SIMULTANEOUS DISSOLUTION OF ZINC FERRITE AND PRECIPITATION OF AMMONIUM JAROSITE

被引:27
作者
ELGERSMA, F [1 ]
WITKAMP, GJ [1 ]
VANROSMALEN, GM [1 ]
机构
[1] DELFT UNIV TECHNOL,PROC EQUIPMENT LAB,2628 CA DELFT,NETHERLANDS
关键词
D O I
10.1016/0304-386X(93)90079-S
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Zinc ferrite (ZnO.Fe2O3) was converted, in a single-step seeded batch process, into ammonium jarosite (NH4Fe3(SO4)2(OH)6) at 95-degrees-C and at a pH which was kept constant at either 1.7 or 1.95. The conversion consists of the dissolution of zinc ferrite, which could be described by a surface reaction controlled shrinking core model, and the simultaneous precipitation of ammonium jarosite, which is also a surface-reaction-controlled process. The supersaturation during conversion for the precipitation of jarosite was calculated from the solution composition. At pH 1.7 virtually 100% conversion of zinc ferrite is achieved. This leads to a residual zinc content of the solids produced of below 0.1 wi%. X-ray diffraction analyses of the product showed correspondingly small amounts of zinc ferrite. This indicates that the zinc incorporation in the jarosite lattice is practically negligible. The advantages of such a controlled conversion process for industrial practice are discussed.
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页码:23 / 47
页数:25
相关论文
共 18 条
[2]  
Dutrizac J.E., 1976, CAN MINERAL, V14, P151, DOI DOI 10.1016/J.HYDROMET.2003.07.009
[3]   BEHAVIOR OF CESIUM AND LITHIUM DURING THE PRECIPITATION OF JAROSITE-TYPE COMPOUNDS [J].
DUTRIZAC, JE ;
JAMBOR, JL .
HYDROMETALLURGY, 1987, 17 (02) :251-265
[4]  
ELDERSMA F, 1993, HYDROMETALLURGY, V33, P313
[5]   ACIDIC DISSOLUTION OF ZINC FERRITE [J].
ELGERSMA, F ;
KAMST, GF ;
WITKAMP, GJ ;
VANROSMALEN, GM .
HYDROMETALLURGY, 1992, 29 (1-3) :173-189
[6]  
ELGERSMA F, 1992, PROCESSING RESIDUES, P413
[7]  
ELGERSMA F, 1990, HYDROMETALLURGY AQUE, P31
[8]  
HUGGARE TL, 1974, WORLD MIN, P36
[9]  
Krauss C.J., 1985, ZINC 85, P467
[10]  
MCANDREW RT, 1975, CIM B, P101