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Gas/particle (G/P) partitioning is an important influencing factor for the environmental fate of semi-volatile organic compounds (SVOCs). The G/P partitioning of polycyclic aromatic hydrocarbons (PAHs) is an integrated complex process due to its formation and growth concurrently with particles. Based on the large dataset of gaseous and particulate samples in a wide ambient temperature range of 50 °C, the simple empirical equations based on ambient temperature were established to predict the G/P partitioning quotient (KP) of PAHs at the temperature range from 252 K to 307 K (−21 °C to 34 °C). The performance of the empirical equations was validated by comparison with the monitoring KP of PAHs worldwide. The empirical equations exhibited good performance for the prediction of KP of PAHs based on ambient temperature. Two deviations with the prediction lines of the previous G/P partitioning models from the monitoring data of KP were observed. It was found that the deviations might be attributed to some non-considered influencing factors with the previous G/P partitioning prediction models. Therefore, further research should be conducted to study the mechanism of the G/P partitioning of PAHs, and more influencing factors should be introduced into the establishment of G/P partitioning models of PAHs. In summary, the result of the present study provided a convenient method for the prediction of KP of PAHs, which should be useful for the study of environmental fate of PAHs in atmosphere.

Concurrent indoor–outdoor fine particulate matter (PM2.5) measurements were conducted at urban, suburban, and rural sites in Harbin, a megacity in the northeast of China. Chemical constituents of indoor–outdoor PM2.5 were determined. Infiltration factors (FINF) of all sites were calculated according to the indoor to outdoor (I/O) ratios of PM2.5 based on the regression analysis. Linear discriminant analysis (LDA) is applied to determine the indoor–outdoor relationship. Secondary organic carbon (SOC) was calculated on the basis of organic carbon to elemental carbon (OC/EC) ratios. The mean concentrations of indoor and outdoor PM2.5 were 166.4 ± 32.5 μg/m3 and 228.4 ± 83.7 μg/m3, respectively, during the heating period. OC/EC and potassium ion to elemental carbon (K+/EC) ratios verified that biomass was an important source in Harbin especially for rural sites. The nitrate to sulfate (NO3−/SO42−) ratio indicates the higher contribution of traffic emissions in urban sites. Cr was the only species that exceeded the guidelines of WHO 2002, which was mainly emitted from coal and oil combustion. SOC/OC and NO3−/SO42− ratios, and ion-balanced acidity (the ratio of cation to anion, R+/−) showed a large urban–rural and indoor–outdoor difference. The highest SOC/OC ratio was found at urban sites, up to 38.3% for indoors. SOC/OC ratios and R+/− values of indoor environments were higher, which is attributed to the conducive condition of forming the secondary pollutants during the heating period. The results of LDA indicated that the distributions of the chemical components of PM2.5 at three sites were statistically dissimilar.

The gas/particle (G/P) partition of organochlorine pesticides (OCPs) has been widely investigated and well documented, but rare at low temperature. In this study, seventy-four pairs of air samples in two sampling sites in northeastern China at a wide ambient temperature range of ~63 °C (−40 to +23 °C) were simultaneously collected in both gaseous and particulate phases and eighteen OCPs in these samples were measured and analyzed, among which, partition quotient (KP) values for fifteen OCPs were determined. Seven models including those have never been used for OCPs were applied to predict the values of KP, and the results were compared with the monitoring data for the fifteen OCPs. It was found out that, L-M-Y model provided advantages over the other models, with the best agreement to the monitoring data for analyzed OCPs (90.1 ± 11.1% data points within ±1 log unit, RMSE: 0.53 ± 0.18). The predicted maximum partition (MP) domain for eleven OCPs was observed with high values of their logarithm of octanol-air partition coefficient (log KOA > 12.5), where the log KP values become a constant (−1.53), indicating that the G/P partition of OCPs is in steady state but not the equilibrium. The Li-Ma-Yang (L-M-Y model) model, considering the wet and dry depositions of particles, elucidates the necessity of non-equilibrium term for the OCPs at low temperature. These results indicate that the L-M-Y model is valid for OCPs, which renders it highly promising for describing the partition behaviors in atmosphere for SVOCs, particularly at low temperature. An equation to calculate the condensation temperature TC was also derived, which gave a new understanding on the situation of chemicals with equal distribution between gaseous and particulate phases of OCPs and other similar SVOCs, especially in Polar Regions.

Organophosphate flame retardants (OPFRs) are widely added to consumer products and building materials, which may pose potential health risk to humans. But information on their contamination and human exposure in the indoor environment especially dormitories in northern China is rare. In this study, twelve OPFRs were investigated in college dormitory dust that collected from Harbin, Shenyang, and Baoding, in northern China. Indoor dust samples were also collected from homes and public microenvironments (PMEs) in Harbin for comparison. The median ∑OPFR concentrations in dormitory dust in Shenyang samples (8690 ng/g) were higher than those in Baoding (6540 ng/g) and Harbin (6190 ng/g). The median ∑OPFR concentrations in home dust (7150 ng/g) were higher than in dormitory and PME dust (5340 ng/g) in Harbin. Tris(2‑chloroethyl) phosphate (TCEP) and tris (2-chloroisopropyl) phosphate (TCIPP) were the most abundant chlorinated OPFRs, while triphenyl phosphate (TPHP) and tris(2‑butoxyethyl) phosphate (TBOEP) were the dominant non-chlorinated OPFRs. The daily intakes of ∑OPFR were estimated, with the median values for female students (2.45 ng/kg-day) higher than those for male students (2.15 ng/kg-day) while were similar to adults (2.45 ng/kg-day) in homes. The estimated daily intakes (EDI) of these OPFRs from indoor dust in Harbin were all below the recommended values. The calculated non-carcinogenic hazard quotients (10−8–10−3) from OPFRs were much lower than the theoretical risk threshold. Meanwhile, carcinogenic risk (CR) of tri‑n‑butyl phosphate (TNBP), TCEP, tris(2‑ethylhexyl) phosphate (TEHP), and tris(1,3‑dichloroisopropyl) phosphate (TDCIPP) were also estimated. The highest carcinogenic risk of TCEP for gender-specific and age-specific category range from 1.75 × 10−7 to 2.46 × 10−7 from exposure to indoor dust indicated a low potential carcinogenic risk for human exposure.

This paper assesses the occurrence, distribution, source, and toxicity of polycyclic aromatic hydrocarbons (PAHs), and their methylated form (Me-PAHs) in sewage sludge from 10 WWTPs in Northeastern China was noted. The concentrations of ∑PAHs, ∑Me-PAHs ranged from 567 to 5040 and 48.1 to 479 ng.g−1dw, which is greater than the safety limit for sludge in agriculture in China. High and low molecular weight 4 and 2-ring PAHs and Me-PAHs in sludge were prevalent. The flux of sludge PAHs and Me-PAHs released from ten WWTPs, in Heilongjiang province, was calculated to be over 100 kg/year. Principal component analysis (PCA), diagnostic ratios and positive matrix factorization (PMF) determined a similar mixed pyrogenic and petrogenic source of sewage sludge. The average values of Benzo[a]pyrene was below the safe value of 600 ng.g−1 dependent on an incremental lifetime cancer risk ILCR of 10−6. Sludge is an important source for the transfer of pollutants into the environment, such as PAHs and Me-PAHs. Consequently, greater consideration should be given to its widespread occurrence.

In this paper, two level III fugacity models are developed and applied using an environmental system containing six compartments, including air, aerosols, soil, water, suspended particulate matters (SPMs), and sediments, as a “unit world”. The first model, assumes equilibrium between air and aerosols and between water and SPMs. These assumptions lead to a four-fugacity model. The second model removes these two assumptions leading to a six-fugacity model. The two models, compared using four PBDE congeners, BDE-28, -99, −153, and −209, with a steady flux of gaseous congeners entering the air, lead to the following conclusions. 1. When the octanol-air partition coefficient (KOA) is less than 1011.4, the two models produce similar results; when KOA > 1011.4, and especially when KOA > 1012.5, the model results diverge significantly. 2. Chemicals are in an imposed equilibrium in the four-fugacity model, but in a steady state and not necessary an equilibrium in the six-fugacity model, between air and aerosols. 3. The results from the six-fugacity model indicate an internally consistent system with chemicals in steady state in all six compartments, whereas the four-fugacity model presents an internally inconsistent system where chemicals are in equilibrium but not a steady state between air and aerosols. 4. Chemicals are mass balanced in air and aerosols predicted by the six-fugacity model but not by the four-fugacity model. If the mass balance in air and aerosols is achieved in the four-fugacity model, the condition of equilibrium between air and aerosols will be no longer valid.

Gas/particle (G/P) partition quotients of semi-volatile organic compounds (SVOCs) for bulk air have been widely discussed in experimental and theoretical contexts, but research on size-resolved G/P partition quotients (KPi) are scarce and limited in scope. To investigate G/P partition behavior of polybrominated diphenyl ethers (PBDEs) for size-segregated particles in the atmosphere, 396 individual size-segregated particulate samples (36 batches × 11 size-ranges), and 108 pairs of concurrent gaseous and bulk particulate samples were collected in Harbin, China. A steady-state equation based on bulk particles is derived to determine G/P partition quotients of PBDEs for size-segregated particles, which depends on the organic matter contents of size-segregated particles (fOMi). This equation can well predict KPi with knowledge of bulk partition quotient (KPS), ambient temperature, and fOMi, the results of which match well with monitoring data in Harbin and other published data collected in Shanghai and Guangzhou of China and Thessaloniki of Greece, and remedies a defect of over-estimate KPi for high-brominated PBDEs by the previous equation. In particular, the new equation contributes to obtaining the PBDEs concentrations in all atmospheric phase from partial phase, then provides a credible path to evaluate healthy exposure dose from the airborne PBDEs, by co-utilization with exposure models.

The study on atmospheric polycyclic aromatic hydrocarbons (PAHs) in China has regional and global significance to understand the large scale atmospheric transport of PAHs. In this study, 16 US EPA priority PAHs were analyzed in more than 500 pairs of gas and particle phases samples, which were collected on the same schedule on a weekly basis from August 2008 to July 2009 at 11 urban sites (6 northern cities and 5 southern cities) across China. The average concentration was 239 ± 329 ng/m3 and 165 ± 164 ng/m3 for the northern cities and the southern cities, respectively. Different seasonal variations of atmospheric PAHs were observed between northern cities and southern cities, which were mainly caused by the different temperature effects in winter. Identified by principal component analysis, coal combustion and vehicle exhaust were the major sources of atmospheric PAHs in northern and southern cities of China, respectively. The temperature dependences of atmospheric PAHs were also different, which were caused by the different influences of temperature on identified sources. To our knowledge, this is the first comprehensive study to report the difference with concentrations, seasonal variations, sources and temperature dependences of atmospheric PAHs between northern cities and southern cities in China.

Gas-particle (G/P) partition is the determining factor to the behaviors of semi-volatile organic compounds (SVOCs) in atmosphere, such as transport and deposition. Based on a case study on the measurement of atmospheric polycyclic aromatic hydrocarbons (PAHs) in Harbin City in China from June 2014 to May 2019, the long-term temporal trend of G/P partition of PAHs and its influencing factors were comprehensively studied. The results indicated that an obvious decreasing temporal trend was observed for total suspended particle (TSP) with the annual mean concentrations of 180, 173, 134, 132, and 119 μg/m3 for the five years. The results demonstrated the effectiveness of the Clean Air Action on decreasing TSP levels in Harbin City. For most PAHs, obvious long-term temporal trends and seasonal variations were observed for the particulate phase fraction (φP) and the G/P partitioning quotient (KP) by fitting with a simple harmonic regression method. Significant correlations between φP with temperature and TSP indicated their influences on the temporal trend of φP. Similarly, the temperature was also the direct influencing factor to the temporal trend of KP. For the five years, non-obvious differences were observed with the linear relationships between log KP vs. log KOA, and between log KP vs. log PL. The comparison between the monitoring data of φP and log KP with the prediction data from the G/P partitioning models indicated that the predictions of the models did not well match all the monitoring data for the period. Therefore, more studies should be conducted to better understand the G/P partitioning mechanism of PAHs in atmosphere and to establish more accurate G/P partitioning models. In summary, the results of the present study provided new insight into the G/P partitioning behavior of PAHs in the atmosphere, especially for the temporal trend of φP and log KP.

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.

Benzotriazoles (BTs) UV filters are widely used as ultraviolet absorbents for our daily products, which received increasing attention in the past decades. Residential wastewater treatment plant (WWTP) is both an important sink for wastewater and a key pollution source for receiving water for these chemicals. In this study, pretreatment and gas chromatography-tandem mass spectrometry analysis method were developed to determine the occurrence and fate of 9 BTs UV filters in wastewater and sludge from the WWTP with anaerobic-oxic treatment process (A/O) and biological aerated filter treatment process (BAF). Totally, 81 wastewater samples and 11 sludge samples were collected in four seasons. In wastewater, UV-326 and UV-329 were frequently detected, while the highest mean concentrations were detected for UV-234 and UV-329. The concentrations were in the range ofLOQs up to several hundred nanograms per liter. The removal efficiency of BTs UV filters was85% in A/O process and 60-77% in BAF process except for UV-350, which was more difficult to remove with lower removal efficiencies of 33.3% for both A/O and BAF. All the target chemicals except for UV-320 were detected in sludge samples with the mean concentration ranging from 0.90 ng/g to 303.39 ng/g. There was no significant difference with concentrations and removal efficiency among different seasons. Higher detection frequency and concentration of BTs UV filters in downstream of the receiving water system indicated the contribution of effluent of the WWTP. Compared with other rivers, the lower concentrations in surface water in the Songhua River indicated light pollution status with of BTs UV filters.

Short-chain chlorinated paraffins (SCCPs) are widely used chemicals in household products and might cause adverse human health effects. However, limited information is available on the occurrence of SCCPs in indoor environments and their exposure risks on humans. In this study the concentrations, profiles and human exposure of SCCPs in indoor dust from five different indoor environments, including commercial stores, residential apartments, dormitories, offices and laboratories were characterized. The SCCPs levels ranged from 10.1 to 173.0 μg/g, with the median and mean concentration of 47.2 and 53.6 μg/g, respectively. No significant difference was found on concentrations among the five microenvironments. The most abundant compounds in indoor dust samples were homologues of C 13 group, Cl 7 group and N 20 (N is the total number of C and Cl) group. In the five microenvironments, commercial stores were more frequently exposed to shorter carbon chained and higher chlorinated homologues. Three potential sources for SCCPs were identified by the multiple linear regression of factor score model and correspondence analysis. The major sources of SCCPs in indoor dust were technical mixtures of CP–42 (42% chlorine, w/w) and CP–52 b (52% chlorine, w/w). The total daily exposure doses and hazard quotients (HQ) were calculated by the human exposure models, and they were all below the reference doses and threshold values, respectively. Monte Carlo simulation was applied to predict the human exposure risk of SCCPs. Infants and toddlers were at risk of SCCPs based on predicted HQ values, which were exceeded the threshold for neoplastic effects in the worst case. Our results on the occurrences, sources and human exposures of SCCPs will be useful to provide a better understanding of SCCPs behaviors in indoor environment in China, and to support environmental risk evaluation and regulation of SCCPs in the world.

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in atmosphere, which attracted more attentions due to their influence on human health. In this study, a national scale cancer risk (CR) assessment with atmospheric PAHs were conducted based on one year monitoring program at 11 cities across China. The annual mean concentrations of benzo[a]pyrene (BaP) and BaP equivalency (BaPeq) were 4.56 ± 7.78 ng/m3 and 8.45 ± 14.1 ng/m3, respectively, which were both higher than the new ambient air quality standards of China (GB 3095–2012, 1 ng/m3). Concentrations of BaP and BaPeq in northern Chinese cities were almost 2 times higher than those in southern Chinese cities. The CR values induced by the dermal contact exposure were two orders of magnitude higher than that by the inhalation exposure. Children and adults were the most sensitive age groups with the dermal contact exposure and the inhalation exposure to atmospheric PAHs, respectively. For the total CR values, 99.7% of its values were higher than the reference level of 10−6. No significant difference of the total CR values was observed between northern Chinese and southern Chinese cities for children and adults. In order to quantify the uncertainties of CR assessment, Monte Carlo Simulation was applied based on the specific distributions of the exposure factors cited from the Exposure Factors Handbook of Chinese Population. The results indicated that almost 90% probability of the total CR values were higher than 10−6, indicating potential cancer risk. Sensitive analysis indicated that atmospheric concentration, outdoor exposure fraction, particle amount adhered to skin, and cancer slope factor should be carefully considered in order to increase the accuracy of CR assessment with PAHs in atmosphere.

Ten polybrominated diphenyl ethers (PBDEs) and 16 novel brominated flame retardants (NBFRs) were measured in air and dust samples collected in a test home in Harbin, China, from January 2017 to June 2018. The PBDE and NBFR concentrations in indoor air were in the ranges of 0.598–14.5 pg m−3 and 9.28–686 pg m−3, respectively. The ranges of the PBDE and NBFR concentrations in indoor dust were 221–1060 ng g−1 and 71.9–1160 ng g−1, respectively. Brominated flame retardant (BFR) concentrations in indoor air were affected by the temperature, relative humidity (RH), and ventilation. The BFR concentrations in indoor dust did not show temperature dependence. All dust samples were sieved into 6 size fractions (F1–F6: 1000–2000 μm, 500–1000 μm, 250–500 μm, 125–250 μm, 63–125 μm, and

Human exposure to formaldehyde, toluene, xylene (FTX) and other volatile organic compounds (VOCs) are associated with negative health impact. To characterize the exposure and health effects of FTX and TVOC from indoor environments, we conducted an extensive monitoring campaign involving 1278 measurements of 472 indoor locations in Harbin, a megacity in China from May 2013 to March 2018. The results showed that household had the highest mean formaldehyde concentration (0.171 ± 0.084 mg m-3) among all types of indoor environments. Meanwhile, there was no significant differences in formaldehyde concentration of the living room, master bedroom, secondary bedroom and study room (p > 0.05), as well as toluene and xylene. The highest mean concentration of toluene, xylene and TVOC was measured in public bath center. Great difference was found between formaldehyde concentrations in 2013 and other years, except 2015. There were great positive nonlinear correlations between the indoor temperature and concentration of formaldehyde (p

The Songhua River is one of the most populated and oldest industrial areas in Northeast China. To understand the sources and distribution of polycyclic aromatic hydrocarbons and their derivatives, such as 16 priority (PAHs), 33 methylated (Me-PAHs), and 12 nitrated (NPAHs) in river water and sediment, were noticed. The concentrations of ∑PAHs, ∑Me-PAHs, and ∑NPAHs in river water scaled from 135 to 563, 9.36 to 711, and 1.26 to 64.7 ng L−1, with mean values of 286, 310, and 17.9 ng L−1, and those in sediments were from 35.8 to 2000 ng g−1, 0.62 to 394 ng g−1, and 0.28 to 176 ng g−1 (dry weight) with mean values of 283, 103, and 21.7 ng g−1. The compositions proved that two-ring and three-ring compounds of PAHs, NPAHs, and four-ring, six-ring of Me-PAHs were prevalent in water samples, in contrast, four-ring dominated in sediments. Principal components analysis (PCA) and diagnostic ratios confirmed that pollutant source was mixed petrogenic and pyrogenic origin. The fugacity fraction (ƒƒ) was also calculated to explain the trend of sediment–water exchange, high ƒƒ values found in summer, for most HMW PAHs and Me-PAHs that these substances acted as a secondary source of emissions from sediment to water. The risk assessment for water was categorized as high.

Phthalates are widely used chemicals in household products, which severely affect human health. However, there were limited studies emphasized on young adults' exposure to phthalates in dormitories. In this study, seven phthalates were extracted from indoor dust that collected in university dormitories in Harbin, Shenyang, and Baoding, in the north of China. Dust samples were also collected in houses in Harbin for comparison. The total concentrations of phthalates in dormitory dust in Harbin and Shenyang samples were significantly higher than those in Baoding samples. The total geometric mean concentration of phthalates in dormitory dust in Harbin was lower than in house dust. Di-(2-ethylhexyl) phthalate (DEHP) was the most abundant phthalate in both dormitory and house dust. The daily intakes of the total phthalates, carcinogenic risk (CR) of DEHP, hazard index (HI) of di-isobutyl phthalate (DiBP), dibutyl phthalate (DBP), and DEHP were estimated, the median values for all students in dormitories were lower than adults who live in the houses. Monte Carlo simulation was applied to predict the human exposure risk of phthalates. HI of DiBP, DBP, and DEHP was predicted according to the reference doses (RfD) provided by the United States Environmental Protection Agency (U.S.EPA) and the reference doses for anti-androgenicity (RfD AA) developed by Kortenkamp and Faust. The results indicated that the risks of some students had exceeded the limitation, however, the measured results were not exceeded the limitation. Risk quotients (RQ) of DEHP were predicted based on China specific No Significant Risk Level (NSRL) and Maximum Allowable Dose Level (MADL). The predicted results of CR and RQ of DEHP suggested that DEHP could pose a health risk through intake of indoor dust.

Simultaneous measurements of fine (PM 2.5 ) and coarse (PM 10 ) particles have been performed during three sampling period: summertime, early winter before the heating period, and during the winter heating. The sampling was done at an urban site, Harbin City, China, to apportion pollution sources and to investigate the impacts of weather parameters and emission sources on distribution patterns of PM 2.5 and PM 10 and their chemical compositions. Two chemometric techniques, hierarchical clustering analysis (HCA) and discriminant analysis (DA), and a receptor model (PMF5) were applied. The average mass concentrations of fine and coarse particles during the whole study period (i.e. annual averages), were 82.4 μg/m 3 and 120.1 μg/m 3 , with relative humidity and wind speed being the main factors influencing distribution patterns of PM 2.5 and PM 10, while sum of major ions ( NO 3 − , NH 4 + , SO 4 2 − ), and organic carbon (OC) were the greater contributor to total mass concentrations. According to DA, the distribution patterns of PM 2.5 and PM 10 during the winter heating period were distinct but overlapping in summer and early winter before heating, implying that, PM 2.5 and PM 10 were originated from different sources during the winter heating period but from similar sources during the other two sampling periods. This claim was further supported by PMF results. Canonical discriminant function coefficients of DA have shown species such as OC, EC, SO 4 2 − , NO 3 − , Cl − , Ti, Sr, Ca 2+ , Ni, and Ba to be good predictors/discriminants responsible for the differences between the three sampling periods. HCA visualized the interrelations among the source markers, while the PMF5 modeling confirmed HCA findings.

In this study we investigated the distribution patterns, infiltration and health risk assessment of PM2.5-bound PAHs in indoor and outdoor air done in Harbin city, northeastern China. Simultaneous indoor and outdoor sampling was done to collect 264 PM2.5 samples from four sites during winter, summer, and spring. Infiltration of PAHs into indoors was estimated using Retene, Benzo [ghi]perylene and Chrysene as reference compounds, where the latter compound was suggested to be a good estimator and subsequently used for further calculation of infiltration factors (IFs). Modeling with positive matrix factorization (PMF5) and estimation of diagnostic isomeric ratios were applied for identifying sources, where coal combustion, crop residues burning and traffic being the major contributors, particularly during winter. Linear discriminant analysis (LDA) has been utilized to show the distribution patterns of individual PAH congeners. LDA showed that, the greatest seasonal variability was attributed to high molecular weight compounds (HMW PAHs). Potential health risk of PAHs exposure was assessed through relative potency factor approach (RPF). The levels of the sum of 16 US EPA priority PAHs during colder months were very high, with average values of 377 ± 228 ng m(-)(3) and 102 ± 75.8 ng m(-)(3), for the outdoors and indoors, respectively. The outdoor levels reported to be 19 times higher than the outdoor concentrations during warmer months (summer + spring), while the indoor concentrations were suggested to be 9 times and 10 times higher than that for indoor summer (average 11.73 ± 4 ng m(-3)) and indoor spring (9.5 ± 3.3 ng m(-3)). During nighttime, outdoor PAHs revealed wider range of values compared to datytime which was likely due to outdoor temperature, a weather parameter with the strongest negative influence on ∑16PAHs compared to low impact of relative humidity and wind speed.

The occurrence and fate of four cyclic (D3 to D6) and 10 linear (L5 to L14) siloxanes were investigated in influent and effluent wastewater, sludge from a wastewater treatment plant (WWTP), and surrounding air and soil within the WWTP in Harbin, Northeast China. The mean concentrations of total siloxanes in influent and effluent were 4780 and 997 ng/L and in excess sludge and aerobic sludge were 25.1 and 32.3 μg/g dw, respectively. The concentrations in air and soil within the WWTP were 243 ng/m(3) and 4960 ng/g dw, respectively. A similar composition profile of siloxanes in influent and sludge suggests their same source. Seasonal variation with concentration was comprehensively studied. It was found that temperature and rainfall are the two important factors for the seasonal variation of siloxanes. Adsorption with sewage sludge was the major way for the removal of siloxanes during the municipal wastewater treatment process. Overall, on a daily basis, the mass loading of the Σsiloxanes into the WWTP, out of the WWTP with the effluent and sludge, were estimated to be 3.0, 0.6 and 1.3 kg, respectively. In general, 21 % of siloxanes were discharged into the receiving body (Songhua River), 43 % of siloxanes were absorbed on sludge, and 36 % of siloxanes were lost during the whole process of WWTP.

Limited studies focus on the occurrence, removal rate and seasonal variation of substituted diphenylamine antioxidants (SDPAs) in surface water and wastewater in China. In this paper, the detection method of SDPAs was established by the ultra-performance liquid chromatography-tandem mass spectrometry. Daily variations suggested that significant variations were found for the concentrations of some SDPAs in the influent. It was found that the SDPAs could be detected in all the effluent samples and C8/C8-DPA was the predominant compound in two WWTPs. The levels of most SDPAs in the effluent were much lower than that of influent, with the removal efficiencies of total SDPAs ranged from 57.9% to 84.2%. There were significant differences with the SDPA concentrations in the influent between different seasons. Higher concentrations of SDPAs were found at downstream than those of upstream. The results of this study provide more environmental occurrence data and new insights into the research on the environmental fate of these compounds.

To investigate the seasonal variation of organophosphate esters (OPEs) in air particulate matter (PM) and the corresponding influence factors in indoor environment, 104 indoor PM samples were collected in a test home, Harbin, China, from March 2017 to March 2018. The Σ12OPEs concentrations ranged from 0.41 ng/m3 to 940 ng/m3. Tris(1-chloro-2-propyl) phosphate (TCIPP) was the most abundant OPE and accounted for 83.2% of the total OPEs. The Σ12OPEs concentrations in spring and summer were higher than those in autumn and winter. Outdoor total suspended particles (TSP) were the main factor that affected the concentration variation of OPEs in PM samples in the test home. Comparisons of the gas/particle (G/P) partitioning equilibrium models indicated that the Dachs-Eisenreich (D-E) model estimates were more reliable than the other models in this study. The particle fractions of OPEs with log KOA > 10.51 that predicted by all four models generally well matched the measured OPE particle fractions in the literatures. To OPEs with lower molecular weight, inhalation was the main exposure route and ingestion contributed mostly to OPEs with higher molecular weight. In addition, the estimated daily intakes (EDIs) and carcinogenic risks (CRs) posed by OPEs were all below the recommended values, indicating that the current OPE levels in the test home were within the safe thresholds.

While infants are developing, they are easily affected by toxic chemicals existing in their environments, such as semi-volatile organic compounds (SVOCs): phthalates, polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), and organophosphate esters (OPEs). However, the specific living environment of infants, including increased plastic products and foam floor mats, may increase the presence of these chemicals. In this study, 68 air, dust, and window film samples were collected from homes, with 3- to 6-month-old infant occupants, to analyze phthalates, PAHs, PBDEs, and OPEs. High detection rates and concentrations suggest that these SVOCs are widespread in infant environments and are associated with cooking methods, smoking habits, the period of time after decoration, and room floors. The partitioning behavior of SVOCs indicates that the logarithms of the dust/gas-phase air partition coefficient (logKD) and the window film/gas-phase air partition coefficient (logKF) in homes are not at an equilibrium state when the logarithm of the octanol/air partition coefficient (logKOA) is less than 8 or greater than 11. Considering the 3 exposure routes, ingestion and dermal absorption have become the main routes of infant exposure to phthalates and OPEs, and ingestion and inhalation have become the dominant routes of exposure to PAHs and PBDEs. The total carcinogenic risk of SVOCs, which have carcinogenic toxicities, via ingestion and dermal absorption for infants in homes exceeds the acceptable value, suggesting that the current levels of these SVOCs in homes might pose a risk to infant health.

The study of indoor organic film on planar surfaces has been shown to be important to assess the transport and fate of organic pollutants in indoor environments. Limited research showed the relationship between equilibrium status of polycyclic aromatic hydrocarbons (PAHs) and the growth days for indoor window films. To accomplish this goal, indoor window film samples were collected in relation to film growth days in Northeast China. PAHs were frequently detected in window films collected during heating season (H-season), with concentrations significantly higher than that of non-heating season (NH-season). Accumulation characteristics of PAH suggested that PAH concentrations (ng/m2 film) were growing near-linearly with time. Partitioning status for PAHs between gas and window films under different accumulation stage from 1 to 11 weeks was investigated during the two seasons. The equilibrium status of PAHs in the films suggested that the octanol–air partition coefficient (logKOA) of the targeted PAHs should be approximately

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.

Emission inventories for polychlorinated biphenyls (PCBs) are crucial input data for atmospheric transport modeling and for the study of source-receptor relationships and the environmental behavior of these chemicals. Three types of primary PCB sources are considered in this study: intentionally produced PCBs (IP-PCBs), unintentionally produced PCBs (UP-PCBs), and PCB emissions from two e-waste sites (EW-PCBs). This study presents the historical emissions of all IP-, UP- and EW-PCBs into the air in China and the gridded Chinese emission inventories at a resolution of 1/6° latitude×1/4° longitude from 1950 to 2010. The UP-TPCB emissions from 1950 to 2010 were re-estimated to be 8.56t from eight emission sources comprising 96.3% of the Chinese UP-TPCB emissions. The EW-TPCB emissions from 1990 to 2010 were estimated to be 103.5 t, of which 7.1t and 12.3t were EW-PCB28 and EW-7PCB congeners (i.e., indicator-PCB28, 52, 101, 118, 138, 153, 180), respectively. The IP-PCB28 and IP-7PCB congener emissions from 1965 to 2010 were estimated to be 57.4 t and 130.1t, respectively. A significant correlation was found between congener PCB28 and 7PCBs (R(2)=0.988 and P=0.000), which suggests that PCB28 is a good marker congener for describing the emission trends of all 7PCB emission sources. The gridded emission data were compared with published measured atmospheric concentrations for 2004 and 2008, and a significant correlation was found between the modeled emissions and monitoring data. To our knowledge, this study presents the first comprehensive gridded emission inventories that include all IP-, UP-, and EW-PCBs on a national scale.

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 (p0.05), 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.

The present study investigated the environmental distribution and fate of low molecular weight (LMW) polychlorinated biphenyls (PCBs) in China using the ChnGIPERM (Chinese Gridded Industrial Pollutants Emission and Residue Model), in which the air-soil exchange, spatial-temporal variations and the heterogeneity of secondary emission and residue in the non-source areas were studied. The model simulated the temporal and spatial variations of the PCB28 concentration in soils and air which agreed well with historical monitoring data across China. The long-range atmospheric transport (LRAT) and temperature was identified as the major factor affecting the distribution patterns of the secondary emissions and residues. Soil residue was considered as important environmental fate of PCB28. However, the intensity of an emissions source and the distance with non-source area strongly affected the spatial and temporal variations of PCB28 residues in soil. Several factors strongly impacted the distribution characteristics and air-soil exchange of PCB28, including emission patterns, atmospheric transport, soil organic carbon (SOC), soil vertical transfer, ambient temperature, and precipitation.

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.

The gas/particle (G/P) partitioning behavior is an important factor for the environmental fate of polycyclic aromatic hydrocarbons (PAHs) in atmosphere. Based on one year monitoring program at 11 urban sites across China, 7647 pairs of gaseous and particulate concentrations were obtained for 16 priority PAHs, which provided a good opportunity to study the G/P partitioning behavior of PAHs. The concentrations of PAHs in both gas and particle phases were not in the same level among the 11 sites with a difference of more than one orders of magnitude. Along with the increase of molar weight of PAHs, the proportion of concentration in particle phase was increasing. In particle phase, the concentrations of ∑16PAHs in northern Chinese cities were significantly (p

Fourteen indoor dust samples were collected in 2010 winter from four cities in Heilongjiang Province, China. Fourteen polybrominated diphenyl ethers (PBDEs) were identified and quantified. Concentration of the total 14 PBDEs ranged from 240 to 9,270 ng/g, with the median of 2,520 ng/g. BDE209 was the dominant congener with concentrations ranged from 234 to 9,190 ng/g, accounting for 97.2 % of the total concentration. Positive correlations (r > 0.8, p

The Songhua River is the third largest river in China and the primary source of drinking and irrigation water for northeastern China. The distribution of 16 priority polycyclic aromatic hydrocarbons (PAHs) in water [dissolved water (DW) and suspended particulate matter (SPM)], sediment, and soil in the river basin was investigated, and the associated risk of cancer from these PAHs was also assessed. The total concentration of PAHs ranged from 13.9 to 161 ng L(-1) in DW, 9.21 to 83.1 ng L(-1) in SPM, 20.5 to 632 ng g(-1) dw (dry weight) in sediment, and from 30.1 to 870 ng g(-1) dw in soil. The compositional pattern of PAHs indicated that three-ring PAHs were predominant in DW and SPM samples, while four-ring PAHs dominated in sediment and soil samples. The spatial distribution of PAHs revealed some site-specific sources along the river, with principal component analysis indicating that these were from pyrogenic sources (such as coal and biomass combustion, and vehicle emissions) and coke oven emission distinguished as the main source of PAHs in the Songhua River Basin. Based on the ingestion of PAH-contaminated drinking water from the Songhua River, cancer risk was quantitatively estimated by combining the Incremental Lifetime Cancer Risk assessment model and BaP-equivalent concentration for five age groups of people (adults, teenagers, children, toddlers, and infants). Overall, the results suggest that the estimated integrated lifetime cancer risk for all groups was in acceptable levels. This study is the first attempt to provide information on the cancer risk of PAHs in drinking water from the Songhua River.

The Tibetan Plateau is suggested to be an important indicator region to study the global long-range atmospheric transport of persistent organic pollutants. In this study, atmospheric polycyclic aromatic hydrocarbons (PAHs) were studied in Lhasa City in the Tibetan Plateau, China. Air samples in gas and particle phases were concurrently collected by a modified high-volume air sampler from 5 August 2008 to 13 July 2009. The concentration of Σ16PAHs ranged from 18 to 160 ng m(-3) (with a geometric mean of 68 ng m(-3)). The most abundant PAHs were phenanthrene and benzo(b)fluoranthene in gas and particle phases, respectively. Compared with other two similar studies in Beijing and Harbin, different temporal trends were found between gas and particle phases PAHs in Lhasa. The influences of meteorological parameters (ambient temperature and relative humidity) and air masses from China, India, Southeast Asia, and West Asia were the two important reasons for explaining the difference, which was confirmed by the 5-day backward trajectories. This is the first comprehensive study to provide the evidence for the different influences of long-range atmospheric transport on gas and particle phases PAHs pollution in the Tibetan Plateau.

Temporal variations of organochlorine pesticides (OCPs) were determined in precipitation and monthly depositional fluxes were calculated in Beijing from February 2009 to March 2011. Compounds which were detected most often included α-HCH and β-HCH, and the volume-weighted mean (VWM) concentration of hexachlorocyclohexanes (HCHs) was 33.0 ng L −1 , accounting for 72.3% of the ∑OCPs in precipitation. The total concentrations of OCPs ranged from 3.73 to 152 ng L −1 (mean: 29.7 ± 3.5 ng L −1 ) for dissolved phase and from 1.61 to 114 ng L −1 (mean: 15.9 ± 2.0 ng L −1 ) for particulate phase, respectively. OCPs in dissolved phase dominated sampled concentrations in precipitation (HCHs: 71.8%, Chlordane: 77.7%, dichlorodiphenyltrichloroethanes-DDTs: 50.1%) with an exception of hexachlorobenzene–HCB (26.3%). Furthermore, the distribution coefficient, K pd , was generally large in low temperature, especially in spring. The abundance of ∑OCPs in the precipitation fluctuated monthly, with high value in late winter and spring. The past farmland near the sampling site was under construction during sampling, which may be an important local re-emission source in this study. The elevated wet deposition flux of 11 selected OCPs was 14.9 μg m −2 yr −1 in Beijing.

Temporal trend of polychlorinated biphenyls (PCBs) was determined in precipitation and monthly depositional fluxes were calculated in Beijing for the first time from February 2009 to March 2011. Total PCBs concentrations ranged from 7.00 to 993 ng L-1 in dissolved phase and from 1.00 to 133 ng L-1 in particulate phase, with a two orders of magnitude variation. Concentrations of PCBs were dominated by dissolved phase, which accounted for 82.5% of the total PCBs in precipitation, implying PCBs enrichment in rainwater due to efficient scavenging of highly contaminated gas phase and nonfilterable submicron particles which easily adsorbed organic contaminants in urban atmosphere. Highest concentrations of PCBs were measured in snow, which were about two times higher than those in rainwater, demonstrating more efficient scavenging of PCBs by snow. The sum of bi-, tri- and tetrachlorinated congeners accounted for 70.5% of total PCBs in precipitation, suggesting that PCBs mainly come from the historical usage of domestic PCB product, e.g., trichlorobiphenyl. PCBs concentrations in both dissolved and particulate phases showed slow rate of decline, with a half-life of 16.9 years in precipitation, suggesting that the atmospheric concentrations of PCBs were decreasing slowly in Beijing. The wet deposition flux of Sigma PCBs ranged from 0.240 to 6.55 mu g m(-2) month(-1) (mean: 1.41 mu g m(-2) month(-1)), indicating a relatively high level of PCBs contamination in Beijing atmosphere. (C) 2012 Elsevier Ltd. All rights reserved.

The Zha Long Wetland, the first water bird conservation area in China, lies on the northern bank of the Song Nen Plain with an area of 2,100 km(2). In many areas of the Zha Long Wetland, water pollution has led to a decrease in the wetland's ecological function, vegetation degradation, a decrease in the number of bird species, and the depletion of fish resources.The sediments used in this study were collected from the surface sediment of seven sites and from different depths in three types of marshes in the Zha Long Wetland in northeast China in late October 2006. The levels and distribution patterns of 17 organochlorine pesticides (OCPs; α-HCH, β-HCH, γ-HCH, δ-HCH, p,p'-DDE, p,p'-DDD, p,p'-DDT, endosulfan I, endosulfan II, endosulfan sulfate, heptachlor, heptachlor epoxide, aldrin, dieldrin, endrin, endrin aldehyde, and methoxychlor) in surface sediments as well as hexachlorocyclohexane (HCH) and 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane (DDT) in vertical sediments were investigated.The concentrations of HCHs, DDTs, endosulfans, heptachlors, aldrin, and methoxychlor in surface sediments ranged from 10.44 to 41.97 ng/g, nd (undetectable levels) to 211.88 ng/g, nd to 69.89 ng/g, nd to 28.10 ng/g, 9.81 to 623.83 ng/g, and from nd to 3.99 ng/g, respectively. The highest levels of OCPs were detected in Tangtugangzi at a total concentration of 727.72 ng/g, where the dominant compound was endrin at a concentration of 483.04 ng/g. In the vertical sediments, the HCHs and DDTs were in the ranges of nd-136.00 and nd-214.06 ng/g, respectively.Different distributions of HCHs, DDTs, and other OCPs indicated that they originated from different contamination sources. Composition analyses in surface sediments indicated recent OCP usage or discharge at some sample sites in the Zha Long Wetland.

This paper reviews the usage and emissions of endosulfan, the newest member of the persistent organic pollutants (POPs), in China, and its fate and behavior in Chinese environment. Endosulfan usage in China has been estimated to be approximately 25700 t between 1994 and 2004. Concentrations of endosulfan in different environmental compartments in China, such as air, soil, water, and biota, but focusing at air and surface soil, have been summarized. Concentrations of total endosulfan in surface soil across China were ranged from below detection limit (BDL) to 19000 pg·g−1 dry weight (dw), with geometric mean of 120 pg·g−1dw. The results indicated that endosulfan sulfate had highest concentration in Chinese soil, followed by β- and α-endosulfan. Air concentrations of endosulfan in China were ranged 0–340 pg·m−3 for α-endosulfan and 0–121 pg·m−3 for β-endosulfan, with high concentrations occurred in the cotton production areas. Gridded usage inventories of endosulfan on a fine gridded system with a 1/4° longitude by 1/6° latitude resolution were compiled, from which, emission to air and residues in soil of endosulfan were calculated in each grid by using a modified simplified gridded pesticide emission and residue model (SGPERM), an integrated modeling system combining mathematical model, database management system, and geographic information system. Total emissions were around 10800 t from 1994 to 2004. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell, which are in general consistent with the published monitoring data.

This study explores long-term environmental fate of α-HCH in China from 1952 to 2007 using ChnGPERM (Chinese Gridded Pesticide Emission and Residue Model). The model captures well the temporal and spatial variations of α-HCH concentration in Chinese soils by comparing with a number of measured data across China in different periods. The results demonstrate α-HCH grasshopping effect in Eastern China and reveal several important features of the chemical in Northeast and Southeast China. It is found that Northeast China is a prominent sink region of α-HCH emitted from Chinese sources and α-HCH contamination in Southwest China is largely attributed to foreign sources. Southeast China is shown to be a major source contributing to α-HCH contamination in Northeast China, incurred by several environmental factors including temperature, soil organic carbon content, wind field and precipitation.

Dechlorane plus (DP) was quantified by gas chromatography/mass spectrometry (GC/MS) in soil and ambient air (collected from Harbin City, a typical northeastern Chinese urban region), water and sediment samples (collected in the segment within Harbin of Songhua River, located in northeast of China). The average concentrations of DP in sediment and soil samples were 123.6 pg g−1 dry weight (dw), and 11.3 pg g−1 dw, respectively. However, the concentration of DP in water was below the method detection limit (MDL). The inter-media comparison between water and sediment suggested that the sediment may be a receptor for DP. For air samples, two methods were used for collecting air in order to compare, active air sampling (AAS) and passive air sampling (PAS). The average concentrations of DP were 0.4 pg m−3 and 6.9 pg m−3 for AAS and PAS samples, respectively. Discrepancies of deployment period and different calculated method for DP concentration may help to explain the remarkable difference between PAS and AAS. Overall, DP in all matrices in Harbin City showed lower concentrations than that in the Great Lakes region. The anti-DP isomer was consistently greater than that of the syn-DP isomer in all matrices. The average fractional abundance of the syn-DP isomer (fsyn) was smaller than the technical DP composition (fsyn=0.35) according to other studies in the Great Lakes region. As we know, this study is the first attempt to comprehensively study DP concentrations in four different matrices (water, ambient air, sediment and soil) in China. Keywords: Dechlorane plus, Water, Sediment, Soil, Air, China

The spatial and seasonal variation of polychlorinated biphenyls (PCBs) were investigated in water and sediment samples collected from Songhua River, China, from 2007 to 2008. The total concentration of PCB congeners ranged from 1.1 to 14 ng/l in water and 0.26-9.7 ng/g dry weight (dw) in sediment. The results of seasonal variation may suggest an impact to PCB concentration in water from its atmospheric input, the dilution to PCBs concentrations of high stream in summer, and a general trend towards increased volatilization in warmer conditions. From PCBs concentrations comparison between upstream and downstream of industrial urban cities, it was obvious that industrial urban cities reflect an important pollutant source for PCBs in our study, also with the evidences of high concentrations of PCBs occurring in high development industry and residential areas. Meanwhile, the homologue profile of PCBs in Songhua was analyzed, whose comparison with published data indicates that the sources of PCBs accumulated in the sediment may also came from the residue of PCBs production in China. Total five dioxin-like PCBs (CB-77, 81, 105, 114, and 126) and nine (CB-77, 81, 105, 114, 118, 123, 126, 156, and 167) were found in Songhua water and sediment.

Understanding the seasonal variations of sources of polycyclic aromatic hydrocarbons (PAHs) in air in urban region is important to the effective control of air pollution in the region. Based on a year round dataset (from August 2008 to July 2009), the sources of atmospheric PAHs in Harbin, a typical Chinese northeastern urban city, were analyzed by principal component analysis (PCA) and positive matrix factorization (PMF). The average total (gas plus particulate) PAH concentration varied from 6.3 ng m −3 to 340 ng m −3 with a mean of 100 ± 94 ng m −3 , with higher concentrations in heating season than those in non-heating season. PCA and PMF identified similar source factors to atmospheric PAHs with obvious seasonal variation. The results obtained by PMF method indicated that the main sources were coal-fired boiler (39%), diesel engine (34%) and coal average (22%) in heating season and traffic emissions (59%), ground evaporation (18%) and coal average (17%) in non-heating season. Excellent correlation coefficients between predicted and measured concentrations of PAHs indicated that PMF was a useful model for source apportionment of PAHs in atmosphere.

Using a dynamic numerical atmospheric transport model for organochlorine pesticides (OCPs), the relationship between the East Asian summer monsoon and the fate of α-hexachlorocyclohexane (α-HCH), a banned OCP, in the atmosphere over Northeast Asia was investigated and assessed. The modeled temporal and spatial patterns and variability of α-HCH air concentrations during the summer months of 2005 revealed a strong link between this chemical in the atmosphere over Northeast Asia and the East Asian summer monsoon. At lower atmospheric levels, easterly and southeasterly winds blowing from relatively cold ocean surface convey α-HCH air concentration from southeast China to northeast China. A monsoon front extending from southeast China to Japan, characterized by a strong wind convergence, carried the air concentration to a high elevation of the atmosphere where it was delivered by southerly monsoon flow to northern China and North Pacific Ocean. This summer monsoon associated northward atmospheric transport caused a reversal of the soil/air exchange from outgassing to net deposition during spring–summer period. The modeled wet deposition fluxes of α-HCH agreed well with the changes in the typical summer monsoon rain bands, designated as Meiyu in China, Changma in Korea, and Baiu in Japan. The major wet deposition flux paralleled with the monsoon front as well as the monsoon rain bands. The temporal change in the fluxes exhibits abrupt northward advances, which is associated with a stepwise northward and northeastward advance of the East Asian summer monsoon. The modeled α-HCH outflow in the atmosphere from China occurs mostly in the summer months and through northeast China, featured strongly by the evolution of the summer month. This study suggests that the East Asian summer monsoon provides a major atmospheric pathway and summer outflows to α-HCH over East Asia.

Surface soil samples were collected surrounding two brominated flame retardants (BFRs) manufacturing plants in China in August 2014 and analyzed for 23 polybrominated diphenyl ethers (PBDEs) and 8 novel brominated flame retardants (NBFRs). BDE209 and decabromodiphenylethane (DBDPE) were the predominant compounds in soil with the median levels of 1600 and 560 ng/g dw, respectively. The PBDEs profiles in soil samples were consistent with that of commercial product (comDecaBDE). The percentage contributions to total PBDEs decreased from higher to lower brominated homologues. Lower concentrations of NBFRs (excluding DBDPE) were detected in soil surrounding the two plants, suggesting they are byproducts or degradation products of the manufacturing activities. The concentrations of most BFRs dropped exponentially within 3-5 km of the manufacturing plants, suggesting recent deposition of these compounds to the soil. Directional distribution indicated that PBDEs and DBDPE concentrations were highest in the north direction of Plants 1. Three-day air parcel forward trajectories confirmed that the air parcel was responsible for the higher concentration of BFRs in the soil of north direction of the plant.

Levels of dechlorane plus (DP) and "DP-like" compounds were measured in indoor dust samples collected across China. The concentrations of ΣDP and "DP-like" compounds ranged from 0.35 to 1,000 ng g(-1) and0.21 to 2.4 ng g(-1), respectively. The total DP concentration in urban sites were significantly higher than those of rural sites, while no significant difference was found for "DP-like" compounds, suggesting different sources of these compounds. Significant positive correlations were found between fsyn and latitude, and between fsyn and longitude. The deleterious risk associated with DP exposure via indoor dust for the general population in China was low and safer than expectation. For estimating human exposure via indoor dust, sensitivity analysis showed that more attention should be given to the influential variables such as the level of pollutants, body weight, and the amount of ingestion and adsorption.

In this study, 16 polycyclic aromatic hydrocarbons (PAHs) were analyzed in 157 concurrently collected soil samples in 2005 over China. Higher concentration of ∑16PAHs was found in urban soil, followed by rural and background soil. The results indicated that PAHs in Chinese surface soil showed a primary distribution pattern, which was confirmed by the positive correlation with emission inventory. Based on the results of literature over the past 10 years (2004–2013) in China, the spatial distribution of PAHs in urban and rural soil was established. An obvious geographical distribution with PAH concentration was found, as higher in Eastern China and lower in Middle and Western China. Furthermore, PAH pollution in Chinese riverbank soil was summarized and showed higher levels, indicating their potential sources from polluted rivers. According to our knowledge, this is the first time to comprehensively study the PAH pollution status in Chinese surface soil on the national scale based on monitoring results.

Indoor environment is an important source of human exposure to several toxicants, such as brominated flame retardants. This study presents the concentrations of 22 Non-BDE brominated flame retardants (NBFRs) in 81 indoor dust samples from 23 provinces across China in the winter of 2010. The concentrations of ΣNBFRs ranged from 6.3 to 20,000 ng/g, with a median concentration of 720 ng/g. DBDPE was the dominated compound, followed by HBCD and BEHTBP. Significant differences of concentrations were found between samples from rural and urban areas, and between family and public houses, indicating different applications of NBFRs. The geographical distribution of NBFRs highlighted several hotspots in North China, suggesting the influence of room temperature (heating). The exposure via dust ingestion of NBFRs was 3.8–14 times higher than that of dermal absorption. The toddlers demonstrated the highest exposure dose (9.6 ng/kg-bw/day) of NBFRs through indoor dust among all life stages.

In order to accurately evaluate the outdoor thermal comfort under hot and humid climatic conditions, the International Low Carbon City (ILCC) of Shenzhen was chosen as the study object. A thermal comfort questionnaire survey and the simultaneous field measurement were carried out in six different places of ILCC. Results derived from the questionnaire survey show that most of the residents in Shenzhen feel comfortable about the hot and humid summer and the thermal dissatisfaction rate expressed the negative correlation with thermal comfort evaluation scales. In addition, the thermal comfort evaluation indices SET* and PET of each questionnaire could be obtained with the results from the questionnaire survey and meteorological parameter measurement. Through combining the thermal comfort evaluation scales, the thermal comfort evaluation range benchmarks of SET* and PET could be thus expressed to quantitatively present the different magnitudes of outdoor thermal comfort in Shenzhen. Furthermore, with the field data collected and processed of the six test sites, the comprehensive impact of building and underlying surface parameters on the thermal comfort can be expressed, which demonstrated that the product of the building floor-area ratio and the green coverage ratio had a strong positive correlation with the thermal comfort.

Atmospheric outflow of alpha-HCH-HCH from China from 1952 to 2009 was investigated using Chinese Gridded Pesticide Emission and Residue Model (ChnGPERM). The model results show that the outflows via the northeast boundary (NEB, longitude 115-135 degrees E along 55 degrees N and latitude 37-55 degrees N along 135 degrees E) and the mid-south boundary (MSB, longitude 100-120 degrees E along 17 degrees N) of China account for 47% and 35% of the total outflow, respectively. Two climate indices based on the statistical association between the time series of modeled alpha-HCH outflow and atmospheric sea-level pressure were developed to predict the outflow on different time scales. The first index explains 70/83% and 10/46% of the intra-annual variability of the outflow via the NEB and MSB during the periods of 1952-1984 and 1985-2009, respectively. The second index explains 16% and 19% of the interannual and longer time scale variability in the outflow through the NEB during June-August and via the MSB during October December for 1991-2009, respectively. Results also revealed that climate warming may potentially result in stronger outflow via the NEB than the MSB. The linkage between the outflow with large scale atmospheric circulation patterns and climate warming trend over China was also discussed.

A comprehensive sampling campaign was carried out to study atmospheric concentration of polycyclic aromatic hydrocarbons (PAHs) in Beijing and to evaluate the effectiveness of source control strategies in reducing PAHs pollution after the 29th Olympic Games. The sub-cooled liquid vapor pressure (logP(L)(o))-based model and octanol-air partition coefficient (K(oa))-based model were applied based on each seasonal dateset. Regression analysis among log K(P), logP(L)(o) and log K(oa) exhibited high significant correlations for four seasons. Source factors were identified by principle component analysis and contributions were further estimated by multiple linear regression. Pyrogenic sources and coke oven emission were identified as major sources for both the non-heating and heating seasons. As compared with literatures, the mean PAH concentrations before and after the 29th Olympic Games were reduced by more than 60%, indicating that the source control measures were effective for reducing PAHs pollution in Beijing.

Polyurethane foam disk passive air samplers were deployed along an urban–rural-background transect in a northeastern Chinese region (Harbin) to investigate the spatial and seasonal variations of polycyclic aromatic hydrocarbons (PAHs). The ∑16PAHs concentrations [ng/(sample·day)] were high at urban sites (315 ± 206), followed by rural sites (222 ± 160), suburban site (142 ± 114) and background site (128 ± 107). The urban fractionation effect was observed along the transect with increasing proportions for low molecular weight PAHs and decreasing proportions for high molecular weight PAHs. PAHs were found to be higher in winter and spring than in summer and autumn, most likely due to the combustion of coal and biomass for domestic heating. Sources of PAHs were investigated by principal component analysis in combination with diagnostic ratios, which both indicated that pyrogenic sources were the main sources of PAHs in the air of Harbin, China.