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  • Result 1-9 of 9
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1.
  • Doliška, A., et al. (author)
  • Antithrombotic properties of sulfated wood-derived galactoglucomannans
  • 2012
  • In: Holzforschung. - 0018-3830 .- 1437-434X. ; 66:2, s. 149-154
  • Journal article (peer-reviewed)abstract
    • Galactoglucomannans (GGMs) are water-soluble polysaccharides released and accumulated in process waters in the production of thermomechanical pulp. The general trend in the forestry industry is moving towards bio-refineries, for example utilizing these hemicelluloses as bioactive substances. At present, there is no industrial use of wood-derived mannans. In this study, GGMs extracted from thermomechanical pulp, as well as further carboxymethyl-ated galactoglucomannans (CM-GGMs), were sulfated to increase their antithrombotic properties. The products were characterized with Fourier transform infrared spectroscopy, nuclear magnetic resonance and capillary electrophoresis. The carbohydrate composition and sulfur amounts were determined. The products' total charges were determined by polyelectrolyte titrations and their antithrombotic effect was measured based on the activated partial thromboplastin time. The results showed a significant increase in the antithrombotic effect of the sulfated galactoglucomannans from spruce wood and thus a potential new use for wood-derived mannans.
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3.
  • Mikkonen, K. S., et al. (author)
  • Glucomannan composite films with cellulose nanowhiskers
  • 2010
  • In: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 17:1, s. 69-81
  • Journal article (peer-reviewed)abstract
    • Spruce galactoglucomannans (GGM) and konjac glucomannan (KGM) were mixed with cellulose nanowhiskers (CNW) to form composite films. Remarkable effects of CNW on the appearance of the films were detected when viewed with regular and polarizing optical microscopes and with a scanning electron microscope. Addition of CNW to KGM-based films induced the formation of fiberlike structures with lengths of several millimeters. In GGM-based films, rodlike structures with lengths of several tens of micrometers were formed. The degree of crystallinity of mannan in the plasticized KGM-based films increased slightly when CNW were added, from 25 to 30%. The tensile strength of the KGM-based films not containing glycerol increased with increasing CNW content from 57 to 74 MPa, but that of glycerol-plasticized KGM and GGM films was not affected. Interestingly, the notable differences in the film structure did not appear to be related to the thermal properties of the films.
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4.
  • Parikka, K., et al. (author)
  • Functional and anionic cellulose-interacting polymers by selective chemo-enzymatic carboxylation of galactose-containing polysaccharides
  • 2012
  • In: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 13:8, s. 2418-2428
  • Journal article (peer-reviewed)abstract
    • Carboxylated, anionic polysaccharides were selectively prepared using a combination of enzymatic and chemical reactions. The galactose-containing polysaccharides studied were spruce galactoglucomannan, guar galactomannan, and tamarind galactoxyloglucan. The galactosyl units of the polysaccharides were first oxidized with galactose oxidase (EC 1.1.3.9) and then selectively carboxylated, resulting in the galacturonic acid derivatives with good conversion and yield. The degrees of oxidation (DO) of the products were determined by gas chromatography-mass spectrometry (GC-MS). A novel feasible electrospray ionization-mass spectrometry (ESI-MS) method was also developed for the determination of DO. The solution properties and charge densities of the products were investigated. The interaction of the products with cellulose was studied by two methods, bulk sorption onto bleached birch kraft pulp and adsorption onto nanocellulose ultrathin films by quartz crystal microbalance with dissipation (QCM-D). To study the effect of the location of the carboxylic acid groups on the physicochemical properties, polysaccharides were also oxidized by 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated reaction producing polyuronic acids. The chemo-enzymatically oxidized galacturonic polysaccharides with an unmodified backbone had a better ability to interact with cellulose than the TEMPO-oxidized products. The selectively carboxylated polysaccharides can be further exploited, as such, or in the targeted functionalization of cellulose surfaces.
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5.
  • Pezoa-Conte, R., et al. (author)
  • Deconstruction of the green alga Ulva rigida in ionic liquids : closing the mass balance
  • 2015
  • In: Algal Research. - : Elsevier. - 2211-9264. ; 12, s. 262-273
  • Journal article (peer-reviewed)abstract
    • Algae are known to grow at high rates compared to terrestrial plants that contain comparable amounts of carbohydrates by weight. Therefore, this renders them attractive in terms of any biorefinery concept. In this work the green alga Ulva rigida, containing 40 wt.% of carbohydrates was pretreated with a switchable ionic liquid (SIL), distillable ionic liquid (DIL) and low-viscosity ionic liquid (LVIL). The SIL DBU–MEA–SO2 was prepared from a mixture of mono-ethanolamine (MEA) and 1,8-diazabicyclo-[5,4,0]-undec-7-ene (DBU) that was coupled with sulfur dioxide (SO2), whereas the DIL [TMGH+][EtCO2−] (1,1,3,3-tetramethylguanidine propionate) was synthesized by a simple acid–base neutralization reaction. Consequently, the LVIL [HDBU+][5OF−] protonated 1,8-diazabicyclo-[5,4,0]-undec-7-ene- 2,2,3,3,4,4,5,5-octafluoro-1-pentoxide was used as received. The treatments were carried out in the temperature range of 100–160 °C for 6 h. The products obtained after the treatments were analyzed using different techniques like ICP, OES, SEM, TEM, TGA, FTIR and carbohydrate determination by GC. Upon treatment with DIL up to 67 wt.% of carbohydrates could be dissolved. For the first time, processing of U. rigida was carried out in ionic liquids so that the mass balance of the process was obtained. It can be concluded that 1,1,3,3-tetramethylguanidine propionate shows significant potential when aiming at releasing carbohydrates from algal biomass that, consequently, can be applied in the production of platform chemicals and/or biofuels such as bioethanol.
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6.
  • Alakalhunmaa, Suvi, et al. (author)
  • Softwood-based sponge gels
  • 2016
  • In: Cellulose. - : Springer Science and Business Media LLC. - 0969-0239 .- 1572-882X. ; 23:5, s. 3221-3238
  • Journal article (peer-reviewed)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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7.
  • Anugwom, I, et al. (author)
  • Selective Extraction of Hemicelluloses from Spruce using Switchable Ionic Liquids
  • 2012
  • In: Carbohydrate Polymers. - : Elsevier. - 0144-8617 .- 1879-1344. ; 87:3, s. 2005-2011
  • Journal article (peer-reviewed)abstract
    • Switchable Ionic Liquids (SILs) made from alcohols, either hexanol or butanol, and CO2 together with an amidine (1,8-diazabicyclo-[5.4.0]-undec-7-ene (DBU)) were investigated as dissolution/fractionation solvents for wood material. Both native spruce (Picea abies), and pre-extracted spruce were treated with either butanol SIL (SIL1) or hexanol SIL (SIL 2) for 5 days at 55 °C under normal pressure. The SILs were formed by bubbling CO2 through an equimolar mixture of either 1-hexanol or 1-butanol and DBU. The viscosity of the mixture increased from 7.1 mPas to 2980 mPas for SIL 2 and 5.1 to 1600 mPas for SIL 1. Melting points of the SILs 1 and 2 were at 8 and 14 °C, respectively. After the treatment time (5 days), the undissolved fraction contained 38 wt % less hemicelluloses compared to native spruce. There was an increase in the glucose content of the milled spruce treated with both SILs, since the milling step reduced the cellulose crystallinity of the wood and facilitated an easier SIL access into the wood. The solvents were very neutral in terms of lignin removal. Consequently, only about 2% of the lignin was removed from native wood. Moreover, a priori removal of the wood extractives did not influence the lignin removal. Highlights► Switchable Ionic Liquids made from, either hexanol or butanol, and CO2 together with an amidine (DBU) were studies as dissolution/fractionation solvents for spruce wood. ► After the treatment undissolved fraction contained 38 wt-% less hemicelluloses. ► We conclude that Switchable ionic liquids are effective solvent for fractionation of wood material, and they are easily recycled and can be reused.
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8.
  • Lozhechnikova, A., et al. (author)
  • Modification of nanofibrillated cellulose using amphiphilic block-structured galactoglucomannans
  • 2014
  • In: Carbohydrate Polymers. - : Elsevier BV. - 0144-8617 .- 1879-1344. ; 110, s. 163-172
  • Journal article (peer-reviewed)abstract
    • Nanofibrillated cellulose (NFC) and hemicelluloses have shown to be highly promising renewable components both as barrier materials and in novel biocomposites. However, the hydrophilic nature of these materials restricts their use in some applications. In this work, the usability of modified O-acetyl galactoglucomannan (GGM) for modification of NFC surface properties was studied. Four GGM-block-structured, amphiphilic derivatives were synthesized using either fatty acids or polydimethylsiloxane as hydrophobic tails. The adsorption of these GGM derivatives was consecutively examined in aqueous solution using a quartz crystal microbalance with dissipation monitoring (QCM-D). It was found that the hydrophobic tails did not hinder adsorption of the GGM derivatives to cellulose, which was concluded to be due to the presence of the native GGM-block with high affinity to cellulose. The layer properties of the adsorbed block-co-polymers were discussed and evaluated. Self-standing NFC films were further prepared and coated with the GGM derivatives and the effect of the surface modification on wetting properties and oxygen permeability (OP) of the modified films was assessed.
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  • Result 1-9 of 9

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