Modifying the flocculation of microfibrillated cellulose suspensions by soluble polysaccharides under conditions unfavorable to adsorption.

Carboxymethylcellulose (CMC) and xanthan gum were studied as dispersants for microfibrillated cellulose (MFC) suspension using a rotational rheometer and imaging methods. The imaging was a combination of photography and optical coherence tomography (OCT). Both polymers dispersed MFC fibers, although CMC was more effective than xanthan gum. The negatively charged polymer chains increased the viscosity of the suspending medium and acted as buffers in between the negatively charged fibers. This behavior decreased the number and strength of contacts between the fibers and subsequently dispersed the flocs. The stronger separation of the fibers was reflected in the frequency sweep where the MFC/polymer suspensions had lower gel strength than pure MFC suspension. Dispersing effect was also observed in the flow measurements, where the floc size was more uniform with polymers in the decelerating flow and after long, slow constant shear, which normally induces a heterogeneous structure with large flocs into the MFC suspension.

Thermoresponsive xylan hydrogels via copper-catalyzed azide-alkyne cycloaddition.

In the present work, hydrogels of birch wood xylan and thermoresponsive poly(ethylene glycol)-b-poly(propylene glycol)-b-poly(ethylene glycol) (PEG-PPG-PEG) were prepared using copper catalyzed alkyne-azide cycloaddition (CuAAC) in aqueous reaction conditions. First, reactive azide groups were introduced on the backbone of xylan by etherification of 1-azido-2,3-epoxypropane in alkaline water/isopropanol-mixture at ambient temperature, providing degree of substitution (DS) values up to 0.28. On the second step, the azide groups were reacted with propargyl bifunctional PEG-PPG-PEG utilizing CuAAC, leading to formation of crosslinked hydrogels. The novel xylan derivatives were characterized with liquid and solid state nuclear magnetic resonance spectroscopy (NMR), Fourier transform infrared spectroscopy (FT-IR) and elemental analysis (EA). The temperature controlled swelling behavior of the developed hydrogels was evaluated in the range of 7-70 °C by water absorption and compressive stress-strain measurements, which showed a reduction in water content and change in stiffness with increasing temperature. The morphology of the hydrogels at different temperatures was studied by scanning electron microscopy (SEM), which showed a reduction in pore size with increasing temperature.