Visible light-induced catalytic activation of peroxymonosulfate using heterogeneous surface complexes of amino acids on TiO2

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Jonghun Lim
  • Dong-yeob Kwak
  • Fabian Sieland
  • Chuhyung Kim
  • Detlef W. Bahnemann
  • Wonyong Choi

Organisationseinheiten

Externe Organisationen

  • Pohang University of Science and Technology
  • Staatliche Universität Sankt Petersburg
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Details

OriginalspracheEnglisch
Seiten (von - bis)406-414
Seitenumfang9
FachzeitschriftApplied Catalysis B: Environmental
Jahrgang225
Frühes Online-Datum11 Dez. 2017
PublikationsstatusVeröffentlicht - 5 Juni 2018

Abstract

Peroxymonosulfate (PMS) is being extensively investigated as an eco-friendly oxidant and various activation methods of PMS have been investigated. Here we demonstrated a new method of catalytic PMS activation, which employed amino acids as both a visible light sensitizer and a substrate to be degraded. Although PMS and amino acids do not absorb any visible light, the surface adsorption of amino acids on titania formed charge-transfer complexes that absorb visible light (λ > 420 nm). Serine and histidine were employed as main target amino acids and their surface complexes on TiO 2 were characterized by various spectroscopic methods The ligand-to-metal charge transfer between amino acids and TiO 2 enabled the absorption of visible light and the subsequent electron transfer catalytically activated PMS with generating sulfate radicals which were detected by electron paramagnetic resonance analysis. Based on various scavenger tests, amino acids seem to be degraded mainly by sulfate radical (radical pathway) and by a non-radical pathway (PMS serving primarily as an electron acceptor) to some extent. Amino acids were degraded with producing ammonium as a sole nitrogenous product in this process, whereas most advanced oxidation processes of amino acid generate not only ammonium but also nitrate and nitrite. The visible light-induced charge transfer characteristics of the amino acid-TiO 2 complexes were demonstrated by the photoelectrochemical characterizations and the time-resolved laser spectroscopic analysis.

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Visible light-induced catalytic activation of peroxymonosulfate using heterogeneous surface complexes of amino acids on TiO2. / Lim, Jonghun; Kwak, Dong-yeob; Sieland, Fabian et al.
in: Applied Catalysis B: Environmental, Jahrgang 225, 05.06.2018, S. 406-414.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Lim J, Kwak D, Sieland F, Kim C, Bahnemann DW, Choi W. Visible light-induced catalytic activation of peroxymonosulfate using heterogeneous surface complexes of amino acids on TiO2. Applied Catalysis B: Environmental. 2018 Jun 5;225:406-414. Epub 2017 Dez 11. doi: 10.1016/j.apcatb.2017.12.025
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abstract = "Peroxymonosulfate (PMS) is being extensively investigated as an eco-friendly oxidant and various activation methods of PMS have been investigated. Here we demonstrated a new method of catalytic PMS activation, which employed amino acids as both a visible light sensitizer and a substrate to be degraded. Although PMS and amino acids do not absorb any visible light, the surface adsorption of amino acids on titania formed charge-transfer complexes that absorb visible light (λ > 420 nm). Serine and histidine were employed as main target amino acids and their surface complexes on TiO 2 were characterized by various spectroscopic methods The ligand-to-metal charge transfer between amino acids and TiO 2 enabled the absorption of visible light and the subsequent electron transfer catalytically activated PMS with generating sulfate radicals which were detected by electron paramagnetic resonance analysis. Based on various scavenger tests, amino acids seem to be degraded mainly by sulfate radical (radical pathway) and by a non-radical pathway (PMS serving primarily as an electron acceptor) to some extent. Amino acids were degraded with producing ammonium as a sole nitrogenous product in this process, whereas most advanced oxidation processes of amino acid generate not only ammonium but also nitrate and nitrite. The visible light-induced charge transfer characteristics of the amino acid-TiO 2 complexes were demonstrated by the photoelectrochemical characterizations and the time-resolved laser spectroscopic analysis. ",
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T1 - Visible light-induced catalytic activation of peroxymonosulfate using heterogeneous surface complexes of amino acids on TiO2

AU - Lim, Jonghun

AU - Kwak, Dong-yeob

AU - Sieland, Fabian

AU - Kim, Chuhyung

AU - Bahnemann, Detlef W.

AU - Choi, Wonyong

N1 - © 2017 Elsevier B.V. All rights reserved.

PY - 2018/6/5

Y1 - 2018/6/5

N2 - Peroxymonosulfate (PMS) is being extensively investigated as an eco-friendly oxidant and various activation methods of PMS have been investigated. Here we demonstrated a new method of catalytic PMS activation, which employed amino acids as both a visible light sensitizer and a substrate to be degraded. Although PMS and amino acids do not absorb any visible light, the surface adsorption of amino acids on titania formed charge-transfer complexes that absorb visible light (λ > 420 nm). Serine and histidine were employed as main target amino acids and their surface complexes on TiO 2 were characterized by various spectroscopic methods The ligand-to-metal charge transfer between amino acids and TiO 2 enabled the absorption of visible light and the subsequent electron transfer catalytically activated PMS with generating sulfate radicals which were detected by electron paramagnetic resonance analysis. Based on various scavenger tests, amino acids seem to be degraded mainly by sulfate radical (radical pathway) and by a non-radical pathway (PMS serving primarily as an electron acceptor) to some extent. Amino acids were degraded with producing ammonium as a sole nitrogenous product in this process, whereas most advanced oxidation processes of amino acid generate not only ammonium but also nitrate and nitrite. The visible light-induced charge transfer characteristics of the amino acid-TiO 2 complexes were demonstrated by the photoelectrochemical characterizations and the time-resolved laser spectroscopic analysis.

AB - Peroxymonosulfate (PMS) is being extensively investigated as an eco-friendly oxidant and various activation methods of PMS have been investigated. Here we demonstrated a new method of catalytic PMS activation, which employed amino acids as both a visible light sensitizer and a substrate to be degraded. Although PMS and amino acids do not absorb any visible light, the surface adsorption of amino acids on titania formed charge-transfer complexes that absorb visible light (λ > 420 nm). Serine and histidine were employed as main target amino acids and their surface complexes on TiO 2 were characterized by various spectroscopic methods The ligand-to-metal charge transfer between amino acids and TiO 2 enabled the absorption of visible light and the subsequent electron transfer catalytically activated PMS with generating sulfate radicals which were detected by electron paramagnetic resonance analysis. Based on various scavenger tests, amino acids seem to be degraded mainly by sulfate radical (radical pathway) and by a non-radical pathway (PMS serving primarily as an electron acceptor) to some extent. Amino acids were degraded with producing ammonium as a sole nitrogenous product in this process, whereas most advanced oxidation processes of amino acid generate not only ammonium but also nitrate and nitrite. The visible light-induced charge transfer characteristics of the amino acid-TiO 2 complexes were demonstrated by the photoelectrochemical characterizations and the time-resolved laser spectroscopic analysis.

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