The Role of Water Loading and Germanium Content in Germanosilicate Hydrolysis

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F21%3A10436085" target="_blank" >RIV/00216208:11310/21:10436085 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Ihl.rJm9ZD" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Ihl.rJm9ZD</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.jpcc.1c06873" target="_blank" >10.1021/acs.jpcc.1c06873</a>

Jazyk výsledku

angličtina

Název v původním jazyce

The Role of Water Loading and Germanium Content in Germanosilicate Hydrolysis

Popis výsledku v původním jazyce

The Assembly-Disassembly-Organization-Reassembly (ADOR) process has been used extensively to prepare new zeolite frameworks based on germanosilicate precursors. The disassembly step exploits the lability of the bonds in the presence of water to selectively disconnect the framework, prior to reorganization into new framework topologies. However, a mechanistic understanding of this crucial step is lacking: specifically, the roles of heteroatom (germanium) content and water loading in zeolite hydrolytic instability. In this work, ab initio free energy simulations, coupled with water vapor adsorption measurements reveal that collectivity effects control the reactivity of the archetypal ADORable zeolite UTL toward water. A transition between reversible and irreversible water adsorption occurs as water loading is increased, leading to reactive transformations. Clustering of germanium is observed to activate hitherto unreported favorable hydrolysis mechanisms beyond a threshold concentration of three atoms per double four ring unit, demonstrating that the heteroatom distribution and collectivity in the hydrolysis mechanism can drastically influence zeolite framework instability. These findings suggest that control over heteroatom content, distribution, and hydration level is important to achieve the controlled partial hydrolysis of zeolitic frameworks and is likely to apply not only to other ADORable germanosilicate zeolites but also to Lewis acidic zeolites in general.

Název v anglickém jazyce

The Role of Water Loading and Germanium Content in Germanosilicate Hydrolysis

Popis výsledku anglicky

The Assembly-Disassembly-Organization-Reassembly (ADOR) process has been used extensively to prepare new zeolite frameworks based on germanosilicate precursors. The disassembly step exploits the lability of the bonds in the presence of water to selectively disconnect the framework, prior to reorganization into new framework topologies. However, a mechanistic understanding of this crucial step is lacking: specifically, the roles of heteroatom (germanium) content and water loading in zeolite hydrolytic instability. In this work, ab initio free energy simulations, coupled with water vapor adsorption measurements reveal that collectivity effects control the reactivity of the archetypal ADORable zeolite UTL toward water. A transition between reversible and irreversible water adsorption occurs as water loading is increased, leading to reactive transformations. Clustering of germanium is observed to activate hitherto unreported favorable hydrolysis mechanisms beyond a threshold concentration of three atoms per double four ring unit, demonstrating that the heteroatom distribution and collectivity in the hydrolysis mechanism can drastically influence zeolite framework instability. These findings suggest that control over heteroatom content, distribution, and hydration level is important to achieve the controlled partial hydrolysis of zeolitic frameworks and is likely to apply not only to other ADORable germanosilicate zeolites but also to Lewis acidic zeolites in general.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Physical Chemistry C

ISSN

1932-7447

e-ISSN

—

Svazek periodika

125

Číslo periodika v rámci svazku

43

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

14

Strana od-do

23744-23757

Kód UT WoS článku

000716453300018

EID výsledku v databázi Scopus

2-s2.0-85118921002