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.     

Dynamics of a pair of coupled nonlinear oscillators

A pair of coupled classical oscillators with a general potential and general form of coupling is investigated. For general potentials, the single-frequency solution is shown to be stable for small excitations. For special potentials, such system remains stable for an arbitrary excitation. In both cases, the stability does not depend on the form of coupling. Transition to the instability regime follows from the way how nonlinear potential entrains the energy transfer between the oscillators. Relation between the existence of multi-frequency quasi-periodic or periodic solutions and the instability of single-frequency ones is discussed.     

Specific high performance liquid chromatographic determination of the molecular weight and concentration of hyaluronic acid in complex mixtures by labelled hyaluronate binding proteins.

A simple High performance liquid chromatographic (HPLC) method for the specific determination of the molecular weight and concentration of hyaluronic acid (HA) in complex mixtures has been developed. Hyaluronate-binding proteins isolated from bovine cartilage labelled by 125I or fluoresceinisothiocyanate were used as specific markers. The specific binding affinities of the markers were compared and were found to have association constants of 1.6 x 10(7) M-1 and 1.2 x 10(7) M-1 respectively. The HA levels and molecular weight distributions can be easily determined in the range 10-500 ng/mL in complex mixtures by the use of markers, molecular sieving HPLC columns and appropriate detectors. It has been demonstrated clearly that the method is useful for the highly specific determination of the parameters in complex biological samples such as serum and synovial fluids and is recommended for clinical applications.     

Use of the Apparent Content Curves for the spectrophotometric identification of substances: identification of amphetamines

The possibility of identification of substances which have similar spectral behaviour by means of Apparent Content Curves has been studied. This study is carried out with absorption, excitation and emission spectra of several amphetamines of widespread pharmaceutical use. Results obtained show that amphetamine, phenylpropanolamine, pseudoephedrine, phenylephrine, epinephrine, dopamine and methoxyamphetamine can be identified with a probability of >95%.     

On theK-property of some planar hyperbolic billiards

TheK-property is demonstrated for a class of planar billiards satisfying Wojtkowski's principles. Their boundary may consist of convex-scattering, concave and linear pieces. Earlier Wojtkowski showed that these billards had non-zero Lyapunov exponents.     

Synchronization Analysis of Coupled Noncoherent Oscillators

We present two different approaches to detect and quantify phase synchronization in the case of coupled non-phase coherent oscillators. The first one is based on the general idea of curvature of an arbitrary curve. The second one is based on recurrences of the trajectory in phase space. We illustrate both methods in the paradigmatic example of the R?ssler system in the funnel regime. We show that the second method is applicable even in the case of noisy data. Furthermore, we extend the second approach to the application of chains of coupled systems, which allows us to detect easily clusters of synchronized oscillators. In order to illustrate the applicability of this approach, we show the results of the algorithm applied to experimental data from a population of 64 electrochemical oscillators.     

Maximal triangle-free graphs with restrictions on the degrees

We investigate the problem that at least how many edges must a maximal triangle-free graph on n vertices have if the maximal valency is ≤D. Denote this minimum value by F(n, D). For large enough n, we determine the exact value of F(n, D) if D ≥ (n ? 2)/2 and we prove that lim F(n, cn)/n = K(c) exists for all 0 < c with the possible exception of a sequence c_k → 0. The determination of K(c) is a finite problem on all intervals [γ, ∞). For D = cn^?, 1/2 < ? < 1, we give upper and lower bounds for F(n, D) differing only in a constant factor. (Clearly, D < (n - 1)^1/2 is impossible in a maximal triangle-free graph.)     

On the resolving power of high-contrast saturated absorption spectroscopy

Recently Svanberg et al. [Optics Lett. 11 (1986) 138; J. Opt. Soc. Am. B 4 (1987) 462] obtained saturated absorption resonances with subnatural linewidth by working in the regime of high pumping intensities and optically thick atomic samples. We analyze here this new spectroscopic regime, within the formalism of Maxwell-Bloch-type equations, in the case of a Doppler broadened medium having two nearly degenerate but uncoupled resonances. We show that even in this most favourable case it is not possible to resolve spectral features that lie within the natural linewidth.     

Highly edge‐connected detachments of graphs and digraphs

Let G = (V,E) be a graph or digraph and r : V → Z₊. An r‐detachment of G is a graph H obtained by ‘splitting’ each vertex ν ∈ V into r(ν) vertices. The vertices ν₁,…,ν_r(ν) obtained by splitting ν are called the pieces of ν in H. Every edge uν ∈ E corresponds to an edge of H connecting some piece of u to some piece of ν. Crispin Nash‐Williams 9 gave necessary and sufficient conditions for a graph to have a k‐edge‐connected r‐detachment. He also solved the version where the degrees of all the pieces are specified. In this paper, we solve the same problems for directed graphs. We also give a simple and self‐contained new proof for the undirected result. © 2003 Wiley Periodicals, Inc. J Graph Theory 43: 67–77, 2003     

Accuracy of the chemical data evaluated from one-atom-at-a-time experiments

Studies of chemistry of the transactinoid elements, which are available only as single atoms, by gas (thermo)chromatographic techniques can provide the adsorption enthalpies of the atoms or molecules. These values serve the ultimate goal—to characterize bulk volatility of the species in terms like sublimation enthalpies. The paper attempts an in-depth discussion of the statistical significance of the adsorption enthalpies derived in such experiments. Usually, the counting statistics are very poor and one faces nonstandard problems in evaluating the confidence intervals for the values of parameters. Here, a most efficient way seems to be the Bayesian approach, realized, when necessary, by Monte Carlo simulations of the counting results. Necessarily, the adsorption enthalpy is not evaluated based on the second law of thermodynamics but through accepting an a priori value of the adsorption entropy. More additional assumptions about the mechanisms and parameters involved are needed. This may produce systematic errors in the quantitative conclusions; the analysis of some recent works with elements 106 and 108 corroborates this concern. Despite such problems, it is possible to reveal qualitative differences in the adsorption behavior of a transactinoid and its expected known congeners as well as to use chemistry for an independent assignment of the atomic numbers of transactinoid nuclides.