JPH0222045B2 - - Google Patents

Info

Publication number
JPH0222045B2
JPH0222045B2 JP56053912A JP5391281A JPH0222045B2 JP H0222045 B2 JPH0222045 B2 JP H0222045B2 JP 56053912 A JP56053912 A JP 56053912A JP 5391281 A JP5391281 A JP 5391281A JP H0222045 B2 JPH0222045 B2 JP H0222045B2
Authority
JP
Japan
Prior art keywords
water
talc
calcined
mica
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
Application number
JP56053912A
Other languages
Japanese (ja)
Other versions
JPS57169412A (en
Inventor
Kazuo Tate
Shigenori Kumagai
Tsutomu Saito
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.)
Shiseido Co Ltd
Original Assignee
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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP5391281A priority Critical patent/JPS57169412A/en
Publication of JPS57169412A publication Critical patent/JPS57169412A/en
Publication of JPH0222045B2 publication Critical patent/JPH0222045B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q13/00Formulations or additives for perfume preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/81Preparation or application process involves irradiation

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)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Description

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

本発明は粘土鉱物、例えばタルク、カオリン、
雲母、モンモリロナイト等から結晶水を脱水した
粉末を配合することを特徴とする新しい使用性及
び優れた安定性を有する化粧料に関する。 化粧料基剤として用いられる体質顔料には、タ
ルク、カオリン、マイカ等のような粘土鉱物があ
り、有色顔料の分散をよくしたり、また皮膚に対
する被覆力(のり)、展延性(のび)、付着性(つ
き)、吸収性などの機能を有し、広く用いられて
いる。しかしながら、従来の粘土鉱物は、化粧料
成分である油脂類、香料等と共存した場合油脂類
を酸敗させたり、あるいは香料を変臭させたりす
るという欠点があつた。さらに、油分と併存させ
た粉末製品において、粉体の凝集を生じたり、ケ
ーキングを生じる等の欠点もあつた。 本発明者らは、これらの欠点を改良すべく鋭意
研究を重ねた結果、従来の粘土鉱物が持つている
結晶水を除くことによつて得られる脱水粘土鉱物
が従来の種々の欠点を解決すると同時に、従来に
ない新しい使用性を持つた化粧料を提供すること
を見い出し、本発明を完成するに至つた。 すなわち、本発明は、単体の状態で結晶水を脱
水し、付着力を低下させたタルク、カオリン及び
マイカから選ばれる粘土鉱物の少なくとも1種を
配合したことを特徴とする化粧料を提供するもの
である。 本発明で用いられる粘土鉱物は、タルク、カオ
リン、マイカ等があり、従来、その化学式から明
らかなように結晶水を含んでいる。たとえば、タ
ルクの化学式は3MgO・4SiO2・H2O、カオリン
の化学式はAl2O3・2SiO2・2H2Oで表わされる。
この結晶水は加熱あるいは真空脱気などによつて
脱水される。例えば熱処理の場合吸着水や層間水
は比較的低い温度(約200℃以下)で脱水するが、
OHの形ではいつているいわゆる結晶水は、種類
によつて500℃位で脱水されるものもあれば900℃
以上でないと脱水されないものもあり、また同じ
粘土鉱物でも産地によつて脱水温度に幅がある。
いずれにしても、高温でないと脱水されない。 本発明者等は、粘土鉱物から結晶水を脱水して
ゆくと、その物性が結晶水を含んだ従来の粘土鉱
物を著しく変化し、それらを配合することによつ
て優れた安定性及び新しい使用性を有する化粧料
を得ることに着目し、本発明を完成したのであ
る。 粘土鉱物から結晶水を脱水する方法は、従来一
般に用いられている方法、たとえば、熱をかけて
焼成する、高周波、マイクロ波等を利用する、真
空脱気、凍結法などが使用できるが、熱処理が一
般的である。脱水条件は結晶水を除く条件が好ま
しく、例えば熱処理の場合は、300℃以上が好ま
しい。結晶水は処理温度や処理時間によつて一部
又は完全に脱水することが出来る。その一例をカ
オリンの示差熱分析により示した。(第1図)未
処理のカオリンは570℃付近に結晶水の脱水に伴
なう吸熱ピークが現れる。500℃と550℃で焼成し
たカオリンの場合は一部残つている結晶水の脱水
による小さな吸熱ピークが未だ見られ、600℃で
焼成すると完全に脱水され、もはや吸熱ピークは
なくなる。脱水粘土鉱物は、熱処理の場合、原鉱
石の段階で焼成した後粉砕して化粧料に配合して
も、粉砕した後に焼成処理したものを配合しても
構わない。 次に、粘土鉱物が結晶水を失なうことによつて
発現する新しい物性について記述する。粉体の表
面粘性は、化粧料成分である油脂類の酸敗、ある
いは香料の変臭の原因として大きな問題を生じさ
せる。 表1は表面活性の変化をイソプロピルアルコー
ルが接触したときの分解によつて生ずるアセト
ン、プロピレン及び水の生成率で表わしたもので
ある。脱水処理によつて表面活性は減少し、特に
結晶水の失なわれ始める900℃でタルクの表面活
性が著しく減少していることが分る。 第2図は、マイカ粉末の付着力に対する熱処理
の影響を示したものである。処理温度300℃まで
はあまり付着力は変化しないが、結晶水の失なわ
れ始める500℃以上の温度で処理すると付着力は
著しく減少し始める。これは層間水などの脱水で
は付着力に大きな影響を与えないけれども、結晶
水の脱水は付着力に大きく影響することを意味し
ている。
The present invention uses clay minerals such as talc, kaolin,
The present invention relates to a cosmetic having new usability and excellent stability, which is characterized by containing powder obtained by dehydrating crystal water from mica, montmorillonite, etc. Extender pigments used as cosmetic bases include clay minerals such as talc, kaolin, mica, etc., which improve the dispersion of colored pigments, and improve skin coverage (glue), spreadability (spreadability), etc. It has functions such as adhesion and absorption, and is widely used. However, conventional clay minerals have had the disadvantage that when they coexist with cosmetic ingredients such as fats and oils and fragrances, they cause the oils and fats to become rancid or cause the fragrances to change odor. Furthermore, in powder products coexisting with oil, there were also drawbacks such as agglomeration of the powder and caking. As a result of intensive research aimed at improving these drawbacks, the present inventors have found that dehydrated clay minerals obtained by removing the crystal water contained in conventional clay minerals solve the various drawbacks of conventional clay minerals. At the same time, the present inventors discovered that it was possible to provide cosmetics with new usability that had never existed before, and thus completed the present invention. That is, the present invention provides a cosmetic product that contains at least one clay mineral selected from talc, kaolin, and mica, which has been dehydrated from crystal water and has reduced adhesion in a single state. It is. Clay minerals used in the present invention include talc, kaolin, mica, etc., and conventionally contain water of crystallization as is clear from their chemical formulas. For example, the chemical formula of talc is 3MgO.4SiO 2 .H 2 O, and the chemical formula of kaolin is Al 2 O 3 .2SiO 2 .2H 2 O.
This crystal water is dehydrated by heating or vacuum degassing. For example, in the case of heat treatment, adsorbed water and interlayer water are dehydrated at relatively low temperatures (approximately 200°C or less);
The so-called water of crystallization, which is present in the form of OH, is dehydrated at around 500℃ and others at 900℃ depending on the type.
There are some clay minerals that cannot be dehydrated unless the temperature is higher than that, and even for the same clay mineral, the dehydration temperature varies depending on the production area.
In any case, dehydration will not occur unless the temperature is high. The present inventors discovered that by dehydrating crystallization water from clay minerals, the physical properties of the clay minerals significantly change compared to conventional clay minerals containing crystallization water, and that by blending them, excellent stability and new uses can be achieved. The present invention was completed by focusing on the purpose of obtaining cosmetics that have specific properties. Methods for dehydrating crystallized water from clay minerals include methods commonly used in the past, such as baking with heat, using high frequency waves, microwaves, etc., vacuum deaeration, and freezing methods. is common. The dehydration conditions are preferably conditions that exclude crystal water, and for example, in the case of heat treatment, the temperature is preferably 300°C or higher. Crystal water can be partially or completely dehydrated depending on the treatment temperature and treatment time. An example of this was shown by differential thermal analysis of kaolin. (Figure 1) In untreated kaolin, an endothermic peak appears around 570°C due to dehydration of crystal water. In the case of kaolin calcined at 500°C and 550°C, a small endothermic peak due to the dehydration of some remaining crystal water is still visible, but when calcined at 600°C, the kaolin is completely dehydrated and there is no longer an endothermic peak. In the case of heat treatment, dehydrated clay minerals may be calcined in the raw ore stage and then crushed and blended into cosmetics, or crushed and then calcined and blended. Next, we will describe new physical properties that appear when clay minerals lose crystallization water. The surface viscosity of the powder causes a major problem as it causes rancidity of oils and fats that are ingredients of cosmetics and odor change of fragrances. Table 1 shows changes in surface activity in terms of production rates of acetone, propylene, and water resulting from decomposition when isopropyl alcohol comes into contact with it. It can be seen that the surface activity of talc decreases with dehydration treatment, especially at 900°C, where water of crystallization begins to be lost. FIG. 2 shows the influence of heat treatment on the adhesion of mica powder. Adhesion does not change much at treatment temperatures up to 300°C, but when treated at temperatures above 500°C, where water of crystallization begins to be lost, adhesion begins to decrease significantly. This means that dehydration of interlayer water does not have a large effect on adhesion, but dehydration of crystalline water has a large effect on adhesion.

【表】 表2には各種粘土鉱物のスクワランの吸油量を
表3には吸水量の熱処理による変化を示した。
900℃で2時間処理した場合、タルク、カオリン
は吸油量、吸水量ともに増加する。一方、マイカ
は吸油量、吸水量ともに減少する。 本発明によつて得られた脱水粘土鉱物はいずれ
も従来配合していた各種化粧料に用いることによ
り、従来の化粧料とは異なつた新しい使用性を与
え、または、安定性を向上させた。 次に実施例によつて本発明をさらに詳細に説明
する。配合量は、重量%である。
[Table] Table 2 shows the oil absorption amount of squalane in various clay minerals, and Table 3 shows the change in water absorption amount due to heat treatment.
When treated at 900°C for 2 hours, both oil absorption and water absorption of talc and kaolin increase. On the other hand, mica decreases both oil absorption and water absorption. When the dehydrated clay minerals obtained according to the present invention are used in various cosmetics that have been conventionally formulated, they provide new usability different from conventional cosmetics or improve stability. Next, the present invention will be explained in more detail with reference to Examples. The blending amount is in weight%.

【表】【table】

【表】【table】

【表】 実施例1は950℃で結晶水を完全に脱水した焼
成タルクを主成分に用いた。比較例1は同一処方
で焼成タルクを従来のタルクに置換したものであ
る。 パヒユームパウダーは香りを目的とするフレグ
ランス製品であるから、経時による香料の劣化が
最大の問題となる。実施例1と比較例1を37℃1
カ月間放置後の勾いを官能で試験した結果、比較
例1は香料の変臭を生じたが、実施例1は全く変
臭が起らなかつた。
[Table] In Example 1, calcined talc whose crystallization water was completely dehydrated at 950°C was used as the main component. Comparative Example 1 uses the same recipe but replaces calcined talc with conventional talc. Since perhyum powder is a fragrance product whose purpose is scent, deterioration of the fragrance over time is the biggest problem. Example 1 and Comparative Example 1 at 37℃1
As a result of a sensory test of the slope after being left for a month, Comparative Example 1 caused a change in fragrance odor, but Example 1 did not cause any change in odor.

【表】 実施例2は500℃で一部結晶水を脱水した焼成
カオリン及び950℃で結晶水を完全に脱水した焼
成タルクを使用した。比較例2は同一処方で焼成
カオリン、焼成タルクの代りに従来のカオリン、
及びタルクを用いた。油性フアウンデイシヨンの
場合には、粉来の表面活性に起因する香料の変臭
に加えて、油脂の酸敗も問題となる。37℃、1カ
間放置後の過酸化物価は実施例2の場合2以下で
あるのに対して比較例2は6〜7であつた。
[Table] In Example 2, calcined kaolin from which crystallization water was partially dehydrated at 500°C and calcined talc from which crystallization water was completely dehydrated at 950°C were used. Comparative Example 2 uses the same recipe with calcined kaolin, conventional kaolin instead of calcined talc,
and talc were used. In the case of oil-based foundations, in addition to the odor of the perfume due to the surface activity of the powder, rancidity of the oil and fat is also a problem. The peroxide value after standing at 37° C. for 1 hour was 2 or less in Example 2, while it was 6 to 7 in Comparative Example 2.

【表】 実施例3は700℃で結晶水を脱水した焼成マイ
カを用いた。比較例3は焼成マイカの代りに従来
のマイカを使用した。この粉白粉は少量の油分が
添加されているが、焼成マイカを用いた実施例3
は粉体間の付着力が非常に小さいため、油分によ
る粉末の凝集が全く起らない。それに対して比較
例3は粉体の凝集を生じ、ルースパウダーとして
の外観を損つた。
[Table] In Example 3, calcined mica whose crystallization water was dehydrated at 700°C was used. Comparative Example 3 used conventional mica instead of calcined mica. This white powder has a small amount of oil added, but Example 3 using calcined mica
Since the adhesion force between the powders is very small, no agglomeration of the powders due to oil occurs. On the other hand, in Comparative Example 3, the powder agglomerated and lost its appearance as a loose powder.

【表】 実施例4は700℃で結晶水を脱水した焼成マイ
カ及び900℃で結晶水を脱水した焼成タルクを用
いた。比較例4,5は従来のマイカ、タルクを使
用した。固形フアウンデイシヨンの場合、油分の
配合量は仕上がり感を左右する重要な因子である
が、少な過ぎる場合には成型性、また多過ぎる場
合にはケーキングという現象から下限と上限があ
る。特に上限については、比較例4に示すように
従来は油分の総量(比較例4では流動パラフイ
ン、ラノリン、ソルビタンセスキオレエートの総
量)として約20%がケーキングしない限度であ
り、これ以上配合するとケーキングがおこつた。
ところが、焼成マイカ、焼成タルクを用いた実施
例4は油分の総量が約40%までケーキングを生じ
なかつた。これは焼成マイカの付着力の減少と、
焼成タルクの吸油量の増加が従来の油分量の限界
を大幅に変えた。専門パネル10名で行なつた実施
例4と比較例4,5の官能による評価結果を表4
に示した。実施例4はつつぱり感、化粧後の肌の
なめらかさなどの点で従来にない特徴が現われて
いる。参考までに実施例4と同じ割合で従来のマ
イカ、タルクを使用した比較例5は、パフへのと
れ、のび、仕上り感等で、製品とはならないもの
である。
[Table] In Example 4, calcined mica whose crystallization water was dehydrated at 700°C and calcined talc whose crystallization water was dehydrated at 900°C were used. Comparative Examples 4 and 5 used conventional mica and talc. In the case of solid foundations, the amount of oil blended is an important factor that affects the finish, but there are lower and upper limits because if it is too little, it will cause moldability, and if it is too much, it will cause caking. In particular, regarding the upper limit, as shown in Comparative Example 4, conventionally the total amount of oil (in Comparative Example 4, the total amount of liquid paraffin, lanolin, and sorbitan sesquioleate) was the limit that would not cause caking, and if more than this was added, caking would occur. I got angry.
However, in Example 4 using calcined mica and calcined talc, caking did not occur until the total oil content was about 40%. This is due to a decrease in the adhesion of fired mica,
The increase in oil absorption of calcined talc has significantly changed the conventional limit of oil content. Table 4 shows the sensory evaluation results of Example 4 and Comparative Examples 4 and 5 conducted by a panel of 10 experts.
It was shown to. Example 4 exhibits unprecedented characteristics in terms of firmness and smoothness of the skin after makeup. For reference, Comparative Example 5, which used conventional mica and talc in the same proportions as Example 4, could not be used as a product due to problems such as adhesion to the puff, spread, and finish.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、末焼成及び焼成カオリンの示差熱分
析の図である。第2図は、マイカの付着力に及ぼ
す熱処理の影響を示した図である。
FIG. 1 is a diagram of differential thermal analysis of uncalcined and calcined kaolin. FIG. 2 is a diagram showing the influence of heat treatment on the adhesion of mica.

Claims (1)

【特許請求の範囲】[Claims] 1 単体の状態で結晶水を脱水し付着力を低下さ
せたタルク、カオリン及びマイカから選ばれる粘
土鉱物の少なくとも1種を配合したことを特徴と
する化粧料。
1. A cosmetic containing at least one clay mineral selected from talc, kaolin, and mica whose adhesion force has been reduced by dehydrating the crystal water in a single substance state.
JP5391281A 1981-04-10 1981-04-10 Cosmetic Granted JPS57169412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5391281A JPS57169412A (en) 1981-04-10 1981-04-10 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5391281A JPS57169412A (en) 1981-04-10 1981-04-10 Cosmetic

Publications (2)

Publication Number Publication Date
JPS57169412A JPS57169412A (en) 1982-10-19
JPH0222045B2 true JPH0222045B2 (en) 1990-05-17

Family

ID=12955920

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5391281A Granted JPS57169412A (en) 1981-04-10 1981-04-10 Cosmetic

Country Status (1)

Country Link
JP (1) JPS57169412A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58180411A (en) * 1982-04-16 1983-10-21 Shiseido Co Ltd Make-up cosmetic
JP5173258B2 (en) * 2006-05-23 2013-04-03 株式会社 資生堂 Powder cosmetics
WO2007097128A2 (en) * 2006-05-23 2007-08-30 Shiseido Company, Ltd. Powder cosmetic composition cotaining humectant in high concentration
JP2009013107A (en) * 2007-07-04 2009-01-22 Shiseido Co Ltd Skin lesion-restoring composition
WO2011121947A1 (en) * 2010-03-30 2011-10-06 パナソニック株式会社 Complex magnetic material, coil-embedded type magnetic element using the same, and manufacturing method thereof
JP5904629B2 (en) * 2011-03-22 2016-04-13 株式会社 資生堂 Solid cosmetic
EP3444233A4 (en) * 2016-04-12 2019-12-04 Suministros de Colombia S.A.S. Ceramic spheres from aluminosilicates
EP3470050A1 (en) * 2017-10-10 2019-04-17 Imertech Sas Use of calcined kaolin as a mattifying agent

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS506726A (en) * 1973-05-30 1975-01-23
JPS5231837A (en) * 1975-10-01 1977-03-10 Pola Chem Ind Inc Cosmetic material
JPS5232024A (en) * 1975-09-05 1977-03-10 Pola Chem Ind Inc Method for the preparation of pigment
JPS5299234A (en) * 1976-02-12 1977-08-19 Pola Kasei Kogyo Kk Cosmetics
JPS53113035A (en) * 1977-03-09 1978-10-03 Pola Kasei Kogyo Kk Cosmetics

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS506726A (en) * 1973-05-30 1975-01-23
JPS5232024A (en) * 1975-09-05 1977-03-10 Pola Chem Ind Inc Method for the preparation of pigment
JPS5231837A (en) * 1975-10-01 1977-03-10 Pola Chem Ind Inc Cosmetic material
JPS5299234A (en) * 1976-02-12 1977-08-19 Pola Kasei Kogyo Kk Cosmetics
JPS53113035A (en) * 1977-03-09 1978-10-03 Pola Kasei Kogyo Kk Cosmetics

Also Published As

Publication number Publication date
JPS57169412A (en) 1982-10-19

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