TY - JOUR
T1 - Accurate observation of black and brown carbon in atmospheric fine particles via a versatile aerosol concentration enrichment system (VACES)
AU - Kang, Huihui
AU - Shang, Xiaona
AU - Abdumutallip, Munira
AU - Chen, Yunqian
AU - Li, Ling
AU - Wang, Xiaofei
AU - Li, Chunlin
AU - Ouyang, Huiling
AU - Tang, Xu
AU - Wang, Lin
AU - Rudich, Yinon
AU - Chen, Jianmin
N1 - Publisher Copyright: © 2022 Elsevier B.V.
PY - 2022/9/1
Y1 - 2022/9/1
N2 - Carbonaceous aerosols (CAs) are major components of fine particulate matter (PM2.5) that dramatically influence the energy budget of Earth. However, accurate assessment of the climatic impacts of CAs is still challenging due to the large uncertainties remaining in the measurement of their optical properties. In this respect, a modified versatile aerosol concentration enrichment system integrated into optical instruments (VACES-OPTS) was set up to increase particle concentration and amplify signal-noise ratio during optical measurement. Based on the novel technique, this study was able to lower the detection limit of CAs by an order of magnitude under high temporal resolution (2 h) and small sampling flow (6 L min−1). Besides, stable and reliable optical data were obtained for absorption apportionment and source identification of black carbon (BC) and brown carbon (BrC). In the field application of the new system, high absorption coefficient of CAs in Shanghai, China was witnessed. Further analysis of the contribution of black carbon BC and BrC to light absorption revealed that BrC could account for over 15% of the total absorption at 370 nm. According to the potential source contribution function model (PSCF) classification, CAs with strong light absorption in urban Shanghai originated not only from highly polluted inland China but also from active marine ship emissions. [Display omitted] •The VACES-OPTS was developed to obtain reliable optical data of BC and BrC.•Accurate and high temporal resolution observations of BC and BrC was realized.•BrC accounted for over 15% of the total absorption at 370 nm in urban Shanghai.•Significant optical impacts of ship emissions on a coastal megacity were found.
AB - Carbonaceous aerosols (CAs) are major components of fine particulate matter (PM2.5) that dramatically influence the energy budget of Earth. However, accurate assessment of the climatic impacts of CAs is still challenging due to the large uncertainties remaining in the measurement of their optical properties. In this respect, a modified versatile aerosol concentration enrichment system integrated into optical instruments (VACES-OPTS) was set up to increase particle concentration and amplify signal-noise ratio during optical measurement. Based on the novel technique, this study was able to lower the detection limit of CAs by an order of magnitude under high temporal resolution (2 h) and small sampling flow (6 L min−1). Besides, stable and reliable optical data were obtained for absorption apportionment and source identification of black carbon (BC) and brown carbon (BrC). In the field application of the new system, high absorption coefficient of CAs in Shanghai, China was witnessed. Further analysis of the contribution of black carbon BC and BrC to light absorption revealed that BrC could account for over 15% of the total absorption at 370 nm. According to the potential source contribution function model (PSCF) classification, CAs with strong light absorption in urban Shanghai originated not only from highly polluted inland China but also from active marine ship emissions. [Display omitted] •The VACES-OPTS was developed to obtain reliable optical data of BC and BrC.•Accurate and high temporal resolution observations of BC and BrC was realized.•BrC accounted for over 15% of the total absorption at 370 nm in urban Shanghai.•Significant optical impacts of ship emissions on a coastal megacity were found.
UR - http://www.scopus.com/inward/record.url?scp=85130186476&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2022.155817
DO - 10.1016/j.scitotenv.2022.155817
M3 - مقالة
SN - 0048-9697
VL - 837
JO - The Science of the total environment
JF - The Science of the total environment
M1 - 155817
ER -