Treatment of Organic Compounds by Activated Persulfate Using Nanoscale Zerovalent Iron

被引:171
作者
Al-Shamsi, Mohammed A. [1 ]
Thomson, Neil R. [1 ]
机构
[1] Univ Waterloo, Dept Civil & Environm Engn, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ZERO-VALENT IRON; HYDROXYL RADICALS; AQUIFER MATERIALS; OXIDIZED PYRITE; FERROUS ION; XPS SPECTRA; OXIDATION; DEGRADATION; SULFATE; SURFACE;
D O I
10.1021/ie400387p
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Recently, persulfate has caught the attention of groundwater remediation practitioners as a promising oxidant for in situ chemical oxidation. In this study, a method was applied to treat a selection of hazardous organic compounds using nanoscale zerovalent iron (nZVI) particles as activators for persulfate. The results show that degradation of these organic compounds using nZVI-activated persulfate is more effective than nZVI alone. For example, the degradation of naphthalene by nZVI-activated persulfate was >99% compared to <10% by nZVI alone. Despite the higher effectiveness, the nZVI particles were passivated quickly following exposure to persulfate, causing the reaction rate to reduce to a magnitude representative of an unactivated persulfate system. X-ray photoelectron spectroscopy analyses indicated that an iron sulfate layer was formed on the nZVI particle surfaces following exposure to persulfate compared to the FeOOH layer that was present on the fresh nZVI surfaces. Although the nZVI particle surfaces are passivated, nZVI appears to be a promising persulfate activator compared to the conventional persulfate activators such as Fe2+ and granular ZVI.
引用
收藏
页码:13564 / 13571
页数:8
相关论文
共 51 条
[1]   A COMPILATION OF SPECIFIC BIMOLECULAR RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS HYDROGEN ATOMS AND HYDROXYL RADICALS WITH INORGANIC AND ORGANIC COMPOUNDS IN AQUEOUS SOLUTION [J].
ANBAR, M ;
NETA, P .
INTERNATIONAL JOURNAL OF APPLIED RADIATION AND ISOTOPES, 1967, 18 (07) :493-&
[2]  
[Anonymous], 2003, ASTMD688903
[3]  
APHA, 1989, Standard methods for the examination of water and wastewater, V17th ed.
[4]  
Baltrus JP, 1997, SURF INTERFACE ANAL, V25, P64, DOI 10.1002/(SICI)1096-9918(199702)25:2<64::AID-SIA203>3.0.CO
[5]  
2-9
[6]   Adsorption of sulfur dioxide on hematite and goethite particle surfaces [J].
Baltrusaitis, Jonas ;
Cwiertny, David M. ;
Grassian, Vicki H. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2007, 9 (41) :5542-5554
[7]   XPS study of the silica-supported Fe-containing catalysts for deep or partial H2S oxidation [J].
Bukhtiyarova, GA ;
Bukhtiyarov, VI ;
Sakaeva, NS ;
Kaichev, VV ;
Zolotovskii, BP .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2000, 158 (01) :251-255
[8]   Methyl Tert-Butyl Ether (MTBE) Degradation by Ferrous Ion-Activated Persulfate Oxidation: Feasibility and Kinetics Studies [J].
Chen, K. F. ;
Kao, C. M. ;
Wu, L. C. ;
Surampalli, R. Y. ;
Liang, S. H. .
WATER ENVIRONMENT RESEARCH, 2009, 81 (07) :687-694
[9]   Nature and distribution of chemical species on oxidized pyrite surface: Complementarity of XPS and nuclear microprobe analysis [J].
Descostes, M ;
Mercier, F ;
Beaucaire, C ;
Zuddas, P ;
Trocellier, P .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 2001, 181 :603-609
[10]   Use of XPS in the determination of chemical environment and oxidation state of iron and sulfur samples: constitution of a data basis in binding energies for Fe and S reference compounds and applications to the evidence of surface species of an oxidized pyrite in a carbonate medium [J].
Descostes, M ;
Mercier, F ;
Thromat, N ;
Beaucaire, C ;
Gautier-Soyer, M .
APPLIED SURFACE SCIENCE, 2000, 165 (04) :288-302