PM2.5 and PM10 concentrations from the Qalabotjha low-smoke fuels macro-scale experiment in South Africa

Citation
Jp. Engelbrecht et al., PM2.5 and PM10 concentrations from the Qalabotjha low-smoke fuels macro-scale experiment in South Africa, ENV MON ASS, 69(1), 2001, pp. 1-15
Citations number
11
Categorie Soggetti
Environment/Ecology
Journal title
ENVIRONMENTAL MONITORING AND ASSESSMENT
ISSN journal
01676369 → ACNP
Volume
69
Issue
1
Year of publication
2001
Pages
1 - 15
Database
ISI
SICI code
0167-6369(200106)69:1<1:PAPCFT>2.0.ZU;2-D
Abstract
This article presents results from the particulate monitoring campaign cond ucted at Qalabotjha in South Africa during the winter of 1997. Combustion o f D-grade domestic coal and low-smoke fuels were compared in a residential neighborhood to evaluate the extent of air quality improvement by switching household cooking and heating fuels. Comparisons are drawn between the gra vimetric results from the two types of filter substrates (Teflon-membrane a nd quartz-fiber) as well as between the integrated and continuous samplers. It is demonstrated that the quartz-fiber filters reported 5 to 10% greater particulate mass than the Teflon-membrane filters, mainly due to the adsor ption of organic gases onto the quartz-fiber filters. Due to heating of sam pling stream to 50 degreesC in the TEOM continuous sampler and the high vol atile content of the samples, approximately 15% of the particulate mass was lost during sampling. The USEPA 24-hr PM2.5 and PM10 National Ambient Air Quality Standards (NAAQS) of 65 mug m(-3) and 150 mug m(-3), respectively, were exceeded on several occasions during the 30-day field campaign. Averag e PM concentrations are highest when D-grade domestic coal was used, and lo west between day 11 and day 20 of the experiment when a majority of the low -smoke fuels were phased in. Source impacts from residential coal combustio n are also found to be influenced by changes in meteorology, especially win d velocity. PM2.5 and PM(1)0 mass, elements, water-soluble cations (sodium, potassium, and ammonium), anions (chloride, nitrate, and sulfate), as well as organic and elemental carbon were measured on 15 selected days during t he field campaign. PM2.5 constituted more than 85% of PM10 at three Qalabot jha residential sites, and more than 70% of PM10 at the gradient site in th e adjacent community of Villiers. Carbonaceous aerosol is by far the most a bundant component, accounting for more than half of PM mass at the three Qa labotjha sites, and for more than a third of PM mass at the gradient site. Secondary aerosols such as sulfate, nitrate, and ammonium are also signific ant, constituting 8 to 12% of PM mass at the three Qalabotjha sites and 15 to 20% at the Villiers gradient site.