Glycerol oxidation over gold supported catalysts - "Two faces" of sulphur based anchoring agent

被引:23
作者
Skrzynska, Elzbieta [1 ,2 ,3 ]
Ftouni, Jamal [2 ,3 ]
Mamede, Anne-Sophie [2 ,3 ]
Addad, Ahmed [3 ,4 ]
Trentesaux, Martine [2 ,3 ]
Girardon, Jean-Sebastien [2 ,3 ]
Capron, Mickael [2 ,3 ]
Dumeignil, Franck [2 ,3 ,5 ]
机构
[1] Cracow Univ Technol, Fac Chem Engn & Technol, PL-31155 Krakow, Poland
[2] UCCS, CNRS, Unite Catalyse & Chim Solide, UMR8181, F-59655 Villeneuve Dascq, France
[3] Univ Lille Nord France, F-590009 Lille, France
[4] CNRS, Unite Mat & Transformat, UMR 8207, F-59655 Villeneuve Dascq, France
[5] Maison Univ, Inst Univ France, F-75005 Paris, France
关键词
Glycerol oxidation; Supported gold catalyst; Au-S interactions; Inhibition by sulphur derivatives; SELF-ASSEMBLED MONOLAYERS; SELECTIVE OXIDATION; AU CATALYSTS; NANOPARTICLES; SURFACE; CO; ANTIOXIDANTS; COMPOSITE; ALCOHOL; METALS;
D O I
10.1016/j.molcata.2013.11.007
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
Three different alumina-supported catalysts were prepared according to 3 different methods, aiming at achieving fine deposition of gold particles. In methods 1 and 2, (3-aminopropyl)triethoxysilane (APTES) and (3-mercaptopropyl)triethoxysilane (MPTES) were respectively used as anchoring agents. In method 3, the gold particles were directly deposited on the support without using any anchoring agent. The performances of the so-obtained catalysts were evaluated in the reaction of glycerol partial oxidation in the liquid phase, and compared to those of a 1 wt.% Au/Al2O3 catalyst provided by Mintek. The best catalyst A3 (method 3) exhibited a 99% conversion at 600 degrees C after 2.5 h, with glyceric and glycolic acids selectivities of 60 and 20%, respectively. These performances were slightly higher than those of the reference commercial catalyst (95% conversion with glyceric and glycolic acids selectivities of 62 and 20%, respectively). In the case of A2 catalyst (method 2), in spite of very good dispersion of small nanoparticles on the surface, which is normally supposed to yield very active materials, a very strong inhibition of glycerol conversion was observed. After 2.5 h of process at 60 degrees C, the glycerol conversion did not exceed 4%. A similar behavior was also observed for TiO2- and ZnO-supported catalysts, prepared in the same manner (using MPTES). In order to get a better understanding of the parameters ruling the reactivity of the various catalytic systems, a series of experiments over the commercial catalyst was performed, in which small quantities of various sulphur derivatives and antioxidants were used in the reaction mixture to simulate the response of the various species that can be present in the lab-prepared samples (method 2). The results, together with XPS analysis, suggests that there are three possible interpretations of the observed inhibition effect: (i) a strong interaction between gold and sulphur leading to the formation of covalent Au-S bonds on nanoparticle's surface; (ii) the formation of so-called SAM's (selfassembled monolayers) blocking access to surface active centers; or (iii) an inhibition of the reactivity due to antioxidation properties of S-derivatives. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
相关论文
共 49 条
[1]  
Afanasev I. B., 2005, OXIDATION ANTIOXIDAN
[2]   How To Prevent the Loss of Surface Functionality Derived from Aminosilanes [J].
Asenath-Smith, Emily ;
Chen, Wei .
LANGMUIR, 2008, 24 (21) :12405-12409
[3]   Controlling the assembly of nanoparticles using surface grafted molecular and macromolecular gradients [J].
Bhat, RR ;
Genzer, J ;
Chaney, BN ;
Sugg, HW ;
Liebmann-Vinson, A .
NANOTECHNOLOGY, 2003, 14 (10) :1145-1152
[4]   Gold-sulfur bonding in 2D and 3D self-assembled monolayers: XPS characterization [J].
Bourg, MC ;
Badia, A ;
Lennox, RB .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (28) :6562-6567
[5]   Influence of Thermal Treatment on Nanostructured Gold Model Catalysts [J].
Bowker, Michael ;
Broughton, Melissa ;
Carley, Albert ;
Davies, Phil ;
Morgan, David ;
Crouch, Jon ;
Lalev, Georgi ;
Dimov, Stefan ;
Pham, Duc-Truong .
LANGMUIR, 2010, 26 (21) :16261-16266
[6]   Oxidation of glycerol using supported Pt, Pd and Au catalysts [J].
Carrettin, S ;
McMorn, P ;
Johnston, P ;
Griffin, K ;
Kiely, CJ ;
Hutchings, GJ .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (06) :1329-1336
[7]   XPS study of supported gold catalysts:: the role of Au0 and Au+δ species as active sites [J].
Casaletto, MP ;
Longo, A ;
Martorana, A ;
Prestianni, A ;
Venezia, AM .
SURFACE AND INTERFACE ANALYSIS, 2006, 38 (04) :215-218
[8]   Hydrogen production by partial oxidation of methanol over gold catalysts supported on TiO2-MOx (M = Fe, Co, Zn) composite oxides [J].
Chang, FW ;
Yu, HY ;
Roselin, LS ;
Yang, HC ;
Ou, TC .
APPLIED CATALYSIS A-GENERAL, 2006, 302 (02) :157-167
[9]   Rectifying nanoscale electron transfer by viologen moieties and hydrophobic electrolyte ions [J].
Chen, S ;
Deng, FJ .
LANGMUIR, 2002, 18 (23) :8942-8948
[10]   Deposition of highly dispersed gold on alumina support [J].
Chen, YJ ;
Yeh, CT .
JOURNAL OF CATALYSIS, 2001, 200 (01) :59-68