| 1. |
- Eriksson, Malin, et al.
(författare)
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Application of polymeric multilayers of starch onto wood fibres to enhance strength properties of paper
- 2005
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 20:3, s. 270-276
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Tidskriftsartikel (refereegranskat)abstract
- Polyelectrolyte multilayers of cationic and anionic starch have been used to enhance the strength properties of paper. All starches used in this investigation had a degree of substitution around 0.065. Optical reflectometry showed that a combination of cationic and anionic starch could form polyelectrolyte multilayers onto silicon oxide surfaces. The same combination of starches was then applied to unbeaten, bleached softwood kraft fibres to form three layers, i.e. a cationic/anionic/cationic starch combination. The results showed a significant increase in the paper strength properties in terms of tensile index, strain at break, and Scott Bond. The adsorbed amount of starch in the sheets, determined using an enzymatic method, was found to increase with each successive starch treatment. The increased paper strength was not only due to the increase in adsorbed amount of starch; rather, the chemical composition of the starch was also important. Cationic starch with high amylose content had a more positive effect on the paper strength properties. Furthermore, it was observed that anionic starch, despite being adsorbed in large amounts, did not contribute to the increase in tensile strength or strain at break to the same extent as did cationic starch. However, the out-of-plane properties, measured as Scott Bond properties, increased with the adsorbed amount, regardless of the chemical composition of the starch used in the outermost layer.
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| 2. |
- Marais, Andrew, et al.
(författare)
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Pilot-scale papermaking using Layer-by-Layer treated fibres; comparison between the effects of beating and of sequential addition of polymeric additives
- 2016
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 31:2, s. 308-314
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Tidskriftsartikel (refereegranskat)abstract
- The Layer-by-Layer (LbL) deposition technique was used to treat fibres before papermaking on a pilot scale. Following a laboratory pre-study performed earlier to determine the adsorption isotherms and the kinetics of formation of multilayers of polyamideamine epichlorydrine (PAE) and carboxymethylated cellulose (CMC) on unbeaten, bleached softwood fibres, online LbL treatment of the furnish was carried out on the EuroFEX pilot paper machine. Papers from fibres coated with up to four layers of polyelectrolytes were produced. Two different LbL systems were investigated, with anionic CMC in combination with either PAE or cationic starch (CS). The results showed that the mechanical strength of the paper significantly increased when the fibres were LbL-treated online. A comparison with conventional beating of the fibres revealed that the LbL treatment was a potential substitute to beating treatment, as the density of the LbL-treated papers remained constant while the mechanical properties were significantly improved. At the same time, the press solids content was significantly higher (2%) when using LbL-treated fibres than with beaten fibres.
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| 3. |
- Wågberg, Lars, et al.
(författare)
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Adsorption of bilayers and multilayers of cationic and anionic co-polymers of acrylamide on silicon oxide
- 2004
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Ingår i: Journal of Colloid and Interface Science. - : Elsevier BV. - 0021-9797 .- 1095-7103. ; 274:2, s. 480-488
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Tidskriftsartikel (refereegranskat)abstract
- Silica surfaces were consecutively treated with copolymers of cationic and anionic polyacrylamides (C-PAM and A-PAM, respectively) and the layer-by-layer build-up was continuously monitored with the aid of stagnation point adsorption reflectometry (SPAR). Four different charge densities of the cationic polymer and one charge density of the anionic polymer were studied. The solid substrate used in the investigation was an oxidized Si wafer, the charge of which was varied by performing the measurements at different pH. Adsorption measurements were performed both in deionized water and with a background electrolyte concentration of 0.01 M NaCl The results show that the adsorption of C-PAM at pH 6 was dominated by electrostatic interactions. However, a significant nonionic contribution to the adsorption of C-PAM on SiO2 was detected-when the results of adsorption measurements conducted in deionized water and in 0.01 M NaCl were compared. At pH 9, the adsorption of C-PAM onto SiO2 was found to be geometrically restricted since the adsorption stoichiometry between the polymer charges and the charges on the surface was less than I irrespective of the charge of the C-PAM. Adsorption of the A-PAM onto the C-PAM covered surface increases as a function of the adsorbed charges in the first layer. Experiments showed that it was possible to form multilayers of polyelectrolytes on the SiO2 surface provided the charge of the C-PAM was high enough. The critical charge of the polyelectrolyte for the formation of multilayers was also dependent on the charge of the substrate; that is, the lower the surface charge the higher the critical charge of the C-PAM. The substrate affected the amount of polyelectrolyte adsorbed up to the fifth layer. For further layers there was almost a stoichiometric relationship between the charges of the polyelectrolytes in consecutive layers. Results from studies of the formed multilayers with a quartz crystal microbalance (QCM-D) indicated that there was a close correlation between energy dissipation into the multilayers and a decrease in the adsorption as detected with SPAR. This in turn indicates that a decrease in the reflectometer signal does not necessarily indicate a decrease in adsorption.
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