Formation of secondary organic aerosols from gas-phase emissions of heated cooking oils
Formation of secondary organic aerosols from gas-phase emissions of heated cooking oils
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加热食用油的气相排放形成二次有机气溶胶
DOI:
10.5194/acp-17-7333-2017
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发表时间:
2017-06
影响因子:
6.3
通讯作者:
Chan Chak K.
中科院分区:
文献类型:
--
作者:
Liu Tengyu;Li Zijun;Chan ManNin;Chan Chak K.
Abstract. Cooking emissions can potentially contribute to secondary organic aerosol (SOA) but remain poorly understood. In this study, formation of SOA from gas-phase emissions of five heated vegetable oils (i.e., corn, canola, sunflower, peanut and olive oils) was investigated in a potential aerosol mass (PAM) chamber. Experiments were conducted at 19–20 °C and 65–70 % relative humidity (RH). The characterization instruments included a scanning mobility particle sizer (SMPS) and a high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS). The efficiency of SOA production, in ascending order, was peanut oil, olive oil, canola oil, corn oil and sunflower oil. The major SOA precursors from heated cooking oils were related to the content of monounsaturated fat and omega-6 fatty acids in cooking oils. The average production rate of SOA, after aging at an OH exposure of 1. 7 × 1011 molecules cm−3 s, was 1. 35 ± 0. 30 µg min−1, 3 orders of magnitude lower compared with emission rates of fine particulate matter (PM2. 5) from heated cooking oils in previous studies. The mass spectra of cooking SOA highly resemble field-derived COA (cooking-related organic aerosol) in ambient air, with R2 ranging from 0.74 to 0.88. The average carbon oxidation state (OSc) of SOA was −1.51 to −0.81, falling in the range between ambient hydrocarbon-like organic aerosol (HOA) and semi-volatile oxygenated organic aerosol (SV-OOA), indicating that SOA in these experiments was lightly oxidized.
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影响因子:
6.3
作者:
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通讯作者:
J. Mao;X. Ren;W. Brune;J. Olson;J. Crawford;A. Fried;L. Huey;R. Cohen;B. Heikes;H. Singh
DOI:
--
发表时间:
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期刊:
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影响因子:
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