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Hydrodechlorination of 4-Chlorophenol on Pd-Fe Catalysts on Mesoporous ZrO

机译:4-氯苯酚对介孔ZRO的PD-Fe催化剂氢化氢化物

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摘要

A mesoporous support based on silica and zirconia (ZS) was used to prepare monometallic 1 wt% Pd/ZS, 10 wt% Fe/ZS, and bimetallic FePd/ZS catalysts. The catalysts were characterized by TPR-H2, XRD, SEM-EDS, TEM, AAS, and DRIFT spectroscopy of adsorbed CO after H2 reduction in situ and tested in hydrodechlorination of environmental pollutant 4-chlorophelol in aqueous solution at 30 °C. The bimetallic catalyst demonstrated an excellent activity, selectivity to phenol and stability in 10 consecutive runs. FePd/ZS has exceptional reducibility due to the high dispersion of palladium and strong interaction between FeOx and palladium, confirmed by TPR-H2, DRIFT spectroscopy, XRD, and TEM. Its reduction occurs during short-time treatment with hydrogen in an aqueous solution at RT. The Pd/ZS was more resistant to reduction but can be activated by aqueous phenol solution and H2. The study by DRIFT spectroscopy of CO adsorbed on Pd/ZS reduced in harsh (H2, 330 °C), medium (H2, 200 °C) and mild conditions (H2 + aqueous solution of phenol) helped to identify the reasons of the reducing action of phenol solution. It was found that phenol provided fast transformation of Pd+ to Pd0. Pd/ZS also can serve as an active and stable catalyst for 4-PhCl transformation to phenol after proper reduction.
机译:基于二氧化硅和氧化锆(ZS)的介孔载体用于制备单金属1wt%pd / zs,10wt%Fe / Zs和双金属FEPD / ZS催化剂。通过TPR-H2,XRD,SEM-EDS,TEM,AAS和漂移光谱在H2降低后的TPR-H2,XRD,SEM-EDS,TEM,AAS和漂移光谱,并在30℃下在水溶液中的环境污染物4-氯酚的水解中进行。双金属催化剂证明了优异的活性,在连续10次运行中对苯酚的选择性和稳定性。 FEPD / ZS由于钯的高分散性和飞钯和钯之间的强互动,通过TPR-H2,漂移光谱,XRD和TEM证实,具有卓越的还原性。其在室温下在水溶液中的氢气处理期间发生的还原。 PD / ZS更耐抗还原,但可以通过酚溶液和H 2激活。在苛刻(H2,330℃),培养基(H2,200℃)和温和条件下(H2 +水溶液)的漂蒸在Pd / Zs上的漂移光谱研究有助于确定还原的原因苯酚溶液的作用。发现苯酚提供了PD +至PD0的快速变换。 Pd / Zs还可以作为4-PHCl转化的活性和稳定的催化剂在适当还原后对苯酚转化。

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