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Chemical speciation of fine airborne particles in Abu Dhabi. NILU OR
PM2.5 was sampled at two urban background sites in Abu Dhabi (Khalifa in the city of Abu Dhabi and Bida Zayed) and analysed chemically for further source identification and quantification. Understanding of source contributions to PM2.5 is a prerequisite for the formulation of effective control strategies for PM2.5 emissions.
For both sites, five source factors were identified. Long-range transported aerosol is the largest contributor (~41%) to average PM2.5 mass concentrations at both sites. It gradually forms from SO2, which is possibly emitted into ambient in the Arabian Gulf area, while it is transported to the sites. Mineral dust was found to be the second most important source, contributing ~25% at both sites. It represents an ubiquitous natural contribution of mainly regional origin to particulate matter in Abu Dhabi.
Other source contributions to particle concentrations found at Khalifa identified were: local traffic (15.1%), shipping/industry (10.5%) and sea salt (4.0%). The latter is a natural contribution.
At Bida Zayed, a mixed traffic/industry factor (13.2%) was found, as well as another two factors of natural origin, explaining 11.4% and 8.7%
2013
2010
2010
Chemical tracers of the origins of Arctic air pollution. Environmental Management Series
1991
2024
Chemicals of emerging concern (CECs) in coastal waters: Environmental impact & Management strategies
2024
2024
2015
Chemistry and thermodynamics of organic aerosols. Report series in aerosol science, vol. 71B
2004
2010
Chiral MVOC's - a new tool for studying moulds in building constructions? Powerpoint presentation. NILU F
2002
2009
2002
Chlorinated alkylbenzenes at Glencore nickel plant. Evaluation of measurement uncertainties. NILU report
2017
Electronic waste is a source of both legacy and emerging flame retardants to the environment, especially in regions where sufficient waste handling systems are lacking. In the present study, we quantified the occurrence of short- and medium chain chlorinated paraffins (SCCPs and MCCPs) and dechloranes in household chicken (Gallus domesticus) eggs and soil collected near waste disposal sites on Zanzibar and the Tanzanian mainland. Sampling locations included an e-waste facility and the active dumpsite of Dar es Salaam, a historical dumpsite in Dar es Salaam, and an informal dumpsite on Zanzibar. We compared concentrations and contaminant profiles between soil and eggs, as free-range chickens ingest a considerable amount of soil during foraging, with potential for maternal transfer to the eggs. We found no correlation between soil and egg concentrations or patterns of dechloranes or CPs. CPs with shorter chain lengths and higher chlorination degree were associated with soil, while longer chain lengths and lower chlorination degree were associated with eggs. MCCPs dominated the CP profile in eggs, with median concentrations ranging from 500 to 900 ng/g lipid weight (lw) among locations. SCCP concentrations in eggs ranged from below the detection limit (LOD) to 370 ng/g lw. Dechlorane Plus was the dominating dechlorane compound in all egg samples, with median concentrations ranging from 0.5 to 2.8 ng/g lw. SCCPs dominated in the soil samples (400–21300 ng/g soil organic matter, SOM), except at the official dumpsite where MCCPs were highest (65000 ng/g SOM). Concentrations of dechloranes in soil ranged from below LOD to 240 ng/g SOM, and the dominating compounds were Dechlorane Plus and Dechlorane 603. Risk assessment of CP levels gave margins of exposure (MOE) close to or below 1000 for SCCPs at one location.
2023
2005