Macroscopic graphite felt containing palladium catalyst for liquid-phase hydrogenation of cinnamaldehyde

[Display omitted] •Structured catalyst consisting of oxygen functionalized graphite felt (OGF) supported highly dispersed Pd nanoparticles.•Abundant oxygenated groups decorated structural defects and porous structure on OGF.•Strong metal-support interaction from charge transfer at Pd-carbon interfac...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2019-05, Vol.244, p.128-139
Hauptverfasser: Xu, Zhenxin, Duong-Viet, Cuong, Liu, Yuefeng, Baaziz, Walid, Li, Bing, Nguyen-Dinh, Lam, Ersen, Ovidiu, Pham-Huu, Cuong
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Sprache:eng
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Zusammenfassung:[Display omitted] •Structured catalyst consisting of oxygen functionalized graphite felt (OGF) supported highly dispersed Pd nanoparticles.•Abundant oxygenated groups decorated structural defects and porous structure on OGF.•Strong metal-support interaction from charge transfer at Pd-carbon interface in Pd/OGF.•Monolith Pd/OGF as efficient catalytic stirrer with easy recyclability for liquid-phase hydrogenation of cinnamaldehyde. Developing of both effective and stable noble metal nanoparticle (NPs) catalysts with easy catalyst-product recovery is still challenging in the liquid-phase catalytic processes. Here, we report on the synthesis of a hierarchical structured catalyst that consisted of oxygen functionalized graphite felt (OGF) support for liquid-phase processes. The monolith palladium-based catalyst was used as catalytic stirrer and displays excellent stability as well as complete recyclability for liquid-phase hydrogenation of α, β-unsaturated cinnamaldehyde. The surface defects decorated with abundant oxygenated groups as well as highly accessible porous structure generated from the acid treatment of carbon support, construct a bridge between Pd and support providing the charge transfer to alter the metal-support interactions. The electron-deficient high-valent Pdδδ+ species, formed on the metal NPs, and defects on the support help to enhance the Pd dispersion and resistance to sintering and/or aggregation during both catalyst preparation and cycling tests, leading to the high and stable hydrogen dissociative adsorption for hydrogenation process.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2018.11.041