Tantalum oxynitride thin films have been deposited by reactive magnetron sputtering, using a fixed proportion reactive gas mixture (85% N2 + 15% O2). To produce the films, the partial pressure of the mixture in the working atmosphere was varied. The characteristics of the produced films were analyzed from three main perspectives and correspondent correlations: the study of the bonding states in the films, the efficiency of photo-degradation, and the antibacterial/antibiofilm capacity of the coatings against Salmonella. X-ray Photoelectron Spectroscopy results suggest that nitride and oxynitride features agree with a constant behavior relative to the tantalum chemistry. The coatings deposited with a higher reactive gas mixture partial pressure exhibit a significantly better antibiofilm capacity. Favorable antibacterial resistance was correlated with the presence of dominant oxynitride contributions. The photocatalytic ability of the deposited films was assessed by measuring the level of degradation of an aqueous solution containing methyl orange, with or without the addition of H2O2, under UV or VIS irradiation. Degradation efficiencies as high as 82% have been obtained, suggesting that tantalum oxynitride films, obtained in certain configurations, are promising materials for the photodegradation of organic pollutants (dyes).
Abstract. The present paper aims at studying the behaviour of the poly(vinyl alcohol) [PVA] cryogel in the presence of 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM] + [BF 4 ] -) aqueous solutions with various concentrations. The gravimetric method showed that the swollen PVA cryogels exhibit mechanically active behaviour. PVA cryogels showed shrinking in the presence of ionic liquid, (IL), and re-swelling in the presence of distilled water. The re-swelling is not completely reversible, due to the influence of the IL ions on the gel morphology. The Fourier transform infrared (FTIR) spectra have indicated no chemical interaction between the PVA and the studied IL, but highlighted the gel crystallinity change as a function of IL concentration, as well as changes in the bound water amount. Rheological analyses showed dominating plastifying effect of the cation at a lower IL concentration and dominating kosmotropic effect of the anion at a higher IL concentration. A phenomenological kinetic equation that takes into account both fluxes of matters, in and out of the gel, is proposed, explaining the alteration of the gel properties when it comes in contact with BMIMBF 4 solutions.
This paper discusses the structure morphology and the thermal and swelling behavior of physically crosslinked hydrogels, obtained from applying four successive freezing–thawing cycles to poly (vinyl alcohol) blended with various amounts of κ-carrageenan. The addition of carrageenan in a weight ratio of 0.5 determines a twofold increase in the swelling degree and the early diffusion coefficients of the hydrogels when immersed in distilled water, due to a decrease in the crystallinity of the polymer matrix. The diffusion of water into the polymer matrix could be considered as a relaxation-controlled transport (anomalous diffusion). The presence of the sulfate groups determines an increased affinity of the hydrogels towards crystal violet cationic dye. A maximum physisorption capacity of up to 121.4 mg/g for this dye was attained at equilibrium.
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