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Partial oxidation of ethane to syngas in an oxygen-permeable membrane reactor

机译:partial oxidation of ethane to syngas in an oxygen-permeable membrane reactor

摘要

A perovskite-type oxide of Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCFO) with mixed electronic and oxygen ionic conductivity at high temperatures was used as an oxygen-permeable membrane. A tubular membrane of BSCFO made by extrusion method has been used in the membrane reactor to exclusively transport oxygen for the partial oxidation of ethane (POE) to syngas with catalyst of LiLaNiO/gamma-Al2O3 at temperatures of 800-900 degreesC. After only 30 min POE reaction in the membrane reactor, the oxygen permeation flux reached at 8.2 ml cm(-2) min(-1). After that, the oxygen permeation flux increased slowly and it took 12 h to reach at 11.0 ml cm(-2) min(-1). SEM and EDS analysis showed that Sr and Ba segregations occurred on the used membrane surface exposed to air while Co slightly enriched on the membrane surface exposed to ethane. The oxygen permeation flux increased with increasing of concentration of C2H6, which was attributed to increasing of the driving force resulting from the more reducing conditions produced with an increase of concentration of C2H6 in the feed gas. The tubular membrane reactor was successfully operated for POE reaction at 875 degreesC for more than 100 h without failure, with ethane conversion of similar to 100%, CO selectivity of >91% and oxygen permeation fluxes of 10-11 ml cm(-2) min(-1). (C) 2002 Elsevier Science B.V. All rights reserved.
机译:具有在高温下具有混合的电子和氧离子导电性的Ba0.5Sr0.5Co0.8Fe0.2O3-δ的钙钛矿型氧化物(BSCFO)用作透氧膜。在膜反应器中已经使用了通过挤出法制成的BSCFO的管状膜,该膜用于在800-900℃的温度下用LiLaNiO /γ-Al2O3催化剂专门输送氧气以将乙烷(POE)部分氧化为合成气。在膜反应器中仅30分钟的POE反应后,氧气渗透通量达到8.2 ml cm(-2)min(-1)。此后,氧气的渗透通量缓慢增加,并花费了12小时达到11.0 ml cm(-2)min(-1)。 SEM和EDS分析表明,Sr和Ba偏析发生在暴露于空气的用过的膜表面上,而Co略微富集于暴露于乙烷的膜表面上。氧气渗透通量随着C2H6浓度的增加而增加,这归因于驱动力的增加,该驱动力是由于进料气体中C2H6浓度的增加而产生的更多还原条件所致。该管式膜反应器已成功在875℃下进行POE反应100多个小时而没有失败,乙烷转化率接近100%,CO选择性> 91%,氧气渗透通量为10-11 ml cm(-2) min(-1)。 (C)2002 Elsevier Science B.V.保留所有权利。

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    Wang HH; Cong Y; Yang WS;

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  • 年度 2002
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