Spatiotemporal variations, sources, and atmospheric transformation potential of volatile organic compounds in an industrial zone based on high-resolution measurements in three plants.

Industrial emissions are significant sources of volatile organic compounds (VOCs). This study conducted a field campaign at high temporal and spatial resolution to monitor VOCs within three plants in an industrial park in southern China. VOC concentrations showed significant spatial variability in this industrial zone, with median concentrations of 75.22, 40.53, and 29.41 µg/m3 for the total VOCs in the three plants, respectively, with oxygenated VOCs (OVOCs) or aromatics being the major VOCs. Spatial variability within each plant was also significant but VOC-dependent. Seasonal variations in the VOC levels were governed by their industrial emissions, meteorological conditions, and photochemical losses, and they were different for the four groups of VOCs. The temporal and spatial variations in the VOC compositions suggest similar sources of each class of VOCs during different periods of the year in each plant. The diurnal patterns of VOCs (unimodal or bimodal) clearly differed from those at most industrial/urban locations previously, reflecting a dependence on industrial activities. The secondary transformation potential of VOCs also varied temporally and spatially, and aromatics generally made the predominant contributions in this industrial park. The loss rate of OH radicals and ozone formation potential were highly correlated, but the linear relationship substantially changed in summer and autumn due to the intensive emissions of an OVOC species. The lifetime cancer and non-cancer risks via occupational inhalation of the VOCs in the plants were acceptable but merit attention. Taking the secondary transformation potential and health risks into consideration, styrene, xylene, toluene, trichloroethylene, and benzene were proposed to be the priority VOCs regulated in the plants.

Disposable Plastic Waste and Associated Antioxidants and Plasticizers Generated by Online Food Delivery Services in China: National Mass Inventories and Environmental Release.

China's online food delivery (OFD) services consume enormous amounts of disposable plastics. Here, we investigated and modeled the national mass inventories and environmental release of plastics and chemical additives in the plastic. The extra-tree regression identified six key descriptors in determining OFD sales in Chinese cities. Approximately 847 kt of OFD plastic waste was generated in 2021 (per capita 1.10 kg/yr in the megacities and 0.39 kg/yr in other cities). Various additives were extensively detected, with geomean concentrations of 140.96, 4.76, and 0.25 µg/g for ∑8antioxidants, ∑21phthalates, and bisphenol A (BPA), respectively. The estimated mass inventory of these additives in the OFD plastics was 164.7 t, of which 51.1 t was released into the atmosphere via incineration plants and 51.0 t was landfilled. The incineration also released 8.07 t of polycyclic aromatic hydrocarbons and 39.1 kt of particulate matter into the atmosphere. Takeout food may increase the dietary intake of phthalates and BPA by 30% to 50% and raise concerns about considerable exposure to antioxidant transformation products. This study provides profound environmental implications for plastic waste in the Chinese OFD industry. We call for a sustainable circular economy action plan for waste disposal, but mitigating the hazardous substance content and their emissions is urgent.

Complex polycyclic aromatic compound mixtures in PM2.5 in a Chinese megacity: Spatio-temporal variations, toxicity, and source apportionment.

Polycyclic aromatic compounds (PACs) are important toxic organic components in fine particulate matter (PM2.5), whereas the links between PM2.5 toxicity and associated PACs in ambient air are poorly understood. This study investigated the spatial-temporal variations of PACs in PM2.5 collected from 11 sampling sites across a Chinese megacity and characterized the reactive oxygen species (ROS) generation and cytotoxicity induced by organic extracts of PM2.5 based on cellular assays. The extra trees regression model based on machine learning and ridge regression were used to identify the key toxicants among complex PAC mixtures. The total concentrations of these PACs varied from 2.12 to 71.7 ng/m3 across the study city, and polycyclic aromatic hydrocarbons (PAHs) are the main PACs. The spatial variations of the toxicological indicators generally resembled those of the PAC concentrations, and the PM2.5 related to waste treatment facilities exhibited the strongest toxic potencies. The ROS generation was highly correlated with high molecular weight PAHs (MW302 PAHs), followed by PAHs with MW<302 amu and oxygenated PAHs, but not with nitrated PAHs and the plastics additives. The cell mortality showed weak correlations with these organic constituents. The associations between the biological endpoints and these PM2.5-bound contaminants were further confirmed by exposure to authentic chemicals. Four primary sources of PACs were identified, among which coal and biomass combustion sources (30.2% of the total PACs) and industrial sources (31.0%) were predominant. PACs emitted from industrial sources were highly associated with ROS generation in this city. Our findings highlight the potent ROS-generating potential of MW302 PAHs and the importance of industrial sources contributing to PM2.5 toxicity in this megacity, raising public concerns and further administration.

Particle size-resolved emission characteristics of complex polycyclic aromatic hydrocarbon (PAH) mixtures from various combustion sources.

Combustion of domestic solid fuels is a significant source of polycyclic aromatic hydrocarbons (PAHs). Some oxygenated PAHs (o-PAHs) and PAHs with molecular weight of 302 (MW302 PAHs) are more toxic than the traditional 16 priority PAHs, whereas their emissions were much less elucidated. This study characterized the size-dependent emissions of parent PAHs (p-PAHs), o-PAHs, and MW302 PAHs from various combustion sources. The estimated emission factors (eEFs) from biomass burning sources were highest for most of the PAHs (391-8928 µg/kg), much higher than that of anthracite coal combustion (43.0-145 µg/kg), both which were operated in an indoor stove. Cigarette smoking had a high eEF of o-PAHs (240 ng/g). MW302 PAHs were not found in the emissions of smoking, cooking, and vehicular exhausts. Particle-size distributions of PAHs were compound- and source-dependent, and the tendency to associate with smaller particles was observed especially in biomass burning and cigarette smoking sources. Furthermore, the inter-source differences in PAH eEFs were associated with their dominance in fine particles. PAH composition profiles also varied with the particle size, showing increasing contributions of large-molecule PAHs with decreasing sizes in most cases. The size distributions of p-PAHs are much more significantly dependent on their n-octanol/air partition coefficients and vapor pressures than those of o-PAHs, suggesting differences in mechanisms governing their distributions. Several molecular diagnostic ratios (MDRs), including two based on MW302 PAHs, specific to these combustion scenarios were identified. However, the MDRs within some sources are also strongly size-dependent, providing a new explanation for the uncertainty in their application for source identification of PAHs. This work also highlights the necessity for understanding the size-resolved atmospheric behaviors and fate of PAHs after their emission.

Accumulation and translocation of traditional and novel organophosphate esters and phthalic acid esters in plants during the whole life cycle.

Organophosphate esters (OPEs) and phthalic acid esters (PAEs) are widespread contaminants in the environment. The variations of these chemicals in plants throughout their life cycle is little known. In this study, OPEs, OPE metabolites, and PAEs in peanut and corn grown under field conditions, soil, and air were measured to understand the uptake and translocation, distributions in the plant compartments, and metabolism in the plants. The soil concentrations showed an enrichment effect of OPEs onto the rhizosphere soil but a depletion effect of PAEs on rhizosphere soils. The PAE concentrations between peanut (with a mean of 1295 ng/g dw) and corn (3339 ng/g dw) were significantly different, but the OPE concentrations were not significantly different (with means of 15.6 and 19.2 ng/g dw, respectively). OPE metabolites were also detected in the plants, with lower concentrations and detection rates. Similarities and differences in the temporal variations of the concentrations of traditional OPEs, novel OPEs, and PAEs in plants during their growth were observed. The variations were dependent on both plant species and particular tissues. The leaf compartment is the most important reservoir of OPEs and PAEs (but not OPE metabolites) for both species, highlighting the importance of an aerial uptake pathway. The chemicals have a low potential to be translocated into peanut and corn kernels, reducing their risks via food consumption. Less hydrophobic compounds have higher root concentration factors in this study. These observations differ from those of previous hydroponic experiments.

PM2.5-bound phthalates and phthalate substitutes in a megacity of southern China: spatioseasonal variations, source apportionment, and risk assessment.

Plasticizers are ubiquitous pollutants in the environment, whereas few efforts have been made to elucidate their emission sources in the atmosphere. In this research, the spatioseasonal variations and sources of particle-bound (PM2.5) phthalates (PAEs) and their substitutes (APs) at residential sites in seven districts and at four potential point-source sites across a megacity in South China were revealed. The total concentrations of PAEs ranging from 10.7 to 528 ng/m3 were substantially higher than those of APs (1.45.58.5 ng/m3). Significant spatial variations in the concentrations of the pollutants were observed, which were generally higher at the sites with intensive industrial activities and the point-source sites. Most atmospheric plasticizer levels peaked in summer, probably due to the temperature-promoted volatilization. Seven sources of plasticizers were identified by the positive matrix factorization (PMF) model. The sources in less industrialized districts are mainly associated with domestic and commercial emissions and with industry in the industrialized districts. Specifically, plastics and personal care products together contributed 60% of the plasticizers in the atmosphere of this city, followed by solvents and polyester industry sources. The incremental lifetime cancer risk of inhalation exposure to bis(2-ethylhexyl) phthalate in the study city is below the acceptable level. Relatively higher risks were found for residents living around sites with intensive industrial activities and around wastewater treatment plant.

Changes in human hair levels of organic contaminants reflecting China's regulations on electronic waste recycling.

To assess the impacts of regulations and laws enhancing the management of e-waste in China, hair samples of local residents and dismantling workers in a former e-waste area in 2016 and 2019, five and eight years after the implementation of legislation and regulations in this area since 2011, respectively. The temporal changes in levels of polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and organophosphorus flame retardants (OPFRs) in the hair samples were investigated. Besides, the levels of these organic contaminants in hair samples collected from the same area in 2009, 2011, and 2015 reported in previous studies were used as comparison. The highest median levels of Σ9PCBs (719 ng/g), Σ3Penta-BDEs (16.1 ng/g), and Σ3Octa-BDEs (8.46 ng/g) in hair were found in 2011, with a significant decrease trend was observed from 2011 to 2019 (p < 0.05). As for Deca-BDE, the levels reached the maximum in 2015 (133 ng/g), following by a significant decrease to 2016 (7.46 ng/g) and 2019 (2.61 ng/g) (p < 0.05). The median levels of Σ8OPFRs, also decreased significantly (p < 0.05) from 2015 (357 ng/g) to 2016 (264 ng/g) and 2019 (112 ng/g). Moreover, a significantly increasing trend was observed for the ratios of triphenyl phosphate (TPHP) and tris(2-chloropropyl) phosphate (TCIPP), two predominant OPFRs, to Deca-BDE from 2015 to 2019 (p < 0.01), suggesting a shift of "legacy" to "emerging" contaminants released from e-waste recycling in this area. The temporal changes in hair levels of typical organic contaminants in residents and dismantling workers indicated the effectiveness of the regulations on informal e-waste recycling activities and solid waste in China.

Traditional and novel organophosphate esters (OPEs) in PM2.5 of a megacity, southern China: Spatioseasonal variations, sources, and influencing factors.

Organophosphate esters (OPEs) are ubiquitous contaminants in the environment, whereas their atmospheric processes and fate are poorly understood. The present study revealed the spatial heterogeneity and seasonal variations of traditional and novel OPEs in PM2.5 (particulate matter with diameters < 2.5 µm) across a megacity (including residential areas and potential source sites) in South China. Potential influencing factors on the contamination levels of OPEs were addressed. The total concentrations of 11 traditional OPEs ranging from 262 to 42,194 pg/m3 (median = 1872 pg/m3) were substantially higher than those of 10 novel OPEs (33.5-3835 pg/m3, median = 318 pg/m3). Significant spatial and temporal variations in the concentrations of most OPEs were observed. The overall district-specific contamination levels in this city showed dependence on the secondary industry sector for non-predominant OPEs and on the tertiary industry for predominant OPEs. The seasonal variations of the OPE concentrations suggest difference in their sources or influence of meteorological conditions. The correlations between the individual OPEs in PM2.5 are determined largely by either their applications or physicochemical properties (in particular vapor pressure). The correlations between OPE concentrations and each meteorological factor (temperature, relative humidity, wind speed, and surface solar radiation) were inconsistent (positive and negative). Wind speed had the greatest effect on the OPE levels; While most OPEs bound to PM2.5 were not efficiently scavenged by below-cloud rainfall. The results suggest that atmospheric half-life and Henry's Law Constant of OPEs are also determining factors for the wind speed and rainfall influence, respectively. However, mechanisms underlying the influence of meteorological conditions on atmospheric OPEs still need further research.

Characterization of airborne particles and cytotoxicity to a human lung cancer cell line in Guangzhou, China.

Air pollution by airborne particles is a serious health problem worldwide. The present study was aimed at investigating the concentrations and composition of total suspended particles (TSPs) and PM2.5 at various industrial/commercial sites of Guangzhou, a megacity of Southern China. Major and trace elements, ions and carbonaceous fraction were determined and main components were calculated. In addition, in order to assess the potential toxic on the respiratory system of these PM, cytotoxicity of size-fractionated particles (PM10-5.6, PM5.6-3.3, PM3.3-1.1, PM1.1-0.43) for a human lung cancer cell line (A549) was also investigated. Correlations between PM constituents and toxicity were assessed. Median levels of TSPs and PM2.5 in industrial/commercial sites were 206 and 57.7 µg/m3, respectively. Nickel, Cu, Mo, Mn, Pb, and Ti were the most abundant metals in TSPs and PM2.5. Industrial activities and coal combustion were the most important sources of carbonaceous particles in the zone. MTT assays showed that PM10-5.6 and PM1.1-0.43 had the highest and the lowest cytotoxicity to A549 cell lines, respectively. Inhalable particles around the manufacturing of metal facilities and formal waste treatment plants showed a high cytotoxicity to A549 cell lines. In general terms, no significant correlations were found between main components of PM and toxicity. However, W showed a significant correlation with cell viability.

Brominated flame retardants (BFRs) in PM2.5 associated with various source sectors in southern China.

The present study investigates legacy and novel brominated flame retardants (BFRs) in atmospheric PM2.5 associated with various urban source sectors in a city and electronic waste (e-waste) recycling facilities in southern China. The concentrations of polybrominated diphenyl ethers (PBDEs) and novel BFRs (∑2NBFRs) at the urban industrial park (UIP) sites varied greatly from 22.0 to 105 pg m-3 and from to 29.7 to 459 pg m-3, respectively, and higher concentrations were generally found at sites involving industrial sectors of electronics, plastics, and machinery. Their spatial variations at other urban potential source sites were small suggesting a lack of strong point emissions. The levels of PBDEs and ∑2NBFRs at the e-waste facilities (220-2356 pg m-3 and 83.6-569 pg m-3) were significantly higher and did not temporally decline, indicating that improvement in e-waste recycling techniques does not significantly reduce emissions of PBDEs. NBFRs dominated the BFRs at the urban sites (55% on average), while PBDEs were still dominant (78%) at the e-waste sites. PBDE congener profiles in PM2.5 were substantially different from those in commercial mixtures. The congener profiles as well as their correlations suggested frequent formation of lower brominated PBDEs from degradation of highly brominated congeners in this region, which became appreciable due to the reduced emissions. The significant correlations among the lower brominated congeners also reflected similar environmental behaviors due to similar physicochemical properties.

Uptake of halogenated organic compounds (HOCs) into peanut and corn during the whole life cycle grown in an agricultural field.

Here, we elucidated the uptake and translocation of numerous halogenated organic compounds (HOCs) into corn and peanut throughout their life cycle cultivated in an agricultural field of an electronic waste recycling area, where plants were simultaneously exposed to contaminants in soil and ambient air. The geometric mean concentrations of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were 22.3 and 11.9 ng/g in peanut and 16.6 and 13.6 ng/g in corn, respectively. Decabromodiphenyl ethane (DBDPE, 6.07 ng/g) and dechlorane plus (DPs, 6.22 ng/g) also showed significant concentrations in peanuts. The plant uptake was initiated from root absorption at the emergence stage but it was subsequently surpassed by leaves absorption from the air since the late seedling stage or early reproductive stage. There was a rapid uptake of lower halogenated HOCs at the early vegetative stages in both species. However, robust uptake of highly halogenated compounds at the reproductive stages suggests a delayed accumulation of them by the plants. PBDE and PCB congener profiles suggest more noticeable tendency for inter-compartment translocation in peanut than in corn during the plant development. The DP and HBCD isomeric compositions in peanut (enriched with syn-DP and γ-HBCD) were different from those in the rhizosphere soils and air, suggesting a more stereoisomer-selective uptake and/or biotransformation in this species compared to corn. The bioaccumulation factors for root-soil and stem-root of these HOCs in most cases were <1. The tissue-distributions demonstrated that leaves serve as a significant reservoir of absorbed HOCs under the field conditions, whereas the low concentrations in peanut and corn kernels indicated translocation of most HOCs into this compartment was significantly hindered (especially for highly halogenated compounds).

Organophosphate esters (OPEs) in fine particulate matter (PM2.5) in urban, e-waste, and background regions of South China.

Organophosphate esters (OPEs) are a focus of research because they are ubiquitous in the environment; however, there is still a limited understanding of the behaviors and fate of OPEs in the environment. In this study, we measured OPEs in fine particulate matter (PM2.5) collected from three regions in South China that have potentially different sources. The concentrations of ∑OPEs in the rural electronic waste (e-waste) recycling area (3852-57,695 pg/m3 with a median of 10,955 pg/m3) were significantly higher than those in the urban and background areas with concentrations of 314-9721 pg/m3 (median = 2346 pg/m3) and 667 and 109,599 pg/m3 (median = 2170 pg/m3), respectively. The OPE compositions in the urban and e-waste areas were generally similar. Correlations analysis with other components of PM2.5 (organic carbon, elemental carbon, and water soluble ions) indicated primary industrial and e-waste sources of OPEs in the urban and e-waste regions, respectively. Correlation analysis also revealed that relative humility played an important role in their air concentrations in the urban and background regions. The air-parcel backward trajectories of the background site demonstrated regional atmospheric transport of OPEs to this region from both the eastern industrial cities and the northern e-waste recycling region.

Characterization and risk assessment of total suspended particles (TSP) and fine particles (PM2.5) in a rural transformational e-waste recycling region of Southern China.

In 2016, total suspended particles (TSP) and fine particles (PM2.5) were collected near four e-waste recycling parks in a region of Southern China. TSP and PM2.5 levels and composition around these industrial activities were determined and the potential risks for human health due to the exposure to toxic elements contained on fine particles (PM2.5) were evaluated. Levels of TSP and PM2.5 were lower with advanced recycling methods than with small recycling e-waste workshops operating in the sampling region. The main trace elements in particles were Cu, Pb, and Ti, the same as those detected before the transition to advanced dismantling methods in e-waste recycling. Significantly higher levels of Cu, Pb, Sn, Te, Tl and NH4+ in TSP and Cu and Te in PM2.5 were found in e-waste recycling areas than in BG site. Taking Cu as the indicative element emitted from e-waste recycling activities, significant high positive correlations between Cu and W, and Cu and Te were found. These elements are present and can be released from electrical and electronical components during e-waste recycling processes. Exposure to elements for the population living near these e-waste recycling parks means carcinogenic risks above the acceptable threshold (>10-5).

Legacy and Currently Used Organic Contaminants in Human Hair and Hand Wipes of Female E-Waste Dismantling Workers and Workplace Dust in South China.

Legacy organic contaminants, such as polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs), and several currently used organic contaminants, such as novel brominated retardants (NBFRs), organophosphate flame retardants (OPFRs), and Dechlorane Plus (DPs), were measured in the segmented hair and hand wipes of e-waste dismantling workers and in the dust from their workplace in an e-waste recycling site in South China to assess the accumulation and sources of organic contaminants in the hair shaft. The median concentrations of DPs, PBDEs, NBFRs, PCBs and OPFRs in hair samples were 23.5, 154, 156, 349, and 371 ng/g, respectively. A linear increase in organic contaminant concentrations was found along the hair shaft, with significant differences among each segment, while the age-related patterns were similar among the 7 hair segments. A linear relationship was found between the accumulation rates and the log KOW, indicating that the accumulation rates of organic contaminants along the hair shaft decreased with increasing log KOW values. Enantiomer fraction (EF) values of PCB-132 in distal segments were close to those in dust and air, while EFs in proximal segments were close to those in serum. The contributions of PCBs from external sources to hair increased with the distance from the scalp of hair segments, from 67.8% in 0-3 cm segments to 95.9% in 18-21 cm segments.

Legacy and emerging contaminants in coastal surface sediments around Hainan Island in South China.

Emerging and legacy hydrophobic pollutants, including halogenated flame retardants (HFRs), organophosphorus FRs (OPFRs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs), as well as polycyclic aromatic hydrocarbons (PAHs) were determined in coastal sediments of Hainan Island, southern China, where little information is known about their contamination. The HFRs were dominated by decabrominated diphenyl ethers (median = 1.32 ng/g) and novel decabromodiphenyl ethane (1.87 ng/g). HFR and PAH concentrations had similar spatial distributions, with higher levels in the river and near the estuary. The concentrations of ∑10OPFRs ranged from 0.74 to 60.0 ng/g (median = 15.3 ng/g), displaying a different spatial distribution. ∑DDTs and ß-HCH, with median concentrations of 1.41 and 3.44 ng/g respectively, were largely from historical inputs, but use of DDT still exists in Hainan. Principal component analysis revealed the associations between most of the pollutants (HFRs, OCPs, and PAHs) and perylene, indicating that terrestrial runoff plays a significant role in their presence in the coastal sediments. OPFRs had different emission sources or entry modes to the coastal ocean.

In vitro oral and inhalation bioaccessibility of hydrophobic organic contaminants (HOCs) in airborne particles and influence of relevant parameters.

The bioaccessibility of environmental contaminants has been assessed widely using in vitro simulation; however, the physiological parameters used vary greatly. In this study, we assessed the influence of various physiological parameters and food material on the oral or inhalation bioaccessibility of PM2.5-bound hydrophobic organic contaminants (HOCs), including halogenated flame retardants (HFRs), organophosphorus flame retardants (OPFRs), and polycyclic aromatic hydrocarbons (PAHs). The results showed that physiologically based pepsin and pancreatin have a small influence on the HOC liberation from particles. The bioaccessibility increased dramatically when the bile salt concentrations exceeding the critical micelle concentration, and application of porcine bile salts probably lead to underestimated bioaccessibility. Protein and carbohydrates significantly increased the bioaccessibility of most HOCs, while a significant bioaccessibility reduction was caused by green tea. The bioaccessibility of most HOCs was not promoted by liquor under normal physiological condition, but was significantly promoted under fast condition. Long residence time of PM2.5 in the lung (15 days) would result in higher mobilization of PAHs into the lung fluid than short time (one day). However, the inverse time-dependence for OPFRs suggests degradation in the lung fluid. A mechanism of hydrolysis of organophosphorus ester is hypothesized, and the half lives ranged from 17 to 90 days.

Organophosphorus esters (OPEs) in PM2.5 in urban and e-waste recycling regions in southern China: concentrations, sources, and emissions.

Organophosphate esters (OPEs) are novel ubiquitous contaminants that are attracting growing concern, but their emissions into the environment are still poorly understood. In this study, 12 OPEs were measured in fine particulate matter (PM2.5) at 20 industrial sites in an urban region and four e-waste recycling facilities in a rural region in southern China. There was no significant difference in the concentrations of ∑OPEs between the urban region (519-62,747 pg/m3, median = 2854 pg/m3) and the rural e-waste region (775-13,823 pg/m3, 3321 pg/m3). High OPE concentrations in urban PM2.5 were generally associated with the electrical, electronic, plastic, and chemical industries. There were no significant correlations between most OPEs in these two regions, suggesting different emission mechanisms. The average emissions of ∑OPEs estimated using a simplified dispersion model were 73.0 kg/yr from the urban industrial point sources and 33.2 kg/yr from the e-waste recycling facilities. The estimated emission inventory from industrial activities in the whole city (3228-4452 kg/yr) was approximately 30-fold higher than that from the e-waste recycling (133 kg/yr) facilities because urban region has a much larger industrial scale. To the best of our knowledge, this is the first effort to model the emissions of OPEs from industrial and e-waste recycling activities to the atmosphere.

Halogenated flame retardants (HFRs) and water-soluble ions (WSIs) in fine particulate matter (PM2.5) in three regions of South China.

Halogenated flame retardants (HFRs) and water-soluble ions (WSIs) were investigated in fine particulate matter (PM2.5) collected from an urban site, a rural e-waste recycling (e-waste) site, and a background site in South China. Generally, the WSI concentrations were highest at the e-waste site and comparable at the other sites and secondary species (SO42-, NH4+, and NO3-) were dominant components at the three sites. The compositions and seasonal variations of WSIs at the e-waste site were distinct from those in the urban and background areas suggesting significant influence of e-waste recycling on PM2.5 components. Polybrominated diphenyl ethers (PBDEs) dominated the HFRs in PM2.5 from the e-waste site, and their concentrations (median = 883 pg/m3) were significantly higher than those at the urban (375 pg/m3) and background site (52.4 pg/m3). However, novel decabromodiphenyl ethane (DBDPE) was the primary HFRs in the urban air, with noticeably elevated concentrations (median = 356 pg/m3) compared to those in the other two areas (medians = 62.3 and 5.09 pg/m3). The composition profiles of HFRs in the background air followed those in the e-waste areas, with substantial contributions of legacy chemicals. This was explained by the prevailing NE wind, which favored atmospheric transport of HFRs from the e-waste recycling area to the background area. Correlation analysis showed that most HFRs in the urban air are associated with Cl-, implying an industrial emission sources. In the e-waste area, HFRs are associated with organic and elemental carbons (OC and EC) and K+, confirming a common source of e-waste recycling. Significant correlations between HFRs and EC and Cl- in the background air suggest that their occurrence in this region was attributed to both the e-waste and urban areas.

Semivolatile Organic Compounds (SOCs) in Fine Particulate Matter (PM2.5) during Clear, Fog, and Haze Episodes in Winter in Beijing, China.

Few efforts have been made to elucidate the influence of weather conditions on the fate of semivolatile organic compounds (SOCs). Here, daily fine particulate matter (PM2.5) during clear, haze, and fog episodes collected in the winter in Beijing, China was analyzed for polycyclic aromatic hydrocarbons (PAHs), brominated flame retardants (BFRs), and organophosphate flame retardants (OPFRs). The total concentrations of PAHs, OPFRs, and BFRs had medians of 45.1 ng/m3 and 1347 and 46.7 pg/m3, respectively. The temporal pattern for PAH concentrations was largely dependent on coal combustion for residential heating. OPFR compositions that change during colder period were related to enhanced indoor emissions due to heating. The mean concentrations of SOCs during haze and fog days were 2-10 times higher than those during clear days. We found that BFRs with lower octanol and air partition coefficients tended to increase during haze and fog episodes, be removed from PM2.5 during clear episodes, or both. For PAHs and OPFRs, pollutants that are more recalcitrant to degradation were prone to accumulate during haze and fog days. The potential source contribution function (PSCF) model indicated that southern and eastern cities were major source regions of SOCs at this site.

Brominated flame retardant (BFRs) and Dechlorane Plus (DP) in paired human serum and segmented hair.

Brominated flame retardants (BFRs) and Dechlorane Plus (DP) were measured in both human hair and paired serum samples from a cohort of university students in South China. Segmental analysis was conducted to explore gender difference and the relationships between the hair and serum. The concentrations of total PBDEs in the hair and serum samples were in a range of 0.28-34.1ng/g dry weight (dw) and 0.16-156ng/g lipid weight (lw), respectively. Concentrations of ∑DPs (sum of the syn-DP and anti-DP isomers) in all hair samples ranged from nd-5.45ng/g dry weight. Concentrations of most PBDEs and decabromodiphenylethane (DBDPE) in distal segments (5-10cm from the scalp) were higher than those in the proximal segments (0-5cm from the scalp) (t-test, p < 0.05), which could be due to the longer exposure time of distal segments. The proximal segments exhibited a unique congener profile, more close to that in the serum rather than the distal segments of hair. An obvious gender difference was found in the levels of ∑PBDEs using integrated hair samples, while the difference disappeared when considering alone the proximal segments of hair (0-5cm from scalp) for both genders. This paper provides supplement to the current knowledge on sources of BFRs and DPs in hair and declares the importance of segmental analysis.