In February 2017 the "Carbonaceous Aerosol in Rome and Environs (CARE)" experiment was carried out in downtown Rome to address the following specific questions: what is the color, size, composition, and toxicity of the carbonaceous aerosol in the Mediterranean urban background area of Rome? The motivation of this experiment is the lack of understanding of what aerosol types are responsible for the severe risks to human health posed by particulate matter (PM) pollution, and how carbonaceous aerosols influence radiative balance. Physicochemical properties of the carbonaceous aerosol were characterised, and relevant toxicological variables assessed. The aerosol characterisation includes: (i) measurements with high time resolution (min to 1-2 h) at a fixed location of black carbon (eBC), elemental carbon (EC), organic carbon (OC), particle number size distribution (0.008-10 µm), major non refractory PM 1 components, elemental composition, wavelength-dependent optical properties, and atmospheric turbulence; (ii) 24-h measurements of PM 10 and PM 2.5 mass concentration, water soluble OC and brown carbon (BrC), and levoglucosan; (iii) mobile measurements of eBC and size distribution around the study area, with computational fluid dynamics modeling; (iv) characterisation of road dust emissions and their EC and OC content. The toxicological assessment includes: (i) preliminary evaluation of the potential impact of ultrafine particles on lung epithelia cells (cultured at the air liquid interface and directly exposed to particles); (ii) assessment of the oxidative stress induced by carbonaceous aerosols; (iii) assessment of particle size dependent number doses deposited in different regions of the human body; (iv) PAHs biomonitoring (from the participants into the mobile measurements). The first experimental results of the CARE experiment are presented in this paper. The objective here is to provide baseline levels of carbonaceous aerosols for Rome, and to address future research directions. First, we found that BC and EC mass concentration in Rome are larger than those measured in similar urban areas across Europe (the urban background mass concentration of eBC in Rome in winter being on average 2.6 ± 2.5 µg · m −3 , mean eBC at the peak level hour being 5.2 (95% CI = 5.0-5.5) µg · m −3 ). Then, we discussed significant variations of carbonaceous aerosol properties occurring with time scales of minutes, and questioned on the data averaging period used in current air quality standard for PM 10 (24-h). Third, we showed that the oxidative potential induced by aerosol depends on particle size and composition, the effects of toxicity being higher with lower mass concentrations and smaller particle size. Albeit this is a preliminary analysis, findings reinforce the need for an urgent update of existing air quality standards for PM 10 and PM 2.5 with regard to particle composition and size distribution, and data averaging period. Our results reinforce existing concerns about the toxicity of carbonaceous aerosols, suppo...

Organo-and hydrogels have been proposed in the restoration field to treat different types of surfaces. The possibility to retain solvents and to have a controlled and superficial action allowed to use these materials for the removal of very thin layers applied on ancient historical objects, when the under paint layers are particularly delicate and water sensitive. In the last years, an increased attention has been devoted to the proposal of more healthy products to guarantee the safeguard of the operators. Few attention has been devoted to the development of green methods which foresee the use of renewable and biodegradable materials. The aim of this paper is to test a green organo-gel for the cleaning of water sensitive surfaces like varnished egg tempera paintings. The gel has been tested experimented on mock ups varnished with natural and synthetic materials and has been validated on a small portion of a Cimabue painting for the removal of two varnishes applied on two different test areas of the painting.

Fully biodegradable novel bio‐based organogels were developed for removing aged protective films from the surfaces of paintings, aiming at providing effective cleaning tools, easily controllable by reducing the solvent permeation into underlying paint layers and not dangerous for human health and the environment. The gels were based on poly‐3‐hydroxybutyrate (PHB) as gelling agent, γ‐valerolactone (GVL) as solvent and triethyl citrate (TEC) as plasticizer. PHB‐gels were able to completely remove protective varnishes on real oil paintings, without affecting the pictorial layer and leaving negligible residues after the application. Moreover, the gels showed good mechanical and handling properties, they were fully composed by non‐toxic ingredients and resulted readily biodegradable in water, therefore easily disposable after the use.

Some studies suggested a role of the atmospheric particulate matter (PM) and of its oxidative potential (OP) in determining adverse health effects. Several works have focused on characterisation of source contributions to PM OP, mainly using three approaches: correlation between OP and chemical markers of specific sources; use of OP as input variable in source apportionment with receptor models; and multi-linear regression (MLR) between OP and source contributions to PM obtained from receptor models. Up to now, comparison of results obtained with different approaches on the same dataset is scarce. This work aims to perform a OP study of PM2.5 collected in an industrial site, located near a biogas production and combustion plant (in southern Italy), comparing different approaches to investigate the contributions of the different sources to OP. The PM2.5 samples were analysed for determining ions, metals, carbonaceous components, and OP activity with the DTT (dithiotreitol) assay. Results showed that OP normalised in volume (DTTV) is correlated with carbonaceous components and some ions (NO3−, and Ca2+) indicating that PM of combustion, secondary, and crustal origin could contribute to the OP activity. The source apportionment, done with the Environmental Protection Agency (EPA)—Positive Matrix Factorization (PMF5.0) model, identified six sources: secondary sulphate; biomass burning; industrial emissions; crustal; vehicle traffic and secondary nitrate; and sea spray. A MLR analysis between the source’s daily contributions and the daily DTTV values showed a reasonable agreement of the two approaches (PMF and MLR), identifying the biomass burning and the vehicle traffic and secondary nitrate as the main sources contributing to DTTV activity.

The concentrations of submicron aerosol particles in maritime regions around Antarctica are influenced by the extent of sea ice. This effect is two ways: on one side, sea ice regulates the production of particles by sea spray (primary aerosols); on the other side, it hosts complex communities of organisms emitting precursors for secondary particles. Past studies documenting the chemical composition of fine aerosols in Antarctica indicate various potential primary and secondary sources active in coastal areas, in offshore marine regions, and in the sea ice itself. In particular, beside the well-known sources of organic and sulfur material originating from the oxidation of dimethylsulfide (DMS) produced by microalgae, recent findings obtained during the 2015 PE-GASO cruise suggest that nitrogen-containing organic compounds are also produced by the microbiota colonizing the marginal ice zone. To complement the aerosol source apportionment performed using online mass spectrometric techniques, here we discuss the outcomes of offline spectroscopic analysis performed by nuclear magnetic resonance (NMR) spectroscopy. In this study we (i) present the composition of ambient aerosols over open-ocean waters across bioregions, and compare it to the composition of (ii) seawater samples and (iii) bubble-bursting aerosols produced in a sea-spray chamber onboard the ship. Our results show that the process of aerosolization in the tank enriches primary marine particles with lipids and sugars while depleting them of free amino acids, providing an explanation for why amino acids occurred only at trace concentrations in the marine aerosol samples analyzed. The analysis of water-soluble organic carbon (WSOC) in ambient submicron aerosol samples shows distinct NMR fingerprints for three bioregions: (1) the open Southern Ocean pelagic environments, in which aerosols are enriched with primary marine particles containing lipids and sugars; (2) sympagic areas in the Weddell Sea, where secondary organic compounds, including methanesulfonic acid and semivolatile amines abound in the aerosol composition; and (3) terrestrial coastal areas, traced by sugars such as sucrose, emitted by land vegetation. Finally, a new biogenic chemical marker, creatinine, was identified in the samples from the Weddell Sea, providing another confirmation of the importance of nitrogen-containing metabolites in Antarctic polar aerosols.