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首页> 外文期刊>Catalysis Letters >Perovskite-Based Lean-Burn NO_x Trap Catalysts Without Using Platinum Group Metals: K/LaCoO3/Ce_(1-x)Zr_xO2
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Perovskite-Based Lean-Burn NO_x Trap Catalysts Without Using Platinum Group Metals: K/LaCoO3/Ce_(1-x)Zr_xO2

机译:不使用铂族金属的钙钛矿基稀燃NO_x陷阱催化剂:K / LaCoO3 / Ce_(1-x)Zr_xO2

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摘要

A series of Ce_(1-x)Zr_xO2 (x = 0, 0.1, 0.2, 0.3) solid solution supported lean-burn NO_x trap (LNT) catalysts K/LaCoO3/Ce_(1-x)Zr_xO2 were prepared by successive impregnation. After sulfation the supported perovsikte LaCoO3 was well maintained; reducing treatment partly destroyed the perovsikte, but it can be well recovered by re-oxidation treatment. Based on NO_x storage and sulfur-resisting performance of the catalysts, the optimal atomic ratio of Zr in Ce_(1-x)Zr_xO2 support is x = 0.2. The catalyst K/LaCoO3/Ce_(0.8)Zr_(0.2)O2 exhibits much better NO_x storage capacity than the Pt-based catalyst Pt/K7Ce_(0.8)Zr_(0.2)O2, which is highly related to its stronger capability for NO to NO2 oxidation. During NO_x storage much larger amounts of nitrate and nitrite species were identified by in situ DRIFTS over perovskite-based catalysts than over Pt-based one. The H2-TPR results reveal that after deep sulfation little sulfur species were deposited on the catalyst K/La-CoO3/Ce_(1-x)Zr_xO2, showing strong sulfur-resisting ability. As a result, it is thought that the full replacement of Pt by perovskite LaCoO3 in the corresponding LNT catalysts is feasible.
机译:通过连续浸渍制备了一系列Ce_(1-x)Zr_xO2(x = 0,0.1,0.2,0.3)固溶负载型稀燃NO_x捕集(LNT)催化剂K / LaCoO3 / Ce_(1-x)Zr_xO2。硫酸化后,负载的过氧化物LaCoO3保持良好。还原处理部分破坏了perovsikte,但可以通过再氧化处理很好地回收。基于NO_x的储存量和催化剂的抗硫性能,Ce_(1-x)Zr_xO2载体中Zr的最佳原子比为x = 0.2。催化剂K / LaCoO3 / Ce_(0.8)Zr_(0.2)O2比Pt基催化剂Pt / K7Ce_(0.8)Zr_(0.2)O2表现出更好的NO_x储存能力,这与它对NO的较强吸附能力高度相关。 NO2氧化。在NO_x储存期间,通过钙钛矿基催化剂上的原位DRIFTS识别出的硝酸盐和亚硝酸盐种类比基于Pt基催化剂上的要多。 H2-TPR结果表明,深度硫酸化后几乎没有硫种类沉积在催化剂K / La-CoO3 / Ce_(1-x)Zr_xO2上,表现出很强的抗硫能力。结果,认为在相应的LNT催化剂中用钙钛矿LaCoO 3完全替代Pt是可行的。

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