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Structure of K-Substituted Zeolite Clinoptillolite and Its Behavior Upon Compression in Penetrating and Non-Penetrating Media. / Seryotkin, Yu V.; Bakakin, V. V.

в: Journal of Structural Chemistry, Том 59, № 6, 01.11.2018, стр. 1392-1399.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Seryotkin YV, Bakakin VV. Structure of K-Substituted Zeolite Clinoptillolite and Its Behavior Upon Compression in Penetrating and Non-Penetrating Media. Journal of Structural Chemistry. 2018 нояб. 1;59(6):1392-1399. doi: 10.1134/S0022476618060203

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Seryotkin, Yu V. ; Bakakin, V. V. / Structure of K-Substituted Zeolite Clinoptillolite and Its Behavior Upon Compression in Penetrating and Non-Penetrating Media. в: Journal of Structural Chemistry. 2018 ; Том 59, № 6. стр. 1392-1399.

BibTeX

@article{e5a2d0b962bb4914b34abfa3831c1cdf,
title = "Structure of K-Substituted Zeolite Clinoptillolite and Its Behavior Upon Compression in Penetrating and Non-Penetrating Media",
abstract = "K6.16Na0.16Ca0.07Mg0.03(H2O)19.2|[Al6.45Si29.55O72] (space group C2/m, a = 17.6490(3) {\AA}, b = 17.9982(2) {\AA}, c = 7.39329(12) {\AA}, β = 116.0655(19)°, V = 2109.63(5) {\AA}3, Z = 1) is studied by the single crystal X-ray diffraction analysis under ambient conditions and also upon compression to 4 GPa in penetrating (water-containing) and non-penetrating (paraffin) media. Compression of Ksubstituted clinoptillolite in a water:ethanol (1:1) mixture results in its additional hydration: inclusion of 2.2 additional H2O molecules into the structure at the initial stage. Upon further compression the H2O concentration increases by two molecules. This is caused by additional occupancy of partially vacant H2O sites. The cation environment practically does not change during overhydration. Changes in the coordination polyhedra of cations during compression in paraffin are reduced to a small (0.02-0.1 {\AA}) decrease in bond lengths. Distinctions in the degree of hydration of the K-form upon compression in penetrating and non-penetrating media are manifested in the features of the compressibility of the compound.",
keywords = "high pressure, K-substituted clinoptillolite, pressure-induced hydration, structure, zeolites, NA, EXCHANGED HEULANDITE, STEPWISE DEHYDRATION, CRYSTAL X-RAY, CLINOPTILOLITE, HIGH-PRESSURE BEHAVIOR",
author = "Seryotkin, {Yu V.} and Bakakin, {V. V.}",
year = "2018",
month = nov,
day = "1",
doi = "10.1134/S0022476618060203",
language = "English",
volume = "59",
pages = "1392--1399",
journal = "Journal of Structural Chemistry",
issn = "0022-4766",
publisher = "Springer GmbH & Co, Auslieferungs-Gesellschaf",
number = "6",

}

RIS

TY - JOUR

T1 - Structure of K-Substituted Zeolite Clinoptillolite and Its Behavior Upon Compression in Penetrating and Non-Penetrating Media

AU - Seryotkin, Yu V.

AU - Bakakin, V. V.

PY - 2018/11/1

Y1 - 2018/11/1

N2 - K6.16Na0.16Ca0.07Mg0.03(H2O)19.2|[Al6.45Si29.55O72] (space group C2/m, a = 17.6490(3) Å, b = 17.9982(2) Å, c = 7.39329(12) Å, β = 116.0655(19)°, V = 2109.63(5) Å3, Z = 1) is studied by the single crystal X-ray diffraction analysis under ambient conditions and also upon compression to 4 GPa in penetrating (water-containing) and non-penetrating (paraffin) media. Compression of Ksubstituted clinoptillolite in a water:ethanol (1:1) mixture results in its additional hydration: inclusion of 2.2 additional H2O molecules into the structure at the initial stage. Upon further compression the H2O concentration increases by two molecules. This is caused by additional occupancy of partially vacant H2O sites. The cation environment practically does not change during overhydration. Changes in the coordination polyhedra of cations during compression in paraffin are reduced to a small (0.02-0.1 Å) decrease in bond lengths. Distinctions in the degree of hydration of the K-form upon compression in penetrating and non-penetrating media are manifested in the features of the compressibility of the compound.

AB - K6.16Na0.16Ca0.07Mg0.03(H2O)19.2|[Al6.45Si29.55O72] (space group C2/m, a = 17.6490(3) Å, b = 17.9982(2) Å, c = 7.39329(12) Å, β = 116.0655(19)°, V = 2109.63(5) Å3, Z = 1) is studied by the single crystal X-ray diffraction analysis under ambient conditions and also upon compression to 4 GPa in penetrating (water-containing) and non-penetrating (paraffin) media. Compression of Ksubstituted clinoptillolite in a water:ethanol (1:1) mixture results in its additional hydration: inclusion of 2.2 additional H2O molecules into the structure at the initial stage. Upon further compression the H2O concentration increases by two molecules. This is caused by additional occupancy of partially vacant H2O sites. The cation environment practically does not change during overhydration. Changes in the coordination polyhedra of cations during compression in paraffin are reduced to a small (0.02-0.1 Å) decrease in bond lengths. Distinctions in the degree of hydration of the K-form upon compression in penetrating and non-penetrating media are manifested in the features of the compressibility of the compound.

KW - high pressure

KW - K-substituted clinoptillolite

KW - pressure-induced hydration

KW - structure

KW - zeolites

KW - NA

KW - EXCHANGED HEULANDITE

KW - STEPWISE DEHYDRATION

KW - CRYSTAL X-RAY

KW - CLINOPTILOLITE

KW - HIGH-PRESSURE BEHAVIOR

UR - http://www.scopus.com/inward/record.url?scp=85058460877&partnerID=8YFLogxK

U2 - 10.1134/S0022476618060203

DO - 10.1134/S0022476618060203

M3 - Article

AN - SCOPUS:85058460877

VL - 59

SP - 1392

EP - 1399

JO - Journal of Structural Chemistry

JF - Journal of Structural Chemistry

SN - 0022-4766

IS - 6

ER -

ID: 17896607