苯甲醇
硼氢化钠
二乙烯基苯
离子液体
介孔材料
共聚物
催化作用
离子键合
苯甲醛
纳米颗粒
材料科学
溶剂
化学工程
酒精氧化
化学
高分子化学
无机化学
有机化学
苯乙烯
离子
纳米技术
聚合物
工程类
作者
Qian Wang,Xiaochun Cai,Yangqing Liu,Jianhui Xie,Yu Zhou,Jun Wang
标识
DOI:10.1016/j.apcatb.2016.02.067
摘要
A series of functional cross-linked mesoporous poly(ionic liquid)s (MPILs) were prepared through the free radical copolymerization of divinylbenzene (DVB) and imidazolium salts based ionic liquids tethered with different groups (−COOH, C4H9, −CN and −NH2). These MPILs were applied as supports to prepare immobilized palladium (Pd) nanoparticles (NPs) through ion exchanging with sodium tetrachloropalladate(II) (Na2PdCl4) and successive reduction by sodium borohydride (NaBH4). Highly uniform and narrow dispersed Pd NPs attained on the carboxyl modified MPIL with large surface area and high ionic density. The obtained materials acted as an efficient and stable recycling heterogeneous catalyst for the atmospheric pressure oxidation of benzyl alcohol to benzaldehyde by using O2 as the oxidant and water as the sole solvent at low temperature (90 °C). The special ionic framework with −COOH group plays a major role in the formation and stabilization of ultrafine Pd NPs. This work indicates that controlling the textural properties of ionic copolymers serves as a facile and efficient way to fabricate immobilized stable metal NPs.
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