Abstract
CaCO3-pulp composite was prepared via precipitation of calcium hydroxide in the presence of pulp. In order to investigate the precipitation selectivity and mechanism, the substrate pulps and the obtained composites were fractionated (R30, R100, R200, R400 and a sedimented fraction that passed the 400 mesh wire) using a Bauer-McNett unit. The main fractionation criterion was therefore fiber length. The pulp used was CTMP (chemithermomechanical pulp), yielding a precipitated calcium carbonate-chemithermomechanical pulp (PCC-CTMP) composite with a targeted PCC-to-CTMP ratio of 1:1. The PCC consisted primarily of nano-sized primary particles which formed aggregates and clusters on the fibers. When the fiber morphology, zeta potential and surface charge density of the fractions were determined, a correlation was found between the surface charge density of the CTMP and the ash content of the corresponding PCC-CTMP fractions. This supports the hypothesis that the precipitation on the CTMP fiber is driven by the charge interparticle interaction. The use of refined CTMP furnishes and fractionation of the PCC-CTMP furnishes demonstrates that PCC is preferably fixed on fines and fibrils since it appears at a higher content in the fines fractions. Fiber activation via fiber split, removal of primary wall and surface defibrillation enhanced the affinity of the PCC for the fibrils. The laboratory handsheets prepared from the material demonstrated the importance of controlling the substrate fiber properties for the mineral-fiber composite, e.g. via refining, as differences between the refining levels and fractions were found to lead to differences in both optical properties and bonding.Graphic abstract
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