In situ Fourier transform infrared measurements of sulfate adsorption on hematite in aqueous solutions

被引:404
作者
Hug, SJ
机构
[1] Swiss Fed. Inst. for Environ. S.
关键词
hematite; sulfate; sulfate adsorption; in situ FTIR; ATR-FTIR; surface complexation;
D O I
10.1006/jcis.1996.4755
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 [物理化学]; 081704 [应用化学];
摘要
An in situ attenuated total reflection (ATR)-Fourier transform infrared (FTIR) method, in which the ATR element is coated with hematite particle layers in direct contact with the aqueous phase, was used to measure sulfate adsorption as a function of aqueous sulfate concentration and pH. Between pH 3 and 6, monitoring the spectral region 900-1300 cm(-1), an IR spectrum with three bands between 950 and 1150 cm(-1), indicative of C-3v symmetry and monodentate sulfate coordination, was observed. The spectral amplitudes varied with sulfate concentration and solution pH in agreement with independent measurements and as described by quantitative surface complexation models. Previous studies on dried samples found a spectrum with a fourth maximum (consistent with C-2v symmetry) at >1200 cm(-1), which has been interpreted as evidence of bidentate coordination. In the present study, a fourth band at 1200 cm(-1) appeared only on drying of the sulfated hematite layer or with an aqueous phase pH <2. Based on these observations and on a comparison with various reported IR measurements, it is suggested that in the presence of an aqueous phase between pH 3 and 5, predominantly monodentate sulfate surface complexes are formed on hematite. Spectral changes on removal of the solvent indicate formation of monodentate bisulfate or of bidentate sulfate on dry hematite. (C) 1997 Academic Press.
引用
收藏
页码:415 / 422
页数:8
相关论文
共 22 条
[1]
Competitive sorption of simple organic acids and sulfate on goethite [J].
Ali, MA ;
Dzombak, DA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (04) :1061-1071
[2]
[Anonymous], AQUATIC SURFACE CHEM
[3]
PREPARATION AND PROPERTIES OF CHELATED SULPHATOBIS-(ETHYLENEDIAMINE)COBALT(III) SALTS [J].
BARRACLOUGH, C ;
TOBE, ML .
JOURNAL OF THE CHEMICAL SOCIETY, 1961, (MAY) :1993-&
[4]
IONIC ADSORPTION AT THE SOLID-SOLUTION INTERPHASE USING 3 INSITU METHODS [J].
BOCKRIS, JO ;
GAMBOAALDECO, M ;
SZKLARCZYK, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1992, 339 (1-2) :355-400
[5]
THE REACTIVITY OF FE(III) (HYDR)OXIDES - EFFECTS OF LIGANDS IN INHIBITING THE DISSOLUTION [J].
BONDIETTI, G ;
SINNIGER, J ;
STUMM, W .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1993, 79 (2-3) :157-167
[6]
SURFACE-IONIZATION AND COMPLEXATION AT THE OXIDE-WATER INTERFACE .3. ADSORPTION OF ANIONS [J].
DAVIS, JA ;
LECKIE, JO .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1980, 74 (01) :32-43
[7]
Dzombak D.A., 1990, SURFACE COMPLEXATION
[8]
An in situ infrared study on the effect of pH on anion adsorption at Pt(111) electrodes from acid sulfate solutions [J].
Faguy, PW ;
Marinkovic, NS ;
Adzic, RR .
LANGMUIR, 1996, 12 (02) :243-247
[9]
PHOTOCATALYTIC OXIDATION OF SULFUR-DIOXIDE IN AQUEOUS SUSPENSIONS OF ALPHA-FE2O3 [J].
FAUST, BC ;
HOFFMANN, MR ;
BAHNEMANN, DW .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (17) :6371-6381
[10]
FOKKINK LGJ, 1987, THESIS U WAGENINGEN