Efficient V2O5/TiO2 composite catalysts for dimethoxymethane synthesis from methanol selective oxidation

被引:41
作者
Fan, Zhihong [1 ,2 ,3 ]
Guo, Heqin [1 ]
Fang, Kegong [1 ]
Sun, Yuhan [4 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Shanxi Agr Univ, Taigu 030801, Shanxi, Peoples R China
[4] Chinese Acad Sci, Shanghai Adv Res Inst, Low Carbon Convers Ctr, Shanghai 201203, Peoples R China
关键词
OXIDE MONOLAYER CATALYSTS; TEMPERATURE-PROGRAMMED REDUCTION; SUPPORTED-VANADIA CATALYSTS; VAPOR-PHASE OXIDATION; REDOX PROPERTIES; V2O5; TITANIUM; NO; FORMALDEHYDE; PERFORMANCE;
D O I
10.1039/c4ra16727a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of V2O5/TiO2 composite catalysts (V2O5-TiO2-Al2O3, V2O5-TiO2-SiO2, V2O5-TiO2-Ce2O3 and V2O5-TiO2-ZrO2) were prepared by an improved rapid sol-gel method and the catalytic behavior for dimethoxymethane (DMM) synthesized from methanol selective oxidation was investigated. The physicochemical properties of catalysts were characterized by X-ray diffraction (XRD), BrunauerEmmett-Teller isotherms (BET), X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H-2-TPR), NH3 temperature programmed desorption (NH3-TPD), infrared spectroscopy of adsorbed pyridine (Py-IR) and transmission electron microscopy (TEM) techniques. The best catalytic performance was obtained on a V2O5-TiO2-SiO2 catalyst with methanol conversion of 51% and DMM selectivity of 99% at 413 K. Furthermore, the V2O5-TiO2-SiO2 catalyst displayed an excellent catalytic stability within 240 h. Results showed that more Bronsted acidic sites were critical to increasing the DMM yield. The activity of V2O5/TiO2 composite catalysts decreased with increasing Bronsted acidity, but the yield of DMM increased with an increasing amount of Bronsted acidic sites. The excellent performance of the V2O5-TiO2-SiO2 catalyst might come from its optimal acidity and redox properties, higher active surface oxygen species, together with more Bronsted acid sites.
引用
收藏
页码:24795 / 24802
页数:8
相关论文
共 54 条
[1]   ESCA INVESTIGATION OF V2O5+TIO2 CATALYSTS FOR THE VAPOR-PHASE OXIDATION OF ALKYLPYRIDINES [J].
ANDERSSON, SLT .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1979, 75 :1356-1370
[2]   Selective electrochemical oxidation of methanol to dimethoxymethane using Ru/Sn catalysts [J].
Anthony, CR ;
McElwee-White, L .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 227 (1-2) :113-117
[3]   Structure and dispersion of supported-vanadia catalysts. Influence of the oxide carrier [J].
Arena, F ;
Frusteri, F ;
Parmaliana, A .
APPLIED CATALYSIS A-GENERAL, 1999, 176 (02) :189-199
[4]   Acidity characterization by microcalorimetry and relationship with reactivity [J].
Auroux, A .
TOPICS IN CATALYSIS, 1997, 4 (1-2) :71-89
[5]   Methanol: a "smart" chemical probe molecule [J].
Badlani, M ;
Wachs, IE .
CATALYSIS LETTERS, 2001, 75 (3-4) :137-149
[6]   INFLUENCE OF GRAIN MORPHOLOGY OF V2O5 ON ITS REDUCIBILITY AND SELECTIVITY FOR METHANOL OXIDATION [J].
BAIKER, A ;
MONTI, D .
JOURNAL OF CATALYSIS, 1985, 91 (02) :361-365
[7]   The role of vanadium oxide on the titania transformation under thermal treatments and surface vanadium states [J].
Banares, MA ;
Alemany, LJ ;
Jimenez, MC ;
Larrubia, MA ;
Delgado, F ;
Granados, VL ;
MartinezArias, A ;
Blasco, JM ;
Fierro, JLG .
JOURNAL OF SOLID STATE CHEMISTRY, 1996, 124 (01) :69-76
[8]   Ionic dispersion of Pt and Pd on CeO2 by combustion method:: Effect of metal-ceria interaction on catalytic activities for NO reduction and CO and hydrocarbon oxidation [J].
Bera, P ;
Patil, KC ;
Jayaram, V ;
Subbanna, GN ;
Hegde, MS .
JOURNAL OF CATALYSIS, 2000, 196 (02) :293-301
[9]   Temperature-programmed reduction and oxidation experiments with V2O5/TiO2 catalysts [J].
Besselmann, S ;
Freitag, C ;
Hinrichsen, O ;
Muhler, M .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2001, 3 (21) :4633-4638
[10]   VANADIUM-OXIDE MONOLAYER CATALYSTS - PREPARATION, CHARACTERIZATION AND CATALYTIC ACTIVITY [J].
BOND, GC ;
TAHIR, SF .
APPLIED CATALYSIS, 1991, 71 (01) :1-31