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Electrostatic Assembly of Porphyrin-Functionalized Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes
[Image: see text] Porphyrin-based catalytic oxidation is one of the most representative biomimetic catalysis. To mimic the biomimetic catalytic oxidation of nature, a positive charged porous membrane, quaternized polysulfone (QPSf) membrane with spongelike structure, was prepared for supporting meso...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178780/ https://www.ncbi.nlm.nih.gov/pubmed/32337433 http://dx.doi.org/10.1021/acsomega.0c00135 |
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author | Fang, Hongbo Wang, Mingxia Yi, Hong Zhang, Yanyan Li, Xiaodan Yan, Feng Zhang, Lu |
author_facet | Fang, Hongbo Wang, Mingxia Yi, Hong Zhang, Yanyan Li, Xiaodan Yan, Feng Zhang, Lu |
author_sort | Fang, Hongbo |
collection | PubMed |
description | [Image: see text] Porphyrin-based catalytic oxidation is one of the most representative biomimetic catalysis. To mimic the biomimetic catalytic oxidation of nature, a positive charged porous membrane, quaternized polysulfone (QPSf) membrane with spongelike structure, was prepared for supporting meso-tetraphenylsulfonato porphyrin (TPPS). The influence of polymer concentration, coagulation bath, and additives on the structure of the substrate membrane was explored, and the optimized membrane with porosity of 87.1% and water flux of 371 L·m(–2)·h(–1) at 0.1 MPa was obtained. Monolayer TPPS was adsorbed on the QPSf membrane surface by the electrostatic self-assembly approach, and the adsorption process followed the pseudo second-order kinetic model and Langmuir adsorption isotherm equation. The resulting TPPS@QPSf membrane showed excellent visible light response, and the photocatalytic performance for dyes was then enhanced dramatically after TPPS was immobilized on the membrane. The removal efficiencies for rhodamine B (RhB), methylene blue (MB), and methyl orange (MO) were 92.1, 94.1, and 92.1% under visible light irradiation, respectively. The primary photocatalytic degradation of the dye was a zero-order reaction, and the secondary reaction of degradation followed pseudo first-order kinetics. Finally, the TPPS@QPSf membrane can be reused for photocatalytic degradation of RhB for 10 cycles with no obvious change on removal efficiency, which indicated that this membrane is a promising material for dyeing water treatment coupled with visible light irradiation. |
format | Online Article Text |
id | pubmed-7178780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71787802020-04-24 Electrostatic Assembly of Porphyrin-Functionalized Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes Fang, Hongbo Wang, Mingxia Yi, Hong Zhang, Yanyan Li, Xiaodan Yan, Feng Zhang, Lu ACS Omega [Image: see text] Porphyrin-based catalytic oxidation is one of the most representative biomimetic catalysis. To mimic the biomimetic catalytic oxidation of nature, a positive charged porous membrane, quaternized polysulfone (QPSf) membrane with spongelike structure, was prepared for supporting meso-tetraphenylsulfonato porphyrin (TPPS). The influence of polymer concentration, coagulation bath, and additives on the structure of the substrate membrane was explored, and the optimized membrane with porosity of 87.1% and water flux of 371 L·m(–2)·h(–1) at 0.1 MPa was obtained. Monolayer TPPS was adsorbed on the QPSf membrane surface by the electrostatic self-assembly approach, and the adsorption process followed the pseudo second-order kinetic model and Langmuir adsorption isotherm equation. The resulting TPPS@QPSf membrane showed excellent visible light response, and the photocatalytic performance for dyes was then enhanced dramatically after TPPS was immobilized on the membrane. The removal efficiencies for rhodamine B (RhB), methylene blue (MB), and methyl orange (MO) were 92.1, 94.1, and 92.1% under visible light irradiation, respectively. The primary photocatalytic degradation of the dye was a zero-order reaction, and the secondary reaction of degradation followed pseudo first-order kinetics. Finally, the TPPS@QPSf membrane can be reused for photocatalytic degradation of RhB for 10 cycles with no obvious change on removal efficiency, which indicated that this membrane is a promising material for dyeing water treatment coupled with visible light irradiation. American Chemical Society 2020-04-10 /pmc/articles/PMC7178780/ /pubmed/32337433 http://dx.doi.org/10.1021/acsomega.0c00135 Text en Copyright © 2020 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 | Fang, Hongbo Wang, Mingxia Yi, Hong Zhang, Yanyan Li, Xiaodan Yan, Feng Zhang, Lu Electrostatic Assembly of Porphyrin-Functionalized Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title | Electrostatic Assembly of Porphyrin-Functionalized
Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title_full | Electrostatic Assembly of Porphyrin-Functionalized
Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title_fullStr | Electrostatic Assembly of Porphyrin-Functionalized
Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title_full_unstemmed | Electrostatic Assembly of Porphyrin-Functionalized
Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title_short | Electrostatic Assembly of Porphyrin-Functionalized
Porous Membrane toward Biomimetic Photocatalytic Degradation Dyes |
title_sort | electrostatic assembly of porphyrin-functionalized
porous membrane toward biomimetic photocatalytic degradation dyes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178780/ https://www.ncbi.nlm.nih.gov/pubmed/32337433 http://dx.doi.org/10.1021/acsomega.0c00135 |
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