JPH0538415A - Filter for decomposing ozone - Google Patents

Filter for decomposing ozone

Info

Publication number
JPH0538415A
JPH0538415A JP3196895A JP19689591A JPH0538415A JP H0538415 A JPH0538415 A JP H0538415A JP 3196895 A JP3196895 A JP 3196895A JP 19689591 A JP19689591 A JP 19689591A JP H0538415 A JPH0538415 A JP H0538415A
Authority
JP
Japan
Prior art keywords
filter
weight
activated carbon
parts
ozone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP3196895A
Other languages
Japanese (ja)
Inventor
Shinro Katsura
真郎 桂
Jiro Fujimura
次郎 藤村
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 Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries 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 Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP3196895A priority Critical patent/JPH0538415A/en
Publication of JPH0538415A publication Critical patent/JPH0538415A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • 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

Landscapes

  • Separation Of Gases By Adsorption (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Treating Waste Gases (AREA)

Abstract

PURPOSE:To provide a filter for decomposing ozone having a lower pressure loss, a high decomposition capacity, and a long life. CONSTITUTION:A cured product of a composition comprising 100 pts.wt. of a resol-type phenolic resin (a), 1-100 pts.wt. of a lipophilic compound (b) which is liquid at room temperature and has a boiling point of 100 deg.C or higher, and 1-100 pts.wt. of a hydrophilic liquid compound (c) having a boiling point of 100 deg.C or higher is carbonized and activated to obtain a porous structure of activated carbon. The structures are allocated in the air passage of a filter for decomposing ozone.

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、オゾン分解などに用い
られるフィルターに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a filter used for ozone decomposition and the like.

【0002】[0002]

【従来の技術】オゾンはその酸化力を利用して水の浄
化、脱臭、漂白等幅広い用途に使用されている。しか
し、オゾン自体は人体に有害であり、作業環境濃度が
0.06ppm以下に規制されている。更に最近は、コ
ピー機のように高圧放電を利用する事務機の普及に伴い
これらの機器から発生するオゾンによる職場環境の破壊
も問題になってきており、オゾンを分解するためのフィ
ルターが設置されている。
2. Description of the Related Art Ozone is used for a wide range of purposes such as water purification, deodorization, and bleaching by utilizing its oxidizing power. However, ozone itself is harmful to the human body, and the working environment concentration is regulated to 0.06 ppm or less. Furthermore, recently, with the spread of office machines such as copiers that use high-voltage discharge, the destruction of the work environment by ozone generated from these devices has become a problem, and a filter for decomposing ozone is installed. ing.

【0003】オゾン分解用フィルターについては、従来
より色々なものが提案されている。例えば特開昭57−
177329号公報に記載されているように活性炭も古
くから簡便で経済的な材料として使用されている。しか
し、事務機用に粒状や粉状の活性炭をフィルター材とし
て使用することは粉塵等の作業環境の面から問題があ
る。このため、ハニカム状の活性炭構造物をオゾン分解
用フィルター使用することは例えば特開昭60−908
03号公報等に記載されているように既に知られてい
る。コピー機等の事務機に設けられるオゾン分解用活性
炭フィルターは、機器に設けられている送風機の能力に
限界があることから、圧力損失が低く、高分解性能が要
求される。
Various types of filters for ozone decomposition have hitherto been proposed. For example, JP-A-57-
As described in Japanese Patent No. 177329, activated carbon has also been used as a simple and economical material for a long time. However, the use of granular or powdery activated carbon as a filter material for office machines has a problem in terms of working environment such as dust. Therefore, the use of a honeycomb-like activated carbon structure filter for ozone decomposition is disclosed in, for example, JP-A-60-908.
It is already known as described in Japanese Patent Publication No. 03, etc. An ozone decomposing activated carbon filter provided in an office machine such as a copying machine is required to have a low pressure loss and a high decomposition performance because the capacity of a blower provided in the equipment is limited.

【0004】オゾン分解用フィルターに使用される活性
炭は、オゾン分解の進行に伴ってある割合で活性炭自身
も消耗することが分かっている。従って、このオゾン分
解用フィルターの寿命は、フィルターを構成している活
性炭の総重量に依存すると考えられている。また、オゾ
ン分解用フィルターの圧力損失は気体流がフィルターを
通過する際のフィルターの抵抗の大きさ、言い替えると
通路の大きさ、つまり開口率に依存すると考えられてい
る。
It is known that the activated carbon used for the ozonolysis filter is also consumed at a certain rate as the ozonolysis proceeds. Therefore, it is considered that the service life of this ozone decomposition filter depends on the total weight of the activated carbon constituting the filter. Further, it is considered that the pressure loss of the ozone decomposing filter depends on the size of the resistance of the filter when the gas flow passes through the filter, in other words, the size of the passage, that is, the aperture ratio.

【0005】コピー機等の事務機に設けられるオゾン分
解用活性炭フィルターは、機器に設けられている送風機
の能力に限界があることから、圧力損失が低く、高分解
性能が要求される。もちろん寿命が長いと保守点検に有
利である。このため、これまで長寿命と低圧力損失のフ
ィルターを得るべく多くの試みがなされているが未だ満
足のいくオゾン分解用フィルターは得られていない。
The ozone decomposing activated carbon filter provided in an office machine such as a copying machine is required to have a low pressure loss and a high decomposition performance because the capacity of the blower provided in the machine is limited. Of course, a long life is advantageous for maintenance inspection. Therefore, many attempts have been made so far to obtain a filter having a long life and a low pressure loss, but a satisfactory filter for ozone decomposition has not been obtained yet.

【0006】[0006]

【発明が解決しようとする問題点】本発明はより低い圧
力損失と高脱臭性能を有し、かつより寿命の長いオゾン
分解用フィルターにつき鋭意検討した結果、本発明に到
達した。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention The present invention has reached the present invention as a result of extensive studies on a filter for ozone decomposition which has lower pressure loss and high deodorizing performance and has a longer life.

【0007】[0007]

【課題を解決するための手段】すなわち本発明は、レゾ
ール型フェノール樹脂(a) 100重量部、親油性で10
0℃以上の沸点を有する常温で液状の化合物(b) 1ない
し100重量部、親水性で100℃以上の沸点を有する
液状の化合物(c) 1ないし100重量部とからなる組成
物の硬化物を炭化、賦活して得た活性炭素多孔体構造物
が空気の通路に配設されていることを特徴とするオゾン
分解用フィルターである。
Means for Solving the Problems That is, the present invention is based on 100 parts by weight of a resol type phenolic resin (a) and 10 parts by lipophilicity.
A cured product of a composition comprising 1 to 100 parts by weight of a liquid compound (b) having a boiling point of 0 ° C. or higher at room temperature and 1 to 100 parts by weight of a hydrophilic liquid compound (c) having a boiling point of 100 ° C. or higher. The filter for ozone decomposition is characterized in that the activated carbon porous material structure obtained by carbonizing and activating is disposed in an air passage.

【0008】本発明を更に詳しく説明する。本発明で用
いられるレゾール型フェノール樹脂(a) とは、例えばフ
ェノール1モルとホルマリン1〜3モルをアルカリ性触
媒、例えばNaOH、KOH、Ca(OH)2、Ba
(OH)2、NH2(CH2CH3) 等の存在下で80〜
100℃に加熱することにより縮合させ、次いで固形分
が60〜80%になるまで減圧下で水を留去して得られ
た、常温での粘度が1000〜20000cpsの液体
である。
The present invention will be described in more detail. The resol type phenolic resin (a) used in the present invention means, for example, 1 mol of phenol and 1 to 3 mol of formalin as an alkaline catalyst such as NaOH, KOH, Ca (OH) 2, Ba.
In the presence of (OH) 2, NH2 (CH2CH3), etc.
It is a liquid having a viscosity at room temperature of 1000 to 20000 cps, which is obtained by condensing by heating at 100 ° C. and then distilling off water under reduced pressure until the solid content becomes 60 to 80%.

【0009】本発明における親油性で100℃以上の沸
点を有する常温で液状の化合物とは、例えば、オクタ
ン、ノナン、デカン、ウンデカン、ドデカン、灯油、鉱
物油、流動パラフィン等の直鎖状、または分岐状アルキ
ル化合物、トルエン、キシレン等の環状アルキレン化合
物等を挙げることができる。これらのうちでは、流動パ
ラフィンがレゾールとの粘度が近似し、混合した際安定
な水中油型分散系を作ることが出来るため、好ましい。
In the present invention, the lipophilic compound having a boiling point of 100 ° C. or higher and being liquid at room temperature is, for example, a straight-chain compound such as octane, nonane, decane, undecane, dodecane, kerosene, mineral oil, liquid paraffin, or the like. Examples thereof include branched alkyl compounds and cyclic alkylene compounds such as toluene and xylene. Among these, liquid paraffin is preferable because it has a viscosity similar to that of resole and a stable oil-in-water dispersion system can be prepared when mixed.

【0010】この親油性化合物(b) のレゾール型フェノ
ール樹脂(a) 100重量部に対する配合量は通常1〜1
00重量部、好ましくは、10〜60重量部の範囲であ
る。親油性化合物(b) の量が少なすぎると、活性炭素多
孔体の多孔構造が少なくなって、吸着性能、液含浸性が
劣るようになる。また、炭化、賦活中に爆裂を生じ、活
性炭を製造しずらくなる。一方上記量を越えると、レゾ
ールの硬化特性が劣るようになる。また、炭化時に硬化
物の収縮が大きく、割れを生じ易くなる。
The lipophilic compound (b) is usually added in an amount of 1 to 1 with respect to 100 parts by weight of the resol type phenol resin (a).
00 parts by weight, preferably 10 to 60 parts by weight. If the amount of the lipophilic compound (b) is too small, the porous structure of the activated carbon porous body will be small, resulting in poor adsorption performance and liquid impregnation property. In addition, explosion occurs during carbonization and activation, making it difficult to produce activated carbon. On the other hand, when the amount exceeds the above range, the curing property of the resole becomes poor. In addition, the shrinkage of the cured product is large during carbonization, and cracking is likely to occur.

【0011】本発明における親水性で100℃以上の沸
点を有する液状の化合物(c) とは、例えば、重合度2以
上のオキシアルキレン化合物、例えば、ジエチレングリ
コール、トリエチレングリコール、分子量1000未満
のポリエチレングリコール、ジプロピレングリコール、
分子量1000未満のポリプロピレングリコール、ある
いはグリセリン等を挙げることが出来る。これらのうち
では、レゾールの粘度に比較的近く、かつ適度な相溶性
がある点から分子量が400〜600のポリエチレング
リコール、または、ジプロピレングリコールが好まし
い。
The liquid compound (c) having a boiling point of 100 ° C. or higher in the present invention means, for example, an oxyalkylene compound having a degree of polymerization of 2 or higher, for example, diethylene glycol, triethylene glycol, polyethylene glycol having a molecular weight of less than 1000. , Dipropylene glycol,
Examples thereof include polypropylene glycol having a molecular weight of less than 1000, glycerin and the like. Among these, polyethylene glycol having a molecular weight of 400 to 600 or dipropylene glycol is preferable because it is relatively close to the viscosity of the resole and has a suitable compatibility.

【0012】この親水性で100℃以上の沸点を有する
液状の化合物(c) のレゾール型フェノール樹脂(a) 10
0重量部に対する配合量は、通常1ないし100重量
部、好ましくは10〜60重量部の範囲である。親水性
化合物(c) の量が少なすぎると、親油性化合物(b) の分
散安定性が劣り、相分離を生じ易くなり、一方上記量を
越えるとレゾールの硬化特性が損なわれ、かつ親水性化
合物とレゾールとが相分離しやすくなる。
Resol type phenolic resin (a) 10 of this liquid compound (c) having a boiling point of 100 ° C. or higher
The compounding amount with respect to 0 part by weight is usually 1 to 100 parts by weight, preferably 10 to 60 parts by weight. When the amount of the hydrophilic compound (c) is too small, the dispersion stability of the lipophilic compound (b) is poor, and phase separation easily occurs. On the other hand, when the amount exceeds the above range, the curing property of the resole is impaired, and the hydrophilicity is high. The compound and the resole are easily phase separated.

【0013】本発明では親油性化合物(b) と、親水性化
合物(c) との配合比は、0.3〜3の範囲にすることが
好ましく、この範囲を外れると混合物が相分離し易くな
る。
In the present invention, the compounding ratio of the lipophilic compound (b) and the hydrophilic compound (c) is preferably in the range of 0.3 to 3, and when it is out of this range, the mixture is likely to undergo phase separation. Become.

【0014】本発明でレゾール型フェノール樹脂(a) の
硬化に用いられる硬化剤としては、公知の種々の強酸性
化合物、例えば塩酸、硫酸、硝酸、リン酸、ピロリン
酸、ポリリン酸等の無機酸、フェノールスルホン酸、ベ
ンゼンスルホン酸、トルエンスルホン酸、メタクレゾー
ルスルホン酸等の有機酸、あるいはこれらの混合物を挙
げることが出来る。硬化剤の使用量は、通常レゾール型
フェノール樹脂100重量部に対し通常1〜30重量部
の範囲である。
As the curing agent used for curing the resol type phenolic resin (a) in the present invention, various known strongly acidic compounds, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, pyrophosphoric acid and polyphosphoric acid are used. , Organic acids such as phenolsulfonic acid, benzenesulfonic acid, toluenesulfonic acid, and metacresolsulfonic acid, or a mixture thereof. The amount of the curing agent used is usually in the range of 1 to 30 parts by weight with respect to 100 parts by weight of the resol type phenol resin.

【0015】本発明のオゾン分解用フィルターに用いる
活性炭素多孔体構造物の原料として使用しうる樹脂組成
物は、上記成分を必須成分とするが、上記以外の少量の
他の成分、例えば活性炭素多孔体の気体吸着性能を向上
するための消失性フィラー、例えばポリエチレン、小麦
粉等、細孔径を多様化するための他の炭素材料、例えば
活性炭、カーボンブラック、メソフェーズピッチ粉、黒
鉛粉等、賦活を促進するための金属塩化合物等を含んで
いてもよい。
The resin composition that can be used as a raw material for the activated carbon porous structure used in the filter for ozone decomposition of the present invention contains the above-mentioned components as essential components, but a small amount of other components other than the above, such as activated carbon. Disintegrating filler for improving the gas adsorption performance of the porous body, such as polyethylene, flour, etc., other carbon materials for diversifying the pore size, such as activated carbon, carbon black, mesophase pitch powder, graphite powder, etc. It may contain a metal salt compound or the like for promoting.

【0016】本発明では、上記レゾール型フェノール樹
脂(a) 親油性で100℃以上の沸点を有する常温で液状
の化合物(b) 、親水性で100℃以上の沸点を有する液
状の化合物(c) 必要に応じて更に界面活性剤、他の充填
剤等を配合したものを攪拌、混合し、ついで/または同
時に硬化剤を混合する。上記成分を混合する方法として
は、好ましくは、高速で回転する攪拌翼を持ったミキサ
ー等で連続的にまたは、回分的に逐次、または同時に混
合する方法を採用することができる。
In the present invention, the resol-type phenolic resin (a) is a lipophilic compound having a boiling point of 100 ° C. or higher and is liquid at room temperature (b), and a hydrophilic liquid compound having a boiling point of 100 ° C. or higher (c) is used. If necessary, a mixture of a surfactant, other filler, etc. is stirred and mixed, and / or at the same time, a curing agent is mixed. As a method of mixing the above components, a method of continuously, batchwise, or simultaneously using a mixer having a stirring blade that rotates at high speed can be preferably used.

【0017】本発明のオゾン分解用フィルターにおいて
は、原料に使用する樹脂組成物の攪拌、混合直後の粘度
は通常5万cps以下の粘度となる。このような低粘度
故に攪拌時に気泡を混入せず、嵩密度等の点で均質な活
性炭素多孔体構造物を得ることができる。
In the ozonolysis filter of the present invention, the viscosity of the resin composition used as a raw material immediately after stirring and mixing is usually 50,000 cps or less. Due to such a low viscosity, bubbles can not be mixed during stirring, and a homogeneous activated carbon porous material structure can be obtained in terms of bulk density and the like.

【0018】本発明のオゾン分解用フィルターに用いる
活性炭素多孔体構造物ではこのようにして得た樹脂硬化
物をそのまま、もしくは切削して板状体とした後、非酸
化性雰囲気下で炭化して炭素多孔体とする。非酸化性雰
囲気とは、例えば、Arガス、Heガス、N2 ガス、ハ
ロゲンガス、アンモニアガス、COガス、水素ガス、あ
るいはこれらの混合ガス、水性ガス等をいう。炭化のた
めの温度は、好ましくは、500℃〜1200℃、特に
600〜900℃の範囲が好ましい。
In the activated carbon porous material structure used for the filter for ozone decomposition of the present invention, the resin cured product thus obtained is used as it is, or after being cut into a plate-like body, it is carbonized in a non-oxidizing atmosphere. To make a carbon porous body. The non-oxidizing atmosphere means, for example, Ar gas, He gas, N2 gas, halogen gas, ammonia gas, CO gas, hydrogen gas, a mixed gas thereof, a water gas or the like. The temperature for carbonization is preferably in the range of 500 ° C to 1200 ° C, particularly 600 to 900 ° C.

【0019】以上のようにして得られた炭素多孔体は、
更に賦活処理を施して活性化する。賦活工程は、炭化工
程に連続していてもよいし、炭化工程と別個の工程とし
てもよい。炭素多孔体の賦活は炭素多孔体を酸化性ガ
ス、または酸化性ガスと不活性ガスとの混合気体の雰囲
気下で加熱して行われる。加熱温度は600℃〜120
0℃、好ましくは750〜1000℃がよい。酸化性ガ
スとしては、公知の酸化性ガス、例えば、水蒸気、二酸
化炭素、酸素、空気等が用いられる。これらは通常調節
しやすいように不活性ガスN2 等と混合して用いる。
The carbon porous body obtained as described above is
Further, activation treatment is applied to activate. The activation step may be continuous with the carbonization step or may be a step separate from the carbonization step. Activation of the carbon porous body is performed by heating the carbon porous body in an atmosphere of an oxidizing gas or a mixed gas of an oxidizing gas and an inert gas. Heating temperature is 600 ° C-120
The temperature is 0 ° C, preferably 750 to 1000 ° C. As the oxidizing gas, known oxidizing gases such as water vapor, carbon dioxide, oxygen, air and the like are used. These are usually mixed with an inert gas such as N2 for easy control.

【0020】以上の方法により製造される活性炭素多孔
体は、嵩密度が好ましくは0.3g/cm3 以上、特に
0.4g/cm3 以上、0.7g/cm 3以下であり、
比表面積が700m2/g以上のものである。
The activated carbon porous body produced by the above method has a bulk density of preferably 0.3 g / cm 3 or more, particularly 0.4 g / cm 3 or more and 0.7 g / cm 3 or less,
It has a specific surface area of 700 m 2 / g or more.

【0021】本発明に係わるオゾン分解用フィルター
は、このような活性炭素多孔体を悪臭成分などを含んだ
空気の流路に配設したものである。
The ozone decomposing filter according to the present invention comprises such an activated carbon porous material arranged in a flow path of air containing a malodorous component and the like.

【0022】この活性炭素多孔体構造物の形状として
は、各種の形状が考えられ、例えば、板状、棒状、ある
いは、穴を形成した板状、ハニカム状などを挙げること
ができる。上記した本発明で用いる樹脂組成物は粘度が
低いため、このような複雑な形状であっても容易に注
型、その他の成形方法で作製することができる。
Various shapes can be considered as the shape of the activated carbon porous material structure, and examples thereof include a plate shape, a rod shape, a plate shape with holes formed therein, and a honeycomb shape. Since the above-mentioned resin composition used in the present invention has a low viscosity, even such a complicated shape can be easily produced by casting or another molding method.

【0023】本発明に係わるオゾン分解用フィルターの
主たる構成材料である活性炭素多孔体構造物は、所定の
間隔を開けて複数並べて構成されるグリッド構造として
もよい。このようなグリッド構造は、製造が容易でかつ
圧力損失が小さいため好ましく、例えば、風速が1m/
sで圧力損失が0.5mmH2O 以下といった基準に達し
得る。
The activated carbon porous material structure, which is the main constituent material of the filter for ozone decomposition according to the present invention, may have a grid structure formed by arranging a plurality of activated carbon porous material structures at predetermined intervals. Such a grid structure is preferable because it is easy to manufacture and the pressure loss is small. For example, the wind speed is 1 m / m.
The pressure loss of 0.5 mmH2O or less can be reached at s.

【0024】[0024]

【実施例】以下、実施例及び比較例により発明を更に具
体的に説明するが、本発明はその要旨を越えない限りこ
れらの実施例になんら制約されるものではない。 実施例1 {活性炭素多孔体構造物の製造}25℃における粘度が
4800cpsのレゾール型フェノール樹脂(略称レゾ
ール)100重量部に界面活性剤として、ヒマシ油のポ
リオキシエチレン2モル付加物の硫酸エステルナトリウ
ム塩5重量部、高沸点親水性化合物として、分子量が6
00のポリエチレングリコール(略称PEG)25重量
部、高沸点親油性化合物として、流動パラフィン(略称
流パラ)25重量部とを3段のピン羽根を有する攪拌器
で6000回転/分の速度で5分間充分に攪拌した。こ
の混合物の粘度は3500cpsであった。
The present invention will be described in more detail below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples unless it exceeds the gist. Example 1 {Production of activated carbon porous material structure} 100 parts by weight of a resole-type phenol resin (abbreviation: resole) having a viscosity at 25 ° C. of 4800 cps was used as a surfactant, and a sulfuric acid ester of a polyoxyethylene 2 mol adduct of castor oil was used. 5 parts by weight of sodium salt, a high boiling point hydrophilic compound having a molecular weight of 6
25 parts by weight of polyethylene glycol (abbreviated as PEG) of 00 and 25 parts by weight of liquid paraffin (abbreviated as flow para) as a high-boiling lipophilic compound are stirred for 5 minutes at a speed of 6000 rpm with a stirrer having three stages of pin blades. Stir well. The viscosity of this mixture was 3500 cps.

【0025】この混合物に硬化剤としてパラトルエンス
ルホン酸20重量部を加えて同様の攪拌速度で1分間攪
拌、混合後70℃エアーオーブン中に5分間放置後取り
出し、間隔が5mmで一方のロールに無数の円柱状突起
が形成されている間を通過させた後、更にエアーオーブ
ン中で完全に硬化させることにより重合体硬化物の多孔
板を製造した。
20 parts by weight of paratoluene sulfonic acid was added to this mixture as a curing agent, stirred at the same stirring speed for 1 minute, mixed and left in an air oven at 70 ° C. for 5 minutes and then taken out. After passing through while a myriad of cylindrical protrusions were formed, the porous plate of the polymer cured product was manufactured by further completely curing it in an air oven.

【0026】この重合体硬化物の多孔板を電気炉に入れ
てN2 雰囲気で1.5℃/分の速度で700℃まで昇温
し、同温度で1時間保持後冷却した。以上の方法で得ら
れた炭素多孔体の板を厚さ3mmのセラミックファイバ
ーボードの箱に入れ、更にこの箱を電気炉に入れてN2
雰囲気3℃/分の速度で900℃まで昇温し、ついでN
2/H2O=9/1の割合で賦活ガスを3時間導入後、冷
却して取り出した。このようにして、比表面積950m
2/g 、嵩密度0.30g/cm3 、厚さ3.5mm、
開口率45%の活性炭素多孔板Aを得た。
The porous plate of the polymer cured product was placed in an electric furnace, heated to 700 ° C. at a rate of 1.5 ° C./min in an N 2 atmosphere, kept at the same temperature for 1 hour, and then cooled. The carbon porous plate obtained by the above method was put in a ceramic fiber board box having a thickness of 3 mm, and this box was put in an electric furnace to obtain N2.
The temperature was raised to 900 ° C at a rate of 3 ° C / min, then N
The activating gas was introduced at a ratio of 2 / H2O = 9/1 for 3 hours, then cooled and taken out. In this way, the specific surface area of 950m
2 / g, bulk density 0.30 g / cm3, thickness 3.5 mm,
An activated carbon porous plate A having an opening ratio of 45% was obtained.

【0027】{フィルターの製造}上記板状活性炭素多
孔体から長さ100mm、幅100mmの板を切り出
し、プラスチックの枠体に固定し、オゾン分解用フィル
ターを製造した。
{Manufacture of Filter} A plate having a length of 100 mm and a width of 100 mm was cut out from the plate-like activated carbon porous body and fixed to a plastic frame to manufacture a filter for ozone decomposition.

【0028】{性能評価} 〔圧力損失〕67mmφの導管の一部に形成されているフ
ィルターホールダーに上記フィルター構造物をセット
し、更にこのホールダーの上下流側各々に圧力計を配設
するとともに、空気を排出する送風機を付設して、これ
らの圧力計と送風機を作動することにより上記フィルタ
ー構造物による圧力損失を下記のようにして測定した。
すなわち、上記ホールダーにフィルター構造物を装着し
た後、送風機を駆動して空気を100cm/sec の速度で
導管を通って排出し、フィルターの上流側と下流側の圧
力を測定し、圧力差を圧力損失(mmH2O) で示すこと
により圧力損失を測定した。
{Performance Evaluation} [Pressure Loss] The above filter structure is set in a filter holder formed in a part of a 67 mmφ conduit, and a pressure gauge is arranged on each of the upstream and downstream sides of the holder. A blower for discharging air was attached, and the pressure loss due to the filter structure was measured as follows by operating these pressure gauges and blowers.
That is, after mounting the filter structure on the above holder, drive the blower to discharge the air through the conduit at a speed of 100 cm / sec, measure the pressure on the upstream side and the downstream side of the filter, and measure the pressure difference. The pressure loss was measured by indicating the loss (mmH2O).

【0029】〔オゾン分解性能〕上記導管の上流部にオ
ゾン発生機を取り付ける。送風機を作動させて系内の空
気を50cm/sの速度で排出しつつ導管内のオゾン濃
度が10ppm になるよう調節する。次に、フィルターを
フィルターホールダーに取り付け、直ちに再び送風機を
作動させる。10分経過後のチャンバー内のオゾンの濃
度をガス検知管により求めた。また、試験開始1時間後
に試験を終了し、試験後のフィルターの重量残存率を測
定した。以上の測定結果を表.1に示す。
[Ozone Decomposing Performance] An ozone generator is attached upstream of the above conduit. Operate the blower to discharge the air in the system at a speed of 50 cm / s and adjust the ozone concentration in the conduit to 10 ppm. Then attach the filter to the filter holder and immediately restart the blower. The concentration of ozone in the chamber after 10 minutes was measured by a gas detector tube. The test was terminated 1 hour after the test was started, and the weight residual ratio of the filter after the test was measured. The above measurement results are shown in the table. Shown in 1.

【0030】実施例2 実施例1のフィルター構造物において、穴径を調節して
開口率を60%にする以外は実施例1と同様にして、性
能評価を行った。結果を表.1に示す。
Example 2 In the filter structure of Example 1, the performance evaluation was performed in the same manner as in Example 1 except that the aperture ratio was adjusted to 60%. The results are shown in the table. Shown in 1.

【0031】実施例3 実施例1で用いた原料樹脂組成物の代わりに、実施例1
で用いたレゾール100重量部、ヒマシ油のポリオキシ
エチレン2モル付加物の硫酸エステルナトリウム塩5重
量部、、分子量が600のPEG25重量部、流動パラ
25重量部、及びメソフェーズピッチ粉50重量部とか
らなる組成物を用いる以外は、実施例1と同様に行い、
活性炭素多孔板Bを得た。この活性炭素多孔板から実施
例1と同様にしてオゾン分解用フィルターを作製し、同
様にしてフィルターの性能を評価した。結果を表.1に
示す。
Example 3 Instead of the raw resin composition used in Example 1, Example 1 was used.
100 parts by weight of the resole used in Example 5, 5 parts by weight of sodium sulfate of a polyoxyethylene 2 mol adduct of castor oil, 25 parts by weight of PEG having a molecular weight of 600, 25 parts by weight of liquid para, and 50 parts by weight of mesophase pitch powder. Example 1 was repeated except that the composition consisting of
Activated carbon porous plate B was obtained. A filter for ozone decomposition was produced from this activated carbon porous plate in the same manner as in Example 1, and the performance of the filter was evaluated in the same manner. The results are shown in the table. Shown in 1.

【0032】比較例1 コピー機用オゾン分解用フィルターとして市販されてい
る、ハニカム活性炭フィルターの性能を実施例1と同様
にして評価した。結果を表.1に示する
Comparative Example 1 The performance of a honeycomb activated carbon filter, which is commercially available as an ozone decomposition filter for a copying machine, was evaluated in the same manner as in Example 1. The results are shown in the table. Shown in 1

【0033】比較例2 実施例1で用いた原料樹脂組成物の代わりに、実施例1
で用いたレゾール100重量部、硬化剤としてパラトル
エンスルホン酸10重量部、及び発泡剤としてフロン1
23b 2重量部とからなる組成物を原料として攪拌し
た組成物を木型内に注入し、その木型を80℃エアーオ
ーブン中に1時間放置して、発泡成形させ、硬化後にブ
ロック状硬化物を切断して厚さ7mmの板にする以外は
実施例1と同様に行い、活性炭素多孔板Cを得た。この
活性炭素多孔板から実施例1と同様の形状のオゾン分解
用フィルターを作り、その性能を評価した。結果を表.
1に示す。
Comparative Example 2 Instead of the raw material resin composition used in Example 1, Example 1 was used.
100 parts by weight of the resol used in step 1, 10 parts by weight of paratoluene sulfonic acid as a curing agent, and CFC 1 as a blowing agent.
23b 2 parts by weight of the composition as a raw material was stirred and poured into a wooden mold, and the wooden mold was left in an air oven at 80 ° C. for 1 hour to be foam-molded. After curing, a block-shaped cured product was obtained. Was cut in the same manner as in Example 1 except that a plate having a thickness of 7 mm was obtained to obtain an activated carbon porous plate C. A filter for ozone decomposition having the same shape as in Example 1 was made from this activated carbon porous plate, and its performance was evaluated. The results are shown in the table.
Shown in 1.

【0034】[0034]

【表1】 [Table 1]

【0035】[0035]

【発明の効果】本発明のオゾン分解用フィルターは、原
料樹脂組成物としてレゾール/親油性化合物/親水性化
合物からなる組成物用いることにより、流動性が優れた
組成物が得られるため、薄肉の樹脂シートが成形でき、
従って厚さ1mm程度の薄肉や様々な形状とすることが
できる。従って、従来より厚さの薄いフィルターである
ことができる。また、本発明のオゾン分解用フィルター
は、本発明で用いる活性炭素多孔体の嵩比重が高いた
め、分解性能及び長期寿命に優れる。また、主たる構成
材料の活性炭素多孔体の強度が大きいため、強度上の問
題を生じない。以上の点から本発明のオゾン分解用フィ
ルターは従来のものに比べよりコンパクトになり、ファ
クシミリ、コピー機等において場所をとらないという利
点を有する。
INDUSTRIAL APPLICABILITY The filter for ozonolysis of the present invention uses a composition comprising resol / lipophilic compound / hydrophilic compound as a raw material resin composition, whereby a composition having excellent fluidity can be obtained. Resin sheet can be molded,
Therefore, it can be formed into a thin wall having a thickness of about 1 mm and various shapes. Therefore, the filter can be thinner than before. In addition, the filter for ozone decomposition of the present invention is excellent in decomposition performance and long life because the activated carbon porous material used in the present invention has a high bulk specific gravity. In addition, since the activated carbon porous body, which is the main constituent material, has a large strength, no strength problem occurs. From the above points, the ozone decomposing filter of the present invention is more compact than the conventional one, and has an advantage that it does not take up a space in a facsimile, a copying machine or the like.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 レゾール型フェノール樹脂(a) 100重
量部、親油性で100℃以上の沸点を有する常温で液状
の化合物(b) 1ないし100重量部、親水性で100℃
以上の沸点を有する液状の化合物(c) 1ないし100重
量部とからなる組成物の硬化物を炭化、賦活して得た活
性炭素多孔体構造物が空気の通路に配設されていること
を特徴とするオゾン分解用フィルター。
1. Resol type phenolic resin (a) 100 parts by weight, lipophilic compound (b) 1 to 100 parts by weight which is liquid at room temperature and has a boiling point of 100 ° C. or more, hydrophilic 100 ° C.
The activated carbon porous structure obtained by carbonizing and activating the cured product of the composition comprising 1 to 100 parts by weight of the liquid compound (c) having the above boiling point is disposed in the air passage. Characteristic ozone decomposition filter.
JP3196895A 1991-08-06 1991-08-06 Filter for decomposing ozone Pending JPH0538415A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3196895A JPH0538415A (en) 1991-08-06 1991-08-06 Filter for decomposing ozone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3196895A JPH0538415A (en) 1991-08-06 1991-08-06 Filter for decomposing ozone

Publications (1)

Publication Number Publication Date
JPH0538415A true JPH0538415A (en) 1993-02-19

Family

ID=16365439

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3196895A Pending JPH0538415A (en) 1991-08-06 1991-08-06 Filter for decomposing ozone

Country Status (1)

Country Link
JP (1) JPH0538415A (en)

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