JPH08281113A - Deodorant - Google Patents

Deodorant

Info

Publication number
JPH08281113A
JPH08281113A JP7109996A JP10999695A JPH08281113A JP H08281113 A JPH08281113 A JP H08281113A JP 7109996 A JP7109996 A JP 7109996A JP 10999695 A JP10999695 A JP 10999695A JP H08281113 A JPH08281113 A JP H08281113A
Authority
JP
Japan
Prior art keywords
deodorant
adsorption carrier
transition element
additive
copper
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.)
Granted
Application number
JP7109996A
Other languages
Japanese (ja)
Other versions
JP3358382B2 (en
Inventor
Kazuhiro Fukumoto
和広 福本
Shigeru Sasaki
慈 佐々木
Mitsumasa Horii
満正 堀井
Seiji Onoda
誠次 小野田
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.)
Toyota Central R&D Labs Inc
Original Assignee
Toyota Central R&D Labs Inc
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 Toyota Central R&D Labs Inc filed Critical Toyota Central R&D Labs Inc
Priority to JP10999695A priority Critical patent/JP3358382B2/en
Publication of JPH08281113A publication Critical patent/JPH08281113A/en
Application granted granted Critical
Publication of JP3358382B2 publication Critical patent/JP3358382B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE: To provide a deodorant capable of displaying excellent deodorization performance in the actual use environment. CONSTITUTION: This deodorant is constituted by carrying both a first additive consisting of either or both of a transition element or a transition element compound and a second additive consisting of at least one kinds of halogen or halide on an adsorption carrier. The transition element is copper or the like. The transition element compound is a copper compound such as copper nitrate. Halogen is bromine or iodine. The halide is KBr or HI3 I2 O5 or the like. The adsorption carrier is desirably active carbon, a hydrated magnesium silicate based clay mineral, silica gel, zeolite or activated alumina. The first additive is desirably carried at 0.5-30 pts.wt. based on 100 pts.wt. adsorption carrier. The second additive is desirably carried at 0.1-60 pts.wt. based on 100 pts.wt. adsorption carrier.

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,トリメチルアミン,メ
チルメルカプタン,硫化水素等の臭気成分を除去するこ
とができる脱臭剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a deodorizing agent capable of removing odorous components such as trimethylamine, methyl mercaptan, hydrogen sulfide and the like.

【0002】[0002]

【従来技術】トイレ,冷蔵庫等の室内における気体中に
は,アミン系の含窒素化合物,硫化水素,メチルメルカ
プタン等の含硫黄化合物等の種々の臭気成分が含まれて
いる。これらの臭気成分は,人間に不快感を与えるた
め,脱臭剤により除去することが求められている。上記
脱臭剤としては,従来,例えば,多孔質で,比表面積が
大きい活性炭が用いられている。
2. Description of the Related Art Various odorous components such as amine-based nitrogen-containing compounds, hydrogen sulfide, and sulfur-containing compounds such as methyl mercaptan are contained in the gas in the room such as toilets and refrigerators. These odorous components are uncomfortable for humans, and thus it is required to remove them with a deodorant. As the deodorant, conventionally, for example, activated carbon that is porous and has a large specific surface area has been used.

【0003】[0003]

【解決しようとする課題】しかしながら,上記の活性炭
だけでは,あらゆる臭気成分を十分に脱臭することはで
きない。そこで,従来,活性炭に添着剤を添着させて,
脱臭性能をより高めることが提案されている(特開平2
─180633号公報,特公平1─42744号公報,
特公昭60─57888号公報,特公昭55─2073
2号公報)。
[Problems to be Solved] However, all the odorous components cannot be sufficiently deodorized by the above-mentioned activated carbon alone. Therefore, conventionally, by impregnating activated carbon with an adhesive,
It has been proposed to further improve the deodorizing performance (Japanese Patent Laid-Open No. HEI-2)
─180633, Japanese Examined Patent Publication No. 1-24744,
Japanese Patent Publication No. 60-57888, Japanese Patent Publication No. 55-2073
No. 2).

【0004】しかし,上記の添着活性炭は,いずれも十
分な脱臭性能を発揮し難いものである。特に,低濃度の
臭気成分が存在する実際の使用環境の下では,その性能
を十分に発揮することができない。
However, all of the above-mentioned impregnated activated carbons are difficult to exert sufficient deodorizing performance. In particular, in an actual use environment in which a low concentration of odorous components is present, the performance cannot be sufficiently exhibited.

【0005】本発明はかかる従来の問題点に鑑み,実使
用環境下において優れた脱臭性能を発揮することができ
る脱臭剤を提供しようとするものである。
In view of the above conventional problems, the present invention aims to provide a deodorant capable of exhibiting excellent deodorizing performance in an actual use environment.

【0006】[0006]

【課題の解決手段】本発明は,吸着担体に,遷移元素或
いは遷移元素化合物の一方又は双方よりなる第1添加
物,及びハロゲン又はハロゲン化合物の1種以上よりな
る第2添加物を担持してなることを特徴とする脱臭剤に
ある。
According to the present invention, an adsorption carrier is loaded with a first additive containing one or both of a transition element and a transition element compound, and a second additive containing one or more halogens or halogen compounds. It is a deodorant characterized by becoming.

【0007】本発明において,第1添加物は,遷移元素
或いは遷移元素化合物のいずれか一方又は双方である。
上記遷移元素としては,例えば,銅,鉄,ニッケル,コ
バルト,マンガンがある。また,上記遷移元素化合物と
しては,例えば,硝酸銅,硫酸銅,塩化第二銅等の銅化
合物がある。
In the present invention, the first additive is either or both of a transition element and a transition element compound.
Examples of the transition element include copper, iron, nickel, cobalt and manganese. Examples of the transition element compound include copper compounds such as copper nitrate, copper sulfate and cupric chloride.

【0008】上記第2添加物は,ハロゲン或いはハロゲ
ン化合物の1種以上よりなる。上記ハロゲンは,例え
ば,フッ素,塩素,臭素,ヨウ素,又はアスタチンであ
り,とりわけ臭素(Br)或いはヨウ素(I)を用いる
ことが好ましい。上記ハロゲン化合物としては,例え
ば,KBr,NaBr,NH4 Br,HIO3 ,I2
5,KI,NaI,NH4 Iがある。
The second additive comprises at least one kind of halogen or halogen compound. The halogen is, for example, fluorine, chlorine, bromine, iodine or astatine, and it is particularly preferable to use bromine (Br) or iodine (I). Examples of the halogen compound include KBr, NaBr, NH 4 Br, HIO 3 , and I 2 O.
There are 5 , KI, NaI, and NH 4 I.

【0009】上記第2添加物は,臭素又はヨウ素を単独
で用いてもよく,とりわけ臭素を用いる場合には,KB
r,NaBr等を用いることが好ましい。また,ヨウ素
を用いる場合にはHIO3 ,I2 5 等のハロゲン化合
物も合わせて用いることが好ましい。その理由は,当該
ハロゲン化合物が臭素又はヨウ素の蒸発を防止するから
である。Br2 ,I2 ,ハロゲン化合物,銅,銅化合物
は,そのままの状態で吸着単体に担持されていると考え
られる。
As the second additive, bromine or iodine may be used alone, and particularly when bromine is used, KB is used.
It is preferable to use r, NaBr or the like. When iodine is used, it is preferable to use halogen compounds such as HIO 3 and I 2 O 5 together. The reason is that the halogen compound prevents evaporation of bromine or iodine. It is considered that Br 2 , I 2 , the halogen compound, copper, and the copper compound are supported as they are on the adsorbing simple substance.

【0010】上記吸着担体としては,活性炭,含水珪酸
マグネシウム質粘土鉱物,シリカゲル,ゼオライト,又
は活性アルミナを用いることができる。この中,特に,
活性炭と含水珪酸マグネシウム質粘土鉱物との混合物を
吸着担体として用いることが好ましい。活性炭は,上述
のように,高い比表面積を有するため,臭気成分との接
触面積が多く,脱臭性能が高いためである。
As the adsorption carrier, activated carbon, hydrous magnesium silicate clay mineral, silica gel, zeolite, or activated alumina can be used. Among these,
It is preferable to use a mixture of activated carbon and hydrous magnesium silicate clay mineral as an adsorption carrier. This is because activated carbon has a high specific surface area as described above, and thus has a large contact area with odorous components and high deodorizing performance.

【0011】活性炭は,主としてメチルメルカプタン,
硫化水素等の含硫黄化合物の吸着除去性能に優れてい
る。一方,含水珪酸マグネシウム質粘土鉱物は,珪酸マ
グネシウムを主成分とする多孔性粘土鉱物であり,山皮
或いはセピオライトを含むものである。このものは,そ
の表面に反応性に富む水酸基を有するため,特にトリメ
チルアミン,アンモニア等の,アミン系化合物の吸着除
去性能に優れている。
Activated carbon is mainly methyl mercaptan,
Excellent adsorption and removal performance for sulfur-containing compounds such as hydrogen sulfide. On the other hand, hydrous magnesium silicate clay minerals are porous clay minerals containing magnesium silicate as a main component, and include mountain crust or sepiolite. Since this product has a highly reactive hydroxyl group on its surface, it is particularly excellent in the adsorptive removal performance of amine compounds such as trimethylamine and ammonia.

【0012】上記第1添加物は,上記吸着担体100重
量部に対して,0.5〜30重量部担持してなることが
好ましい。0.5重量部未満の場合には,硫化水素,メ
チルメルカプタン等の含硫黄化合物の吸着性能が低下す
るおそれがある。一方,30重量部を越える場合には,
吸着担体の細孔が減少して吸着担体本来の性能を損なう
おそれがある。
The first additive is preferably carried in an amount of 0.5 to 30 parts by weight based on 100 parts by weight of the adsorption carrier. If the amount is less than 0.5 parts by weight, the adsorption performance of sulfur-containing compounds such as hydrogen sulfide and methyl mercaptan may deteriorate. On the other hand, if it exceeds 30 parts by weight,
There is a risk that the pores of the adsorption carrier will decrease and the original performance of the adsorption carrier will be impaired.

【0013】上記第2添加物は,上記吸着担体100重
量部に対して,0.1〜60重量部担持してなることが
好ましい。0.1重量部未満の場合には,脱臭成分の分
解能力が低下するおそれがある。一方,60重量部を越
える場合には,吸着担体の細孔が減少して吸着担体本来
の性能を損なうおそれがある。
The second additive is preferably carried in an amount of 0.1 to 60 parts by weight based on 100 parts by weight of the adsorption carrier. If the amount is less than 0.1 part by weight, the ability to decompose the deodorizing component may be reduced. On the other hand, if it exceeds 60 parts by weight, the pores of the adsorption carrier may decrease and the original performance of the adsorption carrier may be impaired.

【0014】[0014]

【作用及び効果】本発明の脱臭剤においては,吸着担体
に,遷移元素又は遷移元素化合物からなる第1添加物,
及びハロゲン又はハロゲン化合物からなる第2添加物を
担持させたものである。遷移元素又は遷移元素化合物
は,硫化水素,メチルメルカプタン等の含硫黄化合物の
除去性能が高い。その理由は,上記遷移元素又は遷移元
素化合物が,硫化物系の臭気成分に対して硫化物を生成
するためであると考えられる。上記遷移元素又は遷移元
素化合物の中,銅又は銅化合物を用いた場合には,上記
の作用効果が更に大きくなる。
[Operation and effect] In the deodorant of the present invention, the adsorbing carrier contains a first additive containing a transition element or a transition element compound,
And a second additive composed of halogen or a halogen compound. A transition element or a transition element compound has high removal performance for sulfur-containing compounds such as hydrogen sulfide and methyl mercaptan. It is considered that the reason is that the above-mentioned transition element or transition element compound forms sulfides with respect to sulfide-based odor components. When copper or a copper compound is used among the above-mentioned transition elements or transition element compounds, the above-mentioned action and effect are further enhanced.

【0015】また,ハロゲン元素又はハロゲン化合物
は,その酸化力により,臭気成分,特にトリメチルアミ
ン,アンモニア等のアミン系臭気成分を酸化分解して,
吸着担体に吸着されやすい物質に変化させる。
The halogen element or halogen compound oxidizes and decomposes odor components, particularly amine odor components such as trimethylamine and ammonia, due to its oxidizing power,
Change to a substance that is easily adsorbed by the adsorption carrier.

【0016】従って,上記添加物は,上記の硫化物生成
反応及び酸化分解反応等の複数の反応が複雑に作用し合
い,多種類の臭気成分を十分に吸着,除去することがで
きる。故に,多成分系の実際の使用環境下において,そ
の脱臭性能を有効に発揮することができる。
Therefore, a plurality of reactions such as the above-mentioned sulfide formation reaction and oxidative decomposition reaction act on each other in a complicated manner, and the above-mentioned additive can sufficiently adsorb and remove various kinds of odorous components. Therefore, the deodorizing performance can be effectively exhibited in the actual use environment of the multi-component system.

【0017】更に,上記の第1,第2添加物は,吸着担
体に担持されているため,臭気成分との接触面積が拡大
して,優れた脱臭性能を発揮することができる。また,
吸着担体自身も臭気成分の吸着性能を有する。従って,
本発明の脱臭剤は,優れた脱臭性能を発揮することがで
きる。特に,臭気成分が,実用レベルの低濃度の場合に
おいても,その脱臭性能が高い(実施例4参照)。その
ため,実際の使用環境において,その脱臭性能を最大限
に発揮することができる。
Further, since the above-mentioned first and second additives are carried on the adsorption carrier, the contact area with the odorous component is expanded, and excellent deodorizing performance can be exhibited. Also,
The adsorption carrier itself also has the ability to adsorb odorous components. Therefore,
The deodorant of the present invention can exhibit excellent deodorizing performance. In particular, the deodorizing performance is high even when the odorous component has a practically low concentration (see Example 4). Therefore, the deodorizing performance can be maximized in the actual use environment.

【0018】上記脱臭剤は,各種工業分野,生活環境等
の多くの環境下において,そこで発生する臭気成分の除
去材として,極めて有用である。
The above deodorant is extremely useful as a material for removing odorous components generated in various environments such as various industrial fields and living environments.

【0019】本発明は,実使用環境下において優れた脱
臭性能を発揮することができる脱臭剤を提供することが
できる。
The present invention can provide a deodorant capable of exhibiting excellent deodorizing performance in an actual use environment.

【0020】[0020]

【実施例】【Example】

実施例1 本発明の実施例にかかる脱臭剤について説明する。本例
の脱臭剤は,吸着担体100重量部に,硝酸銅(Cu
(NO3 2 )5重量部と,臭素(Br2 )2.5重量
部及び臭化カリウム(KBr)1重量部とを担持したも
のである。吸着担体は,含水珪酸マグネシウム質粘土鉱
物(セピオライト)30重量%と活性炭70重量%とか
らなるハニカム成形体である。
Example 1 A deodorant according to an example of the present invention will be described. The deodorant of this example has 100 parts by weight of an adsorption carrier and copper nitrate (Cu).
5 parts by weight of (NO 3 ) 2 ), 2.5 parts by weight of bromine (Br 2 ) and 1 part by weight of potassium bromide (KBr) are supported. The adsorption carrier is a honeycomb molded body composed of 30% by weight of hydrous magnesium silicate clay mineral (sepiolite) and 70% by weight of activated carbon.

【0021】上記脱臭剤を製造するに当たっては,ま
ず,活性炭70重量%と,セピオライト30重量%とを
混合した。次に,当該混合物100重量部に,水140
重量部とメチルセルロース10重量部とを加えて,ニー
ダーにより十分混練する。次に,この混練物を真空押出
機を用いてハニカム状に成形して,吸着担体を得た。次
に,この吸着担体にを室温で乾燥し,その後熱風乾燥し
た。これにより,吸着担体を得た。
In producing the above deodorant, first, 70% by weight of activated carbon and 30% by weight of sepiolite were mixed. Next, 100 parts by weight of the mixture is mixed with 140 parts of water.
1 part by weight and 10 parts by weight of methyl cellulose are added and kneaded sufficiently with a kneader. Next, this kneaded material was formed into a honeycomb shape using a vacuum extruder to obtain an adsorption carrier. Next, this adsorption carrier was dried at room temperature and then dried with hot air. As a result, an adsorption carrier was obtained.

【0022】次に,この吸着担体に,含浸法により,硝
酸銅と,臭素及び臭化カリウムとを担持させた。これに
より,上記脱臭剤を得た。
Next, copper nitrate, bromine and potassium bromide were supported on this adsorption carrier by an impregnation method. As a result, the above deodorant was obtained.

【0023】実施例2 本例の脱臭剤は,吸着担体100重量部に,硝酸銅(C
u(NO3 2 )5重量部と,ヨウ素酸(HIO3 )5
重量部とを担持したものである。上記吸着担体には,含
浸法により,硝酸銅とヨウ素酸とを担持させた。その他
は,実施例1と同様である。
Example 2 The deodorant of this example was prepared by adding 100 parts by weight of an adsorption carrier to copper nitrate (C
u (NO 3 ) 2 ) 5 parts by weight and iodic acid (HIO 3 ) 5
And parts by weight. Copper nitrate and iodic acid were supported on the adsorption carrier by the impregnation method. Others are the same as in the first embodiment.

【0024】実施例3 本例の脱臭剤は,吸着担体100重量部に,硝酸銅(C
u(NO3 2 )5重量部と,五酸化二ヨウ素(I2
5 )5重量部とを担持したものである。上記吸着担体に
は,含浸法により,硝酸銅と五酸化二ヨウ素とを担持さ
せた。その他は,実施例1と同様である。
Example 3 The deodorant of this example was prepared by adding 100 parts by weight of an adsorption carrier to copper nitrate (C
5 parts by weight of u (NO 3 ) 2 and diiodine pentoxide (I 2 O)
5 ) 5 parts by weight. Copper nitrate and diiodine pentoxide were supported on the adsorption carrier by the impregnation method. Others are the same as in the first embodiment.

【0025】実施例4 本例においては,図1〜図4に示すごとく,実施例1の
脱臭剤の脱臭性能について評価した。その測定に当た
り,上記実施例1の脱臭剤を試料1とした。また,比較
例として,鉄とマンガンとを担持した活性炭(実施例1
と同一メッシュ,同一サイズのハニカム)を試料9とし
て用いた。これらの試料1,9についての,臭気成分の
除去率を,図1に示す測定装置7を用いて測定した。
Example 4 In this example, as shown in FIGS. 1 to 4, the deodorizing performance of the deodorant of Example 1 was evaluated. For the measurement, the deodorant of Example 1 was used as Sample 1. As a comparative example, activated carbon carrying iron and manganese (Example 1
The same mesh and honeycomb of the same size) were used as sample 9. The odorous component removal rates of these samples 1 and 9 were measured using the measuring device 7 shown in FIG.

【0026】この測定装置7は,各種臭気成分を収納す
る3本の容器70と,各種臭気成分を混合する混合器7
1と,流量計72と,上記試料1,9をそれぞれ充填し
た2本のカラム73とよりなる。上記試料は,カラム7
3内に載置されている。カラム内のガス流速(SV)
は,1.0×105 hr-1であり,その温度は25℃で
ある。
This measuring device 7 comprises three containers 70 for storing various odor components and a mixer 7 for mixing various odor components.
1, a flow meter 72, and two columns 73 filled with the samples 1 and 9 respectively. The above sample is in column 7
It is placed in 3. Gas flow rate in column (SV)
Is 1.0 × 10 5 hr −1 and its temperature is 25 ° C.

【0027】臭気成分としては,トリメチルアミン
(T),硫化水素(S),メチルメルカプタン(M)の
3種類を含む混合気体を用い,図1に示すごとく,これ
の各容器70を混合器71に接続した。キャリアガスと
しては,空気を用いた。臭気成分の濃度は,カラム73
の入口側A,出口側Bにおいて,それぞれガスクロマト
グラフにより測定した。
As the odorous component, a mixed gas containing three kinds of trimethylamine (T), hydrogen sulfide (S), and methyl mercaptan (M) is used, and each container 70 of the mixed gas is added to a mixer 71 as shown in FIG. Connected Air was used as the carrier gas. Column 73
The measurement was performed by gas chromatography on the inlet side A and the outlet side B, respectively.

【0028】入口側Aにおける各臭気成分は,それぞれ
300ppbと低い濃度とした。そして,出口側の臭気
成分に対する入口側の臭気成分の濃度比を求めた。測定
開始時における濃度(C0 )に対する,時間経過後にお
ける濃度(C)の変化率CX(%) を,CX ={1─
(C/C0 )}×100の式より求め,これを臭気成分
の除去率(%)とした。その結果を図2〜図4に示し
た。図2は,トリメチルアミンの除去率を示す。図3
は,硫化水素の除去率を示す。図4は,メチルメルカプ
タンの除去率を示す。
Each of the odorous components on the inlet side A had a low concentration of 300 ppb. Then, the concentration ratio of the odorous component on the inlet side to the odorous component on the outlet side was obtained. Change rate C X (%) of concentration (C) after the passage of time with respect to concentration (C 0 ) at the start of measurement And C X = {1−
It was obtained from the formula of (C / C 0 )} × 100, and this was taken as the removal rate (%) of odorous components. The results are shown in FIGS. FIG. 2 shows the removal rate of trimethylamine. FIG.
Indicates the removal rate of hydrogen sulfide. FIG. 4 shows the removal rate of methyl mercaptan.

【0029】同図より知られるように,実施例1の脱臭
剤は,いずれの臭気成分に対しても,高い脱臭性能を発
揮した。脱臭性能の経時的劣化も少なかった。このこと
から,実施例1の脱臭剤は,臭気成分濃度が数百ppb
という極く薄い場合においても,特に顕著に高い脱臭効
果を発揮することがわかる。
As can be seen from the figure, the deodorant of Example 1 exhibited high deodorizing performance against any odorous component. Deterioration performance was also less deteriorated over time. From this, the deodorant of Example 1 has an odor component concentration of several hundred ppb.
It can be seen that even in such a very thin case, a particularly high deodorizing effect is exhibited.

【0030】実施例5 本例においては,実施例1〜実施例3に示した脱臭剤に
ついて,その脱臭性能を評価した。評価に当たり,各脱
臭剤の臭気成分の除去率を求めた。ハニカムの試料を破
砕し,粒子状とした。この粒子状試料をカラム内におい
てグラスウール上に載置した。各試料は,それぞれ1.
0cm3 ずつ充填した。カラム内のガス流速(SV)
は,6.0×104 hr-1であり,その温度は25℃で
ある。測定装置には,臭気成分としてのトリメチルアミ
ンを1本の容器に充填した。1本のカラムを用い,各脱
臭剤について,別々に測定した。
Example 5 In this example, the deodorizing performance of the deodorizing agents shown in Examples 1 to 3 was evaluated. For the evaluation, the removal rate of the odorous components of each deodorant was obtained. The honeycomb sample was crushed into particles. The particulate sample was placed on glass wool in the column. Each sample is 1.
Each was filled with 0 cm 3 . Gas flow rate in column (SV)
Is 6.0 × 10 4 hr −1 and its temperature is 25 ° C. In the measuring device, one container was filled with trimethylamine as an odor component. Using one column, each deodorant was measured separately.

【0031】実施例1の脱臭剤の測定においては,キャ
リアガスは空気を用いた。実施例2,3の脱臭剤の測定
においては,キャリアガスは窒素(N2 )を用いた。い
ずれも,入口側Aの臭気成分濃度は,100ppmと,
実施例4の場合よりも高くした。そして,実施例4と同
様に,カラムの入口側,出口側における臭気成分濃度を
測定した。入口側Aの臭気成分濃度に対する出口側Bの
臭気成分濃度の比率を求め,その結果を図5に示した。
In the measurement of the deodorant of Example 1, air was used as the carrier gas. In the measurement of the deodorizing agents of Examples 2 and 3, nitrogen (N 2 ) was used as the carrier gas. In both cases, the odorous component concentration on the inlet side A is 100 ppm,
It was set higher than in the case of Example 4. Then, in the same manner as in Example 4, the odorous component concentrations on the inlet side and the outlet side of the column were measured. The ratio of the odorous component concentration on the outlet side B to the odorous component concentration on the inlet side A was determined, and the result is shown in FIG.

【0032】同図より知られるように,実施例1〜3の
脱臭剤は,臭気成分が100ppmという高濃度におい
ても,いずれも高い脱臭性能を発揮した。
As can be seen from the figure, the deodorants of Examples 1 to 3 exhibited high deodorizing performance even when the odor component was as high as 100 ppm.

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

【図1】実施例4における,脱臭剤の脱臭性能の評価方
法を示す説明図。
FIG. 1 is an explanatory view showing an evaluation method of deodorizing performance of a deodorant in Example 4.

【図2】実施例4における,トリメチルアミンの除去率
を示す線図。
FIG. 2 is a graph showing the removal rate of trimethylamine in Example 4.

【図3】実施例4における,硫化水素の除去率を示す線
図。
FIG. 3 is a diagram showing a hydrogen sulfide removal rate in Example 4.

【図4】実施例4における,メチルメルカプタンの除去
率を示す線図。
FIG. 4 is a graph showing the removal rate of methyl mercaptan in Example 4.

【図5】実施例5における,トリメチルアミンの除去率
を示す線図。
FIG. 5 is a graph showing the removal rate of trimethylamine in Example 5.

【符号の説明】[Explanation of symbols]

1,9...試料, 73...カラム, 7...測定装置, A...カラムの入口側, B...カラムの出口側, 1,9. . . Sample, 73. . . Column, 7. . . Measuring device, A. . . The inlet side of the column, B. . . The outlet side of the column,

───────────────────────────────────────────────────── フロントページの続き (72)発明者 堀井 満正 愛知県愛知郡長久手町大字長湫字横道41番 地の1 株式会社豊田中央研究所内 (72)発明者 小野田 誠次 愛知県愛知郡長久手町大字長湫字横道41番 地の1 株式会社豊田中央研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mitsumasa Horii Aichi Prefecture Nagachite Town, Aichi Prefecture, Nagakute Town, No. 41 Yokomichi 1st Toyota Road Central Research Institute Co., Ltd. (72) Inventor Seiji Onoda Nagachite Town, Aichi Prefecture 1 in 41, Yokomichi, Yokoji Inside Toyota Central Research Institute Co., Ltd.

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 吸着担体に,遷移元素或いは遷移元素化
合物の一方又は双方よりなる第1添加物,及びハロゲン
又はハロゲン化合物の1種以上よりなる第2添加物を担
持してなることを特徴とする脱臭剤。
1. An adsorption carrier carrying a first additive comprising one or both of a transition element and a transition element compound, and a second additive comprising one or more of halogen or a halogen compound. Deodorant to do.
【請求項2】 請求項1において,上記遷移元素或いは
遷移元素化合物の一方又は双方は,銅或いは銅化合物の
一方又は双方であることを特徴とする脱臭剤。
2. The deodorant according to claim 1, wherein one or both of the transition element or the transition element compound is copper or one or both of the copper compound.
【請求項3】 請求項2において,上記銅化合物は,硝
酸銅,硫酸銅,及び塩化第二銅のグループから選ばれる
1種又は2種以上であることを特徴とする脱臭剤。
3. The deodorant according to claim 2, wherein the copper compound is one or more selected from the group consisting of copper nitrate, copper sulfate, and cupric chloride.
【請求項4】 請求項1〜3のいずれか一項において,
上記第1添加物は,上記吸着担体100重量部に対し
て,0.5〜30重量部担持してなることを特徴とする
脱臭剤。
4. The method according to claim 1, wherein
The deodorant, wherein the first additive is carried in an amount of 0.5 to 30 parts by weight based on 100 parts by weight of the adsorption carrier.
【請求項5】 請求項1〜4のいずれか一項において,
上記ハロゲンは,臭素或いはヨウ素であることを特徴と
する脱臭剤。
5. The method according to any one of claims 1 to 4,
A deodorant characterized in that the halogen is bromine or iodine.
【請求項6】 請求項1〜5のいずれか一項において,
上記ハロゲン化合物は,KBr,NaBr,NH4
r,I2 5 ,KI,NaI,NH4 I,及びHIO3
のグループから選ばれる1種又は2種以上であることを
特徴とする脱臭剤。
6. The method according to any one of claims 1 to 5,
The above halogen compounds are KBr, NaBr, NH 4 B
r, I 2 O 5 , KI, NaI, NH 4 I, and HIO 3
The deodorant is one or two or more selected from the group.
【請求項7】 請求項1〜6のいずれか一項において,
上記第2添加物は,上記吸着担体100重量部に対し
て,0.1〜60重量部担持してなることを特徴とする
脱臭剤。
7. The method according to any one of claims 1 to 6,
The deodorant, wherein the second additive is supported in an amount of 0.1 to 60 parts by weight based on 100 parts by weight of the adsorption carrier.
【請求項8】 請求項1〜7のいずれか一項において,
上記吸着担体は,活性炭,含水珪酸マグネシウム質粘土
鉱物,シリカゲル,ゼオライト,及び活性アルミナのグ
ループから選ばれる1種又は2種以上であることを特徴
とする脱臭剤。
8. The method according to any one of claims 1 to 7,
A deodorant characterized in that the adsorption carrier is one or more selected from the group consisting of activated carbon, hydrous magnesium silicate clay mineral, silica gel, zeolite, and activated alumina.
JP10999695A 1995-04-10 1995-04-10 Deodorant Expired - Fee Related JP3358382B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10999695A JP3358382B2 (en) 1995-04-10 1995-04-10 Deodorant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10999695A JP3358382B2 (en) 1995-04-10 1995-04-10 Deodorant

Publications (2)

Publication Number Publication Date
JPH08281113A true JPH08281113A (en) 1996-10-29
JP3358382B2 JP3358382B2 (en) 2002-12-16

Family

ID=14524458

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3358382B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001091896A1 (en) * 2000-05-29 2001-12-06 Three Tec Co., Ltd. Object processing apparatus and plasma facility comprising the same
JP2002369869A (en) * 2001-06-15 2002-12-24 Takeda Chem Ind Ltd Functional porous particle
WO2005032608A1 (en) * 2003-10-02 2005-04-14 Osaka Gas Chemicals Co., Ltd. Gas adsorbing filter
JP2008188437A (en) * 2008-03-14 2008-08-21 Toyota Central R&D Labs Inc Deodorizing molding
JP2009279522A (en) * 2008-05-22 2009-12-03 Kobe Steel Ltd Oxide catalyst and method for preparing oxide catalyst, as well as deodorant and deodorizing filter
KR100937986B1 (en) * 2009-06-16 2010-01-21 주식회사 에이엔씨아이 Method for preparation of high functional activated carbon by electroless copper/iodine surface treatment
JP2012501362A (en) * 2008-09-01 2012-01-19 ビーエーエスエフ ソシエタス・ヨーロピア Adsorbing material and hydrocarbon gas desulfurization method

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001091896A1 (en) * 2000-05-29 2001-12-06 Three Tec Co., Ltd. Object processing apparatus and plasma facility comprising the same
JP2002369869A (en) * 2001-06-15 2002-12-24 Takeda Chem Ind Ltd Functional porous particle
WO2005032608A1 (en) * 2003-10-02 2005-04-14 Osaka Gas Chemicals Co., Ltd. Gas adsorbing filter
JP2008188437A (en) * 2008-03-14 2008-08-21 Toyota Central R&D Labs Inc Deodorizing molding
JP2009279522A (en) * 2008-05-22 2009-12-03 Kobe Steel Ltd Oxide catalyst and method for preparing oxide catalyst, as well as deodorant and deodorizing filter
JP2012501362A (en) * 2008-09-01 2012-01-19 ビーエーエスエフ ソシエタス・ヨーロピア Adsorbing material and hydrocarbon gas desulfurization method
KR100937986B1 (en) * 2009-06-16 2010-01-21 주식회사 에이엔씨아이 Method for preparation of high functional activated carbon by electroless copper/iodine surface treatment

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