Effect of pH on complexation in mixed dilute aqueous solutions of poly(acrylic acid), poly(ethylene glycol), and Cu2+ ions

Abstract

The phase states of mixed dilute solutions of PAA, PEG, and Cu2+ ions largely determines the mechanism governing the growth of metal nanoparticles during the subsequent reduction of copper ions. Mixtures with PAA: PEG > 1 base-mol/base-mol and PAA: Cu2+ ≥ 5 base-mol/mol are studied. It is shown that the simultaneous complexation of PAA with PEG and Cu2+ ions in these mixtures at pH values below the intrinsic pH of a solution is accompanied by phase separation related to insolubility of PAA-PEG interpolymer complexes. A decrease in the pH of the ternary mixture is caused by the release of a strong low-molecular-mass acid due to complexation with Cu2+ ions. The minimum pH value, above which the PAA-PEG-Cu2+ system becomes single-phase (a transparent solution), depends on the concentration ratio between PAA and PEG chains (the mean degree of polymerization). This value is either 6.8–7.0 (if all macromolecules are incorporated in the insoluble interpolymer complex with PEG) or 4.0 (if chains occur in excess). Methods of preparing single-phase systems in the pH range 4.0–7.0 via exchange reactions of the PAA-Cu2+ complex with PEG or the nonstoichiometric soluble interpolymer complex PAA-PEG are developed. Viscometry, electron microscopy, and dynamic light scattering are used to investigate the compositions and structures of soluble complexes, in which either each chain (if the chain is long) may be linked with both PEG and Cu2+ ions or PAA chains are redistributed between two complexes (at comparable lengths of PAA and PEG chains).