Methodology for risk assessment of COVID-19 pandemic propagation.

This paper proposes a methodology to perform risk analysis of the virus spread. It is based on the coupling between CFD modelling of bioaerosol dispersion to the calculation of probability of contact events. CFD model of near-field sneeze droplets dispersion is developed to build the SARS-CoV-2 effect zones and to adequately capture the safe distance. The most shared classification of droplets size distribution of sneezes was used. Droplets were modeled through additive heating/evaporation/boiling laws and their impact on the continuous phase was examined. Larger droplets move behind the droplet nuclei front and exhibit greater vertical drop due to the effect of gravity. CFD simulations provided the iso-risk curves extension (i.e., the maximum distance as well as the angle) enclosed by the incident outcome effect zone. To calculate the risk indexes, a fault tree was developed and the probability of transmission assuming as of the top event "COVID-19 infection" was calculated starting from the virus spread curve, as main base case. Four phases of virus spread evolution were identified: initiation, propagation, generalised propagation and termination. For each phase, the maximum allowable close contact was computed, being fixed the values of the acceptable risk index. In particular, it was found that during the propagation case, the maximum allowable close contacts is two, suggesting that at this point lockdown should be activated. The here developed methodology could drive policy containment design to curb spread COVID-19 infection.

Cyan Hydrogen Process: A New Route for Simultaneous Hydrogen Production and Carbon Valorization.

Hydrogen is expected to largely contribute to the near-future circular economy. Today, most hydrogen is still produced from fossil fuels or renewable pathways with low efficiency and high cost. Herein, a proof of concept for a novel hydrogen production process is proposed, here named cyan hydrogen, inspired by a combination of the green and blue processes, due to the key role played by water and the low carbon content in the gas phase, respectively. The developed novel process, recently patented and demonstrated at the lab scale, is based on successive steps in which ethanol (5.0 mL) and water (10.0 mL) are alternately fed, with a fixed initial amount of sodium metaborate (2.0 g), in a batch reactor at 300 °C. Preliminary results showed the simultaneous production of a 95% v/v hydrogen stream, a polymeric byproduct with a repetitive carbon pattern -CH2-CH2-, and a liquid phase rich in oxygenated chemicals at temperatures lower than conventional hydrogen production processes.

Humic acids on fire? Physico-chemical, thermal, flammability features and extraction process of different humic acids in support of their possible applications.

Humic acids (HA) consist in a multitude of heterogeneous organic molecules surviving the biological and chemical degradation of both vegetal and animal biomasses. The great abundance and chemical richness of these residues make their valorisation one of the most promising approaches to move towards a circular economy. However, the heterogeneity of the biomass from which HA are extracted, as well as the production process, significantly affects the nature and the relative content of functional groups (i.e. quinones, phenols and carboxylic and hydroxyl moieties), eventually changing HA reactivity and ultimately determining their application field. Indeed, depending on their properties, these substances can be used as flame retardants in the case of pronounced resilience degree (i.e., absent or low reactivity), or as antioxidant or antimicrobial agents in the case of pronounced reactivity, thanks to their redox behaviour. In this work we investigated the flammable, the thermal and the physico-chemical features of HA extracted from different composted biomasses to identify the reactivity or the resiliency of these moieties. Several techniques, including flammability characterization (LIT and MIE), laser diffraction granulometry, TG, XRD analyses, FTIR spectroscopy on both solid and gaseous phases, and Raman spectroscopy were integrated to investigate the correlation among the safety parameters, the distributions of particle sizes, as well as the thermal, the chemical properties of HA powders and the influence of post-extraction processes on HA final properties.

Redox behavior of potassium doped and transition metal co-doped Ce0.75Zr0.25O2 for thermochemical H2O/CO2 splitting.

CeO2 slow redox kinetics as well as low oxygen exchange ability limit its application as a catalyst in solar thermochemical two-step cycles. In this study, Ce0.75Zr0.25O2 catalysts doped with potassium or transition metals (Cu, Mn, Fe), as well as co-doped materials were synthesized. Samples were investigated by X-ray diffraction (XRD), N2 sorption (BET), as well as by electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) to gain insight into surface and bulk features, which were connected to redox properties assessed both in a thermogravimetric (TG) balance and in a fixed bed reactor. Obtained results revealed that doping as well as co-doping with non-reducible K cations promoted the increase of both surface and bulk oxygen vacancies. Accordingly, K-doped and Fe-K co-doped materials show the best redox performances evidencing the highest reduction degree, the largest H2 amounts and the fastest kinetics, thus emerging as very interesting materials for solar thermochemical splitting cycles.

K-doped CeO2-ZrO2 for CO2 thermochemical catalytic splitting.

Green syngas production is a sustainable energy-development goal. Thermochemical H2O/CO2 splitting is a very promising sustainable technology allowing the production of H2 and CO with only oxygen as the by-product. CeO2-ZrO2 systems are well known thermochemical splitting catalysts, since they combine stability at high temperature with rapid kinetics and redox cyclability. However, redox performances of these materials must be improved to allow their use in large scale plants. K-doped systems show good redox properties and repeatable performances. In this work, we studied the effect of potassium content on the performances of ceria-zirconia for CO2 splitting. A kinetic model was developed to get insight into the nature of the catalytic sites. Fitting results confirmed the hypothesis about the existence of two types of redox sites in the investigated catalytic systems and their role at different K contents. Moreover, the model was used to predict the influence of key parameters, such as the process conditions.

Synergistic behavior of flammable dust mixtures: A novel classification.

In this work the flammable/explosive behavior of mixtures of flammable dusts is investigated. In particular, minimum ignition temperature, minimum ignition energy, maximum pressure and deflagration index have been measured at varying the relative content of dusts in the mixtures. The thermal behavior of these mixtures has been also studied by means of DSC analysis coupled to chemical analysis performed by HPLC and ATR-FTIR. Depending on the mixtures, a synergistic behavior has been found due to physical and/or chemical reactions. For some mixtures, the more severe behavior has been attributed to the presence of a eutectic point (niacin/anthraquinone, ascorbic acid/niacin), in other cases, to chemical reactions with the formation of volatiles (ascorbic acid/irganox 1222, ascorbic acid/glucose). On this basis, we propose a new classification of dusts mixtures in three mixtures safety classes (MSC): MSC 0 (no synergistic effect, ideal behavior); MSC 1 (deviation from ideality, safety parameters included between those of the pure dusts) and MSC 2 (at least 1 parameter with more sever value than those of pure dusts).