Yuan Cheng

Prof. Dr. Yuan Cheng


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 August 2013 in Atmospheric Chemistry and Physics
Verified
Journal Article
Open access
PDF file
Yuan ChengYuan Cheng
Yuan Cheng
GEG. Engling
G. Engling
KHK.-B. He
K.-B. He
FDF.-K. Duan
F.-K. Duan
YMY.-L. Ma
Y.-L. Ma
RWR. J. Weber
R. J. Weber
Biomass burning, the largest global source of elemental carbon (EC) and primary organic carbon (OC), is strongly associated with many subjects of great scientific concern, such as secondary organic aerosol and brown carbon which exert important effects on the environment and on climate in particular. This study investigated the relationships between levoglucosan and other biomass burning tracers (i.e., water soluble potassium and mannosan) based on both ambient samples collected in Beijing and source samples. Compared with North America and Europe, Beijing was characterized by high ambient levoglucosan concentrations and low winter to summer ratios of levoglucosan, indicating significant impact of biomass burning activities throughout the year in Beijing. Comparison of levoglucosan and water soluble potassium (K+) levels suggested that it was acceptable to use K+ as a biomass burning tracer during summer in Beijing, while the contribution of fireworks to K+ could be significant during winter. Moreover, the levoglucosan to K+ ratio was found to be lower during the typical summer period (0.21 ± 0.16) compared with the typical winter period (0.51 ± 0.15). Levoglucosan correlated strongly with mannosan (R2 = 0.97) throughout the winter and the levoglucosan to mannosan ratio averaged 9.49 ± 1.63, whereas levoglucosan and mannosan exhibited relatively weak correlation (R2 = 0.73) during the typical summer period when the levoglucosan to mannosan ratio averaged 12.65 ± 3.38. Results from positive matrix factorization (PMF) model analysis showed that about 50% of the OC and EC in Beijing were associated with biomass burning processes. In addition, a new source identification method was developed based on the comparison of the levoglucosan to K+ ratio and the levoglucosan to mannosan ratio among different types of biomass. Using this method, the major source of biomass burning aerosol in Beijing was suggested to be the combustion of crop residuals, while the contribution from softwood burning was also non-negligible, especially in winter.

18 November 2011 in Atmospheric Chemistry and Physics
Verified
Journal Article
Open access
PDF file
Yuan ChengYuan Cheng
Yuan Cheng
KHK.-B. He
K.-B. He
MZM. Zheng
M. Zheng
FDF.-K. Duan
F.-K. Duan
ZDZ.-Y. Du
Z.-Y. Du
ARA. G. Russell
A. G. Russell
The mass absorption efficiency (MAE) of elemental carbon (EC) in Beijing was quantified using a thermal-optical carbon analyzer. The MAE measured at 632 nm was 8.45±1.71 and 9.41±1.92 m2 g−1 during winter and summer respectively. The daily variation of MAE was found to coincide with the abundance of organic carbon (OC), especially the OC to EC ratio, perhaps due to the enhancement by coating with organic aerosol (especially secondary organic aerosol, SOA) or the artifacts resulting from the redistribution of liquid-like organic particles during the filter-based absorption measurements. Using a converting approach that accounts for the discrepancy caused by measurements methods of both light absorption and EC concentration, previously published MAE values were converted to the equivalent-MAE, which is the estimated value if using the same measurement methods as used in this study. The equivalent-MAE was found to be much lower in the regions heavily impacted by biomass burning (e.g., below 2.7 m2 g−1 for two Indian cities). Results from source samples (including diesel exhaust samples and biomass smoke samples) also demonstrated that emissions from biomass burning would decrease the MAE of EC. Moreover, optical properties of water-soluble organic carbon (WSOC) in Beijing were presented. Light absorption by WSOC exhibited strong wavelength (λ) dependence such that absorption varied approximately as λ−7, which was characteristic of the brown carbon spectra. The MAE of WSOC (measured at 365 nm) was 1.79±0.24 and 0.71±0.20 m2 g−1 during winter and summer respectively. The large discrepancy between the MAE of WSOC during winter and summer was attributed to the difference in the precursors of SOA such that anthropogenic volatile organic compounds (AVOCs) should be more important as the precursors of SOA in winter. The MAE of WSOC in Beijing was much higher than results from the southeastern United States which were obtained using the same method as used in this study, perhaps due to the stronger emissions of biomass burning in China.

1 February 2016 in Atmospheric Environment
Verified
Journal Article
Closed access
Yuan ChengYuan Cheng
Yuan Cheng
KHKe-Bin He
Ke-Bin He
ZDZhen-Yu Du
Zhen-Yu Du
GEGuenter Engling
Guenter Engling
JLJiu-Meng Liu
Jiu-Meng Liu
RWRodney J. Weber
Rodney J. Weber

1 February 2015 in Environmental Pollution
Verified
Journal Article
Closed access
Yuan ChengYuan Cheng
Yuan Cheng
KHKebin He
Kebin He
ZDZhen-Yu Du
Zhen-Yu Du
MZMei Zheng
Mei Zheng
FDFeng-Kui Duan
Feng-Kui Duan
YMYong-Liang Ma
Yong-Liang Ma

1 June 2014 in Atmospheric Environment
Verified
Journal Article
Closed access
ZDZhenyu Du
Zhenyu Du
KHKebin He
Kebin He
Yuan ChengYuan Cheng
Yuan Cheng
FDFengkui Duan
Fengkui Duan
YMYongliang Ma
Yongliang Ma
RWRodney Weber
Rodney Weber

1 December 2012 in Atmospheric Environment
Verified
Journal Article
Closed access
HZHongliang Zhang
Hongliang Zhang
JLJingyi Li
Jingyi Li
QYQi Ying
Qi Ying
JYJianzhen Yu
Jianzhen Yu
DWDui Wu
Dui Wu
JJJingkun Jiang
Jingkun Jiang