Synthesis and Characterization of Polymer Particles as Metal‐Free Catalysts for Electrooxidation and Methanolysis of Sodium Borohydride

Author:

Gokkus Kutalmis1,Kaya Sefika2ORCID,Yildiz Derya2,Saka Ceren2,Gür Mahmut3,Bütün Vural4,Kivrak Hilal2

Affiliation:

1. Kastamonu University Faculty of Engineering and Architecture Department of Environmental Engineering Kuzeykent Campus 37500 Kastamonu Turkey

2. Eskisehir Osmangazi University Faculty of Engineering and Architectural Sciences Department of Chemical Engineering Meselik Campus 26040 Eskisehir Turkey

3. Kastamonu University Faculty of Forest Department of Forest Industrial Engineering Kuzeykent Campus 37500 Kastamonu Turkey

4. Eskisehir Osmangazi University Faculty of Science Department of Chemistry Meselik Campus 26040 Eskisehir Turkey

Abstract

AbstractIn this study, trimethylolpropane triglycidyl ether/diethylenetriamine (TD) and glutaraldehyde/diethylenetriamine (GD) polymer particles are synthesized as catalysts for hydrogen production from NaBH4 methanolysis and NaBH4 electrooxidation. SEM, FT‐IR and TGA characterization methods are applied to determine the surface morphologies, chemical structures, thermal stability and decomposition of the synthesized polymer particles. The parameters affecting the hydrogen generation rate on NaBH4 methanolysis are investigated and optimum conditions are determined. Under optimum conditions, the hydrogen generation rates of TD and GD polymer particles are obtained as 34903.2 and 97998 mL/min.gcat, respectively. The activation energies of TD and GD polymer particles are also calculated as 16.86 and 18.14 kJ/mol, respectively. The catalytic activities of polymer particles as anode catalysts in NaBH4 electrooxidation are determined by CV, CA, EIS analyses. The specific activities of TD and GD polymer particles are acquired as 0.54 and 0.64 mA/cm2, respectively. These results indicate that the synthesized polymer particles are promising catalysts for electrooxidation and methanolysis of sodium borohydride.

Publisher

Wiley

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