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41.
Abstract

Phosphate-based bioactive glasses and their glass ceramics for 47P2O5– (30.5)CaO–(22.5 ? x)Na2O–xZrO2 for different ZrO2 contents (x = 0, 1.5, 3.0, 4.5, and 6.0 mol%) were prepared through melt quenching and controlled heat treatment procedures. The amorphous nature of glasses and the presence of crystalline phases in glass ceramics were studied by means of X-ray diffraction (XRD) studies. The density, molar volume, ultrasonic velocities, attenuation, elastic constants, and microhardness of glass and glass ceramics were used to study the structural changes. The formation of hydroxyapatite layer on the surface of glasses and glass ceramics after immersion in simulated body fluid (SBF) was explored through XRD, Fourier transform infrared (FTIR), and scanning electron microscopy (SEM) analyses. The results indicate that the added ZrO2 increases the crosslink density of glasses, resulting in network stability, and also induces the formation of an apatite layer on the surface of glasses.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.  相似文献   
42.
Abstract

Palladium(II) acetate has been anchored onto a copolymer support containing pyridyl and carboxyl groups. XPS studies showed the Pd 3d binding energies for the recovered catalyst to be less by 1 eV after being used in hydrogenation studies. However, x-ray studies and a chemical test based on KCN treatment failed to reveal any palladium oxide or palladium metal formation in the recovered catalyst. It is presumed that an acetate ligand is lost during hydrogenation, which could be the reason for the lowering of the palladium 3d binding energies in the recovered catalyst. Results of investigations of the hydrogenation of olefins and selectivity of the catalyst toward the hydrogenation of dienes and alkynes are presented. The loss of palladium due to leaching under the reaction conditions employed was found to be very low (<1%/cycle).  相似文献   
43.
A combination of NaHSO4.H2O and NaNO2 in the presence of wet SiO2 was used as an effective oxidizing agent for the oxidation of dihydropyridines to their corresponding pyridine derivatives at room temperature with excellent yields.  相似文献   
44.
Erbium-165 with 10.3 h physical half-life decays completely by electron capture to the ground state of stable isotope 165Ho and it is an ideal radio lanthanide for Auger electron therapy. Excitation function of 165Er via natEr(p,x)165Tm → 165Er, 166Er(p,2n)165Tm → 165Er, 165Ho(p,n)165Er and 165Ho(d,2n)165Er reactions were calculated using ALICE/ASH (Hybrid and GDH models) and EMPIRE 3.1 codes and then were compared with the reported measurement by experimental data and TENDL-2011. Physical yield and target thickness were evaluated with attention to excitation function, stopping power and SRIM code. 165Er was produced using the sedimentation technique through the natEr (p,x)165Tm → 165Er reaction. The deposited target was irradiated with 15 MeV proton beams at 20 μA current for 1 h. The 165Tm production yield was 26 MBq/μA h at the end of bombardment.  相似文献   
45.
Journal of Thermal Analysis and Calorimetry - The ultimate goal of the present review paper is to summarize and discuss the findings of the most recently published literature on natural convection...  相似文献   
46.
Journal of Cluster Science - Metal oxide nanoparticles (NPs) have gained attention in biomedicine due to their broad spectrum of applications, such as targeted drug delivery, their use as...  相似文献   
47.
48.
In the present study, a series of thiodihydropyrimidine derivatives were synthesized from different substituted aromatic aldehydes, ethyl acetoacetate, and urea/thiourea using a bimetallic TUD-1 catalyst. The structures of all the synthesized compounds were characterized by melting point determination, thin layer chromatography (TLC), infrared (IR), 1HNMR, and 13C-NMR values. All the synthesized compounds were screened for their antimicrobial activities against two gram positive bacteria, two-gram negative bacteria, and two fungal strains.  相似文献   
49.
Abstract

Wound healing is a complex process and it involves restoration of damaged skin tissues. Several wound dressings comprising naturally made substances are constantly investigated to assist wound healing. In this research, a new wound dressing based on polyurethane (PU) supplemented with essence of Channa striatus (CS) fish oil was made by electrospinning. Morphological study depicted the reduction in fiber diameter than PU with the addition of fish oil (0.552?±?0.109?μm for 8:1 v/v% and 0.519?±?0.196?μm 7:2 v/v%) than the pristine PU (0.971?±?0.205?µm). Fourier transform infrared spectroscopy (FTIR) analysis revealed the presence of fish oil in the composite as identified through increasing peak intensity. Fish oil resulted in the hydrophilic behavior (88?±?3 (8:1 v/v) and 70?±?6 (7:2 v/v)) as revealed in the contact angle analysis. Thermal gravimetric analysis (TGA) showed the superior thermal behavior of the wound dressing patch compared to the PU. Atomic force microscopy (AFM) analysis insinuated a decrease in the surface roughness of the pristine polyurethane with the added fish oil. Coagulation assays signified the delay in the blood clotting time portraying its anti-thrombogenic behavior. Hemolytic assay revealed the less toxic nature of the developed nanocomposites with the red blood cells (RBC’s) depicting its safety with blood. Hence, polyurethane nanofibers supplemented with fish oil made them as deserving candidates for wound dressing application.  相似文献   
50.
A new disposable sensitive voltammetric sensor for the determination of Fe(III) based on a graphene (G) and piroxicam (Pir) modified screen printed carbon electrode (Pir/G/SPCE) has been developed. The developed method is based on accumulation of Fe(III) on the surface of the prepared sensor strip, formation a complex with Pir and subsequent reduction the adsorbed chelated Fe(III) at ?0.03 V (vs. Ag/AgCl) coupled with the catalytic enhancement of bromate. Characterizations of the modified electrode surface were performed by field emission scanning electron microscopy (FE‐SEM), energy dispersive X‐ray spectroscopy (EDX) and electrochemical impedance spectroscopy (EIS). Electrochemical behavior of the modified SPCEs was investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under the optimum conditions, the catalytic voltammetric method exhibited linear calibration plot in the concentration ranges of 1–100 ng mL?1 and 100–3500 ng mL?1 Fe(III) with a limit of detection of 0.3 ng mL?1. The sensor strip displayed good reproducibility with 1.7 % relative standard deviation (RSD%). The developed method was successfully applied for the determination of iron in food samples such as vegetables, fruit, and cereal.  相似文献   
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