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作 者:申东明[1,2,3] 程世林[3] 韩冰[3] 钟涛[3] 吕鹏[1,2,3] 邢闯[1,2,3] 盖希坤[1,2,3] 吕成学[1,2,3] 杨瑞芹[1,2,3]
机构地区:[1]浙江省农产品化学与生物加工技术重点实验室,浙江杭州310023 [2]浙江省农业生物资源生化制造协同创新中心,浙江杭州310023 [3]浙江科技学院生物与化学工程学院,浙江杭州310023
出 处:《燃料化学学报》2017年第9期1122-1129,共8页Journal of Fuel Chemistry and Technology
基 金:国家自然科学基金(21528302);浙江省自然科学基金(LQ16B060002);国家级大学生创新训练计划(201611057013)项目资助~~
摘 要:采用共沉淀法制备Cu/ZnO催化剂、水热合成法制备H-β分子筛、通过物理包膜法制备了具有核壳结构的Cu/ZnO@H-β-P催化剂,并用于合成气制备液化石油气(LPG)反应。通过XRD、NH3-TPD、BET和SEM-EDS等手段对催化剂进行了表征,利用固定床连续反应装置对催化剂进行了活性评价。结果表明,Cu/ZnO@H-β-P催化剂是具有中孔的核壳结构材料,其协同作用打破了原有的热力学平衡,促进了甲醇→DME→LPG串联反应的连续进行。与物理混合的Mix-Cu/ZnO-H-β催化剂相比,Cu/ZnO@H-β-P催化剂的CO转化率和LPG选择性更高,空速和反应温度对催化剂活性影响明显,最佳空速和反应温度分别为2 400 h^(-1)和350℃。使用Cu/ZnO@H-β-P催化剂在最佳条件下进行合成气制备LPG反应,CO转化率达到了57.22%,LPG选择性达到了60.52%。The Cu/ZnO catalyst was prepared by the coprecipitation method,and the H-β zeolite was prepared by the hydrothermal synthesis method,and the bifunctional catalyst Cu/ZnO@H-β-P with core shell structure was prepared by the physical envelope method.The catalysts were used in the reactions of LPG preparation from syngas.The catalysts were characterized by the means of XRD,BET,NH3-TPD and SEM-EDS.The activity of the catalysts was evaluated by a continuous flow fixed bed reactor.The results show that the Cu/ZnO@H-β-P catalyst was the mesoporous material with core shell structure,and the acid intensity of H-β zeolite was changed,and the cascade reactions from methanol to dimethyl ether to LPG were promoted by core-shell synergy in the Cu/ZnO@H-β-P catalyst.The CO conversion and LPG selectivity were higher on the Cu/ZnO@H-β-P catalyst with core shell structure than those on the Mix-Cu/ZnO-H-β catalyst.The catalyst activity was affected by the reaction conditions of space velocity and reaction temperature.The best space velocity and reaction temperature were 2 400 h^-1 and 350 ℃.The CO conversion and LPG selectivity achieved respectively 57.22% and 60.52% in the reaction of LPG preparation from syngas at the best reaction conditions using the Cu/ZnO@ H-β-P catalyst.
关 键 词:液化石油气(LPG) 核壳结构 合成气转化 水热合成
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