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The precipitation of lead sulphate was studied from 0.0001 to 0.01 M aqueous solutions (supersaturations 3 to 600) and from 20% aqueous ethanediol, methanol and ethanol solutions, in polypropylene beakers, at ambient temperature: the experimental techniques were conductivity measurements and optical microscopy. The precipitations were heterogeneously nucleated at low supersaturations and homogeneously nucleated at intermediate to high supersaturations. New crystal morphologies generally developed at some what higher supersaturations in the aqueous alcohol systems. The final crystal lengths at first increased with increasing initial metal salt concentration and then decreased with this parameter; the largest crystals at any concentration were obtained from solutions in which lead sulphate solubility was highest. The critical supersaturations (for the onset of homogeneous nucleation) increased from 36 (in water) to 50 (in 20% aqueous ethanol): the surface energies for the formation of nuclei correspondingly increased from 90 to 110 mJ m −2 in good agreement with the Nielsen‐Söhnel relation. The nucleation and crystal growth processes are taking in an aqueous environment of similar water activity to that of the bulk solutions.
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Packter et al. (1980) studied this question.
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