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Chromium carbonitride coatings were deposited by cathodic arc physical vapor deposition technology at a temperature of 300 °C, as were used the reactive gasses CH4 and N2. The structural analysis of the CrN coating showed a polycrystalline structure with mixed CrN and Cr2N phases. All studied coatings, including the CrC exhibits fcc structure. The phases were confirmed by X-ray photoelectron spectroscopy measurements where a surface oxidation was also detected. The increase of the CH4 gas flow during the deposition process leads to a parabolic trend with the highest hardness of 33.5 GPa for the coating deposited at CH4 / N2 = 0.53. At the same time the lowest coefficient of friction for both counterparts Al2O3 and ZrO2 (0.28 and 0.26, respectively) were measured at CH4 / N2 = 1.86. The tribological tests reveal that the wear of the coatings increases with an increasing CH4 flow rate, whereas the coefficient of friction decreases. This observed contradiction is explained by a phenomenon described as the effect of Rebinder.
This paper describes the hydrogenation behavior of Zr-1Nb alloy Ti-implanted by plasma immersion ion implantation (PIII). Hydrogen sorption kinetics of the Ti-modified alloy was investigated under gas-phase hydrogenation at 400 °C for 1 h. The influence of implantation time on the protective properties of the modified layer was shown. The lowest hydrogen absorption as well as the highest hydrogen trapping efficiency was achieved after PIII for 30 min. The main contribution to the reduction of hydrogen permeation is the formation of an oxide layer consisting of mixed TiO2 and ZrO2 on the modified surface of the alloy. X-ray photoelectron spectroscopy (XPS) revealed that PIII titanium oxide exists on the surface in the form of TiO2, which transforms to mixed Ti2O3 and TiO2 after hydrogenation. The thickness of the modified layer increases with implantation time that improves the efficiency of hydrogen trapping. All the absorbed hydrogen is gradually distributed in the modified layer and no hydrides are formed after hydrogenation in Ti-modified Zr-1Nb for 15 and 30 min.