4.7 Article

CO2 utilization as a soft oxidant for the synthesis of styrene from ethylbenzene over Co3O4 supported on magnesium aluminate spinel: role of spinel activation temperature

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SCIENTIFIC REPORTS
卷 10, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41598-020-79188-z

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  1. University Grants Commission (UGC)
  2. Council of Scientific and Industrial Research (CSIR), New Delhi, India
  3. Department of Chemistry (H & S), PACE Institute of Technology & Sciences, Ongole, Andhra Pradesh, India
  4. UKM research grants [DIP-2019-001, GUP-2020-034]

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Magnesium aluminate spinel (MgAl2O4) supported Co3O4 catalysts are synthesized and tested for the oxidative dehydrogenation (ODH) of ethylbenzene using CO2 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 degrees C, the active presence of a single-phase MgAl2O4 spinel is observed. A catalyst series consisting of MgAl2O4 spinel with varying Co loadings (10-20 wt%) were prepared and systematically distinguished by ICP, XRD, BET, TPR, NH3-TPD, UV-Vis DRS, FT-IR, XPS, SEM, and TEM. Among the tested cobalt catalysts, 15Co/800MA sample derived by calcination of MgAl2O4 support at 800 degrees 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 MgAl2O4 spinel at 800 degrees C facilitates a dramatic chemical homogeneity for the alignment of Co3O4 nanoparticles on the surface of the active catalyst. Moreover, the isolated Co3O4 clusters have a strong chemical/electronic interaction with the Mg2+ and Al3+ ions on the support perform a crucial role to achieve the maximum catalytic activity.

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