JPS6339565B2 - - Google Patents
Info
- Publication number
- JPS6339565B2 JPS6339565B2 JP53055219A JP5521978A JPS6339565B2 JP S6339565 B2 JPS6339565 B2 JP S6339565B2 JP 53055219 A JP53055219 A JP 53055219A JP 5521978 A JP5521978 A JP 5521978A JP S6339565 B2 JPS6339565 B2 JP S6339565B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- silica gel
- metal soap
- add
- stirring
- 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
Links
- 239000000843 powder Substances 0.000 claims description 49
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 46
- 229910002027 silica gel Inorganic materials 0.000 claims description 36
- 239000000741 silica gel Substances 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 33
- 239000002537 cosmetic Substances 0.000 claims description 27
- 229910052751 metal Inorganic materials 0.000 claims description 27
- 239000002184 metal Substances 0.000 claims description 27
- 239000000344 soap Substances 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000000576 coating method Methods 0.000 claims description 10
- 238000003756 stirring Methods 0.000 description 27
- 239000004615 ingredient Substances 0.000 description 21
- 239000003205 fragrance Substances 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 9
- 229940063655 aluminum stearate Drugs 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- 238000009472 formulation Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000021355 Stearic acid Nutrition 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 229940057995 liquid paraffin Drugs 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 5
- 238000005096 rolling process Methods 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 238000001179 sorption measurement Methods 0.000 description 5
- 239000008117 stearic acid Substances 0.000 description 5
- 239000004166 Lanolin Substances 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 235000019388 lanolin Nutrition 0.000 description 4
- 229940039717 lanolin Drugs 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 239000004203 carnauba wax Substances 0.000 description 3
- 235000013869 carnauba wax Nutrition 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 3
- 238000000635 electron micrograph Methods 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000003020 moisturizing effect Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 229940099259 vaseline Drugs 0.000 description 2
- 239000012463 white pigment Substances 0.000 description 2
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 1
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- MYOLYOJJHNUECB-UHFFFAOYSA-J C(CCCCCCCCCCC)(=O)[O-].[Zn+2].[Zn+2].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] Chemical compound C(CCCCCCCCCCC)(=O)[O-].[Zn+2].[Zn+2].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] MYOLYOJJHNUECB-UHFFFAOYSA-J 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 208000006981 Skin Abnormalities Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 102000011759 adducin Human genes 0.000 description 1
- 108010076723 adducin Proteins 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- OQNGCCWBHLEQFN-UHFFFAOYSA-N chloroform;hexane Chemical compound ClC(Cl)Cl.CCCCCC OQNGCCWBHLEQFN-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- YGANSGVIUGARFR-UHFFFAOYSA-N dipotassium dioxosilane oxo(oxoalumanyloxy)alumane oxygen(2-) Chemical compound [O--].[K+].[K+].O=[Si]=O.O=[Al]O[Al]=O YGANSGVIUGARFR-UHFFFAOYSA-N 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 230000037336 dry skin Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000008269 hand cream Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229910052627 muscovite Inorganic materials 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 230000037204 skin physiology Effects 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- 229940012185 zinc palmitate Drugs 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
本発明は油性または乳化性のフアンデーシヨ
ン、口紅、ハンドクリーム、アフターシエービン
グクリーム、アイシヤドウなどの化粧料に関する
ものである。
従来、皮膚に塗布する際の伸びならびに滑り感
などを向上させる目的でタルク、カオリン、酸化
チタン、微結晶性セルロース、デンプンなどの微
細な粉体を化粧料に配合させることは周知であ
る。
ところが、前記各種の粉体は一般に不定形を呈
しており、このような粉体を配合した化粧料を皮
膚に塗擦した場合に、粉体の摩擦抵抗力がきわめ
て大きいため充分に滑らかで伸びの軽い感触を得
ることは困難であつた。また、近年望まれている
さつぱり感を有する化粧料を提供する目的でオイ
ル成分として低粘度のものを使用することが検討
されているが、配合する粉体の摩擦抵抗力が大き
いため充分にさらさらとした感触を得ることがで
きないのが現状である。
更に、前記の不定形の粉体の代りに微細球状の
シリカゲルを化粧料に配合することが米国特許第
4000317号公報に提示されているが、このものは
皮脂ならびに汗を吸収する目的で粒径20mμ以下
のシリカゲルをコロイド状に懸濁配合させたせロ
ーシヨンであつて、シリカゲルの有する吸湿性な
らびに乾燥性などのために繰返し使用すると皮膚
の表面が過度に乾燥してカサカサとなり皮膚生理
学上好ましくないばかりか、皮膚に塗布した際の
柔軟性および保湿性が劣るなどの問題がある。
本発明は斯る実情に鑑みてなされたものであつ
て、皮膚に塗擦した場合に充分に滑らかで伸びの
軽い感触を得ることができるとともにカサ付き感
がないばかりか適度のさつぱり感を有し、しかも
皮膚との親和性がよく柔軟で湿潤な感触を得るこ
とのできる化粧料を提供するものである。
即ち、本発明である化粧料は、粒径1〜30μの
球状のシリカゲルに金属石けんをコーテングする
ことにより得られ且つ前記シリカゲルと金属石け
んとの組成比が99:1〜70:30である粉体を含有
していることを特徴としている。
本発明に用いられる球状のシリカゲルは組成式
SiO2・nH2Oで示される多孔質或いは無孔質のも
ので、天然品に限らず乾式ならびに湿式による合
成品も使用可能である。尚、組成式SiO2・nH2O
は本来的に結合水が含まれたものを示すだけでな
く、二酸化ケイ素が自然化下において瞬時に水を
吸着した状態のものも包含しており、これらを総
称した組成式である。また、本発明において球状
は真球状のほかに球に類似の形状のものも包含し
ているものと定義され、粒径1〜30μ、好ましく
は5〜15μのものが使用される。これは1μ未満で
はその転動効果を利用した皮膚に対する滑らかな
伸びを期待することができず、30μを超えるとざ
らついた感触を与え好ましくないためである。
次に、前記のようなシリカゲルをコーテングす
るための金属石けんは一般式(RCOO)nMで示
される化合物(ここで、Rは炭素数6〜8以上の
脂肪族または環状炭化水素基、Mはアルカリ金属
以外の金属、nはその金属の原子価を示す。)の
うちで分散性、潤滑性、柔軟性、付着性に優れ且
つ安全性の高いものが好ましく、例えばステアリ
ン酸アルミニウム、ステアリン酸マグネシウム、
ステアリン酸亜鉛など粉末状のもの或いはロウ状
のものが挙げられる。
金属石けんによるコーテングはシリカゲルの表
面を完全に且つ均一厚さに被覆する状態のみに限
定されるものでなく、不均一厚さであつても完全
に被覆していればよいが、金属石けんがシリカゲ
ルに密着していることが必要である。
更に、粉体を構成するシリカゲルと金属石けん
とは99:1〜70:30の組成比とする。この範囲よ
りも金属石けんが多い場合は金属石けんの特性が
そのまま現出して例えば化粧料基材中に配合して
も転動効果が極端に低下して皮膚に対する感触が
滑らかとならないばかりか、極度に多くなるとシ
リカゲルと金属石けんとが分離し転動効果を生じ
ない。反対に金属石けんが前記範囲よりも少ない
場合にはシリカゲル単体の特性がそのまま現出し
てしまい本発明の効果を期待できない。
更にまた、前記の粉体は化粧料に全重量に対し
て3〜45%、好ましくは5〜35%の範囲で包含さ
せる。殊に油性または乳化性の化粧料において粉
体の配合量を3%未満とした場合には転動効果が
得られにくく、40%を超えると系が過度にゲル化
して好ましくない。
本発明に用いられる化粧料に使用される粉体は
種々の方法によつて製造することができるが、例
えば所定の組成比を有するシリカゲルと金属石け
んとの混合物にヘキサン、オクタン、トルエン、
クロロホルムなどの金属石けん可溶のクロル系溶
剤或いは炭化水素系溶剤の一種或いは複数種を
1:2〜1:200の重量割合で混ぜて、加温下で
溶解、撹拌して浸漬させた後、溶剤を溜去し、次
でエタノールなどの溶剤で洗浄、乾燥することに
よつて得る方法が好適である。
次に、本発明の化粧料に使用される粉体の製造
例を示す。
The present invention relates to cosmetics such as oil-based or emulsifying foundations, lipsticks, hand creams, aftershave creams, and eye shadows. It has been well known that fine powders such as talc, kaolin, titanium oxide, microcrystalline cellulose, and starch are incorporated into cosmetics for the purpose of improving spreadability and smoothness when applied to the skin. However, the various powders mentioned above generally have an irregular shape, and when cosmetics containing such powders are rubbed onto the skin, the frictional resistance of the powders is extremely large, so it is difficult to find a product that is sufficiently smooth and spreadable. It was difficult to obtain a light feel. In addition, in order to provide cosmetics with the refreshing feeling that has been desired in recent years, the use of low-viscosity oil components is being considered, but this is not sufficient due to the high frictional resistance of the powder blended. Currently, it is not possible to obtain a silky smooth feel. Furthermore, in place of the amorphous powder described above, the use of fine spherical silica gel in cosmetics is disclosed in US Patent No.
4000317, this lotion is a colloidal suspension of silica gel with a particle size of 20 mμ or less for the purpose of absorbing sebum and sweat, and the silica gel has hygroscopicity and drying properties. If used repeatedly, the surface of the skin becomes excessively dry and flaky, which is not favorable from the viewpoint of skin physiology, and there are also problems such as poor flexibility and moisturizing properties when applied to the skin. The present invention has been developed in view of the above circumstances, and it is possible to obtain a sufficiently smooth and light feel when rubbed on the skin, as well as not having a feeling of dryness, but also a moderately refreshing feeling. The purpose of the present invention is to provide a cosmetic that has good affinity with the skin and can provide a soft and moist feel. That is, the cosmetic of the present invention is a powder obtained by coating spherical silica gel with a particle size of 1 to 30 μm with metal soap, and in which the composition ratio of the silica gel to metal soap is 99:1 to 70:30. It is characterized by containing a body. The compositional formula of the spherical silica gel used in the present invention is
It is a porous or non-porous material represented by SiO 2 .nH 2 O, and not only natural products but also dry and wet synthetic products can be used. In addition, the composition formula SiO 2・nH 2 O
not only refers to those that inherently contain bound water, but also includes those in which silicon dioxide instantly adsorbs water during naturalization, and is a general compositional formula for these. Furthermore, in the present invention, spherical shape is defined to include not only true spherical shape but also shapes similar to spheres, and particles having a particle size of 1 to 30 μm, preferably 5 to 15 μm are used. This is because if it is less than 1μ, it cannot be expected to spread smoothly on the skin by utilizing its rolling effect, and if it exceeds 30μ, it will give a rough feel, which is undesirable. Next, the metal soap for coating the silica gel as described above is a compound represented by the general formula (RCOO)nM (where R is an aliphatic or cyclic hydrocarbon group having 6 to 8 or more carbon atoms, and M is an alkali Among metals other than metals (n indicates the valence of the metal), those with excellent dispersibility, lubricity, flexibility, adhesion, and high safety are preferred, such as aluminum stearate, magnesium stearate,
Powdered ones such as zinc stearate or waxed ones can be mentioned. Coating with metal soap is not limited to coating the silica gel surface completely and with a uniform thickness; it is sufficient to completely coat the surface of the silica gel even if the thickness is uneven; It is necessary to be in close contact with Furthermore, the composition ratio of silica gel and metal soap constituting the powder is 99:1 to 70:30. If the amount of metal soap is more than this range, the characteristics of metal soap will appear as they are, and even if it is mixed into a cosmetic base material, the rolling effect will be extremely reduced, and the feel on the skin will not be smooth, or it will not be extremely smooth. If the amount increases, the silica gel and the metal soap will separate and no rolling effect will occur. On the other hand, if the amount of metal soap is less than the above range, the properties of the silica gel alone will appear as they are, and the effects of the present invention cannot be expected. Furthermore, the above-mentioned powder is included in the cosmetic composition in an amount of 3 to 45%, preferably 5 to 35%, based on the total weight. Particularly in oil-based or emulsifying cosmetics, if the amount of powder blended is less than 3%, it is difficult to obtain a rolling effect, and if it exceeds 40%, the system will become excessively gelled, which is undesirable. The powder used in the cosmetics used in the present invention can be produced by various methods, but for example, hexane, octane, toluene,
One or more types of chlorine-based solvents or hydrocarbon-based solvents that are soluble in metal soap such as chloroform are mixed in a weight ratio of 1:2 to 1:200, dissolved under heating, stirred and immersed, A preferred method is to distill off the solvent, then wash with a solvent such as ethanol, and dry. Next, an example of manufacturing the powder used in the cosmetic of the present invention will be shown.
【製造例 1】
トルエン500mlに粒径5〜15μの球形のシリカ
ゲルの径が異なるものの混合物95gを加えて60℃
に加温し、緩かに撹拌しながらステアリン酸アル
ミニウム3gを少量ずつ添加して30分間加温、撹
拌を続け、減圧蒸溜(3mmHg)により溶剤を留
去する。次で、15〜20℃の温度に保ちながらエタ
ノール300mlを加えて20分間撹拌し濾過する。か
かる操作を三回繰り返した後、洗浄して60℃にて
減圧乾燥し、ステアリン酸アルミニウムをコーテ
ングした粉体(粒径約5〜15μ)ほぼ100gを得
た。[Production example 1] Add 95 g of a mixture of spherical silica gels with particle sizes of 5 to 15 μm to 500 ml of toluene and heat at 60°C.
3 g of aluminum stearate was added little by little with gentle stirring. The mixture was heated and stirred for 30 minutes, and the solvent was distilled off under reduced pressure (3 mmHg). Next, while maintaining the temperature at 15-20°C, add 300 ml of ethanol, stir for 20 minutes, and filter. After repeating this operation three times, it was washed and dried under reduced pressure at 60° C. to obtain approximately 100 g of aluminum stearate coated powder (particle size: approximately 5 to 15 μm).
【製造例 2】
ヘキサン1000mlに粒径1〜10μの球形のシリカ
ゲルの径が異なるものの混合物95gを加えて50℃
に加温し、緩やかに撹拌しながらステアリン酸亜
鉛5gを少量ずつ添加して30分間加温、撹拌を続
け、溜出温度80℃により溶剤を留去する。次で、
15〜20℃の温度に保ちながらエタノール500mlを
加えて30分間撹拌し濾過する。かかる操作を二回
繰り返した後、洗浄して60℃にて減圧乾燥し、ス
テアリン酸亜鉛をコーテングした粉体(粒径約1
〜10μ)ほぼ100gを得た。[Production Example 2] Add 95g of a mixture of spherical silica gels with particle sizes of 1 to 10μ to 1000ml of hexane and heat at 50°C.
5 g of zinc stearate was added little by little with gentle stirring, continued heating and stirring for 30 minutes, and distilled off the solvent at a distillation temperature of 80°C. Next,
While maintaining the temperature at 15-20°C, add 500 ml of ethanol, stir for 30 minutes, and filter. After repeating this operation twice, it was washed and dried under reduced pressure at 60°C to form a powder coated with zinc stearate (particle size: approx.
~10μ) Almost 100g was obtained.
【製造例 3】
ヘキサン―クロロホルム混合液(1:1)
1000mlに粒径10〜20μの球形のシリカゲルの径
が異なるものの混合物93gを加えて50℃に加温
し、緩やかに撹拌しながらパルミチン酸亜鉛7g
を少量ずつ添加し40分間加温、撹拌を続け、溜出
温度80℃により溶剤を留去する。次で、15〜20℃
の温度に保ちながらエタノール700mlを加えて40
分間撹拌し濾過する。かかる操作を三回繰り返し
た後、洗浄して50℃にて減圧乾燥し、てパルミチ
ン酸亜鉛をコーテングした粉体(粒径約10〜
20μ)ほぼ100gを得た。[Production Example 3] Add 93g of a mixture of spherical silica gel of different diameters with a particle size of 10 to 20μ to 1000ml of a hexane-chloroform mixture (1:1), heat it to 50℃, and add palmitic acid while stirring gently. 7g zinc
was added little by little, heated and stirred for 40 minutes, and the solvent was distilled off at a distillation temperature of 80°C. At 15-20℃
Add 700 ml of ethanol while keeping the temperature at 40
Stir for a minute and filter. After repeating this operation three times, the powder was washed and dried under reduced pressure at 50°C to form a powder coated with zinc palmitate (particle size approx.
20μ) Almost 100g was obtained.
【製造例 4】
トルエン―オクタン混合液(2:1)2000mlに
粒径1〜25μの球形のシリカゲルの径の異なる混
合物90gを加えて70℃に加温し、緩やかに撹拌し
ながらラウリン酸亜鉛5gとオレイン酸亜鉛5g
とを少量ずつ添加し60分間加温、撹拌を続け、減
圧蒸溜(3mmHg、溜出温度70℃)により溶剤を
留去する。次で、15〜20℃の温度に保ちながらエ
タノール1000mlを加えて60分間撹拌し濾過する。
かかる操作を二回繰り返した後、洗浄して70℃に
て減圧乾燥し、ラウリン酸亜鉛―オレイン酸亜鉛
混合物をコーテングした粉体(粒径約1〜25μ)
ほぼ100gを得た。
このようにして得られた粉体は球状のシリカゲ
ルの表面に金属石けんの薄い膜によるコーテング
が施されてシリカゲルの表面を完全に被覆すると
ともに密着し、単一体となつて水系、非水系のい
ずれにおいても分離することなく挙動するもので
ある。また、通常はシリカゲル単体がきわめて飛
散しやすいのに対し、本発明に用いられる粉体は
飛散性がなく分散能が良好であるため、充填性、
生産性においても優れている。
ここで、シリカゲル単体、シリカゲル単体と金
属石けんの混合物、本発明に用いられる粉体につ
いての見掛け密度、気相吸着法による比表面積の
測定結果ならびに電子顕微鏡写真を第1図、第2
図ならびに第3図にそれぞれ示す。見掛け密度の
測定はそれぞれ粒径1〜15μ程度の各試料32gを
容積目盛を施した試料管(口径2cm、長さ30cmの
円筒容器)に一定の条件で流し込み、これを電動
式の見掛け容積測定器(応科工業社製)にセツト
して1分間に30回の落下回数の速さで試料管を高
さ1.5cmの範囲で連続して落下させ、各試料の充
填容積の変化を測定することにより求めた。比表
面積は、吸着測定装置用の試料管(V字形枝付フ
ラスコ 容積2ml)に試料0.5gを入れて、吸着
測定装置(ADS―IB型 株式会社島津制作所製)
にセツトし、窒素ガスとヘリウムガスの混合ガス
(PN2=0.3)を流して液体窒素で冷却し、試料に
混合ガス中の窒素ガスを吸着させて平衡に達した
とき液体窒素を試料管から取除き、試料の温度上
昇により吸着窒素ガスを離脱させ、この吸着、離
脱過程における混合ガス濃度の変化を窒素ガスの
変化量をガスクロマトグラフイ(GC―6AM 株
式会社島津制作所製)の熱伝導形デイテクタで測
定することによつて求めた。また、電子顕微鏡写
真は走査形電子顕微鏡(日立―明石MINI―
SEM,MSM―4型)を用いてそれぞれ直径約
10μの試料を5000倍の倍率で撮影したものであ
り、第3図Xはシリカゲル単体、第3図Yは球状
のシリカゲルに金属石けんをコーテングすること
により得られ且つそれらの組成比が93:7の粉
体、第3図Zは球状のシリカゲルに金属石けんを
コーテングすることにより得られ且つそれらの組
成比が90:10の粉体をそれぞれ示す。
そして、第1図によれば落下回数900回におけ
る見掛け密度はシリカゲル単体よりなる試料(イ)で
は0.775、シリカゲルとステアリン酸アルミニウ
ムとを95:5,90:10の割合で混合した試料(ロ),
(ハ)では0.755、0.710であるのに対し、シリカゲル
にステアリン酸アルミニウムをコーテングして得
られ且つそれらの組成比がそれぞれ99:1,95:
5,90:10である試料(ニ),(ホ),(ヘ)の見掛け密度は
それぞれ0.670,0.630ならびに0.580であり、試料
(ニ),(ホ),(ヘ)の見掛け密度は試料(イ)および(ロ),
(ハ)の
見掛け密度よりも小さい。これらのことより試料
(ニ),(ホ),(ヘ)はシリカゲル表面に被覆されたステア
リン酸アルミニウムの被覆量だけ粒子の表面層が
厚くなつていることならびに試料(ニ),(ホ)とは全く
異なる構造を有していることがわかる。
また、第2図によれば、シリカゲル単体よりな
る試料(a)の比表面積が224.5m2/gであるのに対
して、シリカゲルにステアリン酸アルミニウムを
コーテングして得られ且つそれらの組成比がそれ
ぞれ99:1,97:3,95:5,93:7,90:10で
ある試料(b),(c),(d),(e),(f)の比表面積はいずれ
も(a)よりも小さい。このことから金属石けんがシ
リカゲルの孔部ならびに表面の僅かな窪みを被覆
しているものと推定できる。但し、試料(f)の比表
面積が(c),(d),(e)に比べて大きいが、これは被覆
面が破損したためであると推測される。従つて、
シリカゲルと金属石けんとの組成比は97:3〜
93:7の範囲が最適であるといえる。
次に本発明の実施例を示す。尚、配合割合は重
量部である。
〓実施例1〓 ステイツク状フアンデーシヨン
A 成分
カルナウバロウ 5.0
バチルアルコール 1.5
セレシン 1.5
ワセリン 15.0
流動パラフイン 35.0
着色顔料ペースト
白色顔料ペースト 16.5
B 成分
セリサイト(白雲母) 5.0
製造例1により得られた粉体 20.0
香 料 0.5
A成分を80℃以上に加温し、撹拌しながらB成
分を少しずつ加えてよく分散させ、撹拌しながら
70℃まで放冷し、香料を加えて65℃(±5℃)を
保つてステイツク容器に直接流し込み常温で放冷
して製品を得る。
〓実施例2〓 油性コンパクトフアンデーシヨン
A 成分
カルナウバロウ 2.0
ベヘニルアルコール 9.0
固形パラフイン 3.5
セタノール 4.0
ラノリン 7.0
流動パラフイン 6.0
活性剤 2.0
着色顔料ペースト 26.5
B 成分
タルク 10.0
製造例4により得られた粉体 30.0
香 料 0.5
A成分を85℃以上に加温し、撹拌しながら65℃
まで放冷し、B成分を少しずつ加えてよく分散さ
せ、次で香料を加えて65℃(±5℃)を保つて中
皿容器に直接流し込み常温で放冷して製品を得
る。
〓実施例3〓 乳化タイプフアンデーシヨン
A 成分
ミツロウ 2.0
ステアリン酸 2.5
流動パラフイン 15.0
活性剤 6.0
ラノリン 6.0
着色顔料ペースト
白色顔料ペースト 17.0
B 成分
トリエタノールアミン 1.0
グリセリン 5.0
蒸溜水 39.0
製造例3により得られた粉体 10.0
香 料 0.5
A成分を85℃以上に加温し、撹拌しながら粉体
を少しづつ加えてよく分散させ、次で87℃以上に
加温したB成分を徐々に加えて乳化し、そのまま
撹拌しながら放冷し55〜60℃のときに香料を加え
て更に40℃になるまで撹拌して製品を得る。
〓実施例4〓 練状口紅
A 成分
ミツロウ 6.0
ステアリン酸 8.0
セタノール 5.0
ワセリン 8.0
酸化チタン 12.5
B 成分
タルク 35.0
製造例2により得られた粉体 25.0
香 料 0.5
A成分を90℃に加温し、撹拌しながらB成分を
少しずつ加えてよく分散させ、そのまま撹拌しな
がら放冷し60℃のときに香料を加えて65℃(±5
℃)のときに口紅容器に直接流し込み40℃まで放
冷させて製品を得る。
〓実施例5〓 リキツド状アイシヤドウ
A 成分
カルナウバロウ 5.0
流動パラフイン 5.0
IPM 5.0
ステアリン酸 5.0
活性剤 5.0
着色顔料ペースト 17.0
B 成分
酸化チタン 10.0
製造例1により得られた粉体 5.0
C 成分
トリエタノールアミン 0.5
プロピレングリコール 5.0
蒸溜水 37.0
香 料 0.5
A成分を85℃以上に加温した撹拌しながらB成
分を少しずつ加えてよく分散させ、次で加温した
C成分を徐々に加えて乳化し、そのまま撹拌しな
がら放冷し55〜60℃のときに香料を加えて40℃に
なるまで撹拌を続け製品を得る。
〓実施例6〓 ハンドクリーム
A 成分
ステアリン酸 15.0
セタノール 4.0
ラノリン 2.0
ブチルステアレート 2.0
製造例2により得られた粉体 10.0
防腐剤 0.05
B 成分
活性剤 3.0
プロピレングリコール 5.0
蒸溜水 58.55
香 料 0.5
A成分を80℃以上に加温し、撹拌しながら82℃
以上に加温したB成分を徐々に加えて乳化し、そ
のまま撹拌しながら放冷し60℃のときに香料を加
えて40℃になるまで撹拌を続け、次で常温で放置
して製品を得る。
〓実施例7〓 アフターシエービングクリーム
A 成分
ラノリン 1.0
スクワレン 3.0
流動パラフイン 3.0
ステアリン酸 8.5
セタノール 4.0
鯨ロウ 4.0
パラフインワツクス 2.0
活性剤 4.0
防腐剤 0.2
l―メントール 0.05
製造例2により得られた粉体 4.0
B 成分
ホウ砂 0.5
プロピレングリコール 5.0
蒸溜水 60.25
香 料 0.5
A成分を80℃以上に加温した撹拌しながら82℃
以上に加温したB成分を徐々に加えて乳化し、そ
のまま撹拌しながら放冷し60〜65℃のときに香料
を加えて43℃になるまで撹拌を続け、次で常温で
放置して脱泡し製品を得る。
次に、ステイツク状フアンデーシヨンにおける
本発明品ならびに対照品について専門パネラ5名
を対象として行なつた官能プロフアイルの結果を
第4図に示す。尚、(A)は前記製造例1により得ら
れた粉体(粒径5〜15μ)を用いて前記実施例1
により製造されたステイツク状フアンデーシヨ
ン、(B)は(A)の処方において粉体の代りにセリサイ
トを配合して製造した従来のステイツク状フアン
デーシヨン、(C)は(A)の処方において粉体の代りに
特開昭53−38635号公報中実施例に開示されてい
る超微粒粉シリカ(登録商標「アエロジル」(日
本アエロジル)、粒径40mmμ)のスクワラン(20
部)吸着物を配合して製造したステイツク状フア
ンデーシヨン、(D)は(A)の処方において粉体の代り
に特開昭53−38635号公報に開示されている粉末
化法により製造された前記超微粒粉シリカの金属
石けん(ステアリン酸アルミニウム)吸着物を配
合して製造したステイツク状フアンデーシヨンを
示すものであり、評価方法としては(B)のステイツ
ク状フアンデーシヨンを0の基点とした。
第4図の官能プロフアイルの結果にみられる如
く、本発明に係るステイツク状フアンデーシヨン
(A)は対照品(B)に比べて使用中の伸びが軽くて使用
中の油つぽさがなく、また使用後のつやならびに
透明感があり、しかも、使用後のべたつきがない
など、いずれの評価においても優れている。ま
た、対照品(C),(D)との比較においては、これらが
使用着手時のかたさが硬く、使用中の伸びが重
く、使用後のつやならびに透明感がないなど、本
発明よりも劣る評価であつたのに対し、(a)はいず
れも抜群に良好な結果を得た。特に、使用中のつ
やなどにおいては、本発明品では含有する粉体が
有する転動効果が発揮されて格段の効果が得られ
ている。尚、対照品(C),(D)は使用中の油つぽさや
使用後のべたつきがない評価になつているが、こ
れらは、むしろフアンデーシヨンの粉つぽさが現
れて皮膚にカサつき感を与え、却つて悪い性状を
示した。
以上の通り、本発明は従来のフアンデーシヨン
の長所を保ちながらこれまでになかつた効果、即
ち皮膚に対して軽妙で滑らかな伸びを有するとと
もに使用後のべたつきならびに油つぽさがなく、
しかも粉体の配合割合によつて乾燥感を任意に調
整でき、且つまた適度の柔軟性を有するとともに
保湿性に優れているという効果を有する化粧料を
提供するものである。
更に、次表は年齢18〜40歳の女性80名(18〜25
歳:26〜30歳:31〜40歳=1:2:1の構成割
合)を対象として、後記の各種ステツツク状フア
ンデーシヨンを20日間連日使用し、各回の塗布後
2〜3時間経過後の評価を示すものである。[Production Example 4] Add 90g of a mixture of spherical silica gels with particle sizes of 1 to 25μ to 2000ml of a toluene-octane mixture (2:1), heat to 70°C, and add zinc laurate while stirring gently. 5g and zinc oleate 5g
were added little by little, heating and stirring were continued for 60 minutes, and the solvent was distilled off under reduced pressure (3 mmHg, distillation temperature 70°C). Next, while maintaining the temperature at 15-20°C, add 1000 ml of ethanol, stir for 60 minutes, and filter.
After repeating this operation twice, the powder was washed and dried under reduced pressure at 70°C and coated with a zinc laurate-zinc oleate mixture (particle size of about 1 to 25μ).
I got almost 100g. The powder obtained in this way is coated with a thin film of metal soap on the surface of the spherical silica gel, completely covering the surface of the silica gel and adhering to it, forming a single body that can be used in both aqueous and non-aqueous systems. It also behaves without separation. In addition, while silica gel itself is normally very easy to scatter, the powder used in the present invention has no scattering properties and has good dispersibility, so it has good filling properties and
It is also excellent in productivity. Here, the measurement results of the apparent density, specific surface area by gas phase adsorption method, and electron micrographs of silica gel alone, a mixture of silica gel alone and metal soap, and the powder used in the present invention are shown in Figures 1 and 2.
and FIG. 3, respectively. To measure the apparent density, 32 g of each sample with a particle size of approximately 1 to 15 μm is poured into a sample tube (a cylindrical container with a diameter of 2 cm and a length of 30 cm) with a volume scale under certain conditions, and this is measured using an electric apparent volume measurement method. Set the sample tube in a container (manufactured by Ohka Kogyo Co., Ltd.) and drop the sample tube continuously within a height of 1.5 cm at a rate of 30 drops per minute to measure the change in the filling volume of each sample. I asked for it. To measure the specific surface area, put 0.5 g of the sample into the sample tube for the adsorption measurement device (V-shaped side flask, volume 2 ml) and use the adsorption measurement device (ADS-IB type, manufactured by Shimadzu Corporation).
A mixture of nitrogen and helium gas (PN2 = 0.3) is flowed through the tube, and the sample is cooled with liquid nitrogen. When equilibrium is reached, the sample is adsorbed with nitrogen gas in the mixture, and the liquid nitrogen is removed from the sample tube. The adsorbed nitrogen gas is desorbed by increasing the temperature of the sample, and the change in nitrogen gas concentration during this adsorption and desorption process is measured using a thermal conduction type gas chromatograph (GC-6AM, manufactured by Shimadzu Corporation). It was determined by measuring with a detector. In addition, the electron micrographs were taken using a scanning electron microscope (Hitachi-Akashi MINI-
SEM, MSM-4 type), each with a diameter of approximately
A 10 μ sample was photographed at a magnification of 5000 times. Figure 3 (X) shows silica gel alone, Figure 3 (Y) shows spherical silica gel coated with metal soap, and their composition ratio is 93:7. FIG. 3Z shows a powder obtained by coating spherical silica gel with metal soap and having a composition ratio of 90:10. According to Figure 1, the apparent density after 900 drops is 0.775 for the sample made of silica gel alone (a), and the apparent density for the sample made of silica gel and aluminum stearate mixed at a ratio of 95:5 and 90:10 (b). ,
In (c), they are 0.755 and 0.710, whereas those obtained by coating silica gel with aluminum stearate and whose composition ratios are 99:1 and 95:1, respectively.
The apparent densities of samples (d), (e), and (f), which have a ratio of 5,90:10, are 0.670, 0.630, and 0.580, respectively.
The apparent densities of (d), (e), and (f) are for samples (a) and (b),
It is smaller than the apparent density of (c). From these things, the sample
Samples (d), (e), and (f) have a surface layer that is thicker by the amount of aluminum stearate coated on the silica gel surface, and have a completely different structure from samples (d) and (e). It can be seen that it has. Furthermore, according to FIG. 2, the specific surface area of sample (a) made of silica gel alone is 224.5 m 2 /g, while that of sample (a) obtained by coating silica gel with aluminum stearate and their composition ratio is The specific surface areas of samples (b), (c), (d), (e), and (f), which are 99:1, 97:3, 95:5, 93:7, and 90:10, respectively, are (a ) is smaller than From this, it can be inferred that the metal soap covers the pores of the silica gel as well as the slight depressions on the surface. However, the specific surface area of sample (f) is larger than that of samples (c), (d), and (e), which is presumed to be due to damage to the coated surface. Therefore,
The composition ratio of silica gel and metal soap is 97:3 ~
It can be said that the range of 93:7 is optimal. Next, examples of the present invention will be shown. Incidentally, the blending ratio is in parts by weight. Example 1 Static foundation A Ingredients Carnauba wax 5.0 Bacyl alcohol 1.5 Ceresin 1.5 Vaseline 15.0 Liquid paraffin 35.0 Colored pigment paste White pigment paste 16.5 B Ingredient sericite (muscovite) 5.0 Powder obtained in Production Example 1 20.0 Fragrance 0.5 Heat ingredient A to 80°C or above, add ingredient B little by little while stirring to disperse well, and add ingredient B while stirring.
Allow to cool to 70°C, add fragrance, maintain at 65°C (±5°C), pour directly into a storage container, and leave to cool at room temperature to obtain the product. Example 2 Oil-based compact foundation A Ingredients Carnauba wax 2.0 Behenyl alcohol 9.0 Solid paraffin 3.5 Setanol 4.0 Lanolin 7.0 Liquid paraffin 6.0 Activator 2.0 Color pigment paste 26.5 B Ingredient talc 10.0 Powder obtained according to Production Example 4 30.0 Fragrance 0.5 Heat component A to 85℃ or higher, and then heat to 65℃ while stirring.
Component B is added little by little and dispersed well. Next, the fragrance is added and the temperature is maintained at 65°C (±5°C), and the mixture is poured directly into a medium dish container and left to cool at room temperature to obtain a product. Example 3 Emulsified type foundation A Ingredients Beeswax 2.0 Stearic acid 2.5 Liquid paraffin 15.0 Activator 6.0 Lanolin 6.0 Colored pigment paste White pigment paste 17.0 B Ingredient Triethanolamine 1.0 Glycerin 5.0 Distilled water 39.0 Obtained according to Production Example 3 Powder 10.0 Fragrance 0.5 Heat component A to 85℃ or higher, add the powder little by little while stirring to disperse well, then gradually add component B, which has been heated to 87℃ or higher, to emulsify. The mixture is left to cool while stirring, and when the temperature reaches 55 to 60°C, fragrance is added and further stirred until the temperature reaches 40°C to obtain a product. 〓Example 4〓 Kneaded lipstick A Ingredients Beeswax 6.0 Stearic acid 8.0 Setanol 5.0 Vaseline 8.0 Titanium oxide 12.5 B Ingredient Talc 35.0 Powder obtained in Production Example 2 25.0 Fragrance 0.5 Ingredient A was heated to 90°C and stirred. While stirring, add component B little by little and disperse well. Leave to cool while stirring. When the temperature is 60℃, add the fragrance and heat to 65℃ (±5
℃), pour directly into a lipstick container and leave to cool to 40℃ to obtain the product. 〓Example 5〓 Liquid Eyeshadow A Component Carnauba Wax 5.0 Liquid Paraffin 5.0 IPM 5.0 Stearic Acid 5.0 Activator 5.0 Colored Pigment Paste 17.0 B Component Titanium Oxide 10.0 Powder Obtained in Production Example 1 5.0 C Component Triethanolamine 0.5 Propylene Glycol 5.0 Distilled water 37.0 Fragrance 0.5 Ingredient A is heated to 85°C or higher, and while stirring, add ingredient B little by little and disperse well. Next, gradually add ingredient C, which has been heated, to emulsify it, and continue stirring while stirring. Leave to cool and add fragrance when the temperature reaches 55-60°C and continue stirring until the temperature reaches 40°C to obtain a product. 〓Example 6〓 Hand cream A Ingredients Stearic acid 15.0 Setanol 4.0 Lanolin 2.0 Butyl stearate 2.0 Powder obtained in Production Example 2 10.0 Preservative 0.05 B Ingredient activator 3.0 Propylene glycol 5.0 Distilled water 58.55 Fragrance 0.5 Ingredient A Heat to 80°C or higher, then heat to 82°C while stirring.
Gradually add the heated component B to emulsify it, leave it to cool while stirring, add the fragrance when the temperature is 60℃, continue stirring until it reaches 40℃, and then leave it at room temperature to obtain the product. . 〓Example 7〓 Aftershave Cream A Ingredients Lanolin 1.0 Squalene 3.0 Liquid paraffin 3.0 Stearic acid 8.5 Cetanols 4.0 Sperm wax 4.0 Paraffin wax 2.0 Active agent 4.0 Preservative 0.2 L-menthol 0.05 Powder obtained according to Production Example 2 4.0 Ingredient B Borax 0.5 Propylene Glycol 5.0 Distilled Water 60.25 Fragrance 0.5 Ingredient A was heated to 80°C or higher and heated to 82°C while stirring.
Gradually add the heated component B to emulsify it, leave it to cool while stirring, add the fragrance when the temperature is 60-65℃, continue stirring until it reaches 43℃, then leave it at room temperature to decompose it. Get foamy product. Next, FIG. 4 shows the results of a sensory profile conducted on five expert panelists regarding the present invention product and the control product in the form of stick foundations. Note that (A) was prepared using the powder obtained in Production Example 1 (particle size 5 to 15μ) in Example 1.
(B) is a conventional stick-like foundation manufactured by adding sericite instead of powder in the formulation of (A); (C) is the formulation of (A) In place of the powder, squalane (20
Part) A stick-like foundation manufactured by blending an adsorbent, (D) is manufactured by the powdering method disclosed in JP-A-53-38635 in place of powder in the formulation of (A). This shows a stick-like foundation manufactured by blending the ultrafine powder silica adsorbed with metal soap (aluminum stearate).The evaluation method is to use the stick-like foundation of (B) as a base point of 0. And so. As seen in the sensory profile results in Figure 4, the stake-like foundation according to the present invention
Compared to the control product (B), (A) spreads lightly during use, does not feel oily during use, has a glossy and transparent feel after use, and is not sticky after use. Excellent in all evaluations. In addition, in comparison with control products (C) and (D), these were inferior to the present invention, such as hardness at the beginning of use, heavy elongation during use, and lack of luster and transparency after use. In contrast, (a) obtained extremely good results. In particular, in terms of gloss during use, the product of the present invention exhibits the rolling effect of the powder contained therein, resulting in a remarkable effect. In addition, control products (C) and (D) are rated as having no oily feel during use or stickiness after use, but these products actually appear powdery and dry on the skin. It gave a feeling of stickiness, and showed rather bad properties. As described above, the present invention maintains the advantages of conventional foundations while providing unprecedented effects, namely, it spreads lightly and smoothly on the skin, and there is no stickiness or oiliness after use.
Furthermore, the present invention provides a cosmetic that can adjust the dryness as desired by adjusting the blending ratio of powder, has appropriate flexibility, and has excellent moisturizing properties. In addition, the following table shows 80 women aged 18-40 (18-25
Ages: 26-30 years: 31-40 years old = composition ratio of 1:2:1) Use various stucco foundations listed below every day for 20 days, 2 to 3 hours after each application. This shows the evaluation of
【表】
尚、表中、化粧料Aは前記実施例1のステツク
状フアンデーシヨンの処方において粉体を粒状の
シリカゲル単体に置換させたもの、化粧料Bは前
記実施例1のステツク状フアンデーシヨンの処方
中において粉体を粒状のシリカゲルと金属石けん
との組成比が99.5:0.5である粉体に置換させた
もの、化粧料Cは前記実施例1のステツク状フア
ンデーシヨン、化粧料Dは前記実施例1のステツ
ク状フアンデーシヨンの処方において粉体を粒状
のシリカゲルと金属石けんとの組成比が90:10で
ある粉体に置換させたものである。
この表に示される評価は冬期に実施したが、本
発明の化粧料であるC、Dはほぼ全員が肌の異常
を訴えなかつたのに対して、粒状のシリカゲル単
体を配合したAならびに金属石けんによるコーテ
ングが不充分な粉体を配合したBについてはいず
れも肌の乾燥状態を訴える者が多くみられた。
尚、金属石けんを過度にコーテングした粉体を用
いたDは全員が乾燥感を解消することができたが
同時に皮膚に対する伸びが重いことが確認され
た。
また、前記評価試験と同様の対象者について使
用感の調査を行なつたところ、ほぼ全員が、サ
ラサラとしたさつぱり感、自然のままの素肌
感、肌への塗布後の透明感、化粧の仕上りを
薄くも厚くも自由に調整できるなどの従来存在し
なかつた新しい性状を有するステツク状フアンデ
ーシヨンであるとの評価を得た。
更に前記実施例2に示した油性コンパクトフア
ンデーシヨンとこれから粉体を除いた油性コンパ
クトフアンデーシヨンとを5℃、20℃ならびに40
℃で3ケ月間に亘つて放置したところ、対象品は
ブロツク強度が著しく低下して発汗現象がみられ
たのに対して、実施例2の化粧料は何等の変化も
なく耐温性に優れていることが確認された。
更にまた、前記実施例1に示したステツク状の
フアンデーシヨンを兎6匹を対象として動物経皮
試験を実施し1日目、2日目、3日目、4日目の
計4回に亘つて判定を行ない、その結果何等異常
なく安全性の高いことが実証された。
尚、本発明は殊に例えばステツク状フアンデー
シヨン、クリームコンパクトフアンデーシヨン、
練状口紅などの油性化粧料ならびに例えば乳化形
フアンデーシヨン、ハンドクリーム、アフターシ
エービングクリーム、リキツド状アイシヤドウな
どの乳化性化粧料に実施した場合にその効果を充
分に発揮するものであるが、他の化粧料について
も同様の効果を期待できることは勿論である。
以上のように本発明の化粧料は、粒状のシリカ
ゲルの表面を適度の厚さを有する金属石けんの被
膜で覆つた粉体が配合されているため、皮膚に対
する塗擦性がきわめて滑からかで伸びが軽いばか
りか、皮膚との親和性がよく湿潤な感触が得られ
るとともに塗布後における皮膚表面の過度の乾燥
感を防止して柔軟性、保湿性に優れており、しか
も同時にさつぱりとした感触も得られるものであ
る。[Table] In the table, Cosmetic A is the formulation of the stick-shaped foundation of Example 1 in which the powder is replaced with granular silica gel alone, and Cosmetic B is the formulation of the stick-shaped foundation of Example 1. In the formulation of the foundation, the powder was replaced with powder in which the composition ratio of granular silica gel and metal soap was 99.5:0.5, and Cosmetic C was the same as the stick-shaped foundation of Example 1. D is obtained by replacing the powder in the formulation of the stick-like foundation of Example 1 with a powder having a composition ratio of granular silica gel and metal soap of 90:10. The evaluation shown in this table was carried out in the winter season, and almost all of the cosmetics C and D, which are cosmetics of the present invention, did not complain of skin abnormalities, whereas the cosmetics A, which contains granular silica gel alone, and the metal soap Regarding B, which contained powder with insufficient coating, many people complained of dry skin.
Incidentally, in D, which used a powder excessively coated with metal soap, all the patients were able to eliminate the dry feeling, but at the same time, it was confirmed that it was difficult to spread on the skin. In addition, when we conducted a survey on the feeling of use on the same subjects as in the above evaluation test, almost all of them commented on the smooth and refreshing feeling, the natural feel of bare skin, the transparency after applying it to the skin, and the feeling of makeup. The foundation was praised for having new properties that did not exist before, such as the ability to freely adjust the finish to be thin or thick. Further, the oil-based compact foundation shown in Example 2 and the oil-based compact foundation from which the powder was removed were heated at 5°C, 20°C and 40°C.
When left at ℃ for 3 months, the target product showed a significant decrease in block strength and sweating phenomenon, whereas the cosmetic of Example 2 showed no change and had excellent temperature resistance. It was confirmed that Furthermore, an animal dermal test was conducted using the stick-shaped foundation shown in Example 1 on 6 rabbits, and the test was carried out four times on the 1st, 2nd, 3rd, and 4th days. After repeated evaluations, the results showed no abnormalities and proved to be highly safe. The present invention is particularly applicable to, for example, stick-shaped foundations, cream compact foundations,
It exhibits its full effect when applied to oil-based cosmetics such as powdered lipsticks, as well as emulsifying cosmetics such as emulsified foundations, hand creams, aftershave creams, and liquid eye shadows. Of course, similar effects can be expected with other cosmetics. As described above, the cosmetic of the present invention contains powder in which the surface of granular silica gel is covered with a metal soap film having an appropriate thickness, so it has an extremely smooth application property on the skin and spreads easily. Not only is it light, but it also has good affinity with the skin and provides a moist feel, prevents excessive dryness on the skin surface after application, has excellent flexibility and moisturizing properties, and at the same time leaves a refreshing feeling. You can also feel it.
第1図は本発明に用いられる粉体ならびに比較
品を電動式見掛け容積測定器により測定した際の
落下回数と見掛け密度との関係図、第2図は発明
に用いられる粉体ならびに比較品の比表面積を気
相吸着法により測定した際の比表面積とステアリ
ン酸アルミニウムのコーテング量との関係図、第
3図は本発明に用いられる粉体ならびに比較品の
電子顕微鏡写真、第4図は本発明の実施例の官能
プロフアイルを比較品とともに示したものであ
る。
Figure 1 shows the relationship between the number of falls and the apparent density when the powder used in the invention and a comparative product are measured using an electric apparent volume measuring device, and Figure 2 shows the relationship between the powder used in the invention and the comparative product. A diagram of the relationship between the specific surface area and the coating amount of aluminum stearate when the specific surface area was measured by the gas phase adsorption method. Figure 3 is an electron micrograph of the powder used in the present invention and a comparative product. Figure 4 is the graph of the book. The sensory profile of an example of the invention is shown together with a comparative product.
Claims (1)
んをコーテングすることにより得られ且つ前記シ
リカゲルと金属石けんとの組成比が99:1〜70:
30である粉体を含有していることを特徴とする化
粧料。 2 化粧料が油性または乳化性である特許請求の
範囲第1項記載の化粧料。[Scope of Claims] 1. Obtained by coating spherical silica gel with a particle size of 1 to 30 μm with metal soap, and the composition ratio of the silica gel and metal soap is 99:1 to 70:
A cosmetic characterized by containing powder having a content of 30%. 2. The cosmetic according to claim 1, wherein the cosmetic is oil-based or emulsifiable.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5521978A JPS54151137A (en) | 1978-05-10 | 1978-05-10 | Microospherical silica gel metal soap coating composition and cosmetics containing same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5521978A JPS54151137A (en) | 1978-05-10 | 1978-05-10 | Microospherical silica gel metal soap coating composition and cosmetics containing same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54151137A JPS54151137A (en) | 1979-11-28 |
JPS6339565B2 true JPS6339565B2 (en) | 1988-08-05 |
Family
ID=12992495
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5521978A Granted JPS54151137A (en) | 1978-05-10 | 1978-05-10 | Microospherical silica gel metal soap coating composition and cosmetics containing same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54151137A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04169828A (en) * | 1990-11-01 | 1992-06-17 | Hino Motors Ltd | Method and apparatus for detecting riveting pressure of riveting machine |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5338635A (en) * | 1976-09-20 | 1978-04-08 | Ota Toshuki | Process for pulverization of oily liquid |
-
1978
- 1978-05-10 JP JP5521978A patent/JPS54151137A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5338635A (en) * | 1976-09-20 | 1978-04-08 | Ota Toshuki | Process for pulverization of oily liquid |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04169828A (en) * | 1990-11-01 | 1992-06-17 | Hino Motors Ltd | Method and apparatus for detecting riveting pressure of riveting machine |
Also Published As
Publication number | Publication date |
---|---|
JPS54151137A (en) | 1979-11-28 |
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