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Virginia Tech

Atomic Force Microscopy Study of Clay Mineral Dissolution

Abstract

dc:description.abstract

An integrated program has been developed to explore the reactivity of 2:1 phyllosilicates (biotite and the clays montmorillonite, hectorite, and nontronite) with respect to acid dissolution using in situ atomic force microscopy (AFM). Three techniques are described which make it possible to fix these minerals and other small particles to a suitable substrate for examination in the fluid cell of the atomic force microscope. A suite of macros has also been developed for the Image SXM image analysis environment which make possible the accurate and consistent measurement of the dimensions of clay particles in a series of AFM images, so that dissolution rates can be measured during a fluid cell experiment. Particles of biotite and montmorillonite were dissolved, and their dissolution rates normalized to their reactive surface area, which corresponds to the area of their edge surfaces (A<sub>e</sub>). The A<sub>e</sub>-normalized rates for these minerals between pH 1-2 are all ~10E<sup>-8</sup> mol/m<sup>2</sup>*s, and compare very well to other A<sub>e</sub>-normalized dissolution rates in the literature. Differences between the A<sub>e</sub>-normalized rates for biotite and the BET-normalized rates (derived from solution chemical studies) found in the literature can be easily explained in terms of the proportion of edge surface area and the formation of leached layers. However, the differences between the A<sub>e</sub>-normalized montmorillonite rates and the literature values cannot be explained the same way. Rather, it is demonstrated that rates derived from solution studies of montmorillonite dissolution have been affected by the colloidal behavior of the mineral particles. Finally, the dissolution behavior of hectorite (a trioctahedral smectite) and nontronite ( a dioctahedral smectite) were compared. Based on the differential reactivity of their crystal faces, a model of their surface atomic structures is formulated using Hartman-Perdock crystal growth theory, which explains the observed data if it is assumed that the rate-determining step of the dissolution mechanism is the breaking of connecting bonds between the octahedral and tetrahedral sheets of the mineral structure.

Degree

thesis:*
Name thesis:degree_name
Ph. D.
Level thesis:degree_level
doctoral
Discipline thesis:degree_discipline
Geological Sciences
Department dc:contributor.department
Geological Sciences
Grantor dc:publisher
Virginia Tech
Year dc:date.issued
1999

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Bickmore, Barry Robert
Chair dc:contributor.committeechair
  • Hochella, Michael F. Jr.
Committee members dc:contributor.committeemember
  • Rimstidt, J. Donald
  • Zelazny, Lucian W.
  • Gibbs, Gerald V.
  • Ribbe, Paul H.

Subjects

dc:subject × 13

Rights

dc:rights
Statement dc:rights
  • In Copyright

Identifiers

dc:identifier.*
Dc Identifier Other
etd-0111100-115522
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/25984

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Bickmore, Barry Robert. Atomic Force Microscopy Study of Clay Mineral Dissolution. doctoral thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/25984