Synthesis of magnetically recyclable Fe3O4@NiO nanostructures for styrene epoxidation and adsorption application

被引:27
作者
Li, Tianyong [1 ]
Yang, Chao [1 ]
Rao, Xuehui [1 ]
Xiao, Feng [1 ]
Wang, Jide [1 ]
Su, Xintai [1 ]
机构
[1] Xinjiang Univ, Coll Chem & Chem Engn, Minist Key Lab Oil & Gas Fine Chem, Urumqi 830046, Peoples R China
关键词
Fe3O4@NiO composite; Core-shell nanostructures; Adsorption; Magnetically recyclable; Olefin epoxidation; NEGATIVE-ELECTRODE MATERIALS; LITHIUM-ION BATTERIES; CO OXIDATION; NIO; NANOPARTICLES; CATALYST; REMOVAL; CARBON; GAS; NANOCOMPOSITE;
D O I
10.1016/j.ceramint.2014.10.022
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A solvothermal method combining a calcination process was conducted to synthesize Fe3O4@NiO core-shell hierarchical nanostructures. First, Fe3O4 microspheres were synthesized through a solvothermal method by using ethylene glycol as solvent. Second, Fe3O4@Ni(OH)(2) core-shell hierarchical nanostructures were prepared through an in situ growing procedure. Third, Fe3O4@NiO core-shell hierarchical nanostructures were obtained from the Fe3O4@Ni(OH)(2) precursors by a simple calcination procedure. The results showed that the Fe3O4 core was about 250 nm in diameter and the NiO shell was around 30 nm in thickness. The Fe3O4@NiO core shell nanostructures were used as a magnetically separable adsorbent for the removal of Congo red (CR) dye from aueous solution, which exhibited a high adsorption capacity of 128.9 mg g(-1). Moreover, the Fe3O4@NiO core-shell nanostructures displayed a superior catalytic property for the epoxidation of styrene with an extremely high selectivity (100%), conversion (99%) and yield (99%). Such Fe3O4@NiO catalyst could be conveniently recycled from the reaction system by using a magnet and without any noticeable catalytic deactivation even after five cycles. The results indicate that the as-prepared core-shell materials can be used as a recyclable catalyst for the epoxidation of styrene. (C) 2014 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:2214 / 2220
页数:7
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