JPS59199039A - Deodorant and its manufacture - Google Patents

Deodorant and its manufacture

Info

Publication number
JPS59199039A
JPS59199039A JP58072655A JP7265583A JPS59199039A JP S59199039 A JPS59199039 A JP S59199039A JP 58072655 A JP58072655 A JP 58072655A JP 7265583 A JP7265583 A JP 7265583A JP S59199039 A JPS59199039 A JP S59199039A
Authority
JP
Japan
Prior art keywords
iodine
activated carbon
deodorant
hydrogen sulfide
deodorizing
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
JP58072655A
Other languages
Japanese (ja)
Other versions
JPS629377B2 (en
Inventor
Hisato Yano
矢野 壽人
Shusuke Hashimoto
橋本 修左
Sotaro Yonemura
惣太郎 米村
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.)
Shimizu Construction Co Ltd
Original Assignee
Shimizu Construction Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shimizu Construction Co Ltd filed Critical Shimizu Construction Co Ltd
Priority to JP58072655A priority Critical patent/JPS59199039A/en
Publication of JPS59199039A publication Critical patent/JPS59199039A/en
Publication of JPS629377B2 publication Critical patent/JPS629377B2/ja
Granted legal-status Critical Current

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  • Treating Waste Gases (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

PURPOSE:To manufacture a deodorant having high deodorizing efficiency and long life by adding an oxide of iodine and/or an oxo acid of iodine to active carbon. CONSTITUTION:An aq. soln. of oxo acid of iodine is prepd. by dissolving about 0.01-1.0mol/l oxo acid of iodine such as HIO3 or HIO4 in water. Active carbon is immersed therein for >=5min, and a deodorant is prepd. by drying the immersed active carbon by heating at <=250 deg.C. Since the deodorant comprises an oxide of iodine such as I2O5 and an oxo acid of iodine such as HIO3 or HIO4 adsorbed to the surface of active carbon, a deodorant having superior deodorizing effect an long life is obtd.

Description

【発明の詳細な説明】 この発明は、脱臭の効果が良く寿命の長い脱臭剤および
その製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a deodorizing agent with good deodorizing effect and long life, and a method for producing the same.

今日、悪臭公害は重大な社会問題となっている。Today, odor pollution has become a serious social problem.

この悪臭を規制する悪臭防止法において指定されている
法定悪臭81fiJ分の中でも、硫化水素(Has)は
しばしば悪臭公害の主因物質となっており、この硫化水
素をどの程度除去できるかが脱臭の効果を知るうえで重
要なポイントとされている。
Hydrogen sulfide (Has) is often the main cause of foul odor pollution, and the effectiveness of deodorization depends on how much hydrogen sulfide can be removed. This is considered an important point to know.

悪臭を除去するための脱臭装置の方式には、洗浄・吸収
法、吸着法、燃焼法、酸化法、マスキング法など種々の
方法が用いられているが、吸着脱臭法は設備費が安価で
あること、安全で装置の運転が容易であること、負荷の
変動に強いことなどから、今日広く利用されている。
Various methods are used for deodorizing equipment to remove bad odors, such as cleaning/absorption methods, adsorption methods, combustion methods, oxidation methods, and masking methods, but the adsorption deodorization method has low equipment costs. It is widely used today because it is safe, easy to operate, and resistant to load fluctuations.

従来、この吸着脱臭法に用いる脱臭剤として(ま、主に
活性炭が用いられていたが、悪臭の主因物質である硫化
水素が低分子イi1低沸点極性化合物であるため、活性
炭に吸着されに<<、このため現在では硫化水素を取り
除くためのIIt+!臭剤として次のものが市販されて
いる。
Conventionally, activated carbon was mainly used as a deodorizing agent for this adsorption deodorization method, but since hydrogen sulfide, which is the main cause of bad odors, is a low-molecular, low-boiling, polar compound, it cannot be adsorbed by activated carbon. <<For this reason, the following are currently commercially available as IIt+! odorants for removing hydrogen sulfide.

囚 強アルカリ剤を活性炭に添着させるなど特殊化学処
」1した脱臭剤。
A deodorizer that has undergone special chemical treatment such as impregnating activated carbon with a strong alkaline agent.

(B)  水酸化−2@系脱臭剤。(B) Hydroxylated-2@ type deodorizer.

(0イオン交換樹脂よりなる脱臭剤。(A deodorizing agent made of 0 ion exchange resin.

(2)の脱臭剤は、H2S゛が弱酸性であることに着目
したもので、面の脱臭剤は水酸化第2鉄とfit化水素
との反応に着目したものである。しかし、いずれの脱臭
剤も破過時間すなわち寿命が短かいという欠点があった
The deodorizing agent (2) focuses on the fact that H2S is weakly acidic, and the surface deodorizing agent focuses on the reaction between ferric hydroxide and ferric hydrogen hydride. However, all deodorizers have the disadvantage of short breakthrough times, that is, short lifespans.

この発明は上記事情に鑑みてなされたもので、脱臭効率
が高く寿命の長い脱臭剤およびその製造方法を提供する
ことを目的とするものである。
This invention was made in view of the above circumstances, and aims to provide a deodorizing agent with high deodorizing efficiency and long life, and a method for producing the same.

この発明の脱臭剤は、ヨウ素の酸化物、たとえば五酸化
ニヨウ素(IzOa)およびヨウ素のオキソ酸たとえば
ヨウ素酸(HIO8)や過ヨウ素酸(HI 04;オル
トHJ Oa、メタ丁(I04・2 I20でも表わす
)、あるいはこれらのいずれかがヤシガラ活性炭等の活
性炭の表面に添着されたものである。
The deodorizing agent of the present invention contains oxides of iodine such as niodine pentoxide (IzOa) and oxoacids of iodine such as iodic acid (HIO8) and periodic acid (HI 04; ), or any of these is attached to the surface of activated carbon such as coconut shell activated carbon.

この吸豹剤を製造するには、まず、ヨウ素のオキソ酸、
例えば丁(I Od’ HI 04を0.01〜1.0
mol/J  程度水に溶解してヨウ素のオキソ酸水溶
液を調!((j L、、これに活性炭を5分間以上浸漬
する。
To produce this leopard absorbent, first, iodine oxoacid,
For example, I Od' HI 04 is 0.01 to 1.0
Prepare an oxoacid aqueous solution of iodine by dissolving it in water to the extent of mol/J! ((j L,, immerse activated carbon in this for at least 5 minutes.

次に、この浸漬された活性炭を250’C以下で加熱乾
燥する。
Next, this soaked activated carbon is heated and dried at 250'C or less.

ここでヨウ素のオキソ酸の水溶液の濃度を1. Qmo
l/e以下としたのは、これ以止濃い濃度では、活性炭
の細孔の多くがオキソ酸によって塞さがれ、活性炭の吸
着能が低下し、従って、この発明の脱臭剤の性能が低下
し、しかも、寿命が短かくなるためである。また、ヨウ
素のオキソ酸の水溶液の濃度を0.01 mol/if
f以上としたのは、これ以下の浅度では、活性炭に添着
されるオキソ酸の量が少なく、良好な脱臭性能が得られ
ないためである。
Here, the concentration of the aqueous solution of iodine oxoacid is 1. Qmo
The reason for setting it below 1/e is that if the concentration is higher than this, many of the pores of the activated carbon will be blocked by the oxoacid, the adsorption capacity of the activated carbon will decrease, and the performance of the deodorizer of this invention will therefore decrease. Moreover, the lifespan is shortened. In addition, the concentration of the aqueous solution of iodine oxoacid is 0.01 mol/if
The reason for setting it above f is that at shallower depths than this, the amount of oxoacid impregnated on the activated carbon is small and good deodorizing performance cannot be obtained.

この水溶液のHIO,Wは)rIOμはとんど貸元され
ることなく活性炭の表面に添着される。活性版表面に添
着されたTI I O> HI 04は乾燥に伴いしだ
いに脱水され分解してI2011となるものと考えられ
る。T−I I Os%)r I 04、■す、は強い
酸化作用を有するが、過マンガン酸カリウム、重クロム
酊カリウム、クロム酸カリウムのような通常の41 N
a化剤のように、活性炭中のt元物質や触媒作用によっ
て急速に還元されることがなく、活性炭の表面に添着さ
れた状轄で比較的酸化されやすい硫化水素を酸化する能
力を保持し続ける。
The HIO,W)rIOμ of this aqueous solution is impregnated onto the surface of the activated carbon without being released. It is considered that TI IO> HI 04 attached to the surface of the active plate gradually dehydrates and decomposes as it dries to become I2011. T-I Os%) r I 04, ■ has a strong oxidizing effect, but ordinary 41 N such as potassium permanganate, potassium dichromate, potassium chromate
Unlike the a-oxidizing agent, it is not rapidly reduced by the t-substances in activated carbon or the catalytic action, and retains the ability to oxidize hydrogen sulfide, which is relatively easily oxidized when attached to the surface of activated carbon. continue.

この発明の脱臭剤の脱臭機構は次のように考えられる。The deodorizing mechanism of the deodorizing agent of this invention is considered as follows.

この発明の脱臭剤の活性炭の表面に添着されているIf
Osは、活性炭に吸着される硫化水素(TT2Slを酸
化する。この反応は次式で示される。
If attached to the surface of activated carbon of the deodorizer of this invention
Os oxidizes hydrogen sulfide (TT2Sl) adsorbed on activated carbon. This reaction is shown by the following equation.

I’ ++3 H2S  → I−+(STT−+3S
  ↓このように、この発明の脱臭剤とHβとの吸着反
応Gま、H2Sを単体イオン(S)にまで酸化するもの
と考えられる。このため、この脱臭剤の吸着過程におい
ては吸着作用が主体となり、活性炭に吸着されたH2S
が活性炭から脱離する脱離作用はほとんど関与しないも
のと考えられる。したがってこの発明の脱臭剤は、硫化
水素を吸着する方向に押し進め、硫化水素は継続的に活
性炭の表面に吸着されてゆく。また上式からもわかるよ
うに、1モルのI、O,は6モルの硫化水素を酸化する
ことができるので、この脱臭剤は多量の硫化水素を°処
理できるものとなる。
I' ++3 H2S → I-+(STT-+3S
↓In this way, it is thought that the adsorption reaction between the deodorizer of the present invention and Hβ oxidizes H2S to a simple ion (S). Therefore, in the adsorption process of this deodorizer, the adsorption effect is the main one, and the H2S adsorbed on activated carbon
It is thought that the desorption effect of desorption from activated carbon is hardly involved. Therefore, the deodorizer of the present invention pushes hydrogen sulfide in the direction of adsorption, and hydrogen sulfide is continuously adsorbed on the surface of activated carbon. Furthermore, as can be seen from the above formula, 1 mole of I, O, can oxidize 6 moles of hydrogen sulfide, so this deodorizer can treat a large amount of hydrogen sulfide.

次に実1.曳例により、この発明をさらに詳しく説明す
る。
Next is the fruit 1. This invention will be explained in more detail with reference to examples.

〔実施例1〕 ifα2mol/eのHIOs*溶液に市販のヤシガラ
破砕炭(4〜8mθah、比表面積約110Or71′
/g)を24時間浸漬した後、120℃で3時間加熱乾
燥し、これを脱臭剤(8)とした。
[Example 1] Commercially available crushed coconut husk charcoal (4 to 8 mθah, specific surface area about 110Or71'
/g) for 24 hours, and then heated and dried at 120°C for 3 hours to obtain a deodorizing agent (8).

次に、0.2 mol/gのI(I O,水溶液に上記
の市販ヤシガラ破砕炭を浸漬し、同一の条件で処理を行
ない、これを脱臭剤[F])とした。
Next, the commercially available crushed coconut husk charcoal was immersed in an aqueous solution of 0.2 mol/g of I (IO) and treated under the same conditions to obtain a deodorizing agent [F].

このようにして得られた2種類の脱臭剤1(5)の)と
、比較のために無処理の上記の市販ヤシガラ破砕炭およ
び代表的な3aの市販の脱硫剤+’Q n■(いずれも
活性炭をベースとするもの)を下記の試験に供した。
The two types of deodorizing agent 1 (5)) obtained in this way, the untreated commercially available crushed coconut husk charcoal, and the representative commercially available desulfurizing agent 3a +'Q n■ (both (also based on activated carbon) were subjected to the following tests.

実験装量としては、第1図に示すように、実験ガスが流
される吸着管1をジャケット2で皆ったものを用いた。
As shown in FIG. 1, the experimental equipment used was one in which an adsorption tube 1 through which the experimental gas was passed was covered with a jacket 2.

この1!!i着管1内には、段部3が設けられており、
ここに上記した脱臭剤を投入し厚さ7引の脱臭剤層4を
設は実験を行なった。吸着管1内には、この層4の下か
ら上方に向けて実験ガスを流し、またジャケット2内に
は25℃の温水を流して吸着管1内を25℃に保温した
。実験ガスには、硫化水素濃度をIDQpplnとした
空気を用いて、相対温度約50%、温度約25℃とt7
た。
This one! ! i A stepped portion 3 is provided in the fitting pipe 1,
An experiment was conducted in which the above-mentioned deodorizing agent was added to form a deodorizing agent layer 4 having a thickness of 7 layers. An experimental gas was flowed into the adsorption tube 1 from below this layer 4 upward, and 25° C. hot water was flowed into the jacket 2 to maintain the temperature inside the adsorption tube 1 at 25° C. Air with a hydrogen sulfide concentration of IDQppln was used as the experimental gas, with a relative temperature of about 50%, a temperature of about 25°C, and t7.
Ta.

他の実験条件は次のとうりである。Other experimental conditions were as follows.

吸着塔断面積 12.6CI 空塔筏1速度(LV値3 4 [] Mcc空間速度C
8V値)  20600hr’各脱臭剤の能力を比較す
るために、入口における実験ガス中の硫化水素濃度と出
口における処理済の実験ガス中の研、化水素濃度とを時
間ごとに測定した。
Adsorption tower cross-sectional area 12.6CI Empty column raft 1 velocity (LV value 3 4 [] Mcc space velocity C
8V value) 20,600 hr' In order to compare the performance of each deodorizer, the hydrogen sulfide concentration in the experimental gas at the inlet and the hydrogen sulfide concentration in the treated experimental gas at the outlet were measured every hour.

各脱臭剤の実験ガスの流通時間と、出口硫化水素濃度(
Cou+:)/入口硫化水嚢濃度fcix1)の比(破
過$ = Cout/ C1n XI DO)との関係
を第2図に示す。また、下記の第1表に測定結果から求
めた各脱臭剤の1デ、5%、10%破過時間を示す。
The experimental gas flow time for each deodorizer and the outlet hydrogen sulfide concentration (
The relationship between the ratio of Cou+:)/inlet sulfide water sac concentration fcix1) (breakthrough $=Cout/C1n XI DO) is shown in FIG. In addition, Table 1 below shows the 1%, 5%, and 10% breakthrough times of each deodorizer determined from the measurement results.

第1表 これらの結果からこの発明の脱臭剤(A)■が硫化水素
の脱臭処理を効率良く長時間行えるものであることがわ
かる。
Table 1 From these results, it can be seen that the deodorizing agent (A) (2) of the present invention can efficiently deodorize hydrogen sulfide for a long time.

〔実施例2〕 処理対象とする排ガスの湿度がこの発明の脱臭剤CA)
(B)のメI命に与える影響を見るために実験を行なっ
た。実験は相対湿度0%と80%とについて行ない、そ
の他の実験条件は実権例1における実験条件と同様にし
た。it +2対象としてはカl舌fi 33[!のヤ
シガラ破砕炭、市販の脱硫剤(C)[F]をi1′び、
各々の1%、5%、10%破過時間を測定した結宋を第
2表に示す。
[Example 2] The humidity of the exhaust gas to be treated is the deodorizer CA of the present invention)
An experiment was conducted to see the effect of (B) on life. The experiment was conducted at relative humidity of 0% and 80%, and the other experimental conditions were the same as those in Example 1. It +2 target is cal tongue fi 33[! crushed coconut husk charcoal, commercially available desulfurization agent (C) [F],
Table 2 shows the measured 1%, 5%, and 10% breakthrough times.

第  2  表 (#i位二分j 上記の結果から、この発明の脱臭剤(4)のノは他の脱
硫剤よりも依然として破過時i1が長く、したがってこ
の発明の脱臭剤は処理対象排ガスの湿度の変動にも強い
ものであることがわかる。
Table 2 (#i bisection It can be seen that it is resistant to fluctuations in .

なお上記実施例においては、硫化水素の吸着について述
べたが、この発明の脱臭剤は担体として活性炭を用いて
いるので、他の悪臭物質などの吸着処理に適用すること
もできる。
In the above embodiments, the adsorption of hydrogen sulfide was described, but since the deodorizer of the present invention uses activated carbon as a carrier, it can also be applied to the adsorption treatment of other malodorous substances.

以上説明したように、この発明の脱臭邪1は、活性炭を
ヨウ士のオキソ酸水溶液に浸隨した後加熱乾燥すること
によって製造され、活性炭の表面にヨウ素の酊化物、ヨ
ウ素のオキン酸が吸着されたものなので、製造が容易で
あるとともに、硫化水素による悪臭を脱臭処理するに優
れた効果を発押し、その寿命も長く、シたがってこの脱
臭剤を用いることによって脱臭処理費用を低減すること
ができ°C経済的である。
As explained above, the deodorizing agent 1 of the present invention is produced by soaking activated carbon in an aqueous solution of iodine oxoacid and then heating and drying it, and the iodine alcoholic acid and iodine oxoacid are adsorbed on the surface of the activated carbon. Because it is a deodorizing agent, it is easy to manufacture, has an excellent effect in deodorizing bad odors caused by hydrogen sulfide, and has a long life. Therefore, by using this deodorizing agent, the cost of deodorizing treatment can be reduced. It is economical.

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

第1図は実1租例1.2における実験に用いた吸着脱臭
装置の概略図、第2図は実施例1において求めた出ロ硫
化水゛素濃度/入ロ硫化水素濃度×100−流通時間の
グラフである。
Fig. 1 is a schematic diagram of the adsorption deodorization equipment used in the experiment in Example 1.2, and Fig. 2 shows the output hydrogen sulfide concentration/input hydrogen sulfide concentration x 100 - distribution determined in Example 1. It is a graph of time.

Claims (2)

【特許請求の範囲】[Claims] (1)活性炭にヨウ素の酸化物および/又はヨウ素のオ
キソ酸を添着させたことを特徴とする脱臭剤。
(1) A deodorizing agent characterized in that activated carbon is impregnated with an iodine oxide and/or an iodine oxoacid.
(2)  ヨウ素のオキソ酸の水溶液に活性炭を浸漬し
た徒乾燥することを特徴とする脱臭剤の製造方法。
(2) A method for producing a deodorizing agent, which comprises immersing activated carbon in an aqueous solution of iodine oxoacid and drying it.
JP58072655A 1983-04-25 1983-04-25 Deodorant and its manufacture Granted JPS59199039A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58072655A JPS59199039A (en) 1983-04-25 1983-04-25 Deodorant and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58072655A JPS59199039A (en) 1983-04-25 1983-04-25 Deodorant and its manufacture

Publications (2)

Publication Number Publication Date
JPS59199039A true JPS59199039A (en) 1984-11-12
JPS629377B2 JPS629377B2 (en) 1987-02-27

Family

ID=13495607

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58072655A Granted JPS59199039A (en) 1983-04-25 1983-04-25 Deodorant and its manufacture

Country Status (1)

Country Link
JP (1) JPS59199039A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5403548A (en) * 1992-02-28 1995-04-04 Takeda Chemical Industries Ltd. Activated carbon adsorbent and applications thereof
JPH08196860A (en) * 1995-01-30 1996-08-06 Dia Tec Kk Deodorizing device
JPH10277362A (en) * 1997-04-09 1998-10-20 Fuso Unitec Kk Cleaning system for exhaust gas containing nox
JP2002191968A (en) * 2000-12-27 2002-07-10 Nkk Corp Deodorant and method for manufacturing the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5403548A (en) * 1992-02-28 1995-04-04 Takeda Chemical Industries Ltd. Activated carbon adsorbent and applications thereof
JPH08196860A (en) * 1995-01-30 1996-08-06 Dia Tec Kk Deodorizing device
JPH10277362A (en) * 1997-04-09 1998-10-20 Fuso Unitec Kk Cleaning system for exhaust gas containing nox
JP2002191968A (en) * 2000-12-27 2002-07-10 Nkk Corp Deodorant and method for manufacturing the same

Also Published As

Publication number Publication date
JPS629377B2 (en) 1987-02-27

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