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Greenhouse Gases Mitigation by CO2 Reforming of Methane to Hydrogen-rich Syngas using Praseodymium Oxide Supported Cobalt Catalyst

机译:氧化Pra负载的钴催化剂将甲烷CO2重整为富氢合成气可缓解温室气体

摘要

This study focuses on the potential of hydrogen rich syngas production by CO2 reforming of methane over Co/Pr2O3catalyst. The Co/Pr2O3catalyst was synthesized via wet-impregnation method and characterized for physicochemical properties by TGA, XRD, BET, H2-TPR, FESEM, EDX, and FTIR. The CO2reforming of methane over the as-synthesized catalyst was studied in a tubular stainless steel fixed-bed reactor at feed ratio ranged 0.1–1.0, temperature ranged 923–1023 K, and gas hourly space velocity (GHSV) of 30,000 h-1 under atmospheric pressure condition. The catalyst activity studies showed that the increase in the reaction temperature from 923 to 1023 K and feed ratio from 0.1 to 1.0 resulted in a corresponding increase in the reactant’s conversion and the product’s yields. At 1023 K and feed ratio of 1.0, the activity of the Co/Pr2O3 catalyst climaxed with CH4 and CO2 conversions of 41.49 and 42.36 %. Moreover, the catalyst activity at 1023 K and feed ratio of 1.0 resulted in the production of H2and CO yields of 40.7 and 40.90 %,respectively. The syngas produced was estimated to have H2:CO ratio of 0.995, making it suitable as chemical building blocks for the production of oxygenated fuel and other value-added chemicals. The used Co/Pr2O3 catalyst which was characterized by TPO, XRD, and SEM-EDX show some evidence of carbon formation and deposition on its surface.
机译:这项研究的重点是在Co / Pr2O3催化剂上通过甲烷进行CO2重整来生产富氢合成气的潜力。通过湿浸渍法合成了Co / Pr2O3催化剂,并通过TGA,XRD,BET,H2-TPR,FESEM,EDX和FTIR对其理化性质进行了表征。在管式不锈钢固定床反应器中,在进料比为0.1–1.0,温度为923–1023 K和气体时空速(GHSV)为30,000 h-1的条件下,研究了合成催化剂上甲烷的CO2重整。大气压条件。催化剂活性研究表明,反应温度从923增加到1023 K,进料比从0.1增加到1.0,导致反应物的转化率和产物收率相应增加。在1023 K和1.0的进料比下,Co / Pr2O3催化剂的活性达到最高,CH4和CO2转化率为41.49和42.36%。此外,催化剂在1023 K和进料比为1.0时产生的H2和CO产率分别为40.7和40.90%。估计产生的合成气的H2:CO比为0.995,使其适合用作生产含氧燃料和其他增值化学品的化学构件。用过的TPO,XRD和SEM-EDX表征的Co / Pr2O3催化剂显示出一些碳形成和沉积在其表面的迹象。

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