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Biodiesel production via transesterification of palm oil by using CaO-CeO2 mixed oxide catalysts

机译:使用CaO-CeO2混合氧化物催化剂通过棕榈油的酯交换反应生产生物柴油

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Solid base CaO-CeO2 mixed oxide catalysts have been synthesized via wet impregnation method and characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, temperature-programmed desorption of CO2 (TPD-CO2) and scanning electron microscopy (SEM). The catalytic activity was determined by transesterification of palm oil. Optimum biodiesel yield, 95%, was achieved by 50Ca-Ce catalyst under the reaction conditions of 5 wt.% of catalyst, methanol to oil molar ratio of 12: 1, reaction temperature of 65 degrees C and reaction time of 4 h. The high catalytic activity (95%) of 50Ca-Ce catalyst may be due to strong basicity and high BET surface area, which indicate more number of active sites on the catalyst surface for transesterification process. Besides, 50Ca-Ce catalyst showed better reusability than the bulk CaO where it can be reused up to 6 times without a significant loss of catalytic activity (>80%). The lixiviation of CaO active phase was greatly reduced with the presence of strong synergic interaction between CaO and CeO2. Deactivation of the catalyst was mainly due to the leaching of CaO active phase into the methanolic solution and pore-filling by fatty acid or glycerol. (C) 2015 Elsevier Ltd. All rights reserved.
机译:通过湿法浸渍法合成了固体碱式CaO-CeO2混合氧化物催化剂,并通过X射线衍射(XRD),Brunauer-Emmett-Teller(BET)表面积分析,程序升温的CO2解吸(TPD-CO2)和扫描电子显微镜(SEM)。通过棕榈油的酯交换反应确定催化活性。在催化剂的5 wt%,甲醇与油的摩尔比为12:1,反应温度为65摄氏度,反应时间为4小时的反应条件下,使用50Ca-Ce催化剂可获得95%的最佳生物柴油收率。 50Ca-Ce催化剂的高催化活性(95%)可能归因于强碱性和高BET表面积,这表明在酯交换过程中催化剂表面上有更多的活性位。此外,50Ca-Ce催化剂比散装CaO表现出更好的可重复使用性,在这种情况下,它可以重复使用多达6次,而催化活性却没有显着降低(> 80%)。由于CaO和CeO2之间存在强烈的协同作用,CaO活性相的浸出作用大大降低。催化剂的失活主要是由于CaO活性相浸出到甲醇溶液中,以及脂肪酸或甘油的孔填充。 (C)2015 Elsevier Ltd.保留所有权利。

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