Effects of niobium pentoxide nanoparticles on the tribological properties of electrodeposited ZnNi coatings

Electrodeposited ZnNi coatings are widely used to improve the corrosion resistance of steel substrates, but their tribological properties are also relevant for loaded contacts under relative motion. This work investigates the hypothesis of improving tribological properties of electrodeposited ZnNi coatings via dispersion of niobium pentoxide nanoparticles (1g/L) in the electrolytic bath. The niobium pentoxide nanoparticles were produced via hydrothermal synthesis assisted by microwave. The surface morphology and chemical composition of the coatings were analysed by scanning electron microscopy coupled with X-ray dispersive energy, X-ray diffraction and X-ray photoelectron spectroscopy. The tribological performance of the coatings was assessed using dry reciprocating ball-on-flat tests at normal loads between 3 and 6 N. The use of niobium pentoxide nanoparticles resulted in significantly denser coatings, with some Nb incorporated in the coated surfaces. Under the lowest normal load, all coated specimens showed relatively low friction (~0.2) and negligible damag. As the normal load increased, the coating produced using niobium pentoxide nanoparticles showed stronger adherence, while conventional ZnNi coating showed increased friction and spalling for the highest load. It is believed that the Nb2O5 nanoparticles increased the number of sites for heterogeneous nucleation, refining the microstructure, so that tougher and more adherent coatings were produced.

Evaluation of the Effect of Deposition pH on the Physico-chemical Properties of Electrochemically Deposited Cadmium Telluride for Photovoltaic Device Applications

Two-electrode (2E) configuration was successfully utilised in the electrochemical deposition of cadmium telluride (CdTe) on fluorine-doped tin oxide (FTO) substrate with the main emphasis on the electrolytic bath pH. The electrochemical deposition pH explored is within the range of (1.00 to 6.00)±0.02 for the aqueous electrolyte comprising of tellurium oxide (TeO2) and cadmium nitrate (Cd(NO3)2) which are the respective precursors of Te and Cd. The optical, structural, morphological, compositional, and electrical properties of the electroplated CdTe thin-films were respectively explored using UV-Vis spectrophotometry, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), and photoelectrochemical (PEC) cell measurements. The optical characterisation show that the CdTe samples exhibit dissimilar absorbance depending on the growth pH for both the as-deposited layers and post-growth treated CdTe layers. A decrease in the absorption edge slope and dip in the bandgap was observed away from pH2. The bandgap of the post-growth treated CdTe layers showed enhancement as it leans towards 1.45 eV, with the trend retention of absorption edge slope, similar to the as-deposited CdTe layers. The electrodeposited CdTe thin-films show a dominant orientation along the cubic (111) CdTe plane, while both the the calculated crystallite size and the XRD peak intensity Pi decreases with the electroplating pH outside the (2.00 to 3.00)±0.02 range. The EDX analyses depicts an alteration in the ratio of Cd to Te atomic percentage relative to the pH of the electrolyte. Comparatively high Te atomic ratio was observed at lower pH values and vice versa with increase alkalinity of the electrolyte. The obtained morphology depicts that the underlying FTO layers are well covered with a gradual reduction in the grain size of the CdTe observable away from pH value (2.00 and 3.00). The photoelectrochemical cell study depicts that the conduction type of the CdTe layers can also be attributed to the CdTe-electrolytic bath pH value.

Obtaining Mn-Co Alloys in AISI 430 Steel from Lithium-Ion Battery Recycling: Application in SOFC Interconnectors

The recycling of exhausted lithium-ion batteries from mobile phones originate five solutions with different Co and Mn proportions that were used as electrolytic solutions to obtain Mn-Co spinel coatings on the surface of AISI430 stainless steel. The coatings are intended to contain chromium volatility in the working conditions of Solid Oxide Fuel Cells (SOFC) metallic interconnectors. Potentiostatic electrodeposition was the technique used to obtain Mn-Co coatings from low concentration electrolytes at pH = 3.0 and potential applied −1.3 V. Charge efficiency data were used for sample optimization. Three optimized samples were subjected to oxidation heat treatment at 800 °C for 300 h and then characterized by XRD, SEM and EDS. The results showed that the addition of manganese ions instead of cobalt ions in the electrolytic bath produces more stable and well-distributed deposits as the ratio of the two ions becomes equal in the electrolytic bath. Thin, homogeneous and stable spinel coatings (Mn, Co)3O4 2.8 μm and 3.9 μm thick were able to block chromium volatility when exposed to SOFC operating temperature.

STUDY OF THERMAL INTERFERENCE OF ELEMENTS OF THE UNDERGROUND HEAT EXCHANGER IN ELECTROLYTIC BATH

A study was made of the mutual thermal eff ect of the tube elements of soil heat exchangers. It was determined that the number of pipe elements of the soil heat exchanger has the greatest eff ect on the amount of heat infl ux from the soil mass. It is established that when placing the pipe elements at a distance of one diameter from each other, it causes a signifi cant decrease in the heat infl ux to the soil heat exchanger. Increasing the distance between the pipes reduces the thermal interference of the elements. The coeffi cients of thermal interference are found for various confi gurations of ground heat exchangers, which depending on the number of pipes and the distance between them vary from 0.621 to 0.99.

Physicochemical characterization of PEG-modified PbO2 coatings electrodeposited from a methanesulfonate bath

This study explores the preparation and application of polyethylene glycol (PEG)-modified PbO2 electrodes. The PEG-modified PbO2 coatings were electrodeposited on a Ti/SnO2-Sb substrate from a methanesulfonate electrolytic bath containing different amounts of PEG. Structural and morphologic characterization was carried out for the deposited electrodes. The presence of PEG in the deposition bath represses the nucleation process and grain growth process in PbO2 deposition. Increasing PEG addition results in an increased [Formula: see text]-PbO2 content and decreased crystallite size. At a limited PEG addition [Formula: see text]4 g/L, a rough and pyramidal surface morphology is presented in the PbO2 coatings. A higher PEG addition at 6 g/L leads to a dense and smooth coating surface yet with less uniformity. Electrochemical characterization reveals a great electrocatalytic activity for the modified PbO2 electrodes when the PEG addition is [Formula: see text]4 g/L.