Stability of gold nanocatalysts supported on mesoporous silica for the oxidation of 5-hydroxymethyl furfural to furan-2,5-dicarboxylic acid

被引:29
作者
Masoud, Nazila [1 ]
Donoeva, Baira [1 ]
de Jongh, Petra E. [1 ]
机构
[1] Univ Utrecht, Inorgan Chem & Catalysis, Debye Inst Nanomat Sci, Univ Weg 99, NL-3589 CG Utrecht, Netherlands
基金
欧盟地平线“2020”;
关键词
Gold catalysis; Support morphology; Particle growth; Nanoparticles; Selective oxidation; SELECTIVE AEROBIC OXIDATION; LONG-TERM STABILITY; 2,5-FURANDICARBOXYLIC ACID; MILD CONDITIONS; AU CATALYSTS; AQUEOUS-SOLUTION; HMF; CONVERSION; GLUCOSE; BASE;
D O I
10.1016/j.apcata.2018.05.027
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
The synthesis of furan-2,5-dicarboxylic acid via catalytic oxidation of 5-hydroxymethyl furfural is an important step for the production of bio-sourced polymers. We report on the activity of SiO2 -supported Au catalysts for this reaction. These catalysts reached 74% furan-2,5-dicarboxylic acid yield at 90 degrees C in 5 h when 5-hydroxymethyl furfural to Au molar ratio was 72. We also investigated the influence of the morphologies of the silica supports on the growth of Au nanoparticles under reaction conditions. Pronounced growth of Au nanoparticles occurred on Aerosil, SiO2 with a disordered porosity and 50 nm average pore diameter: Au nanoparticles grew from 2.4 to 10.1 nm. However, by using ordered mesoporous supports, the growth of the gold nanoparticles was successfully minimized. Also the reaction conditions influenced the particle growth; for instance using HCO3- as a base led to more pronounced particle growth than using NaOH. Particle diffusion in solution, and subsequent coalescence and agglomeration was proposed to be the dominant particle growth mechanism. Our results show the importance of support morphology in mitigation of Au particle growth in liquid phase oxidation reactions.
引用
收藏
页码:150 / 157
页数:8
相关论文
共 51 条
[1]   Conversion of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid over Au-based catalysts: Optimization of active phase and metal-support interaction [J].
Albonetti, Stefania ;
Lolli, Alice ;
Morandi, Vittorio ;
Migliori, Andrea ;
Lucarelli, Carlo ;
Cavani, Fabrizio .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2015, 163 :520-530
[2]  
[Anonymous], 2018, SYNVINA JOINT VENTUR
[3]   Selective oxidation of D-glucose on gold catalyst [J].
Biella, S ;
Prati, L ;
Rossi, M .
JOURNAL OF CATALYSIS, 2002, 206 (02) :242-247
[4]   Technology development for the production of biobased products from biorefinery carbohydrates-the US Department of Energy's "Top 10" revisited [J].
Bozell, Joseph J. ;
Petersen, Gene R. .
GREEN CHEMISTRY, 2010, 12 (04) :539-554
[5]   Gold Nanoclusters Confined in a Supercage of Y Zeolite for Aerobic Oxidation of HMF under Mild Conditions [J].
Cai, Jiaying ;
Ma, Hong ;
Zhang, Junjie ;
Song, Qi ;
Du, Zhongtian ;
Huang, Yizheng ;
Xu, Jie .
CHEMISTRY-A EUROPEAN JOURNAL, 2013, 19 (42) :14215-14223
[6]   Biomass into Chemicals: Aerobic Oxidation of 5-Hydroxymethyl-2-furfural into 2,5-Furandicarboxylic Acid with Gold Nanoparticle Catalysts [J].
Casanova, Onofre ;
Iborra, Sara ;
Corma, Avelino .
CHEMSUSCHEM, 2009, 2 (12) :1138-1144
[7]   The catalytic activity of "Naked" gold particles [J].
Comotti, M ;
Della Pina, C ;
Matarrese, R ;
Rossi, M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (43) :5812-5815
[8]  
Cvd J., 2016, LIQUID PHASE AEROBIC, P313
[9]   On the mechanism of selective oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid over supported Pt and Au catalysts [J].
Davis, Sara E. ;
Zope, Bhushan N. ;
Davis, Robert J. .
GREEN CHEMISTRY, 2012, 14 (01) :143-147
[10]   Oxidation of 5-hydroxymethylfurfural over supported Pt, Pd and Au catalysts [J].
Davis, Sara E. ;
Houk, Levi R. ;
Tamargo, Erin C. ;
Datye, Abhaya K. ;
Davis, Robert J. .
CATALYSIS TODAY, 2011, 160 (01) :55-60