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1.
  • Jansson, Mikael, et al. (författare)
  • Upgrading of wood pre-hydrolysis liquor for renewable barrier design : a techno-economic consideration
  • 2014
  • Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 21:3, s. 2045-2062
  • Tidskriftsartikel (refereegranskat)abstract
    • A techno-economic assessment of an upgrading procedure and outtake of a pre-hydrolysate in a presumed dissolving pulp mill was performed. Pre-hydrolysis of spruce wood chips in pilot scale produced input data for energy and mass balances and was performed with and without subsequent membrane filtration to produce hydrolysate fractions rich in galactoglucomannan and with some lignin. The hydrolysate is a viable raw material for the production of renewable thin oxygen barrier films as demonstrated herein in the formulation of free standing films with very low oxygen permeability at both moderate and high relative humidities. Approximately 50,000 ton dry solid upgraded pre-hydrolysate suitable for production of oxygen barriers could be produced according to the presumed dissolving pulp mill producing about 500,000 air dry ton dissolving pulp per year and applying a liquor to wood ratio of 4:1. Utilization of the pre-hydrolysis liquor hence adds value to and realizes the dissolving plant as a biorefinery. A sensitivity analysis indicates that the market price of the upgraded pre-hydrolysate has the largest positive effect on the return on investment for separation and upgrading of a pre-hydrolysate. Increased investment cost and increased annuity factor show negative effects.
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2.
  • Aaen, Ragnhild, et al. (författare)
  • Combining cellulose nanofibrils and galactoglucomannans for enhanced stabilization of future food emulsions
  • 2021
  • Ingår i: Cellulose. - : Springer Science and Business Media B.V.. - 0969-0239 .- 1572-882X. ; 28:16, s. 10485-10500
  • Tidskriftsartikel (refereegranskat)abstract
    • The use of wood-derived cellulose nanofibrils (CNFs) or galactoglucomannans (GGM) for emulsion stabilization may be a way to obtain new environmentally friendly emulsifiers. Both have previously been shown to act as emulsifiers, offering physical, and in the case of GGM, oxidative stability to the emulsions. Oil-in-water emulsions were prepared using highly charged (1352 ± 5 µmol/g) CNFs prepared by TEMPO-mediated oxidation, or a coarser commercial CNF, less charged (≈ 70 µmol/g) quality (Exilva forte), and the physical emulsion stability was evaluated by use of droplet size distributions, micrographs and visual appearance. The highly charged, finely fibrillated CNFs stabilized the emulsions more effectively than the coarser, lower charged CNFs, probably due to higher electrostatic repulsions between the fibrils, and a higher surface coverage of the oil droplets due to thinner fibrils. At a constant CNF/oil ratio, the lowest CNF and oil concentration of 0.01 wt % CNFs and 5 wt % oil gave the most stable emulsion, with good stability toward coalescence, but not towards creaming. GGM (0.5 or 1.0 wt %) stabilized emulsions (5 wt % oil) showed no creaming behavior, but a clear bimodal distribution with some destabilization over the storage time of 1 month. Combinations of CNFs and GGM for stabilization of emulsions with 5 wt % oil, provided good stability towards creaming and a slower emulsion destabilization than for GGM alone. GGM could also improve the stability towards oxidation by delaying the initiation of lipid oxidation. Use of CNFs and combinations of GGM and CNFs can thus be away to obtain stable emulsions, such as mayonnaise and beverage emulsions. © 2021, The Author(s).
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3.
  • Aaen, Ragnhild, et al. (författare)
  • The potential of TEMPO-oxidized cellulose nanofibrils as rheology modifiers in food systems
  • 2019
  • Ingår i: Cellulose. - : Springer Netherlands. - 0969-0239 .- 1572-882X. ; 26:9, s. 5483-5496
  • Tidskriftsartikel (refereegranskat)abstract
    • Abstract: Cellulose nanofibrils (CNFs) have been proposed for use in low-fat food products due to their availability and excellent viscosifying and gel forming abilities. As the CNFs are negatively charged, the presence of other components in foods, such as electrolytes and food additives such as xanthan gum is likely to affect their rheological properties. Hence, the study of these interactions can contribute valuable information of the suitability of CNFs as rheology modifiers and fat replacers. Rheological measurements on aqueous dispersions of TEMPO-oxidized CNFs were performed with variations in concentration of CNFs, concentration of electrolytes and with varying CNF/xanthan ratios. UV–Vis Spectroscopy was used to evaluate the onset of CNF flocculation/aggregation in the presence of electrolytes. The CNF dispersions followed a power-law dependency for viscosity and moduli on CNF concentration. Low electrolyte additions strengthened the CNF network by allowing for stronger interactions, while higher additions led to fibril aggregation, and loss of viscosity, especially under shear. The CNF/xanthan ratio, as well as the presence of electrolytes were shown to be key factors in determining whether the viscosity and storage modulus of CNF dispersions increased or decreased when xanthan was added. Graphical abstract: [Figure not available: see fulltext.].
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4.
  • Agustin, Melissa B., et al. (författare)
  • Lignin nanoparticles as co-stabilizers and modifiers of nanocellulose-based Pickering emulsions and foams
  • 2023
  • Ingår i: Cellulose. - : Springer Nature. - 0969-0239 .- 1572-882X. ; 30:14, s. 8955-8971
  • Tidskriftsartikel (refereegranskat)abstract
    • Nanocellulose is very hydrophilic, preventing interactions with the oil phase in Pickering emulsions. This limitation is herein addressed by incorporating lignin nanoparticles (LNPs) as co-stabilizers of nanocellulose-based Pickering emulsions. LNP addition decreases the oil droplet size and slows creaming at pH 5 and 8 and with increasing LNP content. Emulsification at pH 3 and LNP cationization lead to droplet flocculation and rapid creaming. LNP application for emulsification, prior or simultaneously with nanocellulose, favors stability given the improved interactions with the oil phase. The Pickering emulsions can be freeze–dried, enabling the recovery of a solid macroporous foam that can act as adsorbent for pharmaceutical pollutants. Overall, the properties of nanocellulose-based Pickering emulsions and foams can be tailored by LNP addition. This strategy offers a unique, green approach to stabilize biphasic systems using bio-based nanomaterials without tedious and costly modification procedures.
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5.
  • Alakalhunmaa, Suvi, et al. (författare)
  • Softwood-based sponge gels
  • 2016
  • Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 23:5, s. 3221-3238
  • Tidskriftsartikel (refereegranskat)abstract
    • Crosslinking-aided gelation was utilized to prepare hydrogels from softwood polysaccharides, with spruce galactoglucomannans (GGM)—a group of largely unexploited hemicelluloses—as the main component, aiming at conversion into sponge-like aerogels. Cellulose nanofibrils were used for the formation of a reinforcing network, which was further crosslinked together with a GGM matrix by ammonium zirconium carbonate, an inorganic salt that is regarded as safe for use in food packaging. The hydrogels were freeze-dried into stiff, low-density aerogels with 98 % of their volume composed of air-filled pores. When immersed in water, the aerogels absorbed water up to 37 times their initial weight, demonstrating elasticity and repeatable and reversible sponge capacity. The developed concept reassembles the wood polysaccharides in a new way, creating interesting possibilities for utilizing the abundant “green gold,” GGM. The obtained biobased materials could find application potential, for example, in the field of food packaging and could contribute in the reduction of the usage of petroleum-based plastics in the future.
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6.
  • Albán Reyes, Diana Carolina, et al. (författare)
  • Is there a diffusion of alkali in the activation of dissolving cellulose pulp at low NAOH stoichiometric excess?
  • 2019
  • Ingår i: Cellulose. - : Springer. - 0969-0239 .- 1572-882X. ; 26:2, s. 1297-1308
  • Tidskriftsartikel (refereegranskat)abstract
    • We conducted a quantitative study, following the degree of activation (i.e. the transformation to alkali cellulose, denoted as DoA) over time for dissolving cellulose pulp treated with different [NaOH] at low NaOH/anhydroglucose unit stoichiometric ratio (denoted as (r) ≤ 2.6). Our quantitative approach was based on Raman spectroscopy data, evaluated by partial least squares regression modelling. The results show strong influence of the (r) on DoA (increasing from DoA= 45% at (r) = 0.8, to DoA = 85% at (r) = 2.6), and its complex dependence on [NaOH]. At (r) = 0.8 the highest DoA (DoA ≳ 60%) was found at 30% [NaOH], while at (r) =1.3 it was found at 20% [NaOH] (DoA ≳ 80%). Although activation of cellulose happens in minutes at the studied temperature (30 °C), it was found that the reaction may be slow when a low (r) is used. A gradual increase of the DoA from ≈ 30% to ≈ 70% in time was seen when samples were activated with 30% [NaOH] at (r) = 0.8. At the same (r), a similar increase of DoA from ≈ 30 % to ≈ 60 % was also observed when 40% [NaOH] was used. Slow diffusion of NaOH through poorly swollen cellulose fibres is proposed as an explanation for this phenomenon. Lastly, solid-state CP/MAS NMR measurements suggest that at a fixed temperature, the Na-Cell allomorph mostly depends on [NaOH]. However, in the transition area between Na-Cell I and Na-Cell II, its influence might be affected by (r). 
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7.
  • Albán Reyes, Diana Carolina, et al. (författare)
  • The influence of different parameters on the mercerisation of cellulose for viscose production
  • 2016
  • Ingår i: Cellulose. - : Springer Netherlands. - 0969-0239 .- 1572-882X. ; 23:2, s. 1061-1072
  • Tidskriftsartikel (refereegranskat)abstract
    • A quantitative analysis of degree of transformation from a softwood sulphite dissolving pulp to alkalised material and the yield of this transformation as a function of the simultaneous variation of the NaOH concentration, denoted [NaOH], reaction time and temperature was performed. Samples were analysed with Raman spectroscopy in combination with multivariate data analysis and these results were confirmed by X-ray diffraction. Gravimetry was used to measure the yield. The resulting data were related to the processing conditions in a Partial Least Square regression model, which made it possible to explore the relevance of the three studied variables on the responses. The detailed predictions for the interactive effects of the measured parameters made it possible to determine optimal conditions for both yield and degree of transformation in viscose manufacturing. The yield was positively correlated to the temperature from room temperature up to 45 A degrees C, after which the relation was negative. Temperature was found to be important for the degree of transformation and yield. The time to reach a certain degree of transformation (i.e. mercerisation) depended on both temperature and [NaOH]. At low temperatures and high [NaOH], mercerisation was instantaneous. It was concluded that the size of fibre particles (mesh range 0.25-1 mm) had no influence on degree of transformation in viscose processing conditions, apparently due to the quick reaction with the excess of NaOH.
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8.
  • Aldaeus, Fredrik, et al. (författare)
  • The supramolecular structure of cellulose-rich wood pulps can be a determinative factor for enzymatic hydrolysability
  • 2015
  • Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 22:6, s. 3991-4002
  • Tidskriftsartikel (refereegranskat)abstract
    • The enzymatic hydrolysability of three industrial pulps, five lab made pulps, and one microcrystalline cellulose powder was assessed using commercial cellulolytic enzymes. To gain insight into the factors that influence the hydrolysability, a thorough characterization of the samples was done, including their chemical properties (cellulose content, hemicellulose content, lignin content, and kappa number), their macromolecular properties (peak molar mass, number-average molar mass, weight-average molar mass, polydispersity, and limiting viscosity) and their supramolecular properties (fibre saturation point, specific surface area, average pore size, and crystallinity). The hydrolysability was assessed by determination of initial conversion rate and final conversion yield, with conversion yield defined as the amount of glucose in solution per unit of glucose in the substrate. Multivariate data analysis revealed that for the investigated samples the conversion of cellulose to glucose was mainly dependent on the supramolecular properties, such as specific surface area and average pore size. The molar mass distribution, the crystallinity, and the lignin content of the pulps had no significant effect on the hydrolysability of the investigated samples.
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9.
  • Alexandrescu, Laura C., et al. (författare)
  • Cytotoxicity tests of cellulose nanofibril-based structures
  • 2013
  • Ingår i: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 20:4, s. 1765-1775
  • Tidskriftsartikel (refereegranskat)abstract
    • Cellulose nanofibrils based on wood pulp fibres are most promising for biomedical applications. Bacterial cellulose has been suggested for some medical applications and is presently used as wound dressing. However, cost-efficient processes for mass production of bacterial cellulose are lacking. Hence, fibrillation of cellulose wood fibres is most interesting, as the cellulose nanofibrils can efficiently be produced in large quantities. However, the utilization of cellulose nanofibrils from wood requires a thorough verification of its biocompatibility, especially with fibroblast cells which are important in regenerative tissue and particularly in wound healing. The cellulose nanofibril structures used in this study were based on Eucalyptus and Pinus radiata pulp fibres. The nanofibrillated materials were manufactured using a homogenizer without pre-treatment and with 2,2,6,6-tetramethylpiperidine-1-oxy radical as pre-treatment, thus yielding nanofibrils low and high level of anionic charge, respectively. From these materials, two types of nanofibril-based structures were formed; (1) thin and dense structures and (2) open and porous structures. Cytotoxicity tests were applied on the samples, which demonstrated that the nanofibrils do not exert acute toxic phenomena on the tested fibroblast cells (3T3 cells). The cell membrane, cell mitochondrial activity and the DNA proliferation remained unchanged during the tests, which involved direct and indirect contact between the nano-structured materials and the 3T3 cells. Some samples were modified using the crosslinking agent polyethyleneimine (PEI) or the surfactant cetyl trimethylammonium bromide (CTAB). The sample modified with CTAB showed a clear toxic behaviour, having negative effects on cell survival, viability and proliferation. CTAB is an antimicrobial component, and thus this result was as expected. The sample crosslinked with PEI also had a significant reduction in cell viability indicating a reduction in DNA proliferation. We conclude that the neat cellulose nanostructured materials tested in this study are not toxic against fibroblasts cells. This is most important as nano-structured materials based on nanofibrils from wood pulp fibres are promising as substrate for regenerative medicine and wound healing.
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10.
  • Alimadadi, Majid, et al. (författare)
  • 3D-oriented fiber networks made by foam forming
  • 2016
  • Ingår i: Cellulose. - : Springer Netherlands. - 0969-0239 .- 1572-882X. ; 23:1, s. 661-671
  • Tidskriftsartikel (refereegranskat)abstract
    • In industrial applications, such as paper and nonwovens, cellulose fibers are used in the form of a network where the fibers are oriented more or less in the sheet-plane direction. However, in many biological systems, fibers are instead oriented in a three-dimensional (3D) space, creating a wide variety of functionalities. In this study we created a 3D-oriented fiber network on the laboratory scale and have identified some unique features of its structure and mechanical properties. The 3D fiber network sheets were prepared by using foam-forming as well as modifying consolidation and drying procedures. The fiber orientation and tensile/compression behavior were determined. The resulting sheets were extremely bulky (above 190 cm3/g) and had extremely low stiffness (or high softness) compared to the reference handsheets. Despite this high bulk, the sheets retained good structural integrity. We found that a 3D-oriented fiber network requires much less fiber-fiber contact to create a connected (“percolated”) network than a two-dimensionally oriented network. The compression behavior in the thickness direction was also unique, characterized by extreme compressibility because of its extreme bulk and a long initial increase in the compression load as well as high strain recovery after compression because of its fiber reorientation during compression.
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