A parametric study for thick plates resting on elastic foundation with variable soil depth

The soil depth is generally considered to be constant for the analysis of plates resting on elastic foundation in the literature. However, it is most reasonable to have a variable subsoil depth as the plate dimensions get larger. In present study, linearly varying subsoil depth is considered as well as constant, linear and quadratic variation of modulus of elasticity with subsoil depth. Also, a parametric study is performed to demonstrate the behavior of thick plates on elastic foundations with variable soil depth. Modified Vlasov Model is used for the analysis of the plate foundation system, and 8-noded Mindlin plate element incorporating shear strain throughout plate thickness is used for the finite element model. Numerical examples are obtained from the literature to compare results and to show the influence of variable soil stratum depth on the behavior of plates. Displacements, bending moments, and shear forces are presented in tabular and graphical formats. As far as results are compared, it can be concluded that variable soil depth significantly affects the variation of the displacements and therefore the internal forces of the plate while keeping it constant ends up with unrealistic results.     

Quantum Chemical,Spectroscopic, and X-Ray Diffraction Studies of N-diphenylphosphino-4-methylpiperidine Selenide (1)

The title molecule, N-diphenylphosphino-4-methylpiperidine selenide(1), was prepared and characterized by elemental analysis, ¹H-NMR, ³¹P-{¹H} NMR, IR, and X-ray single-crystal determination. The compound crystallizes in the monoclinic space group P 2₁/c. In addition to the molecular geometry from X-ray determination, vibrational frequencies and gauge, including atomic orbital (GIAO) ¹H- and ³¹P-{¹H} NMR chemical shift values of the title compound (1) in the ground state, were calculated using the Hartree–Fock and density functional methods with the 6-31G(d, p) basis set. The calculated results show that the optimized geometries can well reproduce the crystal structures. Besides, the theoretical vibrational frequencies and chemical shift values show good agreement with experimental values. The predicted nonlinear optical (NLO) properties of the title compound are greater than those of urea. In addition, density functional theory (DFT) calculations of the molecular electrostatic potentials (MEPs), frontier molecular orbitals (FMOs) of the title compound were carried out at the B3LYP/6-31G(d) level of theory.     

Radiostability of Allantoin by Using Electron Spin Resonance Spectroscopy

The radiosterilization potential and dosimetric feature of allantoin were investigated through the molecular degradations produced after ultraviolet and gamma irradiation using electron spin resonance, infrared, and ultraviolet spectroscopies and thermal measurement techniques (differential thermal analysis and the glass transition temperature). Although ultraviolet-irradiated allantoin presents no electron spin resonance signal, gamma irradiation exhibited an electron spin resonance signal of triplet appearance. Room temperature and high-temperature line intensity and spectrum area data and their variations with applied microwave power, storage time, annealing time, annealing temperature, and applied radiation dose were analyzed by assuming the production of two different types of radicals having different spectroscopic and decay characteristics. Based on its relatively stable nature toward gamma and ultraviolet radiations, it was concluded that allantoin itself and the products containing it can be sterilized by gamma and/or ultraviolet radiations without creating a great loss in its beneficial effects in the allowed radiosterilization dose limits.     

Strong Visible and Near-Infrared Cathodoluminescence in Alkali Feldspar

In this study, cathodoluminescence (CL) spectroscopy at direct current and alternating current under the sample temperature condition of 40–293 K using different modulation frequencies is presented for alkali feldspar from the Dartmoor granite (UK). These feldspars contain strain-controlled lamellar crypto- and microperthites that are cross-cut by strain-free deuteric microperthites. The CL spectra of the alkali feldspar at room and low temperature confirm that the observed emission peaked at ～460 nm could be associated with Al-O^?-Al or Ti impurity centers, yellow emission ～560 nm could be associated with the presence of the centers such as radiation-induced defect centers, and ～756 nm emission could be associated with the Fe³⁺ impurity center on T₁ and T₂ sites. The consequence of their association is to produce different luminescence properties such as intensity, peak wavelength, and band shape.     

Cytotoxic effect,enzyme inhibition,and in silico studies of some novel N-substituted sulfonyl amides incorporating 1,3,4-oxadiazol structural motif

Molecular Diversity - The acetylcholinesterase and carbonic anhydrase inhibitors (AChEIs and hCAIs) remain key therapeutic agents for many bioactivities such as anti-Alzheimer and antiobesity...     

Quark and strange quark matter in f(R) gravity for Bianchi type I and V space-times

Behaviors of quark matter and strange quark matter which exist in the first seconds of the early Universe in f(R) gravity are studied for Bianchi I and V universes. In this respect, we obtain exact solutions of the modified Einstein field equations by using anisotropy feature of Bianchi I and V space-times. In particular, we investigate exact f(R) functions for Bianchi I as the contribution of strange quark and quark matter. Also, we have concluded that quark matter may contribute to the early acceleration of the universe since quark matter behaves like phantom-type dark energy. Furthermore, obtained f(R) solutions represents early eras of the Universe since f(R) solutions for quark matter coincide with f(R) equations for inflation. From this point, we can reach the conclusion that quarks may be source of the early dark energy of the universe or source of little inflation due to their repulsive force.     

Structure–reactivity relationships of alkyl α‐hydroxymethacrylate derivatives

A series of alkyl α‐hydroxymethacrylate derivatives with various secondary functionalities (ether, ester, carbonate, and carbamate) and terminal groups (alkyl, cyano, oxetane, cyclic carbonate, phenyl and morpholine) were synthesized to investigate the effect of intermolecular interactions, H‐bonding, π–π interactions, and dipole moment on monomer reactivity. All of the monomers except one ester and one ether derivative are novel. The polymerization rates, determined by using photo‐DSC, showed the average trend (aromatic carbamate > hydroxyl > ester > carbonate ～ aliphatic carbamate ～ ether), with several exceptions due to the differences in terminal groups. There is a correlation between the chemical shift differences of the double bond carbons, the calculated dipole moments, and the reactivities only for nonhydrogen bonded monomers. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011