Rational design of the La-doped CuCoAl hydrotalcite catalyst for selective hydrogenation of furfuryl alcohol to 1,5-pentanediol
1,5-Pentanediol (1,5-PeD) is an important raw material for the preparation of degradable polyesters, polyurethanes and pharmaceutical intermediates. Efficient synthesis of 1,5-PeD from biomass-derived furfuryl alcohol (FFA) by hydrogenation is a green synthetic route instead of using fossil raw mate...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2024-11, Vol.26 (23), p.1168-11624 |
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Zusammenfassung: | 1,5-Pentanediol (1,5-PeD) is an important raw material for the preparation of degradable polyesters, polyurethanes and pharmaceutical intermediates. Efficient synthesis of 1,5-PeD from biomass-derived furfuryl alcohol (FFA) by hydrogenation is a green synthetic route instead of using fossil raw material production. Nevertheless, it suffers from great challenges as the various adsorption configurations of FFA on the catalyst surface induce diverse product distributions and low selectivity for 1,5-PeD. Herein, a CuCoAl hydrotalcite catalyst modified by La was fabricated and applied in the hydrogenation of FFA to 1,5-PeD. The results demonstrated that in the catalyst doped with La
via
deposition-precipitation methods (La/CuCoAl-DP) there appeared a strong Cu-La interaction, and it exhibited superior activity compared with other catalysts. A near 60% yield of 1,5-PeD was achieved under 160 °C, 4 MPa H
2
within 2 h. Extensive characterizations including XRD, HRTEM, N
2
O-TPD and CO
2
-TPD demonstrated that the doping of La improved markedly the dispersion of Cu and the concentration of strong basic sites. Furthermore, HRTEM and the
in situ
XPS characterization verified that the addition of La species promoted the formation of a Cu-La interface with a stable Cu
n
+
-O-La(OH)
3
structure on the catalyst surface. Such Cu
n
+
-O-La(OH)
3
sites can simultaneously activate the furan ring and the -OH group in FFA with an intermediate six-membered ring transition state, leading to high selective cleavage of the C2-O1 bond in the furan ring to 1,5-PeD. Meanwhile, the DFT calculation results corroborated that the modifying by La species remarkably promoted the C2-end tilted adsorption of FFA on the catalyst surface and enhanced the ability of the catalyst to activate hydrogen. This study provided a new strategy for the high-value utilization of biomass resources and the development of multi-center catalysts.
A near 60% yield of 1,5-PeD was achieved over a La/CuCoAl-DP catalyst under 160 °C, 4 MPa H
2
within 2 h. The excellent activity of this catalyst was derived from the synergistic catalysis of the Cu
0
, CoO
x
, La(OH)
3
and Cu-La interface. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/d4gc03974b |