Potentiometric back titration as a robust and simple method for specific surface area estimation of lignocellulosic fibers

The specific surface area (SSA) of cellulosic or lignocellulosic fibers is seldom reported in the recent literature on papermaking, despite its close relation with the degree of refining and other key pulp properties. Amidst outdated assays (Pulmac permeability test) and methods that, while accurate, are of doubtful usefulness for papermaking purposes (N-2 adsorption-desorption), we suggest a methodology based on the cationic demand. A commonly used cationic polyelectrolyte, poly(diallyldimethylammonium chloride) (PDADMAC), became adsorbed onto thermomechanical pulp samples. Then, a potentiometric back titration with an anionic polyelectrolyte measured the cationic demand, expressed as microequivalents of PDADMAC per gram of pulp. Multiplying this value by the surface area of a microequivalent of polymer, considering rod-like conformation in the case of minimum ionic strength, yielded the SSA of the lignocellulosic pulp. Our system assumes that the quaternary ammonium groups were anchored through electrostatic and ion-dipole interactions. Measuring the carboxyl content allowed for discriminating between both kinds of forces. Finally, the model could be validated by plotting the estimated SSA values against the Schopper-Riegler degree, attaining high correlation coefficients (R-2 similar to 0.98). Owing to the high molecular weight of the polyelectrolyte of choice (107 kDa), and more particularly in the case of fine-free pulps, SSA values estimated from the cationic demand were consistently lower than those from dye (Congo red) sorption. Instead of being a drawback, the limited diffusion of PDADMAC through fibers can enable papermakers to attain a more helpful quantification of the available surfaces in operations with low residence times.

Automated summary

This study proposes a methodology for estimating the specific surface area (SSA) of lignocellulosic pulp based on cationic demand, utilizing a commonly used cationic polyelectrolyte. The system assumes that quaternary ammonium groups are anchored through electrostatic and ion-dipole interactions, with the model validated through high correlation coefficients. The SSA values estimated from cationic demand were consistently lower than those from dye sorption, potentially providing a more helpful quantification of available surfaces in papermaking operations with low residence times.