Optimization of electrophoretic deposition technique to control doping and densification of protective spinel coatings for SOC interconnects

Manganese cobaltite spinel coatings have been reported to limit oxidation and Cr-evaporation from ferritic stainless steel interconnects in solid oxide cell stacks; however, the implementation of the functional properties of the base Mn–Co spinel coating and compatibility with the substrate can be pursued through the optimisation of the coating composition, as well as the deposition method and sintering profile. Electrophoretic deposition (EPD) allows to deposit homogeneous layers in few seconds on complexly shaped steel components; it also offers the possibility to produce in-situ doped coatings, avoiding time and energy consuming multi-step processes. In this work, various EPD suspensions are optimised to achieve a single step co-deposition of CuO, Fe2O3 and Mn1,5Co1,5O4 on Crofer 22 APU. Different Fe-Cu doped Mn–Co spinel are successfully obtained by controlling the precursors amount in the EPD suspension and subsequent reactive sintering, as proved by detailed SEM and TEM analyses. Improved functional properties of produced coatings are evaluated in terms of oxidation kinetics and area specific resistance. Both the iron and copper amount in the coating and the sintering process significantly influence the coating densification, with benefits to the protective properties and thermomechanical compatibility with the interconnect

Manganese–cobalt based spinel coatings processed by electrophoretic deposition method: The influence of sintering on degradation issues of solid oxide cell oxygen electrodes at 750◦c

This paper seeks to examine how the Mn–Co spinel interconnect coating microstructure can influence Cr contamination in an oxygen electrode of intermediate temperature solid oxide cells, at an operating temperature of 750◦C. A Mn–Co spinel coating is processed on Crofer 22 APU substrates by electrophoretic deposition, and subsequently sintered, following both the one-step and two-step sintering, in order to obtain significantly different densification levels. The electrochemical characterization is performed on anode-supported cells with an LSCF cathode. The cells were aged prior to the electrochemical characterization in contact with the spinel-coated Crofer 22 APU at 750◦C for 250 h. Current–voltage and impedance spectra of the cells were measured after the exposure with the interconnect. Post-mortem analysis of the interconnect and the cell was carried out, in order to assess the Cr retention capability of coatings with different microstructures

Stereoselective Activity of 1-Propargyl-4-styrylpiperidine-like Analogues That Can Discriminate between Monoamine Oxidase Isoforms A and B

The resurgence of interest in monoamine oxidases (MAOs) has been fueled by recent correlations of this enzymatic activity with cardiovascular, neurological, and oncological disorders. This has promoted increased research into selective MAO-A and MAO-B inhibitors. Here, we shed light on how selective inhibition of MAO-A and MAO-B can be achieved by geometric isomers of cis-and trans-1-propargyl-4-styrylpiperidines. While the cis isomers are potent human MAO-A inhibitors, the trans analogues selectively target only the MAO-B isoform. The inhibition was studied by kinetic analysis, UV-vis spectrum measurements, and X-ray crystallography. The selective inhibition of the MAO-A and MAO-B isoforms was confirmed ex vivo in mouse brain homogenates, and additional in vivo studies in mice show the therapeutic potential of 1-propargyl-4-styrylpiperidines for central nervous system disorders. This study represents a unique case of stereoselective activity of cis/trans isomers that can discriminate between structurally related enzyme isoforms