ATR-FTIR spectroscopic investigation on phosphate adsorption mechanisms at the ferrihydrite-water interface

被引:609
作者
Arai, Y [1 ]
Sparks, DL [1 ]
机构
[1] Univ Delaware, Dept Plant & Soil Sci, Newark, DE 19717 USA
关键词
phosphate; adsorption; ionic strength; ferrihydrite; surface complexation; electrophoretic mobility; ATR-FTIR;
D O I
10.1006/jcis.2001.7773
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
We investigated the phosphate(P) adsorption mechanisms at the ferrihydrite-water interface as a function of pH, ionic strength (I), and loading level, using a combination of adsorption envelopes, electrophoretic mobility (EM) measurements, and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. The P adsorption envelopes show that: (1) adsorption decreases with increasing pH 3.5-9.5 and (2) adsorption is insensitive to changes in I at pH 4-7.5, but it slightly increases with increasing I from 0.01 to 0.8 at pH > 7.5. The EM in 0.1 M NaCl decreases with increasing P concentration from 0 to 50 mu mol L-1 at pH 3-9. The results of these macroscopic studies suggest the formation of inner-sphere complexes. The ATR-FTIR investigation shows that inner-sphere surface complexes are nonprotonated, bidentate binuclear species (=Fe2PO4) at pH greater than or equal to 7.5 and could be associated with Na+ ions at P loading levels of 0.38 mu mol m(-2). At pH 4-6, protonated innersphere complexes are proposed at the loading levels between 0.38 and 2.69 mu mol m(-2). (C) 2001 Academic Press.
引用
收藏
页码:317 / 326
页数:10
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