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.

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.

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.

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.

A preliminary investigation of BDE-209, OCPs, and PAHs in urban road dust from Yangtze River Delta, China.

Urban road dust samples were collected from different land use areas in Suzhou, Wuxi, and Nantong, Yangtze River Delta, China. The dust samples were analyzed for the levels and compositional profiles of deca-polybrominated diphenyl ethers (Deca-BDE), 22 organochlorine pesticides (OCPs), and 16 polycyclic aromatic hydrocarbons (PAHs). The levels of BDE-209, ∑OCPs, and ∑PAHs in samples ranged from 4.01-1,439 µg/kg, 3.15-615 µg/kg, and 2.24-58.2 mg/kg, respectively. PAHs were the predominant target compounds in road dust samples, comprising on average 97.7 % of total compounds. The spatial gradient of the pollutants (commercial/residential area> industrial area > urban park concentrations) was observed in the present study. The results indicated that the levels of BDE-209, OCPs, and PAHs observed in road dust were usually linked to anthropogenic activities in the urban environment. In addition, there might be a reflection of current usage or emissions of OCPs in urban environment.

Levels and seasonal variations of polybrominated diphenyl ethers in the urban atmosphere of Beijing, China.

Year-round air samples were collected at Beijing on a weekly basis from 2009 to 2010, to determine the levels, gas-particle distribution, seasonal variations and compositional profiles of 8 polybrominated diphenyl ether congeners. The annual mean atmospheric concentrations of ∑7PBDEs and BDE-209 were 6.16 pg/m(3)(N.D-23.6 pg/m(3)) and 164 pg/m(3) (30.7-454 pg/m(3)), respectively. The results showed wide consumption of industrial products containing commercial deca-BDE mixtures in Beijing. The seasonal variations showed that lower brominated congeners had higher levels and greater proportions in the gaseous phase at warm sampling periods than the higher brominated counterparts.

PCDD/Fs, PBDD/Fs, and PBDEs in the air of an e-waste recycling area (Taizhou) in China: current levels, composition profiles, and potential cancer risks.

Atmospheric concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs), and polybrominated diphenyl ethers (PBDEs) were measured in Taizhou, a large electronic equipment waste (e-waste) recycling area in East China. The mean concentrations (in summer and winter) of PCDD/Fs (0.45 and 0.39 pg WHO-TEQ m⁻³, where WHO-TEQ is the toxic equivalent set by the World Health Organisation), PBDD/Fs (0.22 and 0.18 pg WHO-TEQ m⁻³), and PBDEs (270 and 225 pg m⁻³) in this region have declined compared with those in 2005, due to regulations on primitive e-waste recycling activities. However, these concentrations remain higher than the historically highest levels in Europe and North America. The congener profiles of 2,3,7,8-substituted PCDD/Fs were similar, with OCDD, 1,2,3,4,6,7,8-HpCDF, OCDF, and 1,2,3,4,6,7,8-HpCDD being the most abundant congeners at all sites. The PCDD/F homologue profiles in the present study were different from those typically observed at non-e-waste locations, indicating a distinct source in this region. Seasonal differences were found in the lower brominated PBDE profiles. These differences indicate that the PBDE emission sources in summer (e.g., strong evaporation sources) differed from those in winter. However, the relatively steady congener profiles of the highly brominated PBDEs suggest that these PBDEs were controlled primarily by similar emission mechanisms. The lifetime excess cancer risks from exposure to PCDD/Fs and PBDD/Fs via inhalation ranged from 0.7 × 10⁻5 to 5.4 × 10⁻5, or approximately 80 cancer cases in the Taizhou population.

Concentration and source identification of polycyclic aromatic hydrocarbons and phthalic acid esters in the surface water of the Yangtze River Delta, China.

The pollution from polycyclic aromatic hydrocarbons (PAHs) and phthalic acid esters (PAEs) in the surface water of the rapidly urbanized Yangtze River Delta region was investigated. Fourteen surface water samples were collected in June 2010. Water samples were liquid-liquid extracted using methylene chloride and analyzed by gas chromatography-mass spectrometry. Concentrations of PAHs and PAEs ranged 12.9-638.1 ng/L and 61-28550 ng/L, respectively. Fluoranthene, naphthalene, pyrene, phenanthrene, di-2-ethylhexyl phthalate, and di-n-butyl phthalate were the most abundant compounds in the samples. The water samples were moderately polluted with benzo[a]pyrene according to China's environmental quality standard for surface water. The two highest concentrations of PAHs and PAEs occurred in samples from Taihu Lake, Wuxi City and the western section of Yangchenghu Lake. Potential sources of pollution at S7 were petroleum combustion and the plastics industry, and at Yangchenghu Lake were petroleum combustion and domestic waste. Pollution in samples from the Beijing-Hangzhou Grand Canal originated from diesel engines. There were no obvious sources of pollution for the other water samples. These results can be used as reference levels for future monitoring programs of pollution from PAHs and PAEs.

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.

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.

Levels, seasonal patterns, and potential sources of organochlorine pesticides in the urban atmosphere of Beijing, China.

Air samples collected monthly on the roof of a building in Beijing were analyzed for the levels, seasonal patterns, and potential sources of organochlorine pesticides (OCPs). A high-volume air sampler with polyurethane foam and quartz fiber filters was used to collect monthly samples from November 2005 to April 2009. Hexachlorobenzene (HCB) and DDT isomers were the most abundant organochlorinated pesticides in the Beijing atmosphere. Higher OCP concentrations were generally found in summer, except for HCB. Coal combustion, waste incineration, and fuel combustion were assumed to be the potential HCB emission sources. Significant input of either of these OCPs during our study period was considered very unlikely.

Organochlorine pesticides in muscle of wild seabass and Chinese prawn from the Bohai Sea and Yellow Sea, China.

Muscle samples from wild seabass and Chinese prawn collected from the Bohai Sea and the Yellow Sea, China were analyzed for 22 organochlorine pesticides. DDTs were the predominant contaminants in all samples. The concentration of DDTs in seabass was 247 µg kg(-1) wet wt (from 4.30 to 2,089 µg kg(-1) wet wt). Significantly, concentration of DDTs in seabass was much higher than that in prawn (6.51 µg kg(-1) wet wt). Very high concentrations of DDTs and high DDT/DDTs ratio were found in seabass samples from some locations, which imply there might be new inputs of DDT into the marine environment.

Mixed polybrominated/chlorinated dibenzo-p-dioxins and dibenzofurans in stack gas emissions from industrial thermal processes.

Very little is known about mixed polybrominated/chlorinated dibenzo-p-dioxins and dibenzofurans (PBCDD/F) in industrial thermal processes. In this study, the occurrences and characteristics of PBCDD/F from various incineration and metallurgical processes were investigated. In addition, PBCDD/F analytical protocols based on HRGC/HRMS were developed and optimized. The sum of isomer group concentrations ranged from 1.7-3740 pmol Nm(-3) for PBCDF and 0.2-582 pmol Nm(-3) for PBCDD. For some metallurgical industries, the amounts of PBDD/F and PBCDD/F emitted were similar to or even higher than the amounts of PCDD/F. The sources of bromine and brominated-precursors in these processes should be evaluated. The PBCDD/F characteristics investigated included isomer group patterns, ratio of bromine and chlorine incorporated in PBCDD/F, and ratio of halogenated furans to dioxins. Lower brominated PBCDD/F were binomially distributed. But in some cases, the concentrations of higher brominated PBCDD/F were much higher than predicted from the binomial distribution. The formation mechanisms of PBDD/F, PBCDD/F, and PCDD/F in these processes were also evaluated.

Concentration and gas-particle partitioning of hexachlorobenzene in the ambient air before and after the Beijing Olympic Games.

Systematic studies of hexachlorobenzene in the ambient air before and after the Beijing Olympic Games were carried out during July 2007 to March 2009. Air samples were collected around 20th monthly on the roof of a building near the Olympic center. The average concentration of hexachlorobenzene was 264 pg x m(-3), which was higher in winter than other seasons. However, hexachlorobenzene concentration was decreased clearly in winter in 2008 compare with in 2007 due to the implementation of a series of "Green Olympic" policies. Gas-particle partitioning shows that the increase of hexachlorobenzene levels in winter time was mainly contributed by the high total suspended particulate from combustion processes such as coal-burning and traffic emission.

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.

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.

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.

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.

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.