Synthesis of molecularly imprinted photocatalysts containing low TiO2 loading: Evaluation for the degradation of pharmaceuticals

•Molecularly imprinted photocatalyst (MIP) containing low TiO2 loading were prepared by acid-catalyzed sol–gel process.•Seven pharmaceutical compounds were evaluated as a template.•Comparing to the P25, MIP has shown an increase of adsorption up to 752%.•Comparing to the P25, MIP has shown an increa...

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Veröffentlicht in:Journal of hazardous materials 2016-04, Vol.306, p.359-366
Hauptverfasser: de Escobar, Cícero Coelho, Lansarin, Marla Azário, Zimnoch dos Santos, João Henrique
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creator de Escobar, Cícero Coelho
Lansarin, Marla Azário
Zimnoch dos Santos, João Henrique
description •Molecularly imprinted photocatalyst (MIP) containing low TiO2 loading were prepared by acid-catalyzed sol–gel process.•Seven pharmaceutical compounds were evaluated as a template.•Comparing to the P25, MIP has shown an increase of adsorption up to 752%.•Comparing to the P25, MIP has shown an increase of degradation up to 427%.•The presence of specific cavities on the silica domain could explain the better results for MIP. A molecularly imprinted (MI) photocatalyst containing a low TiO2 loading (7.00–16.60mgL−1 of TiO2) was prepared via an acid-catalyzed sol–gel route using different classes of pharmaceutical compounds (i.e., Atorvastatin, Diclofenac, Ibuprofen, Tioconazole, Valsartan, Ketoconazole and Gentamicine) as the template. Herein, our main goal was to test the hypothesis that photocatalysts based on molecular imprinting may improve the degradation performance of pharmaceutical compounds compared to that of a commercial sample (Degussa P25) due to presence of specific cavities in the silica domain. To elucidate certain trends between the performance of photocatalysts and their structural and textural properties, as well the effect of the structure of the drugs on molecular imprinting, the data were analyzed in terms of pore diameter, pore volume, surface area, zeta potential and six-membered ring percentage of silica. In comparison to the commercial sample (P25), we have shown that adsorption and degradation were enhanced from 48 to 752% and from 5 to 427%, respectively. A comparison with the control system (non-imprinted) indicates that the increased performance of the MI systems was due to the presence of specific cavities on the silica domain, and the textural and structural aspects also support this conclusion. The MI photocatalyst was reusable for seven cycles of reuse in which approximately 60% of its photocatalytic efficiency was preserved for the system containing Diclofenac as the template.
doi_str_mv 10.1016/j.jhazmat.2015.11.035
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A molecularly imprinted (MI) photocatalyst containing a low TiO2 loading (7.00–16.60mgL−1 of TiO2) was prepared via an acid-catalyzed sol–gel route using different classes of pharmaceutical compounds (i.e., Atorvastatin, Diclofenac, Ibuprofen, Tioconazole, Valsartan, Ketoconazole and Gentamicine) as the template. Herein, our main goal was to test the hypothesis that photocatalysts based on molecular imprinting may improve the degradation performance of pharmaceutical compounds compared to that of a commercial sample (Degussa P25) due to presence of specific cavities in the silica domain. To elucidate certain trends between the performance of photocatalysts and their structural and textural properties, as well the effect of the structure of the drugs on molecular imprinting, the data were analyzed in terms of pore diameter, pore volume, surface area, zeta potential and six-membered ring percentage of silica. In comparison to the commercial sample (P25), we have shown that adsorption and degradation were enhanced from 48 to 752% and from 5 to 427%, respectively. A comparison with the control system (non-imprinted) indicates that the increased performance of the MI systems was due to the presence of specific cavities on the silica domain, and the textural and structural aspects also support this conclusion. 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A molecularly imprinted (MI) photocatalyst containing a low TiO2 loading (7.00–16.60mgL−1 of TiO2) was prepared via an acid-catalyzed sol–gel route using different classes of pharmaceutical compounds (i.e., Atorvastatin, Diclofenac, Ibuprofen, Tioconazole, Valsartan, Ketoconazole and Gentamicine) as the template. Herein, our main goal was to test the hypothesis that photocatalysts based on molecular imprinting may improve the degradation performance of pharmaceutical compounds compared to that of a commercial sample (Degussa P25) due to presence of specific cavities in the silica domain. To elucidate certain trends between the performance of photocatalysts and their structural and textural properties, as well the effect of the structure of the drugs on molecular imprinting, the data were analyzed in terms of pore diameter, pore volume, surface area, zeta potential and six-membered ring percentage of silica. In comparison to the commercial sample (P25), we have shown that adsorption and degradation were enhanced from 48 to 752% and from 5 to 427%, respectively. A comparison with the control system (non-imprinted) indicates that the increased performance of the MI systems was due to the presence of specific cavities on the silica domain, and the textural and structural aspects also support this conclusion. 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subjects Adsorption
Catalysis
Degradation
Diclofenac
Holes
Molecular Imprinting
Pharmaceutical Preparations - chemistry
Pharmaceuticals
Photocatalysis
Photocatalysts
Photolysis
Silicon dioxide
Silicon Dioxide - chemistry
Titanium - chemistry
Titanium - radiation effects
Titanium dioxide
Ultraviolet Rays
title Synthesis of molecularly imprinted photocatalysts containing low TiO2 loading: Evaluation for the degradation of pharmaceuticals
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