for 30 minutes. Next, air was strongly blown through the nozzle from the compressor, concentrated ammonia water was added, stirred for 1 hour, taken out, centrifuged in a centrifugal separator, and decantated repeatedly until the pH reached 7.6.
After drying at ℃, 96 g of pastel blue colored bentonite powder was obtained. The colored processed powder of Production Example 2 was heated in a weakly reducing atmosphere.
When the powder was fired at 700°C for 9 hours, a Cambridge Blue colored processed powder was obtained. Production example 3 Sodium metasilicate 5 in 1000ml of purified water at 70℃
g. Add 3 g of POE sorbitan monolaurate and stir thoroughly with a jet stirrer for 5 minutes to make a homogeneous solution. Gradually add 100g of calcium silicate to this solution and stir for 30 minutes using a jet stirrer to disperse it.
Next, a solution prepared by dissolving 13 g of ferric chloride in 100 ml of purified water is gradually added. After stirring for an additional 20 minutes, add 1N sodium hydroxide solution.
Adjust the pH to 9.5, stir for 1 hour, and then centrifuge.
Decantation was repeated with 1000 ml of water until the pH reached 7.8, followed by drying with hot air at 100°C to obtain 92 g of blue colored calcium silicate powder. The colored processed powder obtained as described above can maintain the surface characteristics of an inorganic powder like never before, and has an extremely excellent coloring effect, so it can be used in cosmetics, especially pressed powders, dusting powders, etc. When incorporated into make-up cosmetics such as foundations, it does not discolor over time and provides cosmetic effects with excellent adhesion to the skin. It prevents makeup from floating, makes it easy to match the external color with the applied color, and has high tinting power, so you can choose from a wide variety of colors, mainly skin tones. Next, we will show the sensory evaluation of the pressed powder () shown in Example 1 below and the conventional pressed powder (*) after 100 women used it for 3 weeks.

【表】 A:非常に良い B:良い C:普通
※ 後記実施例1の着色加工粉末をタ
ルクに置き換えたプレストパウダー
上記結果より理解される如く、本発明実施例1
のプレストパウダー()は、従来のプレストパ
ウダー()に比べ、「肌へのつき具合」、「塗布
色と外観色の一致性」、「経時による色の変化」、
「肌へのなじみ具合(密着性)」、「総合評価」等の
いずれの官能評価項目においても格段に効果が優
れている。また、後記本発明実施例2のダステイ
ングパウダー、同実施例4のフアンデーシヨン、
同実施例7のフエースパウダー等についても、従
来品との比較のもとに官能評価を行つたが、いず
れも本発明の方が良好な結果が得られた。 次の本発明化粧料の実施例を示す。各成分の配
合割合は重量部である。
[Table] A: Very good B: Good C: Fair * Pressed powder in which the colored processed powder of Example 1 described later was replaced with talc As can be understood from the above results, Example 1 of the present invention
Compared to conventional pressed powder (), pressed powder (2018) has improved "adhesion to the skin", "consistency of applied color and external color", "color change over time",
It is extremely effective in all sensory evaluation items such as "adhesion to the skin" and "overall evaluation." In addition, the dusting powder of Example 2 of the present invention described later, the foundation of Example 4 of the same,
The face powder of Example 7 was also subjected to sensory evaluation based on comparison with conventional products, and in all cases, better results were obtained with the present invention. The following examples of the cosmetics of the present invention are shown below. The mixing ratio of each component is in parts by weight.

【表】 取出しシフターに通してプレス
充填して製品とする
[Table] Pass through the take-out sifter and press to make the product.

【表】 シフターにかけ容器に充填し製
品とする。
[Table] Fill the container with a sifter.
It is considered as a product.

【表】 取出しシフターに通してプレス
充填して製品とする。
[Table] Pass through the take-out shifter and press
Fill it and make it into a product.

【表】 シフターにかけ容器に充填し製
品とする。
[Table] Fill the container with a sifter.
It is considered as a product.

Claims (1)

【特許請求の範囲】[Claims] 1 無機粉末を、水溶性珪酸塩及び/又は水溶性
活性剤を加えた精製水に酸を用いずあるいは用い
て分散せしめ、これに酸あるいは精製水にて予め
溶解させておいた有色金属化合物の溶液を加え、
次いでこれを撹拌しながらアルカリを添加しPH
7.5〜13.0として有色金属水酸化物を無機粉末の
表面に沈着せしめ、これを取り出し、水洗、乾燥
させて得られた着色加工粉末を配合することを特
徴とする化粧料。
1 An inorganic powder is dispersed in purified water to which a water-soluble silicate and/or a water-soluble activator has been added, without or using an acid, and a colored metal compound that has been previously dissolved in an acid or purified water is added to the inorganic powder. Add the solution;
Next, add alkali while stirring to adjust the pH.
7.5 to 13.0, a colored metal hydroxide is deposited on the surface of an inorganic powder, the powder is taken out, washed with water and dried, and a colored processed powder is blended therein.
JP15420877A 1977-12-21 1977-12-21 Cosmetics Granted JPS5486633A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15420877A JPS5486633A (en) 1977-12-21 1977-12-21 Cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15420877A JPS5486633A (en) 1977-12-21 1977-12-21 Cosmetics

Publications (2)

Publication Number Publication Date
JPS5486633A JPS5486633A (en) 1979-07-10
JPS6141322B2 true JPS6141322B2 (en) 1986-09-13

Family

ID=15579198

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15420877A Granted JPS5486633A (en) 1977-12-21 1977-12-21 Cosmetics

Country Status (1)

Country Link
JP (1) JPS5486633A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX152670A (en) * 1981-01-14 1985-10-07 Johnson & Johnson IMPROVED TALCO COMPOSITION
JPS5824510A (en) * 1981-08-05 1983-02-14 Shiseido Co Ltd Foundation having transparent feeling
JPS5998009A (en) * 1982-11-29 1984-06-06 Kanebo Ltd Skin cosmetic
JPS59100167A (en) * 1982-11-30 1984-06-09 Shiseido Co Ltd Coated talc and production thereof
JPH0660088B2 (en) * 1983-01-13 1994-08-10 ポーラ化成工業株式会社 Make-up cosmetics
JPS60221465A (en) * 1984-04-17 1985-11-06 Shiseido Co Ltd Coated talc and its preparation
JPS61286309A (en) * 1985-06-12 1986-12-16 Shiseido Co Ltd Makeup cosmetic
JP2007291090A (en) * 2006-03-31 2007-11-08 Kose Corp Powdery cosmetic
CN111154295A (en) * 2020-01-15 2020-05-15 吉安市中意陶瓷化工有限公司 Environment-friendly green inorganic pigment and preparation method thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2244298C3 (en) * 1972-09-09 1975-06-19 Merck Patent Gmbh, 6100 Darmstadt Pearlescent pigments and processes for their manufacture
JPS5287422A (en) * 1976-01-19 1977-07-21 Shiseido Co Ltd Graphite pigment and toiletry containing same
JPS5299234A (en) * 1976-02-12 1977-08-19 Pola Kasei Kogyo Kk Cosmetics

Also Published As

Publication number Publication date
JPS5486633A (en) 1979-07-10

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