Kinetics of exothermal decomposition of some ketone-2,4-dinitrophenylhydrazones

In this study, the thermal stability and exothermal decomposition of some ketone-2,4-dinitrophenylhydrazones have investigated using the DSC technique. The synthesized and purified crystalline solids are thermally stable and start to decompose after melting. Non-isothermal DSC curves, recorded at several heating rates, were used to evaluate the melting properties and the kinetics of thermal decomposition. The isoconversional and model-fitting methods were applied to determine the activation parameters from the common analysis of multiple curves measured at different heating rates. Based on the results of the model??free method, a kinetic model was derived, and the kinetic parameters were obtained by means of a multivariate nonlinear regression. The results are discussed in relation to the effect of the ketone structure.     

Exponential dichotomy and dichotomy radius for difference equations

The aim of this paper is to provide a new approach concerning the characterization of exponential dichotomy of difference equations by means of admissible pair of sequence spaces. We classify the classes of input and output spaces, respectively, and deduce necessary and sufficient conditions for exponential dichotomy applicable for a large variety of systems. By an example we show that the obtained results are the most general in this topic. As an application we deduce a general lower bound for the dichotomy radius of difference equations in terms of input-output operators acting on sequence spaces which are invariant under translations.     

Perron Conditions for Uniform Exponential Expansiveness of Linear Skew-Product Flows

 We present necessary and sufficient conditions for uniform exponential expansiveness of discrete skew-product flows, in terms of uniform complete admissibility of the pair (c ₀(N, X), c ₀(N, X)). We give discrete and continuous characterizations for uniform exponential expansiveness of linear skew-product flows, using the uniform complete admissibility of the pairs (c ₀(N, X), c ₀(N, X)) and (C ₀(R ₊, X), C ₀(R ₊, X)), respectively. We generalize an expansiveness theorem due to Van Minh, R?biger and Schnaubelt, for the case of linear skew-product flows. Received August 10, 2001; in revised form June 25, 2002     

Some further considerations on deriving matrix elements of non-periodic potentials in the basis of the non-degenerate harmonic oscillator wavefunctions

Using the properties of the generating function of the Hermite polynomials, we have calculated the matrix elements for the Gaussian-type potential V_G(x)=A exp{−B(x−C)²} and for the Morse-type potential V_M(x)=D_e[1−exp(−ax)]² in the basis of the non-degenerate harmonic oscillator wavefunctions. The final forms of these matrix elements are very simple to use and hence suitable for the numerical resolution of the Schrödinger equation for multiple-well potentials or anharmonic oscillators.     

Fructose-derived hydrochar: combustion thermochemistry and kinetics assessments

Journal of Thermal Analysis and Calorimetry - The combustion behavior of fructose-derived hydrochar was investigated using a kinetic evaluation protocol that brings about novel elements related to...     

Thermal stabilities of new synthesized <Emphasis Type="Italic">N</Emphasis>-methoxy-polynitroanilines derivatives

The thermal decomposition of new N-methoxy-polynitroanilines was studied using the differential scanning calorimetry (DSC) method. The characteristic melting parameters were measured and the activation parameters of the most probable kinetic models of thermal decomposition were determined using a multivariate non-linear regression method. All investigated compounds followed an autocatalytic decomposition mechanism. Depending on the number and position of substituents on the aromatic ring the thermal decomposition occurs in one, two or three steps.     

Biochemistry of the para-sulfonato-calix[n]arenes

The biochemistry of the para-sulfonato-calix[n]arenes has shown rapid development during the past ten years, the highly diverse biomedical applications of these molecules now include anti-viral, anti-thrombotic activities, enzyme blocking and protein complexation. The future is even more promising as para-sulfonato-calix[n]arenes have, now, been shown to have potential in the diagnosis of prion-based diseases. Their innocuous nature, as far as is known at present, may open up their future use in medications.     

Kinetics of exothermal decomposition of 2-nitrophenylhydrazine and 4-nitrophenylhydrazine using DSC non-isothermal data

Kinetics of exothermal decomposition of 2-nitrophenylhydrazine (2-NPH) and 4-nitrophenylhydrazine (4-NPH) was investigated by differential scanning calorimetry. The isoconversional methods, Friedman and Flynn-Wall-Ozawa, were applied to determine the activation parameters from the common analysis of multiple curves measured at different heating rates. For the processes involving two-step reactions the multivariate non-linear regression was used. A good agreement between the experimental and the fitted data was found.     

The NADH Electrochemical Detection Performed at Carbon Nanofibers Modified Glassy Carbon Electrode

In this work, the capability of carbon nanofibers to be used for the design of catalytic electrochemical biosensors is demonstrated. The direct electrochemistry of NADH was studied at a glassy carbon electrode modified using carbon nanofibers. A decrease of the oxidation potential of NADH by more than 300 mV is observed in the case of the assembled carbon nanofiber‐glassy carbon electrode comparing with a bare glassy carbon electrode. The carbon nanofiber‐modified electrode exhibited a wide linear response range of 3×10^?5 to 2.1×10^?3 mol L^?1 with a correlation coefficient of 0.997 for the detection of NADH, a high specific sensitivity of 3637.65 (μA/M cm²), a low detection of limit (LOD=3σ) of 11 μM, and a fast response time (3 s). These results have confirmed the fact that the carbon nanofibers represent a promising material to assemble electrochemical sensors and biosensors.     

Anionic fullerenes, calixarenes, coronenes, and pyrenes as activators of oligo/polyarginines in model membranes and live cells

We report that the efflux of 5(6)-carboxyfluorescein anions from neutral egg yolk phosphatidylcholine vesicles is mediated by oligo/polyarginines only in the presence of activating amphiphilic anions. Screening of anion activators reveals best synergism for amphiphilic carboxylates (fullerene > calix[4]arene approximately coronene > pyrene > calix[6]arene > alkyl), whereas amphiphilic sulfates show less satisfactory activation despite often lower effective concentrations. The analogous alcohols and one calix[4]arene diphosphate were inactive. These results are discussed in the context of a tentative anion carrier mechanism, where interactions with bilayer (interface-directed translocation) and carrier (arene-templated carboxylate-guanidinium pairing) contribute to activator efficiencies. Applied to HeLa cells, pyrenebutyrate is shown to significantly increase the uptake of a fluorescently labeled octaarginine in a concentration-dependent manner.