Characterization of Organic Acids with Different Atmospheric Particle Sizes

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Atmospheric particulate samples were collected during January, February, April and May 2012, separately. Twenty-one fatty acids and seven dicarboxylic acids were measured by GC-MS. The results show that average mass concentrations of fatty acids are 809.24ng/m³, 545.34ng/m³, 386.96ng/m³ and dicarboxylic acids are 215.14 ng/m³, 156.45 ng/m³, 111.43 ng/m³ in PM10, PM2.5, PM1, respectively. Fatty acids and dicarboxylic acids concentrate mainly in the PM1. C11-C24 of fatty acids exhibit a significant even carbon predominances, but dicarboxylic acids present no parity preponderance. In the fatty acids, the concentration of hexadecanoic acid is the highest with that of octadecanoic acid followed; Nonandioic acid is the highest in dicarboxylic acids. The results of source apportionments indicate that the fatty acids are mainly related with human activities. Coal burning for heating is the most important source in January and February, but its contribution decreases sharply in April and May for fatty acids; The main source of dicarboxylic acids is photochemical reactions.

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14-22

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November 2012

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] Bi X., Simoneit B.R., Sheng G., Ma S., Fu J. Composition and major sources of organic compounds in urban aerosols. Atmospheric Research 88, 256-265(2008).

DOI: 10.1016/j.atmosres.2007.11.017

Google Scholar

[2] Kawamura K., Ikushima K. Seasonal changes in the distribution of dicarboxylic acids in the urban atmosphere. Environmental Science and Technology 27.2227-2235(1993).

DOI: 10.1021/es00047a033

Google Scholar

[3] Sempere K., Kawamura K. Comparative distributions of dicarboxylic acids and related polar compounds in snow, rain and aerosols from urban atmospheres [J].Atmos Environ. 28:449- 459(1994).

DOI: 10.1016/1352-2310(94)90123-6

Google Scholar

[4] X.L. Tang. Analysis and source appointment of extracal organic acids in TSP of Guangdong. Environment science in China.31(10):1592~1599(2001).

Google Scholar

[5] Limbeck A. Organic aids in continental background aerosols[J].Atmos Environ. 33: 1847一1852(2009).

Google Scholar

[6] Zheng M., Fang M., Wang F., To K.L. Characterization of the solvent extractable organic compounds in PM2.5 aerosols in Hong Kong[J].Atmospheric Environment, 34, p.2691~2702 (2000).

DOI: 10.1016/s1352-2310(99)00521-x

Google Scholar

[7] Yu S.,Zhang Y.H. Xie S.D. Zeng L.M. Zheng M.,Salmon Lynn.G.,Shao M.,Slanina Sjaak.Source apportionment of PM2.5 in Beijing by positive matrix factorization[J]. Atmospheric Environment, 40, 006, p.1526~1537(2003)

DOI: 10.1016/j.atmosenv.2005.10.039

Google Scholar

[8] Yan B., Zheng M., Hu Y., Ding X., Sullivan A.P, Weber R.J., Baek J., Edgerton E.S,Russell, A.G., Roadside, urban, and rural comparison of primary and secondary organic molecular markers in ambient PM2.5. Environmental Science and Technology 43, 42874293(2009).

DOI: 10.1021/es900316g

Google Scholar

[9] Decesari S., Facchini E., Matta F.,et al. Chemical features and seasonal variation of fine aerosol water-soluble organic compounds in the Po Valley, Italy. Atmospheric Environment. 35:3691-3699 (2001).

DOI: 10.1016/s1352-2310(00)00509-4

Google Scholar

[10] Li C.L., Fu J.M., Sheng G.Y., Bi X.H., Hao Y.M., Wang X.M., Mai B.X., Vertical distribution of PAHs in the indoor and outdoor PM2.5 in Guangzhou, China[J]. Building and Environment., 40,p.329~341(2005).

DOI: 10.1016/j.buildenv.2004.05.015

Google Scholar

[11] X.Q. Guo, Y.F. Wang, X.R.Li, Y.S. Wang. Characteristics of organic acids in PM2.5 in Beijing during Spring Festival of 2007. The 5th Mainland-Taiwan aresols Conference. Sep.2-6 2008,93~99.

Google Scholar

[12] Jiang Y L, Hou X M, Zhuang G S, et al. The sources and seasonal variations of organic compounds in PM2.5 in Beijing and Shanghai, Journal of Atmospheric Chemistry, 62(3): 175-192(2009).

DOI: 10.1007/s10874-010-9147-0

Google Scholar

[13] Wang Y., Zhuang G.S., Chen S. Characteristics and sources of formic , acetic and oxalic acids in PM2.5 and PM10 aerosols in Beijing, China [J]. Atmospheric Research,84(2):169-181(2007).

DOI: 10.1016/j.atmosres.2006.07.001

Google Scholar

[14] F.K. Duan, K.B.He, X.D. Liu. Characteristics of organic acids of PM2.5 in Beijing[J]. Environment science,29(6):1139-1145(2009).

Google Scholar

[15] C.S. Liu, X.R.Li, S.S. Zhang. X.Q. Guo. S.Y. Wang. Source appointment and seasonal variations of fatty acids in particulate matter of Beijing. Environment science in China. 29(7):673~678(2009).

Google Scholar

[16] Zheng M., Fang M., Wang F., et al. Characterization of the solvent extractable organic compounds in PM2.5 aerosols in Hong Kong [J]. Atmospheric Environment, 34(17):2691-2702 (2000).

DOI: 10.1016/s1352-2310(99)00521-x

Google Scholar

[17] Oliveira C., Alves C., et al. Seasonal distribution of polar organic compounds in the urban atmosphere of two large cities from the north and south of Europe[J]. Atmospheric Euviroumeut, 41( 27): 5555 5570(2007).

DOI: 10.1016/j.atmosenv.2007.03.001

Google Scholar

[18] Norton R. B., Roberts J. M., Huebert B. J. Tropospheric oxalate[J]. Geophys Res Let, 10:517~520(2003).

Google Scholar

[19] Oliveira C, Pio C., Alves C., et al. Seasonal distribution of polar organic compounds in the urban atmosphere of two large cities from the north and south of Europe [J]. Atmospheric Envirorunent,41(27):5555-5570(2007).

DOI: 10.1016/j.atmosenv.2007.03.001

Google Scholar