| [1] Kanakidou M, Seinfeld J H, Pandis S N, et al. Organic aerosol and global climate modeling: a review [J]. Atmospheric Chemistry and Physics, 2005, 5(4): 1053-1123.
[2] Andreae M O, Crutzen P J. Atmospheric aerosols: biogeochemical sources and role in atmospheric chemistry [J]. Science, 1997, 276: 1052-1058.
[3] Zhang R, Suh I, Zhao J, et al. Atmospheric new particle formation enhanced by organic acids [J]. Science, 2004, 304: 1487-1490.
[4] Huang R J, Zhang Y L, Bozzetti C, et al. High secondary aerosol contribution to particulate pollution during haze events in China [J]. Nature, 2014, 514: 218-222.
[5] Zhang R. Getting to the critical nucleus of aerosol formation [J]. Science, 2010, 328: 1366-1367.
[6] Atkinson R, Baulch D L, Cox R A, et al. Evaluated kinetic and photochemical data for atmospheric chemistry: volume Ⅱ—gas phase reaction of organic species [J]. Atmospheric Chemistry and Physics, 2006, 6: 3625-4055.
[7] Nishino N, Arey J, Atkinson R. Formation yields of glyoxal and methylglyoxal from the gas phase OH radical-initiated reactions of toluene, xylenes, and trimethylbenzenes as a function of NO2 concentration [J]. Journal of Physical Chemistry: Atmospheres, 2010, 114: 10140-10147.
[8] Spaulding R S, Schade G W, Goldstein A H, et al. Characterization of secondary atmospheric photooxidation products: evidence for biogenic and anthropogenic sources [J]. Journal
of Geophysical Research, 2003, DOI: 10.1029/2002JD002478.
[9] Betterton E A, Hoffmann M R. Henry’s law constants of some environmentally important aldehydes [J]. Environmental Science and Technology, 1988, 22: 1415-1418.
[10] Blando J D, Turpin B J. Secondary organic aerosol formation in cloud and fog droplets: a literature evaluation of plausibility [J]. Atmospheric Environment, 2000, 34: 1623-1632.
[11] Lim Y B, Turpin B J. Chemical insights, explicit chemistry, and yields of secondary organic aerosol from OH radical oxidation of methylglyoxal and glyoxal in the aqueous phase [J]. Atmospheric Chemistry and Physics, 2013, 13: 8651-8667.
[12] Heald C L, Jacob D J, Park R J, et al. A large organic aerosol source in the free troposphere missing from current models [J]. Geophysical Research Letters, 2005, DOI:
10.1029/2005GL023831.
[13] Volkamer R, Jimenez J L, Martini F S, et al. Secondary organic aerosol formation from anthropogenic air pollution: rapid and higher than expected [J]. Geophysical Research Letters, 2006, DOI: 10.1029/2006GL026899.
[14] Kleinman L I, Daum P H, Lee Y N, et al. Aircraft observations of aerosol composition and ageing in New England and Mid-Atlantic States during the summer 2002 New England air quality study field campaign [J]. Journal of Geophysical Research, 2007, DOI: 10.1029/2006JD007786.
[15] Heald C L, Jacob D J, Turquety S, et al. Concentrations and sources of organic carbon aerosol in the free troposphere over North America [J]. Journal of Geophysical Research, 2006, DOI: 10.1029/2006JD007705.
[16] Fu T M, Jacob D J, Wittrock F, et al. Global budgets of atmospheric glyoxal and methylglyoxal, and implications for formation of secondary organic aerosols [J]. Journal of Geophysical Research: Atmospheres, 2008, DOI: 10.1029/2007JD009505.
[17] Kroll J H, Ng N L, Murphy S M, et al. Chamber studies of secondary organic aerosol growth by reactive uptake of simple carbonyl compounds [J]. Journal of Geophysical Research, 2005, 110: D23207.
[18] Zhao J, Levitt N P, Zhang R, et al. Heterogeneous reactions of methyglyoxal in acidic media: implications for secondary organic aerosol form [J]. Environmental Science and Technology, 2006, 40(24): 7682-7687.
[19] Gomez M E, Lin Y, Guo S, et al. Heterogeneous chemistry of glyoxal on acidic solutions: a oligomerization pathway for secondary organic aerosol formation [J]. Journal of Physical Chemistry: Atmospheres, 2015, 119: 4457-4463.
[20] Liu W, Zhang J, Zhang L, et al. Estimating contribution of indoor and outdoor sources to indoor carbonyl concentration in three urban areas of the United States [J]. Atmospheric Environment, 2006, 40: 2202-2214.
[21] Kalberer M, Paulsen D, Sax M, et al. Identification of polymers as major components of atmospheric organic aerosols [J]. Science, 2004, 303: 1659-1662.
[22] Guenther A B, Karl P T, Harley C, et al. Estimates of global terrestrial isoprene emissions using MEGAN [J]. Atmospheric Chemistry and Physics, 2006, 6: 3181-3210.
[23] Xiao Y, Jacob D J, Turquety S. Atmospheric acetylene and its relationship with CO as an indicator of air mass age [J]. Journal of Geophysical Research, 2007, DOI: 10.1029/2006JD08268.
[24] Yu J, Flagan R C, Seinfeld J H. Identification of products containing −COOH, −OH and −C=O in atmospheric oxidation of hydrocarbons [J]. Environmental Science and Technology,
1998, 32(16): 2357-2370.
[25] Fick J, Pommer C L, Andersson B. Effect of OH radicals, relative humidity, and time on the composition of the products formed in the ozonolysis of -pinene [J]. Atmospheric Environment, 2003, 37: 4087-4096.
[26] Guenther A B, Hewitt C N, Erickson D, et al. A global model of natural volatile organic compounds emissions [J]. Journal of Geophysical Research, 1995, 100(D5): 8873-8892.
[27] Liggio J, Li S M, Mclaren R, et al. Heterogeneous reactions of glyoxal on particulate matter: identification of acetals and sulfate esters [J]. Environmental Science and Technology, 2005, 391: 532-391, 541.
[28] Pankow J F. An absorption model of gas particle partitioning of organic compounds in the atmosphere [J]. Atmospheric Environment, 1994, 28(2): 185-188.
[29] Pankow J F. An absorption model of the gas aerosol partitioning involved in the formation of secondary organic aerosol [J]. Atmospheric Environment, 1994, 28(2): 189-193.
[30] Tsigaridis K, Kanakidou M. Global modeling of secondary organic aerosol in the troposphere: a sensitivity analysis [J]. Atmospheric Chemistry and Physics, 2003, 3: 1849-1869.
[31] Hennigan C J, Bergin M H, Dibb J E, et al. Enhanced secondary organic aerosol formation due to water uptake by fine particles [J]. Geophysical Research Letters, 2008, DOI:
10.1029/2008GL035046.
[32] Weber R, Sullivan A P, Peltier R E, et al. A study of secondary organic aerosol formation in the anthropogenic influenced southeastern United States [J]. Journal of Geophysical Research, 2007, DOI: 10.1029/2007JD008408.
[33] Kawamura K, Okuzawa K, Aggarwal S G, et al. Determination of gaseous and particulate carbonyls (glycolaldehyde, hydroxyacetone, glyoxal, methylglyoxal, nonanal and decanal) in the atmosphere at Mt. Tai [J]. Atmospheric Chemistry and Physics, 2013, 13: 5369-5380.
[34] Warneck P. In-cloud chemistry opens pathway to the formation of oxalic acid in the marine
atmosphere [J]. Atmospheric Environment, 2003, 37: 2423-2427.
[35] Carlton A G, Wiedinmyer C, Kroll J H. A review of secondary organic aerosol (SOA) formation from isoprene [J]. Atmospheric Chemistry and Physics, 2009, 9: 4987-5005.
[36] Carlton A G, Turpin B J, Lim H J, et al. Link between isoprene and secondary organic aerosol(SOA) : pyruvic acid oxidation yields low volatility organic acids in clouds [J]. Geophysical Research Letters, 2006, 33: L06822.
[37] Altieri K E, Carlton A G, Lim H J, et al. Evidence for oligomer formations in clouds: reactions of isoprene oxidation products [J]. Environmental Science and Technology, 2006, 40:
4956-4960.
[38] Lim H J, Carlton A G, Turpin B J. Isoprene forms secondary organic aerosol through cloud processing: model simulations [J]. Environmental Science and Technology, 2005, 39: 4441-4446.
[39] Matsumoto K, Kawai S, Igawa M. Dominant factors controlling concentrations of aldehydes in rain, fog, dew water, and in the gas phase [J]. Atmospheric Environment, 2005, 39: 7321-7329.
[40] Munger J W, Collett J, Daube J R, et al. Fog water chemistry at riverside California [J]. Atmospheric Environment, 1990, 24: 185-205.
[41] Buxton G V, Malone T N, Salmon G A. Oxidation of glyoxal initiated by ·OH in oxygenated aqueous solution [J]. Journal of the Chemical Society, Faraday Transactions, 1997, 93: 2889.
[42] Sareen N, Schwier A N, Shapiro E L, et al. Secondary organic material formed by methylglyoxal in aqueous aerosol mimics [J]. Atmospheric Chemistry and Physics, 2010, 10: 997-1016.
[43] Zhou X, Mopper K. Apparent partition coefficients of 15 carbonyl compounds between air and seawater and between air and freshwater: implications for air-sea exchange [J]. Environmental Science and Technology, 1990, 24: 1864-1869.
[44] Schwier A N, Sareen N, Mitroo D, et al. Glyoxal-methylglyoxal cross-reactions in secondary
organic aerosol formation [J]. Environmental Science and Technology, 2010, 44: 6174-6182.
[45] Jang M, Kamens R M. Atmospheric secondary aerosol formation by heterogeneous reactions of aldehydes in the presence of a sulfuric acid aerosol catalyst [J]. Environmental Science and Technology, 2001, 35(24): 4758-4766.
[46] Jang M, Czoschke N M, Lee S, et al. Heterogeneous atmospheric aerosol production by acidcatalyzed particle phase reaction [J]. Science, 2002, 298(5594): 814-817.
[47] Jang M, Caroll B, Chandromouli B, et al. Particle growth by acid-catalyzed heterogeneous reactions of organic carbonyls on preexisting aerosols [J]. Environmental Science and Technology, 2003, 37(17): 3828-3837.
[48] Schweitzer F, Magi L, Mirabel P, et al. Uptake rate measurements of methanesulfonic acid and glyoxal by aqueous droplets [J]. Journal of Geophysical Research: Atmospheres, 1998, 102(3): 593-600.
[49] Hastings W P, Koehler C A, Bailey E L, et al. Secondary organic aerosol formation by glyoxal hydration and oligomer formation: humidity effects and equilibrium shifts during
analysis [J]. Environmental Science and Technology, 2005, 39: 8728-8735.
[50] Loeffler K W, Koehler C A, Paul N M, et al. Oligomer formation in evaporating aqueous glyoxal and methylglyoxal solutions [J]. Environmental Science and Technology, 2006, 40: 6318-6323.
[51] 祁骞, 周学华, 王文兴. 二次有机气溶胶的水相形成研究[J]. 化学进展, 2014, 26(2/3): 458-466.
[52] De Haan D O, Corrigan A L, Tolbert M A, et al. Secondary organic aerosol formation by self-reactions of methyglyoxal and glyoxal in evaporating droplets [J]. Environmental Science
and Technology, 2009, 43: 8184-8190.
[53] Yasmeen F, Sauret N, Gal J F, et al. Characterization of oligomers from methylglyoxal under dark conditions: a pathway to produce secondary organic aerosol through cloud processing during nighttime [J]. Atmospheric Chemistry and Physics, 2010, 10: 3803-3812.
[54] Rincon A G, Guzman M I, Hoffmann M R, et al. Optical absorptivity versus molecular composition of model organic aerosol matter [J]. Journal of Physical Chemistry: Atmospheres,
2009, 113: 10512-10520.
[55] Andracchio A, Cavicchi C, Tonelli D, et al. A new approach for the fractionation of watersoluble organic carbon in atmospheric aerosols and cloud drops [J]. Atmospheric Environment, 2002, 36: 5097-5107.
[56] Kerminen V M, Lihavainen H, Komppula M, et al. Direct observational evidence linking atmospheric aerosol formation and cloud droplet activation [J]. Geophysical Research Letters, 2005, DOI: 10.1029/2005GL023130.
[57] Ortiz-Montalvo D L, Schwier A N, Lim Y B, et al. Volatility of methyglyoxal cloud SOA formed through OH radical oxidation and droplet evaporation [J]. Atmospheric Environment,
2016, 130: 142-152.
[58] McNeill V F. Aqueous organic chemistry in the atmosphere: sources and chemical processing of organic aerosols [J]. Environmental Science and Technology, 2015, 49: 1237-1244.
[59] Heiinigan C J, Bergin M H, Russell A G, et al. Gas/particle partitioning of water-soluble organic aerosol in Atlanta [J]. Atmospheric Chemistry and Physics, 2009, 9(11): 3613-3628.
[60] Waxman E M, Dzepina K, Ervens B, et al. Secondary organic aerosol formation from semiand intermediate-volatility organic compounds and glyoxal: relevance of O/C as a tracer for aqueous multiphase chemistry [J]. Geophysical Research Letters, 2013, 40(5): 978-982.
[61] Faust B C, Allen J M. Aqueous-phase photochemical formation of hydroxyl radical in authentic cloud waters and fog waters [J]. Environmental Science and Technology, 1993, 27: 1221-1224.
[62] Lim Y B, Tan Y, Perri M J, et al. Aqueous chemistry and its role in secondary organic aerosol(SOA) formation [J]. Atmospheric Chemistry and Physics, 2010, 10: 10521-10539.
[63] Arakaki T, Faust B C. Sources, sinks, and mechanisms of hydroxyl radical (OH) photo production and consumption in authentic acidic continental cloud waters from Whiteface Mountain, New York: the role of Fe(r) (r=Ⅱ, Ⅲ) photochemical cycle [J]. Journal of Geophysical Research, 1998, 103: 3487-3504.
[64] Hullar T, Anastasio C. Yields of hydrogen peroxide from the reaction of hydroxyl radical with organic compounds in solution and ice [J]. Atmospheric Chemistry and Physics, 2011, 11: 7209-7222.
[65] Dong M M, Rosario-Ortiz F L. Photochemical formation of hydroxyl radical from effluent organic matter [J]. Environmental Science and Technology, 2012, 46: 3788-3794.
[66] Volkamer R, Ziemann P J, Molina M J. Secondary organic aerosol formation from acetylene (C2H2): seed effect on SOA yield due to organic photochemistry in the aerosol aqueous
phase [J]. Atmospheric Chemistry and Physics, 2009, 9: 1907-1928.
[67] Monod A, Poulain L, Grybert S, et al. Kinetics of OH-initiated oxidation of oxygenated organic compounds in the aqueous phase: new rate constants, structure-activity relationships
and atmospheric implications [J]. Atmospheric Environment, 2005, 39: 7667-7688.
[68] Monod A, Doussin J F. Structure-activity relationship for the estimation of OH-oxidation rate constants of aliphatic organic compounds in the aqueous phase: alkanes, alcohols, organic acids and bases [J]. Atmospheric Environment, 2008, 42: 7611-7622.
[69] Kampf C J, Bonn B, Hoffmann T. Development and validation of a selective HPLC-ESIMS/ MS method for the quantification of glyoxal and methylglyoxal in atmospheric aerosols
(PM2.5) [J]. Analytical and Bioanalytical Chemistry, 2011, 401(10): 3115-3124.
[70] 邹婷, 冯艳丽, 付正茹, 等. 五氟苄基羟胺衍生与GC/MS 联用分析大气中的单羰基化合物和多羰基化合物[J]. 环境科学学报, 2012, 32(11): 2718-2724.
[71] Pang X B, Lewis A C, Hamilton J F. Determination of airborne carbonyls via pentafluorophenylhydrazine derivatisation by GC-MS and its comparison with HPLC method [J]. Talanta, 2011, 85: 406-414.
[72] Ho S S H, Yu J Z. Determination of airborne carbonyls: comparison of a thermal desorption/GC method with the standard DNPH/HPLC method [J]. Environmental Science and Technology, 2004, 38: 862-870.
[73] 冯艳丽, 牟翠翠, 付正茹, 等. 涂布2, 4- 二硝基苯肼的环形溶蚀器/滤膜系统和高效液相色谱法检测大气中二羰基化合物[J]. 分析化学, 2011, 39(11): 1653-1658.
[74] Temime B, Healy R M, Wenger J C, et al. A denuder-filter sampling technique for the detection of gas and particle phase carbonyl compounds [J]. Environmental Science and Technology, 2007, 41: 6514-6520.
[75] 任青青, 冯艳丽, 王芳, 等. 大气中气相和颗粒相羰基化合物的AD-FP系统采集和GC-MS分析[J]. 上海大学学报: 自然科学版, 2015, 21(6): 672-684.
[76] 王芳, 冯艳丽, 姜知明, 等. 上海大气中气相和颗粒相羰基化合物研究[J]. 科技导报, 2015, 33(6): 13-19.
[77] Ho S H H, Dai W T, Cao J J, et al. Seasonal variations of mono carbonyl and dicarbonyl in urban and sub-urban sites of Xi’an, China [J]. Environ Monit Assess, 2014, 186: 2835-2849.
[78] Dai W T, Ho S H H, Ho K F, et al. Characterization of particulate-phase high molecular weight monocarbonyls and dicarbonyls in urban atmosphere of Xi’an, China [J]. Aerosol and
Air Quality Research, 2012, 12: 892-901.
[79] Matsunaga S, Mochida M, Kawamura K. Variation on the atmospheric concentrations of biogenic carbonyl compounds and their removal processes in the northern forest at Moshiri, Hokkaido Island in Japan [J]. Journal of Geophysical Research: Atmosphere, 2004, 109(D4): 1-9.
[80] Blake R S, Monks P S, Ellis A M. Proton transfer reaction mass spectrometry: principles and applications [J]. Chemical Review, 2009, 109: 861-896.
[81] Macdonald S M, Oetjen H, Mahajan A S, et al. DOAS measurements of formaldehyde and glyoxal above a South-East Asian tropical rainforest [J]. Atmospheric Chemistry and Physics, 2012, 12: 5949-5962.
[82] Profeta L T M, Sams R L, Johnson T J, et al. Quantitative infrared intensity studies of vaporphase glyoxal, methylglyoxal, and 2,3-butanedione (diacetyl) with vibrational assignments [J]. Journal of Physical Chemistry: Atmospheres, 2012, 115: 9886-9900.
[83] Gomez A E, Moreno M V, Gligorovski S, et al. Characterization and calibration of active sampling solid phase microextraction applied to sensitive determination of gaseous
carbonyls [J]. Talanta, 2012, 88: 252-258.
[84] Pang X, Lewis A C, Rickard A R, et al. A smog chamber comparison of a microfluidic derivatisation measurement of gas-phase glyoxal and methylglyoxal with other analytical techniques [J]. Atmospheric Measurement Techniques, 2014, 7: 373-389.
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