Electrochemical synthesis of FexNi1-x nanostructures for environmental remediation

被引:28
作者
Hong, Yongsuk [1 ]
Rheem, Youngwoo [1 ]
Lai, Min [1 ]
Cwiertny, David M. [1 ]
Walker, Sharon L. [1 ]
Myung, Nosang V. [1 ]
机构
[1] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92521 USA
关键词
Nanoparticles; Electrodeposition; FeNi alloy; Environmental remediation; Chlorinated ethane; ZERO-VALENT IRON; COMPLETE DECHLORINATION; NICKEL; REDUCTION; PARTICLES; KINETICS; PATHWAYS; FE; NANOPARTICLES; STABILITY;
D O I
10.1016/j.cej.2009.01.048
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
FexNi1-x nanostructures with different compositions (0 < x < 1.0) were electrodeposited from simple aqueous electrolytes with different ferric ion and nickel ion ratios. Composition, morphology, crystal structure, magnetic properties and electronegativity of the synthesized FexNi1-x nanostructures were systematically investigated. As the composition of Fe (x) in FexNi1-x nanostructures decreased from 1.0 to 0, the morphology changed from dendritic to nanoparticles and thin plates. The X-ray diffraction (XRD) patterns revealed that the dominant crystal structures shifted from metallic body centered cubic (bcc) for iron-rich FexNi1-x to mixed bcc and faced center cubic (fcc) for near equiatomic FeNi to rhombohedral/hexagonal for nickel-rich FeNi. The magnetic saturation and isoelectric point were also strongly dependent on nanostructure composition. Specifically, the magnetic saturation decreased and the isoelectric point increased with decreasing Fe content. When Fe content in FexNi1-x nanostructures was greater than 0.5 (x > 0.5), FexNi1-x nanostructures showed mainly metallic (zero-valent) Fe present as determined by XRD and selected area electron diffraction (SAED) patterns. Accordingly. Fe-1.0, Fe0.71Ni0.29 and Fe0.55Ni0.45 exhibited reactivity toward 1,1,1,2-tetrachloroethane, with Fe-1.0 yielding the greatest rate of reductive dechlorination. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 72
页数:7
相关论文
共 66 条
[21]   Highly efficient endosomal labeling of progenitor and stem cells with large magnetic particles allows magnetic resonance imaging of single cells [J].
Hinds, KA ;
Hill, JM ;
Shapiro, EM ;
Laukkanen, MO ;
Silva, AC ;
Combs, CA ;
Varney, TR ;
Balaban, RS ;
Koretsky, AP ;
Dunbar, CE .
BLOOD, 2003, 102 (03) :867-872
[22]   Kinetics of nitrate reduction by iron at near neutral pH [J].
Huang, YH ;
Zhang, TC .
JOURNAL OF ENVIRONMENTAL ENGINEERING, 2002, 128 (07) :604-611
[23]   Magnetic properties of graphitically encapsulated nickel nanocrystals [J].
Hwang, JH ;
Dravid, VP ;
Teng, MH ;
Host, JJ ;
Elliott, BR ;
Johnson, DL ;
Mason, TO .
JOURNAL OF MATERIALS RESEARCH, 1997, 12 (04) :1076-1082
[24]   Synthesis of highly crystalline and monodisperse maghemite nanocrystallites without a size-selection process [J].
Hyeon, T ;
Lee, SS ;
Park, J ;
Chung, Y ;
Bin Na, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (51) :12798-12801
[25]   The effect of humic acid adsorption on pH-dependent surface charging and aggregation of magnetite nanoparticles [J].
Illés, E ;
Tombácz, E .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2006, 295 (01) :115-123
[26]   Influences of metal ions on the formation of γ-FeOOH and magnetite rusts [J].
Ishikawa, T ;
Kumagai, M ;
Yasukawa, A ;
Kandori, K ;
Nakayama, T ;
Yuse, F .
CORROSION SCIENCE, 2002, 44 (05) :1073-1086
[27]   Factors governing the electrochemical synthesis of α-nickel (II) hydroxide [J].
Jayashree, RS ;
Kamath, PV .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1999, 29 (04) :449-454
[28]   Preparation of nickel hydroxide nanorods/nanotubes and microscopic nanorings under hydrothermal conditions [J].
Jiao, Qing-Ze ;
Tian, Zhou-Ling ;
Zhao, Yun .
JOURNAL OF NANOPARTICLE RESEARCH, 2007, 9 (03) :519-522
[29]   Kinetics of halogenated organic compound degradation by iron metal [J].
Johnson, TL ;
Scherer, MM ;
Tratnyek, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (08) :2634-2640
[30]   Controlling transport and chemical functionality of magnetic nanoparticles [J].
Latham, Andrew H. ;
Williams, Mary Elizabeth .
ACCOUNTS OF CHEMICAL RESEARCH, 2008, 41 (03) :411-420