Optical properties of porous silicon processed in tetraethyl orthosilicate

We investigate the change in the composition and optical properties of porous silicon (por-Si) obtained by electrochemical etching of a palate made of n-type (111) silicon single crystal under high-temperature annealing and processing in tetraethyl orthosilicate (TEOS). It is shown that TEOS processing and annealing prevent contamination of a sample stored for a long time in atmosphere. The processing of por-Si in TEOS does not change the position of the photoluminescence (PL) peak and suppresses PL to a smaller extent as compared to annealing of por-Si. This increases the reliability of optoelectronic devices based on por-Si.     

Chitosan loaded with silver nanoparticles,CS‐AgNPs,using thymus syriacus,wild mint,and rosemary essential oil extracts as reducing and capping agents

The present study describes the green method for the preparation of chitosan loaded with silver nanoparticles (CS‐AgNPs) in the presence of 3 different extracted essential oils. The essential oils play dual roles as reductant and capping agents. The reducing power and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) assay for the 3 essential oils—Thymus syriacus (T), wild mint (M), and rosemary (R)—have been reported. The preparation of CS‐AgNPs was performed by 2 steps. The 3 previously extracted essential oils have been used as reducing and capping agent in the first step, while in the second step, silver nanoparticles were integrated in chitosan. The integration of AgNPs in the structure of chitosan was confirmed by ultraviolet‐visible, Fourier transform infrared spectroscopy, scanning electron microscopy techniques, and energy dispersive X‐ray. Surface plasmon resonance confirmed the formation of CS‐AgNPs with maximum absorbance at λ_max between 405 ‐ 410 and 410 ‐ 430 nm for colloidal and films of CS‐AgNPs, respectively. The intensity of bands at 3408 cm^?1 in the fourier transform infrared spectroscopy measurements was decreased substantially and shifted slightly to lower frequency (?υ = 43 cm^?1). Scanning electron microscopy shows a spherical morphology of AgNPs with size of 62 nm for both colloidal and film samples, and energy dispersive X‐ray analysis shows peaks confirming AgNPs formation.     

Composition and structure of nanoporous silicon layers with galvanically deposited Fe and Co

The morphology and phase composition of porous silicon with galvanically deposited Fe and Co particles were investigated by ultrasoft X-ray emission spectroscopy, X-ray absorption near-edge structure spectroscopy, and scanning electron microscopy. It is shown that iron uniformly covers the surface of porous silicon, whereas cobalt penetrates into pores in the form of nanoparticles. It is established that iron is present mainly in the Fe₂O₃ phase with an admixture of FeO and Fe₃O₄. Cobalt forms a mixture of phases of metallic Co and Co₂O₃.     

Progress in development of Nuclotron accelerator complex

The Nuclotron superconducting synchrotron was constructed in 1987–1992 [1]; it is the world’s first synchrotron based on fast cycling “window frame” electromagnets with a superconducting coil. For a design field of dipole magnets of 2 T, the magnetic rigidity is 45 T m, which corresponds to the energy of heavy nuclei (for example, gold) of 4.5 GeV/nucleon. The Nuclotron accelerator complex is currently being upgraded (the Nuclotron-M project); this upgrade is considered a key part of the first stage of fulfilling the new Joint Institute for Nuclear Research (JINR) project: the Nuclotron-based Ion Collider fAcility and Multi-Purpose Detector (NICA/MPD). The most important task of this new project is the preparation of basic Nuclotron systems for its reliable operation as part of the NICA accelerator complex. Basic results of activity on the project, which started in 2007, are presented and the results of the last Nuclotron runs are analyzed.     

Synthesis,Antibacterial, and Antioxidant Evaluation of Novel Series of Condensed Thiazoloquinazoline with Pyrido,Pyrano, and Benzol Moieties as Five- and Six-Membered Heterocycle Derivatives

A novel synthesis of thiazolo[2,3-b]quinazolines 4(a–e), pyrido[2′,3′:4,5]thiazolo[2,3-b]quinazolines {5(a–e), 6(a–e), and 7(a–e)}, pyrano[2′,3′:4,5]thiazolo[2,3-b]quinazolines 8(a–e), and benzo[4,5]thiazolo[2,3-b]quinazoloine9(a–e) derivatives starting from 2-(Bis-methylsulfanyl-methylene)-5,5-dimethyl-cyclohexane-1,3-dione 2 as efficient α,α dioxoketen dithioacetal is reported and the synthetic approaches of these types of compounds will provide an innovative molecular framework to the designing of new active heterocyclic compounds. In our study, we also present optimization of the synthetic method along with a biological evaluation of these newly synthesized compounds as antioxidants and antibacterial agents against the bacterial strains, like S. aureus, E. coli, and P. aeruginosa. Among all the evaluated compounds, it was found that some showed significant antioxidant activity at 10 μg/mL while the others exhibited better antibacterial activity at 100 μg/mL. The results of this study showed that compound 6(c) possessed remarkable antibacterial activity, whereas compound 9(c) exhibited the highest efficacy as an antioxidant. The structures of the new synthetic compounds were elucidated by elemental analysis, IR, ¹H-NMR, and ¹³C-NMR.     

Cetyl‐alcohol‐reinforced hollow fiber solid/liquid‐phase microextraction and HPLC–DAD analysis of ezetimibe and simvastatin in human plasma and urine

A new cetyl‐alcohol‐reinforced hollow fiber solid/liquid‐phase microextraction (CA–HF–SLPME) followed by high‐performance liquid chromatography–diode array detection (HPLC–DAD) method was developed for simultaneous determination of ezetimibe and simvastatin in human plasma and urine samples. To prepare the CA–HF–SLPME device, the cetyl‐alcohol was immobilized into the pores of a 2.5 cm hollow fiber micro‐tube and the lumen of the micro‐tube was filled with 1‐octanol with the two ends sealed. Afterwards, the prepared device was introduced into 10 mL of the sample solution containing the analytes with agitation. Under optimized conditions, calibration curves plotted in spiked plasma and urine samples were linear in the ranges of 0.363–25/0.49–25 μg L^?1 for ezetimibe/simvastatin and 0.193–25/0.312–25 μg L^?1 for ezetimibe/simvastatin in plasma and urine samples, respectively. The limit of detection was 0.109/0.174 μg L^?1 for ezetimibe/simvastatin in plasma and 0.058/0.093 μg L^?1 for ezetimibe/simvastatin in urine. As a potential application, the proposed method was applied to determine the concentration of selected analytes in patient plasma and urine samples after medication and satisfactory results were achieved. In comparison with reference methods, the CA–HF–SLPME–HPLC–DAD method demonstrates considerable potential in the biopharmaceutical analysis of selected drugs.     

Alteration of Structure and Properties of Thin Polyimide Films and Coatings by Plasma and Thermal Treatment

The influence of alternating radiofrequency-plasma and heat treatment on the structure and bulk properties of polyimide films and coatings with a thickness of 3.5 m was studied. It was shown that plasma treatment leads to the enhancement of the specific surface energy due to the polar component and to an increase in the diffusion coefficient and in the amount of sorbed water. The subsequent thermal treatment leads to the recovery of the polyimide surface and bulk properties to almost their initial magnitudes. It was assumed that these effects are caused by a change in the structure of thin films and coatings and by the buildup of negatively charged particles at the surface and in mesopores of the polymer upon RF plasma treatment and due to annealing upon thermal treatment.