Shweta Yadav, Ankit Tandon, Arun K. Attri

  • School of Environmental Sciences, Jawaharlal Nehru University, New Delhi – 110067, India

Received: January 4, 2012
Revised: July 19, 2012
Accepted: July 19, 2012
Download Citation: ||https://doi.org/10.4209/aaqr.2012.01.0004  

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Cite this article:
Yadav, S., Tandon, A. and Attri, A.K. (2013). Monthly and Seasonal Variations in Aerosol Associated n-alkane Profiles in Relation to Meteorological Parameters in New Delhi, India. Aerosol Air Qual. Res. 13: 287-300. https://doi.org/10.4209/aaqr.2012.01.0004


 

ABSTRACT


A one-year extensive investigation to assess monthly and seasonal variations in the PM10 associated homologous series of n-alkane (C11–C35) profiles was carried out in New Delhi, India. Quantitative estimation of n-alkanes, involving 3–4 PM10 samples/month, was done by using thermal desorption gas chromatography mass spectrometry (TD-GC-MS). Significant seasonal variations were observed, both in mass concentrations (annual mean: 517 ± 256 ng/m3) and mass fractions (annual mean: 4368 ± 2067 ppm) of total n-alkanes (C11–C35). The impact of the Planetary Boundary Layer (PBL) on the n-alkane profiles was the most significant among all the meteorological parameters considered. A strong positive correlation (r = 0.84) between PM10 load (μg/m3) and mass concentrations of total n-alkanes (ng/m3) was observed; whereas a negative correlation (r = –0.72) was seen between the PM10 load and mass fractions of total n-alkanes (ppm). Annual mean values of the Carbon Preference Index (CPI) and Wax n-alkanes percentage (WNA%) stood at 2.2 ± 0.6 and 39 ± 10%, respectively. Established diagnostic tools indicated that during autumn, the dominant inputs of aerosol associated n-alkanes came from petrogenic (vehicular and industrial) emissions (72 ± 7%), with lesser contributions from biogenic activities (28 ± 7%). In other seasons, although petrogenic sources remained a dominant contributor (53 ± 6%–59 ± 14%), the contributions from biological sources were also comparable (41 ± 14%–47 ± 6%). Emissions of total n-alkanes from both petrogenic and biogenic sources were maximum during spring. In the rest of the months, small variations were observed in the emissions of total n-alkanes from petrogenic sources, whereas large variations were noted in the emissions from biogenic sources.


Keywords: Aerosols; n-alkanes; Seasonal variations; TD-GC-MS; Diagnostic parameters


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