JPH02208369A - Ultraviolet absorbing inorganic pigment - Google Patents

Ultraviolet absorbing inorganic pigment

Info

Publication number
JPH02208369A
JPH02208369A JP1030355A JP3035589A JPH02208369A JP H02208369 A JPH02208369 A JP H02208369A JP 1030355 A JP1030355 A JP 1030355A JP 3035589 A JP3035589 A JP 3035589A JP H02208369 A JPH02208369 A JP H02208369A
Authority
JP
Japan
Prior art keywords
zinc oxide
surface area
specific surface
ultraviolet absorbing
zinc
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
JP1030355A
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 JP1030355A priority Critical patent/JPH02208369A/en
Publication of JPH02208369A publication Critical patent/JPH02208369A/en
Pending legal-status Critical Current

Links

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  • Compositions Of Macromolecular Compounds (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To increase the ultraviolet absorbing power and visible ray transmittance by utilizing zinc oxide having a specified specific surface area as the effective component. CONSTITUTION:Fused zinc is heated to about 1000 deg.C in a retort, the resulting zinc vapor is caused to flow at a rate of 0.5-1.5kg/hr, and air is blown against the zinc vapor at a rate of about 1.8Nm<3>/min to oxidize the zinc vapor. The resulting zinc oxide is blown with a blower to a cooling pipe to cool, separated and collected with a collector and a bag filter to give an ultraviolet absorbing inorg. pigment containing zinc oxide having a specific surface area of 20m<2>/g or larger as the effective component.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、紫外線吸収能が要求される分野、例えばプラ
スチックス、塗料、インキ等に配合される紫外線吸収無
機顔料に関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Field of Application> The present invention relates to fields in which ultraviolet absorbing ability is required, such as ultraviolet absorbing inorganic pigments that are incorporated into plastics, paints, inks, and the like.

〈従来の技術〉 従来、例えば塗料の主成分をなずポリマーの紫外線によ
る分解を防止するために、紫外線吸収能を有する体質顔
料すなわち紫外線吸収顔料が用いられている。
<Prior Art> Extender pigments, that is, ultraviolet absorbing pigments, having ultraviolet absorbing ability have been used in the past, for example, in order to prevent polymers, which are the main components of paints, from being decomposed by ultraviolet rays.

紫外線吸収顔料としては、有機顔料と無機顔料とがある
が、有機溶媒に対して不溶であり、また耐熱性に優れる
無機顔料は、独自の利用分野を有している。例えば、陶
磁器の着色には必要不可欠なものであり、プラスチック
ス、塗料、インキなどの分野にも、幅広い用途を有して
いる。
Ultraviolet absorbing pigments include organic pigments and inorganic pigments, but inorganic pigments, which are insoluble in organic solvents and have excellent heat resistance, have unique fields of use. For example, it is essential for coloring ceramics, and has a wide range of uses in fields such as plastics, paints, and inks.

紫外線吸収無機顔料としては、酸化亜鉛、酸化チタンな
どが挙げられるが、酸化亜鉛、とりわけフランス法によ
る高純度酸化亜鉛が、白色顔料中量も大きい紫外線吸収
能を有することから、汎用されている。
Examples of ultraviolet-absorbing inorganic pigments include zinc oxide and titanium oxide, but zinc oxide, especially high-purity zinc oxide produced by the French process, is widely used because it has a large amount of ultraviolet absorbing ability as a white pigment.

従来、紫外線吸収無機顔料として広く用いられている酸
化亜鉛は、比表面積が3〜10 m2/ gのものであ
った。
Zinc oxide, which has been widely used as an ultraviolet absorbing inorganic pigment, has a specific surface area of 3 to 10 m2/g.

〈発明が解決しようとする課題〉 しかしながら、比表面積3〜10m’/gの酸化亜鉛の
紫外線吸収能は未だ充分とは言い難い。
<Problems to be Solved by the Invention> However, the ultraviolet absorption ability of zinc oxide, which has a specific surface area of 3 to 10 m'/g, is still far from sufficient.

また、可視光の透過率が低いため、製品に透明性が要求
される例えばメーキャップ化粧料などの用途には、適さ
ないという問題がある。
Furthermore, since the transmittance of visible light is low, there is a problem that it is not suitable for applications that require transparency in the product, such as makeup cosmetics.

本発明は、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、従来の紫外線吸収無機顔料に比
べて紫外線吸収能に優れ、しかも可視光の透過率が高い
ため、製品の透明性を損なわない紫外線吸収無機顔料を
提供するにある。
The present invention has been made in view of the above circumstances, and its purpose is to provide superior ultraviolet absorption ability compared to conventional ultraviolet-absorbing inorganic pigments, as well as high visible light transmittance. An object of the present invention is to provide an ultraviolet absorbing inorganic pigment that does not impair transparency.

〈課題を解決するための手段及び作用〉上記目的を達成
するための本発明に係る紫外線吸収無機顔料は、比表面
積が20m2/g以上である酸化亜鉛を有効成分とする
ものである。ここで、比表面積の値はBET吸着法に基
ついて測定された値である。
<Means and effects for solving the problems> The ultraviolet absorbing inorganic pigment according to the present invention for achieving the above object contains zinc oxide having a specific surface area of 20 m2/g or more as an active ingredient. Here, the value of the specific surface area is a value measured based on the BET adsorption method.

このように比表面積が特定範囲の酸化亜鉛に特定したの
は、比表面積が20 m2/ g未満の場合、少なくと
も可視光透過率及び紫外線吸収率のいずれか一方が低下
してしまうからである。
The reason why zinc oxide with a specific surface area in a specific range was selected is that when the specific surface area is less than 20 m2/g, at least one of visible light transmittance and ultraviolet absorbance decreases.

酸化亜鉛の製造方法としては、フランス法、湿式法など
があるが、既述したように、不純物の混じらない高純度
の酸化亜鉛を得るためには、フランス法か最適である。
Methods for producing zinc oxide include the French method and the wet method, but as mentioned above, the French method is most suitable for obtaining highly pure zinc oxide free of impurities.

このフランス法は、溶融させた金属亜鉛をしトルトの中
で]、 000℃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。
This French method involves heating molten metal zinc in a tort to about 1,000 degrees Celsius, oxidizing the generated zinc vapor using air, and sending the generated zinc oxide to an air-cooled pipe with a blower to cool it. This method separates and collects the waste using a collector and bag filter.

本発明においては、比表面積は大きい方か好ましいが、
フランス法による場合、比表面積か30を越えるものは
現在のところ得られていない。
In the present invention, a larger specific surface area is preferred;
In the case of the French method, a material with a specific surface area of more than 30 has not been obtained so far.

フランス法により比表面積か20〜30爪2/g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
〜]、5kq/時て流し、これに例えば1.8Nm3/
分程度の割合で空気を吹き付ければよい。
To obtain zinc oxide with a specific surface area of 20 to 30 μg2/g using the French method, metallic zinc vapor is heated at a constant flow rate of, for example, 0.5
~], 5kq/hour, and add, for example, 1.8Nm3/
All you have to do is blow air at a rate of about a minute.

なお、湿式法を用いた場合、比表面積70程度のものも
得ることか可能である。
Note that when a wet method is used, it is possible to obtain a material with a specific surface area of about 70.

湿式法は、塩化亜鉛溶液にソーダ灰を加えて液中に塩枯
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、粒子径か非常に小さく比表面
積が大きいものか得られるか、炭酸イオンが不純物とし
て残留するという欠点かある。
The wet method is a method in which soda ash is added to a zinc chloride solution to precipitate salt-drying zinc carbonate in the solution, which is washed with water, dried, and then calcined. According to this method, particles with a very small particle size and a large specific surface area can be obtained, and the disadvantage is that carbonate ions remain as impurities.

〈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.

(実施例コ) 金属亜鉛蒸気を1.0kq/時の流速で流し、これに1
 、8 N m”/分程度の割合で空気を吹き付けて酸
化し比表面積25m2/gの酸化亜鉛を調製した。
(Example 1) Metallic zinc vapor was flowed at a flow rate of 1.0 kq/hour, and 1
, 8 N m''/min to prepare zinc oxide having a specific surface area of 25 m2/g.

次いで、ニトロセルロース6.3gをトルエン8.9g
、イソプロパツール8.9g及び酢酸エチル8.9gか
らなる混合溶媒に溶かしてバインダー溶液を調製した。
Next, 6.3 g of nitrocellulose was mixed with 8.9 g of toluene.
, 8.9 g of isopropanol, and 8.9 g of ethyl acetate to prepare a binder solution.

次いで、容量100 m flのガラス容器に、先に調
製した酸化亜鉛微粒子3g、バインダー溶液33g1ジ
オクチルフタレート3g1直径3mmの球形のガラスピ
ーズ90gをこの順に入れて、ペイントシェーカーに6
0分間かけて均一に分散させ塗料を作製した。
Next, 3 g of zinc oxide fine particles prepared previously, 33 g of binder solution, 3 g of dioctyl phthalate, 90 g of spherical glass beads with a diameter of 3 mm were placed in a glass container with a capacity of 100 m fl in this order, and the mixture was placed in a paint shaker for 6 hours.
A paint was prepared by uniformly dispersing the mixture over a period of 0 minutes.

この塗料を厚さ30μmのポリプロピレンフィルムに#
4バーコーターにて塗布し、フィルム上に塗膜を形成し
た。
Apply this paint to a 30 μm thick polypropylene film #
It was applied using a 4-bar coater to form a coating film on the film.

この塗膜形成フィルムの可視光透過率及び紫外線吸収率
を分光光度計(日立社製、型式、100]0)にて測定
した。
The visible light transmittance and ultraviolet absorbance of this coating film-forming film were measured using a spectrophotometer (manufactured by Hitachi, model 100]0).

なお、分光光度計の紫外部の吸収波長は370nmを、
また可視部の吸収波長は520nmを用いた。
In addition, the absorption wavelength of the ultraviolet region of the spectrophotometer is 370 nm.
Further, the absorption wavelength in the visible region was 520 nm.

上記各操作は全て常温で行った。All of the above operations were performed at room temperature.

(比較例1) 比表面積25m’/gの酸化亜鉛微粒子3gに代えて市
販されている、比表面積10m2/gの酸化亜鉛微粒子
(堺化学工業社製、微細亜鉛華)3gを配合したこと以
外は、実施例1と同様にして塗料の作製、塗膜形成、可
視光透過率及び紫外線吸収率の測定を行った。
(Comparative Example 1) Except that 3 g of commercially available zinc oxide fine particles (manufactured by Sakai Chemical Industry Co., Ltd., fine zinc white) with a specific surface area of 10 m2/g was blended instead of 3 g of zinc oxide fine particles with a specific surface area of 25 m'/g. In the same manner as in Example 1, a paint was prepared, a coating film was formed, and the visible light transmittance and ultraviolet absorbance were measured.

(比較例2) 比表面積25m2/gの酸化亜鉛微粒子3gに代えて市
販されている、比表面積5 m2/ gの酸化亜鉛微粒
子(堺化学工業社製、亜鉛華1号特製)3gを配合した
こと以外は、実施例1と同様にして塗料の作製、塗膜形
成、可視光透過率及び紫外線吸収率の測定を行った。
(Comparative Example 2) Instead of 3 g of zinc oxide fine particles with a specific surface area of 25 m2/g, 3 g of commercially available zinc oxide fine particles with a specific surface area of 5 m2/g (manufactured by Sakai Chemical Industry Co., Ltd., Zinchua No. 1 special product) was blended. Except for the above, a coating material was prepared, a coating film was formed, and the visible light transmittance and ultraviolet absorbance were measured in the same manner as in Example 1.

上記各塗料の可視光透過率(%)及び紫外線吸収率(%
)を、表に示す。
Visible light transmittance (%) and ultraviolet absorption rate (%) of each of the above paints
) are shown in the table.

表 表より明らかなように、紫外線吸収無機顔料として比表
面積25m2/gの酸化亜鉛を配合した場合は、可視光
透過率及び紫外線吸収率ともに高いのに対して、比表面
積10 m’/ gのものを配合した場合は、紫外線吸
収率は高いものの可視光透過率か低く、また比表面積5
 m2/ gのものを配合した場合は、可視光透過率及
び紫外線吸収率ともに低いことが分る。
As is clear from the table, when zinc oxide with a specific surface area of 25 m2/g is blended as an ultraviolet absorbing inorganic pigment, both visible light transmittance and ultraviolet absorbance are high, whereas with a specific surface area of 10 m'/g When compounded, the ultraviolet absorption rate is high, but the visible light transmittance is low, and the specific surface area is 5.
It can be seen that when m2/g is blended, both visible light transmittance and ultraviolet absorbance are low.

〈発明の効果〉 本発明に係る紫外線吸収無機顔料は、紫外線吸収能に優
れ、また高い可視光透過率を有する等、本発明は優れた
特有の効果を奏する。
<Effects of the Invention> The ultraviolet absorbing inorganic pigment according to the present invention has excellent ultraviolet absorbing ability and high visible light transmittance, and the present invention exhibits excellent unique effects.

Claims (1)

【特許請求の範囲】 1、比表面積が20m^2/g以上である酸化亜鉛を有
効成分とすることを特徴とする 紫外線吸収無機顔料。
[Scope of Claims] 1. An ultraviolet absorbing inorganic pigment characterized by containing as an active ingredient zinc oxide having a specific surface area of 20 m^2/g or more.
JP1030355A 1989-02-08 1989-02-08 Ultraviolet absorbing inorganic pigment Pending JPH02208369A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1030355A JPH02208369A (en) 1989-02-08 1989-02-08 Ultraviolet absorbing inorganic pigment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1030355A JPH02208369A (en) 1989-02-08 1989-02-08 Ultraviolet absorbing inorganic pigment

Publications (1)

Publication Number Publication Date
JPH02208369A true JPH02208369A (en) 1990-08-17

Family

ID=12301551

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1030355A Pending JPH02208369A (en) 1989-02-08 1989-02-08 Ultraviolet absorbing inorganic pigment

Country Status (1)

Country Link
JP (1) JPH02208369A (en)

Cited By (4)

* 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
US5618580A (en) * 1992-12-28 1997-04-08 Kao Corporation Method for producing ceramic fine particles and apparatus used therefor
JP2009191245A (en) * 2008-01-18 2009-08-27 Aisin Chem Co Ltd Water-based coating material
JP6037080B1 (en) * 2016-06-14 2016-11-30 住友大阪セメント株式会社 Zinc oxide powder for cosmetics, dispersions, cosmetics

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62228006A (en) * 1985-12-18 1987-10-06 Kao Corp Sunscreen cosmetic

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62228006A (en) * 1985-12-18 1987-10-06 Kao Corp Sunscreen cosmetic

Cited By (5)

* 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
US5618580A (en) * 1992-12-28 1997-04-08 Kao Corporation Method for producing ceramic fine particles and apparatus used therefor
JP2009191245A (en) * 2008-01-18 2009-08-27 Aisin Chem Co Ltd Water-based coating material
JP6037080B1 (en) * 2016-06-14 2016-11-30 住友大阪セメント株式会社 Zinc oxide powder for cosmetics, dispersions, cosmetics
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, dispersion liquid, and cosmetics

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