Effect of various storage media on the physicochemical properties of plasma-treated dental zirconia.

This study investigated the effect of various storage media on the physicochemical properties of plasma-treated 3-mol% yttria-stabilized tetragonal zirconia: air, vacuum, deionized water (DIW), and plasma-activated water (PAW). Each group was divided into five subgroups based on storage periods: immediately after NTP irradiation (T0), and after 1 week (T1), 2 weeks (T2), 3 weeks (T3), and 4 weeks (T4). The control group (C) received no treatment.

Plasma Surface Modification of 3Y-TZP at Low and Atmospheric Pressures with Different Treatment Times.

The efficiency of plasma surface modifications depends on the operating conditions. This study investigated the effect of chamber pressure and plasma exposure time on the surface properties of 3Y-TZP with N/Ar gas. Plate-shaped zirconia specimens were randomly divided into two categories: vacuum plasma and atmospheric plasma.

Effect of the Plasma Gas Type on the Surface Characteristics of 3Y-TZP Ceramic.

Plasma surface treatment can be an attractive strategy for modifying the chemically inert nature of zirconia to improve its clinical performance. This study aimed to clarify the effect of plasma gas compositions on the physicochemical surface modifications of 3 mol% yttria-stabilized zirconia (3Y-TZP). The cold, atmospheric plasma discharges were carried out by using four different plasma gases, which are He/O, N/Ar, N, and Ar from an application distance of 10 mm for 60 s.

Copper-Catalyzed Oxidative Cleavage of the C-C Bonds of β-Alkoxy Alcohols and β-1 Compounds.

Copper-catalyzed aerobic oxidation conditions were employed to promote the C-C bond cleavage of β-alkoxy alcohols and β-1 compounds (lignin model compounds). Besides these compounds, various 1,2 and 1,3-diols were successfully converted to aldehydes. We propose the Cu(I)-catalyzed mechanism explaining the C-C cleavage of these 1,2 and 1,3-dihydroxy compounds and β-alkoxy alcohols based on XPS data.

Photocurrent Enhancement by a Rapid Thermal Treatment of Nanodisk-Shaped SnS Photocathodes.

Photocathodes made from the earth-abundant, ecofriendly mineral tin monosulfide (SnS) can be promising candidates for p/n-type photoelectrochemical cells because they meet the strict requirements of energy band edges for each individual photoelectrode. Herein we fabricated SnS-based cell that exhibited a prolonged photocurrent for 3 h at -0.3 V vs the reversible hydrogen electrode (RHE) in a 0.

Engineering defects and photocatalytic activity of TiO nanoparticles by thermal treatments in NH and subsequent surface chemical etchings.

TiO nanoparticles with N dopants were prepared by thermal treatments in NH and their surface defects were controlled by post chemical etching in HF to find out the influence of the N dopants on photoactivity. The effect of N-doping is found to enhance the photoactivity of TiO, but is strongly dependent on the degree of N-doping and the detailed distribution of nitrogen species within the TiO nanoparticles. In particular, the N-rich layers formed near the surface are found to contribute to the enhanced photoactivity due to the reduced band gap.

The effect of oxygen vacancies on the binding interactions of NH3 with rutile TiO2(110)-1 × 1.

A series of NH(3) temperature-programmed desorption (TPD) spectra were taken after dosing NH(3) at 70 K on rutile TiO(2)(110)-1 × 1 surfaces with oxygen vacancy (V(O)) concentrations of ~0% (p-TiO(2)) and 5% (r-TiO(2)), respectively, to study the effect of V(O)s on the desorption energy of NH(3) as a function of coverage, θ. Our results show that in the zero coverage limit, the desorption energy of NH(3) on r-TiO(2) is 115 kJ mol(-1), which is 10 kJ mol(-1) less than that on p-TiO(2). The desorption energy from the Ti(4+) sites decreases with increasing θ due to repulsive NH(3)-NH(3) interactions and approaches ~55 kJ mol(-1) upon the saturation of Ti(4+) sites (θ = 1 monolayer, ML) on both p- and r-TiO(2).

Alcohol Dehydration on Monooxo W═O and Dioxo O═W═O Species.

The dehydration of 1-propanol on nanoporous WO3 films prepared via ballistic deposition at ∼20 K has been investigated using temperature-programmed desorption, infrared reflection absorption spectroscopy, and density functional theory. The as-deposited films are extremely efficient in 1-propanol dehydration to propene. This activity is correlated with the presence of dioxo O═W═O groups, whereas monooxo W═O species are shown to be inactive.

Catalytic dehydration of 2-propanol on (WO3)3 clusters on TiO2(110).

Our study of a (WO3)3/TiO2(110) model mixed oxide catalyst shows that this system is an extremely efficient for dehydration of alcohols, effectively lowering the energy barrier as much as possible for an endothermic reaction without yielding a significant concentration of other side products.