| 1. |
- Plackett, David, et al.
(författare)
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Physical Properties and Morphology of Films Prepared from Microfibrillated Cellulose and Microfibrillated Cellulose in Combination with Amylopectin
- 2010
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Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 117:6, s. 3601-3609
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Tidskriftsartikel (refereegranskat)abstract
- Two types of microfibrillated cellulose (MFC) were prepared using either a sulfite pulp containing a high amount of hemicellulose (MFC 1) or a carboxymethylated dissolving pulp (MFC 2). MFC gels were then combined with amylopectin solutions to produce solvent-cast MFC-reinforced amylopectin films. Tensile testing revealed that MFC 2-reinforced films exhibited a more ductile behavior and that MFC 1-reinforced films had higher modulus of elasticity (E-modulus) at MFC loadings of 50 wt % or higher. Pure MFC films had relatively low oxygen permeability values when data were compared with those for a variety of other polymer films. MFC 1 and MFC 2 films had similar opacity but differences in appearance which were attributed to the presence of some larger fibers and nanofiber agglomerates in MFC 2. Field emission scanning electron microscopy (FE-SEM) and atomic force microscopy (AFM) were used to illustrate the morphology of MFC nanofibers in pure films and in an amylopectin matrix.
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| 2. |
- Siró, I., et al.
(författare)
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Highly Transparent Films from Carboxymethylated Microfibrillated Cellulose : The Effect of Multiple Homogenization Steps on Key Properties
- 2011
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Ingår i: Journal of Applied Polymer Science. - : Wiley-Blackwell. - 0021-8995 .- 1097-4628. ; 119:5, s. 2652-2660
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Tidskriftsartikel (refereegranskat)abstract
- We produced microfibrillated cellulose by passing carboxymethylated sulfite-softwood-dissolving pulp with a relatively low hemicellulose content (4.5%) through a high-shear homogenizer. The resulting gel was subjected to as many as three additional homogenization steps and then used to prepare solvent-cast films. The optical, mechanical, and oxygen-barrier properties of these films were determined. A reduction in the quantity and appearance of large fiber fragments and fiber aggregates in the films as a function of increasing homogenization was illustrated with optical microscopy, atomic force microscopy, and scanning electron microscopy. Film opacity decreased with increasing homogenization, and the use of three additional homogenization steps after initial gel production resulted in highly transparent films. The oxygen permeability of the films was not significantly influenced by the degree of homogenization, whereas the mean tensile strength, modulus of elasticity, and strain at break were increased by two or three extra homogenization steps.
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| 3. |
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| 4. |
- Ankerfors, Mikael, et al.
(författare)
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Method for providing a nanocellulose involving modifying cellulose fibers
- 2009
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Patent (populärvet., debatt m.m.)abstract
- The present invention provides a method for the manufacturing of nanocellulose. The method includes a first modification of the cellulose material, where the cellulose fibres are treated with an aqueous electrolyte-containing solution of an amphoteric cellulose derivative. The modification is followed by a mechanical treatment. By using this method for manufacturing nanocellulose, clogging of the mechanical apparatus is avoided. Also disclosed is nanocellulose manufactured in accordance with said method and uses of said cellulose.
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| 5. |
- Ankerfors, Mikael
(författare)
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Microfibrillated cellulose : Energy-efficient preparation techniques and key properties
- 2012
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Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This work describes three alternative processes for producing microfibrillated cellulose (MFC) in which pulp fibres are first pre-treated and then homogenized using a high-pressure homogenizer. In one process, fibre cell wall delamination was facilitated with a combined enzymatic and mechanical pre-treatment. In the two other processes, cell wall delamination was facilitated by pre-treatments that introduced anionically charged groups into the fibre wall, by means of either a carboxymethylation reaction or irreversibly attaching carboxymethyl cellulose (CMC) onto the fibres. All three processes are industrially feasible and enable production with low energy consumption. Using these methods, MFC can be produced with an energy consumption of 500–2300 kWh/tonne, which corresponds to a 91–98% reduction in energy consumption from that presented in earlier studies. These materials have been characterized in various ways and it has been demonstrated that the produced MFCs are approximately 5–30 nm wide and up to several microns long.
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| 6. |
- Ankerfors, Mikael, 1978-
(författare)
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Microfibrillated cellulose: Energy-efficient preparation techniques and applications in paper
- 2015
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This work describes three alternative processes for producing microfibrillated cellulose (MFC; also referred to as cellulose nanofibrils, CNF) in which bleached pulp fibres are first pretreated and then homogenized using a high-pressure homogenizer. In one process, fibre cell wall delamination was facilitated by a combined enzymatic and mechanical pretreatment. In the two other processes, cell wall delamination was facilitated by pretreatments that introduced anionically charged groups into the fibre wall, by means of either a carboxymethylation reaction or irreversibly attaching carboxymethylcellulose (CMC) to the fibres. All three processes are industrially feasible and enable energy-efficient production of MFC. Using these processes, MFC can be produced with an energy consumption of 500–2300 kWh/tonne. These materials have been characterized in various ways and it has been demonstrated that the produced MFCs are approximately 5–30 nm wide and up to several microns long.The MFCs were also evaluated in a number of applications in paper. The carboxymethylated MFC was used to prepare strong free-standing barrier films and to coat wood-containing papers to improve the surface strength and reduce the linting propensity of the papers. MFC, produced with an enzymatic pretreatment, was also produced at pilot scale and was studied in a pilot-scale paper making trial as a strength agent added at the wet-end for highly filled papers.
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| 7. |
- Ankerfors, Mikael, et al.
(författare)
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Multilayer assembly onto pulp fibres using oppositely charged microfibrillated celluloses, starches, and wetstrength resins : Effect on mechanical properties of CTMP-sheets
- 2016
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 31:1, s. 135-141
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Tidskriftsartikel (refereegranskat)abstract
- The effects of multilayering of microfibrillar cellulose (MFC) onto a chemi-thermomechanical pulp (CTMP), from which the fines material had been removed, were investigated with regard to the mechanical properties of hand-sheets. In one series of experiments, the CTMP was multilayered with cationic MFC/anionic MFC (C-MFC/A-MFC) at various addition levels and sheets made in a conventional sheet former, pressed, and dried at room temperature. This experimental series was complemented with a second series, where sheets were made in a Rapid Köthen sheet former. In a third series of experiments, the CTMP was multilayered using a cationic polyamideamine epichlorohydrine resin (PAE) and an AMFC. Sheets were formed using the Rapid Köthen sheet former. Finally, in a fourth series of experiments, the MFC multilayering experiments were compared with multilayering experiments using cationic starch/anionic starch (C-starch/A-Starch). MFC-multilayering (C-MFC/A-MFC) gave inferior strength gain at a low addition level compared to starch multilayering, but (compared on a weight basis) the strength seemed to level off using starches at high addition levels, whereas there were a continuous increase in strength using MFC multilayering. Multilayering using PAE/A-MFC was found to give a higher strength gain than both C-MFC/A-MFC and C-starch/A-starch multilayering. Sheet density was slightly affected (<14%) by the multilayering techniques used in these experiments.
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| 8. |
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| 9. |
- Ankerfors, Mikael, et al.
(författare)
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The effects of different types of wet-end added microfibrillated celluloses on the properties of paper made from bleached kraft pulp
- 2017
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 32:3, s. 336-345
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Tidskriftsartikel (refereegranskat)abstract
- Research has been undertaken to compare the effects of different types of microfibrillated cellulose (MFC) on the mechanical properties of paper. Three types of MFC were produced: Enzyme MFC (low anionic charge density), Carboxymethylated MFC (high anionic charge density) and cationic MFC (high cationic charge density). The different MFCs required different retention aid strategies. The simplest retention strategy was selected to secure a high retention of MFC. Some experiments also focused on dewatering and pressability of wet webs with carboxymethylated MFC. Conventional isotropic laboratory handsheets were made using a never-dried unrefined elemental chlorine free (ECF)-bleached softwood kraft pulp. It has been shown that the evolution of the mechanical properties and scattering coefficients when plotted versus MFC content was very similar for the three types. However, Enzyme MFC gave a significantly better reinforcement effect. All three types of MFC had a similar effect on the sheet consolidation, reflected in sheet density. Evaluation of the dewatering and pressability of the wet sheets showed that if the MFC was aggregated by an appropriate retention strategy, the dewatering and pressability were not detrimental to the practical applicability of MFC.
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| 10. |
- Ankerfors, Mikael, et al.
(författare)
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The use of microfibrillated cellulose in fine paper manufacturing : Results from a pilot scale papermaking trial
- 2014
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 29:3, s. 476-483
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Tidskriftsartikel (refereegranskat)abstract
- In this work the strength enhancing capabilities of microfibrillated cellulose (MFC) in highly filled papers was studied. Both the MFC production and the paper making were done in pilot scale under realistic industrial conditions. The results clearly show that MFC (2.5 - 5.0wt-%) could improve the mechanical properties of highly filled papers (20 - 35 wt-% filler contents). All studied dry mechanical properties were improved and the improvements were most pronounced for Z-strength and fracture toughness. By combining the MFC with a C-starch dosage further improvements in mechanical properties could be achieved. The improvements in mechanical properties enabled increased filler content with retained properties. The filler increase could be achieved at the same time as the sheet formation and the dry content after pressing were improved.
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| 11. |
- Ankerfors, Mikael, et al.
(författare)
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The use of microfibrillated cellulose in fine paper manufacturing : Results from a pilot scale papermaking trial
- 2014
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 29:3, s. 476-483
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Tidskriftsartikel (refereegranskat)abstract
- In this work the strength enhancing capabilities of microfibrillated cellulose (MFC) in highly filled papers was studied. Both the MFC production and the paper making were done in pilot scale under realistic industrial conditions. The results clearly show that MFC (2.5-5.0 wt-%) could improve the mechanical properties of highly filled papers (20-35 wt-% filler contents). All studied dry mechanical properties were improved and the improvements were most pronounced for Z-strength and fracture toughness. By combining the MFC with a C-starch dosage further improvements in mechanical properties could be achieved. The improvements in mechanical properties enabled increased filler content with retained properties. The filler increase could be achieved at the same time as the sheet formation and the dry content after pressing were improved.
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| 12. |
- Ankerfors, Mikael, et al.
(författare)
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Topo-chemical modification of fibres by grafting of carboxymethyl cellulose in pilot scale
- 2013
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Ingår i: Nordic Pulp and Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; :1, s. 6-14
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Tidskriftsartikel (refereegranskat)abstract
- The aim of this study was to graft carboxymethyl cellulose (CMC) on to bleached softwood kraft pulp at temperatures below 100°C and to do a pilot paper machine trial in order to examine the influence of the CMC on dewatering, sheet formation and mechanical properties. During the pilot trial, one CMC grafted pulp was compared to a pulp with 3 different refining degrees. It was shown that CMC-grafting improves the mechanical properties of paper with only a minor effect on the sheet density. It was also shown that the CMC grafting is less detrimental to dewatering than refining and at a certain tensile index a higher dry content after pressing could be reached. The formation number of the paper produced in the FEX trial was not significantly affected by the addition of CMC.
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| 13. |
- Athley, Karin, et al.
(författare)
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Mechanical retention - Influence of filler floc size and grammage of the fibre web
- 2012
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 27:2, s. 202-207
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Tidskriftsartikel (refereegranskat)abstract
- An investigation of the impact of particle size on the mechanical retention of particles in a fibre network has been conducted. The particles used were five sets of quartz particle fractions having fairly narrow particle size distributions with average particle size ranging from a few μm to around 100 μm. The particles were used to model flocculated filler aggregates as part of a larger study of the effect of pre-flocculation on mechanical retention. Pre-flocculation of the filler is a possible strategy to increase the filler content of paper without deterioration of strength properties. A modified laboratory hand sheet former, known as the Rapid Drainage Device (RDD) was used. The major modification consisted of a long pipe that acted as a suction leg, which provides a dewatering vacuum at the same level as on a paper machine. The experimental results showed that mechanical filler retention increased linearly with particle size and grammage of the fibre layer above a critical grammage which depended on particle size. The linear relation was also seen in a pilot scale trial on the FEX pilot-paper machine at Innventia. During this trial fine paper was produced using pre-flocculated filler where the mean particle size of the flocs and fibres was measured in the flow to the headbox. The results from this pilot trial show that mechanical retention is an important part of the total filler retention. Drainage time and therefore drainage resistance increased with the grammage of the fibre layer and amount of quartz particle added. Drainage time, compared at total grammage (i.e. the sum of fibre and quartz particle grammage) was lowest for a fraction of medium-sized particles, with a median size of 35 μm. There was no obvious effect on retention or drainage resistance of a change in the dewatering pressure from 27.5 to 41.5 kPa.
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| 14. |
- Blell, Rebecca, et al.
(författare)
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Generating in-Plane Orientational Order in Multilayer Films Prepared by Spray-Assisted Layer-by-Layer Assembly
- 2017
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 11:1, s. 84-94
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Tidskriftsartikel (refereegranskat)abstract
- We present a simple yet efficient method for orienting cellulose nanofibrils in layer-by-layer assembled films through spray-assisted alignment. While spraying at 90° against a receiving surface produces films with homogeneous in-plane orientation, spraying at smaller angles causes a macroscopic directional surface flow of liquid on the receiving surface and leads to films with substantial in-plane anisotropy when nanoscale objects with anisotropic shapes are used as components. First results with cellulose nanofibrils demonstrate that such fibrils are easily aligned by grazing incidence spraying to yield optically birefringent films over large surface areas. We show that the cellulosic nanofibrils are oriented parallel to the spraying direction and that the orientational order depends for example on the distance of the receiving surface from the spray nozzle. The alignment of the nanofibrils and the in-plane anisotropy of the films were independently confirmed by atomic force microscopy, optical microscopy between crossed polarizers, and the ellipsometric determination of the apparent refractive index of the film as a function of the in-plane rotation of the sample with respect to the plane of incidence of the ellipsometer.
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| 15. |
- Duker, Elisabeth, et al.
(författare)
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The use of CMC as a dry strength agent - the interplay between CMC attachment and drying.
- 2008
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Ingår i: Nordic Pulp & Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 23:1, s. 65-71
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Tidskriftsartikel (refereegranskat)abstract
- This paper deals with the ability to use high molecular weight CMC as a dry strength agent in paper and how the drying of the pulp, either before or after the CMC attachment, affects the mechanical properties of the paper. The effect of the counter-ion form used during drying and reslushing was also investigated. In the case of the calcium and hydrogen counter-ion forms, drying after CMC attachment had no impact on the attached amount. The sodium form did, however, result in some detachment of CMC. When the pulp was dried prior to CMC treatment, the counter-ion form had no effect on the attached amount. It was also shown that drying of a CMC-treated pulp reduced the positive effect of CMC on the mechanical properties. Nevertheless, the mechanical properties were still better than those of paper made from the never-dried reference pulp. The relative effect of CMC on the mechanical properties was independent of the drying strategy used and the counter-ion form did not affect the mechanical properties. However, surface carboxymethylation prior to drying resulted in sheets with better final mechanical properties than sheets made from pulp that had first been dried and then surface carboxymethylated.
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| 16. |
- Fernández, A., et al.
(författare)
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Effects of ionizing radiation in ethylene-vinyl alcohol copolymers and in composites containing microfibrillated cellulose
- 2008
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Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 109:1, s. 126-134
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Tidskriftsartikel (refereegranskat)abstract
- This study reports on the effect of gamma radiation on morphological, thermal, and water barrier properties of pure ethylene vinyl alcohol copolymers (EVOH29 and EVOH44) and its biocomposites with the nanofiller microfibrillated cellulose (2 wt%). Added microfibrillated cellulose (MFC) preserved the transparency of EVOH films but led to a decrease in water barrier properties. Gamma irradiation at low (30 kGy) and high doses (60 kGy) caused some irreversible changes in the phase morphology of EVOH29 and EVOH44 copolymers that could be associated to crosslinking and other chemical alterations. Additionally, the EVOH copolymers and the EVOH composites reduced the number of hygroscopic hydroxyl functionalities during the irradiation processing and novel carbonyl based chemistry was, in turn, detected. As a result of the above alterations, the water barrier properties of both neat materials and composites irradiated at low doses were notably enhanced, counteracting the detrimental effect on water barrier of adding MFC to the EVOH matrix. © 2008 Wiley Periodicals, Inc.
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| 17. |
- Jin, H., et al.
(författare)
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Effects of different drying methods on textural properties of nanocellulose aerogels
- 2009
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Ingår i: ICCM International Conferences on Composite Materials.
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Konferensbidrag (refereegranskat)abstract
- There is increasing research interest in nanocellulose aerogels because they have low density, hierarchical structure and they are biodegradable and biocompatible. Typically, aerogels are made by supercritical drying, freeze drying and vacuum drying. This work will report the effects that different drying methods have on textural properties of aerogels.
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| 18. |
- Jin, Hua, et al.
(författare)
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Ionically interacting nanoclay and nanofibrillated cellulose lead to tough bulk nanocomposites in compression by forced self-assembly
- 2013
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Ingår i: Journal of Materials Chemistry B. - : Royal Society of Chemistry (RSC). - 2050-750X .- 2050-7518. ; 1:6, s. 835-840
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Tidskriftsartikel (refereegranskat)abstract
- Several approaches have recently been shown for self-assembled biomimetic composite films, aiming at combinations of high toughness, strength, and stiffness. However, it remains challenging to achieve high toughness using simple processes especially for bulk materials. We demonstrate that ionically interacting cationic native nanofibrillated cellulose (C-NFC) and anionic nanoclay, i.e. montmorillonite (MTM), allow local self-assemblies by a simple centrifugation process to achieve 3D bulk materials. The composite with MTM/C-NFC of 63/37 w/w has a high compressive strain to failure of 37% with distinct plastic deformation behaviour, a high work to fracture of 23.1 MJ m(-3), and a relatively high compression strength of 76 MPa. Unlike the conventionally used sequential deposition methods to achieve well-defined layers for the oppositely charged units as limited to films, the present one-step method allows quick formation of bulk materials and leads to local self-assemblies, however, having a considerable amount of nanovoids and defects between them. We suggest that the nanovoids and defects promote the plastic deformation and toughness. Considering the simple preparation method and bio-based origin of NFC, we expect that the present tough bulk nanocomposites in compression have potential in applications for sustainable and environmentally friendly materials in construction and transportation.
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| 19. |
- Karabulut, Erdem, 1983-, et al.
(författare)
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Adhesive Layer-by-Layer Films of Carboxymethylated Cellulose Nanofibril Dopamine Covalent Bioconjugates Inspired by Marine Mussel Threads
- 2012
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 6:6, s. 4731-4739
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Tidskriftsartikel (refereegranskat)abstract
- The preparation of multifunctional films and coatings from sustainable, low-cost raw materials has attracted considerable interest during the past decade. In this respect, cellulose-based products possess great promise due not only to the availability of large amounts of cellulose in nature but also to the new classes of nanosized and well-characterized building blocks of cellulose being prepared from trees or annual plants. However, to fully utilize the inherent properties of these nanomaterials, facile and also sustainable preparation routes are needed. In this work, bioinspired hybrid conjugates of carboxymethylated cellulose nanofibrils (CNFC) and dopamine (DOPA) have been prepared and layer-by-layer (LbL) films of these modified nanofibrils have been built up in combination with a branched polyelectrolyte, polyethyleneimine (PEI), to obtain robust, adhesive, and wet-stable nanocoatings on solid surfaces. It is shown that the chemical functionalization of CNFCs with DOPA molecules alters their conventional properties both in liquid dispersion and at the interface and also influences the LbL. film formation by reducing the electrostatic interaction. Although the CNFC-DOPA conjugates show a lower colloidal stability in aqueous dispersions due to charge suppression, it was possible to prepare the LbL films through the consecutive deposition of the building blocks. Adhesive forces between muttilayer films prepared using chemically functionalized CNFCs and a silica probe are much stronger in the presence of Fe3+ than those between a multilayer film prepared from unmodified nanofibrils and a silica probe. The present work demonstrates a facile way to prepare chemically functionalized cellulose nanofibrils whereby more extended applications can produce novel cellulose-based materials with different functionalities.
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| 20. |
- Klemm, Dieter, et al.
(författare)
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Nanocelluloses : A New Family of Nature-Based Materials
- 2011
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Ingår i: Angewandte Chemie International Edition. - : Wiley. - 1433-7851 .- 1521-3773. ; 50:24, s. 5438-5466
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Forskningsöversikt (refereegranskat)abstract
- Cellulose fibrils with widths in the nanometer range are nature-based materials with unique and potentially useful features. Most importantly, these novel nanocelluloses open up the strongly expanding fields of sustainable materials and nanocomposites, as well as medical and life-science devices, to the natural polymer cellulose. The nanodimensions of the structural elements result in a high surface area and hence the powerful interaction of these celluloses with surrounding species, such as water, organic and polymeric compounds, nanoparticles, and living cells. This Review assembles the current knowledge on the isolation of microfibrillated cellulose from wood and its application in nanocomposites; the preparation of nanocrystalline cellulose and its use as a reinforcing agent; and the biofabrication of bacterial nanocellulose, as well as its evaluation as a biomaterial for medical implants.
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| 21. |
- Larsson, Karolina, et al.
(författare)
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Polylactide latex/nanofibrillated cellulose bionanocomposites of high nanofibrillated cellulose content and nanopaper network structure prepared by a papermaking route
- 2012
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Ingår i: Journal of Applied Polymer Science. - : Wiley. - 0021-8995 .- 1097-4628. ; 125:3, s. 2460-2466
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Tidskriftsartikel (refereegranskat)abstract
- Previous attempts to use polylactide (PLA) latex particles and nanofibrillated cellulose (NFC) in papermaking processing have been limited to low NFC content. In the present study, a bionanocomposite material was successfully produced using a PLA latex and NFC. The components were mixed using a wet mixing method and bionanocomposite films were made by filtration followed by hot pressing. In composite materials, the dispersion of the reinforcing component in the matrix is critical for the material properties. Biopolymers such as PLA are non-polar and soluble only in organic solvents; NFC is, however, highly hydrophilic. By utilizing latex, i.e., an aqueous dispersion of biopolymer micro-particles, wet mixing is possible and the problem of aggregation of the hydrophilic nanocellulose in organic solvent is avoided. The properties of the resulting NFC/PLA latex bionanocomposite films were analyzed. Thorough blending resulted in good dispersion of the reinforcing component within the matrix. Adding increasing amounts of NFC improved the Young's modulus, tensile strength, and strain at break of the bionanocomposite material. The increase in the tensile properties was linear with increasing NFC content as a result of the good dispersion. The NFC also improved the thermal stability of the bionanocomposite material.
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| 22. |
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| 23. |
- Lindström, Tom, et al.
(författare)
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On the nature of joint strength of paper : Effect of dry strength agents - Revisiting the Page equation
- 2016
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 31:3, s. 459-468
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Tidskriftsartikel (refereegranskat)abstract
- This report deals with the effects of various chemical-treatments - carboxymethylcellulose-grafted (CMC) pulp in different ionic forms (Na+, Ca2+, and Al3+), cationic starch, anionic polyacrylamide, and microfibrillated cellulose (MFC) as well as PFI-refining on the strength properties of never-dried bleached soft-wood kraft pulp. The general in-plane strength properties were measured together with z-strength and interlaminar shear strength. The sheet density was varied by pressing the wet sheets to various dry solids content. The relative bonded area of the sheets was determined by the BET surface area of the sheets using krypton adsorption. Interlaminar shear strength is introduced as a measure for fibre-fibre bond strength and validates its use in the Page equation from first principles and it was shown to hold over a large range of tensile strengths. Only at very high tensile index values the calculated tensile index deviated from measured tensile index. This was most likely due to a shift from adhesive to cohesive failure of the joint. The various strength reinforcement methods used were all based on carbohydrate based additives and for those additives the specific joint strength was found to be independent of the specific additive, so the strength reinforcement is only related to the increased relative bonded area upon the addition of the strength adjuvant, although the additives consolidate the sheet on various structural levels.
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| 24. |
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| 25. |
- Lôpez-Rubio, A., et al.
(författare)
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Enhanced film forming and film properties of amylopectin using micro-fibrillated cellulose
- 2007
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Ingår i: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617 .- 1879-1344. ; 68:4, s. 718-727
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Tidskriftsartikel (refereegranskat)abstract
- This work describes a novel approach to produce amylopectin films with enhanced properties by the addition of micro fibrillated cellulose (MFC). Aqueous dispersions of gelatinized amylopectin, glycerol (0-38 wt%) and MFC (0-10 wt%) were cast at ambient temperature and 50% relative humidity and, after 10 days of storage, the tensile properties were investigated. The structure of the composite films was revealed by optical, atomic force and transmission electron microscopy. The moisture content was determined by thermogravimetry and the temperature-dependent film rigidity was measured by thermal mechanical analysis. Synchrotron simultaneous small- and wide-angle X-ray measurements revealed that the solutions had to be heated to above 85 degrees C in order to achieve complete gelatinization. Optical microscopy and atomic force microscopy revealed uniformly distributed MFC aggregates in the films, with a length of 10-90 mu m and a width spanning from a few hundred nanometers to several microns. Transmission electron microscopy showed that, in addition to aggregates, single MFC microfibrils were also embedded in the amylopectin matrix. It was impossible to cast antylopectin films of sufficient quality with less than 38 wt% glycerol. However, when MFC was added it was possible to produce high quality films even without glycerol. The film without glycerol was stiff and strong but not brittle. It was suggested that this remarkable effect was due to its comparatively high moisture content. Consequently MFC acted both as a "conventional" reinforcement because of its fibrous structure and also indirectly as a plasticiser because its presence led to an increase in film moisture content.
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| 26. |
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| 27. |
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| 28. |
- Nordqvist, David, et al.
(författare)
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Enhancement of the wet properties of transparent chitosan-acetic-acid-salt films using microfibrillated cellulose
- 2007
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 8:8, s. 2398-2403
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Tidskriftsartikel (refereegranskat)abstract
- This report presents a new route to enhance the wet properties of chitosan-acetic-acid-salt films using microfibrillated cellulose (MFC). The enhancement makes it easier to form chitosan-acetic-acid-salt films into various shapes at room temperature in the wet state. Chitosan with MFC was compared with the well-known buffer treatment. It was observed that films containing 5 wt % MFC were visually identical to the buffered/unbuffered films without MFC. Field-emission scanning electron microscopy indicated that MFC formed a network with uniformly distributed fibrils and fibril bundles in the chitosan matrix. The addition of MFC reduced the risk of creases and deformation in the wet state because of a greater wet stiffness. The wet films containing MFC were also extensible. Although the stiffness, strength and extensibility were highest for the buffered films, the wet strength of the MFC-containing unbuffered films was sufficient for wet forming operations. The effects of MFC on the mechanical properties of the dry chitosan films were small or absent. It was concluded that the addition of MFC is an acceptable alternative to buffering for shaping chitosan films/products in the wet state. The advantages are that the "extra" processing step associated with buffering is unnecessary and that the film matrix remains more water-soluble.
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| 29. |
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| 30. |
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| 31. |
- Pääkkö, M., et al.
(författare)
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Enzymatic hydrolysis combined with mechanical shearing and high-pressure homogenization for nanoscale cellulose fibrils and strong gels
- 2007
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 8:6, s. 1934-1941
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Tidskriftsartikel (refereegranskat)abstract
- Toward exploiting the attractive mechanical properties of cellulose I nanoelements, a novel route is demonstrated, which combines enzymatic hydrolysis and mechanical shearing. Previously, an aggressive acid hydrolysis and sonication of cellulose I containing fibers was shown to lead to a network of weakly hydrogen-bonded rodlike cellulose elements typically with a low aspect ratio. On the other hand, high mechanical shearing resulted in longer and entangled nanoscale cellulose elements leading to stronger networks and gels. Nevertheless, a widespread use of the latter concept has been hindered because of lack of feasible methods of preparation, suggesting a combination of mild hydrolysis and shearing to disintegrate cellulose I containing fibers into high aspect ratio cellulose I nanoscale elements. In this work, mild enzymatic hydrolysis has been introduced and combined with mechanical shearing and a high-pressure homogenization, leading to a controlled fibrillation down to nanoscale and a network of long and highly entangled cellulose I elements. The resulting strong aqueous gels exhibit more than 5 orders of magnitude tunable storage modulus G' upon changing the concentration. Cryotransmission electron microscopy, atomic force microscopy, and cross-polarization/magic-angle spinning (CP/MAS) C-13 NMR suggest that the cellulose I structural elements obtained are dominated by two fractions, one with lateral dimension of 5-6 nm and one with lateral dimensions of about 10-20 nm. The thicker diameter regions may act as the junction zones for the networks. The resulting material will herein be referred to as MFC (microfibrillated cellulose). Dynamical rheology showed that the aqueous suspensions behaved as gels in the whole investigated concentration range 0.125-5.9% w/w, G' ranging from 1.5 Pa to 10(5) Pa. The maximum G' was high, about 2 orders of magnitude larger than typically observed for the corresponding nonentangled low aspect ratio cellulose I gels, and G' scales with concentration with the power of approximately three. The described preparation method of MFC allows control over the final properties that opens novel applications in materials science, for example, as reinforcement in composites and as templates for surface modification.
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| 32. |
- Pääkkö, M., et al.
(författare)
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Long and entangled native cellulose i nanofibers allow flexible aerogels and hierarchically porous templates for functionalities
- 2008
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Ingår i: Soft Matter. - : Royal Society of Chemistry (RSC). - 1744-683X .- 1744-6848. ; 4:12, s. 2492-2499
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Tidskriftsartikel (refereegranskat)abstract
- Recently it was shown that enzymatic and mechanical processing of macroscopic cellulose fibers lead to disintegration of long and entangled native cellulose I nanofibers in order to form mechanically strong aqueous gels (Pääkkö¶ et al., Biomacromolecules, 2007, 8, 1934). Here we demonstrate that (1) such aqueous nanofibrillar gels are unexpectedly robust to allow formation of highly porous aerogels by direct water removal by freeze-drying, (2) they are flexible, unlike most aerogels that suffer from brittleness, and (3) they allow flexible hierarchically porous templates for functionalities, e.g. for electrical conductivity. No crosslinking, solvent exchange nor supercritical drying are required to suppress the collapse during the aerogel preparation, unlike in typical aerogel preparations. The aerogels show a high porosity of ˜98% and a very low density of ca. 0.02 g cm -3. The flexibility of the aerogels manifests as a particularly high compressive strain of ca. 70%. In addition, the structure of the aerogels can be tuned from nanofibrillar to sheet-like skeletons with hierarchical micro- and nanoscale morphology and porosity by modifying the freeze-drying conditions. The porous flexible aerogel scaffold opens new possibilities for templating organic and inorganic matter for various functionalities. This is demonstrated here by dipping the aerogels in an electrically conducting polyaniline-surfactant solution which after rinsing off the unbound conducting polymer and drying leads to electrically conducting flexible aerogels with relatively high conductivity of around 1 ×— 10-2 S cm-1. More generally, we foresee a wide variety of functional applications for highly porous flexible biomatter aerogels, such as for selective delivery/separation, tissue-engineering, nanocomposites upon impregnation by polymers, and other medical and pharmaceutical applications.
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| 33. |
- Svensson, Anna, et al.
(författare)
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3D-shapeable thermoplastic paper materials
- 2013
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Ingår i: Nordic Pulp & Paper Research Journal. - 0283-2631 .- 2000-0669. ; 28:4, s. 602-610
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Tidskriftsartikel (refereegranskat)abstract
- The purpose of this work was to investigate to what extent it is possible to improve the thermoplastic properties of paper materials so that 3D-shapeable paper products can be manufactured. For that purpose, the addition of various chemical adjuvants, known to improve both tensile strength index and strain at break, was investigated. Adding polylactide latex was found to significantly improve both the tensile strength properties and strain at break of paper materials. To enhance their strainability, the paper sheets were cured at an elevated temperature of 150 degrees C. The improved strainability after curing is hypothesized to relate to the spreading of the polylactide latex (minimum film-forming temperature of 90 degrees C) on the fibre surfaces, improving the relative bonded area. Both the tensile strength index and strain at break improved significantly with no densification of the paper sheets. A second aim was to make double-curved board structures in a hydroforming equipment, using the sheets treated with polylactide latex under various conditions. Double-curved sheets with a nominal strain at break of over 20% could be formed by adding 20% polylactide latex. Hydroforming had to be done at temperatures exceeding the minimum film-forming temperature of the polylactide latex to significantly improve the strain at break during the forming operation.
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| 34. |
- Svensson, Anna, et al.
(författare)
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3D-shapeable thermoplastic paper materials
- 2013
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Ingår i: Nordic Pulp and Paper Research Journal. - : Walter de Gruyter GmbH. - 0283-2631 .- 2000-0669. ; 28:4, s. 602-610
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Tidskriftsartikel (refereegranskat)abstract
- The purpose of this work was to investigate to what extent it is possible to improve the thermoplastic properties of paper materials so that 3Dshapeable paper products can be manufactured. For that purpose, the addition of various chemical adjuvants, known to improve both tensile strength index and strain at break, was investigated. Adding polylactide latex was found to significantly improve both the tensile strength properties and strain at break of paper materials. To enhance their strainability, the paper sheets were cured at an elevated temperature of 150°C. The improved strainability after curing is hypothesized to relate to the spreading of the polylactide latex (minimum filmforming temperature of 90°C) on the fibre surfaces, improving the relative bonded area. Both the tensile strength index and strain at break improved significantly with no densification of the paper sheets. A second aim was to make double-curved board structures in a hydroforming equipment, using the sheets treated with polylactide latex under various conditions. Double-curved sheets with a nominal strain at break of over 20% could be formed by adding 20% polylactide latex. Hydroforming had to be done at temperatures exceeding the minimum film-forming temperature of the polylactide latex to significantly improve the strain at break during the forming operation.
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| 35. |
- Wang, Miao, et al.
(författare)
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Colloidal Ionic Assembly between Anionic Native Cellulose Nanofibrils and Cationic Block Copolymer Micelles into Biomimetic Nanocomposites
- 2011
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Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 12:6, s. 2074-2081
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Tidskriftsartikel (refereegranskat)abstract
- We present a facile ionic assembly between fibrillar and spherical colloidal objects toward biomimetic nanocomposites with majority hard and minority soft domains based on anionic reinforcing native cellulose nanofibrils and cationic amphiphilic block copolymer micelles with rubbery core. The concept is based on ionic complexation of carboxymethylated nanofibrillated cellulose (NFC, or also denoted as microfibrillated cellulose, MFC) and micelles formed by aqueous self-assembly of quaternized poly(1,2-butadiene)-block-poly(dimethylaminoethyl methacrylate) with high fraction of the NFC reinforcement. The adsorption of block copolymer micelles onto nanocellulose is shown by quartz crystal microbalance measurements, atomic force microscopy imaging, and fluorescent optical microscopy. The physical properties are elucidated using electron microscopy, thermal analysis, and mechanical testing. The cationic part of the block copolymer serves as a binder to NFC, Whereas the hydrophobic rubbery micellar cores are designed to facilitate energy dissipation and nanoscale lubrication between the NFC domains under deformation. We show that the mechanical properties do not follow the rule of mixtures, and synergistic effects are observed with promoted work of fracture in one composition. As the concept allows wide possibilities for tuning, the work suggests pathways for nanocellulose-based biomimetic nanocomposites combining high toughness with stiffness and strength.
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| 36. |
- Wågberg, Lars, et al.
(författare)
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The build-up of polyelectrolyte multilayers of microfibrillated cellulose and cationic polyelectrolytes
- 2008
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 24:3, s. 784-795
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Tidskriftsartikel (refereegranskat)abstract
- A new type of nanocellulosic material has been prepared by high-pressure homogenization of carboxymethylated cellulose fibers followed by ultrasonication and centrifugation. This material had a cylindrical cross-section as shown by transmission electron microscopy with a diameter of 5-15 nm and a length of up to 1 mu m. Calculations, using the Poisson-Boltzmann equation, showed that the surface potential was between 200 and 250 mV, depending on the pH, the salt concentration, and the size of the fibrils. They also showed that the carboxyl groups on the surface of the nanofibrils are not fully dissociated until the pH has reached pH = similar to 10 in deionized water. Calculations of the interaction between the fibrils using the Derjaguin-Landau-Verwey-Overbeek theory and assuming a cylindrical geometry indicated that there is a large electrostatic repulsion between these fibrils, provided the carboxyl groups are dissociated. If the pH is too low and/or the salt concentration is too high, there will be a large attraction between the fibrils, leading to a rapid aggregation of the fibrils. It is also possible to form polyelectrolyte multilayers (PEMs) by combining different types of polyelectrolytes and microfibrillated cellulose (MFC). In this study, silicon oxide surfaces were first treated with cationic polyelectrolytes before the surfaces were exposed to MFC. The build-up of the layers was monitored with ellipsometry, and they show that it is possible to form very well-defined layers by combinations of MFC and different types of polyelectrolytes and different ionic strengths of the solutions during the adsorption of the polyelectrolyte. A polyelectrolyte with a three-dimensional structure leads to the build-up of thick layers of MFC, whereas the use of a highly charged linear polyelectrolyte leads to the formation of thinner layers of MFC. An increase in the salt concentration during the adsorption of the polyelectrolyte results in the formation of thicker layers of MFC, indicating that the structure of the adsorbed polyelectrolyte has a large influence on the formation of the MFC layer. The films of polyelectrolytes and MFC were so smooth and well-defined that they showed clearly different interference colors, depending on the film thickness. A comparison between the thickness of the films, as measured with ellipsometry, and the thickness estimated from their colors showed good agreement, assuming that the films consisted mainly of solid cellulose with a refractive index of 1.53. Carboxymethylated MFC is thus a new type of nanomaterial that can be combined with oppositely charged polyelectrolytes to form well-defined layers that may be used to form, for example, new types of sensor materials.
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