柴油自热重整用Rh/Al-Ce-Zr催化剂寿命试验

RAN Pub Date : 2016-04-01 DOI:10.11159/ICNNFC16.111
W. Choi, Yeon Baek Seong, Tae Hoon Lee, Changhyun Park, Jin Wook Lee, M. Kim, N. Park, T. Lee
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引用次数: 0

摘要

近年来,能源短缺问题不断出现。因此,对替代能源的研究势在必行[12]。研究了rh基负载型催化剂在柴油自热重整中的催化活性。柴油的自热重整是在800℃以上的高温条件下,由蒸汽、氧气与汽化后的柴油气体发生化学反应而进行的。因此,烧结和炭化会降低催化剂的催化活性。然而,自热重整被认为是柴油重整的合适方法,因为自热重整比其他重整方法结焦少[2-5]。本研究以铑为主要活性物质制备氢,以氧化铝、氧化锆和氧化铈为催化助剂。氧化锆和二氧化锆因其具有较高的热稳定性和抗碳结焦性而被用作催化助剂。将Al-Ce-Zr基催化载体材料包覆在金属泡沫板上,形成纳米结构。通过XRD分析证实,Al-Ce-Zr基催化载体材料中的铈和锆组分被合成为CeZrO2晶体结构。CeZrO2具有较高的晶格氧迁移率,可以防止碳在催化剂活性部位沉积。碳沉积是烃类重整反应中催化失活的一种。随着反应温度的升高,柴油自热重整制氢率提高,在600℃、700℃和800℃时分别达到5%、15%和43%。在相同条件下,燃料转化率分别为20%、85%和100%。在800℃下进行重整反应,在蒸汽碳比为2.5时获得了较高的产氢率。氧碳比的最佳条件为0.25。本研究在最佳自热重整条件下对Rh/AlCe-Zr基催化剂进行了长期活性测试。在500小时内,干产物气体中氢和一氧化碳的组成分别保持在45%和11%左右。在相同条件下,经物料衡算,合成气的理论组成为56%。因此,Rh/Al-Ce-Zr基催化剂对柴油自热重整具有优异的催化活性。反应100、200、300、400和500 h后,EDX分析了催化剂表面的碳含量,未观察到碳沉积。TEM分析也证实,随着反应时间的延长,催化载体材料的晶粒尺寸增大。结果表明,晶粒尺寸的变化是由氧化铝烧结和CeZrO2在高温条件下结晶引起的。然而,在500 h内没有观察到晶体结构变化导致的催化失活。可以预期,CeZrO2的结晶阻止了CeZrO2中晶格氧的碳氧化导致的碳沉积导致的失活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Longevity Tests of Rh/Al-Ce-Zr Catalyst for Auto-thermal Reforming of Diesel Oil
Extended Abstract Recently, energy shortages are appearing constantly. Therefore, the research on alternative energy has demanded [12]. In this study, the catalytic activity of Rh-based supported catalysts was investigated for the auto-thermal reforming of diesel oil. The auto-thermal reforming of diesel oil occur the chemical reaction of steam, oxygen and the vaporized diesel gas, and it was performed at high temperature condition above at 800 °C. Therefore, the catalytic activity can decrease by the sintering and the carbon coking. However, auto-thermal reforming has been considered as the appropriate method for diesel reforming, because auto-thermal reforming has showed less coke formation than other reforming method [2-5]. In this study, rhodium was used as the main active material for the production of hydrogen and the catalytic promoter was used alumina, zirconia, and ceria. Zirconia and ceria has been used as the catalytic promoter due to its high thermal stability and carbon coking resistibility. The Al-Ce-Zr based catalytic support material coated over metal foam plate was formed to the morphology of nano-structure. It was confirmed by XRD analysis that cerium and zirconium components in Al-Ce-Zr based catalytic support material was synthesized to CeZrO2 crystal structure. It was concluded that CeZrO2 prevents carbon deposition on catalyst active site due to their high lattice oxygen mobility. Carbon deposition is one of catalytic deactivation in hydrocarbons reforming reaction. The yield of hydrogen by diesel auto-thermal reforming increased with increasing reaction temperature, and was obtained 5, 15 and 43% at 600, 700 and 800 °C, respectively. The fuel conversions at same conditions were 20, 85 and 100%. The high hydrogen yield was obtained at 2.5 of steam/carbon ratio when reforming reaction was carried out at 800. The optimum condition of oxygen/carbon was also confirmed to 0.25. In this study, long-term activity test of Rh/AlCe-Zr based catalyst was carried out under the optimum auto-thermal reforming condition. The composition of hydrogen and carbon monoxide in dry product gas was maintained to approximately 45% and 11% during 500 h, respectively. The theoretical composition of syn-gas, which is calculated by material balance under same condition, was 56%. Therefore, it was concluded that the catalytic activity of Rh/Al-Ce-Zr based catalysts is very excellent on diesel auto-thermal reforming. The carbon content on the surface of catalysts after 100, 200, 300, 400and 500 h reactions was investigated by EDX analysis and the carbon deposition was not observed. It was also confirmed by TEM analysis that the crystal size of catalytic support materials increased with increasing reaction time. It was concluded that the change of crystal size is occurred by the sintering of alumina and the crystallization of CeZrO2 at high temperature condition. However, catalytic deactivation by the change of crystal structure was not observed for 500 h. It was expected that the crystallization of CeZrO2 prevents the deactivation by carbon deposition due to carbon oxidation of lattice oxygen in CeZrO2.
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