A Biodegradable, Bio-Based Polymer for the Production of Tools for Aquaculture: Processing, Properties and Biodegradation in Sea Water.

Bio-based, biodegradable polymers can dramatically reduce the carbon dioxide released into the environment by substituting fossil-derived polymers in some applications. In this work, prototypes of trays for aquaculture applications were produced via injection molding by using a biodegradable polymer, Mater-Bi®. A characterization carried out via calorimetric, rheological and mechanical tests revealed that the polymer employed shows properties suitable for the production of tools to be used in aquaculture applications. Moreover, the samples were subjected to a biodegradation test in conditions that simulate the marine environment. The as-treated samples were characterized from gravimetrical, morphological and calorimetric point of views. The obtained data showed a relatively low biodegradation rate of the thick molded samples. This behavior is of crucial importance since it implies a long life in marine water for these manufacts before their disappearing.

Theoretical study on the decomposition mechanism of bisphenol A polycarbonate induced by the combined effect of humidity and UV irradiation.

Polycarbonate (PC) is a good material for covering and protecting cultural heritage sites because of its durability, mechanical properties, and transparency. When bisphenol A polycarbonate is subjected to weathering conditions this polymer shows several degradation processes depending on the irradiation wavelength, humidity and temperature. In particular, the combined effects of humidity and UV irradiation speed up the PC molecular weight reduction. In this work, the decomposition mechanisms associated to the hydrolysis process are scrutinized and the effects of UV irradiation on the hydrolysis process are evaluated throughout the Density Functional Theory (DFT) approach. It was found that under UV irradiation the hydrolysis process is speeded up because of the geometrical rearrangement due to the photo-Fries process induced by the UV light.

Understanding memory effects in Li-ion batteries: evidence of a kinetic origin in TiO2 upon hydrogen annealing.

Memory effects in Li-ion battery materials have been explained on the basis of the thermodynamics of many-particles body, however the role of the (de-)intercalation kinetics is not yet clear. We demonstrate that kinetic aspects, specifically Li-ion mobility, are determining the magnitude of the memory effect in TiO2 by studying samples with different levels of oxygen vacancies.

Capturing Cd(ii) and Pb(ii) from contaminated water sources by electro-deposition on hydrotalcite-like compounds.

Two different hydrotalcite-like compounds were prepared and used as substrates for the electrochemical removal of extremely toxic pollutant cations, such as Cd(ii) and Pb(ii), from aqueous solutions, and their subsequent recovery for further potential applications. By deposition on the hydrotalcite electrode, it was possible to remove 75% of Cd(ii) contained in a starting 5.2 mM solution of CdCl2, which was subsequently recovered and concentrated up to 14.3 mM in a single step. A removal of almost 100% was obtained in the case of Pb(ii). Its recovery was largely hindered by the formation of several inert phases, among which is some stable formation of hydroxycarbonate. Our results suggest that the removal of these contaminants by hydrotalcite-like compounds occurs by the combination of two parallel processes: electro-deposition and adsorption. It was possible to achieve a removal capacity for Cd(ii) and Pb(ii) equal to 763 mg ga.m.(-1) and 1039 mg ga.m.(-1), respectively. These removal capacities, accompanied by an excellent posterior eluent-free recovery of Cd(ii), suggest that this new method could be an environmentally friendly alternative to the conventional adsorption wastewater treatment.

Solid electrolyte interphase in semi-solid flow batteries: a wolf in sheep's clothing.

The formation of the alkyl carbonate-derived solid electrolyte interphase (SEI) enables the use of active materials operating at very cathodic potentials in Li-ion batteries. However, the SEI in semi-solid flow batteries results in a hindered electron transfer between a fluid electrode and the current collector restricting the operating potentials to ca. 0.8 V vs. Li/Li(+) for EC-based electrolytes.

Nickel hexacyanoferrate as suitable alternative to Ag for electrochemical lithium recovery.

Currently, Li is mainly produced through evaporation of Li-rich brines obtained from South American countries such as Bolivia, Chile, and Argentina. The most commonly used process, the lime-soda evaporation, requires a long time and several purification steps, which produces a considerable amount of chemical waste. Various electrochemical methods have been proposed as alternatives, but they use expensive metals such as Ag or Pt, thus rendering these methods economically unacceptable. In this work, we present KNiFe(CN)6 , an abundant and environmentally friendly material, as alternative to these expensive components. The Prussian blue derivate has a higher affinity toward cations (Na(+) or K(+) ) than for Li(+) . Additionally, the use of KNiFe(CN)6 permits the utilization of seawater or brine water as recovery solution, thus reducing the consumption of fresh water, which is typically a scarce element in Li production sites.

Aging effects of anatase TiO2 nanoparticles in Li-ion batteries.

Anatase TiO2 nanoparticles with a diameter of 5 nm have been investigated as a negative intercalation electrode material for Li-ion batteries. The focus was on the stability upon cycling within four different potential ranges, namely from 1.5, 1.2, 1.0 and 0.7 V vs. Li/Li(+) as the lower potential limit to 3.0 V vs. Li/Li(+) as the upper potential limit. While a lower cut-off potential allows for a higher amount of charge stored, the irreversible processes induce a faster fading of the specific charge. Galvanostatic cycling (GC), electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) experiments suggest that SEI formation has a negligible contribution to the irreversible processes. It appears more plausible that an irreversible degradation of the bulk phase occurs, leading to a decrease in the amount of active sites. Moreover, it has been observed that this degradation appears as an anodic shift of the thermodynamic potential of (de-)intercalation of Li-ions in the TiO2 structure. The shift is caused by a change in the activity of Li-ions in the solid phase, which is driven by changes in the ionic atmosphere of the crystal.