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Mechanisms behind the Stabilizing Action of Cellulose Nanofibrils in Wet-Stable Cellulose Foams
KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. KTH, School of Chemical Science and Engineering (CHE), Centres, Wallenberg Wood Science Center.
KTH, School of Chemical Science and Engineering (CHE), Fibre and Polymer Technology. KTH, School of Chemical Science and Engineering (CHE), Centres, Wallenberg Wood Science Center.ORCID iD: 0000-0001-8622-0386
2015 (English)In: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 16, no 3, p. 822-831Article in journal (Refereed) Published
Abstract [en]

The principal purpose of the investigation was to clarify the mechanisms behind the stabilizing action of cellulose nanofibrils (CNFs) in wet-stable cellulose foams. Following the basic theories for particle-stabilized foams, the investigation was focused on how the surface energy of the stabilizing CNF particles, their aspect ratio and charge density, and the concentration of CNF particles at the air-water interface affect the foam stability and the mechanical properties of a particle-stabilized air-liquid interface. The foam stability was evaluated from how the foam height changed over time, and the mechanical properties of the interface were evaluated as the complex viscoelastic modulus of the interface using the pendant drop method. The most important results and conclusions are that CNFs can be used as stabilizing particles for aqueous foams already at a concentration as low as 5 g/L. The major reasons for this were the small dimensions of the CNF and their high aspect ratio, which is important for gel-formation and the complex viscoelastic modulus of the particle-filled air-water interface. The influence of the aspect ratio was also demonstrated by a much higher foam stability of foams stabilized with CNFs than of foams stabilized by cellulose nanocrystals (CNC) with the same chemical composition. The charge density of the CNFs affects the level of liberation within larger aggregates and hence also the number of contact points at the interface and the gel formation and complex viscoelastic modulus of the air-water interface. The charges also result in a disjoining pressure related to the long-range repulsive electrostatic pressure between particle-stabilized bubbles and hence contribute to foam stability. (Figure Presented).

Place, publisher, year, edition, pages
2015. Vol. 16, no 3, p. 822-831
Keywords [en]
Air, Aspect ratio, Cellulose, Chemical stability, Density (specific gravity), Mechanical properties, Nanofibers, Stability, Viscoelasticity, Air liquid interfaces, Cellulose nanocrystal (CNC), Cellulose nanofibrils, Cellulose nanofibrils (CNFs), Chemical compositions, Electrostatic pressure, Particle-stabilized foams, Pendant drop methods, Phase interfaces, cellulose nanofibril, decylamine, nanocrystal, unclassified drug, adsorption, adsorption kinetics, Article, chemical composition, controlled study, foam stability, foaming, hydrophobicity, light scattering, priority journal, surface property, thickness
National Category
Polymer Technologies
Identifiers
URN: urn:nbn:se:kth:diva-167761DOI: 10.1021/bm5017173ISI: 000350841100016PubMedID: 25635472Scopus ID: 2-s2.0-84924347671OAI: oai:DiVA.org:kth-167761DiVA, id: diva2:814608
Note

QC 20150527

Available from: 2015-05-27 Created: 2015-05-22 Last updated: 2022-06-23Bibliographically approved
In thesis
1. Porous Materials from Cellulose Nanofibrils
Open this publication in new window or tab >>Porous Materials from Cellulose Nanofibrils
2014 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

In the first part of this work a novel type of low-density, sponge-like material for the separation of mixtures of oil and water has been prepared by vapour deposition of hydrophobic tri-chloro-silanes on ultra-porous cellulose nanofibril (CNF) aerogels. To achieve this, a highly porous (>99%) robust CNF aerogel with high structural flexibility is first formed by freeze-drying an aqueous suspension of the CNFs. The density, pore size distribution and wetting properties of the aerogel can be tuned by selecting the concentration of the CNF suspension before freeze-drying. The hydrophobic light-weight aerogels are almost instantly filled with the oil phase when they selectively absorb oil from water, with a capacity to absorb up to 45 times their own weight. The oil can subsequently be drained from the aerogel and the aerogel can then be subjected to a second absorption cycle.

The second part is about aerogels with different pore structures and manufactured with freeze-drying and supercritical carbon dioxide for the preparation of super slippery surfaces. Tunable super slippery liquid-infused porous surfaces (SLIPS) were fabricated through fluorination of CNFsand subsequent infusion with perfluorinated liquid lubricants. CNF-based self-standing membranes repelled water and hexadecane with roll-off angles of only a few degrees. The lifetime of the slippery surface was controlled by the rate of evaporation of the lubricant, where the low roll-off angle could be regained with additional infusion. Moreover, adjusting the porosity of the membranes allowed the amount of infused lubricant to be tuned and thereby the lifetime. The CNF-based process permitted the expansion of the concept to coatings on glass, steel, paper and silicon. The lubricant-infused films and coatings are optically transparent and also feature self-cleaning and self-repairing abilities.

The third part describes how porous structures from CNFs can be prepared in a new way by using a Pickering foam technique to create CNF-stabilized foams. This technique is promising for up-scaling to enable these porous nanostructured cellulose materials to be produced on a large scale. With this technique, a novel, lightweight and strong porous cellulose material has been prepared by drying aqueous foams stabilized with surface-modified CNFs. Confocal microscopy and high-speed video imaging show that the long-term stability of the wet foams can be attributed to the octylamine-coated, rod-shaped CNF nanoparticles residing at the air-liquid interface which prevent the air bubbles from collapsing or coalescing. Careful removal of the water yields a porous cellulose-based material with a porosity of 98 %, and measurements with an autoporosimeter (APVD) reveal that most pores have a radius in the range of 300 to 500 μm.

In the fourth part, the aim was to clarify the mechanisms behind the stabilizing action of CNFs in wet-stable cellulose foams. Factors that have been investigated are the importance of the surface energy of the stabilizing CNF particles, their aspect ratio and charge density, and the concentration of CNF particles at the air-water interface. In order to investigate these parameters, the viscoelastic properties of the interface have been evaluated using the pendant drop method. The properties of the interface have also been compared by foam stability tests to clarify how the interface properties can be related to the foam stability over time. The most important results and conclusions are that CNFs can be used as stabilizing particles for aqueous foams already at a concentration as low as 5 g/L. The reasons for this are the high aspect ratio which is important for gel formation and the viscoelastic modulus of the air-water interface. Foams stabilized with CNFs are therefore much more stable than foams stabilized by cellulose nanocrystals (CNC). The charge density of the CNFs affects the level of liberation of the CNFs within large CNF aggregates and hence the number of contact points at the interface, and also the gel formation and viscoelastic modulus. The charges also lead to a disjoining pressure related to the long-range repulsive electrostatic interaction between the stabilized bubbles, and this contributes to foam stability.

In the fifth part, the aim was to develop the drying procedure in order to producea dry porous CNF material using the wet foam as a precursor and to evaluate the dry foam properties. The wet foam was dried in an oven while placed on a liquid-filled porous ceramic frit to preserve and enhance the porous structure in the dried material and prevent the formation of larger cavities and disruptions. The cell structure has been studied by SEM microscopy and APVD (automatic pore volume distribution). The mechanical properties have been studied by a tensile tester (Instron 5566) and the liquid absorption ability with the aid of the APVD-equipment. By changing the charge density of the CNFs it is possible to prepare dry foams with different densities and the lowest density was found to be 6 kg m-3with a porosity of 99.6 %. The Young ́s modulus in compression was 50 MPa and the energy absorption was 2340kJ m-3 for foams with a density of 200 kg m-3. The liquid absorption of the foam with a density of 13 kg m-3 is 34 times its own weight. By chemically cross-linking the foam,it wasalso possible to empty the liquid-filled foams by compression and then to reabsorb the liquid to the same degree with maintained foam integrity. This new processing method also shows great promise for preparing low-density cellulose foams continuously and could be very suitable for industrial up-scaling.

Place, publisher, year, edition, pages
Stockholm: KTH Royal Institute of Technology, 2014. p. ix, 64
Series
TRITA-CHE-Report, ISSN 1654-1081 ; 2014:45
Keywords
Poröst material, cellulosa nanofibriller
National Category
Paper, Pulp and Fiber Technology
Research subject
Fibre and Polymer Science
Identifiers
urn:nbn:se:kth:diva-155065 (URN)978-91-7595-315-1 (ISBN)
Public defence
2014-11-21, F3, Lindstedtsvägen 26, KTH, Stockholm, 10:00 (English)
Opponent
Supervisors
Funder
Knut and Alice Wallenberg Foundation
Note

QC 20141103

Available from: 2014-11-03 Created: 2014-10-30 Last updated: 2022-06-23Bibliographically approved

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