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JP3485643B2 - Coated zinc oxide powder and composition containing coated zinc oxide powder - Google Patents

Coated zinc oxide powder and composition containing coated zinc oxide powder

Info

Publication number
JP3485643B2
JP3485643B2 JP24746494A JP24746494A JP3485643B2 JP 3485643 B2 JP3485643 B2 JP 3485643B2 JP 24746494 A JP24746494 A JP 24746494A JP 24746494 A JP24746494 A JP 24746494A JP 3485643 B2 JP3485643 B2 JP 3485643B2
Authority
JP
Japan
Prior art keywords
zinc oxide
oxide powder
coated
photocatalytic activity
coated 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.)
Expired - Lifetime
Application number
JP24746494A
Other languages
Japanese (ja)
Other versions
JPH0859890A (en
Inventor
彰 一柳
靖英 山口
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.)
Mitsui Mining and Smelting Co Ltd
Original Assignee
Mitsui Mining and Smelting 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 Mitsui Mining and Smelting Co Ltd filed Critical Mitsui Mining and Smelting Co Ltd
Priority to JP24746494A priority Critical patent/JP3485643B2/en
Publication of JPH0859890A publication Critical patent/JPH0859890A/en
Application granted granted Critical
Publication of JP3485643B2 publication Critical patent/JP3485643B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Cosmetics (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は紫外線吸収性顔料等とし
て用いられる酸化亜鉛粉末に関し、より詳しくは、表面
にカップリング剤を被覆処理することにより、酸化亜鉛
自体の紫外線吸収、殺菌、抗菌、防黴、脱臭等の作用を
そのまま維持しているが、酸化亜鉛自体の光触媒活性が
抑制されており、且つ樹脂組成物(塗料、塗膜、フィル
ム、樹脂成形品、繊維等)や油脂組成物(化粧料等)へ
の分散性が向上しており、その結果として樹脂組成物や
油脂組成物に配合した場合にそれらの光劣化を効果的に
防止し、保存性を向上させる被覆酸化亜鉛粉末に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to zinc oxide powder used as an ultraviolet absorbing pigment and the like. More specifically, the surface of the zinc oxide powder is coated with a coupling agent to absorb, sterilize, and disinfect the zinc oxide itself. While maintaining the effects of mildew proofing, deodorization, etc., the photocatalytic activity of zinc oxide itself is suppressed, and resin compositions (paints, coatings, films, resin moldings, fibers, etc.) and oil and fat compositions Coated zinc oxide powder that has improved dispersibility in (cosmetics, etc.) and, as a result, effectively prevents their photodegradation when blended in a resin composition or an oil / fat composition and improves storage stability. Regarding

【0002】[0002]

【従来の技術】有機物である樹脂組成物や油脂組成物
は、太陽光などに含まれる紫外線により分解、劣化、変
色等を引き起こす。紫外線吸収剤はこれらの分解、劣
化、変色等を防止することを目的とした添加剤のひとつ
であり、大別するとベンゾフェノン系やベンゾトリアゾ
ール系などの有機系紫外線吸収剤と、酸化亜鉛粉末や酸
化チタン粉末に代表される無機系紫外線吸収剤とに分類
される。
2. Description of the Related Art Organic resin compositions and oil and fat compositions cause decomposition, deterioration, discoloration and the like due to ultraviolet rays contained in sunlight. UV absorbers are one of the additives that are aimed at preventing their decomposition, deterioration, discoloration, etc.These are roughly classified into organic UV absorbers such as benzophenone and benzotriazole, and zinc oxide powder and oxides. It is classified into an inorganic ultraviolet absorber represented by titanium powder.

【0003】有機系の紫外線吸収剤は、有機物であるゆ
えにそれ自身が紫外線照射を受けることにより劣化して
しまうという欠点、及び時間の経過に伴い、塗膜または
成形品の表面に浮き出てくる所謂ブルーミングを起こ
し、徐々に雨水等により流失してしまうという欠点を持
つことは良く知られている。紫外線吸収効果の面のみな
らず、近年高まりを見せている地球環境保護の観点から
も、化学的にも安定であり且つブルーミングも起こさ
ず、古くからその優れた紫外線吸収効果だけでなく、殺
菌、抗菌、防黴、脱臭等の効果も確認されている酸化亜
鉛や酸化チタン等の無機系紫外線吸収剤に再び目が向け
られつつある。
Organic ultraviolet absorbers are disadvantageous in that they are organic substances and therefore deteriorate when they are exposed to ultraviolet light, and with the passage of time, so-called so-called "embosses" appear on the surface of a coating film or a molded article. It is well known that it has the drawback of causing blooming and being gradually washed away by rainwater or the like. Not only in terms of UV absorption effect, but also from the viewpoint of global environmental protection that has been increasing in recent years, it is chemically stable and does not cause blooming, and not only its excellent UV absorption effect from old times, but also sterilization, Inorganic UV absorbers such as zinc oxide and titanium oxide, which have been confirmed to have antibacterial, antifungal, and deodorizing effects, are being revisited.

【0004】しかしながら、酸化亜鉛や酸化チタンは優
れた紫外線吸収作用を示し、それで樹脂組成物や油脂組
成物に配合することにより紫外線照射によるそれらの劣
化を防止できる一方で、紫外線照射により励起される光
触媒活性も高く、樹脂組成物や油脂組成物の分解、劣
化、変色等を促進させるという欠点をも併せ持ち、塗膜
や樹脂成形品等の表面が白亜化する所謂チョーキングを
引き起こすことが良く知られている。換言すれば、紫外
線吸収剤として酸化亜鉛や酸化チタンを使用するには、
その欠点である光触媒活性を如何に抑制せしめるかが技
術課題とされていた。
[0004] However, zinc oxide and titanium oxide exhibit an excellent ultraviolet ray absorbing action, and therefore, when incorporated into a resin composition or an oil and fat composition, their deterioration due to ultraviolet ray irradiation can be prevented, while they are excited by ultraviolet ray irradiation. It has a high photocatalytic activity and also has the drawback of accelerating the decomposition, deterioration, discoloration, etc. of resin compositions and fats and oils compositions, and is well known to cause so-called chalking, which causes the surface of coating films and resin molded products to become chalky. ing. In other words, to use zinc oxide or titanium oxide as a UV absorber,
It has been a technical subject how to suppress the photocatalytic activity which is the defect.

【0005】この課題を解決する手段として、酸化チタ
ンに於いてはAl23、SiO2、ZnO、TiO2
による表面被覆処理が行われており、既に市販されてい
る。酸化亜鉛の表面被覆処理については、特表平4−5
06674号公報にモノカルボン酸の水不溶性金属石鹸
の被覆による紫外線吸収性の化学的に不活性な顔料酸化
亜鉛が開示されているが、混練もしくは成形中の樹脂の
劣化はおきていなかったという実施例6〜10中の効果
の記述内容から判断して特表平4−506674号公報
に記載の発明で言う化学的に不活性な顔料酸化亜鉛とは
溶融混練もしくは熱プレス成形中の熱劣化に対する安定
性を向上せしめた顔料酸化亜鉛の意であり、本発明で言
う紫外線照射により励起される酸化亜鉛の光触媒活性を
抑制することにより樹脂組成物や油脂組成物の劣化を抑
制せんとする試みとは全く別のことである。又、酸化チ
タンの場合と同様に酸化亜鉛粒子表面にAl、Si、Z
rあるいはSnの酸化物もしくは水酸化物を被覆する技
術が特開平3−183620号公報に開示されている。
As a means for solving this problem, titanium oxide is subjected to a surface coating treatment with Al 2 O 3 , SiO 2 , ZnO, TiO 2 or the like, which is already commercially available. For surface treatment of zinc oxide, see Table 4-5
Japanese Patent No. 06674 discloses a UV-absorbing, chemically inactive pigment zinc oxide coated with a water-insoluble metal soap of a monocarboxylic acid, but does not show deterioration of the resin during kneading or molding. Judging from the contents of description of the effects in Examples 6 to 10, the chemically inert pigment zinc oxide referred to in the invention described in JP-A-4-506674 is against the thermal deterioration during melt kneading or hot press molding. It means a pigment zinc oxide having improved stability, and attempts to suppress the deterioration of the resin composition or the oil and fat composition by suppressing the photocatalytic activity of zinc oxide excited by ultraviolet irradiation referred to in the present invention. Is something else. Also, as in the case of titanium oxide, the surface of zinc oxide particles is Al, Si, Z.
A technique for coating an oxide or hydroxide of r or Sn is disclosed in JP-A-3-183620.

【0006】[0006]

【発明が解決しようとする課題】しかしながら、紫外線
吸収剤を含む樹脂組成物や油脂組成物に透明性、有彩色
性を望む最近の市場の要請に答えるため、酸化亜鉛粉末
は一層微粒子化され、粉体比表面積が大きくなる傾向に
ある。比表面積の増加は必要とする被覆量の増加をもた
らすことから、従来技術に基づくAl、Si、Zrある
いはSnの酸化物もしくは水酸化物による表面被覆処理
では光触媒活性を抑制するに必要な被覆量が増大し、肝
腎の紫外線吸収効果に悪影響を及ぼす事が懸念されはじ
めてきた。つまり、より少量の被覆量で、即ち相対的に
酸化亜鉛の含有量を極力減らさずに、光触媒活性を抑制
できるような表面処理技術の開発は、微粒子化を求める
紫外線吸収剤市場の要請に伴い急務となってきている。
However, in order to meet the recent market demands for transparency and chromaticity of resin compositions and oil and fat compositions containing an ultraviolet absorber, zinc oxide powder is further made into fine particles, The powder specific surface area tends to increase. Since the increase of the specific surface area leads to the increase of the required coating amount, the surface coating treatment with the oxide or hydroxide of Al, Si, Zr or Sn based on the conventional technique requires the coating amount required to suppress the photocatalytic activity. It has started to be feared that the UV absorption rate of the liver and kidney may be adversely affected. In other words, the development of surface treatment technology that can suppress photocatalytic activity with a smaller coating amount, that is, without relatively reducing the content of zinc oxide as much as possible, is accompanied by the demand of the ultraviolet absorber market that requires fine particle formation. It has become an urgent task.

【0007】従来技術のもうひとつの課題は、酸化亜鉛
粉末の樹脂組成物や油脂組成物への分散性の向上であ
る。紫外線吸収剤は、添加剤として樹脂組成物や油脂組
成物に分散させて使用される。即ち、樹脂組成物や油脂
組成物となった時の紫外線吸収効果が重要であって、酸
化チタン等に於いても、分散性が悪く凝集が強いほど樹
脂の劣化が速いことは良く知られている。従来技術に基
づくAl、Si、ZrあるいはSnの酸化物もしくは水
酸化物といった無機物による表面被覆処理では、樹脂組
成物や油脂組成物との分散性に課題を残し、折角表面被
覆処理により酸化亜鉛の光触媒活性を抑制せしめても、
分散性が悪いため肝腎の樹脂組成物や油脂組成物となっ
た時の紫外線吸収効果が悪く、樹脂組成物や油脂組成物
の光劣化の防止に充分な効果を発揮できないことが懸念
されている。
Another problem of the prior art is to improve the dispersibility of zinc oxide powder in a resin composition or a fat composition. The ultraviolet absorber is used as an additive dispersed in a resin composition or an oil and fat composition. That is, it is well known that the ultraviolet ray absorbing effect when it becomes a resin composition or an oil and fat composition is important, and even in titanium oxide and the like, the worse the dispersibility and the stronger the aggregation, the faster the deterioration of the resin. There is. The surface coating treatment with an inorganic substance such as Al, Si, Zr, or Sn oxide or hydroxide based on the conventional technique leaves a problem in dispersibility with the resin composition or the oil / fat composition. Even if you suppress the photocatalytic activity,
Due to poor dispersibility, it is feared that the effect of absorbing ultraviolet rays when it becomes a resin composition or oil / fat composition of the liver and kidney is poor, and it is not possible to exert sufficient effect for preventing photodegradation of the resin composition or oil / fat composition. .

【0008】本発明の目的は、酸化亜鉛粉末自体の紫外
線吸収、殺菌、抗菌、防黴、脱臭等の作用、効果に悪影
響を及ぼさない程度の少量の表面被覆量で、且つ紫外線
吸収剤として用いた場合の酸化亜鉛が持つ欠点である樹
脂組成物や油脂組成物を劣化させる光触媒活性を充分に
抑制し、同時に酸化亜鉛の樹脂組成物や油脂組成物への
分散性をも向上せしめる表面被覆量で被覆されており、
樹脂組成物(塗膜、フィルム、樹脂成形品、繊維等)や
油脂組成物(化粧料等)となったときに好適な紫外線吸
収剤、殺菌、抗菌、防黴、脱臭剤等としての働きを示
し、且つ樹脂組成物や油脂組成物の光劣化を抑える被覆
酸化亜鉛粉末、該被覆酸化亜鉛粉末を有効成分とする添
加剤並びに該被覆酸化亜鉛粉末を配合してなる組成物を
提供することにある。
The object of the present invention is to use the zinc oxide powder itself as a UV absorber with a small amount of surface coating which does not adversely affect the UV absorption, sterilization, antibacterial, antifungal and deodorizing effects and effects of the zinc oxide powder itself. The amount of surface coating that sufficiently suppresses the photocatalytic activity that deteriorates the resin composition and the oil and fat composition, which are the disadvantages of zinc oxide when it is present, and at the same time improves the dispersibility of the zinc oxide in the resin composition and the oil and fat composition. Is covered with
When used as a resin composition (coating film, film, resin molded product, fiber, etc.) or oil / fat composition (cosmetics, etc.), it works as a suitable UV absorber, bactericidal, antibacterial, antifungal, deodorant, etc. To provide a coated zinc oxide powder which suppresses photodegradation of a resin composition or an oil and fat composition, an additive containing the coated zinc oxide powder as an active ingredient, and a composition comprising the coated zinc oxide powder. is there.

【0009】[0009]

【課題を解決するための手段】本発明者等は、上記の目
的を達成するために鋭意検討した結果、酸化亜鉛粉末の
粒子表面に少量のカップリング剤を被覆させることによ
り前述の従来技術の課題が解決されることを見出し、本
発明を完成した。即ち、本発明の被覆酸化亜鉛粉末は、
酸化亜鉛粒子表面にカップリング剤を被覆処理して
り、該カップリング剤の被覆量が酸化亜鉛に対して0.
2〜10重量%であることを特徴とするものである。
Means for Solving the Problems The inventors of the present invention have conducted extensive studies in order to achieve the above-mentioned object, and as a result, by coating a small amount of a coupling agent on the surface of zinc oxide powder particles, The inventors have found that the problems can be solved and completed the present invention. That is, the coated zinc oxide powder of the present invention,
The surface of the zinc oxide particles has been coated with a coupling agent .
The coating amount of the coupling agent was 0.
It is characterized by being 2 to 10% by weight .

【0010】また、本発明の添加剤は、上記の被覆酸化
亜鉛粉末を有効成分とし、紫外線吸収、殺菌、抗菌、防
黴、脱臭作用を有するが、光触媒活性の抑制されている
ものである。更に、本発明の樹脂組成物及び油脂組成物
は、それぞれ上記の被覆酸化亜鉛粉末を配合してなるこ
とを特徴とするものである。
Further, the additive of the present invention contains the above-mentioned coated zinc oxide powder as an active ingredient and has ultraviolet absorption, sterilization, antibacterial, antifungal and deodorizing effects, but the photocatalytic activity is suppressed. Furthermore, the resin composition and the oil / fat composition of the present invention are characterized by containing the above-mentioned coated zinc oxide powder.

【0011】以下に本発明について詳細に説明する。本
発明の被覆酸化亜鉛粉末を得るために被覆処理される酸
化亜鉛粉末は、所謂湿式合成法で得られたものであって
も、所謂乾式合成法で得られたものであってもよい。酸
化亜鉛粉粒子表面へのカップリング剤の被覆処理方法と
しては、酸化亜鉛粉末の水中または非水溶媒中のスラリ
ーを攪拌しつつカップリング剤を添加する所謂湿式法で
も良く、また高速回転が可能なヘンシェルミキサーやハ
イスピードミキサー等で酸化亜鉛粉末を高速攪拌しつつ
カップリング剤をスプレーまたは滴下する所謂乾式法で
も良く、また酸化亜鉛粉末を入れた反応容器内に窒素等
の不活性ガスでキャリーしたカップリング剤を導入し、
被覆処理する所謂気相法でも良い。
The present invention will be described in detail below. The zinc oxide powder to be coated to obtain the coated zinc oxide powder of the present invention may be obtained by a so-called wet synthesis method or may be obtained by a so-called dry synthesis method. As a method for coating the surface of the zinc oxide powder particles with the coupling agent, a so-called wet method in which the coupling agent is added while stirring a slurry of zinc oxide powder in water or in a non-aqueous solvent may be used, and high-speed rotation is also possible. A so-called dry method in which the coupling agent is sprayed or dropped while stirring the zinc oxide powder at high speed with a Henschel mixer or high-speed mixer is also possible, and it is also possible to carry in a reaction vessel containing the zinc oxide powder with an inert gas such as nitrogen. Introduced coupling agent,
A so-called vapor-phase method for coating may be used.

【0012】但し、被覆量に関しては、被覆処理される
酸化亜鉛粉末の比表面積を考慮する必要がある。例え
ば、後に詳述する実施例2に於いては、使用した酸化亜
鉛粉末のBET法による比表面積は20m2/gであり、
これにシランカップリング剤を1重量%被覆処理するこ
とによりほぼ完全に酸化亜鉛の持つ光触媒活性を抑制で
きたが、これよりも大きな比表面積を持つより微細な酸
化亜鉛粉末に同様の目的で被覆処理する場合には、その
被覆率を目安として被覆量を増加させないと光触媒活性
を充分に抑制できないことは容易に推察される。
However, regarding the coating amount, it is necessary to consider the specific surface area of the zinc oxide powder to be coated. For example, in Example 2 described in detail later, the zinc oxide powder used has a specific surface area of 20 m 2 / g according to the BET method,
By coating 1% by weight of a silane coupling agent on this, the photocatalytic activity of zinc oxide could be suppressed almost completely, but for the same purpose coating of finer zinc oxide powder with a larger specific surface area was possible. In the case of treatment, it is easily inferred that the photocatalytic activity cannot be sufficiently suppressed unless the coating amount is increased with the coverage as a guide.

【0013】即ち、著しく大きい比表面積を持つ酸化亜
鉛粉末(例えば400m2/g)への被覆処理を行う場合
には20%程度の被覆量が必要となり、逆に、比表面積
が数m2/g程度の比較的粒径の大きい酸化亜鉛粉末に被
覆処理する場合には0.1%程度の被覆量でも充分な効
果が期待できる。従って、被覆量の通常の範囲としては
0.1〜20重量%、分散性を考慮すると好ましくは0.
2〜15重量%、コスト面を考慮すると好ましくは0.
1〜10重量%、総合的には好ましくは0.2〜10重
量%となる。
That is, when coating zinc oxide powder having a remarkably large specific surface area (for example, 400 m 2 / g), a coating amount of about 20% is required, and conversely, the specific surface area is several m 2 / g. When coating zinc oxide powder having a relatively large particle size of about g, a sufficient effect can be expected even with a coating amount of about 0.1%. Therefore, the usual range of the coating amount is 0.1 to 20% by weight, and considering the dispersibility, it is preferably 0.1.
2 to 15% by weight, preferably 0.1 considering the cost.
1 to 10% by weight, preferably 0.2 to 10% by weight in total.

【0014】後記の実施例1〜3に於いては、信越化学
(株)製シランカップリング剤KBM−403(γ−グ
リシドキシプロピルトリメトキシシラン)、KBM−5
03(γ−メタクリロキシプロピルトリメトキシシラ
ン)を被覆処理剤として用いたが、酸化亜鉛のような無
機酸化物粒子表面との反応に主として関与するのは、カ
ップリング剤の加水分解性基が加水分解を受けて生成し
たシラノール基であり、エポキシ基やメタクリル基のよ
うな有機官能基は主として種々の樹脂と反応して結合し
得ることは良く知られている。光触媒活性を抑える目的
に対しては、その他のシランカップリング剤、即ち、ビ
ニル基、メルカプト基、アミノ基等を持つシランカップ
リング剤を使用しても、また、シランカップリング剤以
外のチタン系、アルミニウム系、ジルコニウム系、ジル
コアルミネート系等のその他のカップリング剤あるいは
シラン等を使用しても良い。
In Examples 1 to 3 described later, silane coupling agents KBM-403 (γ-glycidoxypropyltrimethoxysilane) manufactured by Shin-Etsu Chemical Co., Ltd. and KBM-5 were used.
03 (γ-methacryloxypropyltrimethoxysilane) was used as a coating treatment agent, but the main reason for the reaction with the surface of the inorganic oxide particles such as zinc oxide is that the hydrolyzable group of the coupling agent is hydrolyzed. It is well known that a silanol group generated by decomposition and an organic functional group such as an epoxy group or a methacryl group mainly reacts with various resins to be bonded. For the purpose of suppressing the photocatalytic activity, even if other silane coupling agents, that is, silane coupling agents having a vinyl group, a mercapto group, an amino group, etc. are used, titanium-based compounds other than silane coupling agents are also used. Other coupling agents such as aluminum-based, zirconium-based, zirco-aluminate-based, or silane may be used.

【0015】尚、表面被覆剤としてカップリング剤を用
いた場合は、従来技術の無機物を用いた場合よりも何故
少量で酸化亜鉛の光触媒活性を抑制し得るのかは明確で
はないが、酸化亜鉛粒子表面の光触媒活性を司る活性点
とカップリング剤との反応性は、酸化亜鉛粒子表面の光
触媒活性を司る活性点と無機の表面処理剤との反応性に
比較して選択性が一層高く、それ故にカップリング剤は
少量の被覆量で無駄なく酸化亜鉛粒子表面の光触媒活性
を司る活性点を殺しているのではないかと思われる。
Incidentally, it is not clear why the photocatalytic activity of zinc oxide can be suppressed in a small amount when a coupling agent is used as the surface coating agent as compared with the case of using an inorganic material of the prior art, but zinc oxide particles The reactivity between the active site controlling the surface photocatalytic activity and the coupling agent is much higher than the reactivity between the active site controlling the photocatalytic activity on the zinc oxide particle surface and the inorganic surface treatment agent. Therefore, it seems that the coupling agent may kill the active sites controlling the photocatalytic activity on the surface of the zinc oxide particles without waste even with a small coating amount.

【0016】本発明の被覆酸化亜鉛粉末においては、よ
り少量の被覆量で、即ち酸化亜鉛の相対的含有量を極力
減らさずに光触媒活性を抑制できるので、酸化亜鉛自体
の紫外線吸収作用をそのまま維持しており、更に光触媒
活性が抑制されるにも係わらず、殺菌、抗菌、防黴、脱
臭等の作用がそのまま維持されている。この理由は明確
ではないが、一つの仮説として光触媒活性を司る活性点
と殺菌、抗菌、防黴、脱臭等を司る活性点とが異なって
いることが考えられ、この考えに立てば、被覆量を光触
媒活性を司る活性点を殺すことのできる必要且つ最少
量、即ち光触媒活性を抑制できる必要且つ最少量にする
ことにより、殺菌、抗菌、防黴、脱臭等を司る活性点が
残り、殺菌、抗菌、防黴、脱臭等の作用がそのまま維持
されことになる。
In the coated zinc oxide powder of the present invention, the photocatalytic activity can be suppressed with a smaller coating amount, that is, without reducing the relative content of zinc oxide as much as possible, so that the ultraviolet absorbing action of zinc oxide itself is maintained. Although the photocatalytic activity is further suppressed, the bactericidal, antibacterial, antifungal and deodorizing effects are maintained as they are. The reason for this is not clear, but one hypothesis is that the active sites that control photocatalytic activity are different from the active sites that control sterilization, antibacterial, antifungal, deodorizing, etc. The necessary and minimum amount that can kill the active sites that control the photocatalytic activity, that is, the necessary and minimum amount that can suppress the photocatalytic activity, sterilization, antibacterial, antifungal, deodorant active sites that remain, such as sterilization, The effects of antibacterial, mildew-proof, and deodorizing are maintained as they are.

【0017】樹脂への分散性を一層向上させるために
は、使用する樹脂とカップリング剤の有機官能基との相
性を考慮してカップリング剤を選定する必要がある。こ
のことは、従来技術に基づくAl、Si、Zrあるいは
Snの酸化物もしくは水酸化物といった無機物による表
面被覆処理ではなし得なかった分散性向上のポイントで
あり、例えば、後に述べる実施例4〜6に於いては、ポ
リエチレン樹脂を使用するのでKBM−503で表面被
覆処理した酸化亜鉛粉末を用いた。
In order to further improve the dispersibility in the resin, it is necessary to select the coupling agent in consideration of the compatibility between the resin used and the organic functional group of the coupling agent. This is a point of improving the dispersibility which could not be achieved by the surface coating treatment with the inorganic material such as Al, Si, Zr or Sn oxide or hydroxide based on the prior art, and for example, Examples 4 to 6 described later. In this case, since polyethylene resin is used, zinc oxide powder surface-coated with KBM-503 was used.

【0018】本発明の被覆酸化亜鉛粉末は、紫外線吸
収、殺菌、抗菌、防黴、脱臭作用を有するが、光触媒活
性の抑制されている添加剤として用いられ、例えば樹脂
組成物や油脂組成物に添加して用いることにより、紫外
線吸収、殺菌、抗菌、防黴、脱臭等の効果が達成され、
且つ光触媒活性が抑制されているので樹脂組成物や油脂
組成物が分解したり、劣化したり、変色したりすること
がない。本発明において添加剤として用いる場合には被
覆酸化亜鉛粉末単独で用いても、或いは他の成分との混
合物として用いてもよい。
The coated zinc oxide powder of the present invention has ultraviolet absorption, bactericidal, antibacterial, antifungal, and deodorizing effects, but is used as an additive whose photocatalytic activity is suppressed. For example, it is used in resin compositions and oil and fat compositions. By adding and using it, UV absorption, sterilization, antibacterial, antifungal, deodorizing and other effects are achieved.
Moreover, since the photocatalytic activity is suppressed, the resin composition and the oil and fat composition are not decomposed, deteriorated, or discolored. When used as an additive in the present invention, the coated zinc oxide powder may be used alone or as a mixture with other components.

【0019】本発明の添加剤を塗料に添加する場合に
は、塗料に直接添加しても、或いは塗料の一成分と混合
した後に塗料として調合してもよい。このようにして調
製した塗料を壁、床、天井等に塗布した場合には、窓か
ら差し込む太陽光等に含まれる紫外線によって塗膜が変
色したり、劣化したりするのを防止でき、脱臭し、黴の
発生を防止できる。
When the additive of the present invention is added to the paint, it may be added directly to the paint or may be prepared as a paint after being mixed with one component of the paint. When the paint prepared in this way is applied to walls, floors, ceilings, etc., it is possible to prevent the coating film from discoloring or deteriorating due to the ultraviolet rays contained in the sunlight or the like inserted through the window, and to deodorize. , Can prevent the development of mold.

【0020】本発明の添加剤を樹脂組成物に練り込み、
例えばフィルム状に成形し、それを食品等の包装材料と
して用いた場合には、紫外線による食品の変色を防止
し、且つ同時に殺菌、抗菌、防黴作用による腐敗の防止
や脱臭作用による開封時の嫌な臭いも防止できる。また
そのフィルム状物を壁紙等として使用した場合には、窓
から差し込む太陽光等に含まれる紫外線によって壁紙が
変色したり、劣化したりするのを防止でき、脱臭し、黴
の発生を防止できる。
Kneading the additive of the present invention into a resin composition,
For example, when it is formed into a film and used as a packaging material for foods, etc., it prevents discoloration of foods due to ultraviolet rays, and at the same time, sterilization, antibacterial, prevention of decay due to mildew-proofing and deodorization during opening. It can prevent an unpleasant odor. Also, when the film-like material is used as wallpaper or the like, it is possible to prevent the wallpaper from being discolored or deteriorated by ultraviolet rays contained in the sunlight or the like that is inserted through the window, and it is possible to prevent deodorization and the occurrence of mold. .

【0021】本発明の添加剤を樹脂組成物に練り込み、
樹脂成形品とした場合や、本発明の添加剤を樹脂組成物
に練り込み、その後一旦粉砕して樹脂粉末とし、その後
それを用いて基材にコーティングして作成した樹脂成形
品とした場合には、例えば台所用品の場合には、殺菌、
抗菌、防黴作用による腐敗の防止や脱臭作用が達成され
る。
Kneading the additive of the present invention into a resin composition,
When it is used as a resin molded product, or when the additive of the present invention is kneaded into a resin composition and then pulverized once to obtain a resin powder, and a resin molded product prepared by coating a substrate with the powder For example, in the case of kitchen utensils, sterilization,
Antibacterial and antifungal effects prevent spoilage and deodorize.

【0022】本発明の添加剤を繊維に用いる場合には、
紡糸工程で添加剤を練り込んだり、或いは紡糸後にパジ
ングにより後加工することにより、紫外線による繊維製
品の変色を防止し、同時に殺菌、抗菌、防黴、脱臭等の
効果が達成される。本発明の添加剤を化粧料に添加す場
合には、本発明の添加剤をそのまま添加しても、或いは
粉末樹脂等の表面に担持させたものを添加してもよい。
このようにして調製した化粧料は紫外線吸収効果はもと
より汗の臭等を脱臭する効果も達成される。
When the additive of the present invention is used in fibers,
By kneading the additives in the spinning step, or by post-processing by spinning after spinning, discoloration of the textile product due to ultraviolet rays is prevented, and at the same time, effects such as sterilization, antibacterial activity, mildew proofing, and deodorization are achieved. When the additive of the present invention is added to cosmetics, the additive of the present invention may be added as it is, or a powder resin or the like supported on the surface may be added.
The cosmetic thus prepared has not only an ultraviolet absorbing effect but also an effect of deodorizing sweat odor and the like.

【0023】[0023]

【実施例】【Example】

実施例1 BET比表面積が20m2/gである酸化亜鉛粉末の水ス
ラリーを攪拌しつつ被覆量が0.5重量%になるように
所定量のシランカップリング剤KBM−503を滴下し
た。攪拌を暫く続け、次にこのスラリーを濾過し、洗浄
し、さらに乾燥機にて加熱乾燥して被覆酸化亜鉛粉末の
乾粉を得た。
Example 1 While stirring an aqueous slurry of zinc oxide powder having a BET specific surface area of 20 m 2 / g, a predetermined amount of silane coupling agent KBM-503 was added dropwise so that the coating amount was 0.5% by weight. Stirring was continued for a while, and then the slurry was filtered, washed, and further dried by heating in a dryer to obtain a dry powder of coated zinc oxide powder.

【0024】酸化亜鉛粉末の粒子表面を被覆処理したこ
とによる光触媒活性の抑制効果を調べるために、上記の
ようにして得た酸化亜鉛粉末の光触媒活性を調べた。光
触媒活性の抑制効果の目安として、透明密封容器内にア
セトアルデヒド気体と一定量の上記の酸化亜鉛粉末を入
れ、紫外光照射を行い、一定時間経過した時に測定し
た、アセトアルデヒドの自動酸化による分解率を用い
た。その測定結果を表面被覆物及び被覆量と共に表1に
示す。
The photocatalytic activity of the zinc oxide powder obtained as described above was examined in order to investigate the effect of suppressing the photocatalytic activity by coating the surface of the particles of the zinc oxide powder. As a measure of the effect of suppressing photocatalytic activity, put the acetaldehyde gas and a certain amount of the above zinc oxide powder in a transparent sealed container, irradiate with ultraviolet light, and measure the decomposition rate of acetaldehyde due to autoxidation, measured after a certain period of time. Using. The measurement results are shown in Table 1 together with the surface coating and the coating amount.

【0025】実施例2 被覆量が1%になるように所定量のシランカップリング
剤KBM−503を用いた以外は実施例1と同様の操作
を行って被覆酸化亜鉛粉末の乾粉を得た。また実施例1
と同様にして光触媒活性の抑制効果を調べた。その測定
結果を表面被覆物及び被覆量と共に表1に示す。更に、
この実施例で得た被覆酸化亜鉛粉末の脱臭活性を調べ
た。脱臭効果の目安として、透明密封容器内に硫化水素
と被覆酸化亜鉛粉末を入れ、透明密封容器内の残留硫化
水素濃度の経時変化を測定した。その測定結果を図1に
示す。
Example 2 A dry powder of coated zinc oxide powder was obtained in the same manner as in Example 1 except that a predetermined amount of the silane coupling agent KBM-503 was used so that the coating amount was 1%. Example 1
The effect of suppressing the photocatalytic activity was examined in the same manner as in. The measurement results are shown in Table 1 together with the surface coating and the coating amount. Furthermore,
The deodorizing activity of the coated zinc oxide powder obtained in this example was investigated. As a measure of the deodorizing effect, hydrogen sulfide and coated zinc oxide powder were put in a transparent sealed container, and the change with time of the residual hydrogen sulfide concentration in the transparent sealed container was measured. The measurement result is shown in FIG.

【0026】実施例3 シランカップリング剤として前記のKBM−403を用
いた以外は、実施例1と同様の操作を行って被覆酸化亜
鉛粉末の乾粉を得た。また実施例1と同様にして光触媒
活性の抑制効果を調べた。その測定結果を表面被覆物及
び被覆量と共に表1に示す。
Example 3 A dry powder of coated zinc oxide powder was obtained in the same manner as in Example 1 except that KBM-403 was used as the silane coupling agent. Further, the effect of suppressing the photocatalytic activity was examined in the same manner as in Example 1. The measurement results are shown in Table 1 together with the surface coating and the coating amount.

【0027】比較例1〜3 特開平3−183620号公報に記載の方法に従い、S
iO2被覆量がそれぞれ3%、7%及び18%になるよ
うにBET比表面積が20m2/gである酸化亜鉛粉末の
所定量を珪酸ソーダ水溶液中に加え、液のpHに注意し
ながら該水溶液中に塩酸希釈液を徐々に添加した。そし
て、pHが7程度になったら添加をやめて暫く静置し
た。次にこれらの懸濁液を濾過し、洗浄し、さらに乾燥
機にて105℃で加熱乾燥してそれぞれ被覆酸化亜鉛粉
末の乾粉を得た。また実施例1と同様にして光触媒活性
の抑制効果を調べた。その測定結果を表面被覆物及び被
覆量と共に表1に示す。
Comparative Examples 1 to 3 In accordance with the method described in JP-A-3-183620, S
A predetermined amount of zinc oxide powder having a BET specific surface area of 20 m 2 / g was added to an aqueous solution of sodium silicate so that the coverage of io 2 was 3%, 7% and 18%, respectively, and the pH of the solution was carefully monitored. A hydrochloric acid diluted solution was gradually added to the aqueous solution. Then, when the pH reached about 7, the addition was stopped and the mixture was allowed to stand for a while. Next, these suspensions were filtered, washed, and further dried by heating at 105 ° C. in a dryer to obtain dry powders of coated zinc oxide powder. Further, the effect of suppressing the photocatalytic activity was examined in the same manner as in Example 1. The measurement results are shown in Table 1 together with the surface coating and the coating amount.

【0028】比較例4 実施例1〜3及び比較例1〜3で用いた表面被覆処理を
施す前のBET比表面積が20m2/gである無被覆酸化
亜鉛粉末自体を比較対照とした。また実施例1と同様に
して光触媒活性の抑制効果を調べた。その測定結果を表
1に示す。更に、実施例2と同様にして脱臭効果を調べ
た。その測定結果を図1に示す。
Comparative Example 4 The uncoated zinc oxide powder itself having a BET specific surface area of 20 m 2 / g before the surface coating treatment used in Examples 1 to 3 and Comparative Examples 1 to 3 was used as a comparative control. Further, the effect of suppressing the photocatalytic activity was examined in the same manner as in Example 1. The measurement results are shown in Table 1. Further, the deodorizing effect was examined in the same manner as in Example 2. The measurement result is shown in FIG.

【0029】[0029]

【表1】 [Table 1]

【0030】比較例4の表面被覆処理を施す前の無被覆
酸化亜鉛粉末は表1に示すように、アセトアルデヒドの
分解率が86.0%と極めて大きく、光触媒活性が極め
て高いことを示している。本発明に基づく実施例2の被
覆酸化亜鉛粉末(KBM−503の被覆量1%)に於い
ては、アセトアルデヒドの分解率が0.9%であり、酸
化亜鉛の紫外線吸収剤としての欠点である光触媒活性を
ほぼ完全に抑制していることが確認された。
As shown in Table 1, the uncoated zinc oxide powder before the surface coating treatment of Comparative Example 4 has a very high decomposition rate of acetaldehyde of 86.0%, indicating that the photocatalytic activity is extremely high. . In the coated zinc oxide powder of Example 2 based on the present invention (coating amount of KBM-503: 1%), the decomposition rate of acetaldehyde was 0.9%, which is a drawback of zinc oxide as an ultraviolet absorber. It was confirmed that the photocatalytic activity was almost completely suppressed.

【0031】一方、従来技術に基づく比較例1〜3の被
覆酸化亜鉛粉末に於いては、被覆量が3%では分解率が
77.4%であってほとんど効果が無く、被覆量の増加
につれて次第に光触媒活性抑制効果が増加しているが、
被覆量18%に至っても分解率12.6%程度であり、
実施例2の被覆酸化亜鉛粉末の場合の被覆量1%で分解
率0.9%と比較するとその光触媒活性抑制効果は遠く
及ばない。
On the other hand, in the coated zinc oxide powders of Comparative Examples 1 to 3 based on the prior art, when the coating amount was 3%, the decomposition rate was 77.4% and there was almost no effect, and as the coating amount increased. Although the effect of suppressing photocatalytic activity is gradually increasing,
Even if the coating amount reaches 18%, the decomposition rate is about 12.6%,
When the coating amount of the coated zinc oxide powder of Example 2 is 1% and the decomposition rate is 0.9%, the effect of suppressing the photocatalytic activity is far short.

【0032】このように、カップリング剤を被覆処理し
てなる本発明の被覆酸化亜鉛粉末は、無機物を表面被覆
する従来技術に比較して、圧倒的に少量で且つほぼ完全
に酸化亜鉛粉末の光触媒活性を抑制できることが確認で
きた。更に、脱臭効果を示す図1のグラフにおいて、直
線の傾きが大きい程被覆酸化亜鉛による脱臭効果が大き
いことを意味しており、実施例2で調製した被覆酸化亜
鉛粉末は比較例4の無被覆酸化亜鉛粉末自体とほぼ同等
の傾き、即ちほぼ同等の脱臭効果示している。尚、この
脱臭活性試験は紫外光照射を行わないで実施したが、紫
外光照射を行なった場合もほぼ同じ結果であった。光触
媒活性の測定においては、紫外光を照射した場合のみに
光触媒活性を示したことを考慮すると、現象的には、光
触媒活性を司る活性点と殺菌、抗菌、防黴、脱臭等を司
る活性点とが異なっていると考えられる。即ち、本発明
の被覆酸化亜鉛は光触媒活性を抑制するが、酸化亜鉛が
元来持っている紫外線吸収効果や殺菌、抗菌、防黴、脱
臭等の効果は殆ど損なわれないと言える。
As described above, the coated zinc oxide powder of the present invention obtained by coating the coupling agent has an overwhelmingly small amount of zinc oxide powder as compared with the prior art in which the surface of the inorganic material is coated. It was confirmed that the photocatalytic activity can be suppressed. Further, in the graph of FIG. 1 showing the deodorizing effect, it means that the larger the slope of the straight line is, the larger the deodorizing effect of the coated zinc oxide is, and the coated zinc oxide powder prepared in Example 2 is the same as that of Comparative Example 4. It shows almost the same slope as the zinc oxide powder itself, that is, almost the same deodorizing effect. This deodorizing activity test was carried out without irradiation with ultraviolet light, but the result was almost the same when irradiation with ultraviolet light was carried out. In the measurement of photocatalytic activity, considering that it showed photocatalytic activity only when it was irradiated with ultraviolet light, in terms of phenomena, the active point controlling photocatalytic activity and the active point controlling sterilization, antibacterial, antifungal, deodorizing, etc. Are considered to be different. That is, it can be said that the coated zinc oxide of the present invention suppresses the photocatalytic activity, but the effects inherent to the zinc oxide such as the ultraviolet absorbing effect, sterilization, antibacterial, antifungal, deodorizing, etc. are hardly impaired.

【0033】実施例4 実施例1で得られた被覆酸化亜鉛粉末3重量部とポリエ
チレン樹脂100重量部とを溶融混練し、厚さ50μm
のフィルムに成形して、ポリエチレン樹脂に対する被覆
酸化亜鉛粉末の分散性を調べた。 実施例5 実施例2で得られた被覆酸化亜鉛粉末を用いた以外は実
施例4と同様に操作して分散性を調べた。また、酸化亜
鉛粉末が樹脂組成物になったときの紫外線吸収効率を調
べるために、その得られたフィルムの分光透過スペクト
ルを測定した。その結果を図2に示す。
Example 4 3 parts by weight of the coated zinc oxide powder obtained in Example 1 and 100 parts by weight of a polyethylene resin were melt-kneaded to a thickness of 50 μm.
Was formed into a film and the dispersibility of the coated zinc oxide powder in polyethylene resin was examined. Example 5 Dispersibility was examined in the same manner as in Example 4 except that the coated zinc oxide powder obtained in Example 2 was used. Further, in order to investigate the ultraviolet absorption efficiency when the zinc oxide powder became a resin composition, the spectral transmission spectrum of the obtained film was measured. The result is shown in FIG.

【0034】実施例6 実施例3で得られた被覆酸化亜鉛粉末を用いた以外は実
施例4と同様に操作して分散性を調べた。 比較例5 比較例1で得られた被覆酸化亜鉛粉末を用いた以外は実
施例4と同様に操作して分散性を調べた。また、酸化亜
鉛粉末が樹脂組成物になったときの紫外線吸収効率を調
べるために、その得られたフィルムの分光透過スペクト
ルを測定した。その結果を図2に示す。
Example 6 The dispersibility was examined in the same manner as in Example 4 except that the coated zinc oxide powder obtained in Example 3 was used. Comparative Example 5 The dispersibility was examined in the same manner as in Example 4 except that the coated zinc oxide powder obtained in Comparative Example 1 was used. Further, in order to investigate the ultraviolet absorption efficiency when the zinc oxide powder became a resin composition, the spectral transmission spectrum of the obtained film was measured. The result is shown in FIG.

【0035】比較例6 比較例2で得られた被覆酸化亜鉛粉末を用いた以外は実
施例4と同様に操作して分散性を調べた。 比較例7 比較例3で得られた被覆酸化亜鉛粉末を用いた以外は実
施例4と同様に操作して分散性を調べた。また、酸化亜
鉛粉末が樹脂組成物になったときの紫外線吸収効率を調
べるために、その得られたフィルムの分光透過スペクト
ルを測定した。その結果を図2に示す。
Comparative Example 6 Dispersibility was examined in the same manner as in Example 4 except that the coated zinc oxide powder obtained in Comparative Example 2 was used. Comparative Example 7 The dispersibility was examined in the same manner as in Example 4 except that the coated zinc oxide powder obtained in Comparative Example 3 was used. Further, in order to investigate the ultraviolet absorption efficiency when the zinc oxide powder became a resin composition, the spectral transmission spectrum of the obtained film was measured. The result is shown in FIG.

【0036】比較例8 比較例4の酸化亜鉛粉末を用いた以外は実施例4と同様
に操作して分散性を調べた。また、酸化亜鉛粉末が樹脂
組成物になったときの紫外線吸収効率を調べるために、
その得られたフィルムの分光透過スペクトルを測定し
た。その結果を図2に示す。
Comparative Example 8 The dispersibility was examined in the same manner as in Example 4 except that the zinc oxide powder of Comparative Example 4 was used. In addition, in order to investigate the ultraviolet absorption efficiency when the zinc oxide powder becomes a resin composition,
The spectral transmission spectrum of the obtained film was measured. The result is shown in FIG.

【0037】比較例9 酸化亜鉛粉末を添加しなかった以外は実施例4と同様に
操作してフィルムに成形し、酸化亜鉛粉末が樹脂組成物
になったときの紫外線吸収効率を調べるために、その得
られたフィルムの分光透過スペクトルを測定した。その
結果を図2に示す。
COMPARATIVE EXAMPLE 9 A film was formed in the same manner as in Example 4 except that the zinc oxide powder was not added, and the ultraviolet absorption efficiency when the zinc oxide powder became a resin composition was examined. The spectral transmission spectrum of the obtained film was measured. The result is shown in FIG.

【0038】SiO2で被覆された酸化亜鉛粉末を用い
た比較例5〜7に於いては、目視に於いても、いずれも
未分散凝集塊が観察され、無被覆酸化亜鉛粉末を用いた
比較例8の場合よりも分散性が悪化していた。カップリ
ング剤で被覆された酸化亜鉛粉末を用いた実施例4〜6
の場合と比較例5〜8の場合とを比較すると、分散性の
差は目視でも歴然としていたが、それぞれのフィルムの
SEM写真(組成像写真)及びEPMA写真を撮り、凝
集塊が酸化亜鉛であるかないかを確認した。図3は実施
例5で得られたフィルムのSEM写真(40倍)、図4
は実施例5で得られたフィルムのSEM写真(1000
倍)、図5は実施例5で得られたフィルムのEPMA写
真(1000倍)である。図6は比較例5で得られたフ
ィルムのSEM写真(40倍)、図7は比較例5で得ら
れたフィルムのSEM写真(1000倍)、図8は比較
例5で得られたフィルムのEPMA写真(1000倍)
である。図3〜図5の写真からも明らかなように、本発
明の被覆酸化亜鉛粉末を用いた場合には凝集塊もなく一
様に分散されていた。これに対して、図6〜図8の写真
からも明らかなように比較例5の場合には大きな凝集塊
があり、なかには数百μm径のものが見られ、明らかに
分散性が劣っていることが明確になった。
In Comparative Examples 5 to 7 in which the zinc oxide powder coated with SiO 2 was used, undispersed agglomerates were visually observed, and comparison was made using uncoated zinc oxide powder. The dispersibility was worse than in the case of Example 8. Examples 4 to 6 using zinc oxide powder coated with a coupling agent
Comparing the case of No. 2 and the cases of Comparative Examples 5 to 8, the difference in dispersibility was visually apparent, but SEM photographs (composition image photographs) and EPMA photographs of the respective films were taken, and the agglomerates were zinc oxide. I checked if there was one. FIG. 3 is a SEM photograph (40 times) of the film obtained in Example 5, FIG.
Is a SEM photograph of the film obtained in Example 5 (1000
5) is an EPMA photograph (1000 times) of the film obtained in Example 5. FIG. 6 is a SEM photograph (40 times) of the film obtained in Comparative Example 5, FIG. 7 is a SEM photograph (1000 times) of the film obtained in Comparative Example 5, and FIG. 8 is a photograph of the film obtained in Comparative Example 5. EPMA photograph (1000 times)
Is. As is clear from the photographs of FIGS. 3 to 5, when the coated zinc oxide powder of the present invention was used, it was uniformly dispersed without aggregates. On the other hand, as is clear from the photographs of FIGS. 6 to 8, in the case of Comparative Example 5, there were large aggregates, some of which had a diameter of several hundreds of μm, and the dispersibility was obviously poor. It became clear.

【0039】また、比較例8(無被覆酸化亜鉛粉末を使
用)の場合には、混練及び成形中に所謂焼けや変色が観
察された。これに対して実施例4〜6の場合には、焼け
や変色は全く観察されず、従って本発明に基づいて表面
被覆処理された酸化亜鉛は光触媒活性を抑制するのみな
らず、混練及び成形中の熱劣化に関する酸化亜鉛の光触
媒活性をも抑制していることが確認された。尚、比較例
5〜7に於いては若干焼けや変色が観察され、熱劣化に
対しても本発明は従来技術を上回ることが確認された。
In the case of Comparative Example 8 (using uncoated zinc oxide powder), so-called burning and discoloration were observed during kneading and molding. On the other hand, in the case of Examples 4 to 6, no burning or discoloration was observed, so that the zinc oxide surface-coated according to the present invention not only suppresses the photocatalytic activity, but also during kneading and molding. It was confirmed that the photocatalytic activity of zinc oxide with respect to the thermal deterioration of the is also suppressed. It should be noted that in Comparative Examples 5 to 7, slight burning and discoloration were observed, and it was confirmed that the present invention is superior to the prior art even with respect to thermal deterioration.

【0040】尚、実施例4〜6及び比較例5〜8におい
ては、便宜的に樹脂に混練することにより樹脂との分散
性を調べたが、塗料にして分散性を調べても基本的には
同様の結果が得られる。また、油脂に分散させる場合に
も基本的には同様の結果が得られる。図2のグラフより
明らかなように、本発明に基づく実施例5のフィルムは
紫外線(約400nm以下)をほとんど吸収し、透過さ
せていない。実施例5のフィルムには、実施例2で作成
した僅か1%のカップリング剤被覆量で酸化亜鉛の紫外
線吸収剤としての欠点である光触媒活性をほぼ完全に抑
制している酸化亜鉛粉が含有されている。即ち、本発明
が目的とした酸化亜鉛粉末の紫外線吸収効率に影響しな
い少量の被覆量で、酸化亜鉛が持つ紫外線吸収剤として
の欠点である光触媒活性を充分に抑制し、同時に酸化亜
鉛の樹脂への分散性を向上せしめ、樹脂組成物となった
ときに好適な紫外線吸収剤としての働きを示す被覆酸化
亜鉛粉末を開発できたことを確認した。
In Examples 4 to 6 and Comparative Examples 5 to 8, the dispersibility with the resin was examined by kneading with the resin for the sake of convenience. Produces similar results. In addition, basically the same result can be obtained even when dispersed in oil and fat. As is clear from the graph of FIG. 2, the film of Example 5 according to the present invention absorbs almost no ultraviolet rays (about 400 nm or less) and does not transmit it. The film of Example 5 contains zinc oxide powder prepared in Example 2 which almost completely suppresses the photocatalytic activity which is a drawback of zinc oxide as an ultraviolet absorber with a coating amount of the coupling agent of 1%. Has been done. That is, a small coating amount that does not affect the ultraviolet absorption efficiency of the zinc oxide powder aimed at by the present invention sufficiently suppresses the photocatalytic activity, which is a drawback of zinc oxide as an ultraviolet absorber, and at the same time makes it a resin of zinc oxide. It was confirmed that a coated zinc oxide powder having improved dispersibility and exhibiting a suitable action as an ultraviolet absorber when it became a resin composition was developed.

【0041】一方、従来技術に基づく比較例5、7のフ
ィルムは、比較例8(無被覆酸化亜鉛粉末を使用)のフ
ィルムよりも紫外線吸収能が低下している。この理由
は、前述したようにSiO2表面被覆処理により分散性
の低下をきたしたことに起因すると思われる。即ち、従
来技術の難点は、光触媒活性を抑制するために被覆量を
多くすると、樹脂組成物となった場合に分散性の低下を
招き、図2の比較例5、7のスペクトルが示すように紫
外線吸収効率が悪化することである。本発明は、一言で
言えば、従来技術の抱えていたこの課題をカップリング
剤を用いることにより一気に解決したと言える。
On the other hand, the films of Comparative Examples 5 and 7 based on the prior art have lower ultraviolet absorption ability than the film of Comparative Example 8 (using uncoated zinc oxide powder). The reason for this is considered to be that the dispersibility was lowered by the SiO 2 surface coating treatment as described above. That is, the drawback of the prior art is that when the coating amount is increased in order to suppress the photocatalytic activity, the dispersibility of the resin composition decreases, and as shown by the spectra of Comparative Examples 5 and 7 in FIG. That is, the ultraviolet absorption efficiency is deteriorated. In a word, the present invention can be said to have solved this problem, which the conventional technique had, at once by using a coupling agent.

【0042】実施例7 酸化亜鉛粉末(比較例4)のn−ヘキサンスラリーを撹
拌しつつ被覆量が1重量%になるように所定量のチタン
カップリング剤KR TTS(味の素株式会社製)を滴
下した。撹拌をしばらく続け、次にこのスラリーを濾過
し、洗浄し、更に一夜風乾して被覆酸化亜鉛粉末の乾粉
を得た。このようにして得た被覆酸化亜鉛粉末について
実施例1と同様にして光触媒活性の抑制効果を調べた。
また、実施例4と同様にしてフィルムに成形し、ポリエ
チレン樹脂に対する被覆酸化亜鉛粉末の分散性を調べ
た。更に、実施例5と同様にして紫外線吸収効率を調べ
た。それらの測定結果を表面被覆物及び被覆量と共に表
2に示す。
Example 7 While stirring an n-hexane slurry of zinc oxide powder (Comparative Example 4), a predetermined amount of titanium coupling agent KR TTS (manufactured by Ajinomoto Co., Inc.) was dropped so that the coating amount was 1% by weight. did. Stirring was continued for a while, then the slurry was filtered, washed and air dried overnight to give a dry powder of coated zinc oxide powder. With respect to the coated zinc oxide powder thus obtained, the effect of suppressing the photocatalytic activity was examined in the same manner as in Example 1.
Also, a film was formed in the same manner as in Example 4, and the dispersibility of the coated zinc oxide powder in the polyethylene resin was examined. Further, the ultraviolet absorption efficiency was examined in the same manner as in Example 5. The measurement results are shown in Table 2 together with the surface coating and the coating amount.

【0043】実施例8 酸化亜鉛粉末(比較例4)の水スラリーを撹拌しつつ被
覆量が1重量%になるように所定量のジルコアルミネー
ト系カップリング剤M(CAVEDON CHEMICAL CO.INC.製)
を滴下した。撹拌をしばらく続け、次にこのスラリーを
濾過し、洗浄し、更に乾燥機にて加熱乾燥して被覆酸化
亜鉛粉末の乾粉を得た。このようにして得た被覆酸化亜
鉛粉末について実施例1と同様にして光触媒活性の抑制
効果を調べた。また、実施例4と同様にしてフィルムに
成形し、ポリエチレン樹脂に対する被覆酸化亜鉛粉末の
分散性を調べた。更に、実施例5と同様にして紫外線吸
収効率を調べた。それらの測定結果を表面被覆物及び被
覆量と共に表2に示す。
Example 8 A predetermined amount of a zircoaluminate coupling agent M (made by CAVEDON CHEMICAL CO. INC. Was added so that the coating amount was 1% by weight while stirring an aqueous slurry of zinc oxide powder (Comparative Example 4). )
Was dripped. Stirring was continued for a while, and then the slurry was filtered, washed, and further dried by heating in a dryer to obtain a dry powder of coated zinc oxide powder. With respect to the coated zinc oxide powder thus obtained, the effect of suppressing the photocatalytic activity was examined in the same manner as in Example 1. Also, a film was formed in the same manner as in Example 4, and the dispersibility of the coated zinc oxide powder in the polyethylene resin was examined. Further, the ultraviolet absorption efficiency was examined in the same manner as in Example 5. The measurement results are shown in Table 2 together with the surface coating and the coating amount.

【0044】尚、表2には実施例2で得た被覆酸化亜鉛
粉末、比較例1及び3で得た被覆酸化亜鉛粉末及び比較
例4の無被覆酸化亜鉛粉末を用いた場合についても合わ
せて示す。
Table 2 also shows the cases where the coated zinc oxide powder obtained in Example 2, the coated zinc oxide powder obtained in Comparative Examples 1 and 3 and the uncoated zinc oxide powder obtained in Comparative Example 4 were used. Show.

【0045】[0045]

【表2】 樹脂への分散性の判断基準は次の通りである:10mm
×10mmの範囲内に存在する約30μm以上の凝集塊
の数で ◎:全くなし、○:10個未満、△:10〜20個、
×:20個超
[Table 2] The criteria for determining dispersibility in resin are as follows: 10 mm
In the number of aggregates of about 30 μm or more existing in the range of × 10 mm, ⊚: none, ∘: less than 10, Δ: 10 to 20
×: Over 20

【0046】表2に示すデータからも明らかなように、
本発明に基づく実施例2、7及び8で得た被覆酸化亜鉛
粉末が紫外線吸収剤として従来技術に基づく酸化亜鉛粉
末よりもはるかに優れたものであることが確認された。
本発明は、カップリング剤を被覆処理してなる被覆酸化
亜鉛粉末に関連するものであるが、酸化チタンも紫外線
吸収剤としては酸化亜鉛以上に光触媒活性が強いという
欠点を持っており、またカップリング剤の無機酸化物の
表面との反応機構から考えて、酸化チタンをカップリン
グ剤で被覆処理した場合にも本発明と同様の効果が得ら
れる。
As is clear from the data shown in Table 2,
It was confirmed that the coated zinc oxide powders obtained in Examples 2, 7 and 8 according to the present invention were far superior to the zinc oxide powders according to the prior art as UV absorbers.
The present invention relates to a coated zinc oxide powder obtained by coating a coupling agent, but titanium oxide also has a drawback that it has a stronger photocatalytic activity than zinc oxide as an ultraviolet absorber, and a cup Considering the reaction mechanism of the ring agent with the surface of the inorganic oxide, the same effect as that of the present invention can be obtained when titanium oxide is coated with the coupling agent.

【0047】[0047]

【発明の効果】本発明の被覆酸化亜鉛においては、酸化
亜鉛粉末自体の紫外線吸収、殺菌、抗菌、防黴、脱臭等
の作用、効果に悪影響を及ぼさない程度の少量の表面被
覆量で、且つ紫外線吸収剤として用いた場合の酸化亜鉛
が持つ欠点である樹脂組成物や油脂組成物を劣化させる
光触媒活性を充分に抑制し、同時に酸化亜鉛の樹脂組成
物や油脂組成物への分散性をも向上せしめる表面被覆量
で被覆されており、樹脂組成物(塗膜、フィルム、樹脂
成形品、繊維等)や油脂組成物(化粧料等)となったと
きに好適な紫外線吸収剤、殺菌、抗菌、防黴、脱臭剤等
としての働きを示し、且つ樹脂組成物や油脂組成物の光
劣化を抑える。
INDUSTRIAL APPLICABILITY The coated zinc oxide of the present invention has a small amount of surface coating which does not adversely affect the action and effects of ultraviolet absorption, sterilization, antibacterial, mildew, deodorization, etc. of the zinc oxide powder itself, and Sufficiently suppresses the photocatalytic activity that deteriorates the resin composition and the oil and fat composition, which are the drawbacks of zinc oxide when used as an ultraviolet absorber, and at the same time, disperses the zinc oxide in the resin composition and the oil and fat composition. It is coated with an improved surface coating amount, and it is suitable as a UV absorber, sterilizer, antibacterial when it becomes a resin composition (coating film, film, resin molded product, fiber, etc.) or fat composition (cosmetics, etc.). , Acts as an antifungal agent, a deodorant, etc., and suppresses the photodegradation of resin compositions and oil and fat compositions.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例2の被覆酸化亜鉛粉末及び比較例4無被
覆酸化亜鉛粉末の脱臭効果を示すグラフである。
FIG. 1 is a graph showing the deodorizing effect of a coated zinc oxide powder of Example 2 and an uncoated zinc oxide powder of Comparative Example 4.

【図2】実施例5、比較例5、7、8及び9で得られた
ポリエチレンフィルムの分光透過スペクトルである。
2 is a spectral transmission spectrum of polyethylene films obtained in Example 5 and Comparative Examples 5, 7, 8 and 9. FIG.

【図3】実施例5で得られたフィルムのSEM写真(4
0倍)である。
FIG. 3 is a SEM photograph of the film obtained in Example 5 (4
0 times).

【図4】実施例5で得られたフィルムのSEM写真(1
000倍)である。
FIG. 4 is a SEM photograph of the film obtained in Example 5 (1
000 times).

【図5】実施例5で得られたフィルムのEPMA写真
(1000倍)である。
5 is an EPMA photograph (1000 ×) of the film obtained in Example 5. FIG.

【図6】比較例5で得られたフィルムのSEM写真(4
0倍)である。
6 is a SEM photograph of the film obtained in Comparative Example 5 (4
0 times).

【図7】比較例5で得られたフィルムのSEM写真(1
000倍)である。
7 is a SEM photograph of the film obtained in Comparative Example 5 (1
000 times).

【図8】比較例5で得られたフィルムのEPMA写真
(1000倍)である。
8 is an EPMA photograph (1000 times) of the film obtained in Comparative Example 5. FIG.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) A61K 7/00 C08L 1/00 - 101/16 ─────────────────────────────────────────────────── ─── Continuation of the front page (58) Fields surveyed (Int.Cl. 7 , DB name) A61K 7/00 C08L 1/00-101/16

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 酸化亜鉛粒子表面にカップリング剤を被
覆処理しており、該カップリング剤の被覆量が酸化亜鉛
に対して0.2〜10重量%であることを特徴とする被
覆酸化亜鉛粉末。
1. A zinc oxide particle surface is coated with a coupling agent, and the coating amount of the coupling agent is zinc oxide.
0.2 to 10% by weight of the coated zinc oxide powder.
【請求項2】 カップリング剤がシランカップリング剤
である請求項1記載の被覆酸化亜鉛粉末。
2. The coated zinc oxide powder according to claim 1, wherein the coupling agent is a silane coupling agent.
【請求項3】 請求項1又は2記載の被覆酸化亜鉛粉末
を有効成分とし、紫外線吸収、殺菌、抗菌、防黴、脱臭
作用を有するが、光触媒活性の抑制されている添加剤。
3. An additive having the coated zinc oxide powder according to claim 1 or 2 as an active ingredient, which has ultraviolet absorption, bactericidal, antibacterial, antifungal and deodorizing properties, but has suppressed photocatalytic activity.
【請求項4】 請求項3記載の添加剤を配合してなるこ
とを特徴とする樹脂組成物。
4. A resin composition containing the additive according to claim 3.
【請求項5】 請求項3記載の添加剤を配合してなるこ
とを特徴とする油脂組成物。
5. An oil and fat composition comprising the additive according to claim 3.
JP24746494A 1994-06-16 1994-10-13 Coated zinc oxide powder and composition containing coated zinc oxide powder Expired - Lifetime JP3485643B2 (en)

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JP6-133465 1994-06-16
JP13346594 1994-06-16
JP24746494A JP3485643B2 (en) 1994-06-16 1994-10-13 Coated zinc oxide powder and composition containing coated zinc oxide powder

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JPH0859890A JPH0859890A (en) 1996-03-05
JP3485643B2 true JP3485643B2 (en) 2004-01-13

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JP2002104823A (en) * 2000-09-28 2002-04-10 Hakusui Tech Co Ltd Anti-bacteria.anti-mildew agent
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JP4923345B2 (en) * 2001-07-13 2012-04-25 大日本印刷株式会社 Coating composition, coating film thereof, antireflection film, and antireflection film
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