JPH0565237B2 - - Google Patents
Info
- Publication number
- JPH0565237B2 JPH0565237B2 JP1171439A JP17143989A JPH0565237B2 JP H0565237 B2 JPH0565237 B2 JP H0565237B2 JP 1171439 A JP1171439 A JP 1171439A JP 17143989 A JP17143989 A JP 17143989A JP H0565237 B2 JPH0565237 B2 JP H0565237B2
- Authority
- JP
- Japan
- Prior art keywords
- tetrachlorethylene
- ozone
- trichlorethylene
- mol
- amount
- 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.)
- Expired - Lifetime
Links
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 35
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims description 35
- 229950011008 tetrachloroethylene Drugs 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 8
- 238000005273 aeration Methods 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 3
- 239000002351 wastewater Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
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、近年問題となつてい
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つた物質に
より吸着除去する方法。 A method of adsorption and removal using substances such as activated carbon and cyclodextrin.
酢酸セルロース膜を使つた加圧逆浸透による
分離方法。 A separation method using pressurized reverse osmosis using a 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。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 to expel 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, and the separated trichlorethylene and tetrachlorethylene may volatilize into the atmosphere or remain as waste in the environment, potentially causing secondary pollution. The present invention has been made in consideration of the above circumstances,
The object of the present invention is to provide a method for treating water contaminated with trichlorethylene and tetrachlorethylene, which prevents trichlorethylene and tetrachlorethylene from remaining in the environment by decomposing the trichlorethylene and tetrachlorethylene into low molecules.
[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イルタを通して
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 that 0.01 mol to 1 mol of trichlorethylene or tetrachlorethylene contained in water.
The second claim is characterized in that 1.2 mol of ozone is delivered, and the second claim is 0.01 mol of ozone per 1 mol of trichlorethylene or tetrachlorethylene contained in water.
It is characterized by feeding between mol and 1.2 mol of ozone through a fine filter.
上記微細フイルターとしては、孔径0.2mm前後
のガラスフイ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レ
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 mol per mol of trichlorethylene or tetrachloroethylene, it is not practical, and if the amount exceeds 1.2 mol, 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。ま
た、微細フイ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。[Operation] When ozone generated by discharge is brought 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. Furthermore, 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、微細ガラスフイルタ
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ツプ、8は脱気
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 carrying out 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, 7
8 is a trap containing hexane, and 8 is a degassing device, which is 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。 By adding distilled water to cleaning factory waste liquid, approximately
A 0.1% tetrachlorethylene solution was prepared and used as a sample.
この試料液1を処理水槽2に入れ、オゾン
10、20、60ppmを含む空気を散気管4から毎分
2.5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ツプ5〜7内のヘキサンに
捕集される。 This sample solution 1 is put into the treated water tank 2, and ozone
Air containing 10, 20, and 60 ppm is supplied from diffuser pipe 4 every minute.
When the removal rate of tetrachlorethylene was investigated at room temperature (approximately 20°C) by blowing at 2.5, 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つた。 In Figure 2, the amount of ozone injected is expressed as a logarithm, but it was found that, regardless of the ozone concentration, if approximately 2 μmol or more 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, even with only air without ozone,
If the ozone is blown in at 2.5 for 10 minutes, it will volatilize due to the aeration effect, so to calculate the amount of ozone decomposition, 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。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倍まで続く。したが
つて、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
From 2 μmol to approximately 25 μmol, approximately 250 μmol of tetrachlorethylene can be decomposed and processed within 10 minutes.
When the amount of ozone is 25 μmol or more, the amount of tetrachlorethylene decomposed increases slightly. Although not shown, this slight increasing tendency continues until the amount of ozone is 1.2 times the amount of decomposed tetrachlorethylene in terms of molar ratio. Therefore, expressed in equivalent ratio, 0.01 to 1.2 moles of ozone can decompose and decompose 1 mole of tetrachlorethylene.
It can be said that processing is possible.
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
増すにしたがつて、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0.1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 0.1 mol to 1.2 mol per 1 mol 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, and it was found that tetrachlorethylene and trichlorethylene contained in water can be decomposed and treated in a very short time through a chemical reaction with ozone.
[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、オゾンを微細フイ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.
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(微細フイルター付)。
FIG. 1 is a schematic diagram showing an example of an apparatus for implementing the present invention, FIG. 2 is a diagram showing the removal rate of tetrachlorethylene by ozone blowing, and FIG.
The figure shows the amount of tetrachlorethylene decomposed by ozone. 2...Treatment water tank, 3...Ozone generator, 4...
...Air diffuser (with fine filter).
Claims (1)
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。 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イ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。[Claims] 1 0.01 mol to 1 mol of trichlorethylene or tetrachlorethylene contained in water
A method for treating water contaminated with trichlorethylene and tetrachlorethylene, characterized by introducing 1.2 mol of ozone. 2 0.01 mol to 1 mol of trichlorethylene or tetrachlorethylene contained in water
A method for treating water contaminated with trichlorethylene and tetrachlorethylene, which comprises sending 1.2 mol of ozone through a fine filter.
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 JPH0338297A (en) | 1991-02-19 |
JPH0565237B2 true 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) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69942497D1 (en) | 1998-06-22 | 2010-07-29 | Canon Kk | Process for the decomposition of halogenated aliphatic and aromatic compounds |
US6610178B2 (en) | 1998-11-30 | 2003-08-26 | Canon Kabushiki Kaisha | Method for decomposing halogenated aliphatic hydrocarbon compounds or aromatic compounds, method for cleaning medium contaminated with at least one of these compounds, and apparatus for these |
US6497795B1 (en) | 1998-12-16 | 2002-12-24 | Canon Kabushiki Kaisha | Method and apparatus for decomposing gaseous aliphatic hydrocarbon halide compound |
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 |
JP3825959B2 (en) | 2000-06-16 | 2006-09-27 | キヤノン株式会社 | Pollutant decomposition method and apparatus |
JP2003205221A (en) | 2001-11-12 | 2003-07-22 | Canon Inc | Chlorinated organic compound treating method and apparatus and soil restoring method and apparatus |
US7018514B2 (en) | 2001-11-12 | 2006-03-28 | Canon Kabushiki Kaisha | Method and apparatus for processing substances to be decomposed |
Citations (1)
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 |
-
1989
- 1989-07-03 JP JP17143989A patent/JPH0338297A/en active Granted
Patent Citations (1)
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 |
Also Published As
Publication number | Publication date |
---|---|
JPH0338297A (en) | 1991-02-19 |
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