Facile synthesis of Fe3O4@Cu(OH)2 composites and their arsenic adsorption application

被引:104
作者
Peng, Bing [1 ,2 ]
Song, Tingting [1 ]
Wang, Ting [3 ]
Chai, Liyuan [1 ,2 ]
Yang, Weichun [1 ,2 ]
Li, Xiaorui [1 ]
Li, Chaofang [1 ]
Wang, Haiying [1 ,2 ]
机构
[1] Cent S Univ, Sch Met & Environm, Dept Environm Engn, Changsha 410083, Hunan, Peoples R China
[2] Chinese Natl Engn Res Ctr Control & Treatment Hea, Changsha 410083, Peoples R China
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
基金
中国国家自然科学基金;
关键词
Magnetic composites; Fe3O4@Cu(OH)(2); Arsenic; Adsorption; Magnetic separation; HETEROGENEOUS CATALYST; ONE-POT; REMOVAL; OXIDE; WATER; METAL; PARTICLES; NANOSTRUCTURES; NANOPARTICLES; MICROSPHERES;
D O I
10.1016/j.cej.2016.03.135
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A directly coating method, controlled double jet precipitation (CDJP), was developed for synthesizing magnetic Fe3O4@Cu(OH)(2) composites in combination of advantages of magnetic rapid separation and satisfactory adsorption performance. The morphology and structure of the composites were analyzed by SEM, TEM, XRD, FTIR, XPS and VSM techniques. Through controlling the reaction on Fe3O4 particles, directly coating of Cu(OH)(2) was successfully realized without the extra complicated procedures. The obtained Fe3O4@Cu(OH)(2) consists of micro particles of size around 250 nm coated with special leaflike nanomorphologies, possessing high saturation magnetization (from 56.5 to 98.84 emu g(-1)). As the amount of loaded Cu increased, As(V) removal of the composites augmented from 11.11 to 35.71 mg g(-1) far beyond that of reported traditional magnetic adsorbents. The adsorption isotherm was best fitted by Langmuir adsorption mode and the mechanism was mainly ascribed to the -OH functionality of the Fe3O4@Cu(OH)(2) composites and electrostatic attraction between As(V) species and Fe3O4@Cu(OH)(2) composites. The Fe3O4@Cu(OH)(2) composites is a promising candidate for treating arsenic contaminated water. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:15 / 22
页数:8
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