• Title/Summary/Keyword: UV-$H_2O_2$ Oxidation

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UV/H2O2 Advanced Oxidation of Photo Processing Chemicals in a UV-free Reflecting Reactor (사진현상폐수의 UV-자유반사 반응조에서의 UV/H2O2 고급산화처리)

  • Choi, Kyung-Ae;Kim, Young-Ju
    • Journal of Korean Society of Environmental Engineers
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    • v.22 no.2
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    • pp.241-249
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    • 2000
  • In this study, UV-catalyzed $H_2O_2$ oxidation and $H_2O_2$ oxidation to remove contaminants from photo processing chemicals were investigated at various conditions. Photo processing chemicals contains high concentrations of organic compounds and has very low biodegradability. Hydrogen peroxide is subjected to gradual decomposition as metastable substance. In the process, short-lived and highly reactive hydroxyl radicals are formed. The decomposition can be significantly accelerated by use of appropriate catalyst, such as ultraviolet radiation. The experiments were conducted in a UV-free reflecting reactor in batch and a high-pressure mercury lamp was used as UV source. Mixing, cooling and ventilation of the reactor were operated during experiments. In $UV/H_2O_2$ oxidation and $H_2O_2$ oxidation, the removal efficiencies of $COD_{Cr}$, TOC and chromaticity increased with the increase of $H_2O_2$ dosage and were higher in the controlled pH condition of 3 than in original pH condition of 8. In $UV/H_2O_2$ oxidation under the optimum condition of pH 8 and 1.3 stoichiometric $H_2O_2$ dosage, the removal efficiencies of $COD_{Cr}$, TOC and chromaticity were 47.5%, 75.0% and 91.5% respectively and $BOD/COD_{Cr}$ ratio was significantly increased from 0.04 to 0.21.

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Comparative Studies Of the $UV/H_2O_2,\;UV/TiO_2/H_2O_2$ and Photo-Fenton Oxidation for Degradation of Citric Acid ($UV/H_2O_2,\;UV/TiO_2/H_2O_2$, Photo-Fenton 산화방법에 의한 Citric Acid의 분해효율 비교)

  • Seo, Min-Hye;Cho, Soon-Haing;Ha, Dong-Yun
    • Journal of Korean Society of Environmental Engineers
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    • v.28 no.4
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    • pp.429-437
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    • 2006
  • To establish the efficient treatment technology of chemical cleaning wastewater from power plant, several AOPs($UV/H_2O_2,\;UV/TiO_2/H_2O_2$, Photo-Fenton oxidation) were investigated. Treatment efficiencies and the electrical energy requirements based on the EE/O parameter(the electrical energy, required per order of pollutant removal in $1m^3$ wastewater) were evaluated. TOC removal efficiencies of $UV/H_2O_2,\;UV/TiO_2/H_2O_2$, Photo-Fenton oxidation at the optimum conditions were 95.5%, 92.3%, 91.5%, respectively. The electrical energy requirements of $UV/H_2O_2,\;UV/TiO_2/H_2O_2$, Photo-Fenton oxidation were $11.26kWh/m^3,\;3.85kWh/m^3,\;0.799kWh/m^3$, respectively. From these results, it could be concluded that all of the three oxidation processes were effective for the degradation of citric acid. Considering the treatment efficiency and economical aspect, photo-Fenton oxidation was the most efficient treatment process among the three processes tested.

Removal of Tetracycline Antibiotics Using UV and UV/H2O2 Systems in Water (UV 및 UV/H2O2 시스템을 이용한 수중의 Tetracycline계 항생물질 제거)

  • Son, Hee-Jong;Yoom, Hoon-Sik;Jang, Seong-Ho;Kim, Han-Soo;Hong, Soon-Heon;Park, Woo-Sik;Song, Young-Chae
    • Journal of Environmental Science International
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    • v.23 no.7
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    • pp.1359-1366
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    • 2014
  • Seven tetracycline classes of antibiotics were treated using ultraviolet (UV) and $UV/H_2O_2$ oxidation. Two different UV lamps were used for the UV and $UV/H_2O_2$ oxidation. The performance of the UV oxidation was different depending on the lamp type. The medium pressure lamp showed better performance than the low pressure lamp. Combining the low pressure lamp with hydrogen peroxide ($H_2O_2$) improved the removal performance substantially. The by-products formation of tetracycline by UV and $UV/H_2O_2$ were investigated. The protonated form ($[1+H]^+$) of tetracycline was m/z 445, reacted to yield almost exclusively two oxidation by-products by UV and $UV/H_2O_2$ oxidation. Their protonated forms of by-products were m/z 461 and m/z 477. The structures of tetracycline's by-products in UV and $UV/H_2O_2$ system were similar.

Degradation of Dye Wastewater by Advanced Oxidation Process: A Comparative Study (고급산화공정에 의한 안료폐수 처리: 비교 연구)

  • Park Young-Seek
    • Journal of Environmental Science International
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    • v.15 no.1
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    • pp.67-75
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    • 2006
  • The degradation of Rhodamine B (RhB) in water was investigated in laboratory-scale experiments, using five advanced oxidation Processes (AOPs) $UV/H_2O_2$, lenten, photo-lenten, $UV/TiO_2,\;UV/TiO_2/H_2O_2$. The photodegradation experiments were carried out in a fluidized bed photoreactor equipped with an immersed 32 W UV-C lamp as light source. initial decolorization rate and COD removal efficiency were evaluated and compared. The results obtained showed that the initial decolorization rate constant was quite different for each oxidation process. The relative order of decolorization was: photo-fenton > $UV/TiO_2/H_2O_2$ > fenton > $UV/H_2O_2$ > $UV/TiO_2$ > UV > $H_2O_2$. The relative order of COD removal was different from decolorization: photo-fenten ${\fallingdotseq}$ $UV/TiO_2/H_2O_2\;>\;UV/TiO_2\;>\;fenton\;>\;UV/H_2O_2$. The Photo-lenten and $UV/TiO_2/H_2O_2$ processes seem to be appropriate for decolorization and COD removal of dye wastewater.

Degradation Characteristics of Oxalic Acid and Citric Acid by UV/H2O2 Oxidation (Oxalic Acid와 Citric Acid UV/H2O2에 의한 분해특성 조사)

  • Ha, Dong-Yun;Cho, Soon-Haing;Choi, Young-Soo;Kyung, Gyu-Seok;Kim, Dong-Hyun
    • Journal of Korean Society of Environmental Engineers
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    • v.22 no.7
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    • pp.1307-1318
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    • 2000
  • The purpose of this study is to investigate the degradation characteristics of oxalic acid and citric acid by $UV/H_2O_2$ oxidation. For this purpose, the effects of pH, $H_2O_2$ dosage and the concentration of each compounds on the degradation of oxalic acid and citric acid by $UV/H_2O_2$ were investigated. Oxalic acid was effectively degraded at the wavelength of 254 nm, while the degradation efficiency of citric acid was very low at the same wavelength. It was also found that both organic substances were not degraded by the injection of $H_2O_2$ only. The optimum pH of degradation of oxalic acid and citric acid was 4 and 4 to 6, respectively. In the case of $UV/H_2O_2$ oxidation, the degradation efficiency was increased by increasing $H_2O_2$ dosage. The degradation efficiency decreased when the dose of $H_2O_2$ exceeds 200 mg/L. From these results, it can be concluded that the optimum reaction conditions for the degradation of oxalic acid and citric acid by $UV/H_2O_2$ oxidation were pH 4 and 200mg/L of $H_2O_2$.

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Characterization of Humic Acid in the Chemical Oxidation Technology(I) - Characteristics by Photocatalytic Oxidation Process - (화학적 산화법에 의한 부식산의 분해 처리기술에 관한 연구(I) - 광산화공정을 통한 부식산의 분해특성 분석 -)

  • Kim, Jong Boo;Rhee, Dong Seok
    • Analytical Science and Technology
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    • v.13 no.2
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    • pp.234-240
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    • 2000
  • The efficiency of Photocatalytic Oxidation Process were investigated for the treatment of Aquatic Humic Substances (AHS). In UV-only system, pH 7-9 was the optimum pH range for TOC removal, and alkali range was the optimum pH for absorbance decrease. In UV/$TiO_2$ system, the optimum $TiO_2$ dosage was 50ppm and over 50ppm of $TiO_2$ dosage was not effective for removal of AHS. In UV/$H_2O_2$ system, optimum $H_2O_2$ dosage was 20mM, when over 20mM dosage, removal of TOC (Total Organic Carbon) and absorbance was decreased. Radical scavenger affected on the photo-oxidation of AHS. Removal rate of TOC and absorbance was decreased by addition of carbonate ions and TOC removal was more effected than that of absorbance.

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KINETICS OF ATRAZINE OXIDATION BY UV RADIATION AND OXALATE ASSISTED H2O2/UV PROCESSES

  • Choi, Hyun-Jin;Choi, Jong-Duck;Kim, Hyun-Kab;Lee, Tae-Jin
    • Environmental Engineering Research
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    • v.11 no.1
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    • pp.28-32
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    • 2006
  • The degradation of atrazine was explored using UV alone, $H_2O_2/UV$, oxalate/UV and oxalate-assisted $H_2O_2/UV$. The addition of oxalate to the $H_2O_2/UV$ (oxalate-assisted $H_2O_2/UV$) process was the most effective method for the degradation of atrazine. The overall kinetic rate constant was split into the direct oxidation due to photolysis and that by the radicals from hydrogen peroxide or oxalate. In semi-empirical terms, the initial concentration of hydrogen peroxide had a greater contribution than that of oxalate for atrazine oxidation.

Destruction of Acetic Acid Using Various Combinations of Oxidants by an Advanced Oxidation Processes (다양한 산화반응을 조합한 고급산화공정의 아세트산 분해에 관한 연구)

  • Kwon, Tae Ouk;Park, Bo Bae;Moon, Jang Soo;Moon, Il Shik
    • Applied Chemistry for Engineering
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    • v.18 no.4
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    • pp.314-319
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    • 2007
  • The destruction of synthetic acetic acid wastewater was carried out using UV, $O_3$, $H_2O_2$, $Fe^{2+}$ oxidants in various combinations by the advanced oxidation processes. $UV/H_2O_2$, $UV/H_2O_2/Fe^{2+}$, $O_3$, $O_3/H_2O_2$, $UV/O_3/H_2O_2$, $UV/O_3/H_2O_2/Fe^{2+}$ processes were tested. $UV/H_2O_2/Fe^{2+}$, $O_3/H_2O_2$, $UV/O_3/H_2O_2$, $UV/O_3/H_2O_2/Fe^{2+}$ processes shows the most effective destruction efficiency at low pH (3.5) condition of wastewater, but $UV/H_2O_2$ and $O_3$ processes were observed less than 20%. Destruction efficiency was gradually increased with the reaction time in the $O_3/H_2O_2$ and $UV/O_3/H_2O_2$ processes, in case of the $UV/H_2O_2/Fe^{2+}$ and $UV/O_3/H_2O_2/Fe^{2+}$ processes shows rapid increasing of destruction efficiency within 90 min, then slightly decreasing with time. The destruction efficiencies of $UV/H_2O_2/Fe^{2+}$, $O_3/H_2O_2$, $UV/O_3/H_2O_2$ and $UV/O_3/H_2O_2/Fe^{2+}$ processes were observed 55, 66, 66 and 64%, respectively.

UV/H2O2 Oxidation for Treatment of Organic Compound-spilled Water (UV/H2O2 산화를 활용한 유기오염물질 유출수 처리용 공정 연구)

  • Kim, Nahee;Lee, Sangbin;Park, Gunn;Park, Jae-Woo
    • Journal of the Korean GEO-environmental Society
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    • v.23 no.10
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    • pp.5-12
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    • 2022
  • In this study, we investigated the UV/H2O2 process to treat organic compound-spilled water. In consideration of usage and properties, benzene, toluene, phenol, and methyl ethyl ketone were selected as representative organic compounds. The selected material was first removed by natural volatilization and aeration that simulated the pretreatment of the prcoess. After that, UV/H2O2 oxidation experiments were conducted under various H2O2 concentration conditions. Benzene and toluene were mostly volatilized before reaching the oxidation process due to high volatility. Considering the volatility, oxidation experiments were performed at an initial concentration of 5 mg/L for benzene and toluene. The UV/H2O2 oxidation process achieved 100% of benzene and toluene removal after 20 minutes under all hydrogen peroxide concentration conditions. The phenol was rarely removed from the volatile experiments and oxidation tests were performed at an initial concentration of 50 mg/L. The process showed 100 % phenol removal after 30 minutes under 0.12 v/v% of hydrogen peroxide concentration condition. Methyl ethyl ketone was removed 58 % after 2 hours of volatile experiments. The process showed 99.7% Methyl ethyl ketone removal after 40 minutes under 0.08 v/v% of hydrogen peroxide concentration condition. It was confirmed that the UV/H2O2 process showed high decomposition efficiency for the four selected organic compounds, and identified the amount of hydrogen peroxide in classified organic contaminants.

Removal of Tetrachloroethylene using Advanced Oxidation Processes (고급산화법을 이용한 Tetrachloroethylene의 처리)

  • Shin, Hang-Sik;Lim, Jae-Lim
    • Journal of Korean Society of Water and Wastewater
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    • v.10 no.4
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    • pp.64-72
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    • 1996
  • The effect of $O_3$, $O_3/pH$, and $O_3/H_2O_2$, $O_3/UV$, and $H_2O_2/UV$ advanced oxidation process(AOP) were investigated for the treatment of tetrachloroethylen(PCE) at various condition. The removal efficiency of 10, 20, and 30ppm PCE by ozonation were almost same, only about 60%. And pseudo first-order rate constants, ko for overall oxidation was about 0.097($min^{-1}$). In the $O_3/pH$ AOP experiment for the 20ppm PCE, the removal rate of PCE increased with the increase of pH. However, mineralization rate of PCE at pH 7 was higher than at pH 10. In the $O_3/H_2O_2$ AOP, the removal rate of PCE was the highest at peroxide-to-ozone dosage ratio of about 0.9, which PCE was removed over 99.95%. Despite 42% of PCE was directly photolyzed by the UV irradiation, the removal efficiency of PCE by $O_3/UV$ AOP was only about 70%. In $H_2O_2/UV$ AOP, the removal efficiency of PCE increased to about 98% in proportion to the $H_2O_2$ injection concentration at constant UV intensity of 5W/l.

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