A State-of-the-Art Review on SARS-CoV-2 Virus Removal Using DifferentWastewater Treatment Strategies

In addition to the numerous health effects caused by the COVID-19 pandemic, the scientific community has considered other emerging effects such as water-related impacts worthy of deep investigation. In this regard, the transmission cycles of the SARS-CoV-2 virus from fecal, vomiting, and sputum routes to sewage have led health authorities to diagnose, prevent, and use novel wastewater treatment technologies. Once they enter the gastrointestinal canal of a healthy person, viral particles can infect via the nominal amount of Angiotensin-Converting Enzyme 2 (ACE2) present in alimentary canal epithelial cell surfaces and further infect lung, heart, kidney, and other organs. The current review highlights the detection, status, and fate of SARS-CoV-2 from sewage treatment facilities to water bodies. Besides, it addresses the potential wastewater treatment processes to cope with various viruses, especially SARS-CoV-2. Many processes can manage contaminated wastewater and solid wastes over the long term, including membrane technologies, disinfectants, UV-light and advanced oxidation methods like photocatalysis, ozonation, hydrogen peroxide, nanomaterials, and algae. Future work must focus on implementing the selected actions for the treatment of the wastewater released from the COVID-19 hospitals and self-quarantine centers to better regulate future waves of SARS-CoV-2

Comparison of Physical-chemical and Mechanical Properties of Chlorapatite and Hydroxyapatite Plasma Sprayed Coatings

Chlorapatite can be considered a potential biomaterial for orthopaedic applications. Its use as plasma-sprayed coating could be of interest considering its thermal properties and particularly its ability to melt without decomposition unlike hydroxyapatite. Chlorapatite (ClA) was synthesized by a high-temperature ion exchange reaction starting from commercial stoichiometric hydroxyapatites (HA). The ClA powder showed similar characteristics as the original industrial HA powder, and was obtained in the monoclinic form. The HA and ClA powders were plasma-sprayed using a low-energy plasma spraying system with identical processing parameters. The coatings were characterized by physical-chemical methods, i.e. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy, including distribution mapping of the main phases detected such as amorphous calcium phosphate (ACP), oxyapatite (OA), and HA or ClA. The unexpected formation of oxyapatite in ClA coatings was assigned to a side reaction with contaminating oxygenated species (O2, H2O). ClA coatings exhibited characteristics different from HA, showing a lower content of oxyapatite and amorphous phase. Although their adhesion strength was found to be lower than that of HA coatings, their application could be an interesting alternative, offering, in particular, a larger range of spraying conditions without formation of massive impurities.This study was carried out under a MNT ERA-Net Project named NANOMED. The authors gratefully thank the Midi-Pyrénées region (MNT ERA Net Midi-Pyrénées Région, NANOMED2 project) and the Institute National Polytechnique de Toulouse (BQR INPT 2011, BIOREVE project) for supporting this research work, especially the financial support for research carried out in the CIRIMAT and the LGP laboratories (France), and the Basque government and Tratamientos Superficiales Iontech, S.A. for their financial and technical support under the IG-2007/0000381 grant for the development of the LEPS device and deposition of the coatings carried out in Inasmet-Tecnalia. The French industrial collaborators (TEKNIMED SA and 2PS SA) were financed by the OSEO programs

Microstructural characterization of Co-based coating deposited by low power pulse laser cladding

<p>A detailed microstructural study of Stellite 6 coating deposited on a low carbon ferritic steel substrate using preplaced powder method and low power Nd:YAG pulse laser is performed. The grain structure and solidification texture of the coating are investigated by orientation imaging microscopy (OIM) and scanning electron microscopy. In addition, the effect of consecutive pulses on the microstructure of the coating is examined. The orientation relationship (OR) at coating/substrate interface and the solid state phase transformation in heat-affected zone are studied as well as the Vickers microhardness profile measurement in order to support the microstructural observations. An important conclusion is reached that the shape of solidification front during pulsed laser cladding is similar to the shape of solidification front during continuous cladding with a doubled laser beam scanning speed. Further, OIM reveals the Greninger-Troiano OR between the face centered cubic coating and bcc substrate grains. It is concluded that at the moment of solidification epitaxial growth of the grains in the coating occur on the austenitic grains of the substrate and that an austenite-ferrite transformation occurs in the heat-affected zone upon subsequent cooling.</p>

Influence of Noncovalent Cation/Anion−π Interactions on the Magnetic Exchange Phenomenon

The role of noncovalent ion-π interactions in controlling the intramolecular magnetic exchange interaction in 1,3-phenylene-based bis(aminoxyl) diradical has been investigated computationally through deploying an external ion in the vicinity of the π-cloud of the phenylene coupler. Using spin-polarized hybrid density functional theory-based calculations, we observe that the anions drastically enhance the magnetic exchange interaction for distances below the equilibrium distance. The phenomenon could be understood by two simultaneously occurring effects, which influence the intramolecular magnetic exchange interaction. The first one is the enhancement of the paratropic current density on the aryl couplers due to a small amount of charge transfer. The other one is the attainment of magnetization density on the anionic species due to such charge transfer, favorably altering the magnetic exchange pathway. The achieved understanding provides prospects of a completely new strategy of enhancing the intramolecular ferromagnetic coupling through the assistance of external ionic species inserted in molecular crystals. © 2011 American Chemical Society