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Cyclodextrin‐Based Polymer‐Assisted Ru Nanoparticles for the Aqueous Hydrogenation of Biomass‐Derived Platform Molecules
25
Citations
62
References
2017
Year
EngineeringPolymer NanotechnologyGreen ChemistryLevulinic AcidChemistryPolymersChemical EngineeringBiomass ConversionRu NanoparticlesMacromolecular EngineeringBiomass‐derived Platform MoleculesHybrid MaterialsPlatform ChemicalPolymer ChemistryAqueous HydrogenationNatural PolymerBiopolymersHydrogen Production TechnologyCatalysisHydrogenDispersed Ru NpsCyclodextrin ProductionPolymer SciencePolymer ReactionPolymer SynthesisCo‐ploymer Peg‐cd Matrix
Abstract A green water‐soluble cyclodextrin polymer has been prepared through cross‐linking of β‐cyclodextrin (β‐CD) and polyethylene glycol diglycidyl ether (PEGDE). The as‐synthesized co‐polymer (PEG‐CD) showed an excellent ability to stabilize and constrain the size of Ru‐Nanoparticles in aqueous phase, as compared with other polymer stabilizer used in this work such as polyvinyl pyrrolidone (PVP−K30) and polyethylene glycol diglycidyl ether (PEGDE). The co‐ploymer PEG‐CD‐stabilizied Ru NPs have been found to be a highly efficient catalyst in the aqueous hydrogenation of levulinic acid into γ‐valerolactone under mild reaction condition. This catalyst system can be easily extended to the selective hydrogenation of other lignocellulose‐derived platform molecule including 5‐hydroxymethylfurfural, furfural, phenol, 2‐methoxy‐4‐methyl phenol and 2‐methoxy‐4‐ethyl phenol, etc. The further characterization analysis indicated that the small‐sized and highly dispersed Ru NPs (1.2‐2.0 nm) embedded in co‐ploymer PEG‐CD matrix were highly stable for the consecutive catalytic recycles. Additionally, the inclusion interaction of substrate molecules and β‐CD units within polymer matrix played a crucial role in the enhancement of catalytic performance.
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