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Gaseous pollutants in Beijing urban area during the heating period 2007-2008: variability, sources, meteorological, and chemical impacts.

Authors :
Lin, W.
Xu, X.
Ge, B.
Liu, X.
Source :
Atmospheric Chemistry & Physics; 2011, Vol. 11 Issue 15, p8157-8170, 14p
Publication Year :
2011

Abstract

Gaseous pollutants, NO<subscript>y</subscript>/NO<subscript>x</subscript>, SO<subscript>2</subscript>, CO, and O<subscript>3</subscript>, were measured at an urban site in Beijing from 17 November 2007 to 15 March 2008. The average concentrations (with ±1σ) of NO<subscript>y</subscript>, SO<subscript>2</subscript>, CO, and O<subscript>3</subscript> were 29.0±2.7 ppb, 33.7±1.4 ppb, 62.7±4.0 ppb, 72.8±4.5 ppb, 1.99±0.13 ppm, 31.9±2.0 ppb, and 11.9±0.8 ppb, respectively, with hourly maxima of 200.7 ppb, 113.5 ppb, 303.9 ppb, 323.2 ppb, 15.06 ppm, 147.3 ppb, and 69.7 ppb, respectively. The concentrations of the pollutants show "saw-toothed" patterns, which are attributable mainly to changes in wind direction and speed. The frequency distributions of the hourly mean concentrations of NO<subscript>y</subscript>, SO<subscript>2</subscript>, CO, and O<subscript>3</subscript> can all be decomposed in the two Lorentz curves, with their peak concentrations representing background levels under different conditions. During the observation period, the average ratio NO<subscript>x</subscript>/NO<subscript>y</subscript> was 0.86±0.10, suggesting that the gaseous pollutants in Beijing in winter are mainly from local emissions. Data of O<subscript>3</subscript>, NO<subscript>z</subscript>, and NO<subscript>x</subscript>/NO<subscript>y</subscript> indicate that photochemistry can take place in Beijing even in the cold winter period. Based on the measurements of O<subscript>3</subscript>, NO<subscript>x</subscript>, and NO<subscript>y</subscript>, ozone production efficiency (OPE) is estimated to be in the range of 0-8.9 (ppb ppb<superscript>-1</superscript>) with the mean(±1σ) and median values being 1.1(±1.6) and 0.5 (ppb ppb<superscript>-1</superscript>), respectively, for the winter 2007--2008 in Beijing. This low OPE would cause a photochemical O<subscript>3</subscript> source of 5 ppb day<superscript>-1</superscript>, which is small but significant for surface O<subscript>3</subscript> in winter in Beijing. Downward transport of O<subscript>3</subscript>-rich air from the free troposphere is the more important factor for the enhancement of the O<subscript>3</subscript> level in the surface layer, while high NO level for the destruction of O<subscript>3</subscript>. The concentrations of SO<subscript>2</subscript>, CO, and NO<subscript>x</subscript> are strongly correlated among each other, indicating that they are emitted by some common sources. Multiple linear regression analysis is applied to the concentrations of NO<subscript>y</subscript>, SO<subscript>2</subscript>, and CO and empirical equations are obtained for the NO<subscript>3</subscript> concentration. Based the equations, the relative contributions from mobile and point sources to NO<subscript>y</subscript> is estimated to be 66±30% and 40±16%, respectively, suggesting that even in the heating period, mobile sources in Beijing contribute more to NO<subscript>y</subscript> than point sources. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16807316
Volume :
11
Issue :
15
Database :
Complementary Index
Journal :
Atmospheric Chemistry & Physics
Publication Type :
Academic Journal
Accession number :
66465906
Full Text :
https://doi.org/10.5194/acp-11-8157-2011