WO2002079096A1 - Procede et dispositif de decomposition de polluants environnementaux - Google Patents
Procede et dispositif de decomposition de polluants environnementaux Download PDFInfo
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- WO2002079096A1 WO2002079096A1 PCT/JP2002/003070 JP0203070W WO02079096A1 WO 2002079096 A1 WO2002079096 A1 WO 2002079096A1 JP 0203070 W JP0203070 W JP 0203070W WO 02079096 A1 WO02079096 A1 WO 02079096A1
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- solution
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- reaction vessel
- ultrasonic
- environmental pollutants
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- 239000003344 environmental pollutant Substances 0.000 title claims abstract description 109
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- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
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- C—CHEMISTRY; METALLURGY
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- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
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- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
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- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D2203/00—Aspects of processes for making harmful chemical substances harmless, or less harmful, by effecting chemical change in the substances
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- B01J2219/00049—Controlling or regulating processes
- B01J2219/00051—Controlling the temperature
- B01J2219/00132—Controlling the temperature using electric heating or cooling elements
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- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/0873—Materials to be treated
- B01J2219/0877—Liquid
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/72—Treatment of water, waste water, or sewage by oxidation
- C02F1/722—Oxidation by peroxides
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
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- C02F2101/32—Hydrocarbons, e.g. oil
- C02F2101/322—Volatile compounds, e.g. benzene
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
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- C02F2101/36—Organic compounds containing halogen
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
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- C02F2101/363—PCB's; PCP's
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/36—Organic compounds containing halogen
- C02F2101/366—Dioxine; Furan
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/06—Contaminated groundwater or leachate
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/32—Details relating to UV-irradiation devices
- C02F2201/322—Lamp arrangement
- C02F2201/3227—Units with two or more lamps
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/32—Details relating to UV-irradiation devices
- C02F2201/322—Lamp arrangement
- C02F2201/3228—Units having reflectors, e.g. coatings, baffles, plates, mirrors
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2209/00—Controlling or monitoring parameters in water treatment
- C02F2209/02—Temperature
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- C—CHEMISTRY; METALLURGY
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- C02F2209/00—Controlling or monitoring parameters in water treatment
- C02F2209/06—Controlling or monitoring parameters in water treatment pH
Definitions
- the present invention relates to a method and an apparatus for decomposing and detoxifying various pollutants in the environment. More specifically, the present invention relates to organic solvents such as organic halogen compounds contained in soil, groundwater, industrial wastewater, and the like, and river water, lakes and marshes. The present invention relates to a method and an apparatus for easily and efficiently decomposing organic substances, nitrogen-phosphorus compounds, and the like contained in water. Background art
- organic solvents especially organic halogen compounds such as tetrachloroethylene, trichloroethylene, and dichloromethane have been used in various manufacturing and laundry industries as cleaning agents having excellent solubility in oils and fats. Recently, its carcinogenicity has been pointed out, and its release into the environment has been restricted. However, the pollution of the environment such as air, public waters, and soil by organic chlorine compounds has not been solved yet, and the use of alternative solvents or detoxification after the use of solvents has been required.
- refrigerants such as chlorofluorocarbon and polychlorinated biphenyl (PCB) that have been used as refrigerants and insulating oils, and dioxins that are generated in the presence of chlorine compounds in garbage incinerators and the like when the incineration temperature is low, include organic halogen compounds. And its persistence in the environment poses a problem due to its toxicity and indegradability.
- PCB polychlorinated biphenyl
- organohalogen compounds are volatile and easily volatilize into the atmosphere as a gas. Utilizing this property, as a method for removing organic halogen compounds contained in contaminated soil ⁇ groundwater or industrial wastewater, there are methods such as air-ventilation and air-dissipation, and air-dissipation. Many methods of transferring organic halides into the gas phase, recovering them with an adsorbent such as activated carbon, and incinerating them as waste are now being practiced in terms of cost and simplicity.
- the aeration method has a problem that harmful substances are diffused into the atmosphere as it is, thus causing air pollution.
- the activated carbon adsorption method Since the amount of adsorption per hour is limited, in the case of wastewater treatment containing high-concentration pollutants, the frequency of replacement increases, resulting in higher costs. There are issues such as the possibility of leakage. Furthermore, both methods merely transfer the pollutants, and the harmful substances themselves do not chemically change.Especially, when incinerating the activated carbon that has adsorbed the pollutants, the highly toxic dioxin is generated. Both of the above methods have caused problems.
- OH radicals have a higher oxidizing power than ozone, as shown in Table 1, and have a low selectivity for the reactants and a high activity, so they are the main components of the reaction, and the volatile substances and cavitation bubbles mentioned above. Evaporates and oxidizes and decomposes non-volatile substances such as ionic substances that are difficult to enter into harmless substances. table 1
- the decomposition rate depends on the frequency of the irradiated ultrasonic waves.
- the formation of cavitation bubbles and crushing, that is, thermal decomposition and oxidative decomposition by radicals take a cycle of several seconds to several 10 / X seconds. The decomposition is performed efficiently.
- the oxidizing power of hydrogen peroxide is weaker than that of OH radical or ozone, so that the decomposition rate decreases at the end of the reaction.
- an object of the present invention is to process and decompose volatile substances such as organic halogen compounds in wastewater in a short time in a large amount up to a low concentration range that can be discharged to sewage or the like as wastewater.
- An object of the present invention is to provide a method and an apparatus capable of decomposing even a substance which is particularly difficult to oxidatively decompose, such as an organic substance, a nitrogen-phosphorus compound, and the like. Disclosure of the invention
- the present inventors have conducted intensive studies to solve the above-mentioned problems, and found that the combination of ultrasonic irradiation treatment and ultraviolet irradiation treatment improved the decomposition rate of organic halogen compounds, etc. It has been found that the nitrogen-phosphorus compound can be decomposed, and the present invention has been completed.
- one of the methods for decomposing environmental pollutants of the present invention is to introduce a solution to be treated containing an environmental pollutant into a reaction vessel, and apply ultrasonic waves and ultraviolet rays to the solution to be treated stored in the reaction vessel.
- ultrasonic irradiation means is attached to the reaction vessel to irradiate ultrasonic waves, and ultraviolet rays are irradiated to a position which does not substantially interfere with the traveling path of the ultrasonic waves.
- the method is characterized in that ultraviolet light is applied to the solution to be treated stored in the traveling path of the ultrasonic wave.
- the hydrogen peroxide generated by the ultrasonic waves is irradiated with the ultraviolet rays, thereby achieving high activity. Since OH radicals are generated with low selectivity, contaminated water containing volatile substances such as organic halogen compounds can be easily, without reagents, and efficiently, from high concentration levels to low concentration levels that are equivalent to the standard levels for environmental emissions. It can be decomposed into water, drained to public sewage, etc., and used as reused water.
- the ultraviolet irradiation means is installed at a position that does not substantially interfere with the traveling path of the ultrasonic waves, the ultraviolet irradiation means does not hinder the progress of the ultrasonic waves, and suppresses the attenuation of the ultrasonic waves and efficiently irradiates the ultrasonic waves.
- a decomposition process can be performed.
- Another method for decomposing environmental pollutants of the present invention is a method for decomposing environmental pollutants.
- a treatment solution introduced into the reaction vessel, and irradiating the solution to be treated stored in the reaction vessel with ultrasonic waves and ultraviolet rays to decompose the environmental pollutants. And irradiating the solution with ultrasonic waves, and then introducing the solution subjected to ultrasonic treatment into a second reaction vessel and irradiating the solution with ultraviolet rays.
- ultrasonic irradiation of an aqueous solution containing contaminants first generates hydrogen peroxide in the liquid phase, followed by irradiation with ultraviolet rays to generate OH radicals from hydrogen peroxide. Therefore, it is possible to decompose volatile substances in a low concentration range or substances that are difficult to oxidatively decompose in the liquid phase.
- the environmental pollutants are organic halogen compounds. Since organic halogen compounds such as low molecular weight ethylene tetrachloride are volatile, they are easily decomposed by ultrasonic irradiation, so that the method of the present invention can be particularly preferably used.
- the solution to be treated is a dry cleaning waste liquid. Since the dry cleaning waste liquid contains a volatile organic halogen compound such as tetrachloroethylene, it is easily decomposed by ultrasonic irradiation, and the method of the present invention can be particularly preferably used.
- a volatile organic halogen compound such as tetrachloroethylene
- simultaneous or sequential irradiation of the ultrasonic irradiation and the ultraviolet irradiation is repeated for a plurality of cycles.
- continuous treatment can be performed while flowing the solution to be treated, and treatment can be performed in accordance with the final target concentration of the treated water.
- an apparatus having a high processing effect can be configured, and production is easy and cost reduction is achieved. . That is, for example, by using a cascade-connected configuration or a multi-stage configuration using a plurality of large-sized reaction vessels, scale-up of processing capacity or continuous processing can be realized easily and at low cost.
- the ultrasonic irradiation and / or the ultraviolet ray irradiation are performed while the pH of the solution to be treated is adjusted to 2 to 6. According to this method, the oxidizing power of OH radicals in the solution to be treated is increased, so that the decomposition treatment can be performed efficiently.
- the ultrasonic irradiation and the Z or ultraviolet irradiation are performed after or while adding hydrogen peroxide to the solution to be treated.
- the added hydrogen peroxide is decomposed by ultraviolet rays to generate OH radicals, and a large amount of OH radicals is present even in the initial stage of decomposition, so that the decomposition treatment can be performed efficiently. it can.
- the ultrasonic irradiation and the Z or ultraviolet irradiation are performed while maintaining the temperature of the solution to be treated at 40 to 60 ° C. .
- the vapor pressure of volatile environmental pollutants in the solution to be treated is increased, so that the number of molecules of environmental pollutants migrating into the cavitation bubbles increases, and unnecessary boiling phenomenon does not occur. . Therefore, the decomposition speed is improved, and the treatment can be performed efficiently.
- the temperature of the solution to be treated is maintained at 40 to 60 ° C. by intermittently irradiating the ultrasonic waves and Z or the ultraviolet rays. I do. According to this method, it is not necessary to provide a new temperature adjusting means, and the temperature can be controlled only by the electric ONZOFF, so that the temperature of the solution to be treated can be easily maintained at low cost.
- a reflection surface is formed on a peripheral wall of the reaction vessel to which the ultraviolet irradiation means is attached, so that the irradiated ultraviolet rays hardly leak out of the reaction vessel. I do. According to this method, since the entire surface of the reaction vessel can be irradiated with ultraviolet rays by using the reflecting surface, the generation of O H radicals in the solution to be treated is promoted, and the decomposition treatment can be performed efficiently.
- one of the devices for decomposing environmental pollutants of the present invention comprises: a reaction vessel for storing a solution to be treated containing environmental pollutants; and means for irradiating the solution to be treated in the reaction vessel with ultrasonic waves.
- An apparatus for decomposing environmental pollutants comprising: means for irradiating the solution to be treated in the reaction vessel with ultraviolet light, wherein the apparatus does not substantially interfere with the traveling path of the ultrasonic waves irradiated by the ultrasonic irradiation means.
- the ultraviolet irradiation means is arranged at a position where the solution to be processed stored in the traveling path of the ultrasonic waves can be irradiated with ultraviolet rays.
- Ultrasonic irradiation and ultraviolet irradiation of environmental pollutants In the same manner as above, contaminated water containing volatile substances such as organic halogen compounds can be easily and without reagent from high-concentration levels to low-concentration levels at the level of environmental emission standards. It can be decomposed efficiently and can be drained to public sewage and used as reused water on an industrial scale.
- the ultraviolet irradiation means does not substantially interfere with the traveling path of the ultrasonic wave and is located at a position where the ultraviolet light can be irradiated to the solution to be treated, when the ultrasonic wave and the ultraviolet light are simultaneously irradiated, The ultraviolet irradiation means does not hinder the progress of the ultrasonic wave, the processing efficiency of the apparatus is improved, and the decomposition treatment can be performed to a low concentration in a short time.
- the ultraviolet irradiation means is arranged on an outer circumference of a traveling path of the ultrasonic wave. Therefore, when simultaneously irradiating the ultrasonic wave and the ultraviolet light, the ultraviolet irradiation means does not hinder the progress of the ultrasonic wave, so that the decomposing process can be performed efficiently.
- the ultraviolet irradiation means is disposed in the reaction vessel along a traveling path of the ultrasonic wave, and the ultrasonic irradiation means is superposed along an outer periphery of the ultraviolet irradiation means. It is attached to the reaction vessel so that a sound wave can travel. Also in this case, when simultaneously irradiating the ultrasonic waves and the ultraviolet rays as described above, the ultraviolet irradiation means does not hinder the progress of the ultrasonic waves, so that the decomposition treatment can be performed efficiently.
- the ultrasonic irradiation means and the ultraviolet irradiation means are arranged such that the ultrasonic waves irradiated by the ultrasonic irradiation means travel along the surface of the ultraviolet irradiation means. ing. According to this, when the ultraviolet irradiation means is immersed in the solution to be treated, the adhesion of dirt to the ultraviolet lamp or the like is prevented by the ultrasonic waves, so that a decrease in ultraviolet transmittance can be prevented.
- Another of the apparatus for decomposing environmental pollutants of the present invention is a reaction vessel for storing a solution to be treated containing an environmental pollutant, means for irradiating the solution to be treated in the reaction vessel with ultrasonic waves,
- An environmental pollutant decomposing apparatus comprising: means for irradiating the solution to be treated in the reaction vessel with ultraviolet light; a first reaction vessel storing the solution to be treated; and an outflow from the first reaction vessel.
- a second reaction vessel for storing the solution to be treated, wherein the first reaction vessel is provided with ultrasonic irradiation means for irradiating the treatment solution with ultrasonic waves; and In the reaction vessel, the ultrasonically treated Ultraviolet irradiation means for irradiating the treatment solution with ultraviolet rays is provided.
- the ultraviolet irradiation means does not interfere with the traveling path of the ultrasonic wave. For this reason, it is possible to efficiently irradiate ultrasonic waves, and the dissolving capacity of the apparatus is improved.
- the apparatus for decomposing environmental pollutants of the present invention has a pH adjusting agent adding means for adjusting the pH of the solution to be treated to 2 to 6.
- a pH adjusting agent adding means for adjusting the pH of the solution to be treated to 2 to 6.
- the ultrasonic irradiation and the UV irradiation or the UV irradiation can be performed with the pH of the solution to be treated adjusted to an optimal range, for example, pH 2 to 6.
- the oxidizing power of OH radicals in the solution to be treated is increased, the decomposition treatment can be performed efficiently.
- a hydrogen peroxide adding means for adding hydrogen peroxide to the solution to be treated.
- ultrasonic irradiation and Z or the ultraviolet irradiation can be performed after or while adding hydrogen peroxide to the solution to be treated. It is decomposed by ultraviolet rays to generate OH radicals, and a large amount of OH radicals is present even in the initial stage of decomposition, so that the decomposition process can be performed efficiently.
- a temperature adjusting means for maintaining the temperature of the solution to be treated at 40 to 60 ° C. According to this, as described above, the decomposition speed is improved, and the processing can be performed efficiently.
- an irradiation control means for intermittently irradiating the ultrasonic waves and / or the ultraviolet rays to maintain the temperature of the solution to be treated at 40 to 60 ° C. preferable.
- the temperature can be adjusted only by controlling the irradiation of ultrasonic waves and / or ultraviolet rays without providing a heating or cooling means, so that the cost of the apparatus can be reduced.
- a reflecting surface is formed on a peripheral wall of the reaction vessel to which the ultraviolet irradiation means is attached. According to this, the ultraviolet light radiated from the ultraviolet irradiating means is reflected by the reflecting surface and is effectively irradiated to the solution to be treated, so that the decomposition efficiency can be improved.
- the ultrasonic irradiation means and the ultraviolet irradiation means may be provided. Is preferred. According to this, since the ultrasonic irradiation and the ultraviolet irradiation can be repeated a plurality of times, the liquid to be treated can be treated to a target level. Further, it is preferably used for treating a solution to be treated containing an organic halogen compound as the environmental pollutant. According to this, the organic halogen compound can be effectively decomposed.
- FIG. 1 is a schematic configuration diagram showing an embodiment of an apparatus for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along line AA ′ of (a).
- FIG. 2 is a schematic configuration diagram showing another embodiment of the apparatus for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along line BB ′ of (a).
- FIG. 3 is a schematic configuration diagram showing still another embodiment of the environmental pollutant decomposition device according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along the line CC ′ of (a). .
- FIG. 4 is a schematic configuration diagram showing another embodiment of the device for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view, and (b) is a D_D and cross-sectional view of (a).
- FIG. 5 is a schematic configuration diagram showing another embodiment of the apparatus for decomposing environmental pollutants according to the present invention, where (a) is a plan view and (b) is a cross-sectional view taken along line E-E of (a).
- FIG. 6 is a schematic configuration diagram showing another embodiment of the device for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view, and (b) is a cross-sectional view taken along line FF of (a).
- FIG. 7 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 8 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 9 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 10 is a schematic diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- FIG. 10 is a schematic diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- FIGS. 11A and 11B are schematic structural views showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention, wherein FIG. 11A is a plan view, and FIG. 11B is a sectional view taken along line GG ′ of FIG. It is.
- FIG. 12 is a schematic configuration diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along the line ⁇ _ ⁇ ′ of (a). .
- FIG. 12 is a schematic configuration diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along the line ⁇ _ ⁇ ′ of (a). .
- FIG. 13 is a schematic configuration diagram showing still another embodiment of the environmental pollutant decomposition apparatus according to the present invention, wherein (a) is a plan view and (b) is a cross-sectional view taken along the line I-I ′ of (a). It is.
- FIG. 14 is a schematic configuration diagram showing still another embodiment of the environmental pollutant decomposing device according to the present invention, wherein (a) is a plan view, (b) is a J_J of (a), and a cross-sectional view. It is.
- FIG. 15 is a schematic configuration diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- FIG. 16 is a schematic configuration diagram showing still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- FIG. 17 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 18 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 19 is a schematic configuration diagram showing still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- FIG. 20 is a diagram showing an example of temperature control by intermittent irradiation of ultrasonic waves and ultraviolet rays in FIG.
- FIG. 21 is a graph showing the relationship between the treatment time and the residual tetrachloroethylene concentration in Example 1 and Comparative Examples 1 and 2 of the present invention.
- FIG. 22 is a graph showing the relationship between the treatment time and the nitrogen decomposition rate in Example 2 of the present invention and Comparative Examples 3 and 4.
- FIG. 23 is a graph showing the relationship between the treatment time and the residual tetrachloroethylene concentration in Examples 3 and 4 and Comparative Examples 5 and 6 of the present invention.
- FIG. 24 is a graph showing the relationship between the treatment time and the residual tetrachloroethylene concentration in Example 5 and Comparative Example 7 of the present invention.
- FIG. 25 is a graph showing the relationship between the treatment time in Examples 6 and 7 and Comparative Examples 8 to 11 of the present invention and the concentration of residual tetrataroethylene.
- FIG. 1 shows an embodiment of an apparatus for decomposing environmental pollutants of the present invention.
- a solution to be treated 20 which is an aqueous solution containing environmental pollutants is contained in a reaction vessel 10a.
- the inside of the reaction vessel 10a is mostly filled with the solution 20 to be treated, and is shut off from outside air to form a closed system.
- a disk-shaped ultrasonic oscillator 30 a is provided at the center bottom of the reaction vessel 10 a, and is connected to the oscillator 31.
- a plurality of rod-shaped ultraviolet lamps 40a are arranged around the vibrator 30a in the solution 20 to be treated so as to surround the vibrator 30a around the vibrator 30a. As shown in (a), in this embodiment, four ultraviolet lamps are arranged.
- the material of the reaction vessel 10 can be appropriately selected from metals, glass, plastics, and the like, but is preferably a material that does not leak ultraviolet rays to the outside of the reaction vessel 10. In addition, measures may be taken to prevent ultraviolet rays from leaking to the outside. Further, since ultrasonic waves are irradiated from the outside of the reaction vessel 10, it is preferable that the material and the thickness be such that the propagation of the ultrasonic waves is not hindered.
- the cylindrical ultraviolet lamp 40a is mounted vertically downward so that it can be easily replaced at the end of its life, and a single ultraviolet lamp has a range from near the water surface to near the bottom surface of the container.
- Fig. 1 (a) when the effective area of ultrasonic waves is cylindrical in the center of the container as shown in Fig. 1 (a), the ultraviolet rays are irradiated in the radial direction of the lamp tube. It is desirable to attach two or more.
- the ultraviolet lamp 40a does not hinder the progress of the ultrasonic waves, and the effective region of the ultrasonic waves is irradiated with the maximum amount of ultraviolet light in consideration of the overlap of the ultraviolet rays radiated from each of the ultraviolet lamps 40a. Mounting in position It is preferred that
- the ultrasonic irradiation means a conventionally known ultrasonic apparatus using the piezoelectric effect of a crystal can be used, and is not particularly limited.
- the vibrator 30a may be arranged outside the bottom of the reaction vessel 10a as shown in FIG. 1 (b), or may be arranged at the bottom inside the reaction vessel 10a.
- the reaction vessel 10a is filled with the solution 20 to be treated, and the irradiation of the ultraviolet lamp 40a is started, and at the same time, the ultrasonic oscillator 31 is operated to start the irradiation of ultrasonic waves from the vibrator 30a. You. Then, ultraviolet rays (not shown) are emitted from the ultraviolet lamp 40a toward the radially inner side of the reaction vessel. On the other hand, the ultrasonic waves 50 are emitted from the vibrator 30a in the axial direction (vertical direction) of the reaction vessel 10a as shown by the phantom line in FIG. 1 (b).
- the ultrasonic irradiation causes instantaneous adiabatic compression of the cavitation bubbles, as described above, and a high temperature of several thousand degrees and several thousand atmospheres. Decomposes into harmless carbon dioxide and halogen ions.
- OH radicals are generated by thermal decomposition of water molecules and oxidative decomposition is also performed by OH radicals.On the contrary, hydrogen peroxide is generated by recombination of OH radicals Also progresses.
- the hydrogen peroxide generated in the liquid phase of the solution to be treated 20 by ultraviolet irradiation from the ultraviolet lamp 40a is again decomposed into OH radicals.
- OH radicals are newly generated in the liquid phase, not at the interface of the cavitation bubbles.
- the high oxidizing power of these OH radicals improves the decomposition rate of volatile substances in wastewater in low-concentration regions.
- the UV irradiation intensity and the ultrasonic frequency can be appropriately selected depending on the type, amount, initial concentration, final target decomposition concentration, etc. of the target solution to be treated, and are not particularly limited.
- the irradiation intensity is preferably from 0.1 to 100 mWZ cm 2 , while the irradiation frequency of the ultrasonic wave is less than that due to the cavitation effect.
- FIG. 2 shows another embodiment of the apparatus for decomposing environmental pollutants according to the present invention. In the following description of the embodiment, substantially the same parts as those of the above embodiment are denoted by the same reference numerals, and description thereof will be omitted.
- this decomposition apparatus is different in that an ultraviolet lamp 40a is disposed outside a reaction vessel 10b.
- the reaction vessel 10b is preferably made of a material such as quartz glass through which ultraviolet rays pass.
- the ultraviolet lamp 40a can be easily replaced and the maintenance is easy, and the ultraviolet lamp 40a is not directly immersed in the solution 20 to be treated, so that the safety is improved. I do.
- FIG. 3 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the ultraviolet lamp 40b has a cylindrical shape and is attached vertically downward so as to surround a cylindrical central portion of the container, which is an effective area of ultrasonic waves, as shown in FIG. Is different from the embodiment.
- the number of ultraviolet lamps 40a is considered in consideration of the overlap of the ultraviolet light emitted as in the first embodiment. Since there is no need to determine the location and location, the efficiency of decomposing environmental pollutants can be further improved.
- FIG. 4 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention. This embodiment differs from FIG. 3 only in that an ultraviolet lamp 40b is arranged outside the reaction vessel 10b as in FIG.
- FIG. 5 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- This embodiment is different from the first embodiment in that the positional relationship between the ultrasonic irradiation unit and the ultraviolet irradiation unit is reversed. Therefore, the transducer 30 b of the ultrasonic wave 50 is It has a ring shape and is provided at the bottom of a cylindrical reaction vessel 10c. Further, a cylindrical ultraviolet lamp 40a is attached to the center of the reaction vessel 10c vertically downward.
- FIG. 6 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the ultraviolet lamp 40a is arranged inside the reaction vessel 10d so that the ultraviolet lamp 40a does not directly immerse in the solution 20 to be treated is shown in FIG. Is different.
- FIG. 7 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- this apparatus is composed of two types of reaction vessels, a reaction vessel 10e for ultrasonic irradiation and a reaction vessel 10f for irradiation with ultraviolet rays.
- a disk-shaped vibrator 30a is provided at the bottom of the center of the reaction vessel 10e, and a rod-shaped ultraviolet lamp 40a is mounted vertically downward in the center of the reaction vessel 10f. ing.
- the solution 20 to be treated is injected into the reaction vessel 10f, and is irradiated with ultrasonic waves by a timer (not shown) for a certain period of time.
- volatile substances such as organic halogen compounds contained in the solution to be treated 20 are rapidly decomposed up to a high to medium concentration range by the effect of the above-mentioned cavitation bubbles.
- the decomposition rate decreases, and instead, the thermal decomposition of water vapor generates OH radicals and recombination to generate hydrogen peroxide.
- the solution 20 to be treated is an organic substance or a nitrogen-phosphorus compound in environmental water, and particularly contains a substance that is non-volatile and difficult to oxidatively decompose, direct decomposition only by the above-mentioned cavitation bubbles cannot be performed.
- Hydrogen peroxide is mainly generated by thermal decomposition of steam.
- the solution 20 to be treated containing the hydrogen peroxide and the unreacted substance generated by the treatment in the reaction vessel 10 e is subsequently introduced into the reaction vessel 10 f and irradiated by the ultraviolet lamp 40 a. Processing is performed. As a result, the hydrogen peroxide is decomposed by ultraviolet rays to regenerate OH radicals, and unreacted substances that could not be decomposed in the reaction vessel 10e can be oxidized and decomposed in the reaction vessel 10f.
- the introduction of the solution to be treated from the reaction vessel 10e into the reaction vessel 10f can be performed manually or automatically using a liquid sending pump or the like.
- reaction vessels 10e and 10f can be connected and circulated in a loop as shown in Fig. 7. According to the present embodiment, it is also possible to repeat the processing until the target decomposition rate is achieved.
- FIG. 8 shows still another embodiment of the device for decomposing environmental pollutants according to the present invention.
- the apparatus of the embodiment shown in FIG. 5 is connected in a plurality of cascades.
- simultaneous processing of ultrasonic irradiation and ultraviolet irradiation is continuously performed in each of the reaction vessels 10c, 10c ', and 10c "..., thereby increasing the processing capacity and shortening the continuous processing. It is possible in a short time, and it is possible to reliably achieve the target decomposition rate in the final treated water 20a.
- each reaction vessel is not particularly limited as long as it can perform a combination treatment of ultrasonic irradiation and ultraviolet irradiation, and any of the embodiments 10a to 10c according to the embodiment of the present invention is applicable. Is also usable and is not particularly limited. Further, a combination of the reaction vessels 10e and 10f as shown in FIG. 7 may be used to form a cascade.
- FIG. 9 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- a plurality of sets of means for simultaneously irradiating ultrasonic waves and ultraviolet rays are provided, and a means for controlling the direction of the flow of the solution to be treated is provided between each pair. Is possible.
- this decomposition apparatus has a plurality of compartments partitioned by a plurality of partition walls 61 in 10 g of a reaction vessel.
- an ultraviolet lamp 40a and an ultrasonic vibrator 30b are arranged to form an ultrasonic / ultraviolet processing section 62.
- a partition wall 61 extending from the bottom wall of the reaction vessel 10 g to below the water surface and a partition wall 61 extending from the top of the reaction vessel 10 g to the vicinity of the bottom wall are provided between the processing units 62.
- the flow adjustment section 60 is sandwiched therebetween.
- the solution to be treated 20 was added to the first ultrasonic / ultraviolet treatment section 6 2 of the reaction vessel 10 g (Fig. 9
- the flow of the solution to be treated 20 goes to the upper part from the lower part in Fig. 9 in the ultrasonic / ultraviolet processing part 62, and to the lower part from the upper part by the partition wall 61 in the flow adjusting part 60.
- continuous treatment of the solution to be treated 20 becomes possible, and the final target decomposition rate in the treated water 20a can be achieved.
- the decomposition apparatus can be made more compact.
- FIG. 10 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the reaction vessel 1Oh of this embodiment includes a plurality of sets of means for simultaneously irradiating ultrasonic waves and ultraviolet rays as in the above-described embodiment, but omits means for controlling the flow direction of the solution to be treated. This is different from the embodiment of FIG.
- a plurality of sets of the ultrasonic / ultraviolet processing unit 62 including the ultraviolet lamp 40a and the ultrasonic vibrator 30b are arranged in the reaction vessel 10h.
- Each wall is not provided between them, and the solution to be treated 20 is configured to pass through each of the ultrasonic wave processing sections 62 in the lateral direction.
- the apparatus can be further integrated and compacted, so that a large-volume treatment solution 20 can be subjected to both ultrasonic irradiation and ultraviolet irradiation.
- a large-volume treatment solution 20 can be subjected to both ultrasonic irradiation and ultraviolet irradiation.
- adjacent ultrasonic waves interfere with each other with a traveling wave, a reflected wave, or the like. It is desirable that they should be placed at an appropriate distance from each other.
- 11 to 13 show other different embodiments of the apparatus for decomposing environmental pollutants according to the present invention.
- an ultrasonic vibrator 30a for treating the solution 20 to be treated is arranged at the center of the bottom wall of the reaction vessel 10a.
- four ultraviolet lamps 40a are arranged at equal intervals.
- the bottom wall of the reaction vessel 10a is surrounded by an ultrasonic vibrator 30a for treating the solution 20 to be treated, and is provided with an annular cleaning for cleaning the ultraviolet lamp 40a.
- a transducer 30 c is provided.
- the decomposition device shown in FIG. 12 is similar to the decomposition device shown in FIG. The difference is that a cylindrical ultraviolet lamp 40b is used instead. Also in this disassembly apparatus, an annular cleaning oscillator 30d is provided on the bottom wall of the reaction vessel 10a just below the ultraviolet lamp 40b.
- a rod-shaped ultraviolet lamp 40 a is disposed at the center of the reaction vessel 10 a, and an ultrasonic vibrator 30 a for treating the solution 20 to be treated is provided in the reaction vessel 1 a. It is arranged in an annular shape on the periphery of the bottom wall of 0a. At the center of the bottom wall of the reaction vessel 10a, a disc-shaped cleaning vibrator 30e for cleaning the ultraviolet lamp 40a is provided.
- the water immersion type ultraviolet lamp 40a emits ultraviolet light due to the adhesion or coloring of physical dirt such as particles contained in the solution 20 to be treated on the tube surface.
- separate washing vibrators 30 c, 30 d, and 30 e are provided on the bottom of the reaction vessel 10 a and directly below the ultraviolet lamp 40. Therefore, it is possible to use the oscillation of the cavitation caused by irradiation of the cleaning ultrasonic waves 50a, the oxidative decomposition by hydrogen peroxide or OH radicals, and the bleaching action. Therefore, it is possible to maintain a stable treatment effect for a long time.
- the ultrasonic 50a has the advantage that the wavelength becomes shorter as the frequency becomes higher and the reaction area increases with the increase of cavitation bubbles, but the drawback is that the directivity and attenuation are increased. Therefore, the frequency of the cleaning ultrasonic wave applied to the ultraviolet lamp 40a is preferably a low frequency of 20 to 100 kHz. If the frequency is lower than 20 kHz, the reaction region accompanying the increase in cavitation bubbles is reduced and the cleaning effect is not sufficient, and if the frequency is higher than 100 kHz, high directivity and high attenuation are obtained. As a result, effective ultrasonic intensity cannot be obtained at and near the tube bottom of the ultraviolet lamp 40a, and a sufficient cleaning effect may not be obtained, which is not preferable.
- the timing of irradiating the reaction ultrasonic wave and the cleaning ultrasonic wave is determined by the reaction ultrasonic wave and the degree of coloring of the solution to be treated 20 or the degree of adhesion of the ultraviolet lamp 40a.
- Ultrasonic waves for cleaning may be constantly applied during processing, or ultrasonic waves for cleaning may be applied after the processing such as maintenance is completed.
- the ultrasonic waves for treatment may be alternately irradiated during the treatment.
- FIG. 14 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- This embodiment differs from the embodiment of FIG. 5 in that the relationship between the ring inner diameter D T of the vibrator 30 f and the tube diameter DL of the ultraviolet lamp 40 is opposite to that of D L ⁇ D T. ing. That is, the ultrasonic irradiation area partially overlaps from the tube surface of the ultraviolet lamp 40a toward the center of the tube diameter. -By irradiating ultrasonic waves 50 with a part of the reaction ultrasonic waves in contact with the ultraviolet lamp 40a and using the vibrator 30f in this way, the reaction due to ultrasonic turbulence is resolved.
- the efficiency is slightly reduced, the prevention of a decrease in the UV transmittance due to the adhesion of physical stains such as particles contained in the solution to be treated 20 to the tube surface or the coloring is performed simultaneously with the decomposition treatment.
- the structure can be simplified.
- the difference between and DT can be set as appropriate, but from the viewpoint of preventing the decomposition efficiency of the reaction due to the disturbance of the ultrasonic wave as much as possible, the smaller the better, the better, preferably between 0 and 0.1 mm. It is.
- FIG. 15 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the basic configuration of the apparatus is the same as that of the embodiment of FIG. 5, and the transducer 30 b of the ultrasonic wave 50 has a ring shape, and the cylindrical reaction vessel 10 c It is provided at the bottom.
- the cylindrical ultraviolet lamp 40a is mounted vertically downward on the center of the reaction vessel 10c.
- a pH adjusting agent adding means 70 for adjusting the pH of the sample solution 20 is provided.
- the pH adjusting agent adding means 70 includes a pH sensor 71, a solenoid valve 72, and a solution tank 73.
- the solution tank 73 contains a pH adjusting agent such as an acid, an alkali, or a phosphate buffer solution.
- a required amount of the pH adjuster is set according to the pH of the solution 20 to be treated. It is injected into the sample solution to enable constant pH adjustment.
- the oxidizing power of OH radicals generated by simultaneous irradiation of ultrasonic waves and ultraviolet rays is acidic>alkali> neutral
- the oxidizing power of OH radicals in the solution to be treated is increased, especially in the acidic region, making the decomposition process efficient. Can be done.
- the pH adjusting agent addition means as shown in FIG. 15 is not used, and the pH is separately and manually shown in FIG. Another embodiment is shown.
- the basic configuration of the device is the same as that of the embodiment of FIG. 15 except that a hydrogen peroxide adding unit 80 is provided instead of the pH adjusting agent adding unit. It differs from the embodiment of FIG.
- the hydrogen peroxide adding means 80 includes a hydrogen peroxide sensor 81, a solenoid valve 82, and a solution tank 83, and the solution tank 83 contains hydrogen peroxide.
- a required amount of hydrogen peroxide is injected into the reaction vessel 10c sample solution by opening and closing the solenoid valve 82 by a control signal from the hydrogen peroxide sensor 81, and a certain amount of hydrogen peroxide is supplied.
- the density can be adjusted.
- the ultrasonic irradiation and / or the ultraviolet irradiation can be performed after or while adding hydrogen peroxide to the solution 20 to be treated.
- the amount of hydrogen peroxide generated in the initial stage of decomposition is small, so the amount of O H radical generated by irradiation with ultraviolet light is small, and ultrasonic decomposition is mainly performed in the initial stage of decomposition.
- the added hydrogen peroxide is decomposed by ultraviolet rays to generate OH radicals separately, so that the decomposition treatment can be performed efficiently even in the initial stage. it can.
- the amount of hydrogen peroxide to be added is preferably 10 to 100 times the molar concentration of environmental pollutants in the solution 20 to be treated. Further, in the present invention, the hydrogen peroxide adding means as shown in FIG. 16 may not be used, and hydrogen peroxide may be separately added manually or the like.
- FIG. 17 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the basic configuration of the device is the same as that of the embodiment of FIG. 5.
- the point that a heater or a cooler 91 is provided on the outer periphery of the force reaction vessel 10c is different from that of FIG. It is different from the form.
- the temperature adjusting means 90a includes a heater or a cooler 91 and a temperature sensor 92.
- a heater or the cooler 91 a conventionally known heater or a cooler such as a Peltier element can be used.
- the heater or cooler 91 is controlled by the control signal from the temperature sensor 92 so that the temperature of the solution to be treated 20 can be maintained at a preset target liquid temperature.
- the temperature of the solution to be treated in the range of 40 to 60 ° C. If the temperature of the solution to be treated is less than 40 ° C, the vapor pressure of liquid or environmental pollutants in the cavitation bubbles will be low due to the low vapor pressure of the liquid at low water temperature in the ultrasonic reaction mechanism. ⁇ Since the amount of transfer is small, the number of molecules thermally decomposed or oxidatively decomposed by OH radicals is decreased, which is not preferable. On the other hand, when the temperature exceeds 60 ° C., a boiling phenomenon occurs, and the reaction tends to be nonuniform, and the cost is uneconomical.
- the temperature of the solution to be treated 20 is preliminarily heated until it reaches 40 to 60 ° C, and then irradiation of ultrasonic waves and ultraviolet rays is started. Is preferred.
- FIG. 18 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the basic configuration of the device is the same as that of the above-described embodiment of FIG. 17, except that the temperature adjusting means 9 Ob includes a temperature sensor 92, a heating or cooling jacket 93, and a solenoid valve. The difference is that it consists of 94.
- a heating liquid or a cooling liquid supplied from the outside flows into the heating or cooling jacket 93 along the direction of the arrow in FIG.
- the temperature of the solution to be treated 20 can be maintained at 40 to 60 ° C.
- the temperature of the heating liquid or the cooling liquid may be adjusted using the control signal from the temperature sensor 92.
- FIG. 19 shows still another embodiment of the apparatus for decomposing environmental pollutants according to the present invention.
- the basic configuration of the device is the same as that of the embodiment of FIG. 5.
- a temperature adjusting means of the solution to be treated 20 a temperature sensor 92 in a reaction vessel 10 c, an ultrasonic wave and Ultrasonic / ultraviolet control circuit 95 that can control O NZ OFF of ultraviolet irradiation is installed. Then, the signal of the temperature sensor 92 is input to the ultrasonic wave / ultraviolet ray control circuit 92, and the ultrasonic wave / ultraviolet ray control circuit 92 sets the driving power to the oscillator 31 so that the temperature falls within a preset temperature range.
- the drive power supply to the UV lamp 40a is intermittently turned ON / OFF.
- FIG. 20 shows an example of temperature control by intermittent driving of ultrasonic and ultraviolet irradiation using the apparatus of FIG.
- Tb is the upper limit of the set temperature
- Ta is the lower limit of the set temperature
- T. Is the initial temperature before the treatment of the solution 20 to be treated.
- drive power P at the start of processing. Is supplied, ultrasonic waves and ultraviolet rays are irradiated on the solution to be treated 20, and the temperature of the solution to be treated 20 detected by the temperature sensor 92 is T. To Tb.
- the ultrasonic wave / ultraviolet ray control circuit 92 is operated to stop the irradiation of the ultrasonic wave and the ultraviolet ray with the driving power to OFF, the temperature of the solution to be treated 20 gradually decreases.
- the drive power P is again increased. Is supplied, and ultrasonic waves and ultraviolet rays are irradiated to the solution to be treated. In this way, the temperature of the solution to be treated 20 can be maintained by repeating the intermittent irradiation of ultrasonic waves and ultraviolet rays.
- the drive power P 0 , the drive power supply time lt on, and the drive power non-supply time lt off can be appropriately set according to the set temperatures Ta and Tb.
- the driving power P may not always be constant, for example, the initial temperature T of the solution 20 to be treated. When the temperature is low, the initial decomposition rate decreases. Therefore, the driving power P may be increased and the time ta may be shortened until the set temperature reaches the upper limit Tb.
- Example 1 The time-dependent change in the concentration of the remaining ethylene tetrachloride was measured under the same conditions as in Example 1 except that only the ultraviolet rays were irradiated and the ultrasonic waves were not irradiated.
- the results are shown in FIG. From Fig. 21, it can be seen that in Example 1 in which simultaneous irradiation with ultrasonic waves and ultraviolet rays was performed, the decomposition rate hardly decreased even when the ethylene concentration in the residual tetrachloride decreased, and the time was only 2 hours, and the decomposition rate was as short as 15 hours. It was possible to decompose from a high concentration level of O mg / L to a low concentration level of 0.1 mg ZL, which is the standard value for sewage drainage.
- Example 2 Under the same conditions as in Example 2 except that only the ultraviolet rays were irradiated and the ultrasonic waves were not irradiated, the change over time in the generation rate of the decomposition product nitrate ion was measured. The results are shown in FIG. As can be seen from FIG. 22, in Example 2 in which simultaneous irradiation with ultrasonic waves and ultraviolet rays was performed, the decomposition rate increased with the elapse of the processing time, and the decomposition rate was about 40% in one hour. On the other hand, in Comparative Examples 3 and 4 of the single treatment, the decomposition rate after 1 hour was 0.5% or less, and almost no decomposition was performed. Therefore, it can be seen that the present invention is also effective for non-volatile and hardly decomposable substances, for example, organic substances and nitrogen-phosphorus compounds which are difficult to oxidatively decompose.
- non-volatile and hardly decomposable substances for example, organic substances and nitrogen-phosphorus compounds which are difficult to oxid
- Example 9 From FIG. 24, it can be seen that in Example 7 in which hydrogen peroxide was added to the solution to be treated, both the decomposition rate and decomposition rate were higher than in Example 8 in which hydrogen peroxide was not added.
- a high concentration aqueous solution of tetrachlorethylene 4 Omg / L (3 L) was used as the solution to be treated, and the temperature of the solution to be treated was 40 ° C. While maintaining the temperature at 200 kHz, an ultrasonic wave of 200 kHz and 50 W and an ultraviolet ray having a maximum ultraviolet ray intensity at a wavelength of about 260 nm were simultaneously irradiated, and the time-dependent change in the concentration of the remaining tetrachloroethylene was measured. The results are shown in FIG.
- Example 9 Under the same conditions as in Example 9 except that the temperature of the solution to be treated was maintained at 60 ° C, the remaining The change over time in the ethylene concentration of the tracloth was measured. The results are shown in FIG.
- the solution to be treated was 10 ° C., 25 ° C., 80 ° C. It can be seen that the decomposition rate was higher than in Examples 11 to 14 in which the temperature was maintained at 90 ° C, and the processing was performed in a short time.
- the solution to be treated is irradiated with ultrasonic waves and ultraviolet rays simultaneously, or after the ultrasonic waves are irradiated, the combined treatment of ultrasonic waves and ultraviolet rays such as irradiation with ultraviolet rays is carried out,
- an ultraviolet irradiation means at a position that does not substantially interfere with the route, contaminated water containing volatile substances such as organic halogen compounds can be easily and simply removed from high-concentration levels to low-concentration levels at the level of environmental emission standards. It can be decomposed efficiently with reagents, and can be drained to public sewage and used as reused water.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mechanical Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Physical Water Treatments (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Accessory Of Washing/Drying Machine, Commercial Washing/Drying Machine, Other Washing/Drying Machine (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
- Fire-Extinguishing Compositions (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/473,644 US20040170538A1 (en) | 2001-03-28 | 2002-03-28 | Method and device for decomposing environmental pollutants |
KR10-2003-7012376A KR20030083752A (ko) | 2001-03-28 | 2002-03-28 | 환경 오염 물질의 분해 방법 및 장치 |
EP02713224A EP1375432A4 (en) | 2001-03-28 | 2002-03-28 | METHOD AND DEVICE FOR DECOMPOSING ENVIRONMENTAL POLLUTANTS |
Applications Claiming Priority (4)
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JP2001092353 | 2001-03-28 | ||
JP2001-92353 | 2001-03-28 | ||
JP2001-324766 | 2001-10-23 | ||
JP2001324766A JP2002355551A (ja) | 2001-03-28 | 2001-10-23 | 環境汚染物質の分解方法及び装置 |
Publications (1)
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WO2002079096A1 true WO2002079096A1 (fr) | 2002-10-10 |
Family
ID=26612333
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PCT/JP2002/003070 WO2002079096A1 (fr) | 2001-03-28 | 2002-03-28 | Procede et dispositif de decomposition de polluants environnementaux |
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---|---|
US (1) | US20040170538A1 (ja) |
EP (1) | EP1375432A4 (ja) |
JP (1) | JP2002355551A (ja) |
KR (1) | KR20030083752A (ja) |
CN (1) | CN1535249A (ja) |
WO (1) | WO2002079096A1 (ja) |
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Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3672823A (en) * | 1970-03-25 | 1972-06-27 | Wave Energy Systems | Method of sterilizing liquids |
JPH04166283A (ja) * | 1990-10-30 | 1992-06-12 | Furuno Aqua Toreede:Kk | 殺菌装置 |
JPH05228480A (ja) * | 1992-02-24 | 1993-09-07 | Kubota Corp | 生物難分解性物質の処理装置 |
JPH0655196A (ja) * | 1992-08-06 | 1994-03-01 | F Tex:Kk | 汚水浄化処理方法およびその装置 |
JPH07108285A (ja) * | 1993-10-12 | 1995-04-25 | Kubota Corp | 汚水中のダイオキシン類除去方法 |
JPH11300345A (ja) * | 1998-04-20 | 1999-11-02 | Kubota Corp | 埋立浸出水中のダイオキシン類等の有機塩素化合物の分解方法および分解装置 |
JP2000334447A (ja) * | 1999-05-28 | 2000-12-05 | Hitachi Metals Ltd | 循環水浄化滅菌装置 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE855521C (de) * | 1950-12-28 | 1952-11-13 | Siemens Ag | Verfahren und Einrichtung zum Behandeln, vorzugsweise Reinigen von Abwaessern und anderen Fluessigkeiten |
US5130031A (en) * | 1990-11-01 | 1992-07-14 | Sri International | Method of treating aqueous liquids using light energy, ultrasonic energy, and a photocatalyst |
GB9206079D0 (en) * | 1992-03-20 | 1992-05-06 | Biwater Treatment Ltd | Treatment of water |
SE504204C2 (sv) * | 1994-12-28 | 1996-12-09 | Rune Soeremark | Förfarande och anordning för behandling av fluida samt användning av detta fluidum |
-
2001
- 2001-10-23 JP JP2001324766A patent/JP2002355551A/ja not_active Withdrawn
-
2002
- 2002-03-28 CN CNA028073770A patent/CN1535249A/zh active Pending
- 2002-03-28 US US10/473,644 patent/US20040170538A1/en not_active Abandoned
- 2002-03-28 WO PCT/JP2002/003070 patent/WO2002079096A1/ja not_active Application Discontinuation
- 2002-03-28 EP EP02713224A patent/EP1375432A4/en not_active Withdrawn
- 2002-03-28 KR KR10-2003-7012376A patent/KR20030083752A/ko not_active Application Discontinuation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3672823A (en) * | 1970-03-25 | 1972-06-27 | Wave Energy Systems | Method of sterilizing liquids |
JPH04166283A (ja) * | 1990-10-30 | 1992-06-12 | Furuno Aqua Toreede:Kk | 殺菌装置 |
JPH05228480A (ja) * | 1992-02-24 | 1993-09-07 | Kubota Corp | 生物難分解性物質の処理装置 |
JPH0655196A (ja) * | 1992-08-06 | 1994-03-01 | F Tex:Kk | 汚水浄化処理方法およびその装置 |
JPH07108285A (ja) * | 1993-10-12 | 1995-04-25 | Kubota Corp | 汚水中のダイオキシン類除去方法 |
JPH11300345A (ja) * | 1998-04-20 | 1999-11-02 | Kubota Corp | 埋立浸出水中のダイオキシン類等の有機塩素化合物の分解方法および分解装置 |
JP2000334447A (ja) * | 1999-05-28 | 2000-12-05 | Hitachi Metals Ltd | 循環水浄化滅菌装置 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1375432A4 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005014489A1 (de) * | 2003-08-08 | 2005-02-17 | Buettner Klaus | Verfahren zur desinfektion von flüssigkeiten |
WO2005039754A1 (de) * | 2003-09-26 | 2005-05-06 | Ultrawaves Wasser- Und Umwelttechnologie Gmbh | Ultraschallreaktor |
DE10351184B4 (de) * | 2003-11-03 | 2015-02-19 | Klaus Büttner | Verfahren zur Behandlung einer wässrigen Lösung oder Flüssigkeit |
US8889075B2 (en) | 2007-09-26 | 2014-11-18 | Kitakyushu Foundation For The Advancement Of Industry, Science And Technology | Apparatus for producing water having redox activity |
Also Published As
Publication number | Publication date |
---|---|
JP2002355551A (ja) | 2002-12-10 |
KR20030083752A (ko) | 2003-10-30 |
CN1535249A (zh) | 2004-10-06 |
EP1375432A4 (en) | 2004-12-15 |
US20040170538A1 (en) | 2004-09-02 |
EP1375432A1 (en) | 2004-01-02 |
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