The application of ultrasound radiation to the synthesis of nanocrystalline metal oxide in a non-aqueous solvent

Highly crystalline metal oxide nanoparticles of TiO₂, WO₃, and V₂O₅ were synthesized in just a few minutes by reacting transition metal chloride with benzyl alcohol using ultrasonic irradiation under argon atmosphere in a non-aqueous solvent. The sonochemical process was conducted at a relatively low temperature, 363 K. A unique crystallization process of these nanoparticles has been observed and characterized by powder X-ray diffraction (PXRD), high resolution scanning electron microscopy (HRSEM), and BET. The particles’ size and shape measured from HRSEM reveal “quasi” zero-dimensional, spherical TiO₂ particles in the range of 3–7 nm. The V₂O₅ particles have a “quasi” one-dimensional ellipsoidal morphology, with lengths in the range of 150–200 nm and widths varying between 40 and 60 nm. The WO₃ particles were obtained as “quasi” two-dimensional platelets with square shapes having facets ranging from 30 to 50 nm. The thickness of these platelets was between 2 and 7 nm. The mechanism of the reactions leading to these three metal oxide nanoparticles in a non-aqueous system is substantiated by Nuclear Magnetic Resonance (NMR), and Electron Spin Resonance (ESR).     

Holographic entropy packing inside a black hole

If general relativity is spontaneously induced, the black hole limit is governed by a phase transition which occurs precisely at the would-have-been horizon. The exterior Schwarzschild solution then connects with a novel core of vanishing spatial volume. The Kruskal structure, admitting the exact Hawking imaginary time periodicity, is recovered, with the conic defect defused at the origin, rather than at the horizon. The entropy stored inside any interior sphere is universal, equal to a quarter of its surface area, thus locally saturating the 't Hooft-Susskind holographic bound. The associated Komar mass and material energy functions are nonsingular.     

Preparation of enzyme nanoparticles and studying the catalytic activity of the immobilized nanoparticles on polyethylene films

Using high-intensity ultrasound, in situ generated α-amylase nanoparticles (NPs) were immobilized on polyethylene (PE) films. The α-amylase NP-coated PE films have been characterized by E-SEM, FTIR, DLS, XPS and RBS. The PE was reacted with HNO₃ and NPs of the α-amylase were also deposited on the activated PE. The PE impregnated with α-amylase (4 μg per 1 mg PE) was used for hydrolyzing soluble potato starch to maltose. The immobilization improved the catalytic activity of α-amylase at all the reaction conditions studied. The kinetic parameters, K_m (5 and 4 g L^?1 for the regular and activated PE, respectively) and V_max (5 × 10^?7 mol ml^?1 min^?1, almost the same numbers were obtained for the regular and activated PEs) for the immobilized amylase were found to slightly favor the respective values obtained for the free enzyme (K_m = 6.6 g L^?1, V_max = 3.7 × 10^?7 mol ml^?1 min^?1). The enzyme remained bound to PE even after soaking the PE in a starch solution for 72 h and was still found to be weakly active.     

Sonochemical deposition of magnetite on silver nanocrystals

Sonochemical irradiation of iron (II) acetate aqueous solution in presence of silver nanopowder resulted in deposition of magnetite nanoparticles on silver nanocrystals, and imparted them with magnetic properties. The Ag-Fe(3)O(4) nanocomposite is well attracted to a permanent magnet, and demonstrates superparamagnetic behavior typical of nanomaterials in a magnetic field. The characterization of the product by X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HR TEM), energy-dispersive X-ray analysis (EDX), and X-ray photoelectron spectroscopy (XPS) reveal the presence of two phases of the silver and the magnetite, but no chemical interaction between them has been found. The strong anchoring of magnetite to the nanosilver surface was explained as a result of local melting of silver when the magnetite nucleus is thrown at the silver surface by high speed sonochemical microjets.     

Loading magnetic nanoparticles into sperm cells does not affect their functionality

The spontaneous loading of magnetite nanoparticles into sperm cell was carried out by mixing an aqueous colloidal solution of Fe3O4-PVA with sperm cells (10(8) cells/ml) for 2 h at 37 degrees C suspended in glucose-free modified Tyrode solution. The penetration of the magnetite nanoparticles into the sperm cells was monitored by conventional analytical chemistry. We have demonstrated that the motility and the ability to undergo the acrosome reaction (i.e., the ability to fertilize the egg) were not affected by the presence of the magnetite nanoparticles.     

Electroholographic tunable volume grating in the g44 configuration

The g(44) grating is an electroholographic transmission grating in which the applied field is perpendicular to both the grating vector and the wave vector of the incident beam. It is argued that in this configuration the incident beam traverses through a periodically rotating index ellipsoid. It is shown that in the g(44) configuration the Bragg condition is fulfilled for a specific value of the applied field and for a diffracting beam polarization that is perpendicular to that of the incident beam. Consequently, the g(44) grating can be used as an electrically controlled filter. Tunability of 7 nm is demonstrated in a 2mm thick grating.     

The CoMirror algorithm for solving nonsmooth constrained convex problems

We introduce a first-order Mirror-Descent (MD) type algorithm for solving nondifferentiable convex problems having a combination of simple constraint set X (ball, simplex, etc.) and an additional functional constraint. The method is tuned to exploit the structure of X by employing an appropriate non-Euclidean distance-like function. Convergence results and efficiency estimates are derived. The performance of the algorithm is demonstrated by solving certain image deblurring problems.     

Electroinitiated oligomerization of methyl acrylate in methanol solution

The electroinitiated oligomerization of methyl acrylate in methanol solution in the presence of lithium acetate was studied. It was found that in this system the initiator is the methyl radical (obtained from anodic oxidation of acetate ion), and the major termination step is the abstraction of hydrogen radical from methanol by the growing oligomer chain. Eleven compounds were found to be formed in the reaction. A reaction sequence for their formation together with an electric balance for the reactions is given.     

The horizontal axion alternative: The interplay of vacuum structure and flavor interactions

We classify all minimal N-generational SU(3) × SU(2) × U(1) axion models according to the structure of their vacuum manifold M, showing that n ≡ π₀(M) is such that 1 ? n ? N. For n < N, the purely axial U(1)_A must be explicitly broken in the Yukawa sector, implying that U(1)_PQ necessarily distinguishes some quark families. In fact, a complete distinction, i.e. a fully horizontal realization of U(1)_PQ does exist for arbitrary N, leading to definite flavor interaction patterns with non-trivial relative structure of the mass matrices M_u versus M_d. For each n, in particular for the domain-wall-free n = 1 case, we find a unique Yukawa pattern embeddable in unified SU(5), whereas SO(10) can only host n = N. It is emphasized that axion invisibility guarantees the invisibility of flavor changing neutral currents.