Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation

Abstract Chlormayenite Ca12Al14O32[♦4Cl2] (♦-vacancy) is partially hydrated micro porouss mineral with hydroxide groups situated at various crystallographic sites. There are few mechanisms describing its hydration. The first one assumes Cl− substitution by OH− at the center of the structural cages (...

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Autores principales: Mateusz Dulski, Katarzyna M. Marzec, Joachim Kusz, Irina Galuskina, Katarzyna Majzner, Evgeny Galuskin
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:8cec503ecc854d73890d18d5e80d998b2021-12-02T11:53:01ZDifferent route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation10.1038/s41598-017-08152-12045-2322https://doaj.org/article/8cec503ecc854d73890d18d5e80d998b2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08152-1https://doaj.org/toc/2045-2322Abstract Chlormayenite Ca12Al14O32[♦4Cl2] (♦-vacancy) is partially hydrated micro porouss mineral with hydroxide groups situated at various crystallographic sites. There are few mechanisms describing its hydration. The first one assumes Cl− substitution by OH− at the center of the structural cages (W-site). The second one determines the converting a T1O4 tetrahedron to a T1O3(OH)3 octahedron due to the replacement of oxygen at the O2 site by three OH-groups according to the scheme: (O2O2− +  W Cl−) → 3 ×  O2aOH. The third mechanism, not considered so far in the case of zeolite-like minerals, includes the hydroxide incorporation in form of hydrogarnet defect due to the arrangement of tetrahedral (OH)4 in vacant cages. This yields a strong hydrated phase containing even up to 35% of water more than in any currently known mineral applicable to Portland cement. Moreover, water molecules present in different structural cages are stable up to 355 K while dehydroxylation linked to the gradual loss of only 8% of OH− groups according to 3 O2aOH− → O2O2− + W OH− + gH2O occurs at temperature range from 355 K to 598 K.Mateusz DulskiKatarzyna M. MarzecJoachim KuszIrina GaluskinaKatarzyna MajznerEvgeny GaluskinNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mateusz Dulski
Katarzyna M. Marzec
Joachim Kusz
Irina Galuskina
Katarzyna Majzner
Evgeny Galuskin
Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
description Abstract Chlormayenite Ca12Al14O32[♦4Cl2] (♦-vacancy) is partially hydrated micro porouss mineral with hydroxide groups situated at various crystallographic sites. There are few mechanisms describing its hydration. The first one assumes Cl− substitution by OH− at the center of the structural cages (W-site). The second one determines the converting a T1O4 tetrahedron to a T1O3(OH)3 octahedron due to the replacement of oxygen at the O2 site by three OH-groups according to the scheme: (O2O2− +  W Cl−) → 3 ×  O2aOH. The third mechanism, not considered so far in the case of zeolite-like minerals, includes the hydroxide incorporation in form of hydrogarnet defect due to the arrangement of tetrahedral (OH)4 in vacant cages. This yields a strong hydrated phase containing even up to 35% of water more than in any currently known mineral applicable to Portland cement. Moreover, water molecules present in different structural cages are stable up to 355 K while dehydroxylation linked to the gradual loss of only 8% of OH− groups according to 3 O2aOH− → O2O2− + W OH− + gH2O occurs at temperature range from 355 K to 598 K.
format article
author Mateusz Dulski
Katarzyna M. Marzec
Joachim Kusz
Irina Galuskina
Katarzyna Majzner
Evgeny Galuskin
author_facet Mateusz Dulski
Katarzyna M. Marzec
Joachim Kusz
Irina Galuskina
Katarzyna Majzner
Evgeny Galuskin
author_sort Mateusz Dulski
title Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
title_short Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
title_full Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
title_fullStr Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
title_full_unstemmed Different route of hydroxide incorporation and thermal stability of new type of water clathrate: X-ray single crystal and Raman investigation
title_sort different route of hydroxide incorporation and thermal stability of new type of water clathrate: x-ray single crystal and raman investigation
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/8cec503ecc854d73890d18d5e80d998b
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