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Trace metals in atmospheric fine particles in one industrial urban city: Spatial variations, sources, and health implications 被引量:25

Trace metals in atmospheric fine particles in one industrial urban city: Spatial variations, sources, and health implications
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摘要 Trace metals in PM2.5 were measured at one industrial site and one urban site during September, 2010 in Ji'nan, eastern China. Individual aerosol particles and PM2.5 samples were collected concurrently at both sites. Mass concentrations of eleven trace metals (i.e., Al, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Sr, Ba, and Pb) and one metalloid (i.e., As) were measured by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The result shows that mass concentrations of PM2.5 (130μg/m3) and trace metals (4.03 μg/m3) at the industrial site were 1.3 times and 1.7 times higher than those at the urban site, respectively, indicating that industrial activities nearby the city can emit trace metals into the surrounding atmosphere. Fe concentrations were the highest among all the measured trace metals at both sites, with concentrations of 1.04 ixg/m 3 at the urban site and 2.41 Itg/m3 at the industrial site, respectively. In addition, Pb showed the highest enrichment factors at both sites, suggesting the emissions from anthropogenic activities existed around the city. Correlation coefficient analysis and principal component analysis revealed that Cu, Fe, Mn, Pb, and Zn were originated from vehicular traffic and industrial emissions at both sites; As, Cr, and part of Pb from coal-fired power plant; Ba and Ti from natural soil. Based on the transmission electron microscopy analysis, we found that most of the trace metals were internally mixed with secondary sulfate/organic particles. These internally mixed trace metals in the urban air may have different toxic abilities compared with externally mixed trace metals. Trace metals in PM2.5 were measured at one industrial site and one urban site during September, 2010 in Ji'nan, eastern China. Individual aerosol particles and PM2.5 samples were collected concurrently at both sites. Mass concentrations of eleven trace metals (i.e., Al, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Sr, Ba, and Pb) and one metalloid (i.e., As) were measured by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The result shows that mass concentrations of PM2.5 (130μg/m3) and trace metals (4.03 μg/m3) at the industrial site were 1.3 times and 1.7 times higher than those at the urban site, respectively, indicating that industrial activities nearby the city can emit trace metals into the surrounding atmosphere. Fe concentrations were the highest among all the measured trace metals at both sites, with concentrations of 1.04 ixg/m 3 at the urban site and 2.41 Itg/m3 at the industrial site, respectively. In addition, Pb showed the highest enrichment factors at both sites, suggesting the emissions from anthropogenic activities existed around the city. Correlation coefficient analysis and principal component analysis revealed that Cu, Fe, Mn, Pb, and Zn were originated from vehicular traffic and industrial emissions at both sites; As, Cr, and part of Pb from coal-fired power plant; Ba and Ti from natural soil. Based on the transmission electron microscopy analysis, we found that most of the trace metals were internally mixed with secondary sulfate/organic particles. These internally mixed trace metals in the urban air may have different toxic abilities compared with externally mixed trace metals.
出处 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2014年第1期205-213,共9页 环境科学学报(英文版)
基金 supported by the National Basic Research Program(973)of China(No.2011CB403401) the National Natural Science Foundation of China(No.41105088,41275141) the Natural Science Foundation of Shandong Province(No.ZR2011DQ001) the State Key Laboratory for Coal Resources and Safe Mining(No.SKLCRSM11KFB03)
关键词 trace metals PM2.5 enrichment factors principal component analysis (PCA) industrial sources trace metals PM2.5 enrichment factors principal component analysis (PCA) industrial sources
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