聚磷腈
微球
纳米材料基催化剂
材料科学
化学
纳米技术
化学工程
有机化学
纳米颗粒
聚合物
工程类
作者
Xiufang Chen,Qingguang Xiao,Yiguo Yang,Bo Dong,Zhengping Zhao
出处
期刊:Catalysts
[MDPI AG]
日期:2024-05-27
卷期号:14 (6): 345-345
被引量:2
标识
DOI:10.3390/catal14060345
摘要
The efficient hydrogenation of N-heterocycles with H2 under mild conditions remains a significant challenge. In this work, polyphosphazene (PZs) microspheres, novel organic–inorganic hybrid materials possessing unique –P=N– structural units and a diverse range of side groups, were used to serve as support for the design of a stable and efficient Pd nanocatalyst (Pd/PZs). The PZs microspheres were prepared by self-assembly induced by precipitation polymerization, and Pd nanoparticles were grown and loaded on the support by a chemical reduction process. Several characterization techniques, including XRD, FTIR, SEM, TEM, XPS, BET and TGA, were used to study the structural features of the nanocomposites. The results revealed that Pd nanoparticles were uniformly distributed on the PZs microspheres, with primary sizes ranging from 4 to 9 nm based on the abundance of functional P/N/O groups in PZs. Remarkably high catalytic activity and stability were observed for the hydrogenation of quinoline compounds using the Pd/PZs nanocatalyst under mild conditions. Rates of 98.9% quinoline conversion and 98.5% 1,2,3,4-tetrahydroquinoline selectivity could be achieved at a low H2 pressure (1.5 bar) and temperature (40 °C). A possible reaction mechanism for quinoline hydrogenation over Pd/PZs was proposed. This work presents an innovative approach utilizing a Pd-based nanocatalyst for highly efficient multifunctional hydrogenation.
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