检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]中国石油大学重质油国家重点实验室CNPC催化重点实验室,山东青岛266580 [2]洛阳瑞泽石化工程有限公司
出 处:《石油炼制与化工》2015年第4期40-45,共6页Petroleum Processing and Petrochemicals
基 金:国家重点基础研究发展计划(973计划)项目(2010CB226905);教育部自主创新科研计划新项目(13CX06050A)
摘 要:以硝酸镍和碱式碳酸镍为Ni前躯体,采用水热合成法制备了一系列Ni-Mo-W复合氧化物,并采用BET,XRD,SEM等手段对合成的复合氧化物进行表征,考察Ni前躯体对Ni-Mo-W复合氧化物结构的影响。采用混捏法制备了非负载型Ni-Mo-W催化剂,在20 mL高压加氢微反装置上以劣质催化裂化柴油为原料考察了非负载型催化剂的加氢性能。结果表明:以硝酸镍为Ni前躯体合成的复合氧化物的比表面积和孔体积较小,Ni-Mo-W复合程度较低,而以碱式碳酸镍为Ni前躯体时则倾向于形成晶相弥散且晶粒尺寸较小的介孔Ni-Mo-W复合氧化物;以大孔体积低比表面积的碱式碳酸镍为Ni前躯体制备的非负载催化剂具有较高的加氢脱硫、加氢脱氮活性,脱硫率高达99.91%,脱氮率高达99.94%。A series of Ni-Mo-W composite oxides were prepared through hydrothermal synthesis method by changing nickel precursors. The influence of nickel precursors on structure and activity of unsupported catalysts was investigated and the composite oxides were characterized by BET, XRD and SEM. Unsupported catalysts were prepared through wet-mixing-kneading method, and the fluid catalytic cracking (FCC) diesel was used as a feedstock for activity evaluation of the unsupported catalysts in a 20 mL high-pressure hydrotreating unit. The experiment results show that the composite oxides from nickel nitrate have less BET surface area and pore volume. While crystal phase of Ni-Mo-W composite oxide from basic nickel carbonate precursor tends to be amorphous, and particle size is smaller than that from nickel nitrate precursor. The experiments also reveal that surface area and pore volume of the com- posite oxide synthesized by basic nickel carbonate precursor are improved a lot. The activity evaluation results show that the catalyst prepared hy basic nickel carbonate with larger pore volume and lower sur- face area performs the highest activity of hydrodesulfurization (HDS), hydrodenitrogeneration (HDN) and aromatics saturation. The sulfur and nitrogen removal rate reaches to 99.91% and 99.94%, respec- tively.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.216