Monitoring and ecological risk assessment of contaminants in freshwater bodies by bioindicators in China: a proposed framework.

Bioindicators can provide pollution information with longer temporal duration and larger spatial scale. It is an ideal strategy for long-term monitoring of bioaccumulative contaminants. Bioindicator monitoring has been widely used; however, there were seldom detailed studies about bioindicator methodology in literature. The present study proposed a bioindicator framework suitable for the local conditions of China, including selection of bioindicator species, evaluation of impact factors, and derivation of threshold values using per- and polyfluoroalkyl substances (PFASs) as an example. The criteria that proper bioindicator species should meet and the procedure how the bioindicator species is selected were proposed, under which crucian carp (Carassius auratus) was selected as the local bioindicator for studied PFASs. Several factors which may affect accumulation of contaminants in bioindicators were suggested to produce reliable and comparable results. Derivation method of bioindicator thresholds for ecological risk assessment of aquatic ecosystems was firstly developed. The long-term and short-term ecological thresholds of perfluorooctanesulfonate using crucian carp as bioindicator are 3.329 and 1.402 µg/g wet weight respectively. Using the long-term thresholds derived from chronic toxicity data and the accumulative concentrations of contaminants obtained by bioindicator results, the bioindicator monitoring can be used for long-term ecological risk surveillance. The threshold derivation method can extend the application of bioindicator monitoring from the occurrence study to ecological risk surveillance, which is especially important for China who has made progresses on regular contaminant control and starts to be concerned about the ecological risks of the emerging contaminants. The framework can be used to create national and regional long-term freshwater bioindicator monitoring programs, with the purposes of ecological risk assessment, occurrence and temporal trend study, pollution source identification, international convention fulfillment, retrospective study, etc. The bioindicator framework will benefit the aquatic environmental safety and the hazardous chemical management in China.

6:2 Chlorinated polyfluoroalkyl ether sulfonate as perfluorooctanesulfonate alternative in the electroplating industry and the receiving environment.

Electroplating industry is an important application field of per- and polyfluoroalkyl substances (PFASs) as the chromium mist suppressants. 6:2 chlorinated polyfluoroalkyl ether sulfonate (6:2 Cl-PFAES) and perfluorooctanesulfonate (PFOS) have been the two widely used mist suppressants, and after the ban of PFOS, 6:2 Cl-PFAES will become the dominant suppressant. The behavior and mechanisms of 6:2 Cl-PFAES in the electroplating industry and the receiving environment were studied and compared with PFOS. 6:2 Cl-PFAES behaved similarly with PFOS due to their similar chemical structure. However, some difference exists for the relatively stronger hydrophobicity of 6:2 Cl-PFAES. Up to 35.7 mg/L of PFOS and 13.4 mg/L of 6:2 Cl-PFAES were found in the industrial wastewater influents, and were effectively reduced to 0.3-0.8 mg/L by the interaction with chromium hydroxide through hydrophobic interaction and ligand exchange. The stronger hydrophobicity of 6:2 Cl-PFAES than PFOS resulted in its accumulation in the surface of foams and comparable or less removal during the industrial and municipal wastewater treatment. 6:2 Cl-PFAES exhibited higher bioaccumulation potential than PFOS in the surface water. 6:2 Cl-PFAES emitted by both mists and water may pose health risks to humans. More attentions towards 6:2 Cl-PFAES are needed after the replacement of PFOS by it in the electroplating industry as a global contaminant of emerging concerns.

Spatial distribution and profile of atmospheric short-chain chlorinated paraffins in the Yangtze River Delta.

Research on the atmospheric occurrence of short chain chlorinated paraffins (SCCPs) in industrialized areas is scarce. In this study, we investigated the concentrations, profile, and spatial distribution of SCCPs in the highly industrialized and developed areas of the Yangtze River Delta (YRD) in China using polyurethane foam passive air samplers. Sampling was performed during two separate periods in 2011. The concentrations of atmospheric SCCPs ranged from 6.1 to 63 ng m-3 in summer and 6.2-42 ng m-3 in winter. The C10 and C11 groups were the predominant carbon groups in all the samples. Different congener patterns between summer and winter were found, indicating that congeners in the air in winter may be influenced by local and external sources. The highest level of SCCPs was found in Suzhou, which is a highly industrialized area with many manufactories including electronic industries and plastic factories. Higher levels of SCCPs were found in the air than polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and polybrominated diphenyl ether (PBDEs), suggesting that the production and use of SCCPs were much higher than prohibited or restricted persistent organic pollutants (e.g., PCBs, OCPs, and PBDEs). Future studies should investigate the different sources of atmospheric SCCPs by conducting a comprehensive assessment of SCCP exposure.

Occurrence, composition, source, and regional distribution of halogenated flame retardants and polybrominated dibenzo-p-dioxin/dibenzofuran in the soils of Guiyu, China.

Guiyu, China, is well-known for the crude disposal of electronic waste (EW) and severe persistent organic pollutants (POPs). Therefore, in this study, the occurrence, composition, and source of polybrominated diphenyl ethers (PBDEs), 2,2',4,4',5,5'-hexabromobiphenyl (BB153), some novel brominated flame retardants (NBFRs), Dechlorane Plus (DP) and polybrominated dibenzo-p-dioxins/dibenzofurans (PBDD/Fs) in farmland soils covering Guiyu were studied. In EW disposal area soils, PBDEs were the most abundant FRs, with concentrations of 13-1014 ng g-1. The primary PBDE sources were technical Penta- and Deca-BDE mixtures in northern and southern Guiyu, respectively. The levels of BB153 were relatively low, possibly because it has been banned in the 1970s. The concentrations of hexabromobenzene (HBB) were 0.048-3.3 ng g-1, while pentabromoethylbenzene (PBEB) was almost not detected in the soils. Two alternatives to commercial PBDEs, decabromodiphenyl ethane (DBDPE) and 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), were the primary NBFRs, with concentrations of 1.8-153 ng g-1 and 0.43-15 ng g-1, respectively. DP was another primary FR, with concentrations of 0.57-146 ng g-1. Moreover, syn-DP and anti-DP isomers were not stereoselectively decomposed during the EW disposal process and were therefore present in their original fractions in the soils. The levels of PBDD/Fs in EW disposal area soils were 2.5-17 pg TEQ g-1. 1,2,3,4,6,7,8-HpBDF and OBDF were the dominant congeners, mainly derived from processing, pyrolysis and combustion of BFRs. The regional distribution of pollutants was shown to be related to the disposal manner of EW, with their open thermal disposal tending to release more highly brominated compounds such as BDE209, DBDPE, and 1,2,3,4,6,7,8-HpBDF. Additionally, some riverbank sites were heavily polluted because of nearby point sources, downwind Simapu (SMP) town without EW disposal activity was also contaminated by these pollutants.

Temporal and spatial distribution, sources, and potential health risks of ambient polycyclic aromatic hydrocarbons in the Yangtze River Delta (YRD) of eastern China.

In this study, from July 2011 to June 2012, 31 sampling sites were identified in order to investigate the concentrations and sources of polycyclic aromatic hydrocarbons (PAHs), as well as to evaluate their potential health risks in the cities of Suzhou, Wuxi, and Nantong, which are located in the Yangtze River Delta (YRD). The samples were collected by means of passive air sampling (PAS), and the contents of 15 PAHs were detected by gas chromatography-mass spectrometry. The ∑15PAHs concentrations were found to range from 6.48 to 154 ng m-3, with an average value of 56.8 ± 14.8 ng m-3. The pollution levels in Suzhou and Nantong were higher than those in Wuxi. Furthermore, the concentrations of the PAHs in the urban sites were determined to be higher than those in the suburban sites for ambient air. The seasonal average contents were found to be at a maximum in autumn, with concentrations reaching 74.1 ng m-3. Vehicle emissions and coal/biomass combustion were the dominant sources of the PAHs in the ambient air, with the contributions of 48% and 46%, respectively. The BaP TEQ (0.88 ng m-3) was found to have surpassed the Chinese and Japanese dioxin emission limit, and in doing so, may have caused a certain degree of risk to human health.

[Pollution Characteristics of PCDD/Fs in Ambient Air and Exposure Risk Assessment Around a Municipal Solid Waste Incinerator in Beijing].

Ambient air was sampled and analyzed around a municipal solid waste incinerator (MSWI) in Beijing from April 2014 to January 2015 to investigate the concentrations, profiles and seasonal variations of PCDD/Fs in the region using HRGC-HRMS technique. The mass concentrations and TEQ of 2,3,7,8-substituted PCDD/Fs in the air samples ranged from 8.9 to 140 pg·m-3 and from 0.11 to 1.8 pg·m-3, respectively. The concentration values at 4 sampling sites in haze day in autumn and all 7 sampling sites in winter were higher than the ambient air standard of 0.6 pg·m-3 for dioxins regulated in Japan. 1,2,3,4,6,7,8-HpCDF and OCDD dominated PCDD/Fs in all the samples for all four seasons with average contribution fractions of 20.5% and 14.0%, respectively, while 2,3,4,7,8-PeCDF was the dominant congener contributing to TEQ (43.3%). The spatial distribution basically exhibited a trend that the concentrations at all sites were comparable and not related to the distances from the source. Seasonal variation showed obviously higher concentration in winter than the other three seasons, which may attribute to the high concentration of ambient particulate matter due to domestic heating and worse atmospheric dispersion that occurred in winter. The homologue and congener profiles of PCDD/Fs in the air samples differed from those of the flue gas emission from the MSWI, consistent with the principle component analysis results. Dioxin inhalation exposure dose estimation showed that the dioxin inhalation exposure risk of residents living in the studied area was at a relatively safe level[0.060-0.224 pg·(kg·d)-1]. However, the dioxin inhalation exposure risk in heavily polluted seasons still needs great concerns.

Polycyclic aromatic hydrocarbon concentrations, compositions, sources, and associated carcinogenic risks to humans in farmland soils and riverine sediments from Guiyu, China.

The concentrations of 16 priority polycyclic aromatic hydrocarbons (PAHs) were measured in 23 farmland soil samples and 10 riverine sediment samples from Guiyu, China, and the carcinogenic risks associated with PAHs in the samples were evaluated. Guiyu is the largest electronic waste (EW) dismantling area globally, and has been well known for the primitive and crude manner in which EWs are disposed, such as by open burning and roasting. The total PAH concentrations were 56-567 ng/g in the soils and 181-3034 ng/g in the sediments. The Shanglian and Huamei districts were found to be more contaminated with PAHs than the north of Guiyu. The soils were relatively weakly contaminated but the sediments were more contaminated, and sediments in some river sections might cause carcinogenic risks to the groundwater system. The PAHs in the soils were derived from combustion sources, but the PAHs in the sediments were derived from both combustion and petroleum sources.

Concentrations and patterns of polychlorinated naphthalenes in urban air in Beijing, China.

Air samples were collected, using a high-volume air sampler, at an urban site in Beijing from April 2014 to March 2015. The polychlorinated naphthalene (PCN) concentration in the atmosphere in each season was determined. The total PCN (total target tri- to octachloronaphthalene congeners) concentrations were 1.99-19.0 pg/m(3), and the mean was 7.20 pg/m(3). The PCN concentrations were higher in fall than summer, indicating that the concentrations varied significantly over time. The trichloronaphthalene homolog was the predominant PCN homolog in all four seasons. The PCN toxic equivalent (TEQ) concentrations were 0.42-6.89 fg/m(3), and the mean was 1.74 fg/m(3). The CN-66/67 and CN-73 congeners were the predominant contributors to the TEQ concentrations. The mean seasonal TEQ concentration decreased in the order fall (3.18 fg/m(3)) > winter (1.41 fg/m(3)) > summer (1.11 fg/m(3)) > spring (1.03 fg/m(3)). The TEQ concentrations and the PCN concentrations did not follow the same seasonal trends, but the highest TEQ and PCN concentrations were both found in fall. Correlation analysis, ratio analysis, and principal component analysis were used to investigate the sources of PCNs to the Beijing atmosphere. The results suggested that combustion processes may be the main sources of PCNs to the Beijing atmosphere.

Seasonality in polybrominated diphenyl ether concentrations in the atmosphere of the Yangtze River Delta, China.

Polybrominated diphenyl ether (PBDE) concentrations in the atmosphere in rapidly developing parts of China have been studied little. In this study, polyurethane foam disk passive air samplers were used to comprehensively investigate PBDE concentrations in the atmosphere of the Yangtze River Delta in different seasons in 2010 and 2011. The mean sum of the concentrations of 13 PBDE congeners was 3.3 pg/m(3) in spring, 7.3 pg/m(3) in summer, 1.0 pg/m(3) in autumn, and 12 pg/m(3) in winter. Higher PBDE concentrations were found in urban areas than in rural areas. The PBDE concentrations were comparable to concentrations that have been found in cities around the world. BDE28, BDE47, BDE99, BDE153, and BDE183 were the dominant PBDE congeners in all seasons. High PBDE concentrations were found in satellite cities, such as Changshu, Wujiang, and Zhangjiagang, suggesting that commercial PBDEs (including pentabromodiphenyl ether products) are produced and/or used in those cities. The PBDE concentrations in the atmosphere were used to estimate daily doses through the inhalation of outdoor air. The most severe risks posed by exposure to PBDEs were found to occur in winter, for both adults and children, but the PBDE concentrations were found not to pose appreciable risks to human health.

Simultaneous determination of three alternative flame retardants (dechlorane plus, 1,2-bis(2,4,6-tribromophenoxy) ethane, and decabromodiphenyl ethane) in soils by gas chromatography-high resolution mass spectrometry.

A gas chromatography-high resolution mass spectrometry (GC-HRMS) method has been developed for the simultaneous determination of three alternative flame retardants, dechlorane plus (DP), 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), and decabromodiphenyl ethane (DBDPE) in soils. The soil samples were extracted by accelerated solvent extraction, followed by purification with concentrated sulfuric acid partitioning combined with acid-base silica gel column separation. The gas chromatography featured with a thermostable capillary column of short length and a thin stationary phase was operated in pulse injection mode. A double-focusing magnetic sector high resolution mass spectrometer with electron impact ionization was used for quantification of the analytes. The method detection limits were 0.27-0.33 pg for DPs, 0.41 pg for BTBPE, and 36 pg for DBDPE. The mean recoveries for DPs, BTBPE, and DBDPE in spiked soils were 88-107%, 78-97%, and 74-113%, respectively, with relative standard deviations ranging from 5.2% to 18%. The recoveries of (13)C-labeled standards for DPs, BTBPE, and DBDPE in soil samples were 45-110%, 67-118%, and 27-82%, respectively. These results met the acceptable range of labeled standards for analysis of polybrominated diphenyl ethers as specified by the USEPA 1614 method.

Tree bark as a biomonitor for the determination of polychlorinated biphenyls and polybrominated diphenyl ethers from Southern Jiangsu, China: levels, distribution, and possible sources.

Tree bark was used as the passive air sampler to evaluate polychlorinated biphenyl (PCB) and polybrominated diphenyl ether (PBDE) pollution and possible sources in Southern Jiangsu. The concentrations of PCBs and Σ7PBDEs were in the range of 0.58-5.19 ng/g dry weight (dw; mean 1.79 ng/g dw) and 17.9-243 pg/g dw (mean 74.7 pg/g dw), respectively. Tri-PCBs were the major PCB homologs, and technical PCB product Ar1242 was identified as the main source. BDE209 concentrations (4.29-456 ng/g dw) were relatively high, indicating that BDE209 pollution was serious in this region. The deca-BDE commercial mixture was the predominant commercial PBDE product used in this region. A good correlation was found between tree bark and polyurethane foam (PUF) disks in Σ6PCB monitoring, suggesting that both of them respond well to the gas-phase PCB monitoring.

Concentrations and patterns of polychlorinated naphthalenes in surface sediment samples from Wuxi, Suzhou, and Nantong, in East China.

The concentrations and patterns of polychlorinated naphthalenes (PCNs) were determined in surface sediment samples from Wuxi, Suzhou, and Nantong, in the Yangtze River Delta (East China), which has become urbanized rapidly. The total PCN (tri- to octachlorinated naphthalenes) concentrations in the samples from Wuxi, Suzhou, and Nantong were 0.89-40, 2.8-4600, and 0.60-34 ng/gdry weight, respectively. Unexpectedly high PCN concentrations were found in four of the sediment samples. The PCN concentrations were much higher in the samples from the Beijing-Hangzhou Grand Canal than in the samples from the Yangtze River. The toxic equivalent (TEQ) concentrations (determined from the concentrations of the "dioxin-like" PCNs) ranged from 1.45×10(-7) to 2.16 ng TEQ/g, and the congeners CN-66/67 and CN-73 were the predominant contributors to the TEQs. Independent samples t-tests were performed, and no significant differences were found between the PCN concentrations in the samples from the metropolitan area and the development zone when the four development-zone samples that contained very high PCN concentrations were excluded. The PCN profiles were dominated by the hexa- to octachlorinated naphthalene homologs. The CN-66/67 to CN-71/72 and CN-66 to CN-67 concentration ratios were used to identify specific PCN sources. Emissions from chemical and other industrial plants were found to have strongly influenced the PCN concentrations in sediment in the study area.

Changes of polybrominated diphenyl ethers and polychlorinated biphenyls in surface soils from urban agglomeration of the Yangtze River Delta, in China between 2003 and 2012.

Surface soil samples were collected from urban agglomeration of the Yangtze River Delta (YRD), China in 2003 and 2012, respectively. Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were analyzed to determine if there were any changes in their levels and compositional profiles between the two sampling years. The concentrations of Σ8PBDEs ranged from 0.553 to 13.0 µg kg(-1)(with the mean of 3.31 µg kg(-1)) in the 2003 samples and from 1.01 to 43.2 µg/kg (with the mean of 10.0 µg kg(-1)) in the 2012 samples. The concentrations of Σ32PCBs ranged from 0.301 to 3.29 µg kg(-1)(with the mean of 1.01 µg kg(-1)) in the 2003 samples and from 0.205 to 3.96 µg/kg (with the mean of 0.991 µg kg(-1)) in the 2012 samples. The comparisons between the 2012 and 2003 data showed that PBDEs concentrations increased over the years, but PCB concentrations did not change much. BDE-209 was the major BDE congener in both the 2003 and 2012 samples, indicating that the dominant PBDE mixture production and usage in the YRD had been the commercial deca-BDE mixture. Investigation of the PBDE congener profiles indicated that there had been new input of octa-BDEs in this region in recent years. Little change was found for the pattern of PCBs congener profiles between 2 years' samples. As such, spatial distributions of PBDEs or PCBs in surface soil samples reflected a gradient (from high to low) from the central cities out to rural areas in both the 2003 and 2012 data. In addition, high concentrations of PBDEs were observed in the industrial and residential areas, whereas high concentrations of PCBs were only observed in the industrial areas.

Levels and spatial distribution of polybrominated diphenyl ethers (PBDEs) in surface soil from the Yangtze River Delta, China.

Surface soil samples were collected from Suzhou, Wuxi and Nantong in the Yangtze River Delta (YRD), China. Eight BDE congeners (BDE-28, 47, 99, 100, 153, 154, 183 and 209) were measured to determine the levels and compositional profiles in the samples. The concentrations of Σ7PBDEs and BDE-209 ranged from 0.04 to 2.23 µg/kg dw and 1.48 to 41.7 µg/kg dw in the samples, respectively. BDE-209 was the predominant congener (contributing to 69.2 %-99.8 % of Σ8PBDEs) in all samples. It was found that small towns and rural economic development zones in this region had also become sources of polybrominated diphenyl ethers pollutants to surrounding areas. Investigation of the pattern of BDE congener profiles showed that deca- and octa- technical formulations as emission sources were identified in the samples collected from the YRD.

[Determination of kepone in water by liquid chromatography-tandem mass spectrometry].

An analytical procedure for the determination of kepone in water was described. Water samples were extracted by liquid-liquid extraction, and then cleaned-up. Chromatographic separation was performed on an Eclipse plus C18 column (100 mm x 2.1 mm, 3.5 microm) with gradient elution using acetonitrile and water at a flow rate of 0.3 mL/min. The target compounds were determined in multiple reaction monitoring (MRM) mode via negative electrospray ionization (ESI(-)) and quantified by isotopic-dilution technique. Results showed that kepone existed as diol form and hemiacetal in acetone/acetonitrile and methanol respectively, the structures of which were confirmed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Due to the polar nature of kepone, it was difficult to be eluted during clean-up procedure and it may be decomposed during sulfuric acid washing. Therefore, it could not be analyzed together with the other organochlorine pesticides. The calibration curve showed good linearity in the range of 5-100 microg/L with correlation coefficient (r2) of 0.999. The limit of detection was 0.70 ng/L and the limit of quantification was 2.8 ng/L in water. The average recoveries when spiked at 5, 40 and 100 ng/L in water were 95.1%-98.9%, and the relative standard deviations (RSDs) were 3.85%-4.72%. The method can be used to the determination of kepone in water due to its high sensitivity, good recovery and reproducibility.

[Levels and possible sources of organochlorine pesticides (OCPs) in camphor (Cinnamomum camphora) tree bark from Southern Jiangsu, China].

Thirty-three camphor tree bark samples were collected from Southern Jiangsu in August 2012. They were analyzed for organochlorine pesticides (OCPs), including hexachlorobenzene (HCB), DDTs (o,p'-DDE, p,p'-DDE, o,p'-DDD, p,p'-DDD, o,p'-DDT and p,p'-DDT), trans-chlordane and cis-chlordane. The concentrations of HCB, sigma6 DDTs and sigma Chlordanes ranged (dw) from 0.31 ng x g(-1) to 1.81 ng x g(-1), 0.40 ng x g(-1) to 17.3 ng x g(-1) and n. d. to 1.03 ng x g(-1), respectively. Due to the high volatility, the spatial distribution of HCB in Southern Jiangsu was uniform. Compared to the other results, the HCB concentration in Southern Jiangsu was lower. The historical usage of technical DDT mixture and the dicofol-type DDT were the major sources of DDTs in southern Jiangsu. The TC/CC ratio is usually used to distinguish between aged and fresh chlordane. According to the ratio of TC/CC, the chlordane in the urban area was derived from the fresh application of technical chlordane, and that in the rural area was attributed to the historical usage.

Occurrence, sources, and ecological risks of PBDEs, PCBs, OCPs, and PAHs in surface sediments of the Yangtze River Delta city cluster, China.

Polybrominated diphenyl ethers (PBDEs), organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polycyclic aromatic hydrocarbons (PAHs) in 25 surface sediments in three cities (Nantong, Wuxi, and Suzhou) in the Yangtze River Delta, eastern China were measured. The mean concentrations were 378, 45.8, 1.98, 4,002 ng/g for PBDEs, OCPs, PCBs, and PAHs, respectively. Their levels in the sediments in the three cities were generally consistent with the city industrialization. PBDEs and OCPs were markedly dominated by deca-BDE (>90 %) and DDTs (>70 %). A principle component analysis of the analytes identified three major factors suggesting different sources of the contaminants in the sediments. PBDEs and the organic carbon in the sediments have common sources from industrial activities; whereas OCPs and PCBs, correlated with the second factor, were mainly from historical sources. The third factor with loadings of PAHs is indicative of various combustion sources. Ecological risk assessment indicated that the potential highest risk is from DDTs, for which 22 sites exceed the effects range low (ERL) values and three sites exceed the effects range median (ERM) value.

Spatial distribution and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in Camphor (Cinnamomum camphora) tree bark from Southern Jiangsu, China.

The concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) were investigated in Camphor tree bark from Southern Jiangsu, China. Tree bark samples were collected in August 2012. The Σ15PAHs concentrations were ranged from 6.18 to 1560 ng g(-1)dry weight (dw), with an average value of 407 ng g(-1)dw. Generally, the concentrations of PAHs in the suburban areas were the highest, followed by urban and rural areas. Principal component analysis and diagnostic ratios results showed that vehicle emission, biomass and coal combustion and industrial emission were the major sources of PAHs in tree bark from Southern Jiangsu. Good correlation was found between tree bark and polyurethane foam (PUF) samplers, indicating that both of them respond well to the gas-phase PAHs monitoring.

Simple and rapid determination of PCDD/Fs in flue gases from various waste incinerators in China using DR-EcoScreen cells.

In developing countries such as China, there is a strong need for simple and rapid bioassays for the determination of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in environmental samples; i.e., flue gas and fly ash from waste incinerators. In this study, we applied the DR-EcoScreen cell (DR-cell) assay to determination of PCDD/Fs in 78 flue gas samples obtained from various waste incinerators in China between 2009 and 2011. The flue gas samples were obtained from four kinds of incinerators, classified into hazardous, medical and municipal-solid waste, and iron ore sintering, and the flue gas extracts were cleaned up using an SPD-600 automated-sample preparation device for DR-cell assay. The PCDD/Fs values obtained from the DR-cell assay were compared with those obtained from conventional high resolution gas chromatography-high resolution mass spectrometry (HRGC-HRMS) analysis. The bioanalytical equivalent (BEQ) values obtained from the DR-cell assay were very closely correlated with the international toxicity equivalent (I-TEQ) values from HRGC-HRMS analysis (r2=0.98, n=78), while the BEQ values were 5.52-fold higher than the I-TEQ values, as the PCDFs, which account for 80% of the total I-TEQ value, were overestimated by DR cell-assay. Therefore, we multiplied the BEQ values from the DR-cell assay by a conversion coefficient (0.181, the reciprocal of 5.52), and could approximate the TEQ values from the HRGC-HRMS analysis. These results suggest that the DR-cell assay combined with SPD-600 cleanup provides a promising method for the simple and rapid screening of PCDD/Fs levels in flue gas samples, such as those from various waste incinerators in China.

[Uncertainty evaluation of the determination of toxic equivalent quantity of polychlorinated dibenzo-p-dioxins and dibenzofurans in soil by isotope dilution high resolution gas chromatography and high resolution mass spectrometry].

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in soil samples were analyzed by isotope dilution method with high resolution gas chromatography and high resolution mass spectrometry (ID-HRGC/HRMS), and the toxic equivalent quantity (TEQ) were calculated. The impacts of major source of measurement uncertainty are discussed, and the combined relative standard uncertainties were calculated for each 2, 3, 7, 8 substituted con- gener. Furthermore, the concentration, combined uncertainty and expanded uncertainty for TEQ of PCDD/Fs in a soil sample in I-TEF, WHO-1998-TEF and WHO-2005-TEF schemes are provided as an example. I-TEF, WHO-1998-TEF and WHO-2005-TEF are the evaluation schemes of toxic equivalent factor (TEF), and are all currently used to describe 2,3,7,8 sub- stituted relative potencies.