Molecular characterization and spatial distribution of dicarboxylic acids and related compounds in fresh snow in China

2021 ◽  
pp. 118114
Author(s):  
Zhimin Zhang ◽  
Wanyu Zhao ◽  
Wei Hu ◽  
Junjun Deng ◽  
Lujie Ren ◽  
...  
2013 ◽  
Vol 122 (4) ◽  
pp. 651-665 ◽  
Author(s):  
Takayuki KURAMOTO ◽  
Daichi SUZUKI ◽  
Akihiko SASAKI ◽  
Keisuke SUZUKI

2009 ◽  
Vol 9 (6) ◽  
pp. 2097-2112 ◽  
Author(s):  
R. Winterhalter ◽  
M. Kippenberger ◽  
J. Williams ◽  
E. Fries ◽  
K. Sieg ◽  
...  

Abstract. Samples of freshly fallen snow were collected at the high alpine research station Jungfraujoch (Switzerland) in February and March 2006 and 2007, during the Cloud and Aerosol Characterization Experiments (CLACE) 5 and 6. In this study a new technique has been developed and demonstrated for the measurement of organic acids in fresh snow. The melted snow samples were subjected to solid phase extraction and resulting solutions analysed for organic acids by HPLC-MS-TOF using negative electrospray ionization. A series of linear dicarboxylic acids from C5 to C13 and phthalic acid, were identified and quantified. In several samples the biogenic acid pinonic acid was also observed. In fresh snow the median concentration of the most abundant acid, adipic acid, was 0.69 μg L−1 in 2006 and 0.70 μg L−1 in 2007. Glutaric acid was the second most abundant dicarboxylic acid found with median values of 0.46 μg L−1 in 2006 and 0.61 μg L−1 in 2007, while the aromatic acid phthalic acid showed a median concentration of 0.34 μg L−1 in 2006 and 0.45 μg L−1 in 2007. The concentrations in the samples from various snowfall events varied significantly, and were found to be dependent on the back trajectory of the air mass arriving at Jungfraujoch. Air masses of marine origin showed the lowest concentrations of acids whereas the highest concentrations were measured when the air mass was strongly influenced by boundary layer air.


2010 ◽  
Vol 10 (5) ◽  
pp. 2209-2225 ◽  
Author(s):  
S. Kundu ◽  
K. Kawamura ◽  
T. W. Andreae ◽  
A. Hoffer ◽  
M. O. Andreae

Abstract. Aerosols in the size class <2.5 μm (6 daytime and 9 nighttime samples) were collected at a pasture site in Rondônia, Brazil, during the intensive biomass burning period of 16–26 September 2002 as part of the Large-Scale Biosphere-Atmosphere Experiment in Amazonia – Smoke, Aerosols, Clouds, Rainfall and Climate (LBA-SMOCC). Homologous series of dicarboxylic acids (C2–C11) and related compounds (ketocarboxylic acids and α-dicarbonyls) were identified using gas chromatography (GC) and GC/mass spectrometry (GC/MS). Among the species detected, oxalic acid was found to be the most abundant, followed by succinic, malonic and glyoxylic acids. Average concentrations of total dicarboxylic acids, ketocarboxylic acids and α-dicarbonyls in the aerosol samples were 2180, 167 and 56 ng m−3, respectively. These are 2–8, 3–11 and 2–16 times higher, respectively, than those reported in urban aerosols, such as in 14 Chinese megacities. Higher ratios of dicarboxylic acids and related compounds to biomass burning tracers (levoglucosan and K+) were found in the daytime than in the nighttime, suggesting the importance of photochemical production. On the other hand, higher ratios of oxalic acid to other dicarboxylic acids and related compounds normalized to biomass burning tracers (levoglucosan and K+) in the daytime provide evidence for the possible degradation of dicarboxylic acids (≥C3) in this smoke-polluted environment. Assuming that these and related compounds are photo-chemically oxidized to oxalic acid in the daytime, and given their linear relationship, they could account for, on average, 77% of the formation of oxalic acid. The remaining portion of oxalic acid may have been directly emitted from biomass burning as suggested by a good correlation with the biomass burning tracers (K+, CO and ECa) and organic carbon (OC). However, photochemical production from other precursors could not be excluded.


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