Volume 227, Issue 1 pp. 27-38
Article

Light, Small Angle Neutron and X-Ray Scattering from Gels

Erik Geissler

Erik Geissler

Laboratoire de Spectrométrie Physique CNRS UMR 5588, Université J. Fourier de Grenoble, B.P. 87, 38402 St Martin d'Hères cedex, France

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Anne-Marie Hecht

Anne-Marie Hecht

Laboratoire de Spectrométrie Physique CNRS UMR 5588, Université J. Fourier de Grenoble, B.P. 87, 38402 St Martin d'Hères cedex, France

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Cyrille Rochas

Cyrille Rochas

Laboratoire de Spectrométrie Physique CNRS UMR 5588, Université J. Fourier de Grenoble, B.P. 87, 38402 St Martin d'Hères cedex, France

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Ferenc Horkay

Ferenc Horkay

Section on Tissue Biophysics and Biomimetics, Laboratory of Integrative and Medical Biophysics, NICHD, National Institutes of Health, 13 South Drive, Bethesda, MD 20892, USA

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Peter J. Basser

Peter J. Basser

Section on Tissue Biophysics and Biomimetics, Laboratory of Integrative and Medical Biophysics, NICHD, National Institutes of Health, 13 South Drive, Bethesda, MD 20892, USA

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First published: 04 August 2005
Citations: 9

Abstract

This paper gives two examples of experiments that demonstrate the power of small angle scattering techniques in the study of swollen polymer networks. First, it is shown how the partly ergodic character of these systems is directly detected by neutron spin echo experiments. The observed total field correlation function of the intensity scattered from a neutral gel allows the ergodic contribution to be directly distinguished from the non ergodic part, at values of transfer wave vector q that lie well beyond the range of dynamic light scattering. The results can be compared with those obtained at much lower q from visible light scattering.

Second, a recent application of small angle X-ray (SAXS) and neutron (SANS) scattering is described for a polyelectrolyte molecule, DNA, in semi-dilute solutions under near-physiological conditions. For these observations, the divalent ion normally present, calcium, is replaced by an equivalent ion, strontium. The comparison between SANS and SAXS yields a quantitative picture of the cloud of divalent counter-ions around the central DNA core. At physiological conditions, the cloud is thinner than that predicted on the basis of the Debye screening length but thicker than if the counter-ions were condensed on the DNA chain.

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