High-temperature stability and saturation magnetization of superparamagnetic nickel nanoparticles in microporous polysilazane-derived ceramics and their gas permeation properties.

Superparamagnetic Ni nanoparticles with diameters of about 3 nm are formed in situ at room temperature in a polysilazane matrix, forming Ni/polysilazane nanocomposite, in the reaction between a polysilazane and trans-bis(aceto-kO)bis(2-aminoethanol-k(2)N,O)nickel(II). The thermolysis of the Ni/polysilazane nanocomposite at 700 °C in an argon atmosphere results in a microporous superparamagnetic Ni/silicon oxycarbonitride (Ni/SiCNO) ceramic nanocomposite. The growth of Ni nanoparticles in Ni/SiCNO ceramic nanocomposite is totally suppressed even after thermolysis at 700 °C, as confirmed by HRTEM and SQUID characterizations. The analysis of saturation magnetization of Ni nanoparticles in Ni/polysilazane and Ni/SiCNO nanocomposites indicates that the saturation magnetization of Ni nanoparticles is higher than expected values and infers that the surfaces of Ni nanoparticles are not oxidized. The microporous superparamagnetic Ni/SiCNO nanocomposite is shaped as a free-standing monolith and foam. In addition, Ni/SiCNO membranes are fabricated by the dip-coating of a tubular alumina substrate in a dispersion of Ni/polysilazane in THF followed by a thermolysis at 700 °C under an argon atmosphere. The gas separation performance of Ni/SiCNO membranes at 25 and 300 °C is assessed by the single gas permeance (pressure rise technique) using He, H2, CO2, N2, CH4, n-propene, n-propane, n-butene, n-butane, and SF6 as probe molecules. After hydrothermal treatment, the higher increase in the hydrogen permeance compared to the permeance of other gases as a function of temperature indicates that the hydrogen affinity of Ni nanoparticles influences the transport of hydrogen in the Ni/SiCNO membrane and Ni nanoparticles stabilize the structure against hydrothermal corrosion.

Visible light photocatalysis with c-WO(3-x)/WO3×H2O nanoheterostructures in situ formed in mesoporous polycarbosilane-siloxane polymer.

In recent years, there have been significant efforts to find novel photocatalytic materials with improved properties. Thus, there is an active ongoing search for new materials that can operate at a broad range of wavelengths for photocatalytic reactions. Among photocatalytically active semiconductors, considerable attention has been given to tungsten oxide with a band gap of E(g) ≈ 2.6 eV, which provides the opportunity to harvest visible light. In the present work, we report on a one-step synthesis of c-WO(3-x)/WO3×H2O nanowhiskers dispersed in a hydrolytically stable mesoporous polycarbosilane-siloxane ([-Si(O)CH2-]n) matrix. The as-synthesized nanocomposites possess high photocatalytic activity for the degradation of methylene blue (MB) under visible light irradiation. The enhanced photocatalytic activity is due to (i) the reduction in the electron-hole recombination rate because of the reduced dimensions of nanowhiskers, (ii) more efficient consumption of photogenerated electrons and holes as a result of the high surface-to-bulk-ratio of the nanowhiskers, and (iii) better electron-hole pair separation due to the formation of c-WO(3-x)/WO3×H2O nanoheterostructures.

trans-Bis(acetato-κO)bis-(2-amino-ethanol-κ(2)N,O)nickel(II).

In the title compound, [Ni(CH(3)CO(2))(2)(C(2)H(7)NO)(2)], the Ni(II) cation, located on an inversion center, is N,O-chelated by two 2-amino-ethanol mol-ecules and further coordinated by two monodendate acetate anions in a slightly distorted octa-hedral geometry. The latter is stabilized by intra-molecular O-H⋯O hydrogen bonds involving the non-coordinated O atom of the acetate and the H atom of the hy-droxy group of the 2-amino-ethanol ligand. In the crystal, N-H⋯O hydrogen bonds link the mol-ecules into a three-dimensional supra-molecular framework that involves (a) the coordinated acetate O atom and one of the H atoms of the amino group and (b) the non-coordinated acetate O atom and the other H atom of the amino group.