Introduction to Soil Chemistry
Introduction to Soil Chemistry
Introduction to Soil Chemistry
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Incoming<br />
X-ray<br />
x-ray fluorescence 151<br />
Electron falling <strong>to</strong><br />
lower level<br />
Ejected<br />
electron<br />
Fluorescence<br />
pho<strong>to</strong>n<br />
Figure 8.3. Diagram showing the source of X-ray fluorescence pho<strong>to</strong>ns.<br />
often a metal, will, in part, determine the range of elements that can be<br />
detected.<br />
When used in direct soil analysis, X-ray fluorescence suffers from the fact<br />
that it is largely a surface phenomenon. For this reason, only surface elements<br />
will be determined. However, because it is a surface phenomenon, it has been<br />
extensively used <strong>to</strong> study sorption on the surfaces of soil components. An<br />
extensive list of investigations using XRF <strong>to</strong> investigate various sorption<br />
mechanisms is given in the text by Sparks [6].<br />
Other characteristics of XRF that can limit its usefulness are the surface<br />
area observed and surface contamination. In XRF the surface area measured<br />
is small, meaning that a large number of determinations must be made in order<br />
<strong>to</strong> obtain a representative sample of the elements present. In addition, transport<br />
and s<strong>to</strong>rage of uncovered soil samples can lead <strong>to</strong> surface contamination<br />
that will subsequently appear as part of the soil constituents.<br />
The sensitivity of X-ray fluorescence determinations is better for elements<br />
with higher mass number and less for lighter elements. Often in soil analysis<br />
lighter elements are of greater interest, and this makes application of this<br />
method more difficult. Typically determination of elemental composition in<br />
the part per million (ppm) range is, however, achievable.<br />
Fluorescence determinations are best made on samples of homogeneous<br />
particle size, and this is not the normal state of soil. Grinding and carefully<br />
sieving soil before analysis can minimize problems associated with particle size<br />
heterogeneity. Another approach has been <strong>to</strong> fuse soil with borate or dilute it