双金属片
三聚氰胺
催化作用
化学工程
材料科学
选择性
化学
无机化学
核化学
有机化学
复合材料
工程类
作者
Xinzheng Ma,Luyao Guo,Ziang Zhao,Yu Meng,Xiaoling Mou,Ronghe Lin,Yihui Li,Yan Li,Hejun Zhu,Yunjie Ding
出处
期刊:Chemcatchem
[Wiley]
日期:2023-08-25
卷期号:15 (19)
被引量:1
标识
DOI:10.1002/cctc.202300703
摘要
Abstract Different bimetallic platinum and bismuth catalysts supported on melamine‐modified activated carbon (AC) are designed by a co‐impregnation method. Through controlling the activation temperatures of the melamine−AC mixture, a series of N‐doped and C 3 N 4 ‐modified AC (N−AC and C 3 N 4 −AC) are prepared. Combined powder X‐ray diffractions, X‐ray photoelectron spectroscopic, and high‐angle annual dark‐field scanning transmission electron microscopic studies demonstrate that the introduction of C 3 N 4 favors the formation of PtBi alloy and leads to increased particle sizes in comparison to the pristine and N‐doped AC‐supported bimetallics. The catalytic performance of the developed catalysts is evaluated in the oxidation of n ‐heptanol oxidation in a batch mode using O 2 as the oxidant. PtBi/C 3 N 4 −AC exhibits significantly boosted activity as well as selectivity to heptanoic acid as compared with the other catalysts. A high yield of heptanoic acid of 69 % can be achieved under the optimized reaction conditions. Furthermore, our work points to the PtBi alloy as the most active sites for the alcohol oxidation. Catalyst deactivation occurs in the cycling tests, mainly due to the collapse of the alloy phase and likely the decrease in particle sizes.
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