以Al^3+/(Al^3++Mg^2+)摩尔比为0.2的水滑石(HT)为载体,采用还原浸渍法制备了负载型Pd—Ce—B/HT催化剂,并将其应用于液相苯酚选择性加氢制环己酮.与Pd—Ce—B/Al2O3,Pd—Ce—B/MgO和Pd—Ce—B/SiO2相比,Pd—Ce-B/HT催化剂具有高活性和高环己酮选择性.5.8%Pd—Ce—B/HT上苯酚的转化率和环己酮的选择性分别达82.0%和80.3%,显示了其潜在的工业化应用前景.根据多种表征结果,初步讨论了催化剂的构效关系以及添加剂Ce^3+和载体酸碱性对催化性能的促进作用.
Supported Pd-Ce-B catalysts were prepared by chemical reduction of Pd and Ce ions deposited on hydrotalcite (HT) with an Al^3+/(Al^3+ + Mg^2+ ) molar ratio of 0.2. In the reaction of liquid-phase selective hydrogenation of phenol, the as-prepared Pd-Ce-B/HT catalyst exhibited much higher activity and selectivity for cyclohexanone than Pd-Ce-B/Al2O3, Pd-Ce-B/MgO, and Pd-Ce-B/SiO2. The maximum phenol conversion and selectivity for cyclohexanone over 5.8 % Pd-Ce-B/HT reached 82.0 % and 80.3 %, respectively. Based on the results of various characterizations, the catalyst structure-activity correlation and the promoting effects of the Ce dopant and acidic-basic properties of the support on the catalyst behavior were discussed.