JP2008114109A - Flame-retardant ozone/voc removing filter - Google Patents

Flame-retardant ozone/voc removing filter Download PDF

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JP2008114109A
JP2008114109A JP2006297604A JP2006297604A JP2008114109A JP 2008114109 A JP2008114109 A JP 2008114109A JP 2006297604 A JP2006297604 A JP 2006297604A JP 2006297604 A JP2006297604 A JP 2006297604A JP 2008114109 A JP2008114109 A JP 2008114109A
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ozone
flame
activated carbon
filter
flame retardant
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JP5150090B2 (en
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Akiko Kosaka
明子 小阪
Tatsuro Nakamura
達郎 中村
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Japan Vilene Co Ltd
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Japan Vilene Co Ltd
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

Abstract

<P>PROBLEM TO BE SOLVED: To provide a flame-retardant ozone/VOC removing filter which is excellent in fire retardance, ozone decomposition and VOC removal, and can exhibit excellent properties in various electronic apparatuses, air conditioners, etc. without inhibiting fire retardance especially applied according to design. <P>SOLUTION: The flame-retardant ozone/VOC removing filter is made by carrying activated carbon particles impregnated with potassium carbonate on a cover material containing a fire retardant and made of fabric. The amount of the impregnated potassium carbonate is 1-3 mass%. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、レーザープリンターを始めとする電子機器や、種々の空調機器などに組み込んでオゾン及びVOCを除去するためのフィルタに関するものであり、特に、難燃剤の効力低下を来すことなく、1つのフィルタで、オゾンの分解機能と揮発性有機化合物の吸着機能の両方の機能を有する難燃性オゾンVOC除去フィルタに関するものである。 The present invention relates to a filter for removing ozone and VOC by being incorporated in electronic devices such as laser printers and various air conditioners, and in particular, without reducing the effectiveness of flame retardants. The present invention relates to a flame retardant ozone VOC removal filter having both functions of decomposing ozone and adsorbing volatile organic compounds.

従来、電子機器の使用に際して、機器内の放電現象等に伴って発生するオゾンが人体に対して悪影響を及ぼすことが問題視されてきた。このようなオゾンを電子機器内で分解し、排出する技術として、例えば特開2006−119313号公報(以下、特許文献1)では、画像形成装置本体内の空気を外部に排出する排気排出路と、当該排出路に設けられ、排出する空気中の化合物を吸着によって除去を行える吸着フィルタと、前述の排気排出路に設けられ、排出する空気中の化合物を触媒により分解して除去する触媒フィルタと、を備え、排気方向に沿っての上流側に前述した吸着フィルタを配置し、下流側に前記触媒フィルタを配置したことを要旨とする排気装置、並びに、当該排気装置を備える画像形成装置が提案されている。   Conventionally, it has been regarded as a problem that ozone generated due to a discharge phenomenon or the like in an apparatus adversely affects a human body when the electronic apparatus is used. As a technique for decomposing and discharging such ozone in an electronic device, for example, in Japanese Patent Laid-Open No. 2006-119313 (hereinafter referred to as Patent Document 1), an exhaust discharge path for discharging the air inside the image forming apparatus main body to the outside An adsorption filter that is provided in the exhaust passage and can remove the compounds in the exhausted air by adsorption; and a catalyst filter that is provided in the exhaust exhaust passage and that decomposes and removes the compounds in the exhausted air with a catalyst; The above-described adsorption filter is disposed on the upstream side in the exhaust direction, and the catalyst filter is disposed on the downstream side, and an image forming apparatus including the exhaust device is proposed. Has been.

この特許文献1によれば、所謂、トナー像を記録材に加熱定着するプリンタ、複写機、ファクシミリ等の画像形成装置においては、インクを使用したものと同様に、高精細なドットの細かい画像が求められている。このような背景の下、上質紙の表面を化学物質でコートし、グロス調やマット調に仕上げたコート紙の利用が拡大しており、例えば180℃程度の上述したトナー像の加熱定着に際して、コート紙から揮発性有機化合物(以下、VOC[Volatile Organic Compound]と称する)が発生し、前述したオゾンと共に、当該装置の使用環境の悪化を招いていた。従って、この文献技術では、画像形成装置本体内の空気を外部に排出する排気排出路と、この排気排出路に設けられ、排出する空気中の化合物を吸着によって除去し得る吸着フィルタと、上記排気排出路に設けられ、排出する空気中の化合物を触媒により分解して除去する触媒フィルタと、を備え、この排気方向に沿っての上流側に上記吸着フィルタを配置し、下流側に上述の触媒フィルタを配置するとの構成を採用している。また、これらフィルタを構成する素材として、活性炭を織布、不織布、薄板に担持した機械的除去作用を利用したもの、或いは、白金、パラジウム等の貴金属系、又は、マンガン、鉄等の卑金属系の酸化触媒を織布、不織布、薄板などの基材で担持した化学的除去作用を利用したものが開示されている。   According to this Patent Document 1, in a so-called image forming apparatus such as a printer, a copying machine, or a facsimile that heats and fixes a toner image on a recording material, a fine image of high-definition dots is obtained as in the case of using ink. It has been demanded. Under such a background, the use of coated paper coated with a chemical substance on the surface of high-quality paper and finished in a glossy or matte tone is expanding. For example, when the above-described toner image is heated and fixed at about 180 ° C. Volatile organic compounds (hereinafter referred to as VOC [Volatile Organic Compound]) were generated from the coated paper, and together with the ozone described above, the use environment of the apparatus was deteriorated. Therefore, in this document technique, an exhaust discharge path that discharges air inside the image forming apparatus main body to the outside, an adsorption filter that is provided in the exhaust discharge path and can remove compounds in the discharged air by adsorption, and the exhaust A catalyst filter that is provided in the discharge path and decomposes and removes the compounds in the discharged air with a catalyst, and the adsorption filter is disposed on the upstream side along the exhaust direction, and the catalyst described above is disposed on the downstream side. A configuration in which a filter is arranged is adopted. In addition, as a material constituting these filters, activated carbon is woven fabric, non-woven fabric, a material using a mechanical removal action carried on a thin plate, or a precious metal system such as platinum or palladium, or a base metal system such as manganese or iron. The thing using the chemical removal effect | action which carry | supported the oxidation catalyst with base materials, such as a woven fabric, a nonwoven fabric, and a thin plate, is disclosed.

また、このような画像形成装置で発生するオゾンを分解するためのフィルタとして、特開2004−313880号公報(以下、特許文献2)では、排気経路、上流側にトルエン吸着量が5mg/cc以上の活性炭担持フィルターを配置し、下流側に酢酸吸着量が2.5mg/cc以上の金属酸化物担持フィルターを配置する構成を採用したオゾンフィルターが提案されている。この公報技術では、活性炭担持フィルターとして例えば木材(木炭)やのこ屑、果実殻(ヤシ殻、もみ殻、コーヒー豆など)、セルロース、リグニン、パルプなどの植物系原料;褐炭、亜炭、泥炭、無煙炭、石油スラッジなどの鉱物系原料等を素材とし、塩化亜鉛などを使用した薬品賦活あるいは水蒸気などを用いたガス賦活等を施すことにより得られた活性炭を採用することが開示されており、また、金属酸化物担持フィルターとしては、マンガン、銅、コバルト、ニッケル、鉄、ニッケル、チタン、銀等の単一酸化物、複合酸化物とし、特に、マンガンの単一酸化物、複合酸化物が好適に採用される旨の開示がある。そして、各担持フィルターのより具体的な態様として、ウレタンまたは不織布等を基材として、プリーツ加工若しくはハニカム加工を行うことが好適であるとの記載がある。   In addition, as a filter for decomposing ozone generated in such an image forming apparatus, Japanese Patent Laid-Open No. 2004-313880 (hereinafter referred to as Patent Document 2) has a toluene adsorption amount of 5 mg / cc or more on the exhaust path and upstream side. Has been proposed, and an ozone filter employing a configuration in which a metal oxide-carrying filter having an acetic acid adsorption amount of 2.5 mg / cc or more is arranged downstream is proposed. In this technology, for example, wood (charcoal), sawdust, fruit husk (coconut husk, rice husk, coffee beans, etc.), cellulose, lignin, pulp, and other plant materials such as lignite, lignite, peat, It is disclosed to employ activated carbon obtained by using mineral raw materials such as anthracite and petroleum sludge as raw materials, chemical activation using zinc chloride or gas activation using water vapor, etc. As a metal oxide-carrying filter, a single oxide or composite oxide such as manganese, copper, cobalt, nickel, iron, nickel, titanium or silver is used, and a single oxide or composite oxide of manganese is particularly preferable. Is disclosed to be adopted. As a more specific embodiment of each supported filter, there is a description that it is preferable to perform pleating or honeycomb processing using urethane or nonwoven fabric as a base material.

さらに、上述した特許文献2と同様な技術として、特開2000−157827号公報(以下、特許文献3)では、シート基材の両面に、ガス吸着層を形成してなるガス吸着用シートであって、前記ガス吸着層が、活性炭と、アルカリ金属化合物及びアルカリ土類金属化合物の少なくとも一方と、難溶性難燃剤とを含んでなるガス吸着用シートが開示されている。この公報では、活性炭によるオゾン除去性能自体を向上させるために活性炭にカリウム化合物とナトリウム化合物とを混合した活性炭成形体、或いは、特定の活性炭にアルカリ金属化合物またはアルカリ土類金属化合物を添着、熱処理した活性炭を用いた技術を従前の背景技術として開示している。そして、前述の画像形成装置を始めとする事務用機器では、UL(Underwriters Laboratories Inc.)の発行する燃焼性試験に関する規格『UL 94:Standard for Safety Tests for Flammability of Plastic Materials for Parts in Devices and Appliances』(以下、非特許文献1)を満足する必要があるものの、オゾン分解機能を補助するために活性炭に添着されたアルカリ金属化合物及びアルカリ土類金属は、活性炭の燃焼性を促進してしまい、実用性に乏しいと記載されている。さらに、従前、リン酸アンモニウムなどの水溶性無機系化合物を含有する従来技術を挙げ、難燃性の面から一応の成果は得ているものの、当該無機系化合物によって活性炭上のオゾン分解活性点が減少するという問題を提起し、難燃剤とアルカリ金属とが反応し、例えばリン酸ナトリウムの如き物質を形成して、活性炭上のオゾン分解活性点が被覆されると記載されている。   Furthermore, as a technique similar to Patent Document 2 described above, Japanese Patent Application Laid-Open No. 2000-1557827 (hereinafter, Patent Document 3) is a gas adsorption sheet in which a gas adsorption layer is formed on both surfaces of a sheet base material. In addition, a gas adsorption sheet is disclosed in which the gas adsorption layer includes activated carbon, at least one of an alkali metal compound and an alkaline earth metal compound, and a hardly soluble flame retardant. In this publication, in order to improve the ozone removal performance itself by activated carbon, an activated carbon molded body in which potassium compound and sodium compound are mixed with activated carbon, or an alkali metal compound or alkaline earth metal compound is attached to a specific activated carbon and heat-treated. A technique using activated carbon is disclosed as a conventional background art. And in office equipment such as the above-described image forming apparatus, the standard “UL 94: Standard for Safety of Plastics of Plastics of the Standards for Flammability Test” issued by UL (Underwriters Laboratories Inc.). (Hereinafter referred to as Non-Patent Document 1), the alkali metal compound and alkaline earth metal added to the activated carbon to assist the ozonolysis function promote the flammability of the activated carbon, It is described as being impractical. In addition, the conventional technology containing water-soluble inorganic compounds such as ammonium phosphate has been mentioned, and although some achievements have been obtained from the viewpoint of flame retardancy, the ozonolysis active sites on activated carbon have been obtained by the inorganic compounds. It raises the problem of decreasing, and it is described that a flame retardant reacts with an alkali metal to form a substance such as sodium phosphate to coat an ozonolysis active site on activated carbon.

この特許文献3に適用されるアルカリ金属化合物およびアルカリ土類金属化合物の具体例として、アルカリ金属化合物としては、ナトリウム、カリウム、リチウムなどのアルカリ金属類の水酸化物;酸化物;炭酸塩、炭酸水素塩、酢酸塩、シュウ酸塩、リン酸塩、硫酸塩、コハク酸、フタル酸、フタル酸水素などの水溶性の塩;ハロゲン化物など、そして、アルカリ土類金属化合物としては、カルシウム、マグネシウム、バリウムなどのアルカリ土類金属の水酸化物;酸化物;炭酸塩、酢酸塩、シュウ酸塩、リン酸塩などの水溶性の塩;ハロゲン化物などが列挙されている。これら金属化合物の添加量は、ガス吸着層中の活性炭に対して10〜100wt%が好適であるとの記載が認められる。   Specific examples of the alkali metal compound and the alkaline earth metal compound applied to Patent Document 3 include alkali metal hydroxides such as sodium, potassium and lithium; oxides; carbonates and carbonates. Water-soluble salts such as hydrogen salt, acetate salt, oxalate salt, phosphate salt, sulfate salt, succinic acid, phthalic acid, hydrogen phthalate; halides, etc., and alkaline earth metal compounds include calcium, magnesium And alkaline earth metal hydroxides such as barium; oxides; water-soluble salts such as carbonates, acetates, oxalates and phosphates; halides and the like. It is recognized that the addition amount of these metal compounds is preferably 10 to 100 wt% with respect to the activated carbon in the gas adsorption layer.

また、特許文献3の技術で用いられる難燃剤として、前述したオゾン分解活性点への被覆を回避する必要性から、難溶性難燃剤であり、例えばメタリン酸アルミニウム、リン酸メラミン、リン酸マグネシウム、縮合リン酸アミドなどのリン系難燃剤;水酸化アルミニウム、水酸化マグネシウムなどの無機系の難溶性難燃剤を一種または二種以上併用し得るとの開示がある。   In addition, as a flame retardant used in the technology of Patent Document 3, from the need to avoid the coating on the ozonolysis active sites described above, it is a hardly soluble flame retardant, such as aluminum metaphosphate, melamine phosphate, magnesium phosphate, There is a disclosure that one or two or more inorganic flame retardants such as condensed phosphoric acid amides; inorganic flame retardants such as aluminum hydroxide and magnesium hydroxide may be used in combination.

一方、本出願人は、特開平11−57467号公報(以下、特許文献4)において、複数の積層単位で構成され、この積層単位がホットメルト樹脂からなる連結部と樹脂凝集部とで構成されたウエブの一方の表面に、前記樹脂凝集部を介して脱臭粉粒体を固着して成り、かつ相異なる2種類以上の脱臭粉粒体を担持してなる積層型濾材であって、脱臭粉粒体を被覆してしまうバインダーを用いずに、1つの積層単位に1種類の脱臭粉粒体のみを担持して成る積層型脱臭濾材を提案している。この公報技術では、例えば酸性臭気とアルカリ性臭気とに分類される臭気物質を、その荷電状態を利用して捕捉する化学的作用、即ち、電気的に中和することで脱臭を図る、互いに異なる2種類以上の脱臭粉粒体を具えた脱臭濾材に関し、夫々の脱臭粉粒体同士が接触することで失活を来しやすいことに着目したものである。このような技術に用いて好適な脱臭粉粒体としては、臭気に直接作用する化学脱臭剤を主体とする造粒体のみならず、例えば活性炭やゼオライトなど、物理的吸着作用を持つ粉粒体の表面に、化学脱臭剤を付着させた、所謂、添着炭などが記載されている。さらに、より具体的な態様について、酸性臭気用粉粒体を構成する化学脱臭剤として、炭酸カリウム、炭酸水素カリウム、炭酸ナトリウム、炭酸水素ナトリウムなどのアルカリ金属炭酸塩や、エタノールアミン、ヘキサメチレンジアミン、ピペラジンなどのアミン化合物、アルカリ臭気用粉粒体を構成する化学脱臭剤としては、燐酸、硫酸、硝酸、リンゴ酸、クエン酸、アスコルビン酸などが開示されている。   On the other hand, the present applicant, in Japanese Patent Laid-Open No. 11-57467 (hereinafter referred to as Patent Document 4), is composed of a plurality of laminated units, and this laminated unit is composed of a connecting portion made of hot-melt resin and a resin aggregating portion. A deodorized powder, comprising a deodorized powder granule formed by adhering a deodorized powder granule to one surface of a web through the resin agglomerated part and carrying two or more different types of deodorized powder granule. A multilayer deodorizing filter medium is proposed in which only one type of deodorized powder granule is supported in one laminating unit without using a binder that covers the granule. In this publication technique, for example, a chemical action of capturing odorous substances classified into acidic odor and alkaline odor using their charged state, that is, deodorizing by electrically neutralizing, is different from each other. With regard to a deodorizing filter medium having more than one type of deodorized powder particles, attention is paid to the fact that each deodorized powder particle is liable to be deactivated. Deodorant powder suitable for use in such a technique is not only a granule mainly composed of a chemical deodorant that directly acts on odor, but also a powder having a physical adsorption action such as activated carbon and zeolite. In other words, so-called impregnated charcoal, in which a chemical deodorant is attached to the surface, is described. Furthermore, for a more specific embodiment, as a chemical deodorant constituting the powder for acidic odor, alkali metal carbonates such as potassium carbonate, potassium bicarbonate, sodium carbonate, sodium bicarbonate, ethanolamine, hexamethylenediamine As chemical deodorizers constituting amine compounds such as piperazine and powders for alkaline odor, phosphoric acid, sulfuric acid, nitric acid, malic acid, citric acid, ascorbic acid and the like are disclosed.

さらに、本出願人は、特開2004−3070号公報(以下、特許文献5)において、種々の機能を有する固体粒子の表面特性を有効に保持したまま、しかも均一に固着した固体粒子担持繊維及び繊維シートを提供する技術を提案している。この公報技術は、少なくとも表面が熱可塑性樹脂から主としてなる繊維の表面に、この熱可塑性樹脂の融点より高い温度に維持された状態の加熱固体粒子を接触させ、そして固体粒子融着繊維を冷却することによって、当該固体粒子を繊維表面に固着させる態様を含むものである。係る繊維の態様として、その表面を構成する熱可塑性樹脂としては、所定の芯成分を構成する繊維に、鞘成分としてコーティングによって塗布形成された熱可塑性樹脂であっても良いとの開示が有る。   Furthermore, the present applicant, in Japanese Patent Application Laid-Open No. 2004-3070 (hereinafter referred to as Patent Document 5), while maintaining the surface characteristics of the solid particles having various functions effectively, the solid particle-supporting fibers that are uniformly fixed and A technology to provide fiber sheets is proposed. In this publication technique, at least the surface of a fiber mainly composed of a thermoplastic resin is brought into contact with heated solid particles maintained at a temperature higher than the melting point of the thermoplastic resin, and the solid-particle fused fiber is cooled. This includes a mode in which the solid particles are fixed to the fiber surface. As an aspect of such a fiber, there is a disclosure that the thermoplastic resin constituting the surface thereof may be a thermoplastic resin coated and formed as a sheath component on a fiber constituting a predetermined core component.

特開2006−119313号公報([特許請求の範囲]、[背景技術]、[発明を実施するための最良の形態])JP-A-2006-119313 ([Claims], [Background Art], [Best Mode for Carrying Out the Invention]) 特開2004−313880号公報([特許請求の範囲]、[発明の実施の形態])JP-A-2004-313880 ([Claims], [Embodiments of the Invention]) 特開2000−157827号公報([特許請求の範囲]、[0006]〜[0008]、[0014]、[0022]〜[0025])JP 2000-157827 A ([Claims], [0006] to [0008], [0014], [0022] to [0025]) UL 94(国際標準図書番号:ISBN1−55989−150−5)UL 94 (International Standard Book Number: ISBN1-55989-150-5) 特開平11−57467号公報([特許請求の範囲]、[0003]、[0006]、[0013])JP-A-11-57467 ([Claims], [0003], [0006], [0013]) 特開2004−3070号公報([特許請求の範囲]、[0006]、[0012]〜[0016])JP 2004-3070 A ([Claims], [0006], [0012] to [0016])

上述した背景技術からも理解できるように、画像形成装置内で発生するオゾンやVOCを装置内で分解若しくは吸着によって解消を図るため、触媒作用と吸着作用とを併用した濾材が知られている。そして、吸着作用を担う素材については、VOC吸着を主眼に従前用いられてきた活性炭を始めとする比表面積の大きな素材に対して、化学的なオゾン処理機能を付加するために種々の化学物質を添着させる手法が採られるに至っている。さらには、実用上、所定の特性を満たす難燃剤を組み合わせることによって、所期の難燃性を濾材に期待する提案も認められる。しかし、従来技術の手法では、所詮、難燃剤を濾材に付与しても、活性炭に添着する化学物質の添着量は制限されなければならず、その結果オゾン処理機能は満足するものにはならなかった。そのため、従来技術では、全体の除去性能をあげるためにVOC吸着を主眼としたフィルタと、オゾン分解を主眼としたフィルタを別々にしているものが多かった。しかし、2種類の濾材を入れると装置内の圧損上昇につながり、かさばるために装置設計が制限される場合もあった。また、オゾン分解フィルタは金属酸化物を添着したハニカムタイプが主流であるが高価で、コストアップの原因にもなるという問題点があった。   As can be understood from the background art described above, a filter medium that uses both a catalytic action and an adsorbing action is known in order to eliminate ozone or VOC generated in the image forming apparatus by decomposing or adsorbing in the apparatus. And for the material responsible for the adsorption action, various chemical substances are added to add a chemical ozone treatment function to materials with a large specific surface area such as activated carbon which has been used mainly for VOC adsorption. The method of attaching has come to be taken. Furthermore, in practice, a proposal for expecting the desired flame retardancy to the filter medium by combining a flame retardant satisfying predetermined characteristics is also recognized. However, according to the conventional technique, even if a flame retardant is applied to the filter medium, the amount of chemical substances attached to the activated carbon must be limited, and as a result, the ozone treatment function cannot be satisfied. It was. For this reason, in the prior art, in order to improve the overall removal performance, a filter mainly focusing on VOC adsorption and a filter mainly focusing on ozonolysis are often separated. However, when two types of filter media are inserted, the pressure loss in the apparatus increases, and the apparatus design may be limited due to its bulk. In addition, the ozonolysis filter is mainly a honeycomb type with a metal oxide attached, but it is expensive and causes a cost increase.

そこで、本出願にかかる発明者は、このような種々の素材を組み合わせて、鋭意検討した結果、VOCもオゾンも高効率で除去可能なフィルタで、且つ難燃性を阻害しないフィルタ構成を見出し、本発明を完成されたものである。   Therefore, the inventors of the present application combined such various materials, and as a result of extensive studies, found a filter configuration that can remove both VOC and ozone with high efficiency and that does not impair flame retardancy, The present invention has been completed.

本発明は上述した従来の技術の問題点に鑑み成されたものであり、従って、本発明の目的は、難燃性、オゾン分解並びにVOC除去に優れ、特に設計に応じて適用された難燃性を阻害することなく、種々の電子機器や空調装置等において、優れた特性を発揮し得る難燃性オゾンVOC除去フィルタを提供することにある。   The present invention has been made in view of the above-mentioned problems of the prior art, and therefore, the object of the present invention is excellent in flame retardancy, ozonolysis and VOC removal, and particularly flame retardant applied according to the design. An object of the present invention is to provide a flame retardant ozone VOC removal filter capable of exhibiting excellent characteristics in various electronic devices, air conditioners and the like without impairing the properties.

この目的の達成を図るため、本発明の構成によれば、難燃剤を含有し、かつ布帛からなるカバー材に、炭酸カリウムを添着した活性炭粒子を担持してなる難燃性オゾン分解フィルタであって、上述した炭酸カリウムの添着量を1〜3質量%としたことを特徴としている。尚、ここに言う「添着量」とは、次式で示される添着前の活性炭質量に対する炭酸カリウムの添加質量の割合を百分率とした値を表す。
添着量[%]=炭酸カリウムの添加質量[g]/添着前の活性炭質量[g]×100
また、この発明の実施に当たり、前述したカバー材と活性炭粒子とは、ホットメルト樹脂からなる樹脂凝集部を介して接着され、前述した難燃剤と炭酸カリウムを添着した活性炭粒子とは離間配置されていることが好適である。
In order to achieve this object, according to the configuration of the present invention, there is provided a flame retardant ozonolysis filter comprising activated carbon particles containing a flame retardant and having potassium carbonate attached to a cover material made of a fabric. The amount of potassium carbonate mentioned above is 1 to 3% by mass. The “adhesion amount” referred to here represents a value obtained by expressing the ratio of the addition mass of potassium carbonate to the mass of activated carbon before the attachment represented by the following formula as a percentage.
Amount of addition [%] = addition mass of potassium carbonate [g] / active carbon mass before addition [g] × 100
In carrying out the present invention, the cover material and the activated carbon particles described above are bonded via a resin agglomeration portion made of a hot melt resin, and the above-described flame retardant and activated carbon particles impregnated with potassium carbonate are spaced apart. It is preferable that

さらに、上述した難燃剤として、前述したカバー材の構成繊維に被着したバインダーに含有されていることが好ましい。加えて、当該カバー材の構成繊維に被着したバインダーに金属酸化物からなるオゾン分解触媒粒子が担持されているのが好ましい。   Furthermore, it is preferable that the flame retardant described above is contained in a binder attached to the constituent fibers of the cover material described above. In addition, it is preferable that ozonolysis catalyst particles made of a metal oxide are supported on a binder attached to the constituent fibers of the cover material.

上述した本発明の構成を採用することにより、オゾン分解並びにVOC除去性能に優れると共に、所期の難燃性を阻害することが少ない、難燃性オゾンVOC除去フィルタを実現することができる。   By adopting the above-described configuration of the present invention, it is possible to realize a flame-retardant ozone VOC removal filter that is excellent in ozonolysis and VOC removal performance and that hardly inhibits the desired flame retardancy.

以下、本発明の実施に最良な形態について、好適例としての難燃性オゾンVOC除去フィルタを模式的な断面により示す図1を参照し、その作製工程例に従って説明する。尚、同図においては、同一の機能を有する構成成分には同一の符号並びにハッチングを付して示すと共に、一部の構成成分については、その断面構成等を省略してある。   Hereinafter, the best mode for carrying out the present invention will be described with reference to FIG. 1 showing a flame retardant ozone VOC removal filter as a preferred example in a schematic section, according to an example of its production process. In the figure, components having the same function are indicated by the same reference numerals and hatching, and the cross-sectional configuration and the like of some components are omitted.

まず、カバー材を構成する布帛として、不織布、編物若しくは織物からなる任意好適な通気性を有する素材に、所期の難燃性を賦与するための難燃剤を含有した熱可塑性樹脂からなるバインダーを塗布、乾燥して被着させる。然る後、例えば前述した特許文献5の技術を適用することによって、金属酸化物からなるオゾン分解触媒粒子を加熱状態で、上記熱可塑性樹脂からなる表面を有する布帛に接触させ、当該オゾン分解触媒粒子が担持された状態のカバー材11を作製する。尚、このカバー材には、図示を省略したオゾン分解触媒粒子を担持するのが好ましいが、当該触媒粒子は、本願発明に必須の構成成分である炭酸カリウムが添着された活性炭粒子のオゾン分解機能を補助する構成成分として選択的に用いられるものである。   First, as a fabric constituting the cover material, a binder made of a thermoplastic resin containing a flame retardant for imparting desired flame retardancy to an arbitrary suitable breathable material made of nonwoven fabric, knitted fabric or woven fabric. Apply, dry and apply. Thereafter, for example, by applying the technique of Patent Document 5 described above, the ozone decomposition catalyst particles made of a metal oxide are brought into contact with a fabric having a surface made of the thermoplastic resin in a heated state, and the ozone decomposition catalyst The cover material 11 in a state where the particles are supported is produced. The cover material preferably carries ozonolysis catalyst particles (not shown), but the catalyst particles have an ozonolysis function of activated carbon particles to which potassium carbonate, which is an essential component of the present invention, is attached. It is used selectively as a component for assisting.

以下、この作製工程と、用いられる箇々の構成材料とに着目して詳細に説明する。上述したカバー材を構成する布帛としては、前述した種々の構造である通気性の素材を用いることができるが、空調機器に組み込む場合は勿論のこと、画像形成装置などに適用する場合には、例えばトナー若しくは記録材への加熱定着時に生じる煙などの塵埃を捕集する目的で、物理的な濾過作用を考慮して任意好適に選択することができる。また、本発明に適用される難燃剤は、このような布帛を構成する繊維に練り込んで紡糸されたものを用いることができるが、オゾン分解を効果的に行なうためのオゾン分解触媒粒子を担持する態様として、上述した特許文献5の技術を採用した構成とすることが望ましい。   Hereinafter, the manufacturing process and the various constituent materials used will be described in detail. As the fabric constituting the cover material described above, the air-permeable material having the various structures described above can be used, but when applied to an air conditioner, of course, when applied to an image forming apparatus, For example, for the purpose of collecting dust such as smoke generated at the time of heat-fixing on toner or a recording material, it can be arbitrarily selected in consideration of a physical filtering action. Further, the flame retardant applied to the present invention may be a fiber kneaded and spun into the fibers constituting such a fabric, but supports the ozone decomposition catalyst particles for effective ozone decomposition. It is desirable to adopt a configuration that employs the technique of Patent Document 5 described above as an aspect to perform.

この点について詳述すれば、加熱されたオゾン分解触媒粒子を担持する下地となる熱可塑性樹脂として、布帛を構成する繊維の融点若しくは軟化点よりも低い温度で熱可塑性を有するバインダーを用い、このバインダーに、所期の難燃性を有する難燃剤を含有させる。このようなバインダーとしては、アクリル酸エステル系樹脂、SBR系樹脂、NBR系樹脂、尿素系樹脂、ポリ塩化ビニル、ポリ塩化ビニリデンなどをあげることができる。そのなかでも、ハロゲンを含まないアクリル酸エステル系樹脂、SBR系樹脂、NBR系樹脂、尿素系樹脂などがより好ましく、従来周知の熱可塑性樹脂で構成されたものを任意好適に選択して用いれば良い。これらバインダーは、カバー材を構成する布帛の構成繊維の全表面に被着している必要はなく、用いる難燃剤の含有量や、特許文献5の技術を採用する場合に必要となるオゾン分解触媒粒子の被着量といったフィルター設計に応じ、任意好適な被着量とすることができる。   If this point is explained in detail, a binder having thermoplasticity at a temperature lower than the melting point or softening point of the fibers constituting the fabric is used as a thermoplastic resin as a base for supporting the heated ozone decomposition catalyst particles. The binder contains a flame retardant having the desired flame retardancy. Examples of such a binder include acrylate resin, SBR resin, NBR resin, urea resin, polyvinyl chloride, and polyvinylidene chloride. Among them, acrylic ester resins not containing halogen, SBR resins, NBR resins, urea resins, and the like are more preferable, and those made of conventionally known thermoplastic resins can be arbitrarily selected and used. good. These binders do not need to be attached to the entire surface of the constituent fibers of the fabric constituting the cover material, but the content of the flame retardant used and the ozone decomposition catalyst required when the technique of Patent Document 5 is adopted. Depending on the filter design, such as the amount of particles deposited, any suitable amount can be achieved.

さらに、難燃剤についても、例えば前述の特許文献3に開示される種々のリン酸系難燃剤や無機系難燃剤などの周知の材料を用いることができ、特に、近年の環境指向から非ハロゲン系の難燃剤が好ましい。加えて、本発明の構成として、上述したカバー材11の厚さ方向にオゾンを含む処理空気が通過する様にフィルターを配置することで塵埃の捕集効果を期待するため、好適な難燃性の指標として、前述の非特許文献1に記載されている発泡材料水平燃焼試験(Horizontal Burning Foamed Material Test:以下、水平燃焼試験と略記すると共に、具体的な試験法については後段で詳述)に準ずる評価が「94HF−1」の基準条件を満たすことが望ましい。従って、このような基準条件を満たす難燃剤としては、メタリン酸アルミニウム、リン酸メラミン、リン酸マグネシウム、ポリリン酸アンモニウム、水酸化アルミニウム、水酸化マグネシウムなどが最適である。   Further, for the flame retardant, well-known materials such as various phosphoric flame retardants and inorganic flame retardants disclosed in, for example, the above-mentioned Patent Document 3, can be used. These flame retardants are preferred. In addition, as a configuration of the present invention, since a filter is disposed so that the processing air containing ozone passes in the thickness direction of the cover material 11 described above, a dust collection effect is expected, so that suitable flame retardancy is achieved. As an index of the above, in the horizontal burning test (Horizontal Burning Foamed Material Test: hereinafter, abbreviated as a horizontal combustion test, and a specific test method will be described in detail later) It is desirable that the equivalent evaluation satisfies the criterion of “94HF-1”. Therefore, as a flame retardant satisfying such a standard, aluminum metaphosphate, melamine phosphate, magnesium phosphate, ammonium polyphosphate, aluminum hydroxide, magnesium hydroxide and the like are optimal.

上述した難燃剤を含有するバインダーが布帛に塗布、乾燥された状態のカバー材に対して、オゾン分解能を賦与するために担持されるオゾン分解触媒粒子としては、前述した特許文献1並びに特許文献2に例示されるような周知の材料を選択し得るが、当該触媒粒子自体として難燃性を有し、しかも、オゾン分解能に優れた金属酸化物からなるものが好ましく、特に、その比表面積が大きい二酸化マンガンからなるものが好適である。また、既に述べたとおり、本願発明のフィルターを構成するに当たって、上述したバインダーを使用せずに、カバー材を構成する構成繊維に難燃剤を練り込んだ形態とすることもできるが、係る場合には、当該構成繊維の表面が、特許文献5の技術適用が可能な熱可塑性を有することが好ましい。   As the ozonolysis catalyst particles supported for imparting ozone resolution to the cover material in which the binder containing the flame retardant described above is applied to the fabric and dried, the above-mentioned Patent Document 1 and Patent Document 2 are used. However, the catalyst particles themselves are preferably made of a metal oxide having flame retardancy and excellent ozone decomposability, and particularly having a large specific surface area. What consists of manganese dioxide is suitable. In addition, as described above, in configuring the filter of the present invention, a flame retardant can be incorporated into the constituent fibers constituting the cover material without using the binder described above. It is preferable that the surface of the constituent fiber has thermoplasticity to which the technology of Patent Document 5 can be applied.

次いで、このようなカバー材に担持する活性炭粒子は、従来知られている添着技術、例えば、炭酸カリウム水溶液に活性炭粒子を浸漬、乾燥することによって調製することができる。尚、本発明は、難燃剤を含有するカバー材に担持された当該活性炭粒子における炭酸カリウムの添着量を1〜3質量%、より好ましくは1〜2質量%の範囲内とするのがよい。これによって、使用する活性炭の粒径のばらつきや炭酸カリウムの添着ムラなどに由来するフィルタのロットばらつきが生じた場合にも確実に難燃性を期待することができる。この範囲よりも添着量が少ない場合には、オゾン分解能を期待することが難しく、また、この好適範囲を超えて炭酸カリウムの添着量を採用する場合には、フィルタの難燃性を阻害する場合がある。   Next, the activated carbon particles supported on such a cover material can be prepared by a conventionally known attachment technique, for example, by immersing the activated carbon particles in a potassium carbonate aqueous solution and drying. In the present invention, the amount of potassium carbonate attached to the activated carbon particles supported on the cover material containing a flame retardant is preferably 1 to 3% by mass, more preferably 1 to 2% by mass. This makes it possible to reliably expect flame retardancy even when filter lot variations occur due to variations in the particle size of the activated carbon used or potassium carbonate adhesion irregularities. When the amount of adhering is less than this range, it is difficult to expect ozone resolution, and when the amount of adhering potassium carbonate exceeding this preferred range is used, the flame retardancy of the filter is inhibited. There is.

また、上述した活性炭粒子として市販のものを任意好適に選択し、種々の技術で担持することができるが、当該粒子が担持されるカバー材の厚さ方向での圧力損失を抑える目的で、前述した特許文献4の技術を採用するのが最適である。具体的な作製工程としては、前述した図1におけるカバー材11に、例えば熱可塑性ポリアミド系樹脂、熱可塑性ポリエステル樹脂、熱可塑性ウレタン樹脂、ポリオレフィン樹脂、エチレン−酢酸ビニル共重合体樹脂などのホットメルト樹脂を単独、若しくは混合して、例えばメルトブロー法などの周知の紡糸技術で調製されたホットメルト不織布を積層した状態で、当該積層物に上記添着後の活性炭粒子13を散布する。然る後、この状態の積層物を乾熱若しくは湿熱による加熱を行うことによって、ホットメルト樹脂が可塑化し、その一部は繊維形態を残したまま連結部15となり、原材料であるホットメルト不織布を構成していた比較的細い繊維成分は溶融切断されて、活性炭粒子13との接触部分に凝集して樹脂凝集部17を構成することとなる。   Also, commercially available activated carbon particles described above can be arbitrarily selected and supported by various techniques, but for the purpose of suppressing pressure loss in the thickness direction of the cover material on which the particles are supported, It is optimal to adopt the technique of Patent Document 4 described above. As a specific production process, for example, a hot melt such as a thermoplastic polyamide resin, a thermoplastic polyester resin, a thermoplastic urethane resin, a polyolefin resin, or an ethylene-vinyl acetate copolymer resin is applied to the cover material 11 in FIG. In the state where a hot melt nonwoven fabric prepared by a known spinning technique such as a melt blow method is laminated, for example, resin is singly or mixed, and the activated carbon particles 13 after the attachment are sprayed on the laminate. Thereafter, by heating the laminate in this state with dry heat or wet heat, the hot melt resin is plasticized, and a part thereof becomes the connecting portion 15 while leaving the fiber form, and the hot melt nonwoven fabric as the raw material is removed. The relatively thin fiber component that has been configured is melt-cut and aggregated at the contact portion with the activated carbon particles 13 to form the resin aggregation portion 17.

上述した担持技術を採用する場合、難燃剤を含有するカバー材11と活性炭粒子13との配置関係は、樹脂凝集部17を介して離間する構造となる。このため、活性炭粒子13に添着されている炭酸カリウムと難燃剤とは隔絶された配置関係となり、吸湿性若しくは水溶性を有する難燃剤を用いた場合であっても、活性炭粒子に対するオゾン分解機能の低下を回避する効果を有する。   When the above-described supporting technology is adopted, the arrangement relationship between the cover material 11 containing the flame retardant and the activated carbon particles 13 is a structure that is separated via the resin agglomeration portion 17. For this reason, the potassium carbonate attached to the activated carbon particles 13 and the flame retardant are separated from each other, and even when a flame retardant having hygroscopicity or water solubility is used, the ozone decomposing function for the activated carbon particles is reduced. It has the effect of avoiding the decrease.

また、活性炭粒子13が樹脂凝集部17を介して、カバー材11と離間した状態で担持される図1の具体的形態を採用する場合、樹脂凝集部17を形成する加熱工程で、その前段において作製したカバー材11に担持したオゾン分解触媒粒子が脱落しない材料条件、即ち、前述した夫々のホットメルト樹脂が有する融点若しくは軟化点に相当する温度では、カバー材に被着されたバインダーに由来する樹脂成分の軟化しない条件を採用する必要がある。   Further, when adopting the specific form of FIG. 1 in which the activated carbon particles 13 are supported in a state of being separated from the cover material 11 via the resin agglomeration part 17, in the heating step for forming the resin agglomeration part 17, Under the material conditions that the ozone decomposition catalyst particles carried on the produced cover material 11 do not fall off, that is, at the temperature corresponding to the melting point or softening point of each of the above-mentioned hot melt resins, it is derived from the binder applied to the cover material. It is necessary to adopt conditions that do not soften the resin component.

このような一連の工程を順次経ることによって、図1の形態では、2つのカバー材11に挟持された状態で、活性炭粒子13からなる2つの層が、樹脂凝集部17並びに連結部によって構成された難燃性オゾンVOC除去フィルタが得られる。尚、本発明は、このような形態に限定されるものではなく、例えば、図示のフィルタをジグザグに折り加工し、周縁に枠を取り付けたユニットとして種々の機器に組み込むことができる。上述した折り加工の場合、折ることにより濾材面積を効率的に向上させることができ、比較的風速の早い複写機内でも低圧損化を図ることができる。また、図示の形態のように、シート状のフィルタの表面を何れもカバー材11で構成することにより、上述した折り加工に際して、活性炭粒子の脱落を防ぐことが可能である。また、上述した形態においては、カバー材自体に濾過機能を期待する場合を例示したが、本発明の主たる構成を具えたフィルタに対して、従来知られている種々のフィルタを別途積層することもできる。   By sequentially performing such a series of steps, in the form of FIG. 1, the two layers made of the activated carbon particles 13 are constituted by the resin agglomeration portion 17 and the connection portion while being sandwiched between the two cover materials 11. A flame retardant ozone VOC removal filter is obtained. In addition, this invention is not limited to such a form, For example, the filter of illustration can be folded in zigzag and it can incorporate in various apparatuses as a unit which attached the frame to the periphery. In the case of the folding process described above, the area of the filter medium can be efficiently improved by folding, and low pressure loss can be achieved even in a copying machine having a relatively high wind speed. Moreover, by forming the surface of the sheet-like filter with the cover material 11 as in the illustrated embodiment, it is possible to prevent the activated carbon particles from falling off during the above-described folding process. Further, in the above-described embodiment, the case where the cover material itself is expected to have a filtering function is exemplified, but various conventionally known filters may be separately laminated on the filter having the main configuration of the present invention. it can.

以下、本発明の実施例として、特定の条件で作製したフィルタを試験評価した結果につき説明する。尚、以下の説明では、特定の形状、配置関係、並びにその他の数値的条件を挙げるが、これら条件は本発明を理解し得る程度の好適例に過ぎず、本発明はこれら実施例の内容にのみ限定されるものではなく、本発明の目的の範囲内で任意好適な設計の変更及び変形を行うことができる。   Hereinafter, as an example of the present invention, results of test evaluation of a filter manufactured under specific conditions will be described. In the following description, specific shapes, arrangement relationships, and other numerical conditions will be described. However, these conditions are only suitable examples for understanding the present invention, and the present invention is not limited to the contents of these examples. However, the present invention is not limited thereto, and any suitable design changes and modifications can be made within the scope of the object of the present invention.

(フィルタ作製)
始めに、この評価試験では、既に説明した図1の構造のフィルタを種々の材料条件で作製した。まず、カバー材11に被着するための難燃剤を含有するバインダーとして、先に述べた「HF−1」の難燃性規格を期待し得る市販のリン系難燃剤液(難溶性のポリリン酸アンモニウムが固形分として54質量%含有する水分散液)37重量部と、アクリル系樹脂エマルジョン型接着剤(固形分45質量%の水分散液)4.4重量部と、周知の増粘剤0.4重量部と、水58.2重量部とを混合調製した。
(Filter production)
First, in this evaluation test, the filter having the structure shown in FIG. 1 described above was manufactured under various material conditions. First, as a binder containing a flame retardant for adhering to the cover material 11, a commercially available phosphorus-based flame retardant liquid (a hardly soluble polyphosphoric acid that can be expected to meet the flame retardancy standard of “HF-1” described above) 37 parts by weight of an aqueous dispersion containing 54% by mass of ammonium as a solid content), 4.4 parts by weight of an acrylic resin emulsion type adhesive (an aqueous dispersion having a solid content of 45% by mass), and a known thickener 0 4 parts by weight and 58.2 parts by weight of water were mixed and prepared.

次いで、面密度20g/mのポリオレフィン繊維からなる湿式不織布に、上述した難燃剤を含有するバインダーを含浸、乾燥させて、面密度30g/mの基材となるカバー材を得た。このカバー材は、布帛である湿式不織布の繊維表面に被着されたバインダーに由来する熱可塑性樹脂成分中に、29.7質量%のリン系難燃剤を固形分として含有するものであった。 Next, a wet nonwoven fabric composed of polyolefin fibers having a surface density of 20 g / m 2 was impregnated with the binder containing the above-mentioned flame retardant and dried to obtain a cover material serving as a base material having a surface density of 30 g / m 2 . This cover material contained 29.7% by mass of a phosphorus-based flame retardant as a solid content in a thermoplastic resin component derived from a binder applied to the fiber surface of a wet nonwoven fabric as a fabric.

上述した状態のカバー材に、市販の二酸化マンガン『CMD−K200』(中央電気工業(株)製,商品名;比表面積250g/m,平均粒子径4.8μm)を前述した特許文献5の技術によって担持し、最終的に34g/mのカバー材11を用意した。 In the above-described cover material, commercially available manganese dioxide “CMD-K200” (manufactured by Chuo Denki Kogyo Co., Ltd., trade name: specific surface area 250 g / m 2 , average particle diameter 4.8 μm) A cover material 11 of 34 g / m 2 was finally prepared.

また、市販の活性炭である『クラレコール GW20/40』(クラレケミカル(株)製,商品名;粒径範囲0.35〜0.85mm,平均粒径0.61mm)に対し、炭酸カリウム水溶液を用いて種々の添着量(後述)の活性炭粒子を別途調製した。然る後、上述したカバー材11に、熱可塑性ポリアミド系のホットメルト樹脂(190℃におけるメルトインデックスは約80)からなる蜘蛛の巣状のホットメルト不織布(面密度20g/m)を積層した。この状態の積層物に対して、前述の特許文献4の技術により、種々の添着量とした活性炭粒子を散布し、約5Kg/cmの水蒸気処理を約7秒間行い、ホットメルト樹脂からなる連結部15と樹脂凝集部17とを形成することにより、カバー材11に上記活性炭粒子13を固着担持させた。続いて、固着した活性炭粒子以外を除去し、この工程を繰り返すことにより、2層目の活性炭粒子が固着担持した構成成分、及び、別途作製した、フィルタの他面を構成する前述と同一構成のカバー材11を順次に積層接着することにより、図1に示すように、厚さ方向に対称な層構成を有する断面構造のフィルタを得た。このようにして得られた、活性炭粒子の添着量が異なることを除いて実質的に同一条件で作製した4種類のフィルタに関し、主な構成成分の詳細、先に述べた各活性炭粒子における炭酸カリウムの添着量、平板状態での圧力損失(面風速0.5m/秒での測定値)、フィルタとしての面密度並びにフィルタの厚さ(20g/cm荷重時の測定値)を表1に示す。 In addition, an aqueous potassium carbonate solution was added to “Kuraray Coal GW20 / 40” (trade name; particle size range: 0.35 to 0.85 mm, average particle size: 0.61 mm), which is a commercially available activated carbon. The activated carbon particles having various amounts of adhesion (described later) were separately prepared. Thereafter, a spider web-shaped hot melt nonwoven fabric (surface density 20 g / m 2 ) made of a thermoplastic polyamide-based hot melt resin (melt index at 190 ° C. is about 80) was laminated on the cover material 11 described above. . In this state, activated carbon particles with various amounts of adhesion are dispersed by the technique of Patent Document 4 described above, steam treatment at about 5 Kg / cm 2 is performed for about 7 seconds, and a connection made of hot melt resin is performed. By forming the part 15 and the resin aggregation part 17, the activated carbon particles 13 were fixedly supported on the cover material 11. Subsequently, components other than the fixed activated carbon particles are removed, and by repeating this step, the component having the second layer of activated carbon particles fixed and supported, and a separately prepared filter having the same configuration as described above constituting the other surface of the filter are prepared. By sequentially laminating and adhering the cover material 11, as shown in FIG. 1, a filter having a cross-sectional structure having a symmetrical layer structure in the thickness direction was obtained. Regarding the four types of filters prepared under substantially the same conditions except that the amount of the activated carbon particles added is different, the details of the main components and the potassium carbonate in each activated carbon particle described above are obtained. Table 1 shows the amount of adhesion, the pressure loss in a flat plate state (measured value at a surface wind speed of 0.5 m / sec), the surface density as a filter, and the thickness of the filter (measured value at 20 g / cm 2 load). .

Figure 2008114109
Figure 2008114109

(難燃性の試験評価)
次に、上記各フィルタ試料について、前述した難燃性を試験評価した結果について説明する。先に述べたとおり、本発明に係るフィルタは、その厚さ方向に処理すべき空気を通過させることで使用するのが好ましいことから、非特許文献1に規定された水平燃焼試験により評価を実施した。この水平燃焼試験では、所定の高さに試験片を配置しておくことができる支持用金網を用い、この金網の下方に175±25mmの距離で脱脂綿(標識綿と称される)を配置しておく。この金網に、長さ150±1mm、幅50±1mmの短冊状に裁断され、しかも長さ方向の一方の端部から、25mm、60mm及び125mmの各位置に合計3つの標線を予め書き込んだ試験片を載置する。燃焼試験は、試験片を水平に載置した状態で上述した端部に金網の下方から炎を60±1秒間当てたのち、炎を試験片から離す。この時点から計時し、
[a]炎が消えた(残炎)時間
[b]炎と赤熱が消えた(残じん)時間
[c]炎又は赤熱の前線が125mm標線に達した時間、若しくは試験片が125mm標線の手前で燃焼又は赤熱が止まった時間
の3種類の時間を記録する。このような評価試験を5回実施した結果に応じて、夫々の難燃性基準条件は、下記の表2に示すような「94HF−1」若しくは「94HF−2」の2つに分類評価される。
(Flame retardancy test evaluation)
Next, the results of the test evaluation of the above-described flame retardancy for each filter sample will be described. As described above, since the filter according to the present invention is preferably used by passing air to be processed in the thickness direction, the filter is evaluated by the horizontal combustion test defined in Non-Patent Document 1. did. In this horizontal combustion test, a supporting wire net that can place a test piece at a predetermined height is used, and absorbent cotton (referred to as labeled cotton) is placed under the wire net at a distance of 175 ± 25 mm. Keep it. This wire net was cut into strips having a length of 150 ± 1 mm and a width of 50 ± 1 mm, and a total of three marked lines were previously written at each of 25 mm, 60 mm and 125 mm from one end in the length direction. Place the specimen. In the combustion test, a flame is applied for 60 ± 1 second from below the wire mesh to the above-described end portion with the test piece placed horizontally, and then the flame is separated from the test piece. Timing from this point,
[A] Time when flame disappeared (residual flame) [b] Time when flame and red heat disappeared (residual dust) [c] Time when flame or red heat front reached 125 mm mark, or test specimen marked 125 mm Record three types of time, the time when combustion or red heat stopped before. According to the results of performing such evaluation tests five times, each flame retardant standard condition is classified and evaluated into two types of “94HF-1” or “94HF-2” as shown in Table 2 below. The

Figure 2008114109
Figure 2008114109

各試験片について、上述した水平燃焼試験を行った。その結果、実施例1、実施例2並びに比較例1に係る各フィルタについては、用いた難燃剤の特性に応じ、「94HF−1」の基準条件に適合することが確認された。しかしながら、比較例2に係るフィルタでは「94HF−2」にしか適合しなかった。これらの結果を総合して、活性炭粒子の炭酸カリウム添着量を9質量%としたために、難燃剤の効果が阻害されたものであることが理解できる。   The horizontal combustion test mentioned above was done about each test piece. As a result, it was confirmed that the filters according to Example 1, Example 2, and Comparative Example 1 were adapted to the standard conditions of “94HF-1” according to the characteristics of the flame retardant used. However, the filter according to Comparative Example 2 was only compatible with “94HF-2”. By combining these results, it can be understood that the effect of the flame retardant is hindered because the amount of potassium carbonate attached to the activated carbon particles was 9 mass%.

続いて、上述した各フィルタに関し、オゾン分解並びにVOC除去の各性能の評価方法について説明する。   Next, an evaluation method for each performance of ozonolysis and VOC removal will be described for each filter described above.

(オゾン分解の性能評価方法)
この実施例では、表1で説明した4種類のフィルタを30mmφの円盤状に裁断し、円筒状ガラス製測定ホルダーにセットした。この測定ホルダーに対して、市販のオゾン発生機でオゾン濃度2.7ppm、セットされたフィルタ表面での面風速17cm/秒、相対湿度35%の条件によりオゾン雰囲気を連続8時間流し、ホルダーの流入側および流出側の各オゾン濃度を経時的に測定した。この際、オゾン濃度の測定には、『MODEL1200』(ダイレック(株)製,商品名)を用い、オゾン分解性能は、下記の式1からオゾン除去率(%)として算出した。尚、試験開始後10分でのオゾン除去率を初期効率とした。
(Ozone decomposition performance evaluation method)
In this example, the four types of filters described in Table 1 were cut into a 30 mmφ disk shape and set in a cylindrical glass measurement holder. For this measurement holder, an ozone atmosphere was passed for 8 hours continuously with a commercially available ozone generator under the conditions of ozone concentration of 2.7 ppm, surface wind speed on the set filter surface of 17 cm / sec, and relative humidity of 35%. The ozone concentrations on the side and outflow side were measured over time. At this time, the ozone concentration was measured using “MODEL 1200” (trade name, manufactured by Directec Co., Ltd.), and the ozonolysis performance was calculated as the ozone removal rate (%) from Equation 1 below. The ozone removal rate 10 minutes after the start of the test was defined as the initial efficiency.

Figure 2008114109
Figure 2008114109

(VOC除去の性能評価方法)
この実施例では、ガス吸着フィルタ試験法として「DIN 71460−II」に準拠し、VOCをトルエンとした性能評価を実施した。この性能評価では、表1の4種類のフィルタを折高さ60mmのプリーツフィルタとし、周知の枠材によって間口面積;縦56mm×横112mm×高さ60mm、間口面積当たりの濾材面積;1880cmの寸法条件でユニットを作製し、定格風量1.8m/秒、流入側トルエン濃度80ppm一定の条件下でトルエンガスを流し続け、経時的にユニットの流出側のトルエン濃度を脱臭フィルタ用ガス除去性能測定装置にて測定した。このVOC除去の性能評価は、流出側におけるトルエンの濃度が流入側の95%になった破過点(効率としては5%にまで低下した時点)までのトルエン吸着容量を間口面積当たりの値として(g/m)の単位で求めた。さらに、この試験においては、試験開始後、1分後の測定値を初期効率として算出した。
(VOC removal performance evaluation method)
In this example, based on “DIN 71460-II” as a gas adsorption filter test method, performance evaluation was performed using VOC as toluene. In this performance evaluation, the four types of filters in Table 1 are pleated filters with a folding height of 60 mm, and a well-known frame material has a frontage area; length 56 mm × width 112 mm × height 60 mm, filter medium area per frontage area; 1880 cm 2 Units were manufactured under dimensional conditions, and the toluene flow was continued under the conditions of a rated air flow of 1.8 m / sec and a constant inflow side toluene concentration of 80 ppm. Over time, the concentration of toluene on the outflow side of the unit was measured for deodorizing filter gas removal performance. Measured with an apparatus. The performance evaluation of this VOC removal is based on the toluene adsorption capacity up to the breakthrough point where the toluene concentration on the outflow side becomes 95% on the inflow side (when the efficiency drops to 5%) as the value per frontage area. It calculated | required in the unit of (g / m < 2 >). Furthermore, in this test, the measured value 1 minute after the start of the test was calculated as the initial efficiency.

これらオゾン分解並びにVOC除去の性能評価結果について、下記の表3に示す。尚、同表においては、先に述べた難燃性試験の評価結果、並びに炭酸カリウムの添着量についても記載してある。   The performance evaluation results of these ozonolysis and VOC removal are shown in Table 3 below. In the table, the evaluation results of the flame retardancy test described above and the amount of potassium carbonate attached are also described.

Figure 2008114109
Figure 2008114109

上記表3から理解できるように、本発明の構成を適用し、活性炭粒子の添着量を所定範囲として作製した実施例1並びに実施例2では複写機用フィルタの難燃性基準条件である「94HF−1」をクリアできる難燃性を有した濾材であり、オゾン分解能力が高く且つ揮発性有機化合物の除去機能も有することができた。比較例1は、「94HF−1」をクリアできる濾材であったもののオゾン分解能力が低かった。また、比較例2は炭酸カリウム添着量が多かった為に難燃性を阻害したことを示す「94HF−2」と判定され、さらにトルエン吸着容量に劣るものであった。これらの結果から、本出願に係る構成を採用することにより、オゾン分解とVOC除去に優れ、しかも、難燃性を阻害しないフィルタを実現可能であることが確認された。   As can be understood from Table 3 above, in Example 1 and Example 2 in which the configuration of the present invention was applied and the amount of activated carbon particles applied was made in a predetermined range, “94HF, which is a flame retardance standard condition for a copier filter, is used. It was a filter medium having flame retardancy capable of clearing "-1", having a high ozone decomposing ability and a function of removing volatile organic compounds. Although the comparative example 1 was a filter medium which can clear "94HF-1", its ozonolysis ability was low. Further, Comparative Example 2 was determined to be “94HF-2” indicating that the flame retardance was inhibited due to the large amount of potassium carbonate adhering, and was further inferior in toluene adsorption capacity. From these results, it was confirmed that by adopting the configuration according to the present application, it is possible to realize a filter that is excellent in ozonolysis and VOC removal and that does not impair flame retardancy.

本発明の好適実施形態を説明するため、模式的な概略断面により示す図である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic sectional view for explaining a preferred embodiment of the present invention.

符号の説明Explanation of symbols

11:カバー材、
13:(炭酸カリウムが添着された)活性炭粒子、
15:(ホットメルト樹脂からなる)連結部、
17:(ホットメルト樹脂からなる)樹脂凝集部。
11: Cover material
13: Activated carbon particles (impregnated with potassium carbonate),
15: connecting part (made of hot melt resin),
17: Resin aggregation part (consisting of hot melt resin).

Claims (4)

難燃剤を含有し、かつ布帛からなるカバー材に、炭酸カリウムを添着した活性炭粒子を担持してなる難燃性オゾンVOC除去フィルタであって、前記炭酸カリウムの添着量を1〜3質量%としたことを特徴とする難燃性オゾンVOC除去フィルタ。 A flame-retardant ozone VOC removal filter comprising activated carbon particles loaded with potassium carbonate on a cover material comprising a flame retardant and comprising a fabric, wherein the amount of potassium carbonate added is 1 to 3% by mass A flame retardant ozone VOC removal filter characterized by the above. 前記カバー材と前記活性炭粒子とが、ホットメルト樹脂からなる樹脂凝集部を介して接着され、前記難燃剤と前記炭酸カリウムを添着した活性炭粒子とが離間配置されていることを特徴とする請求項1に記載の難燃性オゾンVOC除去フィルタ。 The cover material and the activated carbon particles are bonded via a resin agglomeration portion made of a hot melt resin, and the flame retardant and the activated carbon particles impregnated with the potassium carbonate are spaced apart. The flame-retardant ozone VOC removal filter according to 1. 前記難燃剤は、前記カバー材の構成繊維に被着したバインダーに含有されてなることを特徴とする請求項1または請求項2の何れかに記載の難燃性オゾンVOC除去フィルタ。 The flame retardant ozone VOC removal filter according to claim 1, wherein the flame retardant is contained in a binder attached to a constituent fiber of the cover material. 前記カバー材の構成繊維に被着したバインダーに金属酸化物からなるオゾン分解触媒粒子が担持されてなることを特徴とする請求項3に記載の難燃性オゾンVOC除去フィルタ。 The flame retardant ozone VOC removal filter according to claim 3, wherein ozone decomposition catalyst particles made of a metal oxide are supported on a binder adhered to the constituent fibers of the cover material.
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