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Achieving high ethylene yield in non-oxidative ethane dehydrogenation

脱氢 焦炭 乙烯 催化作用 产量(工程) 化学工程 材料科学 催化裂化 石英 化学 冶金 有机化学 工程类
作者
Christopher Riley,Andrew DeLaRiva,Isabel L. Ibarra,Abhaya K. Datye,Stanley S. Chou
出处
期刊:Applied Catalysis A-general [Elsevier BV]
卷期号:624: 118309-118309 被引量:22
标识
DOI:10.1016/j.apcata.2021.118309
摘要

Steam cracking of ethane, a non-catalytic thermochemical process, remains the dominant means of ethylene production. The severe reaction conditions and energy expenditure involved in this process incentivize the search for alternative reaction pathways and reactor designs which maximize ethylene yield while minimizing cost and energy input. Herein, we report a comparison of catalytic and non-catalytic non-oxidative dehydrogenation of ethane. We achieve ethylene yields as high as 67 % with an open tube quartz reactor without the use of a catalyst at residence times ∼4 s. The open tube reactor design promotes simplicity, low cost, and negligible coke formation. Pristine quartz tubes were most effective, since coke formation was detected when defects were introduced by scratching the surface of the quartz. Surprisingly, the addition of solids to the quartz tube, such as quartz sand, alumina powder, or even Pt-based intermetallic catalysts, led to lower ethylene yield. Pt alloy catalysts are effective at lower temperatures, such as at 575 °C, but conversion is limited due to thermodynamic constraints. When operated at industrially relevant temperatures, such as 700 °C and above, these catalysts were not stable in our tests, causing ethylene yield to drop below that of the open tube. These results suggest that future research on non-oxidative dehydrogenation should be directed at optimizing reactor designs to improve the conversion of ethane to ethylene, since this approach shows promise for decentralized production of ethylene from natural gas deposits.
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