The adsorption of ten selected C3, C4, C5 and C6 acyclic polyols on hydrate
d alumina, under Bayer liquor-like conditions, has been studied. It is foun
d that adsorption is particularly sensitive to the polyhydroxy configuratio
n and that it parallels the trends observed for polyol complexation with me
tal cations and oxyanions. In particular, adsorption increases with increas
ing numbers of vicinal hydroxy groups; threo-threo sequences promote adsorp
tion whilst erythro-erythro sequences have little effect. A strong correlat
ion is found between adsorption and the degree of gibbsite crystallisation
inhibition reported for these compounds. Their effects on gibbsite morpholo
gies in relation to mechanisms of crystal growth inhibition are discussed.
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