Creation of Highly Reducible CuO Species by High-Temperature Calcination of a Cu-Al Layered Double Hydroxide: Selective Hydrogenation of Furfural into Furfuryl Alcohol with Formic Acid

  • Enggah Kurniawan
    Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi, Inage, Chiba 263-8522 , Japan
  • Takayoshi Hara
    Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi, Inage, Chiba 263-8522 , Japan
  • Yessi Permana
    Inorganic and Physical Chemistry Research Division, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesha 10 Bandung, 40132, Indonesia
  • Takashi Kojima
    Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi, Inage, Chiba 263-8522 , Japan
  • Nobuyuki Ichikuni
    Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi, Inage, Chiba 263-8522 , Japan
  • Shogo Shimazu
    Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi, Inage, Chiba 263-8522 , Japan

抄録

<jats:title>Abstract</jats:title> <jats:p>Highly reducible CuO species were created by the calcination of a Cu-Al layered double hydroxide (CuAl LDH) at 1073 K under air. After this heat treatment, the original layered double hydroxide structure was completely transformed into CuO and CuAl2O4 phases. The synthesized calcined CuAl LDH (calc-CuAl LDH) promoted the catalytic hydrogenation of furfural (FALD) into furfuryl alcohol (FOL) with formic acid (FA) as a hydrogen donor. In the initial stage of the above catalytic reaction, the CuO species in the calc-CuAl LDH matrix transformed into active Cu0 species via the formation of a Cu(HCOO)2-1,4-dioxane complex in the liquid phase. The spent catalyst was also reusable without loss of its high catalytic performance.</jats:p>

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