Size effect in reactivity of copper nanoparticles to carbon tetrachloride degradation

被引:35
作者
Liou, Ya Hsuan [1 ]
Lo, Shang Lien [1 ]
Lin, Chin Jung [1 ]
机构
[1] Natl Taiwan Univ, Res Ctr Environm Pollut Prevent & Control Technol, Grad Inst Environm Engn, Taipei 106, Taiwan
关键词
carbon tetrachloride; nanoparticle; size effect; zero valent metal;
D O I
10.1016/j.watres.2007.01.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Surface area-normalized rate constants (k(SA)) of reaction between metallic nanoparticles and reducible contaminants, such as chlorinated hydrocarbons, heavy metals, and nitrate, have been reported to be dramatically increased as compared to that of commercial metallic powder. However, k(SA) for individual pollutants in previously published data vary by as much as 1-2 orders of magnitude and much of this variability is due to the effect of various sizes. The size dependence of the reactivity of nanoparticles is not yet fully understood; however, yielding nanoparticles with uniform size and without agglomeration during the period of reaction would demonstrate the effect of varying particle size. In this study, resin-supported zerovalent copper with average particle size of 7, 10, 18, 26, and 29, respectively, were successfully synthesized and evidenced no agglomeration during the reaction period of 10 h. The k(SA) of copper nanoparticles (k(n,SA)) was 110-120 times higher than that of powdered copper particles (k(p,SA)) when the copper particle size was about 10 nm. However, for diameters of 18-29 nm, the ratio of k(n,SA)/k(p,SA) was around 10-20, indicating that the reactivity of small copper nanoparticles (similar to 10 nm) varies discontinuously. Thus, most variability in previous kSA is attributed to the presence of small nanoparticles. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1705 / 1712
页数:8
相关论文
共 29 条
[1]   Reduction of nitro aromatic compounds by zero-valent iron metal [J].
Agrawal, A ;
Tratnyek, PG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (01) :153-160
[2]   AN IMPROVED PROCEDURE FOR ESTIMATING THE METAL-SURFACE AREA OF SUPPORTED COPPER-CATALYSTS [J].
BOND, GC ;
NAMIJO, SN .
JOURNAL OF CATALYSIS, 1989, 118 (02) :507-510
[3]  
BOUNDART M, 1984, KINETICS HETEROGENEO, P20
[4]   Chlorinated ethene reduction by cast iron: Sorption and mass transfer [J].
Burris, DR ;
Allen-King, RM ;
Manoranjan, VS ;
Campbell, TJ ;
Loraine, GA ;
Deng, BL .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1998, 124 (10) :1012-1019
[5]   Injection of colloidal Fe-0 particles in sand with shear-thinning fluids [J].
Cantrell, KJ ;
Kaplan, DI ;
Gilmore, TJ .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1997, 123 (08) :786-791
[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]   Rapid reductive destruction of hazardous organic compounds by nanoscale Fe0 [J].
Choe, S ;
Lee, SH ;
Chang, YY ;
Hwang, KY ;
Khim, J .
CHEMOSPHERE, 2001, 42 (04) :367-372
[8]   ON THE DETERMINATION OF COPPER SURFACE-AREA BY REACTION WITH NITROUS-OXIDE [J].
EVANS, JW ;
WAINWRIGHT, MS ;
BRIDGEWATER, AJ ;
YOUNG, DJ .
APPLIED CATALYSIS, 1983, 7 (01) :75-83
[9]   Pathways and kinetics of carbon tetrachloride and chloroform reductions by nano-scale Fe and Fe/Ni particles: comparison with commercial micro-scale Fe and Zn [J].
Feng, J ;
Lim, TT .
CHEMOSPHERE, 2005, 59 (09) :1267-1277
[10]   ENHANCED DEGRADATION OF HALOGENATED ALIPHATICS BY ZERO-VALENT IRON [J].
GILLHAM, RW ;
OHANNESIN, SF .
GROUND WATER, 1994, 32 (06) :958-967