Novel nanobiocomposite hydrogels based on sage seed gum-Laponite: Physico-chemical and rheological characterization

In this study, the physico-chemical and rheo-mechanical properties of sage seed gum hydrogel, reinforced by various ratios (0-25 wt.%) of Laponite, were investigated. Particles size measurements indicated the formation of large SSG-Laponite microstructures upon nanoparticle adding, due to the interactions generated between the anionic SSG and the charged surfaces of clay platelets. Laponite affected the surface tension and density of the SSG-based systems significantly, but only influenced the-potential above 20 wt.%. The dynamic rheological behavior of SSG-based nanocomposites reflected the reinforcing effect of secondary structures and percolated three-dimensional network, suggested a structural modification of the hydrogels with the Laponite loading. An improvement in texture profile analysis parameters was observed in Laponite content 5 wt.%, whereas for nanoparticles > 5 wt.%, a significant decrease was obtained. In conclusion, Laponite improved the rheological and physico-chemical properties of SSG-based hydrogel and extended its potential as promising future bio-products for industrial applications.Peer reviewe

Determination of physical emulsion stabilization mechanisms of wood hemicelluloses via rheological and interfacial characterization

Materials manufacturing industries seek efficient, economic, and sustainable compounds for stabilizing dispersed systems such as emulsions. In this study, novel, abundant biobased hydrocolloids spruce galactoglucomannans (GGM) and birch glucuronoxylans (GX) were obtained from a forestry biorefining process and characterized as versatile stabilizers of rapeseed oil-in-water emulsions. For the first time, GGM and GX isolated by pressurized hot water extraction (PHWE) of spruce and birch saw meal, respectively, were studied in emulsions. The PHWE wood hemicelluloses—polysaccharides with relatively low molar mass—facilitated the formation of emulsions with small average droplet size and efficiently prevented droplet coalescence. GGM and GX lowered the surface tension of emulsions’ oil–water interface and increased the viscosity of the continuous phase. However, viscosity of the wood hemicellulose-based systems was low compared to that of commercial polymeric stabilizers. GGMstabilized emulsions with varying oil volume fractions were characterized in terms of their rheological properties, including large amplitude oscillation shear (LAOS) measurements, and compared to emulsions prepared with a classical small-molecular surfactant, Tween20. The physical emulsion stabilization mechanisms of GGM and GX are suggested as steric repulsion assisted by Pickering-type stabilization. Wood hemicelluloses have potential as highly promising future bioproducts for versatile industrial applications involving colloidal systems and soft materials.Peer reviewe

Long-term physical stability of plasticized hemicellulose films

Peer reviewe

Long-Term Physical Stability of Plasticized Hemicellulose Films

Oat spelt arabinoxylan (OsAX) and spruce galactoglucomannan (GGM) are hemicelluloses that can be extracted in large quantities from side-streams of the agriculture and forest industries. They both form self-standing films, making them potential future packaging materials. This systematic study focuses on the effect of long-term storage on the physical stability of hemicellulose-based films. OsAX and GGM films were plasticized with 40% (w/w of the polysaccharide) of glycerol, sorbitol, or their blends, and their stability was followed for four months. Ageing especially affected the glycerol-containing films, in which the tensile strength and Young’s modulus increased and elongation at break decreased. Although the mechanical properties were altered, storage did not affect crystallinity of the films. Oxygen gas permeability (OP) and water vapor permeability (WVP) properties were monitored in OsAX films. Interestingly WVP decreased during storage; more than a 40% decrease was seen when plasticizer blends contained 50% or more glycerol. In contrast, there were no drastic changes in the OP during storage; all the OPs obtained were between 3.7 and 8.9 [cm3 µm/ (m2 d kPa)]