The use of secondary ion mass spectrometry coupled with image analysis to identify and locate chemical elements in soil minerals: The example of phosphorus

Citation
I. Bertrand et al., The use of secondary ion mass spectrometry coupled with image analysis to identify and locate chemical elements in soil minerals: The example of phosphorus, SCANNING, 23(4), 2001, pp. 279-291
Citations number
54
Categorie Soggetti
Multidisciplinary,"Spectroscopy /Instrumentation/Analytical Sciences
Journal title
SCANNING
ISSN journal
01610457 → ACNP
Volume
23
Issue
4
Year of publication
2001
Pages
279 - 291
Database
ISI
SICI code
0161-0457(200107/08)23:4<279:TUOSIM>2.0.ZU;2-N
Abstract
The mobility and bioavailability of elements in soils and sediments largely depends on their distribution on the diverse inorganic and organic constit uents. This work addresses the example of phosphorus (P) associated to goet hite and calcite, that is, to the major minerals involved in the retention of P in soils and sediments in calcareous environments. Synthetic goethite (FeOOH) and calcite (CaCO3) were reacted with P prior to being analysed by dynamic secondary ion mass spectrometry (SIMS). Powdery samples were embedd ed in resin, cut in thin sections, and imaged with a CAMECA IMS 4F ion micr oscope used in scanning mode with a primary ion beam of caesium that produc ed negatively charged secondary ions ((-)) (Cameca, Cedex, France). Carbon, O, P, and calcium (Ca) were directly imaged at m/z 12, 16 31, and 40, resp ectively, while Fe was imaged via the polyatomic ion FeO- ion at m/z 72. Th e SIMS data were treated by image analysis procedures. The visual compariso n of images and the scatterplot method showed that P strongly interacted wi th goethite, probably following an adsorption process, and was thus evenly distributed at its surface. Conversely, P was not evenly distributed at the surface of calcite which rather suggests a precipitation process, and the scatterplot method confirmed a poor relationship between P and Ca. For the goethite-calcite mixture, visual examination suggested that P occurred as c lusters which were largely associated with calcite, whereas a statistical a nalysis of the various images showed that the distribution of P was largely related to that of goethite particles. This work confirms the potential co ntribution of iron oxides in the retention of P in calcareous environments and shows that coupling image analysis to sensitive analytical techniques s uch as SIMS is a powerful approach for providing quantitative information o n the location of elements at low bulk concentrations.