Amines in boreal forest air at SMEAR II station in Finland

摘要

We measured amines in boreal forest air in Finland both in gas and particle phases with 1h time resolution using an online ion chromatograph (instrument for Measuring AeRosols and Gases in Ambient Air – MARGA) connected to an electrospray ionization quadrupole mass spectrometer (MS). The developed MARGA-MS method was able to separate and detect seven different amines: monomethylamine (MMA), dimethylamine (DMA), trimethylamine (TMA), ethylamine (EA), diethylamine (DEA), propylamine (PA), and butylamine (BA). The detection limits of the method for amines were low (0.2–3.1ngm?3), the accuracy of IC-MS analysis was 11–37%, and the precision 10–15%. The proper measurements in the boreal forest covered about 8 weeks between March and December?2015. The amines were found to be an inhomogeneous group of compounds, showing different seasonal and diurnal variability. Total MMA (MMA(tot)) peaked together with the sum of ammonia and ammonium ions already in March. In March, monthly means for MMA were 2.4 and 6.8±9.1ngm?3 in gas and aerosol phases, respectively, and for NH3 and NH4+ these were 52±16 and 425±371ngm?3, respectively. Monthly medians in March for MMA(tot), NH3, and NH4+ were 2.4, 19 and 90ngm?3, respectively. DMA(tot) and TMA(tot) had summer maxima indicating biogenic sources. We observed diurnal variation for DMA(tot) but not for TMA(tot). The highest concentrations of these compounds were measured in July. Then, monthly means for DMA were 3.1 and 8.4±3.1ngm?3 in gas and aerosol phases, respectively, and for TMA these were 0.4±0.1 and 1.8±0.5ngm?3. Monthly medians in July for DMA were below the detection limit (DL) and 4.9ngm?3 in gas and aerosol phases, respectively, and for TMA these were 0.4 and 1.4ngm?3. When relative humidity of air was 90%, gas-phase DMA correlated well with 1.1–2nm particle number concentration (R2=0.63) suggesting that it participates in atmospheric clustering. EA concentrations were low all the time. Its July means were 0.36 and 0.4±0.4ngm?3 in gas and aerosol phases, respectively, but individual concentration data correlated well with monoterpene concentrations in July. Monthly means of PA and BA were below detection limits at all times.