Deoxygenation of oleic acid: Influence of the synthesis route of Pd/mesoporous carbon nanocatalysts onto their activity and selectivity

被引:42
作者
Dragu, A. [1 ]
Kinayyigit, S. [2 ,3 ,4 ]
Garcia-Suarez, E. J. [2 ,3 ,5 ]
Florea, M. [1 ]
Stepan, E. [6 ]
Velea, S. [6 ]
Tanase, L. [7 ]
Colliere, V. [2 ,3 ]
Philippot, K. [2 ,3 ]
Granger, P. [7 ]
Parvulescu, V. I. [1 ]
机构
[1] Univ Bucharest, Fac Chem, Dept Organ Chem Biochem & Catalysis, Bucharest 030016, Romania
[2] CNRS, LCC, F-31077 Toulouse 4, France
[3] Univ Toulouse, UPS, INPT, LCC, F-31077 Toulouse, France
[4] Sabanci Univ, Nanotechnol Res & Applicat Ctr, TR-34956 Istanbul, Turkey
[5] INCAR CSIC, Inst Nacl Carbon, E-33080 Oviedo, Spain
[6] Sci Res & Technol Dev Chem & Petrochem Ind, Bucharest 060021, Romania
[7] Univ Lille1 Sci & Technol, Unite Catalyse & Chim Solide, UMR 8181, F-59650 Villeneuve Dascq, France
关键词
Palladium; Supported nanoparticle; Mesoporous carbon; Catalysis; Oleic acid; Deoxygenation reaction; CATALYTIC DEOXYGENATION; DIESEL FUEL; FATTY-ACID; PALLADIUM CATALYSTS; REACTION PATHWAYS; PROPANOIC ACID; STEARIC-ACID; DECARBOXYLATION; OIL; PD;
D O I
10.1016/j.apcata.2015.01.008
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
Supported Pd nanocatalysts were prepared by deposition of Pd nanoparticles (NPs) onto spherical mesoporous carbon beads (MB) functionalized by thermal or acidic treatement The Pd NPs were synthesized by decomposition of [Pd-2(dba)(3)] (dba: dibenzylideneacetone) under dihydrogen either directly on the carbon supports without stabilizer leading to naked Pd NPs (Pd/MB series) or in solution in the presence of a stabilizer (polymer (PVP series) or triphenylphosphine (TPP series)) to obtain stable colloidal solutions that were further used to impregnate the carbon materials to have carbon-deposited Pd NPs. The NPs deposited on carbon displayed a Pd loading from 0.5 to 14.8 wt.% and were characterized by different techniques (nitrogen physisorption at 77 K, H-2-chemissorption and TPD, XRD, XPS and HRTEM). Their catalytic performance in deoxygenation of oleic acid was evaluated in batch and flow reaction conditions. Flow conditions led to superior results compared to batch. No aromatic compounds were detected as side products, but in the case of the Pd/MB series, octadecanol and octadecane were significantly formed suggesting the involvement of a deoxygenation mechanism in which the hydrocarbons were produced via both decarbonylation/decarboxylation and dehydration steps. Further experiments carried out in H-2/N-2 mixture or in pure N-2 highlighted the key role of hydrogen. For a N-2/H-2 of 2.5:1 the dehydration route was crossing out and even no traces of octadecanol nor octadecane were detected. Then, complete removal of H-2 produced heptadecene in a high excess compared to heptadecane (almost 7-1) thus suggesting the decarbonylation/decarboxylation steps as the main route. ICP-OES measurements indicated no leaching of palladium and simple washing of catalysts with mesitylene allowed recycling without any change in conversion or product distribution. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:81 / 91
页数:11
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