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CO(2) utilization as a soft oxidant for the synthesis of styrene from ethylbenzene over Co(3)O(4) supported on magnesium aluminate spinel: role of spinel activation temperature
Magnesium aluminate spinel (MgAl(2)O(4)) supported Co(3)O(4) catalysts are synthesized and tested for the oxidative dehydrogenation (ODH) of ethylbenzene using CO(2) as a soft oxidant. The effect of spinel calcination temperature on the catalytic performance has been systematically investigated. Wit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747735/ https://www.ncbi.nlm.nih.gov/pubmed/33335173 http://dx.doi.org/10.1038/s41598-020-79188-z |
Sumario: | Magnesium aluminate spinel (MgAl(2)O(4)) supported Co(3)O(4) catalysts are synthesized and tested for the oxidative dehydrogenation (ODH) of ethylbenzene using CO(2) as a soft oxidant. The effect of spinel calcination temperature on the catalytic performance has been systematically investigated. With an increase in the activation temperature from 600 to 900 °C, the active presence of a single-phase MgAl(2)O(4) spinel is observed. A catalyst series consisting of MgAl(2)O(4) spinel with varying Co loadings (10–20 wt%) were prepared and systematically distinguished by ICP, XRD, BET, TPR, NH(3)-TPD, UV–Vis DRS, FT-IR, XPS, SEM, and TEM. Among the tested cobalt catalysts, 15Co/800MA sample derived by calcination of MgAl(2)O(4) support at 800 °C exhibits the most excellent catalytic performance with the maximum ethylbenzene conversion (≥ 82%). Also, high yields of styrene (≥ 81%) could be consistently achieved on the same active catalyst. Further, the catalyst exhibited almost stable activity during 20 h time-on-stream with a slow decrease in the ethylbenzene conversion from 82 to 59%. However, the selectivity of styrene (98%) stayed almost constant during the reaction. Activation of the MgAl(2)O(4) spinel at 800 °C facilitates a dramatic chemical homogeneity for the alignment of Co(3)O(4) nanoparticles on the surface of the active catalyst. Moreover, the isolated Co(3)O(4) clusters have a strong chemical/electronic interaction with the Mg(2+) and Al(3+) ions on the support perform a crucial role to achieve the maximum catalytic activity. |
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