Liquid chromatographic analysis of mexiletine in serum, with alternate application to tocainide, procainamide, and N-acetylprocainamide.

A simple and precise high performance liquid chromatographic method for the determination of mexiletine in human serum or plasma is described. Following addition of N-propionylprocainamide as internal standard the specimens are extracted, under basic conditions, into methylene chloride. After removal of the aqueous layer the drug is back-extracted into dilute acid, which is then injected directly for analysis. The extraction efficiency is 79% for both mexiletine and internal standard, and the assay is linear to 4 mg/L (twice upper therapeutic concentration). Inter-run coefficients of variation are 3.0% or less. The relative retention time of mexiletine to internal standard averages 1.3. An adaptation of this method is described for an alternate application to the analysis of tocainide, procainamide and N-acetylprocainamide.     

Oscillatory kinetics and mechanism of the chromate catalyzed decomposition of hydrogen peroxide

Oscillatory change of pH occurs during the chromate-catalyzed decomposition of hydrogen peroxide in a weakly acidic medium at elevated temperature and at high initial concentration of hydrogen peroxide. In a closed system, there are only two or three periods, but sustained oscillation occurs in a CSTR. In a CSTR bistability is also found. In closed systems the temperature exhibits a great maximum (up to 15°C increase), in a CSTR sustained oscillation occurs at a constant stationary temperature.     

The Kosterlitz-Thouless model in Perovskite superconductors

Il Nuovo Cimento D - The applicability of the Kosterlitz-Thouless theory to HTSC is examined. The model initially presented in its general lines for bidimensional systems is then applied to...     

Effect of Finite Spectral Width on the Modulational Instability of Langmuir Waves described by a Nonlinear Schrödinger Equation

By using the two-point space correlation function an equation for the power spectral density for a random Langmuir field has been derived. The dispersion relation for a monochromatic wave is regained for a delta spectrum. For a Gaussian spectrum, the maximum growth rate is less than that for a monochromatic wave. For a “meander spectrum”, the growth rate is increased with the width of the spectrum in the first stage then decreased for further increase of the width.     

The combined effects of evaporation and quench steps on asymmetric membrane formation by phase inversion

An analysis of the effects of combined evaporation and quench periods on the formation of asymmetric membranes by the phase inversion technique is presented. The model for the evaporation period assumes binary diffusion and includes composition dependence in the mutual diffusion coefficient and free convection mass transfer in the gas phase. The quench period model includes the use of 4 composition-dependent diffusion coefficients and incorporates a modified from of the interface jump mass balance which enables efficient numerical analysis of composition gradients in the film at the beginning of the quench period. Results for the effects of evaporation-period variable, including: evaporation time, initial cast film thickness, casting surface dimension, and vapor-phase composition, clearly indicate that significant effects of the evaporation period on membrane structure formation and its reproducibility occur within 20 seconds.     

Investigations of potassium-cerium phosphates rich in P2O5

In the ternary system Ce₂O₃-K₂O-P₂O₅, the partial system Ce(PO₃)₃-KPO₃-P₂O₅ was examined by means of differential thermal analysis and powder X-ray diffraction. The phase compositions of the products obtained on various thermal treatments were investigated. The phase diagram of the system Ce(PO₃)₃-KPO₃-P₂O₅ is suggested.

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Zusammenfassung Mittels DTA und Röntgendiffraktion wurde im ternären System Ce₂O₃-K₂O-P₂O₅ das Teilsystem Ce(PO₃)₃-KPO₃-P₂O₅ untersucht. Die Phasenzusammensetzungen der durch verschiedene Erhitzungsvorgänge erhaltenen Produkte wurden untersucht und ein Phasendiagramm für das System Ce(PO₃)₃-KPO₃-P₂O₅ erstellt.

     

Inertia-preserving secant updates

Corrections to the last two equations of Ref. 1 are given.     

Intersegmental interaction and critical concentrations in PET–HFIP solutions

Spectroscopic determinations of the concentrations associated with the onset of intermolecular interaction in solutions of poly(ethylene terephthalate) (PET) are described. The intersegment forces perturb the electronic spectra and induce ground-state aggregation. These phenomena become observable at different chain densities, reflecting the influence of concentration on the coil dimensions, as well as the dynamical nature of the interactions. An estimate of the equilibrium constant for PET dimer formation in hexafluoroisopropanol is reported.     

Step-strain deformations for viscoelastic fluids: Formulation of a strain-coupling constitutive equation

An integral constitutive equation which includes strain-coupling effects is proposed. The constitutive equation is more general than the K-BKZ equation, and it is shown that this equation can explain various important aspects of double-step stress-relaxation data.     

A composite methodology for multistage degradation of polymers

Five different analytical schemes for examining isothermal and nonisothermal degradation of polymers were reviewed and found inadequate for describing multistage decomposition. The different schemes were experimentally tested using thermogravimetric analysis data for an ethylene-vinyl acetate (EVA) copolymer, which exhibited a well-behaved two-step decomposition process in a nitrogen environment. Based on these experimental and analytical findings, a generalized methodology was developed capable of describing the exhibited complex decomposition behavior of polymers by combining two or more kinetic mechanisms in a series or parallel arrangement. This composite of combinational methodology thus extends established analytical schemes for describing complex decomposition of polymers in a rational manner, incorporating both experimental and theoretical considerations.