Ling Chen

Find an error

Name:
Organization: Tongji University
Department: 1 State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering
Title:
Co-reporter:Ying Liu, Ling Chen, Jianfu Zhao, Yanping Wei, Zhaoyu Pan, Xiang-Zhou Meng, Qinghui Huang, Weiying Li
Organic Geochemistry 2010 Volume 41(Issue 4) pp:355-362
Publication Date(Web):April 2010
DOI:10.1016/j.orggeochem.2009.12.009
We quantified 18 polycyclic aromatic hydrocarbons (PAHs) in 54 surface soil samples covering an area of 6400 km2 in Shanghai. An isopleth map of total concentrations of the 18 PAHs, which was constructed using an ordinary Kriging approach with log transformed data, clarified the regional variability and identified regional hot spots in the urban and industrial areas of Shanghai. These hot spots all suffer from high PAH pollution, suggesting that local human activities (e.g., vehicular traffic, petrochemical industry and coal combustion) may be the main contributors. Coal or oil fired power plants and their locations seem to be a significant factor controlling the PAH concentrations in surface soil. The higher molecular weight PAHs are often accumulated near pollution sources and are more heterogeneous in Shanghai soil, because they are less easily transported and biodegraded than 2 ring PAHs. The total concentrations are not correlated with soil total organic carbon. We successfully applied hierarchical cluster analysis (HCA) and principal components analysis (PCA) based on a centered log ratio procedure to explore the characteristics and possible sources of soil PAHs. The high PAH contamination in the Shanghai surface soil is mainly attributed to the contribution of pyrogenic sources (vehicular traffic pollution and combustion of coal and biomass). Furthermore, we applied PAH percentages by ring number, isopleth maps of total concentrations of 18 PAHs and source diagnostic ratios of PAHs to help assign the pyrogenic sources in Shanghai soils. Such map based approaches have only rarely been applied in investigations published in Organic Geochemistry.
Co-reporter:Fan Huang;Xiangzhou Meng;Nan Xiang;Ying Liu ;Guangming Li
Chinese Journal of Chemistry 2010 Volume 28( Issue 8) pp:1475-1481
Publication Date(Web):
DOI:10.1002/cjoc.201090252

Abstract

A fast sample pretreatment method was developed to determine polybrominated diphenyl ethers (PBDEs) in polymers from waste electrical and electronic equipment (WEEE). Polymers were firstly prepared into "polymer film" to facilitate a complete Soxtec extraction. Then, three extraction parameters (including hot plate temperature, boiling time, and rinsing time) were optimized based on the recovery of target in reference polymer samples. The proposed method was successfully applied to the analysis of PBDEs in standard plastic materials from WEEE and the extraction yields of PBDEs ranged from 78.9% to 91.3%. The detection limits of PBDEs were 0.05–0.10 µg/g, indicating this method can be used as a quality assurance and quality control procedure of PBDEs in the production of electrical and electronic equipment.

Co-reporter:Xian Zhang;Rong Shen
Chinese Journal of Chemistry 2009 Volume 27( Issue 11) pp:2267-2272
Publication Date(Web):
DOI:10.1002/cjoc.200990380

Abstract

Health risk from exposure of perfluorochemicals to wildlife and human has been a subject of concern in many fields such as environmental ecology, toxicology, pathology and life sciences. The interactions of perfluorooctanoic acid (PFOA) with DNA were investigated by equilibrium dialysis, circular dichroism and isothermal titration calorimetry techniques under normal physiological conditions in vitro. The binding of PFOA to DNA was a non-covalent interaction and corresponded to the Langmuir adsorption isotherm in a two-step binding model, in which PFOA climbed along the backbones of DNA and then interacted with the homolateral bases via hydrophobic interactions. The saturation number of PFOA was calculated to be 0.64 per base-pair of DNA. Such an interaction caused the enhancement of circular dichroism spectra of DNA at both 245 and 275 nm, indicating the change of DNA conformation. The acidic media, low electrolyte and temperature ≦35°C are comparatively more favorable for PFOA binding to DNA. This work provides a useful experimental strategy for studying the interactions of perfluorochemicals with biomacromolecules, aiming at a better understanding of the gene toxicity mechanism of perfluorochemicals.

C N
Formamide, N,N-dimethyl-
12,15,48,51-Tetraoxahexacyclo[67.3.1.12,5.122,25.138,41.158,61]heptaheptacontane-13,49-dimethanol, 9,18,26,30,33,37,45,54,62,66,69-undecamethyl-, (1S,2S,5S,9R,13R,18R,22S,25S,26R,30S,33S,37R,38S,41S,45R,49R,54R,58S,61S,62R,66S,69R)-
2,3',4,4',5-Pentachlorobiphenyl ether
2,3,4,6-Tetrabromodiphenyl Ether in Isooctane
1,3-DIBROMO-5-(4-BROMOPHENOXY)BENZENE
Benzene,1,2,3-tribromo-5-(3,4-dibromophenoxy)-
Benzene,1,3,5-tribromo-2-(3,4-dibromophenoxy)-