Mechanism of Persulfate Activation by Phenols

被引:423
作者
Ahmad, Mushtaque [1 ]
Teel, Amy L. [1 ]
Watts, Richard J. [1 ]
机构
[1] Washington State Univ, Dept Civil & Environm Engn, Pullman, WA 99163 USA
关键词
RATE CONSTANTS; CHLORINATED PHENOLS; HYDROXYL RADICALS; OXIDATION; SULFATE;
D O I
10.1021/es400728c
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The activation of persulfate by phenols was investigated to further the understanding of persulfate chemistry for in situ chemical oxidation (ISCO). Phenol (pK(a) = 10.0) activated persulfate at pH 12 but not at pH 8, suggesting activation occurred only via the, phenoxide form. Evaluation of the phenoxide activation,mechanism was complicated by the concurrent activation of persulfate by hydroperoxide anion, which is generated by the base catalyzed hydrolysis of persulfate. Therefore, phenoxide activation was investigated using pentachlorophenoxide at pH 8.3, midway between the pK(a) of pentachlorophenol (pK(a) = 4.8) and that of hydrogen peroxide (pK(a) = 11.8). Of the two possible mechanisms for phenoxide activation of persulfate (reduction or nucleophilic attack) the results were consistent with reduction of persulfate by phenoxide with oxidation of the phenoxide. The concentration of phenoxide required for maximum persulfate activation was low (1 mM). The results of this research document at phenoxides activate persulfate via reduction; phenolic, moieties ubiquitous to soil organic matter in the subsurface may have a significant role in the activation of persulfate during its injection into the subsurface for ISCO. Furthermore, the results provide the foundation for activation of persulfate by other organic anions without the toxicity of phenols, such as keto acids.
引用
收藏
页码:5864 / 5871
页数:8
相关论文
共 28 条
[1]   Oxidative and Reductive Pathways in Iron-Ethylenediaminetetraacetic Acid-Activated Persulfate Systems [J].
Ahmad, Mushtaque ;
Teel, Amy L. ;
Furman, Olha S. ;
Reed, Joshua I. ;
Watts, Richard J. .
JOURNAL OF ENVIRONMENTAL ENGINEERING, 2012, 138 (04) :411-418
[2]   Persulfate activation by subsurface minerals [J].
Ahmad, Mushtaque ;
Teel, Amy L. ;
Watts, Richard J. .
JOURNAL OF CONTAMINANT HYDROLOGY, 2010, 115 (1-4) :34-45
[3]   The Elbs and Boyland-Sims peroxydisulfate oxidations [J].
Behrman, E. J. .
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2006, 2
[4]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[5]   RATE CONSTANTS FOR HYDROGEN ABSTRACTION REACTIONS OF THE SULFATE RADICAL, SO4- - ALCOHOLS [J].
CLIFTON, CL ;
HUIE, RE .
INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 1989, 21 (08) :677-687
[6]   SPECTROPHOTOMETRIC DETERMINATION OF HYDROGEN PEROXIDE WITH 8-QUINOLINOL [J].
COHEN, IR ;
PURCELL, TC .
ANALYTICAL CHEMISTRY, 1967, 39 (01) :131-&
[7]   Effect of Basicity on Persulfate Reactivity [J].
Furman, Olha S. ;
Teel, Amy L. ;
Ahmad, Mushtaque ;
Merker, Marissa C. ;
Watts, Richard J. .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 2011, 137 (04) :241-247
[8]   Mechanism of Base Activation of Persulfate [J].
Furman, Olha S. ;
Teel, Amy L. ;
Watts, Richard J. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (16) :6423-6428
[9]   CHLORINATED BY-PRODUCTS FROM THE TIO2-MEDIATED PHOTODEGRADATION OF TRICHLOROETHYLENE AND TETRACHLOROETHYLENE IN WATER [J].
GLAZE, WH ;
KENNEKE, JF ;
FERRY, JL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (01) :177-184
[10]  
Haynes W., 2012, CRC Handbook of Chemistry and Physics