HYDROGEN BONDING IN IKAITE, CACO3.6H2O
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dc.contributor.author | Swainson I.P. | |
dc.contributor.author | Hammond R.P. | |
dc.date.accessioned | 2021-11-28T04:25:38Z | |
dc.date.available | 2021-11-28T04:25:38Z | |
dc.date.issued | 2003 | |
dc.identifier | https://www.elibrary.ru/item.asp?id=14256569 | |
dc.identifier.citation | Mineralogical Magazine, 2003, 67, 3, 555-562 | |
dc.identifier.issn | 0026-461X | |
dc.identifier.uri | https://repository.geologyscience.ru/handle/123456789/32572 | |
dc.description.abstract | Ikaite is a metastable hexahydrate of calcium carbonate, forming in aqueous conditions near freezing conditions. Neutron powder diffraction data of synthetic deuterated ikaite, collected at seven temperatures from 4 to 270 K, were refined. The linear thermal expansion coefficients are quite anisotropic, being smaller in the direction of the C-O bond. A review of the hydrogen-bonding scheme around the (CaCO03) ion pair is given and an additional weak potential hydrogen bond is suggested. Temperature-dependent growth of the atomic displacement factors of the carbonate O1 atom agrees with the previous suggestion of a possible low-frequency, hindered librational mode of the carbonate group. | |
dc.subject | Ikaite | |
dc.title | HYDROGEN BONDING IN IKAITE, CACO3.6H2O | |
dc.type | Статья |
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