Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons

A variety of dimensional-structured nanocarbons were applied for the first time as metal-free catalysts to activate persulfate (PS) for catalytic oxidation of phenolics and dyes as well as their degradation intermediates. Singlewalled carbon nanotubes (SWCNTs), reduced graphene oxide (rGO), and meso...

Full description

Bibliographic Details
Main Authors: Duan, X., Sun, Hongqi, Kang, J., Wang, Yuxian, Indrawirawan, S., Wang, Shaobin
Format: Journal Article
Published: American Chemical Society 2015
Online Access:http://purl.org/au-research/grants/arc/DP130101319
http://hdl.handle.net/20.500.11937/30308
_version_ 1848753051670675456
author Duan, X.
Sun, Hongqi
Kang, J.
Wang, Yuxian
Indrawirawan, S.
Wang, Shaobin
author_facet Duan, X.
Sun, Hongqi
Kang, J.
Wang, Yuxian
Indrawirawan, S.
Wang, Shaobin
author_sort Duan, X.
building Curtin Institutional Repository
collection Online Access
description A variety of dimensional-structured nanocarbons were applied for the first time as metal-free catalysts to activate persulfate (PS) for catalytic oxidation of phenolics and dyes as well as their degradation intermediates. Singlewalled carbon nanotubes (SWCNTs), reduced graphene oxide (rGO), and mesoporous carbon (CMK-8) demonstrated superior catalytic activities for heterogeneous PS activation, whereas fullerene (C60), nanodiamonds, and graphitic carbon nitride (g-C3N4) presented low efficiencies. Moreover, the carbocatalysts presented even better catalytic performances than activated carbon and metal oxides, such as Fe3O4, CuO, Co3O4, and MnO2. The activity of prepared rGO-900 was further competing to the most efficient electron donor ofzerovalent iron (ZVI). Both characterization and oxidation results suggested that the catalytic performances of the nanocarbons are determined by the intrinsic atom arrangements of carbon hybridization, pore structure, defective sites, and functional groups (especially the carbonyl groups). Electron paramagnetic resonance (EPR) spectra revealed that carbocatalysts might act as an excellent electron bridge in activation of PS to oxidize adsorbed water directly to generate hydroxyl radicals, distinct from homogeneous and metal-based catalytic activation. This study discovers several efficient nanocarbons for heterogeneous PS activation, and it presents new insights into the catalytic activation processes, providing a fascinating strategy to develop metal-free catalysts for green remediation.
first_indexed 2025-11-14T08:18:22Z
format Journal Article
id curtin-20.500.11937-30308
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T08:18:22Z
publishDate 2015
publisher American Chemical Society
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-303082017-09-13T15:31:39Z Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons Duan, X. Sun, Hongqi Kang, J. Wang, Yuxian Indrawirawan, S. Wang, Shaobin A variety of dimensional-structured nanocarbons were applied for the first time as metal-free catalysts to activate persulfate (PS) for catalytic oxidation of phenolics and dyes as well as their degradation intermediates. Singlewalled carbon nanotubes (SWCNTs), reduced graphene oxide (rGO), and mesoporous carbon (CMK-8) demonstrated superior catalytic activities for heterogeneous PS activation, whereas fullerene (C60), nanodiamonds, and graphitic carbon nitride (g-C3N4) presented low efficiencies. Moreover, the carbocatalysts presented even better catalytic performances than activated carbon and metal oxides, such as Fe3O4, CuO, Co3O4, and MnO2. The activity of prepared rGO-900 was further competing to the most efficient electron donor ofzerovalent iron (ZVI). Both characterization and oxidation results suggested that the catalytic performances of the nanocarbons are determined by the intrinsic atom arrangements of carbon hybridization, pore structure, defective sites, and functional groups (especially the carbonyl groups). Electron paramagnetic resonance (EPR) spectra revealed that carbocatalysts might act as an excellent electron bridge in activation of PS to oxidize adsorbed water directly to generate hydroxyl radicals, distinct from homogeneous and metal-based catalytic activation. This study discovers several efficient nanocarbons for heterogeneous PS activation, and it presents new insights into the catalytic activation processes, providing a fascinating strategy to develop metal-free catalysts for green remediation. 2015 Journal Article http://hdl.handle.net/20.500.11937/30308 10.1021/acscatal.5b00774 http://purl.org/au-research/grants/arc/DP130101319 American Chemical Society restricted
spellingShingle Duan, X.
Sun, Hongqi
Kang, J.
Wang, Yuxian
Indrawirawan, S.
Wang, Shaobin
Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title_full Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title_fullStr Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title_full_unstemmed Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title_short Insights into Heterogeneous Catalysis of Persulfate Activation on Dimensional-Structured Nanocarbons
title_sort insights into heterogeneous catalysis of persulfate activation on dimensional-structured nanocarbons
url http://purl.org/au-research/grants/arc/DP130101319
http://hdl.handle.net/20.500.11937/30308