Graphene Oxide from Graphite of Spent Batteries as Support of Nanocatalysts for Fuel Hydrogen Production

The increasing production of electronic waste and the rising demand for renewable energy are currently subjects of debate. Sustainable processes based on a circular economy are required. Then, electronic devices could be the main source for the synthesis of new materials. Thus, this work aimed to sy...

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Published inProcesses Vol. 11; no. 11; p. 3250
Main Authors Sperandio, Gabriel, Junior, Iterlandes Machado, Bernardo, Esteefany, Moreira, Renata
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 01.11.2023
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ISSN2227-9717
2227-9717
DOI10.3390/pr11113250

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Summary:The increasing production of electronic waste and the rising demand for renewable energy are currently subjects of debate. Sustainable processes based on a circular economy are required. Then, electronic devices could be the main source for the synthesis of new materials. Thus, this work aimed to synthesize graphene oxide (GO) from graphite rod of spent Zn-C batteries. This was used as support for Ni/Co bimetallic nanocatalysts in the evolution of hydrogen from NaBH4 for the first time. The graphene oxide (GO) exhibited a diffraction peak at 2θ = 9.1°, as observed using X-ray diffraction (XRD), along with the presence of oxygenated groups as identified using FTIR. Characteristic bands at 1345 and 1574 cm−1 were observed using Raman spectroscopy. A leaf-shaped morphology was observed using SEM. GO sheets was observed using TEM, with an interplanar distance of 0.680 nm. Ni/Co nanoparticles, with an approximate size of 2 nm, were observed after deposition on GO. The material was used in the evolution of hydrogen from NaBH4, obtaining an efficiency close to 90%, with a kinetic constant of 0.0230 s−1 at 296.15 K and activation energy of 46.7 kJ mol−1. The material showed an efficiency in seven reuse cycles. Therefore, a route of a new material with added value from electronic waste was obtained from an eco-friendly process, which can be used in NaBH4 hydrolysis.
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ISSN:2227-9717
2227-9717
DOI:10.3390/pr11113250