High {001} faceted TiO2 nanoparticles for the valorization of oxygenated compounds present in aqueous biomass-derived feedstocks

被引:18
作者
Fernandez-Arroyo, A. [1 ]
Lara, M. A. [2 ]
Domine, M. E. [1 ]
Sayagues, M. J. [2 ]
Navio, J. A. [2 ]
Hidalgo, M. C. [2 ]
机构
[1] Univ Politecn Valencia, CSIC, UPV, Consejo Super Invest Cient,Inst Tecnol Quim, Avda Naranjos S-N, E-46022 Valencia, Spain
[2] Univ Seville, CSIC, ICMS, Consejo Super Invest Cient, Amer Vespucio 49, Seville 41092, Spain
关键词
{001} faceted TiO2; Bio-oils; Condensation; Oxygenated compounds; Aqueous effluents; SITE REQUIREMENTS; CARBOXYLIC-ACIDS; PYROLYSIS OIL; HYDROCARBONS; CATALYSTS; FUELS; TRANSFORMATION; DEACTIVATION; KETONIZATION; CONDENSATION;
D O I
10.1016/j.jcat.2017.12.018
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
{0 0 1} faceted TiO2 catalysts are hydrothermally synthesized by using titanium(IV) isopropoxide and butoxide precursors (ISO and BUT TiO2 samples) together with HF addition. Their activity and stability are evaluated in the catalytic condensation of light oxygenated organic compounds present in an aqueous model mixture simulating a real bio-refinery effluent, under moderate operation conditions. High {0 0 1} faceted TiO2 catalysts show organic products yields superior to those attained with other TiO2 samples (anatase, rutile, and P25). This enhanced catalytic activity relates to their physico-chemical and textural properties, such as high surface area (approximate to 100 m(2)/g), regular morphology (platelets conformed by partially agglomerated TiO2 nanoparticles), and adequate Lewis acidity. XRD and Raman measurements evidence the unique presence of anatase crystalline phase in both ISO and BUT materials, in which the use of HF during synthesis produces the preferential growth of TiO2 crystals mainly exposing the {0 0 1} plane. This effective {0 0 1} facet exposition directly determines catalytic results. Moreover, TiO2 ISO catalyst shows outstanding stability under reaction conditions, maintaining practically unaltered their activity after several re-uses. In particular, Lewis acid sites present in TiO2 faceted materials are more stable in the presence of organic acids under aqueous environments. This opens new possibilities for the application of these materials in the valorization of light oxygenated compounds present in biomass-derived aqueous effluents. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:266 / 276
页数:11
相关论文
共 40 条
  • [1] Catalytic conversion of biomass to biofuels
    Alonso, David Martin
    Bond, Jesse Q.
    Dumesic, James A.
    [J]. GREEN CHEMISTRY, 2010, 12 (09) : 1493 - 1513
  • [2] Enhanced activity and stability of Ru-TiO2 rutile for liquid phase ketonization
    Aranda-Perez, Nicolds
    Pilar Ruiz, M.
    Echave, Javier
    Faria, Jimmy
    [J]. APPLIED CATALYSIS A-GENERAL, 2017, 531 : 106 - 118
  • [3] Model compound approach to design process and select catalysts for in-situ bio-oil upgrading
    Asadieraghi, Masoud
    Daud, Wan Mohd Ashri Wan
    Abbas, Hazzim F.
    [J]. RENEWABLE & SUSTAINABLE ENERGY REVIEWS, 2014, 36 : 286 - 303
  • [4] Review of fast pyrolysis of biomass and product upgrading
    Bridgwater, A. V.
    [J]. BIOMASS & BIOENERGY, 2012, 38 : 68 - 94
  • [5] Co-processing of pyrolisis bio oils and gas oil for new generation of bio-fuels: Hydrodeoxygenation of guaiacol and SRGO mixed feed
    Bui, Van Ngoc
    Toussaint, Guy
    Laurenti, Dorothee
    Mirodatos, Claude
    Geantet, Christophe
    [J]. CATALYSIS TODAY, 2009, 143 (1-2) : 172 - 178
  • [6] Liquid-phase catalytic processing of biomass-derived oxygenated hydrocarbons to fuels and chemicals
    Chheda, Juben N.
    Huber, George W.
    Dumesic, James A.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (38) : 7164 - 7183
  • [7] Climent MJ, 2002, ADV SYNTH CATAL, V344, P1090, DOI 10.1002/1615-4169(200212)344:10<1090::AID-ADSC1090>3.0.CO
  • [8] 2-X
  • [9] Hydrogen from catalytic reforming of biomass-derived hydrocarbons in liquid water
    Cortright, RD
    Davda, RR
    Dumesic, JA
    [J]. NATURE, 2002, 418 (6901) : 964 - 967
  • [10] Domine M. E., 2017, [No title captured], Patent No. [WO2017/162900A1, 2017162900]