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Mechanochemically assisted hydrolysis in the ADOR process

The ADOR (Assembly-Disassembly-Organisation-Reassembly) process for zeolites has been shown to produce a number of previously unknown frameworks inaccessible through conventional synthesis methods. Here, we present successful mechanochemically assisted hydrolysis of germanosilicate zeolite UTL leadi...

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Autores principales: Rainer, Daniel N., Rice, Cameron M., Warrender, Stewart J., Ashbrook, Sharon E., Morris, Russell E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499815/
https://www.ncbi.nlm.nih.gov/pubmed/33033606
http://dx.doi.org/10.1039/d0sc02547j
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author Rainer, Daniel N.
Rice, Cameron M.
Warrender, Stewart J.
Ashbrook, Sharon E.
Morris, Russell E.
author_facet Rainer, Daniel N.
Rice, Cameron M.
Warrender, Stewart J.
Ashbrook, Sharon E.
Morris, Russell E.
author_sort Rainer, Daniel N.
collection PubMed
description The ADOR (Assembly-Disassembly-Organisation-Reassembly) process for zeolites has been shown to produce a number of previously unknown frameworks inaccessible through conventional synthesis methods. Here, we present successful mechanochemically assisted hydrolysis of germanosilicate zeolite UTL leading to ADOR products under mild conditions, low amounts of solvent and in short reaction times. The expansion of zeolite synthesis into the realm of mechanochemistry opens up feasible pathways regarding the production of these materials, especially for industrial purposes, as well as an exciting application for economical enrichment of materials with the low natural abundance NMR-active isotope of oxygen, (17)O. The results from mechanochemically assisted hydrolysis differ from those seen in the traditional ADOR approach: differences that can be attributed to a change in solvent availability.
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spelling pubmed-74998152020-10-07 Mechanochemically assisted hydrolysis in the ADOR process Rainer, Daniel N. Rice, Cameron M. Warrender, Stewart J. Ashbrook, Sharon E. Morris, Russell E. Chem Sci Chemistry The ADOR (Assembly-Disassembly-Organisation-Reassembly) process for zeolites has been shown to produce a number of previously unknown frameworks inaccessible through conventional synthesis methods. Here, we present successful mechanochemically assisted hydrolysis of germanosilicate zeolite UTL leading to ADOR products under mild conditions, low amounts of solvent and in short reaction times. The expansion of zeolite synthesis into the realm of mechanochemistry opens up feasible pathways regarding the production of these materials, especially for industrial purposes, as well as an exciting application for economical enrichment of materials with the low natural abundance NMR-active isotope of oxygen, (17)O. The results from mechanochemically assisted hydrolysis differ from those seen in the traditional ADOR approach: differences that can be attributed to a change in solvent availability. Royal Society of Chemistry 2020-06-15 /pmc/articles/PMC7499815/ /pubmed/33033606 http://dx.doi.org/10.1039/d0sc02547j Text en This journal is © The Royal Society of Chemistry 2020 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Rainer, Daniel N.
Rice, Cameron M.
Warrender, Stewart J.
Ashbrook, Sharon E.
Morris, Russell E.
Mechanochemically assisted hydrolysis in the ADOR process
title Mechanochemically assisted hydrolysis in the ADOR process
title_full Mechanochemically assisted hydrolysis in the ADOR process
title_fullStr Mechanochemically assisted hydrolysis in the ADOR process
title_full_unstemmed Mechanochemically assisted hydrolysis in the ADOR process
title_short Mechanochemically assisted hydrolysis in the ADOR process
title_sort mechanochemically assisted hydrolysis in the ador process
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499815/
https://www.ncbi.nlm.nih.gov/pubmed/33033606
http://dx.doi.org/10.1039/d0sc02547j
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