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K. Amos

Publications and source records attributed to K. Amos.

111 records · Page 7Linked to original sources

Microscopic model analyses of the elastic scattering of 65 MeV protons from targets of diverse mass

Nonlocal coordinate space optical potentials for the scattering of 65 MeV protons from nuclei ranging in mass from 6Li to 238U have been defined by folding a complex, medium dependent effective interaction with the density matrix elements of each target. The effective interaction is based upon solutions of the Lippmann--Schwinger and Brueckner--Bethe--Goldstone equations having the Paris potential as input. The nuclear structure information required in our folding model are the one body density matrix elements for the target and the single nucleon bound state wave functions that they weight. For light mass nuclei, very large basis shell model calculations have been made to obtain the one body density matrix elements. For medium and heavy mass nuclei, a very simple shell model prescription has been used. The bound state single particle wave functions that complete the nuclear density matrices are either Woods--Saxon or harmonic oscillator functions. The former are employed in most cases when large basis structure is available. For light nuclei (A < 16) Woods--Saxon potential parameters and harmonic oscillator lengths are determined from fits to electron scattering form factors. For all other nuclei, we use harmonic oscillator functions with the oscillator lengths set from an A^{1/6} mass law. Using this microscopic model, optical potentials result from which differential cross sections, analyzing powers and spin rotations are found. In general the calculated results compare very well with data when the effective interactions are determined from a mapping of nucleon--nucleon g matrices. This is not the case when effective interactions built from a mapping of (free) t matrices are used.

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A METHOD OF CALCULATING THE JOST FUNCTION FOR ANALYTIC POTENTIALS

A combination of the variable-constant and complex coordinate rotation methods is used to solve the two-body Schrödinger equation. The latter is replaced by a system of linear first-order differential equations, which enables one to perform direct calculation of the Jost function for all complex momenta of physical interest, including the spectral points corresponding to bound and resonance states. Explicit forms of the equations, appropriate for central, noncentral, and Coulomb-tailed potentials are given. Within the proposed method, the scattering, bound, virtual, and resonance state problems can be treated in a unified way. The effectiveness of the method is demonstrated by a numerical example.

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Complex Conjugate Pairs in Stationary Sturmians

Sturmian eigenstates specified by stationary scattering boundary conditions are particularly useful in contexts such as forming simple separable two nucleon t matrices, and are determined via solution of generalised eigenvalue equation using real and symmetric matrices. In general, the spectrum of such an equation may contain complex eigenvalues. But to each complex eigenvalue there is a corresponding conjugate partner. In studies using realistic nucleon--nucleon potentials, and in certain positive energy intervals, these complex conjugated pairs indeed appear in the Sturmian spectrum. However, as we demonstrate herein, it is possible to recombine the complex conjugate pairs and corresponding states into a new, sign--definite pair of real quantities with which to effect separable expansions of the (real) nucleon--nucleon reactance matrices.

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