首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Dry reforming of methane over 5 wt% Ni/Ce(1-x)Pr(x)o(2-delta) catalysts: Performance and characterisation of active and inactive carbon by transient isotopic techniques
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Dry reforming of methane over 5 wt% Ni/Ce(1-x)Pr(x)o(2-delta) catalysts: Performance and characterisation of active and inactive carbon by transient isotopic techniques

机译:在5 wt%Ni / Ce(1-x)Pr(x)o(2-delta)催化剂上进行甲烷干重整:通过瞬时同位素技术对活性炭和非活性炭进行性能和表征

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摘要

The effects of Ce1-xPrxO2-delta support composition (x = 0.0-0.8) and reaction temperature (550-750 degrees C) on the catalytic activity and selectivity and important features of the mechanism of the dry reforming of methane (DRM) over supported Ni (5 wt%) were investigated. Of particular interest were the effects on the concentration of active and inactive carbon formed, the relative contribution of CH4 and CO2 activation routes towards carbon formation and the structure and morphology of the inactive carbon which was formed. For these carbon characterization studies, steady-state isotopic transient kinetic analysis ((CO2)-C-13-SSITKA), temperature-programmed oxidation (TPO) following (CO2)-C-13/(CH4)-C-12/He dry reforming, thermal gravimetric analysis coupled with TPO (TGA-TPO), scanning electron miscroscopy (SEM-EDX) and transmission electron microscopy with atomic resolution (HRTEM) and powder X-ray diffraction (XRD) were employed. The relative amount of inactive carbon formed via the CH4 and CO2 activation routes was found to strongly depend on reaction temperature and Pr-dopant support composition. At 550 degrees C, the contribution of the CO2 activation route to the inactive carbon formation (besides that of the CH4 activation route) was 65.7 and 60.1%, respectively, for Ni supported on CeO2 and Ce0.2Pr0.8O2 carriers, whereas at 750 degrees C the respective values were 54.0 and 50.9%. Filamentous carbon and thin layers of graphitic carbon were identified as the main morphologies of inactive carbon. The surface coverage of active carbon that truly participates in the formation of CO was found to depend on support composition and reaction temperature (theta(C) = 0.03-0.15 at 550 degrees C and 0.07-3.4 at 750 degrees C). A pool of inactive reversibly adsorbed CO2 was measured (theta= 1.5-4.1) for the first time, which was dependent on support composition and reaction T. The introduction of 20 atom-% Pr in the ceria lattice caused a significant reduction in the rate of inactive carbon formation with marginal decrease in catalyst's activity and stability after 25 h on stream. Further introduction of Pr-dopant (80 atom-%) caused drastic reduction in the deposited carbon after 25 h on the reaction stream at 750 degrees C (0.07 wt%C) but with appreciable decrease in CH4- and CO2-conversions and H-2/CO gas-product ratio (a drop by a factor of 1.85, 1.45 and 1.47, respectively). The latter decrease in catalyst's performance is correlated with the increase in the pool of inactive adsorbed CO2 in the form of carbonate-like species. (C) 2016 Elsevier B.V. All rights reserved.
机译:Ce1-xPrxO2-δ载体组成(x = 0.0-0.8)和反应温度(550-750摄氏度)对载体上甲烷(DRM)干重整的催化活性和选择性的影响以及机理的重要特征研究了Ni(5重量%)。特别令人感兴趣的是对形成的活性碳和惰性碳浓度,CH4和CO2活化途径对碳形成的相对贡献以及形成的惰性碳的结构和形态的影响。对于这些碳表征研究,进行稳态同位素瞬态动力学分析((CO2)-C-13-SSITKA),在(CO2)-C-13 /(CH4)-C-12 / He之后进行程序升温氧化(TPO)采用了干重整,热重分析和TPO(TGA-TPO),扫描电子显微镜(SEM-EDX)和具有原子分辨率的透射电子显微镜(HRTEM)和粉末X射线衍射(XRD)。发现通过CH4和CO2活化途径形成的惰性碳的相对量在很大程度上取决于反应温度和Pr-掺杂剂载体组成。在550摄氏度下,负载在CeO2和Ce0.2Pr0.8O2载体上的Ni的CO2活化途径对无活性碳形成的贡献(除了CH4活化途径之外)分别为65.7%和60.1%。 ℃分别为54.0和50.9%。丝状碳和石墨碳薄层被确定为惰性碳的主要形态。发现真正参与CO形成的活性炭的表面覆盖率取决于载体组成和反应温度(theta(C)在550摄氏度下为0.03-0.15,在750摄氏度下为0.07-3.4)。首次测量了无活性可逆吸附的CO2池(θ= 1.5-4.1),这取决于载体的组成和反应T。在二氧化铈晶格中引入20%(原子)的Pr导致速率显着降低运转25 h后,惰性碳的形成与催化剂活性和稳定性的少量降低有关。在750摄氏度(0.07 wt%C)下反应流25小时后,进一步引入Pr掺杂剂(80原子%)导致沉积碳急剧减少,但CH4-和CO2-转化率和H- 2 / CO气产比(分别下降1.85、1.45和1.47倍)。后者催化剂性能的下降与呈碳酸盐状物质形式的惰性吸附的CO2库增加相关。 (C)2016 Elsevier B.V.保留所有权利。

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