• Journal of Korean Society of Environmental Engineers
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• v.30 no.7
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• pp.735-742
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• 2008

In order to evaluate the levels and distribution patterns, the concentrations of PAHs and chlorophenols were investigated in sludge samples discharged from 6 WWTPs located along Nak-dong river and 7 STPs in Busan, Korea. Levels of 16 PAHs and 19 chlorophenols in sludge samples ranged from 1.28 to 44.9 mg/kg dry wt. and from 213 to 3,850 $\mu$g/kg dry wt., respectively. Levels of PAHs in sludge samples except I5 and S4 were detected lower than those of previous studies. The distribution patterns of PAHs and chlorophenols varied with industrial wastewater sludge samples because industrial wastewater sludge had different industrial input sources. However, the distribution patterns of PAHs and chlorophenols in sewage sludge were pretty similar. Phenanthrene, fluoranthene and pyrene were dominant and the fractions of these 3 PAHs relative to 16 PAHs in sewage sludge ranged from 30.8 to 50.7%. 2-chlorophenol is dominated in most sewage sludge samples and the fraction ranged from 36.0 to 66.8%.

• Journal of the Korea Organic Resources Recycling Association
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• v.11 no.4
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• pp.49-56
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• 2003

The strain Ralstonia eutopha JMP134 (formerly Alcaligenes eutrophus JMP134) can degrade trichloroethylene(TCE) through a chromosomal phenol-dependent pathway. The phenol hydroxylase was previously found to be a single responsible enzyme for TEC degradation. Here, we demonstrate that a recombinant bacterium, R. eutopha AEK301, one of Tn5-induced mutants of JMP134 containing a recombinant plasmid pYK3011, degrades TCE in the absence of inducer, phenol and in the presence of various carbon sources. Complete removal of TCE ($50{\mu}M$) was observed in minimal medium containing only 0.05% ethanol as a carbon source within 24 hours. The bacterium removed $200{\mu}M$ of TCE to below detectable level within two days under non-selective pressure. When TCE concentration was increased up to $400{\mu}M$, the degradation had been continued until two days, then ceased with removal of 70% of detectable TCE.

• Journal of Korean Society of Water and Wastewater
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• v.27 no.1
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• pp.31-38
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• 2013

The degradation of 4-chlorophenol(4-CP) by various AOPs(Advanced Oxidation Processes) with continuous feeding of $H_2O_2$, including the ultraviolet/hydrogen peroxide, the Fenton and the photo-Fenton process has been investigated. The photo-Fenton process showed the highest removal efficiency for degradation of 4-chlorophenol than those of other AOPs including the Fenton process and the combined UV process with continuous feeding of $H_2O_2$. In the photo-Fenton process, the optimal experimental condition for 4-CP degradation was obtained at pH 3. Also the 4-CP removal efficiency increased with decreasing of the initial 4-CP concentration. 4-chlorocatechol and 4-chlororesorcinol were identified as photo-Fenton reaction intermediates, and the degradation pathways of 4-CP in the aqueous phase during the photo-Fenton reaction were proposed.

• Journal of Korean Society of Environmental Engineers
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• v.28 no.5
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• pp.511-521
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• 2006

Homologue and isomer patterns of polychlorinated dibenzo-p-dioxins(PCDDs) and polychlorinated dibenzofurans(PCDFs) congeners formed from phenols in the gas-phase at $600{\sim}700^{\circ}C$ and via particle-mediated reactions at $400^{\circ}C$ were studied in an isothermal flow reactor. A mixture of 20 phenols in relative concentrations found in a municipal waste incinerator(MWI) stack gas was used for this study. PCDDs and PCDFs homologue and isomer patterns obtained from the phenol. From the phenol experiments, gas-phase formation at $600{\sim}700^{\circ}C$ favors PCDFs formation whereas particle-mediated formation at $400^{\circ}C$ favors PCDDs formation. DD and DF were most abundant homologue groups, PCDDs and PCDFs homologue fraction decreased with increasing number of chlorine substituents. PCDDs and PCDFs homologue and isomer fractions were almost constant from gas-phase formation and particle-mediated formation. Unsubstituted phenol, which was present in high concentration, played a significant role in the formation of PCDD/Fs congeners under both sets of experimental conditions.

• Analytical Science and Technology
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• v.14 no.4
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• pp.349-355
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• 2001

A series of micro- and mesoporous activated carbons were prepared from phenolic resin using a metal treated chemical activation methodology. $N_2$-adsorption data were used to characterize the surface properties of the produced activated carbons. Results of the surface properties and pore distribution analysis showed that phenolic resin can be successfully converted to micro- and mesoporous activated carbons with specific surface areas higher than $962.3m^2/g$. Activated carbons with porous structure were produced by controlling the amount of metal chlorides($CdCl_2$, $CuCl_2$). Pore evolvement was shown to be most effected by the incremental addition of metal chloride. From the thermodynamic DSC data, enthalpy formations(${\Delta}H$) of first endothermic reaction were increase with the incremental addition of metal chloride.

• Analytical Science and Technology
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• v.12 no.6
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• pp.540-549
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• 1999

The combustion temperature was controlled between $880^{\circ}C$ to $1070^{\circ}C$ to find the relation the combustion temperature and emission amount of PCDDs/PCDFs in the Municipal solid waste incinerator. The emission amount of PCDDs/PCDFs decreased when the temperature increased in the rear of the boiler. The PCDDs/PCDFs concentration were detected $7.82ng-TEQ/Nm^3$ at $880^{\circ}C$, $6.97ng-TEQ/Nm^3$ at $970^{\circ}C$ and $6.13ng-TEQ/Nm^3$ at $1070^{\circ}C$. Also, The chlorophenols, chlorobenzenes, and PCB concentration decreased by increasing the temperature from $880^{\circ}C$ to at $1070^{\circ}C$, and the isomer of the prescsors had a tendency to emit the higbly cbiorinated compounds.

• Journal of Soil and Groundwater Environment
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• v.11 no.3
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• pp.59-65
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• 2006

Reductive dechlorination of chlorophenols by nickel coated iron was investigated to understand the feasibility of using Ni/Fe for the in situ remediation of contaminated groundwater. Zero valent iron (ZVI) was amended with Ni(II) ions to form bimetal (Ni/Fe). Dechlorination of 4-chlorophenol and formation of intermediates was studied using Ni/Fe. Effects of initial contaminant concentration, bimetal loading, presence of humic acid, and solution chemistry were also evaluated. Experimental results showed that Ni/Fe bimetal was so effective that more than 95% of 4-CP degradation was achieved within 240 minutes. Pseudo first-order rate constant for the dechlorination reaction was well correlated with bimetal loading. Humic acid competed for the reactive sites on the nickel coated iron with chlorophenols, lowering the dechlorination efficiency. No significant changes in solution pH were observed in the dechlorination of chlorophenols with Ni/Fe in the absence of buffer, indicating that reactivity of bimetal (Ni/Fe) could be prolonged. Phenol was found as a dechlorination intermediate of the conversion of 4-chlorophenol compound by Ni/Fe.

• Analytical Science and Technology
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• v.12 no.1
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• pp.68-74
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• 1999

The Concentrations of PCDDs/PCDFs and their precusors(chlorophenols, chlorobenzenes, PCB) were analyzed from the dioxin control device such as EP and SCR to know the emission patterns of these compounds and find the dioxin index compounds. The dioxin concentration increased 7 times in outlet part than inlet part of EP and the concentration of CBs, CPs and PCBs also were increased through this control device. These phenomia may be related to the operating temperature of Electroprecipitator(EP), which the operating temperature is near the $300^{\circ}C$, the method of the decreasing the operating temperature need to consider to prevent the formation of these compounds. In the selected catalytic reactor with wet scrubber(SCR+WS), these compounds were removed after passing the device over 90% for CPs, 30~40% for CBs and 60% for PCBs. But, the systematic study have to perform to reduce the formation of PCDDs/PCDFs and precusors.

• Resources Recycling
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• v.10 no.4
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• pp.18-23
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• 2001

Air pollutants, phenol was generated in case of thermal regeneration of used activated carbon loaded with phenol and because of this problem, removal process of phenol were studied. Electrolytic oxidation of samples, used S.company granular activated carbon (WS-GAC), used C.company granular activated carbon (WC-GAC) and used L.company granular activated carbon (WL-GAC) loaded with phenol carried out by potentiostatic method in this study. In case of experiment was to come into operation in condition of samples containing 100 mg/g phenol, supporting electrolyte was 1.0% sodium chloride solution, Ti-Ir (10$\times$10$\textrm{cm}^2$) electrode and electrode distance was 2 cm, current density was $1.25 A/dm^2$, Obtained from the results of electrolytic oxidation experiments were not detected residual phenol. And then we knew about reaction time of electrolytic oxidation, current density, concentration of supporting electrolyte and electrode and electrode distance were 60 minutes, 1.25 A/dm$^2$, 1.0%, 2 cm.

• Journal of Environmental Science International
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• v.22 no.9
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• pp.1089-1095
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• 2013

The degradation of 3-chlorophenol(3-CP) by various AOPs(Advanced Oxidation Processes) including the ultraviolet / hydrogen peroxide, the Fenton and the ultraviolet(UV)-Fenton process has been conducted. The highest removal efficiency for 3-CP in the aqueous phase was obtained by the UV-Fenton process among the AOPs. In the UV-Fenton process, The removal efficiency of 3-CP decreased with increasing pH in the range of 3 to 6, and it decreased with increasing initial concentration. As the intermediates of 3-CP by UV-Fenton reaction, 3-chlorocatechol, 4-chlorocatechol, and chlorohydroquinone were detected thus the degradation pathways were proposed.