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Structure of K,Na-Exchanged Stellerite Zeolite and its Evolution under High Pressures. / Seryotkin, Yu V.; Bakakin, V. V.

In: Journal of Structural Chemistry, Vol. 60, No. 10, 01.10.2019, p. 1612-1621.

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Seryotkin YV, Bakakin VV. Structure of K,Na-Exchanged Stellerite Zeolite and its Evolution under High Pressures. Journal of Structural Chemistry. 2019 Oct 1;60(10):1612-1621. doi: 10.1134/S0022476619100068

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Seryotkin, Yu V. ; Bakakin, V. V. / Structure of K,Na-Exchanged Stellerite Zeolite and its Evolution under High Pressures. In: Journal of Structural Chemistry. 2019 ; Vol. 60, No. 10. pp. 1612-1621.

BibTeX

@article{b9968cb14a5d4111962d95c2726b4901,
title = "Structure of K,Na-Exchanged Stellerite Zeolite and its Evolution under High Pressures",
abstract = "K,Na-exchanged stellerite |K6.35Na1.53(H2O)25|[Al7.89Si28.11O72], space group F2/m, a = 13.6212(5) {\AA}, b = 18.1589(7) {\AA}, c = 17.8495(5) {\AA}, β = 90.202(3)°, V = 4415.0(3) {\AA}3, Z = 2, is studied by single-crystal X-ray diffraction under ambient conditions and upon compression to 3.5 GPa in water-containing penetrating and non-penetrating (paraffin) media. A specific property of the structure of the K,Na-exchanged form is a vacancy at the site that is occupied by Ca2+ cations in initial stellerite. The cations are distributed over six main positions with a local coordination 7–10 for K+ and 5 for Na+. The compression of K,Na-exchanged stellerite in the 4:1 ethanol:water mixture causes its additional hydration: initially, due to the occupation of partially vacant H2O sites and then, upon further compression, due to the occupation of initially vacant positions. The environment of the cations in other positions is not changed substantially in the course of overhydration. The differences in the degree of hydration of the K,Na-exchanged form under compression in penetrating and non-penetrating media are manifested in the characteristics of the compound{\textquoteright}s compressibility.",
keywords = "high pressure, K,Na-exchanged stellerite, pressure-induced hydration, structure, zeolites, BEHAVIOR, X-RAY-DIFFRACTION, STI, K, POLYMORPHISM, Na-exchanged stellerite, REFINEMENT, DEHYDRATION, INDUCED PENETRATION, CLINOPTILOLITE, BARRERITE",
author = "Seryotkin, {Yu V.} and Bakakin, {V. V.}",
year = "2019",
month = oct,
day = "1",
doi = "10.1134/S0022476619100068",
language = "English",
volume = "60",
pages = "1612--1621",
journal = "Journal of Structural Chemistry",
issn = "0022-4766",
publisher = "Springer GmbH & Co, Auslieferungs-Gesellschaf",
number = "10",

}

RIS

TY - JOUR

T1 - Structure of K,Na-Exchanged Stellerite Zeolite and its Evolution under High Pressures

AU - Seryotkin, Yu V.

AU - Bakakin, V. V.

PY - 2019/10/1

Y1 - 2019/10/1

N2 - K,Na-exchanged stellerite |K6.35Na1.53(H2O)25|[Al7.89Si28.11O72], space group F2/m, a = 13.6212(5) Å, b = 18.1589(7) Å, c = 17.8495(5) Å, β = 90.202(3)°, V = 4415.0(3) Å3, Z = 2, is studied by single-crystal X-ray diffraction under ambient conditions and upon compression to 3.5 GPa in water-containing penetrating and non-penetrating (paraffin) media. A specific property of the structure of the K,Na-exchanged form is a vacancy at the site that is occupied by Ca2+ cations in initial stellerite. The cations are distributed over six main positions with a local coordination 7–10 for K+ and 5 for Na+. The compression of K,Na-exchanged stellerite in the 4:1 ethanol:water mixture causes its additional hydration: initially, due to the occupation of partially vacant H2O sites and then, upon further compression, due to the occupation of initially vacant positions. The environment of the cations in other positions is not changed substantially in the course of overhydration. The differences in the degree of hydration of the K,Na-exchanged form under compression in penetrating and non-penetrating media are manifested in the characteristics of the compound’s compressibility.

AB - K,Na-exchanged stellerite |K6.35Na1.53(H2O)25|[Al7.89Si28.11O72], space group F2/m, a = 13.6212(5) Å, b = 18.1589(7) Å, c = 17.8495(5) Å, β = 90.202(3)°, V = 4415.0(3) Å3, Z = 2, is studied by single-crystal X-ray diffraction under ambient conditions and upon compression to 3.5 GPa in water-containing penetrating and non-penetrating (paraffin) media. A specific property of the structure of the K,Na-exchanged form is a vacancy at the site that is occupied by Ca2+ cations in initial stellerite. The cations are distributed over six main positions with a local coordination 7–10 for K+ and 5 for Na+. The compression of K,Na-exchanged stellerite in the 4:1 ethanol:water mixture causes its additional hydration: initially, due to the occupation of partially vacant H2O sites and then, upon further compression, due to the occupation of initially vacant positions. The environment of the cations in other positions is not changed substantially in the course of overhydration. The differences in the degree of hydration of the K,Na-exchanged form under compression in penetrating and non-penetrating media are manifested in the characteristics of the compound’s compressibility.

KW - high pressure

KW - K,Na-exchanged stellerite

KW - pressure-induced hydration

KW - structure

KW - zeolites

KW - BEHAVIOR

KW - X-RAY-DIFFRACTION

KW - STI

KW - K

KW - POLYMORPHISM

KW - Na-exchanged stellerite

KW - REFINEMENT

KW - DEHYDRATION

KW - INDUCED PENETRATION

KW - CLINOPTILOLITE

KW - BARRERITE

UR - http://www.scopus.com/inward/record.url?scp=85074629858&partnerID=8YFLogxK

U2 - 10.1134/S0022476619100068

DO - 10.1134/S0022476619100068

M3 - Article

AN - SCOPUS:85074629858

VL - 60

SP - 1612

EP - 1621

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 10

ER -

ID: 22363225