Mittuniversitetet

miun.sePublikationer
Driftstörningar
Det förekommer återkommande driftstörningar på några av sök-portalerna på grund av hög belastning. Vi arbetar på att lösa problemet, ni kan tillfälligt mötas av ett felmeddelande.
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • 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
Emulsion formation and stabilization by biomolecules: The leading role of cellulose
Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för kemiteknik. (FSCN)
Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för kemiteknik. University of Algarve, Faro, Portugal.
University of Algarve, Faro, Portugal.
RISE, Stockholm.
Visa övriga samt affilieringar
2019 (Engelska)Ingår i: Polymers, E-ISSN 2073-4360, Vol. 11, nr 10, artikel-id 1570Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Emulsion stabilization by native cellulose has been mainly hampered because of its insolubility in water. Chemical modification is normally needed to obtain water-soluble cellulose derivatives. These modified celluloses have been widely used for a range of applications by the food, cosmetic, pharmaceutic, paint and construction industries. In most cases, the modified celluloses are used as rheology modifiers (thickeners) or as emulsifying agents. In the last decade, the structural features of cellulose have been revisited, with particular focus on its structural anisotropy (amphiphilicity) and the molecular interactions leading to its resistance to dissolution. The amphiphilic behavior of native cellulose is evidenced by its capacity to adsorb at the interface between oil and aqueous solvent solutions, thus being capable of stabilizing emulsions. In this overview, the fundamentals of emulsion formation and stabilization by biomolecules are briefly revisited before different aspects around the emerging role of cellulose as emulsion stabilizer are addressed in detail. Particular focus is given to systems stabilized by native cellulose, either molecularly-dissolved or not (Pickering-like effect). 

Ort, förlag, år, upplaga, sidor
2019. Vol. 11, nr 10, artikel-id 1570
Nyckelord [en]
Adsorption, Amphiphilicity, Cellulose, Emulsion stability, Oil-water interface
Nationell ämneskategori
Kemiteknik
Identifikatorer
URN: urn:nbn:se:miun:diva-37680DOI: 10.3390/polym11101570ISI: 000495382700039PubMedID: 31561633Scopus ID: 2-s2.0-85073478887OAI: oai:DiVA.org:miun-37680DiVA, id: diva2:1370313
Tillgänglig från: 2019-11-14 Skapad: 2019-11-14 Senast uppdaterad: 2025-09-25Bibliografiskt granskad
Ingår i avhandling
1. Cellulose Dissolution and Amphiphilicity: Insights on the Emulsion Formation and Stabilization
Öppna denna publikation i ny flik eller fönster >>Cellulose Dissolution and Amphiphilicity: Insights on the Emulsion Formation and Stabilization
2021 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

An amphiphilic polymer is expected to adsorb at the oil-water interface and be capable of stabilizing emulsions. Cellulose derivatives, cellulose nanoparticles and regenerated cellulose particles show an intrinsic amphiphilic character by self-assembling at oil-water interfaces and stabilizing emulsions without the aid of surfactants or any other co-stabilizers. In its polymeric form, the native cellulose chains could be expected to share similar emulsifying abilities. However, cellulose dissolution is the main issue when it comes to its direct application in emulsion technology and, therefore, there is a lack of knowledge when it comes to this type of approach on making emulsions. Cellulose does not dissolve in either oil or water, but it can be dissolved in water based-solvents at extreme pH's. In this thesis, the interfacial behaviour of cellulose was studied at oil-water interfaces by having cellulose dissolved in aqueous solutions of H3PO4 (very low pH) and NaOH/NaOH-urea and TBAH (very high pH). 

In its dissolved state, cellulose was seen to substantially decrease the interfacial tension (IFT) between the oil phase and the aqueous media, which was a consequence of the adsorption of cellulose at oil-water interfaces. The extent of the IFT reduction was shown to be dependent on the solvent quality. The optimal solvency conditions for cellulose were found for the alkaline solvent with an intermediate polarity (NaOH-urea), which is in line with the favourable conditions for adsorption of an amphiphilic polymer. However, in stabilizing oil-in-water emulsions (O/W), to achieve long-term stability and prevent oil separation from the emulsions, further reduction in cellulose's solvency was needed. This was achieved by a change in the pH of the emulsions that induced the regeneration of cellulose on the surface of the oil droplets (in-situ regeneration) in the form of a continuous film, which was revealed by cryogenic scanning electron microscopy (cryo-SEM). The topography of the droplets surface was found to be very different from what has been reported for cellulose Pickering emulsions. Upon in-situ regeneration, the rate of droplets coalescence was dramatically reduced and emulsions showed a remarkable stability against oil-separation. Finally, the combination of cellulose with lignin as an amphiphilic natural co-stabilizer was studied regarding their compatibility in solution. Lignin was found to improve cellulose dissolution in NaOH (aq.) and delay the gelation kinetics upon ageing or temperature increase in the solutions. Data suggests lignin as an amphiphilic additive able to weaken the hydrophobic interactions among cellulose molecules. 

Ort, förlag, år, upplaga, sidor
Sundsvall: Mid Sweden University, 2021. s. 61
Serie
Mid Sweden University doctoral thesis, ISSN 1652-893X ; 353
Nationell ämneskategori
Kemiteknik
Identifikatorer
urn:nbn:se:miun:diva-43531 (URN)978-91-89341-30-2 (ISBN)
Disputation
2021-10-29, C312, Holmgatan 10, Sundsvall, 10:00 (Engelska)
Opponent
Handledare
Forskningsfinansiär
Vetenskapsrådet, 2015-04290
Anmärkning

Vid tidpunkten för disputationen var följande delarbete opublicerat: delarbete 5 manuskript.

At the time of the doctoral defence the following paper was unpublished: paper 5 in manuscript.

Tillgänglig från: 2021-10-25 Skapad: 2021-10-25 Senast uppdaterad: 2025-09-25Bibliografiskt granskad

Open Access i DiVA

fulltext(1284 kB)1005 nedladdningar
Filinformation
Filnamn FULLTEXT01.pdfFilstorlek 1284 kBChecksumma SHA-512
2f90a60433c5aa7afaa14aceda780eff92060d2ae5ea60a8b80a23cf4259aa21ed935300a25758284c7c2c91912d96f0644fd7b21950f27d377ece409c9082e4
Typ fulltextMimetyp application/pdf

Övriga länkar

Förlagets fulltextPubMedScopus

Person

Costa, CarolinaMedronho, BrunoLindman, BjörnEdlund, HåkanNorgren, Magnus

Sök vidare i DiVA

Av författaren/redaktören
Costa, CarolinaMedronho, BrunoLindman, BjörnEdlund, HåkanNorgren, Magnus
Av organisationen
Institutionen för kemiteknik
I samma tidskrift
Polymers
Kemiteknik

Sök vidare utanför DiVA

GoogleGoogle Scholar
Totalt: 1006 nedladdningar
Antalet nedladdningar är summan av nedladdningar för alla fulltexter. Det kan inkludera t.ex tidigare versioner som nu inte längre är tillgängliga.

doi
pubmed
urn-nbn

Altmetricpoäng

doi
pubmed
urn-nbn
Totalt: 723 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • 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