Magnetic field dependence of the relative critical current density in γ‐irradiated polycrystalline YBa2Cu3O7

The effect of different doses of γ‐rays on the behavior of the critical current density, J_c in an YBa₂Cu₃O₇ polycrystalline sample has been investigated at high temperatures. The samples were irradiated at room temperature by a ⁶⁰Co γ‐ray source at a dose rate of 0.5 MR/h. J_c was found to increase significantly with after irradiation dose of 10 MR. Further irradiation dose of 50 MR produced a slight and field dependent enhancement of J_c above its values at 10 MR. The most interesting result is that the relative change in the critical current density was found to have a non‐monotonic behavior with the applied magnetic field. These results are discussed in terms of the roles of several mechanisms created by γ‐rays in the regions of the grain boundaries combined with the effect of the magnetic field on these mechanisms. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Experimental and Numerical Study of Structural Identification Using Non-Linear Resonant Decay Method

One of the practical approaches in identifying structures is the non-linear resonant decay method which identifies a non-linear dynamic system utilizing a model based on linear modal space containing the underlying linear system and a small number of extra terms that exhibit the non-linear effects. In this paper, the method is illustrated in a simulated system and an experimental structure. The main objective of the non-linear resonant decay method is to identify the non-linear dynamic systems based on the use of a multi-shaker excitation using appropriated excitation which is obtained from the force appropriation approach. The experimental application of the method is indicated to provide suitable estimates of modal parameters for the identification of non-linear models of structures.     

Performance enhancement of thin‐film composite membranes in water desalination process by wood sawdust

In this study, polysulfone/wood sawdust (PSf/WSD) mixed matrix membrane (MMM) was prepared as a novel substrate layer of thin‐film composite (TFC) membrane in water desalination. The main aim was to evaluate how different amounts of WSD (0‐5 wt%) and PSf concentrations (12‐16 wt%) in the porous substrate affect the properties of the final TFC membranes in the separation of organic and inorganic compounds. Morphological and wettability studies demonstrated that the addition of small amount of WSD (less than or equal to 1 wt%) in the casting solution resulted in more porous but similar hydrophobic substrates, while high loading (greater than or equal to 2 wt%) of WSD not only changed the substrate wettability and morphology but also increased and decreased the swelling and mechanical properties of substrate layer. Therefore, PA layer formed thereon displayed extensively varying film morphology, interfacial properties, and separation performance. Based on approximately stable permeate flux (ASPF) and apparent salt rejection efficiency (ASRE), the best TFC membrane was prepared over the substrate with 12 to 14 wt% of PSf and around 0.5 to 1 wt% of WSD. Although notable improvements in permeate flux were obtained by adding a small amount of sawdust, the results clearly indicate that the salt rejection mechanism of TFC membrane was different from the glycerin rejection mechanism. Furthermore, durability results of TFC membranes showed that in continuous operation for 30 days, TFC‐14/0.5 and TFC‐14/01 have the maximum plateau levels of stable permeate flux and salt rejection among the all TFC membranes.     

A Genetically Encoded,Phage‐Displayed Cyclic‐Peptide Library

Superior to linear peptides in biological activities, cyclic peptides are considered to have great potential as therapeutic agents. To identify cyclic‐peptide ligands for therapeutic targets, phage‐displayed peptide libraries in which cyclization is achieved by the covalent conjugation of cysteines have been widely used. To resolve drawbacks related to cysteine conjugation, we have invented a phage‐display technique in which its displayed peptides are cyclized through a proximity‐driven Michael addition reaction between a cysteine and an amber‐codon‐encoded N^?‐acryloyl‐lysine (AcrK). Using a randomized 6‐mer library in which peptides were cyclized at two ends through a cysteine–AcrK linker, we demonstrated the successful selection of potent ligands for TEV protease and HDAC8. All selected cyclic peptide ligands showed 4‐ to 6‐fold stronger affinity to their protein targets than their linear counterparts. We believe this approach will find broad applications in drug discovery.     

On thermoelastic fields of a multi-phase inhomogeneity system with perfectly/imperfectly bonded interfaces

The stress fields of cylindrical and spherical multi-phase inhomogeneity systems with perfect or imperfect interfaces under uniform thermal and far-field mechanical loading conditions are investigated by use of the Boussinesq displacement potentials. The radius of the core inhomogeneity and the thickness of its surrounding coatings are arbitrary. The discontinuities in the tangential and normal components of the displacement at the imperfect interfaces are assumed to be proportional to the associated tractions. In this work, for the problems where the phases of the inhomogeneity system are homogeneous, the exact closed-form thermo-elastic solutions are presented. These solutions along with a systematic numerical methodology are utilized to solve various problems of physical importance, where the constituent phases of the inhomogeneity system may be made of a number of different functionally graded (FG) and homogeneous materials, and each interface may have a perfect or imperfect boundary condition, as desired. Also, the effect of the interfacial sliding and debonding on the stress field and elastic energy of an FG-coated inhomogeneity is examined.     

Effect of phosphatidylserine content on the partition coefficients of diazepam and flurazepam between phosphatidylcholine-phosphatidylserine bilayer of small unilamellar vesicles and water studied by second derivative spectrophotometry

The affinity of the psychotropic benzodiazepine drugs diazepam (DZ) and flurazepam (FZ) to phosphatidylserine (PS) was examined since PS is abundantly contained in brain membranes. The effect of PS content on the partition coefficients (K(p)s) of these drugs between phosphatidylcholine (PC)-PS bilayer membranes of small unilamellar vesicles (SUV) and water was measured using second derivative spectrophotometry. The second derivative spectra of DZ and FZ measured in the solutions containing various amounts of PC-PS SUV clearly showed derivative isosbestic points and a distinct derivative intensity change depending on the amount of the SUV added. The derivative intensity differences (AD) of the drugs before and after addition of the SUV suspension were measured at a specific wavelength. Using the AD values, the Kp values were calculated and obtained with relative standard deviation of below 10%. The Kp values of both drugs increased according to the PS content in the PS-PC bilayer membranes of the SUV proving that both have higher affinity to the PC-PS bilayer membranes than to PC membranes. The effect was much larger for FZ, i.e., the Kp value of FZ at 30 mol% PS content increased to about five times the value for the PC SUV. This can be explained by the fact that at the experimental pH of 7.4, 80% of FZ molecules are in a cationic form (pKa=8.1), so that these molecules are highly accessible to the negatively charged PS molecules. The results support the rapid and high distribution of DZ and FZ in the central nervous system after their administration.     

Cyclodextrin-enclosed substances of Brazilian propolis

By using beta-cyclodextrin-inclusion as a unique technique, an efficient separation of pharmacologically active phenolic compounds from Brazilian propolis was achieved to provide one new compound, 3-(3-hydroxy-3-methyl-butyl)-5-prenyl-4-hydroxycinnamic acid, together with two common cinnamic acid derivatives, artepillin C and capillartemisin A, and two known flavanols, aromadendrin and 3,5,7-trihydroxy-4'-methoxyflavanol.     

A molecular orbital treatment of the electronic spectra of some tryptamines

The electronic absorption spectra of tryptamine, 5-methoxytryptamine, 6-fluorotryptamine, N-acetyl-5-hydroxytryptamine, gramine, and melatonin were investigated. The observed transitions were π–π*, and the values of band maxima and intensity reflected an extent of interaction between the indole ring and the alkylamine side chain. Molecular orbital calculations at the level of INDO /S –CI were performed on all the studied molecules. State functions and transition energies were calculated. The correspondence between the experimental and theoretical results was satisfactory. © 1992 John Wiley & Sons, Inc.     

Single exposure photography applied to a slow flow field

A speckle photography technique has been applied to measuring the velocity profiles of laminar and turbulent flow through pipes of circular cross-section. A single exposure photography technique has been used to visualize slow fluid flow. The fluids used were seeded with tracer particles whose size range from 20 to about 120 μm in diameter. A mathematical expression representing the recorded intensity is presented. A single exposure with a long exposure time was taken on a holographic film material. The recorded intensity was represented by the convolution product of the image formed and a rectangular function representing a one-dimensional continuous motion. The analysis shows that the intensity distribution of the Fourier spectrum of the diffracted image follows a sinc² function on a noise background representing the scattered light of the tracer particles.     

Relationship between the cohesive strength and the tack of elastomers

The autohesion (tack) and cohesion of a random styrene-butadiene elastomer have been examined as a function of test temperature and speed using a T-peel geometry. Both properties have been reduced to a single master curve by horizontally shifting the data with the same set of shift factors. The cohesive strength increases with increasing reduced test rate Ra_T and appears to approach a plateau at the highest rates. Tack also increases with Ra_T but decreases abruptly at a critical rate and peeling the occurs in a stick-slip fashion. Tack again increases at sufficiently high test rates. In the range of rates where tack is maximized, its value is essentially the same as its cohesive strength. Above or below this range, tack is substantially less than the elastomer's cohesive strength. Mechanisms are proposed to explain why relative tack (i.e., tack divided by cohesive strength) is not a simple measure of the extent of completion of a tack bond and may indeed be equal to one in spite of incomplete tack bond formation.