The application of zero-valent iron nanoparticles for the remediation of a uranium-contaminated waste effluent

被引:198
作者
Dickinson, Michelle [1 ]
Scott, Thomas B. [1 ]
机构
[1] Univ Bristol, Interface Anal Ctr, Bristol BS8 1TH, Avon, England
关键词
Iron; Nanoparticles; Uranium; Remediation; Zero-valent; RAY PHOTOELECTRON-SPECTROSCOPY; SUPPORTED ZEROVALENT IRON; REACTIVE BARRIER; REDUCTION; PARTICLES; REMOVAL; GROUNDWATER; KINETICS; SURFACE; METAL;
D O I
10.1016/j.jhazmat.2010.01.060
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Zero-valent iron nanoparticles (INP) were investigated as a remediation strategy for a uranium-contaminated waste effluent from AWE, Aldermaston. Nanoparticles were introduced to the effluent, under both oxic and anoxic conditions, and allowed to react for a 28-d period during which the liquid and nanoparticle solids were periodically sampled. Analysis of the solution indicated that under both conditions U was removed to <1.5% of its initial concentration within 1 h of introduction and remained at similar concentrations until approximately 48 h. A rapid release of Fe into solution was also recorded during this initial period; attributed to the limited partial dissolution of the INP. XPS analyses of the reacted nanoparticulate solids between 1 and 48 h showed an increased Fe(III):Fe(II) ratio, consistent with the detection of iron oxidation products (akaganeite and magnetite) by XRD and FIB. XPS analysis also recorded uranium on the recovered particulates indicating the chemical reduction of U(VI) to U(IV) within 1 h. Following the initial retention period U-dissolution of U was recorded from 48 h, and attributed to reoxidation. The efficient uptake and retention of U on the INP for periods up to 48 h provide proof that INP may be effectively used for the remediation of complex U-contaminated effluents. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 179
页数:9
相关论文
共 52 条
[1]  
ALLEN GC, 1974, J CHEM SOC DA, V14, P1525
[2]   Kinetics of nitrate, nitrite, and Cr(VI) reduction by iron metal [J].
Alowitz, MJ ;
Scherer, MM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (03) :299-306
[3]   Zero-valent iron for water treatment [J].
Bigg, T ;
Judd, SJ .
ENVIRONMENTAL TECHNOLOGY, 2000, 21 (06) :661-670
[4]   Immobilization of uranium and arsenic by injectible iron and hydrogen stimulated autotrophic sulphate reduction [J].
Burghardt, D. ;
Simon, E. ;
Knoeller, K. ;
Kassahun, A. .
JOURNAL OF CONTAMINANT HYDROLOGY, 2007, 94 (3-4) :305-314
[5]   ZERO-VALENT IRON FOR THE IN-SITU REMEDIATION OF SELECTED METALS IN GROUNDWATER [J].
CANTRELL, KJ ;
KAPLAN, DI ;
WIETSMA, TW .
JOURNAL OF HAZARDOUS MATERIALS, 1995, 42 (02) :201-212
[6]   Perchlorate reduction by nanoscale iron particles [J].
Cao, JS ;
Elliott, D ;
Zhang, WX .
JOURNAL OF NANOPARTICLE RESEARCH, 2005, 7 (4-5) :499-506
[7]   A radiotracer study of the adsorption behavior of aqueous Ba2+ ions on nanoparticles of zero-valent iron [J].
Celebi, O. ;
Uezuem, C. ;
Shahwan, T. ;
Erten, H. N. .
JOURNAL OF HAZARDOUS MATERIALS, 2007, 148 (03) :761-767
[8]   Decontamination of TCE- and U-rich waters by granular iron: Role of sorbed Fe(II) [J].
Charlet, L ;
Liger, E ;
Gerasimo, P .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1998, 124 (01) :25-30
[9]   Comparison of reductive dechlorination of p-chlorophenol using Fe0 and nanosized Fe0 [J].
Cheng, Rong ;
Wang, Jian-long ;
Zhang, Wei-xian .
JOURNAL OF HAZARDOUS MATERIALS, 2007, 144 (1-2) :334-339
[10]   Kinetics of reductive denitrification by nanoscale zero-valent iron [J].
Choe, S ;
Chang, YY ;
Hwang, KY ;
Khim, J .
CHEMOSPHERE, 2000, 41 (08) :1307-1311