DEHYDRATION AND REHYDRATION PROCESS IN BOGGSITE: AN IN SITU X-RAY SINGLE-CRYSTAL STUDY

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dc.contributor.author Zanardi S.
dc.contributor.author Cruciani G.
dc.contributor.author Alberti A.
dc.contributor.author Galli E.
dc.date.accessioned 2022-04-18T05:17:15Z
dc.date.available 2022-04-18T05:17:15Z
dc.date.issued 2004
dc.identifier https://www.elibrary.ru/item.asp?id=14482240
dc.identifier.citation American Mineralogist, 2004, 89, 7, 1033-1042
dc.identifier.issn 0003-004X
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/37233
dc.description.abstract The dehydration-rehydration process in boggsite |K0.06Na0.36Sr0.01Ca7.00Mg1.20Fe0.05(H2O)70| [Al17.52Si78.62O192]-BOG, a rare natural pentasil zeolite characterized by a 3D channel system of 10- and 12-rings, occurs in space group Imma with cell parameters a = 20.291(1), b = 23.840(1), c = 12.807(1) Å, and V = 6195.2 Å3 at 25 °C. Single-crystal X-ray data collections were carried out at room temperature, at 150, 350, and 500 °C in a hot nitrogen stream, and after the crystal was cooled down to 150 °C and then again at room temperature. During these processes, the variation in the unit-cell volume was always less than 1.4%. At room conditions boggsite is characterized by strong disorder in cation and H2O molecule distribution, with many partially occupied sites weakly interacting with the framework. At 150 °C, where most of the water is lost, three extraframework cation sites were located. At 350 °C boggsite is fully dehydrated and five cation sites are present; three of these are fourfold coordinated and the others are sixfold coordinated. As a consequence of the migration of the cations, at 500 °C only four cation sites are present. The rehydration process causes distortion of the boggsite channels; the 10-ring reduces its free area by about 1 Å2, whereas the area of the 12-ring channel grows from 40 to 42 Å2. The dehydration process is rapid and completely reversible.
dc.subject boggsite
dc.title DEHYDRATION AND REHYDRATION PROCESS IN BOGGSITE: AN IN SITU X-RAY SINGLE-CRYSTAL STUDY
dc.type Статья


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