Embedding Pd-Cu Alloy Nanoparticles in Shell of Surface-Porous N-Doped Carbon Nanosphere for Selective Hydrogenation of p-Chloronitrobenzene

被引:10
作者
Liu, Yingcen [1 ]
Ye, Wanyue [1 ]
Lin, Hua [1 ]
Song, Caicheng [1 ]
Rong, Zeming [1 ]
Lu, Rongwen [1 ]
Zhang, Hao [1 ]
Huang, He [1 ]
Tang, Zhicheng [1 ]
Zhang, Shufen [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116024, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Alloys; Supported catalysts; Chemoselectivity; p-Chloronitrobenzene; Superficially embedding; CATALYTIC-HYDROGENATION; ACETYLENE HYDROGENATION; INTERMETALLIC COMPOUND; METAL NANOPARTICLES; NANOCRYSTALS; REDUCTION; ENHANCEMENT; PERFORMANCE; EFFICIENT; NANOSHEET;
D O I
10.1002/cjoc.202100261
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Main observation and conclusion A catalyst PdxCuy/NC in which Pd-Cu alloy nanoparticles are superficially embeded in shell of surface-porous N-doped carbon nanosphere was successfully devised for p-chloronitrobenzene (p-CNB) selective hydrogenation. Bimetal ions were loaded in shell of a m-phenylenediamine derived core-shell polymer sphere and the catalyst was obtained after calcination under reducing atmosphere. The as synthesized catalyst exhibited high selectivity in hydrogenation of p-CNB to p-chloroaniline (p-CAN) (up to 98.8%) under full conversion and the performance was basically remained after 6 cyclic experiments. The reasons for the high selectivity were discussed based on the characterization results of catalyst. The interaction between N-doped support and metal atoms affected the electron distribution in alloy, electron-deficient Pd and electron-rich Cu, and thus improved hydrogenation selectivity. In addition, the alloy nanoparticles were distributed only in the porous shell of support, which benefits to prevent side reactions. This work described a scheme for tactfully designing catalyst for selective hydrogenation, which can provide experience and inspiration for relevant works and fields.
引用
收藏
页码:2843 / 2851
页数:9
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