The seventh International Conference on Urban Climate, 29 June - 3 July 2009, Yokohama, Japan THE ATMOSPHERIC POLLUTION IN URBAN ITALIAN CITIES P. Avino*1 *ISPESL, Rome, Italy. Abstract This contribution regards three fundamental aspects of the urban pollution, sources, diffusion and chemical composition with relative speciation, pointing out the anthropogenic activities and their relationship with the environmental sustainability. The chemical parameters ruled by laws (conventional pollutants) are evidenced together with other species not ruled (no conventional pollutants) but important: scientific researches are addressed to investigate secondary pollutants and micro-inorganic contaminants in atmosphere. Further, a task is devoted to the evaluation and characterization of the carbonaceous component (elemental and organic carbon, EC and OC): in fact, EC can be used as tracer for a speed evaluation of pollution state of an urban environment. Key words: Primary pollutants; Anthropogenic sources; Urban atmosphere. 1. INTRODUCTION The study of atmospheric pollution is one of the more interesting field for the different implications: in fact, the knowledge of the chemical-physical reactions occurring in atmosphere and the relative effects of pollutants on the human health are still objects of deep studies. This contribution would like to show what the main contaminations are in urban air of Rome (Itsaly) and what contributions are due to anthropogenic activities. Primary pollutants are defined directly emitted from emission sources both in gaseous and particle phase whereas secondary pollutants derive from chemical and/or photochemical reactions of primary pollutants among them and/or other atmospheric species (Table 1) (Lepore et al., 2001). Primary Pollutant CO NOx (95% NO, 5% NO2) SO2 VOC (benzene, etc.) PAHs Secondary Pollutant Ozone NO2, HNO3, HNO2 Peroxyacetylnitrate HCHO Nanoparticles PM10 Organic nitroderivates Nitrates Sulfates Table 1. Main primary and secondary pollutants present in the urban air of Rome The primary and secondary pollutants for which the Italian legislation defines acceptable maximum levels, are known as conventional pollutants whereas for the non conventional species (e.g., HCHO) no limits are fixed. Finally, photochemical pollution is related to the presence in atmosphere of secondary pollutants (O3, HNO2, peroxyacetylnitrate, etc.) generated by radical reactions of nitrogen oxides and hydrocarbons and occurring in presence of strong UV radiation (Lepore et al., 2001). 2. EXPERIMENTAL PART From an analytical and methodological point of view, the air quality evaluation is performed by means of dedicated equipments to determine gaseous (i.d., SO2, NOx, O3, CO, benzene, toluene and xylene, BTX) and particulate matter (PM10) concentration levels. Further, techniques of remote-sensing can be used (e.g., Differential Optical Absorption Spectrometry, DOAS; Fourier Transformed Infrared spectroscopy, FT-IR) for measuring some pollutants not subjected to high spatial-temporal difference and for evaluating species such as nitrous acid and HCHO. 3. RESULTS AND DISCUSSION 1 Corresponding author: DIPIA-ISPESL, via Urbana 167, 00184 Rome (Italy). E-mail: [email protected] The seventh International Conference on Urban Climate, 29 June - 3 July 2009, Yokohama, Japan 3.1. Boundary layer evolution The interpretation of atmospheric pollution phenomena is complex for the contemporary presence of both emission and chemical-physical processes and diffusion and transport phenomena. The meteorological measurements give information not too much sufficient for describing the evolution of the boundary layer. A parameter of easy interpretation and able to describe the behavior of pollutants and boundary layer t the same time, is developed: the natural radioactivity (Avino et al., 2003). This measures allow to identify the variations of atmospheric pollutant concentrations, expecially primary pollutants because they depends strictly on the emission fluxes (autovehicular traffic). 3.2. Trends of primary pollutants in Rome In Rome, during ’90-years the pollution scenarios are well-studied and interpreted: the different structural operations and the introductions of catalytic pots and the limitations in the benzene and sulfur content in fuels have caused a sharp reduction in benzene (Figura 1) and SO2 (Figura 2) levels since 1994. Figura 1. Monthly (bar) and annual (lines) average levels of benzene measured in downtown Rome. Figura 2. Monthly (bar) and annual (lines) average levels of SO2 measured in downtown Rome. For primary pollutants a clear decreasing trend is observed whereas it results more attenuated for secondary pollutants. These last species show fluctuations in a range compatible with the atmospheric reactivity conditions in relationship with the atmospheric stability conditions during the complex phenomena of HC-NOx-UV reactions not directly correlated with the emission sources (Monod et al., 2001). A particolar look should be dedicated to pariculate matter pollutant: this is a very difficult pollutant for both its physical properties (granulometric size) (Avino and Brocco, 2005) and natural and/or anthropogenic sources (Avino et al., 2006). The main natural sources are vulcan eruption, rock erosion, marine aerosol, biogenic emission, etc., whereas the main anthropogenic are specific industrial activities and combustion processes. From a chemical point of view, Table 3 shows the elemental composition of PM10 in downtown Rome. In urban area, expecially a megacity such as Rome can be compared, the major contribution to PM10 level is due to anthropogenic sources like domestic heating and autovehicular traffic. In fact, to these last sources the elemental carbon (EC) fraction is related: EC can be used as a new tool for evaluating the contamination of an environment (Avino et al., 2003). The seventh International Conference on Urban Climate, 29 June - 3 July 2009, Yokohama, Japan Ag 0.176 Eu* 12.3 Ni 4.54 Zn 80.0 As 1.35 Fe** 0.566 Pb 92 Au 0.008 Hf 0.020 Rb 2.19 Ba 12.8 Hg 1.07 Sb 9.22 OC 30% Br 22.2 K 1100 Sc* 46.1 EC 70% Ca 1500 La* 188 Se 0.687 PAHs 2% Cd 0.526 Mg 240 Sm* 53.4 Sulfate 40% Ce 0.843 Mn 40.0 Th 0.204 Nitrate 25% Co 0.379 Mo 2.10 V 4.02 Ammon 20% Cr 7.28 Na 420 W 1.25 Cs 0.151 Nd 0.245 Yb 0.015 Table 2. Average levels (ng/m3) of elements determined in PM10 fraction in downtown Rome (*: expressed as 3 3 pg/m ; **: expressed as µg/m ). 5. ACKNOWLEDGEMENTS This work was supported under the grant ISPESL/DIPIA/P06 “Identificazione, analisi e valutazione delle conseguenze delle attività antropiche (Identification, analysis and evaluation of consequences of anthropogenic activities)” L06, 2008-2010. References Avino, P., Brocco, D., Lepore, L., Pareti, S., 2003. Interpretation of atmospheric pollution phenomena in relationship with the vertical atmospheric remixing by means of natural radioactivity measurements (Radon) of particulate matter. Annali di Chimica, 93, 589-594. Avino, P., Brocco, D., 2005. Studio delle particelle carboniose in atmosfera in relazione alle varie frazioni granulometriche ed al contenuto di carbonio organico. Fogli d’Informazione, 3, 107-113. Avino, P., Capannesi, G., Rosada, A., 2006. Characterization and distribution of mineral content in fine and coarse airborne particle fractions by Neutron Activation Analysis. Toxicological and Environmental Chemistry, 88, 633-647. Lepore, L. , Ventrone, I., Brocco, D., Avino, P., Sallusti, F., 2001. Studio dell’inquinamento atmosferico nell’area urbana di Roma: Risultati di dieci anni di attività svolta presso la “Stazione Pilota” dell’ISPESL. Fogli di Informazione ISPESL, 1, 62-103. Monod, A., Sive, B.C., Avino, P., Chen, T., Blake, D.R., Rowland, F.S., 2001. Monoaromatic compounds in ambient air of various cities: a focus on correlations between the xylenes and ethylbenzene. Atmospheric Environment, 35, 135-149.
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