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  • 1.
    Atoufi, Zhaleh
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Ciftci, Göksu Cinar
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Green Ambient-Dried Aerogels with a Facile pH-Tunable Surface Charge for Adsorption of Cationic and Anionic Contaminants with High Selectivity2022Inngår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 23, nr 11, s. 4934-4947Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The fabrication of reusable, sustainable adsorbents from low-cost, renewable resources via energy efficient methods is challenging. This paper presents wet-stable, carboxymethylated cellulose nanofibril (CNF) and amyloid nanofibril (ANF) based aerogel-like adsorbents prepared through efficient and green processes for the removal of metal ions and dyes from water. The aerogels exhibit tunable densities (18-28 kg m-3), wet resilience, and an interconnected porous structure (99% porosity), with a pH controllable surface charge for adsorption of both cationic (methylene blue and Pb(II)) and anionic (brilliant blue, congo red, and Cr(VI)) model contaminants. The Langmuir saturation adsorption capacity of the aerogel was calculated to be 68, 79, and 42 mg g-1for brilliant blue, Pb(II), and Cr(VI), respectively. Adsorption kinetic studies for the adsorption of brilliant blue as a model contaminant demonstrated that a pseudo-second-order model best fitted the experimental data and that an intraparticle diffusion model suggests that there are three adsorption stages in the adsorption of brilliant blue on the aerogel. Following three cycles of adsorption and regeneration, the aerogels maintained nearly 97 and 96% of their adsorption capacity for methylene blue and Pb(II) as cationic contaminants and 89 and 80% for brilliant blue and Cr(VI) as anionic contaminants. Moreover, the aerogels showed remarkable selectivity for Pb(II) in the presence of calcium and magnesium as background ions, with a selectivity coefficient more than 2 orders of magnitude higher than calcium and magnesium. Overall, the energy-efficient and sustainable fabrication procedure, along with good structural stability, reusability, and selectivity, makes these aerogels very promising for water purification applications.

  • 2.
    Atoufi, Zhaleh
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Gordeyeva, Korneliya
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberprocesser.
    Cortes Ruiz, Maria F.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Hall, Stephen A
    KTH, Skolan för teknikvetenskap (SCI), Teknisk mekanik, Farkostteknik och Solidmekanik, Hållfasthetslära.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wet-resilient foams based on heat-treated β-lactoglobulin and cellulose nanofibrilsManuskript (preprint) (Annet vitenskapelig)
  • 3.
    Atoufi, Zhaleh
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Gordeyeva, Korneliya
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberprocesser.
    Cortes Ruiz, Maria F.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Synergistically stabilized wet foams from heat treated β-lactoglobulin and cellulose nanofibrils and their application for green foam productionManuskript (preprint) (Annet vitenskapelig)
  • 4.
    Atoufi, Zhaleh
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Gordeyeva, Korneliya
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberprocesser.
    Cortes Ruiz, Maria F.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Synergistically stabilized wet foams from heat treated β-lactoglobulin and cellulose nanofibrils and their application for green foam production2024Inngår i: Applied Materials Today, ISSN 2352-9407, Vol. 39, artikkel-id 102251Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Achieving a sustainable foam production requires a complete substitution of synthetic components with natural and renewable alternatives, as well as development of an environment-friendly production process. This work demonstrates a synergetic combination of heat-treated beta-lactoglobulin proteins and cellulose nanofibrils (CNFs) to create fully bio-based and highly-stable wet foams. Furthermore, a gradual reduction in the pH, enabled oven-drying of the wet foams without any major structural collapse of the foam, resulting in the preparation of lightweight solid foams with the density of 10.2 kg.m(-3). First, the foaming behavior of heat-treated beta-lactoglobulin systems (HBSs) containing amyloid nanofibrils (ANFs) and non-converted peptides was investigated at different pHs. Subsequently, the HBS foams were stabilized using CNFs, followed by a gradual acidification of the system to a final pH of 4.5. To gain a deeper understanding of the stabilization mechanism of the foam, the interactions between the foam's components, their positioning in the foam structure, and the viscoelasticity of the fibrillar network were investigated using quartz crystal microgravimetry, confocal microscopy and rheology. The analysis of the obtained data suggests that the stability of the foams was associated with the accumulation of CNFs and ANFs at the air-water interface, and that the concomitant formation of an intertwined network surrounding the air bubbles. This together resulted in a significant decrease in drainage rate of the liquid in the foam lamellae, bubble coarsening and bubble coalescence within the foams. The results also show that the major surface-active component participating in the creation of the foam is the free peptide left in solution after the formation of the ANFs. A slow reduction in pH to 4.5 lead to further gelation of the fibrillar network and an improved storage modulus of the foam lamellae. This resulted in a strong coherent structure that could withstand oven-drying without collapse. The density, porosity, microstructure and compressive mechanical properties of such prepared dry foams were assessed. Overall, the results demonstrate the potential of HBSs to replace synthetic surfactants and outlines a sustainable preparation protocol for the preparation of light-weight porous composite structures of ANFs and CNFs.

  • 5.
    Atoufi, Zhaleh
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Surface tailoring of cellulose aerogel-like structures with ultrathin coatings using molecular layer-by-layer assembly2022Inngår i: Carbohydrate Polymers, ISSN 0144-8617, E-ISSN 1879-1344, Vol. 282, artikkel-id 119098Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose nanofibril-based aerogels have promising applicability in various fields; however, developing an effi-cient technique to functionalize and tune their surface properties is challenging. In this study, physically and covalently crosslinked cellulose nanofibril-based aerogel-like structures were prepared and modified by a mo-lecular layer-by-layer (m-LBL) deposition method. Following three m-LBL depositions, an ultrathin polyamide layer was formed throughout the aerogel and its structure and chemical composition was studied in detail. Analysis of model cellulose surfaces showed that the thickness of the deposited layer after three m-LBLs was approximately 1 nm. Although the deposited layer was extremely thin, it led to a 2.6-fold increase in the wet specific modulus, improved the acid-base resistance, and changed the aerogels from hydrophilic to hydrophobic making them suitable materials for oil absorption with the absorption capacity of 16-36 g/g. Thus, demon-strating m-LBL assembly is a powerful technique for tailoring surface properties and functionality of cellulose substrates.

  • 6.
    Carrick, Christopher
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Brismar, Hjalmar
    KTH, Skolan för teknikvetenskap (SCI), Tillämpad fysik, Cellens fysik. KTH, Centra, Science for Life Laboratory, SciLifeLab.
    Aidun, Cyrus
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Native and functionalized micrometre-sized cellulose capsules prepared by microfluidic flow focusing2014Inngår i: RSC Advances, E-ISSN 2046-2069, Vol. 4, nr 37, s. 19061-19067Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose capsules with average outer and inner radii of approximately 44 mu m and 29 mm respectively were prepared from cellulose dissolved in a mixture of lithium chloride and dimethylacetamide using a microfluidic flow focusing device (MFFD). The MFFD had three inlets where octane oil in a cellulose solution in silicone oil was used to produce a double emulsion containing a cellulose capsule. This technique enables the formation of capsules with a narrow size distribution which can be beneficial for drug delivery or controlled release capsules. In this respect, cellulose is a highly interesting material since it is known to cause no autoimmune reactions when used in contact with human tissue. Furthermore, by controlling the chemical properties of the cellulose, it is possible to trigger a swelling of the capsules and consequentially the release of an encapsulated substance, e. g. a model drug, when the capsule becomes exposed to an external stimulus. To demonstrate this, capsules were functionalized by carboxymethylation to be pH- responsive and to expand approximately 10% when subjected to a change in pH from 3 to 10. The diffusion constant of a model drug, a 4 kDa fluorescently labelled dextran, through the native capsule wall was estimated to be 6.5 X 10(-14) m(2) s(-1) by fitting fluorescence intensity data to Fick's second law.

  • 7.
    Carrick, Christopher
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Immunoselective cellulose nanospheres: a versatile platform for nanotheranostics2014Inngår i: ACS Macro Letters, E-ISSN 2161-1653, Vol. 3, nr 11, s. 1117-1120Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This paper describes a novel route for the preparation and functionalization of perfectly spherical cellulose nanospheres (CNSs), ranging from 100 to 400 nrn with a typical diameter of 160-170 nrn,for use in theranostics. The method of preparation enables both surface and interior bulk functionalization, and this presumably also makes the CNSs suitable for use in end-use applications other than theranostics. Surface functionalization was here demonstrated by antibody conjugation with an antibody specific toward the epidermal growth factor receptor (EGFR) protein, i.e., facilitating interaction with cancer cells having the EGFR. Besides showing specificity, the CNS-antibody conjugates showed a very low nonspecific binding. The CNSs could easily be bulk functionalized by embedding gold nanoparticles in the cellulose sphere matrix during CNS preparation to provide imaging contrast for diagnostic purposes.

  • 8.
    Carrick, Christopher
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Immunoselective cellulose nanospheres by antibody conjugation2014Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 247, s. 727-COLL-Artikkel i tidsskrift (Annet vitenskapelig)
  • 9.
    Cervin, Nicholas Tchang
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Johanson, Erik
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Strong, Water-Durable, and Wet-Resilient Cellulose Nanofibril-Stabilized Foams from Oven Drying2016Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 8, nr 18, s. 11682-11689Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Porous materials from cellulose nanofibrils (CNFs) have been prepared using Pickering foams from aqueous dispersions. Stable wet foams were first produced using surface-modified CNFs as stabilizing particles. To better maintain the homogeneous pore structure of the foam after drying, the foams were dried in an oven on a liquid-filled porous ceramic frit. The cell structure was studied by scanning electron microscopy and liquid porosimetry, the mechanical properties were studied by compression testing, and the liquid absorption capacity was determined both with liquid porosimetry and by soaking in water. By controlling the charge density of the CNFs, it was possible to prepare dry foams with different densities, the lowest density being 6 kg m(-3), that is, a porosity of 99.6%. For a foam with a density of 200 kg m(-3) the compressive Young's modulus was 50 MPa and the energy absorption to 70% strain was 2.3 MJ M-3. The use of chemically modified CNFs made it possible to prepare cross-linked foams with water-durable and wet-resilient properties. These foams absorbed liquid up to 34 times their own weight and were able to release this liquid under compression and to reabsorb the same amount when the pressure was released.

  • 10.
    Ciftci, Göksu Cinar
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Riazanova, Anastasiia
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Øvrebø, H.H.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Berglund, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Tailoring of rheological properties and structural polydispersity effects in microfibrillated cellulose suspensions2020Inngår i: Cellulose, ISSN 0969-0239, E-ISSN 1572-882X, Vol. 27, nr 16, s. 9227-9241Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Abstract: Industrial production of low-charge microfibrillated cellulose (MFC) typically results in wide fibril size distributions. This polydispersity influences viscosity, overall colloidal stability, and rheological properties of MFC suspensions and gels in aqueous systems. In this work, a systematic rheological analysis is performed for industrially prepared MFC and fractions of different size distributions. Gel formation and flow characteristics (e.g., shear-thinning) of each fraction are examined under neutral and acidic conditions and compared with the unfractionated MFC suspension. The effects of size, aspect ratio, and surface charge on the rheology of semi-dilute MFC suspensions are discussed. The results demonstrate that particle size and aspect ratio distribution control the viscoelasticity and shear-thinning properties of MFC suspensions. An increased fraction of small diameter nanofibrils, by ex situ addition of the fine particles with high aspect ratio or removal of the coarsest particles (with lower aspect ratio) by fractionation, significantly enhances the storage modulus and the yield stress of the complex mixture, compared to the properties of the coarser fractions. New insights are also reported on the tailoring of the rheology of highly polydisperse fibrillar mixtures, where the rheological contributions of each fraction are discussed. Graphic abstract: [Figure not available: see fulltext.].

  • 11.
    Ciftci, Göksu Cinar
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Riazanova, Anastasia
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Karppinen, Anni
    Borregaard AS, Sarpsborg, Norway..
    Ovrebo, Hans Henrik
    Borregaard AS, Sarpsborg, Norway..
    Berglund, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Influence of microfibrillated cellulose fractions on the rheology of water suspensions: Colloidal interactions and viscoelastic properties2018Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 256Artikkel i tidsskrift (Annet vitenskapelig)
  • 12.
    Elf, Patric
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Polymera material.
    Özeren, Hüsamettin Deniz
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Polymera material.
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Anette
    Chalmers Univ Technol, Dept Chem & Chem Engn, SE-41296 Gothenburg, Sweden.;Chalmers Univ Technol, FibRe Ctr Lignocellulose Based Thermoplast, SE-41296 Gothenburg, Sweden..
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Nilsson, Robin
    Chalmers Univ Technol, Dept Chem & Chem Engn, SE-41296 Gothenburg, Sweden.;Chalmers Univ Technol, FibRe Ctr Lignocellulose Based Thermoplast, SE-41296 Gothenburg, Sweden..
    Chaiyupatham, Poppy Thanaporn
    Chalmers Univ Technol, Dept Chem & Chem Engn, SE-41296 Gothenburg, Sweden..
    Hedenqvist, Mikael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Nilsson, Fritjof
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. Mid Sweden Univ, FSCN Res Ctr, S-85170 Sundsvall, Sweden..
    Molecular Dynamics Simulations of Cellulose and Dialcohol Cellulose under Dry and Moist Conditions2023Inngår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 24, nr 6, s. 2706-2720Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The development of wood-based thermoplastic polymersthat can replacesynthetic plastics is of high environmental importance, and previousstudies have indicated that cellulose-rich fiber containing dialcoholcellulose (ring-opened cellulose) is a very promising candidate material.In this study, molecular dynamics simulations, complemented with experiments,were used to investigate how and why the degree of ring opening influencesthe properties of dialcohol cellulose, and how temperature and presenceof water affect the material properties. Mechanical tensile properties,diffusion/mobility-related properties, densities, glass-transitiontemperatures, potential energies, hydrogen bonds, and free volumeswere simulated for amorphous cellulosic materials with 0-100%ring opening, at ambient and high (150 degrees C) temperatures, withand without water. The simulations showed that the impact of ringopenings, with respect to providing molecular mobility, was higherat high temperatures. This was also observed experimentally. Hence,the ring opening had the strongest beneficial effect on "processability"(reduced stiffness and strength) above the glass-transition temperatureand in wet conditions. It also had the effect of lowering the glass-transitiontemperature. The results here showed that molecular dynamics is avaluable tool in the development of wood-based materials with optimalthermoplastic properties.

  • 13.
    Erlandsson, Johan
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    López Durán, Veronica
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Granberg, Hjalmar
    Innventia AB.
    Sandberg, Mats
    Acreo Swedish ICT AB.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Macro- and mesoporous nanocellulose beads for use in energy storage devices2016Inngår i: APPLIED MATERIALS TODAY, ISSN 2352-9407, Vol. 5, s. 246-254Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Chemically cross-linked, wet-stable cellulose nanofibril (CNF) aerogel beads were fabricated using a novel procedure. The procedure facilitated controlled production of millimetre-sized CNF aerogel beads without freeze-drying or critical point drying, while still retaining a highly porous structure with low density. The aerogel beads were mechanically robust in the dry state, supporting loads of 1.3 N at 70% compression, even after being soaked in water and re-dried. Furthermore, they displayed both a good stability in water and a remarkably good shape recovery after wet compression. Owing to the stability in water, the entire surface of the highly porous aerogel beads could be successfully functionalized with polyelectrolytes and carboxyl-functionalized single-wall carbon nanotubes (CF-SWCNTs) using the Layer-by-Layer technique, introducing a significant electrical conductivity (1.6 mS/cm) to the aerogel beads. The functionalized, electrically conducting aerogel beads could carry as much as 2 kA/cm(2) and act as electrodes in a supercapacitor displaying a stabilized charge storage capacity of 9.8 F/g after 50 charging-discharging cycles.

  • 14.
    Erlandsson, Johan
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Pettersson, Torbjörn
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Ingverud, Tobias
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Ytbehandlingsteknik. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Granberg, H.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Malkoch, Michael
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Ytbehandlingsteknik.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    On the mechanism behind freezing-induced chemical crosslinking in ice-templated cellulose nanofibril aerogels2018Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 6, nr 40, s. 19371-19380Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The underlying mechanism related to freezing-induced crosslinking of aldehyde-containing cellulose nanofibrils (CNFs) has been investigated, and the critical parameters behind this process have been identified. The aldehydes introduced by periodate oxidation allows for formation of hemiacetal bonds between the CNFs provided the fibrils are in sufficiently close contact before the water is removed. This is achieved during the freezing process where the cellulose components are initially separated, and the growth of ice crystals forces the CNFs to come into contact in the thin lamellae between the ice crystals. The crosslinked 3-D structure of the CNFs can subsequently be dried under ambient conditions after solvent exchange and still maintain a remarkably low density of 35 kg m-3, i.e. a porosity greater than 98%. A lower critical amount of aldehydes, 0.6 mmol g-1, was found necessary in order to generate a crosslinked 3-D CNF structure of sufficient strength not to collapse during the ambient drying. The chemical stability of the 3-D structure can be further enhanced by converting the hemiacetals to acetals by treatment with an alcohol under acidic conditions.

  • 15. Fall, A. B.
    et al.
    Hagel, F.
    Edberg, J.
    Malti, Abdellah
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. Digital Cellulose Center, Drottning Kristinas Väg 61, SE-114 86 Stockholm, Sweden.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Granberg, H.
    Håkansson, K. M. O.
    Spinning of Stiff and Conductive Filaments from Cellulose Nanofibrils and PEDOT:PSS Nanocomplexes2022Inngår i: ACS Applied Polymer Materials, ISSN 2637-6105, Vol. 4, nr 6, s. 4119-4130Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Research in smart textiles is growing due to the increased demand from the healthcare sector and people's urge to keep track of and analyze the signals and metrics from their bodies. Electrically conductive filaments are the most fundamental material for smart textiles. These filaments can be imbued with functionalities and useful in fields like energy storage, sensing, and actuation. To be able to meet the requirements that the latter applications require, fabrication techniques must be developed to provide better processability and sustainability in a cost-effective manner. Here, a mixture of a conductive polymer, poly(3,4-ethylenedioxythiophene) (PEDOT), and biobased cellulose nanofibrils (CNFs) was used to spin filaments utilizing a water-based process. These filaments show electrical conductivities up to 150 S/cm and tensile stiffness of 20 GPa. Interestingly, the PEDOT aligned to a similar degree as the CNFs during the spinning process without a drawing step, which is hypothesized to be caused by the attachment of PEDOT on the CNFs. Lastly, the filaments were tested in an organic electrochemical transistor (OECT) configuration, which resulted in a working device with an on/off ratio approaching 1500. Furthermore, the OECT exhibited stable behavior when changing temperature (20-80 °C) and relative humidity (40-80%). This aqueous spinning method, resulting in filaments with robust electronic properties in different temperature and humidity environments, show greats promise for future innovative smart textiles. 

  • 16.
    Francon, Hugo
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Benselfelt, Tobias
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Ytbehandlingsteknik.
    Granberg, Hjalmar
    RISE Bioecon, Stockholm, Sweden..
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Fibre & Polymer Technol, Stockholm, Sweden..
    3D printable nanocellulose aerogels via a green crosslinking approach and a facile evaporation procedure2019Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 257Artikkel i tidsskrift (Annet vitenskapelig)
  • 17.
    Francon, Hugo
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Görür, Yunus Can
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för teknikvetenskap (SCI), Centra, Linné Flow Center, FLOW. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Toward commercial Li-ion graphite anodes with enhanced mechanical and electrochemical properties using binders from chemically modified cellulose fibersManuskript (preprint) (Annet vitenskapelig)
  • 18.
    Francon, Hugo
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Görür, Yunus Can
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Biokompositer.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Toward Li-ion Graphite Anodes with Enhanced Mechanical and Electrochemical Properties Using Binders from Chemically Modified Cellulose Fibers2022Inngår i: ACS Applied Energy Materials, E-ISSN 2574-0962, Vol. 5, nr 8, s. 9333-9342Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose nanofibers (CNFs) are bio-sourced nanomaterials, which, after proper chemical modification, exhibit a unique ability to disperse carbon-rich micro- and nanomaterials and can be used in the design of mechanically strong functional nanocomposites. When used in the preparation of graphite anodes for Li-ion batteries, they have the potential to outperform conventional binders such as carboxymethyl cellulose (CMC) and styrene-butadiene rubber (SBR) both electrochemically and mechanically. In this study, cellulose-rich fibers were subjected to three different chemical modifications (including carbonyl-, carboxyl-, and aldehyde-functionalization) to facilitate their fibrillation into CNFs during the preparation of aqueous slurries of graphite and carbon black. Using these binders, graphite anodes were prepared through conventional blade coating. Compared to CMC/SBR reference anodes, all anodes prepared with modified cellulosic fibers as binders performed better in the galvanostatic cycling experiments and in the mechanical cohesion tests they were subjected to. Among them, the aldehyde- and carboxyl-rich fibers performed the best and resulted in a 10% increase in specific capacity with a simultaneous two- and three-fold increase of the electrode material's stress-at-failure and strain-at-break, respectively. In-depth characterizations attributed these results to the distinctive nanostructure and surface chemistry of the composites formed between graphite and these fiber-based binders. 

  • 19.
    Francon, Hugo
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Wang, Zhen
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Marais, Andrew
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Mystek, Katarzyna
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Piper, Andrew
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Granberg, Hjalmar
    RISE Innventia AB, Papermaking & Packaging, Box 5604, SE-11486 Stockholm, Sweden..
    Malti, Abdellah
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Gatenholm, Paul
    Chalmers Univ Technol, Dept Chem & Chem Engn, Kemigarden 4, SE-41269 Gothenburg, Sweden..
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH Royal Inst Technol, Dept Fibre & Polymer Technol, Tekn Ringen 58, SE-10044 Stockholm, Sweden..
    Ambient-Dried, 3D-Printable and Electrically Conducting Cellulose Nanofiber Aerogels by Inclusion of Functional Polymers2020Inngår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 30, nr 12, artikkel-id 1909383Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This study presents a novel, green, and efficient way of preparing crosslinked aerogels from cellulose nanofibers (CNFs) and alginate using non-covalent chemistry. This new process can ultimately facilitate the fast, continuous, and large-scale production of porous, light-weight materials as it does not require freeze-drying, supercritical CO2 drying, or any environmentally harmful crosslinking chemistries. The reported preparation procedure relies solely on the successive freezing, solvent-exchange, and ambient drying of composite CNF-alginate gels. The presented findings suggest that a highly-porous structure can be preserved throughout the process by simply controlling the ionic strength of the gel. Aerogels with tunable densities (23-38 kg m(-3)) and compressive moduli (97-275 kPa) can be prepared by using different CNF concentrations. These low-density networks have a unique combination of formability (using molding or 3D-printing) and wet-stability (when ion exchanged to calcium ions). To demonstrate their use in advanced wet applications, the printed aerogels are functionalized with very high loadings of conducting poly(3,4-ethylenedioxythiophene):tosylate (PEDOT:TOS) polymer by using a novel in situ polymerization approach. In-depth material characterization reveals that these aerogels have the potential to be used in not only energy storage applications (specific capacitance of 78 F g(-1)), but also as mechanical-strain and humidity sensors.

  • 20.
    Ghanadpour, Maryam
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Carosio, Federico
    Politecn Torino, Dipartimento Sci Applicata & Technol, Alessandria, Italy..
    Larsson, Per
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center. Innventia AB, Stockholm, Sweden..
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Use of phosphorylated cellulose nanofibrils in preparation of an all cellulose flame-retardant material2016Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 251Artikkel i tidsskrift (Annet vitenskapelig)
  • 21.
    Gustafsson, Emil
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Hedberg, Jonas
    KTH, Skolan för kemivetenskap (CHE), Kemi, Yt- och korrosionsvetenskap.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Johnson, C. Magnus
    KTH, Skolan för kemivetenskap (CHE), Kemi, Yt- och korrosionsvetenskap.
    Vibrational sum frequency spectroscopy on polyelectrolyte multilayers: Effect of molecular surface structure on macroscopic wetting properties2015Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 31, nr 15, s. 4435-4442Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Adsorption of a single layer of molecules on a surface, or even a reorientation of already present molecules, can significantly affect the surface properties of a material. In this study, vibrational sum frequency spectroscopy (VSFS) has been used to study the change in molecular structure at the solid-air interface following thermal curing of polyelectrolyte multilayers of poly(allylamine hydrochloride) and poly(acrylic acid). Significant changes in the VSF spectra were observed after curing. These changes were accompanied by a distinct increase in the static water contact angle, showing how the properties of the layer-by-layer molecular structure are controlled not just by the polyelectrolyte in the outermost layer but ultimately by the orientation of the chemical constituents in the outermost layers.

  • 22.
    Gustafsson, Emil
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Hedberg, Jonas
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Johnson, C. Magnus
    Vibrational sum frequency spectroscopy on polyelectrolyte multilayers: modelling of hydrophobic fibresManuskript (preprint) (Annet vitenskapelig)
  • 23.
    Gustafsson, Emil
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Treatment of cellulose fibres with polyelectrolytes and wax colloids to create tailored highly hydrophobic fibrous networks2012Inngår i: Colloids and Surfaces A: Physicochemical and Engineering Aspects, ISSN 0927-7757, E-ISSN 1873-4359, Vol. 414, s. 415-421Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Paper is a versatile material with obvious advantages in being both inexpensive and environment friendly. However, a major drawback compared with many other materials, such as plastics, is that it is sensitive to both liquid water and moist air. Traditionally paper is protected from liquid water by sizing. The present work presents a new way to make paper water resistant by combining the layer-by-layer (LbL) technique with the adsorption of a colloidal wax onto the multilayer structure. After the adsorption of five layers of poly(allylamine hydrochloride) and poly(acrylic acid) followed by the adsorption of 8. mg paraffin wax per gram fibre, the contact angle measured 60. s after a drop of water was applied to the sheet was about 138°. If the sheets were cured for 30. min at 160. °C after sheet making, the contact angle was ca. 150°. The heat treatment of sheets prepared from LbL-modified fibres without the addition of wax gave a contact angle of about 113°. To decouple structural effects from changes in surface energy upon heat treatment of PAH/PAA LbL films, model experiments were carried out where LbL assemblies were prepared on silicon oxide and cellulose model surfaces. The contact angle increased when these films were heat treated but it did not exceed 90°. The reason for this is due to the lack of structure of the model surfaces on a micrometre scale. The adsorption of wax impaired the mechanical properties of paper sheets made from modified fibres compared to sheets from the LbL-modified fibres. However, at an adsorption of 8. mg paraffin wax per gram fibre there was still an increase by 37 ± 1% in tensile strength index compared to the untreated reference pulp (33.8 ± 0.7 and 24.7 ± 0.6. kNm/kg respectively).

  • 24.
    Görür, Yunus Can
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Francon, Hugo
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Sethi, Jatin
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Maddalena, L.
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Biokompositer.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Erlandsson, Johan
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Carosio, F.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Rapidly Prepared Nanocellulose Hybrids as Gas Barrier, Flame Retardant, and Energy Storage Materials2022Inngår i: ACS Applied Nano Materials, E-ISSN 2574-0970, Vol. 5, nr 7, s. 9188-9200Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose nanofibril (CNF) hybrid materials show great promise as sustainable alternatives to oil-based plastics owing to their abundance and renewability. Nonetheless, despite the enormous success achieved in preparing CNF hybrids at the laboratory scale, feasible implementation of these materials remains a major challenge due to the time-consuming and energy-intensive extraction and processing of CNFs. Here, we describe a scalable materials processing platform for rapid preparation (<10 min) of homogeneously distributed functional CNF-gibbsite and CNF-graphite hybrids through a pH-responsive self-assembly mechanism, followed by their application in gas barrier, flame retardancy, and energy storage materials. Incorporation of 5 wt % gibbsite results in strong, transparent, and oxygen barrier CNF-gibbsite hybrid films in 9 min. Increasing the gibbsite content to 20 wt % affords them self-extinguishing properties, while further lowering their dewatering time to 5 min. The strategy described herein also allows for the preparation of freestanding CNF-graphite hybrids (90 wt % graphite) that match the energy storage performance (330 mA h/g at low cycling rates) and processing speed (3 min dewatering) of commercial graphite anodes. Furthermore, these ecofriendly electrodes can be fully recycled, reformed, and reused while maintaining their initial performance. Overall, this versatile concept combines a green outlook with high processing speed and material performance, paving the way toward scalable processing of advanced ecofriendly hybrid materials. 

  • 25.
    Görür, Yunus Can
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Francon, Hugo
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Sethi, Jatin
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Maddalena, Lorenza
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Erlandsson, Johan
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Carosio, Federico
    Politecn Torino, Dipartimento Sci Applicata & Tecnol, Alessandria Campus,Viale Teresa Michel 5, I-15121 Alessandria, Italy..
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för teknikvetenskap (SCI), Centra, Linné Flow Center, FLOW. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Rapid Processing of Functional Hybrids via Reversible Self-Assembly of NanocellulosesManuskript (preprint) (Annet vitenskapelig)
  • 26.
    Görür, Yunus Can
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Francon, Hugo
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Sethi, Jatin
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Maddalena, Lorenza
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Erlandsson, Johan
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Carosio, Federico
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, Linné Flow Center, FLOW. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Rapid processing of functional nanocellulose hybrids for gas barrier, flame retardant and energy storage materialsManuskript (preprint) (Annet vitenskapelig)
  • 27.
    Görür, Yunus Can
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Self-Fibrillating Cellulose Fibers: Rapid In Situ Nanofibrillation to Prepare Strong, Transparent, and Gas Barrier Nanopapers2020Inngår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 21, nr 4, s. 1480-1488Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose nanofibrils (CNFs) prepared from wood biomass are promising candidates to replace oil-based materials in, for example, packaging applications. However, CNFs' affinity for water combined with their small size leads to very slow and energy-demanding processes for handling and removal of water. To a large extent, this is the major roadblock that prevents a feasible production of dry CNF-based materials on an industrial scale. In this work, self-fibrillating fibers (SFFs) from wood, where the fibrils can be liberated by external stimuli, were prepared via sequential TEMPO and periodate oxidation reactions. Papers made from these modified fibers using conventional laboratory papermaking methods were then in situ nanofibrillated via a modest pH increase. With a dewatering time of less than 10 s for a 3 g/L dispersion, SFFs represent a major improvement over conventional CNF nanopapers that take approximately 6 h to dewater. Moreover, 100 g/m2 nanopapers obtained through in situ fibrillation exhibited comparable, if not superior, properties to those reported for conventionally made CNF films. A tensile strength of 184 MPa, a Young's modulus of 5.2 GPa, a strain at break of 4.6%, 90% optical transmittance, and an oxygen permeability of 0.7 cm3 μm m-2 d-1 kPa-1 at 50% RH were measured for SFF nanopapers. Furthermore, in situ nanofibrillation of the SFFs can also be achieved from already dried papers, facilitating numerous possibilities in terms of logistics and handling for an industrial scale-up and transportation of nanomaterials. Overall, stimuli-induced SFFs indeed enable a rapid production of strong, transparent, gas barrier nanopapers, which likely can be industrially scaled up and eventually compete with the oil-based plastics in the market for packaging materials.

    Fulltekst (pdf)
    fulltext
  • 28.
    Görür, Yunus Can
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Montanari, Celine
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per Tomas
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Advanced Characterization of Self-Fibrillating Cellulose Fibers and Their Use in Tunable Filters2021Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 13, nr 27, s. 32467-32478Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Thorough characterization and fundamental understanding of cellulose fibers can help us develop new, sustainable material streams and advanced functional materials. As an emerging nanomaterial, cellulose nanofibrils (CNFs) have high specific surface area and good mechanical properties; however, handling and processing challenges have limited their widespread use. This work reports an in-depth characterization of self-fibrillating cellulose fibers (SFFs) and their use in smart, responsive filters capable of regulating flow and retaining nanoscale particles. By combining direct and indirect characterization methods with polyelectrolyte swelling theories, it was shown that introduction of charges and decreased supramolecular order in the fiber wall were responsible for the exceptional swelling and nanofibrillation of SFFs. Different microscopy techniques were used to visualize the swelling of SFFs before, during, and after nanofibrillation. Through filtration and pH adjustment, smart filters prepared via in situ nanofibrillation showed an ability to regulate the flow rate through the filter and a capacity of retaining 95% of 300 nm (diameter) silica nanoparticles. This exceptionally rapid and efficient approach for making smart filters directly addresses the challenges associated with dewatering of CNFs and bridges the gap between science and technology, making the widespread use of CNFs in high-performance materials a not-so-distant reality.

    Fulltekst (pdf)
    fulltext
  • 29.
    Henschen, Jonatan
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Illergård, Josefin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Träkemi och massateknologi.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Ek, Monica
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Träkemi och massateknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Contact-active antibacterial aerogels from cellulose nanofibrils2016Inngår i: Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, E-ISSN 1873-4367, Vol. 146, s. 415-422Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The use of cellulose aerogels as antibacterial materials has been investigated by applying a contact-active layer-by-layer modification to the aerogel surface. Studying the adsorption of multilayers of polyvinylamine (PVAm) and polyacrylic acid to aerogels comprising crosslinked cellulose nanofibrils and monitoring the subsequent bacterial adhesion revealed that up to 26 mg PVAm g aerogel−1 was adsorbed without noticeably affecting the aerogel structure. The antibacterial effect was tested by measuring the reduction of viable bacteria in solution when the aerogels were present. The results show that >99.9% of the bacteria adhered to the surface of the aerogels. Microscopy further showed adherence of bacteria to the surfaces of the modified aerogels. These results indicate that it is possible to create materials with three-dimensional cellulose structures that adsorb bacteria with very high efficiency utilizing the high specific surface area of the aerogels in combination with their open structure.

  • 30.
    Henschen, Jonatan
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Illergård, Josefin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Larsson, Per
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Ek, Monica
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Antibacterial aerogels from cellulose nanofibrils2016Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 251Artikkel i tidsskrift (Annet vitenskapelig)
  • 31.
    Henschen, Jonatan
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Illergård, Josefin
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Ek, Monica
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Antibacterial surface modification of nanocellulosic materials2015Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 249Artikkel i tidsskrift (Annet vitenskapelig)
  • 32.
    Henschen, Jonatan
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Illergård, Josefin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Träkemi och massateknologi.
    Ek, Monica
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Träkemi och massateknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Bacterial adhesion to polyvinyl-amine-modified nanocellulose filmsManuskript (preprint) (Annet vitenskapelig)
  • 33.
    Henschen, Jonatan
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Illergård, Josefin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Ek, Monica
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Bacterial adhesion to polyvinylamine-modified nanocellulose films2017Inngår i: Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, E-ISSN 1873-4367, Vol. 151, s. 224-231Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose nanofibril (CNF) materials have been widely studied in recent years and are suggested for a wide range of applications, e.g., medical and hygiene products. One property not very well studied is the interaction between bacteria and these materials and how this can be controlled. The current work studies how bacteria adhere to different CNF materials modified with polyelectrolyte multilayers. The tested materials were TEMPO-oxidized to have different surface charges, periodate-oxidized to vary the water interaction and hot-pressed to alter the surface structure. Then, multilayers were constructed using polyvinylamine (PVAm) and polyacrylic acid. Both the material surface charge and water interaction affect the amount of polymer adsorbed to the surfaces. Increasing the surface charge decreases the adsorption after the first PVAm layer, possibly due to conformational changes. Periodate-oxidized and crosslinked films have low initial polymer adsorptions; the decreased swelling prevents polymer diffusion into the CNF micropore structure. Microscopic analysis after incubating the samples with bacterial suspensions show that only the materials with the lowest surface charge enable bacteria to adhere to the surface because, when adsorbing up to 5 layers PVAm/PAA, the increased anionic surface charge appears to decrease the net surface charge. Both the amounts of PVAm and PAA influence the net surface charge and thus the bacterial adhesion. The structure generated by the hot-pressing of the films also strongly increases the number of bacteria adhering to the surfaces. These results indicate that the bacterial adhesion to CNF materials can be tailored using polyelectrolyte multilayers on different CNF substrates.

  • 34.
    Hollertz, Rebecca
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    López Durán, Vernica
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Larsson, Per A.
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Chemically modified cellulose micro- and nanofibrils as paper-strength additives2017Inngår i: Cellulose, ISSN 0969-0239, E-ISSN 1572-882X, Vol. 24, nr 9, s. 3883-3899Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Chemically modified cellulose micro- and nanofibrils were successfully used as paper strength additives. Three different kinds of cellulose nanofibrils (CNFs) were studied: carboxymethylated CNFs, periodate-oxidised carboxymethylated CNFs and dopamine-grafted carboxymethylated CNFs, all prepared from bleached chemical fibres of dissolving grade, and one microfibrillated cellulose from unbleached kraft fibres. In addition to mechanical characterization of the final paper sheets the fibril retention, sheet density and sheet morphology were also studied as a function of addition of the four different cellulose fibrils. In general, the cellulose fibrils, when used as additives, significantly increased the tensile strength, Young’s modulus and strain-at-break of the paper sheets. The effects of the different fibrils on these properties were compared and evaluated and used to analyse the underlying mechanisms behind the strengthening effect. The strength-enhancing effect was most pronounced for the periodate-oxidised CNFs when they were added together with polyvinyl amine (PVAm) or poly(dimethyldiallylammonium chloride) (pDADMAC). The addition of periodate-oxidised CNFs, with pDADMAC as retention aid, resulted in a 37% increase in tensile strength at a 2 wt% addition and an 89% increase at a 15 wt% addition (from 67 to 92 and 125 kNm/kg, respectively) compared to a reference with only pDADMAC. Wet-strong sheets with a wet tensile index of 30 kNm/kg were also obtained when periodate-oxidised CNFs and PVAm were combined. This significant increase in wet strength is suggested to be the result of a formation of cross-links between the aldehyde groups, introduced by the periodate oxidation, and hydroxyl groups on the lignocellulosic fibres and the primary amines of PVAm. Even though less significant, there was also an increase in wet tensile strength when pDADMAC was used together with periodate-oxidised fibrils which shows that the aldehyde groups are able to increase the wet strength without the presence of the primary amines of the PVAm. As an alternative method to strengthen the fibre network, carboxymethylated CNFs grafted with dopamine, by an ethyl dimethylaminopropyl carbodiimide coupling, were used as a strength additive. When used as an additive, these CNFs showed a strong propensity to form films on and around the fibres and significantly increased the mechanical properties of the sheets. Their addition resulted in an increase in the Young´s modulus by 41%, from 5.1 to 7.2 GPa, and an increase in the tensile strength index of 98% (from 53 to 105 kNm/kg) with 5 wt% retained dopamine-grafted CNFs.

  • 35.
    Hollertz, Rebecca
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    López Durán, Verónica
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Larsson, Per
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Chemically modified cellulose micro- and nanofibrils as paper-strength additivesManuskript (preprint) (Annet vitenskapelig)
  • 36.
    Jain, Karishma
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Reid, Michael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    On the interaction between PEDOT:PSS and cellulose: Adsorption mechanisms and controlling factors2021Inngår i: Carbohydrate Polymers, ISSN 0144-8617, E-ISSN 1879-1344, Vol. 260, artikkel-id 117818Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a conducting polymer frequently used with cellulose, to develop advanced electronic materials. To understand the fundamental interactions between cellulose and PEDOT:PSS, a quartz crystal microbalance with dissipation (QCM-D) was used to study the adsorption of PEDOT:PSS onto model films of cellulose-nanofibrils (CNFs) and regenerated cellulose. The results show that PEDOT:PSS adsorbs spontaneously onto anionically charged cellulose wherein the adsorbed amount can be tuned by altering solution parameters such as pH, ionic strength and counterion to the charges on the CNF. Temperature-dependent QCM-D studies indicate that an entropy gain is the driving force for adsorption, as the adsorbed amount of PEDOT:PSS increased with increasing temperature. Colloidal probe AFM, in accordance with QCM-D results, also showed an increased adhesion between cellulose and PEDOT:PSS at low pH. AFM images show bead-like PEDOT:PSS particles on CNF surfaces, while no such organization was observed on the regenerated cellulose surfaces. This work provides insight into the interaction of PEDOT:PSS/cellulose that will aid in the design of sustainable electronic devices.

  • 37.
    Jain, Karishma
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wang, Zhen
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Garma, Leonardo D.
    Karolinska Inst, Med Biochem & Biophys, Stockholm, Sweden..
    Engel, Emile
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Ciftci, Göksu Cinar
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Fager, Cecilia
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Centra, Wallenberg Wood Science Center.
    3D printable composites of modified cellulose fibers and conductive polymers and their use in wearable electronics2023Inngår i: APPLIED MATERIALS TODAY, ISSN 2352-9407, Vol. 30, artikkel-id 101703Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    There are many bioelectronic applications where the additive manufacturing of conductive polymers may be of use. This method is cheap, versatile and allows fine control over the design of wearable electronic devices. Nanocellulose has been widely used as a rheology modifier in bio-based inks that are used to print electrical components and devices. However, the preparation of nanocellulose is energy and time consuming. In this work an easy-to-prepare, 3D-printable, conductive bio-ink; based on modified cellulose fibers and poly(3,4-ethylene dioxythiophene) poly(styrene sulfonate) (PEDOT:PSS), is presented. The ink shows excellent printability, the printed samples are wet stable and show excellent electrical and electrochemical performance. The printed structures have a conductivity of 30 S/cm, high tensile strains (>40%), and specific capacitances of 211 F/g; even though the PEDOT:PSS only accounts for 40 wt% of the total ink composition. Scanning electron microscopy (SEM), wide-angle X-ray scattering (WAXS), and Raman spectroscopy data show that the modified cellulose fibers induce conformational changes and phase separation in PEDOT:PSS. It is also demonstrated that wearable supercapacitors and biopotential-monitoring devices can be prepared using this ink.

  • 38.
    Kotov, Nikolay
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi.
    Larsson, Per A.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Jain, Karishma
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Abitbol, Tiffany
    RISE Res Inst Sweden, Drottning Kristinas Vag 55, SE-11428 Stockholm, Sweden..
    Cernescu, Adrian
    Attocube Syst AG, Neaspec, Eglfinger Weg 2, D-85540 Haar, Germany..
    Wågberg, Lars
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Johnson, C. Magnus
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Yt- och korrosionsvetenskap.
    Elucidating the fine-scale structural morphology of nanocellulose by nano infrared spectroscopy2023Inngår i: Carbohydrate Polymers, ISSN 0144-8617, E-ISSN 1879-1344, Vol. 302, artikkel-id 120320Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Nanoscale infrared (IR) spectroscopy and microscopy, enabling the acquisition of IR spectra and images with a lateral resolution of 20 nm, is employed to chemically characterize individual cellulose nanocrystals (CNCs) and cellulose nanofibrils (CNFs) to elucidate if the CNCs and CNFs consist of alternating crystalline and amorphous domains along the CNF/CNC. The high lateral resolution enables studies of the nanoscale morphology at different domains of the CNFs/CNCs: flat segments, kinks, twisted areas, and end points. The types of nano-cellulose investigated are CNFs from tunicate, CNCs from cotton, and anionic and cationic wood-derived CNFs. All nano-FTIR spectra acquired from the different samples and different domains of the individual nanocellulose particles resemble a spectrum of crystalline cellulose, suggesting that the non-crystalline cellulose signal observed in macroscopic measurements of nanocellulose most likely originate from cellulose chains present at the surface of the nanocellulose particles.

  • 39.
    Larsson, Per
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberteknologi.
    Chemical modification of cellulose fibres and nanofibrils for an expanded material property space and novel applications2019Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 257Artikkel i tidsskrift (Annet vitenskapelig)
  • 40.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Dimensional Stability of Paper: Influence of Fibre-Fibre Joints and Fibre Wall Oxidation2008Licentiatavhandling, med artikler (Annet vitenskapelig)
    Abstract [sv]

    Papper är ett mycket mångsidigt material. Trots detta finns det ett flertal egenskaper som begränsar papperets användbarhet. Ett av de större problemen med cellulosa- och lignocellulosafibrer är att de sänker sin fria energi genom att sorbera vatten, och denna sorption förändrar papperets dimensioner. Detta fenomen kallas vanligtvis för bristfällig dimensionsstabilitet och uppträder i form av registerfel vid flerfärgstryck eller som krullning, buckling och vågiga papperskanter vid utskrift, kopiering och lagring, eller med en vidare definition som förkortad livslängd hos lådor på grund av mekanosorptivt kryp.

    Avsikten med denna avhandling har varit att studera och kvantifiera vilka egenskaper som styr, och hur de påverkar, den vatteninducerade dimensionsförändringen som sker hos ett fibernätverk, samt hur dess dimensionsstabilitet kan förbättras. Detta har studerats både genom att ändra fiberns fuktsorptionsegenskaper och genom att förändra adhesionen och kontaktgraden mellan fibrerna i fiber-fiberfogarna. Fogegenskaperna har också varierats genom att tillverka laboratorieark torkade under inspänning samt ark torkade fritt för att minimera mängden inbyggda spänningar i arket.

    Blekt kraftmassa har behandlats med polyelektrolytmultilager (PEM) för att förbättra adhesionen mellan fibrerna och för att öka kontaktgraden mellan fibrerna i fogen. Kontaktgraden har även minskats genom förhorning av fibrerna före arkformning. För de ark som fick torka fritt gav PEM-behandlingen en ökad hygroexpansionskoefficient, det vill säga dimensionsförändringen normaliserad mot förändringen i fuktinnehåll, vid samma förändring i relativ luftfuktighet medan förhorningen minskade hygroexpansionskoefficienten något. Om arken emellertid torkades under inspänning observerades ingen skillnad i hygroexpansionskoefficient mellan de olika fibermodifieringarna. Detta tolkades som ett resultat av en ökad kontaktzon och en större utbredning ut ur fogens plan, när arken torkades utan inspänning. En utbredning som medför att en större del av fiberns transversella expansion överförs som expansion i pappersplanet.

    Fibrernas fuktsorptionsegenskaper förändrades genom natriumperjodatoxidering av 1,4-glukanernas C2-C3-bindning. Detta skapade sannolikt tvärbindningar i fiberväggen som förbättrade fiberväggens tålighet både genom att låsa fibrillerna närmare varandra och genom att ta bort potentiella adsorptionssäten som annars är tillgängliga för vattenadsorption. Perjodatoxidationen minskar också fibrernas kristallinitet och således frigjorde oxidationen hydroxylgrupper där vattenmolekyler kan adsorbera. Detta innebar att oxidationen både minskade och ökade interaktionen mellan vatten och fibervägg, men dock på olika strukturell nivå. Tvärbindningarna visade sig också märkbart reducera sorptionshastigheten när arken utsattes för en förändrad luftfuktighet så länge de inte tidigare utsatts för relativa luftfuktigheter nära mättnad. Som ett resultat av den lägre förändringen i fuktinnehåll vid en förändring i luftfuktighet från 20 till 85 % RF minskade dimensionsförändringens amplitud för de tvärbundna arken upp till 30 %. Emellertid uppvisade de tvärbundna arken en högre hygroexpansionskoefficeint, vilket innebär att de blev mer känsliga för absoluta förändringar i fuktinnehåll.

    Fulltekst (pdf)
    FULLTEXT01
  • 41.
    Larsson, Per A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Hygro- and hydroexpansion of paper: Influence of fibre-joint formation and fibre sorptivity2010Doktoravhandling, med artikler (Annet vitenskapelig)
    Abstract [en]

    Paper is a versatile, cheap and environment-friendly material. Nevertheless, there are several factors limiting its usefulness, and one of the major issues is that cellulosic and ligno-cellulosic fibres spontaneously sorb water. At the same time, the water uptake changes the dimensions of the paper. This phenomenon is usually referred to as a lack of dimensional stability and is often evident as misregister during multicolour printing, or curl, cockle and wavy edges during printing, copying, and storage, or, in a widerperspective, as a shortened lifetime of boxes during storage due to mechano-sorptivecreep.

    This thesis aims to improve the understanding of the mechanisms behind the dimensional(in)stability of paper. It looks beyond finding the best starting material and explores what can be done chemically to further improve the dimensional stability. Furthermore, it compares traditional hygroexpansion measurements, where the dimensional change is measured as a function of atmospheric relative humidity, and dimensional changes caused by liquid water, referred to here as hydroexpansion.

    The main parameters which have been studied are the ability of the fibres to join together and their ability to sorb water. In other words, how the degree of molecular contact within the fibre joints, as well as how the fibres are dried, affect the dimensional stability of the final paper, and whether it is possible to reduce the sorptivity of the fibres, and thus their ability to expand, by chemically cross-linking the fibre-wall.

    It was found that the degree of fibre-fibre contact, modified by drying or adsorption of polyelectrolyte multilayers, had little influence on the hygroexpansion or on the hydroexpansion if the sheets were dried under restraint, whereas freely dried sheets with a reduced degree of contact showed a slightly better dimensional stability, at least during hygroexpansion. What, however, had a positive effect on both hygro- and hydroexpansion was the fibre-wall cross-linking. In this work, cross-linking was achieved by oxidising the cellulose to dialdehydecellulose which can form cross-links with adjacent cellulose molecules, and thus reduce the rate of water diffusion into the fibre and hence the uptake of water. In the case of the most oxidised and cross-linked fibres, the diffusion coefficient was found to be 2–3 times lower than that of the non-oxidisedreference. The effect of the cross-linking was, however, the most prominent the first time the moisture content of the paper was increased since cycled samples no longer show this lower adsorption rate. It is suggested that this is due to the formation of a new pore system when the moisture content is increased, and the slow creation of this pore system reduces the moisture uptake of the sample.

    If hygroexpansion is compared with hydroexpansion, it is evident that a given change in moisture content does not correspond to the same absolute expansion, the maximum hydroexpansion being lower by a factor of 2–3 than the hygroexpansion of the same paper. This is probably because the applied liquid water is never equally distributed in the fibre network before it evaporates. Another effect of the more dynamic absorption of liquid water and the subsequent hydroexpansion is that at least in non-restrained samples there is first a rapid initial expansion which is followed 5 to 15 seconds later by a rapid in-plane contraction. It is suggested that this contraction is due to a combination of the release of dried-in strains, drying, and an increase in surface roughness.

    Fulltekst (pdf)
    FULLTEXT01
  • 42.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Berglund, Lars A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Ductile All-Cellulose Nanocomposite Films Fabricated from Core-Shell Structured Cellulose Nanofibrils2014Inngår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 15, nr 6, s. 2218-2223Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulosic materials have many desirable properties such as high mechanical strength and low oxygen permeability and will be an important component in a sustainable biomaterial-based society, but unfortunately they often lack the ductility and formability offered by petroleum-based materials. This paper describes the fabrication and characterization of nanocomposite films made of core-shell modified cellulose nanofibrils (CNEs) surrounded by a shell of ductile dialcohol cellulose, created by heterogeneous periodate oxidation followed by borohydride reduction of the native cellulose in the external parts of the individual fibrils. The oxidation with periodate selectively produces dialdehyde cellulose, and the process does not increase the charge density of the material. Yet the modified cellulose fibers could easily be homogenized to CNFs. Prior to film fabrication, the CNF was shown by atomic force microscopy to be 0.5-2 mu m long and 4-10 nm wide. The films were fabricated by filtration, and besides uniaxial tensile testing at different relative humidities, they were characterized by scanning electron microscopy and oxygen permeability. The strength-at-break at 23 degrees C and 50% RH was 175 MPa, and the films could, before rupture, be strained, mainly by plastic deformation, to about 15% and 37% at 50% RH and 90% RH, respectively. This moisture plasticization was further utilized to form a demonstrator consisting of a double-curved structure with a nominal strain of 24% over the curvature. At a relative humidity of 80%, the films still acted as a good oxygen barrier, having an oxygen permeability of 5.5 mL-mu L/(m(2).24 h.kPa). These properties indicate that this new material has a potential for use as a barrier in complex-shaped structures and hence ultimately reduce the need for petroleum-based plastics.

  • 43.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Berglund, Lars A.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Highly ductile fibres and sheets by core-shell structuring of the cellulose nanofibrils2014Inngår i: Cellulose, ISSN 0969-0239, E-ISSN 1572-882X, Vol. 21, nr 1, s. 323-333Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A greater ductility of cellulosic materials is important if they are to be used in increasingly advanced applications. This study explores the potential for using chemical core-shell structuring on the nanofibril level to alter the mechanical properties of cellulose fibres and sheets made thereof. The structuring was achieved by a selective oxidation of the cellulose C2-C3 bonds with sodium periodate, followed by a reduction of the aldehydes formed with sodium borohydride, i.e. locally transforming cellulose to dialcohol cellulose. The resulting fibres were morphologically characterised and the sheets made of these modified fibres were mechanically tested. These analyses showed a minor decrease in the degree of polymerisation, a significantly reduced cellulose crystal width and a greater ductility. At 27 % conversion of the available C2-C3 bonds, sheets could be strained 11 %, having a stress at break of about 90 MPa, and consequently a remarkable tensile energy absorption at rupture of about 9 kJ/kg, i.e. 3-4 times higher than a strong conventional paper. Zero-span tensile measurements indicated that the treatment increased the ductility not only of sheets but also of individual fibres. This suggests that the amorphous and molecularly more mobile dialcohol cellulose is located as a shell surrounding the crystalline core of the cellulose fibrils, and that, at deformations beyond the yield point, this facilitates plastic deformation both within and between individual fibres.

  • 44.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Berglund, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Ductile cellulose nanocomposite films fabricated from nanofibrillated cellulose after partial conversion to dialcohol cellulose2013Konferansepaper (Fagfellevurdert)
    Abstract [en]

    Ductile nanofibrillar nanocomposite films with a strain at break of 18%, and a tensile strength of 185 MPa, have been fabricated from nanofibrillated bleached kraft fibres partially converted to dialcohol cellulose prior to homogenisation. The conversion to dialcohol cellulose was performed by oxidation with sodium periodate to a degree of oxidation of ca. 30%, followed by reduction with sodium borohydride, and the fabricated films consequentially had one stiff cellulose phase and one flexible dialcohol cellulose phase. The liberated nanofibrils were characterised by AFM, after adsorption onto a silica surface, and imaging in tapping mode showed a blend of elementary fibrils with a width of 5 nm and inter-entangled fibril aggregates with a width of 15-20 nm. Besides good mechanical properties, the films also provided good barrier properties; at 0% RH the oxygen permeability was 2 ml·µm/(m2·d·kPa).

  • 45.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Gimaker, Magnus
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    The influence of periodate oxidation on the moisture sorptivity and dimensional stability of paper2008Inngår i: Cellulose, ISSN 0969-0239, E-ISSN 1572-882X, Vol. 15, nr 6, s. 837-847Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The hygroexpansion of paper was significantly reduced, up to 28% lower amplitude of change when the paper was subjected to a change in relative humidity from 20 to 85% RH, by oxidation of the fibre wall. Never-dried bleached kraft fibres were oxidised with sodium periodate, which specifically oxidises the C2-C3 bond of 1,4-glucans so that the cellulose is partly converted into dialdehyde cellulose. Since both the dry and wet strength of laboratory sheets were significantly improved, the dry tensile strength increased from 24 kNm/kg up to 66 kNm/kg and the relative wet tensile strength increased from 1.5% up to 40%, it is suggested that the aldehydes form hemiacetal linkages within the fibre wall during the consolidation and drying of the sheets. The mechanical, hygroexpansive and moisture sorptive properties of the sheets made from the oxidised fibres were studied. The results showed that the main reason for the reduced hygroexpansion was a decrease in moisture sorptivity, i.e. when the sheets made of fibres with different degrees of cross-linking were subjected to the same change in relative humidity, the more cross-linked fibres showed a smaller change in moisture content. It was also shown that the hygroexpansion coefficient, i.e. the moisture-normalised dimensional change, was not significantly changed by the periodate oxidation, i.e. indicating that there are no improvement in dimensional stability if the paper is subjected to a specific amount of water.

  • 46.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Hoc, Miroslav
    Innventia AB, Stockholm.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    A novel approach to study the hydroexpansion mechanisms of paper using spray technique2009Inngår i: Nordic Pulp & Paper Research Journal, ISSN 0283-2631, E-ISSN 2000-0669, Vol. 24, nr 4, s. 371-380Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A new method has been developed to measure the dimensional stability of printing paper by measuring the impact of liquid water on the in-plane dimensional change, i.e. the hydroexpansion, without any simultaneous mechanical interference that can occur when water is pressed into the sheet. This was achieved by using a specially developed spray technique and using electronic speckle photography to continuously measure the dimensional change as water is applied.

    The in-plane expansion for a given change in moisture content was found to be lower in the case of hydroexpansion than for earlier reported hygroexpansion. After the initial expansion following the water application, it was found that sheets rapidly start to contract again already 10-20 seconds after being wetted, i.e. despite still having a fairly constant and significantly higher moisture content than the initial moisture content before water application. These effects suggest that there are different mechanisms behind hydroexpansion than hygroexpansion of paper, and that hygroexpansion measurements should be extrapolated with caution when evaluating papers with respect to printability.

  • 47.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    Hoc, Miroslav
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi.
    The Influence Of Grammage, Moisture Content, Fibre Furnish And Chemical Modifications On The Hygro- And Hydro-Expansion Of Paper2009Inngår i: ADVANCES IN PULP AND PAPER RESEARCH, OXFORD 2009, VOLS 1-3 / [ed] IAnson, SJ, 2009, s. 355-388Konferansepaper (Fagfellevurdert)
    Abstract [en]

    The conventional way to evaluate dimensional stability, regardless of end-use purpose, is to measure the change in dimensions when the moisture content is changed by changing the relative humidity. Sorption of moisture from moist air is a relatively slow process and for the evaluation of printing papers this may not be the most appropriate method. In the present work, data from conventional hygroexpansion measurements has been compared with data from hydroexpansion measurements, i.e. expansions caused by the sorption of liquid water, sprayed onto papers printed with a random speckle pattern, the expansion being monitored by electronic speckle photography. Sheets made from different pulps, with different fines contents and different modifications were studied at different grammages and water-transfer levels. The effect of drying-mode, i.e. restrained drying or free drying, was also studied. It was concluded that sheets expand less with a given amount of adsorbed water when it is sorbed in liquid form rather than from moist air. Chemical treatments known to increase both the dry and the wet strength, e.g. polyelectrolyte multilayers and cross-linking through periodate oxidation, did not significantly improve the dimensional stability when the papers were exposed to liquid water.

  • 48.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Kochumalayil, Joby J.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Biokompositer. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Fiberteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemivetenskap (CHE), Centra, Wallenberg Wood Science Center.
    Oxygen and water vapour barrier films with low moisture sensitivity fabricated from self-crosslinking fibrillated cellulose2013Inngår i: Advances in pulp and paper research, Cambridge 2013: transactions of the 15th Fundamental Research Symposium held in Cambridge: September 2013, Lancashire, UK: Bury, Lancashire : The Pulp Fundamental Research Society , 2013, , s. 16s. 851-866Konferansepaper (Fagfellevurdert)
    Abstract [en]

    To replace petroleum-based barriers used in, for example, packaging applications with a bio-based alternative, the sensitivity to moisture must be lowered. The present work describes the fabrication and characterisation of cellulose-based films with remarkably improved oxygen and water-vapour-barrier properties at 80% relative humidity. This was achieved by fabricating films of self-cross-linking fibrillated cellulose after partial periodate oxidation to dialdehyde cellulose. At a relative humidity of 80%, films made of 27% and 44% oxidised cellulose, respectively, showed less than half the permeability of the untreated reference; 3.8 g·mm/(m2·24 h·kPa) and 3.7 g·mm/(m2·24 h·kPa) compared to 8.0 g·mm/(m2·24 h·kPa). This was presumably due to a lower moisture uptake in the films, and consequently less swelling. In the absence of moisture, films from both unmodified and modified fibrillated cellulose were ideal oxygen barriers, but at a relative humidity of 80%, films based on 27% and 44% converted cellulose had an oxygen permeability of 2.2 ml·µm/(m2·24 h·kPa) and 1.8 ml·µm/(m2·24 h·kPa), respectively, compared to 9.2 ml·µm/(m2·24 h·kPa) for the non-oxidised material.

    The cross-linking resulted in an embrittlement of the films, but the 27% oxidised material still had a tensile strength of 148 MPa and a tensile strain at break of 2.0%, which is sufficient in, for example, many packaging applications.

  • 49.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Linvill, Eric
    KTH, Skolan för teknikvetenskap (SCI), Hållfasthetslära (Inst.). KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Lo Re, Giada
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Östlund, Sören
    KTH, Skolan för teknikvetenskap (SCI), Hållfasthetslära (Inst.). KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation. KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Ductile and thermoplastic cellulose with novel application and design opportunities2018Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 255Artikkel i tidsskrift (Annet vitenskapelig)
  • 50.
    Larsson, Per A.
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Pettersson, Torbjörn
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Wågberg, Lars
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi. KTH, Skolan för teknikvetenskap (SCI), Centra, VinnExcellens Centrum BiMaC Innovation.
    Cross-linked barrier films with low sensitivity to relative humidity fabricated from nanofibrillated cellulose2014Inngår i: Abstracts of Papers of the American Chemical Society, ISSN 0065-7727, Vol. 247, s. 256-CELL-Artikkel i tidsskrift (Annet vitenskapelig)
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