首页> 外文会议>Natural Gas Conversion Symposium; 20040606-10; Dalian(CN) >Middle pressure methane conversion into C_2 hydrocarbons on supported Pt-Co catalysts
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Middle pressure methane conversion into C_2 hydrocarbons on supported Pt-Co catalysts

机译:在负载的Pt-Co催化剂上将中压甲烷转化为C_2烃

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摘要

Pt-Co bimetallic catalysts were prepared by incipient wetness technique on alumina or NaY zeolite and were characterized by XRF, XRD, TPR, CO chemisorption and X-ray photoelectron spectroscopy. Methane conversion to higher hydrocarbons was investigated in a flow system by high temperature one-step, constant flow mode at 750℃ and by two-step low temperature pulse mode at 250℃ under non-oxidative conditions. Catalytic activity in oxygen-free transformations at atmospheric pressure is stable only for a short time. The simultaneous use of higher pressure and high temperature weakens the poisoning effect and makes the process possible to form primarily ethane (and ethene) which is predicted from thermodynamic calculations. The nature of support also significantly affects the amount of C_(2+) products, which can be attributed to structural differences of metal particles (location, reducibility, dispersion).
机译:通过初期润湿技术在氧化铝或NaY沸石上制备了Pt-Co双金属催化剂,并通过XRF,XRD,TPR,CO化学吸附和X射线光电子能谱对其进行了表征。在非氧化条件下,通过在高温下以750℃的高温单步恒定流动模式和在250℃以250℃的两步低温脉冲模式研究了在流动系统中甲烷向高级烃的转化。大气压下无氧转化的催化活性仅在短时间内稳定。同时使用高压和高温会削弱中毒效果,并使该过程可能主要形成乙烷(和乙烯),这是根据热力学计算得出的。载体的性质也显着影响C_(2+)产物的数量,这可归因于金属颗粒的结构差异(位置,还原性,分散性)。

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