苯甲腈
双金属片
催化作用
苄胺
选择性
化学
吸附
甲苯
化学选择性
多相催化
氢解
钯
组合化学
无机化学
产量(工程)
有机化学
光化学
材料科学
化学稳定性
化学工程
选择性吸附
协同催化
作者
Li Ma,Feng Zhang,Minghao Sun,Z X Chen,Shuxing Bai
摘要
ABSTRACT Benzylamine (BA), a vital chemical intermediate, is traditionally synthesized via the hydrogenation of benzonitrile (BN). However, this process often suffers from poor selectivity toward BA over monometallic Pd catalysts, leading to by‐products like toluene and dibenzylamine (DBA). Herein, we report a series of Pd–Ni bimetallic heterogeneous catalysts for the highly selective hydrogenation of BN to BA under mild conditions. The optimized Pd 3 Ni/TiO 2 catalyst exhibited exceptional performance at 50 °C and 0.2 MPa H 2 , achieving a BN conversion of 97.0% and a BA selectivity of 95.0%, significantly outperforming its monometallic Pd/TiO 2 counterpart. Comprehensive characterization revealed that alloying Pd with Ni modulates the electronic structure of Pd, enhancing the activation of BN while weakening the strong adsorption of the BA product and key intermediates. This differential adsorption tuning effectively suppresses over‐hydrogenation and coupling side reactions. Furthermore, the Pd 3 Ni/TiO 2 catalyst demonstrated excellent stability over 10 catalytic cycles. This work provides an effective strategy for designing efficient and selective hydrogenation catalysts through bimetallic synergy.
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