Arsenic removal from aqueous solution via ferrihydrite crystallization control

被引:123
作者
Richmond, WR [1 ]
Loan, M [1 ]
Morton, J [1 ]
Parkinson, GM [1 ]
机构
[1] Curtin Univ Technol, Nanochem Res Inst, Perth, WA 6845, Australia
关键词
D O I
10.1021/es0353154
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Removal of arsenate anion from aqueous solution by coprecipitation with ferrihydrite has been studied under conditions in which the Fe/As ratio is maintained at a constant level, while the degree of supersaturation with respect to the iron oxide precipitate is varied. An Fe/As ratio of 12 was chosen, and supersaturation was controlled by varying the iron concentration or the pH. The relationship between supersaturation and arsenic removal was found to follow an exponential curve, with greater arsenic removal occurring at higher supersaturation ratios for each of the pH values tested. Higher supersaturation ratios were required to achieve a given level of arsenic removal at pH 7 than would be required to achieve the same level of removal at pH 3.5. The results provide important guidelines for selection of appropriate concentrations of iron(III) required for arsenic removal under various circumstances. Powder XRD analysis of the arsenate-ferrihydrite precipitates showed an increasing degree of structural order with decreasing levels of supersaturation. TEM images of the precipitates revealed that aggregates with a morphology similar to that of schwertmannite are formed in some samples at low supersaturation levels. The results described in this paper indicate that the overall efficiency of arsenic removal involves a combination of both supersaturation and pH effects, with pH controlling the affinity of arsenate for the ferrihydrite surface, and supersaturation controlling the surface area and physical properties of the ferrihydrite product.
引用
收藏
页码:2368 / 2372
页数:5
相关论文
共 17 条
[1]   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
[2]   Scavenging of as from acid mine drainage by schwertmannite and ferrihydrite: A comparison with synthetic analogues [J].
Carlson, L ;
Bigham, JM ;
Schwertmann, U ;
Kyek, A ;
Wagner, F .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (08) :1712-1719
[3]  
Cornell R.M., 2003, IRON OXIDES
[4]   Sorption of As(V) by some oxyhydroxides and clay minerals.: Application to its immobilization in two polluted mining soils [J].
García-Sanchez-, A ;
Alvarez-Ayuso, E ;
Rodriguez-Martin, F .
CLAY MINERALS, 2002, 37 (01) :187-194
[5]   Occurrence and constitution of natural and synthetic ferrihydrite, a widespread iron oxyhydroxide [J].
Jambor, JL ;
Dutrizac, JE .
CHEMICAL REVIEWS, 1998, 98 (07) :2549-2585
[6]  
KRAUSE E, 1987, INT S CRYST PREC, P195
[7]  
KRAUSE E, 1985, IMPURITY CONTROL DIS, P5
[8]   Iron oxy-hydroxide crystallization in a hyd ro metallurgical residue [J].
Loan, M ;
Parkinson, G ;
Newman, M ;
Farrow, J .
JOURNAL OF CRYSTAL GROWTH, 2002, 235 (1-4) :482-488
[9]  
LOAN M, IN PRESS AM MINER
[10]  
LOAN M, UNPUB