Poincaré-Invariant Markov Processes and Gaussian Random Fields on Relativistic Phase Space

We give a complete characterization, including a Lévy–Itô decomposition, of Poincaré-invariant Markov processes on , the relativistic phase space in 1+1 spacetime dimensions. Then, by means of such processes, we construct Poincaré-invariant Gaussian random fields, and we prove a no-go theorem for the random fields corresponding to Brownian motions on .     

Complex formation between a nanoparticle and a weak polyelectrolyte chain: Monte Carlo simulations

Understanding the complexation processes between nanoparticles and polyelectrolytes is an essential aspect in many branches of nanotechnology, nanoscience, chemistry, and biology to describe processes such as nanoparticle stabilization/destabilization and dispersion, water treatment, microencapsulation, complexation with biomolecules for example, and evolution of the interface of many natural and synthetic systems. In view of the complexity of such processes, applications are often based on empirical or semiempirical observations rather than on predictions based on theoretical or analytical models. In this study, the complex formation between an isolated weak polyelectrolyte and an oppositely charged nanoparticle is investigated using Monte Carlo simulations with screened Coulomb potentials in the grand canonical ensemble. The roles of the nanoparticle surface charge density , solution pH and ionic concentration C_i are systematically investigated. The phase diagrams of complex conformations are also presented. It is shown that the polyelectrolyte conformation at the surface of the nanoparticle is controlled by the attractive interactions with the nanoparticle but also by the repulsive interactions between the monomers. To bridge the gap with experiments titration curves are calculated. We clearly demonstrate that an oppositely charged nanoparticle can significantly modify the acid/base properties of a weak polyelectrolyte.     

Quantum-classical correspondence for motion on a plane with deficit angle

A particle constrained to move on a cone and bound to its tip by harmonic oscillator and Coulomb-Kepler potentials is considered both in the classical as well as in the quantum formulations. The SU(2) coherent states are formally derived for the former model and used for showing some relations between closed classical orbits and quantum probability densities. Similar relations are shown for the Coulomb-Kepler problem. In both cases a perfect localization of the densities on the classical solutions is obtained even for low values of quantum numbers.     

Electromagnetically induced transparency and evolution of a two-level system under chaotic field of arbitrary intensity

The electromagnetically induced transparency (EIT) with a (near-)resonant chaotic (amplitude-phase fluctuating, Gaussian-Markovian) coupling field is studied theoretically. The Fourier transform of the steady-state EIT spectrum, which determines a nonstationary probe absorption, is also considered. This quantity equals the average diagonal element of the (reduced) evolution operator of the coupled transition (the evolution function). The exact solution in the form of a continued fraction is obtained and used to perform numerical calculations. Moreover, a number of approximate analytical results are obtained, which, together with the results of previous publications, describe the EIT and the evolution function in all possible regimes. In particular, in the constructive-interference case the EIT increases with the coupling-field bandwidth ν at sufficiently small ν. For a strong field, the maximum of the transparency as a function of ν is less than that for a monochromatic field of the same average intensity. In contrast, for a weak field, there is a range of ν values, where the field fluctuations do not affect the EIT. The latter result is shown to hold for a broad class of stochastic fields. Received 31 December 2000 and Received in final form 14 May 2001     

差分方程解对初值连续性问题

本文讨论了差分方程的解对初值的连续性问题，对较一般的方程给出了保证解对初值连续的充分条件，对线性方程（组）利用系数矩阵的特征值给出其解对初值连续的条件．     

格上度量理论

通过对格上两种度量理论,即M．A．Erceg意义下的度量理论与史福贵意义下的度量理论的介绍与评述,展现出格上拓扑学中有关度量理论发展的概况,从这里可以看到,这一般拓扑学听度量理论比较,格上度量理论的研究有基本思想和研究方法上都有其独到之处。     

Ab initio calculations of small hydrides including electron correlation

Five different structures of CH₅ ⁺ and one structure of CH₅ ^– are calculated using a gaussian basis both in the SCF approximation and with the inclusion of electron correlation in the independent electron pair approximation (IEPA). While on SCF level the C _sstructure of CH₅ ⁺ has to lowest energy, the energy difference between the C _sand C _2vstructures becomes negligible if correlation is included. In contrast to this the approach of a proton to CH₄ at large and intermediate distances is most favorable towards a corner of the CH₄ tetrahedron which means a structure. The decomposition of CH₅ ⁺ into CH₃ ⁺ and H₂ requires 20kcal/mol on SCF level and 40 kcal/mol if correlation is included.     

The ‘Temperature Integral’ — Its use and abuse

This paper first reviews the history of the temperature dependence of reaction rate in reaction kinetics. The various equations which are in use today for expressing this dependence were delineated by van't Hoff almost one hundred years ago. Since an exponential form best describes this dependence for most thermal analysis reactions and, due to the fact that the simple Arrhenius equation (with a temperature-independent preexponential factor) has traditionally been used for this purpose, the mathematically intractable temperature integral often has become a necessary evil in the analysis of thermal analysis kinetics. Methods which avoid the temperature integral in kinetics analysis are discussed. The merits of various evaluations and approximations for the temperature integral are described and assessed in this paper.     

Preparation and properties of sclerotium rolfsii invertase immobilized on indion 48-R

Crude extracellular invertase fromSclerotium rolfsii, when coupled to glutaraldehyde activated Indion 48-R, retained 70–80% activity of the soluble enzyme. Immobilization resulted in a decrease in the pH and temperature optima but it increased the temperature stability. K_m and V_max also increased as a result of immobilization. Both soluble and immobilized invertase showed inhibition at high substrate concentrations. The bound enzyme showed excellent stability to repeated use and retained approx 90% of its initial activity after 8 cycles of use.