N-doped carbon supported Pt catalyst for base-free oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid

被引:97
|
作者
Han, Xuewang [1 ]
Li, Chaoqun [1 ]
Guo, Yong [2 ]
Liu, Xiaohui [1 ]
Zhang, Yongguang [2 ]
Wang, Yanqin [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Res Inst Ind Catalysis, Meilong Rd 130, Shanghai 200237, Peoples R China
[2] Sinopec, RIPP, 18 Xueyuan Rd 18,POB 914-12, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
N-doped carbon; Base-free oxidation; 2,5-Furandicarboxylic acid; SELECTIVE AEROBIC OXIDATION; BIOMASS; NANOPARTICLES; CHEMICALS; PHASE; AU; NITROGEN; FUELS; CONVERSION; MECHANISM;
D O I
10.1016/j.apcata.2016.07.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new kind of N-doped carbon supported Pt catalyst (Pt/C) has been prepared for the selective oxidation of 5-Hydroxymethylfurfural (HMF) to 2,5-Furandicarboxylic Acid (FDCA) in base-free conditions. The catalyst (Pt/C-EDA-x) prepared by using ethylenediamine (EDA) as nitrogen source showed higher activity than those prepared by N,N-dimethylaniline (DMA), ammonia (NH3) or acetonitrile (ACN) as nitrogen sources. The Pt/C-EDA-4.1 catalyst showed the highest activity in the oxidation of HMF to FDCA and as high as 96.0% FDCA was obtained under optimal reaction conditions (110 degrees C, 1.0 MPa O-2, 12 h). The samples were characterized by XRD, XPS, CO2-TPD, TEM, SEM, and elemental analysis. XPS results showed that the pyridine-type nitrogen (N-6) played a key role in the selective oxidation of HMF, which can be attributed to the basicity of N-6 site. CO2-TPD measurements also showed that the involving of N elements in catalyst preparation introduced a new kind of medium basic site on the support surface. The influence of reaction time, catalyst dosage, and temperature on the HMF oxidation to FDCA catalyzed by Pt/C-EDA-4.1 was studied. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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