TY - JOUR
T1 - Sources and formation of carbonaceous aerosols in Xi'an, China
T2 - Primary emissions and secondary formation constrained by radiocarbon
AU - Ni, Haiyan
AU - Huang, Ru-Jin
AU - Cao, Junji
AU - Guo, Jie
AU - Deng, Haoyue
AU - Dusek, Ulrike
PY - 2019/12/20
Y1 - 2019/12/20
N2 - To investigate the sources and formation mechanisms of carbonaceous aerosols, a major contributor to severe particulate air pollution, radiocarbon (C-14) measurements were conducted on aerosols sampled from November 2015 to November 2016 in Xi'an, China. Based on the C-14 content in elemental carbon (EC), organic carbon (OC) and water-insoluble OC (WIOC), contributions of major sources to carbonaceous aerosols are estimated over a whole seasonal cycle: primary and secondary fossil sources, primary biomass burning, and other non-fossil carbon formed mainly from secondary processes. Primary fossil sources of EC were further sub-divided into coal and liquid fossil fuel combustion by complementing C-14 data with stable carbon isotopic signatures.The dominant EC source was liquid fossil fuel combustion (i.e., vehicle emissions), accounting for 64 % (median; 45 %-74 %, interquartile range) of EC in autumn, 60 % (41 %-72 %) in summer, 53 % (33 %-69 %) in spring and 46 % (29 %-59 %) in winter. An increased contribution from biomass burning to EC was observed in winter (similar to 28 %) compared to other seasons (warm period; similar to 15 %). In winter, coal combustion (similar to 25 %) and biomass burning equally contributed to EC, whereas in the warm period, coal combustion accounted for a larger fraction of EC than biomass burning. The relative contribution of fossil sources to OC was consistently lower than that to EC, with an annual average of 47 +/- 4 %. Non-fossil OC of secondary origin was an important contributor to total OC (35 +/- 4 %) and accounted for more than half of non-fossil OC (67 +/- 6 %) throughout the year. Secondary fossil OC (SOCfossil) concentrations were higher than primary fossil OC (POCfossil) concentrations in winter but lower than POCfossil in the warm period.Fossil WIOC and water-soluble OC (WSOC) have been widely used as proxies for POCfossil and SOCfossil, respectively. This assumption was evaluated by (1) comparing their mass concentrations with POCfossil and SOCfossil and (2) comparing ratios of fossil WIOC to fossil EC to typical primary OC-to-EC ratios from fossil sources including both coal combustion and vehicle emissions. The results suggest that fossil WIOC and fossil WSOC are probably a better approximation for primary and secondary fossil OC, respectively, than POCfossil and SOCfossil estimated using the EC tracer method.
AB - To investigate the sources and formation mechanisms of carbonaceous aerosols, a major contributor to severe particulate air pollution, radiocarbon (C-14) measurements were conducted on aerosols sampled from November 2015 to November 2016 in Xi'an, China. Based on the C-14 content in elemental carbon (EC), organic carbon (OC) and water-insoluble OC (WIOC), contributions of major sources to carbonaceous aerosols are estimated over a whole seasonal cycle: primary and secondary fossil sources, primary biomass burning, and other non-fossil carbon formed mainly from secondary processes. Primary fossil sources of EC were further sub-divided into coal and liquid fossil fuel combustion by complementing C-14 data with stable carbon isotopic signatures.The dominant EC source was liquid fossil fuel combustion (i.e., vehicle emissions), accounting for 64 % (median; 45 %-74 %, interquartile range) of EC in autumn, 60 % (41 %-72 %) in summer, 53 % (33 %-69 %) in spring and 46 % (29 %-59 %) in winter. An increased contribution from biomass burning to EC was observed in winter (similar to 28 %) compared to other seasons (warm period; similar to 15 %). In winter, coal combustion (similar to 25 %) and biomass burning equally contributed to EC, whereas in the warm period, coal combustion accounted for a larger fraction of EC than biomass burning. The relative contribution of fossil sources to OC was consistently lower than that to EC, with an annual average of 47 +/- 4 %. Non-fossil OC of secondary origin was an important contributor to total OC (35 +/- 4 %) and accounted for more than half of non-fossil OC (67 +/- 6 %) throughout the year. Secondary fossil OC (SOCfossil) concentrations were higher than primary fossil OC (POCfossil) concentrations in winter but lower than POCfossil in the warm period.Fossil WIOC and water-soluble OC (WSOC) have been widely used as proxies for POCfossil and SOCfossil, respectively. This assumption was evaluated by (1) comparing their mass concentrations with POCfossil and SOCfossil and (2) comparing ratios of fossil WIOC to fossil EC to typical primary OC-to-EC ratios from fossil sources including both coal combustion and vehicle emissions. The results suggest that fossil WIOC and fossil WSOC are probably a better approximation for primary and secondary fossil OC, respectively, than POCfossil and SOCfossil estimated using the EC tracer method.
KW - NON-FOSSIL SOURCES
KW - PM2.5 CHEMICAL-COMPOSITION
KW - REGIONAL BACKGROUND SITE
KW - SOLUBLE ORGANIC-CARBON
KW - WINTER HAZE EPISODE
KW - SOURCE APPORTIONMENT
KW - ELEMENTAL CARBON
KW - ATMOSPHERIC AEROSOLS
KW - SEASONAL-VARIATIONS
KW - PARTICULATE MATTER
U2 - 10.5194/acp-19-15609-2019
DO - 10.5194/acp-19-15609-2019
M3 - Article
SN - 1680-7316
VL - 19
SP - 15609
EP - 15628
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 24
ER -