Hydrogen ion-selective poly(vinyl chloride) membrane electrode based on a calix[4]arene.

A hydrogen ion-selective poly(vinyl chloride) membrane electrode was constructed using 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetracyanomethoxycalix[4]arene as a neutral carrier. The electrode showed an apparent Nernstian response in the 2-11.5 pH range with a slope of 54.0 +/- 0.2 mV/pH at 20 +/- degrees C. This electrode showed a rapid response of the emf to changes in the pH, high ion selectivity with respect to lithium, sodium and potassium, and characteristics similar to those reported for the conventional pH glass membrane electrode. It can be used as a potentiometric indicator electrode in hydrofluoric acid solutions. The effects of iodide, thiocyanate, perchlorate and bromide on the characteristics of the electrode were also considered.     

Oligomeric calix[4]arene‐thiacrown ether for toxic heavy metals

A new oligomeric calix[4]arene‐thiacrown‐4 ( 5 ) was synthesized via a condensation reaction of 5,11,17,23‐tetra‐tert‐butyl‐25,27‐bis‐(4‐aminobenzyloxy)‐calix[4]arene‐thiacrown‐4 ( 4 ) with adipoyl dichloride. In this oligomerization reaction only five/six calix[4]arene‐thiacrown‐4 units were linked in the oligomeric chain. The complexation studies of 5 were made with liquid–liquid‐ extraction and solid–liquid‐sorption procedures. For comparison, the extraction efficiencies of monomers 1 , 3 , and 4 to selected transition metals are reported. The selectivity of monomers 3 and 4 toward Cu²⁺, Hg²⁺, and Pb²⁺ was lost after oligomerization in the two‐phase extraction systems. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 186–193, 2004     

Permanganate-impregnated packed capillary columns for group separation of triacylglycerols using supercritical media as mobile phases

Capillary columns packed with a silica-based anion exchanger were treated in situ with a solution of potassium permanganate. These columns showed highly reproducible retention times when used under supercritical conditions. Column temperatures up to 140°C could be applied. This type of column was successfully used for the group separation of triacylglycerols from vegetable oils according to their degree of unsaturation.     

A direct search method for determination of DAEM kinetic parameters from nonisothermal TGA data (note)

In this study, a simple direct search method to be used for the determination of distributed activation energy model (DAEM) kinetic parameters from the nonisothermal thermogravimetric analysis (TGA) data of coals has been introduced. Process steps of direct search method that depends on the grid technique have been given. The method has been applied to the nonisothermal TGA data of one Turkish coal and one imported coal, and DAEM kinetic parameters of these coal samples have been determined. Calculated model results from determined kinetic parameters have been compared with nonisothermal TGA data of the coals.     

A novel, ultra sensible biosensor built by layer-by-layer covalent attachment of a receptor for diagnosis of tumor growth

In the presented research, a novel, ultra sensitive biosensor for the impedimetric detection of vascular endothelial growth factor (VEGF) is introduced. The human vascular endothelial growth factor receptor 1 (VEGF-R1, Flt-1) was used as a biorecognition element for the first time. The immobilization of VEGF-R1 on glassy carbon electrodes was carried out using layer-by-layer covalent attachment of VEGF-R1. The electrochemical properties of the layers constructed on the electrodes were characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The differences in electron transfer resistance (R_et) between the working solution and the biosensor surface, recorded by the redox probe K₃[Fe(CN)₆]/K₄[Fe(CN)₆], confirmed the binding of VEGF to VEGF-R1. The new biosensor allowed a detection limit of 100 fg mL⁻¹ with a linear range of 100–600 fg mL⁻¹ to be obtained. The biosensor also exhibited good repeatability (with a correlation coefficient of 1.95%), and reproducibility.     

Uniform stability for thermoelastic systems with boundary time-varying delay

In this paper we consider a thermoelastic system with boundary time-varying delay. Using the energy method, we show, under suitable assumptions, that the damping effect through heat conduction is still strong enough to uniformly stabilize the system even in the presence of boundary time-varying delay. Our result improves earlier results existing in the literature.     

The main and modified CUPRAC methods of antioxidant measurement

The antioxidant activity/capacity levels of biological fluids and foods are measured for the diagnosis and the treatment of oxidative stress-associated diseases in clinical biochemistry, and for meaningful comparison of the antioxidant content of foods. Currently, there is no “total antioxidant” as a nutritional index available for food labeling and biological fluids due to the lack of standardized quantitative methods.The CUPRAC (CUPric Reducing Antioxidant Capacity) method of antioxidant measurement, introduced by our research group, is based on the absorbance measurement of Cu(I)-neocuproine (Nc) chelate formed as a result of the redox reaction of chain-breaking antioxidants with the CUPRAC reagent, Cu(II)-Nc, where absorbance is recorded at the maximal light-absorption wavelength of 450 nm.We introduce the main CUPRAC method and describe modifications to it in the past six years.     

Study of the Coordination Properties of 1,2-Bis(2,6-dimethphenylamino) Glyoxime and Determine the Stability Constant of Its Complexes with Ni(II), Cu(II) and Zn(II) Metal Ions in Solution

This study aims to investigate the nature and type of complexes formed in solution between 1,2-bis(2,6-dimethphenylamino) glyoxime (DPG) and the ions Ni²⁺, Cu²⁺ and Zn²⁺. Potentiometric titration was used to follow the formation of complexes.The complexes formed were studied through the determination of stability constants of these complexes in mixed ethanol–aqueous solution at 25±0.1?°C and ionic strength of 0.1 mol?dm^?3 NaCl. The basicity of the ligand was also assessed by the determination of the dissociation constants of the ligand. All of the constants were determined by computer refinement of pH–volume data using the SUPERQUAD program. The species distribution diagrams were also calculated.Comparison with other vic-dioximes was made to provide reliable support for the formation of the proposed complexes in solution.     

Synthesis of isoxazoline N-oxides via [hydroxy(tosyloxy)iodo]benzene (HTIB)-mediated oxidative N-O coupling

An HTIB mediated oxidative N-O coupling strategy for the synthesis of some isoxazoline N-oxide derivatives from β-hydroxyketoximes is described, along with a comparative study of the efficiency of N-O coupling in two different solvents. A plausible mechanism for the conversion is proposed.     

Humidity sensing properties of ZnO-based fibers by electrospinning

Zinc oxide (ZnO) based fibers with a diameter of 80-100 nm were prepared by electrospinning. Polyvinyl alcohol (PVA) and zinc acetate dihydrate were dissolved in water and the polymer/salt solution was electrospun at 2.5 kV cm⁻¹. The resulting electrospun fibers were subjected to calcination at 500 °C for 2 h to obtain ZnO-based fibers. Humidity sensing properties of the fiber mats were investigated by quartz crystal microbalance (QCM) method and electrical measurements. The adsorption kinetics under constant relative humidity (RH) between 10% and 90% were explained using Langmuir adsorption model. Results of the measurements showed that ZnO-based fibers were found to be promising candidate for humidity sensing applications at room temperature.