Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Polyelectrolyte complexes for tailoring of wood fibre surfaces
RISE - Research Institutes of Sweden, Swerea, Swerea KIMAB AB.ORCID-id: 0000-0001-8168-6785
KTH Royal Institute of Technology.
2014 (Engelska)Ingår i: Advances in Polymer Science, ISSN 0065-3195, E-ISSN 1436-5030, Vol. 256, s. s.1-24Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The use of polyelectrolyte complexes (PECs) provides new opportunities for surface engineering of solid particles in aqueous environments to functionalize the solids either for use in interactive products or to tailor their adhesive interactions in the dry and/or wet state. This chapter describes the use of PECs in paper-making applications where the PECs are used for tailoring the surfaces of wood-based fibres. Initially a detailed description of the adsorption process is given, in more general terms, and in this respect both in situ formed and pre-formed complexes are considered. When using in situ formed complexes, which were intentionally formed by the addition of oppositely charged polymers, it was established that the order of addition of the two polyelectrolytes was important, and by adding the polycation first a more extensive fibre flocculation was found. PECs can also form in situ by the interaction between polyelectrolytes added and polyelectrolytes already present in the fibre suspension originating from the wood material, e.g. lignosulphonates or hemicelluloses. In this respect the complexation can be detrimental for process efficiency and/or product quality depending on the charge balance between the components, and when using the PECs for fibre engineering it is not recommended to rely on in situ PEC formation. Instead the PECs should be pre-formed before addition to the fibres. The use of pre-formed PECs in the paper-making process is described as three sub-processes: PEC formation, adsorption onto surfaces, and the effect on the adhesion between surfaces. The addition of PECs, and adsorption to the fibres, prior to formation of the paper network structure has shown to result in a significant increase in joint strength between the fibres and to an increased strength of the paper made from the fibres. The increased joint strength between the fibres is due to both an increased molecular contact area between the fibres and an increased molecular adhesion. The increased paper strength is also a result of an increased number of fibre/fibre contacts/unit volume of the paper network. © Springer-Verlag Berlin Heidelberg 2013.

Ort, förlag, år, upplaga, sidor
2014. Vol. 256, s. s.1-24
Nationell ämneskategori
Materialteknik
Identifikatorer
URN: urn:nbn:se:ri:diva-12799DOI: 10.1007/12-2012-206Scopus ID: 2-s2.0-84890926502ISBN: 9783642407451 (tryckt)OAI: oai:DiVA.org:ri-12799DiVA, id: diva2:972992
Tillgänglig från: 2016-09-22 Skapad: 2016-09-22 Senast uppdaterad: 2018-07-19Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Övriga länkar

Förlagets fulltextScopushttp://rd.springer.com/chapter/10.1007/12_2012_206

Personposter BETA

Ankerfors, Caroline

Sök vidare i DiVA

Av författaren/redaktören
Ankerfors, Caroline
Av organisationen
Swerea KIMAB AB
I samma tidskrift
Advances in Polymer Science
Materialteknik

Sök vidare utanför DiVA

GoogleGoogle Scholar

doi
isbn
urn-nbn

Altmetricpoäng

doi
isbn
urn-nbn
Totalt: 50 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
v. 2.35.8