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Although wastewater treatment plants (WWTPs) can purify wastewater, they also discharge numerous contaminants into the environment through effluent discharge and sludge disposal. The occurrence, emission flux, and risk assessment of traditional pollutants (e.g., heavy metals [HMs]), and emerging pollutants (e.g., perfluoroalkyl substances [PFASs] and pharmaceutical and personal care products [PPCPs]) in WWTP emissions are of important concern. The present study analyzed 17 PFASs, 25 PPCPs, and 8 HMs in influent, effluent, and excess sludge from six WWTPs along the Yanghe River, North China. Samples were collected during four sampling campaigns from November 2016 to July 2017. The mean concentrations of PFASs and PPCPs in influent were 46.4 ng L -1 and 6.57 μg L -1 , respectively; while those in effluent were 38.5 ng L -1 and 2.14 μg L - 1 , respectively. The highest concentrations of HMs was detected of Zn in influent (2,866 μg L - 1 ) and effluent (3,960 μg L - 1 ). According to the concentration composition, short-chain PFASs, fluoroquinolones (FQs), and Zn were the predominant components in both influents and effluents. The mean PFAS and PPCP concentrations in excess sludge were 5.95 ng g - 1 and 3.74 μg g - 1 dry weight (dw). Zn was the most abundant HMs in excess sludge with the concentration range of 156-14,271 μg g - 1 dw. The compositions of PFASs, PPCPs and HMs differed between wastewater and excess sludge. The estimated emission flux of these pollutants was ordered as HMs > PPCPs > PFASs through effluent discharge and sludge disposal. Sludge disposal discharged more PPCPs and HMs into the environment than effluent discharge, which was contrary for PFASs. Relative risk of each pollutant is calculated by comparing the mean effluent concentration with the median effective concentration. Algae and fish were selected as recipient organisms to calculate the relative risk of 23 selected pollutants towards aquatic organisms. The highest-risk pollutant was Zn on both algae and fish, while perfluorobutane sulfonate (PFBS) and atenolol (ATE) posed the lowest risk. In general, HMs (regarded as traditional pollutants) presented higher risks in effluent, followed by the emerging pollutants (PPCPs and PFASs). Therefore, control of traditional pollutants should be prioritized in WWTPs in this region. This study presents an overall assessment of the current status of traditional and emerging pollutants in WWTPs and provides useful information for upgrading wastewater treatment processes., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

The production of polychlorinated biphenyls (PCBs) has been banned globally for decades, but PCB concentrations in environmental media remain relatively high, especially in urban areas. Emissions estimates, studies of soil gradients between urban and rural areas, and quantitative identification of regional sources of PCBs in soils are necessary for understanding the environmental behavior of PCBs. In this study, regional PCB emissions were estimated at a resolution of 10 km × 10 km, and the spatial distribution of soil PCBs from urban to rural areas was studied along the Bohai and Yellow Sea regions. Compared with rural areas, mean PCB concentrations in urban soils (20.7 ng/g) were found to be higher, and concentrations decreased with distance from the city. Across both latitude and longitude directions, high PCB emissions in urban areas matched the distribution of total PCB concentrations in soils. The concentrations of the pollutants PCB28, PCB52, PCB101, PCB118, PCB138, PCB153, and PCB180 in soils originated from 5-year emissions, and accounted for 97%, 95%, 84%, 81%, 58%, 57%, and 27% of the total emissions, respectively. Unintentionally produced PCB (UP-PCB) emissions, which are mainly derived from cement (42%), pig iron (37%), crude steel (18%), and rolled steel (3%) industries, are the major contributors to PCBs in soils. Further identification of the sources and fates of PCBs requires a combination of field, laboratory, and modeling efforts., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Methodology to quantify and distinguish the spatial distribution of the risks from multiple pollutants within the region was developed in this paper. An integrated quantitative risk assessment was conducted by utilizing a large amount of information available to explore spatial distribution of risk by single and multiple pollutants, and the magnitude of the overall risk from multiple pollutants based on the current concentrations of pollutants and toxicity data. Two target criteria levels - level I (NOEC/LOEC based) and level II (LC/EC/IC 50 based) - were employed, and thus, the regional and sub-regional risks were evaluated according to these two levels. The risk of multiple toxic metals (As, Cd, Cr, Hg and Pb) to a terrestrial ecosystem for the region around the Bohai Sea and the Yellow Sea were evaluated as a case. The total overall ecological risks from heavy metals in the region for level I and level II were 21.73% and 12.53%, respectively. The risks were ranked in the order of Cr > As > Pb > Cd > Hg with Cr posing the greatest ecological risk, which was 61.12% for level I. The top three cities according to the level II ecological risk were Cangzhou > Lianyungang > Panjin, while the top three cities of level I ecological risk were Cangzhou > Panjin > Lianyungang. This method provides a quantitative risk assessment with multiple and clear protection levels for risk management., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Between 1945 and 1983, China was the world's largest producer of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs), and the second largest producer of hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs). The provinces of Liaoning, Hebei, Tianjin, Shandong, and Jiangsu around the Yellow and Bohai Seas have a long history of production and usage of OCPs and PCBs. To investigate their residual concentration, distribution, risk level, and temporal degradation, 7 OCPs and 7 indicator PCBs were determined in surface soils collected around the Yellow and Bohai Seas. Residues of the 7 OCPs and 7 PCBs were in the range of 5.89-179.96 ng g -1 dry weight (dw) and non-detectable (ND)-385.67 ng g -1 dw, respectively. Tianjin and Hebei provinces recorded the highest concentrations of OCPs and PCBs, respectively. Moreover, OCPs residues had a significant relationship with agriculture and orchard land-use types, whereas PCBs residues occurred more in wasteland. Lifetime carcinogenic and non-carcinogenic risks of OCPs and PCBs through ingestion, inhalation, and dermal contact indicated that OCPs and PCBs residues in surface soils are at a low risk level., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Perfluoroalkyl acids (PFAAs) are being increasingly reported as emerging contaminants in riverine and marine settings. This study investigated the contamination level and spatial distribution of 17 PFAAs within the depth profile of the Bohai and Yellow Seas using newly detected sampling data from 49 sites (June 29 to July 14, 2016). Moreover, the riverine flux of 11 selected PFAAs in 33 rivers draining into the Bohai and Yellow Seas was estimated from previous studies (2002-2014) in order to establish the relationship between riverine sources and marine sinks. The results showed that the Bohai and Yellow Seas were commonly contaminated with PFAAs: total concentrations of PFAAs in the surface, middle, and bottom zones ranged from 4.55 to 556 ng L -1 , 4.61-575 ng L -1 , and 4.94-572 ng L -1 , respectively. The predominant compounds were PFOA (0.55-449 ng L -1 ), PFBA (-1 ), and PFPeA (-1 ), accounting for 10.1-87.0%, 5.2-59.5%, and 0.6-68.6% of the total PFAAs, respectively. In general, the ∑PFAA concentrations showed a slightly decreasing trend with sampling depth. Contamination was particularly severe in Laizhou Bay, fed by the Xiaoqing River and an industrial park known for PFAA production. The total riverine PFAA mass flux into the Bohai and Yellow Seas was estimated to be 72.2 t y -1 , of which 94.8% was carried by the Yangtze and Xiaoqing Rivers. As the concentration of short-chain PFAAs begins to rise in seawater, further studies on the occurrence and fate of short-chain PFAAs with special focus on effective control measures would be very timely, particularly in the Xiaoqing River and Laizhou Bay., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

With the shift of fluorine chemical industry from developed countries to China and increasing demand for fluorine chemical products, occurrence of perfluoroalkyl substances (PFASs) in production and application areas has attracted more attention. In this study, 153 soil samples were collected from 21 cities along the urbanizing coastal area of the Bohai and Yellow Seas. PFASs in this area were relatively higher, compared with other study areas. The concentrations ranged from 2.76 to 64.0 ng g -1 , and those in most sites were between 2.76 and 13.9 ng g -1 , with a predominance of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). Among the 21 coastal cities, contaminations of PFASs in Zibo, Nantong and Binzhou were elevated, which was likely affected by local fluorine chemical plants, equipment manufacturing and chemical industry, respectively. The total emissions of PFOA and PFOS were similar, with amount of 4431 kg and 4335 kg, respectively. Atmospheric deposition was the largest source, accounting for 93.2% of total PFOA and 69.6% of PFOS, respectively. In addition, due to application of aqueous film-forming foams (AFFFs) and sulfluramid, disposal of sewage sludge and stacking of solid waste, emission of PFOA and PFOS to soil was 1617 kg, accounting for 9.29% of the whole China. In general, pollution in Jiangsu, Shandong and Tianjin was more serious than those in Liaoning and Hebei, which was consistent with industrialization level and size of industrial sectors emitting PFASs., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Eutrophication has become one of the most serious threats to aquatic ecosystems in the world. With the combined drivers of climate change and human activities, eutrophication has expanded from warm shallow lakes to cold-water lakes in relatively high latitude regions and has raised greater concerns over lake aquatic ecosystem health. A two-year field study was carried out to investigate water quality, phytoplankton characteristics and eutrophication status in a typical alpine glacial lake of Tianchi, a scenic area and an important drinking water source in the Xinjiang Autonomous Region of China, in 2014 and 2015. Clear seasonal and annual variations of nutrients and organic pollutants were found especially during rainy seasons. For the phytoplankton community, Bacillariophyta held the dominant position in terms of both species and biomass throughout the year, suggesting the dominant characteristics of diatoms in the phytoplankton structure in such a high-altitude cold-water lake. This was quite different from plain and warm lakes troubled with cyanobacterial blooming. Moreover, the dominant abundance of Cyclotella sp. in Tianchi might suggest regional warming caused by climate change, which might have profound effects on the local ecosystems and hydrological cycle. Based on water quality parameters, a comprehensive trophic level index TLI (Σ) was calculated to estimate the current status of eutrophication, and the results inferred emerging eutrophication in Tianchi. Results from Canonical Correspondence Analysis (CCA) and correlation analysis of phytoplankton genera and physico-chemical variables of water indicated that abiotic factors significantly influenced the phytoplankton community and its succession in Tianchi Lake. These abiotic factors could explain 77.82% of the total variance, and ammonium was identified as the most discriminant variable, which could explain 41% of the total variance followed by TP (29%). An estimation of annual nutrient loadings to Tianchi was made, and the results indicated that about 212.97 t of total nitrogen and 32.14 t of total phosphorus were transported into Tianchi Lake annually. Human socio-economic activities (runoff caused by historical overgrazing and increasing tourism) were identified as the most important contributors to Tianchi nutrient loadings.

Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are extremely persistent in the environment, and have the potential for long-range transport. The present study focused on the Daling River and its tributary, a larger river flowing into Liaodong Bay of the Bohai Sea. Recent studies have shown the elevated levels of PFOS and PFOA in the Daling River. Hence, the objective of this study was to investigate the seasonal changes, fate and transport modeling of PFOS and PFOA concentrations using one-dimensional DHI MIKE-11 river model. We designed three scenarios to assess the risk of PFOS and PFOA in surface water: the measured concentrations, constant maximum and the magnitude of a continuous constant load. The mean absolute errors divided by the mean of measured concentrations were 41-64% for PFOS and 29-36% for PFOA. The result indicated that PFOS and PFOA in the downstream of the Daling River would not reach a harmful level with the current load. The fluorochemical parks contributed an average of 44.57% of the total PFOS and 95.44% of the total PFOA flow that reached the estuary. The mass flow was observed as 1.74 kg y -1 for PFOS and 40.57 kg y -1 for PFOA to the Bohai Sea. These modeling results may be useful for monitoring the status and trends of emerging POPs and will help the determination of the risk to both humans and wildlife, in the estuarine and coastal areas of the Bohai Sea, China., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Short chain perfluoroalkyl acids (PFAAs) have been developed since 2002 by the major manufacturers to replace the conventional C8 and higher homologues, with much of the world production shifted to China in recent years. In this study, we conducted a continuous monitoring program over the period 2011-2014 with seasonal monitoring in 2013 for PFAAs emitted from two rapidly developing fluorochemical industry parks located in the Daling River Basin, Northern China. The trend of PFAA contamination was identified, dominated by perfluorobutane sulfonic acid (PFBS), perfluorobutanoic acid (PFBA) and perfluorooctanoic acid (PFOA), with the maximum concentrations of 3.78 μg/L, 3.70 μg/L, and 1.95 μg/L, respectively. Seasonal monitoring uncovered the occasional emission of perfluorooctane sulfonic acid (PFOS). Construction trends of new facilities and associated manufacturing capacity of the main products were also analyzed to assess correlations with PFAA emissions. An assessment of the data over the period 2011-2014 found a positive correlation with fluorocarbon alcohol (FCA) production and emission of PFAAs. Groundwater and tap water around the main source indicated that the dominant PFAAs had different diffusion behaviors. PFBS levels were higher in surface water, while PFBA was dominant in groundwater and tap water, with PFOA levels being higher in downstream groundwater. Considering the continuous expansion and development of fluorochemical industry in the Daling River Basin, this study will provide abundant information on the effectiveness of risk assessment and management., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

The manufacture of fluorochemicals can lead to high levels of perfluoroalkyl acids (PFAAs) contaminating the surrounding environment and consequently elevated exposure to the local residents. In this study, measurements of PFAAs associated with indoor and outdoor dusts around a mega fluorochemical industrial park (FIP) were made. Perfluorooctanoic acid (PFOA) and short-chain perfluoroalkyl carboxylic acids (C4-C7 PFCAs) were the predominant forms in all samples. The signature of the PFAAs in dusts in the local area matched that found within the FIP complex. The contamination plume in the local area could be linked to the prevailing wind direction starting from the FIP. The dust concentrations decreased exponentially with distance from the FIP (noticeably in the first 5km). PFAAs contamination could be detected at the furthest location, 20km away from the FIP. The concentrations of PFAAs were higher in indoor dust (73-13,500ng/g, median: 979ng/g) than those in outdoor dust (5-9495ng/g, median: 62ng/g) at every location. The highest estimated daily intake of PFOA via dust ingestion (26.0ng/kg·bw/day) was for toddlers (2-5years) living 2km away from the FIP, which is posing human health risk, though exposure remains within the provisional tolerable daily intake values., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

After global commercialization of short-chain perfluoroalkyl acids (PFAAs) as substitutes to conventional long-chain PFAAs by the major manufacturers, two fluorine industry parks for production of short-chain PFAAs located in the Daling River Basin of northern China have developed rapidly in the last few years. This study provides a systematic assessment of sources, emissions, transportation, and potential risks of the PFAAs in this area. The C4 perfluorobutane sulfonic acid (PFBS) and perfluorobutanoic acid (PFBA) were the predominant short-chain PFAAs in river water, with maximum concentrations of 2.90 and 1.35 μg/L, respectively. Park 1 equipped with a telomerization process was identified to be the source of linear and branched mixtures of PFBS, PFBA, and perfluorooctanoic acid (PFOA), while park 2 with an electrochemical fluorination process (ECF) was identified to be the source of linear and branched mixtures of PFBS and PFOA. Partition coefficients between water and sediment were consistent for C4-C8 perfluoroalkyl carboxylic acids (PFCAs) but directly proportional to C9-C11 PFCAs and perfluoroalkyl sulfonic acids (PFSAs). Analysis on the health risk of PFBS and PFBA suggested that they were not without risk since short chain PFAAs are known to be recalcitrant during water treatment.

In the present study, we investigated concentrations and composition profiles of perfluoroalkyl substances (PFASs) in surface water from the Daling River in different seasons. The highest concentration of ΣPFASs (9540 ng L(-1)) and dominant homologues were found in surface water collected in summer. Perfluorobutanoic acid (PFBA), perfluorobutane sulfonate (PFBS), and perfluorooctanoic acid (PFOA) were the dominant PFASs in four seasons with a total contribution of over 90%. The discharge of two fluorine chemical industry parks was predicted to be the main contamination source of PFASs in the study area. The daily and annual mass flows were calculated according to data of detected PFAS concentrations and water discharge, and the annual mass loading of PFASs into the Bohai Sea from the Daling River reached to 461 kg year(-1). Hazard assessment indicated that concentrations of PFASs in study area had little risk to aquatic organisms and wildlife. However, the multiple health risk would be relatively high if the water was served as drinking water in the study area.

Concentrations of 13 perfluoroalkyl substances (PFASs) were quantified in 79 surface soil samples from 17 coastal cities in three provinces and one municipality along the Bohai and Yellow Seas. The ∑PFASs concentrations ranged from less than limitation of quantification (LOQ) to 13.97 ng/g dry weight (dw), with a mean of 0.98 ng/g dw. The highest concentration was observed along the Xiaoqing River from Shandong province, followed by that from the Haihe River in Tianjin (10.62 ng/g dw). Among four regions, ∑PFASs concentrations decreased in the order of Tianjin, Shandong, Liaoning and Hebei, which was consistent with levels of urbanization. Fluorine chemical industries allocated in Shandong and Liaoning played important roles in terms of point emission and contamination of PFASs, dominated by perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS). Intensive anthropogenic activities involved in urbanization possibly resulted in increasing releases of PFASs from industrial and domestic sources., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

The pollution level and source of perfluoroalkyl substances (PFASs) in mainstream and tributary of Daling River in northeast China were investigated in present study. Concentrations of PFASs in surface water and sediment ranged from 4.6 to 3,410 ng/L and from 0.08 to 2.6 ng/g dry weight, respectively. The lowest levels of PFASs were found in vicinity of a drinking water source located in upstream of Daling River. Xihe tributary, which is adjacent to two local fluorine industrial parks, contained the highest level of PFASs. Short-chain PFASs, including perfluorobutanoic acid and perfluorobutane sulfonate, were of higher levels due to their emerging as alternative products for perfluorooctane sulfonate. High level of perfluorooctanoic acid was also found in Daling River. Based on these results, it can be concluded that the relatively severe pollutions of Xihe tributary were caused by long-term development of the two local fluorine industry parks.