The activity of the aluminum hydroxide-montmorillonite complex as an adsorbent, Al
2.09 (OH)
5.68Cl
0.44+0.23·nH
2O/unit formula weight of montmorillonite, to organic substances has been investigated by
dye
adsorption from aqueous solution. The relations between the soluble components of the complex and the mechanisms of anionic and of basic
dye
adsorptions have been discussed.
When the complex is suspended in water, aluminum and chlorine ions dissolve in the ratio of 1: 3 (AlCl
3). The aluminum ion in solution changes by hydrolytic polymerization into polynuclear hydroxy-aluminum ion, resulting in the formation of H
+ ions. Most of
dye
anions are probably adsorbed by electrostatic attraction onto Al-OH
+2 sites of the complex formed by protonation. The rest of the
dye
anions is bonded with the polymeric hydroxy-aluminum ion. Another important function of H
+ ions is that the H
+ ions give a favorable circumstance for adsorption of anionic
dye
since the solubility of
dye
anion is lowered. The adsorption of anionic
dye
is of Langmuir type and its amount of saturated adsorption is measured to be about 3×10
-4eq/g of charge which is nearly equivalent to the dissolved aluminum ion from the complex.
The adsorption of basic
dye
is a competitive cation-exchange reaction with the aluminum ion or H
+ ion at the negatively charged surface of the complex. Therefore the adsorbed amount of basic
dye
increases in case that some parts of these cations drain out from the adsorption system as a column bed type apparatus is employed. A part of
dye
cations penetrates into the interlayer of the complex to be strongly adsorbed and the rest exchanges the H
+ ions to be weakly adsorbed on the surface. The adsorption of basic
dye
is slow and of Freundlich type. The adsorbed amount of basic
dye
in isothermal adsorption is more temperature-dependent than that of anionic
dye
adsorption. This is mainly attributed to the strongly aggregated structure of the adsorbent particles which may be peptized at elevated temperatures.
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