Characterization of carbonaceous materials in PM2.5 and PM10 size fractions in Morogoro, Tanzania, during 2006 wet season campaign

被引:7
作者
Mkoma, Stelyus L. [1 ]
Chi, Xuguang [2 ]
Maenhaut, Willy [2 ]
机构
[1] Sokoine Univ Agr, Fac Sci, Dept Phys Sci, Morogoro, Tanzania
[2] Univ Ghent, Inst Nucl Sci, Dept Analyt Chem, B-9000 Ghent, Belgium
关键词
Thermal-optical transmission; Total organic carbon analyser; Atmospheric aerosols; PM2.5; PM10; Sampling artifacts; SECONDARY ORGANIC AEROSOL; ELEMENTAL CARBON; CHEMICAL-COMPOSITION; MASS CLOSURE; EAST-AFRICA; SITES; URBAN; EC; OC;
D O I
10.1016/j.nimb.2010.03.001
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Atmospheric aerosol samples in PM10 and PM2.5 size fractions were collected in parallel at a rural site in Morogoro during wet season in March and April 2006. All samples were analysed for the particulate matter mass, for organic, elemental, and total carbon (OC. EC, and TC), and for water-soluble OC (WSOC). The average PM10 and PM2.5 mass concentrations and associated standard deviations were 14 +/- 13 mu g/m(3) and 7.3 +/- 4 mu g/m(3) respectively. On average, TC accounted for 33% of the PM10 mass and 44% of the PM2.5 mass for the campaign. The average OC/PM percentage ratios were 27% and 33% in PM10 and PM2.5 size fractions respectively and a larger fraction of the OC was water-soluble. The observed low EC/TC mean percentage ratios of 10-14% respectively for PM10 and PM2.5 fractions indicate that the carbonaceous aerosol originates mainly from biogenic aerosols and/or biomass burning. A simple source apportionment approach was used to apportion the OC to biofuel and charcoal burning. On average, 93% of the PM10 OC was attributed to biofuel and 7% to charcoal burning in the 2006 wet season campaign. However, it is suggested that a contribution to the OC at Morogoro could also come from other natural biogenic matter, and/or biomass burning aerosols. The results for the sources of OC at Morogoro should therefore be considered with great caution. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1665 / 1670
页数:6
相关论文
共 24 条
[1]   Emission of trace gases and aerosols from biomass burning [J].
Andreae, MO ;
Merlet, P .
GLOBAL BIOGEOCHEMICAL CYCLES, 2001, 15 (04) :955-966
[2]  
[Anonymous], 2020, Gothenburg Protocol to reduce transboundary air pollution, DOI DOI 10.5860/CHOICE.44-4512
[3]   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
[4]   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
[5]   Black carbon and total carbon measurements at urban and rural sites in Kenya, East Africa [J].
Gatari, MJ ;
Boman, J .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (08) :1149-1154
[6]   Intercomparison of methods to measure the mass concentration of the atmospheric aerosol during INTERCOMP2000 -: influence of instrumentation and size cuts [J].
Hitzenberger, R ;
Berner, A ;
Galambos, Z ;
Maenhaut, W ;
Cafmeyer, J ;
Schwarz, J ;
Müller, K ;
Spindler, G ;
Wieprecht, W ;
Acker, K ;
Hillamo, R ;
Mäkelä, T .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (38) :6467-6476
[7]  
Intergovernmental Panel on Climate Change, 2007, 4 IPCC
[8]   Sampling methods used for the collection of particle-phase organic and elemental carbon during ACE-Asia [J].
Mader, BT ;
Schauer, JJ ;
Seinfeld, JH ;
Flagan, RC ;
Yu, JZ ;
Yang, H ;
Lim, HJ ;
Turpin, BJ ;
Deminter, JT ;
Heidemann, G ;
Bae, MS ;
Quinn, P ;
Bates, T ;
Eatough, DJ ;
Huebert, BJ ;
Bertram, T ;
Howell, S .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (11) :1435-1449
[9]   Aerosol chemical mass closure during the EUROTRAC-2 AEROSOL Intercomparison 2000 [J].
Maenhaut, W ;
Schwarz, J ;
Cafmeyer, J ;
Chi, XG .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 2002, 189 :233-237
[10]  
MAENHAUT W, 2007, EV11 SPSD 2, P92