The interaction of dolomite surfaces with metal impurities: a computer simulation study
This study investigates the behaviour of selected, morphologically important surfaces of dolomite (CaMg(CO3)2), using computational modelling techniques. Interatomic potential methods have been used to examine impurity substitution at cationic sites in these surfaces. Environmentally prevalent catio...
| Main Authors: | , , , |
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| Format: | Journal Article |
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Royal Society of Chemistry
2005
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| Online Access: | http://hdl.handle.net/20.500.11937/24060 |
| _version_ | 1848751324539125760 |
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| author | Wright, Kathleen Gale, Julian Slater, B. Austen, K. |
| author_facet | Wright, Kathleen Gale, Julian Slater, B. Austen, K. |
| author_sort | Wright, Kathleen |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | This study investigates the behaviour of selected, morphologically important surfaces of dolomite (CaMg(CO3)2), using computational modelling techniques. Interatomic potential methods have been used to examine impurity substitution at cationic sites in these surfaces. Environmentally prevalent cations were studied to this end, namely Ni21, Co21, Zn21, Fe21, Mn21 and Cd21, all of which are also found as end-member carbonate minerals. Solid?solution substitution was investigated and showed that Cd and Mn will substitute from their end-member carbonate phase at either dolomite cation site. Mn is found to preferentially substitute at Mg sites, in agreement with experimental findings. For Ni21, Co21 and Zn21, the magnitude of substitution energies is approximately equal for all surfaces, with the exception of the (1014) surface. However, for the larger cations, a far greater disparity in substitution energies is observed. At a stepped surface, analogous substitutions were performed and it was found that substitution energies for all impurity cations were reduced, indicating that uptake is more viable during growth. The predominant surface, the (1014), was solvated with a monolayer of water in order to investigate the influence of hydration on substitution energetics. The addition of water changes the relative preference for substitution of the different cations. Under aqueous conditions, the substitution energy is determined by three competing factors, the relative importance of which cannot be predicted without this type of computational investigation. |
| first_indexed | 2025-11-14T07:50:55Z |
| format | Journal Article |
| id | curtin-20.500.11937-24060 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T07:50:55Z |
| publishDate | 2005 |
| publisher | Royal Society of Chemistry |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-240602017-09-13T15:58:25Z The interaction of dolomite surfaces with metal impurities: a computer simulation study Wright, Kathleen Gale, Julian Slater, B. Austen, K. This study investigates the behaviour of selected, morphologically important surfaces of dolomite (CaMg(CO3)2), using computational modelling techniques. Interatomic potential methods have been used to examine impurity substitution at cationic sites in these surfaces. Environmentally prevalent cations were studied to this end, namely Ni21, Co21, Zn21, Fe21, Mn21 and Cd21, all of which are also found as end-member carbonate minerals. Solid?solution substitution was investigated and showed that Cd and Mn will substitute from their end-member carbonate phase at either dolomite cation site. Mn is found to preferentially substitute at Mg sites, in agreement with experimental findings. For Ni21, Co21 and Zn21, the magnitude of substitution energies is approximately equal for all surfaces, with the exception of the (1014) surface. However, for the larger cations, a far greater disparity in substitution energies is observed. At a stepped surface, analogous substitutions were performed and it was found that substitution energies for all impurity cations were reduced, indicating that uptake is more viable during growth. The predominant surface, the (1014), was solvated with a monolayer of water in order to investigate the influence of hydration on substitution energetics. The addition of water changes the relative preference for substitution of the different cations. Under aqueous conditions, the substitution energy is determined by three competing factors, the relative importance of which cannot be predicted without this type of computational investigation. 2005 Journal Article http://hdl.handle.net/20.500.11937/24060 10.1039/b510454h Royal Society of Chemistry fulltext |
| spellingShingle | Wright, Kathleen Gale, Julian Slater, B. Austen, K. The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title | The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title_full | The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title_fullStr | The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title_full_unstemmed | The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title_short | The interaction of dolomite surfaces with metal impurities: a computer simulation study |
| title_sort | interaction of dolomite surfaces with metal impurities: a computer simulation study |
| url | http://hdl.handle.net/20.500.11937/24060 |