JP6652241B2 - Solid powder cosmetics - Google Patents
Solid powder cosmetics Download PDFInfo
- Publication number
- JP6652241B2 JP6652241B2 JP2016047844A JP2016047844A JP6652241B2 JP 6652241 B2 JP6652241 B2 JP 6652241B2 JP 2016047844 A JP2016047844 A JP 2016047844A JP 2016047844 A JP2016047844 A JP 2016047844A JP 6652241 B2 JP6652241 B2 JP 6652241B2
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- Prior art keywords
- powder
- mass
- cosmetic
- component
- solid powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000843 powder Substances 0.000 title claims description 79
- 239000002537 cosmetic Substances 0.000 title claims description 57
- 239000007787 solid Substances 0.000 title claims description 21
- 239000003921 oil Substances 0.000 claims description 27
- 239000000463 material Substances 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000003125 aqueous solvent Substances 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- 239000002002 slurry Substances 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000010703 silicon Substances 0.000 claims description 10
- 238000003682 fluorination reaction Methods 0.000 claims description 7
- -1 isostearyl Chemical group 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 claims description 6
- 239000000539 dimer Substances 0.000 claims description 6
- 229920001296 polysiloxane Polymers 0.000 claims description 6
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims description 5
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 5
- 229920006037 cross link polymer Polymers 0.000 claims description 5
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 230000000887 hydrating effect Effects 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- 230000033444 hydroxylation Effects 0.000 claims description 2
- 238000005805 hydroxylation reaction Methods 0.000 claims description 2
- 235000019198 oils Nutrition 0.000 description 24
- 238000000034 method Methods 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000004205 dimethyl polysiloxane Substances 0.000 description 6
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
- 229940008099 dimethicone Drugs 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000003755 preservative agent Substances 0.000 description 5
- 238000010298 pulverizing process Methods 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000010445 mica Substances 0.000 description 3
- 229910052618 mica group Inorganic materials 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 240000002871 Tectona grandis Species 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229940032094 squalane Drugs 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- WFXHUBZUIFLWCV-UHFFFAOYSA-N (2,2-dimethyl-3-octanoyloxypropyl) octanoate Chemical compound CCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCC WFXHUBZUIFLWCV-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-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
- BJDAUCLANVMIOB-UHFFFAOYSA-N (3-decanoyloxy-2,2-dimethylpropyl) decanoate Chemical compound CCCCCCCCCC(=O)OCC(C)(C)COC(=O)CCCCCCCCC BJDAUCLANVMIOB-UHFFFAOYSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 1
- LBPNCQGSZHRGME-UHFFFAOYSA-N 2,2,3,3,4,4-hexahydroxyoctadecanoic acid Chemical compound CCCCCCCCCCCCCCC(O)(O)C(O)(O)C(O)(O)C(O)=O LBPNCQGSZHRGME-UHFFFAOYSA-N 0.000 description 1
- RKJGFHYCZPZJPE-UHFFFAOYSA-N 2,2-bis(16-methylheptadecanoyloxymethyl)butyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(CC)(COC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C RKJGFHYCZPZJPE-UHFFFAOYSA-N 0.000 description 1
- JNAYPSWVMNJOPQ-UHFFFAOYSA-N 2,3-bis(16-methylheptadecanoyloxy)propyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C JNAYPSWVMNJOPQ-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 235000018330 Macadamia integrifolia Nutrition 0.000 description 1
- 240000000912 Macadamia tetraphylla Species 0.000 description 1
- 235000003800 Macadamia tetraphylla Nutrition 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- HGKOWIQVWAQWDS-UHFFFAOYSA-N bis(16-methylheptadecyl) 2-hydroxybutanedioate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CC(O)C(=O)OCCCCCCCCCCCCCCCC(C)C HGKOWIQVWAQWDS-UHFFFAOYSA-N 0.000 description 1
- WMNULTDOANGXRT-UHFFFAOYSA-N bis(2-ethylhexyl) butanedioate Chemical compound CCCCC(CC)COC(=O)CCC(=O)OCC(CC)CCCC WMNULTDOANGXRT-UHFFFAOYSA-N 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229940105984 diethylhexyl succinate Drugs 0.000 description 1
- 229940090934 diphenylsiloxy phenyl trimethicone Drugs 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- XJNUECKWDBNFJV-UHFFFAOYSA-N hexadecyl 2-ethylhexanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(CC)CCCC XJNUECKWDBNFJV-UHFFFAOYSA-N 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 229940114937 microcrystalline wax Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 229910052604 silicate mineral Inorganic materials 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229940118594 trimethylolpropane triisostearate Drugs 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
本発明は、粉末と油剤を混合することによって調製される化粧料基材を、水性溶剤と混合してスラリー状とし、容器に充填した後、該溶剤を除去することを特徴とする固形粉末化粧料の製造方法において、特定の粉末及び油剤を含有することにより、使用感が良好で、充分な耐衝撃性を有した固形粉末化粧料に関する。 The present invention provides a solid powder cosmetic comprising the steps of mixing a cosmetic base material prepared by mixing a powder and an oil agent with an aqueous solvent to form a slurry, filling the container, and removing the solvent. The present invention relates to a solid powder cosmetic having a good feeling of use and sufficient impact resistance by containing a specific powder and an oil agent in a method for producing a cosmetic.
固形粉末化粧料の製造方法には、粉末と油剤を混合したのち圧密成型する乾式成型方法と、粉末と油剤を混合した化粧料基材に揮発性溶剤を加えてスラリーとし、容器に充填した後、揮発性溶剤を乾燥除去して化粧料を得る湿式成型方法がある。湿式成型方法においては、従来、揮発性シリコーンや低沸点炭化水素等の揮発性油剤を溶剤として用いてきたが、近年、環境保護の観点から、水性溶剤を用いる必要がでてきた。しかし、水性溶剤を用いた場合、得られる製品は粉の取れ量や塗布時の滑らかさが不充分であったり、耐衝撃性に劣るといった問題点があった。 The method of manufacturing a solid powder cosmetic includes a dry molding method in which powder and an oil agent are mixed and then compacting, and a method in which a volatile solvent is added to a cosmetic base material in which the powder and the oil agent are mixed to form a slurry, which is then filled in a container. There is a wet molding method for obtaining a cosmetic by drying and removing a volatile solvent. In the wet molding method, volatile oils such as volatile silicones and low-boiling hydrocarbons have been used as solvents, but in recent years, from the viewpoint of environmental protection, it has become necessary to use aqueous solvents. However, when an aqueous solvent is used, the resulting product has problems such as insufficient powder removal and insufficient smoothness at the time of application, and poor impact resistance.
このような課題を解決するため、結合成型性のある粉末と特定の複合粉末、炭化水素油を配合する方法(特許文献1)、疎水化処理粉末と多価アルコール、特定のシリコーンゲル組成物、特定の活性剤を配合する方法(特許文献2)、疎水化処理粉末と多価アルコール、特定の柔軟性有機樹脂粉末、特定の活性剤を配合する方法(特許文献3)、疎水化処理粉末と多価アルコール、抱水性油剤、特定の活性剤を配合する方法(特許文献4)、層状ケイ酸塩鉱物と親水性球状粉末、特定の油剤を配合する方法(特許文献5)が知られている。 In order to solve such a problem, a method of blending a powder having bonding moldability and a specific composite powder, a hydrocarbon oil (Patent Document 1), a hydrophobized powder and a polyhydric alcohol, a specific silicone gel composition, A method of blending a specific activator (Patent Document 2), a method of blending a hydrophobized powder with a polyhydric alcohol, a specific flexible organic resin powder, and a method of blending a specific activator (Patent Document 3). There are known a method of blending a polyhydric alcohol, a water hydrating agent, and a specific activator (Patent Document 4), and a method of blending a layered silicate mineral, a hydrophilic spherical powder, and a specific oil agent (Patent Document 5). .
しかしながら、上記湿式成型法で得られた固形粉末化粧料は、いずれも耐衝撃性の点で充分ではなく、優れた使用感と耐衝撃性の両立の点でいまだに満足のいく固形粉末化粧料が得られていないのが現状であった。 However, the solid powder cosmetics obtained by the above wet molding method are not sufficient in terms of impact resistance, and solid powder cosmetics that are still satisfactory in terms of both excellent usability and impact resistance have been developed. At present, it has not been obtained.
本願発明者らは、上記の課題を解決するために鋭意検討を行った結果、下記成分(A)〜(C)を化粧料基材に含有することにより、水性溶剤を用いた湿式成型方法により、使用感及び耐衝撃性に優れた固形粉末化粧料が得られることを見出し、本願発明を完成するに至った。すなわち、本願発明は、下記成分(A)〜(C)を含有する化粧料基材と、水性溶剤とを混合してスラリー状とし、容器に充填した後、該溶剤を除去することを特徴とする固形粉末化粧料の製造方法、及び該製造方法により得られた固形粉末化粧料を提供するものである。
(A)(フッ化/水酸化/酸化)/(Mg/K/ケイ素)
(B)疎水性及び柔軟性を備えた粉末
(C)常温で抱水させたとき、自重と等量以上の水を抱水することが可能な抱水性油剤
The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, by including the following components (A) to (C) in a cosmetic base material, a wet molding method using an aqueous solvent is used. It has been found that a solid powder cosmetic having excellent usability and impact resistance can be obtained, and the present invention has been completed. That is, the present invention is characterized in that a cosmetic base material containing the following components (A) to (C) and an aqueous solvent are mixed to form a slurry, which is then filled in a container, and then the solvent is removed. The present invention provides a method for producing a solid powder cosmetic to be used, and a solid powder cosmetic obtained by the production method.
(A) (fluorination / hydroxylation / oxidation) / (Mg / K / silicon)
(B) a powder having hydrophobicity and flexibility (C) a hydrated oil agent capable of hydrated water equal to or more than its own weight when hydrated at normal temperature
本願発明の固形粉末化粧料は、溶剤として水性溶剤を用いた湿式成型方法において、優れた使用感と耐衝撃性を有するものである。 The solid powder cosmetic composition of the present invention has excellent usability and impact resistance in a wet molding method using an aqueous solvent as a solvent.
以下、本願発明を詳細に説明する。本願発明に用いられる成分(A)の(フッ化/水酸化/酸化)/(Mg/K/ケイ素)は体質顔料であり、通常化粧料に用いられるものであれば良く、形状や粒径においても特に限定されない。このような粉末の市販品として、ソフトセリサイト T−6、ソフトセリサイト SH(大日本化成社製)等が挙げられる。
また本願発明に用いられる成分(A)は、表面処理を施して用いても未処理であってもよいが、耐衝撃性の観点からシリコーン化合物により表面処理したものが好ましい。
Hereinafter, the present invention will be described in detail. The component (A) (fluorinated / hydroxylated / oxidized) / (Mg / K / silicon) used in the present invention is an extender, and may be any of those commonly used in cosmetics. Is not particularly limited. Commercial products of such powder include Soft Sericite T-6 and Soft Sericite SH (manufactured by Dainippon Kasei Co., Ltd.).
The component (A) used in the present invention may be used after being subjected to a surface treatment, or may be untreated, but is preferably subjected to a surface treatment with a silicone compound from the viewpoint of impact resistance.
本願発明で用いられる成分(A)の含有量は、より滑らかでしっとりとした使用感が得られる点から、化粧料基材中に5質量%以上が好ましく、10質量%以上がより好ましい。 The content of the component (A) used in the present invention is preferably 5% by mass or more, more preferably 10% by mass or more in the cosmetic base material, from the viewpoint that a smooth and moist feeling is obtained.
本願発明に用いられる成分(B)の疎水性及び柔軟性を備えた粉末とは、下記の疎水性試験により疎水性と判断され、且つ、圧縮強度が1.0MPa以下の粉末である。疎水性試験とは、水10gと評価粉末0.1gをガラス瓶に入れてから蓋をして激しく上下に撹拌した後、1日静置し、観察する。その結果、評価粉末の大部分が水表面に存在するものを疎水性とする。また、圧縮強度とは、微小硬度計にて粉末粒子の直径が10%変形するのに要した力を測定し、次の式、圧縮強度(MPa)=27.5×P/πd2(P=粒子を10%変形させるのに必要な荷重(N)、d=粒子径(mm))によって求められる値である。
また本願発明に用いられる成分(B)は、通常化粧料に使用されるものであればいずれのものも使用することができ、1種又は2種以上を組み合わせて使用してもよい。例えば、(アクリレーツ/アクリル酸エチルヘキシル)クロスポリマーやナイロン等の疎水性粉末や、元来は親水性である表面にシリコーン化合物やフッ素化合物を処理して疎水化したウレタン等も使用することができるが、使用感の観点から(アクリレーツ/アクリル酸エチルヘキシル)クロスポリマーが好ましい。このような粉末の市販品としては、テクポリマーACX−806C、テクポリマーACX−1502C(積水化成品工業社製)等が挙げられる。
The powder having hydrophobicity and flexibility of the component (B) used in the present invention is a powder determined to be hydrophobic by the following hydrophobicity test and having a compressive strength of 1.0 MPa or less. In the hydrophobicity test, 10 g of water and 0.1 g of the evaluation powder are put into a glass bottle, covered with a lid, vigorously stirred up and down, allowed to stand for one day, and observed. As a result, those in which most of the evaluation powder exists on the water surface are made hydrophobic. Further, the compressive strength, the diameter of the powder particles to measure the force required to deform 10% by microhardness tester, the following equation, compressive strength (MPa) = 27.5 × P / πd 2 (P = Load (N) required to deform the particles by 10%, d = particle diameter (mm).
As the component (B) used in the present invention, any one can be used as long as it is commonly used in cosmetics, and one or two or more types may be used in combination. For example, hydrophobic powders such as (Acrylates / ethylhexyl acrylate) crosspolymer and nylon, and urethanes that have been hydrophobicized by treating a silicone compound or a fluorine compound on a surface that is originally hydrophilic can be used. From the viewpoint of feeling of use, (acrylates / ethylhexyl acrylate) crosspolymer is preferred. Commercial products of such powders include Techpolymer ACX-806C and Techpolymer ACX-1502C (manufactured by Sekisui Plastics Co., Ltd.).
本願発明に用いられる成分(B)の含有量は、より優れた耐衝撃性が得られる点から化粧料基材中に10質量%以上が好ましく、15質量%以上がより好ましい。また、塗布時に適度な密着感が得られるという点から、50質量%以下が好ましく、30質量%以下がより好ましい。 The content of the component (B) used in the present invention is preferably 10% by mass or more, more preferably 15% by mass or more in the cosmetic base material, from the viewpoint of obtaining more excellent impact resistance. Further, from the viewpoint that a proper feeling of adhesion can be obtained at the time of coating, the content is preferably 50% by mass or less, and more preferably 30% by mass or less.
本願発明に用いられる成分(B)の形状や粒径は特に限定されないが、平均粒子径が2〜10μmの球状粉末が好ましい。平均粒子径が2μm以上で球状であると、より滑らかな使用感が得られ、10μm以下であると、より優れた耐衝撃性が得られるためである。尚、本願発明において平均粒子径は、レーザー回折粒子径測定装置(LA−920:ホリバ製作所製)を用いて、粉末をエタノールに分散させて測定したメジアン径の値である。また、球状粉末とは形状が略球形の粉末をいい、球状粉末の長径/短径の比が1.2以下のものが好ましい。 The shape and particle size of the component (B) used in the present invention are not particularly limited, but a spherical powder having an average particle size of 2 to 10 μm is preferable. When the average particle diameter is 2 μm or more and the particles are spherical, a smoother feeling of use is obtained, and when the average particle diameter is 10 μm or less, more excellent impact resistance is obtained. In the present invention, the average particle diameter is a value of a median diameter measured by dispersing a powder in ethanol using a laser diffraction particle diameter measuring apparatus (LA-920: manufactured by Horiba Seisakusho). In addition, the spherical powder refers to a powder having a substantially spherical shape, and preferably has a ratio of the major axis / minor axis of the spherical powder of 1.2 or less.
本願発明に用いられる成分(C)の抱水性油剤は、下記の抱水性試験にて、自重と等量以上の抱水力のある油剤であればいずれのものも使用することができ、1種又は2種以上を組み合わせて使用してもよい。抱水性試験とは、常温で評価油剤10gに精製水を徐々に滴下しながら練り込み、水が入らなくなった点を終点する。例えば、ダイマージリノール酸(フィトステリル/イソステアリル/セチル/ステアリル/ベヘニル)、ダイマージリノール酸ジ(イソステアリル/フィトステリル)、(イソステアリン酸/ベヘン酸)(グリセリル/ポリグリセリル−6)エステルズ、ヘキサ(ヒドロキシステアリン酸/ステアリン酸/ロジン酸)ジペンタエリスリチル等が挙げられ、使用感の観点からダイマージリノール酸(フィトステリル/イソステアリル/セチル/ステアリル/ベヘニル)が好ましい。このような油剤の市販品としては、Plandool−H(日本精化社製)等が挙げられる。 As the water-containing oil agent of the component (C) used in the present invention, any oil agent having a water-holding power equal to or more than its own weight can be used in the following water-holding test. Two or more kinds may be used in combination. The water retention test is performed by gradually kneading purified water into 10 g of the evaluation oil at room temperature while gradually dropping the kneaded water, and ending the point where water does not enter. For example, dimer dilinoleic acid (phytosteryl / isostearyl / cetyl / stearyl / behenyl), di dimer dilinoleic acid (isostearyl / phytosteryl), (isostearic acid / behenic acid) (glyceryl / polyglyceryl-6) esters, hexa (hydroxy) Stearic acid / stearic acid / rosin acid) dipentaerythrityl and the like, and dimer dilinoleic acid (phytosteryl / isostearyl / cetyl / stearyl / behenyl) is preferable from the viewpoint of feeling of use. Commercially available products of such oils include Planool-H (manufactured by Nippon Seika).
本願発明に用いられる成分(C)の含有量は、より優れた耐衝撃性が得られる点から化粧料基材中に0.5質量%以上が好ましく、1質量%以上がより好ましい。また、滑らかな使用感が得られるという点から、5質量%以下が好ましく、3質量%以下がより好ましい。 The content of the component (C) used in the present invention is preferably 0.5% by mass or more, more preferably 1% by mass or more in the cosmetic base material, from the viewpoint of obtaining more excellent impact resistance. Further, from the viewpoint that a smooth feeling in use can be obtained, the content is preferably 5% by mass or less, more preferably 3% by mass or less.
本願発明の固形粉末化粧料において、上記成分以外の化粧料基材は、通常の化粧料に用いられるものであればいずれも使用することができ、上記以外の粉末及び油剤等を用いることができる。 In the solid powder cosmetic of the present invention, any cosmetic base other than the above components can be used as long as it is used for ordinary cosmetics, and powders and oils other than the above can be used. .
上記以外の粉末としては、例えば、タルク、セリサイト、マイカ、合成マイカ、シリカ、硫酸バリウム、アルミナ、窒化ホウ素、酸化チタン、酸化鉄、酸化亜鉛等の無機粉末、シルクパウダー、結晶セルロースパウダー等の有機粉末等が挙げられ、これらより1種又は2種以上を用いることができる。また、これら粉末はフッ素化合物、シリコーン化合物、界面活性剤等の通常公知の処理剤により表面処理を施して用いてもよい。 Examples of the powder other than the above include, for example, talc, sericite, mica, synthetic mica, silica, barium sulfate, alumina, boron nitride, titanium oxide, iron oxide, inorganic powder such as zinc oxide, silk powder, crystalline cellulose powder, and the like. Organic powders and the like can be mentioned, and one or more of these can be used. These powders may be subjected to a surface treatment with a generally known treating agent such as a fluorine compound, a silicone compound, and a surfactant.
上記以外の油剤としては、流動パラフィン、スクワラン、マイクロクリスタリンワックス、セレシン、セチルアルコール、イソステアリルアルコール、オレイルアルコール、2−ヘキシルデカノール、2−エチルヘキサン酸セチル、パルミチン酸2−エチルヘキシル、ジ2−エチルヘキサン酸ネオペンチルグリコール、ジカプリル酸ネオペンチルグリコール、ジカプリン酸ネオペンチルグリコール、トリ2−エチルヘキサン酸グリセリン、トリイソステアリン酸グリセリン、オリーブ油、マカデミアナッツ油、ヒマワリ油、ラノリン、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、ビーズワックス、キャンデリラロウ、カルナウバロウ、鎖状又は環状のジメチルポリシロキサン、メチルフェニルポリシロキサン等の油剤が挙げられる。 Other oils include liquid paraffin, squalane, microcrystalline wax, ceresin, cetyl alcohol, isostearyl alcohol, oleyl alcohol, 2-hexyldecanol, cetyl 2-ethylhexanoate, 2-ethylhexyl palmitate, di-2-ethylhexane Neopentyl glycol acid, neopentyl glycol dicaprylate, neopentyl glycol dicaprate, glycerin tri-2-ethylhexanoate, glycerin triisostearate, olive oil, macadamia nut oil, sunflower oil, lanolin, lauric acid, myristic acid, palmitic acid, stearin Examples include oils such as acids, beeswax, candelilla wax, carnauba wax, linear or cyclic dimethylpolysiloxane, methylphenylpolysiloxane, and the like. That.
また上記成分に加えて、化粧料において一般的に用いられるその他の成分を含有してもよく、例えば、界面活性剤、香料、薬効成分、清涼剤、紫外線吸収剤、安定化剤、酸化防止剤、防腐剤、pH調整剤、粘度調整剤、防腐剤、美容成分等が挙げられる。 Further, in addition to the above components, other components commonly used in cosmetics may be contained, for example, surfactants, fragrances, medicinal ingredients, cooling agents, ultraviolet absorbers, stabilizers, antioxidants , Preservatives, pH adjusters, viscosity adjusters, preservatives, cosmetic ingredients and the like.
本願発明の化粧料基材は、通常の粉末化粧料を製造する装置を使用し、上記成分を攪拌混合して、調製される。具体的には、まず成分(C)を含む油剤を混合し、必要に応じて加熱溶解する。一方、成分(A)及び(B)を含む粉末を均一に混合する。この粉末に油剤を加えて均一に分散させ、粉砕することにより調製される。
このようにして得られる化粧料基材と、水性溶剤とを混合してスラリー状とし、容器に充填した後、該溶剤を除去することにより、固形粉末化粧料を得ることができる。
The cosmetic base material of the present invention is prepared by stirring and mixing the above components using an ordinary apparatus for producing powder cosmetics. Specifically, first, an oil agent containing the component (C) is mixed and, if necessary, dissolved by heating. On the other hand, a powder containing the components (A) and (B) is uniformly mixed. It is prepared by adding an oil agent to the powder, dispersing the powder uniformly, and pulverizing the powder.
The thus-obtained cosmetic base material and an aqueous solvent are mixed to form a slurry, filled into a container, and then the solvent is removed to obtain a solid powder cosmetic.
化粧料基材との混合に用いる水性溶剤は、水又は、エチルアルコール、プロピルアルコール、イソプロピルアルコール、ブチルアルコール等の低沸点アルコールから選ばれる1種又は2種以上の水溶液が好ましく、水単独又はエチルアルコールを水に溶解したエチルアルコール水溶液がより好ましい。 The aqueous solvent used for mixing with the cosmetic base material is preferably water or one or more aqueous solutions selected from low-boiling alcohols such as ethyl alcohol, propyl alcohol, isopropyl alcohol, and butyl alcohol. An ethyl alcohol aqueous solution in which alcohol is dissolved in water is more preferable.
本願発明において、化粧料基材と水性溶剤を用いてスラリーを調製する場合、スラリーが充填に適した流動性を有する点から、化粧料基材100質量部に対して水性溶剤50〜100質量部を用いることが好ましい。 In the present invention, when preparing a slurry using a cosmetic base material and an aqueous solvent, from the viewpoint that the slurry has fluidity suitable for filling, 50 to 100 parts by weight of the aqueous solvent with respect to 100 parts by weight of the cosmetic base material. It is preferable to use
本願発明において、化粧料基材と水性溶剤を混合した後、容器に充填し、加熱乾燥によって溶剤を除去する際、加熱温度及び装置は限定されないが、全ての溶剤を乾燥留去するためには50℃以上であるのが好ましい。 In the present invention, after mixing the cosmetic base material and the aqueous solvent, filling the container, when removing the solvent by heating and drying, the heating temperature and equipment is not limited, in order to dry and distill all the solvent The temperature is preferably 50 ° C. or higher.
本願発明における固形粉末化粧料は、ファンデーション、プレストパウダー、アイカラー、フェイスカラー等として適用することができる。特に、先行技術と比較して耐衝撃性が非常に優れているため、成型品の面積が大きく、持ち運び使用する機会の多いファンデーションに好適である。 The solid powder cosmetic according to the present invention can be applied as a foundation, a pressed powder, an eye color, a face color and the like. In particular, since the impact resistance is very excellent as compared with the prior art, it is suitable for a foundation in which the area of a molded product is large, and there are many opportunities to carry and use.
次に、実施例をあげて、本願発明をより詳細に説明する。本願発明はこれにより制限されるものではない。尚、表中の数値は、含有量(質量%)を示す。
実施例1〜11及び比較例1〜7:パウダーファンデーション
表1に示す処方及び下記製法により、パウダーファンデーションを調製し、以下に示す評価方法及び判定基準により評価した。これらの結果を併せて表1に示した。
Next, the present invention will be described in more detail with reference to examples. The present invention is not limited by this. In addition, the numerical value in a table | surface shows content (mass%).
Examples 1 to 11 and Comparative Examples 1 to 7: Powder foundation A powder foundation was prepared according to the formulation shown in Table 1 and the following production method, and evaluated according to the following evaluation methods and criteria. Table 1 also shows these results.
(製造方法)
A:油剤成分15〜17を混合し、80℃まで加熱して溶解する。
B:粉末成分1〜14を均一に混合する。
C:BにAを加えて均一分散させ、粉砕後、化粧料基材を得る。
D:Cの化粧料基材100質量部と水性溶剤80質量部を均一混合してスラリーを調製した。前記水性溶剤は、水90質量部とエタノール10質量部をあらかじめ混合し使用した。
E:Dを金皿(54mm×42mmの長方形、厚さ5mm)に充填し、真空吸引しながら圧縮成型した。
F:成型品は70℃乾燥機内で10時間乾燥して、パウダーファンデーションを得た。
(Production method)
A: The oil agent components 15 to 17 are mixed and heated to 80 ° C. to dissolve.
B: Powder components 1 to 14 are uniformly mixed.
C: A is added to B and uniformly dispersed, and after pulverization, a cosmetic base material is obtained.
D: 100 parts by mass of the cosmetic base material of C and 80 parts by mass of the aqueous solvent were uniformly mixed to prepare a slurry. As the aqueous solvent, 90 parts by mass of water and 10 parts by mass of ethanol were previously mixed and used.
E: D was filled in a metal plate (a rectangle of 54 mm × 42 mm, thickness of 5 mm), and compression-molded while vacuum suctioning.
F: The molded product was dried in a dryer at 70 ° C. for 10 hours to obtain a powder foundation.
(評価方法1;使用感)
20〜40代の化粧品専門パネル5名に、上記実施例及び比較例のパウダーファンデーションを使用してもらい、パフへの取れや塗布時の滑らかさ等使用感について、以下の評価基準により評点を付し、パウダーファンデーションごとに評点の平均点を算出して、以下に示す判定基準に従って判定した。
<評価基準>
〔使用感〕 〔評点〕
非常に良好 :5
良好 :4
普通 :3
やや不良 :2
不良 :1
<判定基準>
〔評点の平均点〕 〔判定〕
4.5以上 ◎
3.5以上4.5未満 ○
2以上3.5未満 △
2未満 ×
(Evaluation method 1; feeling of use)
Five panelists specializing in cosmetics in their 20s and 40s were asked to use the powder foundations of the above examples and comparative examples. Then, an average score was calculated for each powder foundation, and determined according to the following criteria.
<Evaluation criteria>
[Usability] [Score]
Very good: 5
Good : 4
Normal: 3
Somewhat bad: 2
Bad: 1
<Judgment criteria>
[Average score] [Judgment]
4.5 or more ◎
3.5 or more and less than 4.5 ○
2 or more and less than 3.5 △
Less than 2 ×
(評価方法2;耐衝撃性)
上記実施例及び比較例のパウダーファンデーション各5枚について、100cmの高さから塩ビ板上に水平に落下させた。これをひびや割れが生じるまで繰り返し、ひびや割れが生じるまでの落下回数について5枚で平均をとり、以下の判定基準に従って判定した。
<判定基準>
◎:3.0回以上
○:2.0以上3.0回未満
△:1.0以上2.0回未満
×:1.0回未満
(Evaluation method 2: impact resistance)
Five powder foundations of each of the above Examples and Comparative Examples were horizontally dropped on a PVC plate from a height of 100 cm. This was repeated until cracks and cracks were formed, and the number of drops until cracks and cracks were formed was averaged for five sheets, and judged according to the following criteria.
<Judgment criteria>
◎: 3.0 times or more ○: 2.0 or more and less than 3.0 times Δ: 1.0 or more and less than 2.0 times ×: less than 1.0 times
実施例1〜11は、使用感及び耐衝撃性ともに良好であった。それに対し、(フッ化/水酸化/酸化)/(Mg/K/ケイ素)を含有していない比較例1〜3及び抱水性油剤を7質量%含有した比較例7は、使用感が不良であり、親水性の弾力性粉末であるポリウレタンを含有した比較例5は耐衝撃性が充分ではなかった。また、弾力性粉末を含有していない比較例4及び抱水性油剤を含有していない比較例6は、使用感及び耐衝撃性が充分ではなかった。このことから、(フッ化/水酸化/酸化)/(Mg/K/ケイ素)、疎水性及び柔軟性を備えた粉末、並びに抱水性油剤を含有することの必然性が明らかとなった。 In Examples 1 to 11, both the usability and the impact resistance were good. On the other hand, Comparative Examples 1 to 3 containing no (fluorination / hydroxide / oxidation) / (Mg / K / silicon) and Comparative Example 7 containing 7% by mass of the hydrated oil had a poor feeling in use. Comparative Example 5 containing polyurethane, which is a hydrophilic elastic powder, did not have sufficient impact resistance. Further, Comparative Example 4 containing no elastic powder and Comparative Example 6 containing no hydrating oil agent were not satisfactory in feeling in use and impact resistance. From this, it became clear that it was necessary to contain (fluorinated / hydroxylated / oxidized) / (Mg / K / silicon), a powder having hydrophobicity and flexibility, and an oil hydrate.
実施例12
プレストパウダー処方
成分 含有量(質量%)
(1) ハイドロゲンジメチコン3%処理(フッ化/水酸化/酸化)/(Mg/K/ケイ素)※1 55.00
(2) 合成マイカ 残量
(3) 黄酸化鉄 0.20
(4) ベンガラ 0.25
(5) 黒酸化鉄 0.05
(6) (アクリレーツ/アクリル酸エチルヘキシル)クロスポリマー※6 20.00
(7) 防腐剤 0.50
(8) コハク酸ジエチルヘキシル 4.00
(9) リンゴ酸ジイソステアリル 1.00
(10)ダイマージリノール酸ジ(イソステアリル/フィトステリル)※12 1.00
(11)酸化防止剤 適量
(12)香料 適量
合計 100.00
※12:LUSPLAN PI−DA(日本精化社製)
(製造方法)
A:油剤成分8〜11を混合し、加熱して溶解する。冷却後、成分12を加える。
B:粉末成分1〜7を均一に混合する。
C:BにAを加えて均一分散させ、粉砕後、化粧料基材を得る。
D:Cの化粧料基材100質量部と水70質量部を均一混合してスラリーを調製した。
E:Dを金皿に充填し、真空吸引しながら圧縮成型した。
F:成型品は70℃乾燥機内で10時間乾燥して、プレストパウダーを得た。
Example 12
Presto powder formulation Ingredient Content (% by mass)
(1) Hydrogen dimethicone 3% treatment (fluorination / hydration / oxidation) / (Mg / K / silicon) * 1 55.00
(2) Residual synthetic mica (3) Yellow iron oxide 0.20
(4) Bengala 0.25
(5) Black iron oxide 0.05
(6) (Acrylates / ethylhexyl acrylate) crosspolymer * 6 20.00
(7) Preservative 0.50
(8) diethylhexyl succinate 4.00
(9) Diisostearyl malate 1.00
(10) Dimer dilinoleic acid di (isostearyl / phytosteryl) * 12 1.00
(11) Suitable amount of antioxidant (12) Suitable amount of fragrance
Total 100.00
* 12: LUSPLAN PI-DA (manufactured by Nippon Seika)
(Production method)
A: The oil components 8 to 11 are mixed and heated to dissolve. After cooling, component 12 is added.
B: Powder components 1 to 7 are uniformly mixed.
C: A is added to B and uniformly dispersed, and after pulverization, a cosmetic base material is obtained.
D: 100 parts by mass of the cosmetic base material of C and 70 parts by mass of water were uniformly mixed to prepare a slurry.
E: D was filled in a metal plate and compression molded while vacuum suctioning.
F: The molded product was dried in a dryer at 70 ° C. for 10 hours to obtain a pressed powder.
実施例13
アイシャドウ処方
成分 含有量(質量%)
(1) ハイドロゲンジメチコン3%処理(フッ化/水酸化/酸化)/(Mg/K/ケイ素)※1 20.00
(2) ジメチコン3%処理セリサイト 残量
(3) ナイロン−12※8 18.00
(4) シリカ 1.00
(5) 赤色226号 0.30
(6) グンジョウ 1.00
(7) 雲母チタン 10.00
(8) 防腐剤 0.50
(9) ジメチコン 5.00
(10)スクワラン 6.00
(11)ヘキサ(ヒドロキシステアリン酸/ステアリン酸/ロジン酸)ジペンタエリスリチル※13 2.00
(12)酸化防止剤 適量
(13)香料 適量
合計 100.00
※13:コスモール168ARV(日清オイリオグループ社製)
(製法)
A:油剤成分9〜12を混合し、加熱して溶解する。冷却後、成分13を加える。
B:粉末成分1〜8を均一に混合する。
C:BにAを加えて均一分散させ、粉砕後、化粧料基材を得る。
D:Cの化粧料基材100質量部と水70質量部を均一混合してスラリーを調製した。
E:Dを樹脂皿に充填し、真空吸引しながら圧縮成型した。
F:成型品は70℃乾燥機内で10時間乾燥して、アイシャドウを得た。
Example 13
Eye shadow formulation Ingredient Content (% by mass)
(1) Hydrogen dimethicone 3% treatment (fluorination / hydration / oxidation) / (Mg / K / silicon) * 1 20.00
(2) Sericite remaining 3% treated with dimethicone (3) Nylon-12 * 8 18.00
(4) Silica 1.00
(5) Red No. 226 0.30
(6) Gunjo 1.00
(7) Titanium mica 10.00
(8) Preservative 0.50
(9) Dimethicone 5.00
(10) Squalane 6.00
(11) Hexa (hydroxystearic acid / stearic acid / rosinic acid) dipentaerythrityl * 13 2.00
(12) Suitable amount of antioxidant (13) Suitable amount of fragrance
Total 100.00
* 13: Cosmall 168ARV (manufactured by Nisshin Oillio Group)
(Production method)
A: The oil components 9 to 12 are mixed and heated to dissolve. After cooling, component 13 is added.
B: Powder components 1 to 8 are uniformly mixed.
C: A is added to B and uniformly dispersed, and after pulverization, a cosmetic base material is obtained.
D: 100 parts by mass of the cosmetic base material of C and 70 parts by mass of water were uniformly mixed to prepare a slurry.
E: D was filled in a resin dish, and compression molded while suctioning under vacuum.
F: The molded product was dried in a dryer at 70 ° C. for 10 hours to obtain an eye shadow.
実施例14
チークカラー
成分 含有量(質量%)
(1) ハイドロゲンジメチコン3%処理(フッ化/水酸化/酸化)/(Mg/K/ケイ素)※1 30.00
(2) タルク 残量
(3) アクリレーツ/アクリル酸エチルヘキシル)クロスポリマー※6 30.00
(4) シリカ 1.50
(5) 赤色226号 0.30
(6) 黄色5号 0.35
(7) ベンガラ 0.80
(8) ベンガラ被覆雲母チタン 5.00
(9) 防腐剤 0.20
(10)ジフェニルシロキシフェニルトリメチコン 10.00
(11)トリイソステアリン酸トリメチロールプロパン 0.50
(12)セスキイソステアリン酸ソルビタン 0.50
(13)ダイマージリノール酸(フィトステリル/イソステアリル/セチル/ステアリル/ベヘニル)※10 1.50
(14)酸化防止剤 適量
(15)香料 適量
合計 100.00
(製法)
A:油剤成分10〜14を混合し、加熱して溶解する。冷却後、成分15を加える。
B:粉末成分1〜9を均一に混合する。
C:BにAを加えて均一分散させ、粉砕後、化粧料基材を得る。
D:Cの化粧料基材100質量部と水80質量部を均一混合してスラリーを調製した。
E:Dを樹脂皿に充填し、真空吸引しながら圧縮成型した。
F:成型品は70℃乾燥機内で10時間乾燥して、チークカラーを得た。
Example 14
Teak color Ingredient Content (% by mass)
(1) Hydrogen dimethicone 3% treatment (fluorination / hydration / oxidation) / (Mg / K / silicon) * 1 30.00
(2) Residual amount of talc (3) Acrylates / ethylhexyl acrylate) crosspolymer * 6 30.00
(4) Silica 1.50
(5) Red No. 226 0.30
(6) Yellow No. 5 0.35
(7) Bengala 0.80
(8) Bengala-coated mica titanium 5.00
(9) Preservative 0.20
(10) diphenylsiloxyphenyltrimethicone 10.00
(11) Trimethylolpropane triisostearate 0.50
(12) Sorbitan sesquiisostearate 0.50
(13) dimer dilinoleic acid (phytosteryl / isostearyl / cetyl / stearyl / behenyl) * 10 1.50
(14) Antioxidant appropriate amount (15) Fragrance appropriate amount
Total 100.00
(Production method)
A: Oil components 10 to 14 are mixed and heated to dissolve. After cooling, component 15 is added.
B: Powder components 1 to 9 are uniformly mixed.
C: A is added to B and uniformly dispersed, and after pulverization, a cosmetic base material is obtained.
D: 100 parts by mass of the cosmetic base material of C and 80 parts by mass of water were uniformly mixed to prepare a slurry.
E: D was filled in a resin dish, and compression molded while suctioning under vacuum.
F: The molded product was dried in a dryer at 70 ° C. for 10 hours to obtain a teak color.
実施例12〜14はいずれも、使用感、耐衝撃性ともに良好な化粧料であった。 All of Examples 12 to 14 were cosmetics having good usability and impact resistance.
本願発明の固形粉末化粧料は、(フッ化/水酸化/酸化)/(Mg/K/ケイ素)、疎水性及び柔軟性を備えた粉末、並びに抱水性油剤を化粧料基材に含有することにより、溶剤として水性溶剤を用いた湿式成型方法において、優れた使用感と耐衝撃性を有することができる。
The solid powder cosmetic of the present invention contains (fluorinated / hydroxylated / oxidized) / (Mg / K / silicon), a powder having hydrophobicity and flexibility, and a water-retaining oil agent in a cosmetic base material. Thereby, in a wet molding method using an aqueous solvent as a solvent, excellent usability and impact resistance can be obtained.
Claims (8)
(A)(フッ化/水酸化/酸化)/(Mg/K/ケイ素)
(B)疎水性及び柔軟性を備えた粉末:10質量%以上
(C)自重と等量以上の水を抱水することが可能な抱水性油剤:5質量%以下 A cosmetic base material prepared by mixing a powder containing the following components (A) and (B) with an oil agent containing (C) is mixed with an aqueous solvent to form a slurry, which is filled in a container. And then removing the solvent.
(A) (fluorination / hydroxylation / oxidation) / (Mg / K / silicon)
(B) Powder having hydrophobicity and flexibility : 10% by mass or more (C) Water-containing oil agent capable of hydrating water equal to or more than its own weight : 5% by mass or less
A solid powder cosmetic produced by the production method according to claim 1.
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