JPH072619A - Mica powder and cosmetic blending the same therein - Google Patents

Mica powder and cosmetic blending the same therein

Info

Publication number
JPH072619A
JPH072619A JP16978693A JP16978693A JPH072619A JP H072619 A JPH072619 A JP H072619A JP 16978693 A JP16978693 A JP 16978693A JP 16978693 A JP16978693 A JP 16978693A JP H072619 A JPH072619 A JP H072619A
Authority
JP
Japan
Prior art keywords
acid
average particle
powder
mica
mica powder
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
JP16978693A
Other languages
Japanese (ja)
Other versions
JP3582662B2 (en
Inventor
Kazuhisa Ono
和久 大野
Shigenori Kumagai
重則 熊谷
Katsumoto Ogawa
克基 小川
Masaru Yamamoto
勝 山本
Kenichiro Sugimori
健一郎 杉森
Akira Suzumura
亮 鈴村
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.)
Topy Industries Ltd
Shiseido Co Ltd
Original Assignee
Topy Industries Ltd
Shiseido 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 Topy Industries Ltd, Shiseido Co Ltd filed Critical Topy Industries Ltd
Priority to JP16978693A priority Critical patent/JP3582662B2/en
Publication of JPH072619A publication Critical patent/JPH072619A/en
Application granted granted Critical
Publication of JP3582662B2 publication Critical patent/JP3582662B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To obtain mica powder excellent in feeling of use and forming properties and replaceable by sericite having hardly any gloss. CONSTITUTION:The mica powder is characterized in that mica is dolomite, phlogopite, biotite or synthetic mica and average particle diameter (A) by laser diffraction method is in the range of the formula 5mum<=A<=20mum and the thickness index (A/B) expressed by a ratio of the above diameter (A) to average particle diameter (B) by sedimentation method is in the range of the formula 1.5<=A/B<=3.5.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、成型性が良好でしか
も光沢が低い性質があるため化粧料の基材として極めて
優れた雲母粉体及び該雲母粉体を配合した使用性及び仕
上がりに優れた化粧料に関するものである。
INDUSTRIAL APPLICABILITY The present invention has excellent moldability and low gloss, and therefore is extremely excellent as a base material for cosmetics. Mica powder is excellent in usability and finish mixed with the mica powder. Cosmetics.

【0002】[0002]

【従来の技術】化粧料には、製品の伸展性、付着性、隠
蔽力及び成形性等を向上させる目的で、各種の体質顔料
が使用されている。このような体質顔料としては、タル
ク、カオリン、セリサイト、雲母等の無機粉末及びナイ
ロンパウダー、ポリエチレンパウダー、アクリル樹脂パ
ウダー及びエポキシ樹脂パウダー等の有機粉末が挙げら
れる。これらの中で雲母は、透明感に優れ、艶があり、
使用感触に優れ伸展性がある等の利点があることから多
く使用されている。最近では、天然雲母だけでなく、合
成雲母も開発されてきた。化粧料用合成雲母について
は、例えば特開昭63−183962号、特開昭63−
185810号及び特開昭63−241072号に開示
されている。
2. Description of the Related Art Various extender pigments are used in cosmetics for the purpose of improving the extensibility, adhesion, hiding power and moldability of products. Examples of such extender pigments include inorganic powders such as talc, kaolin, sericite and mica, and organic powders such as nylon powder, polyethylene powder, acrylic resin powder and epoxy resin powder. Among them, mica has excellent transparency and gloss,
It is often used because of its excellent feel and extensibility. Recently, not only natural mica but also synthetic mica has been developed. Synthetic mica for cosmetics is disclosed, for example, in JP-A-63-183962 and JP-A-63-183962.
No. 185810 and JP-A-63-241072.

【0003】上記したように、雲母は、化粧料の基材と
して優れた性質を持つ反面、光沢が高く、成型性が劣る
欠点があった。それ故、化粧料に配合した場合、化粧料
の艶が高すぎ、しわが目立ち、仕上がりが奇麗でないと
か、耐衝撃性が悪い等の傾向があった。一方、天然雲母
の1種であるセリサイトは、成型性に優れ、且つ光沢が
少ない性質があり、しかも使用感触にも優れているた
め、化粧料の基材として広く使用されている。しかしな
がら、近年は、セリサイトの良質品は枯渇してきてお
り、セリサイトに代替し得る材料の要求は強くなってき
ているが、使用感触、成型性に優れ、且つ光沢の少ない
セリサイトに代替できる雲母粉体は未だ知られていな
い。
As described above, mica has excellent properties as a base material for cosmetics, but has the drawbacks of high gloss and poor moldability. Therefore, when blended in cosmetics, the gloss of the cosmetics was too high, wrinkles were noticeable, the finish was not beautiful, and the impact resistance was poor. On the other hand, sericite, which is one type of natural mica, is widely used as a base material for cosmetics because it has excellent moldability, low gloss, and excellent feeling in use. However, in recent years, the quality products of sericite have been depleted, and the demand for materials that can substitute for sericite is increasing, but it is possible to substitute sericite with excellent feel and moldability and low gloss. Mica powder is not yet known.

【0004】[0004]

【発明が解決しようとする課題】この発明は、このよう
な点に着目してなされたものであり、使用感触、成型性
に優れ、且つ光沢の少ないセリサイトに代替できる化粧
料に好適な雲母粉体を提供することを目的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of the above points, and is suitable for cosmetics which can be replaced with sericite which is excellent in touch and moldability and has low gloss. The purpose is to provide a powder.

【0005】[0005]

【課題を解決するための手段】上記目的を達成するため
本発明者等は鋭意研究の結果、レ−ザー回折法平均粒子
径(A)及び(A)と沈降法平均粒子径(B)の比で示さ
れる厚み指数(A/B)を特定の範囲内とすることによ
り、使用感触、成型性に優れ、且つ光沢の少ないセリサ
イトに代替できる化粧料用雲母粉体が得られるという画
期的な事実を見いだし、本発明に到達した。
In order to achieve the above object, the inventors of the present invention have earnestly studied, and as a result, the average particle diameters (A) and (A) of the laser diffraction method and the average particle diameter (B) of the precipitation method were determined. By setting the thickness index (A / B) indicated by the ratio within a specific range, it is possible to obtain a mica powder for cosmetics that can be used as a substitute for sericite, which has excellent feel and moldability and low gloss. The present invention has been reached by discovering such facts.

【0006】即ち本発明は、白雲母、金雲母、黒雲母若
しくは合成雲母で、レ−ザー回折法平均粒子径(A)が、
5μm≦A≦20μmで、且つ上記(A)と沈降法平均
粒子径(B)の比で示される厚み指数(A/B)が、
1.5≦A/B≦3.5更に好ましくは2.0≦A/B
≦3.0であることを特徴とする雲母粉体及び該雲母粉
体を含有する化粧料である。
That is, the present invention is muscovite, phlogopite, biotite or synthetic mica and has a laser diffraction average particle size (A) of
5 μm ≦ A ≦ 20 μm, and the thickness index (A / B) indicated by the ratio of the above (A) and the average particle diameter by the sedimentation method (B) is
1.5 ≦ A / B ≦ 3.5, more preferably 2.0 ≦ A / B
A mica powder and a cosmetic containing the mica powder, wherein ≦ 3.0.

【0007】本発明の雲母は、白雲母、金雲母、黒雲母
若しくは合成雲母であり、合成雲母は、鉄等の着色元素
を含有しないため、白色度の高い本発明の合成雲母が得
られると共に、成型性、光沢及び使用感触の全てが著し
く改善されるため特に好ましい。白雲母、金雲母若しく
は黒雲母の場合は、成型性及び光沢はかなり改善される
が、感触は多少改善される程度である。合成雲母は、溶
融法、水熱法若しくは固体間反応法によって得られるフ
エロケイ酸塩鉱物であり、良質の結晶の合成雲母粉体
は、カリウム、ナトリウム、マグネシウム、アルミニウ
ム、ケイ素、フッ素等を含有する化合物を一定の割合で
混合し、これを溶融、晶出、冷却後、機械的粉砕を行う
ことにより得られる。代表的な合成雲母としては、次の
ようなものが挙げられる。 KMg3(AlSi310)F2 カリウムフッ素金
雲母 KMg2.5(Si410)F2 カリウム4ケイ素
雲母 NaMg3(AlSi310)F2 ナトリウムフッ素
金雲母
The mica of the present invention is muscovite, phlogopite, biotite or synthetic mica. Since the synthetic mica does not contain a coloring element such as iron, the synthetic mica of the present invention with high whiteness can be obtained. , The moldability, gloss and feel of use are all significantly improved, which is particularly preferable. In the case of muscovite, phlogopite or biotite, the moldability and gloss are considerably improved, but the feel is only slightly improved. Synthetic mica is a ferrosilicate mineral obtained by a melting method, a hydrothermal method, or an inter-solid reaction method, and a high quality crystalline synthetic mica powder contains potassium, sodium, magnesium, aluminum, silicon, fluorine, etc. The compound is obtained by mixing the compounds at a constant ratio, melting, crystallizing, cooling and mechanically pulverizing the mixture. Examples of typical synthetic mica include the following. KMg 3 (AlSi 3 O 10 ) F 2 Potassium Fluoro phlogopite KMg 2.5 (Si 4 O 10 ) F 2 Potassium 4-silicon mica NaMg 3 (AlSi 3 O 10 ) F 2 Sodium Fluoro phlogopite

【0008】本発明の雲母のレザー回折法平均粒子径
(A)は、5μm≦A≦20μmである必要があり、5μ
m未満であると、使用感触が悪く、20μmを越える
と、成型性が悪く、光沢も強くなるため、本発明の効果
を発揮しない。また、本発明の雲母は、上記(A)と沈
降法平均粒子径(B)の比で示される厚み指数(A/
B)が、1.5≦A/B≦3.5である必要があり、
1.5未満であると、使用感触が悪く、また3.5を越
えると、成型性が悪く、光沢も強くなり、本発明の効果
を発揮しない。
Average particle size of the mica of the present invention by the laser diffraction method
(A) needs to be 5 μm ≦ A ≦ 20 μm, and 5 μm
If it is less than m, the feeling of use is bad, and if it exceeds 20 μm, the moldability is poor and the gloss is strong, so that the effect of the present invention is not exhibited. Further, the mica of the present invention has a thickness index (A /
B) must be 1.5 ≦ A / B ≦ 3.5,
When it is less than 1.5, the feeling of use is poor, and when it exceeds 3.5, the moldability is poor and the gloss is strong, so that the effect of the present invention is not exhibited.

【0009】次に、本発明の雲母粉体の製造方法を説明
する。原料雲母は、白雲母、金雲母、黒雲母若しくは合
成雲母である。合成雲母は、公知の方法で製造すればよ
く、例えば合成フッ素金雲母の場合、無水ケイ酸約40
部、無水マグネシウム約30部、酸化アルミニウム約1
3部及びケイフッ化カリウム約17部を配合した後、1
400℃〜1500℃で溶融し、次いで1300℃〜1
400℃で晶出させて、合成フッ素金雲母を得る。これ
らの原料雲母を、順次粗砕機、中粉砕機、微粉砕機にか
けた後、レザー回折法平均粒子径(A)が、5μm≦A≦
20μmで、且つ上記(A)と沈降法平均粒子径(B)
の比で示される厚み指数(A/B)が、1.5≦A/B
≦3.5であるように分級して、本発明の雲母粉体を得
る。
Next, a method for producing the mica powder of the present invention will be described. The raw mica is muscovite, phlogopite, biotite or synthetic mica. The synthetic mica may be produced by a known method. For example, in the case of synthetic fluorine phlogopite, the silicic acid anhydride is about 40
Part, anhydrous magnesium about 30 parts, aluminum oxide about 1
After blending 3 parts and about 17 parts potassium silicofluoride, 1
Melt at 400 ° C-1500 ° C, then 1300 ° C-1
Crystallization is performed at 400 ° C. to obtain synthetic fluorophlogopite. These raw materials mica were sequentially subjected to a coarse crusher, a medium crusher, and a fine crusher, and then the laser diffraction average particle diameter (A) was 5 μm ≦ A ≦
20 μm, and (A) and the average particle size by precipitation method (B)
The thickness index (A / B) indicated by the ratio is 1.5 ≦ A / B
The mica powder of the present invention is obtained by classification so that ≦ 3.5.

【0010】粗砕機、中粉砕機としては、圧縮破砕機、
せん断粗砕機、衝撃破砕機、ロール式,スタンプ式の粗
砕機,中粉砕機等が使用できるが、特にこれらに限定さ
れない。微粉砕機としては、ボール媒体ミル、媒体撹拌
式媒体ミル、ジエツト粉砕機、湿式高速回転ミル、石臼
式ミル等が使用できるが、特にこれらに限定されない。
分級方法は、自然沈降法、遠心沈降法、サイクロン法等
により行えば良い。分級後若しくは分級前に、酸処理、
熱処理若しくは酸処理と熱処理との併用処理を行っても
良い。合成雲母は、酸処理により粒子端面を薄葉化する
ことができ、また熱処理により、フッ素イオンの溶出が
なく、表面活性を少なくすることができる。
As the coarse crusher and the medium crusher, a compression crusher,
A shearing crusher, an impact crusher, a roll type, a stamp type crusher, a medium crusher, etc. can be used, but not limited to these. As the fine pulverizer, a ball medium mill, a medium agitating medium mill, a jet pulverizer, a wet high-speed rotary mill, a stone mill type mill, etc. can be used, but not particularly limited thereto.
The classification method may be a natural sedimentation method, a centrifugal sedimentation method, a cyclone method, or the like. Acid treatment after or before classification,
A heat treatment or a combined treatment of an acid treatment and a heat treatment may be performed. Synthetic mica can be thinned at the end faces of particles by acid treatment, and can be reduced in surface activity by heat treatment without elution of fluorine ions.

【0011】上記酸処理に使用する酸は、無機酸、有機
酸のいずれであってもであっても良いが、強酸を用いた
場合は、雲母の構造が破壊されることがあるので、弱酸
を使用するのが好ましい。無機酸としては、例えば、塩
酸、硝酸、硫酸、塩素酸、過塩素酸、過ヨウ素酸、臭素
酸、リン酸、ホウ酸、炭酸等が挙げられる。有機酸とし
ては、例えば、ギ酸,酢酸、アクリル酸,安息香酸,シ
ュウ酸,マロン酸,コハク酸,グルタル酸,アジピン
酸,ピメリン酸,フタル酸等のカルボン酸、乳酸,リン
ゴ酸,酒石酸,クエン酸等のオキシカルボン酸、グリシ
ン,アラニン,バリン,ロイシン,チロシン,トレオニ
ン,セリン,プロリン,トリプトフアン,メチオニン,
シスチン,チロキシン,アスパラギン酸,グルタミン
酸,リジン,アルギン等のアミノ酸等が挙げられる。
The acid used in the above acid treatment may be either an inorganic acid or an organic acid. However, when a strong acid is used, the structure of mica may be destroyed. Is preferably used. Examples of the inorganic acid include hydrochloric acid, nitric acid, sulfuric acid, chloric acid, perchloric acid, periodic acid, bromic acid, phosphoric acid, boric acid, carbonic acid and the like. Examples of organic acids include formic acid, acetic acid, acrylic acid, benzoic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, phthalic acid, and other carboxylic acids, lactic acid, malic acid, tartaric acid, and citric acid. Oxycarboxylic acids such as acids, glycine, alanine, valine, leucine, tyrosine, threonine, serine, proline, tryptophan, methionine,
Examples thereof include amino acids such as cystine, thyroxine, aspartic acid, glutamic acid, lysine and algin.

【0012】雲母を熱処理する設備方式は、例えば外熱
式加熱炉、内熱式加熱炉、ロータリーキルン等公知のあ
らゆる方法を適用することができる。熱処理雰囲気は、
酸化雰囲気、還元雰囲気、アルゴンガス雰囲気、窒素ガ
ス雰囲気、アンモニアガス雰囲気、真空中等のいずれで
も、或はこれらを組み合わせても良く、目的とする雲母
粉体の用途、機能等に応じて適宜選択すれば良い。雲母
の熱処理温度は、600〜1350℃、好ましくは70
0〜1200℃である。
As a facility system for heat-treating the mica, for example, any known method such as an external heating furnace, an internal heating furnace, a rotary kiln can be applied. The heat treatment atmosphere is
Any of an oxidizing atmosphere, a reducing atmosphere, an argon gas atmosphere, a nitrogen gas atmosphere, an ammonia gas atmosphere, a vacuum, etc., or a combination thereof may be selected as appropriate according to the intended use and function of the mica powder. Good. The heat treatment temperature of mica is 600 to 1350 ° C., preferably 70.
It is 0-1200 degreeC.

【0013】本発明の雲母粉体の化粧料への配合量は、
化粧料全量中の1〜100重量%である。本発明の化粧
料としては、フエーシャル化粧料、メーキャップ化粧
料、ヘア化粧料、浴用剤等広い範囲の化粧料が含まれる
が、特にメーキャップ化粧料、例えばフアンデーショ
ン、粉白粉、アイシャドー、ブラッシャー、化粧下地、
ネイルエナメル、アイライナー、マスカラ、口紅、フア
ンシーパウダー等に好適である。本発明の雲母粉体は、
化粧料に配合されるに当たって必要に応じ、シリコーン
処理、フッ素処理、金属石鹸処理、脂肪酸処理、界面活
性剤処理、或は酸、アルカリ、無機酸類による処理、更
にはこれらの複合処理を行った後配合させても良い。
The content of the mica powder of the present invention in cosmetics is
It is 1 to 100% by weight in the total amount of the cosmetic. The cosmetics of the present invention include a wide range of cosmetics such as facial cosmetics, makeup cosmetics, hair cosmetics and bath agents, but especially makeup cosmetics such as foundation, white powder, eye shadow, blusher, Makeup base,
It is suitable for nail enamel, eyeliner, mascara, lipstick, fanci powder and the like. The mica powder of the present invention is
After being treated with silicone, fluorine, metal soap, fatty acid, surfactant, or with acid, alkali, or inorganic acid, or a combination of these treatments, if necessary before being incorporated into cosmetics. You may mix.

【0014】本発明の化粧料には、本発明の合成雲母粉
体の他に、通常化粧料に用いられる他の成分を必要に応
じて適宜配合することができる。例えばタルク,カオリ
ン,セリサイト,白雲母,金雲母,紅雲母,黒雲母,合
成雲母,リチア雲母,バーミキュライト,炭酸マグネシ
ウム,炭酸カルシウム,珪ソウ土,ケイ酸マグネシウ
ム,ケイ酸カルシウム,ケイ酸アルミニウム,ケイ酸バ
リウム,硫酸バリウム,ケイ酸ストロンチウム,タング
ステン酸金属塩,シリカ,ヒドロキシアパタイト,ゼオ
ライト,窒化ホウ素,セラミックスパウダー等の無機粉
末、ナイロンパウダー,ポリエチレンパウダー,ポリス
チレンパウダー,ベンゾグアナミンパウダー,ポリ四弗
化エチレンパウダー,ジスチレンベンゼンポリマーパウ
ダー,エポキシパウダー,アクリルパウダー,シリコ−
ンパウダー,微結晶性セルロース等の有機粉体、酸化チ
タン,酸化亜鉛等の無機白色顔料、酸化鉄(ベンガ
ラ),チタン酸鉄等の無機赤色系顔料、γ酸化鉄等の無
機褐色系顔料、黄酸鉄,黄土等の
In the cosmetic of the present invention, in addition to the synthetic mica powder of the present invention, other components usually used in cosmetics can be appropriately blended if necessary. For example, talc, kaolin, sericite, muscovite, phlogopite, phlogopite, biotite, synthetic mica, lithia mica, vermiculite, magnesium carbonate, calcium carbonate, diatomaceous earth, magnesium silicate, calcium silicate, aluminum silicate, Inorganic powder such as barium silicate, barium sulfate, strontium silicate, tungstic acid metal salt, silica, hydroxyapatite, zeolite, boron nitride, ceramics powder, nylon powder, polyethylene powder, polystyrene powder, benzoguanamine powder, polytetrafluoroethylene Powder, distyrenebenzene polymer powder, epoxy powder, acrylic powder, silicone
Powder, organic powders such as microcrystalline cellulose, inorganic white pigments such as titanium oxide and zinc oxide, iron oxide (red iron oxide), inorganic red pigments such as iron titanate, inorganic brown pigments such as γ iron oxide, Such as iron citrate and loess

【0015】無機黄色系顔料、四酸酸化鉄,カーボンブ
ラック等の無機黒色系顔料,マンゴバイオレット,コバ
ルトバイオレット等の無機紫色系顔料、酸化クロム,水
酸化クロム,チタン酸コバルト等の無機緑色顔料,群
青,紺青等の無機青色系顔料、酸化チタン被覆雲母,酸
化チタン被覆オキシ塩化ビスマス,オキシ塩化ビスマ
ス,酸化チタン被覆タルク,魚鱗箔,着色酸化チタン被
覆雲母等のパール顔料、アルミニウムパウダー,カッパ
ーパウダー等の金属粉末顔料、赤色201号,赤色20
2号,赤色204号,赤色205号,赤色220号,赤
色226号,赤色228号,赤色405号,橙色203
号,橙色204号,黄色205号,黄色401号及び青
色404号等の有機顔料、赤色3号,赤色104号,赤
色106号,赤
Inorganic yellow pigments, iron tetraoxide, inorganic black pigments such as carbon black, inorganic purple pigments such as mango violet and cobalt violet, inorganic green pigments such as chromium oxide, chromium hydroxide and cobalt titanate, Inorganic blue pigments such as ultramarine blue and navy blue, titanium oxide-coated mica, titanium oxide-coated bismuth oxychloride, bismuth oxychloride, titanium oxide-coated talc, fish scale foil, pearl pigments such as colored titanium oxide-coated mica, aluminum powder, copper powder, etc. Metallic powder pigment, Red No. 201, Red 20
No. 2, Red No. 204, Red No. 205, Red No. 220, Red No. 226, Red No. 228, Red No. 405, Orange No. 203
No. 204, Orange No. 204, Yellow No. 205, Yellow No. 401, Blue No. 404 and other organic pigments, Red No. 3, Red No. 104, Red No. 106, Red

【0016】色227号,赤色230号,赤色401
号,赤色505号,橙色205号,黄色4号,黄色5
号,黄色202号,黄色203号,橙色3号及び青色1
号のジルコニウム,バリウム,若しくはアルミニウムレ
ーキ等の有機顔料、クロロフイル,β−カロチン等の天
然色素、スクワラン,流動パラフイン,ワセリン,マイ
クロクリスタリンワックス,オゾケライト,セレシン,
ミリスチン酸,パルミチン酸,ステアリン酸,オレイン
酸,イソステアリン酸,セチルアルコール,ヘキサデシ
ルアルコール,オレイルアルコール,2−エチルヘキサ
ン酸セチル,パルミチン酸2−エチルヘキシル,ミリス
チン酸2ーオクチルドデシル,ジ2ーエチルヘキサン酸
ネオペンチルグリコール,トリ−2−エチルヘキサン酸
グリセロール,オレイン酸2ーオクチルドデシル,ミリ
スチン酸イソプロピル,トリイソステアリン酸グリセロ
ール,トリヤシ油脂肪酸グリセロール,オリーブ油,ア
ボガド油,ミツロウ,ミリスチン酸ミリスチル,ミンク
油,ラノリン等の各種炭化水素、シリコーン油,高級脂
肪酸,油脂類のエステル類、高級アルコール,ロウ類等
の油性成分、アセトン,トルエン,酢酸ブチル,酢酸エ
ステル等の有機溶剤、アル
Color 227, red 230, red 401
No., Red No. 505, Orange No. 205, Yellow No. 4, Yellow 5
No., Yellow No. 202, Yellow No. 203, Orange No. 3 and Blue No. 1
, Organic pigments such as zirconium, barium or aluminum lake, natural pigments such as chlorophyll, β-carotene, squalane, liquid paraffin, petrolatum, microcrystalline wax, ozokerite, ceresin,
Myristic acid, palmitic acid, stearic acid, oleic acid, isostearic acid, cetyl alcohol, hexadecyl alcohol, oleyl alcohol, cetyl 2-ethylhexanoate, 2-ethylhexyl palmitate, 2-octyldodecyl myristate, di-2-ethylhexanoate neo Pentyl glycol, glycerol tri-2-ethylhexanoate, 2-octyldodecyl oleate, isopropyl myristate, glycerol triisostearate, tricoconut oil fatty acid glycerol, olive oil, avocado oil, beeswax, myristyl myristate, mink oil, lanolin, etc. Various hydrocarbons, silicone oils, higher fatty acids, esters of oils and fats, oily components such as higher alcohols and waxes, organic solvents such as acetone, toluene, butyl acetate and acetic acid esters , Al

【0017】キッド樹脂,尿素樹脂等の樹脂、カンフア
ー,クエン酸アセトルトリブチル等の可塑剤、紫外線吸
収剤、酸化防止剤、防腐剤、界面活性剤、保湿剤、香
料、水、アルコール、増粘剤等が挙げられる。本発明に
よる化粧料の形態は、特に限定されず、例えば粉末状、
ケーキ状、ペンシル状、スチック状、ペレット状、軟膏
状、液状、乳液状、クリーム状等とすることができる。
本発明の雲母粉体は、化粧料用として特に有用なもので
あるが、塗料、プラスチック、ゴム等の添加剤、ゴム等
の離型剤、潤滑剤として使用することもできる。
Resins such as kid resin and urea resin, plasticizers such as camphor and acetoltributyl citrate, ultraviolet absorbers, antioxidants, preservatives, surfactants, humectants, fragrances, water, alcohols, thickeners Agents and the like. The form of the cosmetic according to the present invention is not particularly limited, and for example, powder form,
It can be cake-shaped, pencil-shaped, stick-shaped, pellet-shaped, ointment-shaped, liquid, emulsion, cream-shaped and the like.
The mica powder of the present invention is particularly useful for cosmetics, but it can also be used as an additive for paints, plastics, rubber and the like, a release agent for rubber and the like, and a lubricant.

【0018】[0018]

【実施例】次に、実施例、参考例を挙げて本発明を更に
説明するが、本発明はこれら実施例に限定されない。実
施例、参考例中のレーザー回折法平均粒子径、沈降法平
均粒子径、成型性、光沢の測定値は、以下の方法により
測定したものである。 (レーザー回折法平均粒子径)レーザー回折法平均粒子
径は、体積基準のメジアン径、累積分布の50%に相当
する粒子径であり、レーザー回折式粒度分布測定装置
(堀場製作所製、型式LAー500)により測定した。
The present invention will be further described with reference to Examples and Reference Examples, but the present invention is not limited to these Examples. The measured values of the average particle diameter by laser diffraction method, the average particle diameter by sedimentation method, moldability, and gloss in Examples and Reference Examples are measured by the following methods. (Laser Diffraction Method Average Particle Diameter) The laser diffraction method average particle diameter is a volume-based median diameter, a particle diameter corresponding to 50% of cumulative distribution, and is a laser diffraction type particle size distribution measuring device (manufactured by Horiba Ltd., model LA- 500).

【0019】(沈降法平均粒子径)沈降法平均粒子径
は、体積基準のメジアン径、累積分布の50%に相当す
る粒子径であり、超遠心式自動粒度分布測定装置(堀場
製作所製、 型式CAPAー700)により測定した。 (成型性)雲母粉60部に対し、タルク30部、流動パ
ラフイン9部、界面活性剤1部を混合した。これを、8
0kg/cm2の圧力でプレス成型し、表面硬度をオル
ゼン硬度計(針入硬度)で測定した。評価は、下記基準
により行った。 ◎ 40未満 ○ 40以上50未満 × 50以上 (光沢)アート紙に張り付けたセロテープ粘着面に粉体
を塗布し、日本電色製デジタル携帯用光沢計VG−2P
型で60°ー60°の光沢を測定した。評価は、下記基
準により行った。 −× 3.0未満 −○ 3.0以上3.5未満 ◎ 3.5以上4.5未満 +○ 4.5以上5.0未満 +× 5.0以上
(Average particle diameter of sedimentation method) The average particle diameter of sedimentation method is a volume-based median diameter, a particle diameter corresponding to 50% of cumulative distribution, and is an ultracentrifugal automatic particle size distribution measuring apparatus (manufactured by Horiba, Ltd., model CAPA-700). (Moldability) 30 parts of talc, 9 parts of fluid paraffin, and 1 part of surfactant were mixed with 60 parts of mica powder. This is 8
Press molding was carried out at a pressure of 0 kg / cm 2 , and the surface hardness was measured with an Olsen hardness meter (penetration hardness). The evaluation was performed according to the following criteria. ◎ Less than 40 ○ 40 or more and less than 50 × 50 or more (Gloss) Digital adhesive gloss meter VG-2P made by Nippon Denshoku Co., Ltd. by applying powder to the adhesive surface of cellophane tape attached to art paper.
The 60 ° -60 ° gloss was measured with a mold. The evaluation was performed according to the following criteria. − × less than 3.0 − ○ 3.0 to less than 3.5 ◎ 3.5 to less than 4.5 + ○ 4.5 to less than 5.0 + × 5.0 or more

【0020】実施例 1 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、湿式媒
体ミルで粉砕した後、0.2Mクエン酸により1時間酸
処理し、マッフル炉で900℃、1時間熱処理した。そ
の後、自然沈降法により分級し、レーザー回折法平均粒
子径(A)10.9μm、沈降法平均粒子径(B)4.
0μm、厚み指数(A/B)2.7の本発明の雲母粉体
900gを得た。評価結果を後記表ー1に示す。
Example 1 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were blended, melted at 1400 ° C-1500 ° C, and then 1300 ° C-1400 ° C. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorophlogopite was pulverized with a wet medium mill, then acid-treated with 0.2 M citric acid for 1 hour, and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, the particles were classified by a natural sedimentation method, a laser diffraction method average particle diameter (A) of 10.9 μm, and a sedimentation method average particle diameter (B) of 4.
900 g of the mica powder of the present invention having a thickness of 0 μm and a thickness index (A / B) of 2.7 was obtained. The evaluation results are shown in Table 1 below.

【0021】実施例 2 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、湿式高
速回転ミルで粉砕した後、0.3Mクエン酸により30
分間酸処理し、マッフル炉で900℃、1時間熱処理し
た。その後、自然沈降法により分級し、レーザー回折法
平均粒子径(A)11.5μm、沈降法平均粒子径
(B)4.3μm、厚み指数(A/B)2.7の本発明
の雲母粉体950gを得た。評価結果を後記表ー1に示
す。
Example 2 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were blended, melted at 1400 ° C-1500 ° C, and then 1300 ° C-1400 ° C. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorophlogopite was crushed with a wet high-speed rotary mill, and then 30% with 0.3 M citric acid.
It was acid-treated for a minute and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, the mica powder of the present invention is classified by a natural sedimentation method and has a laser diffraction average particle diameter (A) of 11.5 μm, a sedimentation average particle diameter (B) of 4.3 μm and a thickness index (A / B) of 2.7. 950 g of body were obtained. The evaluation results are shown in Table 1 below.

【0022】実施例 3 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、湿式媒
体ミルで粉砕した後、1N塩酸により1時間酸処理し、
マッフル炉で900℃、1時間熱処理した。その後、自
然沈降法により分級し、レーザー回折法平均粒子径
(A)20.0μm、沈降法平均粒子径(B)5.7μ
m、厚み指数(A/B)3.5の本発明の雲母粉体1K
gを得た。評価結果を後記表ー1に示す。
Example 3 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were blended, melted at 1400 ° C-1500 ° C, and then 1300 ° C-1400 ° C. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorine phlogopite was crushed with a wet medium mill and then acid-treated with 1N hydrochloric acid for 1 hour,
It heat-processed at 900 degreeC for 1 hour in a muffle furnace. Then, classification was carried out by a natural sedimentation method, and a laser diffraction method average particle diameter (A) of 20.0 μm and a sedimentation method average particle diameter (B) of 5.7 μm.
m of the present invention having a thickness index (A / B) of 3.5 m
g was obtained. The evaluation results are shown in Table 1 below.

【0023】実施例 4 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、ボール
媒体ミルで粉砕した後、1N塩酸により1時間酸処理
し、マッフル炉で900℃、1時間熱処理した。その
後、自然沈降法により分級し、レーザー回折法平均粒子
径(A)5.0μm、沈降法平均粒子径(B)3.3μ
m、厚み指数(A/B)1.5の本発明の雲母粉体1K
gを得た。評価結果を後記表ー1に示す。
Example 4 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were blended, melted at 1400 ° C-1500 ° C, and then 1300 ° C-1400 ° C. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorophlogopite was crushed with a ball medium mill, then acid-treated with 1N hydrochloric acid for 1 hour, and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, classification was carried out by a natural sedimentation method, and a laser diffraction method average particle diameter (A) of 5.0 μm and a sedimentation method average particle diameter (B) of 3.3 μm.
m, a mica powder of the present invention having a thickness index (A / B) of 1.5, 1K
g was obtained. The evaluation results are shown in Table 1 below.

【0024】実施例 5 白雲母2kgを、ボール媒体ミルで粉砕した後、自然沈
降法により分級し、レーザー回折法平均粒子径(A)1
0.3μm、沈降法平均粒子径(B)4.3μm、厚み
指数(A/B)4.3の本発明の雲母粉体300gを得
た。評価結果を後記表ー1に示す。 実施例 6 金雲母2kgを、湿式高速回転ミルで粉砕した後、自然
沈降法により分級し、レーザー回折法平均粒子径(A)
12.5μm、沈降法平均粒子径(B)5.0μm、厚
み指数(A/B)2.5の本発明の雲母粉体300gを
得た。評価結果を後記表ー1に示す。
Example 5 2 kg of muscovite was crushed by a ball medium mill and classified by a natural sedimentation method, and a laser diffraction method average particle diameter (A) 1
300 g of the mica powder of the present invention having a particle size of 0.3 μm, an average particle size by sedimentation method (B) of 4.3 μm and a thickness index (A / B) of 4.3 was obtained. The evaluation results are shown in Table 1 below. Example 6 2 kg of phlogopite was pulverized by a wet high-speed rotary mill, and then classified by a natural sedimentation method, and a laser diffraction method average particle diameter (A)
300 g of the mica powder of the present invention having a particle size of 12.5 μm, an average particle size by sedimentation method (B) of 5.0 μm and a thickness index (A / B) of 2.5 was obtained. The evaluation results are shown in Table 1 below.

【0025】比較例 1 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、湿式媒
体ミルで粉砕した後、0.3Mクエン酸により1時間酸
処理し、マッフル炉で900℃、1時間熱処理した。そ
の後、自然沈降法により分級し、レーザー回折法平均粒
子径(A)11.0μm、沈降法平均粒子径(B)2.
5μm、厚み指数(A/B)4.4の雲母粉体1Kgを
得た。評価結果を後記表ー1に示す。
Comparative Example 1 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were mixed and then melted at 1400 ° C to 1500 ° C, and then 1300 ° C to 1400. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorophlogopite was pulverized with a wet medium mill, then acid-treated with 0.3 M citric acid for 1 hour, and heat-treated in a muffle furnace at 900 ° C. for 1 hour. Then, classification was carried out by a natural sedimentation method, and a laser diffraction method average particle diameter (A) of 11.0 μm and a sedimentation method average particle diameter (B) of 2.
1 Kg of mica powder having a thickness of 5 μm and a thickness index (A / B) of 4.4 was obtained. The evaluation results are shown in Table 1 below.

【0026】比較例 2 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母10kgを、湿式高
速回転ミルで粉砕した後、1N塩酸により1時間酸処理
し、マッフル炉で900℃、1時間熱処理した。その
後、自然沈降法により分級し、レーザー回折法平均粒子
径(A)10.0μm、沈降法平均粒子径(B)7.0
μm、厚み指数(A/B)1.4の雲母粉体1Kgを得
た。評価結果を後記表ー1に示す。
Comparative Example 2 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were blended, melted at 1400 ° C-1500 ° C, and then 1300 ° C-1400 ° C. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 10 kg of this synthetic fluorophlogopite was crushed with a wet high-speed rotary mill, then acid-treated with 1N hydrochloric acid for 1 hour, and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, classification was carried out by a natural sedimentation method, and a laser diffraction method average particle diameter (A) of 10.0 μm and a sedimentation method average particle diameter (B) of 7.0.
1 Kg of mica powder having a thickness of μm and a thickness index (A / B) of 1.4 was obtained. The evaluation results are shown in Table 1 below.

【0027】比較例 3 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母5kgを、湿式媒体
ミルで粉砕した後、1N塩酸により1時間酸処理し、マ
ッフル炉で900℃、1時間熱処理した。その後、自然
沈降法により分級し、レーザー回折法平均粒子径(A)
25μm、沈降法平均粒子径(B)10μm、厚み指数
(A/B)2.5の雲母粉体500gを得た。評価結果
を後記表ー1に示す。
Comparative Example 3 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were mixed and then melted at 1400 ° C to 1500 ° C, and then 1300 ° C to 1400. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 5 kg of this synthetic fluorophlogopite was crushed by a wet medium mill, then acid-treated with 1N hydrochloric acid for 1 hour, and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, the particles were classified by the natural sedimentation method, and the average particle diameter (A) by the laser diffraction method was measured.
500 g of mica powder having a particle size of 25 μm, an average particle size by sedimentation method (B) of 10 μm and a thickness index (A / B) of 2.5 was obtained. The evaluation results are shown in Table 1 below.

【0028】比較例 4 無水ケイ酸約40部、酸化マグネシウム約30部、酸化
アルミニウム約13部及びケイフッ化カリウム約17部
を配合した後、1400℃〜1500℃で溶融し、次い
で1300℃〜1400℃で晶出させて、合成フッ素金
雲母を得た。この合成フッ素金雲母5kgを、湿式媒体
ミルで粉砕した後、1N塩酸により1時間酸処理し、マ
ッフル炉で900℃、1時間熱処理した。その後、自然
沈降法により分級し、レーザー回折法平均粒子径(A)
4.4μm、沈降法平均粒子径(B)1.2μm、厚み
指数(A/B)3.3の雲母粉体500gを得た。評価
結果を後記表ー1に示す。
Comparative Example 4 About 40 parts of silicic acid anhydride, about 30 parts of magnesium oxide, about 13 parts of aluminum oxide and about 17 parts of potassium silicofluoride were mixed and then melted at 1400 ° C to 1500 ° C, and then 1300 ° C to 1400. Crystallization was performed at ° C to obtain synthetic fluorophlogopite. 5 kg of this synthetic fluorophlogopite was crushed by a wet medium mill, then acid-treated with 1N hydrochloric acid for 1 hour, and heat-treated at 900 ° C. for 1 hour in a muffle furnace. Then, the particles were classified by the natural sedimentation method, and the average particle diameter (A) by the laser diffraction method was measured.
Thus, 500 g of mica powder having a particle size of 4.4 μm, an average particle size by sedimentation method (B) of 1.2 μm and a thickness index (A / B) of 3.3 was obtained. The evaluation results are shown in Table 1 below.

【0029】[0029]

【表−1】[Table-1]

【0030】次に、本発明の合成雲母粉体を配合した化
粧料の実施例を示す。なお、化粧料の性能は、次表−2
に挙げた項目について、専門パネル20名による5段階
官能評価を行い、20名の平均値に基づき、下記の記号
によって示した。
Next, examples of cosmetics containing the synthetic mica powder of the present invention will be shown. The performance of the cosmetics is shown in Table 2 below.
With respect to the items listed in (1), a five-level sensory evaluation was conducted by 20 specialist panels, and based on the average value of 20 persons, the following symbols were used.

【0031】[0031]

【表−2】 [Table-2]

【0032】(1)つやの評価基準 +× 4.5以上5.0まで +△ 3.5以上4.5未満 ◎ 2.5以上3.5未満 −△ 1.5以上2.5未満 −× 1.0以上1.5未満 (2)のび、つき、なめらかな使用感、化粧肌のきれい
さ、なじみ、密着感の評価基準 ◎ 4.5以上5.0まで ○ 3.5以上4.5未満 □ 2.5以上3.5未満 △ 1.5以上2.5未満 × 1.0以上1.5未満
(1) Shine Evaluation Criteria + × 4.5 to 5.0 + Δ 3.5 to less than 4.5 ◎ 2.5 to less than 3.5 −Δ 1.5 to less than 2.5 − × 1.0 or more and less than 1.5 (2) Evaluation criteria for spread, stickiness, smooth feeling of use, cleanliness of makeup skin, familiarity, and adhesion ◎ 4.5 to 5.0 ○ 3.5 to 4.5 Less than □ 2.5 or more and less than 3.5 △ 1.5 or more and less than 2.5 × 1.0 or more and less than 1.5

【0033】実施例7〜12:両用フアンデション 以下の各成分から、本発明の両用フアンデション7〜1
2を調製した。 (重量%) 1 酸化チタン 7 2 シリコーン処理微粒子酸化チタン※ 10 3 白雲母 8 4 実施例1〜6それぞれの雲母粉体のシリコーン処理品※ 65 5 ナイロンパウダー 2 6 赤色酸化鉄 0.5 7 黄色酸化鉄 1 8 黒色酸化鉄 0.1 9 シリコ−ンオイル 1 10 パルミチン酸2ーエチルヘキシル 9 11 セスキオレイン酸ソルビタン 1 12 防腐剤 0.3 13 香料 0.1 ※ 3部のメチルハイドロジエンポリシロキサンを5部
のジクロルメタンに溶解したものに、粉体97部を混合
し、乾燥後180℃で3時間熱処理した。
Examples 7-12: Dual-purpose fundation From the following components, the dual-purpose foundation 7-1 of the present invention.
2 was prepared. (Wt%) 1 Titanium oxide 7 2 Silicone-treated fine particle titanium oxide * 10 3 Muscovite 8 4 Silicone-treated product of each mica powder of Examples 1 to 6 * 6 5 Nylon powder 2 6 Red iron oxide 0.5 7 Yellow Iron oxide 18 Black iron oxide 0.1 9 Silicone oil 1 10 2-Ethylhexyl palmitate 9 11 Sorbitan sesquioleate 1 12 Preservative 0.3 13 Perfume 0.1 * 3 parts of methylhydrogenpolysiloxane 5 97 parts of the powder was mixed with that dissolved in 1 part of dichloromethane, dried and then heat-treated at 180 ° C. for 3 hours.

【0034】上記成分1〜8をヘンシエルミキサーで混
合し、この混合物に、加熱溶解混合した成分9〜13を
添加混合した後、5HPパルベライザー(細川ミクロン
製)で粉砕し、これを直径5.3cmの中皿中160k
g/cm2の圧力で成形して両用フアンデションを得
た。上記成分4の雲母粉体の代わりに、比較例1〜4の
雲母粉体及び絹雲母のシリコーン処理した粉体を上記と
同量使用する以外は上記と同様にして、比較用両用フア
ンデション5〜9を調製した。
The above components 1 to 8 were mixed with a Henschel mixer, and the components 9 to 13 which had been heated and dissolved and mixed were added to and mixed with this mixture, which was then pulverized with a 5HP pulsarizer (manufactured by Hosokawa Micron) to obtain a diameter of 5. 160k in a medium dish of 3cm
Molding was performed at a pressure of g / cm 2 to obtain a dual-purpose foundation. Comparative dual-purpose foundation 5 in the same manner as above except that the same amount of the mica powder of Comparative Examples 1 to 4 and the sericite-treated silicone powder were used in place of the component 4 mica powder. ~ 9 were prepared.

【0035】上記のように調製した両用フアンデション
の官能評価及び成型したときの針入硬度(オルゼン硬度
計、荷重1ポンド)を測定した。針入硬度は、成型性に
対応し、評価は下記基準により行った。 ◎ 20未満 ○ 20以上30未満 □ 30以上40未満 △ 40以上50未満 × 50以上 結果を次表ー3に示す。
The sensory evaluation of the dual-purpose foundation prepared as described above and the needle penetration hardness (Olsen hardness meter, load 1 pound) at the time of molding were measured. The penetration hardness corresponds to the moldability, and the evaluation was performed according to the following criteria. ◎ Less than 20 ○ 20 or more and less than 30 □ 30 or more and less than 40 △ 40 or more and less than 50 × 50 or more The results are shown in Table 3 below.

【0036】[0036]

【表−3】 [Table-3]

【0037】上記表の結果から、本発明の両用フアンデ
ションは、比較例の両用フアンデションよりも、高い評
価を受けていることがわかる。 実施例13:ブラッシャー 以下の各成分から本発明のブラッシャー13を調製し
た。 (重量%) 1 タルク 15.1 2 絹雲母 8.1 3 マイカ 5.0 4 実施例1の合成雲母粉体 60.0 5 赤色226号 0.4 6 チタンマイカ 3.0 7 スクワラン 3.0 8 パルミチン酸2ーエチルヘキシル 5.0 9 防腐剤 0.3 10 香料 0.2
From the results in the above table, it can be seen that the dual-purpose foundation of the present invention received a higher evaluation than the dual-purpose foundation of the comparative example. Example 13: Blusher A brusher 13 of the present invention was prepared from the following components. (Wt%) 1 Talc 15.1 2 Sericite 8.1 3 Mica 5.0 4 Synthetic mica powder of Example 1 60.0 5 Red 226 0.4 6 Titanium mica 3.0 7 Squalane 3.0 8 2-Ethylhexyl palmitate 5.0 9 Preservative 0.3 10 Perfume 0.2

【0038】上記成分1〜5をヘンシエルミキサーで混
合し、この混合物に、加熱溶解混合した成分7〜10を
吹き付け、更に混合した後、5HPパルベライザー(細
川ミクロン製)で粉砕し、更に成分6を加えて混合した
後、4×6cmの中皿中120kg/cm2の圧力で成
形して、本発明のブラッシャー13を得た。上記成分4
の合成雲母粉60.0重量%をセリサイト60.0重量
%に置換する以外は、上記と同様にして、比較用ブラッ
シャー10を調製した。上記のように調製したブラッシ
ャーの官能評価を前記実施例と同様に行い、結果を次表
ー4に示す。
The above components 1 to 5 were mixed with a Henschel mixer, and the components 7 to 10 which had been heated and dissolved and mixed were sprayed onto this mixture, which was further mixed, and then pulverized with a 5HP pulsarizer (manufactured by Hosokawa Micron), and further the component 6 was added. Was added and mixed, and then molded in a medium dish of 4 × 6 cm at a pressure of 120 kg / cm 2 to obtain a blusher 13 of the present invention. Component 4 above
Comparative blusher 10 was prepared in the same manner as described above except that 60.0% by weight of synthetic mica powder was replaced with 60.0% by weight of sericite. The blusher prepared as described above was subjected to sensory evaluation in the same manner as in the above example, and the results are shown in Table 4 below.

【0039】[0039]

【表−4】 [Table-4]

【0040】上記表から明らかなように、本発明のブラ
ッシャー13は、官能評価項目のいずれにおいても優れ
ていることがわかる。またブラッシャーの硬度は、本発
明のブラッシャー13が25であり、比較用ブラッシャ
ー10が35であり、本発明のブラッシャーの方が成形
性が良いことがわかる。更に成形品の外観色を日立カラ
ーアナライザー607で測定した結果、本発明のブラッ
シャーが彩度11.8、比較用ブラッシャーが彩度1
0.6であり、本発明のブラッシャーのほうが彩度が高
く、あざやかな外観色であることがわかった。
As is apparent from the above table, the blusher 13 of the present invention is excellent in all sensory evaluation items. The hardness of the blusher is 25 for the blusher 13 of the present invention and 35 for the comparative blusher 10, and it can be seen that the blusher of the present invention has better moldability. Furthermore, as a result of measuring the appearance color of the molded product with a Hitachi Color Analyzer 607, the color saturation of the brusher of the present invention was 11.8 and that of the comparative brusher was 1
It was 0.6, and it was found that the brusher of the present invention had a higher saturation and a vivid appearance color.

【0041】実施例14:フアンシーパウダー 以下の各成分から本発明のフアンシーパウダー14を調
製した。 (重量%) 1 実施例2の合成雲母粉体 95 2 タルク 4 3 香料 1 4 酸化鉄顔料 適量
Example 14: Fanci powder The fanci powder 14 of the present invention was prepared from the following components. (Wt%) 1 Synthetic mica powder of Example 2 95 2 Talc 4 3 Perfume 1 4 Iron oxide pigment Appropriate amount

【0042】上記成分1、2、4を混合した後、これに
成分3を加えて更に混合し、容器に充填して本発明のフ
アンシーパウダー14を得た。上記成分1の合成雲母粉
95重量%の代わりにタルク同量(従ってタルク合計9
9重量%)を使用する以外は、上記と同様にして、比較
用フアンシーパウダー11を調製した。上記のように調
製したフアンシーパウダーを、37℃の恒温槽に1ケ月
保存したサンプルと、各々のコントロール(同じ処方で
製造したフアンシーパウダーの製造直後のもの)とにつ
いて、官能評価により匂い安定性を比較した。結果は、
本発明のフアンシーパウダーは、1ケ月保存後のサンプ
ルとコントロールとは殆ど変わらなかったが、比較用フ
アンシーパウダーの場合は、1ケ月保存後のサンプル
は、コントロールと比べてかなりの変臭していた。
After mixing the above components 1, 2 and 4, the component 3 was added thereto and further mixed and filled in a container to obtain the fancy powder 14 of the present invention. Instead of 95% by weight of the synthetic mica powder of the above component 1, the same amount of talc is used (thus totaling 9 talcs).
Comparative Fancy Powder 11 was prepared in the same manner as above, except that 9% by weight) was used. The fancy powder prepared as described above was stored in a 37 ° C. thermostat for one month, and each control (immediately after the production of fancy powder manufactured with the same formulation) was odor-stabilized by sensory evaluation. Sex was compared. Result is,
The fanci powder of the present invention was almost the same as the control and the sample after storage for 1 month, but in the case of the comparative fanci powder, the sample after storage for 1 month had a considerably strange odor compared with the control. Was there.

【0043】実施例15:ネイルエナメル 以下の各成分から本発明のネイルエナメルを調製した。 (重量%) 1 ニトロセルロース 12 2 変性アルキッド樹脂 12 3 クエン酸アセチルトリブチル 5 4 酢酸n−ブチル 36.4 5 酢酸エチル 6 6 n−ブチルアルコール 2 7 トルエン 21 8 酸化鉄顔料 0.5 9 二酸化チタン 0.1 10 パール顔料 2 11 実施例4の合成雲母粉体 2 12 有機変性モンモリロナイト 1Example 15: Nail enamel A nail enamel of the present invention was prepared from the following components. (% By weight) 1 Nitrocellulose 12 2 Modified alkyd resin 12 3 Acetyltributyl citrate 5 4 n-Butyl acetate 36.4 5 Ethyl acetate 6 6 n-Butyl alcohol 2 7 Toluene 21 8 Iron oxide pigment 0.5 9 Titanium dioxide 0.1 10 Pearl pigment 2 11 Synthetic mica powder of Example 4 2 12 Organically modified montmorillonite 1

【0044】上記成分1〜7(但し、成分4は一部分)
を溶解し、この溶液に、成分12と成分4の残分とを混
合してゲル状にしたものを添加混合し、更に成分8〜1
1を添加混合し、容器に充填し、本発明のネイルエナメ
ル15を得た。上記成分11の合成雲母粉体の代わりに
セリサイト同量を使用する以外は、上記と同様にして、
比較用ネイルエナメル12を調製した。上記のように調
製したネイルエナメルの官能評価を次表ー5に示す。
Components 1 to 7 above (however, component 4 is a part)
Was dissolved in the solution, and a gel-like mixture of ingredient 12 and the remainder of ingredient 4 was added and mixed, and ingredients 8 to 1 were added.
1 was added and mixed and filled in a container to obtain a nail enamel 15 of the present invention. In the same manner as above, except that the same amount of sericite was used instead of the synthetic mica powder of the above component 11,
A comparative nail enamel 12 was prepared. The sensory evaluation of the nail enamel prepared as described above is shown in Table 5 below.

【0045】[0045]

【表−5】 [Table-5]

【0046】上記表から明らかなように、本発明のネイ
ルエナメルは、官能評価においても優れていることがわ
かる。 実施例16:乳化フアンデーション 以下の各成分から本発明の乳化フアンデーションを調製
した。 (重量%) 1 ステアリン酸 0.4 2 イソステアリン酸 0.3 3 2−エチルヘキサン酸セチル 4 4 流動パラフイン 11 5 ポリオキシエチレン(10)ステアリルエーテル 2 6 タルク 15 7 顔料 4 8 セチルアルコール 0.3 9 防腐剤 0.07 10 実施例5の雲母粉体 3 11 トリエタノールアミン 0.42 12 プロピレングリコール 5 13 防腐剤 0.02 14 イオン交換水 54.19 15 香料 0.3
As is apparent from the above table, the nail enamel of the present invention is also excellent in sensory evaluation. Example 16: Emulsion foundation An emulsion foundation of the present invention was prepared from the following components. (% By weight) 1 stearic acid 0.4 2 isostearic acid 0.3 3 cetyl 2-ethylhexanoate 4 4 liquid paraffin 11 5 polyoxyethylene (10) stearyl ether 2 6 talc 15 7 pigments 4 8 cetyl alcohol 0.3 9 Preservative 0.07 10 Mica powder of Example 5 3 11 Triethanolamine 0.42 12 Propylene glycol 5 13 Preservative 0.02 14 Ion-exchanged water 54.19 15 Perfume 0.3

【0047】上記成分1〜9を85℃で加熱溶解混合し
た後、成分10を添加して均一に分散させた。これに、
85℃で加熱溶解混合した成分11〜14の混合物を徐
々に添加して乳化させた。乳化時の温度を10分間保持
して撹拌した後、撹拌しながら冷却して45℃にした。
これに成分15を加え、35℃まで撹拌冷却を続けた
後、生成物を取り出し、容器に充填して、本発明の乳化
フアンデーション15を得た。上記成分10の雲母粉体
の代わりにタルク同量を使用する以外は、前記と同様の
方法により、比較用乳化フアンデーション13を調製し
た。上記のように調製した乳化フアンデーションの官能
評価を次表ー6に示す。
After the above components 1 to 9 were heated and dissolved and mixed at 85 ° C., the component 10 was added and uniformly dispersed. to this,
The mixture of components 11 to 14 which had been heated and dissolved and mixed at 85 ° C. was gradually added to emulsify. The temperature at the time of emulsification was maintained for 10 minutes and stirred, and then cooled to 45 ° C while stirring.
Ingredient 15 was added to this, and after stirring and cooling to 35 ° C, the product was taken out and filled in a container to obtain an emulsion foundation 15 of the present invention. A comparative emulsified foundation 13 was prepared in the same manner as described above, except that the same amount of talc was used instead of the mica powder of Component 10. The sensory evaluation of the emulsion foundation prepared as described above is shown in Table 6 below.

【0048】[0048]

【表−6】 [Table-6]

【0049】上記表から明らかなように、本発明の乳化
フアンデーション15は、比較用乳化フアンデーション1
3に比べて優れていることがわかる。 実施例17:浴用剤 以下の各成分から本発明の錠剤タイプの浴用剤を調製し
た。 (重量%) 1 硫酸ナトリウム 45 2 炭酸水素ナトリウム 15 3 炭酸ナトリウム 8 4 コハク酸 22 5 実施例1の合成雲母粉体 15 6 色素 適量 7 顔料 適量 上記成分をヘンシエルミキサーで均一に混合し、打錠機
にて円形に成型し、本発明の浴用剤を調製した。
As is clear from the above table, the emulsion foundation 15 of the present invention is the emulsion foundation 1 for comparison.
It turns out that it is superior to 3. Example 17: Bath Agent A tablet-type bath agent of the present invention was prepared from the following components. (% By weight) 1 Sodium sulfate 45 2 Sodium hydrogen carbonate 15 3 Sodium carbonate 8 4 Succinic acid 22 5 Synthetic mica powder of Example 1 15 6 Dye proper amount 7 Pigment proper amount The above components are uniformly mixed with a Henschel mixer, and the mixture is cast. The bath agent of the present invention was prepared by molding it into a circular shape with a tablet machine.

【0050】[0050]

【効果】以上述べた如く、本発明の雲母粉末は、使用感
触、成型性に優れ、しかも光沢が少ないので、化粧品の
基材として、従来の雲母粉を使用した場合と比べて、画
期的な効果を奏するものであるから、良質品が枯渇し、
その代替品の要求が強い、セリサイトに十分代替できる
ものであり、この業界に貢献するところ極めて大きい。
[Effects] As described above, the mica powder of the present invention has an excellent feeling in use, moldability, and low gloss, so that it is epoch-making compared with the case of using conventional mica powder as a base material for cosmetics. Because it has such a great effect, quality products are exhausted,
It is a strong substitute for sericite, which is highly demanded as a substitute, and it is extremely important to contribute to this industry.

【表1】 [Table 1]

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小川 克基 神奈川県横浜市港北区新羽町1050番地 株 式会社資生堂研究所内 (72)発明者 山本 勝 愛知県豊橋市明海町1番地トピー工業株式 会社豊橋製造所内 (72)発明者 杉森 健一郎 愛知県豊橋市明海町1番地トピー工業株式 会社豊橋製造所内 (72)発明者 鈴村 亮 愛知県豊橋市明海町1番地トピー工業株式 会社豊橋製造所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Katsuji Ogawa 1050 Shinba-cho, Kohoku-ku, Yokohama-shi, Kanagawa Prefecture Shiseido Research Institute Co., Ltd. (72) Inventor Kenichiro Sugimori 1 Toyami, Toyohashi, Toyohashi, Aichi Prefecture Topy Industries Ltd. (72) Inventor, Ryo Suzumura 1, Akemi, Toyohashi, Aichi Toyoi, Ltd.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】合成雲母粉体で、レーザー回折法平均粒子
径(A)が、5μm≦A≦20μmで、且つ上記(A)と
沈降法平均粒子径(B)の比で示される厚み指数(A/
B)が、1.5≦A/B≦3.5であることを特徴とし
た雲母粉体。
1. A synthetic mica powder having a laser diffraction average particle size (A) of 5 μm ≦ A ≦ 20 μm, and a thickness index indicated by the ratio of the above (A) and the sedimentation average particle size (B). (A /
B) is a mica powder characterized in that 1.5 ≦ A / B ≦ 3.5.
【請求項2】白雲母、金雲母若しくは黒雲母で、レ−ザ
ー回折法平均粒子径(A)が、5μm≦A≦20μmで、
且つ上記(A)と沈降法平均粒子径(B)の比で示され
る厚み指数(A/B)が、1.5≦A/B≦3.5であ
ることを特徴とした雲母粉体。
2. A muscovite, phlogopite or biotite having a laser diffraction average particle diameter (A) of 5 μm ≦ A ≦ 20 μm,
A mica powder having a thickness index (A / B) represented by the ratio of (A) to the average particle size by sedimentation method (B) is 1.5 ≦ A / B ≦ 3.5.
【請求項3】合成雲母粉体で、レ−ザー回折法平均粒子
径(A)が、5μm≦A≦20μmで、且つ上記(A)と
沈降法平均粒子径(B)の比で示される厚み指数(A/
B)が、1.5≦A/B≦3.5である雲母粉体を配合
したことを特徴とする化粧料。
3. A synthetic mica powder having a laser diffraction average particle size (A) of 5 μm ≦ A ≦ 20 μm and a ratio of (A) to the sedimentation average particle size (B). Thickness index (A /
A cosmetic composition characterized in that B) is blended with a mica powder with 1.5 ≦ A / B ≦ 3.5.
【請求項4】白雲母、金雲母若しくは黒雲母で、レ−ザ
ー回折法平均粒子径(A)が、5μm≦A≦20μmで、
且つ上記(A)と沈降法平均粒子径(B)の比で示され
る厚み指数(A/B)が、1.5≦A/B≦3.5であ
る雲母粉体を配合したことを特徴とする化粧料。
4. A muscovite, phlogopite or biotite having a laser diffraction average particle diameter (A) of 5 μm ≦ A ≦ 20 μm,
A mica powder having a thickness index (A / B) represented by the ratio of (A) and the average particle size by sedimentation method (B) of 1.5 ≦ A / B ≦ 3.5 is blended. And cosmetics.
JP16978693A 1993-06-17 1993-06-17 Mica powder and cosmetics containing the mica powder Expired - Lifetime JP3582662B2 (en)

Priority Applications (1)

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JP3582662B2 JP3582662B2 (en) 2004-10-27

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6416573B2 (en) 2000-02-14 2002-07-09 Miyoshi Kasei, Inc. Composite pigment and cosmetics containing the same
KR100467034B1 (en) * 1996-12-27 2006-04-07 주식회사 엘지생활건강 Compression Molding Oil Cake Cosmetic and Its Manufacturing Method
JP2014065692A (en) * 2012-09-27 2014-04-17 Mandom Corp Gel skin cosmetic material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100467034B1 (en) * 1996-12-27 2006-04-07 주식회사 엘지생활건강 Compression Molding Oil Cake Cosmetic and Its Manufacturing Method
US6416573B2 (en) 2000-02-14 2002-07-09 Miyoshi Kasei, Inc. Composite pigment and cosmetics containing the same
JP2014065692A (en) * 2012-09-27 2014-04-17 Mandom Corp Gel skin cosmetic material

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