Adsorption mechanism of mixed cationic/anionic collectors in feldspar-quartz flotation system

被引:159
作者
Vidyadhar, A.
Rao, K. Hanumantha [1 ]
机构
[1] Lulea Univ Technol, Div Mineral Proc, SE-97187 Lulea, Sweden
[2] Natl Met Lab, Mineral Proc Div, Jamshedpur 831007, Bihar, India
关键词
microcline; quartz; adsorption; flotation; zeta-potential; FTIR; LONG-CHAIN ALKYLAMINES; SURFACTANT MIXTURES; SILICATES; ALUMINA; ALBITE;
D O I
10.1016/j.jcis.2006.10.047
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 ; 081704 ;
摘要
The adsorption mechanism of mixed cationic alkyl diamine and anionic sulfonate/oleate collectors at acidic pH values was investigated on microcline and quartz minerals through Hallimond flotation, electrokinetic and diffuse reflectance FTIR studies. In the presence of anionic collectors, neither of the minerals responded to flotation but the diamine flotation of the minerals was observed to be pH and concentration dependent. The presence of sulfonate enhanced the diamine flotation of the minerals by its co-adsorption. The difference in surface charge between the minerals at pH 2 was found to be the basis for preferential feldspar flotation from quartz in mixed diamine/sulfonate collectors. The infrared spectra revealed no adsorption of sulfonate collector when used alone but displayed its co-adsorption as diamine-sulfonate complex when used with diamine. The presence of sulfonate increased the diamine adsorption due to a decrease in the electrostatic head-head repulsion between the adjacent surface ammonium ions and thereby increasing the lateral tail-tail hydrophobic bonds. The mole ratio of diamine/sulfonate was found to be an important factor in the orientation of alkyl chains and thus the flotation response of minerals. The increase in sulfonate concentration beyond diamine concentration leads to the formation of soluble 1:2 diamine-sulfonate complex or precipitate and the adsorption of these species decreased the flotation since the alkyl chains are in chaotical orientation with a conceivable number of head groups directing towards the solution phase. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
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