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首页> 外文期刊>Ultrasonics sonochemistry >CO2-enhanced dehydrogenation of ethane over sonochemically synthesized Cr/clinoptilolite-ZrO2 nanocatalyst: Effects of ultrasound irradiation and ZrO2 loading on catalytic activity and stability
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CO2-enhanced dehydrogenation of ethane over sonochemically synthesized Cr/clinoptilolite-ZrO2 nanocatalyst: Effects of ultrasound irradiation and ZrO2 loading on catalytic activity and stability

机译:超声化学合成Cr /斜发沸石-ZrO2纳米催化剂上乙烷的CO2增强脱氢:超声辐射和ZrO2负载量对催化活性和稳定性的影响

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CO2-enhanced oxidative dehydrogenation of ethane was investigated over sonochemically synthesized Cr/clinoptilolite-ZrO2 nanocatalyst with the aim of assessing the effect of composite support and ultrasonic irradiation on the nanocatalyst reactivity and stability. To this aim, ZrO2 promoted clinoptilolite supports varying in zirconia content (0, 25, 50 wt%) were synthesized by hydrothermally precipitation method and impregnated with chromium nitrate under ultrasound irradiation. The samples were characterized by XRD, FESEM, EDX, TEM, ICP, BET, FTIR, TPR-H-2 and TPD-NH3 techniques. The characterization results indicated that ultrasound irradiation could not only reduce the formation of Cr2O3 and decrease submicron particle size of chromium oxide to nanometer scale, but also promote the distribution of metallic particles and strengthen the chromium-support interaction. As a result, utilizing ultrasound irradiation in the synthesis of Cr/Clinoptilolite helped to maintain a high and stable catalytic activity. These features were more prominent in the presence of zirconia. It was found that the metal oxide nanopartides with about 4-8 nm are dispersed uniformly on the surface of composite support containing 25 wt% ZrO2 (CLT-Z25). Moreover, the addition of ZrO2 resulted in the formation of new strong acid sites and a significant modification in the reducibility of chromium species, which alongside homogenous and small Cr nanoparticles account for the superior catalytic performance of ZrO2 containing samples. However, excessive loading of ZrO2 (50 wt%) severely covered the surface of clinoptilolite, afforded the aggregations of metallic particles and thereupon, weakened the contact between clinoptilolite and ZrO2, which together with more acid strength seriously resulted in the deactivation of catalyst. In spite of superior initial activity of ZrO2-rich sample among the catalysts tested, ultrasonic synthesized Cr/CLT-Z25 nanocatalyst showed the best catalytic performance after 5 h-catalytic reaction. (C) 2016 Elsevier B.V. All rights reserved.
机译:以超声化学合成的Cr /斜发沸石-ZrO2纳米催化剂为研究对象,研究了CO2促进乙烷的氧化脱氢,目的是评估复合载体和超声辐照对纳米催化剂反应性和稳定性的影响。为此,通过水热沉淀法合成了氧化锆含量(0、25、50 wt%)的ZrO2促进斜发沸石载体,并在超声辐射下浸渍了硝酸铬。通过XRD,FESEM,EDX,TEM,ICP,BET,FTIR,TPR-H-2和TPD-NH3技术对样品进行表征。表征结果表明,超声辐照不仅可以减少Cr2O3的形成,并将氧化铬的亚微米粒径减小至纳米级,而且可以促进金属颗粒的分布并增强铬-载体的相互作用。结果,在Cr /斜发沸石的合成中利用超声辐射有助于保持高且稳定的催化活性。在氧化锆存在下,这些特征更为突出。发现具有约4-8nm的金属氧化物纳米粒子均匀地分散在包含25wt%的ZrO 2(CLT-Z25)的复合载体的表面上。此外,ZrO2的添加导致形成新的强酸位点,并显着改变了铬的还原性,这与均匀且小的Cr纳米颗粒共同构成了含ZrO2样品的优异催化性能。然而,过量的ZrO 2(50wt%)的负载严重覆盖了斜发沸石的表面,使金属颗粒聚集并且随后,减弱了斜发沸石与ZrO 2之间的接触,这与更高的酸强度一起严重导致了催化剂的失活。尽管所测试的催化剂中富含ZrO2的样品具有优异的初始活性,但超声合成的Cr / CLT-Z25纳米催化剂在5 h催化反应后仍表现出最佳的催化性能。 (C)2016 Elsevier B.V.保留所有权利。

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