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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Key factors in Sr-doped LaBO3 (B = Co or Mn) perovskites for NO oxidation in efficient diesel exhaust purification
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Key factors in Sr-doped LaBO3 (B = Co or Mn) perovskites for NO oxidation in efficient diesel exhaust purification

机译:SR掺杂Labo3(B = Co或Mn)钙钛矿在高效柴油机排气净化中没有氧化的关键因素

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Perovskites have attracted attention in recent years as an economic alternative to noble metals in oxidation processes. Synthesis conditions of LaCoO3 and LaMnO3 perovskites have been studied varying citrate to nitrate molar ratio in the starting solution, pH and calcination protocol, with the aim of obtaining high purity perovskites, absence of impurities, and with enhanced textural properties. Once synthesis conditions were established, strontium was incorporated in the perovskite lattice as a textural and structural promoter, by substituting lanthanum with different doping levels, i.e. La0.9Sr0.1BO3, La0.8Sr0.2BO3, La0.7Sr0.3BO3, La0.6Sr0.4BO3 and La0.5Sr0.5BO3 with B = Co or Mn. The prepared solids were characterized in terms of crystalline phase identification (XRD), specific surface area (N-2 adsorption-desorption at -196 degrees C), reducibility and oxidation state of transition metal ions (H-2-TPR), quantification of adsorbed oxygen species (O-2-TPD) and surface elemental composition (XPS). Charge imbalance associated to strontium (Sr2+) incorporation in the perovskite lattice in substitution of lanthanum (La3+) was preferentially balanced by Mn4+ promotion in La1-xSrxMnO3 perovskites, whereas formation of oxygen vacancies seems to be the mechanism for charge compensation in La1-xSrxCoO3 perovskites, where Co ions remained as Co3+ ions. Strontium doped perovskites further improved NO conversion compared to the non-substituted formulations. The best NO oxidation performance was obtained with La0.7Sr0.3CoO3 and La0.9Sr0.1MnO3 samples, achieving maximum NO conversion of 83 and 65% at 300 and 325 degrees C, respectively. Higher oxidation capacity of La0.7Sr0.3CoO3 sample was associated to the higher oxygen mobility and exchange capacity between oxygen in the lattice and gas phase oxygen. It is worth noting that prepared perovskites presented far higher NO oxidation capacity than platinum-based NSR model catalysts, confirming perovskites as an economic alternative to catalyze NO oxidation reactions in automotive catalysis. (C) 2017 Elsevier B.V. All rights reserved.
机译:近年来佩洛夫斯基特引起了关注作为氧化过程中贵金属的经济替代品。已经研究了LACOO3和LAMNO3 PEROVSKITE的合成条件,其在起始溶液,pH和煅烧方案中改变柠檬酸盐,其目的是获得高纯度钙酸盐,不存在杂质,并且具有增强的纹理性质。一旦建立了合成条件,通过用不同掺杂水平的镧作为纹理和结构启动子将锶掺入Perovskite晶格中,即La0.9sr0.1bO3,La0.8sr0.2bo3,La0.6sr0 .4bo3和la0.5sr0.5bo3与b = co或mn。在结晶相鉴定(XRD),比表面积(在-196℃下的N-2吸附 - 解吸),过渡金属离子(H-2-TPR)的再氧化和氧化状态,表征制备的固体。吸附的氧气(O-2-TPD)和表面元素组成(XPS)。在La1-XSRXMNO3钙钛矿中的MN4 +促进,优先通过Mn4 +促进术中掺入与锶(SR2 +)掺入的电荷不平衡掺入镧(La3 +)中的钙钛晶片,而氧空位的形成似乎是La1-XsrxCoO3钙钛矿的电荷补偿机制,Co离子保持为CO 3 +离子。与未取代的制剂相比,掺杂掺杂的钙酸盐进一步改善了转化。使用La0.7SR0.3COO3和LA0.9SR0.1MNO3样品获得最佳氧化性能,分别在300和325摄氏度下实现最大的83和65%的最大转化率。 La0.7SR0.3COO3样品的较高氧化能力与晶格和气相氧中的氧气之间的较高的氧气迁移率和交换能力相关。值得注意的是,制备的Perovskites呈现比基于铂的NSR模型催化剂更高的氧化能力,确认钙酸盐作为催化在汽车催化中没有氧化反应的经济替代品。 (c)2017 Elsevier B.v.保留所有权利。

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