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Light absorption properties of water-soluble organic carbon (WSOC) were investigated in the urban area of Guangzhou. The fine particulate matter (PM₂.₅) and size-segregated samples were collected in September and December of 2014 and January of 2015. The variation of absorption with wavelength of WSOC was characterized by the absorption Angström exponent (AAEabs). The AAE values of WSOC in PM₂.₅ were 3.72 ± 0.41 in autumn and 3.91 ± 0.70 in winter, which were lower than those in Beijing and north America. The mass absorption efficiency (MAE) of WSOC at 365 nm wavelength was 0.52 m² · g⁻¹ in autumn and 0.92 m² · g⁻¹ in winter, exhibiting distinct variations between autumn and winter. In winter, the MAEwsoc values exhibited a decreasing trend with increasing particle size, and all size-segregated MAE(WSOC) values in autumn were lower than those in winter, particularly for the particles0.95 µm, suggesting more contribution of the secondary formation to WSOC. Comparing the MAE values of elemental carbon (EC) and WSOC, it could be found that the contribution of WSOC to the light extinction of particles couldn't be ignored when the particles were mainly emitted from primary sources.

A sensitive and reliable method has been developed for the simultaneous determination of 20 airborne carbonyl compounds in the C 1 –C 10 range. The carbonyls were collected onto solid sorbent coated with pentafluorophenyl hydrazine (PFPH), followed by solvent extraction and gas chromatographic (GC)/mass spectrometric (MS) analysis of the PFPH derivatives. The sorbent is packed into two separate sections in a glass sampling tube. The two-section design allows convenient checking of collection efficiency and breakthrough. The sampling tube, with a coating amount of 971 nmol PFPH per 100 mg Tenax TA and operated at a sampling flow rate of 80 mL min −1 , collects the 20 carbonyls with efficiencies above 95%. Hexane extracts the collected carbonyls in their PFPH derivatives in the sampling tube with better than 95% extraction efficiency. It is necessary to let the sampling tube sit at ambient temperature for 3 days before solvent extraction to ensure complete derivatization of the carbonyls. The limits of detection (LODs) of the tested carbonyls are in the range of 3.7–11.6 ng per sample. The method has been field-tested both in ambient environment and in an indoor environment from burning mosquito-repellent incense. Eighteen carbonyls were detected in the ambient air samples with the exception of o -tolualdehyde and m -tolualdehyde, while all the 20 target carbonyls were found in the incense smoke. Compare field test with classical DNPH–HPLC/UV method, good agreement exited between the two methods for lower molecular carbonyls but PFPH method is found to be a better analytical method for determination of high molecular weight carbonyls.

Forty surface sediment samples from the Hunhe River in Northeast China were evaluated for contamination by polybrominated diphenyl ethers (PBDEs) and hexabromocyclododecane (HBCD). The results showed that decabromodiphenyl ether (BDE-209) was the predominant congener, accounting for >98 % of PBDEs in all sediment. The concentrations of BDE-209 and HBCD ranged from 3.96 to 327 ng/g dry weight and 0.05 to 25.8 ng/g dry weight, respectively, suggesting that BDE-209 was more widely applied in the study area. The mean concentrations of BDE-209 and HBCD in the downstream portion of the Hunhe River (BDE-209 148 ng/g dry weight and HBCD 3.74 ng/g dry weight) were found to be relatively higher than those in the upstream portion of the Hunhe River and the Dahuofang Reservoir, revealing an association with municipal sewage and industrial effluent received from the cities of Fushun and Shenyang. γ-HBCD was the most abundant diastereoisomer of all three analyzed HBCD isomers; however, marked elevations of α-HBCD were also found in most sediment samples. Surprisingly, the relative abundance (mean 38 %) of α-HBCD in sediment from the upstream portion of the Hunhe River was significantly higher (p

In July to September 2003, particulates in the oceanic atmosphere from the Bohai Sea to the high Arctic (37 degrees N to 80 degrees N) were collected aboard a research expedition icebreaker, Xuelong (Snow Dragon), under the 2003 Chinese Arctic Research Expedition Program (CHINARE 2003). These samples were analyzed to elucidate the atmospheric distributions of polybrominated diphenyl ethers (PBDEs) in the North Pacific Ocean and adjacent Arctic region. The levels of 11 PBDE congeners (BDE-28, -47, -66, -100, -99, -85, -154, -153, -138, -183, and -209; the sum was defined as sigma11PBDE) in the oceanic atmosphere of Far East Asia (34-48 degrees N/122-148 degrees E) ranged from 2.25 to 198.9 pg/m3 with a mean of 58.3 pg/m3. BDE-47, -99, -100, and -209 were the dominant congeners in all the samples, suggesting that the widely used commercial penta- and deca-BDE products were the original sources. The PBDE levels exhibited a decreasing trend from the mid- to high-latitudinal regions of the North Pacific Ocean, probably resulting from dilution, deposition, and decomposition of PBDEs during long-range transport of air masses. On the other hand, no apparent geographical pattern of PBDE distribution was observed within the Arctic, attributable to unstable air circulation and strong air mixing. Correlations among the PBDE congeners suggested that air masses collected from the North Pacific Ocean were relatively fresh, whereas those from the Arctic were aged as a result of photodecompoisiton. The higher average level (17.3 pg/m3) of PBDE congeners in the Arctic than those in the adjacent North Pacific Ocean (12.8 pg/m3) or other remote areas reported in the literature was attributed to the impact of the North American continent and temperature effects, which was consistent with the hypotheses of global fractionation.

The concentrations of 144 polychlorinated biphenyls (PCBs) in the river sediments from Luqiao were analyzed by GC-muECD. The objectives of this study were to understand the contents, spatial distribution and possible sources of PCBs. The Sigma PCBs concentrations detected in the river sediments were in the range of 1.66 to 5 930 ng x g(-1), with a mean of 763 ng x g(-1). Tri-CBs, tetra-CBs and penta-CBs were the primary PCB congeners in all samples, accounting for 2.63%-57.6%, 10.4%-54.6% and 7.82%-46.1%, respectively. Octa-CBs and deca-CBs were the minor PCB congeners in all samples, with the percentages of 0-8.57% and 0-11.0%, respectively. The hierarchical cluster analysis (HCA) showed that 22 samples were mainly polluted by Ar1248, 9 samples were polluted by Ar1254, and 6 samples were contaminated by Ar1016, Ar1232 and Ar1242. The PCBs concentrations found in the present study were at an upper-middle level compared with those in other studies in the world. The PCBs pollution in the present area had a high ecological risk.

A total of 175 samples of 18 types of food were collected from markets in Shanghai, China, and the concentrations and bioaccessibility of 15 priority-controlled polycyclic aromatic hydrocarbons (PAHs) in these samples were determined. The mean concentrations of PAHs varied between 2.4 and 47.1 ng g(-1) wet weight, with the highest being observed in snail and lowest in chicken. The concentrations were lower than the maximum levels of PAH allowed for food per EU regulations. Among the PAHs measured, phenanthrene was the predominant one. Most of the PAHs originated from pyrogenic sources, analysed using molecular indices. The mean bioaccessibility of PAHs varied from 29.0% to 61.2% as measured by simulating the human gastrointestinal digestion process. Linear relationships between the bioaccessibility and lipid contents were observed for most PAH congeners. The daily intake of PAHs by an average Shanghai resident was 848 ng day(-1) and decreased to 297 ng day(-1) when the bioaccessibility of PAHs were considered, demonstrating that most intake might have been overestimated. According to the potency equivalent concentrations and screening values of PAHs, consumption of snail and clam, especially snail, should be limited.

The concentrations of 144 polychlorinated biphenyls (PCBs) in the soils from Luqiao were analyzed by GC-microECD. The objectives of this study were to understand the contents, spatial distribution and sources. The sigma PCBs concentrations in soils samples were in the range of 0.779 ng x g(-1) to 937 ng x g(-1), with a mean of 75.7 ng x g(-1), and the relatively high level of PCBs were mainly distributed in the south central area. Penta-CBs, hexa-CBs and tetra-CBs were the primary homologues in 38 samples, with the range of 13.0% - 61.1%, 4.59% - 48.8% and 10.1% - 31.5%, respectively. Di-CBs was the most predominant homologues in other samples, with the range of 47.1% - 75.2%. The hierarchical cluster analysis (HCA) showed that most of samples were mainly polluted by Ar1254, few samples were polluted by Ar1221. Significant correlations were observed between sigma PCBs and TOC, which suggested PCBs were affected by TOC in soils. The correlation analysis also showed significant correlation among the PCBs homologues (except di-CBs and nona-CBs), which suggested PCBs might have the similar sources. Compared to other studies from different countries and regions, the PCBs concentrations in the present study were at an upper-middle level.

The concentration of 46 polychlorinated naphthalenes (PCNs) in the agricultural soils from Luqiao was analyzed by GC-NCI-MS. The objectives of this study were to investigate the contents, spatial distribution and sources of PCNs. The total concentrations of PCNs (sigma PCNs) in soil samples were in the range of 0.062 to 2.92 ng x g(-1), with a mean of 0.630 ng x g(-1). Tetra-CNs and penta-CNs were the predominant homologues in most of the samples, accounting for 18.4% - 88.8% and 8.40% - 53.1%, with average values of 46.7% and 30.7%, respectively, followed by tri-CNs, accounting for 0 - 47.3%, with a mean of 10.6%. Cluster analysis and combustion marker analysis showed that the sampling sites were mainly polluted by Halowax 1014 and Halowax 1013, also possibly polluted by PCBs mixtures and e-waste combustion process. Compared to other studies, the PCNs concentration in this study was at a medium level.

The concentrations of 41 polybrominated diphenyl ethers (PBDEs) in the river sediments from Luqiao were analyzed by GC-NCI-MS. The objectives of this study were to understand the contents, spatial distribution and sources. The Sigma40 PBDEs (excluding BDE209) concentrations in sediments sampled were in the range of 0.177 to 161 ng x g(-1), with a mean of 22.5 ng x g(-1), and the concentrations of BDE209 were from 0.36 to 958 ng x g(-1), with a mean of 148 ng x g(-1). Deca-BDE was the most predominant in 9 PBDE homologues in most of samples, accounting for 38.4%-96.0%, with an average of 74.4% nona-BDEs and hepta-BDEs, accounting for 3.3%-25.8% and 0.01%-14.1%, respectively. Significant correlations were observed among all of PBDEs congeners, which suggested these PBDEs might have the similar sources. The homologue composition of PBDEs and hierarchical cluster analysis (HCA) showed that most of sampling sites were mainly polluted by deca-BDE formulation, and others polluted by deca-BDE and octa-BDE formulations. Compared to other studies from different countries and regions, the PBDEs concentrations in the present study were at a medium-to-low level. But it should be concerned that a few of sampling sites were highly contaminated by point sources.

The 55 soil samples were collected from Shanghai urban areas in March 2007. The residues and distribution characteristics of organochlorine pesticides (OCPs) in the soil samples were investigated with gas chromatography. The results showed that HCHs, DDTs, and HCB were in the ranges of nd-38.58 microg x kg(-1), 1.81-79.61 microg x kg(-1) and 0.16-40.25 microg x kg(-1), respectively. The total OCPs concentrations in urban soil of Shanghai ranged from 3.12 microg x kg(-1) to 91.07 microg x kg(-1) with a mean of 22.33 microg x kg(-1), and the p,p'-DDE took over 60% of the total OCPs. The main contaminated areas were distributed in the park and greenbelts. The composition of OCPs indicated that OCPs in soil samples mainly came from historical application. Compared to the reference data, the pollution burden in soil of Shanghai was lower than those in other areas of China and in German, Argentina and Poland.

Indoor dry deposition of eight homes and offices in the urban area of Shanghai, China were sampled with clean glass plate during July to August of 2008 to study the indoor deposition flux and congener profiles of polybrominated diphenyl ethers (PBDEs). 16 PBDEs congeners which including BDE-17, -28, -71, 47, -66, -77, -100, -99, -85, -118, -154, -153, -138, -183, -190 and BDE-209 were measured by GC-MS with negative chemical ionization (NCI) in selected ion monitoring (SIM) mode. The particulate deposition flux of PBDEs in homes and offices were (10.9 +/- 8.2) and (14.2 +/- 11.9) ng x (m2 x d)(-1) respectively. Deca-BDE (BDE-209) was the major compound, accounting for 88.2% -99.2% of the quantified PBDEs. The particulate deposition flux in the offices [(3.1 +/- 2.0) mg x (m2 x d)(-1)] was relatively lower than that of homes, but the concentration of PBDEs in the particles [(3361.6 +/- 1987.4) ng x g(-1)] was significantly higher than that of homes [(1169.1 +/- 647.1) ng x g(-1)]. The concentration of PBDEs in the indoor dry deposition of Shanghai ranked in the middle level comparing with other cities around the world. The indoor deposition flux of PBDEs was mainly correlated with the flux of particle deposition and the usage of electrical and electronic products, but not the interior decoration and the amount of furniture.

The concentrations of 16 US EPA PAHs in 37 sediment samples collected from Luqiao were analyzed by isotope dilution gas chromatograph/mass spectrometer (GC/MS), and their distribution characters,sources and ecological risk were further investigated. Each of the 16 PAHs could be detected in all of the sediment samples, the total concentrations of the 16 PAHs in the sediments ranged from 59.3 microg/kg to 3 180 microg/kg,with a mean of 722 microg/kg. The pollution level of PAHs can be categorized as low to moderate when compared with other studies around the world. SigmaPAHs were significantly correlated with TOC (r = 0.699, p0.001), indicating that TOC was a key soil property affecting the level and fate of PAHs in sediments. The isomeric ratios and factor analysis revealed that PAHs in the Luqiao sediments were originated from mixed sources, and combustion source was dominant. Six sampling sites had the mean PAH ERL quotient1, indicating that some sediments in Luqiao may have potential ecological risk. The toxic benzo[a]pyrene equivalents (TEQ(BaP)) of the 16 PAHs ranged from 3.41 microg/kg to 485 microg/kg, 98.4% of which was contributed by 7 carcinogenic PAHs, indicating that 7 PAHs were the main influential factors to the ecological risk.

A ternary-mobile phase program with acetonitrile, water and tetrahydrofuran was developed to identify and quantify 22 carbonyl compounds species by HPLC-UV. The analytical method succeeded in separating acrolein from acetone. Two sampling sites (industrial district and business district) were chosen to study carbonyl compounds levels in ambient air of Shanghai. The results indicated that formaldehyde, acetaldehyde, acetone and 2-butanone (C1-C4 carbonyl compounds) were the most abundant carbonyl compounds in ambient air of Shanghai. The four carbonyls together accounted for 78.95% (industrial district) and 77.63% (business district) of the total carbonyl compounds, respectively. In industrial district, the mean concentrations of formaldehyde, acetaldehyde, acetone and 2-butanone were 10.36, 15.32, 9.95 and 4.56 microg/m3, respectively; in business district, their mean levels were 10.00, 10.04, 7.80 and 2.81 microg/m3, respectively. So the mean levels of C1-C4 carbonyl compounds in industrial district were higher than in business district. The higher concentrations of the total carbonyls were also found in industrial district (53.64 microg/m3) than in business district (41.96 microg/m3). A similar diel variation occurred to the two districts that higher carbonyl concentrations were shown in morning peak and nighttime than in other three periods.

The characteristics of occurrence and distribution of 8 synthetic musks in 15 sewage sludges in Shanghai were studied. The results indicated that HHCB and AHTN were the two main components in all sludges, with the mean concentration of 2.92 mg x kg(-1) (0.81-6.39 mg x kg(-1)) and 1.96 mg x kg(-1) (0.35-3.11 mg x kg(-1)), respectively; and the concentrations of ADBI, AHMI, MK were less. The distributions detected in sludges are in accordance with the usage patterns in China. Total concentrations of 8 synthetic musks were ranged from 1.16-9.57 mg x kg(-1), which were lower than the results in previous studies. Concentrations in sludges are influenced by ratio of domestic wastewater in influent, sewage load and sewage treatment methods. The good linear relationships among HHCB, AHTN and ADBI indicate that these components have the same source: domestic wastewater. The consumption rates of HHCB and AHTN connected to per inhabitant in Shanghai region were estimated, which are low compared with those found in European. The potential impacts on agricultural soil were also assessed.

To obtain the temporal and spatial distribution and partition of PAH between water and particles in coastal area, water samples were collected from the Pearl River Estuary in July 2002 (summer) and April 2003 (spring) and polycyclic aromatic hydrocarbons (PAHs) were analysed with GC-MS in the present study. Total PAH concentrations in water samples were higher in spring (c(p): 4.0-39.1 ng/L; c(w): 15.9-184.2 ng/L) than in summer (c(p): 2.6-26.6 ng/L; c(w): 13.0-28.3 ng/L). Suspended particle matter (SPM) content, photogradation and riverine discharge were the major factors controlling the PAH concentrations in water. The 3-ring PAHs were the dominant PAHs in water samples. The 5 and 6 ring PAHs are more enriched in the inner estuary samples than in outside estuary samples, and the 3 ring PAHs are more enriched in summer samples than in spring samples. The differences in composition and source of SPM might be responsible for this observation. The partition coefficient (Kp) increased with the particular organic carbon content of SPM and salinity of water and decreased with the SPM content of samples, which were consistent with the PAH partition theory. A linear correlation between IgK(OC) and lgK(OW) were found in two sampling periods. The observed values of lgK(OC) exceed their predicted values calculated form linear free energy relationship between lgK(OC) and lgK(OW).

The vapor-phase and particulate-phase samples were collected from the E-waste dismantling region (E) and a reference region (S), which is located in the upwind direction of the E and where the costume industry is developed. The aim was to acquire information about the concentrations, gas/particle partitioning and distribution of polybrominated diphenyt ethers (PBDEs). 11 congeners PBDEs were detected with GC-NCI-MS. The results showed that E-waste dismantling has resulted in serious pollution and the PBDE concentrations (from tri-to deca-BDE) ranged from 51.1 pg x m(-3) to 2685 pg x m(-3) (mean:830 pg x m(-3)), while the PBDE concentrations (from tri-to deca-BDE) in S were in the range of 1.00 pg x m(-3) to 98.9 pg x m(-3) (mean: 28.7 pg x m(-3)). The gas/particle partitioning of PBDEs exhibited a strong dependence on bromine number. Low-brominated PBDEs tend to have a higher concentration in the gas-phase while highly brominated PBDEs are mostly associated with the particulate. The mass distribution of PBDEs in E (including vapor-phase and particulate-phase) was dominated by penta-BDE, accounting for 54.3% of the total PBDEs, followed by deca-BDE, accounting for 23.8%. This pollution characters validated that the E-waste did not only come from Asia, but also from North America and Europe.

During the 2003 Chinese Arctic Research Expedition (CHINARE2003) from the Bohai Sea to the high Arctic (37 degrees N to 80 degrees N) aboard the icebreaker Xuelong (Snow Dragon), air samples were collected for the analysis of hexachlorocyclohexanes (HCHs) in the North Pacific Ocean and adjacent Arctic region. The sigma HCHs (alpha-HCH + gamma-HCH) ranged from 2.3 to 95.1 pg/m3 with the highest levels observed in Far East Asia (32.5 pg/m3), followed by the North Pacific Ocean (17.0 pg/m3) and the Arctic (7.3 pg/ m3). Compared to previous studies in the same areas in 1990s, our measurements were approximately 1 order of magnitude lower. Because of disproportionate chemical reduction and physical fractioning during long-range transport, the ratios of alpha-HCH to gamma-HCH (alpha/gamma-HCH) showed a significant increasing trend from low to high latitudes, suggesting thatthe alpha/gamma-HCH range of 4-7 could not be used to identify sources of technical HCHs especially in remote areas. The ratios of (+)-alpha-HCH to the sum of (+)-alpha-HCH and (-)-alpha-HCH were on average much more biased from 0.5 compared to previous observations in mid-1990s, indicating the exchange of atmospheric alpha-HCH with those in the oceans, where (+)-alpha-HCH was selectively depleted in biological degradation processes. Estimated fugacity ratios based on available data for both alpha-HCH and gamma-HCH further implied their net volatilization from seawater to air in the Arctic Ocean.

PM(2.5) was collected at Shanghai urban and suburban sites during spring and autumn. PIXE (Proton Induced X-ray Emission) was used to investigate mass concentration of 15 elements (S, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Sr, Pb) in Shanghai PM(2.5). The total mass concentration of the 15 chemical elements was higher in spring (5 038.6 ng x m(-3)) than in summer (3 810.6 ng x m(-3)). In spring, mass concentrations of these elements in urban and suburban samples were in the same level. In summer, concentration of the elements in urban samples were lower than in suburban samples, however, the elements which were originated from anthropogenic resources were in higher level in urban samples. The results of FESEM showed that Shanghai PM(2.5) was consisted of soot aggregates, coal fly ashes, minerals, bio-particles and unidentified particles. The result of Plasmid DNA assay demonstrated bioreactivity of urban PM(2.5) was more reactive than that of suburban PM(2.5), this phenomenon probably was explained by higher mass level of heavy metals and more proportion of soot aggregates in urban PM(2.5).

Biofitlers inoculated P. putida strain and packed respectively with ACOF and ceramic pellets were employed to purify the chlorobenzene contained gases. An anionic surfactant, sodium dodecyl sulfonate (SDS) was introduced to trickling liquid to investigate its effect on the performance of biofilters. The result of microorganism cultivation shows that the inhibition to P. putida will be occurred when the SDS concentration in culture medium exceeded 35 mg/L. Addition of SDS in trickling liquid at concentration of 25 mg/L reduce the acclimatization periods and improve the performance of biofilter at stable condition. For the ACOF biofilter, the optimum SDS addition concentration is 25 mg/L, and the maximum elimination capacity of 234.7 g/(m3 x h) could be achieved. 18% - 20% of SDS in trickling liquid was lost after five days operation, but the lose could not reduce the efficiency of biofilter evidently.

A method of compound-specific stable carbon isotopic analysis for the research about the sources of atmospheric formaldehyde was preliminary studied using gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS) via 2, 4-dinitrophenylhydrazine (DNPH) derivatization. In order to evaluate the reproducibility, the accuracy and the carbon isotope effects of the method, formaldehyde with different delta 13C values were used to simulate the sampling procedure. The results show that the maximal analytical deviation for all formaldehyde 2, 4-dinitrophenylhydrazone is 0.3 per thousand and the average deviations between the determined and theoretical delta 13C values of them are 0.24 per thousand +/- 0.14per thousand (ranged from 0.03 per thousand to 0.35 per thousand), less than 0.5 per thousand the technical specifications of the GC/C/IRMS system. These mean that no carbon isotopic fractionation occurred during the procedure. The study for the indoor and outdoor atmospheric formaldehyde in the restaurant show that the stable carbon isotopic compositions are significant different for different sources of formaldehyde. The present method could provide valuable information about the sources of atmospheric formaldehyde.

Size distribution of aerosol samples collected from two urban locations (Liwan and Wushan) and a suburban location (Xinken) in Guangzhou (South China) in autumn using Micro-Orifice Uniform Deposit Impactor (MOUDI) were analyzed for 13 polycyclic aromatic hydrocarbons (PAHs) by gas chromatography with mass selective detection (GC-MS). Bimodal distribution was found for 3- and 4-ring PAHs and unimodal for 5-, 6- and 7-ring PAHs. Different PAH size distribution models were found for urban and suburban. PAHs associated with larger particles in suburban than in urban, and different aging processes of aerosols can account for it. Adsorption behavior may be the main mechanism controlled the size distribution of PAHs in urban, and adsorption, absorption and multilayer adsorption may all play a part in suburban. For the diagnostic ratios of PAHs with the same molecular weight, large differences were found between the range of 1-2.5 microm and 0.1-0.56 microm. The concentrations of 13 PAHs were 39 ng/m3 in Xinken, 71-94 ng/m3 in Wushan and 32-154 ng/m3 in Liwan, and 5-7 ring PAHs were the most abundant.

To study the posts-depositional behaviors of organic pollutants in natural conditions, concentrations and distributions of free and bound PAHs in a sediment core from Nam Van artificial Lake of Macao were investigated. Result indicate that free PAHs are predominated by 4-ring, 6,7-ring, and 5-ring PAHs, with the mass percentages of 28.7% to approximately 40.6%, 17.6% to approximately 29.6%, and 13.2% to approximately 28.2%, respectively, and for bound PAHs, the main components are 4-ring, 3-ring, and 2-ring ones, with mass percentages 42.3% to approximately 55.8%, 20.2% to approximately 35.8%, and 7.8% to approximately 18.8%, respectively, which suggeste that PAHs with low molecular weight are more prone to entering the micro-pores of sediment organic matters. Vertical profile of free PAHs concentrations in sediment core, to some degree, is correlated with the degree of regional economy development and the proceeding of environmental management. The concentrations of bound PAHs in the sediment core are controlled by the total PAHs mass input to the sediments and the structure (especially the polymerization) of sediment organic mater. The sediment burying favors the transformation of free form to bound form for PAH compounds.

Monoaromatic hydrocarbons (MAHs) from indigenous and industrial coking processes are studied in Shanxi province. They are sampled on the top of coke ovens and in the chimneys using stainless steel canister and determined by GC/MSD after preconcentration with liquid nitrogen. Benzene, toluene and xylene are the main components among MAHs emitted from coking processes. Benzene and the total MAHs concentrations were as high as 3421.0 microg/m3 and 4 865.9 microg/m3 in the air from indigenous coking, 548.7 microg/m3 and 1 054.8 microg/m3 in the oventop air from industrial coking, and 1 376.4 microg/m3 and 1 819.4 microg/m3 in stack gas from industrial coking, respectively. The MAHs concentrations vary greatly during the indigenous coking process, which in the prophase (from firing to 10 days) is obviously higher than in the anaphase (10 days to quenching the coke). In industrial coking the MAHs in the oventop air are highest when charging the coal and next when transferring the hot coke, but in stack gas they are highest when charging coal and lowest when transferring the coke. Benzene, toluene, ethylbenzene and xylene (BTEX) in industrial coking samples show good linearity, indicating that MAHs in industrial coking might come predominantly from coal pyrolysis; but BTEX distribute dispersedly in indigenous coking samples, indicating that its emission might be affected by many factors. In all samples BTEX ratios especially high B/E ratio, is unique among MAHs sources, and might be helpful to characterize pollution from coking.

Polycyclic aromatic hydrocarbons (PAHs) are measured in surface sediments from rivers and estuary of Pearl River Delta and its nearby South China Sea. Total PAH concentration varied from 255.9 - 16 670.3 ng/g and a moderate to low level compare to relevant areas worldwide. The order of PAHs concentration in sediments was: rivers of Pearl River DeltaestuarySouth China Sea, and the most significant PAH contamination was at Guangzhou channel of Zhujiang river. A decrease trend for PAHs concentration with distance from estuary to open sea can be sees in South China Sea. Coal and biomass combustion is the major source of PAHs in nearshore of South China Sea, and petroleum combustion is the main source of pyrolytic PAHs in rivers and estuary of Pearl River Delta according to PAHs diagnostic ratios. Petroleum PAHs are revealed have a high contribution to PAHs in Xijiang River, estuary and some stations in Zhujiang River. A comparison of data from study in 1997 with data from present study indicates that there is no clear change in the PAH concentration over time but the source of PAHs in Pearl River Delta have been change from a main coal combustion to petroleum combustion and being reflect in the sediments in rivers and estuary of Pearl River Delta where there have high sedimentation rate.

To understand the intercorrelation between the heterogeneity of kerogen and sorptive-desorptive characteristics, the sorption and desorption equilibria of phenanthrene and 1,3,5-trichlorobenzene were measured for three different types of coal (lignite, bark coal and fusinite) using a batch technique. The results show that the sorption and desorption of phenanthrene and 1,3,5-trichlorobenzene are highly nonlinear and significantly hysteretic. The observed sorptive differences among the three coals are explained viathe structural and chemical heterogeneity of kerogen.

The summer contamination of dissolved nonylphenols (NPs) and octylphenol (OP) in surface water of Zhujiang estuary and other rivers of Zhujiang Delta was analyzed. The result reveals that NPs concentration in The Pearl River remains20-40 ng/L, apart from the NPs concentrations of the mouth of The Pingzhou Channel the mouth of The Shawan Channel and Hutiaomen reaching a higher level of 98.84, 129.82 and 164.98 ng/L respectively. The Lingding Sea and open sea surface water keep at a lower level with the NPs concentration of10-14 ng/L. In terms of OP concentration in The Pearl River, any other sampling location is below LOD 2 ng/L, except for Baiertan, the mouth of The Shawan Channel and Hutiaomen being 2.89, 2.44, 2.12 ng/L respectively and inside Macao harbor being the highest level of 8.54 ng/L. The OP concentrations of The Lingding Sea and open sea surface water are lower than LOD 1 ng/L.

Six water samples were collected, and twenty-one compounds of organochlorine pesticides (OCPs) in surface water from the Pearl River Artery estuary were analyzed quantitatively, based on USEPA 8000 series methods and under quality assurance and quality control (QA/QC). The total (particulate plus dissolved phase) concentration of OCPs in surface water from the Pearl River Artery estuary in both high flow season and low flow season were 9.7 ng/L-26.3 ng/L and 41.7 ng/L-122.5 ng/L respectively. The concentration of total HCHs and total other OCPs was much higher than that of DDTs. The seasonality of the concentration of OCPs was significantly, and the level of OCPs in low flow season was higher than that of OCPs in high flow season. The spatial and temporal distribution of OCPs suggested that there were significant differences of OCPs between the East River (Dongjiang) network and Guangzhou channel and the nonpoint-source pollution of OCPs was found in the Pearl River Artery estuary, particularly in high flow season.

The coastal region off Macao is a known depositional zone for persistent organic pollutants (POPs) in the Pearl River Delta and Estuary of southern China and an important gateway for the regional contributions of contamination to the globe. This paper presents a comprehensive assessment of the input sources and transport pathways of polycyclic aromatic hydrocarbons (PAHs) found in the coastal sediments of Macao, based on measurements of 48 2-7 ring PAHs and 7 sulfur/oxygenated (S/O) PAH derivatives in 45 sediment, 13 street dust, and 68 aerosol samples. Total sediment PAHs concentrations ranged from 294 to 12741 ng/g, categorized as moderate contamination compared to other regions of Asia and the world. In addition, the PAH compounds appeared to be bound more strongly to aromatics-rich soot particles than to natural organic matter, implying a prevailing atmospheric transport route for PAHs to Macao's coast. Compositional analysis and principal component analysis (PCA) suggested that different classes of PAHs in the coastal sediments of Macao may have been derived from different input sources via various transport pathways. For example, alkylated and S/O PAHs were likely derived from fossil fuel leakage and transported to sediments by both aerosols particles and street runoff. High-molecular-weight parent PAHs were predominantly originated from automobile exhausts and distributed by direct and indirect atmospheric deposition. Low-molecular-weight parent PAHs, on the other hand, may have stemmed from lower temperature combustion and fossil fuel (such as diesel) spillage from ships and boats and were transported to sediments by river runoff or direct discharge as well as by air-water exchange.