Platinum catalysed aerobic selective oxidation of cinnamaldehyde to cinnamic acid

被引:19
作者
Durndell, Lee J. [1 ]
Cucuzzella, Costanza [1 ]
Parlett, Christopher M. A. [1 ]
Isaacs, Mark A. [1 ]
Wilson, Karen [2 ]
Lee, Adam F. [2 ]
机构
[1] Aston Univ, European Bioenergy Res Inst, Birmingham B4 7ET, W Midlands, England
[2] RMIT Univ, Sch Sci, Melbourne, Vic 3001, Australia
基金
英国工程与自然科学研究理事会;
关键词
Platinum; Cinnamaldehyde; Oxidation; Porous; Silica; ALCOHOL OXIDATION; 2,5-FURANDICARBOXYLIC ACID; CARBONYL-COMPOUNDS; MOLECULAR-OXYGEN; PHASE OXIDATION; AIR; GLYCEROL; DEHYDROGENATION; ALDEHYDES; BASE;
D O I
10.1016/j.cattod.2018.02.052
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Aerobic selective oxidation of allylic aldehydes offers an atom and energy efficient route to unsaturated carboxylic acids, however suitable heterogeneous catalysts offering high selectivity and productivity have to date proved elusive. Herein, we demonstrate the direct aerobic oxidation of cinnamaldehyde to cinnamic acid employing silica supported Pt nanoparticles under base-free, batch and continuous flow operation. Surface and bulk characterisation of four families of related Pt/silica catalysts by XRD, XPS, HRTEM, CO chemisorption and N-2 porosimetry evidence surface PtO2 as the common active site for cinnamaldehyde oxidation, with a common turnover frequency of 49,000 +/- 600 h(-1); competing cinnamaldehyde hydrogenolysis is favoured over metallic Pt. High area mesoporous (SBA-15 or KIT-6) and macroporous-mesoporous SBA-15 silicas confer significant rate and cinnamic acid yield enhancements versus low area fumed silica, due to superior platinum dispersion. High oxygen partial pressures and continuous flow operation stabilise PtO2 active sites against in-situ reduction and concomitant deactivation, further enhancing cinnamic acid productivity.
引用
收藏
页码:161 / 168
页数:8
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