Two-Step Pressure-Induced Superhydration in Small Pore Natrolite with Divalent Extra-Framework Cations

被引:18
|
作者
Seoung, Donghoon [1 ,2 ]
Lee, Yongmoon [1 ]
Kao, Chi-Chang [2 ]
Vogt, Thomas [3 ,4 ]
Lee, Yongjae [1 ]
机构
[1] Yonsei Univ, Dept Earth Syst Sci, Seoul 120749, South Korea
[2] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA 94025 USA
[3] Univ S Carolina, NanoCtr, Columbia, SC 29208 USA
[4] Univ S Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
关键词
EXCHANGED NATROLITES; INDUCED HYDRATION; VOLUME EXPANSION; ALKALINE-EARTH; ZEOLITE; INSERTION; WATER; DIFFRACTION; REFINEMENT; SCOLECITE;
D O I
10.1021/acs.chemmater.5b00506
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In situ high pressure X-ray powder diffraction studies of natrolite (NAT) containing the divalent extra-framework cations (EFC) Sr2+, Ca2+, Pb2+, and Cd2+ reveal that they can be superhydrated in the presence of water. In the case of Ca-NAT, Sr-NAT, and Pb-NAT pressure-induced hydration (PIH) inserts 40 H2O/unit cell into the zeolite compared to 32 in superhydrated natrolites containing monovalent EFC. Cd-NAT is superhydrated in one step to a zeolite containing 32 H2O/unit cell. PIH of Ca-NAT and Sr-NAT occurs in two steps. During PIH of Pb-NAT three distinct steps have been observed. The excess H2O in natrolites with divalent EFC are accommodated on sites no longer required for charge compensation. Two distinct families with ordered and disordered EFCwater topologies have been found. Our work established the importance of both size and charge of the EFC in PIH.
引用
收藏
页码:3874 / 3880
页数:7
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