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The behavior of nitrosyl chloride (ClNO) exposed to ionizing radiation was studied by direct probing valence-shell electrons in temporal coincidence with ions originating from the fragmentation process of the transient ClNO2+. Such a molecular dication was produced by double photoionization with synchrotron radiation in the 24–70 eV photon energy range. The experiment has been conducted at the Elettra Synchrotron Facility of Basovizza (Trieste, Italy) using a light beam linearly polarized with the direction of the polarization vector parallel to the ClNO molecular beam axis. ClNO molecules crossing the photon beam at right angles in the scattering region are generated by effusive expansion and randomly oriented. The threshold energy for the double ionization of ClNO (30.1 ± 0.1 eV) and six dissociation channels producing NO+/Cl+, N+/Cl+, N+/O+, O+/Cl+, ClN+/O+, NO+/Cl2+ ion pairs, with their relative abundance and threshold energies, have been measured. [ABSTRACT FROM AUTHOR]

In surficial sediments of Lake Piediluco, a small, riverine, regulated and heavily modified water body in the Central Italian Apennines, contamination by persistent organochlorine pollutants (POPs) was assessed. During spring and autumn, six representative points were investigated. Reflecting a substantial zonation of pollution within this aquatic ecosystem, concentrations were found to vary from site to site. OCPs, particularly DDT and its metabolites DDE and DDD, were detected at varying frequencies and concentrations from 0.301 to 8.185 ng/g d.w., whilst total PCBs (Σ50 congeners) were from 0.570 to 10.206 ng/g d.w. Although both PCB congener-specific and homolog patterns suggest a prevalent presence of Aroclors 1254 and 1260, a more limited likely contribution of 1248 technical mixture is not to be excluded. In the western area of the lake, affected daily by continuous basin water remixing for hydroelectricity production, major seasonal differences in OCP concentrations were found. Conversely, the eastern area was typified by low seasonal fluctuation and small variation among sites. Regardless of either collection site or seasonality, polychlorinated-p-dioxin and furan (PCDD/Fs) contamination were below 8.3 pg WHO-TEQ/g. In contrast to the present study, POP pollution from PCBs, PCDD/Fs and some DDT-derived pollutants has not been investigated so far. Nevertheless, the concentrations are typical of low-polluted or pristine area lakes and are consistently lower than those of other Italian lakes of greater size and depth (e.g., Como, Garda and Maggiore). The physical and chemical properties of investigated analytes are more consistent with probable diffuse point source contamination originating from the catchment area, rather than from atmospheric depositions by regional or long-range transports. Finally, according to the international sediment quality guidelines (SQGs), Piediluco sediments pose a low risk to sediment-dwelling organisms and, more generally, to the wildlife of such aquatic ecosystems. [ABSTRACT FROM AUTHOR]

Fundamental properties of multiply charged molecular ions, such as energetics, structure, stability, lifetime and fragmentation dynamics, are relevant to understand and model the behavior of gaseous plasmas as well as ionosphere and astrophysical environments. Experimental determinations of the Kinetic Energy Released (KER) for ions originating from dissociations reactions, induced by Coulomb explosion of doubly charged molecular ions (molecular dications) produced by double photoionization of CO2, N2O and C2H2 molecules of interest in planetary atmospheres, are reported. The KER measurement as a function of the ultraviolet (UV) photon energy in the range of 28-65 eV was extracted from the electron-ion-ion coincidence spectra obtained by using tunable synchrotron radiation coupled with ion imaging techniques at the ELETTRA Synchrotron Light Laboratory Trieste, Italy. These experiments, coupled with a computational analysis based on a Monte Carlo trajectory simulation, allow assessing the probability of escape for simple ionic species in the upper atmosphere of Mars, Venus and Titan. The measured KER in the case of H+, C+, CH+, CH2 +, N2+, O+, CO+, N2 + and NO+ fragment ions range between 1.0 and 5.5 eV, being large enough to allow these ionic species to participate in the atmospheric escape from such planets into space. In the case of Mars, we suggest a possible explanation for the observed behavior of the O+ and CO22+ ion density profiles. [ABSTRACT FROM AUTHOR]

In this paper we suggest Penning ionization as an important route of formation for ionic species in upper planetary atmospheres. Our goal is to provide relevant tools to researchers working on kinetic models of atmospheric interest, in order to include Penning ionizations in their calculations as fast processes promoting reactions that cannot be neglected. Ions are extremely important for the transmission of radio and satellite signals, and they govern the chemistry of planetary ionospheres. Molecular ions have also been detected in comet tails. In this paper recent experimental results concerning production of simple ionic species of atmospheric interest are presented and discussed. Such results concern the formation of free ions in collisional ionization of H2O, H2S, and NH3 induced by highly excited species (Penning ionization) as metastable noble gas atoms. The effect of Penning ionization still has not been considered in the modeling of terrestrial and extraterrestrial objects so far, even, though metastable helium is formed by radiative recombination of He+ ions with electrons. Because helium is the second most abundant element of the universe, Penning ionization of atomic or molecular species by He*(2³S1) is plausibly an active route of ionization in relatively dense environments exposed to cosmic rays. [ABSTRACT FROM AUTHOR]

In this paper, a review of cold plasma setups and the physical and chemical processes leading to the generation of active species is presented. The emphasis is given to the interaction of cold plasmas with materials used in medical applications, especially medical implants as well as live cells. An overview of the different kinds of plasmas and techniques used for generation of active species, which significantly alter the surface properties of biomaterials is presented. The elemental processes responsible for the observed changes in the physio-chemical properties of surfaces when exposed to plasma are described. Examples of ongoing research in the field are given to illustrate the state-of-the-art at the more conceptual level. [ABSTRACT FROM AUTHOR]

A jointed experimental and theoretical investigation pointing out new insights about the microscopic mechanism of the volatile organic compounds (VOCs) photocatalytic elimination by TiO2 was done. Methane, hexane, isooctane, acetone and methanol were photomineralized in a batch reactor. Values of K (adsorption constant on TiO2) and k (mineralization rate constant) of the five VOCs (treating the kinetic data through a Langmuir–Hinshelwood approach) were determined. Recorded K (in the range of 0.74 × 10−2–1.11 × 10−2 ppm−1) and k (in the range of 1.9–9.9 ppm min−1) values and performed theoretical calculations allowed us to suggest the involvement of an electron transfer step between the VOC and the hole, TiO2(h+), as the rate-determining one. [ABSTRACT FROM AUTHOR]

Molecular dications are doubly charged cations of importance in flames, plasma chemistry and physics and in the chemistry of the upper atmosphere of Planets. Furthermore, they are exotic species able to store a considerable amount of energy at a molecular level. This high energy content of several eV can be easily released as translational energy of the two fragment monocations generated by their Coulomb explosion. For such a reason, they were proposed as a new kind of alternative propellant. The present topic review paper reports on an overview of the main contributions made by the authors' research groups in the generation and characterization of simple molecular dications during the last 40 years of coupling experimental and theoretical efforts. [ABSTRACT FROM AUTHOR]

The nature, strength, range and role of the bonds in adducts of noble gas atoms with both neutral and ionic partners have been investigated by exploiting a fine-tuned integrated phenomenological–theoretical approach. The identification of the leading interaction components in the noble gases adducts and their modeling allows the encompassing of the transitions from pure noncovalent to covalent bound aggregates and to rationalize the anomalous behavior (deviations from noncovalent type interaction) pointed out in peculiar cases. Selected adducts affected by a weak chemical bond, as those promoting the formation of the intermolecular halogen bond, are also properly rationalized. The behavior of noble gas atoms excited in their long-life metastable states, showing a strongly enhanced reactivity, has been also enclosed in the present investigation. [ABSTRACT FROM AUTHOR]