Oxidation of cysteine and glutathione by soluble polymeric MnO2

被引:57
作者
Herszage, J
Afonso, MD
Luther, GW
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, INQUIMAE, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Inorgan Analit & Quim Fis, RA-1428 Buenos Aires, DF, Argentina
[3] Univ Delaware, Coll Marine Studies, Lewes, DE 19956 USA
关键词
D O I
10.1021/es0340634
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The kinetics of reduction of soluble polymeric MnO2 by cysteine and glutathione has been studied in the pH range of 4.0-9.0. The concentration of thiols was varied between 1 and 2 mM, while the MnO2 concentration was varied between 2 and 12 muM. In this pH range, the reaction products were identified as Mn(II) and the corresponding disulfides (cystine and glutathione disulfide) Cysteic or cysteinesulfonic acid was formed only when pH < 2. Experimental data indicate that the rate law over the pH range of 4-9 is first-order in both MnO2 and thiol concentration. Eyring plots for both thiols reacting with MnO2 indicate that the reaction is associative (DeltaS(#) similar to -160 J mol(-1) K-1) and proceeds via an inner-sphere redox process. The reaction proceeds via the formation of two different inner-sphere complexes equivalent toMn(IV)SR(-) and equivalent toMn(IV)SR and their further reaction to products. Both surface species are linked to each other via acid-base equilibria, and the rate constant decreases as pH increases. The presence of two ligand surface species is determined using surface complexation modeling. A reaction mechanism in agreement with the experimental results is proposed.
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页码:3332 / 3338
页数:7
相关论文
共 64 条
[1]  
AFONSO MD, 1992, LANGMUIR, V8, P1671
[2]   Thiols in coastal waters of the western North Sea and English Channel [J].
Al-Farawati, R ;
Van Den Berg, CMG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (10) :1902-1911
[3]   Reductive dissolution of Fe(III) (hydr)oxides by cysteine: Kinetics and mechanism [J].
Amirbahman, A ;
Sigg, L ;
vonGunten, U .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 194 (01) :194-206
[4]  
[Anonymous], ADV CHEM SERIES
[5]  
Atwood J.D., 1985, INORGANIC ORGANOMETA
[6]   Oxidation of aqueous Cr(III) at birnessite surfaces: Constraints on reaction mechanism [J].
Banerjee, D ;
Nesbitt, HW .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1999, 63 (11-12) :1671-1687
[7]   XPS study of reductive dissolution of birnessite by oxalate: Rates and mechanistic aspects of dissolution and redox processes [J].
Banerjee, D ;
Nesbitt, HW .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1999, 63 (19-20) :3025-3038
[8]   XPS study of reductive dissolution of birnessite by H2SeO3 with constraints on reaction mechanism [J].
Banerjee, D ;
Nesbitt, HW .
AMERICAN MINERALOGIST, 2000, 85 (5-6) :817-825
[9]   XPS study of dissolution of birnessite by humate with constraints on reaction mechanism [J].
Banerjee, D ;
Nesbitt, HW .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (11) :1703-1714
[10]   KINETICS OF THE DISSOLUTION OF MAGNETITE IN THIOGLYCOLIC ACID-SOLUTIONS [J].
BAUMGARTNER, E ;
BLESA, MA ;
MAROTO, AJG .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1982, (09) :1649-1654