• Journal of Korean Society for Atmospheric Environment
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• v.22 no.6
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• pp.842-850
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• 2006

The role of chlorination reactions in the formation of polychlorinated dibenzofurans (PCDFs) in a municipal waste incinerator was assessed using a chlorination model for predicting PCDF isomer distributions. Complete distributions of PCDF congeners were obtained from a stoker-type municipal waste incinerator operated under 13 test conditions. Samples were collected from the flue gas prior to the gas cleaning system. While total PCDF yields varied by a factor of five to six, the distributions of congeners were similar. A chlorination model, dependent only on the observed distribution of monochlorinated isomers, was developed to predict the distributions of poly-chlorinated isomers formed by chlorination of dibenzofuran (DF). Agreement between predicted and measured PCDF isomer distributions was high for all homologues, supporting the hypothesis that DF chlorination can play an important role in the formation of PCDF byproducts.

• 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.17 no.4
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• pp.295-301
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• 2004

In this study, static and dynamic solvent extractions are compared for more efficient extraction of polychlorinated dibenzofurans (PCDFs) from fly ash. Static solvent extraction rather than dynamic extraction showed a higher recovery of PCDFs, which was adsorbed strongly with fly ash. The effects of parameters, such as temperature, toluene-isopropyl alcohol mixture, static and dynamic time flow rate, and solvent volume on the extraction were investigated and the variations in average recoveries of PCDFs were explained. In both extractions, temperature was an effective parameter because the higher temperature gave the higher recoveries. In dynamic solvent extraction, dynamic time was more effective than flow rate and solvent volume for the extraction of PCDFs from fly ash. Multi-layer column chromatography on neutral and acidic silica gel with n-hexane was used for cleaning up the extracts. The quantification of the PCDFs extracted was performed using HPLC-UV.

• Environmental Engineering Research
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• v.11 no.4
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• pp.232-240
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• 2006

Polychlorinated naphthalenes (PCNs) formed along with dibenzo-p-dioxin and dibenzofuran products in the slow combustion of dichlorophenols (DCPs) at $600^{\circ}C$ were identified. Each DCP reactant produced a unique set of PCN products. Major PCN congeners observed in the experiments were consistent with products predicted from a mechanism involving an intermediate formed by ortho-ortho carbon coupling of phenoxy radicals; polychlorinated dibenzofurans (PCDFs) are formed from the same interemediate. Tautomerization of the intermediate and $H_2O$ elimination produces PCDFs; alternatively, CO elimination to form dihydrofulvalene and fusion produces naphthalenes. Only trace amounts of tetrachloronaphthalene congeners were formed, suggesting that the preferred PCN formation pathways from chlorinated phenols involve loss of chlorine. 3,4-DCP produced the largest yields of PCDF and PCN products with two or more chlorine substituents. 2,6-DCP did not produce tri- or tetra-chlorinated PCDF or PCN congeners. It did produce 1,8-DCN, however, which could not be explained.

• Journal of Environmental Science International
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• v.21 no.4
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• pp.451-459
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• 2012

PCDDs(Polychlorinated dibenzo-$p$-dioxins) and PCDFs(polychlorinated dibenzofurans) are measured in soil of Yeungju and Sangju on North Gyeongbuk to investigate the risk assessment of dioxins. Dioxins are analyzed by HRGC/HRMS(high resolution gas chromatography - high resolution mass spectrometer). 2,3,7,8-T4CDD and 1,2,3,7,8-Pe5CDD in soil on Yeungju and Sangju are not detected. Also, 2,3,7,8-T4CDF is not detected in soil on Yeungju and Sangju. PCDDs and PCDFs in Yeungju soil are 1.957 pg/g and 0.294 pg/g, respectively. Total of dioxins in Yeungju soil are 2.251 pg/g. PCDDs and PCDFs in Sangju soil are 1.220 pg/g and 0.420 pg/g, respectively. Total of dioxins in Sangju soil are 1.640 pg/g. PCDDs and PCDFs in Yeungju soil are 0.0049 pg WHO-TEQ/g and 0.0123 pg WHO-TEQ/g, respectively. Total of dioxins with PCDDs and PCDFs in Yeungju soil are 0.0172 pg WHO-TEQ/g. PCDDs and PCDFs in Sangju soil are 0.0065 pg WHO-TEQ/g and 0.0213 pg WHO-TEQ/g, respectively. Total of dioxins with PCDDs and PCDFs in Sangju soil are 0.0278 pg WHO-TEQ/g. Amount for pg/g concentration unit of PCDDs is higher than amount of PCDFs in soil. But, WHO-TEQ of PCDFs is higher than WHO-TEQ of PCDDs in soil.

• Fisheries and Aquatic Sciences
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• v.4 no.2
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• pp.51-57
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• 2001

Polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) were measured in sediment samples from 19 stations in the coastal areas of Korea from February to July 2000. PCDDs and PCDFs were detected in all sediment samples. The concentrations of these con­taminants ranged from 18.2 to 804.0 pg/g dry weight and I-TEQ concentrations varied from 0.1 to 5.5 pg/g dry weight. Examination of homologue groups showed that octachlorinated dibenzo-p-dioxin (OCDD) was predominant congener in Korean coast. This pattern was similar to homologue profiles of marine sediments in which the main source of PCDDs/DFs was derived from the atmospheric deposition of particulate matters generated from various industrial activities. Grain size and total organic carbon (TOC) distribution are one of the important factors governing PCDDs/DFs concentration in this study.

• Proceedings of the Korean Society of Toxicology Conference
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• 2003.10b
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• pp.172-173
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• 2003

There are growing concerns about human health effects of dioxin and dioxin like compounds such as polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and polychlorinated biphenyls (PCBs). Earlier studies recognized that 2.3.7.8-tetrachloro dibenzo-p-dioxin (TCDD) and structually related dioxin like compounds invoke a number of common toxic responses that are mediated through a high-affinity cytosolic receptor protein, the AhR.(omitted)

• Journal of Environmental Health Sciences
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• v.33 no.1 s.94
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• pp.11-15
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• 2007

This study was performed to evaluate the congeners of polychlorinated dibenzo-p-dioxins(PCDDS) and polychlorinated dibenzofurans(PCDFs) in Korean foods among children in Korea, in comparison with the findings in their mothers. The PCDDs and PCDFs intakes of 24-h diet duplicates were estimated from the previous Korean reports. In Korean children and their mothers of this study, major sources of lipid intake were plant-based foods(62% for children, 66% for their mothers). The women took 34% of lipid from animal sources, among which meats were leading sources of animal lipids(30%). Fish and shellfish were accounted for 4% in total lipid intake. Daily intake of PCDDs and PCDFs in the children md their mothers were 0.002-3.188 and 0.002-2.717 pg WHO-TEQ/day in animal sources and ND-0.283 and ND-0.296 pg WHO-TEQ/day in plant sources, respectively. PCDDs/PCDFs intake from animal origin was the major exposure source for both children and their mothers in Korea. Among the 17 PCDD/Fs congeners, 2,3,4,7,8-pentachlorodibenzofuran was assumed to be the effective exposure marker for diet intake.

• Korean Journal of Veterinary Research
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• v.48 no.1
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• pp.39-48
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• 2008

Polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) are ubiquitous and can contaminate the food chain. A study monitoring PCDD/Fs in imported meat was conducted at the National Veterinary Research and Quarantine Service (NVRQS, Republic of Korea) in order to maintain food safety from the bioaccumulative PCDD/Fs. Seventeen PCDD/Fs with toxic equivalency factors (TEFs) established by World Health Organization (WHO, 1998) were analyzed in imported beef, pork, and chicken by high resolution gas chromatography/mass spectrometry (HR-GC/MS). Results of the monitoring for the last 5 years are presented. The levels of PCDD/Fs were similar to other studies except two unusually high concentrations in pork and beef. Excessive levels greater than the Korean provisional maximum residue limit of PCDD/Fs were found in a sample of pork imported from Chile and a sample of beef imported from U.S, and those products were rejected and returned. There was no obvious trend or differences with respect to time or origin of meat in this study.

• Journal of Environmental Science International
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• v.16 no.1
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• pp.9-19
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• 2007

Comparing predicted PCDF isomer patterns with those obtained from a municipal waste incinerator assessed the role of two-phenol condensation pathways in the formation of PCDFs. Complete PCDF homologue and isomer distributions were obtained from a Fluidized Bed Incinerator (FBI). Two-phenol condensation model, dependent only on the distributions of phenols, was developed to predict the PCDF congeners produced from phenol precursors. R-squared values from linear correlations are presented for the dichlorinated through hexa-chlorinated isomer distributions between measured and predicted. They range from 0.00: to 0.1 far the di-chlorinated through hexa-chlorinated isomer sets. Agreement between predicted and measured PCDF isomer distributions was very poor for all homologues. Two-phenol condensation pathways are not likely to be the pre-dominant pathways in the formation of PCDF in a FBI. However, dibenzofuran (DF) is likely to be produced from a condensation of two phenols. This work demonstrates the use of PCDF homologue and isomer patterns for testing PCDF formation mechanism from two-phenol condensation pathways in municipal waste incinerators.