Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant

Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant

Background: Substitution of different types of B-site metal cations in the perovskite structure led to a significant change in the catalytic reactivity of the resulting catalysts. In this work, the functional role of B-site substitution on the catalytic reactivity of mixed oxides containing B-site s...

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Published in:Journal of the Taiwan Institute of Chemical Engineers
Main Author: Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
Format: Article
Language:English
Published: Taiwan Institute of Chemical Engineers 2023
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146451859&doi=10.1016%2fj.jtice.2023.104675&partnerID=40&md5=71c41a86d830f50b363c88fc29a2aeb6
id 2-s2.0-85146451859
spelling 2-s2.0-85146451859
Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
2023
Journal of the Taiwan Institute of Chemical Engineers
143

10.1016/j.jtice.2023.104675
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146451859&doi=10.1016%2fj.jtice.2023.104675&partnerID=40&md5=71c41a86d830f50b363c88fc29a2aeb6
Background: Substitution of different types of B-site metal cations in the perovskite structure led to a significant change in the catalytic reactivity of the resulting catalysts. In this work, the functional role of B-site substitution on the catalytic reactivity of mixed oxides containing B-site substituted CaMFeO3 (M = Cu, Mo and Co) perovskite catalysts is investigated. Methods: The catalysts were synthesized via a modified EDTA-citric acid complexation method and tested for the heterogeneous Fenton-like reaction for oxidative degradation of acid orange II (AOII) dye in the presence of H2O2. Significant findings: CaCuFeO3 exhibited the highest AOII degradation (97%) followed by CaMoFeO3 (90%), CaFeO3 (64%) and CaCoFeO3 (40%) within 60 min of reaction, and the reaction followed a pseudo-second-order kinetics model. Interestingly, the partial substitution of Cu in the B-site of CaFeO3 enhanced the reaction rate constant achieving a k value of 1.9 × 10−2 L mg−1 min−1, approximately twenty-one times higher than that of the blank catalyst CaFeO3. The enhanced catalytic reactivity of CaCuFeO3 is associated with the high reducibility of copper/iron ions within the B-site structure in the presence of oxidant which facilitated fast redox cycling of the active sites during catalysis. The fast redox cycling is attributed to the decent electron mobility due to low electron transfer resistance between the active sites. © 2023
Taiwan Institute of Chemical Engineers
18761070
English
Article
author Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
spellingShingle Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
author_facet Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
author_sort Alrozi R.; Zubir N.A.; Bakar N.F.A.; Ladewig B.P.; Motuzas J.; Bakar N.H.H.A.; Wang D.K.; da Costa J.C.D.
title Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
title_short Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
title_full Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
title_fullStr Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
title_full_unstemmed Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
title_sort Functional role of B-site substitution on the reactivity of CaMFeO3 (M = Cu, Mo, Co) perovskite catalysts in heterogeneous Fenton-like degradation of organic pollutant
publishDate 2023
container_title Journal of the Taiwan Institute of Chemical Engineers
container_volume 143
container_issue
doi_str_mv 10.1016/j.jtice.2023.104675
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146451859&doi=10.1016%2fj.jtice.2023.104675&partnerID=40&md5=71c41a86d830f50b363c88fc29a2aeb6
description Background: Substitution of different types of B-site metal cations in the perovskite structure led to a significant change in the catalytic reactivity of the resulting catalysts. In this work, the functional role of B-site substitution on the catalytic reactivity of mixed oxides containing B-site substituted CaMFeO3 (M = Cu, Mo and Co) perovskite catalysts is investigated. Methods: The catalysts were synthesized via a modified EDTA-citric acid complexation method and tested for the heterogeneous Fenton-like reaction for oxidative degradation of acid orange II (AOII) dye in the presence of H2O2. Significant findings: CaCuFeO3 exhibited the highest AOII degradation (97%) followed by CaMoFeO3 (90%), CaFeO3 (64%) and CaCoFeO3 (40%) within 60 min of reaction, and the reaction followed a pseudo-second-order kinetics model. Interestingly, the partial substitution of Cu in the B-site of CaFeO3 enhanced the reaction rate constant achieving a k value of 1.9 × 10−2 L mg−1 min−1, approximately twenty-one times higher than that of the blank catalyst CaFeO3. The enhanced catalytic reactivity of CaCuFeO3 is associated with the high reducibility of copper/iron ions within the B-site structure in the presence of oxidant which facilitated fast redox cycling of the active sites during catalysis. The fast redox cycling is attributed to the decent electron mobility due to low electron transfer resistance between the active sites. © 2023
publisher Taiwan Institute of Chemical Engineers
issn 18761070
language English
format Article
accesstype
record_format scopus
collection Scopus
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