JP2001002529A - Cosmetics compounded with fine powder of conductive zinc oxide - Google Patents
Cosmetics compounded with fine powder of conductive zinc oxideInfo
- Publication number
- JP2001002529A JP2001002529A JP11169125A JP16912599A JP2001002529A JP 2001002529 A JP2001002529 A JP 2001002529A JP 11169125 A JP11169125 A JP 11169125A JP 16912599 A JP16912599 A JP 16912599A JP 2001002529 A JP2001002529 A JP 2001002529A
- Authority
- JP
- Japan
- Prior art keywords
- zinc oxide
- conductive zinc
- parts
- cosmetics
- skin
- 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.)
- Pending
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 title claims abstract description 194
- 239000011787 zinc oxide Substances 0.000 title claims abstract description 97
- 239000002537 cosmetic Substances 0.000 title claims abstract description 46
- 239000000843 powder Substances 0.000 title claims abstract description 27
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 8
- -1 Ti4+ Inorganic materials 0.000 abstract description 7
- 239000002245 particle Substances 0.000 abstract description 4
- 238000013329 compounding Methods 0.000 abstract description 3
- 239000013078 crystal Substances 0.000 abstract description 3
- 230000002045 lasting effect Effects 0.000 abstract description 3
- 239000002019 doping agent Substances 0.000 abstract 1
- 210000003491 skin Anatomy 0.000 description 28
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 24
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 16
- 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 15
- 238000000034 method Methods 0.000 description 14
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- 239000006071 cream Substances 0.000 description 8
- 239000004166 Lanolin Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 7
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- 238000002360 preparation method Methods 0.000 description 7
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- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 5
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
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- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 4
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
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- 238000010438 heat treatment Methods 0.000 description 4
- 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 4
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 4
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- 239000011701 zinc Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
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- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
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- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 2
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
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- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
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- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
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- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
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- 239000003607 modifier Substances 0.000 description 1
- 229940074096 monoolein Drugs 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229940073665 octyldodecyl myristate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229960002969 oleic acid Drugs 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
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 229940056211 paraffin Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- 239000000600 sorbitol Substances 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
- 239000007858 starting material Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/27—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、導電性酸化亜鉛微
粉末を配合した紫外線吸収能及び化粧もちに優れた化粧
料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cosmetic composition which is blended with a conductive zinc oxide fine powder and which has an excellent ultraviolet absorbing ability and excellent makeup.
【0002】[0002]
【従来の技術】ファンデーション、化粧水、乳液、クリ
ームなどのメーキャップ化粧品や基礎化粧品は、皮膚の
シミやシワなどを隠し、好みの色彩を与え、魅力的な容
貌を与えて美しく見せるという美的役割とともに皮膚に
対しての保護的な役割も持っている。2. Description of the Related Art Makeup cosmetics and foundation cosmetics such as foundations, lotions, emulsions and creams have the aesthetic role of hiding skin spots and wrinkles, giving them the desired color, and giving them an attractive appearance and giving them a beautiful appearance. It also has a protective role on the skin.
【0003】特に近年、オゾン層破壊という環境問題が
大きくとりあげられる様になるとともに、最近の皮膚科
学の研究結果から、紫外線に曝されると、シミ、ソバカ
スの発生や皮膚の老化の原因になるほか、皮膚細胞の遺
伝子を傷つける等紫外線が予想以上の悪影響を肌に及ぼ
すことが明らかになり、肌を有害な紫外線から守るとい
うことに大きな関心が持たれる様になってきた。このた
め、化粧料にも、紫外線から肌を守る紫外線遮蔽作用を
持つことが求められ、これに対応するために酸化亜鉛等
の紫外線吸収剤を配合したメーキャップ化粧品、基礎化
粧品などの化粧料が開発されてきた。In particular, in recent years, the environmental problem of ozone layer depletion has become a major issue, and recent dermatological studies have shown that exposure to ultraviolet radiation causes spots, freckles, and aging of the skin. In addition, it has been found that ultraviolet rays have an unexpectedly adverse effect on skin, such as damaging skin cell genes, and there has been a great interest in protecting skin from harmful ultraviolet rays. For this reason, cosmetics are also required to have an ultraviolet shielding effect that protects the skin from ultraviolet rays, and in order to respond to this, cosmetics such as makeup cosmetics and basic cosmetics that contain an ultraviolet absorber such as zinc oxide have been developed. It has been.
【0004】なかでも、酸化亜鉛粒子は、基本的に優れ
た紫外線吸収能を有し、これを紫外線吸収剤として配合
した化粧料又は配合用に適した酸化亜鉛がいくつか提案
されている( 特開平5−17329号、特開平5−24
6823号、特開平5−213618号、特開平7−1
18133号、特開平7−10538号、特開平8−5
3568号 )。この結果、酸化亜鉛を紫外線吸収剤とし
て配合した化粧料により化粧を施した場合に、紫外線か
ら肌を守るという役割に対してはほぼ満足するものが得
られている。[0004] Among them, zinc oxide particles basically have an excellent ultraviolet absorbing ability, and some cosmetics or zinc oxide suitable for blending the same as an ultraviolet absorber have been proposed. JP-A-5-17329, JP-A-5-24
No. 6823, JP-A-5-213618, JP-A-7-1
No. 18133, JP-A-7-10538, JP-A-8-5
No. 3568). As a result, when makeup is applied with a cosmetic in which zinc oxide is blended as an ultraviolet absorber, there is obtained an almost satisfactory role of protecting the skin from ultraviolet rays.
【0005】しかしながら、実際に肌に塗って化粧した
場合、時間の経過とともに、発汗などにより化粧料が剥
がれ落ちるため、その効果を長時間に渡り持続させるこ
とは必ずしも容易ではなかった。効果が長時間持続する
こと、すなわち化粧もちが良いことは、酸化亜鉛の本来
の効果を充分に発揮させて肌を保護する点で、非常に重
要なファクターなのである。また、化粧もちのよい化粧
品であれば、しばしば化粧直しをしなくてよいことを意
味し、この点からも現在化粧もちのよい化粧品に対する
ニーズはきわめて高い。[0005] However, when the makeup is actually applied to the skin, the cosmetics peel off due to sweating or the like over time, and it is not always easy to maintain the effect for a long time. The long-lasting effect, that is, good makeup lasting, is a very important factor in protecting the skin by making full use of the original effect of zinc oxide. In addition, cosmetics that have good makeup often mean that makeup does not need to be redressed. From this point of view, the need for cosmetics with good makeup is extremely high.
【0006】なお、酸化亜鉛配合化粧料において紫外線
から肌を守る効果を長時間に渡って維持させることに対
して、例えば特開平7−118133号には、特定の比
表面積で不純物元素含量が少ない酸化亜鉛を使用するこ
とにより、皮脂中に存在する遊離脂肪酸との反応性を上
げ皮脂をゲル化させることなどが提案されている。しか
しながら、この方法においては、確かにある程度皮脂中
に存在する遊離脂肪酸との反応性を上げることができる
が、その事のみでは、化粧もちを大きく改善することは
困難であり、更なる改善が求められている。On the other hand, while the effect of protecting the skin from ultraviolet rays is maintained for a long time in a zinc oxide-containing cosmetic, for example, Japanese Patent Application Laid-Open No. Hei 7-118133 discloses a specific specific surface area and a low impurity element content. It has been proposed to increase the reactivity with free fatty acids present in sebum by using zinc oxide to gel the sebum. However, in this method, it is possible to increase the reactivity with free fatty acids present in sebum to some extent, but it is difficult to greatly improve the makeup stickiness by itself, and further improvement is required. Have been.
【0007】[0007]
【発明が解決しようとする課題】本発明は、上記に鑑み
てなされたもので、その目的は紫外線から肌を長時間に
渡って守る化粧もちのよい化粧料を提供することにあ
る。SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a cosmetic composition having good makeup and protecting skin from ultraviolet rays for a long time.
【0008】[0008]
【課題を解決するための手段】本発明者らは、従来技術
の問題点である化粧もちを改善する方法について鋭意検
討した結果、導電性の酸化亜鉛微粉末を化粧料に配合す
ることにより、紫外線を吸収するのみならず、赤外線の
透過を防止し、肌に対する熱線を和らげる事ができるこ
とを見出した。このため皮膚の感じる温度を下げ、いわ
ゆるほてり感を少なくし、発汗を押さえ、従来の化粧料
に比べて汗による化粧崩れがずっと少なくなり、化粧が
長時間維持されるのである。本発明は、かかる知見に基
づきなされるに到ったものである。Means for Solving the Problems The present inventors have conducted intensive studies on a method of improving the cosmetic moistness, which is a problem of the prior art, and as a result, by adding conductive zinc oxide fine powder to cosmetics, It has been found that it not only absorbs ultraviolet rays, but also prevents transmission of infrared rays, and can reduce heat rays to the skin. For this reason, the temperature felt by the skin is reduced, so-called hot flash feeling is reduced, sweating is suppressed, makeup collapse due to sweat is much less than conventional cosmetics, and makeup is maintained for a long time. The present invention has been made based on such findings.
【0009】すなわち本発明に従えば、以下の発明が提
供される。 (1) 比表面積が2〜100m2 /g、体積抵抗率5
00Ωcm以下である導電性酸化亜鉛微粉末を配合して
なることを特徴とする化粧料。That is, according to the present invention, the following inventions are provided. (1) Specific surface area of 2 to 100 m 2 / g, volume resistivity 5
A cosmetic comprising a conductive zinc oxide fine powder having a size of not more than 00 Ωcm.
【0010】(2) 導電性酸化亜鉛微粉末の配合量
が、揮発分を除いた皮膚への残留成分として重量百分率
で5%以上であることを特徴とする (1) 記載の化粧
料。(2) The cosmetic according to (1), wherein the amount of the conductive zinc oxide fine powder is at least 5% by weight as a residual component on the skin excluding volatile components.
【0011】(3) 導電性酸化亜鉛微粉末が、導電性
付与成分としてアルミニウムを用いた酸化亜鉛微粉末で
あることを特徴とする (1) または (2) 記載の化粧
料。(3) The cosmetic according to (1) or (2), wherein the conductive zinc oxide fine powder is a zinc oxide fine powder using aluminum as a conductivity-imparting component.
【0012】[0012]
【発明の実施の形態】以下、本発明について詳細に説明
する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
【0013】本発明で用いられる導電性酸化亜鉛として
は、比表面積が2〜100m2 /g、より好ましくは1
0〜100m2 /g、さらに好ましくは20〜100m
2 /gの微粉末状のものが望ましい。比表面積が2より
あまり小さくなると、紫外線吸収能等の性能は変わらな
いものの、添加された化粧料に透明感がなくなり、化粧
本来の目的に合わなくなり好ましくない。また、比表面
積が100m2 /gより大きいものは、現在の技術では
製造が困難であり、製造コストが高くなり実質的に実用
化が困難である。The conductive zinc oxide used in the present invention has a specific surface area of 2 to 100 m 2 / g, more preferably 1 to 100 m 2 / g.
0 to 100 m 2 / g, more preferably 20 to 100 m
A fine powder of 2 / g is desirable. When the specific surface area is much smaller than 2, although the performance such as ultraviolet absorption ability does not change, the added cosmetic does not have a transparent feeling, and it is not suitable for the original purpose of the makeup, which is not preferable. Further, those having a specific surface area of more than 100 m 2 / g are difficult to manufacture with the current technology, the manufacturing cost is high, and practical use is practically difficult.
【0014】本発明における比表面積は、公知のBET
法により測定された値である。なお、これらの比表面積
を粒径に換算すると0.01〜0.5μm、好ましくは
0.01〜0.1μm程度である。In the present invention, the specific surface area is determined by a known BET.
It is a value measured by the method. When these specific surface areas are converted into particle diameters, they are about 0.01 to 0.5 μm, preferably about 0.01 to 0.1 μm.
【0015】また、本発明で用いられる導電性酸化亜鉛
の導電性としては、少なくても体積抵抗率500Ωcm
以下、さらに好ましくは100Ωcm以下である。一方
この体積抵抗率の下限は、より低い方が好ましいが、実
際に製造が容易な範囲としては10〜100Ωcm程度
である。体積抵抗率が500Ωcmを越えて大きくなる
と、本発明の目的である赤外線透過防止能が小さくな
り、肌の発汗を押さえる効果が小さくなる。The conductivity of the conductive zinc oxide used in the present invention is at least 500 Ωcm in volume resistivity.
Or less, more preferably 100 Ωcm or less. On the other hand, the lower limit of the volume resistivity is preferably lower, but the range in which the production is practically easy is about 10 to 100 Ωcm. When the volume resistivity exceeds 500 Ωcm, the ability to prevent infrared transmission, which is the object of the present invention, decreases, and the effect of suppressing perspiration of the skin decreases.
【0016】本発明において導電性酸化亜鉛の体積抵抗
率は、試料10gを内径25mmのテフロン加工した円
筒に入れ、100kg/cm2 の加圧を行い、テスター
で測定した値( Ωcm )である。In the present invention, the volume resistivity of the conductive zinc oxide is a value (Ωcm) obtained by placing a 10 g sample in a Teflon-coated cylinder having an inner diameter of 25 mm, applying a pressure of 100 kg / cm 2 and measuring with a tester.
【0017】本発明で使用する導電性酸化亜鉛は、酸化
亜鉛の結晶格子中にAl3+、In3+、Ti4+、Sn4+な
どをドーピングし導電性を付与したもので、ドーパント
( 導電性付与成分 )としてはアルミニウムがドーピング
性能及びコストの面で最も好ましい。The conductive zinc oxide used in the present invention is obtained by doping the crystal lattice of zinc oxide with Al 3+ , In 3+ , Ti 4+ , Sn 4+, etc. to impart conductivity.
As the (conductivity-imparting component), aluminum is most preferable in terms of doping performance and cost.
【0018】本発明で用いられる導電性酸化亜鉛の製造
方法としては、特に限定されるものでなく比表面積が2
〜100m2 /g、体積抵抗率が500Ωcm以下の導
電性酸化亜鉛微粉末が得られる方法であれば、基本的に
は、いかなる方法も用いられうるが、実施の容易性から
以下の方法が最も好ましい。The method of producing the conductive zinc oxide used in the present invention is not particularly limited, and the specific surface area is 2
Basically, any method can be used as long as a conductive zinc oxide fine powder having a volume resistivity of up to 100 m 2 / g and a volume resistivity of 500 Ωcm or less can be obtained. preferable.
【0019】出発原料の酸化亜鉛としては、亜鉛を溶融
・蒸発させ気相で酸化するフランス法、亜鉛鉱石を仮焼
・コークス還元・酸化するアメリカ法、亜鉛塩溶液にソ
ーダ灰を加えて塩基性炭酸亜鉛を沈殿させ、乾燥・仮焼
する湿式法等のいずれでもよいが、比表面積が上記範囲
のものであることが好ましい。Examples of the zinc oxide as a starting material include a French method in which zinc is melted and evaporated and oxidized in a gas phase, an American method in which zinc ore is calcined, coke reduced and oxidized, and a basic method in which soda ash is added to a zinc salt solution. Any of a wet method of precipitating zinc carbonate, drying and calcining may be used, but the specific surface area is preferably in the above range.
【0020】これら一般的な製法により製造された酸化
亜鉛微粒子を、例えば特公昭62−41171号に開示
されているようにして、炭酸アンモニウム等のアンモニ
ウム塩及びアルミニウムやチタンの水溶性塩を含む水溶
液中に投入・分散処理し、生成ケーキを水洗・乾燥後、
水素等の還元性雰囲気中で400〜1,000℃程度の
温度で0.2〜3時間程度還元焼成する。かくして、酸
化亜鉛の結晶格子中にAl3+、In3+又はTi4+などが
充分ドーピングされた、比表面積が2〜100m2 /
g、体積抵抗率が500Ωcm以下である導電性酸化亜
鉛微粉末が得られる。The zinc oxide fine particles produced by these general production methods can be used, for example, in an aqueous solution containing an ammonium salt such as ammonium carbonate and a water-soluble salt of aluminum or titanium as disclosed in JP-B-62-41171. After pouring and dispersing into the product, washing and drying the resulting cake,
Reduction firing is performed in a reducing atmosphere such as hydrogen at a temperature of about 400 to 1,000 ° C. for about 0.2 to 3 hours. Thus, the zinc oxide crystal lattice is sufficiently doped with Al 3+ , In 3+ or Ti 4+, and has a specific surface area of 2 to 100 m 2 /
g, a conductive zinc oxide fine powder having a volume resistivity of 500 Ωcm or less is obtained.
【0021】使用する導電性酸化亜鉛微粉末の粒子形状
としては、球状、鱗片状、薄片状、板状、破砕状、不定
形状、板状、針状等いずれであっても構わない。The particle shape of the conductive zinc oxide fine powder to be used may be any of a spherical shape, a scale shape, a flake shape, a plate shape, a crushed shape, an irregular shape, a plate shape, a needle shape and the like.
【0022】本発明の化粧料としては、特に限定される
ものでなく、肌を紫外線から守る目的であれば、いかな
る化粧料であっても良いが、肌を整えるための基礎化粧
品、ベースメイクやポイントメイクに用いられるメーキ
ャップ化粧品が特に好ましい。具体的には、白粉、ファ
ンデーション、プレストパウダー、口紅、頬紅、アイシ
ャドウ、サンオイル、日焼けどめクリーム、ルースパウ
ダー、乳液、化粧水等が挙げられる。The cosmetic of the present invention is not particularly limited, and any cosmetic may be used as long as it protects the skin from ultraviolet rays. Basic cosmetics, base makeup, Makeup cosmetics used for point makeup are particularly preferred. Specific examples include white powder, foundation, pressed powder, lipstick, blusher, eyeshadow, sun oil, sunburn cream, loose powder, milky lotion, lotion and the like.
【0023】本発明の導電性酸化亜鉛微粉末が配合され
る化粧料の成分としては、通常の化粧料に配合される成
分、例えば一般に化粧料に用いられる基剤成分や、一般
的な薬効付与成分( 例えば保湿剤、消炎剤、血行促進剤
など )、油分、色素、香料等が用いられる。The components of the cosmetic to which the conductive zinc oxide fine powder of the present invention is blended include components to be blended with ordinary cosmetics, for example, a base component generally used for cosmetics and a general drug effect imparting agent. Components (eg, humectants, anti-inflammatory agents, blood circulation promoters, etc.), oils, pigments, fragrances and the like are used.
【0024】例えば、シリカ、タルク、ベンガラ、クレ
ー、マイカ、ベントナイト、酸化チタン、炭酸カルシウ
ム、硫酸バリウム、炭酸マグネシウム、CIピグメント
イエロー、酸化鉄、シルクパウダー、ナイロンパウダー
等の有機及び無機充填剤や顔料;ラノリン、ワセリン、
パラフィン、ワックス、カルナバロウ、キャンデリラロ
ウ、セレシン、ラウリルアルコール、ラウリン酸、セチ
ルアルコール等の固形又は半固形油;オリーブ油、ホホ
バ油、オレイン酸、オレイルアルコール、イソヘキサデ
シルアルコール、ジメチルポリシロキサン、流動パラフ
ィン、スクワレン、ミリスチン酸オクタドデシル、スク
ワラン等の液体油;メチルセルロース、カルボキシメチ
ルセルロース、ヒドロキシメチルセルロース、キサンタ
ンガム、デキストリン、ゼラチン、アルギン酸ナトリウ
ム等の水溶性高分子;ポリオキシエチレンステアリン酸
エステル、トリエタノールアミン、モノオレイン酸ソル
ビタン、グリセリン脂肪酸エステル、塩化ベヘニルトリ
メチルアンモニウム等の界面活性剤;ソルビトール、マ
ンニトール、グリセリン、乳酸、ベタイン、ヒアルロン
酸ナトリウム、プロピレングリコール等の保湿剤、その
他防腐剤、香料、pH調節剤、各種アミノ酸、殺菌剤、
酸化防止剤等が挙げられる。For example, organic and inorganic fillers and pigments such as silica, talc, red iron oxide, clay, mica, bentonite, titanium oxide, calcium carbonate, barium sulfate, magnesium carbonate, CI Pigment Yellow, iron oxide, silk powder, nylon powder and the like. Lanolin, vaseline,
Solid or semi-solid oil such as paraffin, wax, carnauba wax, candelilla wax, ceresin, lauryl alcohol, lauric acid, cetyl alcohol; olive oil, jojoba oil, oleic acid, oleyl alcohol, isohexadecyl alcohol, dimethylpolysiloxane, liquid paraffin , Squalene, octadodecyl myristate, squalane, etc .; water-soluble polymers such as methylcellulose, carboxymethylcellulose, hydroxymethylcellulose, xanthan gum, dextrin, gelatin, sodium alginate; polyoxyethylene stearate, triethanolamine, monoolein Surfactants such as sorbitan acid, glycerin fatty acid ester, and behenyltrimethylammonium chloride; sorbitol, mannitol, Phosphoric, lactic, betaine, sodium hyaluronate, humectants such as propylene glycol, other preservatives, fragrances, pH regulators include various amino acids, fungicides,
Antioxidants and the like.
【0025】また、導電性酸化亜鉛の化粧料への配合割
合は、用いられる化粧料の種類や性状によって異なるた
めに一概には言えないが、成分のうち水やアルコールな
どの揮発分を除いた皮膚への残留成分重量のうち5%(
重量%、以下同じ。 )以上を含むことが望ましい。5%
未満の場合、他の紫外線吸収剤( 紫外線遮蔽剤 )を併用
することにより、紫外線吸収能は維持できるとしても赤
外線透過防止能が不十分となるためである。配合割合
は、より好ましくは、10%〜80%、さらに好ましく
は、15〜65%、最も好ましくは、15〜50%であ
る。あまり多量に化粧料に配合した場合使用感が悪くな
る。Further, the mixing ratio of the conductive zinc oxide to the cosmetic cannot be determined unconditionally because it varies depending on the type and properties of the cosmetic used, but volatile components such as water and alcohol are excluded from the components. 5% of the weight of residual ingredients on the skin (
Wt%, the same applies hereinafter. ) It is desirable to include the above. 5%
If the ratio is less than the above, the combined use of another ultraviolet absorber (ultraviolet ray shielding agent) will result in insufficient infrared transmission preventing ability even if the ultraviolet absorbing ability can be maintained. The mixing ratio is more preferably 10% to 80%, further preferably 15 to 65%, and most preferably 15 to 50%. When used in a cosmetic in an excessive amount, the feeling of use becomes worse.
【0026】本発明の導電性酸化亜鉛を化粧料に配合す
るに当たっては、配合成分とのなじみをよくするために
配合に先立って、例えばシランカップリング剤、シリコ
ーンオイル、チタネートカップリング剤、アルコール、
界面活性剤その他の公知の表面処理剤や表面改質剤によ
る表面処理を行っても、酸化亜鉛の性質を損なわない限
り問題ない。In blending the conductive zinc oxide of the present invention into cosmetics, for example, a silane coupling agent, a silicone oil, a titanate coupling agent, an alcohol,
There is no problem even if surface treatment is performed with a surfactant or other known surface treatment agents or surface modifiers, as long as the properties of zinc oxide are not impaired.
【0027】なお化粧料とする場合、本発明の導電性酸
化亜鉛は、上記したように他の紫外線吸収剤と併用する
ことは何ら問題を生じない。このような紫外線吸収剤と
しては酸化チタン、酸化セリウム、酸化鉄、ベンゾフェ
ノン系紫外線吸収剤、ベンズイミダゾール系紫外線吸収
剤、ベンゾトリアゾール系紫外線吸収剤等の有機又は無
機化合物が挙げられる。In the case of a cosmetic, the conductive zinc oxide of the present invention causes no problem when used in combination with another ultraviolet absorbent as described above. Examples of such UV absorbers include organic or inorganic compounds such as titanium oxide, cerium oxide, iron oxide, benzophenone UV absorber, benzimidazole UV absorber, and benzotriazole UV absorber.
【0028】[0028]
【実施例】以下、実施例により本発明を説明する。ただ
し、これらは単なる実施の態様の一例であり、本発明の
技術的範囲がこれらになんら限定されるものではない。The present invention will be described below with reference to examples. However, these are merely examples of the embodiments, and the technical scope of the present invention is not limited thereto.
【0029】(I) サンプル化粧料の作製 〔実施例1〕 (I) Preparation of Sample Cosmetic [Example 1]
【0030】( パウダリーファンデーションの作製 )導
電性酸化亜鉛として比表面積が10m2 /g、体積抵抗
率が90Ωcmのもの( ハクスイテック株式会社製:導
電性酸化亜鉛23−K )を使用した。(Preparation of Powdery Foundation) A conductive zinc oxide having a specific surface area of 10 m 2 / g and a volume resistivity of 90 Ωcm (manufactured by Hakusuitek Co., Ltd .: conductive zinc oxide 23-K) was used.
【0031】導電性酸化亜鉛50部、タルク10部、マ
イカ10部、ベンガラ1部、黄酸化鉄3部、黒酸化鉄
0.2部及びナイロンパウダ10部の粉体成分を混合機
により混合し、混合粉を得た。Powder components of 50 parts of conductive zinc oxide, 10 parts of talc, 10 parts of mica, 1 part of red iron oxide, 3 parts of yellow iron oxide, 0.2 parts of black iron oxide and 10 parts of nylon powder are mixed by a mixer. , To obtain a mixed powder.
【0032】この混合紛に流動パラフィン5部、スクワ
ラン6部、ミリスチン酸オクチルドデシル2部、ジイソ
オクタン酸ネオペンチルグリコール2部、モノオレイン
酸ソルビタン0.8部及び香料適量を加え、十分に攪拌
混合しパウダリーファンデーションを製造した。ファン
デーション中の導電性酸化亜鉛の配合量は、揮発分を除
いた皮膚への残留成分として重量百分率で50%であっ
た。To this mixed powder, 5 parts of liquid paraffin, 6 parts of squalane, 2 parts of octyldodecyl myristate, 2 parts of neopentyl glycol diisooctanoate, 0.8 parts of sorbitan monooleate and an appropriate amount of flavor are added, and the mixture is thoroughly stirred and mixed. A powdery foundation was produced. The content of the conductive zinc oxide in the foundation was 50% by weight as a residual component on the skin excluding volatile components.
【0033】〔比較例1〕酸化亜鉛として比表面積が1
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー10( SUPER−
10 ) )を使用した以外は実施例1と同様にしてパウダ
リーファンデーションを製造した。ファンデーション中
の酸化亜鉛の配合量は、揮発分を除いた皮膚への残留成
分として重量百分率で50%であった。[Comparative Example 1] Zinc oxide having a specific surface area of 1
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuiteku Co., Ltd .: Zinc oxide super 10 (SUPER-
A powdery foundation was produced in the same manner as in Example 1 except that 10))) was used. The amount of zinc oxide in the foundation was 50% by weight as a residual component on the skin excluding volatile components.
【0034】〔実施例2〕( ケーキファンデーションの作製 ) 導電性酸化亜鉛とし
て比表面積が10m2 /g、体積抵抗率が90Ωcmの
もの( ハクスイテック株式会社製:導電性酸化亜鉛23
−K )を使用した。Example 2 (Preparation of Cake Foundation) Conductive zinc oxide having a specific surface area of 10 m 2 / g and a volume resistivity of 90 Ωcm (Hakusui Tech Co., Ltd .: conductive zinc oxide 23)
-K) was used.
【0035】導電性酸化亜鉛32部、タルク15部、マ
イカ16部、ベンガラ1部、黄酸化鉄2.8部、黒酸化
鉄0.2部及びナイロンパウダ15部の粉体成分を混合
機にて混合し、混合粉を得た。Powder components of 32 parts of conductive zinc oxide, 15 parts of talc, 16 parts of mica, 1 part of bengara, 2.8 parts of yellow iron oxide, 0.2 parts of black iron oxide and 15 parts of nylon powder are mixed in a mixer. And mixed to obtain a mixed powder.
【0036】この混合紛にモノオレイン酸POEソルビ
タン4部、スクワラン8部、シリコン油6部、香料適量
を加え十分に攪拌混合しケーキファンデーションを製造
した。ケーキファンデーション中の導電性酸化亜鉛の配
合量は、揮発分を除いた皮膚への残留成分として重量百
分率で32%であった。To this mixed powder, 4 parts of POE sorbitan monooleate, 8 parts of squalane, 6 parts of silicone oil, and an appropriate amount of flavor were added, and the mixture was sufficiently stirred and mixed to produce a cake foundation. The content of the conductive zinc oxide in the cake foundation was 32% by weight as a residual component on the skin excluding volatile components.
【0037】〔比較例2〕酸化亜鉛として比表面積が1
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー10( SUPER−
10 ) )を使用した以外は実施例2と同様にしてケーキ
ファンデーションを製造した。ケーキファンデーション
中の酸化亜鉛の配合量は、揮発分を除いた皮膚への残留
成分として重量百分率で32%であった。Comparative Example 2 The specific surface area of zinc oxide was 1
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuiteku Co., Ltd .: Zinc oxide super 10 (SUPER-
A cake foundation was produced in the same manner as in Example 2 except that 10))) was used. The content of zinc oxide in the cake foundation was 32% by weight as a residual component on the skin excluding volatile components.
【0038】〔実施例3〕( O/W乳化型ファンデーションの作製 ) Example 3 (Preparation of O / W emulsion type foundation)
【0039】導電性酸化亜鉛として比表面積が10m2
/g、体積抵抗率が90Ωcmのもの( ハクスイテック
株式会社製:導電性酸化亜鉛23−K )を使用した。The conductive zinc oxide has a specific surface area of 10 m 2.
/ G, having a volume resistivity of 90 Ωcm (manufactured by Hakusui Tech Co., Ltd .: conductive zinc oxide 23-K).
【0040】導電性酸化亜鉛10部、ベンガラ0.5
部、黄酸化鉄1.4部、黒酸化鉄0.1部、ベントナイ
ト0.5部、精製水55部、トリエタノールアミン1
部、プロピレングリコール10部、モノステアリン酸ポ
リオキシエチレンソルビタン1部、モノステアリン酸グ
リセリン2部、流動パラフィン7.5部、ラノリン2
部、ステアリン酸2部及びイソヘキサデシルアルコール
7部を用い、次の手順によりO/W乳化型ファンデーシ
ョンを製造した。Conductive zinc oxide 10 parts, Bengala 0.5
Parts, yellow iron oxide 1.4 parts, black iron oxide 0.1 part, bentonite 0.5 part, purified water 55 parts, triethanolamine 1
Parts, propylene glycol 10 parts, polyoxyethylene sorbitan monostearate 1 part, glycerin monostearate 2 parts, liquid paraffin 7.5 parts, lanolin 2
, A 2 / part of stearic acid and 7 parts of isohexadecyl alcohol were used to produce an O / W emulsified foundation according to the following procedure.
【0041】すなわち、まずベントナイトを分散したプ
ロピレングリコールを精製水に加え、攪拌混合した後、
さらにトリエタノールアミン、モノステアリン酸ポリオ
キシエチレンソルビタン加えて混合した。これに、導電
性酸化亜鉛、ベンガラ、黄酸化鉄、黒酸化鉄を混合機に
て混合して得た混合紛を添加し、ホモミキサーにより処
理した。That is, first, propylene glycol in which bentonite is dispersed is added to purified water and mixed with stirring.
Further, triethanolamine and polyoxyethylene sorbitan monostearate were added and mixed. To this, a mixed powder obtained by mixing conductive zinc oxide, red iron oxide, yellow iron oxide, and black iron oxide with a mixer was added, and the mixture was treated with a homomixer.
【0042】更にモノステアリン酸グリセリン、流動パ
ラフィン、ラノリン、ステアリン酸及びイソヘキサデシ
ルアルコールを加え、ホモミキサーにて処理し、最後に
香料適量を加え十分に攪拌混合し、O/W乳化型ファン
デーション製造した。O/W乳化型ファンデーション中
の導電性酸化亜鉛の配合量は、揮発分を除いた皮膚への
残留成分として重量百分率で22%であった。Further, glycerin monostearate, liquid paraffin, lanolin, stearic acid and isohexadecyl alcohol were added, and the mixture was treated with a homomixer. Finally, an appropriate amount of a flavor was added and thoroughly stirred and mixed to produce an O / W emulsion type foundation. did. The compounding amount of the conductive zinc oxide in the O / W emulsified foundation was 22% by weight as a residual component on the skin excluding volatile components.
【0043】〔比較例3〕酸化亜鉛として比表面積が1
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー10( SUPER−
10 ) )を使用した以外は実施例3と同様にしてO/W
乳化型ファンデーションを製造した。O/W乳化型ファ
ンデーション中の酸化亜鉛の配合量は、揮発分を除いた
皮膚への残留成分として重量百分率で22%であった。Comparative Example 3 The specific surface area of zinc oxide was 1
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuiteku Co., Ltd .: Zinc oxide super 10 (SUPER-
10) O / W in the same manner as in Example 3 except that) was used.
An emulsion type foundation was manufactured. The amount of zinc oxide in the O / W emulsion type foundation was 22% by weight as a residual component on the skin excluding volatile components.
【0044】〔実施例4〕( 導電性酸化亜鉛の製造 ) まず、導電性酸化亜鉛を次の
ようにして製造した。すなわち、Example 4 (Production of Conductive Zinc Oxide ) First, conductive zinc oxide was produced as follows. That is,
【0045】試薬1級炭酸アンモニウム30gを水50
0ccに溶解し、別に50ccの水に硫酸アルミニウム
5gを溶解した溶液を上記炭酸アンモニウム溶液中に投
入した。この溶液を、別にフランス法亜鉛華100gを
200ccの水に分散して作った分散液中に入れ、60
℃に加温・攪拌し、1時間後濾過水洗し、このケーキを
乾燥後、水素雰囲気中で760℃、120分焼成して導
電性酸化亜鉛を得た。Reagent 30 g of primary ammonium carbonate was added to water 50
A solution of 5 g of aluminum sulfate dissolved in 50 cc of water was added to the above ammonium carbonate solution. This solution was separately placed in a dispersion prepared by dispersing 100 g of French method zinc flower in 200 cc of water.
After heating and stirring at 1 ° C. for 1 hour, the mixture was filtered and washed with water. The cake was dried and calcined in a hydrogen atmosphere at 760 ° C. for 120 minutes to obtain conductive zinc oxide.
【0046】得られた導電性酸化亜鉛は、比表面積が2
5m2 /g、体積抵抗率が40Ωcmのものであった。The resulting conductive zinc oxide has a specific surface area of 2
It had a volume resistivity of 5 m 2 / g and a volume resistivity of 40 Ωcm.
【0047】( 化粧水の作製 )酸化亜鉛として上述の導
電性酸化亜鉛( 比表面積が25m2 /g、体積抵抗率が
40Ωcm )を使用した。(Preparation of lotion) As the zinc oxide, the above-described conductive zinc oxide (having a specific surface area of 25 m 2 / g and a volume resistivity of 40 Ωcm) was used.
【0048】導電性酸化亜鉛1.6部、ベンガラ0.1
部、黄酸化鉄0.1部、グリセリン2部、1,3ブチレ
ングリコール2部、プロピレングリコール1部、カンフ
ァー0.2部、エタノール15部、精製水78部、香料
適量を用い、次の手順により化粧水を製造した。1.6 parts of conductive zinc oxide, 0.1 parts of red iron oxide
Parts, yellow iron oxide 0.1 part, glycerin 2 parts, 1,3 butylene glycol 2 parts, propylene glycol 1 part, camphor 0.2 parts, ethanol 15 parts, purified water 78 parts, perfume appropriate amount, the following procedure Produced a lotion.
【0049】まずエタノール、グリセリン、1,3ブチ
レングリコール、プロピレングリコール及び香料からな
る有機分を混合する。次に精製水、カンファー、導電性
酸化亜鉛、ベンガラ、黄酸化鉄を攪拌分散した後、この
分散液に、先に混合した有機混合分を添加、攪拌して化
粧水を作製した。化粧水中の導電性酸化亜鉛の配合量
は、揮発分を除いた皮膚への残留成分として重量百分率
で22%であった。First, an organic component consisting of ethanol, glycerin, 1,3 butylene glycol, propylene glycol and a fragrance is mixed. Next, purified water, camphor, conductive zinc oxide, red iron oxide and yellow iron oxide were stirred and dispersed, and the organic mixture previously mixed was added to the dispersion and stirred to prepare a lotion. The content of the conductive zinc oxide in the lotion was 22% by weight as a residual component on the skin excluding volatile components.
【0050】〔比較例4〕酸化亜鉛として比表面積が3
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー30( SUPER−
30 ) )を使用した以外は実施例4と同様にして化粧水
を製造した。化粧水中の酸化亜鉛の配合量は、揮発分を
除いた皮膚への残留成分として重量百分率で22%であ
った。Comparative Example 4 Specific surface area of zinc oxide was 3
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuitek Co., Ltd .: Zinc oxide super 30 (SUPER-
A lotion was produced in the same manner as in Example 4, except that 30)) was used. The content of zinc oxide in the lotion was 22% by weight as a residual component on the skin excluding volatile components.
【0051】〔実施例5〕( 導電性酸化亜鉛の製造 ) まず、導電性酸化亜鉛を次の
ようにして製造した。すなわち、Example 5 (Production of Conductive Zinc Oxide ) First, conductive zinc oxide was produced as follows. That is,
【0052】試薬1級炭酸アンモニウム30gを水50
0ccに溶解し、別に50ccの水に硫酸アルミニウム
5gを溶解した溶液を上記炭酸アンモニウム溶液中に投
入した。この溶液を別にフランス法亜鉛華100gを2
00ccの水に分散して作った分散液中に入れ、60℃
に加温・攪拌し、1時間後濾過水洗し、このケーキを乾
燥後、水素雰囲気中で780℃、60分焼成して導電性
酸化亜鉛を得た。Reagent 30 g of primary ammonium carbonate was added to water 50
A solution of 5 g of aluminum sulfate dissolved in 50 cc of water was added to the above ammonium carbonate solution. Separate this solution into 100 g of French zinc
Put into a dispersion prepared by dispersing in
After heating and stirring for 1 hour, the mixture was filtered and washed with water, and the cake was dried and calcined at 780 ° C. for 60 minutes in a hydrogen atmosphere to obtain conductive zinc oxide.
【0053】得られた導電性酸化亜鉛は、比表面積が1
8m2 /g、体積抵抗率が120Ωcmのものであっ
た。The obtained conductive zinc oxide has a specific surface area of 1
The volume resistivity was 8 m 2 / g and the volume resistivity was 120 Ωcm.
【0054】( 乳液の作製 )酸化亜鉛として上述の導電
性酸化亜鉛( 比表面積が18m2 /g、体積抵抗率が1
20Ωcm )を使用した。 (Preparation of Emulsion) As the zinc oxide, the above-mentioned conductive zinc oxide (having a specific surface area of 18 m 2 / g and a volume resistivity of 1
20 Ωcm 2).
【0055】導電性酸化亜鉛10部、精製水50部、プ
ロピレングリコール7部、ソルビタンセスキオレイン酸
エステル4部、POE( 20 )ソルビタンモノオレイン
酸エステル1部、流動パラフィン15部、ラノリン2
部、スクワラン8部、シリコン油1部、ビーズワックス
2部を用い、次の手順により乳液を製造した。10 parts of conductive zinc oxide, 50 parts of purified water, 7 parts of propylene glycol, 4 parts of sorbitan sesquioleate, 1 part of POE (20) sorbitan monooleate, 15 parts of liquid paraffin, 2 parts of lanolin
, Squalane 8 parts, silicone oil 1 part and beeswax 2 parts, an emulsion was prepared by the following procedure.
【0056】まず精製水にプロピレングリコール及び導
電性酸化亜鉛を加え、70℃に加熱・混合する。流動パ
ラフィン、ラノリン、スクワラン、シリコン油及びビー
ズワックスを加熱溶解後、ソルビタンセスキオレイン酸
エステル、POE( 20 )ソルビタンモノオレイン酸エ
ステルを加え70℃に調整後、上記プロピレングリコー
ル及び導電性酸化亜鉛を含む精製水を徐々に添加し、乳
化させて乳液を製造した。乳液中の導電性酸化亜鉛の配
合量は、揮発分を除いた皮膚への残留成分として重量百
分率で20%であった。First, propylene glycol and conductive zinc oxide are added to purified water, and heated to 70 ° C. and mixed. After heating and dissolving liquid paraffin, lanolin, squalane, silicone oil and beeswax, adding sorbitan sesquioleate and POE (20) sorbitan monooleate and adjusting to 70 ° C., containing the above propylene glycol and conductive zinc oxide Purified water was gradually added and emulsified to produce an emulsion. The content of the conductive zinc oxide in the emulsion was 20% by weight as a residual component on the skin excluding volatile components.
【0057】〔比較例5〕酸化亜鉛として比表面積が3
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー30( SUPER−
30 ) )を使用した以外は実施例4と同様にして乳液を
作製した。乳液中の酸化亜鉛の配合量は、揮発分を除い
た皮膚への残留成分として重量百分率で20%であっ
た。Comparative Example 5 Zinc oxide having a specific surface area of 3
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuitek Co., Ltd .: Zinc oxide super 30 (SUPER-
An emulsion was prepared in the same manner as in Example 4 except that 30))) was used. The content of zinc oxide in the emulsion was 20% by weight as a residual component on the skin excluding volatile components.
【0058】〔実施例6〕( クリームの作製 ) 導電性酸化亜鉛として比表面積が1
0m2 /g、体積抵抗率が90Ωcmのもの( ハクスイ
テック株式会社製:導電性酸化亜鉛23−K )を使用し
た。Example 6 (Preparation of cream) The conductive zinc oxide has a specific surface area of 1
0 m 2 / g, as the volume resistivity of 90Omucm (Hakusui Tech Co., Ltd. Conductive zinc oxide 23-K) was used.
【0059】導電性酸化亜鉛10部、精製水45部、セ
タノール2部、グリセリン8部、モノステアリン酸プロ
ピレングリコール2部、ステアリン酸2部、シリコン油
5部、ラノリン2部、スクワラン15部、オクタン酸セ
チル8部、マイクロクリスタリンワックス1部を用い、
次の手順によりクリームを製造した。10 parts of conductive zinc oxide, 45 parts of purified water, 2 parts of cetanol, 8 parts of glycerin, 2 parts of propylene glycol monostearate, 2 parts of stearic acid, 5 parts of silicone oil, 2 parts of lanolin, 15 parts of squalane, 15 parts of octane Using 8 parts of cetyl acid and 1 part of microcrystalline wax,
The cream was manufactured according to the following procedure.
【0060】モノステアリン酸プロピレングリコール、
セタノール、ラノリン、シリコン油、オクタン酸セチ
ル、ステアリン酸、スクワラン及びマイクロクリスタリ
ンワックスからなる油分を70℃で加熱攪拌混合した。Propylene glycol monostearate,
An oil composed of cetanol, lanolin, silicone oil, cetyl octanoate, stearic acid, squalane and microcrystalline wax was heated and mixed at 70 ° C.
【0061】グリセリンを精製水に溶解させた後、導電
性酸化亜鉛を攪拌混合し、70℃とした後、上記加熱混
合した油分を添加してホモミキサーで乳化し、クリーム
を作製した。クリーム中の導電性酸化亜鉛の配合量は、
揮発分を除いた皮膚への残留成分として重量百分率で1
8%であった。After dissolving glycerin in purified water, conductive zinc oxide was stirred and mixed, and the mixture was heated to 70 ° C., and the oil mixed by heating was added and emulsified with a homomixer to prepare a cream. The amount of conductive zinc oxide in the cream is
1% by weight as residual components on the skin excluding volatile components
8%.
【0062】〔比較例6〕酸化亜鉛として比表面積が1
0m2 /g、体積抵抗率が100MΩcm( ハクスイテ
ック株式会社製:酸化亜鉛スーパー10( SUPER−
10 ) )を使用した以外は実施例6と同様にして乳液を
作製した。クリーム中の酸化亜鉛の配合量は、揮発分を
除いた皮膚への残留成分として重量百分率で18%であ
った。Comparative Example 6 The specific surface area of zinc oxide was 1
0 m 2 / g, volume resistivity 100 MΩcm (manufactured by Hakusuiteku Co., Ltd .: Zinc oxide super 10 (SUPER-
An emulsion was prepared in the same manner as in Example 6 except that 10))) was used. The content of zinc oxide in the cream was 18% by weight as a residual component on the skin excluding volatile components.
【0063】(II) サンプルの評価 (I) で作製した実施例と比較例の各種化粧料を用いて
紫外線不透過性と赤外線不透過性並びに化粧もち及びほ
てり感を測定した。 (II) Evaluation of Samples Using the various cosmetics of the examples and the comparative examples prepared in (I), ultraviolet impermeability and infrared impermeability, and makeup stickiness and hot flash were measured.
【0064】紫外線不透過性、赤外線不透過性:作製
した化粧料のうち、パウダリーファンデーション、ケー
キファンデーションは、PETフィルム上にパフを用い
て塗布し、乳化型ファンデーション、化粧水、乳液、ク
リームについては、PETフィルム上に塗布し、それぞ
れ分光器(日本分光V-570 型 )にて測定した。UV impermeability, infrared impermeability: Among the cosmetics prepared, powdery foundation and cake foundation are applied on a PET film using a puff, and emulsified foundation, lotion, lotion, and cream are applied. , And applied to a PET film, and each was measured using a spectroscope (JASCO Corporation V-570 type).
【0065】測定結果を紫外、可視、赤外領域での各波
長における透過率として〔表1〕にまとめた。The measurement results are summarized in Table 1 as the transmittance at each wavelength in the ultraviolet, visible, and infrared regions.
【0066】化粧もち、ほてり感: i)化粧もちについては、10名の女性パネラーに実施
例、比較例の化粧料を用いて官能試験を行ってもらっ
た。その結果、8〜10名が実施例のほうが良いとした
ものを○、5〜7名が良いとしたものを△、それ以外の
ものを×とした。Makeup Stickiness, Hot Flashiness: i) With regard to makeup stickiness, 10 female panelists were subjected to a sensory test using the cosmetics of Examples and Comparative Examples. As a result, 8 to 10 persons judged that the example was better, ○, 5 to 7 persons judged better, Δ, and others indicated X.
【0067】ii) ほてり感については、同じく10名の
女性パネラーに実施例、比較例の化粧料を用いて晴天下
の屋外に出てもらい、官能試験による熱感を聴取した。
その結果、8〜10名が実施例のほうが少ないとしたも
のを○、5〜7名が少ないとしたものを△、それ以外を
×とした。以上の官能試験の結果を〔表2〕に示した。Ii) Regarding the feeling of hot flashes, ten female panelists were asked to come out outdoors under the fine weather using the cosmetics of Examples and Comparative Examples, and the heat of the sensory test was heard.
As a result, ○ indicates that 8 to 10 persons were smaller in the example, Δ indicates that 5 to 7 persons were smaller, and X indicates the others. The results of the above sensory tests are shown in [Table 2].
【0068】〔表1〕における各波長での透過率からわ
かるように、すべての例において実施例と比較例は、可
視領域における透過率についての差が殆どないが、紫
外、赤外領域においては、実施例は、いずれも比較例よ
り透過率が低く、比較例に比べて紫外線防止効果及び赤
外線防止効果が大きいことがが分かる。As can be seen from the transmittance at each wavelength in Table 1, there is almost no difference in the transmittance in the visible region between the example and the comparative example in all the examples, but there is little difference in the transmittance in the ultraviolet and infrared regions. In each of the examples, it can be seen that the transmittance is lower than that of the comparative example, and the ultraviolet ray preventing effect and the infrared ray preventing effect are larger than those of the comparative example.
【0069】また、〔表2〕の官能試験結果より実施例
は、程度の差はあるものの、すべての例において化粧持
ちが良く、かつ、ほてり感が少ないという本発明の導電
性酸化亜鉛を化粧料に配合した効果が確認された。Further, from the results of the sensory tests shown in Table 2, the conductive zinc oxide of the present invention, which has good makeup lasting and little hot flash, was applied to all the examples, although the degree was different. The effect of mixing with the ingredients was confirmed.
【0070】[0070]
【表1】 [Table 1]
【0071】[0071]
【表2】 [Table 2]
【0072】[0072]
【発明の効果】本発明に従えば、導電性酸化亜鉛微粉末
を配合した紫外線吸収能を備えるとともに、化粧もちに
優れた化粧料が提供される。この化粧崩れが少ないとい
うことは、当然ながら紫外線防止効果のみならず、化粧
の本来の目的である美しく見せるという美的役割をも長
時間に渡り維持でき、非常に好都合なものである。According to the present invention, it is possible to provide a cosmetic which has an ultraviolet absorbing ability blended with a conductive zinc oxide fine powder and which is excellent in makeup. The fact that the makeup collapse is small is, of course, not only an effect of preventing ultraviolet rays, but also the aesthetic role of showing the beauty, which is the original purpose of makeup, can be maintained for a long time, which is very convenient.
フロントページの続き (72)発明者 田中 隆夫 福岡県飯塚市大字横田669番地 ハクスイ テック株式会社内 Fターム(参考) 4C083 AA082 AB211 AB212 AB221 AB222 AB232 AB432 AB442 AB501 AB502 AC012 AC022 AC072 AC092 AC102 AC122 AC242 AC352 AC372 AC392 AC422 AC442 AC542 AD072 AD152 AD512 AD532 CC01 CC04 CC05 CC12 DD17 DD21 DD23 DD31 DD33 EE17 FF01Continued on the front page (72) Inventor Takao Tanaka 669, Yokota, Iizuka-shi, Fukuoka F-term (reference) 4C083 AA082 AB211 AB212 AB221 AB222 AB232 AB432 AB442 AB501 AB502 AC012 AC022 AC072 AC092 AC102 AC122 AC242 AC352 AC372 AC392 AC422 AC442 AC542 AD072 AD152 AD512 AD532 CC01 CC04 CC05 CC12 DD17 DD21 DD23 DD31 DD33 EE17 FF01
Claims (3)
抗率500Ωcm以下である導電性酸化亜鉛微粉末を配
合してなることを特徴とする化粧料。1. A cosmetic comprising a conductive zinc oxide fine powder having a specific surface area of 2 to 100 m 2 / g and a volume resistivity of 500 Ωcm or less.
分を除いた皮膚への残留成分として重量百分率で5%以
上であることを特徴とする請求項1記載の化粧料。2. The cosmetic according to claim 1, wherein the amount of the conductive zinc oxide fine powder is at least 5% by weight as a residual component on the skin excluding volatile components.
分としてアルミニウムを用いた酸化亜鉛微粉末であるこ
とを特徴とする請求項1または2記載の化粧料。3. The cosmetic according to claim 1, wherein the conductive zinc oxide fine powder is a zinc oxide fine powder using aluminum as a conductivity-imparting component.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11169125A JP2001002529A (en) | 1999-06-16 | 1999-06-16 | Cosmetics compounded with fine powder of conductive zinc oxide |
| PCT/JP2000/008783 WO2002047640A1 (en) | 1999-06-16 | 2000-12-13 | Cosmetic comprising fine zinc oxide powder having electrically conductivity |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11169125A JP2001002529A (en) | 1999-06-16 | 1999-06-16 | Cosmetics compounded with fine powder of conductive zinc oxide |
| PCT/JP2000/008783 WO2002047640A1 (en) | 1999-06-16 | 2000-12-13 | Cosmetic comprising fine zinc oxide powder having electrically conductivity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2001002529A true JP2001002529A (en) | 2001-01-09 |
Family
ID=26344995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11169125A Pending JP2001002529A (en) | 1999-06-16 | 1999-06-16 | Cosmetics compounded with fine powder of conductive zinc oxide |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JP2001002529A (en) |
| WO (1) | WO2002047640A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002047640A1 (en) * | 1999-06-16 | 2002-06-20 | Hakusui Tech Co., Ltd. | Cosmetic comprising fine zinc oxide powder having electrically conductivity |
| JP2005162695A (en) * | 2003-12-04 | 2005-06-23 | Lion Corp | Infrared shielding substance-containing cosmetics |
| JP2013193960A (en) * | 2012-03-16 | 2013-09-30 | Goshu Yakuhin Kk | Hand cream |
| US10675229B2 (en) | 2015-03-24 | 2020-06-09 | Landa Labs (2012) Ltd. | UV-protective compositions and their use |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58161923A (en) * | 1982-03-17 | 1983-09-26 | Hakusui Kagaku Kogyo Kk | Manufacture of electrically conductive zinc oxide |
| JPH086055B2 (en) * | 1987-12-11 | 1996-01-24 | 白水化学工業株式会社 | Zinc oxide-based transparent conductive film-forming composition |
| JP3521934B2 (en) * | 1992-06-30 | 2004-04-26 | 朝日化学工業株式会社 | Cosmetic and method for producing flaky zinc oxide powder used therefor |
| JP3559293B2 (en) * | 1992-06-30 | 2004-08-25 | 朝日化学工業株式会社 | Flaky zinc oxide powder and method for producing the same |
| JP3398829B2 (en) * | 1994-12-13 | 2003-04-21 | 株式会社日本触媒 | Method for producing zinc oxide-based fine particles |
| JP2001002529A (en) * | 1999-06-16 | 2001-01-09 | Hakusui Tech Co Ltd | Cosmetics compounded with fine powder of conductive zinc oxide |
-
1999
- 1999-06-16 JP JP11169125A patent/JP2001002529A/en active Pending
-
2000
- 2000-12-13 WO PCT/JP2000/008783 patent/WO2002047640A1/en not_active Ceased
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002047640A1 (en) * | 1999-06-16 | 2002-06-20 | Hakusui Tech Co., Ltd. | Cosmetic comprising fine zinc oxide powder having electrically conductivity |
| JP2005162695A (en) * | 2003-12-04 | 2005-06-23 | Lion Corp | Infrared shielding substance-containing cosmetics |
| JP2013193960A (en) * | 2012-03-16 | 2013-09-30 | Goshu Yakuhin Kk | Hand cream |
| US10675229B2 (en) | 2015-03-24 | 2020-06-09 | Landa Labs (2012) Ltd. | UV-protective compositions and their use |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2002047640A1 (en) | 2002-06-20 |
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