Franco Belosi

The direct influence of ship traffic on atmospheric PM2.5, PM10 and PAH in Venice.

The direct influence of ship traffic on atmospheric levels of coarse and fine particulate matter (PM(2.5), PM(10)) and fifteen polycyclic aromatic hydrocarbons (PAHs) has been estimated in the urban area of Venice. Data analysis has been performed on results collected at three sites over the summer, when ship traffic is at a maximum. Results indicate that monitoring of the PM daily concentrations is not sufficiently detailed for the evaluation of this contribution, even though it could be useful for specific markers such as PAHs. Therefore a new methodology, based on high temporal resolution measurements coupled with wind direction information and the database of ship passages of the Harbour Authority of Venice has been developed. The sampling sites were monitored with optical detectors (DustTrack(®) and Mie pDR-1200) operating at a high temporal resolution (20s and 1s respectively) for PM(2.5) and PM(10). PAH in the particulate and gas phases were recovered from quartz fibre filters and polyurethane foam plugs using pressurised solvent extraction, the extracts were then analysed by gas chromatography- high-resolution mass spectrometry. Our results shows that the direct contribution of ships traffic to PAHs in the gas phase is 10% while the contribution to PM(2.5) and to PM(10) is from 1% up to 8%.

Comparison of PM10 concentrations and metal content in three different sites of the Venice Lagoon： An analysis of possible aerosol sources

The Venice Lagoon is exposed to atmospheric pollutants from industrial activities, thermoelectric power plants, petrochemical plants, incinerator, domestic heating, ship traffic, glass factories and vehicular emissions on the mainland. In 2005, construction began on the mobile dams (MOSE), one dam for each channel connecting the lagoon to the Adriatic Sea as a barrier against high tide. These construction works could represent an additional source of pollutants. PM10 samples were taken on random days between 2007 and 2010 at three different sites: Punta Sabbioni, Chioggia and Malamocco, located near the respective dam construction worksites. Chemical analyses of V, Cr, Fe, Co, Ni, Cu, Zn, As, Mo, Cd, Sb, Tl and Pb in PM10 samples were performed by Inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS) and results were used to identify the main aerosol sources. The correlation of measured data with meteorology, and source apportionment, failed to highlight a contribution specifically associated to the emissions of the MOSE construction works. The comparison of the measurements at the three sites showed a substantial homogeneity of metal concentrations in the area. Source apportionment with principal component analysis (PCA) and positive matrix factorization (PMF) showed that a four principal factors model could describe the sources of metals in PM10. Three of them were assigned to specific sources in the area and one was characterised as a source of mixed origin (anthropogenic and crustal). A specific anthropogenic source of PM10 rich in Ni and Cr, active at the Chioggia site, was also identified.

Organic micropollutants in wet and dry depositions in the Venice Lagoon.

Atmospheric transport is an important route by which pollutants are conveyed from the continents to both coastal and open sea. The role of aerosol deposition in the transport of polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs) and polybromodiphenyls ethers (PBDEs) to water and soil systems has been evaluated by measuring their concentrations in wet and dry depositions to the Venice Lagoon. The organic micropollutant flux data indicate that they contribute to the total deposition flux in different ways through wet and dry deposition, showing that the prevalent contribution derives from wet deposition. The fluxes calculated for PBDEs, showed the prevalence of 47, 99, 100 and 183 congeners, both in dry and wet fluxes. With regard to PCBs, the flux of summation operatorPCB for wet deposition is in the same order of magnitude of the diffusive flux at the air-water interface. The PAH fluxes obtained in the present study are similar to those obtained in previous studies on the atmospheric bulk deposition to the Venice Lagoon. The ratios between Phe/Ant and Fl/Py indicate that the pollutants sources are pyrolytic, deriving from combustion fuels.

Characterisation of PM2,5 concentrations and turbulent fluxes on a island of the Venice Lagoon using high temporal resolution measurements

This work presents an analysis of PM2.5 concentrations and vertical turbulent fluxes on an island of the Venice lagoon. Data were collected during three measurement campaigns in spring, summer and winter periods. Measurements were taken with a high-resolution optical PM2.5 detector, coupled with a micrometeorological station that allowed the evaluation of the vertical turbulent fluxes of PM2.5 using the eddy-correlation technique. The main objective of this paper is to analyse the daily and seasonal pattern in PM2.5 concentrations and fluxes and to discuss their correlation with the main meteorological and micrometeorological parameters using high temporal resolution measurements. Observed data showed a seasonal pattern in turbulent fluxes with daytime average positive value during winter and negative during summer. Deposition velocities, ranged from –60 to 20 mm/s, appeared to be mainly influenced by atmospheric stability. There were larger emissions in cases of high wind velocities blowing from water sector indicating a significant potential contribution of sea spray to PM2.5 fluxes. The local atmospheric circulation, due to the orography of the area, was characterised by diurnal winds coming from the Adriatic Sea and nocturnal wind coming from the Alps. This circulation influenced deposition velocity creating an increase of negative fluxes in the morning at the starting of the sea breeze. A diurnal pattern in concentration has been observed and it is similar for all three measurement campaigns, with higher concentrations in nocturnal periods. The daily pattern was investigated in terms of its correlation with meteorological and micro-meteorological parameters, and was found highly correlated with the diurnal pattern of boundary layer height (BLH) and with relative humidity.

The Mystery of Ice Crystal Multiplication in a Laboratory Experiment

AbstractThis paper addresses the problem of the large discrepancies between ice crystal concentrations in clouds and the number of ice nuclei in nearby clear air reported in published papers. Such discrepancies cannot always be explained, even by taking into account both primary and secondary ice formation processes. A laboratory experiment was performed in a cylindrical column placed in a cold room at atmospheric pressure and temperature in the −12° to −14°C range. Supercooled droplets were nucleated in the column, in the absence of aerosol ice nuclei, by injecting ice crystals generated outside in a small syringe. A rapid increase in the ice crystal concentration was observed in the absence of any known ice multiplication. The ratio between the mean number of ice crystals in the column, after complete droplet vaporization, and the number of ice crystals introduced in the column was about 10:1. The presence of small ice crystals (introduced at the top of the column) in the unstable system (supercooled dr...

Influence of supersaturation on the concentration of ice nucleating particles

Abstract There is a consensus on the increase in ice nucleating particles (INP) concentration from subsaturated to supersaturated water conditions typically associated with clouds (1 ÷ 2%). However, it is important to evaluate the INP concentration trend when water supersaturation further increases, as supercooled clouds contain pockets of high water vapor supersaturation. Three laboratory dry-generated aerosols, two biological (microcrystalline and fibrous cellulose) and one mineral (Arizona test dust), and a field aerosol, sampled on filters, were investigated. Atmospheric aerosol (PM1 and PM10 fractions) was sampled at Capo Granitola (CG, coastal site in Sicily) and the National Research Council (CNR) research area in Bologna (urban background site). The dynamic filter processing chamber (DFPC) was used to explore the ice nucleation of the sampled aerosol in the deposition and condensation freezing modes. Experiments were performed from water subsaturated conditions (water saturation ratio Sw = 0.94) to Sw = 1.1, at T = −22 °C. At CG we considered separately events with a prevalent contribution of marine aerosol, and those showing a contribution of both marine and continental aerosols. An increase in INP concentration, the aerosol activated fraction (AF) and ice nucleation active surface site density (ns) from water subsaturated conditions to Sw = 1.02 was measured in both laboratory and field campaigns. This increase is due to the transition from deposition nucleation to condensation freezing. The highest increases in AF and ns from Sw = 1.02 to Sw = 1.1 were obtained for urban and mixed aerosol and the lowest for marine aerosol. Samplings performed in Bologna showed a high increase in the average INP concentration from PM1 to PM10. Our results show the importance of performing measurements of ice nucleation efficiency for continental aerosol even at supersaturation values higher than those typically associated with clouds, and also considering the contribution of coarse aerosol particles.

Aerosol Scavenging during the Early Growth Stage of Ice Crystal Formation

This paper investigated the possibility that aerosol particles are scavenged during the first and fast diffusional growth of small ice crystals. After ice phase formation, riming, scavenging and aggregation may lead to the collection of additional aerosol particles. Therefore, particles left after ice evaporation in hydrometeors, called ice residuals, may not currently be identical to ice nucleating particles. To overcome this problem, the largest ice crystals are removed during sampling in clouds and only crystals in the initial phase of growth, with diameters lower than 20 - 30 μm, are usually considered. Published papers assume that no aerosol scavenging takes place during the initial phase of growth of small ice crystals. The aim of this paper was to ascertain if this assumption is valid. Experiments were performed in a cold laboratory by considering ice crystals growing in the presence of supercooled droplets. Results showed that crystals can scavenge aerosol even in the first stage of growth. Theoretical considerations show that aerosol scavenging cannot be explained by Brownian diffusion, inertial impaction or interception processes. We suggest that the presence of aerosol in the pristine ice crystals may be due to diffusiophoretic force. During diffusive crystal growth, a flow called Stefan’s flow exists near the hydrometeor surface, driving the nearby aerosol particles towards the surface of the growing hydrometeors.

Further Laboratory Experiments on Aerosol Scavenging in Mixed Clouds to Assess the Role of Phoretic Forces and Particle Solubility

Scavenging experiments have been performed in a cloud chamber inside a cold room with different aerosol particles: Paraffin particles, NaCl particles, Magnesium oxide particles, Carbon particles, Sahara dust particles. Essentially the experimental tests were carried on following the sequence of operations: the generation of the aerosol particles, their injection in the lower part of the cloud chamber, injection of water droplets in the whole chamber volume, nucleation of ice crystals, collection of ice crystals and their examination as for resulting scavenging efficiency. Evidence is given of the peculiar behaviour of soluble particles, individual and eventually inside mixed particles, leading to very much important scavenging efficiency, probably to be ascribed to aerodynamic capture. The evident peculiar behaviour of deliquescent particles can be oriented towards applications to an efficient abatement of specific effluents, on one side, and to weather modification experiments, both rain enhancement and hail prevention experiments.

Evaluation of Heat and Moisture Exchanger Performance with Two Different Methods in the Same Test Apparatus

Abstract: This paper presents a new test apparatus for the evaluation of the humidification efficiency of heat and moisture exchangers (HMEs). These devices are widely used in invasive ventilation conditions to humidify and to heat medical gases inhaled by the patients. The new custom-made test apparatus allows simultaneous measurements with the two most common methods for in vitro tests: gravimetric, which is considered the reference method by the international standard ISO 9360, and hygrometric. In the reference method, the absolute humidity of the inhaled gas (HME moisture output) is determined by subtracting, from the absolute humidity of the exhaled gas (AHexh), the moisture loss measured with a precision balance. Consequently, AHexh is supposed to be stable throughout the test. In addition, ISO 9360 does not set a limit for the maximum value of AHexh in the measuring process. In the new experimental test apparatus, AHexh is constantly monitored and the humidification efficiency of an HME is expressed as the ratio of the HME moisture output with respect to AHexh, the so-called relative efficiency. Results show that average values of AHexh and of the relative efficiency are very similar with both methods, confirming the reliability of the new test apparatus.

Natural Polymers as Heat and Moisture Exchange Devices for Medical Applications

In recent decades, Heat and Moisture Exchange (HME) devices have been employed increasingly for short-term use in anaesthesia and long-term use in intensive care units. These devices work as heat exchangers, accumulating the patient’s expired heat and moisture and returning them to the patient during the inhalation phase. Porous matrices obtained from freeze-drying of blends of natural polymers exhibit high open and interconnected porosity and water vapour intake characteristics which make them possible candidates for HME devices. Preliminary tests were conducted on specimens made of gelatine blended with chitosan and treated with a non-toxic cross-linking agent. The tests were carried out in cyclic flow conditions with saturated and dried air. Results show water vapour retention comparable with accepted standards for HME devices.