The effect of phosphate group replacement by sulfate groups on the phase formation in the synthesis of hydroxyapatite

Sulfate-substituted hydroxyapatite materials with a degree of substitution of up to 20 mol % (Ca₁₀(PO₄)_{(6 – 0.06x)}(SO₄)_0.09x (OH)₂, x = 0, 0.1, 0.5, 1, 5, 10, and 20) were synthesized. For substitutions of 0, 0.1, 0.5, and 1 mol %, a single-phase material with the apatite structure is formed. On further increase in the concentration of SO₄ ^2? groups up to 20 mol %, a second phase, CaSO₄, is formed; the amount of this phase increases for higher degrees of substitution. The unit cell parameters of hydroxyapatite-based materials change slightly upon the replacement of phosphate groups by sulfate groups: the parameter a tends to increase, while c tends to decrease. The introduction of sulfate groups results in decreasing particle size.     

New polymer composites based on keratin and polyethylene

New biodegradable composites based on keratin and polyethylene have been produced under shear deformation. It has been demonstrated that the introduction of keratin leads to an increase in elastic modulus and to a decrease in ultimate tensile strength and elongation at break of the compositions. Elongation at break ε_b depends on the keratin dispersity; the highest ε_b values are observed for the compositions containing the smallest keratin particles. It has been shown that the compositions are susceptible to mold fungi; i.e., they are biodegradable.     

Experimental study of gasification of vacuum residue in metal melt by alternating reactor feeding with carbonaceous feedstock and oxidant

Processes occurring in a metal melt during plasma-assisted melt gasification of carbonaceous feedstock have been studied in the mode of alternating feeding the reactor with the carbonaceous feedstock and oxidant. Vacuum residue was used as an oxygen-free carbonaceous material, and air and steam were used as an oxidant. The results of the study show that by alternating the carbonaceous-feedstock pyrolysis step and the step of carbon oxidation in the metal melt, it is possible to produce synthesis gas with any desired H₂/CO ratio.     

Ammonolysis of magnesiothermic tantalum powders

Tantalum nitrides are synthesized by ammonolysis of a mesoporous magnesiothermic tantalum powders. The effect of specific surface area of the powders and synthesis temperature on product composition is shown. Nitrogen content in the ammonolysis product of tantalum powder with a specific surface area of 56 m² g^–1 corresponds to oxynitride TaON exposed to 600°C for 1 h. The specific surface area of the oxynitride is 35 m² g^–1.     

Dielectric relaxation of Tripropylene glycol–water mixture using time domain reflectometry

The complex permittivity spectra of tripropylene glycol and water solutions have been obtained by time domain reflectometry (TDR) technique in the frequency range from 10 MHz to 30 GHz and the temperature range 20°C–05°C. The dielectric relaxation parameters such as static dielectric constant and relaxation time were obtained by using the non-linear least square fit method. The intermolecular hydrogen bonding of tripropylene glycol–water has been discussed using the Kirkwood correlation factor and thermodynamic parameters. The activation energy decreases with increase in water content in the mixture as expected in the Arrhenius behaviour. The dielectric constant for mixtures has been fitted to the Bruggeman mixture formula in the non-linear case.     

Time‐Resolved Energetics of Photoprocesses in Prokaryotic Phytochrome‐Related Photoreceptors

Time‐resolved photoacoustics (PA) is uniquely able to explore the energy landscape of photoactive proteins and concomitantly detects light‐induced volumetric changes (ΔV) accompanying the formation and decay of transient species in a time window between ca. 20 ns and 5 μs. Here, we report PA measurements on diverse photochromic bilin‐binding photoreceptors of prokaryotic origin: (1) the chromophore‐binding GAF3 domain of the red (R)/green (G) switching cyanobacteriochrome 1393 (Slr1393g3) from Synechocystis; (2) the red/far red (R/FR) Synechocystis Cph1 phytochrome; (3) full‐length and truncated constructs of Xanthomonas campestris bacteriophytochrome (XccBphP), absorbing up to the NIR spectral region. In almost all cases, photoisomerization results in a large fraction of energy dissipated as heat (up to 90%) on the sub‐ns scale, reflecting the low photoisomerization quantum yield (<0.2). This “prompt” step is accompanied by a positive ΔV₁ = 5–12.5 mL mol^?1. Formation of the first intermediate is the sole process accessible to PA, with the notable exception of Slr1393g3‐G for which ΔV₁ = +4.5 mL mol^?1 is followed by a time‐resolved, energy‐conserving contraction ΔV₂ = ?11.4 mL mol^?1, τ₂ = 180 ns at 2.4°C. This peculiarity is possibly due to a larger solvent occupancy of the chromophore cavity for Slr1393g3‐G.