Hydrogeological characterization of peculiar Apenninic springs

Abstract. In the northern Apennines of Italy, springs are quite widespread over the slopes. Due to the outcropping of low-permeability geologic units, they are generally characterized by low-yield capacities and high discharge variability during the hydrologic year. In addition, low-flow periods (discharge lower than 1 Ls-1) reflect rainfall and snowmelt distribution and generally occur in summer seasons. These features strongly condition the management for water-supply purposes, making it particularly complex. The "Mulino delle Vene" springs (420 m a.s.l., Reggio Emilia Province, Italy) are one of the largest in the Apennines for mean annual discharge and dynamic storage and are considered as the main water resource in the area. They flow out from several joints and fractures at the bottom of an arenite rock mass outcrop in the vicinity of the Tresinaro River. To date, these springs have not yet been exploited, as the knowledge about the hydrogeological characteristics of the aquifer and their hydrological behaviour is not fully achieved. This study aims to describe the recharge processes and to define the hydrogeological boundaries of the aquifer. It is based on river and spring discharge monitoring and groundwater balance assessment carried out during the period 2012–2013. Results confirm the effectiveness of the approach, as it allowed the total aliquot of discharge of the springs to be assessed. Moreover, by comparing the observed discharge volume with the one calculated with the groundwater balance, the aquifer has been identified with the arenite slab (mean altitude of 580 m a.s.l.), extended about 5.5 km2 and located 1 km west of the monitored springs

Electron transfer in polyaromatic hydrocarbons and molecular carbon nanostructures

Planar and curved polycyclic aromatic hydrocarbons (PAHs) represent an interesting class of compounds with physical chemical properties particularly appealing, as good organic semiconductors and molecular model of larger carbon nano- structures. Investigation of the heterogeneous electron transfer in these systems lets to probe their electronic properties and the reactivity of the corresponding generated carbanions and carbocations that can form new bonds, thus leading to different carbon systems. A particular focus is on the intrinsically high reactivity of carbocations which induces a series of reactions building up new carbon–carbon bonds, thus allowing to enlarge the initial molecular unit into a nanostructure. This represents a new and convenient way to exploit the electro- chemically triggered reactivity into the synthesis of carbon nanostructured materials

Electrochemical Characterization and CO2 Reduction Reaction of a Family of Pyridazine-Bridged Dinuclear Mn(I) Carbonyl Complexes

Three recently synthesized neutral dinuclear carbonyl manganese complexes with the pyridazine bridging ligand, of general formula [Mn2(μ-ER)2(CO)6(μ-pydz)] (pydz = pyridazine; E = O or S; R = methyl or phenyl), have been investigated by cyclic voltammetry in dimethylformamide and acetonitrile both under an inert argon atmosphere and in the presence of carbon dioxide. This family of Mn(I) compounds behaves interestingly at negative potentials in the presence of CO2. Based on this behavior, which is herein discussed, a rather efficient catalytic mechanism for the CO2 reduction reaction toward the generation of CO has been hypothesized

Dinuclear Re(I) Complexes as New Electrocatalytic Systems for CO2 Reduction

A family of dinuclear tricarbonyl rhenium (I) complexes containing bridging 1,2-diazine ligand and halide anions as ancillary ligands and able to catalyze CO2 reduction is presented. Electrochemical studies show that the highest catalytic efficiency is obtained for the complex containing the 4,5-bipenthyl-pyridazine and iodide as ancillary halogen ligands. This complex gives rise to TOF=15 s−1 that clearly outperforms the values reported for the benchmark mononuclear Re(CO)3Cl(bpy) (11.1 s−1). The role of the substituents on the pyridazine ligand and the nature of the bridging halide ligands on the catalytic activity have been deeply investigated through a systematic study on the structure-properties relationship to understand the improved catalytic efficiencies of this class of complexes

Extremely fast triplet formation by charge recombination in a Nile Red/fullerene flexible dyad

A donor/acceptor dyad was obtained by linking Nile Red and fullerene to a calix[4]arene scaffold. The dyad was spectroscopically characterized, both with steady-state and ultrafast transient absorption experiments, as well as with electrochemical and spectroelectrochemical techniques. We demonstrate extremely fast and efficient formation of a long-lived excited triplet localized on the fullerene moiety in this system, occurring in about 80 ps in toluene and 220 ps in chloroform. The mechanism of this process is investigated and discussed. The spectroscopic and electrochemical characterization suggests the occurrence of electron transfer from Nile Red to fullerene, leading to the formation of a charge-separated state. This state lives very briefly and, because of the small interaction between the electron donor and acceptor, promotes a singlet/triplet state mixing, inducing charge recombination and efficient triplet formation

Three electrodes and a cage: an account of electrochemical research on C60, C70 and their derivatives

An overview of the electrochemistry of C60, C70 and higher fullerenes, and of their derivatives and relatives is given together with highlights on possible future studies and applications. A general introduction gives the idea of the size and importance of this field that embraces classic solution and surface electrochemistry, materials chemistry, interlocked molecular architectures, biosensors and solar-energy conversion. A description of the general electrochemical behaviour for several fullerene derivatives is given together with insights on possible applications

Electrochemistry

This reference combines fundamental research, recent breakthroughs and real-life applications in one well-organized treatise concerning Carbon's special structures, such as diamond, graphite, and in particular fullerenes and nanotubes