JPH02289506A - Zinc oxide for cosmetic - Google Patents

Zinc oxide for cosmetic

Info

Publication number
JPH02289506A
JPH02289506A JP20905589A JP20905589A JPH02289506A JP H02289506 A JPH02289506 A JP H02289506A JP 20905589 A JP20905589 A JP 20905589A JP 20905589 A JP20905589 A JP 20905589A JP H02289506 A JPH02289506 A JP H02289506A
Authority
JP
Japan
Prior art keywords
zinc oxide
cosmetics
zinc
surface area
cosmetic
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
Application number
JP20905589A
Other languages
Japanese (ja)
Inventor
Teruo Fujiwara
藤原 輝男
Hirobumi Yamamoto
博文 山本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sakai Chemical Industry Co Ltd
Original Assignee
Sakai Chemical Industry Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sakai Chemical Industry Co Ltd filed Critical Sakai Chemical Industry Co Ltd
Priority to JP20905589A priority Critical patent/JPH02289506A/en
Publication of JPH02289506A publication Critical patent/JPH02289506A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain the title zinc oxide which is made through the dry process, having prescribed values of specific surface area and ultraviolet absorptivity, and is admixed to cosmetics to improve clearness and make up duration and protect skins effectively from ultraviolet rays. CONSTITUTION:The zinc oxide for cosmetics is produced through the dry process, and has 20 to 30m<2>/g, about 0.1mum particle size and more than 90% ultraviolet absorptivity. The zinc oxide is prepared by heating molten zinc metal in a retort at about 100 deg.C, allowing the generated zinc vapor to flow at a certain rate, for example, 0.5 to 1.5kg/hour and oxidizing the vapor with a constant amount of air, sending the zinc oxide formed to the cooling tube with a blower and collecting the cooled zinc oxide with the collector and bag filters whereby zinc oxide of high purity is obtained. The zinc oxide is excellent in dispersion to increase the luster of cosmetic and is used as a pigment and added to cosmetics such as foundation or cheek rouge.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 この発明は、メーキャップ化粧料に配合されることによ
り、透明感および化粧もちを改善することができ、しか
も高い紫外線吸収能を有する化粧料用酸化亜鉛に関する
[Detailed Description of the Invention] <Industrial Application Field> The present invention provides a cosmetic product that can be incorporated into makeup cosmetics to improve transparency and makeup durability, and also has high ultraviolet absorption ability. Regarding zinc oxide.

〈従来の技術〉 ファウンデーション、アイシャドー、頬紅、口紅などの
化粧t4は、目もと、頬、口もとなどにみずみずしさを
与え、容姿を美しく、魅力的なものにするためのもので
あり、美が求められる女性の必需品である。
<Conventional technology> Makeup T4, such as foundation, eye shadow, blusher, and lipstick, is used to add freshness to the eyes, cheeks, and mouth, to make one's appearance beautiful and attractive. It is a must-have item for women.

かかる化粧料は、通常、粉末、油、水、フックスなどか
らなり、このうち粉末は、着色顔料と、タルク、カオリ
ン、マイカ、二酸化チタン、硫酸バリウムなどの体質顔
料とからなる。
Such cosmetics usually consist of powder, oil, water, fuchs, etc., of which the powder consists of coloring pigments and extender pigments such as talc, kaolin, mica, titanium dioxide, barium sulfate, etc.

また、化粧料には、紫外線から女性の肌を保護するため
紫外線吸収剤が配合されたものもある。
Additionally, some cosmetics contain UV absorbers to protect women's skin from UV rays.

〈発明が解決しようとする課題〉 しかし、従来の化粧料においては、長時間塗膜の美しさ
を維持するのは困難であった。また、紫外線吸収能も未
だ充分なものとは言い難かった。
<Problems to be Solved by the Invention> However, with conventional cosmetics, it has been difficult to maintain the beauty of the coating film for a long time. Furthermore, the ultraviolet absorbing ability was still far from sufficient.

この発明は、以上の事情に鑑みなされたものであって、
その目的とするところは、化粧料に配合されることによ
り、透明感がよく、化粧もちを改善することができ、し
かも紫外線から肌を有効に保護しうる化粧料用酸化亜鉛
を提供するにある。
This invention was made in view of the above circumstances, and
The purpose is to provide zinc oxide for cosmetics that, when incorporated into cosmetics, provides good transparency, improves makeup retention, and can effectively protect the skin from ultraviolet rays. .

〈課題を解決するための手段および作用〉上記問題を解
決するためのこの発明の化粧料用酸化亜鉛は、乾式法で
製造されるものであって、比表面積20〜30 m’ 
/ g 、紫外線吸収率90%以上を有するものである
<Means and effects for solving the problems> The zinc oxide for cosmetics of the present invention for solving the above problems is produced by a dry method, and has a specific surface area of 20 to 30 m'
/g, and has an ultraviolet absorption rate of 90% or more.

ここで、比表面積の値はBET吸着法に基づく値である
。また、紫外線吸収率の値は、吸収波長が370nmの
場合の値である。
Here, the value of the specific surface area is a value based on the BET adsorption method. Moreover, the value of ultraviolet absorption rate is the value when the absorption wavelength is 370 nm.

酸化亜鉛の製造方法としては、一般に乾式法(フランス
法)と湿式法とがある。
There are generally two methods for producing zinc oxide: a dry method (French method) and a wet method.

湿式法は、塩化亜鉛溶液にソーダ灰を加えて液中に塩基
性炭酸亜鉛を沈澱させ、水洗、乾燥後、仮焼する方法で
ある。この方法によると、比表面積が70 m’ / 
g程度のものしか得られず、また、炭酸イオンが不純物
として残留し、さらに紫外線吸収能が充分でないという
欠点がある。
The wet method is a method in which basic zinc carbonate is precipitated by adding soda ash to a zinc chloride solution, followed by washing with water, drying, and calcining. According to this method, the specific surface area is 70 m'/
However, there are disadvantages in that only about 1.5 g of carbonate ions can be obtained, carbonate ions remain as impurities, and ultraviolet absorption ability is not sufficient.

これに対して、この発明における乾式法は、溶融させた
金属亜鉛をレトルトの中で1000℃程度に加熱し、発
生する亜鉛蒸気を空気を用いて酸化し、生成した酸化亜
鉛を送風機で空冷管に送って冷却し、コレクター及びバ
グフィルタ−で分離、捕集する方法である。
On the other hand, in the dry method of this invention, molten metal zinc is heated to about 1000°C in a retort, the generated zinc vapor is oxidized using air, and the generated zinc oxide is transferred to an air-cooled tube using a blower. In this method, the waste is sent to a refrigerator, cooled, and separated and collected using a collector and bag filter.

この乾式法によれば、不純物の混じらない高純度の酸化
亜鉛を得ることができる。さらに、乾式法で得られた酸
化亜鉛は、湿式法で得られたものに比べて、紫外線吸収
能が高く、分散性に秀れ、化粧料の光沢をより向上させ
る。
According to this dry method, highly pure zinc oxide without any impurities can be obtained. Furthermore, zinc oxide obtained by the dry method has higher ultraviolet absorption ability and excellent dispersibility than that obtained by the wet method, and improves the gloss of cosmetics.

かかる乾式法により比表面積か20〜30m27gおよ
び紫外線吸収率90%以上の酸化亜鉛を得るには、金属
亜鉛蒸気を一定流速、例えば0.5〜1.5ki/時で
流し、これに一定量例えば1.8Nm’/分程度の割合
で空気を吹き付ければよい。
In order to obtain zinc oxide having a specific surface area of 20 to 30 m27g and an ultraviolet absorption rate of 90% or more by such a dry method, metallic zinc vapor is flowed at a constant flow rate, for example, 0.5 to 1.5 ki/hour, and a certain amount of, for example, Air may be blown at a rate of about 1.8 Nm'/min.

ここで、比表面積を20〜30 m2/ gの範囲に特
定したのは、比表面積が20 m’ / g未満の酸化
亜鉛では、これを化粧料に配合した場合、化粧しちが悪
くなり、さらに可視光線透過率や紫外線吸収率も低下す
るためであり、また比表面積が30m’/gを越えるも
のは現在の乾式法では工業的に製造することができない
からである。
Here, the reason why the specific surface area is specified to be in the range of 20 to 30 m2/g is because zinc oxide with a specific surface area of less than 20 m'/g will have poor makeup application when added to cosmetics. Furthermore, the visible light transmittance and ultraviolet absorption rate are also lowered, and the specific surface area exceeding 30 m'/g cannot be industrially produced using the current dry method.

また、紫外線吸収率を90%以上としたのは、紫外線吸
収率が90%未満の酸化亜鉛では、これを化粧料に配合
した場合、十分な紫外線吸収能を示さなくなるためであ
る。
Further, the reason why the ultraviolet absorption rate is set to 90% or more is because zinc oxide with an ultraviolet absorption rate of less than 90% does not exhibit sufficient ultraviolet absorption ability when added to cosmetics.

この発明の化粧料用酸化亜鉛は顔料として、従来既知の
他の配合成分と共に、ファウンデーション、アイシャド
ー、頬紅、口紅等の化粧料に配合される。
The zinc oxide for cosmetics of the present invention is blended as a pigment into cosmetics such as foundations, eye shadows, blushers, lipsticks, etc., along with other conventionally known ingredients.

他の配合成分としては、タルク、マイカ、カオリン、二
酸化チタン、青色顔料などの粉末、油分、アルコール、
8f4が例示される。
Other ingredients include talc, mica, kaolin, titanium dioxide, blue pigment powder, oil, alcohol,
8f4 is exemplified.

この場合、酸化亜鉛の微粒子は、粒子そのまま又は油分
と混合してローラなどにより混練りしてペースト状にし
て化粧料に配合することができる。
In this case, the fine particles of zinc oxide can be blended into the cosmetic as they are or mixed with oil and kneaded with a roller or the like to form a paste.

この発明の酸化亜鉛の化粧料への配合量は、1〜50重
量%の割合であるのが好ましい。これは、1重量%未満
の場合、添加効果が殆どみられないからであり、50重
量%を越えた場合、化粧料の透明感が損なわれるからで
ある。
The amount of zinc oxide of this invention incorporated into the cosmetic is preferably 1 to 50% by weight. This is because when the amount is less than 1% by weight, there is almost no effect of addition, and when it exceeds 50% by weight, the transparency of the cosmetic is impaired.

なお、比表面積20 m’ / gの酸化亜鉛の場合、
その粒径は、0゜1μ−程度である。
In addition, in the case of zinc oxide with a specific surface area of 20 m'/g,
Its particle size is approximately 0°1μ.

〈実施例〉 以下、本発明を実施例に基づいて詳細に説明する。但し
、本発明は下記の実施例に限定されるものではない。
<Examples> Hereinafter, the present invention will be described in detail based on Examples. However, the present invention is not limited to the following examples.

実施例1 ノズルから金属亜鉛蒸気を1kcJ/時の流速で流し、
これに2.ONm’/分の割合で空気を吹き付けて金属
亜鉛を酸化し、酸化亜鉛の微粒子を作製した。その比表
面積をBET吸着法によって測定したところ、22. 
1 m2/ gであった。
Example 1 Metal zinc vapor was flowed from a nozzle at a flow rate of 1 kcJ/hour,
2. Metal zinc was oxidized by blowing air at a rate of ON m'/min to produce fine particles of zinc oxide. When its specific surface area was measured by BET adsorption method, it was found to be 22.
It was 1 m2/g.

実施例2 ノズルから金属亜鉛蒸気を1−7時の流速で流し、これ
に1.8Nm’/分の割合で空気を吹き付けて金属亜鉛
を酸化し、酸化亜鉛の微粒子を作製した。その比表面積
をBET吸着法によって測定したところ、25.0m’
/gであった。
Example 2 Metallic zinc vapor was flowed from a nozzle at a flow rate of 1 to 7 hours, and air was blown thereto at a rate of 1.8 Nm'/min to oxidize metal zinc to produce fine particles of zinc oxide. When its specific surface area was measured by BET adsorption method, it was found to be 25.0 m'
/g.

実施例3 ノズルから金属亜鉛蒸気を10−7時の流速で流し、こ
れに15.ONm’/分の割合で空気を吹き付けて金属
亜鉛を酸化し、酸化亜鉛の微粒子を作製した。その比表
面積をBET吸着法によって測定したところ、29.6
m’/gであった。
Example 3 Metallic zinc vapor was flowed from a nozzle at a flow rate of 10-7 hours, and 15. Metal zinc was oxidized by blowing air at a rate of ON m'/min to produce fine particles of zinc oxide. When its specific surface area was measured by BET adsorption method, it was found to be 29.6
m'/g.

評価試験 前記実施例1〜3で得た酸化亜鉛の可視光透過率(%)
及び紫外線吸収率(%)を、分光光度計([1立社製、
型式1θ0−10)にてJlll定した。
Evaluation test Visible light transmittance (%) of zinc oxide obtained in Examples 1 to 3 above
and ultraviolet absorption rate (%) using a spectrophotometer ([1 Ritsusha,
Jllll was determined using the model 1θ0-10).

結果を表1に示す。The results are shown in Table 1.

なお、分光光度1;1の紫外部の吸収波長として370
nmを、またi’J N部の吸収波長として52θnm
を用いt二。
In addition, the absorption wavelength in the ultraviolet region with a spectrophotometric intensity of 1:1 is 370
nm, and 52θnm as the absorption wavelength of the i'J N part.
Use t2.

また、表中には、比表面積60 m’ / gの湿式法
で得られた酸化亜鉛(堺化学工業株式会社製、ZINC
A−20)(比較例1)および表面積2、4 m’/ 
Hの従来既知の硫酸バリウム(比較例2)の可視光透過
率(%)及び紫外線吸収率(%)を比較参照のため併記
した。
In addition, in the table, zinc oxide obtained by a wet method with a specific surface area of 60 m'/g (manufactured by Sakai Chemical Industry Co., Ltd., ZINC
A-20) (Comparative Example 1) and surface area 2.4 m'/
The visible light transmittance (%) and ultraviolet absorption rate (%) of conventionally known barium sulfate (Comparative Example 2) of H are also listed for comparison and reference.

表1 表1より、実施例1〜3は、比較例1〜2に比べてi’
+J視光L3過率及び紫外線吸収率がともに高いことか
分る。
Table 1 From Table 1, Examples 1 to 3 have i'
It can be seen that both the +J visible light L3 pass rate and ultraviolet absorption rate are high.

このように、実施例1〜3で得た酸化亜鉛は、可視光透
過率か高いため、メーキャップ化粧料に配合しても化粧
料の透明性を損なうことか少なくなる。また、紫外線吸
収率が高いので、紫外線吸収顔料として、化粧料に配合
することができる。
As described above, since the zinc oxide obtained in Examples 1 to 3 has a high visible light transmittance, even if it is incorporated into makeup cosmetics, the transparency of the cosmetics is less likely to be impaired. Furthermore, since it has a high ultraviolet absorption rate, it can be incorporated into cosmetics as an ultraviolet absorbing pigment.

使用例1〜3(口紅の作製) ヒマシ油15部(重量部、以下同じ)、ジー2−ヘプチ
ルウンデカン酸グリセリン30部、流動パラフィン15
部、ポリエチレンワックス15.8部、カルナバロウ3
部を加熱混合して溶解させた。次いて、この溶液に予め
調製しておいた、前記実施例1〜3で得た各酸化亜鉛1
0部をヒマシ浦10部にそれぞれ分散させた液と、着色
顔料とを加えて攪拌し、均一に分散させた。次いで、減
圧して脱気し、口紅容器に移した後、冷却固化させて口
紅を作製した。実施例1の酸化亜鉛を用いて作製した口
紅を使用例1、実施例2の酸化亜鉛を用いて作製した口
紅を使用例2、実施例′3の酸化亜鉛を用いて作製した
口紅を使用例3として、透明性及び化粧もちについての
官能テストを10人の女性パネラ−により行った。
Usage Examples 1 to 3 (Preparation of lipstick) 15 parts of castor oil (parts by weight, same hereinafter), 30 parts of glycerin di-2-heptylundecanoate, 15 parts of liquid paraffin
15.8 parts of polyethylene wax, 3 parts of carnauba wax
The mixture was heated and mixed to dissolve. Next, each zinc oxide 1 obtained in Examples 1 to 3, which had been prepared in advance, was added to this solution.
A solution obtained by dispersing 0 part in 10 parts of Castor porridge and a coloring pigment were added and stirred to uniformly disperse them. Next, the mixture was degassed under reduced pressure, transferred to a lipstick container, and then cooled and solidified to produce a lipstick. Example 1 of using a lipstick made using zinc oxide of Example 1, Example 2 of using a lipstick made using zinc oxide of Example 2, and Example 2 of using a lipstick made using zinc oxide of Example '3. As part 3, a sensory test regarding transparency and makeup durability was conducted by 10 female panelists.

参考例 実施例1で得た酸化亜鉛に代えて湿式法で得た前記比較
例1の酸化亜鉛10部を用いたこと以外は、使用例1と
同様にして口紅の作製及び官能テストを行った。
Reference Example A lipstick was prepared and a sensory test was conducted in the same manner as in Use Example 1, except that 10 parts of the zinc oxide obtained in Comparative Example 1 obtained by a wet method was used in place of the zinc oxide obtained in Example 1. .

上記テスト結果を表2に示す。The above test results are shown in Table 2.

表2 表中、透明性Oは透明感があったこと(10人中10人
)を、透明性△はややくすみがあったこと(10人中8
人)を示す。また、化粧ちちOは、4時間経過後の化粧
もちがよいこと(10人中10人)を、化粧もち△は、
やや化粧もちがよくない(10人中9人)を示す。
Table 2 In the table, Transparency O means that it was transparent (10 out of 10 people), and Transparency △ means that it was a little dull (8 out of 10 people).
person). In addition, makeup Chichi O said that the makeup lasted for 4 hours (10 out of 10 people), and makeup longevity △
Indicates that makeup does not last long (9 out of 10 people).

表2より明らかなように、使用例1〜3の場合、得られ
た口紅は参考例で得られたものに比べて透明性に優れて
おり、また化粧もちが良いことが分る。
As is clear from Table 2, in the case of Usage Examples 1 to 3, the obtained lipsticks had better transparency and better makeup retention than those obtained in Reference Examples.

使用例4(バウダリーファウンデーションの作製)実施
例2で得られた酸化亜鉛50部、タルク18部、マイカ
15部、赤色酸化鉄0.5部、黄色酸化鉄1.0部、黒
色酸化鉄0.2部及び酸化チタン6.3部を攪拌して混
合した。この混合顔料にシリコーン浦3部、流動パラフ
ィン5部、ソルビタンセスキオレート1部、及び適宜量
の防腐剤及び香料を加えて加熱しながら攪拌混合して溶
解させ、混合粉砕した。この粉砕物を所定形状に成形し
てパウダリーファウンデーションを作製した。
Use example 4 (preparation of border foundation) 50 parts of zinc oxide obtained in Example 2, 18 parts of talc, 15 parts of mica, 0.5 part of red iron oxide, 1.0 part of yellow iron oxide, 0 part of black iron oxide. .2 parts and 6.3 parts of titanium oxide were mixed with stirring. To this mixed pigment were added 3 parts of silicone ura, 5 parts of liquid paraffin, 1 part of sorbitan sesquiolate, and appropriate amounts of preservatives and fragrances, stirred and mixed while heating to dissolve, and mixed and pulverized. This pulverized product was molded into a predetermined shape to produce a powder foundation.

得られたファウンデーションは、従来のものに比べて化
粧のびがよく、肌へのフィツト感かあり、化粧もちもき
わめて良かった。
The obtained foundation applied makeup better than conventional products, had a good fit to the skin, and had extremely good makeup retention.

〈発明の効果〉 以上のようにこの発明の化粧料用酸化亜鉛は、乾式法で
つくられ、特定の比表面積および紫外線吸収率を有する
ため、これを化粧料に配合した場合に化粧料の化粧もち
を向上させ、しかも化粧料の紫外線吸収能を高めること
ができる。また、この発明の化粧料用酸化亜鉛は、可視
光線透過率にも秀れているので、化粧料の透明性を損な
わず、さらに分散性に秀れ、光沢等がよいので、化粧料
の配合剤として特に好適に使用できるという効果を奏す
る。
<Effects of the Invention> As described above, the zinc oxide for cosmetics of this invention is produced by a dry process and has a specific specific surface area and ultraviolet absorption rate, so when it is blended into cosmetics, It is possible to improve the durability of the cosmetic and also to increase the ultraviolet absorption ability of the cosmetic. In addition, the zinc oxide for cosmetics of this invention has excellent visible light transmittance, so it does not impair the transparency of cosmetics, and has excellent dispersibility and gloss, so it can be used in cosmetic formulations. It has the advantage that it can be particularly suitably used as a drug.

、I!lF(自発) 平成1年 第209055号 化粧料用酸化亜鉛 3、補正をする者 事件との関係,I! IF (spontaneous) 1999 No. 209055 Zinc oxide for cosmetics 3. Person who makes corrections Relationship with the incident

Claims (1)

【特許請求の範囲】 1、比表面積が20〜30m^2/g、紫外線吸収率が
90%以上であることを特徴と する乾式法で得られた化粧料用酸化亜鉛。
[Scope of Claims] 1. Zinc oxide for cosmetics obtained by a dry process, characterized by having a specific surface area of 20 to 30 m^2/g and an ultraviolet absorption rate of 90% or more.
JP20905589A 1989-02-08 1989-08-11 Zinc oxide for cosmetic Pending JPH02289506A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20905589A JPH02289506A (en) 1989-02-08 1989-08-11 Zinc oxide for cosmetic

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP1-30356 1989-02-08
JP3035689 1989-02-08
JP20905589A JPH02289506A (en) 1989-02-08 1989-08-11 Zinc oxide for cosmetic

Publications (1)

Publication Number Publication Date
JPH02289506A true JPH02289506A (en) 1990-11-29

Family

ID=26368686

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20905589A Pending JPH02289506A (en) 1989-02-08 1989-08-11 Zinc oxide for cosmetic

Country Status (1)

Country Link
JP (1) JPH02289506A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH069363A (en) * 1992-06-29 1994-01-18 Fuiru Internatl:Kk Medicinal cosmetic
US5366660A (en) * 1991-10-04 1994-11-22 Tioxide Specialties Limited Dispersions
US5573753A (en) * 1991-10-04 1996-11-12 Tioxide Specialties Limited Method of preparing sunscreens
WO1999059540A1 (en) * 1998-05-21 1999-11-25 The Boots Company Plc Antimicrobial agent
US7390355B2 (en) * 2003-06-11 2008-06-24 Croda International Plc Zinc oxide
WO2012036082A1 (en) 2010-09-13 2012-03-22 堺化学工業株式会社 Zinc oxide particles and cosmetic material
JP2017222589A (en) * 2016-06-14 2017-12-21 住友大阪セメント株式会社 Zinc oxide powder for cosmetics, dispersions, cosmetics

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JPS57205319A (en) * 1981-06-15 1982-12-16 Mitsubishi Metal Corp Manufacture of very fine zinc oxide powder
JPS61236708A (en) * 1985-04-12 1986-10-22 Shiseido Co Ltd Cosmetic
JPS61257909A (en) * 1985-05-10 1986-11-15 Shiseido Co Ltd Cosmetic
JPS62228006A (en) * 1985-12-18 1987-10-06 Kao Corp Sunscreen cosmetic

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Publication number Priority date Publication date Assignee Title
JPS57205319A (en) * 1981-06-15 1982-12-16 Mitsubishi Metal Corp Manufacture of very fine zinc oxide powder
JPS61236708A (en) * 1985-04-12 1986-10-22 Shiseido Co Ltd Cosmetic
JPS61257909A (en) * 1985-05-10 1986-11-15 Shiseido Co Ltd Cosmetic
JPS62228006A (en) * 1985-12-18 1987-10-06 Kao Corp Sunscreen cosmetic

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5366660A (en) * 1991-10-04 1994-11-22 Tioxide Specialties Limited Dispersions
US5573753A (en) * 1991-10-04 1996-11-12 Tioxide Specialties Limited Method of preparing sunscreens
US5605652A (en) * 1991-10-04 1997-02-25 Tioxide Specialties Limited Method of preparing sunscreens
JPH069363A (en) * 1992-06-29 1994-01-18 Fuiru Internatl:Kk Medicinal cosmetic
WO1999059540A1 (en) * 1998-05-21 1999-11-25 The Boots Company Plc Antimicrobial agent
AU745253B2 (en) * 1998-05-21 2002-03-14 Boots Company Plc, The Antimicrobial agent
US7390355B2 (en) * 2003-06-11 2008-06-24 Croda International Plc Zinc oxide
WO2012036082A1 (en) 2010-09-13 2012-03-22 堺化学工業株式会社 Zinc oxide particles and cosmetic material
JP2017222589A (en) * 2016-06-14 2017-12-21 住友大阪セメント株式会社 Zinc oxide powder for cosmetics, dispersions, cosmetics
WO2017216989A1 (en) * 2016-06-14 2017-12-21 住友大阪セメント株式会社 Zinc oxide powder, dispersion, and cosmetics
US11364185B2 (en) 2016-06-14 2022-06-21 Sumitomo Osaka Cement Co., Ltd. Zinc oxide powder, dispersion, and cosmetics

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