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]辽宁石油化工大学,抚顺113001 [2]中国石化抚顺石油化工研究院,抚顺113001
出 处:《中国科学:化学》2013年第11期1548-1556,共9页SCIENTIA SINICA Chimica
摘 要:本文提出了第三次纳米自组装的正向胶束、反向胶束法,并利用其制备了一种大孔主客体催化材料.以二次纳米自组装Al2O3为主体,根据压汞法,正向胶束法制备的催化材料孔容为0.62~0.80cm^3/g、比表面积为123~137mZ/g、平均孔径为20~23.3nm,孔径分布大于30nm范围的可达58.69%,堆积密度为0.43—0.55g/cm^3,活性金属负载量可达36.99%;由氮气吸附法,反向胶柬法制备的催化材料具有0.74cm^3/g的孔容、262m2/g的比表面积、11.8nm的平均孔径.结果显示,活性金属以球形或棒状的结晶态存在于主体表面,其中,正向胶束法中为直径2-3nm的微晶态纳米粒子,反向胶束法中为直径0.1μm、长1-2.5μm的棒状体.采用催化裂化柴油和催化裂化重循环油(1:2,体积比)混合而得油品对FA.Z20进行50h加氢评价实验,其单位体积活性金属的脱硫率、脱氮率、脱芳烃率(四环、五环)分别为参比剂的4.6、2.1和4.7倍,初活性良好,具有较强的抗结焦性能.A macroporous catalytic host-guest material based on secondary self-assembly alumina was synthesized by micellar method and reverse micellar method of the third nano self-assembly. Characterization showed that the macrostructure of catalytic materials by micellar method with a pore volume of 0.62-0.80 cm^3/g, a specific surface area (BET) of 123-127 m^2/g, a average pore diameter of 20-23.3 nm and pore diameter lager than 30 nm reached to 58.69% (mercury intrusion porosimetry, MIP) were 2-3 nm microcrystal nanoparticles, processed a bulk density of 0.43-0.55 g/cm3 and a active metal of 36.99%. Meanwhile, the catalytic material by reverse micellar method possessed rod-like structure of a 2.5 ~tm long and 0.1 ~tm diameter, which owned a pore volume of 0.74 cm3/g, a specific surface area (BET) of 262 m2/g and a average pore diameter of 11.8 nm (nitrogen adsorption method, NAM). A mixed oil of FCC diesel and FCC-HCO (2:1, volume ratio) was used in HDAr (four ring and five ring aromatic hydrocarbon) 50 h hydrogenation evaluation investigating the HDS, HDN and properties of FA-Z20. The catalytic performance of active metal per unit volume was as 4.6, 2.1 and 4.7 times as reference catalyst, which indicated a high initial activity and strong coking inhibitor ability.
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:216.73.216.3