Cobalt loaded organic acid modified kaolin clay for the enhanced catalytic activity of hydrogen release via hydrolysis of sodium borohydride
Autor: | Cafer Saka, Mustafa Salih Eygi, Asım Balbay |
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Rok vydání: | 2021 |
Předmět: |
chemistry.chemical_classification
Renewable Energy Sustainability and the Environment Energy Engineering and Power Technology chemistry.chemical_element Hydrochloric acid 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences 0104 chemical sciences Catalysis Sodium borohydride chemistry.chemical_compound Hydrolysis Fuel Technology chemistry Nitric acid Fourier transform infrared spectroscopy 0210 nano-technology Cobalt Organic acid Nuclear chemistry |
Zdroj: | International Journal of Hydrogen Energy. 46:3876-3886 |
ISSN: | 0360-3199 |
DOI: | 10.1016/j.ijhydene.2020.10.201 |
Popis: | Inorganic acids such as hydrochloric acid (HCl), nitric acid (HNO3) and sulphuric acid (H2SO4) are generally used in the acid modification of clays. Here, CoB catalyst was synthesized on the acetic acid-activated kaolin support material (CH3COOH -kaolin- CoB) with an alternative approach. This prepared catalyst, firstly, was used to catalyze the hydrolysis of NaBH4 (NaBH4-HR). The structure of the raw kaolin, kaolin-CH3COOH, and CH3COOH-kaolin-CoB samples were characterized by X-ray diffraction spectroscopy (XRD), Fourier transforms infrared spectroscopy (FTIR), scanning electron microscope (SEM), and nitrogen adsorption. At the same time, this catalyst performance was examined by Co loading, NaBH4 concentration, NaOH concentration, temperature and reusability parameters. The end times of this hydrolysis reaction using raw kaolin-CoB and CH3COOH-kaolin-CoB were found to be approximately 140 and 245 min, respectively. The maximum hydrogen generation rates (HGRs) obtained at temperatures 30 °C and 50 °C were 1533 and 3400 mL/min/gcatalyst, respectively. At the same time, the activation energy was found to be 49.41 kJ/mol. |
Databáze: | OpenAIRE |
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