Gamma-ray spectrometry for the self-attenuation correction factor of the sand samples from Antalya in Turkey

In this paper, we attempt to determine the self-attenuation correction factor for 37 different sand samples collected from Antalya region of Turkey with densities changing from 2.205 to 2.679 g  \(\hbox {cm}^{-3}.\) Transmission method has been used in order to obtain self-attenuation correction factor in comparison with the air and ultrapure water samples for each case. Self-attenuation correction factor versus energy fit curve is obtained. While the self-attenuation correction factor has large values at low energies, it becomes smaller at high energies and tends to become constant thereafter.     

Peleg and Weibull models for water absorption of copolymer gels crosslinked on polyethylene glycol dimethacrylates

In this study, the super-absorbent copolymer gels were obtained from the aqueous solution of monomers dispersed in a continuous organic phase. The inverse suspension polymerization was accomplished with the use of aqueous solutions of partly neutralized acrylic acid with a predetermined crosslinker agent, polyethylene glycol dimethacrylates (PEGDMA)/monomer ratio in cyclohexan. The copolymer gels synthesized using PEGDMA crosslinker with three different molecular weights (PEGDMA₃₃₀, PEGDMA₅₅₀, and PEGDMA₇₅₀) were characterized by ?nfrared spectroscopy and scanning electron microscopy. Water absorption capacities of the copolymer gels were determined. The water absorption capacity of 1 g copolymer gels in water was respectively obtained as 232, 255, and 316 g water/g polymer gel for PEGDMA₃₃₀, PEGDMA₅₅₀, and PEGDMA₇₅₀, respectively. The Peleg and Weibull models were used to describe the water absorption behavior of the copolymer gels. The highest values of R ² and the lowest values of χ ² and RMSE for copolymer gels were observed with the Weibull model.     

Electroanalysis of Benazepril Hydrochloride Antihypertensive Drug Using an Ionic Liquid Crystal Modified Carbon Paste Electrode

Electroanalysis of benazepril HCl was successful using a carbon paste electrode modified with an ionic liquid crystal ( 1‐butyl‐1‐methylpiperidinium hexafluorophosphate) in presence of sodium dodecyl sulfate. The electrode performance was compared to ionic liquids (1‐n‐hexyl‐3‐methyl imidazolium tetrafluoroborate and 1‐butyl‐4‐methyl pyridinium tetrafluoroborate). Electrochemical determination of benazepril HCl was in the linear dynamic range of 8.89×10^?7 to 1.77×10^?5 mol L^?1 (correlation coefficient 0.999) and LOD 7.17×10^?9 mol L^?1. benazepril HCl was determined using this sensor in presence of urine metabolites such as uric acid, ascorbic acid. Binary mixtures of dopamine/benazepril and amlodipine/benazepril were also determined successfully.     

Fabrication of an Electrochemical E. coli Biosensor in Biowells Using Bimetallic Nanoparticle‐Labelled Antibodies

An electrochemical biosensor was developed for the determination of Escherichia coli (E. coli) in water. For this purpose, silver‐gold core‐shell (Ag@Au) bioconjugates and anti‐E. coli modified PS‐microwells were designed in a sandwich‐type format in order to obtain higher sensitivity and selectivity. Ag@Au bimetallic nanoparticles were synthesized by co‐reduction method. The core‐shell formation was analyzed by using UV‐Vis spectroscopy and transmission electron microscopy. Biotin labeled anti‐E. coli antibodies were coupled with Ag@Au nanoparticles to form bioconjugates. The electrochemical immunosensor was prepared by immobilizing anti‐E. coli on polystyrene (PS)‐microwells via chemical bonding. These modified microwells were identified with X‐ray photoelectron spectroscopy and surface enhanced Raman spectroscopy. E. coli was sandwiched between Ag@Au bioconjugates and anti‐E. coli on PS‐microwells at different concentrations. The relationship between the E. coli concentration and stripping current of gold ions (Au³⁺) were investigated by square wave anodic stripping voltammetry at pencil graphite electrode. The proposed method can provide some advantages such as lower detection limit and shorter detection time. The electrochemical response for the immunosensor was linear with the concentration of the E. coli in the range of 10¹ and 10⁵ cfu/mL with a limit of detection 3 cfu/mL. The procedure maintains good sensitivity and repeatability and also offers utility in the fields of environmental monitoring and clinical diagnosis.     

PC expansion for material parameters using artificial data and statistical methods

This paper investigates the uncertainty of a hyper-elastic model by random material parameters as stochastic variables. For its stochastic discretization a polynomial chaos (PC) is used to expand the coefficients into deterministic and stochastic parts. Then, from experimental data in combination with artificial data for elastomers the distribution of the force-displacement curves are known. In the numerical example the PC-based stochastic and the deterministic parameter identification are used for generation of the distribution of Ogden's material parameters. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Elastic moduli and step-like elastic anomalies in Ce-substituted Tl0.9Bi0.1Sr2−xCexCa0.9Y0.1Cu1.99Fe0.01O7−δ (x = 0–0.20) superconductors

Ultrasonic velocity measurements have been performed on polycrystalline Tl_0.9Bi_0.1Sr_2?xCe_xCa_0.9Y_0.1Cu_1.99Fe_0.01O_7?δ superconductor to study the influence of Ce substitution on elastic properties of the samples. Ce was observed to influence elastic moduli at 80 K which showed the largest value obtained at x = 0.10 where, coincidentally, the highest superconducting temperature T_c among samples was also shown. A longitudinal velocity anomaly was observed at around 260 K for the unsubstituted sample (x = 0). Ce substitution caused the temperature of the elastic anomaly to shift to 250 K (x = 0.1) and 262 K (x = 0.2). The existence of the step-like elastic anomaly was suggested to be due to oxygen ordering taking place in Tl–O planes. The analysis of elastic behavior in the vicinity of the elastic anomalies using the Landau free-energy model suggests that the anomaly is due to a phase transition which involves oxygen ordering.     

Ruthenium N‐heterocyclic–carbene catalyzed diarylation of arene C?H bond

Novel ruthenium‐1,3‐dialkylimidazolin‐2‐ylidene complexes ( 2a–e ) have been prepared and characterized by C, H, N analysis, ¹H‐NMR and ¹³C‐NMR. The ortho position of the aromatic ring of pyridyl group substituted aromatic compound was directly arylated with aryl bromides and chlorides in the presence of a catalytic amount of [RuCl₂(1,3‐dialkylimidazolin‐2‐ylidene)] complexes. Copyright © 2008 John Wiley & Sons, Ltd.     

Flow-through chloroquine sensor and its applications in pharmaceutical analysis.

Poly (vinyl chloride) membrane electrodes that responded selectively towards the antimalarial drug chloroquine are described. The electrodes were based on the use of the lipophilic potassium tetrakis(4-chlorophenyl)borate as ion-exchanger and bis(2-ethylhexyl)adipate (BEHA), or trioctylphosphate (TOP) or dioctylphenylphosphonate (DOPP) as plasticizing solvent mediator. All electrodes produced good quality characteristics such as Nernstian- and rapid responses, and are minimally interfered with by the alkali and alkaline earth metal ions tested. The membranes were next applied to a flow-through device, enabling it to function as flow-injection analysis (FIA) detector. The performance of the sensor after undergoing the FIA optimization was further evaluated for its selectivity characteristics and lifetime. Results for the determination of chloroquine in synthetic samples that contained common tablet excipients such as glucose, starch, and cellulose, and other foreign species such as cations, citric acid or lactic acid were generally satisfactory. The sensor was also successfully used for the determination of the active ingredients in mock tablets, synthetic fluids and biological fluids. The sensor was applied for the determination of active ingredients and the dissolution profile of commercial tablets was also established.     

Synthesis and use of mono- or bisxylyl linked bis(benzimidazolium) bromides as carbene precursors for C-C bond formation reactions

Two benzimidazolium moieties linked by one or two xylyls (m- and p-) have been synthesized, characterized and then they were used for Heck coupling reactions as in situ formed catalysts. Mono bridged salts are more efficient as compared to bisbridged salts. In addition, mono bridged salts were converted to Rh-NHC complexes which were tested as catalysts for the arylation of aldehydes.