An in situ ATR-FTIR investigation of sulfate bonding mechanisms on goethite

被引:465
作者
Peak, D [1 ]
Ford, RG [1 ]
Sparks, DL [1 ]
机构
[1] Univ Delaware, Dept Plant & Soil Sci, Newark, DE 19717 USA
关键词
sulfate; surface complexation; ATR-FTIR; goethite; bonding mechanisms; in situ spectroscopy; schwertmannite;
D O I
10.1006/jcis.1999.6405
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The mechanism of sulfate adsorption on goethite was investigated in situ using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Sulfate adsorption was investigated at ionic strengths between 0.005 and 0.1 M, reactant concentrations between 5 and 500 mu M, and pH values between 3.5 and 9.0. It was determined that sulfate forms both outer-sphere and inner-sphere surface complexes on goethite at pH less than 6. At pH values greater than 6, sulfate adsorbs on goethite only as an outer-sphere complex. The relative amount of outer-sphere sulfate surface complexation increased with decreasing ionic strength. The spectrum of sulfate adsorbed on goethite was also compared to the infrared spectrum of synthetic schwertmannite, an iron(III) oxy-hydroxy-sulfate. It was determined that in situ spectra of both schwertmannite and adsorbed sulfate are quite similar, suggesting that a continuum of outer- and inner-sphere sulfate occurs in both cases. (C) 1999 Academic Press.
引用
收藏
页码:289 / 299
页数:11
相关论文
共 22 条
[21]   MECHANISM OF ANION ADSORPTION AT FERRIC AND CHROMIC OXIDE - WATER INTERFACES [J].
YATES, DE ;
HEALY, TW .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1975, 52 (02) :222-228
[22]   KINETICS AND MECHANISMS OF SULFATE ADSORPTION DESORPTION ON GOETHITE USING PRESSURE-JUMP RELAXATION [J].
ZHANG, PC ;
SPARKS, DL .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1990, 54 (05) :1266-1273