In the high-surface-potential Schulze-Hardy rule, the critical coagulation concentration scales approximately as with the counterion valence. Hence
The more highly charged counterion therefore requires about eleven times less concentration in this idealized estimate. This assumes the cations are the counterions of a negatively charged surface, the surface-potential regime is appropriate, and the only changing mechanism is electrostatic stabilization. Specific adsorption and hydrolysis of aluminium ions can invalidate this scaling; matching ionic strengths instead is not the same prediction.

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