10 research outputs found

    Volatile Organic Compounds in the Po Basin. Part B: Biogenic VOCs

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    Measurements of volatile organic compounds (VOCs) were performed in the Po Basin, northern Italy in early summer 1998, summer 2002, and autumn 2003. During the three campaigns, trace gases and meteorological parameters were measured at a semi-rural station, around 35 km north of the city center of Milan. Bimodal diurnal cycles of isoprene with highest concentrations in the morning and evening were found and could be explained by the interaction of emissions, chemical reactions, and vertical mixing. The diurnal cycle could be qualitatively reproduced by a three-dimensional Eulerian model. The nighttime decay of isoprene could be attributed mostly to reactions with NO3, while the decay of the isoprene oxidation products could not be explained with the considered chemical reactions. Methanol reached very high mixing ratios, up to 150 ppb. High concentrations with considerable variability occurred during nights with high relative humidities and low wind speeds. The origin of these nighttime methanol concentrations is most likely local and biogenic but the specific source could not be identifie

    Photochemical modelling in the Po basin with focus on formaldehyde and ozone

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    As part of the EU project FORMAT ( Formaldehyde as a Tracer of Oxidation in the Troposphere), a field campaign was carried out in the vicinity of Milan during the summer of 2002. Results from a 3-D regional chemical transport model (NILU RCTM) were used to interpret the observations focusing primarily on HCHO and ozone. The performance of the model was assessed by comparing model results with ground based and aircraft measurements. The model results show good agreement with surface measurements, and the model is able to reproduce the photochemical episodes during fair weather days. The comparison indicates that the model can represent well the HCHO concentrations as well as their temporal and spatial variability. The relationship between HCHO and (O-3 x H2O) was used to validate the model ability to predict the HCHO concentrations. Further analysis revealed the importance of the representativeness of different instruments: in-situ concentrations might be locally enhanced by emissions, while long path measurements over a forest can be influenced by rapid formation of HCHO from isoprene. The model is able to capture the plume from the city of Milan and the modelled levels agree generally well with the aircraft measurements, although the wind fields used in the model can lead to a displacement of the ozone plume. During the campaign period, O3 levels were seldom higher than 80 ppb, the peak surface ozone maxima reached 90 ppb. Those relatively low values can be explained by low emissions during the August vacation and unstable weather conditions in this period. The modelled Delta O-3/Delta NOz slope at Alzate of 5.1 agrees well with the measured slope of 4.9

    A photochemical modelling study of ozone and formaldehyde generation and budget in the Po basin

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    In this work, a photochemical dispersion model, CAMx (Comprehensive Air quality Model with eXtensions) was used to simulate a high ozone episode observed in the Po basin during the 2003 FORMAT (Formaldehyde as a Tracer of Oxidation in the Troposphere) campaign. The study focuses on formaldehyde and ozone, and a budget analysis was set up for interpreting the importance of different processes, namely emission, chemistry, transport and deposition, for three different areas (urban, downwind, suburban) around the Milan metropolitan region. In addition, a sensitivity study was carried out based on 11 different VOC emission scenarios. The results of the budget study show that the strongest O-3 production rate (4 ppbv/hour) occurs in the downwind area of the city of Milan, and that accumulated O3 is transported back to Milan city during nighttime. More than 80% of the HCHO concentration over the Milan metropolitan region is secondary, i. e., photochemically produced from other VOCs. The sensitivity study shows that the emissions of isoprene are not, on average, a controlling factor for the peak concentrations of O3 and HCHO over the model domain because of very few oak trees in this region. Although the paraffinic (PAR) emissions are fairly large, a 20% reduction of PAR yields only 1.7% of HCHO reduction and 2.7% reduction of the O3 peak. The largest reduction of O3 levels can be obtained by reduced xylene (XYL) emissions. A 20% reduction of the total anthropogenic VOC emissions leads to 15.5% (20.3 ppbv) reduction of O3 peak levels over the Milan metropolitan region
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