(NH4)2[Co(H2O)4]2[Mo8O27]∙6H2O型杂多化合物催化乙烯的效率

N. A. Panurin, Natalya Yu. Isaeva, E. Markova, T. F. Sheshko, Alexander G. Cherednechenko, A. S. Savchenko, Y. Samoilenko, G. Z. Kaziev
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引用次数: 0

摘要

利用杂多化合物进行多相酸催化因其具有巨大的经济效益和环境效益而受到广泛关注。尽管如此,它的工业应用受到限制,因为它的热稳定性相对较低,导致催化剂再生(沉淀)困难。本工作的目的是寻找和选择与丙烷裂解相关的杂多化合物类型的催化剂,测试其工艺的选择性,并探讨解决催化剂失活问题的可能方法,从而有助于实现固体杂多催化剂的稳定特性。这些方法包括:开发具有高热稳定性的新型催化剂,对催化剂进行改性以促进焦炭燃烧,抑制杂多化合物催化剂在反应过程中生成焦炭,在超临界介质中进行反应,以及使用多功能杂多催化剂进行级联反应。用物理化学方法对所得催化剂进行了研究,以深入了解这些化合物的哪些特性对催化活性有影响。合成了一种高活性、选择性的八钼钴酸铵(II)铵(NH4)2[Co(H2O)4]2[Mo8O27]∙6H2O裂解伴生石油气体催化剂。通过x射线衍射、x射线物相和荧光分析等方法确定了催化剂的定性、定量、结构组成和比表面积。结果表明,八钼钴酸铵(II)的晶型为三斜晶型,晶型参数为:α = 8.6292(9) Å b = 9.4795(10) Å c = 12.2071(13) Å α = 104.326(2)°β = 109.910(2)°γ = 100.820(2)°。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficiency of using heteropoly compounds of the type (NH4)2[Co(H2O)4]2[Mo8O27]∙6H2O as catalysts for the production of ethylene
Carrying out heterogeneous acid catalysis with the use of heteropoly compounds has received considerable attention due to the great economic and environmental benefits. In spite of this, its industrial application is limited as there are difficulties in catalyst regeneration (settling) caused by its relatively low thermal stability. The aim of present work was to search and select catalysts related to the class of heteropoly compounds for propane cracking, to test the selectivity of the prosses as well as to discuss possible approaches for solving the problem of catalyst deactivation, that can contribute to achieve stable characteristics of solid heteropoly catalysts. Among these approaches are: the development of new catalysts with high thermal stability, the modification of catalysts to promote coke combustion, the inhibition of coke formation on heteropoly compound catalysts during the process, carrying out the reactions in supercritical media and also the cascade reactions using a multifunctional heteropoly catalyst. The obtained catalyst was also studied by physicochemical methods to get deep knowledge about which features of these compounds influence on the catalytic activity. A highly active and selective catalyst for ammonium octomolybdenocobaltate(II) ammonium (NH4)2[Co(H2O)4]2[Mo8O27]∙6H2O was synthesized for cracking associated petroleum gases. The qualitative, quantitative, and structural composition as well as the specific surface area of the obtained catalyst was established by the methods of X-ray diffraction, X-ray phase and fluorescence analysis. It was revealed that ammonium octomolybdenocobaltate(II) crystallizes in a triclinic syngony with cell parameters: а = 8.6292(9) Å b = 9.4795(10) Å c = 12.2071(13) Å α = 104.326(2)° β = 109.910(2)° γ = 100.820(2)°.
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