Mineralization versus photoreduction of 4-nitrophenol under the influence of surface functionalized CeO2 nanoparticles, hosted by versatile cellulose supports

Multiple cellulose-derived platforms were designed for the immobilization of pristine/functionalized CeO2 nanoparticles with efficient photocatalytic activity under UV light. CeO2 nanoparticles were synthesized at two different pH values (pH = 6 and pH = 9) observing that those prepared at basic pH have better defined shapes and, by modifying their surface with silane moieties, the band gap values decreased from 3.27 eV to 2.89 eV. The synthesized CeO2 NPs were embedded in cellulose acetate matrix in various amounts and the achieved nanocomposites were tested as photocatalysts under UV irradiation in the photodegradation of hazardous pollutants, the optimal results being obtained at nanoparticle loading of 5 wt%. Also, the matrix type strongly influences the reaction pathway for 4-nitrophenol, from mineralization to photoreduction to 4-aminophenol. The cellulose acetate film containing functionalized CeO2 NPs was deacetylated under alkaline medium, to regenerate the cellulose structure, and subsequently oxidized using TEMPO mediated protocol. Experiments on 4-nitrophenol photodegradation, in the presence of oxidized cellulose bearing CeO2 NPs showed that this is completely converted to 4-aminophenol and proved the versatility of the proposed materials. Nanocomposites have good reusability results and the film containing silane-functionalized CeO2 NPs displayed encouraging efficiency as photocatalyst under visible light.

Automated summary

Multiple cellulose-derived platforms were designed to immobilize CeO2 nanoparticles, showing efficient photocatalytic activity under UV light. Synthesized CeO2 nanoparticles at different pH values exhibited varying shapes and band gap values, with better results obtained at basic pH. The nanocomposites tested as photocatalysts in the photodegradation of pollutants showed promising reusability and efficiency under visible light.