Highly dispersed uniformly sized Pt nanoparticles on mesoporous Al-SBA-15 by solid state impregnation

被引:46
作者
Medina-Mendoza, Ana K. [1 ,2 ]
Cortes-Jacome, Maria A. [1 ]
Toledo-Antonio, Jose A. [1 ]
Angeles-Chavez, Carlos [1 ]
Lopez-Salinas, Esteban [1 ]
Cuauhtemoc-Lopez, Ignacio [1 ]
Barrera, Maria C. [1 ]
Escobar, Jose [1 ]
Navarrete, Juan [1 ]
Hernandez, Isaias [2 ]
机构
[1] Inst Mexicano Petr, Programa Ingn Mol, Mexico City 07730, DF, Mexico
[2] Univ Autonoma Metropolitana Azcapotzalco, Dept Ciencias Basicas, Mexico City 02200, DF, Mexico
关键词
Pt nanoparticles; Al-SBA-15; Solid state impregnation; Chemical grafting; Naphthalene hydrogenation; ATR-FTIRAS METHODS; PLATINUM CATALYSTS; PARTICLE-SIZE; ELECTRON-MICROSCOPY; TITANIA NANOTUBES; SBA-15; SILICA; BASE METALS; HYDROGEN; OXIDATION; SURFACE;
D O I
10.1016/j.apcatb.2011.04.031
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
Highly dispersed Pt nanoparticles on modified mesoporous Al-SBA-15 were obtained by a solid state impregnation (SSI) methodology, which consisted of a physical mixture of Al-SBA-15 support with a given amount of Pt(acac)(2) in order to have 1 wt.% of Pt on the final solid. The solid mixture was ground vigorously and annealed at 180 degrees C (e.g. the sublimation point of Pt(acac)(2)) for 0.5 h and then at 400 degrees C in inert atmosphere, to decompose the organic ligand. The materials were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) by applying high angle annular dark field (HAADF) technique, nitrogen physisorption, pyridine adsorption by infrared spectroscopy (FTIR), X-ray photoelectronic spectroscopy (XPS) and FUR of CO adsorption. Catalytic activity of Pt nanoparticles was evaluated in naphthalene hydrogenation (HYD) as test reaction. The results were compared with those obtained on Pt nanoparticles dispersed on Al-SBA-15 by wet impregnation (WI) method. Both SSI and WI methods produce significant differences in the population of flat and edge sites on the Pt nanoparticles with dimensions around 1.0 nm. However, Pt nanoparticles obtained by SSI showed higher activity upon naphthalene HYD than those obtained by WI method, which was explained by the higher density of edge sites measured by FTIR of CO adsorption. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 25
页数:12
相关论文
共 106 条
  • [1] Anderson J.R., 1975, Structure of metallic catalysts
  • [2] THEORY AND PRACTICE OF THE FORMULATION OF HETEROGENEOUS CATALYSTS
    ANDREW, SPS
    [J]. CHEMICAL ENGINEERING SCIENCE, 1981, 36 (09) : 1431 - 1445
  • [3] An XPS study on oxidation states of Pt and its alloys with Co and Cr and its relevance to electroreduction of oxygen
    Aricò, AS
    Shukla, AK
    Kim, H
    Park, S
    Min, M
    Antonucci, V
    [J]. APPLIED SURFACE SCIENCE, 2001, 172 (1-2) : 33 - 40
  • [4] Poly(amidoamine) dendrimer-templated nanocomposites. 1. Synthesis of zerovalent copper nanoclusters
    Balogh, L
    Tomalia, DA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (29) : 7355 - 7356
  • [5] STUDY OF BENZENE HYDROGENATION AND IDENTIFICATION OF ADSORBED SPECIES WITH PT-AL2O3 CATALYSTS
    BASSET, JM
    DALMAIIMELIK, G
    PRIMET, M
    MUTIN, R
    [J]. JOURNAL OF CATALYSIS, 1975, 37 (01) : 22 - 36
  • [6] PREPARATION OF HIGHLY DISPERSED CATALYTIC METALS - PLATINUM SUPPORTED ON SILICA GEL
    BENESI, HA
    CURTIS, RM
    STUDER, HP
    [J]. JOURNAL OF CATALYSIS, 1968, 10 (04) : 328 - &
  • [7] THE INTERPRETATION OF CO ADSORBED ON PT/SIO2 OF 2 DIFFERENT PARTICLE-SIZE DISTRIBUTIONS
    BRANDT, RK
    HUGHES, MR
    BOURGET, LP
    TRUSZKOWSKA, K
    GREENLER, RG
    [J]. SURFACE SCIENCE, 1993, 286 (1-2) : 15 - 25
  • [8] Gas-phase hydrogenation of acetonitrile over Pt and Pt-Pd supported on mesoporous solids:: influence of the metallic precursor
    Carrión, MC
    Manzano, BR
    Jalón, FA
    Fuentes-Perujo, I
    Maireles-Torres, P
    Rodríguez-Castellón, E
    Jiménez-López, A
    [J]. APPLIED CATALYSIS A-GENERAL, 2005, 288 (1-2) : 34 - 42
  • [9] Carrott MMLR, 1999, LANGMUIR, V15, P8895
  • [10] Colin B.G., 2005, METAL CATALYSED REAC