期刊
JOURNAL OF CATALYSIS
卷 225, 期 2, 页码 359-368出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2004.03.046
关键词
kinetic modeling; ammonia synthesise; promotion of ruthenium; cesium; barium; lanthanum; magnesium oxide
The kinetics of ammonia synthesis over unpromoted and Cs-, Ba-, and La-promoted Ru/MgO (similar to 2 wt%) were studied in a tubular reactor at 20.7 atm. The reaction over all of the catalysts was nearly first order in N-2 and nearly zero order in NH3. However, the order of reaction in H-2) was largely dependent on the choice of promoter, with Ba and La significantly reducing the inhibition by dihydrogen seen oil Cs-promoted Ru/MgO. The turnover frequencies on Ba- and La-promoted Ru/M-O under stoichiometric conditions and 673 K were almost an order of magnitude greater than that on Cs-promoted Ru/MgO. Two kinetic models with optimized parameters were used to describe the Outlet ammonia pressures determined experimentally both close to and far from equilibrium. Although Cs promotion of Ru lowered the activation barrier for N-2 dissociation. the enthalpy of dihydrogen adsorption and therefore the H atom surface coverage increased. Thus, promotion of Ru catalysts with bases cannot be attributed solely to an effect on dinitrogen dissociation, which is the rate-determining step. Base promotion is a trade-off between lowering the activation barrier for N-2 dissociation and increasing the competitive adsorption of H-2. The coverages of nitrogen-containing species determined by an optimized kinetic model matched well those determined experimentally by isotopic transient analysis over the same catalysts. (C) 2004 Elsevier Inc. All rights reserved.
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