Enhanced visible-light photocatalytic performance of Fe3O4 nanopyramids for water splitting and dye degradation

Journal of Solid State Electrochemistry - Iron oxide (Fe3O4) pyramid nanostructures were synthesized via a co-precipitation method, without using surfactants or template, for photocatalytic and...     

Synthesis and reactions of 2-[α-(3,4-disubstituted phenacyl)-p-substituted styryl]-4H-3,1-benzoxazin-4-ones

Science Department, Faculty of Teachers, P.O.Box 2313, Al Hasa, 31982, Saudi Arabia Faculty of Engineering, Ain Shames University, EgyptChemistry Department, Faculty of Science, Ain Shames University, Egypt     

Exact solutions and conservation laws of Zakharov-Kuznetsov modified equal width equation with power law nonlinearity

This paper obtains solutions to the Zakharov-Kuznetsov modified equal width equation with power law nonlinearity. The Lie symmetry approach and the simplest equation method are used to obtain these solutions. Moreover, conservation laws are derived for the underlying equation by employing two approaches: the new conservation theorem and the multiplier method.     

Flow injection spectrophotometric determination of iron(III) using diphenylamine-4-sulfonic acid sodium salt

A highly sensitive and very simple spectrophotometric flow-injection analysis (FIA) method for the determination of iron(III) at low concentration levels is presented. The method is based on the measurement of absorbance intensity of the red complex at 410 nm formed by iron(III) and diphenylamine-4-sulfonic acid sodium salt (DPA-4-SA). It is a simple, highly sensitive, fast, and low cost alternative method using the color developing reagent DPA-4-SA in acetate buffer at pH 5.50 and the flow-rate of 1 mL min⁻¹ with the sample throughput of 60 h⁻¹. The method provided a linear determination range between 5 μg L⁻¹ and 200 μg L⁻¹ with the detection limit (3S) of 1 μg L⁻¹ of iron(III) using the injection volume of 20 μL. FIA variables influencing the system performance were optimized. The amount of iron(III) and total iron in river and seawater samples was successfully determined. Repeatability of the measurements was satisfactory at the relative standard deviation of 3.5 % for 5 determinations of 10 μg L⁻¹ iron(III). The accuracy of the method was evaluated using the standard addition method and checked by the analysis of the certified material Std Zn/Al/Cu 43 XZ3F.     

Pyrene-BODIPY-substituted novel water-soluble cyclotriphosphazenes: synthesis,characterization, and photophysical properties

In the present work, pyrene-boron-dipyrromethene (BODIPY)-substituted novel water-soluble cyclotriphosphazene derivatives (6 and 7) were synthesized by click reactions between a cyclotriphosphazene derivative with a hydrophilic glycol side group (2) and BODIPYs (4 and 5). All of the new compounds (2, 6, and 7) were characterized by Fourier-transform infrared and nuclear magnetic resonance spectroscopy, as well as mass spectrometry and elemental analysis. The photophysical properties of the BODIPY-substituted cyclotriphosphazenes (6 and 7) were investigated by UV-Vis and fluorescence emission spectroscopy in water and water/solvent mixtures. It was found that the target compounds were soluble in water and could be potential candidates as water-soluble fluorescent dyes for the desired applications.     

Synthesis,characterization, and biological activities of some novel thienylpyrido[3′,2′:4,5]thieno[3,2-d]pyrimidines and related heterocycles

3-Cyano-5-ethoxycarbonyl-6-methyl-4-(2′-thienyl)-pyridine-2(1H)-thione ( 1 ) is synthesized and reacted with chloroacetamide or chloroacetonitrile to give 3-amino-5-ethoxycarbonyl-6-methyl-4(2′-thienyl)-thieno[2,3-b]pyridine-2-carboxamide 3a or its 2-carbonitrile analog 3b , respectively. Cyclocondensation of 3a with triethylorthoformate produced the corresponding pyridothienopyrimidineone 4 , which on heating with phosphorus oxychloride gave 4-chloropyrimidine derivative 5 . Compound 5 was used as key intermediate for synthesizing compounds 6 , 9 , 10 , 11 , and 12 upon treatment with some nucleophilic reagents such as thiourea, 5-phenyl-s-triazole-3(1H)-thione, piperidine, morpholine, or hydrazine hydrate, respectively. Reaction of pyridothienopyrimidinethione 6 with N-(4-tolyl)-2-chloroacetamide or ethyl bromoacetate afforded the corresponding S-substituted methylsulfanylpyrimidines 7 or 8 . The condensation of 3b with triethylorthoformate gave azomethine derivative 13 , which was reacted with hydrazine hydrate to give ethyl 3-amino-3,4-dihydro-4-imino-7-methyl-9-(2′-thienyl)pyrido[3′,2′:4,5]thieno[3,2-d]pyrimidine-8-carboxylate ( 14 ). Compounds 12 and 14 were used as precursors for synthesizing other new thienylpyridothienopyrimidines as well as isomeric thienyl-s-triazolopyridothieno- pyrimidines. All synthesized compounds were characterized by elemental and spectral analyses such as IR, ¹H NMR, and ¹³C NMR. In addition, majority of synthesized compounds were tested for their antifungal activity against five strains of fungi. Moreover, compounds 3a , 5 , 6 , 8 , and 22 were screened for their anticancer activity against HEPG-2 and MCF-7 cell lines.     

A note on defining singular integral as distribution and partial differential equations with convolution term

In this study first we consider the singular integrals as generalized functions in two dimensions and then we solve the non-homogeneous wave equation with convolutional term by using the generalized functions as boundary conditions.     

Holograms in CaF2 crystals with high content of alkaline impurities

Similarities and dissimilarities of holograms recorded in fluorite crystals with color centers that are pure or contain relatively high concentrations of an alkaline impurity (sodium) are considered. It is shown that, in these two cases, the mechanism of recording is the same, but formation of the impurity-vacancy complexes in heavily doped crystals causes certain peculiarities in the types of color centers in the initial crystals and those with holograms and determines specific features of spatial redistribution of centers in the process of recording. These features reduce the diffraction efficiency of holograms in heavily doped crystals compared to pure and weakly activated crystals.     

Impacts of uniaxial elongation on the bandstructures of two-dimensional sonic crystals and associated applications

Influences of uniaxial elongation along the [11] direction of triangular and [10] direction of square sonic crystals under the constraint of conserved unit cell area are investigated by examining band structures and equi-frequency contours. Lowest-lying band gap of the triangular lattice observed at high filling fractions diminishes for negative elongation (compression), whereas another band gap develops at lower frequencies whose width reaches appreciable values for moderate elongation. The band gap of the square lattice, which appears at high filling fractions, is modified slightly with elongation. Frequency ranges of the bands, and thus the group velocities along the high-symmetry directions, vary with elongation which may be useful in applications like slow sound propagation. Elongation is observed to modify the equi-frequency contours significantly through reducing the lattice symmetry. The most prominent impact is the transformation of closed contours into open ones, whereas the rest are stretched either along or normal to the elongation axis of the 1st Brillouin Zone. This observation is utilized to implement wide-band all-angle self-collimation and superprism effect, which are demonstrated through Finite-Element computations.