Chemometric Strategies to Develop a Nanocomposite Electrode for Simultaneous Determination of Ascorbic Acid,Dopamine, and Uric Acid

A simple and sensitive method for simultaneously measuring dopamine (DA), ascorbic acid (AA), and uric acid (UA) using a poly(1‐aminoanthracene) and carbon nanotubes nanocomposite electrode is presented. The experimental parameters for composite film synthesis as well as the variables related to simultaneous determination of DA, AA, and UA were optimized at the same time using fractional factorial and Doehlert designs. The use of carbon nanotubes and poly(1‐aminoanthracene) in association with a cathodic pretreatment led to three well‐defined oxidation peaks at potentials around ?0.039, 0.180 and 0.351 V (vs. Ag/AgCl) for AA, DA, and UA, respectively. Using differential pulse voltammetry, calibration curves for AA, DA, and UA were obtained over the range of 0.16–3.12×10^?3 mol L^?1, 3.54–136×10^?6 mol L^?1, and 0.76–2.92×10^?3 mol L^?1, with detection limits of 3.95×10^?5 mol L^?1, 2.90×10^?7 mol L^?1, and 4.22×10^?5 mol L^?1, respectively. The proposed method was successfully applied to determine DA, AA, and UA in biological samples with good results.     

Field-induced structural ordering in electrorheological fluids

Structural relaxations of an electrorheological fluid (ERF) due to changes in the applied electrical field strength or shear rate are observed on time scales 1 s<t<40 000 s. Commercial ERFs consisting of mesoscopic polyurethane particles in a silicone oil matrix were studied by three different experimental techniques in order to obtain and compare the characteristic relaxation times. It is demonstrated that dielectric spectroscopy, viscosimetry and light transmission experiments represent the same results concerning the structural relaxation phenomena of ERFs when electrical fields are applied. The tendency of strong induced dipoles to align the particles in the direction of the field increases the effective dipole moment and therefore , the shear viscosity and the amount of light transmitted along the field direction in an ITO/glass sandwich cell. The optical experiment is capable of resolving fast processes within the first 1 ms if large electrical fields are applied. The effects of electrophoresis and shearing, which both counteract the field induced structures, are also addressed.     

Oil Base Mud. Part I: Synthesis of Some Local Surfactants Used as Primary Emulsifiers for Oil Base Mud and Evaluation of Their Rheology Properties

Six oil soluble nonionic surfactants with different HLBs have been prepared. Their HLBs situate between 3.9 and 6.7. Transesterification was carried out for glycerol and triethanol amine with oleic acid at different moles to obtain six emusilifiers. They named glycerol momooleate (I), glycerol diooleate (II), glycerol trioleate (III), triethanol amine mono-, di- and tri-oleate (IV), (V,) and (VI). The chemical structure was confirmed using; the elemental analysis, FTIR and ¹HNMR. They were evaluated as a primary emulsifiers (PE) for thdrilling fluids (oil base mud) comparing with a currently used primary emulsifier (Fc). The water in oil base mud (w/o emulsions) was prepared. The concentration of emulsifiers and their HLB exhibited interesting rheology properties including shear-thinning behavior, yield value, viscoelastic effects, thixtropy, gel strength, and filtration loss. The rheology properties of such emulsions strongly depended on the average size distribution of the dispersed droplets that could be varied both with the bulk concentration and HLB value of the emulsifiers. The interfacial and surface properties of these emulsifiers suggest that the droplet size of the dispersed phase and bulk concentration are strongly related to the HLB value of emulsifiers. The w/o emulsion (mud formulation) stability is sensitive to the droplet size of the dispersed phase and HLB value of the used emulsifier. The results were discussed on the light the chemical structure of the primary emulsifiers and the emulsion ingredients.     

Multicommuted flow-through fluorescence optosensor for determination of furosemide and triamterene

Multicommutation implemented with flow-through optosensors is a very promising area of research. This recent approach benefits from the advantages of both methods and results in high sensitivity, selectivity, and speed, and little waste generation. This paper reports the simultaneous determination of furosemide and triamterene, two widely used diuretics, by measurement of their native fluorescence. The system has been proved to be useful for determination of both analytes in pharmaceutical preparations and for determination of triamterene in human urine and serum. A minicolumn filled with Sephadex SPC-25 microbeads was used to achieve separation of both analytes before detection in a flow-through cell filled with the same resin. The sensor is linear in the range 50–1200 and 0.4–8 ng mL⁻¹ with detection limits of 15 and 0.1 ng mL⁻¹ for furosemide and triamterene, respectively.     

Heck coupling reaction of iodobenzene and styrene using supercritical water in the absence of a catalyst

Heck coupling reaction of iodobenzene and styrene proceeds rapidly and selectively in supercritical water even without any catalyst in the presence of base. Both the choice of base and the reaction conditions had a significant effect on the conversion and the selectivity of the coupling products. The addition of a relatively mild base such as potassium acetate facilitated the cross-coupling reaction, while the hydrolysis of phenyl halide was favored in the presence of a strong base. The conversion and the yields of coupling products increased with increasing temperature, reaching a maximum at 650 K near the critical temperature of water, and then decreased as the temperature was further increased. Water density had a significant influence on the reaction rate, showing nearly 30% augmentation with a slight increase in density from 0.45 to 0.56 g cm(-3), but had less effect on the product selectivity. Two possibilities of the role of water responsible for the noncatalytic Heck coupling reaction in supercritical water, that is, ion and water-catalyzed mechanisms have been considered.     

Colorimetric Determination of Propofol in Bulk form,Dosage Form and Biological Fluids

ABSTRACT

Propofol is coupled with 2, 6-dichloroquinone-4-chlorimide (DCQ) in a reaction buffered at pH 9.6 to give a colored product having an analytically useful maximum at 635 nm. The factors affecting the color generation were optimized and incorporated in the procedure. The reacted propofol has a molar absorptivity of 3.9 × 10^?4 L mol^?1 cm^?1, and Beer's law is obeyed for concentrations 1-5 μg ml^?1 with detection limit 0.25 μg ml^?1. The method was found applicable to biological fluids (plasma and urine) spiked with propofol at concentration levels 1-5 μg ml^?1 for plasma and 1-5 μg 0.5 ml^?1 urine (less sensitivity is obtained with urine volumes above 0.5 ml) with detection limits 0.28 μg ml^?1 for plasma and 0.4 μg 0.5 ml^?1 urine. The average recovery for the commercial preparation (1% w/v propofol emulsion intravenous injection for infusion) was 99.54% with an RSD of 1.05%. The method was validated by an adopted HPLC method. The results obtained by the HPLC method for the commercial preparation were statistically compared with the proposed method and evaluated at the 95% confidence limits.     

Hard and Soft - Core Equations of State for Simple Fluids: VI. General Theory of Termination Temperatures,and a Validity Criterion for the Second Virial Coefficient

Abstract

A general proof is given that the classical second virial coefficient satisfies the requirement for the non-existence of a termination point of any locus of C_v extrema. This validity criterion is applied to some proposed forms for the second virial coefficient. The order of the termination temperatures is verified for a fairly general intermolecular potential. In particular a proof is given that T_F lies between T_C and T_A. Also the hard-core limit of the ratio T_D/T_A(～2) is examined briefly.     

Highly Selective Potentiometric Sensor for Determining Phenazopyridine Hydrochloride in Biological Fluids Using N,N′-(Pyromellitoyl)-bis-L-tyrosine Dimethyl Ester

A new membrane selective electrode based on the potentiometric method was developed for the determination of phenazopyridine. The membrane signal is based on the interaction of N,N′-(pyromellitoyl)-bis-L-tyrosine dimethyl ester with phenazopyridine. The sensor displays a linear response with a slope of 61.1 mV decade^?1 for phenazopyridine concentrations in the range of 1.0 × 10^?2–1.0 × 10^?5 mol L^?1 and with detection limit of 8.0 × 10^?6 mol L^?1 of phenazopyridine. The electrode enjoys a fast response time. Application of this potentiometric sensor for phenazopyridine determination in pharmaceuticals, urine, and blood serum samples is reported without any special pretreatment required.     

Synthesis,Characterization and Electrorheological Properties of Polyindene/Kaolinite Composites

In this study, synthesis, characterization and electrorheological (ER) properties of polyindene (PIN) and polyindene/kaolinite composites were carried out by cationic radical polymerization using FeCl₃ as the oxidizing agent. The homopolymer and composites, containing different amounts of PIN were characterized by FTIR spectroscopy, thermo‐gravimetric (TGA) analyses, scanning electron microscopy (SEM) and dynamic light scattering (DLS) methods. The conductivity and dielectric properties of PIN and PIN/kaolinite composites were determined. Suspensions of PIN and PIN/kaolinite composites were prepared in silicone oil (SO), at a series of concentrations (c=5–25 m/m %). The effects of concentration, shear rate, electric field strength, frequency, temperature and promoter on ER activities of suspensions were investigated.