Abstract

Efficient and applicable catalysts are highly desirable for advanced biomass transformation industry, here, we fabricated a series of Nd-Co-P catalysts for hydrogenation of furfural (FAL) to furfuryl alcohol (FOH). By comprehensive characterizations, it is demonstrated that the prepared Nd-Co-P samples are structured as (NdPO4)m/Co2P nanocomposites with molar ratio (m) in range of 0.24–1.1; by manipulating m, the outstanding catalytic efficiency comparable with the performance of precious metal catalysts, such as turnover frequency (TOF) up to 0.50 s−1 (being ten-fold higher than Co2P) and FOH yield up to 97%, is achieved on the reusable (NdPO4)m/Co2P composites. Temperature programmed desorption (TPD), in-situ infrared spectroscopy (IR) and kinetic-mechanism studies further disclose that Co2P is decisive for activating FAL, instead, NdPO4 possesses unique capability of activating hydrogen which readily facilitate the selective hydrogenation of FAL to FOH through a rapid Langmuir–Hinshelwood process over (NdPO4)m/Co2P catalyst. These results indicate that rare-earth phosphates like NdPO4 can act as the promising and reliable catalytic component to activate hydrogen, which can be of interest not only for innovating novel and applicable non-metallic catalysts for sustainable biomass transformation analogous to hydrogenation of FAL, but also for expanding material base for other green mass transformation techniques involving hydrogen.

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