Gel strength and swelling of acrylamide‐protic acid superabsorbent copolymers

Abstract

Abstract The viscoelastic and swelling properties of polyacrylamide‐based superabsorbent copolymers were investigated as a function of the ionic comonomer structure. Superabsorbent copolymers were synthesized by free‐radical crosslinking copolymerization of acrylamide and one of the monoprotic acids (acrylic acid and crotonic acid) or the diprotic acids (maleic acid and itaconic acid) as the investigated ionic comonomer. The reaction composition of all components, i.e. monomer, comonomer, initiator, co‐initiator, and crosslinker, was fixed to be the same for the synthesis of all four superabsorbent copolymer systems. Viscoelastic measurements were performed in all systems where the particles were closely packed. The network structures of all systems were evaluated via viscoelastic and swelling measurements. The results indicated that superabsorbent polymers (SAPs) with high water absorbency were accompanied by low gel strength and the calculated high value of molecular weight between crosslinks ( $\bar {M}{}_c$ ) and low value of effective crosslinking density ( ν e ). Diprotic acid‐containing SAPs showed higher water absorbency over monoprotic acid‐containing and non‐ionic ones. The differences in $\bar {M}{}_c$ and ν e values of each system were explained with respect to the differences in the monomer reactivity ratio and hydrophilicity of the comonomers. Copyright © 2010 John Wiley & Sons, Ltd.