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机构地区:[1]鲁东大学化学与材料科学学院,山东烟台264025
出 处:《合成化学》2016年第5期409-413,共5页Chinese Journal of Synthetic Chemistry
摘 要:以分子筛HZSM-5为前驱体,氨气为氮源,直接高温氮化制得掺氮分子筛HZSM-5-N(1);以Pd(OAc)_2为钯源,1为载体,采用溶胶-固载法制备了一系列不同钯负载量(α)的新型Pd~α/1催化剂,其结构和性质经SEM,FT-IR,元素分析,XRD,N_2-BET和ICP表征。以苯甲醇氧化成苯甲醛反应为探针反应,研究了α,Pd~α/1用量,反应时间和反应温度对Pd~α/1催化性能的影响。结果表明:在最优反应条件(Pd^2/1 40 mg,于120℃反应180min)下,苯甲醇转化率为66.7%,苯甲醛选择性为92.9%。Pd^2/1重复使用性能较好,循环使用5次,催化活性保持不变。The doped nitrogen molecular sieve,HZSM-5-N( 1),was obtained by directly high temperature nitridation,using molecular sieve HZSM-5 as precursor and ammonia as nitrogen source. A series of catalysts( Pd~α/1) with different Pa loading( α) were prepared by sol-immobilization method,using 1as supporter and Pd( OAc)_2as Pd source. The structures and properties of Pd~α/1 were characterized by SEM,FT-IR,elemental analysis,XRD,N_2-BET and ICP. Effects of α,Pd~α/1 dosage,reaction time and temperature on catalytic performances of Pd~α/1 were investgated,using benzyl alcohol oxidation as the template reaction. The results showed that conversion of benzyl alcohol was 66. 7% and selectivity of benzaldehyde was 92. 9% under the optimum reaction conditions( Pd^2/1 40 mg,reacted at120 ℃ for 180 min). The catalytic performance of Pd^2/1 remain stable after recycling for five times.
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