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Paramagnetic relaxation of spin polarized 3He at bare glass surfaces.

Authors :
Schmiedeskamp, J.
Heil, W.
Otten, E. W.
Kremer, R. K.
Simon, A.
Zimmer, J.
Source :
European Physical Journal D (EPJ D); Jun2006, Vol. 38 Issue 3, p427-438, 12p, 1 Color Photograph, 2 Charts, 6 Graphs
Publication Year :
2006

Abstract

In this first in a series of three papers on wall relaxation of spin polarized, gaseous <superscript>3</superscript>He we investigate both by theory and by experiment surface-induced spin relaxation due to paramagnetic sites in the containing glass. We present experimental and theoretical evidence that — contrary to the traditional opinion — distant dipolar coupling to paramagnetic impurities in the glass, in particular iron ions, cannot be the dominant relaxation mechanism of <superscript>3</superscript>He-spins, although iron dominates the bulk static permeability. Instead dangling-bond type defects in the glass matrix are found to interact much stronger via the isotropic Fermi contact interaction. A model of paramagnetic site controlled <superscript>3</superscript>He relaxation including the Fermi contact interaction is presented. With reasonable semi-empirical assumptions our model allows to describe satisfactorily the measured relaxivities, both in the dissolution-dominated regime of fused silica or borosilicate glasses of the Pyrex type as well as in the surface dominated situation of aluminosilicate glasses which have only a low permeability for He atoms. In a large sample of 1.1 litre cells, built from various aluminosilicate glasses, an average relaxation time of 150 h is reached in case contaminant ferromagnetic particles have been demagnetized beforehand. From the maximum observed value of 250 h we derive after subtraction of dipolar relaxation in the gas phase a paramagnetic surface relaxivity of ρ<0.005 cm/h at room temperature. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14346060
Volume :
38
Issue :
3
Database :
Complementary Index
Journal :
European Physical Journal D (EPJ D)
Publication Type :
Academic Journal
Accession number :
20667491
Full Text :
https://doi.org/10.1140/epjd/e2006-00050-2