EXAFS study of the nature of zinc complexation sites in humic substances as a function of Zn concentration

被引:32
作者
Sarret, G
Manceau, A
Hazemann, JL
Gomez, A
Mench, M
机构
[1] CNRS, F-38041 GRENOBLE, FRANCE
[2] INRA, UNITE RECH AGRON, CTR BORDEAUX, F-33883 VILLENAVE DORNON, FRANCE
来源
JOURNAL DE PHYSIQUE IV | 1997年 / 7卷 / C2期
关键词
D O I
10.1051/jp4:1997239
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Humic substances are known to play a key role in the immobilisation of metals in soils. The main complexing ligands that are supposed to interact with metals are carboxylic and phenolic. The complexation mechanism of zinc by two natural humic acids (T and F) was studied by EXAFS spectroscopy at the Zn-K edge over a wide range of zinc concentration. The ligation mechanism of Zn was found to vary with the metal concentration and the nature of the humic acid. As Zn concentration is raised, the amplitude of EXAFS spectra decreases, which is interpreted as an increased distribution of Ligand sites. At low Zn concentration (300-5000 mg/Kg), zinc forms inner sphere complexes in octahedral coordination for T humic acid, and in octahedral and tetrahedral coordinations for F humic acid. At intermediate Zn concentration (32 g/Kg), a large number of different sites are observed and only octahedral coordination is detected. At high Zn concentration (500 g/Kg), most Zn forms outer sphere complexes. The difference of complexation mechanisms between humic acids F and T can be related to differences in their structure as indicated by C-13-NMR spectroscopy.
引用
收藏
页码:799 / 802
页数:4
相关论文
共 11 条
[1]   ATOMIC DISPLACEMENT, ANHARMONIC THERMAL VIBRATION, EXPANSIVITY AND PYROELECTRIC COEFFICIENT THERMAL DEPENDENCES IN ZNO [J].
ALBERTSSON, J ;
ABRAHAMS, SC ;
KVICK, A .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1989, 45 :34-40
[2]  
ARROUAYS D, 1994, SCI SOL, V30, P227
[3]   METAL-ION BINDING TO HUMIC SUBSTANCES - APPLICATION OF THE NONIDEAL COMPETITIVE ADSORPTION MODEL [J].
BENEDETTI, MF ;
MILNE, CJ ;
KINNIBURGH, DG ;
VANRIEMSDIJK, WH ;
KOOPAL, LK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (02) :446-457
[4]  
BUFFLE J, 1984, MET IONS BIOL SYST, V18, P165
[5]  
BURGESS J, 1988, IONS SOLUTION, P36
[6]   MONOCLINIC ANHYDROUS ZINC(II) ACETATE [J].
CLEGG, W ;
LITTLE, IR ;
STRAUGHAN, BP .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1986, 42 :1701-1703
[7]   Direct determination of lead speciation in contaminated soils by EXAFS spectroscopy [J].
Manceau, A ;
Boisset, MC ;
Sarret, G ;
Hazemann, RL ;
Mench, M ;
Cambier, P ;
Prost, R .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (05) :1540-1552
[8]  
SENESI N, 1992, ADV TR SUB, P429
[9]  
SENESI N, 1977, GEOCHIM COSMOCHIM AC, V41, P1131
[10]  
Stevenson F.J., 1994, HUMUS CHEM, V2, P378