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 in | Chemistry of materials Vol. 29; no. 21; pp. 9030 - 9042 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: Paul Scherrer Institut (PSI) – name: Institute for Integrated Catalysis and Physical Sciences Division – name: TU München – name: Environmental Molecular Sciences Laboratory – name: Swiss Light Source – name: Department of Chemistry and Catalysis Research Institute |
Author_xml | – sequence: 1 givenname: Aleksei surname: Vjunov fullname: Vjunov, Aleksei organization: Institute for Integrated Catalysis and Physical Sciences Division – sequence: 2 givenname: Meng orcidid: 0000-0002-3380-3534 surname: Wang fullname: Wang, Meng organization: Institute for Integrated Catalysis and Physical Sciences Division – sequence: 3 givenname: Niranjan surname: Govind fullname: Govind, Niranjan organization: Environmental Molecular Sciences Laboratory – sequence: 4 givenname: Thomas surname: Huthwelker fullname: Huthwelker, Thomas organization: Paul Scherrer Institut (PSI) – sequence: 5 givenname: Hui orcidid: 0000-0003-1180-7443 surname: Shi fullname: Shi, Hui organization: Institute for Integrated Catalysis and Physical Sciences Division – sequence: 6 givenname: Donghai orcidid: 0000-0002-0286-4182 surname: Mei fullname: Mei, Donghai email: Donghai.Mei@pnnl.gov organization: Institute for Integrated Catalysis and Physical Sciences Division – sequence: 7 givenname: John L orcidid: 0000-0001-9361-9803 surname: Fulton fullname: Fulton, John L email: John.Fulton@pnnl.gov organization: Institute for Integrated Catalysis and Physical Sciences Division – sequence: 8 givenname: Johannes A orcidid: 0000-0002-2495-1404 surname: Lercher fullname: Lercher, Johannes A email: Johannes.Lercher@pnnl.gov organization: TU München |
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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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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 |
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