Small-Angle X-ray Scattering and Rheological Characterization of Aqueous Lignosulfonate Solutions

Abstract

Lignosulfonate is a colloidal polyelectrolyte widely used as a dispersant in various industrial applications and produced during chemical pulping of wood chips. Here we present a systematic small-angle X-ray scattering (SAXS) and rheological study of fractionated lignosulfonate (mass weighted molar mass M w 18 000 g/mol) dissolved in water and 0.2 M NaCl. The concentration range varied from semidilute to concentrated regime. SAXS intensity of all solutions followed the Porod law at all concentrations, which is a clear indication of a compact shape of the lignosulfonate particle. In water, below 10 mass % lignosulfonate, the average interparticle distance obtained from SAXS patterns relates to concentration via a power law with exponent -0.28. Deviation of the power law exponent from ideal -0.33 and a linear decrease in volume fraction normalized Porod constant as a function of concentration are taken as indications of self-association of lignosulfonate. In saline solutions at high lignosulfonate mass fractions the average distance between lignosulfonate particles was longer and the average particle size was larger than those in aqueous solutions. The intrinsic viscosity in saline solution also was larger than that in aqueous solution. Lignosulfonate solutions showed Newtonian viscosity, except at very high concentrations. The variation of the relative zero-shear viscosity eta(0),r) with concentration was interpreted with the Krieger-Dougherty equation. An oblate spheroid shape with an axial ratio of 3.5 describes the average shape of the lignosulfonate particles in saline solutions based on SAXS intensities, the size distribution obtained using gel permeation chromatography, and rheological characterization. The largest dimension of the particles was about 8 nm. SAXS and rheology studies as a function of temperature reveal indications of temperature-dependent self-association.