Title page for ETD etd-07212007-104241


Document Type Doctoral Thesis
Author Morkel, Jacqueline
Email Jacqueline.morkel@debeersgroup.com
URN etd-07212007-104241
Document Title Kimberlite weathering : mineralogy and mechanism
Degree PhD (Metallurgical Engineering)
Department Materials Science and Metallurgical Engineering
Supervisor
Advisor Name Title
Prof P C Pistorius Committee Chair
Prof T J Napier-Munn Committee Chair
Dr M K G Vermaak Committee Co-Chair
Keywords
  • cation exchange
  • accelerated weathering
  • clay minerals
  • mineralogy
  • kimberlite
  • swelling
  • weathering
Date 2007-04-24
Availability unrestricted
Abstract
The aim of this study was to arrive at a fundamental understanding of kimberlite weathering and of factors which affect the rate and extent of weathering. Weathering was evaluated by measuring the change in size distribution after immersing crushed kimberlite in solutions of various compositions. Reproducibility of the measurements was found to be good, with the cumulative mass passing a given size differing by 7% or less, as tested for various weathering conditions.

Kimberlite mineralogy, specifically the swelling clay content, was found to play a central role: kimberlite ores containing no swelling clay were not prone to weathering under any of the conditions tested.

The cation exchange capacity (CEC) correlates well with the swelling clay content and with the weathering behaviour. The cation exchange capacity may be used in conjunction with the swelling clay content, as a predictor of possible kimberlite behaviour; however, given the relative complexity and cost of measuring swelling clay content (by X-ray diffraction), the CEC is the preferred parameter for practical use.

Cations in the weathering solution have a strong effect on kimberlite weathering; the strength of the effect followed the series Cu2+ > Li+ > Fe2+ > Ca2+ > Fe3+ > Mg2+, whereas K+ and NH4+ stabilised the kimberlite somewhat against weathering. This sequence was in reasonable correlation with the ionic potential (ratio of valency to ionic radius), but with exceptionally strong weathering effects of Cu2+, and (to a lesser extent) of Li+ and Fe2+. The strong effect of the latter group of cations may be related to their tendency to adsorb onto other crystal sites in addition to the interlayer the associated change in surface energy can change the fracture behaviour of the kimberlite.

Measurement of the layer spacing of the swelling clay (by X-ray diffraction) showed no correlation between the weathering effect of a cation and the associated thickness of the interlayer. For solutions of cupric ions, the identity of the anion (chloride or sulphate) has little effect on weathering. The size of the crushed kimberlite ore similarly has little effect on the relative extent of size degradation by weathering.

The concentration of cupric ions affects weathering, as does the weathering time although 85% of the weathering caused by 30 days' exposure was found to occur within the first 24 hours. Increasing the temperature to 40C (in a magnesium chloride solution) also increased weathering strongly. The kinetics of exchange of cuprous and potassium ions was measured (for two different kimberlites); the apparent reaction order (with respect to the concentration of exchanging cations in solution) varied between 1 and 3.5, and exchange of potassium was more rapid.

This work has practical implications for in-plant processing of kimberlite, possible alternative kimberlite processing routes which eliminate one or more crushing steps, and for the stability of mine tunnels which pass through kimberlite.

University of Pretoria

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  00front.pdf 237.57 Kb 00:01:05 00:00:33 00:00:29 00:00:14 00:00:01
  01chapters1-2.pdf 568.50 Kb 00:02:37 00:01:21 00:01:11 00:00:35 00:00:03
  02chapters3-5.pdf 423.69 Kb 00:01:57 00:01:00 00:00:52 00:00:26 00:00:02
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  04chapters8-9-references.pdf 155.72 Kb 00:00:43 00:00:22 00:00:19 00:00:09 < 00:00:01
  05appendices.pdf 896.76 Kb 00:04:09 00:02:08 00:01:52 00:00:56 00:00:04

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