Wen-Long Li

Polybrominated diphenyl ethers (PBDEs) in the indoor dust in China: Levels, spatial distribution and human exposure

Indoor environment is an important source of human exposure to several toxicants, such as brominated flame retardants. Indoor dust samples were collected in winter season in 2010, which covered 23 provinces across China, for the analysis of polybrominated diphenyl ethers (PBDEs). Concentrations of PBDEs (Σ14PBDEs) ranged from 8.92 to 37,500 ng/g, with the mean of 3520 ng/g. BDE-209 was the most dominate congener, followed by BDE-183, BDE-47 and BDE-99. PBDE concentrations and the longitude were significantly correlated (p<0.05), which was consistent with the status of social-economic development and human activities. The results of exposure to PBDEs through dust ingestion and dermal absorption indicated that the toddlers had the highest exposure dose, with the median value of 6.0 ng/kg-bw/day. According to the hazard quotients, health risk of PBDEs via dust ingestion in China is currently acceptable. Monte Carlo simulation was implemented to quantify the uncertainty and sensitivity of exposure models for determining the most influential variables. The results suggested that more specific and accurate parameters should be used for dust ingestion and dermal absorption exposure models in future.

Concentrations and sources of polycyclic aromatic hydrocarbons in indoor dust in China.

Indoor dust samples were collected across China in the winter of 2010 from 45 private domiciles and 36 public buildings. 16 polycyclic aromatic hydrocarbons (PAHs) were determined by GC-MS. Total concentrations of PAHs ranged from 1.00 μg/g to 470 μg/g with a mean value of 30.9 μg/g. High-molecular weight (HMW) PAHs (4 to 6 rings) are the predominant PAHs found in indoor dust, accounting for 68% of the total PAH concentration in private domiciles, and 84.6% in public buildings. Traffic conditions and cooking methods were the two key factors controlling PAH levels, especially for coal combustion and vehicular traffic emission sources. A significant positive correlation was observed between PAH concentrations in indoor dust and based on location (latitude and longitude). The latitudinal distribution indicated a higher usage of coal for heating in Northern China than in Southern China. The longitudinal distribution indicated that the usage of oil and mineral fuels as well as economic development and population density increased from West China to East China. In addition, diagnostic ratios and principal component analysis (PCA) were used to explore source apportion, as indicated in both the pyrogenic and petrogenic sources of PAHs in indoor dust in China. Furthermore, the BaP equivalent was applied to assess the carcinogenic risk of PAHs, which also indicated that traffic emissions and coal combustion were the two major contributions to carcinogenic risk of PAHs in indoor dust in China.

Brominated flame retardants in the urban atmosphere of Northeast China: Concentrations, temperature dependence and gas–particle partitioning

57 pairs of air samples (gas and particle phases) were collected using a high volume air sampler in a typical city of Northeast China. Brominated flame retardants (BFRs) including 13 polybrominated diphenyl ethers (PBDEs, including BDEs 17, 28, 47, 49, 66, 85, 99, 100, 138, 153, 154, 183, and 209) and 9 alternative BFRs (p-TBX, PBBZ, PBT, PBEB, DPTE, HBBZ, γ-HBCD, BTBPE, and DBDPE) were analyzed. The annual average total concentrations of the 13 PBDEs and the 9 alternative BFRs were 69 pg/m(3) and 180 pg/m(3), respectively. BDE 209 and γ-HBCD were the dominant congeners, according to the one-year study. The partial pressure of BFRs in the gas phase was significantly correlated with the ambient temperature, except for BDE 85, γ-HBCD and DBDPE, indicating the important influence of ambient temperature on the behavior of BFRs in the atmosphere. It was found that the gas-particle partitioning coefficients (logKp) for most low molecular weight BFRs were highly temperature dependent as well. Gas-particle partitioning coefficients (logKp) also correlated with the sub-cooled liquid vapor pressure (logPL(o)). Our results indicated that absorption into organic matter is the main control mechanism for the gas-particle partitioning of atmospheric PBDEs.

Five-year trends of selected halogenated flame retardants in the atmosphere of Northeast China.

This study collected 227 pairs of gas phase and particle phase air samples in a typical urban city of Northeast China from 2008 to 2013. Four alternative halogenated flame retardants for polybrominated diphenyl ethers (PBDEs) were analyzed, namely 2-ethylhexyl 2,3,4,5-tetrabromobenzoate (EHTBB), bis (2-ethylhexyl) tetrabromophthalate (BEHTBP), syn-dechlorane plus (syn-DP) and anti-dechlorane plus (anti-DP). The average concentrations for EHTBB and BEHTBP were 5.2 ± 20 and 30 ± 200 pg/m3, respectively, while for syn-DP and anti-DPwere 1.9±5.1 and 5.8±18 pg/m3, respectively. Generally, they were frequently detected in the particle phase, and the gas/particle partitioning suggested they were the maximum partition chemicals. The fractional abundance of EHTBB (fEHTBB) and syn-DP (fsyn)were comparablewith those in other studies. Strong local sources were identified based on the air parcel backward trajectories and the potential source contribution function. The concentrations of these chemicals were significantly increased during this sampling campaign, possibly suggesting their increasing usages from 2008 to 2013 in China.

Spatial–temporal variation, possible source and ecological risk of PCBs in sediments from Songhua River, China: Effects of PCB elimination policy and reverse management framework

The spatial variation, possible sources and ecological risk of polychlorinated biphenyls (PCBs) in the sediment from the Songhua River, China were investigated and evaluated in this paper. The total concentration of PCBs ranged from 0.59 to 12.38ng/gdw, with a mean value of 3.82ng/gdw. The seven indicators of PCB concentrations are significantly correlated with the total PCB concentrations (R=0.950, p=0.000). The temporal trend of PCBs in sediments showed that the total PCBs in the Songhua River have decreased since 2008. Point source pollution, discharge of historical usage and industrial sewage, and emissions of unintentionally produced PCBs were the predominant sources in sediment. A risk assessment indicated that most of the sampling sites in the sediment were at low potential ecological risk. The apparent decrease of PCBs in the sediment appeared after the China National Coordination Group for Implementation of the Stockholm Convention was established. A conceptual reverse management framework for PCBs and other organic pollutants was established in this study.

Multi-year air monitoring of legacy and current-use brominated flame retardants in an urban center in northeastern China

The occurrence and temporal trends of polybrominated diphenyl ethers (PBDEs) and non-PBDE brominated flame retardants (NBFRs) were investigated in an urban atmosphere of Northeast China in consecutive six years (2008-2013). Among all chemicals, BDE-209, l,2,5,6,9,10-hexabromocyclododecane (HBCD), and decabromodiphenylethane (DBDPE) were the three most dominant compounds. During the period, the levels of pentabromodiphenyl ethers in the gas-phase and octabromodiphenyl ethers in the particle-phase significantly decreased, while the levels of BDE-209 and NBFRs increased in either the gas-phase or particle-phase. Ambient temperature was the most significant variable that influenced the gas-phase and particle-phase concentrations of BFRs, followed by wind speed and relative humidity. A stronger temperature dependence of the atmospheric concentrations was found for lower mass BFRs. Gas-particle partitioning studies suggested PBDEs in the urban atmosphere of Northeast China were at steady-state. Steady-state equation can also well describe the partitioning behavior for NBFRs, suggesting that the atmospheric partitioning behaviors of NBFRs were similar to those of PBDEs.

Trends in indoor–outdoor PM2.5 research: A systematic review of studies conducted during the last decade (2003–2013)

There has been growing concern about potential health risks from exposure to PM2.5 (fine particulate matter). The importance of conducting simultaneous indoor and outdoor measurements emerged because people, especially in developed countries, spend more than 90% of their time indoors. Great spatial and temporal variations in human exposure to PM2.5 have recently been reported. This review aims to identify the main research areas that have attracted recent attention, any possible gaps in the measurements of PM2.5 in various microenvironments, and the relationships between indoor and outdoor concentrations. This study also provides recommendations for further studies on PM2.5 measurement methods and exposure levels. To achieve these goals, this review included articles published online from 2003 to 2013 in the Science Direct and Web of Science databases. In the initial screening stage, 113 abstracts selected while 61 articles were remained for full review. The reviewed studies consistently showed positive correlations between indoor and outdoor PM2.5. Sulfate/sulfur concentrations were used intensively for calculating the infiltration factor (FINF). The higher FINF indicated high infiltration of outdoor PM2.5 into indoor areas. Great percentage (42%) of the reviewed filter–based studies was conducted in Europe, followed by a similar amount (38%) in the USA, and 20% in Asia, indicating a lack in PM2.5 research in other parts of the world. It was difficult to conclude that ambient fixed–site monitoring provided accurate estimations of actual exposure to PM2.5– Studies shown trends of higher personal concentrations compared to indoor and outdoor ones. Higher indoor levels of OC (organic carbon), compared to outdoor levels, were consistently reported. The opposite trend was true for EC (elemental carbon), and there were higher indoor OC/EC ratios than outdoor OC/EC ratios. There was a consistent general trend of a high (r>0.70) correlation between indoor and outdoor EC, while the correlation between indoor and outdoor OC was much weaker (r=022–0.75). The higher indoor OC/EC ratios, compared to the outdoor OC/EC ratios, reflects multiple sources of indoor OC. Sulfate (SO42–), nitrate (NO3–), and ammonium (NH4+) were primary contributors to PM2.5 mass.

Occurrence and source apportionment of atmospheric halogenated flame retardants in Lhasa City in the Tibetan Plateau, China

Active air samples were collected in Lhasa, one of the highest cities in the world (3650m above sea level) located in the Tibetan Plateau, and were analyzed for 38 halogenated flame retardants (HFRs), including polybrominated diphenyl ethers (PBDEs), non-PBDE brominated flame retardants (NBFRs) and dechlorane plus (DPs). The median concentrations of PBDEs, NBFRs and DPs were 40, 23 and 0.21pg/m3, respectively. Correlation analysis indicated the common source and/or similar environmental behavior for several HFRs. The Clausius-Clapeyron equation was applied to diagnose the sources of lower molecular weight HFRs (LMW-HFRs), which suggested that the gaseous LMW-HFRs at Lhasa were more controlled by regional or long-range atmospheric transport rather than the temperature-driven evaporation from local contaminated surfaces. Finally, the potential source contribution function model was applied to assess the influences of air parcels on the atmospheric concentrations of HFRs in Lhasa, which suggested that the sources of higher molecular weight HFRs (HMW-HFRs) were mostly originated from local emissions, while the others were originated from long-range atmospheric transport.

An evaluation on the intra-day dynamics, seasonal variations and removal of selected pharmaceuticals and personal care products from urban wastewater treatment plants

Pharmaceuticals and personal care products (PPCPs) in wastewater have become an emerging issue due to their negative effects on human health and aquatic ecosystems. Two full-scale municipal and industrial wastewater treatment plants (WWTPs) along the Songhua River were chosen to evaluate the intra-day dynamics, seasonal variations and removal of 12 selected PPCPs. Our results suggested that the selected PPCPs were frequently detected in the influent and effluent. Caffeine was the predominant compound in the influent; while the selected PPCPs was dominated by TCS in the effluent, suggesting the different fates of selected PPCPs in the WWTPs. The intra-day dynamics of PPCPs in the influent were evaluated, suggesting that the 12 PPCPs can be grouped into three categories because of their different use patterns. The analysis of seasonal changes of PPCPs concentrations in the WWTPs suggested that the concentrations of some PPCPs were influenced by the chemical usage, degradation and temperature. The removal efficiency for the PPCPs were very high with the values ranged from 70.0% to 99.7% for WWTP#1, and from 62.5% to 99.4% for WWTP#2. Significant seasonal variations of PPCPs removal efficiency were observed. Base on the mass loading of PPCPs in the two WWTPs, our results suggested that WWTP#1 in the urban core received much more PPCPs in comparison to WWTP#2 in the suburban regions, suggesting that influences of the service population.

Removal characteristic of surfactants in typical industrial and domestic wastewater treatment plants in Northeast China

Surfactants are widely used in household and industrial products for cleaning and/or solubilization in our daily life. Therefore, they are finally discharged into wastewater treatment plants (WWTPs), which may be the major point pollution source for environment if they were not completely removed during wastewater treatment. In this study, two typical industrial and domestic WWTPs with different wastewater treatment technologies were considered for the topic. Totally, two types of surfactants were analyzed in 24 h influent and each processing unit effluent. Four linear alkylbenzene sulfonates (LASs) with the alkyl chain from C10 to C13, and two benzalkonium chlorides (BACs) with the alkyl chain of C12 and C14 were selected as target compounds. The total concentrations of LASs in influent varied from 19.2 to 1889 μg/L and LAS-C11 and LAS-C12 were the predominant compounds with the concentration from 6.01 to 641 μg/L and 8.02-674 μg/L, respectively. The total concentrations of BACs were much lower than those of LASs, with the concentration ranging from 0.00935 to 1.85 μg/L. Significant positive correlations were observed between concentrations of LASs and BACs in influent, indicating their same and/or similar sources. Compared with the concentration of influent, the concentration of effluent was much lower, indicating the high removal efficiency by the two wastewater treatment processes. Biological treatment unit and cyclic activated sludge system were the main treatment units for the removing of surfactants, which suggested that these two types of surfactants can be easily degraded under aerobic condition. Seasonal variation indicated that the removal efficiencies of surfactants in autumn were a little higher than those in winter. The results of this study provided new insights into the environmental fate of surfactants in wastewater treatment system.