Preparation and characterization of compounds of the system FeAs2−xSex

Compounds of the system FeAs_2?xSe_x were ynthesized both as polycrystalline powders by direct combination of the elements and as single crystals by chemical vapor transport. Electrical and magnetic measurements were made on well-characterized samples. These measurements showed that the substitution of selenium for arsenic in the diamagnetic semiconductor FeAs₂ results in metallic, paramagnetic behavior. These results are consistent with a band model proposed by Goodenough for compounds crystallizing in the marcasite structure.     

The amounts Fe, Ba, Sr, K, Ca and Ti in some lichens growing in Erzurum province (Turkey)

The amounts of Fe, Ba, Sr, K, Ca and Ti were determined qualitatively and quantitatively by using energy-dispersive X-ray fluorescence in eight lichen species, Pinus sylvestris, rock and soil in district of Erzurum province (Turkey). Lichen species were Cetraria pinastri (Scop.) Gray, Dermatocarpon miniatum (L.) W. Mann, Lecanora muralis (Schreb.) Rabenh., Pseudevernia furfuracea (L.) Zopf., Ramalina capitata (Ach.) Nyl., Rhizoplaca chrysoleuca (sm.) Zopf., Rhizoplaca melanophthalma (DC.) Leuckert & Poelt, and Xanthoparmelia somloensis (Gyeln.) Hale. The standard addition method was used for the determination of the concentration of Fe, Ba, Sr, K, Ca and Ti. The experimental setup consists of a Si(Li) detector with a resolution of at and annular ⁵⁵Fe and ²⁴¹Am radioactive sources. By the use of intersite, interelement and interspecies comparisons, it is concluded that some metals within the thalli of lichens in Erzurum province may reach high levels even when these plants are growing in rural and isolated sites.     

Structural and electronic properties of InNxP1-x alloy in full range (0 ≤ x ≤1)

We have performed first-principles method to investigate structural and electronic properties of InN_xP_1?x ternary semiconductor alloy in full range (0 ≤ x ≤ 1) using density functional theory. We have used modified Becke–Johnson potential to obtain accurate band gap results. From the electronic band structure calculation we have found that InN_xP_1?x become metal between 47 and 80% of nitrogen concentration. Additional to our band gap calculations, we have also used the band anticrossing model. The band anticrossing model supplies a simple, analytical expression to calculate the physical properties, such as the electronic and optical properties, of III-N_xV_1?x alloys. The knowledge of the electron density of states is required to understand and clarify some properties of materials such as the band structures, bonding character and dielectric function. In order to have a deeper understanding of these properties of the studied materials, the total and partial density of states has been calculated. Finally, we have calculated the total bowing parameter b of studied alloys, together with three contributions b_VD, b_CE, and b_SR due to volume deformation, different atomic electron negativities and structural relaxation, respectively.     

A Novel and Selective Methylene Blue Imprinted Polymer Modified Carbon Paste Electrode

In this study, methylene blue (MB) imprinted microbeads were synthesized and characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM).Differential pulse voltammetric responses of carbon paste electrodes modified with MB imprinted polymer were used to evaluate the adsorption and selectivity features of the polymer. For selectivity studies two basic dyestuffs (thionine blue and toluidine blue) which have similar structure to MB were chosen. Comparison of the voltammetric responses obtained with pure carbon paste and carbon paste modified with either imprinted or nonimprinted polymer electrodes revealed that MB imprinted polymer presented a higher selectivity to the template molecule MB in contrast to structurally similar molecules, thionine blue and toluidine blue.     

Exact and explicit solutions to nonlinear evolution equations using the division theorem

In this paper, we show the applicability of the first integral method, which is based on the ring theory of commutative algebra, to the regularized long-wave Burgers equation and the Gilson-Pickering equation under a parameter condition. Our method provides polynomial first integrals for autonomous planar systems. Through the established first integrals, exact traveling wave solutions are derived in a concise manner.     

Highly Active Cobalt Sulfide/Carbon Nanotube Catalyst for Hydrogen Evolution at Soft Interfaces

Hydrogen evolution at polarized liquid–liquid interfaces [water/1,2‐dichloroethane (DCE)] by the electron donor decamethylferrocene (DMFc) is catalyzed efficiently by the fabricated cobalt sulfide (CoS) nanoparticles and nanocomposites of CoS nanoparticles formed on multi‐walled carbon nanotubes (CoS/CNT). The suspended CoS/CNT nanocomposite catalysts at the interface show a higher catalytic activity for the hydrogen evolution reaction (HER) than the CoS nanoparticles due to the high dispersity and conductivity of the CNT materials, which can serve as the main charge transport pathways for the injection of electrons to attain the catalytic sites of the nanoparticles. The reaction rate increased more than 1000‐fold and 300‐fold by using CoS/CNT and CoS catalysts, respectively, when compared to a non‐catalyzed reaction.     

Synthesis,Characterization, and Spectroscopic Properties of Hexa(4-Bromo-2-Formyl-Phenoxy)Cyclotriphosphazene and Hexa(4-Chloro-2-Formyl-Phenoxy)Cyclotriphosphazene and Fully Substituted Cyclotriphosphazene Derivatives Bearing a Schiff Base at Room Temperature

Abstract

Hexa(4-bromo-2-formyl-phenoxy)cyclotriphosphazene (2) and hexa(4-chloro-2- formyl-phenoxy)cyclotriphosphazene (3) were obtained from the reactions of hexachloro- cyclotriphosphazene (1) with 5-bromosalicylaldehyde and 5-chlorosalicylaldehyde in the presence of (C₂H₅)₃N and K₂CO₃ at room temperature, respectively. The new two organocyclotriphosphazenes bearing formyl groups were reacted with 4-cyano aniline, 2-phenyl aniline, 4-aceto aniline, 5-chloro-2-hydroxy aniline, 2-hydroxy aniline, 4-hydroxy aniline, 2-(4-morpholino)ethyl amine, 4-carboxy aniline, 4-carbomoyl aniline, 2-mercapto aniline, and 5-amino isoquonoline to prepare cyclotriphosphazene derivatives containing a Schiff base at room temperature. However, fully phenoxy-substituted cyclotriphosphazenes containing a Schiff base were isolated from the reactions of the compound 2 and 3 with 5-chloro-2-hydroxy aniline, 2-hydroxy aniline, 4-hydroxy aniline, and 2-(4-morpholino)ethyl amine. The structures of the synthesized compounds were characterized by elemental analysis, IR, and NMR (¹H, ¹³C, ³¹P) spectroscopy. According to the results of the analysis, all synthesized compounds were found to be fully substituted organocyclotriphosphazenes, such as hexa[4-bromo-2-(5-chloro-2-hydroxy-pheyliminomethyl)phenoxy]cyclotriphosphaze (2a). All cyclotriphosphazene derivatives synthesized gave fluorescence emission peaks in range between 300 nm and 410 nm.