Xiangying Zeng

Levels and distributions of organophosphate flame retardants and plasticizers in sediment from Taihu Lake, China

The concentrations and distribution of seven organophosphate flame retardants and plasticizers (OPs) were investigated in 28 sediment samples collected from Taihu Lake. The analytes were ultrasonically extracted, enriched using solid-phase extraction, and determined by gas chromatography-mass spectrometry. The results indicated that the analytes were all detected in the sediments. The total concentrations of seven OPs ranged from 3.38 to 14.25 µg/kg, and tris (2-chloroiso-propyl) phosphate (TCPP), tris (2-chloroethyl) phosphate (TCEP), and tris (2-butoxyethyl) phosphate (TBEP) were the dominant compounds, with concentrations ranging from<limit of quantification to 2.27 µg/kg, 0.62 to 3.17 µg/kg, and 1.03 to 5.00 µg/kg, respectively. The highest concentration of total assessed OPs (14.25 µg/kg) was found at GH-5, with tris (1,3-dichloro-2-propyl) phosphate (TDCPP) as the main component at the sampling site. This result implied that there is an obvious emission source nearby at Suzhou City; in addition, human activities also play an important role in the concentration of OPs in the sediment.

Synthetic musks in the aquatic environment and personal care products in Shanghai, China

The concentrations and distributions of six polycyclic musks and two nitro musks in Suzhou Creek, influent/effluent of a sewage treatment plant (STP), and household commodities were investigated and discussed in this study. The levels of 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexa-methylcyclopenta(g)-2-benzopyran (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN) in Suzhou Creek were 3-78 ng g(-1) (dry weight) and 2-31 ng g(-1) (dry weight) in sediments, while 20-93 ng l(-1) and 8-20 ng l(-1) in surface waters. The results indicated a low proportion of wastewater burden in this river. The concentrations of HHCB and AHTN in the effluent of the STP were 5- to 6-fold higher than those in Suzhou Creek. The amounts discharged into the aquatic environment from sewage in Shanghai are 1.26 t (HHCB) and 0.38 t (AHTN) in 2007, and the input into the STPs is estimated to be HHCB 0.2 g y(-1) and AHTN 0.06 g y(-1) per inhabitant, respectively. A broad concentration range of HHCB and AHTN could be observed in household commodities. The distributions are in accordance with the profiles of musks in aquatic environment, with HHCB and AHTN being the major components.

Levels and isomer profiles of Dechlorane Plus in the surface soils from e-waste recycling areas and industrial areas in South China

Dechlorane Plus (DP) is a highly chlorinated flame retardant. Levels of DP were measured in surface soils from e-waste recycling areas and industrial areas in South China. Higher DP levels were found in e-waste recycling areas (undetectable-47.4 ng/g) than those in industrial areas (0.0336-4.65 ng/g) in South China. The highest DP concentration (3327 ng/g) was found at the e-waste recycling site in Qingyuan, while DP levels fell dramatically with increasing distance away from the recycling site, suggesting that the e-waste recycling activities are an important source of DP emissions. The mean ratios of anti-DP to total DP (fanti) for different sampling areas ranged from 0.58 to 0.76 and showed no significant difference from the ratio for the technical DP products (t-test, p>0.05). Further intensive studies are needed to investigate the process of DP degradation and its degradation products.

Particle-bound Dechlorane Plus and polybrominated diphenyl ethers in ambient air around Shanghai, China

In present study, atmospheric particles from Shanghai, the biggest city and the most important industrial base in China, were analyzed for polybrominated diphenyl ethers (PBDEs) and Dechlorane Plus (DP). Concentrations of ∑(20)PBDEs and DP both exhibited the changing trend of industrial area > urban areas. Jiading District had the highest levels of particulate PBDEs and DP with values of 744 ± 152 pg/m(3) and 5.48 ± 1.28 pg/m(3), respectively. Compared with similar data in other areas of the world, PBDEs in Shanghai were at medium pollution level, while DP was at lower level, which reflected their different production and use in Shanghai. The results from multiple linear regression analysis suggested that deca-BDE mixture was the most important contributor of particulate PBDEs in Shanghai. The fractions of anti-DP showed no significant differences to those of the technical mixtures (p > 0.05), which suggested that no obviously stereoselective process occurred in ambient air around Shanghai.

Occurrence and distribution of organophosphate flame retardants/plasticizers in wastewater treatment plant sludges from the Pearl River Delta, China

Organophosphate esters (OPs) are widely used as flame retardants or plasticizers and are ubiquitously distributed in the environment. In the present study, the occurrence and distribution of 7 widely used OPs were analyzed in sludge samples collected from 19 municipal wastewater treatment plants in the Pearl River Delta, South China. All analytes were detected in these samples, and the total concentration of OPs ranged from 96.7 µg/kg to 1312.9 µg/kg dry weight, with a mean value of 420.1 µg/kg dry weight. In most sludge samples OPs exhibited a similar distribution pattern, for example, tris(2-butoxyethyl) phosphate (TBEP) and triphenyl phosphate (TPhP) were identified as the dominant compounds. However, the results also indicated significantly higher levels of OPs in specific sludges, such as tri-n-butyl phosphate (804.9 µg/kg), TBEP (783.7 µg/kg), TPhP (656.7 µg/kg), and tritolyl phosphate (265.0 µg/kg), which implied different discharge sources in the studied areas.

Distribution of polycyclic musks in surface sediments from the Pearl River Delta and Macao Coastal Region, South china.

Polycyclic musks were measured in surface sediments collected from the Pearl River Delta and Macao coastal region, South China, to investigate contamination from domestic sewage. Three polycyclic musk compounds-4-acetyl-1,1-dimethyl-6-tert-butylindan, 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran (HHCB), and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN)-were detected in sediment samples. Two polycyclic musks, HHCB and AHTN, were dominant components in sediment, consistent with the use pattern of polycyclic musks by perfume industries in the Pearl River Delta region. The concentrations of total polycyclic musks ranged from 5.76 to 167 microg/kg. Because of the large amount of domestic sewage and industrial wastewater discharged from the city of Guangzhou, the highest concentration of polycyclic musks was found in sediments from the Zhujiang River. The significant positive correlation between the HHCB to AHTN ratios and the concentrations of polycyclic musks suggested that the HHCB to AHTN ratio could be used as a tracer for source discrimination and for the degree of degradation in the environment.

Comparative study of the eliminating of waste gas containing toluene in twin biotrickling filters packed with molecular sieve and polyurethane foam.

Two kinds of packing materials, molecular sieve (MS) and polyurethane foam (PUF), were loaded into two identical biotrickling filters respectively to compare the microbial removal efficiency of waste gas containing toluene by seeding with same bacteria. The affecting parameters of the removal performance, such as gas flow rates, inlet toluene concentrations, periods of starvation, were investigated in detail in biotrickling filters. The results demonstrated that both of the packing materials exhibited high toluene degradation efficiency when the gas flow rates ranged from 100 L h(-1) to 600 L h(-1). For MS, the total maximum removal efficiency (RE) of toluene maintained 100% when the gas flow rates increased from 100 L h(-1) to 200 L h(-1) accompanied with the decrease of empty bed residence time (EBRT) from 266s to 133s. However, as for PUF, merely 97.64% RE was obtained at the gas flow rate of 100 L h(-1) and the EBRT of 266s. With further increasing the gas flow rates (to 600 L h(-1)) and decreasing the EBRTs (to 44s), both the total REs of toluene for MS and PUF decreased to 70.68% and 63.18%, respectively. When varying the inlet toluene concentrations, the REs for MS are able to maintain nearly 100% at the inlet concentration of 9.19 mg L(-1) or below, and with the maximum elimination capacity (EC) of 373.24 gm(-3)h(-1) (RE=100%) at the inlet concentration of 9.19 mg L(-1). Contrastively, the maximum EC of PUF was only 119.41 gm(-3)h(-1) (RE=56.66%) at the inlet concentration of 5.19 mg L(-1). As illustrated by different starvation period (2, 10 and 60 days), MS possessed shorter recovery time (9h for 2 days, 17 h for 10 days and 324 h for 60 days starvation, respectively) than PUF (14 h for 2 days, 24h for 10 days and 324 h for 60 days starvation, respectively). Based on its higher removal capacity of toluene and shorter recovery time, MS would be a better choice than PUF for packing material used for biotrickling filter.

Mutagenicity assessment of produced water during photoelectrocatalytic degradation.

Oilfield produced water was treated by photocatalysis, electro-oxidation, and photoelectrocatalysis, respectively. The chemical composition and toxicity of the raw effluent and treated products were assessed by chemical and mutagenicity analysis. The raw effluent exhibited mutagenic activity in both strains of Salmonella typhimurium. The lowest concentration of the dichloromethane extract capable of inducing a positive response in strains TA98 and TA100 were as low as 4 and 5 microg/plate, respectively. All three technologies could detoxify direct-acting mutagenic organic pollutants efficiently, although they could not completely eliminate mutagenicity in the water after 60 min of treatment. At equivalent doses, photoelectrocatalysis exhibited the greatest capability to reduce genotoxicity, whereas photocatalysis was the least effective and did not cause appreciable change in mutagenicity. The gas chromatography-mass spectrometry (GC-MS) analysis revealed that n-alkanes (259.4 ng/L) and phenolic compounds (2,501.4 ng/L) were the main organic constituents in the oilfield produced water. Thus, the results of both biological and chemical analysis indicate that photoelectocatalysis was the most effective technology for degradation of oilfield wastewater.

Source identification and health risk of polycyclic aromatic hydrocarbons associated with electronic dismantling in Guiyu town, South China

In this study the concentrations and distribution of sixteen polycyclic aromatic hydrocarbons (PAHs) were investigated in gas and total suspended particle (TSP) samples collected during daytime and night time. The sampling locations included an electronic waste dismantling workshop (EW), a plastic recycling workshop (PW) and a waste incineration field (WF) in Guiyu, China. A large residential area (RA) in this region was used as a control site. In the daytime, the highest concentration was found at WF (1041 ng m(-3)); while in the night time the highest concentration was found outside of EW (744 ng m(-3)). Comparison between work hours (daytime) and rest hours (night time) displayed that the total PAHs (gas+particulate phase) concentrations and the percentages of PAHs associated with TSP were higher at night than those in the daytime in all sampling workshops except WF. Source diagnostic-ratio analysis revealed that unwanted materials and smoldering honeycomb coals were the main sources of PAHs in EW, WF and PW. Benzo[a]pyrene equivalent [BaPeq] concentrations calculated by using the toxic equivalent factors [TEFs] suggested that the occupational exposure levels were not significantly high when compared with other occupational exposure. Additionally, our study suggested that the smoldering of unwanted materials could produce much more toxic PAHs compounds.

Levels of synthetic musk fragrances in human milk from three cities in the Yangtze River Delta in Eastern China

Synthetic musks are used as additives in many household products. After absorption into the human body, they accumulate and their concentrations in human milk reflect both the mother and her infants exposure level. Concentrations of four synthetic musks, musk xylene (1-tert-butyl-2,6-dimethyl-2,4,6-trinitrobenzene, MX), musk ketone (4-tert-butyl-2,6-dimethyl-3,5-dinitroacetophenone, MK), 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta[gamma]-2-benzopyran (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyl- 1,2,3,4-tetrahydronaphthalene (AHTN), were determined in human milk samples collected from Shanghai, Wuxi, and Shaoxing in Eastern China. The four synthetic musks were found in most samples analyzed, with HHCB the dominant component followed by MX. The median (mean) values for HHCB, AHTN, MX and MK concentrations were 63 (82), 5 (12), 17 (24) and 4 (9) ng/g lipid weight, respectively. These data suggested the total synthetic musk contamination was low, and the distribution percentage was HHCB > MX > AHTN approximately MK. The relative high ratio of nitro to polycylic musk indicated that nitro musks were still widely used. The musk concentrations in these cities were not significantly different from each other (p > 0.05). Principal components score plots were obtained, which showed similar exposure sources. The amount of total synthetic musks in human milk were not associated with mothers age, although HHCB was significantly correlated with AHTN (p < 0.05). Daily ingestion of HHCB, AHTN, MX and MK for infants from human milk were estimated as (2526 +/- 2926), (370 +/- 524), (7391 +/- 832), and (277 +/- 462) ng/day, respectively. Those doses were 1-2 orders of magnitude below the provisional tolerable daily intakes.