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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.
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页码:289 / 299
页数:11
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