A method for the in situ measurement of fine aerosol water content of ambient aerosols: The dry-ambient aerosol size spectrometer (DAASS)

被引:46
作者
Stanier, CO [1 ]
Khlystov, AY [1 ]
Chan, WR [1 ]
Mandiro, M [1 ]
Pandis, SN [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
D O I
10.1080/02786820390229525
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hygroscopic growth of atmospheric particles affects a number of environmentally important aerosol properties. Due to the hysteresis exhibited by the aerosol hygroscopic growth, the physical state of particles and the amount of aerosol water are uncertain within a wide range of relative humidities (RHs) found in the troposphere, leading to uncertainties in optical and chemical properties of the aerosol. Here we report the design and tests of an automated system that was built to assess the amount of aerosol water at atmospheric conditions. The system consists of two scanning mobility particle sizers (SMPS) and an aerodynamic particle sizer (APS) that measure the aerosol size distribution between 3 nm and 10 mum in diameter. The inlets of the instruments and their sheath air lines are equipped with computer-controlled valves that direct air through Nation dryers or bypass them. The Nation dryers dehydrate the air streams to below 30% RH at which point ambient particles are expected to lose most or all water. The switch between the dried and the ambient conditions occurs every 7 min and is synchronized with the scan times of the aerosol spectrometers. In this way the system measures alternatively dried (below 30% RH) and ambient aerosol size distributions. A comparison of the ambient RH and the dried RH size distributions and the corresponding integrated volume concentrations provides a measure of the physical state of particles and the amount of aerosol water. The aerosol water content can be treated as a growth factor or as an absolute quantity and can be calculated as a time series or as a function of RH (humidigram). When combined with aerosol composition measurements, the DAASS can be used to compare hygroscopic growth models and measurements.
引用
收藏
页码:215 / 228
页数:14
相关论文
共 48 条
[1]   Sources and composition of PM2.5 at the National Energy Technology Laboratory in Pittsburgh during July and August 2000 [J].
Anderson, RR ;
Martello, DV ;
Rohar, PC ;
Strazisar, BR ;
Tamilia, JP ;
Waldner, K ;
White, CM ;
Modey, WK ;
Mangelson, NF ;
Eatough, DJ .
ENERGY & FUELS, 2002, 16 (02) :261-269
[2]   Prediction of multicomponent inorganic atmospheric aerosol behavior [J].
Ansari, AS ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (05) :745-757
[3]   Water absorption by secondary organic aerosol and its effect on inorganic aerosol behavior [J].
Ansari, AS ;
Pandis, SN .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (01) :71-77
[4]   Concentration measurement and counting efficiency for the aerodynamic particle sizer 3320 [J].
Armendariz, AJ ;
Leith, D .
JOURNAL OF AEROSOL SCIENCE, 2002, 33 (01) :133-148
[5]   Hygroscopic growth of aerosol particles in the marine boundary layer over the Pacific and Southern Oceans during the First Aerosol Characterization Experiment (ACE 1) [J].
Berg, OH ;
Swietlicki, E ;
Krejci, R .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D13) :16535-16545
[6]   Deliquescence behavior of organic/ammonium sulfate aerosol [J].
Brooks, SD ;
Wise, ME ;
Cushing, M ;
Tolbert, MA .
GEOPHYSICAL RESEARCH LETTERS, 2002, 29 (19) :23-1
[7]   Sources of atmospheric carbonaceous particulate matter in Pittsburgh, Pennsylvania [J].
Cabada, JC ;
Pandis, SN ;
Robinson, AL .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2002, 52 (06) :732-741
[8]   WATER ACTIVITIES OF NH4NO3/(NH4)2SO4 SOLUTIONS [J].
CHAN, CK ;
FLAGAN, RC ;
SEINFELD, JH .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1992, 26 (09) :1661-1673
[9]   Thermodynamic modelling of aqueous aerosols containing electrolytes and dissolved organic compounds [J].
Clegg, SL ;
Seinfeld, JH ;
Brimblecombe, P .
JOURNAL OF AEROSOL SCIENCE, 2001, 32 (06) :713-738
[10]   The effect of water on gas-particle partitioning of secondary organic aerosol:: II.: m-xylene and 1,3,5-trimethylbenzene photooxidation systems [J].
Cocker, DR ;
Mader, BT ;
Kalberer, M ;
Flagan, RC ;
Seinfeld, JH .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (35) :6073-6085