4.7 Article

Magnetic field-enhanced catalytic CO2 hydrogenation and selective conversion to light hydrocarbons over Fe/MCM-41 catalysts

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 306, Issue -, Pages 866-875

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2016.08.029

Keywords

Carbon dioxide; Hydrogenation; Magnetic flux density; Magnetic field orientation; Ferro/ferrimagnetic property; Green catalysis

Funding

  1. Thailand Research Fund (TRF)
  2. Kasetsart University through the Royal Golden Jubilee Ph.D. Fellowship [PHD/0283/2552]
  3. Kasetsart University Research and Development Institute (KURDI)
  4. Synchrotron Light Research Institute (Public Organization), Thailand
  5. Institute of Materials Chemistry, Vienna University of Technology

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Based on green and efficient utilization concepts, an external magnetic field is applied with an attempt to improve the catalytic performance in CO2 hydrogenation reaction. In this research, effects of magnetic field orientation and magnetic flux density on activity and selectivity of xFe/MCM-41 catalysts with ferro/ferrimagnetic property were investigated. With external magnetic field, especially in north-to south (N-S) direction, CO2 conversions were significantly improved by 1.5-1.8 times; meanwhile, the activation energy was decreased by 1.12-1.15 times, compared to those of without magnetic field. Upon changing the magnetic flux density, CO2 conversion increased with increasing the magnetic flux density followed the order of 27.7 mT > 25.1 mT > 20.8 mT. Furthermore, higher selectivities to C-2-C-3 hydrocarbons (2.5-5.3 times), and CH3OH (1.6 times) were observed at 180-200 degrees C and 220 degrees C, respectively. Among all the conditions with magnetic field, the highest CO2 conversion and selectivity to CH3OH and C-2-C-3 hydrocarbons were obtained at -27.7 mT in N-S direction. These outstanding catalytic activities could be attributed to the fact that magnetic field help facilitate the reactant adsorption and surface reaction over the magnetized Fe catalysts, leading to the decrease of apparent activation energy, and also the increase of selectivities to hydrocarbons and CH3OH. (C) 2016 Elsevier B.V. All rights reserved.

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