2006
DOI: 10.1016/j.molcata.2006.01.060
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A Fe-promoted Ni–P amorphous alloy catalyst (Ni–Fe–P) for liquid phase hydrogenation of m- and p-chloronitrobenzene

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Cited by 89 publications
(31 citation statements)
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“…Thus, it is possible to generate the efficient H * from water/ethanol donor for the hydrogenation of halogenated nitrobenzenes under the appropriate conditions. The H * on the active sites of the catalyst transferred from water/ethanol donor could be promptly removed by reacting with halogenated nitrobenzene immediately to form the stable amine, which lead to the novel hydrogenation of aromatic nitro compounds in a more efficient way [17] also found that the catalytic activity and selectivity could be enhanced by the Fe-doped catalyst. The electron-deficient Fe promoted the activity of the Ru atoms by activating the polar NO 2 groups of halogenated nitrobenzene and coordinating with the NH 2 groups of produced of aromatic aniline [18,19], and which also could weaken the extent of electron feedback from the Ru atoms to the aromatic ring in aromatic aniline thereby promoting the hydrogenation of halogenated nitrobenzene and further depressing the hydrodehalogenation of aromatic aniline.…”
Section: The Novel Catalytic Transfer Hydrogenation Of Halogenated Nimentioning
confidence: 95%
“…Thus, it is possible to generate the efficient H * from water/ethanol donor for the hydrogenation of halogenated nitrobenzenes under the appropriate conditions. The H * on the active sites of the catalyst transferred from water/ethanol donor could be promptly removed by reacting with halogenated nitrobenzene immediately to form the stable amine, which lead to the novel hydrogenation of aromatic nitro compounds in a more efficient way [17] also found that the catalytic activity and selectivity could be enhanced by the Fe-doped catalyst. The electron-deficient Fe promoted the activity of the Ru atoms by activating the polar NO 2 groups of halogenated nitrobenzene and coordinating with the NH 2 groups of produced of aromatic aniline [18,19], and which also could weaken the extent of electron feedback from the Ru atoms to the aromatic ring in aromatic aniline thereby promoting the hydrogenation of halogenated nitrobenzene and further depressing the hydrodehalogenation of aromatic aniline.…”
Section: The Novel Catalytic Transfer Hydrogenation Of Halogenated Nimentioning
confidence: 95%
“…However, excessive load of Fe x O y led to the overconsumption of ethanol water during FTS, leading to reformed active hydrogen. Meanwhile, a part of Pt-Fe active sites were covered by Fe x O y , which reduced the effective utilization rate of active components [26]. On the contrary, the Fe-in/CNTs did not show the m-CNB in-situ hydrogenation activity, while the catalytic activity of Pt-in-Fe-out/CNTs was improved only to 16.7 h −1 .…”
Section: Introductionmentioning
confidence: 95%
“…Dragieva et al focused on developing amorphous alloys as electrode or catalytic oxidation materials [38][39][40][41][42][43], while Chen and coworkers prepared MPB alloy nanoparticle catalysts for various selective hydrogenation reactions [44][45][46][47][48][49][50]. Amorphous alloy nanoparticulate catalysts have been widely studied by different research groups in China [51][52][53][54][55][56][57][58][59][60]. Among them, our group has attempted to develop NiB and NiP industrial amorphous alloy catalysts in various catalytic hydrogenation reactions [61][62][63][64][65][66][67][68][69][70][71][72].…”
Section: History Of Amorphous Alloy Catalystmentioning
confidence: 99%