Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination
An α-Fe2O3-supported HY zeolite (α-Fe2O3/HY) was prepared by introducing nanosized α-Fe2O3 into an HY zeolite support through in situ (α-Fe2O3/HYIS) and ion-exchange (α-Fe2O3/HYIE) methods. The effect of the preparation methods on the physicochemical properties of the catalyst were studied via XRD,...
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my.utm.473782018-10-14T08:21:43Z http://eprints.utm.my/id/eprint/47378/ Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination Jaafar, Nur Farhana Abdul Jalil, Aishah Triwahyono, Sugeng Muhd. Muhid, Muhd. Nazlan Sapawe, Norzahir Satar, Mohammad Azrul Hisham Asaari, Hanak TP Chemical technology An α-Fe2O3-supported HY zeolite (α-Fe2O3/HY) was prepared by introducing nanosized α-Fe2O3 into an HY zeolite support through in situ (α-Fe2O3/HYIS) and ion-exchange (α-Fe2O3/HYIE) methods. The effect of the preparation methods on the physicochemical properties of the catalyst were studied via XRD, FESEM-EDX, TEM, UV–vis DRS, FTIR, XPS, 29Si and 27Al MAS NMR, ESR and BET surface area analysis. In this study, dealumination was accomplished by using a facile electrolysis system without any strong acids, reactive compounds and/or hydrothermal treatment. Dealumination accompanied by ion exchange of Al with Fe3+ ions in the HY zeolite framework resulted in the formation of an active species that had a higher photoactivity towards the decolorization of methyl orange (MO). A 5 wt% α-Fe2O3/HYIS was found to produce an 80% photodecolorization of 30 mg L−1 of MO at pH 2 with 0.375 g L−1 catalyst, while 5 wt% α-Fe2O3/HYIE only produced 23% photodecolorization under similar conditions (2 h reaction time). This study showed that the kinetics follow a pseudo-first order Langmuir–Hinshelwood model with an activation energy (Ea) calculated for both 5 wt% α-Fe2O3/HYIS and 5 wt% α-Fe2O3/HYIE to be 45.8 kJ mol−1 and 70.2 kJ mol−1, respectively. Measurements of the mineralization of MO by COD, BOD5 and TOC analysis were 27.0%, 69.6% and 16.9%, respectively, after 2 h of contact time. The Fe dissolution from the catalyst showed insignificant leaching of Fe (<1%) when subjected to AAS. A reusability study demonstrated that α-Fe2O3/HYIS could be a promising photocatalyst for the degradation of various dyes in wastewater. Elsevier B. V. 2012-05-15 Article PeerReviewed Jaafar, Nur Farhana and Abdul Jalil, Aishah and Triwahyono, Sugeng and Muhd. Muhid, Muhd. Nazlan and Sapawe, Norzahir and Satar, Mohammad Azrul Hisham and Asaari, Hanak (2012) Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination. Chemical Engineering Journal, 191 . pp. 112-122. ISSN 1385-8947 https://www.sciencedirect.com/science/article/pii/S1385894712003105?via%3Dihub DOI:10.1016/j.cej.2012.02.077 |
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TP Chemical technology Jaafar, Nur Farhana Abdul Jalil, Aishah Triwahyono, Sugeng Muhd. Muhid, Muhd. Nazlan Sapawe, Norzahir Satar, Mohammad Azrul Hisham Asaari, Hanak Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
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An α-Fe2O3-supported HY zeolite (α-Fe2O3/HY) was prepared by introducing nanosized α-Fe2O3 into an HY zeolite support through in situ (α-Fe2O3/HYIS) and ion-exchange (α-Fe2O3/HYIE) methods. The effect of the preparation methods on the physicochemical properties of the catalyst were studied via XRD, FESEM-EDX, TEM, UV–vis DRS, FTIR, XPS, 29Si and 27Al MAS NMR, ESR and BET surface area analysis. In this study, dealumination was accomplished by using a facile electrolysis system without any strong acids, reactive compounds and/or hydrothermal treatment. Dealumination accompanied by ion exchange of Al with Fe3+ ions in the HY zeolite framework resulted in the formation of an active species that had a higher photoactivity towards the decolorization of methyl orange (MO). A 5 wt% α-Fe2O3/HYIS was found to produce an 80% photodecolorization of 30 mg L−1 of MO at pH 2 with 0.375 g L−1 catalyst, while 5 wt% α-Fe2O3/HYIE only produced 23% photodecolorization under similar conditions (2 h reaction time). This study showed that the kinetics follow a pseudo-first order Langmuir–Hinshelwood model with an activation energy (Ea) calculated for both 5 wt% α-Fe2O3/HYIS and 5 wt% α-Fe2O3/HYIE to be 45.8 kJ mol−1 and 70.2 kJ mol−1, respectively. Measurements of the mineralization of MO by COD, BOD5 and TOC analysis were 27.0%, 69.6% and 16.9%, respectively, after 2 h of contact time. The Fe dissolution from the catalyst showed insignificant leaching of Fe (<1%) when subjected to AAS. A reusability study demonstrated that α-Fe2O3/HYIS could be a promising photocatalyst for the degradation of various dyes in wastewater. |
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Jaafar, Nur Farhana Abdul Jalil, Aishah Triwahyono, Sugeng Muhd. Muhid, Muhd. Nazlan Sapawe, Norzahir Satar, Mohammad Azrul Hisham Asaari, Hanak |
author_facet |
Jaafar, Nur Farhana Abdul Jalil, Aishah Triwahyono, Sugeng Muhd. Muhid, Muhd. Nazlan Sapawe, Norzahir Satar, Mohammad Azrul Hisham Asaari, Hanak |
author_sort |
Jaafar, Nur Farhana |
title |
Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
title_short |
Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
title_full |
Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
title_fullStr |
Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
title_full_unstemmed |
Photodecolorization of methyl orange over α-Fe2O3-supported HY catalysts: the effects of catalyst preparation and dealumination |
title_sort |
photodecolorization of methyl orange over α-fe2o3-supported hy catalysts: the effects of catalyst preparation and dealumination |
publisher |
Elsevier B. V. |
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2012 |
url |
http://eprints.utm.my/id/eprint/47378/ https://www.sciencedirect.com/science/article/pii/S1385894712003105?via%3Dihub |
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1643652301974405120 |
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13.211869 |