Introduction
To
investigate an actinide or other alpha-emitter at the low concentrations
encountered in many environmental samples necessitates chemical separation
of the actinide of interest from the bulk matrix, purification by the
elimination of other interferants, mounting onto suitable substrates for
counting, and quantification by radiometric, mass spectrometric or other
means.

Background:
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The
actinide series of the periodic table comprises the
naturally-occurring thorium, protactinium and uranium nuclides, and
the transuranium elements neptunium to lawrencium, inclusive.
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Small
traces of naturally-produced transuranium nuclides remain or are being
generated in nature, but the overwhelming ‘weight’ of present
environmental inventories of these elements derive from human
activities, related mainly to the nuclear fuel and to military
applications.
The Need for Radiochemical
Procedures:
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Although
direct quantitative measurement of some of these nuclides is possible
by non-destructive techniques such as gamma and X-ray spectrometry,
most of them decay by the emission of alpha or beta particles.
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For
these nuclides, direct measurement in the presence of the host matrix
(e.g water, soil) is not possible, as the particles emitted are
rapidly absorbed by the matrix before they can be detected.
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At
environmental levels, even those nuclides with gamma and X-ray
emissions may be difficult to detect, given the minute concentrations
involved, the comparatively low sensitivity of gamma and X-ray
detection systems, and interference from other photon-emitters in the
sample.
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In such
cases, radiochemical separation of the nuclides of interest from the
bulk matrix, purification by the elimination of other interferants and
preparation in a form suitable for counting is essential.
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Accurate
determination of actinide concentrations at these low levels depends
heavily on the analyst's ability to prepare extremely pure analytes,
free of any gravimetric or radiometric interferences which could lead
to complications in the interpretation of the measured spectra.
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Since
most of the actinides spontaneously decay by alpha-emission,
high-resolution alpha spectrometry has become the most widely used
technique for the determination of these nuclides.
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Over
the years, numerous radiochemical separation schemes, based primarily
on coprecipitation, ion exchange or solvent extraction, have been
proposed and adapted for different matrices and types of analysis.
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