JPH05253581A - Treatment of waste water - Google Patents

Treatment of waste water

Info

Publication number
JPH05253581A
JPH05253581A JP4086301A JP8630192A JPH05253581A JP H05253581 A JPH05253581 A JP H05253581A JP 4086301 A JP4086301 A JP 4086301A JP 8630192 A JP8630192 A JP 8630192A JP H05253581 A JPH05253581 A JP H05253581A
Authority
JP
Japan
Prior art keywords
water
treated
hydrogen peroxide
titanium oxide
light
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
JP4086301A
Other languages
Japanese (ja)
Other versions
JPH0714516B2 (en
Inventor
Hiroshi Taoda
垰田博史
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP4086301A priority Critical patent/JPH0714516B2/en
Publication of JPH05253581A publication Critical patent/JPH05253581A/en
Publication of JPH0714516B2 publication Critical patent/JPH0714516B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Treatment Of Water By Oxidation Or Reduction (AREA)
  • Physical Water Treatments (AREA)

Abstract

PURPOSE:To economically treat waste water to obtain safe water by easily and rapidly treating agricultural chemicals, an org. solvent (especially, halocarbon) or a surfactant (especially, one having a side chain) hard to treat by a present activated sludge method under a mild condition in order to take measures to meet serious water pollution. CONSTITUTION:Water to be treated such as waste water is received in a container whose inside is coated with a titanium oxide film and hydrogen peroxide and a copper ion or a copper salt are added to the water to be treated to irradiate said water with light such as solar rays or water to be treated and hydrogen peroxide are received in a container whose inside is coated with a titanium oxide film containing a copper ion to be irradiated with light. By this method, the org. matter contained in the water to be treated is rapidly and perfectly oxidized and decomposed to carbon dioxide and water to obtain purified water. This waste water treatment method is extremely economical because hydrogen peroxide is inexpensive and the use amount of the copper salt is extremely small and a waste fluid containing a copper ion can be also utilized.

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、下水などの廃水処理法
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating wastewater such as sewage.

【0002】[0002]

【従来の技術】水は、空気や土、太陽などとともに人間
の生命維持に不可欠であるが、最近、その貴重な水の汚
染が広範囲に進行しており、大きな問題となっている。
特に問題になっているのは、1)ハイテク産業やクリー
ニング業で使われている有機溶剤による地下水や水源の
汚染、2)合成洗剤(界面活性剤)など、生活排水によ
る湖・河川の富栄養化や水源の汚染、3)ゴルフ場で使
用される農薬の流出による水質の汚染、3)浄水処理に
使われる塩素が被処理水中に含まれる有機物と反応する
ことによる有害物質の生成である。
2. Description of the Related Art Water, together with air, soil, the sun, etc., is indispensable for maintaining human life, but recently, valuable water pollution has become widespread and has become a major problem.
Of particular concern are 1) pollution of groundwater and water sources by organic solvents used in high-tech industry and cleaning industry, 2) eutrophication of lakes and rivers by domestic wastewater such as synthetic detergents (surfactants). And pollution of water sources, 3) pollution of water quality due to outflow of pesticides used at golf courses, and 3) generation of harmful substances by reacting chlorine used for water purification treatment with organic substances contained in the water to be treated.

【0003】現在広く行われている廃水処理法は活性汚
泥法であるが、この方法は微生物という生き物を用いる
ため、温度、PH、ガス雰囲気、毒性などの反応条件が
厳しく、しかも上述の農薬や有機溶剤(特にハロカーボ
ン)、界面活性剤(特に側鎖の付いたもの)などを分解
・除去しにくく、それらに対して無力であるという欠点
を持っている。このような生物学的に難分解性の有機物
の処理方法としては、活性炭吸着法、化学酸化法、逆浸
透法、焼却処理などがあるが、いずれも処理効果や経済
性などの点で問題が多い。化学酸化法において用いられ
る酸化剤としては塩素とオゾンが代表的なものである
が、塩素は酸化力の点や、アンモニウムイオンとの反応
性や過剰注入による残留塩素などの点、あるいは被処理
水中に含まれる有機物と反応して発ガン性を持つトリハ
ロメタンや有機塩素化合物を生成するなどの問題があ
る。また、オゾンの場合は設備費、運転費がともに高価
であるという欠点を持っている(例えば、北尾高嶺、八
橋亮介、水処理技術、Vol.8, No.8, 35 (1976))。そし
て、焼却処理は希薄溶液の場合、現実的ではない。
The currently widely used wastewater treatment method is the activated sludge method, but since this method uses living things called microorganisms, the reaction conditions such as temperature, pH, gas atmosphere, and toxicity are severe, and the above-mentioned pesticides and It has the drawback that it is difficult to decompose and remove organic solvents (especially halocarbons) and surfactants (especially those with side chains), and it is ineffective against them. Methods for treating such biologically difficult-to-decompose organic substances include activated carbon adsorption method, chemical oxidation method, reverse osmosis method, and incineration treatment, but all of them have problems in terms of treatment effect and economical efficiency. Many. Although chlorine and ozone are typical oxidants used in the chemical oxidation method, chlorine has a point of oxidizing power, reactivity with ammonium ions, residual chlorine due to excessive injection, and the like, or water to be treated. There is a problem that it reacts with the organic substances contained in to produce trihalomethane and organochlorine compounds that have carcinogenicity. In addition, ozone has the drawback that both equipment and operating costs are high (for example, Takamine Kitao, Ryosuke Yahashi, Water Treatment Technology, Vol.8, No.8, 35 (1976)). And incineration is not practical for dilute solutions.

【0004】光触媒による排水処理法は、二酸化チタン
などの半導体粉末に光を照射することによって生じる電
子と正孔の酸化還元作用を利用して被処理水中に含まれ
る有機物を分解処理するものであり、無機物を用いるた
め温度、PH、ガス雰囲気、毒性などの反応条件が厳し
くなく、しかも活性汚泥法では処理しにくい有機溶剤の
ようなものでも容易に分解・除去できるという長所を持
っている(例えば、A.L. Pruden and D. F. Ollis, Jou
rnal of Catalysis, Vol.82, 404 (1983))。しかしな
がら、この方法は反応が遅いため処理に時間がかかり、
しかも被処理水中に含まれる溶存酸素が無くなると反応
が止まってしまうという欠点を持っていた。さらに、光
触媒である二酸化チタンなどの半導体粉末を回収するた
め、処理した水を濾過しなければならないが、光触媒は
微粉末であるため目詰まりを起こし、濾過が容易でない
という問題があった。
The wastewater treatment method using a photocatalyst is a method for decomposing organic substances contained in the water to be treated by utilizing the redox action of electrons and holes generated by irradiating semiconductor powder such as titanium dioxide with light. However, since inorganic substances are used, the reaction conditions such as temperature, pH, gas atmosphere, and toxicity are not strict, and it has the advantage that even organic solvents that are difficult to process by the activated sludge method can be easily decomposed and removed (for example, , AL Pruden and DF Ollis, Jou
rnal of Catalysis, Vol.82, 404 (1983)). However, this method takes a long time because of the slow reaction,
Moreover, it has a drawback that the reaction stops when the dissolved oxygen contained in the water to be treated disappears. Further, the treated water has to be filtered in order to recover the semiconductor powder such as titanium dioxide which is a photocatalyst, but the photocatalyst is a fine powder, which causes clogging, and there is a problem that filtration is not easy.

【0005】[0005]

【発明が解決しようとする課題】本発明は上記の点に鑑
み、深刻な水質汚染に対処して、活性汚泥法では処理し
にくい農薬や有機溶剤(特にハロカーボン)、界面活性
剤(特に側鎖の付いたもの)などを温和な条件で容易か
つ迅速に処理する経済的な廃水処理法の提供を目的とす
るものである。
SUMMARY OF THE INVENTION In view of the above points, the present invention addresses serious water pollution by treating pesticides and organic solvents (especially halocarbons) and surface active agents (especially halocarbons) that are difficult to treat by the activated sludge method. It is intended to provide an economical wastewater treatment method that easily and quickly treats (such as those with chains) under mild conditions.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上述の難
分解性の汚染物質の迅速な処理法を開発するために鋭意
研究を重ねた結果、二酸化チタンなどの半導体粉末の代
わりに酸化チタン膜を用い、それに過酸化水素と銅イオ
ンを加えて光を照射するとOHラジカルが効率良く発生
し、それによって難分解性の汚染物質が容易かつ迅速に
分解されるという予想外の事実を見い出した。本発明は
この知見に基づいてなされたものである。すなわち、内
側に酸化チタン膜を被覆した容器に廃水などの被処理水
を入れ、過酸化水素と銅塩を加えて太陽光などの光を照
射すること、あるいは、鉄イオンを添加した酸化チタン
膜を内側に被覆した容器に被処理水と過酸化水素を入れ
て光を照射することによって難分解性の汚染物質が容易
かつ迅速に分解される。この場合、粉末の代わりに酸化
チタン膜を使用するため、濾過の必要がなく、過酸化水
素はオゾンよりも単位有効酸素量当りの価格がかなり低
廉で、高価な設備を必要としないという大きな利点を持
っている。
DISCLOSURE OF THE INVENTION The inventors of the present invention have conducted extensive research to develop a rapid treatment method for the above-mentioned persistent pollutants, and as a result, oxidize instead of semiconductor powder such as titanium dioxide. We found an unexpected fact that OH radicals are efficiently generated when a titanium film is used and hydrogen peroxide and copper ions are added to the film to irradiate light, thereby easily and rapidly decomposing persistent pollutants. It was The present invention was made based on this finding. That is, water to be treated such as wastewater is placed in a container coated with a titanium oxide film on the inside, hydrogen peroxide and a copper salt are added, and light such as sunlight is irradiated, or a titanium oxide film added with iron ions. By putting the water to be treated and hydrogen peroxide in a container coated with water and irradiating it with light, persistent pollutants are easily and quickly decomposed. In this case, since the titanium oxide film is used instead of the powder, there is no need for filtration, hydrogen peroxide has a considerably lower price per unit effective oxygen amount than ozone, and a great advantage that expensive equipment is not required. have.

【0007】本発明による方法で用いられる容器の材質
は、必要な強度を持っていればコンクリート、ガラス、
プラスチック、セラミックス、金属など、何でもよい。
また、本発明に用いられる容器は透明であっても不透明
であってもよいが、容器内側に被覆した酸化チタン膜が
無色透明の場合は、容器も透明の方が光が外側から壁を
透過して酸化チタン膜に入射できるため、好都合であ
る。
The material of the container used in the method according to the invention may be concrete, glass, if it has the required strength.
Anything such as plastic, ceramics, metal, etc. may be used.
The container used in the present invention may be transparent or opaque, but when the titanium oxide film coated on the inside of the container is colorless and transparent, the transparent container also allows light to pass through the wall from the outside. This is convenient because it can be incident on the titanium oxide film.

【0008】本発明による方法で用いられる容器の形状
は、角柱状、円柱状、球状、円錐状、瓢箪型、ラグビー
ボール型など、どのような形であってもよい。また、容
器が閉じた形であっても、蓋があってもなくてもよく、
円管状や角管状で反応液が流れ出すような形であっても
よい。
The shape of the container used in the method according to the present invention may be any shape such as prismatic shape, cylindrical shape, spherical shape, conical shape, gourd shape and rugby ball shape. Also, the container may be closed, with or without a lid,
The reaction liquid may flow out in a circular tube shape or a rectangular tube shape.

【0009】本発明による方法で用いられる内側に酸化
チタン膜を被覆した容器は、四塩化チタンとアルコール
との反応などによって得られるチタンのアルコキシドか
らゾル−ゲル法によってゲルを作り、ディップコーティ
ング法やスピンコーティング法、塗布法などによって容
器の内側にコートした後、焼成して製作してもよいし、
チタン製の容器の内側をガス炎などで加熱・酸化して酸
化チタンにして製作してもよい。また、CVD法、PV
D法、スパッタリング法などによって容器の内側に酸化
チタン膜を作製してもよいし、超微粒子の酸化チタンの
懸濁液をディップコーティング法やスピンコーティング
法、塗布法などによって容器の内側にコートした後、焼
成して製作してもよい。その時の焼成温度は500℃程
度が最も好ましい。さらに、上述の方法によって製造し
た酸化チタンを被覆した板あるいは酸化チタン板を組み
立てて、容器を製作してもよい。
The container coated with a titanium oxide film used in the method according to the present invention forms a gel by a sol-gel method from an alkoxide of titanium obtained by a reaction between titanium tetrachloride and alcohol, and a dip coating method or It may be manufactured by coating on the inside of the container by a spin coating method, a coating method or the like, and then firing.
The inside of a titanium container may be heated and oxidized with a gas flame to form titanium oxide. Also, CVD method, PV
A titanium oxide film may be formed on the inside of the container by a D method, a sputtering method, or the like, or a suspension of ultrafine titanium oxide may be coated on the inside of the container by a dip coating method, a spin coating method, a coating method, or the like. After that, you may bake and manufacture. The firing temperature at that time is most preferably about 500 ° C. Further, the titanium oxide-coated plate or the titanium oxide plate manufactured by the above method may be assembled to manufacture the container.

【0010】こうして得られた、内側に酸化チタン膜を
被覆した容器に、廃水などの被処理水を入れ、過酸化水
素と銅イオンを加えて太陽光などの光を照射すると、被
処理水に含まれていた有機物が速やかに分解され、炭酸
ガスと水などに完全酸化される。この場合は、酸化チタ
ン膜を使用しており、過酸化水素も最終的には水に変わ
るため、処理された水は濾過などの操作がいらず、その
まま放水できる。
The treated water such as waste water is put into the container thus obtained, which is coated with a titanium oxide film, and hydrogen peroxide and copper ions are added to the container to irradiate it with light such as sunlight. The contained organic matter is rapidly decomposed and completely oxidized into carbon dioxide gas and water. In this case, a titanium oxide film is used, and hydrogen peroxide is finally converted into water, so that the treated water can be discharged as it is without any operation such as filtration.

【0011】本発明による方法で用いられる銅イオン
は、一価の銅イオンだけでなく、二価の銅イオンや、一
価の銅イオンと二価の銅イオンの混合物なども挙げられ
る。本発明による方法で汚染物質を含んだ被処理水に銅
イオンを加える方法としては、銅塩を加えたり、銅イオ
ンを含んだ溶液あるいは廃液を加える方法が挙げられ
る。
The copper ions used in the method according to the present invention include not only monovalent copper ions, but also divalent copper ions and a mixture of monovalent copper ions and divalent copper ions. Examples of the method of adding copper ions to the water to be treated containing pollutants by the method of the present invention include a method of adding a copper salt or a solution or a waste solution containing copper ions.

【0012】本発明による方法で用いられる銅塩は、第
一銅塩だけでなく、第二銅塩や、第一銅塩と第二銅塩の
混合物などが挙げられ、硫酸塩、硝酸塩、炭酸塩、酢酸
塩、アンモニウム塩、塩化物や臭化物などのハロゲン化
物など、いろいろな塩が使用できるが、ハロゲン化物、
硝酸塩あるいは硫酸塩が好ましく、その中でも特に塩化
物が好ましい。これは塩素イオンによって反応が加速さ
れるためである。また、本発明による方法で用いられる
銅塩は無水塩であっても含水塩であってもよい。
The copper salts used in the method of the present invention include not only cuprous salts but also cupric salts and mixtures of cuprous and cupric salts, such as sulfates, nitrates and carbonates. Various salts such as salts, acetates, ammonium salts, and halides such as chloride and bromide can be used.
Nitrate or sulfate is preferable, and chloride is particularly preferable. This is because chlorine ions accelerate the reaction. The copper salt used in the method of the present invention may be an anhydrous salt or a hydrated salt.

【0013】本発明による方法で用いられる、銅イオン
を添加した酸化チタン膜を内側に被覆した容器は、上述
の方法によって得られた酸化チタン膜を被覆した容器を
第一銅塩または第二銅塩またはそれらの混合物の水溶液
に浸した後、乾燥して製作してもよいし、イオン注入法
などによって銅イオンを注入して製作してもよい。ま
た、チタンのアルコキシドからゾル−ゲル法によって作
ったゲルに銅塩またはその水溶液を添加し、ディップコ
ーティング法やスピンコーティング法、塗布法などによ
って容器の内側にコートした後、焼成して製作してもよ
いし、超微粒子の酸化チタンの懸濁液に銅塩またはその
水溶液を添加し、ディップコーティング法やスピンコー
ティング法、塗布法などによって容器の内側にコートし
た後、焼成して製作してもよい。その時の焼成温度は5
00℃程度が最も好ましい。
The container coated with a titanium oxide film to which copper ions are added, which is used in the method according to the present invention, is the container coated with the titanium oxide film obtained by the above-mentioned method, which is a cuprous salt or cupric acid. It may be manufactured by immersing it in an aqueous solution of a salt or a mixture thereof and then drying it, or may be manufactured by implanting copper ions by an ion implantation method or the like. In addition, copper salt or its aqueous solution was added to the gel made from titanium alkoxide by sol-gel method, coated on the inside of the container by dip coating method, spin coating method, coating method, etc. Alternatively, it may be manufactured by adding copper salt or its aqueous solution to a suspension of ultrafine titanium oxide, coating the inside of the container by a dip coating method, a spin coating method, a coating method, etc., and then firing. Good. The firing temperature at that time is 5
Most preferred is about 00 ° C.

【0014】こうして得られた、銅イオンを添加した酸
化チタン膜をその内側に被覆した容器に、廃水などの被
処理水を入れ、過酸化水素を加えて太陽光などの光を照
射すると、被処理水に含まれていた有機物が速やかに分
解され、炭酸ガスと水などに完全に酸化される。この場
合は、銅イオンが酸化チタン膜に含まれているため、銅
イオンや銅塩をほとんど加える必要がない。
When water to be treated such as waste water is placed in a container having a copper oxide-added titanium oxide film coated on its inside, which is obtained in this manner, and hydrogen peroxide is added to the container to irradiate it with light such as sunlight, Organic substances contained in the treated water are quickly decomposed and completely oxidized into carbon dioxide gas and water. In this case, since copper ions are contained in the titanium oxide film, it is almost unnecessary to add copper ions or copper salts.

【0015】本発明による方法で用いられる光の光源と
しては、太陽や白熱灯、蛍光灯、ハロゲンランプ、キセ
ノンランプ、水銀灯、UVランプなどが挙げられる。照
射する光は可視光のような波長の長い光でもよいが、水
の処理速度を上げたい場合には紫外線など、短波長の光
を多く含む光を用いてもよい。光の照射は、不透明容器
の場合には容器の内部あるいは開口部から行い、透明容
器の場合には容器の内部あるいは開口部、外側から行
う。このとき、光の照射と同時に加熱を行うと処理速度
を上げることができるが、その温度は70℃程度が最も
好ましい。また、その際、攪拌を行うと処理速度をさら
に上げることができる。
Examples of light sources used in the method according to the present invention include the sun, incandescent lamps, fluorescent lamps, halogen lamps, xenon lamps, mercury lamps and UV lamps. The light to be irradiated may be light having a long wavelength such as visible light, but light including a large amount of light having a short wavelength such as ultraviolet light may be used to increase the treatment speed of water. The light irradiation is performed from the inside or the opening of the container in the case of an opaque container, and from the inside or the opening or the outside of the container in the case of a transparent container. At this time, the processing speed can be increased by heating at the same time as the irradiation of light, but the temperature is most preferably about 70 ° C. Further, at that time, if stirring is performed, the processing speed can be further increased.

【0016】本発明による方法で用いられる過酸化水素
の添加量は、被処理水に含まれている有機物が炭酸ガス
や水などに無機化される反応式から化学量論的に求めら
れる。酸化チタン膜を用いる本発明の方法では光の照射
によって過酸化水素が生成し、無駄に分解して失われて
しまう過酸化水素が少なく、被処理水に含まれている有
機物の分解反応が効率的に行われるので、過酸化水素の
添加量はほぼ化学量論量でよい。さらに反応効率を上げ
るためには、マグネシウムやニオブ、チタン、鉄などを
ドープした酸化チタン膜を用いてもよいし、さらに色素
や白金膜などをコートしてもよい。また、本発明による
方法では銅イオンが光の照射により過酸化水素と連鎖的
に反応するので、銅イオンあるいは銅塩の添加量は極く
微量の触媒量でよい。廃水などの被処理水は既に銅イオ
ンを含んでいることが多いので、銅イオンあるいは銅塩
の添加が必要でないこともある。
The amount of hydrogen peroxide used in the method of the present invention is stoichiometrically determined from the reaction formula in which the organic matter contained in the water to be treated is mineralized into carbon dioxide gas or water. In the method of the present invention using a titanium oxide film, hydrogen peroxide is generated by irradiation of light and less hydrogen peroxide is wastefully decomposed and lost, and the decomposition reaction of organic substances contained in the water to be treated is efficient. The amount of hydrogen peroxide added may be approximately stoichiometric. In order to further increase the reaction efficiency, a titanium oxide film doped with magnesium, niobium, titanium, iron or the like may be used, or a dye or a platinum film may be coated. Further, in the method according to the present invention, since copper ions react with hydrogen peroxide in a chain reaction by irradiation with light, the addition amount of copper ions or copper salt may be a very small amount of catalyst. Since treated water such as waste water often already contains copper ions, it may not be necessary to add copper ions or copper salts.

【0017】こうして廃水などの被処理水に過酸化水素
と銅塩を加えて太陽光などの光を照射すると、被処理水
に含まれていた有機物が速やかに分解され、炭酸ガスと
水などに完全に酸化される。本発明による方法では第一
銅塩だけでなく第二銅塩でも第一銅塩と第二銅塩の混合
物でも銅イオンを含んだ溶液あるいは廃液でも使用する
ことができ、反応条件に制限がなく、光を照射するとい
う簡単な方法で廃水を迅速に処理できる。このとき、光
の照射と同時に加熱を行うと処理速度を上げることがで
きるが、その温度は70℃程度が最も好ましい。また、
その際、攪拌を行うと処理速度をさらに上げることがで
きる。
When hydrogen peroxide and copper salts are added to water to be treated such as wastewater and light such as sunlight is irradiated, organic substances contained in the water to be treated are rapidly decomposed to carbon dioxide gas and water. It is completely oxidized. In the method according to the present invention, not only the cuprous salt but also the cupric salt, the mixture of the cuprous salt and the cupric salt, or the solution or the waste solution containing copper ions can be used, and the reaction conditions are not limited. The wastewater can be treated quickly by the simple method of irradiating with light. At this time, the processing speed can be increased by heating at the same time as the irradiation of light, but the temperature is most preferably about 70 ° C. Also,
At that time, if stirring is performed, the processing speed can be further increased.

【0018】[0018]

【実施例】本発明の実施例の内で特に代表的なものを以
下に示す。
EXAMPLES Among the examples of the present invention, particularly representative ones are shown below.

【0019】実施例1 有機リン系の農薬である4−ニトロフェニルエチルフェ
ニルホスフィナートの4000ppmの濃度の水溶液
を、内側に酸化チタン膜を被覆した硬質ガラス製容器に
入れ、12000ppmの過酸化水素と150ppmの
塩化第二銅・二水和物を添加し、マグネチックスターラ
ーで攪拌しながら、500Wのキセノンランプの光を1
時間20分間照射した。得られた反応液の全有機炭素の
量(TOC値)を全有機炭素計を用いて分析した結果、
反応液のTOC値は80%減少していた。
Example 1 An aqueous solution of 4-nitrophenylethylphenylphosphinate, an organophosphorus pesticide, at a concentration of 4000 ppm was placed in a hard glass container coated with a titanium oxide film on the inside, and 12000 ppm of hydrogen peroxide was added. And 150 ppm cupric chloride dihydrate are added, and the light of a 500 W xenon lamp is adjusted to 1 while stirring with a magnetic stirrer.
Irradiation for 20 minutes. As a result of analyzing the total organic carbon amount (TOC value) of the obtained reaction liquid using a total organic carbon meter,
The TOC value of the reaction solution was reduced by 80%.

【0020】比較例 4−ニトロフェニルエチルフェニルホスフィナートの4
000ppmの濃度の水溶液を、内側に酸化チタン膜を
被覆した硬質ガラス製容器に入れ、150ppmの塩化
第二銅・二水和物を添加し、マグネチックスターラーで
攪拌しながら、500Wのキセノンランプの光を1時間
20分間照射した。得られた反応液のTOC値を全有機
炭素計を用いて分析した結果、反応液のTOC値は10
%しか減少していなかった。また、実施例1で塩化第二
銅・二水和物を添加しない場合には反応液のTOC値は
40%しか減少していなかった。他の有機リン系の農薬
である4−ニトロフェニルジエチルホスフェートや、ジ
エチルベンジルホスフォナート、ジエチル−p−ニトロ
フェニル チオホスフェート、0,0−ジメチル−S−
(1,2−ジカルベトキシエチル)ホスフォロジチオエ
ートの場合も、同様の結果が得られた。
Comparative Example 4 of 4-nitrophenylethylphenylphosphinate
An aqueous solution having a concentration of 000 ppm was placed in a hard glass container coated with a titanium oxide film on the inside, 150 ppm of cupric chloride dihydrate was added, and the mixture was stirred with a magnetic stirrer while stirring with a 500 W xenon lamp. The light was irradiated for 1 hour and 20 minutes. As a result of analyzing the TOC value of the obtained reaction liquid using a total organic carbon meter, the TOC value of the reaction liquid was 10
Only%. Further, in Example 1, when the cupric chloride dihydrate was not added, the TOC value of the reaction solution was reduced by only 40%. Other organophosphorus pesticides such as 4-nitrophenyl diethyl phosphate, diethyl benzyl phosphate, diethyl-p-nitrophenyl thiophosphate, 0.0-dimethyl-S-
Similar results were obtained with (1,2-dicarbetoxyethyl) phosphorodithioate.

【0021】実施例2 内側に酸化チタン膜を被覆した鉛ガラス製容器を2g/
lの塩化白金酸カリウムのエタノール水溶液に入れ、マ
グネチックスターラーで攪拌しながら、100Wの水銀
ランプの光を4時間照射し、酸化チタン膜の表面に白金
をコートした。この容器にトリクロロエチレンの400
ppmの濃度の水溶液を入れ、600ppmの過酸化水
素と20ppmの酢酸銅を添加して、マグネチックスタ
ーラーで攪拌しながら500Wの白熱灯の光を1時間照
射した。得られた反応液に含まれるTOC値を全有機炭
素計を用いて分析した結果、反応液のTOC値が95%
減少しており、トリクロロエチレンの95%が分解して
いることが分かった。
Example 2 A lead glass container coated with a titanium oxide film on the inside was 2 g /
It was put in an aqueous ethanol solution of potassium chloroplatinate (1) and stirred with a magnetic stirrer, and was irradiated with light of a 100 W mercury lamp for 4 hours to coat the surface of the titanium oxide film with platinum. 400 ml of trichlorethylene in this container
An aqueous solution having a concentration of ppm was added, hydrogen peroxide of 600 ppm and copper acetate of 20 ppm were added, and light of an incandescent lamp of 500 W was irradiated for 1 hour while stirring with a magnetic stirrer. As a result of analyzing the TOC value contained in the obtained reaction solution using a total organic carbon meter, the TOC value of the reaction solution was 95%.
It was found that 95% of trichlorethylene had decomposed.

【0022】比較例 実施例2で作製した容器に400ppmの濃度のトリク
ロロエチレンの水溶液と20ppmの酢酸銅を入れ、マ
グネチックスターラーで攪拌しながら500Wの白熱灯
の光を1時間照射した。得られた反応液のTOC値を全
有機炭素計を用いて分析した結果、反応液のTOC値は
11%しか減少していなかった。また、実施例2で酢酸
銅を添加しなかった場合には反応液のTOC値は45%
しか減少しなかった。
Comparative Example A container prepared in Example 2 was charged with an aqueous solution of trichloroethylene having a concentration of 400 ppm and 20 ppm of copper acetate, and irradiated with light of a 500 W incandescent lamp for 1 hour while stirring with a magnetic stirrer. As a result of analyzing the TOC value of the obtained reaction solution using a total organic carbon meter, the TOC value of the reaction solution was reduced by only 11%. Further, in the case where copper acetate was not added in Example 2, the TOC value of the reaction solution was 45%.
Only decreased.

【0023】実施例3 内側に酸化チタン膜を被覆した直径8mm長さ30cm
の石英ガラス製の円管を硫酸第二銅の10%溶液に浸し
て乾燥した後、その中を300ppmの濃度のテトラク
ロロエチレンの水溶液に500ppmの過酸化水素を添
加した50℃の溶液をゆっくり流下させながら、外側か
ら500Wのキセノンランプの光を1時間照射した。得
られた反応液のTOC値を全有機炭素計を用いて分析し
た結果、反応液のTOC値は93%減少していた。
Example 3 Titanium oxide film coated on the inside 8 mm in diameter and 30 cm in length
The quartz glass circular tube is immersed in a 10% solution of cupric sulfate and dried, and then a solution of tetrachloroethylene having a concentration of 300 ppm and 500 ppm of hydrogen peroxide added thereto is slowly flowed down at 50 ° C. Meanwhile, the light of a 500 W xenon lamp was irradiated from the outside for 1 hour. As a result of analyzing the TOC value of the obtained reaction solution using a total organic carbon meter, the TOC value of the reaction solution was reduced by 93%.

【0024】比較例 実施例3と同様にして300ppmの濃度のテトラクロ
ロエチレンの水溶液の50℃に加熱した溶液をゆっくり
流下させながら外側から500Wのキセノンランプの光
を1時間照射した。得られた反応液のTOC値を全有機
炭素計を用いて分析した結果、反応液のTOC値は20
%しか減少していなかった。
Comparative Example In the same manner as in Example 3, a solution of an aqueous solution of tetrachloroethylene having a concentration of 300 ppm heated to 50 ° C. was slowly flowed down and irradiated with 500 W of a xenon lamp from the outside for 1 hour. As a result of analyzing the TOC value of the obtained reaction liquid using a total organic carbon meter, the TOC value of the reaction liquid was 20.
Only%.

【0025】実施例4 硝酸第二銅を添加した酸化チタン膜をその内側に被覆し
たアルミナ容器に、活性汚泥処理が困難なエチレンジア
ミン四酢酸二ナトリウムの1%溶液を入れ、3%の過酸
化水素を添加し、攪拌しながら、500WのUVランプ
の光を1時間照射した。得られた反応液のTOC値を全
有機炭素計を用いて、また、COD値(化学的酸素要求
量)をCOD測定装置によって分析した結果、反応液の
TOC値は85%、また、COD値も80%減少してい
た。
Example 4 A 1% solution of disodium ethylenediaminetetraacetate, which is difficult to treat with activated sludge, was placed in an alumina container whose inside was coated with a titanium oxide film containing cupric nitrate, and 3% hydrogen peroxide was added. Was added, and the mixture was irradiated with light from a 500 W UV lamp for 1 hour while stirring. The TOC value of the obtained reaction solution was analyzed by using a total organic carbon meter, and the COD value (chemical oxygen demand) was analyzed by a COD measuring device. As a result, the TOC value of the reaction solution was 85%, and the COD value was Also decreased by 80%.

【0026】比較例 実施例4と同様の容器に、エチレンジアミン四酢酸二ナ
トリウムの1%溶液を入れ、攪拌しながら、500Wの
UVランプの光を1時間照射した。得られた反応液のT
OC値を全有機炭素計を用いて、また、COD値をCO
D測定装置によって分析した結果、反応液のTOC値
も、COD値も約10%しか減少していなかった。
Comparative Example A 1% solution of ethylenediaminetetraacetic acid disodium was placed in the same container as in Example 4 and irradiated with a 500 W UV lamp for 1 hour while stirring. T of the obtained reaction solution
The OC value was measured using a total organic carbon meter, and the COD value was measured using CO
As a result of analysis by a D measuring device, both the TOC value and the COD value of the reaction solution were reduced by about 10%.

【0027】実施例5 80ppmの濃度の合成洗剤(アルキルベンゼンスルホ
ン酸)の水溶液を、内側にニオブドープの酸化チタン膜
を被覆した硬質ガラス製容器に入れ、300ppmの過
酸化水素と20ppmの銅イオンを含んだ廃水を加え、
マグネチックスターラーで攪拌しながら太陽光を1時間
半照射した。得られた反応液のTOC値を全有機炭素計
を用いて、また、アルキルベンゼンスルホン酸の濃度を
メチレンブルー法によって分析した。その結果、反応液
のアルキルベンゼンスルホン酸の濃度は8ppmに減
り、TOC値も90%減少していた。
Example 5 An aqueous solution of a synthetic detergent (alkylbenzene sulfonic acid) having a concentration of 80 ppm was placed in a hard glass container coated with a niobium-doped titanium oxide film on the inside, and 300 ppm hydrogen peroxide and 20 ppm copper ions were contained therein. Add wastewater,
While stirring with a magnetic stirrer, sunlight was irradiated for one and a half hours. The TOC value of the obtained reaction solution was analyzed using a total organic carbon meter, and the concentration of alkylbenzene sulfonic acid was analyzed by the methylene blue method. As a result, the concentration of alkylbenzenesulfonic acid in the reaction solution was reduced to 8 ppm, and the TOC value was also reduced by 90%.

【0028】比較例 実施例5と同様の容器に80ppmの濃度の合成洗剤
(アルキルベンゼンスルホン酸)の水溶液を入れ、マグ
ネチックスターラーで攪拌しながら太陽光を1時間半照
射した。得られた反応液のTOC値を全有機炭素計を用
いて、また、アルキルベンゼンスルホン酸の濃度をメチ
レンブルー法によって分析した。その結果、反応液のア
ルキルベンゼンスルホン酸の濃度は70ppmとあまり
変わらず、TOC値も13%しか減少していなかった。
また、実施例5で銅イオンを含んだ廃水を添加しなかっ
た場合には反応液のTOC値及びアルキルベンゼンスル
ホン酸の濃度が55%しか減少しなかった。
Comparative Example An aqueous solution of a synthetic detergent (alkylbenzene sulfonic acid) having a concentration of 80 ppm was placed in the same container as in Example 5, and the mixture was irradiated with sunlight for 1 hour and a half while stirring with a magnetic stirrer. The TOC value of the obtained reaction solution was analyzed using a total organic carbon meter, and the concentration of alkylbenzene sulfonic acid was analyzed by the methylene blue method. As a result, the concentration of the alkylbenzene sulfonic acid in the reaction solution did not change much to 70 ppm, and the TOC value was reduced only by 13%.
Further, when the waste water containing copper ions was not added in Example 5, the TOC value of the reaction solution and the concentration of alkylbenzene sulfonic acid were reduced by only 55%.

【0029】実施例6 300ppmの濃度のクロロホルムの水溶液を、内側に
酸化チタン膜を被覆した硬質ガラス製容器に入れ、25
0ppmの過酸化水素と25ppmの塩化第一銅を添加
し、マグネチックスターラーで攪拌しながら30Wの蛍
光灯を10本用いて光を1時間20分間照射した。得ら
れた反応液のTOC値を全有機炭素計を用いて分析した
結果、反応液のTOC値は83%減少していた。
Example 6 An aqueous solution of chloroform having a concentration of 300 ppm was placed in a hard glass container having a titanium oxide film coated on the inside thereof, and was put at 25
0 ppm of hydrogen peroxide and 25 ppm of cuprous chloride were added, and light was irradiated for 1 hour and 20 minutes using 10 fluorescent lamps of 30 W while stirring with a magnetic stirrer. As a result of analyzing the TOC value of the obtained reaction liquid using a total organic carbon meter, the TOC value of the reaction liquid was reduced by 83%.

【0030】比較例 実施例6と同様の容器に300ppmの濃度のクロロホ
ルムの水溶液と25ppmの塩化第一銅を入れ、マグネ
チックスターラーで攪拌しながら30Wの蛍光灯を10
本用いて光を1時間20分間照射した。得られた反応液
のTOC値を全有機炭素計を用いて分析した結果、反応
液のTOC値は12%しか減少していなかった。また、
実施例6で塩化第一銅を添加しない場合には反応液のT
OC値が41%しか減少しなかった。
COMPARATIVE EXAMPLE A container similar to that used in Example 6 was charged with an aqueous solution of chloroform having a concentration of 300 ppm and 25 ppm of cuprous chloride and stirred with a magnetic stirrer to obtain a 10 W fluorescent lamp.
The book was used and irradiated with light for 1 hour and 20 minutes. As a result of analyzing the TOC value of the obtained reaction liquid using a total organic carbon meter, the TOC value of the reaction liquid was reduced by only 12%. Also,
When cuprous chloride was not added in Example 6, T of the reaction solution
The OC value decreased only 41%.

【0031】[0031]

【発明の効果】本発明は以上説明したように、深刻な水
質汚染に対処して、活性汚泥法では処理しにくい農薬や
有機溶剤(特にハロカーボン)、界面活性剤(特に側鎖
の付いたもの)などを温和な条件で容易にかつ迅速に処
理できる経済的な廃水処理方法を提供するものである。
内側に酸化チタン膜を被覆した容器に廃水などの被処理
水を入れ、過酸化水素と銅イオンまたは銅塩を添加して
太陽光などの光を照射すること、あるいは、銅イオンを
添加した酸化チタン膜を内側に被覆した容器に被処理水
と過酸化水素を入れて加熱あるいは無加熱で光を照射す
ることにより、被処理水に含まれていた有機物を速やか
に炭酸ガスと水などに分解し、浄化された水を得ること
ができる。本発明による方法で用いられる過酸化水素は
安価であり、使用される銅塩は極く微量で、銅イオンを
含んだ廃液も利用できるため、非常に経済的である。ま
た、本発明による廃水処理プロセスを行って難分解性の
物質を分解した後、活性汚泥法による水処理を行えば、
水の浄化効果がさらに大きい。
INDUSTRIAL APPLICABILITY As described above, the present invention copes with serious water pollution, and pesticides and organic solvents (especially halocarbons) which are difficult to treat by the activated sludge method, and surfactants (especially those having a side chain). The present invention provides an economical wastewater treatment method capable of easily and quickly treating such substances) under mild conditions.
Put water to be treated such as waste water in a container coated with titanium oxide film inside, add hydrogen peroxide and copper ion or copper salt and irradiate with light such as sunlight, or oxidize by adding copper ion By putting the water to be treated and hydrogen peroxide into a container coated with a titanium film inside and irradiating it with or without heating, the organic substances contained in the water to be treated are rapidly decomposed into carbon dioxide gas and water. And you can get purified water. Hydrogen peroxide used in the method according to the present invention is inexpensive, the amount of copper salt used is very small, and a waste liquid containing copper ions can be used, which is very economical. In addition, if the wastewater treatment process according to the present invention is carried out to decompose hardly-decomposable substances, then water treatment by the activated sludge method is performed
Greater water purification effect.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 内側に酸化チタン膜を被覆した容器に被
処理水を入れ、過酸化水素と銅イオンを添加し、光を照
射することを特徴とする廃水処理方法。
1. A method for treating waste water, which comprises placing water to be treated in a container coated with a titanium oxide film, adding hydrogen peroxide and copper ions, and irradiating with light.
【請求項2】 内側に酸化チタン膜を被覆した容器に被
処理水と過酸化水素と銅塩を入れ、光を照射することを
特徴とする廃水処理方法。
2. A method for treating waste water, which comprises irradiating light with water to be treated, hydrogen peroxide and copper salt being placed in a container coated with a titanium oxide film on the inside.
【請求項3】 内側に酸化チタン膜を被覆した容器に被
処理水と過酸化水素と銅イオンを含んだ廃水を入れ、光
を照射することを特徴とする廃水処理方法。
3. A method for treating wastewater, which comprises irradiating light with water to be treated, wastewater containing hydrogen peroxide and copper ions being placed in a container coated with a titanium oxide film.
【請求項4】 銅イオンを添加した酸化チタン膜を内側
に被覆した容器に、被処理水と過酸化水素を入れ、光を
照射することを特徴とする廃水処理方法。
4. A method for treating waste water, which comprises irradiating light with water to be treated and hydrogen peroxide placed in a container whose inside is coated with a titanium oxide film added with copper ions.
【請求項5】 光を照射すると同時に加熱や攪拌を行う
ことを特徴とする請求項1または2または3または4記
載の廃水処理方法。
5. The wastewater treatment method according to claim 1, wherein heating and stirring are performed at the same time as irradiating with light.
JP4086301A 1992-03-10 1992-03-10 Wastewater treatment method Expired - Lifetime JPH0714516B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4086301A JPH0714516B2 (en) 1992-03-10 1992-03-10 Wastewater treatment method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4086301A JPH0714516B2 (en) 1992-03-10 1992-03-10 Wastewater treatment method

Publications (2)

Publication Number Publication Date
JPH05253581A true JPH05253581A (en) 1993-10-05
JPH0714516B2 JPH0714516B2 (en) 1995-02-22

Family

ID=13883018

Family Applications (1)

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

Country Link
JP (1) JPH0714516B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7485259B2 (en) * 2002-10-08 2009-02-03 Eldred Bradley J Organic compound and metal ion synergistic disinfection and purification system and method of manufacture
WO2014195686A1 (en) * 2013-06-03 2014-12-11 Managed Technologies Limited Water treatment apparatus

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7485259B2 (en) * 2002-10-08 2009-02-03 Eldred Bradley J Organic compound and metal ion synergistic disinfection and purification system and method of manufacture
US8173067B2 (en) 2002-10-08 2012-05-08 Bradley J. Eldred Organic compound and metal ion synergistic disinfection and purification system and method of manufacture
WO2014195686A1 (en) * 2013-06-03 2014-12-11 Managed Technologies Limited Water treatment apparatus
GB2517546A (en) * 2013-06-03 2015-02-25 Managed Technologies Ltd Water treatment apparatus
GB2517546B (en) * 2013-06-03 2017-01-04 Managed Tech Ltd Water treatment apparatus

Also Published As

Publication number Publication date
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