Phase transitions of malonic and oxalic acid aerosols

被引:93
作者
Braban, CF [1 ]
Carroll, MF [1 ]
Styler, SA [1 ]
Abbatt, JPD [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
关键词
D O I
10.1021/jp034483f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Atmospheric aerosol has been shown to contain an organic component that includes a significant fraction of small dicarboxylic acids, particularly in the urban environment. As an initial step toward understanding the phase in which particles may exist, a detailed study into the phase transitions of malonic and oxalic acid aerosols has been carried out. Both the aerosol phase transitions (deliquescence and efflorescence) and bulk solution properties (equilibrium water vapor pressure and the solubility and freezing curves of the aqueous solutions) are reported. An aerosol flow tube-FTIR and a static mode chamber-FTIR have been used to identify particulate phase transitions. In the latter the particles can be observed under ice-supersaturated conditions, allowing investigation of behavior at subeutectic temperatures. We report that both malonic and oxalic acid aerosols sustain a substantial level of solute supersaturation before efflorescence occurs, whereas deliquescence occurs at the thermodynamically predicted relative humidity. At room temperature, malonic acid efflorescence is observed at RH = 6% +/- 3% and oxalic acid efflorescence occurs at RH less than or equal to 5%. Malonic acid particles deliquesce between 69% and 91% RH over the temperature range 293-252 K, and for oxalic acid conditions close to 100% RH are required. We report the first observation of the phase transition of oxalic acid between the anhydrous and dihydrate form and discuss our results in the context of recently published data.
引用
收藏
页码:6594 / 6602
页数:9
相关论文
共 29 条
[1]   The aqueous pressure of some hydrated crystals. Oxalic acid, strontium chloride and sodium sulfate. [J].
Baxter, GP ;
Lansing, JE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1920, 42 :419-426
[2]   Deliquescence of ammonium sulfate particles at sub-eutectic temperatures [J].
Braban, CF ;
Abbatt, JPD ;
Cziczo, DJ .
GEOPHYSICAL RESEARCH LETTERS, 2001, 28 (20) :3879-3882
[3]   Deliquescence behavior of organic/ammonium sulfate aerosol [J].
Brooks, SD ;
Wise, ME ;
Cushing, M ;
Tolbert, MA .
GEOPHYSICAL RESEARCH LETTERS, 2002, 29 (19) :23-1
[4]   The effects of organic species on the hygroscopic behaviors of inorganic aerosols [J].
Choi, MY ;
Chan, CK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (11) :2422-2428
[5]   A study of the ability of pure secondary organic aerosol to act as cloud condensation nuclei [J].
Cruz, CN ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (15) :2205-2214
[6]   Infrared observations of the response of NaCl, MgCl2, NH4HSO4, and NH4NO3 aerosols to changes in relative humidity from 298 to 238 K [J].
Cziczo, DJ ;
Abbatt, JPD .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (10) :2038-2047
[7]   Infrared spectroscopy of model tropospheric aerosols as a function of relative humidity: Observation of deliquescence and crystallization [J].
Cziczo, DJ ;
Nowak, JB ;
Hu, JH ;
Abbatt, JPD .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D15) :18843-18850
[8]   Deliquescence, efflorescence, and supercooling of ammonium sulfate aerosols at low temperature: Implications for cirrus cloud formation and aerosol phase in the atmosphere [J].
Cziczo, DJ ;
Abbatt, JPD .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D11) :13781-13790
[9]   Infrared spectroscopic study of the low-temperature phase behavior of ammonium sulfate [J].
Fortin, TJ ;
Shilling, JE ;
Tolbert, MA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D10)
[10]   Heterogeneous nucleation of the efflorescence of (NH4)2SO4 particles internally mixed with Al2O3, TiO2, and ZrO2 [J].
Han, JH ;
Martin, ST .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D3) :3543-3553