4.7 Article

Fabrication of PdZn alloy catalysts supported on ZnFe composite oxide for CO2 hydrogenation to methanol

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 597, Issue -, Pages 260-268

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.03.135

Keywords

CO2 hydrogenation; Methanol synthesis; PdZn alloy; ZnFe2O4 spinel

Funding

  1. National Natural Science Foundation of China [21872106]
  2. China National Key Research and Development Plan Project [2018YFB1502000]
  3. Fundamental Research Funds for Central Universities [2042019kf0019]

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The use of supported Pd catalysts with PdZn alloy on ZnO-enriched support is an effective strategy for efficient CO2 hydrogenation to methanol. The amount of formed PdZn alloy and catalyst structure influenced by ZnO concentration on ZnFe2O4 were explored to obtain the best Pd-Z(1)FO catalyst, achieving high methanol space-time yield (STY).
The conversion of CO2 to methanol is of great significance for providing a means of CO2 fixation and the development of future fuels. Supported Pd catalysts have been demonstrated to be active for CO2 hydrogenation to methanol and PdZn alloy plays a key role in this reaction. Therefore, using ZnO-enriched support to increase the amount of nanometric PdZn alloy particles on the surface is an effective strategy to develop ideal catalysts. Herein, we fabricated a PdZn alloy catalyst supported on ZnO-enriched ZnFe2O4 spinel for efficient CO2 hydrogenation to methanol. The amount of formed PdZn alloy and catalyst structure influenced by ZnO concentration on ZnFe2O4 were explored to obtain the best Pd-Z(1)FO catalyst, which achieves a methanol space-time yield (STY) of 593 g kg(cat)(-1) h(-1) (12 g gPd(-1) h(-1)) with CO2 conversion of 14% under reaction conditions of 290 degrees C, 4.5 MPa and 21600 mL g(-1) h(-1). Furthermore, the amount of exposed PdZn alloy sites were measured by using CO-pulse chemisorption and we find a linearity between methanol production rate and PdZn alloy sites. (C) 2021 Elsevier Inc. All rights reserved.

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