Tracking the Chemical Transformations at the Brønsted Acid Site upon Water-Induced Deprotonation in a Zeolite Pore

The structural changes induced by reversible formation of Brønsted acidic sites and hydronium ions with water in a zeolite with MFI structure are reported as a function of temperature using a combination of physicochemical methods and theory. In the presence of an ample concentration of water, the p...

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Published inChemistry of materials Vol. 29; no. 21; pp. 9030 - 9042
Main Authors Vjunov, Aleksei, Wang, Meng, Govind, Niranjan, Huthwelker, Thomas, Shi, Hui, Mei, Donghai, Fulton, John L, Lercher, Johannes A
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 14.11.2017
American Chemical Society (ACS)
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Abstract The structural changes induced by reversible formation of Brønsted acidic sites and hydronium ions with water in a zeolite with MFI structure are reported as a function of temperature using a combination of physicochemical methods and theory. In the presence of an ample concentration of water, the protons are present as hydrated hydronium ions (H3O+(H2O) n ) that are ion-paired to the zeolite. Loss of water molecules hydrating the hydronium ions leads to an unstable free hydronium ion that dissociates to form the hydroxylated T-site. The formation of this SiOHAl species leads to the elongation of one of the four Al–O bonds and causes significant distortion of the tetrahedral symmetry about the Al atom. This distortion leads to the appearance of new pre-edge features in the Al K-edge X-ray absorption near edge structure (XANES) spectra. The pre-edge peak assignment is confirmed by time-dependent density functional theory calculation of the XANES spectrum. The XANES spectra are also sensitive to solutes or solvents that are in proximity to the T-site. As temperature increases, the minor fraction of extra-framework Al present in the sample at ambient conditions in octahedral coordination is converted to tetrahedral coordination through the decoordination of H2O ligands.
AbstractList We report the structural changes induced by Brønsted acidic site deprotonation in a zeolite with MFI structure as a function of temperature up to 430°C using in situ Al K-edge X-ray absorption fine structure spectroscopy (XAFS). At ambient conditions, the protons are present as hydrated hydronium ions (H3O+(H2O)n) that are ion-paired to the anionic, Al tetrahedral (T) site. At elevated temperatures, loss of water molecules hydrating the hydronium ions leads to an unstable free hydronium ion that disso-ciates to form the hydroxylated T-site. The formation of this (-O3)-Al-(OH-) species leads to the elongation of one of the four Al-O bonds and causes significant distortion of the tetrahedral symmetry about the Al atom. This distortion leads to the appearance of new pre-edge features in the Al K-edge X-ray absorption near edge structure (XANES) spectra. The pre-edge peak assignment is confirmed by time-dependent density functional theory calculation of the XANES spectrum. The XANES spectra are also sensitive to solutes or solvent that are in proximity to the T-site. A second structural transition occurs at about the same temperature, namely the conversion of a minor fraction of extra-framework octahedral Al present in the sample at ambient conditions to a tetrahedral species through the de-coordination of H2O-ligands. Both IR spectroscopy and thermogravimetric analysis (TGA) are further used to confirm the overall chemical transformation of the T-site.
The structural changes induced by reversible formation of Brønsted acidic sites and hydronium ions with water in a zeolite with MFI structure are reported as a function of temperature using a combination of physicochemical methods and theory. In the presence of an ample concentration of water, the protons are present as hydrated hydronium ions (H3O+(H2O) n ) that are ion-paired to the zeolite. Loss of water molecules hydrating the hydronium ions leads to an unstable free hydronium ion that dissociates to form the hydroxylated T-site. The formation of this SiOHAl species leads to the elongation of one of the four Al–O bonds and causes significant distortion of the tetrahedral symmetry about the Al atom. This distortion leads to the appearance of new pre-edge features in the Al K-edge X-ray absorption near edge structure (XANES) spectra. The pre-edge peak assignment is confirmed by time-dependent density functional theory calculation of the XANES spectrum. The XANES spectra are also sensitive to solutes or solvents that are in proximity to the T-site. As temperature increases, the minor fraction of extra-framework Al present in the sample at ambient conditions in octahedral coordination is converted to tetrahedral coordination through the decoordination of H2O ligands.
Author Lercher, Johannes A
Shi, Hui
Mei, Donghai
Huthwelker, Thomas
Fulton, John L
Wang, Meng
Govind, Niranjan
Vjunov, Aleksei
AuthorAffiliation TU München
Institute for Integrated Catalysis and Physical Sciences Division
Environmental Molecular Sciences Laboratory
Paul Scherrer Institut (PSI)
Swiss Light Source
Department of Chemistry and Catalysis Research Institute
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BackLink https://www.osti.gov/biblio/1411916$$D View this record in Osti.gov
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Snippet The structural changes induced by reversible formation of Brønsted acidic sites and hydronium ions with water in a zeolite with MFI structure are reported as a...
We report the structural changes induced by Brønsted acidic site deprotonation in a zeolite with MFI structure as a function of temperature up to 430°C using...
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acs
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StartPage 9030
SubjectTerms Bronsted acid sites
Environmental Molecular Sciences Laboratory
hydronium ion
INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
pore dehydration
zeolite MFI
Title Tracking the Chemical Transformations at the Brønsted Acid Site upon Water-Induced Deprotonation in a Zeolite Pore
URI http://dx.doi.org/10.1021/acs.chemmater.7b02133
https://www.osti.gov/biblio/1411916
Volume 29
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