Highly porous Zr-MCM-48 immobilized Cu-porphyrin for photocatalytic reduction of CO2 to methanol in a slurry reactor
This study involves the development of novel mesoporous Zr-MCM-48 photocatalyst impregnated with Cu-porphyrin (CuTPP) having Si/Zr ratio of 100, 50 and 25. The synthesized materials were applied as hybrid photocatalyst affording mid-gap energy states and Zi3+ sites for reduction of CO2 into methanol...
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| Main Authors: | , , , , |
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| Format: | Article |
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Springer
2021
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| Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85111739170&doi=10.1007%2fs10854-021-06676-x&partnerID=40&md5=1cd1609f9bc3faca62a25b83f46f13d3 http://eprints.utp.edu.my/23837/ |
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| Summary: | This study involves the development of novel mesoporous Zr-MCM-48 photocatalyst impregnated with Cu-porphyrin (CuTPP) having Si/Zr ratio of 100, 50 and 25. The synthesized materials were applied as hybrid photocatalyst affording mid-gap energy states and Zi3+ sites for reduction of CO2 into methanol selectively using UV�Visible light treatment. Interestingly, Zr-MCM-48 displayed significant photocatalytic reduction ability under UV�Vis wavelength. The bare Zr-based MCM-48(25) matrix with maximum Zr content in catalyst enhanced the photocatalytic activity with 47.5 µmol methanol formation, possessing high surface area SBET of 1324 m2 g�1, under UV�Visible light irradiation. The characterization results highlighted the influence of visible light active Cu-porphyrin interaction over Zr-MCM-48 silica frameworks due to transition of electrons from the porphyrin centres to the active Zr sites as evident from DRS analysis. Moreover, the impregnation of Cu-porphyrin over Zr-MCM-48(25) displayed methanol formation about 365.11 µmol under UV�Visible light using 0.1 M NaOH and 0.1 M Na2SO3. Also, the effect of varying reaction conditions shown that catalyst concentration, metal loading, light intensity and stirring speed pronouncedly impact the formation of methanol. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. |
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