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Fluorine Doping of Microporous Organosilica Membranes for Pore Size Control and Enhanced Hydrophobic Properties
[Image: see text] Fluorine-doped organosilica membranes for gas and pervaporation (PV) separation were fabricated using a sol–gel method. NH(4)F and bis(triethoxysilyl)methane (BTESM) were selected as the dopant and Si precursor, respectively, for the fabrication of fluorine-doped organosilica membr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644774/ https://www.ncbi.nlm.nih.gov/pubmed/31458991 http://dx.doi.org/10.1021/acsomega.8b01370 |
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author | Kanezashi, Masakoto Murata, Masaaki Nagasawa, Hiroki Tsuru, Toshinori |
author_facet | Kanezashi, Masakoto Murata, Masaaki Nagasawa, Hiroki Tsuru, Toshinori |
author_sort | Kanezashi, Masakoto |
collection | PubMed |
description | [Image: see text] Fluorine-doped organosilica membranes for gas and pervaporation (PV) separation were fabricated using a sol–gel method. NH(4)F and bis(triethoxysilyl)methane (BTESM) were selected as the dopant and Si precursor, respectively, for the fabrication of fluorine-doped organosilica membranes. Doping with fluorine was evaluated for its effect on the physicochemical properties of organosilica (hydrophobicity/hydrophilicity and network size). Fluorine doping dramatically eliminated the formation of Si–OH groups in the sol, so that the condensation of Si–OH groups during the calcination process was suppressed. It is possible that fluorine doping enlarged the network pore sizes in organosilica, because the F-BTESM (F/Si = 1/9) membrane showed superior He and H(2) permeance with a low H(2)/N(2) permeance ratio that corresponded to the network pore size by comparison with an undoped BTESM membrane. The F-BTESM (F/Si = 1/9) membranes clearly showed a high level of C(3)H(6) permeance (>3.0 × 10(–7) mol m(–2) s(–1) Pa(–1)) with a high C(3)H(6)/SF(6) permeance ratio (∼250), which suggests that the network pore size of F-BTESM is suitable for the separation of large molecules such as hydrocarbon gases (C3/C4, C4 isomer, etc.). Organosilica membranes both with and without fluorine doping showed stable PV performance because of the fact that H(2)O permeance and each permeance ratio under different separation systems was approximately constant over 10 h at 70 °C. Fluorine doping enhanced the hydrophobic nature of the organosilica, which was confirmed by the H(2)O adsorption and PV properties. |
format | Online Article Text |
id | pubmed-6644774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66447742019-08-27 Fluorine Doping of Microporous Organosilica Membranes for Pore Size Control and Enhanced Hydrophobic Properties Kanezashi, Masakoto Murata, Masaaki Nagasawa, Hiroki Tsuru, Toshinori ACS Omega [Image: see text] Fluorine-doped organosilica membranes for gas and pervaporation (PV) separation were fabricated using a sol–gel method. NH(4)F and bis(triethoxysilyl)methane (BTESM) were selected as the dopant and Si precursor, respectively, for the fabrication of fluorine-doped organosilica membranes. Doping with fluorine was evaluated for its effect on the physicochemical properties of organosilica (hydrophobicity/hydrophilicity and network size). Fluorine doping dramatically eliminated the formation of Si–OH groups in the sol, so that the condensation of Si–OH groups during the calcination process was suppressed. It is possible that fluorine doping enlarged the network pore sizes in organosilica, because the F-BTESM (F/Si = 1/9) membrane showed superior He and H(2) permeance with a low H(2)/N(2) permeance ratio that corresponded to the network pore size by comparison with an undoped BTESM membrane. The F-BTESM (F/Si = 1/9) membranes clearly showed a high level of C(3)H(6) permeance (>3.0 × 10(–7) mol m(–2) s(–1) Pa(–1)) with a high C(3)H(6)/SF(6) permeance ratio (∼250), which suggests that the network pore size of F-BTESM is suitable for the separation of large molecules such as hydrocarbon gases (C3/C4, C4 isomer, etc.). Organosilica membranes both with and without fluorine doping showed stable PV performance because of the fact that H(2)O permeance and each permeance ratio under different separation systems was approximately constant over 10 h at 70 °C. Fluorine doping enhanced the hydrophobic nature of the organosilica, which was confirmed by the H(2)O adsorption and PV properties. American Chemical Society 2018-08-02 /pmc/articles/PMC6644774/ /pubmed/31458991 http://dx.doi.org/10.1021/acsomega.8b01370 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kanezashi, Masakoto Murata, Masaaki Nagasawa, Hiroki Tsuru, Toshinori Fluorine Doping of Microporous Organosilica Membranes for Pore Size Control and Enhanced Hydrophobic Properties |
title | Fluorine Doping of Microporous Organosilica Membranes
for Pore Size Control and Enhanced Hydrophobic Properties |
title_full | Fluorine Doping of Microporous Organosilica Membranes
for Pore Size Control and Enhanced Hydrophobic Properties |
title_fullStr | Fluorine Doping of Microporous Organosilica Membranes
for Pore Size Control and Enhanced Hydrophobic Properties |
title_full_unstemmed | Fluorine Doping of Microporous Organosilica Membranes
for Pore Size Control and Enhanced Hydrophobic Properties |
title_short | Fluorine Doping of Microporous Organosilica Membranes
for Pore Size Control and Enhanced Hydrophobic Properties |
title_sort | fluorine doping of microporous organosilica membranes
for pore size control and enhanced hydrophobic properties |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644774/ https://www.ncbi.nlm.nih.gov/pubmed/31458991 http://dx.doi.org/10.1021/acsomega.8b01370 |
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