V. Bobacka et D. Eklund, The influence of charge density of cationic starch on dissolved and colloidal material from peroxide bleached thermomechanical pulp, COLL SURF A, 152(3), 1999, pp. 285-291
Citations number
26
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
The interaction between anionically charged colloidal and dissolved materia
l (anionic trash) from peroxide bleached thermomechanical pulp and cationic
starches of different charge densities has been examined. The evaluated de
grees of substitution, DS, were 0.015, 0.035, 0.05 and 0.08. For comparison
, a starch of considerably higher degree of substitution, called fixative,
was also evaluated. A higher amount of the cationic starch of DS 0.015 was
needed than that of DS 0.035 to achieve complete destabilisation of colloid
al material. However, lower dosages of the starches with DS 0.035 and 0.05
were needed than of the starch of DS 0.08. A lower dosage of fixative than
of the common starch of DS 0.08 was also needed. The fixative recharged the
particles upon an overdose. Measurements of residual turbidity and zeta po
tential indicate that the common starches destabilised the colloidal lipoph
ilic extractives by interparticle bridging. The fixative starch of consider
ably higher charge density, DS 0.8, may have destabilised the colloids by t
he patch flocculation mechanism. The common cationic starches also formed c
omplexes with dissolved pectic substances, which are anionically charged wo
od polymers consisting of galacturonic acid units. The amount of starch nee
ded to achieve complete destabilisation of pectic substances decreased with
increasing charge density, probably due to intensified electrostatic inter
action. Still lower amounts of fixative were needed. An overdose of fixativ
e restablized the pectic substances. (C) 1999 Elsevier Science B.V. All rig
hts reserved.