ANALYSIS OF CATION DISTRIBUTION IN THE OCTAHEDRAL SHEET OF DIOCTAHEDRAL 2:1 PHYLLOSILICATES BY USING INVERSE MONTE CARLO METHODS

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dc.contributor.author Sainz-Díaz C.I.
dc.contributor.author Cuadros J.
dc.contributor.author Hernández-Laguna A.
dc.date.accessioned 2021-03-05T03:25:25Z
dc.date.available 2021-03-05T03:25:25Z
dc.date.issued 2001
dc.identifier https://elibrary.ru/item.asp?id=13836766
dc.identifier.citation Physics and Chemistry of Minerals, 2001, 28, 7, 445-454
dc.identifier.issn 0342-1791
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/26294
dc.description.abstract An inverse Monte Carlo (MC) method was developed to determine the distribution of octahedral cations (Al3+, Fe3+, and Mg2+) in bentonite illite–smectite (I–S) samples (dioctahedral 2:1 phyllosilicates) using FT–IR and 27Al MAS NMR spectroscopies. FT–IR allows determination of the nature and proportion of different cation pairs bound to OH groups measuring the intensities of OH-bending bands. 27Al MAS NMR data provide information about cation configuration because 27Al MAS NMR intensity depends on Fe distribution. MC calculations based on FT–IR data alone show Fe segregation by short-range ordering (Fe clusters within 9 to 15 Å from a given Fe atom). Fe segregation increases with illite proportion. MC calculations based on IR and 27Al NMR simultaneously yield similar configurations in which Fe clusters are smaller. The latter calculations fail to build appropriate cation distributions for those samples with higher number of illite layers and significant Fe content, which is indicative of long-range Fe ordering that cannot be detected by FT–IR and 27Al MAS NMR. The proportion of Mg–Mg pairs is negligible in all samples, and calculations, in which the number of Mg atoms, as second neighbours, is minimised, create appropriate configurations.
dc.title ANALYSIS OF CATION DISTRIBUTION IN THE OCTAHEDRAL SHEET OF DIOCTAHEDRAL 2:1 PHYLLOSILICATES BY USING INVERSE MONTE CARLO METHODS
dc.type Статья


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