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Lignin, as a structurally complex biomaterial, offers a valuable resource for the production of aromatic chemicals; however, its selective conversion into desired products remains a challenging task. In this study, we prepared three types of Pd-based nano-catalysts and explored their application in the depolymerization of alkali lignin, under both H-free (hydrogen transfer) conditions and H atmosphere conditions. The materials were well characterized with TEM, XRD, and XPS and others, and the electronic interactions among Pd, Ni, and P were analyzed. The results of lignin depolymerization experiments revealed that the ternary Pd-Ni-P catalyst exhibited remarkable performance and guaiacols could be produced under H atmosphere conditions in 14.2 wt.% yield with a selectivity of 89%. In contrast, Pd-Ni and Pd-P catalysts resulted in a dispersed product distribution. Considering the incorporation of P and the Pd-Ni synergistic effect in the Pd-Ni-P catalyst, a possible water-involved transformation route of lignin depolymerization was proposed. This work indicates that metal phosphides could be promising catalysts for the conversion of lignin and lignin-derived feedstocks into value-added chemicals.
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http://dx.doi.org/10.3390/ma16145198 | DOI Listing |
Materials (Basel)
July 2023
Department of Materials and Biology, National Institute of Technology, Akita College, Akita 011-8511, Japan.
Lignin, as a structurally complex biomaterial, offers a valuable resource for the production of aromatic chemicals; however, its selective conversion into desired products remains a challenging task. In this study, we prepared three types of Pd-based nano-catalysts and explored their application in the depolymerization of alkali lignin, under both H-free (hydrogen transfer) conditions and H atmosphere conditions. The materials were well characterized with TEM, XRD, and XPS and others, and the electronic interactions among Pd, Ni, and P were analyzed.
View Article and Find Full Text PDFMolecules
March 2023
Laboratory for Development & Application of Cold Plasma Technology, College of Chemistry and Chemical Engineering, Luoyang Normal University, Luoyang 471022, China.
Selective semi-hydrogenation of acetylene is an extremely important reaction from both industrial and theoretical perspectives. Palladium, due to its unique chemical and physical properties, is the most active and currently irreplaceable metal for this reaction in industry, but the poor catalytic selectivity towards ethylene is also its inherent shortcoming. Introducing a secondary metal to tune a geometric and electronic structures of Pd nanoparticles and to create a synergistic effect is the most widely used strategy to effectively improve the overall catalytic performance of Pd-based catalysts.
View Article and Find Full Text PDFInt J Biol Macromol
December 2021
Department of Chemistry, Iran University of Science and Technology, Tehran 16846-13114, Iran.
Heck cross-coupling reaction (HCR) is one of the few transition metal catalyzed CC bond-forming reactions, which has been considered as the most effective, direct, and atom economical synthetic method using various catalytic systems. Heck reaction is widely employed in numerous syntheses including preparation of pharmaceutical and biologically active compounds, agrochemicals, natural products, fine chemicals, etc. Commonly, Pd-based catalysts have been used in HCR.
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