JPH0716465A - Deodorizing member - Google Patents

Deodorizing member

Info

Publication number
JPH0716465A
JPH0716465A JP5164875A JP16487593A JPH0716465A JP H0716465 A JPH0716465 A JP H0716465A JP 5164875 A JP5164875 A JP 5164875A JP 16487593 A JP16487593 A JP 16487593A JP H0716465 A JPH0716465 A JP H0716465A
Authority
JP
Japan
Prior art keywords
activated carbon
deodorizing
deodorizing member
weight
gas
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
JP5164875A
Other languages
Japanese (ja)
Inventor
Tatsuo Ando
達男 安藤
Kiyoshi Arai
喜代志 荒井
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel 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 Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP5164875A priority Critical patent/JPH0716465A/en
Publication of JPH0716465A publication Critical patent/JPH0716465A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a deodorizing member capable of efficiently reducing the concn. of gaseous malodorous components to be removed, capable of preventing secondary emission of a malodor and excellent in the rate of deodorization and durability. CONSTITUTION:This deodorizing member contains 10-70wt.% manganese dioxide, 25-85wt.% activated carbon and/or activated carbon fibers and 3-20wt.% one or more kinds of oxides selected from among oxides of Cu, Fe, Ni, Co, V, Pt and Au. It is obtd. by firing in the temp. range of 200-350 deg.C in the final working process.

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、悪臭の原因となる悪臭
成分ガスを分解し、又は改質することにより脱臭する脱
臭部材に関し、特に、高活性触媒物質と活性炭又は活性
炭繊維を必須構成要素として、脱臭部材からの二次的な
悪臭の発生を伴うことなく優れた脱臭性能を発揮する脱
臭部材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a deodorizing member that deodorizes by decomposing or modifying a malodorous component gas that causes a malodor, and in particular, a highly active catalyst substance and activated carbon or activated carbon fiber are essential constituent elements. As a result, the present invention relates to a deodorizing member that exhibits excellent deodorizing performance without generating a secondary malodor from the deodorizing member.

【0002】[0002]

【従来の技術】従来のこの種の脱臭部材は、各種担持体
の表面に活性炭、金属酸化物若しくは貴金属等の触媒作
用を有する物質を担持したり、又はそれらの物質を各種
バインダーと共に混練し、成形した後、乾燥することに
より製造されている。このように構成される従来の脱臭
部材は、脱臭の対象となる悪臭成分ガス濃度の低減に
は、所望の効果を発揮している。
2. Description of the Related Art Conventional deodorizing members of this type carry various substances having a catalytic action such as activated carbon, metal oxides or noble metals on the surface of various carriers, or knead these substances with various binders, It is manufactured by molding and then drying. The conventional deodorizing member thus configured exerts a desired effect in reducing the concentration of the malodorous component gas to be deodorized.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、これら
の従来の脱臭部材は、脱臭部材を悪臭成分ガス中に位置
させて、その悪臭ガス成分を吸着又は分解により脱臭す
る脱臭作用中に、別のガス成分が副次的に生成してしま
うという難点がある。そして、この副次的に生成するガ
ス成分が新たな悪臭原因となったり、副次的に生成する
悪臭ガス及び元来大気中に含まれている微量悪臭成分が
脱臭部材中に蓄積したり、脱臭部材中に含まれる有機物
が変質したりすることによって、結果的に従来の脱臭部
材は脱臭効果が十分に発揮できず、耐久性が悪いという
問題点がある。
However, these conventional deodorizing members are arranged so that the deodorizing member is placed in the malodorous component gas and another gas is deodorized during the deodorizing action by adsorbing or decomposing the malodorous gas component. There is a drawback that components are generated secondarily. Then, this secondary gas component causes a new malodor, or secondary malodor gas and a trace amount of malodor component originally contained in the atmosphere accumulate in the deodorizing member, As a result, the organic substances contained in the deodorizing member may be deteriorated, and as a result, the conventional deodorizing member cannot sufficiently exert the deodorizing effect, resulting in poor durability.

【0004】本発明はかかる問題点に鑑みてなされたも
のであって、脱臭すべき悪臭成分ガスの濃度を高効率で
低減することができると共に、副次的な悪臭の発生を防
止することができ、悪臭除去率及び耐久性が優れた脱臭
部材を提供することを目的とする。
The present invention has been made in view of such problems, and it is possible to reduce the concentration of the malodorous component gas to be deodorized with high efficiency and prevent the generation of secondary malodors. It is an object of the present invention to provide a deodorizing member that can be manufactured and has excellent malodor removal rate and excellent durability.

【0005】[0005]

【課題を解決するための手段】本発明に係る脱臭部材
は、主要成分として、二酸化マンガンを10乃至70重
量%、活性炭及び/又は活性炭繊維を25乃至85重量
%含有し、微量添加成分として、銅、鉄、ニッケル、コ
バルト、バナジウム、白金及び金の各酸化物からなる群
から選択された少なくとも1種以上の酸化物を3乃至2
0重量%含有することを特徴とする。
The deodorizing member according to the present invention contains 10 to 70% by weight of manganese dioxide and 25 to 85% by weight of activated carbon and / or activated carbon fiber as main components, and as a minor addition component, 3 to 2 of at least one oxide selected from the group consisting of oxides of copper, iron, nickel, cobalt, vanadium, platinum and gold.
It is characterized by containing 0% by weight.

【0006】また、この脱臭部材は、最終加工工程で2
00乃至350℃の温度域で焼成されたものであること
が好ましい。
Further, this deodorizing member has two steps in the final processing step.
It is preferably baked in a temperature range of 00 to 350 ° C.

【0007】[0007]

【作用】本発明においては、二酸化マンガンという高活
性触媒物質によって悪臭成分ガスの分解・改質を高反応
速度で行う。一方、副次的に生成し悪臭源となるガス成
分は活性炭又は活性炭繊維によって捕捉する。副次的に
生成したガス成分は脱臭速度が遅いため、これを活性炭
又は活性炭繊維に捕捉することにより、高活性触媒物質
との十分な接触時間を与える。これにより、この副次的
に発生した悪臭成分ガスは、無臭物質に変換され、優れ
た脱臭効果が得られる。
In the present invention, the malodorous component gas is decomposed and reformed at a high reaction rate by using a highly active catalytic substance called manganese dioxide. On the other hand, the gas component that is secondarily generated and becomes a malodor source is captured by activated carbon or activated carbon fiber. Since the gas component generated as a by-product has a slow deodorization rate, it is trapped on activated carbon or activated carbon fiber to provide sufficient contact time with the highly active catalyst substance. As a result, the offensive odor component gas generated as a result is converted into an odorless substance, and an excellent deodorizing effect is obtained.

【0008】更に、脱臭部材の製造過程の最終工程で、
200℃から350℃の温度域で焼成工程を行うことに
より、触媒物質の高活性化を行うと共に、脱臭部材内の
有機物を除去し、脱臭部材全体を無機化する。これによ
り、脱臭効率を向上すると共に、脱臭部材の変質と、大
気中の微量悪臭物質の蓄積を抑制した。焼成温度が35
0℃を超えると、一部の酸化物が変質し、性能が劣化す
る傾向にある。
Furthermore, in the final step of the manufacturing process of the deodorizing member,
By performing the calcination process in the temperature range of 200 ° C. to 350 ° C., the catalyst substance is highly activated, the organic substances in the deodorizing member are removed, and the entire deodorizing member is made inorganic. As a result, the deodorizing efficiency was improved and the deterioration of the deodorizing member and the accumulation of a trace amount of malodorous substances in the atmosphere were suppressed. Firing temperature is 35
If the temperature exceeds 0 ° C, some oxides will deteriorate and the performance tends to deteriorate.

【0009】触媒利用による悪臭の分解脱臭において
は、触媒の時間的な処理能力を超える条件のもとでは、
触媒反応速度が追いつかなくなり、必然的に未処理の悪
臭成分が脱臭部材から排出され、脱臭効果が上がらな
い。また、脱臭対象となるガス成分が触媒成分によって
別の悪臭成分ガスに変換し、この新たに生成したガス成
分の無臭化に長時間を要すると、脱臭効果が上がらな
い。
In the decomposition and deodorization of a bad odor by utilizing a catalyst, under the condition that the treatment capacity of the catalyst is exceeded,
The catalytic reaction rate cannot catch up, and untreated malodorous components are inevitably discharged from the deodorizing member, and the deodorizing effect does not improve. Further, if the gas component to be deodorized is converted into another malodorous component gas by the catalyst component and it takes a long time to deodorize the newly generated gas component, the deodorizing effect is not enhanced.

【0010】しかしながら、本発明の脱臭部材によれ
ば、時間的処理能力を超える副次生成悪臭成分について
は、物理吸着能が優れた活性炭又は活性炭繊維によりこ
の副次生成悪臭成分を捕捉し、悪臭を発生させることが
ない。そして、この活性炭又は活性炭繊維に吸着した悪
臭成分は触媒反応によって分解されるまで活性炭又は活
性炭繊維に吸着保持することができる。これによって触
媒反応速度が追いつかない場合でも、脱臭効果の低下を
防ぐことができる。
However, according to the deodorizing member of the present invention, with respect to the offensive odor component produced by the secondary treatment which exceeds the processing capacity over time, the offensive odor component produced by the secondary reaction is captured by activated carbon or activated carbon fiber having an excellent physical adsorption ability. Does not occur. The malodorous component adsorbed on the activated carbon or the activated carbon fiber can be adsorbed and retained on the activated carbon or the activated carbon fiber until it is decomposed by the catalytic reaction. This makes it possible to prevent the deodorizing effect from decreasing even if the catalytic reaction rate cannot catch up.

【0011】脱臭部材に含まれる有機物は長時間の使用
により、大気中の水、酸素及び微生物等によって、腐敗
し、変質し、それ自体悪臭源となる。また、水を含んだ
有機物は大気中の微量悪臭物質を吸着し易くなり、脱臭
部材が悪臭源となる傾向を強める。そこで、脱臭部材の
製造過程の最終工程で200℃から350℃の温度域で
焼成することにより、脱臭部材内の有機物を炭化し、脱
臭部材全体を無機化する。更に、焼成温度を200℃か
ら350℃に設定することにより、触媒物質の高活性化
を、活性炭又は活性炭繊維の機能劣化を生じることなく
実現することができる。焼成時間は2時間以上8時間以
下が適当である。焼成時間が2時間未満であると、有機
物が十分に炭化せず、脱臭部材を無機化できない。ま
た、焼成時間が8時間あれば、十分無機化を完了するこ
とが可能であり、8時間を超える焼成は加工コストの増
大をもたらし、実用的ではない。
The organic substances contained in the deodorizing member are decomposed and deteriorated by water, oxygen, microorganisms and the like in the atmosphere after being used for a long time, and become an odor source itself. In addition, organic substances containing water are more likely to adsorb a trace amount of malodorous substances in the atmosphere, and the deodorizing member becomes more likely to become a source of malodorous substances. Therefore, by firing in the temperature range of 200 ° C. to 350 ° C. in the final step of the manufacturing process of the deodorizing member, the organic substances in the deodorizing member are carbonized and the entire deodorizing member is made inorganic. Furthermore, by setting the calcination temperature to 200 ° C. to 350 ° C., high activation of the catalyst substance can be realized without causing functional deterioration of the activated carbon or activated carbon fiber. A firing time of 2 hours or more and 8 hours or less is suitable. If the firing time is less than 2 hours, the organic substances are not sufficiently carbonized and the deodorizing member cannot be made inorganic. Further, if the firing time is 8 hours, it is possible to sufficiently complete the mineralization, and firing for more than 8 hours causes an increase in processing cost and is not practical.

【0012】また、本発明においては、銅、鉄、ニッケ
ル、コバルト、バナジウム、白金及び金の各酸化物から
なる群から選択された少なくとも一種以上の酸化物を3
乃至20重量%含有する。これらの各酸化物はいずれも
二酸化マンガンと共存させることによって、脱臭部材と
しての処理能力を向上させる。しかし、これらの酸化物
はその含有量が10重量%を超えたところから、その添
加効果が少なくなり、20重量%を超えて含有しても処
理能力の向上は認められない。このため、これらの酸化
物の添加量は総量で3乃至20重量%であり、好ましく
は3乃至10重量%である。
Further, in the present invention, at least one oxide selected from the group consisting of copper, iron, nickel, cobalt, vanadium, platinum and gold oxides is used.
To 20% by weight. By making each of these oxides coexist with manganese dioxide, the processing ability as a deodorizing member is improved. However, since the content of these oxides exceeds 10% by weight, the effect of addition becomes small, and even if the content of these oxides exceeds 20% by weight, no improvement in treatment capacity is observed. Therefore, the total amount of these oxides added is 3 to 20% by weight, preferably 3 to 10% by weight.

【0013】二酸化マンガンは、高活性触媒物質として
の作用を有するためには、10乃至70重量%含有する
必要があり、好ましくは15乃至40重量%とする。
Manganese dioxide must be contained in an amount of 10 to 70% by weight, preferably 15 to 40% by weight, in order to function as a highly active catalyst substance.

【0014】また、活性炭及び活性炭繊維は、夫々単独
で含有しても良いし、同時に含有しても良い。この活性
炭及び活性炭繊維の含有量は、十分な吸着作用を得るた
めに、総量で25乃至85重量%、好ましい範囲は40
乃至85重量%にする。
The activated carbon and the activated carbon fiber may be contained individually or simultaneously. The content of the activated carbon and the activated carbon fiber is 25 to 85% by weight in order to obtain a sufficient adsorption action, and the preferable range is 40.
To 85% by weight.

【0015】なお、活性炭及び/又は活性炭繊維の含有
量と、二酸化マンガンの含有量との比R1を1.2乃至
4.5とすることにより両者の作用をより効果的に発揮
させることができる。
By setting the ratio R 1 of the content of activated carbon and / or activated carbon fiber to the content of manganese dioxide to 1.2 to 4.5, both effects can be exhibited more effectively. it can.

【0016】また、二酸化マンガンの含有量と、銅、ニ
ッケル、コバルト、バナジウム、白金及び金の各酸化物
からなる群から選択された少なくとも1種以上の酸化物
の含有量との比R2を2.0乃至6.0とすることによ
り、処理能力を更に向上させることができる。
Further, the ratio R 2 of the content of manganese dioxide and the content of at least one oxide selected from the group consisting of oxides of copper, nickel, cobalt, vanadium, platinum and gold is set to R 2 . By setting 2.0 to 6.0, the processing capacity can be further improved.

【0017】この脱臭部材の成形方法は、押出加工によ
ればよく、この押出加工により、ハニカム成形体、ペレ
ット状成形体、抄紙状成形体又はコルゲート成形体な
ど、種々の形状に成形することができる。また、特に成
形せずに、混合粉体として反応容器内に充填しても効果
がある。
The deodorizing member may be molded by extrusion, and the extrusion can be formed into various shapes such as a honeycomb molded body, a pellet-shaped molded body, a paper-shaped molded body or a corrugated molded body. it can. Further, it is also effective to fill the inside of the reaction vessel as a mixed powder without particularly molding.

【0018】一方、成形加工に必要な各種の有機系又は
無機系バインダー、活性炭及び金属酸化物を効率よく保
持するパルプ等の有機系繊維類、ガラス等の無機系繊維
類、及びコージュライト又はセピオライト等の鉱物系資
材は極力少量とすることが、単位容積当たりの脱臭性能
を高めるためには望ましく、特許請求の範囲に規定した
必須構成成分の総含有量の3乃至55重量%とすること
が好ましい。このバインダの添加量が55重量%を上回
ると、処理対象の悪臭ガス量に対して、投入すべき脱臭
部材の最低必要量が増加してしまい、ハンドリング上不
利となる。
On the other hand, various organic or inorganic binders required for molding, organic fibers such as pulp that efficiently retains activated carbon and metal oxides, inorganic fibers such as glass, and cordierite or sepiolite. It is desirable to minimize the amount of the mineral-based materials such as, for improving the deodorizing performance per unit volume, and the content is 3 to 55% by weight of the total content of the essential constituents defined in the claims. preferable. If the added amount of the binder exceeds 55% by weight, the minimum required amount of the deodorizing member to be added increases with respect to the amount of the malodorous gas to be treated, which is disadvantageous in handling.

【0019】[0019]

【実施例】以下、本発明をメチルメルカプタンの脱臭に
適用した実施例について説明する。本発明の実施例の脱
臭部材の加工方法の一例として、ハニカム成形した脱臭
部材を脱臭試験に供した。この脱臭部材は、脱臭部材の
全重量に対して二酸化マンガンを22%、活性炭を55
%、酸化銅をCuO換算で8%、セルロース系有機バイ
ンダーを3%、粘土鉱物系無機バインダーを17%配合
したものであり、これらの成分を混練し、押出しハニカ
ム成型し、乾燥後、300℃で3時間の焼成を行った
(サンプル1)。また、比較例として、脱臭部材全重量
に対して二酸化マンガンを80%、セルロース系有機バ
インダーを3%、粘土鉱物系無機バインダーを17%配
合したもの(サンプル2)と、活性炭を80%、セルロ
ース系有機バインダーを3%、粘土鉱物無機バインダー
を17%配合したもの(サンプル3)を同様の方法で成
形し、その後焼成した。これらのサンプル1乃至3の性
能評価を行った。
EXAMPLES Examples in which the present invention is applied to deodorization of methyl mercaptan will be described below. As an example of a method for processing the deodorizing member of the example of the present invention, a honeycomb-molded deodorizing member was subjected to a deodorizing test. This deodorizing member contains 22% of manganese dioxide and 55% of activated carbon based on the total weight of the deodorizing member.
%, Copper oxide 8% in terms of CuO, cellulosic organic binder 3%, clay mineral inorganic binder 17%. These components are kneaded, extruded into honeycomb, and dried at 300 ° C. Was fired for 3 hours (Sample 1). As a comparative example, 80% of activated carbon and 80% of activated carbon and cellulose were mixed with 80% of manganese dioxide, 3% of a cellulose-based organic binder and 17% of a clay mineral-based inorganic binder with respect to the total weight of the deodorizing member. A mixture containing 3% of a system organic binder and 17% of a clay mineral inorganic binder (Sample 3) was molded by the same method, and then fired. The performance of these samples 1 to 3 was evaluated.

【0020】この性能試験方法は図3に示すようにして
行った。即ち、サンプル1乃至3の脱臭部材を測定治具
2に装着した。そして、この測定治具2に、常温及び常
湿で悪臭ガス(メチルメルカプタン)を流し、所定の時
間毎に測定治具2の入り口側のA点及び出口側のB点に
てガスを採取し、採取したガスの濃度をガスクロマトグ
ラフィー法により分析し、A点とB点との濃度差から脱
臭部材の吸着能を求めた。但し、入り口濃度は5pp
m、ガス流速は1リットル/分である。また、悪臭物質吸着
能の測定値は20分経過後の除去率である。
This performance test method was performed as shown in FIG. That is, the deodorizing members of Samples 1 to 3 were attached to the measuring jig 2. Then, a malodorous gas (methyl mercaptan) is caused to flow into the measuring jig 2 at room temperature and normal humidity, and the gas is sampled at a point A on the inlet side and a point B on the outlet side of the measuring jig 2 every predetermined time. The concentration of the collected gas was analyzed by a gas chromatography method, and the adsorption capacity of the deodorizing member was determined from the difference in concentration between points A and B. However, the entrance concentration is 5pp
m, the gas flow rate is 1 liter / min. The measured value of the malodorous substance adsorption capacity is the removal rate after 20 minutes have elapsed.

【0021】図1はこれらのサンプル1〜3のメチルメ
ルカプタンの脱臭性能の試験結果を示すグラフ図であ
る。また、図2は出口側で検出されたジメチルジサルフ
ァイドの濃度を示すグラフ図である。図1から明らかな
ように、本発明の実施例に係るサンプル1及び比較例の
サンプル2のメチルメルカプタン除去率が100%であ
るのに対し、比較例のサンプル3は時間の経過と共に、
除去率が低下している。また、図2に示すように、比較
例のサンプル3においては、脱臭部材の脱臭過程で生成
するジメチルジサルファイドが1〜2ppm存在するの
に対し、本発明の実施例に係るサンプル1及び比較例2
の場合にはジメチルジサルファイドの濃度は0ppmで
ある。このように、本発明の実施例に係るサンプル1に
おいては、悪臭成分の除去率が高いと共に、副次的に発
生する悪臭ガスも存在せず、総合的に本実施例の脱臭部
材は脱臭性能が高いことがわかる。
FIG. 1 is a graph showing the test results of the deodorizing performance of these methyl mercaptans of Samples 1 to 3. 2 is a graph showing the concentration of dimethyldisulfide detected on the outlet side. As is clear from FIG. 1, the methyl mercaptan removal rate of sample 1 according to the example of the present invention and sample 2 of the comparative example is 100%, whereas sample 3 of the comparative example,
The removal rate is decreasing. Further, as shown in FIG. 2, in the sample 3 of the comparative example, dimethyldisulfide produced in the deodorizing process of the deodorizing member is present in an amount of 1 to 2 ppm, whereas the sample 1 according to the example of the present invention and the comparative example. Two
In this case, the concentration of dimethyl disulfide is 0 ppm. As described above, in Sample 1 according to the example of the present invention, the removal rate of the malodorous component is high, and the malodorous gas that is generated secondarily does not exist. It turns out that is high.

【0022】なお、他の加工方法によって製造された脱
臭部材も上記実施例と同様の効果が得られ、また本発明
の実施例の脱臭部材は、メチルメルカプタン以外の種々
の悪臭成分ガス及び混合悪臭成分ガスに対しても優れた
脱臭効果を表す。
A deodorizing member manufactured by another processing method can obtain the same effect as that of the above-mentioned embodiment, and the deodorizing member of the embodiment of the present invention can produce various malodorous component gases and mixed malodors other than methyl mercaptan. It also has an excellent deodorizing effect on component gases.

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

【図1】メチルメルカプタンの除去率の経時変化を示す
グラフ図である。
FIG. 1 is a graph showing the change over time in the removal rate of methyl mercaptan.

【図2】副次的に発生したジメチルジサルファイドの濃
度の経時変化を示す図である。
FIG. 2 is a diagram showing a time-dependent change in the concentration of dimethyldisulfide generated as a by-product.

【図3】脱臭性能試験方法を示す模式図である。FIG. 3 is a schematic diagram showing a deodorizing performance test method.

【符号の説明】[Explanation of symbols]

2;測定治具 A;入口 B;出口 2; Measuring jig A; Inlet B; Outlet

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B01D 53/81 53/86 ZAB B01J 23/34 ZAB A 8017−4G 23/64 ZAB 8017−4G 23/656 23/84 ZAB 8017−4G B01D 53/36 ZAB H 8017−4G B01J 23/64 104 A ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location B01D 53/81 53/86 ZAB B01J 23/34 ZAB A 8017-4G 23/64 ZAB 8017-4G 23 / 656 23/84 ZAB 8017-4G B01D 53/36 ZAB H 8017-4G B01J 23/64 104 A

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 二酸化マンガンを10乃至70重量%、
活性炭及び/又は活性炭繊維を25乃至85重量%、
銅、鉄、ニッケル、コバルト、バナジウム、白金及び金
の各酸化物からなる群から選択された少なくとも1種以
上の酸化物を3乃至20重量%含有することを特徴とす
る脱臭部材。
1. Manganese dioxide in an amount of 10 to 70% by weight,
25 to 85% by weight of activated carbon and / or activated carbon fiber,
A deodorizing member containing 3 to 20% by weight of at least one oxide selected from the group consisting of oxides of copper, iron, nickel, cobalt, vanadium, platinum and gold.
【請求項2】 最終加工工程で200乃至350℃の温
度域で焼成されたものであることを特徴とする請求項1
に記載の脱臭部材。
2. The final processing step is performed by firing in a temperature range of 200 to 350 ° C.
The deodorizing member described in.
JP5164875A 1993-07-02 1993-07-02 Deodorizing member Pending JPH0716465A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5164875A JPH0716465A (en) 1993-07-02 1993-07-02 Deodorizing member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5164875A JPH0716465A (en) 1993-07-02 1993-07-02 Deodorizing member

Publications (1)

Publication Number Publication Date
JPH0716465A true JPH0716465A (en) 1995-01-20

Family

ID=15801582

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5164875A Pending JPH0716465A (en) 1993-07-02 1993-07-02 Deodorizing member

Country Status (1)

Country Link
JP (1) JPH0716465A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0761239A1 (en) * 1995-03-23 1997-03-12 Toto Ltd. Deodorizing method, deodorant, process for the preparation of deodorant, and deodorizing equipment
KR100457699B1 (en) * 2001-10-09 2004-11-18 (주)대동 에이씨 Deodorant and method for making the same using multiporous adsorbent
JP2006271966A (en) * 2005-03-29 2006-10-12 Kocat Inc Chemical filter using metal compounds and manufacturing method thereof
JP2016179127A (en) * 2015-03-25 2016-10-13 株式会社 日本リモナイト Deodorant, and production method of deodorant

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0761239A1 (en) * 1995-03-23 1997-03-12 Toto Ltd. Deodorizing method, deodorant, process for the preparation of deodorant, and deodorizing equipment
EP0761239A4 (en) * 1995-03-23 1998-07-08 Toto Ltd Deodorizing method, deodorant, process for the preparation of deodorant, and deodorizing equipment
US6010666A (en) * 1995-03-23 2000-01-04 Toto, Ltd. Deodorizing method, deodorizer, method of manufacturing deodorizer, and deodorizing apparatus
US6207106B1 (en) 1995-03-23 2001-03-27 Toto, Ltd. Room temperature deodorizing method based on a polymerization reaction, an oxidation reaction and adsorption
KR100457699B1 (en) * 2001-10-09 2004-11-18 (주)대동 에이씨 Deodorant and method for making the same using multiporous adsorbent
JP2006271966A (en) * 2005-03-29 2006-10-12 Kocat Inc Chemical filter using metal compounds and manufacturing method thereof
JP2016179127A (en) * 2015-03-25 2016-10-13 株式会社 日本リモナイト Deodorant, and production method of deodorant

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