g-C3N4 anchored Cu(Ⅰ) highly selective catalytic synthesis of 2,4,4,4-tetrachlorobutyronitrile using CCl4 and acrylonitrile

被引:0
|
作者
Xiao Z. [1 ,2 ]
Li J. [1 ,2 ]
Chen Y. [1 ,2 ]
Lan Z. [1 ,2 ]
Yin D. [1 ,2 ]
机构
[1] College of Chemistry and Chemical Engineering, Hunan Normal University, Hunan, Changsha
[2] National & Local Joint Engineering Laboratory for New Petro-Chemical Materials and Fine Utilization of Resources, Hunan, Changsha
关键词
2,4,4,4-tetrachloronitrile; atom transfer radical addition (ATRA); Cu/CN catalyst; g-C[!sub]3[!/sub]N[!sub]4[!/sub;
D O I
10.16085/j.issn.1000-6613.2023-0762
中图分类号
学科分类号
摘要
CuCNn (n=1, 2, 3) catalysts with different Cu loading amounts were prepared by thermal condensation using urea and Cu(NO3)2·3H2O as precursors, The structures and morphology of the catalysts were characterized by XRD, FTIR, XPS, BET, SEM and TEM. The catalytic performance of Cu/CNn with different Cu loading amounts was compared in the atom transfer radical addition (ATRA) reaction of CCl4 with acrylonitrile (AN) to synthesize 2,4,4,4-tetrachlorobutanitrile (TBN). The results showed that the Cu/CN1 exhibited excellent catalytic performance. Using acetonitrile (MeCN) as a solvent, n(Cu/CN1)∶n(AN)= 1∶1000, 120℃, for 12h, the selectivity and yield of TBN can reach 96.5% and 83.3%, respectively. As a heterogeneous catalyst, Cu/CN can be reused only after filtration treatment, and its catalytic activity can still be stably maintained after 7 times of use. Based on the relevant experimental results, the oxidation-reduction cycle ATRA reaction mechanism of CCl4 and AN catalyzed by Cu/CN was proposed. The results of experiments revealed the synergistic mechanism of Cu and g-C3N4, providing a new idea for the development of efficient catalytic systems for CCl4 deep processing. © 2024 Chemical Industry Press Co., Ltd.. All rights reserved.
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页码:3293 / 3300
页数:7
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