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High-silica, heulandite-type zeolites prepared by direct synthesis and topotactic condensation

Schmidt, Joel E. and Xie, Dan and Davis, Mark E. (2015) High-silica, heulandite-type zeolites prepared by direct synthesis and topotactic condensation. Journal of Materials Chemistry A, 3 (24). pp. 12890-12897. ISSN 2050-7488. doi:10.1039/c5ta02354h. https://resolver.caltech.edu/CaltechAUTHORS:20150608-082630276

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Abstract

There are both natural minerals and synthetic zeolites that possess the HEU framework topology. These materials have a limited compositional range (Si/Al < 6), and the natural zeolites often contain a large amount of impurities such as Fe^(3+). The preparation of impurity-free HEU-type zeolites with higher Si/Al ratio could open many areas of application, particularly in catalysis. Here, we report the first high-silica HEU-type zeolite that can be prepared via two different procedures. In the first method high-silica HEU (denoted CIT-8) is prepared using a topotactic condensation mechanism (layered precursor denoted CIT-8P); CIT-8P is obtained from a low-water synthesis in fluoride media. CIT-8 prepared in this manner has a product Si/Al ratio of 9.8 ± 0.7 and a micropore volume of 0.10 cm^3 g^(−1) (measured by nitrogen adsorption). The variable temperature powder X-ray diffraction shows that CIT-8 forms via topotactic condensation from CIT-8P along the b axis. Additionally, high-silica heulandite can be synthesized directly from a hydroxide-mediated reaction mixture (denoted CIT-8H), and has a Si/Al ratio of 6.4 ± 0.3 and a micropore volume of 0.10 cm^3 g^(−1). Both synthesis methods produce zeolites that expand the compositional range of HEU-type zeolites. These synthetic methods allow for the addition of other heteroatoms, and titanium-containing CIT-8 is prepared as an illustrative example.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1039/c5ta02354hDOIArticle
http://pubs.rsc.org/en/Content/ArticleLanding/2015/TA/C5TA02354HPublisherArticle
http://www.rsc.org/suppdata/c5/ta/c5ta02354h/c5ta02354h1.pdfPublisherSupplementary Information
ORCID:
AuthorORCID
Xie, Dan0000-0003-2467-976X
Davis, Mark E.0000-0001-8294-1477
Additional Information:© 2015 The Royal Society of Chemistry. Received 31st March 2015; Accepted 19th May 2015; First published online 27 May 2015. We would like to thank Thomas Rea (Chevron Energy Technology Company) for collecting the RED data and Dr Stacey Zones (Chevron Energy Technology Company) for insightful discussions. Also, we would like to thank Dr Sonjong Hwang (Caltech) for assistance with solid-state NMR collection and interpretation. Chevron Energy Technology Company provided funding for this work. J.E.S. would like to thank the NDSEG for their support through a fellowship. PQ Corporation is thanked for providing us with sodium silicate.
Funders:
Funding AgencyGrant Number
Chevron Energy Technology CompanyUNSPECIFIED
National Defense Science and Engineering Graduate (NDSEG) FellowshipUNSPECIFIED
Issue or Number:24
DOI:10.1039/c5ta02354h
Record Number:CaltechAUTHORS:20150608-082630276
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20150608-082630276
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:58069
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:08 Jun 2015 15:43
Last Modified:10 Nov 2021 21:58

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