Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate

In this paper, we report an in-situ method for one-pot synthesis of carbon microspheres supported cobalt catalysts (Co/CMS) by a hydrothermal process, followed by calcination at 300, 400 and 500 oC, respectively. Cobalt would distribute three-dimensionally in the spheres. Many characterization techn...

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Main Authors: Zhou, Guanliang, Sun, Hongqi, Ang, Ming, Tade, Moses, Wang, Shaobin
Other Authors: CHEMECA Editorial Board
Format: Conference Paper
Published: CHEMECA 2014
Online Access:http://hdl.handle.net/20.500.11937/24920
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author Zhou, Guanliang
Sun, Hongqi
Ang, Ming
Tade, Moses
Wang, Shaobin
author2 CHEMECA Editorial Board
author_facet CHEMECA Editorial Board
Zhou, Guanliang
Sun, Hongqi
Ang, Ming
Tade, Moses
Wang, Shaobin
author_sort Zhou, Guanliang
building Curtin Institutional Repository
collection Online Access
description In this paper, we report an in-situ method for one-pot synthesis of carbon microspheres supported cobalt catalysts (Co/CMS) by a hydrothermal process, followed by calcination at 300, 400 and 500 oC, respectively. Cobalt would distribute three-dimensionally in the spheres. Many characterization techniques, such as XRD, SEM, EDS and elemental mapping were applied to investigate the physicochemical properties of the supported catalysts. The catalytic activities were evaluated by decomposition of 20 ppm phenol solutions with sulfate radicals. It was found that the Co/CMS catalysts were able to efficiently decompose phenol by activation of PMS. Co/CMS-300, 400 and 500 can completely decompose 20 ppm phenol in 15, 5 and 10 min, respectively. Kinetics studies were carried out to investigate the effects of catalyst loading, PMS amount, and reaction temperature on phenol degradation efficiency. Deactivation and regeneration were also discussed.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:54:42Z
publishDate 2014
publisher CHEMECA
recordtype eprints
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spelling curtin-20.500.11937-249202017-01-30T12:45:43Z Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate Zhou, Guanliang Sun, Hongqi Ang, Ming Tade, Moses Wang, Shaobin CHEMECA Editorial Board In this paper, we report an in-situ method for one-pot synthesis of carbon microspheres supported cobalt catalysts (Co/CMS) by a hydrothermal process, followed by calcination at 300, 400 and 500 oC, respectively. Cobalt would distribute three-dimensionally in the spheres. Many characterization techniques, such as XRD, SEM, EDS and elemental mapping were applied to investigate the physicochemical properties of the supported catalysts. The catalytic activities were evaluated by decomposition of 20 ppm phenol solutions with sulfate radicals. It was found that the Co/CMS catalysts were able to efficiently decompose phenol by activation of PMS. Co/CMS-300, 400 and 500 can completely decompose 20 ppm phenol in 15, 5 and 10 min, respectively. Kinetics studies were carried out to investigate the effects of catalyst loading, PMS amount, and reaction temperature on phenol degradation efficiency. Deactivation and regeneration were also discussed. 2014 Conference Paper http://hdl.handle.net/20.500.11937/24920 CHEMECA restricted
spellingShingle Zhou, Guanliang
Sun, Hongqi
Ang, Ming
Tade, Moses
Wang, Shaobin
Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title_full Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title_fullStr Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title_full_unstemmed Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title_short Carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
title_sort carbon microspheres supported cobalt catalysts for phenol oxidation with peroxymonosulfate
url http://hdl.handle.net/20.500.11937/24920