Abstract

Palladium nanoparticles were grown on sub-millimeter activated Al2O3 particle support by spraying H2PdCl4 solution evenly onto the support, followed with a thermal reduction under H2 atmosphere. Compared with its counterpart created by the conventional impregnation method, the Pd/Al2O3 catalyst created by the spray process could enrich the existence of active Pd nanoparticles on the surface of the catalyst support and increase their degree of dispersion, resulting in a much higher activity in the catalytic reduction of bromate in water. The effect of Al2O3 support particle size on the bromate removal rate was also investigated, which demonstrated that smaller support particle size could have higher activity in the catalytic reduction of bromate in water because of its larger exposed surface. This Pd/Al2O3 catalyst could be easily used in the fixed bed reactor due to its large support size and demonstrated excellent stability in the catalytic reduction of bromate in mineral water. This Pd/Al2O3 catalyst also exhibited a good catalytic reduction performance on azo dyes as demonstrated by its effective catalytic hydrogenation of methyl orange. Thus, catalysts prepared by the spray method developed in this work could have the potential to be used in fixed bed reactors for various water treatment practices.

Highlights

  • Bromate is not normally present in natural water, it could be readily formed as a toxic disinfection by-product during the drinking water disinfection with ozone when bromide ion is present in the raw water[1,2]

  • Pd was loaded onto carbon nanofibers grown on various macroscopic supports[43,44,45,46], which could be utilized in the fixed-bed reactors for the catalytic bromate reduction

  • For Pd/Al2O3 catalysts, the diffraction peaks of AlO(OH) could not be observed because activated Al2O3 was dehydrated in the calcination step during the Pd/Al2O3 catalyst synthesis process

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Summary

Results and Discussion

For both samples, the binding energy of Pd 3d3/2 and 3d5/2 peaks was determined at ~341.3 eV and ~336 eV, respectively, which demonstrated clearly metallic Pd32,40 was successfully loaded by both methods after the thermal reduction at 300 °C under H2 atmosphere. 0.104%Pd/Fe3O4 2.0%Pd/amino functionalized magnetic MCM-41 0.3%Pd/10%CNF/monolith 0.3%Pd/CNFs/Sintered Metal Fibers 0.3%Pd/CNFs/Carbon Cloth

Reaction Conditions
Natural Mineral Water
Methods
Additional Information
Full Text
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