We investigated the As(III) and As(V) adsorption complexes forming at the γ -Al 2 O 3 /water interface as a function of pH and ionic strength (I), using a combination of adsorption envelopes, electrophoretic mobility (EM) measurements, and X-ray absorption spectroscopy (XAS). The As adsorption envel
ATR–FTIR Spectroscopic Investigation on Phosphate Adsorption Mechanisms at the Ferrihydrite–Water Interface
✍ Scribed by Yuji Arai; D.L. Sparks
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 148 KB
- Volume
- 241
- Category
- Article
- ISSN
- 0021-9797
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✦ Synopsis
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 µmol 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 (≡Fe 2 PO 4 ) at pH ≥ 7.5 and could be associated with Na + ions at P loading levels of 0.38 µmol m -2 . At pH 4-6, protonated innersphere complexes are proposed at the loading levels between 0.38 and 2.69 µmol m -2 .
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