For the first time to the knowledge of the authors, well-defined and stable lignin model surfaces have been utilized as substrates in polyelectrolyte adsorption studies. The adsorption of polyallylamine (PAH), poly(acrylic acid) (PAA), and polyelectrolyte complexes (PECs) was monitored using quartz crystal microgravimetry with dissipation (QCM-D). The PECs were prepared by mixing PAH and PAA at different ratios and sequences, creating both cationic and anionic PECs with different charge levels. The adsorption experiments were performed in 1 and 10 mM sodium chloride solutions at pH 5 and 7.5. The highest adsorption of PAH and cationic PECs was found at pH 7.5, where the slightly negatively charged nature of the lignin substrate is more pronounced, governing electrostatic attraction of oppositely charged polymeric substances. An increase in the adsorption was further found when the electrolyte concentration was increased. In comparison, both PAA and the anionic PEC showed remarkably high adsorption to the lignin model film. The adsorption of PAA was further studied on silica and was found to be relatively low even at high electrolyte concentrations. This indicated that the high PAA adsorption on the lignin films was not induced by a decreased solubility of the anionic polyelectrolyte. The high levels of adsorption on lignin model surfaces found both for PAA and the anionic PAA-PAH polyelectrolyte complex points to the presence of strong nonionic interactions in these systems.
Fines are an essential component in the papermaking process because they have a profound influence on the behaviour of the wet web and on the mechanical properties of the final sheet. Primary fines are present in the pulp prior to refining, and secondary fines are produced during refining. In the present investigation, two commercially manufactured unbleached pulps with kappa numbers of 45 and 90 were studied in terms of how they responded to refining with respect to the quality of fibre and fines. Primary and secondary fines were collected and characterised and their impact on sheet strength was evaluated by addition of known amounts to a refined and decrilled pulp. All the measured paper strength properties improved when primary and secondary fines were added. The strength improvement was generally somewhat higher in the second case. The effect was more pronounced at a higher level of addition. We attribute the main strength improvements associated with fines to improved consolidation by the creation of capillary forces between the surfaces.
SynopsisThe dynamic mechanical properties of paper during restrained drying are reported in this article. The apparatus used was a servohydraulic material testing system (MTS), connected to a computer unit. It has been found that the ratio of drying stress to elastic modulus at a given dry solids content corresponds to the instantaneous linear contraction of the sheet when the drying stress is relieved. It is therefore deduced that paper behaves as a linear viscoelastic body during restrained drying. The finding of a maximum loss coefficient and the drastic change in elastic modulus during drying of paper are interpreted in terms of a transitional change in the amorphous regions of wood polymers plasticized by water.
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