Temperature-responsive random copolymers based on poly(N-isopropyl acrylamide) (PNIPAM) with 15 mol% of either acrylic acid or dimethylaminoethyl acrylate quaternary chloride were prepared. The effect of the charge and its sign were investigated in the solid-liquid separation of silica and alumina mineral suspensions. The results were compared to PNIPAM homopolymer of similar molecular weight. PNIPAM copolymers of the same charge as the particles (co-ionic PNIPAM) act as dispersants at both 25 degrees C and 50 degrees C. Flocculation occurs when counter-ionic PNIPAM facilitates selective aggregation and rapid sedimentation of minerals at both 25 degrees C and 50 degrees C. Adsorption and desorption studies showed that, unlike non-ionic PNIPAM, little desorption of the counter-ionic copolymers from the oxides occurred after cooling a suspension from 50 degrees C to below the lower critical solution temperature. Thus, incorporation of counter-ionic charge into the temperature sensitive polymer PNIPAM was found to reduce the sediment bed consolidation upon cooling when compared to PNIPAM homopolymers. The lack of secondary consolidation upon cooling is attributed to attractive inter-particle forces, such as conventional polyelectrolyte flocculation mechanisms (bridging, charge neutralization or charge patch) which persist at both 25 degrees C and 50 degrees C when counter-ionic PNIPAM is used. On the other hand, it was possible to obtain rapid sedimentation with the counter-ionic PNIAPMs even when they were added to the suspension already at 50 degrees C, a process which has not been possible with neutral PNIPAM homopolymers. (C) 2011 Elsevier Inc. All rights reserved.