Importance of the oxygen bond strength for catalytic activity in soot oxidation

被引:35
作者
Christensen, Jakob M. [1 ]
Grunwaldt, Jan-Dierk [1 ,2 ]
Jensen, Anker D. [1 ]
机构
[1] Tech Univ Denmark, Dept Chem & Biochem Engn, Soltofts Plads B229, DK-2800 Lyngby, Denmark
[2] Karlsruhe Inst Technol, Inst Chem Technol & Polymer Chem ITCP, Engesserstr 20, D-76131 Karlsruhe, Germany
关键词
Soot oxidation; Oxygen bond strength; Heat of chemisorption; Volcano curve; Bronsted-Evans-Polanyi relationship; TRANSITION-METAL; ISOTOPIC-EXCHANGE; DIESEL EXHAUST; EQUILIBRIUM PRESSURE; VANADIUM PENTOXIDE; ACTIVATED OXYGEN; CARBON-MONOXIDE; PARTICULATE; SURFACE; OXIDE;
D O I
10.1016/j.apcatb.2016.01.068
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
The oxygen bond strength on a catalyst, as measured by the heat of oxygen chemisorption, is observed to be a very important parameter for the activity of the catalyst in soot oxidation. With both intimate contact between soot and catalyst (tight contact) and with the solids stirred loosely together (loose contact) the rate constants for a number of catalytic materials outline a volcano curve when plotted against their heats of oxygen chemisorption. However, the optima of the volcanoes correspond to different heats of chemisorption for the two contact situations. In both cases the activation energies for soot oxidation follow linear Bronsted-Evans-Polanyi relationships with the heat of oxygen chemisorption. Among the tested metal or metal oxide catalysts Co3O4 and CeO2 were nearest to the optimal bond strength in tight contact oxidation, while Cr2O3 was nearest to the optimum in loose contact oxidation. The optimum of the volcano curve in loose contact is estimated to occur between the bond strengths of alpha-Fe2O3 and alpha-Cr2O3. Guided by an interpolation principle FeaCrb Ox binary oxides were tested, and the activity of these oxides was observed to pass through an optimum for an FeaCr2Ox binary oxide catalyst, which exhibited a rate constant at 550 degrees C that was 2.3 times higher than the one for pure alpha-Cr2O3 and 29 times higher than the one for pure alpha-Fe2O3. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 244
页数:10
相关论文
共 111 条
[1]   Ceramic diesel particulate filters [J].
Adler, J .
INTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, 2005, 2 (06) :429-439
[2]   Climate's Dark Forcings [J].
Andreae, Meinrat O. ;
Ramanathan, V. .
SCIENCE, 2013, 340 (6130) :280-281
[3]   The formation of nanodomains of Ce6O11 in ceria catalyzed soot combustion [J].
Aneggi, Eleonora ;
Divins, Nuria J. ;
de Leitenburg, Carla ;
Llorca, Jordi ;
Trovarelli, Alessandro .
JOURNAL OF CATALYSIS, 2014, 312 :191-194
[4]  
Antoshin G. V., 1967, VESTN AN SSSR+, V16, P1793
[5]   STANDARD ENTHALPY OF FORMATION OF CRYSTALLINE GOLD (III) OXIDE [J].
ASHCROFT, SJ ;
SCHWARZM.E .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1972, 68 (07) :1360-&
[6]   CATALYTIC GASIFICATION OF GRAPHITE BY CHROMIUM AND COPPER IN OXYGEN, STEAM AND HYDROGEN [J].
BAKER, RTK ;
CHLUDZINSKI, JJ .
CARBON, 1981, 19 (02) :75-82
[7]  
Balandin A. A., 1969, ADV CATAL, V19, P1, DOI [10.1016/S0360-0564(08)60029-2, DOI 10.1016/S0360-0564(08)60029-2]
[8]   SURFACE STUDIES ON GRAPHITE - ACIDIC SURFACE OXIDES [J].
BARTON, SS ;
BOULTON, GL ;
HARRISON, BH .
CARBON, 1972, 10 (04) :395-&
[9]   SURFACE STUDIES ON GRAPHITE - DESORPTION OF SURFACE OXIDE [J].
BARTON, SS ;
HARRISON, BH ;
DOLLIMOR.J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1973, 69 :1039-1048
[10]   SURFACE STUDIES ON GRAPHITE - DESORPTION OF SURFACE OXIDES FORMED ON CLEAN SURFACE AT 300-K [J].
BARTON, SS ;
HARRISON, BH ;
DOLLIMORE, J .
JOURNAL OF PHYSICAL CHEMISTRY, 1978, 82 (03) :290-294