首页> 外文会议>International conference on energy and sustainability >Synthesis of novel catalysts for hydrodeoxygenation of bio-oil: guaiacol as a model component
【24h】

Synthesis of novel catalysts for hydrodeoxygenation of bio-oil: guaiacol as a model component

机译:合成用于生物油加氢脱氧的新型催化剂:愈创木酚为模型组分

获取原文

摘要

In this work, NiMo/Support catalysts have been prepared by impregnation technique and evaluated for hydrodeoxygneation (HDO) reaction of guaiacol (GUA) aiming at the identification of active catalysts. Among various catalysts, NiMo/TiO_2 was chosen to understand the influence of reaction parameters, such as temperature, reaction time, H_2 pressure, and quantity of the catalyst. The influence of the metal components on guaiacol conversion is determined by comparing mono (Ni and Mo) metals deposited TiO_2. These results signify the alloying nature of metal components. GCMS results showed that phenol is a major component in all the conditions. As there is an increase in the temperature (200, 250, 300, 350°C), reaction time (1, 5, 8, 24 h), H_2/guaiacol molar feed ratio (0, 1:2, 1:1, and 2:1), and catalyst amount (0, 25, 50, 100 mg), the conversion has increased significantly while maintaining the high selectivity to HDO products without ring opening reactions. Under optimized conditions (350°C and 2:1 of H_2:guaiacol ratio), 98% guaiacol is converted on NiMo/TiO_2 resulting phenol, poly methyl substituted phenols, and traces of cyclohexanone and benzene. It is remarkable that a low amount of catechol dimethyl ether and no indication of catechol and creosol were detected.
机译:在这项工作中,已通过浸渍技术制备了NiMo /载体催化剂,并针对愈创木酚(GUA)的加氢脱氧(HDO)反应进行了评估,旨在鉴定活性催化剂。在各种催化剂中,选择NiMo / TiO_2以了解反应参数的影响,例如温度,反应时间,H_2压力和催化剂的量。通过比较单(Ni和Mo)金属沉积的TiO_2,可以确定金属组分对愈创木酚转化率的影响。这些结果表明金属成分的合金化性质。 GCMS结果表明,在所有条件下,苯酚都是主要成分。随着温度(200、250、300、350°C),反应时间(1、5、8、24小时),H_2 /愈创木酚摩尔进料比(0、1:2、1:1,和2:1)和催化剂用量(0、25、50、100毫克),转化率显着提高,同时保持了对HDO产物的高选择性而无开环反应。在最佳条件下(350°C和2:1的H_2:愈创木酚比率),NiMo / TiO_2上转化了98%愈创木酚,得到苯酚,聚甲基取代的苯酚以及痕量的环己酮和苯。值得注意的是,未检测到少量的邻苯二酚二甲醚,也没有检测到邻苯二酚和甲酚的迹象。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号