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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Development of cobalt catalysts for the steam reforming of naphthalene as a model compound of tar derived from biomass gasification
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Development of cobalt catalysts for the steam reforming of naphthalene as a model compound of tar derived from biomass gasification

机译:用于萘蒸汽重整的钴催化剂的开发,该催化剂是生物质气化衍生的焦油的典型化合物

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摘要

The catalytic performances of Co/MgO catalysts for the steam reforming of naphthalene were investigated. The results of characterizations (TPR, XRD, CO adsorption, and CO-TPD) showed that large-sized Co metal particles were formed over the catalysts pre-calcined at 873 K with high Co loading via reduction Of Co-3-O-4 and MgCo2O4 phases. A few Co metal particles were obtained over the catalysts pre-calcined at 1173 K with all Co loading values after reduction.The catalytic performances data showed that 12 wt.% Co/MgO catalyst pre-calcined at 873 K exhibited the best catalytic performance (conv., 23%, 3 h) for the steam reforming of naphthalene among the catalysts tested in this study, due to the existence of Co metal and the low amounts of coke deposition. On the other hand, the data also revealed that the reaction of steam reforming of naphthalene proceeds over all Co-loaded catalyst pre-calcined at 1173 K initially; however, the deposition of the polymer of Q,H radicals and the oxidation of catalysts by H2O led to the decrease of activity.It should be noted that 12 wt.% Co/MgO catalyst pre-calcined at 873 K showed high and stable activity under the low steam/carbon mole ratio (0.6), with H-2 and CO2 as main products. These two excellent advantages serve to increase the overall biomass gasification system energy efficiency and allow using the product gas for fuel cell system. Thus, Co catalyst is a promising system for the steam reforming of naphthalene derived from biomass gasification as a second fixed catalytic bed. (C) 2004 Elsevier B.V. All rights reserved.
机译:研究了Co / MgO催化剂对萘的蒸汽重整反应的催化性能。表征结果(TPR,XRD,CO吸附和CO-TPD)表明,通过还原Co-3-O-4,在高K负载下于873 K预煅烧的催化剂上形成了大尺寸的Co金属颗粒。和MgCo2O4相。在1173 K下预煅烧的催化剂上获得了一些Co金属颗粒,还原后所有的Co载量值。催化性能数据表明,在873 K下预煅烧的12 wt。%Co / MgO催化剂表现出最佳的催化性能(由于存在金属钴和少量的焦炭沉积,本研究中测试的催化剂中萘的蒸汽重整转化率分别为23%,3小时)。另一方面,该数据还表明,萘的蒸汽重整反应在最初于1173 K下预煅烧的所有负载于Co的催化剂上进行。然而,Q,H自由基的聚合物沉积和H 2 O对催化剂的氧化导致活性降低。应注意的是,在873 K下预煅烧的12 wt。%Co / MgO催化剂显示出高而稳定的活性。在低蒸汽/碳摩尔比(0.6)下,以H-2和CO2为主要产物。这两个优异的优势可提高整体生物质气化系统的能源效率,并允许将产物气用于燃料电池系统。因此,Co催化剂是用于将来自生物质气化的萘蒸汽重整作为第二固定催化床的有前途的系统。 (C)2004 Elsevier B.V.保留所有权利。

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