JPS6019281B2 - cosmetics - Google Patents

cosmetics

Info

Publication number
JPS6019281B2
JPS6019281B2 JP9000276A JP9000276A JPS6019281B2 JP S6019281 B2 JPS6019281 B2 JP S6019281B2 JP 9000276 A JP9000276 A JP 9000276A JP 9000276 A JP9000276 A JP 9000276A JP S6019281 B2 JPS6019281 B2 JP S6019281B2
Authority
JP
Japan
Prior art keywords
powder
particle size
porous powder
parts
carbonate
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
JP9000276A
Other languages
Japanese (ja)
Other versions
JPS5315433A (en
Inventor
政章 堀野
公一 萱生
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 JP9000276A priority Critical patent/JPS6019281B2/en
Publication of JPS5315433A publication Critical patent/JPS5315433A/en
Publication of JPS6019281B2 publication Critical patent/JPS6019281B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は化粧料、詳しくは新規に作られた多孔性粉体
が配合され、保香性、保湿性、通気性、感触性、耐光性
、分散性「充填性に陵れ、且つ肌に負担をかけずにしっ
とりとし滑らかにして密着性に優れている化舷料に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is a cosmetic, in particular, a newly created porous powder that is blended with a cosmetic that has excellent fragrance retention, moisture retention, breathability, texture, light resistance, dispersibility, and filling properties. The present invention relates to a skin material that is moist and smooth and has excellent adhesion without causing any strain on the skin.

従来、化粧料に使用されている粉体は、結晶の生長過程
が複雑であるため結晶作用により構造が形成されるとき
に既に欠陥が生じている場合が多く、特に天然鉱物では
、例えば原子配列の乱雑性、原子の脱落、結晶内の均質
性の欠如などによって不連続的なブロックの集合からな
る構造を呈していて理想的配列を有する結晶は殆んどな
い。
Conventionally, powders used in cosmetics have a complex crystal growth process, so defects often already occur when the structure is formed by crystallization, especially in natural minerals, for example, due to the atomic arrangement. Due to the randomness of the crystals, the dropout of atoms, and the lack of homogeneity within the crystal, crystals exhibit a structure consisting of a discontinuous collection of blocks, and there are almost no crystals that have an ideal arrangement.

このような天然鉱物からなる粉体は通常の粉体がもつ諸
物性の内で弾性、比熱、比重、透明度、硬度、電磁性、
展延性、耐熱性、男関性、操曲性などに固有の特性をも
ち、結晶構造およびその繊密性、結晶形から種々の性質
を与えるものである。例えば、鱗片状で三層構造をなし
た鉱物は眉間の結合が弱く完全な男開が発達しているた
め滑り感を与え弾性に富んでいるが、逆にこれを製造充
填する場合は充填性を欠いているために製造上のトラブ
ルの一つの原因となっている。また二層構造のものは努
関性の優れたものはごく一部にすぎないとともに、結晶
が不定形であるため粉体の有する榛曲性、結晶形の繊密
性の面から最密充填構造をとりにくく、充填性に劣ると
同時に滑り感において満足し得るものを入手することは
できない。一方、天然鉱物には水分や不純物が存在し、
また生成条件に対し影響を受ける敏感性のものと影響を
受けない非敏感性のものとがある。結晶構造内の水分に
は自由水、付着水、吸着水、結合水があるが、自由水、
付着水、吸着水は外的条件により容易に脱着、付着また
は吸着するものであり、特に綜合水は脱着すると結晶構
造に変化を及ぼすものである。以上から理解されるよう
に天然鉱物は、本来保温性の低いものが殆んどである。
このように構造面から捉えると、天然鉱物は水分、香料
の保持性が低く、僅かの経時で香料の匂いが弱くなる欠
点を有していることが立証される。また、天然鉱物は一
層、二層或いは三層構造を示しているのが殆んどである
が、それらは多孔性を有しないため通気性に乏しく、イ
Q荘料に配合して皮膚に塗布したとき皮膚呼吸を阻害し
やすく、皮膚に負担をかける原因となっている。本発明
は前記のような従来の諸問題を解決し、優れた性質の化
粧料を提供するものである。
Powders made of natural minerals have the physical properties of ordinary powders, such as elasticity, specific heat, specific gravity, transparency, hardness, electromagnetic properties,
It has unique characteristics such as malleability, heat resistance, virility, and flexibility, and it has various properties depending on its crystal structure, its fineness, and crystal shape. For example, minerals that are scaly and have a three-layer structure have weak connections between the eyebrows and a fully developed penis, giving them a slippery feel and being rich in elasticity. The lack of this is one of the causes of manufacturing troubles. In addition, only a few of the two-layered structures have excellent interlocking properties, and because the crystals are amorphous, close-packed packing is required due to the elasticity of the powder and the fineness of the crystalline form. It is difficult to obtain a structure, poor in filling properties, and at the same time, it is not possible to obtain a material that is satisfactory in terms of sliding feel. On the other hand, natural minerals contain water and impurities,
There are also sensitive types that are affected by the generation conditions and non-sensitive types that are not affected. There are three types of water in a crystal structure: free water, attached water, adsorbed water, and bound water.
Adhered water and adsorbed water are easily desorbed, attached, or adsorbed depending on external conditions, and in particular, when adsorbed water is desorbed, the crystal structure changes. As can be understood from the above, most natural minerals inherently have low heat retention properties.
Viewed from a structural standpoint, it is proven that natural minerals have the disadvantage that they have a low ability to retain moisture and fragrance, and the fragrance of the fragrance weakens over a short period of time. In addition, most natural minerals have a one-, two-, or three-layer structure, but since they do not have porosity, they have poor breathability, so they are often mixed with IQ shoyo and applied to the skin. When this occurs, it tends to impede the skin's ability to breathe, causing stress on the skin. The present invention solves the conventional problems as described above and provides cosmetics with excellent properties.

即ち、本発明に係る化粧料は無水珪酸化合物、アルミ/
珪酸化合物、マグネシウム珪酸化合物の一種または二種
以上の微粉末からなる被覆物質を金属炭酸化合物、水以
外の揮発性成分を含有する無水アルミノ珪酸化合物、薄
発性物質、燃焼性物質の一種または二種以上の微粉末か
らなる内芯核物質の表面に付着凝集して得られた多孔性
粉体をイa荘料成分に配合したことを特徴としている。
以下、本発明の詳細を具体的に説明すると、先ず多孔性
粉体の被覆物質を構成する天然鉱物として好ましい具体
例は次表の通りであって、平均粒蓬1〜50仏程度のも
のを一種または二種以上混合して用いる。次に、内芯核
物質を構成する金属炭酸化合物としては炭酸マグネシウ
ム、炭酸ベリリウム、炭酸カルシウム、炭酸第二鉄、炭
酸バリウム、炭酸マンガン、炭酸リチウム、炭酸コバル
ト、炭酸水素マグネシウムカリウム、炭酸ストロンチウ
ム、炭酸水素リチウム、炭酸亜鉛、炭酸クロムなどが例
示され、天然鉱物として存在する金属炭酸化合物として
は、ドロマイト、方解石、アラレ石、ストロンチアン石
、リョクドウ石、ドクジュウド石などが例示される。
That is, the cosmetic according to the present invention contains anhydrous silicic acid compound, aluminum/
A coating material consisting of one or more fine powders of a silicic acid compound, a magnesium silicate compound, a metal carbonate compound, an anhydrous aluminosilicate compound containing a volatile component other than water, a low-emitting substance, or one or two combustible substances. It is characterized in that a porous powder obtained by adhering and aggregating on the surface of an inner core material consisting of a fine powder of more than 100% is blended into the ionizing material component.
Hereinafter, to explain the details of the present invention in detail, first, preferred specific examples of natural minerals constituting the coating material of the porous powder are as shown in the table below. Use one type or a mixture of two or more types. Next, the metal carbonate compounds that make up the inner core material include magnesium carbonate, beryllium carbonate, calcium carbonate, ferric carbonate, barium carbonate, manganese carbonate, lithium carbonate, cobalt carbonate, magnesium potassium hydrogen carbonate, strontium carbonate, carbonate Examples include lithium hydrogen, zinc carbonate, and chromium carbonate. Examples of metal carbonate compounds existing as natural minerals include dolomite, calcite, aralite, strontianite, munganite, and dokujudoite.

水以外の揮発性成分を含む無水アルミノ珪酸化合物とし
ては角閃石、黒雲母、黄玉、デユモリチーフライト、ズ
ニ石などが例示され、これらは加熱によって揮発成分を
失い容易にムライトに移化し体積を収縮する鉱物であり
、加熱によって膨張する真珠石、黒滋石、松脂石等は好
ましくないので使用しない。また、揮発性物質としては
平均粒径1〜50仏のものが好ましく、メントール、カ
ンフル、メチル/ぐラベン、エチル/ぐラベン、プロピ
ル/ゞラベン、ブチルパラベン、ナフタリン、イオウソ
ルビン酸、デヒドロ酷酸、安息香酸、サリチル酸、ケイ
皮酸、パラクロル安息香酸、パラオキシ安息香酸などが
例示され、更に燃焼性物質としてはナイロン、ポリスチ
レン、テフロン、ポリエチレン、ポリプoピレン、ポリ
オレフイン、デルリン、ジスチルベンゼンピンホールポ
リマ、ベンゾグアナミパウダなどの合成樹脂あるいはこ
れらの共重合体、または澱粉、炭素、イオウなどが例示
され、これらは球体または多孔性球体のものが好ましい
Examples of anhydrous aluminosilicate compounds containing volatile components other than water include amphibole, biotite, jadeite, dumolychieflite, and zunite, which lose their volatile components when heated and easily transform into mullite, increasing their volume. Minerals that contract and expand when heated, such as pearlite, blackstone, and pinestone, are undesirable and should not be used. In addition, the volatile substances preferably have an average particle size of 1 to 50 French, and include menthol, camphor, methyl/graben, ethyl/graben, propyl/graben, butylparaben, naphthalene, sulfurobic acid, dehydroboric acid, etc. , benzoic acid, salicylic acid, cinnamic acid, parachlorobenzoic acid, paraoxybenzoic acid, etc.Furthermore, flammable substances include nylon, polystyrene, Teflon, polyethylene, polypropylene, polyolefin, Delrin, and distylbenzene pinhole polymer. , synthetic resins such as benzoguanami powder, copolymers thereof, starch, carbon, sulfur, etc., and these are preferably spherical or porous spherical.

本発明に使用される多孔性粉体を製造する場合、被覆物
質と内芯核物質との重量割合は8:2〜1:9程度であ
り、これらを水系中で常温にして好ましくは700〜7
60肌Hg程度の減圧下で鷹拝すると、内芯核物質の表
面に吸着イオン層を生じ、これらに被覆物質である負電
荷の鉱物が吸引され内芯核物質の表面に被覆物が付着凝
集して平均粒径1〜50〃程度の内芯核物質を含有する
有芯の多孔性粉体が作られるのである。
When producing the porous powder used in the present invention, the weight ratio of the coating material and the inner core material is about 8:2 to 1:9, and it is preferably 700 to 7
When worshiped under a reduced pressure of about 60 Hg, an adsorbed ion layer is formed on the surface of the inner core material, and the negatively charged minerals that are the coating material are attracted to these layers, causing the coating to adhere and coagulate on the surface of the inner core material. As a result, a cored porous powder containing an inner core material having an average particle size of about 1 to 50 mm is produced.

また、このような多孔性粉体を水系中の代りに不活性溶
媒を用いて製造することもできる。この場合は被覆物質
と内芯核物質との重量割合は8:2〜2:8であり、被
覆物質および内芯核物質と不活性溶媒との重量割合を9
:1〜6:4、好ましくは8.3:1.7とする。不活
性溶媒としてはシリコンオイル、ポリブラン、ポリオキ
シェチレントール油誘導体などが例示され、これらの不
活性溶媒に被覆物質と内芯核物質とを加え、常温にして
好ましくは700〜760脚Hg程度の減圧下で強力に
鷹拝すると被覆物質と内芯核物質とが不活性溶媒で包囲
され物理的に合一化し、それらを吸引炉過する−と有芯
の多孔性粉体を得られるのである。次で、この粉体を酸
化気流中で50〜150000程度で1〜24時間程度
加熱乾燥乃至焼成すると、被覆物質を構成する微粉末の
粒子が互いに強固に結着すると同時に内芯核物質とも互
いに強固に結着し容易に破砕しない粉体となる。ここで
内芯核物質が揮発性物質を含有している場合は加熱時に
これが揮発し、更に金属炭酸化合物を含有している場合
には濃度1〜2の重量%程度の塩酸、硝酸、硫酸等の酸
液で洗浄することによってこれが熔出し、半中空の有芯
多孔性粉体とすることができる。また内芯核物質が燃焼
性物質特に合成樹脂を含有している場合は、被覆物質と
内芯核物質とを7:3〜3:7の割合で遠心ボールミル
の鷹梓粉砕機内で1〜2独特間摩擦混合し被覆物質のみ
を摩砕して更にこれを微細化すると同時に内芯核物質を
摩擦によって帯電させ、内芯核物質の表面に微細化した
被覆物を付着凝集させる。
Moreover, such porous powders can also be produced using an inert solvent instead of in an aqueous system. In this case, the weight ratio of the coating material and the inner core material is 8:2 to 2:8, and the weight ratio of the coating material, the inner core material, and the inert solvent is 9:2 to 2:8.
:1 to 6:4, preferably 8.3:1.7. Examples of inert solvents include silicone oil, polybran, polyoxyethylene tall oil derivatives, etc. The coating material and the inner core material are added to these inert solvents, and the mixture is preferably heated to about 700 to 760 legs Hg at room temperature. When the coating material and the inner core material are surrounded by an inert solvent and physically united under reduced pressure, a cored porous powder can be obtained by passing them through a suction furnace. be. Next, when this powder is dried or fired by heating at about 50 to 150,000 in an oxidizing gas flow for about 1 to 24 hours, the particles of the fine powder constituting the coating material will firmly bind to each other, and at the same time, the inner core material will also bond to each other. It becomes a powder that binds tightly and does not easily shatter. If the inner core material contains a volatile substance, it will volatilize during heating, and if it further contains a metal carbonate compound, it may contain hydrochloric acid, nitric acid, sulfuric acid, etc. at a concentration of about 1 to 2% by weight. This can be melted by washing with an acid solution to form a semi-hollow cored porous powder. In addition, if the inner core core material contains a combustible substance, especially a synthetic resin, the coating material and the inner core core material are mixed in a ratio of 7:3 to 3:7 in the Takaazusa crusher of a centrifugal ball mill. Unique frictional mixing is performed to grind only the coating material and further refine it, and at the same time, the inner core material is charged by friction, and the finer coating material is adhered and aggregated on the surface of the inner core material.

次でこの有芯多孔性粉体を酸化気硫中で、常圧下で15
0〜1600℃間にて徐々に昇温加熱することによって
、燃焼性物質を燃焼するとともに被覆物質を構成する微
粉末の粒子を互いに強固に結着させ、容易に破砕しない
半中空の有芯多孔性粉体とすることができる。更に、内
芯核物質が水以外の揮発性成分を含有する無水アルミ/
珪酸化合物で構成されている場合は前記の如き燃焼処理
、酸処理を施すことによって体積を収縮させ半中空の有
芯多孔性粉体とすることができる。次に本発明に使用さ
れる多孔性粉体の製造例を示す。
Next, this cored porous powder was placed in oxidized gas and sulfur under normal pressure for 15 minutes.
By gradually increasing the temperature between 0 and 1,600 degrees Celsius, the combustible material is burned and the fine powder particles that make up the coating material are firmly bound to each other, creating a semi-hollow cored porous structure that does not easily shatter. It can be made into a powder. Furthermore, anhydrous aluminum whose inner core material contains volatile components other than water
If it is made of a silicic acid compound, it can be subjected to the combustion treatment and acid treatment as described above to shrink its volume and form a semi-hollow cored porous powder. Next, an example of manufacturing the porous powder used in the present invention will be shown.

製造例 1 粒径3〜8uの黒雲母5部と粒径2〜5山のセリサイト
4$部とをcpsのジメチルシロキサン250部中に鷹
拝しながら徐々に添加し、2時間常温で鷹拝して取出し
吸引アスピレータで炉過し、850℃で1時間焼成した
後急冷して粒径5〜14仏の有芯の多孔性粉体4碇部を
得た。
Production Example 1 5 parts of biotite with a particle size of 3 to 8 μm and 4 parts of sericite with a particle size of 2 to 5 particles were gradually added to 250 parts of CPS dimethylsiloxane while stirring, and the mixture was incubated at room temperature for 2 hours. The mixture was taken out, filtered through a furnace using a suction aspirator, fired at 850° C. for 1 hour, and then rapidly cooled to obtain 4 portions of cored porous powder with a particle size of 5 to 14 mm.

製造例 2 粒径2〜8仏の炭酸マグネシウム15部と粒径1〜3仏
のカリ長石45部と精製水1500叫中に分散し、アジ
タ−で1時間額拝した後取出して吸引アスピレータで吸
引炉過し、950q○で1糊時間焼成し粒径6〜15仏
の有芯多孔性粉体55部を得た。
Production Example 2 15 parts of magnesium carbonate with a particle size of 2 to 8 degrees and 45 parts of potassium feldspar with a particle size of 1 to 3 degrees are dispersed in 1,500 g of purified water, and after worshiping in an agitator for 1 hour, it is taken out and pumped with a suction aspirator. The mixture was passed through a suction furnace and fired at 950 q○ for 1 hour to obtain 55 parts of cored porous powder with a particle size of 6 to 15 mm.

製造例 3粒径2〜5rのカオリオナィト15部と粒径
3〜5仏の珪藻±15部と粒径8〜10仏の炭酸カルシ
ウム1碇部と粒径5〜9仏の炭酸マグネシウム1碇都と
を精製水500の【中に分散し、アジターで1時間婿拝
した後に取出し、吸引アスピレータで吸引炉遇し100
0ooで1観時間焼成し粒径9〜18一の有芯の多孔性
粉体4碇部を得た。
Production Example 3: 15 parts of kaolionite with a particle size of 2 to 5R, 15 parts of diatom with a particle size of 3 to 5 degrees, 1 part of calcium carbonate with a particle size of 8 to 10 degrees, and 1 part of magnesium carbonate with a particle size of 5 to 9 degrees. Disperse it in 500ml of purified water, worship it in an agitator for 1 hour, take it out, put it in a suction furnace with a suction aspirator,
The powder was fired at 0oo for 1 hour to obtain 4 anchor portions of cored porous powder having a particle size of 9 to 18 mm.

製造例 4 粒径2〜5りのカオリン7の都と粒蓬3〜8〃の炭酸第
二鉄3碇部とを精製水82の【中に分散し、遠心回転形
ボールミルに投入して9時間濠合摩砕して取出し、80
ooで2御嵩間乾燥して粒径5〜16山の有芯の多孔性
粉体91部を得た。
Production Example 4 Disperse 7 parts of kaolin with a particle size of 2 to 5 mm and 3 parts of ferric carbonate of 3 to 8 particles of grain size in 82 of purified water, and put it into a centrifugal rotating ball mill. Grind and remove for an hour, 80
The powder was dried for 2 mounds at OO to obtain 91 parts of cored porous powder having a particle size of 5 to 16 grains.

製造例 5 粒径2〜5一の金雲母7礎都と粒径3〜8仏の炭酸第二
鉄3碇部とを精製水82の‘中に分散し、遠心回転形ボ
ールミルに投入して9時間混合摩砕して取出し、80q
oで2独特間乾燥して粒径5〜16仏の有芯の多孔性粉
体91部を得た。
Production Example 5 7 pieces of phlogopite with a particle size of 2 to 5 and 3 pieces of ferric carbonate with a particle size of 3 to 8 were dispersed in 82 of purified water and put into a centrifugal rotating ball mill. Mix and grind for 9 hours, take out, 80q
The powder was dried for 2 hours at 100 ℃ to obtain 91 parts of cored porous powder having a particle size of 5 to 16 mm.

製造例 6 粒径2〜8ムのカリ長石1礎部と粒径2〜5〃の炭酸カ
ルシウム5碇部とを50%エチレンアルコール水溶液8
6の‘に加え遠心回転形ボールミルに投入し6.報時間
混合鰹砕して敬出し、70℃で48時間燥して粒径5〜
17仏の有芯の多孔性粉体46部を得た。
Production Example 6 One cornerstone of potassium feldspar with a grain size of 2 to 8 μm and 5 anchor parts of calcium carbonate with a grain size of 2 to 5 mm are mixed in 8 parts of a 50% ethylene alcohol aqueous solution.
In addition to step 6, put it into a centrifugal rotary ball mill. The dried bonito is crushed and drained for a long time, and dried at 70℃ for 48 hours until the particle size is 5~
46 parts of porous powder with a core of 17 mm was obtained.

製造例 7粒径2〜8山の金雲母1碇部と粒径2〜5山
の黒雲母5碇部とを50%エチルアルコール水溶液86
の‘に加え遠心回転形ボールミルに投入し、6.糊時間
混合摩砕して取出し、70午0で4鞘時間乾燥して粒径
5〜17〃の有芯の多孔性粉体46部を得た。
Production example 1 part of phlogopite with 7 grain sizes of 2 to 8 grains and 5 parts of biotite with grain sizes of 2 to 5 grains were mixed into 86 parts of a 50% ethyl alcohol aqueous solution.
In addition to '', put it into a centrifugal rotary ball mill, 6. The mixture was mixed and ground for a long time, taken out, and dried at 70:00 for 4 hours to obtain 46 parts of cored porous powder with a particle size of 5 to 17 mm.

製造例 8粒径2〜5仏のカオリオナィト15部と粒径
3〜5仏の珪藻士15部と粒径8〜10の炭酸カルシウ
ム1碇部と粒径5〜9山の炭酸マグネシウム1碇都とを
精製水500の上中に分散し、アジタ−によって激しく
1時間燭拝して敬出し、吸引アスピレータで吸引炉過し
、100000で1細時間焼成し、粒径9〜18仏の有
芯の多孔性粉体4碇部を得た。
Production example: 15 parts of kaolionite with a grain size of 8 to 5 grains, 15 parts of diatomite with a grain size of 3 to 5 grains, 1 part of calcium carbonate with a grain size of 8 to 10 grains, and 1 part of magnesium carbonate with a grain size of 5 to 9 grains Dispersed in 500ml of purified water, vigorously worshiped with an agitator for 1 hour, filtered through a suction furnace with a suction aspirator, fired at 100,000°C for 1 minute, and made into a core with a particle size of 9 to 18 Buddhas. Four anchor portions of porous powder were obtained.

製造例 9 前記製造例7で得られた多孔性粉体4碇部を5%の塩酸
300肌中に3時間浸潰して敬出し吸引アスピレータで
吸引炉過し乾燥して半中空の有芯の多孔性粉体を得た。
Production Example 9 Four anchor parts of the porous powder obtained in Production Example 7 were soaked in 5% hydrochloric acid (300%) for 3 hours, taken out, passed through a suction oven with a suction aspirator, dried, and made into a semi-hollow cored material. A porous powder was obtained.

製造例 10粒径2〜5山のカオリン2碇部と粒径2〜
8〃炭酸マグネシウム2の部とを50%エチルアルコー
ル水溶液100Mに加え遠心回転形ボールミルに投入し
7.幼時間激しく燈拝して取出し、70℃で4即時間乾
燥して粒径5〜17仏の有芯の多孔性粉体を得た。
Production example: 10 particle sizes of 2 to 5 kaolin anchors and particle sizes of 2 to 5 particles.
8. Add 2 parts of magnesium carbonate to 100M of 50% ethyl alcohol aqueous solution and put it into a centrifugal rotating ball mill.7. The powder was heated vigorously for a while, then taken out, and immediately dried at 70° C. for 4 hours to obtain a cored porous powder with a particle size of 5 to 17 mm.

製造例 11粒径2〜5仏のカオリン2碇部と粒径2〜
8仏のメチルパラベン1碇部とジスチルベンゼンピンホ
ールポリマ10部とを50%エチルアルコール水溶液l
oo似に加え遠心回転形ボ−ルミルに投入し7.2時間
激しく縄拝して取出し、70q0で4錨時間乾燥して粒
径5〜17山の有芯の多孔性粉体を得た。
Production example 11 Kaolin 2 anchors with particle size 2-5 and particle size 2-5
8 parts of methylparaben and 10 parts of distylbenzene pinhole polymer in a 50% aqueous solution of ethyl alcohol.
In addition, the powder was placed in a centrifugal rotary ball mill, stirred vigorously for 7.2 hours, taken out, and dried at 70q0 for 4 hours to obtain a cored porous powder with a particle size of 5 to 17 grains.

製造例 12前記製造例10によって得られた多孔性粉
体36部を300ooで20時間焼成して粒径5〜15
一の有芯多孔性粉体を得た。
Production Example 12 36 parts of the porous powder obtained in Production Example 10 was fired at 300 oo for 20 hours to obtain a particle size of 5 to 15.
A cored porous powder was obtained.

このようにして製造された多孔性粉体は電子顕微鏡観察
(略)によると、微細な被覆物質である天然鉱物が粒径
1〜50山程度の球状、楕円球状に近い形状で互いに貼
り合さつた集合体となって居り、各被覆物質間に大小の
空隙が認められ、この空隙またはこの空隙と所望により
内芯に形成した空洞とによって液体、気体の吸湿放散能
力が優れていることが判明した。
According to electron microscopic observation (omitted), the porous powder produced in this way has a fine coating of natural minerals stuck together in a shape close to a spherical or ellipsoidal shape with a grain size of about 1 to 50 peaks. It was found that large and small voids were observed between each coating material, and that these voids, or the cavities formed in the inner core as required, had excellent moisture absorption and dissipation ability for liquids and gases. did.

そして、表層部は被覆物質の永久収縮、一部結晶質への
転化などにより高強度の膜体を形成している。また、本
発明に使用される有芯の多孔性粉体は構成成分が無機物
質であるから、耐熱性、耐光性に優れて居り、水系、非
水系において見掛けの比重が軽く且つ溶媒との親和性が
あり、そのため混合系では非沈降性を有するものであり
、単一体として挙動し分散性に優れているため従来の粉
体にないしっとりとした感触を与え、感触がなめらかで
、密着性のよい化粧料が提供できるのである。
The surface layer forms a high-strength film due to permanent shrinkage of the coating material and partial conversion to crystalline material. In addition, since the cored porous powder used in the present invention is composed of inorganic substances, it has excellent heat resistance and light resistance, has a light apparent specific gravity in aqueous and non-aqueous systems, and is compatible with solvents. As a result, it has non-sedimenting properties in a mixed system, behaves as a single body, and has excellent dispersibility, giving it a moist feel that is not found in conventional powders. We can provide good cosmetics.

また、容器へ充填した場合最密充填構造をつくりやすく
、パッキング性にも優れているものである。さらに、本
発明に使用される多孔性粉体は皮膚刺激性、毒性が全く
なく、健康肌の女性102名の前縛部における貼布試験
においても2餌寺間、7幼時間後の判定で何等の異常も
認められなかった。
Furthermore, when filled into a container, it is easy to create a close-packed structure and has excellent packing properties. Furthermore, the porous powder used in the present invention has no skin irritation or toxicity, and in a patch test on the anterior bound area of 102 women with healthy skin, it was judged after 2 hours and 7 hours. No abnormality was observed.

即ち、本発明に係る化粧料は、配合されている多孔性粉
体の特性によって肌に負担をかけずにしっとりとし滑ら
かにして密着性に陵れ、しかも保香力があり長時間に亘
つて芳香を発しすぐれた化粧効果を有するものばかりか
、充填性を大きく向上させるものである。また、本発明
に使用される多孔性粉体は被覆物質と内芯核物質との結
合時における両者の配合割合を変化させることによって
粒径、被覆物質層の強度を自由に調整することができる
ものである。
In other words, the cosmetics according to the present invention moisturizes and smooths the skin without putting a burden on the skin due to the characteristics of the porous powder contained in it, and has good adhesion, and also has a fragrance-retaining ability that lasts for a long time. Not only does it emit a fragrance and have excellent cosmetic effects, but it also greatly improves filling properties. In addition, the porous powder used in the present invention can freely adjust the particle size and the strength of the coating material layer by changing the mixing ratio of the coating material and the inner core material when they are combined. It is something.

尚また、多孔性粉体は粒径1〜100仏程度であり、且
つ2〜75重量%を配合して化粧料とする。次に調香師
10名による各試料についての保青性の官能試験結果を
示す。各試料に用いられたプレストパウダは前記各製造
例によって製造された有芯の多孔性粉体または天然鉱物
微粉末(タルク)6う タルク15.1、ナイロンパウ
ダ10.0 シルクパウダ3.0、赤色系酸化鉄0.1
6、黄色水和酸化鉄0.11、黒色酸化鉄0.03(重
量%)の混合物をへンシェルミキサで2分間(180仇
.p.m)混合して粉砕機で粉砕した後、この粉砕物を
再びへンシヱルミキサに移し、これにトリー2エチルヘ
キサングリセリン3.5、オレイン酸オクチドデシル2
.0、ィソステアリン酸グリセリン0.5(重量%)を
加えて8分間(180仇.p.m)混合し、この健拝混
合物に香料レモン0.6重量%を加えて更に2分間(1
80比.p.m)混合して取出し、ブロアシフタを通し
て容器に充填した。
Furthermore, the porous powder has a particle size of about 1 to 100 F, and is blended in an amount of 2 to 75% by weight to form a cosmetic. Next, we will show the results of a sensory test of the retention properties of each sample conducted by 10 perfumers. The pressed powders used for each sample were cored porous powders or natural mineral fine powders (talc) manufactured by the above-mentioned manufacturing examples. Talc 15.1, nylon powder 10.0, silk powder 3.0, red. Iron oxide 0.1
6. A mixture of 0.11 yellow hydrated iron oxide and 0.03 (wt%) black iron oxide was mixed in a Henschel mixer for 2 minutes (180 p.m.) and pulverized in a pulverizer. was transferred to the hensyl mixer again, and to this was added 3.5% of tri2-ethylhexane glycerin and 2.5% of octidodecyl oleate.
.. 0.0, glyceryl isostearate 0.5 (wt%) was added and mixed for 8 minutes (180 m.p.m.), and 0.6 wt% of lemon flavor was added to this health mixture and further mixed for 2 minutes (1
80 ratio. p. m) Mixed, taken out and filled into a container through a blower sifter.

試料A−【a’乃至A−(k)はそれぞれ製造例1乃至
11によって作られた多孔性粉体を用いたものであり、
試料Bはタルクを用いたものである。(1)常 温 評
価 (20〜250C)第1表(2)40℃評価 第2表 注,±は揮発強度を示す。
Samples A-[a' to A-(k) are those using porous powders made according to Production Examples 1 to 11, respectively.
Sample B uses talc. (1) Room temperature evaluation (20-250C) Table 1 (2) 40°C evaluation Table 2 Note: ± indicates volatilization strength.

(一なし,十あり)これらの官能試験の結果によると、
常温において従釆の天然鉱物の微粉末を用いた試料Bは
3ケ月後から次第に保香性が失われているのに対し、本
発明である有芯の多孔性粉体を含有した試料Aは少なく
とも1年間に亘つて保苔性を維持して居り、本発明のイ
Q舷料が従釆品に比べて格段に保香性に優れていること
は明白である。
(No 1, 10) According to the results of these sensory tests,
Sample B, which used a fine powder of a natural mineral as a substructure at room temperature, gradually lost its fragrance retention after three months, whereas sample A, which contained a cored porous powder according to the present invention, It maintains its moss retention properties for at least one year, and it is clear that the IQ sheathing of the present invention has much better fragrance retention than the subordinate products.

また、40oCにおける官能試験結果におけても本発明
は従来品よりも保香性に優れていることが確認できる。
Furthermore, the results of the sensory test at 40oC also confirm that the present invention has superior fragrance retention compared to conventional products.

以下に本発明の実施例を示す。但し、配合割合は重量部
である。実施例 1 油性ファンデーション 製造例1による多孔性粉体 30オゾ
ケライト 80セ
レシン 90マ
イクロクリスタルワックス 30スク
ワラン 710活性剤
3ラノリン
40無機顔料
2ジブチルヒドロキシトルエン
0.5上記の各成分を溶解釜に仕込
み80qoで完全溶解、分散を行なった後、80o0に
保持してゆっくりと蝿拝しながら溶解釜より容器に充填
し、放冷して製品とする。
Examples of the present invention are shown below. However, the blending ratio is in parts by weight. Example 1 Porous powder according to oil-based foundation production example 1 30 Ozokerite 80 Ceresin 90 Microcrystal wax 30 Squalane 710 Activator
3 lanolin
40 inorganic pigments
2-dibutylhydroxytoluene
0.5 Each of the above-mentioned components is charged into a dissolving pot and completely dissolved and dispersed at 80 qo.Then, the mixture is maintained at 80 qo and slowly poured into a container from the dissolving pot, and left to cool to form a product.

実施例 2 水おしるし、 Aをアジターで1時間燈拝し、更にBを加えて30分間
縄拝した後に取出して容器に充填し製品とする。
Example 2 Mizu Oshishi A is heated in an agitator for 1 hour, B is added and stirred for 30 minutes, then taken out and filled into containers to produce a product.

実施例 3 ダステイグパウダ Aをへンシェルミキサに仕込み高速回転で1ぴ分間縄拝
混合し、更にBを加え1び分間縄梓混合して取出し、シ
フターにかけ容器に充填して製品とする。
Example 3 Dusting powder A is charged into a Henschel mixer and mixed at high speed for 1 minute, then B is added and mixed for 1 minute, taken out, passed through a sifter, and filled into containers to produce a product.

実施例 4 プレストパウダ Aをへンシェルミキサで2分間鷹拝混合し粉砕機で粉砕
混合して再びへンシェルミキサにBと一緒に入れ5分間
蝿梓混合して出し、シフターに通しプレス充填して製品
とする。
Example 4 Pressed powder A is mixed for 2 minutes in a Henschel mixer, pulverized and mixed in a pulverizer, put into the Henschel mixer together with B again, mixed for 5 minutes, taken out, passed through a sifter, press filled, and made into a product. do.

実施例 5 フエースカラ 製造例5による多孔性粉体 5.0Aをへン
シェルミキサで5分間混合し粉砕機で粉体温合して再び
へンシェルミキサにBと一緒に入れ10分間溜梓混合し
て取出し、ブロワーシフターを通しプレス充填して製品
とする。
Example 5 Porous powder 5.0 A according to Phase Scara Production Example 5 was mixed in a Henschel mixer for 5 minutes, the powder was mixed in a pulverizer, put into the Henschel mixer together with B again, mixed for 10 minutes, taken out, and then removed using a blower. The product is press-filled through a sifter.

実施例 6 アイベンシノレ 製造例3による多孔性粉体 21.0木
ロウ 8.0セレ
シン 12.
0力ルナバ 1
0.0活性剤 5.
0金属石けん 20.0マ
イクロクリスタリンワツクス 30ステアリン
酸 15.0流動パラフィン
4.0イソプロピルミリス
テート 2.0上記の各成分を80
qoに加熱しながらニーダーで30分間混練した後に成
形金型に充填し成形して製品とする。
Example 6 Porous powder according to Ibensinole Production Example 3 21.0 Wood wax 8.0 Ceresin 12.
0 power lunaba 1
0.0 activator 5.
0 Metal soap 20.0 Microcrystalline wax 30 Stearic acid 15.0 Liquid paraffin
4.0 Isopropyl myristate 2.0 80% of each of the above ingredients
After kneading with a kneader for 30 minutes while heating to qo, the mixture is filled into a mold and molded to form a product.

実施例 7 クリームルージュ B 香 料 0.5A
を溶解釜で80ooにて完全溶解し分散させてBを添加
し、ゆっくり縄拝しながら溶解釜より取出し容器に充填
し放冷して製品とする。
Example 7 Cream Rouge B Fragrance 0.5A
Completely dissolve and disperse in a melting pot at 80 oo, add B, and slowly remove from the melting pot, fill in a container, and leave to cool to obtain a product.

実施例 8 力ラミローシヨン AにBを添加してアジターで1時間鷹梓混合し、更にC
を添加し30分間縄拝混合した後にDを添加して20分
間燈拝し、取出し容器に充填し製品とする。
Example 8 Add B to the lotion A, mix in an agitator for 1 hour, and then add C.
After adding and mixing for 30 minutes, add D and stir for 20 minutes, then take out and fill in a container to make a product.

実施例 9 油性ファンデーション 製造例9による多孔性粉体 30オゾケ
ライト 80セレシン
90マイクロ
クリスタリンワツクス 30スクワラン
710活性剤
3ラ/リン
40無機顔料
2ジブチルヒドロキシトルエン
0.5上記の各成分を溶解釜に仕込み80午○
で完全溶解し分散させた後、80ooに保持してゆっく
りと蝿拝しながら溶解釜より容器に充填し、放冷して製
品とする。
Example 9 Porous powder according to oil-based foundation production example 9 30 Ozokerite 80 Ceresin
90 microcrystalline wax 30 squalane
710 activator
3 la/rin
40 inorganic pigments
2-dibutylhydroxytoluene
0.5 Place each of the above ingredients into a melting pot and heat at 80pm.
After complete dissolution and dispersion, the mixture is maintained at 80 oo and slowly poured into a container from the melting pot, and left to cool to form a product.

実施例 10 水おしるし、 Aをアジタ−で1時間蝿拝し、更にBを加えて30分間
損拝した後に取出し、容器に充填して製品とする。
Example 10 Mizu Oshishi: A was soaked in an agitator for 1 hour, B was added thereto and stirred for 30 minutes, then taken out and filled into containers to produce a product.

実施例 11 ダステインパウダ Aをへンシェルミキサに仕込高速回転で10分間蝿梓混
合し、更にBを加え10分間損梓混合して取出し、シフ
ターにかけ容器に充填して製品とする。
Example 11 Dustin powder A is charged into a Henschel mixer and mixed at high speed for 10 minutes, then B is added and mixed for 10 minutes, taken out, passed through a sifter, and filled into containers to produce a product.

Claims (1)

【特許請求の範囲】[Claims] 1 無水珪酸化合物、アルミノ珪酸化合物、マグネシウ
ム珪酸化合物の一種または二種以上の微粉末からなる被
覆物質を金属炭酸化合物、水以外の揮発性成分を含有す
る無水アルミノ珪酸化合物、揮発性物質、燃焼性物質の
一種または二種以上の微粉末からなる内芯核物質の表面
に付着凝集して得られた多孔性粉体を化粧料成分に配合
したことを特徴とする化粧料。
1 Coating material consisting of fine powder of one or more types of anhydrous silicic acid compound, aluminosilicate compound, and magnesium silicate compound is coated with a metal carbonate compound, an anhydrous aluminosilicate compound containing volatile components other than water, volatile substances, and flammability. 1. A cosmetic comprising a cosmetic ingredient containing porous powder obtained by adhering and agglomerating on the surface of an inner core material consisting of fine powder of one or more kinds of substances.
JP9000276A 1976-07-28 1976-07-28 cosmetics Expired JPS6019281B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9000276A JPS6019281B2 (en) 1976-07-28 1976-07-28 cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9000276A JPS6019281B2 (en) 1976-07-28 1976-07-28 cosmetics

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP20329684A Division JPS60100509A (en) 1984-09-28 1984-09-28 Cosmetic

Publications (2)

Publication Number Publication Date
JPS5315433A JPS5315433A (en) 1978-02-13
JPS6019281B2 true JPS6019281B2 (en) 1985-05-15

Family

ID=13986386

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9000276A Expired JPS6019281B2 (en) 1976-07-28 1976-07-28 cosmetics

Country Status (1)

Country Link
JP (1) JPS6019281B2 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54163830A (en) * 1978-06-16 1979-12-26 Pola Kasei Kogyo Kk Cosmetics
JPS56142131A (en) * 1979-11-30 1981-11-06 Eesupatsuku Kk Molding device for flat top type catron
JPS60141842U (en) * 1984-03-01 1985-09-19 桐灰化学工業株式会社 Flavored holder for abrasive or scorching tools
JPS60228406A (en) * 1984-04-27 1985-11-13 Pola Chem Ind Inc Cosmetic
JPS6147410A (en) * 1984-08-14 1986-03-07 Agency Of Ind Science & Technol Cosmetic
JPS63222108A (en) * 1987-03-11 1988-09-16 Noebia:Kk Cosmetic
JP6543575B2 (en) * 2013-05-14 2019-07-10 ロレアル Cosmetic composition

Also Published As

Publication number Publication date
JPS5315433A (en) 1978-02-13

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