Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B

Nanocatalysts prepared by immobilizing Pd nanoparticles on mesoporous iron oxides (ferrihydrite, goethite and α-hematite) were used in persulfate activation for the rapid oxidative degradation of an organic dye, Rhodamine B. Pd nanoparticles were prepared by dendrimer encapsulation and were then imm...

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Main Authors: Batsile M. Mogudi, Phendukani Ncube, Malose C. Nong, Matumuene J. Ndolomingo, Reinout Meijboom
Format: Article
Language:English
Published: Elsevier 2025-10-01
Series:Applied Catalysis O: Open
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Online Access:http://www.sciencedirect.com/science/article/pii/S2950648425000434
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author Batsile M. Mogudi
Phendukani Ncube
Malose C. Nong
Matumuene J. Ndolomingo
Reinout Meijboom
author_facet Batsile M. Mogudi
Phendukani Ncube
Malose C. Nong
Matumuene J. Ndolomingo
Reinout Meijboom
author_sort Batsile M. Mogudi
collection DOAJ
description Nanocatalysts prepared by immobilizing Pd nanoparticles on mesoporous iron oxides (ferrihydrite, goethite and α-hematite) were used in persulfate activation for the rapid oxidative degradation of an organic dye, Rhodamine B. Pd nanoparticles were prepared by dendrimer encapsulation and were then immobilized on the three iron oxide supports by wet impregnation. The Pd nanoparticles were seen to be on the surface of mono-dispersed iron oxide nanoparticle aggregates as characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The nanomaterials were active catalysts for the rapid oxidation of the organic dye Rhodamine B with persulfate as the oxidant in a Fenton-like mechanism. Under optimized conditions Pd on ferrihydrite was the most active catalyst followed by Pd/α-hematite then Pd/goethite. The activation energies (EA) were 43.3 kJ·mol−1, 98.6 kJ·mol−1 and 75.1 kJ·mol−1 for Pd/ferrihydrite, Pd/α-hematite and Pd/goethite, respectively, correlating with the observed order of activity. The reaction followed Langmuir-Hinshelwood kinetics with surface rate constants of k = 3.35 × 10−5 mol·m−2·s−1, 1.55 × 10−5 mol·m−2·s−1 and 2.80 × 10−5 mol·m−2·s−1 for the three catalysts, respectively.
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institution Kabale University
issn 2950-6484
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spelling doaj-art-18f4ff5da0204208a4bc2eb617c068852025-08-25T04:15:00ZengElsevierApplied Catalysis O: Open2950-64842025-10-0120720706810.1016/j.apcato.2025.207068Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine BBatsile M. Mogudi0Phendukani Ncube1Malose C. Nong2Matumuene J. Ndolomingo3Reinout Meijboom4Department of Chemistry, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South AfricaDepartment of Chemistry, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South AfricaDepartment of Chemistry, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South AfricaDepartment of Chemistry, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South AfricaCorresponding author.; Department of Chemistry, University of Johannesburg, PO Box 524, Auckland Park, Johannesburg 2006, South AfricaNanocatalysts prepared by immobilizing Pd nanoparticles on mesoporous iron oxides (ferrihydrite, goethite and α-hematite) were used in persulfate activation for the rapid oxidative degradation of an organic dye, Rhodamine B. Pd nanoparticles were prepared by dendrimer encapsulation and were then immobilized on the three iron oxide supports by wet impregnation. The Pd nanoparticles were seen to be on the surface of mono-dispersed iron oxide nanoparticle aggregates as characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The nanomaterials were active catalysts for the rapid oxidation of the organic dye Rhodamine B with persulfate as the oxidant in a Fenton-like mechanism. Under optimized conditions Pd on ferrihydrite was the most active catalyst followed by Pd/α-hematite then Pd/goethite. The activation energies (EA) were 43.3 kJ·mol−1, 98.6 kJ·mol−1 and 75.1 kJ·mol−1 for Pd/ferrihydrite, Pd/α-hematite and Pd/goethite, respectively, correlating with the observed order of activity. The reaction followed Langmuir-Hinshelwood kinetics with surface rate constants of k = 3.35 × 10−5 mol·m−2·s−1, 1.55 × 10−5 mol·m−2·s−1 and 2.80 × 10−5 mol·m−2·s−1 for the three catalysts, respectively.http://www.sciencedirect.com/science/article/pii/S2950648425000434Advanced oxidation processHeterogeneous catalysisPersulfate activationPd/Fe nanocatalystsRhodamine B degradation
spellingShingle Batsile M. Mogudi
Phendukani Ncube
Malose C. Nong
Matumuene J. Ndolomingo
Reinout Meijboom
Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
Applied Catalysis O: Open
Advanced oxidation process
Heterogeneous catalysis
Persulfate activation
Pd/Fe nanocatalysts
Rhodamine B degradation
title Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
title_full Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
title_fullStr Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
title_full_unstemmed Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
title_short Heterogeneous persulfate activation by mesoporous Pd/FexOy nanocatalysts for the rapid degradation of Rhodamine B
title_sort heterogeneous persulfate activation by mesoporous pd fexoy nanocatalysts for the rapid degradation of rhodamine b
topic Advanced oxidation process
Heterogeneous catalysis
Persulfate activation
Pd/Fe nanocatalysts
Rhodamine B degradation
url http://www.sciencedirect.com/science/article/pii/S2950648425000434
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