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Parasitic Light Absorption, Rate Laws and Heterojunctions in the Photocatalytic Oxidation of Arsenic(III) Using Composite TiO 2 /Fe 2 O 3
Composite photocatalyst-adsorbents such as TiO /Fe O are promising materials for the one-step treatment of arsenite contaminated water. However, no previous study has investigated how coupling TiO with Fe O influences the photocatalytic oxidation of arsenic(III). Herein, we develop new hybrid experi...
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Published in: | Chemistry : a European journal 2022-03, Vol.28 (16), p.e202104181 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Composite photocatalyst-adsorbents such as TiO
/Fe
O
are promising materials for the one-step treatment of arsenite contaminated water. However, no previous study has investigated how coupling TiO
with Fe
O
influences the photocatalytic oxidation of arsenic(III). Herein, we develop new hybrid experiment/modelling approaches to study light absorption, charge carrier behaviour and changes in the rate law of the TiO
/Fe
O
system, using UV-Vis spectroscopy, transient absorption spectroscopy (TAS), and kinetic analysis. Whilst coupling TiO
with Fe
O
improves total arsenic removal by adsorption, oxidation rates significantly decrease (up to a factor of 60), primarily due to the parasitic absorption of light by Fe
O
(88 % of photons at 368 nm) and secondly due to changes in the rate law from disguised zero-order kinetics to first-order kinetics. Charge transfer across this TiO
-Fe
O
heterojunction is not observed. Our study demonstrates the first application of a multi-adsorbate surface complexation model (SCM) towards describing As(III) oxidation kinetics which, unlike Langmuir-Hinshelwood kinetics, includes the competitive adsorption of As(V). We further highlight the importance of parasitic light absorption and catalyst fouling when designing heterogeneous photocatalysts for As(III) remediation. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.202104181 |