Journal
CATALYSIS LETTERS
Volume 153, Issue 4, Pages 1215-1226Publisher
SPRINGER
DOI: 10.1007/s10562-022-04035-x
Keywords
1-Octanol amination; Ni3P; Acid-base sites; In situ FTIR
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In this study, Ni phosphide and Lewis acid-base pair site of Al2O3 were combined as a highly efficient catalyst for the direct amination of 1-octanol to 1-octylamine. The Ni3P/Al2O3-TPP catalyst prepared by organophosphorus exhibited 4.0 times higher activity than Ni/Al2O3, leading to increased selectivity to 1-octylamine from 71.4% to 92.8% at 0.4 MPa NH3.
Ni phosphide and Lewis acid-base pair site of Al2O3 were combined as highly efficient catalyst for direct amination of 1-octanol to 1-octylamine. Due to the higher dehydrogenation activity and the site isolation effect, Ni3P/Al2O3-TPP prepared by organophosphorus was 4.0 times more active than Ni/Al2O3 and increased the selectivity to 1-octylamine from 71.4 to 92.8% at 0.4 MPa NH3. [GRAPHICS] .
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