Journal: Carbohydrate Polymers

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Abbreviation

Carbohydr. Polym.

Publisher

Elsevier

Journal Volumes

ISSN

0144-8617
1879-1344

Description

Search Results

Publications1 - 10 of 39
  • Gulfi, M.; Ariggoni, Eva; Amado, Renato (2005)
    Carbohydrate Polymers
  • Faure, Audrey M.; Andersen, Mogens L.; Nyström, Laura (2012)
    Carbohydrate Polymers
  • Spies, Paul-Antoine; Keplinger, Tobias; Horbelt, Nils; et al. (2022)
    Carbohydrate Polymers
    Small specimens of spruce wood with different degrees of delignification were studied using in-situ tensile tests and simultaneous synchrotron X-ray diffraction to reveal the effect of delignification and densification on their tensile properties at relative humidities of 70–80 %. In addition to mechanical properties, these analyses yield the ratio of strains in the cellulose crystals and in the bulk, which reflects the stress-transfer to crystalline cellulose. While the specific modulus of elasticity slightly increases from native wood by partial or complete delignification, the lattice strain ratio does not show a significant change. This could indicate a compensatory effect from the decomposition of the amorphous matrix by delignification and from a tighter packing of cellulose crystals that would increase the stress transfer. The reduced strain to failure and maximum lattice strain of delignified specimens suggests that the removal of lignin affects the stress-strain behavior with fracture at lower strain levels.
  • Iron(II) binding by cereal beta-glucan
    Item type: Journal Article
    Faure, Audrey M.; Koppenol, Willem H.; Nyström, Laura (2015)
    Carbohydrate Polymers
  • Loebel, Claudia; D'Este, Matteo; Alini, Mauro; et al. (2015)
    Carbohydrate Polymers
  • Ahmadi Heidari, Nadia; Hamdami, Nasser; Siqueira, Gilberto; et al. (2025)
    Carbohydrate Polymers
    Global concerns about food and energy waste call for new sustainable solutions. Phase changing materials (PCM) are promising thermal storage and management materials which have potential to mitigate food waste, yet they often suffer from leakage and non-shape stability. Here, a green shape-stabilized polyethylene glycol 300 (PEG) nanocellulose-based composite was developed using readily available and cost-effective side streams from the brewery industry. Two different routes were examined for the incorporation of PEG into the cellulose nanofiber (CNF) cryogel including adding different dry mass ratios of PEG in the sol stage, with or without physical crosslinking, or adding the PEG after CNF gelation. FTIR and TGA analysis revealed the improved thermal stability of PEG after incorporation into the CNF cryogel. The PEG/CNF composite produced by adding PEG in the gel stage outperformed the other material formulations by demonstrating the highest enthalpy value (93.2 J/g) and the best mechanical properties (Young's modulus of 140 kPa). The package containing the PEG/CNF composite could maintain the meat temperature below 0 °C around 4 times longer than the control package when the cold system was interrupted. Furthermore, the PEG/CNF composite showed a positive effect on the color and drip loss values of frozen meat.
  • Pollard, Michael; Eder, Barbara; Fischer, Peter; et al. (2010)
    Carbohydrate Polymers
    Galactomannans isolated from legume seed endosperms, including those of commercial interest, have been characterized by multidetection aqueous SEC. Galactomannans derived from seeds of the Faboideae subfamily had substantially higher Mw than those from Caesalpinioideae seeds (Mw,Fab = 2.4–3.1 × 106 g/mol, Mw,Caes. = 0.86–2.1 × 106 g/mol) and within the latter botanical subfamily, an apparent correlation between Mw and the degree of galactose substitution DG was found. The molar mass distributions were unimodal and differed primarily by a scale factor, with distributional widths narrower than a true Flory ‘most-probable distribution’; good fits to Schulz–Zimm model were obtained. Across subfamilies no differences were found in the exponents of [η]–M and Rv–M relationships (0.61 ± 0.02, 0.54 ± 0.01, respectively), the Flory chain stiffness ratio (C∞ = 20 ± 1 (BSF analysis)), or the persistence length (Lp = 5.5 ± 0.2 nm) obtained from SEC fraction data. However, it was found that prefactors in the [η]–M and Rv–M relationships as well as the unperturbed parameter KΘ decrease in proportion to DG and therefore chain density. Generalized relationships incorporating galactose-dependent prefactors were therefore developed to model SEC fraction data of native galactomannans ([η]GM = (1800 ± 200) × Mo−1.61 × M0.61±0.02, Rv,GM = 0.63 ± 0.05 × Mo−0.54 × M0.54±0.01) as well as lower-M fractions obtained by ultrasonication ([η]GM = (730 ± 100) × Mo−1.71 × Mw0.71±0.02, Rv,GM = 0.49 ± 0.05 × Mo−0.57 × Mw0.57±0.01, M ≈ 1 × 105-native). As a consequence of this dependence and the observed patterns in molar mass variation, [η] varies within a narrow range for galactomannans as a whole despite substantial Mw differences.
  • Wu, Tingting; Kummer, Nico; De France, Kevin J.; et al. (2021)
    Carbohydrate Polymers
    Biohybrid colloids were fabricated based on electrostatic complexation between anionic TEMPO-oxidized cellulose nanofibrils (TO-CNF) and cationic hen egg white lysozyme (HEWL). By altering the loading of HEWL, physical colloidal complexes can be obtained at a relatively low concentration of TO-CNF (0.1 wt%). At neutral pH, increasing the HEWL loading induces an increase in charge screening, as probed by zeta-potential, resulting in enhanced TO-CNF aggregation and colloidal gel formation. Systematic rheological testing shows that mechanical reinforcement of the prepared biohybrid gels is easily achieved by increasing the loading of HEWL. However, due to the relatively weak nature of electrostatic complexation, the formed colloidal gels exhibit partial destruction when subjected to cyclic shear stresses. Still, they resist thermo-cycling up to 90 °C. Finally, the pH responsiveness of the colloidal complex gels was demonstrated by adjusting pH to above and below the isoelectric point of HEWL, representing a facile mechanism to tune the gelation of TO-CNF/HEWL complexes. This work highlights the potential of using electrostatic complexation between HEWL and TO-CNF to form hybrid colloids, and demonstrates the tunability of the colloidal morphology and rheology by adjusting the ratio between the two components and the pH.
  • Wu, Xiaowen; Boulos, Samy; Yulikov, Maxim; et al. (2022)
    Carbohydrate Polymers
    Use of spin labels to study structures of polymers has been widely spread in polymer science. However, for the studies of neutral water-soluble dietary fibers (DFs), labelling efficiencies in past studies have only been sufficient for application of continuous wave electron paramagnetic resonance spectroscopy (CW-EPR), but still insufficient for some advanced methods such as pulse EPR. Thus, in this paper, two spin labelling strategies, namely, site-selective mono-spin-labelling and stochastic multi-spin-labelling, were examined on linear cereal β-glucan, as well as linearly branched arabinoxylan and galactomannan. The effects of both methods in DF properties were evaluated. For the mono-labelling pathway, labelling efficiency could reach up to 46 %. In the stochastic labelling strategy, a degree of substitution (DS) up to 150 % could be reached, whereas optimized conditions for this strategy were achieved at DS = 3 % to obtain DFs whose bioactivity properties were still preserved while spin labelling efficiency was still sufficient for CW and pulse EPR experiments.
  • Bösiger, Peter; Richard, Isabelle M.T.; Le Gat, Luce; et al. (2018)
    Carbohydrate Polymers
Publications1 - 10 of 39