Controls on schwertmannite transformation rates and products

被引:94
作者
Knorr, Klaus-Holger
Blodau, Christian
机构
[1] Univ Bayreuth, Limnol Res Stn, D-95440 Bayreuth, Germany
[2] Univ Bayreuth, Dept Hydrol, D-95440 Bayreuth, Germany
关键词
D O I
10.1016/j.apgeochem.2007.04.017
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
To study the impact of geochemical conditions on the fate of schwertmannite in AMD polluted sediments, pH, concentrations of SO42- and DOC, and temperature were varied in batch experiments. Schwertmannite transformation was quantified by titration of released acidity and the product investigated with FTIR, XRD, SEM/EDX, and chemical extraction. Rates ranged from 0.0002 d(-1) to 0.13 d(-1) (transformed fraction/incubation time.). Raising pH from 3 to 5 increased transformation by a factor of 5.8 (+/- 2.1) and temperature from 10 to 20 C by a factor 3.8 (+/- 1.6). Sulphate (20 mmol L-1) and DOC (20 mg L-1) lowered transformation by a factor of 2.5 (+/- 0.4) and 2.4 (+/- 0.5), respectively. The Fe phase was less dissolvable in 1 N HCl but goethite was not detected by XRD. The morphology changed little, even in SO42- -poor Fe phases. An amorphous, SO4 depleted Fe phase thus formed. Most of the SO4 released from the schwertmannite tunnel structure remained within this phase but changes in IR bands at 1108 cm(-1) (nu(3)) and 984 cm(-1) (nu(1)) suggested a relocation of SO4. The study documents the high potential of schwertmannite to buffer pH increase in sediments, particularly at low SO42- concentrations, and high temperatures. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2006 / 2015
页数:10
相关论文
共 28 条
[1]  
[Anonymous], 2002, WATER AIR SOIL POLL, DOI DOI 10.1023/A:1019959814202
[2]  
BIGHAM JM, 1990, GEOCHIM COSMOCHIM AC, V54, P2743
[3]   Schwertmannite and the chemical modeling of iron in acid sulfate waters [J].
Bigham, JM ;
Schwertmann, U ;
Traina, SJ ;
Winland, RL ;
Wolf, M .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1996, 60 (12) :2111-2121
[4]   SCHWERTMANNITE, A NEW IRON OXYHYDROXYSULPHATE FROM PYHASALMI, FINLAND, AND OTHER LOCALITIES [J].
BIGHAM, JM ;
CARLSON, L ;
MURAD, E .
MINERALOGICAL MAGAZINE, 1994, 58 (393) :641-648
[5]   Influence of pH on mineral speciation in a bioreactor simulating acid mine drainage [J].
Bigham, JM ;
Schwertmann, U ;
Pfab, G .
APPLIED GEOCHEMISTRY, 1996, 11 (06) :845-849
[6]   Thermodynamics and organic matter: constraints on neutralization processes in sediments of highly acidic waters [J].
Blodau, C ;
Peiffer, S .
APPLIED GEOCHEMISTRY, 2003, 18 (01) :25-36
[7]   Evidence for a hydrologically controlled iron cycle in acidic and iron rich sediments [J].
Blodau, C .
AQUATIC SCIENCES, 2004, 66 (01) :47-59
[8]  
Cornell R. M., 1996, The Iron Oxides
[9]   COMPARISON AND CLASSIFICATION OF THE EFFECTS OF SIMPLE IONS AND MOLECULES UPON THE TRANSFORMATION OF FERRIHYDRITE INTO MORE CRYSTALLINE PRODUCTS [J].
CORNELL, RM .
ZEITSCHRIFT FUR PFLANZENERNAHRUNG UND BODENKUNDE, 1987, 150 (05) :304-307
[10]   A natural attenuation of arsenic in drainage from an abandoned arsenic mine dump [J].
Fukushi, K ;
Sasaki, M ;
Sato, T ;
Yanase, N ;
Amano, H ;
Ikeda, H .
APPLIED GEOCHEMISTRY, 2003, 18 (08) :1267-1278