JPH0338297A - Method for treating water contaminated by trichloroethylene and tetrachloroethylene - Google Patents

Method for treating water contaminated by trichloroethylene and tetrachloroethylene

Info

Publication number
JPH0338297A
JPH0338297A JP17143989A JP17143989A JPH0338297A JP H0338297 A JPH0338297 A JP H0338297A JP 17143989 A JP17143989 A JP 17143989A JP 17143989 A JP17143989 A JP 17143989A JP H0338297 A JPH0338297 A JP H0338297A
Authority
JP
Japan
Prior art keywords
ozone
tetrachlorethylene
trichloroethylene
water
trichlorethylene
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
JP17143989A
Other languages
Japanese (ja)
Other versions
JPH0565237B2 (en
Inventor
Yoshitaka Nitta
新田 義孝
Koushichi Suzuki
鈴木 弘七
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.)
SHIN NIPPON KISHIYOU KAIYO KK
Central Research Institute of Electric Power Industry
Original Assignee
SHIN NIPPON KISHIYOU KAIYO KK
Central Research Institute of Electric Power Industry
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 SHIN NIPPON KISHIYOU KAIYO KK, Central Research Institute of Electric Power Industry filed Critical SHIN NIPPON KISHIYOU KAIYO KK
Priority to JP17143989A priority Critical patent/JPH0338297A/en
Publication of JPH0338297A publication Critical patent/JPH0338297A/en
Publication of JPH0565237B2 publication Critical patent/JPH0565237B2/ja
Granted legal-status Critical Current

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  • Treatment Of Water By Oxidation Or Reduction (AREA)

Abstract

PURPOSE:To decompose trichloroethylene or tetrachloroethylene contained in water to low molecular compounds so as not to remain in the environment by injecting a specified amount of ozone into water containing trichloroethylene, etc. CONSTITUTION:A gas dispersion pipe 4 equipped with fine glass filters is fitted to the tip of an ozone injection pipe 1 connected to an ozone generator 3, and this ozone injection pipe 4 is inserted into a treatment tank 2. 0.01 to 1.2mol ozone is injected for 1mol trichloroethylene or tetrachloroethylene contained in water. It is possible to decompose trichloroethylene or tetrachloroethylene in a very short time by the injected ozone and to prevent them from remaining in the environment.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明はクリーニング業や電子機器部品製造業などで洗
浄剤として使用されているトリクロロエチレン、テトラ
クロロエチレンの混入排水や飲料水等、トリクロロエチ
レン及びテトラクロロエチレン汚染水の処理方法に関す
る。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is applicable to trichlorethylene- and tetrachlorethylene-contaminated water, such as trichlorethylene- and tetrachlorethylene-contaminated wastewater and drinking water, which are used as cleaning agents in the cleaning industry and electronic device parts manufacturing industry. Regarding the processing method.

[従来の技術] トリクロロエチレンやテトラクロロエチレンが排水に混
じると、長期間に人体に入り込んで健康を害する恐れが
あることが、近年問題となっている。
[Prior Art] In recent years, it has become a problem that if trichlorethylene or tetrachlorethylene is mixed with wastewater, it may enter the human body for a long period of time and harm health.

上記汚染水からトリクロロエチレン及びテトラクロロエ
チレンを除去する方法として、従来、次のような方法が
提案されている。
Conventionally, the following methods have been proposed as methods for removing trichlorethylene and tetrachlorethylene from the contaminated water.

■活性炭、シクロデキストリンといった物質により吸着
除去する方法。
■Method of adsorption and removal using substances such as activated carbon and cyclodextrin.

■酢酸セルロース膜を使った加圧逆浸透による分離方法
■Separation method using pressurized reverse osmosis using cellulose acetate membrane.

■汚染水を空気曝気して、水中から追い出す方法 [発明が解決しようとする課題] しかしながら、上記のいずれの方法もトリクロロエチレ
ン、テトラクロロエチレンを水から物理的に分離するだ
けに留まり、分離されたトリクロロエチレン、テトラク
ロロエチレンは大気中に揮散したり、廃棄物として、そ
のまま環境中に残存することになり、二次的な汚染の原
因となる可能性がある1本発明は上記事情を考慮してな
され、トリクロロエチレン、テトラクロロエチレンを低
分子に分解することにより環境中に残存させないように
したトリクロロエチレン及びテトラクロロエチレン汚染
水の処理方法を提供することを目的とする。
■A method of aerating contaminated water and expelling it from the water [Problem to be solved by the invention] However, all of the above methods only physically separate trichlorethylene and tetrachlorethylene from water; Tetrachlorethylene may volatilize into the atmosphere or remain as waste in the environment, potentially causing secondary pollution.1 The present invention was made in consideration of the above circumstances, and An object of the present invention is to provide a method for treating trichlorethylene and tetrachlorethylene-contaminated water by decomposing tetrachlorethylene into low molecules so that they do not remain in the environment.

[課題を解決するための手段] 上記目的を達成するために本発明の第1の請求項は、水
中に含まれるトリクロロエチレンあるいはテトラクロロ
エチレン1モルに対し0.01モル〜1.2モルのオゾ
ンを送り込むことを特徴とし、第2の請求項は水中に含
まれるトリクロロエチレンあるいはテトラクロロエチレ
ン1モルに対し0.01モル〜1.2モルのオゾンを微
細フィルタを通して送り込むことを特徴とする。
[Means for Solving the Problems] In order to achieve the above object, the first claim of the present invention provides a method for feeding 0.01 mol to 1.2 mol of ozone per 1 mol of trichlorethylene or tetrachlorethylene contained in water. The second claim is characterized in that 0.01 mol to 1.2 mol of ozone is sent through a fine filter per 1 mol of trichlorethylene or tetrachlorethylene contained in water.

上記微細フィルターとしては、孔径0.2mm前後のガ
ラスフィルターが好適である。
As the fine filter, a glass filter with a pore diameter of about 0.2 mm is suitable.

トリクロロエチレンあるいはテトラクロロチジン1モル
に対しオゾンの量が0.01モル未満では実用に供さず
、また1、2モルを超える量では分解量は増大しない。
If the amount of ozone is less than 0.01 mole per mole of trichlorethylene or tetrachlorotidine, it is not practical, and if it exceeds 1 or 2 moles, the amount of decomposition will not increase.

[作 用] 放電で発生するオゾンを汚染水に接触させると、オゾン
による直接酸化やオゾンが水と反応して生成するラジカ
ルにより汚染水のトリクロロエチレン及びテトラクロロ
エチレンを分解する。
[Operation] When ozone generated by discharge comes into contact with contaminated water, trichlorethylene and tetrachlorethylene in the contaminated water are decomposed by direct oxidation by ozone and by radicals generated by ozone reacting with water.

また、微細フィルターを使用することによりオゾンと汚
染水の接触面積が増大し、分解効率が向上する。
In addition, by using a fine filter, the contact area between ozone and contaminated water increases, improving decomposition efficiency.

[実施例] 第1図は本発明を実施するための処理装置の一例を示し
たもので、オゾン発生装置3に接続されたオゾン注入管
1の先端に、微細ガラスフィルターを備えた散気管4が
取り付けてあり、この散気管4が処理水槽2に挿入され
ている。5.6.7はそれぞれヘキサンを入れたトラッ
プ、8は脱気管で、図示しない吸着装置に接続されてい
る。
[Example] Fig. 1 shows an example of a processing apparatus for implementing the present invention, in which an aeration pipe 4 equipped with a fine glass filter is installed at the tip of an ozone injection pipe 1 connected to an ozone generator 3. is attached, and this aeration pipe 4 is inserted into the treated water tank 2. 5, 6, and 7 are traps each containing hexane, and 8 is a degassing pipe, which are connected to an adsorption device (not shown).

クリーニング工場廃液に蒸溜水を加えて、約0.1%の
テトラクロロエチレン溶液を作製し、試料とした。
Distilled water was added to cleaning factory waste liquid to prepare an approximately 0.1% tetrachlorethylene solution, which was used as a sample.

この試料液IJ2を処理水槽2に入れ、オゾン10.2
0.60ppmを含む空気を散気管4から毎分2.54
で吹き込み、室温(約20℃)でのテトラクロロエチレ
ンの除去率を調べたところ、第2図のような結果が得ら
れた。なお、除去されたテトラクロロエチレンはトラッ
プ5〜7内のヘキサンに捕集される。
This sample solution IJ2 was put into the treated water tank 2, and the ozone 10.2
Air containing 0.60 ppm is supplied from diffuser pipe 4 at 2.54 per minute.
When the removal rate of tetrachlorethylene was investigated at room temperature (approximately 20°C), the results shown in Figure 2 were obtained. Note that the removed tetrachlorethylene is collected in hexane in traps 5 to 7.

第2図では吹き込んだオゾン量を対数で表わしているが
、オゾン濃度にかかわらず、約2μモル以上のオゾンが
吹き込まれると、80%以上のテトラクロロエチレンが
除去されることがわかった。
In Figure 2, the amount of ozone injected is expressed in logarithms, but it was found that, regardless of the ozone concentration, if more than about 2 μmol of ozone was injected, more than 80% of tetrachlorethylene was removed.

しかし、オゾンを含まない空気のみでも毎分2.5氾で
10分吹き込むと、曝気効果により揮散するので、オゾ
ンによる分解量を求めるには曝気による揮散量を補正す
る必要がある。
However, if only air containing no ozone is blown at 2.5 floods per minute for 10 minutes, it will volatilize due to the aeration effect, so in order to determine the amount of decomposition due to ozone, it is necessary to correct the amount of volatilization due to aeration.

第3図はオゾン・空気によるテトラクロロエチレンの除
去率から空気のみを吹き込んだ場合の除去率を補正して
、テトラクロロエチレンの分解量として表わしたもので
ある。
FIG. 3 shows the amount of tetrachlorethylene decomposed by correcting the removal rate when only air is blown from the removal rate of tetrachlorethylene using ozone and air.

オゾン濃度にかかわらず、吹き込んだオゾン約2μモル
〜約25μモルまでは約250μモル前後のテトラクロ
ロエチレンが10分以内で分解・処理でき、オゾン量が
25μモル以上ではテトラクロロエチレンの分解量は微
増となる0図示していないが、この微増傾向はテトラク
ロロエチレンの分解量に対し、オゾン量はモル比で1.
2倍まで続<、シたがって、当量比で表すと、1モルの
テトラクロロエチレンに対し、0.01〜1.2モルの
オゾンで分解・処理が可能と言える。
Regardless of the ozone concentration, approximately 250 μmol of tetrachlorethylene can be decomposed and processed within 10 minutes when the ozone is blown in from approximately 2 μmol to approximately 25 μmol, and when the amount of ozone is 25 μmol or more, the amount of tetrachlorethylene decomposed increases slightly. Although not shown in the figure, this slight increase trend indicates that the molar ratio of ozone to the decomposed amount of tetrachlorethylene is 1.
Therefore, in terms of equivalent ratio, it can be said that 1 mole of tetrachlorethylene can be decomposed and treated with 0.01 to 1.2 moles of ozone.

オゾン量に対し10倍以上のテトラクロロエチレンが系
内から消失するということは、分解生成した化合物がさ
らにテトラクロロエチレンと化学反応することを示唆し
ている。また、吹き込み量が増すにしたがって、曝気効
果により廃水中からテトラクロロエチレンが揮散して系
内のテトラクロロエチレン量が少なくなる。このため相
対的にオゾンとの接触が小さくなり、テトラクロロエチ
レン1モルに対しオゾン量がO,1モル〜1.2モルの
範囲では分解量は微増になるものと推定される。
The fact that more than 10 times as much tetrachlorethylene as the amount of ozone disappears from the system suggests that the decomposed compounds further chemically react with tetrachlorethylene. Moreover, as the amount of injection increases, tetrachlorethylene is volatilized from the wastewater due to the aeration effect, and the amount of tetrachlorethylene in the system decreases. Therefore, the contact with ozone becomes relatively small, and it is estimated that the amount of decomposition increases slightly when the amount of ozone is in the range of 1 to 1.2 moles of O per 1 mole of tetrachlorethylene.

トリクロロエチレンについてもほぼ同様な結果が得られ
、水中に含まれるテトラクロロエチレン、トリクロロエ
チレンがオゾンとの化学反応によりごく短時間に分解・
処理できることが判明した。
Almost the same results were obtained for trichlorethylene, indicating that tetrachlorethylene and trichlorethylene contained in water decompose and decompose in a very short time due to a chemical reaction with ozone.
It turns out that it can be handled.

[発明の効果] 上記のように本発明によれば、吹き込んだオゾンにより
極めて短時間でトリクロロエチレン、テトラクロロエチ
レンを分解することができ、それらが、環境中に残存す
ることを防止できる。また、オゾンを微細フィルターを
通して吹き込めば、オゾンの分解能力に加え散気による
微細なオゾンの気泡の作用との相乗効果により、トリク
ロロエチレン、テトラクロロエチレンの分解効率が向上
する。
[Effects of the Invention] As described above, according to the present invention, trichlorethylene and tetrachlorethylene can be decomposed in a very short time by the blown ozone, and it is possible to prevent them from remaining in the environment. Furthermore, if ozone is blown through a fine filter, the decomposition efficiency of trichlorethylene and tetrachlorethylene will be improved due to the synergistic effect of the ozone decomposition ability and the action of fine ozone bubbles caused by aeration.

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

第1図は本発明を実施するための装置の一例を示す概略
構成図、第2図はオゾンの吹き込みによるテトラクロロ
エチレンの除去率を示す図、第3図はオゾンによるテト
ラクロロエチレンの分解量を示す図である。 2・・・処理水槽、3・・・オゾン発生装置、4・・・
散気管(微細フィルター付)。
Figure 1 is a schematic configuration diagram showing an example of an apparatus for implementing the present invention, Figure 2 is a diagram showing the removal rate of tetrachlorethylene by ozone blowing, and Figure 3 is a diagram showing the amount of tetrachlorethylene decomposed by ozone. be. 2... Treated water tank, 3... Ozone generator, 4...
Air diffuser (with fine filter).

Claims (2)

【特許請求の範囲】[Claims] (1)水中に含まれるトリクロロエチレンあるいはテト
ラクロロエチレン1モルに対し0.01モル〜1.2モ
ルのオゾンを送り込むことを特徴とするトリクロロエチ
レン及びテトラクロロエチレン汚染水の処理方法。
(1) A method for treating water contaminated with trichlorethylene and tetrachlorethylene, which comprises feeding 0.01 to 1.2 moles of ozone per 1 mole of trichlorethylene or tetrachlorethylene contained in water.
(2)水中に含まれるトリクロロエチレンあるいはテト
ラクロロエチレンに1モル対し0.01モル〜1.2モ
ルのオゾンを微細フィルターを通して送り込むことを特
徴とするトリクロロエチレン及びテトラクロロエチレン
汚染水の処理方法。
(2) A method for treating trichlorethylene- and tetrachlorethylene-contaminated water, which comprises sending 0.01 to 1.2 moles of ozone per mole of trichlorethylene or tetrachlorethylene contained in water through a fine filter.
JP17143989A 1989-07-03 1989-07-03 Method for treating water contaminated by trichloroethylene and tetrachloroethylene Granted JPH0338297A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17143989A JPH0338297A (en) 1989-07-03 1989-07-03 Method for treating water contaminated by trichloroethylene and tetrachloroethylene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17143989A JPH0338297A (en) 1989-07-03 1989-07-03 Method for treating water contaminated by trichloroethylene and tetrachloroethylene

Publications (2)

Publication Number Publication Date
JPH0338297A true JPH0338297A (en) 1991-02-19
JPH0565237B2 JPH0565237B2 (en) 1993-09-17

Family

ID=15923143

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17143989A Granted JPH0338297A (en) 1989-07-03 1989-07-03 Method for treating water contaminated by trichloroethylene and tetrachloroethylene

Country Status (1)

Country Link
JP (1) JPH0338297A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6462250B1 (en) 1999-06-22 2002-10-08 Canon Kabushiki Kaisha Method for decomposing halogenated aliphatic hydrocarbon compounds having adsorption process and apparatus for decomposition having adsorption means
US6497795B1 (en) 1998-12-16 2002-12-24 Canon Kabushiki Kaisha Method and apparatus for decomposing gaseous aliphatic hydrocarbon halide compound
US6616815B2 (en) 1998-06-22 2003-09-09 Canon Kabushiki Kaisha Method of decomposing halogenated aliphatic hydrocarbon compounds or aromatic compounds and apparatus to be used for the same as well as method of clarifying exhaust gas and apparatus to be used for the same
US6699370B2 (en) 2000-06-16 2004-03-02 Canon Kabushiki Kaisha Process and system for decomposing pollutants
US6716399B2 (en) 1998-11-30 2004-04-06 Canon Kabushiki Kaisha Apparatus for decomposing halogenated aliphatic hydrocarbon compounds or aromatic compounds
US7018514B2 (en) 2001-11-12 2006-03-28 Canon Kabushiki Kaisha Method and apparatus for processing substances to be decomposed
US7163615B2 (en) 2001-11-12 2007-01-16 Canon Kabushiki Kaisha Method of treating substance to be degraded and its apparatus

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5750595A (en) * 1980-09-12 1982-03-25 Mitsubishi Electric Corp Treatment of waste water dissolved trichloroethylene

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5750595A (en) * 1980-09-12 1982-03-25 Mitsubishi Electric Corp Treatment of waste water dissolved trichloroethylene

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6616815B2 (en) 1998-06-22 2003-09-09 Canon Kabushiki Kaisha Method of decomposing halogenated aliphatic hydrocarbon compounds or aromatic compounds and apparatus to be used for the same as well as method of clarifying exhaust gas and apparatus to be used for the same
US6716399B2 (en) 1998-11-30 2004-04-06 Canon Kabushiki Kaisha Apparatus for decomposing halogenated aliphatic hydrocarbon compounds or aromatic compounds
US6497795B1 (en) 1998-12-16 2002-12-24 Canon Kabushiki Kaisha Method and apparatus for decomposing gaseous aliphatic hydrocarbon halide compound
US7163665B2 (en) 1998-12-16 2007-01-16 Canon Kabushiki Kaisha Apparatus for decomposing gaseous aliphatic hydrocarbon halide compounds
US6462250B1 (en) 1999-06-22 2002-10-08 Canon Kabushiki Kaisha Method for decomposing halogenated aliphatic hydrocarbon compounds having adsorption process and apparatus for decomposition having adsorption means
US6699370B2 (en) 2000-06-16 2004-03-02 Canon Kabushiki Kaisha Process and system for decomposing pollutants
US7018514B2 (en) 2001-11-12 2006-03-28 Canon Kabushiki Kaisha Method and apparatus for processing substances to be decomposed
US7163615B2 (en) 2001-11-12 2007-01-16 Canon Kabushiki Kaisha Method of treating substance to be degraded and its apparatus

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Publication number Publication date
JPH0565237B2 (en) 1993-09-17

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