Journal
CHEMICAL ENGINEERING JOURNAL
Volume 293, Issue -, Pages 327-336Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2016.02.069
Keywords
CO2 hydrogenation; Methanol synthesis; Cu-based catalyst's; H-2 to CO2 ratio
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Funding
- Thailand Research Fund
- Center of Excellence on Petrochemical and Materials Technology (PETROMAT)
- National Research University Project of Thailand (NRU)
- Nanotechnology Center (NANOTEC)
- NSTDA
- Ministry of Science and Technology, Thailand through its program of Center of Excellence Network
- Kasetsart University Research and Development Institute (KURDI)
- Faculty of Engineering, Kasetsart University
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Structure-activity relationships of amorphous (a-), tetragonal (t-), monoclinic (m-) ZrO2 phase supported copper catalysts for methanol synthesis from CO2 hydrogenation were investigated with X-ray diffraction (XRD), high resolution transmission electron microscopy (HR-TEM), N2O chemisorption, H-2-temperature programmed reduction (H-2-TPR), X-ray absorption spectroscopy (XAS), H-2 and CO2 temperature programmed desorption (H-2- and CO2-TPD). The order of copper surface area is found to be as follows: Cu/a-ZrO2 > Cu/t-ZrO2> Cu/m-ZrO2. The increased yield of methanol is correlated to the increase of copper surface area. However, normalization of the copper site specific activity (TOFmethanol) of Cu/t-ZrO2 is about 1.10-1.50 times and 1.62-3.59 times higher than Cu/a-ZrO2 and Cu/a-ZrO2, respectively. The high TOFmethanol is caused by a strong Cu-ZrO2 interaction and a high surface concentration of atomic hydrogen to CO2. (C) 2016 Elsevier B.V. All rights reserved.
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