Hao Zhang , Tianyu Gao , Qizhao Zhang , Bang Gu , Qinghu Tang , Qiue Cao , Wenhao Fang
{"title":"Synergistic catalysis in loaded PtRu alloy nanoparticles to boost base-free aerobic oxidation of 5-hydroxymethylfurfural","authors":"Hao Zhang , Tianyu Gao , Qizhao Zhang , Bang Gu , Qinghu Tang , Qiue Cao , Wenhao Fang","doi":"10.1016/j.mtcata.2023.100013","DOIUrl":null,"url":null,"abstract":"<div><p>The synergistic catalysis of dual metal sites is vital for selective activation of complicated chemical bonds in biomass compounds. The base-free selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) using air as oxidant and water as solvent is a highly sustainable upgrading process for cellulosic carbohydrates. In this work, a series of Pt<sub><em>x</em></sub>Ru-MgAlO (<em>x</em> = 0.5, 1, 2 and 3, in mole) nanocatalysts with controlled particle sizes (<em>ca.</em> 2 nm) were synthesized by a PVP-assisted adsorption method. The Pt<sub>2</sub>Ru-MgAlO catalyst showed 99% selectivity of FDCA with full conversion of HMF at only 100 °C under 0.2 MPa of air. In the meantime, an initial reaction rate of HMF of 2.8 mmol mol<sub>M</sub><sup>−1</sup> s<sup>−1</sup> and an intrinsic turnover frequency of 61.5 h<sup>−1</sup> were attained, respectively. Besides, this catalyst exhibited superior stability during five consecutive reuses without metal leaching. It was disclosed that the Pt-Ru interaction played critical roles in determining the intrinsic activity and the C<img>O bond activation of the prepared Pt<sub><em>x</em></sub>Ru-MgAlO catalysts. Kinetic experiments combined with <em>in situ</em> chemisorption techniques clearly unraveled adsorption and activation processes of C<img>O bond on Pt<sup>0</sup>-Ru<sup>0</sup> sites. To the best of our knowledge, this work firstly reported a PtRu bimetallic catalyst for aerobic oxidation of HMF and provided insight into synergistic catalysis.</p></div>","PeriodicalId":100892,"journal":{"name":"Materials Today Catalysis","volume":"3 ","pages":"Article 100013"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949754X23000133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
The synergistic catalysis of dual metal sites is vital for selective activation of complicated chemical bonds in biomass compounds. The base-free selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) using air as oxidant and water as solvent is a highly sustainable upgrading process for cellulosic carbohydrates. In this work, a series of PtxRu-MgAlO (x = 0.5, 1, 2 and 3, in mole) nanocatalysts with controlled particle sizes (ca. 2 nm) were synthesized by a PVP-assisted adsorption method. The Pt2Ru-MgAlO catalyst showed 99% selectivity of FDCA with full conversion of HMF at only 100 °C under 0.2 MPa of air. In the meantime, an initial reaction rate of HMF of 2.8 mmol molM−1 s−1 and an intrinsic turnover frequency of 61.5 h−1 were attained, respectively. Besides, this catalyst exhibited superior stability during five consecutive reuses without metal leaching. It was disclosed that the Pt-Ru interaction played critical roles in determining the intrinsic activity and the CO bond activation of the prepared PtxRu-MgAlO catalysts. Kinetic experiments combined with in situ chemisorption techniques clearly unraveled adsorption and activation processes of CO bond on Pt0-Ru0 sites. To the best of our knowledge, this work firstly reported a PtRu bimetallic catalyst for aerobic oxidation of HMF and provided insight into synergistic catalysis.