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- Colson, Jérôme, et al.
(author)
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Adhesion properties of regenerated lignocellulosic fibres towards poly(lactic acid) microspheres assessed by colloidal probe technique
- 2018
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In: Journal of Colloid and Interface Science. - : Elsevier BV. - 1095-7103 .- 0021-9797. ; 532, s. 819-829
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Journal article (peer-reviewed)abstract
- In the field of polymer reinforcement, it is important to understand the interactions involved between the polymer matrix and the reinforcing component. This paper is a contribution to the fundamental understanding of the adhesion mechanisms involved in natural fibre reinforced composites. We report on the use of the colloidal probe technique for the assessment of the adhesion behaviour between poly(lactic acid) microspheres and embedded cross-sections of regenerated lignocellulosic fibres. These fibres consisted of tailored mixtures of cellulose, lignin and xylan, the amount of which was determined beforehand. The influence of the chemical composition of the fibres on the adhesion behaviour was studied in ambient air and in dry atmosphere. In ambient air, capillary forces resulted in larger adhesion between the sphere and the fibres. Changing the ambient medium to a dry nitrogen atmosphere allowed reducing the capillary forces, leading to a drop in the adhesion forces. Differences between fibres of distinct chemical compositions could be measured only on freshly cut surfaces. Moreover, the surface energy of the fibres was assessed by inverse gas chromatography. Compared to fibres containing solely cellulose, the presence of lignin and/or hemicellulose led to higher adhesion and lower surface energy, suggesting that these chemicals could serve as natural coupling agents between hydrophobic and hydrophilic components.
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- Nypelö, Tiina, 1982, et al.
(author)
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Conversion of wood-biopolymers into macrofibers with tunable surface energy via dry-jet wet-spinning
- 2018
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In: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 25:9, s. 5297-5307
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Journal article (peer-reviewed)abstract
- Surface chemistry of regenerated all-wood-biopolymer fibers that are fine-tuned by composition of cellulose, lignin and xylan is elucidated via revealing their surface energy and adhesion. Xylan additive resulted in thin fibers and decreased surface energy of the fiber outer surfaces compared to the cellulose fibers, or when lignin was used as an additive. Lignin increased the water contact angle on the fiber surface and decreased adhesion force between the fiber cross section and a hydrophilic probe, confirming that lignin reduced fiber surface affinity to water. Lignin and xylan enabled fiber decoration with charged groups that could tune the adhesion force between the fiber and an AFM probe. The fibers swelled in water: the neat cellulose fiber cross section area increased 9.2%, the fibers with lignin as the main additive 9.1%, with xylan 6.8%, and the 3-component fibers 5.5%. This indicates that dimensional stability in elevated humidity is improved in the case of 3-component fiber compared to 2-component fibers. Xylan or lignin as an additive neither improved strength nor elongation at break. However, improved deformability was achieved when all the three components were incorporated into the fibers. Graphical Abstract: [Figure not available: see fulltext.].
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- Nypelö, Tiina, 1982, et al.
(author)
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Self-Standing Nanocellulose Janus-Type Films with Aldehyde and Carboxyl Functionalities
- 2018
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In: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 19:3, s. 973-979
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Journal article (peer-reviewed)abstract
- Nanocellulose-based self-standing films are becoming a substrate for flexible electronics, diagnostics, and sensors. Strength and surface chemistry are vital variables for these film-based endeavors, the former is one of the assets of nanocellulose. To contribute to the latter, nanocellulose films are tuned with a side-specific functionalization, having an aldehyde and a carboxyl side. The functionalities were obtained combining premodification of the film components by periodate oxidation with ozone post-treatment. Periodate oxidation of cellulose nanocrystals results in film components that interact through intra- and intermolecular hemiacetals and lead to films with an elastic modulus of 11 GPa. The ozone treatment of one film side induces conversion of the aldehyde into carboxyl functionalities. The ozone treatment on individual crystals was largely destructive. Remarkably, such degradation is not observed for the self-standing film, and the film strength at break is preserved. Preserving a physically intact film despite ozone treatment is a credit to using the dry film structure held together by interparticle covalent linkages. Additionally, gas-phase post-treatment avoids disintegration that could result from immersion into solvents. The crystalline cellulose "Janus" film is suggested as an interfacial component in biomaterial engineering, separation technology, or in layered composite materials for tunable affinity between the layers.
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