LC-MS methods with use of ion-trap and time-of-flight mass spectrometers were developed for the determination of organic acids in aerosol samples collected by a high-volume sampler in a Finnish coniferous forest. Comparison was made of the composition of samples collected during atmospheric formation of new aerosol particles and on days when this formation did not occur. A dynamic sonication-assisted solvent extraction system was developed for fast and quantitative extraction of the filter samples. Several organic acids, including pinonic acid, pinic acid, and homologous series of n-alkanoic acids, n-alkenoic acids, and aliphatic dicarboxylic acids, were identified. In samples collected between 08:00 and 16:00 hours the concentration of pinonic acid ranged from 0.5 ng m(-3) to 3.7 ng m(-3) and that of pinic acid from 0.2 ng m(-3) to 1.5 ng m(-3). For most of the compounds identified, the trends in concentration could be explained by the differences in temperature during collection. However, concentrations of short-chain n-alkanoic acids were clearly higher on the days when new aerosol particle formation occurred.
The estimated average annual exposures to asbestos, coal tar-derived PAHs and quartz dust in the bitumen waterproofing industry in Finland and Denmark were significant in the past but have a clear declining trend. Exposure to bitumen fume was found to follow a similar trend.
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