Critical concentrations of α-(1→3)-D-glucan L-FV-Ⅱ from Lentinus edodes were studied by viscometry andfluorescence probe techniques. The dependence of the reduced viscosity on concentration of the glucan in 0.5 mol/L NaOHaqueous solutions with or without urea showed two turning points corresponding to the dynamic contact concentration cs andthe overlap concentration c* of the polymer. The values of cs and c* were found to be 1×10-3 g cm-3 and 1.1×10-2 g cm-3
respectively
for L-FV-II in 0.5 mol/L NaOH aqueous solutions.The two critical concentrations of L-FV-II in 0.5 mol/L NaOH aqueous solutions were also found to be 1.2×10-3g cm-3 for cs and 9.2×10-3g cm-3 for c8 from the concentration dependence of phenanthrene fluorescence intensities.The overlap concentration c* of L-FV-II in 0.5 mol/L NaOH aqueous solutions was lower than that of polystyrene with same molecular weight in benzene
owing to the fact that polysaccharide rends to undergo aggregation caused by intermolecular hydrogen bonding.A normal viscosity behavior of L-FV-II in 0.5mol/L urea/0.5 mol/L NaOH aqueous solutions can still be observed in an extremelt low concentration range at 25℃.
Abstract
Critical concentrations of α-(1→3)-D-glucan L-FV-Ⅱ from Lentinus edodes were studied by viscometry andfluorescence probe techniques. The dependence of the reduced viscosity on concentration of the glucan in 0.5 mol/L NaOHaqueous solutions with or without urea showed two turning points corresponding to the dynamic contact concentration cs andthe overlap concentration c* of the polymer. The values of cs and c* were found to be 1×10-3 g cm-3 and 1.1×10-2 g cm-3
respectively
for L-FV-II in 0.5 mol/L NaOH aqueous solutions.The two critical concentrations of L-FV-II in 0.5 mol/L NaOH aqueous solutions were also found to be 1.2×10-3g cm-3 for cs and 9.2×10-3g cm-3 for c8 from the concentration dependence of phenanthrene fluorescence intensities.The overlap concentration c* of L-FV-II in 0.5 mol/L NaOH aqueous solutions was lower than that of polystyrene with same molecular weight in benzene
owing to the fact that polysaccharide rends to undergo aggregation caused by intermolecular hydrogen bonding.A normal viscosity behavior of L-FV-II in 0.5mol/L urea/0.5 mol/L NaOH aqueous solutions can still be observed in an extremelt low concentration range at 25℃.
关键词
Keywords
references
The trial reading is over, you can activate your VIP account to continue reading.
Sliding Dynamics of Ring Chain on a Rod-Coil Block Copolymer in Rotaxane
Upgrading Commercially Available Polyethylene to High-value Materials with Strong Mechanical Performance and Hydrophilicity by Blending with Ethylene/meta-Methoxystyrene Copolymers
Silk Sericin-inspired Poly-β-homoserine for Protein Protection
Highly Regio- and trans-Selective Ring-opening Metathesis Polymerization of Chiral Aza-norbornene with a Simple Phenylimido-Tungsten Catalyst
Two-way Shape Memory Effect of Polycaprolactone-based Polyurethane via Synergistic Role of Hydrogen Bonding and Crystallization Tuned by Malic Acid