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« Previous AbstractAdsorption of multicomponent VOCs on various biomass-derived hierarchical porous carbon: A study on adsorption mechanism and competitive effect    Next AbstractAbundant Biogenic Oxygenated Organic Aerosol in Atmospheric Coarse Particles: Plausible Sources and Atmospheric Implications »

Environ Pollut


Title:Exploration of sources of OVOCs in various atmospheres in southern China
Author(s):Huang XF; Wang C; Zhu B; Lin LL; He LY;
Address:"Key Laboratory for Urban Habitat Environmental Science and Technology, School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China. Key Laboratory for Urban Habitat Environmental Science and Technology, School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen, 518055, China. Electronic address: hely@pku.edu.cn"
Journal Title:Environ Pollut
Year:2019
Volume:20190327
Issue:
Page Number:831 - 842
DOI: 10.1016/j.envpol.2019.03.106
ISSN/ISBN:1873-6424 (Electronic) 0269-7491 (Linking)
Abstract:"Oxygenated volatile organic compounds (OVOCs) are critical atmospheric ozone and secondary organic aerosol (SOA) precursors and radical sources, while understanding of OVOC sources in the atmosphere, especially with large anthropogenic emissions, still has large uncertainties. A high-sensitivity proton transfer reaction mass spectrometer (PTR-MS) was deployed in vastly different atmospheres in southern China, including an urban site (SZ-U), a regional site (NA-R), and a background site (NL-B). Four critical OVOCs, i.e., methanol, acetone, methyl ethyl ketone (MEK) and acetaldehyde, five groups of aromatic hydrocarbons, isoprene and acetonitrile were measured with a high time resolution. The featured relative abundance and diurnal variations of the OVOCs indicated that methanol, acetone and MEK had prominent contributions from urban industrial activities, while acetaldehyde was closely related to the photochemical formation at all three sites. The photochemical age-based parameterization method was improved locally and then applied to quantify different sources of daytime OVOCs: anthropogenic secondary and biogenic sources (together 60-73%) were always the dominant source for acetaldehyde in various atmospheres; in addition to a significant background for methanol, acetone and MEK, anthropogenic primary emissions (mostly industrial) were their dominant source at SZ-U (38-73%), while biogenic sources played the key role for them at NL-B (30-43%); biomass burning contributed a small fraction of 5-17% for the four OVOCs at the three sites"
Keywords:Air Pollutants/*analysis Atmosphere/*analysis/chemistry China Environmental Monitoring Human Activities Industrial Development Photochemical Processes Volatile Organic Compounds/*analysis OVOCs Ptr-ms Photochemical age Source apportionment;
Notes:"MedlineHuang, Xiao-Feng Wang, Chuan Zhu, Bo Lin, Li-Liang He, Ling-Yan eng England 2019/04/07 Environ Pollut. 2019 Jun; 249:831-842. doi: 10.1016/j.envpol.2019.03.106. Epub 2019 Mar 27"

 
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