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21.
Ohne Zusammenfassung k (s) = ((s)) k , und ebenso in allen analogen Fällen.  相似文献   
22.
For any self-adjoint realization S of a singular Sturm-Liouville equation on an interval (a,b) with limit-circle endpoints, we construct a family of self-adjoint realizations S r ,r ∈ (0,∞), of this equation on subintervals (a r ,b r ) of (a,b) such that every eigenvalue of S is the limit of a continuous eigenvalue branch of this family. Of particular interest are the cases when at least one endpoint is oscillatory or the leading coefficient function changes sign. In these cases, we show that the index determining each continuous eigenvalue branch has an infinite number of jump discontinuities and give an explicit characterization of these discontinuities.  相似文献   
23.
Reuther  H.  Arnold  T.  Krawczyk-Bärsch  E. 《Hyperfine Interactions》2004,156(1-4):439-443
Hyperfine Interactions - During batch sorption experiments of heavy metals on chlorite not only sorption reactions take place, but also reactions of chemical weathering leading to mineral...  相似文献   
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25.
Polarization dynamics are considered in the presence of an anisotropic Kerr non-linearity in the most common semiconductor waveguide geometry. The equations of motion are formulated in terms of Stokes polarization parameters and their Hamiltonian form is derived. Stationary solutions and their stability are found for plane-wave propagation. It is found that the non-integrable problem of mixed-polarization spatial soliton dynamics can be largely explained in terms of the equivalent plane-wave solutions.  相似文献   
26.
Novel oscillatory flow results of phenoxy/organoclay nanocomposites are analysed considering the blocking effect of nanostructure on polymer chain mobility. The modification provoked by this hindering effect on loss tangent spectrum is investigated. The study of three different systems, involving a pristine montmorillonite and two montmorillonites modified with one alkyl tail and two alkyl tails, respectively, leads to conclude that polymer-alkyl repulsive interactions play the most important role in the chain mobility obstruction process. Our results suggest that polymer-alkyl interactions increase with temperature.  相似文献   
27.
The thermochemical transformation of electrostatically formed complexes of methyl orange (MO) with polycations containing primary amine groups such as ammonium salts afforded new polymers with a high concentration of covalently bound 4‐N,N‐dimethylaminoazobenzene groups in the side chain. Poly(allylamine hydrochloride) and poly(β‐aminoethylene acrylamide hydrochloride) were employed as support polycations for MO. The transformation of sulfonate–ammonium ion pairs into sulfonamide bonds, via heating at an elevated temperature, was supported by the polymer properties before and after the thermal treatment. The polymer structure changes were monitored with elemental analysis, Fourier transform infrared, 1H NMR, and ultraviolet–visible absorption spectroscopy, and thermogravimetric analysis. The spacer length between the backbone and azobenzene structures used as side chains strongly influenced the polymer properties before and after the heat‐induced reaction. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5898–5908, 2006  相似文献   
28.
In this paper,Lefschetz formulae for torus actions on p-adic groups are proven. These are similar to comparable formulae for real Lie groups.Applications lie in the realm of dynamical zeta functions.  相似文献   
29.
Summary For the numerical solution of non-stiff semi-explicit differentialalgebraic equations (DAEs) of index 1 half-explicit Runge-Kutta methods (HERK) are considered that combine an explicit Runge-Kutta method for the differential part with a simplified Newton method for the (approximate) solution of the algebraic part of the DAE. Two principles for the choice of the initial guesses and the number of Newton steps at each stage are given that allow to construct HERK of the same order as the underlying explicit Runge-Kutta method. Numerical tests illustrate the efficiency of these methods.  相似文献   
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