Charring characteristics of atmospheric organic particulate matter in thermal analysis

被引:168
作者
Yu, JZ [1 ]
Xu, JH [1 ]
Yang, H [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
关键词
D O I
10.1021/es015540q
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The charring of organic materials during carbon analysis bythermal methods makes it difficult to differentiate elemental carbon (EC) from organic carbon (OC). Failure to correct for charring results in the overestimation of EC and the underestimation of OC. The charring characteristics and thermal behaviors of aerosol OC are studied by subjecting hexane and water extracts of ambient aerosols to various analysis conditions. The complete evolution of water-soluble organic carbon (WSOC) aerosol materials is found to require a temperature as high as 850 degreesC and the presence of oxygen. EC would be oxidized under these thermal conditions as well. As a result, thermal methods relying only on temperature for the differentiation of EC and OC would give unreliable OC and EC concentrations. Our investigation also reveals that WSOC accounts for a large fraction (13-66%) of charring, while hexane extractable organic compounds produce little charring. The extent of charring from WSOC, defined as the ratio between pyrolytically generated EC to the total WSOC, is found to increase with the WSOC loading in each analysis when the loadings are below a certain value, This ratio remains constant when the loadings are above this value. This may account for the high variability in the extent of charring among aerosol samples from different locations as well as among samples from a single location collected at different times. Charring is reduced if the residence time at each temperature step in a helium atmosphere is sufficiently long to allow for maximum C evolution at each step. Charring is also influenced by the presence of inorganic constituents such as ammonium bisulfate. For the few tested organic materials, it is observed that ammonium bisulfate enhances the charring of starch and cellulose but reduces the charring of levoglucosan.
引用
收藏
页码:754 / 761
页数:8
相关论文
共 25 条
[1]  
[Anonymous], P 2 INT CLEAN AIR C
[2]   ANALYSIS OF ORGANIC-MATTER FROM CLOUD PARTICLES [J].
BANK, S ;
CASTILLO, R .
GEOPHYSICAL RESEARCH LETTERS, 1987, 14 (03) :210-212
[3]  
Birch ME, 1998, ANALYST, V123, P851
[4]   Elemental carbon-based method for monitoring occupational exposures to particulate diesel exhaust [J].
Birch, ME ;
Cary, RA .
AEROSOL SCIENCE AND TECHNOLOGY, 1996, 25 (03) :221-241
[5]   AUTOMATED CARBON ANALYZER FOR PARTICULATE SAMPLES [J].
CADLE, SH ;
GROBLICKI, PJ ;
STROUP, DP .
ANALYTICAL CHEMISTRY, 1980, 52 (13) :2201-2206
[6]   Organic molecular tracers for particulate air pollution sources [J].
Cass, GR .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1998, 17 (06) :356-366
[7]   Comparison of IMPROVE and NIOSH carbon measurements [J].
Chow, JC ;
Watson, JG ;
Crow, D ;
Lowenthal, DH ;
Merrifield, T .
AEROSOL SCIENCE AND TECHNOLOGY, 2001, 34 (01) :23-34
[8]   THE DRI THERMAL OPTICAL REFLECTANCE CARBON ANALYSIS SYSTEM - DESCRIPTION, EVALUATION AND APPLICATIONS IN UNITED-STATES AIR-QUALITY STUDIES [J].
CHOW, JC ;
WATSON, JG ;
PRITCHETT, LC ;
PIERSON, WR ;
FRAZIER, CA ;
PURCELL, RG .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (08) :1185-1201
[9]   INTERLABORATORY ANALYSES OF CARBONACEOUS AEROSOL SAMPLES [J].
COUNTESS, RJ .
AEROSOL SCIENCE AND TECHNOLOGY, 1990, 12 (01) :114-121
[10]  
Goldberg E. D., 1985, Black carbon in the environment. Properties and distribution