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Surface interactions in polyelectrolyte-cellulose systems and their implications for flocculation mechanisms

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dc.contributor Aalto-yliopisto fi
dc.contributor Aalto University en
dc.contributor.author Salmi, Jani
dc.date.accessioned 2012-08-21T12:42:39Z
dc.date.available 2012-08-21T12:42:39Z
dc.date.issued 2009
dc.identifier.isbn 978-951-22-9877-8
dc.identifier.isbn 978-951-22-9876-1 (printed) #8195;
dc.identifier.issn 1797-5093
dc.identifier.uri https://aaltodoc.aalto.fi/handle/123456789/4611
dc.description.abstract The overall purpose of this work was to gain a better understanding on how the different polyelectrolyte systems affect on the interactions between cellulose surfaces, and thus how the different flocculation systems worked on a molecular level. The focus was on studying the effect of cationic polyelectrolytes, polyelectrolyte complexes and architectures formed by polyelectrolyte and nanoparticles on interactions. The main part of the results was obtained using atomic force microscope (AFM). The forces between cellulose surfaces in cationic polyelectrolyte solutions depended on the molecular weight and charge density of the polyelectrolyte. Repulsion at high polymer concentrations was mainly steric in the solution of high molecular weight, low charged polyelectrolyte, whereas repulsion was mainly electrostatic in the solution of the low molecular weight, high charged polyelectrolyte. Also forces on separation were different. While a sharp minimum was found in the presence of a polyelectrolyte with high charge density and low molecular weight close to charge neutralization point, the detachment was gradual and long ranged for a polyelectrolyte with low charge density and high molecular weight. The main mechanism for flocculation was bridging in both cases. The interactions between adsorbed polyelectrolyte complex layers were mainly steric and repulsion was long ranged, even at low polymer concentration. The largest complex, formed by high molecular weight, low charged polyelectrolytes, showed the longest ranged repulsion and the best dewatering behaviour. In contrast to single polymer systems, the pull-off force was long ranged even in high polymer concentrations. It was concluded that the flexible and large complex was beneficial for flocculation, when the anionic polyelectrolyte can act as a link between the complex layers. The stratifying of silica nanoparticles and cellulose nanofibrils (NFC) with polyelectrolyte were compared. The adsorption and repulsion increased during the layer formation in the silica nanoparticle systems, whereas the second addition of cationic polyelectrolyte decreased repulsion in the case of nanofibrillar cellulose multilayer formation due to the collapse of the topmost nanofibrils. A high repulsion between nanofibril covered surfaces indicated together with high dissipation changes that NFC formed loose and thick layer containing a large amount of water. Silica nanoparticles were concluded to be able to penetrate inside the loose polyelectrolyte structure due to their small size. On the other hand, NFC formed individual layers between the polyelectrolyte layers. en
dc.format.extent Verkkokirja (3675 KB, 75 s.)
dc.format.mimetype application/pdf
dc.language.iso en en
dc.publisher Teknillinen korkeakoulu en
dc.relation.ispartofseries TKK reports in forest products technology, Series A, 9 en
dc.relation.haspart [Publication 1]: Jani Salmi, Monika Österberg, Per Stenius, and Janne Laine. 2007. Surface forces between cellulose surfaces in cationic polyelectrolyte solutions: The effect of polymer molecular weight and charge density. Nordic Pulp and Paper Research Journal, volume 22, number 2, pages 249-257. © 2007 by authors. en
dc.relation.haspart [Publication 2]: Jani Salmi, Monika Österberg, and Janne Laine. 2007. The effect of cationic polyelectrolyte complexes on interactions between cellulose surfaces. Colloids and Surfaces A: Physicochemical and Engineering Aspects, volume 297, numbers 1-3, pages 122-130. © 2007 Elsevier Science. By permission. en
dc.relation.haspart [Publication 3]: S. Ahola, J. Salmi, L.-S. Johansson, J. Laine, and M. Österberg. 2008. Model films from native cellulose nanofibrils. Preparation, swelling, and surface interactions. Biomacromolecules, volume 9, number 4, pages 1273-1282. en
dc.relation.haspart [Publication 4]: Jani Salmi, Tiina Nypelö, Monika Österberg, and Janne Laine. 2009. Layer structures formed by silica nanoparticles and cellulose nanofibrils with cationic polyacrylamide (C-PAM) on cellulose surface and their influence on interactions. BioResources, volume 4, number 2, pages 602-625. © 2009 by authors. en
dc.relation.haspart [Publication 5]: Lihua Xiao, Jani Salmi, Janne Laine, and Per Stenius. 2009. The effects of polyelectrolyte complexes on dewatering of cellulose suspension. Nordic Pulp and Paper Research Journal, accepted for publication. © 2009 by authors. en
dc.subject.other Paper technology en
dc.title Surface interactions in polyelectrolyte-cellulose systems and their implications for flocculation mechanisms en
dc.type G5 Artikkeliväitöskirja fi
dc.contributor.department Puunjalostustekniikan laitos fi
dc.subject.keyword surface core en
dc.subject.keyword surface force en
dc.subject.keyword AFM en
dc.subject.keyword flocculation en
dc.subject.keyword cellulose en
dc.subject.keyword polyelectrolyte en
dc.subject.keyword polyelectrolyte complex en
dc.subject.keyword polyelectrolyte multilayer en
dc.subject.keyword nanoparticle en
dc.identifier.urn URN:ISBN:978-951-22-9877-8
dc.type.dcmitype text en
dc.type.ontasot Väitöskirja (artikkeli) fi
dc.type.ontasot Doctoral dissertation (article-based) en
local.aalto.digifolder Aalto_67656
local.aalto.digiauth ask


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