Nickel sulfide nanoparticles on alumina and unsupported for p-chloroaniline production

被引:0
|
作者
Olivas, A. [1 ]
Rodriguez, J. R. [2 ]
Cardenas-Lizana, F. [3 ]
Cota-Leal, M. [1 ]
Keane, M. A. [3 ]
机构
[1] Natl Autonomous Univ Mexico CNyN UNAM, Ctr Nanosci & Nanotechnol, Carretera Tijuana Ensenada Km 107, Ensenada 22860, Baja California, Mexico
[2] CNyN UNAM, PCeIM, Carretera Tijuana Ensenada Km 107, Ensenada 22860, Baja California, Mexico
[3] Heriot Watt Univ, Sch Engn & Phys Sci, Chem Engn, Edinburgh EH14 4AS, Midlothian, Scotland
来源
CHALCOGENIDE LETTERS | 2022年 / 19卷 / 05期
关键词
Ni-based catalysts; Sol-gel method; Solvothermal method; p-chloronitrobenzene (p-CNB); Hydrogenation; p-chloroaniline (p-CA); GAS-PHASE HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; CATALYTIC-HYDROGENATION; SELECTIVE HYDROGENATION; M-CHLORONITROBENZENE; SUPPORTED PLATINUM; EFFICIENT CATALYST; NI; NITROARENES; REDUCTION;
D O I
10.15251/CL.2022.195.337
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Due to the need for producing intermediate chemicals such as p-chloroaniline (p-CA) using more environmentally friendly and efficient processes, nanostructured nickel and nickel sulfide-based catalysts were synthesized and studied. The selective pchloronitrobenzene (p-CNB) gas-phase hydrogenation to produce p-CA was tested. The catalysts were characterized by N-2 physisorption (S-BET), temperature-programmed reduction (TPR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The catalytic activity was evaluated in terms of conversion and selectivity towards p-CNB and p-CA, respectively. Based on the experimental results, the addition of sulfur promoted the selectivity towards p-CA in a range of temperature from 120 to 220 degrees C. The selectivity towards p-CA was close to 100 %, avoiding the formation of undesirable side products. Therefore, it is suggested that sulfured-Ni based catalysts increase the surface acidity, which allowed improved hydrogenolysis of the N-O bond.
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页码:337 / 352
页数:16
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