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Sökning: WFRF:(Larsson Lars) > Wågberg Lars

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41.
  • Francon, Hugo, et al. (författare)
  • Ambient-Dried, 3D-Printable and Electrically Conducting Cellulose Nanofiber Aerogels by Inclusion of Functional Polymers
  • 2020
  • Ingår i: Advanced Functional Materials. - : Wiley-VCH Verlag. - 1616-301X .- 1616-3028.
  • Tidskriftsartikel (refereegranskat)abstract
    • 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. © 2020 The Authors. 
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42.
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43.
  • Francon, Hugo, et al. (författare)
  • Toward Li-ion Graphite Anodes with Enhanced Mechanical and Electrochemical Properties Using Binders from Chemically Modified Cellulose Fibers
  • 2022
  • Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 5:8, s. 9333-9342
  • Tidskriftsartikel (refereegranskat)abstract
    • 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. 
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44.
  • Fält, Susanna, et al. (författare)
  • Model films of cellulose II - improved preparation method and characterization of the cellulose film
  • 2004
  • Ingår i: Cellulose. - 0969-0239 .- 1572-882X. ; 11:2, s. 151-162
  • Tidskriftsartikel (refereegranskat)abstract
    • An optimization study of the preparation of spin-coated cellulose model films from the NMMO/DMSO system on silicon wafers has been made. The study shows that the cellulose concentration in the solution determines the cellulose film thickness and that the temperature of the solution affects the surface roughness. A lower solution temperature results in a lower surface roughness at cellulose concentrations below 0.8%. Using the described method, it is possible to prepare films with thicknesses of 30-90 nm with a constant surface roughness by changing the cellulose concentration, i.e. by dilution with DMSO. On these films, water has a contact angle less than 20degrees and about 50% of the material can, according to CP/MAS C-13-NMR spectroscopy on corresponding fibrous material, be considered to consist of crystalline cellulose II type material. It has further been shown that AFM can be used to determine the thickness of cellulose films, in both dry and wet states. In this method, the difference in height between the top surface and the underlying wafer has been measured at an incision made into the cellulose film. The cellulose films have also been spin-coated with the same technique as on the silicon oxide wafer onto the crystal in a quartz crystal microbalance (QCM). These model films were found to be suitable for swelling measurements with the QCM. The films were very stable during this type of measurement and films with different amounts of charges gave different swelling responses depending on their charges. As expected, films with a higher charge showed a higher swelling.
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45.
  • Ghanadpour, Maryam, 1984-, et al. (författare)
  • Phosphorylated Cellulose Nanofibrils : A Renewable Nanomaterial for the Preparation of Intrinsically Flame-Retardant Materials
  • 2015
  • Ingår i: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 16:10, s. 3399-3410
  • Tidskriftsartikel (refereegranskat)abstract
    • Cellulose from wood fibers can be modified for use in flame-retardant composites as an alternative to halogen-based compounds. For this purpose, sulfite dissolving pulp fibers have been chemically modified by phosphorylation, and the resulting material has been used to prepare cellulose nanofibrils (CNF) that have a width of approximately 3 nm. The phosphorylation was achieved using (NH4)(2)HPO4 in the presence of urea, and the degree of substitution by phosphorus was determined by X-ray photoelectron spectroscopy, conductometric titration, and nuclear magnetic resonance spectroscopy. The presence of phosphate groups in the structure of CNF has been found to noticeably improve the flame retardancy of this material. The nanopaper sheets prepared from phosphorylated CNF showed self-extinguishing properties after consecutive applications of a methane flame for 3 s and did not ignite under a heat flux of 35 kW/m(2), as shown by flammability and cone calorimetry measurements, respectively.
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46.
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47.
  • Gustafsson, Emil, et al. (författare)
  • Treatment of cellulose fibres with polyelectrolytes and wax colloids to create tailored highly hydrophobic fibrous networks
  • 2012
  • Ingår i: Colloids and Surfaces A. - : Elsevier BV. - 0927-7757 .- 1873-4359. ; 414, s. 415-421
  • Tidskriftsartikel (refereegranskat)abstract
    • 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).
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48.
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49.
  • Gustafsson, Emil, et al. (författare)
  • Vibrational sum frequency spectroscopy on polyelectrolyte multilayers : Effect of molecular surface structure on macroscopic wetting properties
  • 2015
  • Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 31:15, s. 4435-4442
  • Tidskriftsartikel (refereegranskat)abstract
    • 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.
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