Evaluation of H2 effect on NO oxidation over a diesel oxidation catalyst

被引:19
作者
Azis, Muhammad Mufti [1 ]
Auvray, Xavier [1 ]
Olsson, Louise [1 ]
Creaser, Derek [1 ]
机构
[1] Chalmers Univ Technol, Dept Chem & Chem Engn, Competence Ctr Catalysis, SE-41296 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
Hydrogen; Diesel oxidation catalyst; NO oxidation; Pt oxide; Exhaust emission; PLATINUM OXIDE FORMATION; EXCESS OXYGEN; PT/AL2O3; REDUCTION; CO; TEMPERATURE; DISPERSION; PD;
D O I
10.1016/j.apcatb.2015.05.054
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 influence of H-2 on NO oxidation over Pt/Al2O3 as a model DOC catalyst was evaluated with various DOC feed mixtures. Discrimination of surface chemistry and exothermal effects due to addition of H-2 was made based on differences in time scales of transient responses. H-2 was proposed to retard Pt oxide formation mainly at low temperatures (ca. <200 degrees C), whereas, at higher temperatures Pt oxide formation was unhindered by H-2. As a result, a temporal enhancement in NO2 yield due to H-2 was obtained during temperature ramp experiments. In C3H6 containing mixtures, it was evident that the promotional role of H-2 was to weaken the inhibition effect of C3H6 by lowering the light-off temperature for C3H6 oxidation. The results from transient experiments clearly showed an increase in NO2 yield that resulted from effects of H-2 on surface chemistry and/or reactions. H-2 decreased the blocking effect of adsorbed C3H6 species and prevented the reaction of C(3)H(6)with NO2 forming NO. For a complete DOC feed mixture (containing NO, CO, C3H6), an addition of ca. 250 ppm of H-2 appeared to be optimal, while higher H-2 concentrations were disadvantageous due to NO2 consumption by H-2. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:542 / 550
页数:9
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