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The properties oť potato starch saturated with Na, K, Ca and H cations were studied in extrudates cooked at 60°-65°-75°C, 90°-105°-120°C and 140°-155°-170°C. The morphological features of the extrudates, their specific gravity and expansion ratio as well as starch properties depended on the temperature of extrusion and type of saturating cations. The higher were the temperatures of extrusion, the higher was the solubility of the extrudates, but lower rétrogradation degree and the amount of sediment obtained from centrifuged pastes. The starches saturated with Na, K, Ca and H cations, either non-extruded or extruded at 60°-65°-75°C and 90°-105o-120°C exhibited different solubility and rétrogradation degree; the starches extruded at 140°-155o-170°C were totally soluble and their rétrogradation degree was similar. Some differences in water absorption capacity of the extruded starches saturated with different cations were observed - the extrudates of Na, K and Ca starches exhibited higher water absorption capacity than non-extruded starches, while the water absorption capacity of extruded hydrogen starch was lower than before extrusion.
Buckwheat starch was subjected to cycles of high pressure-cooling (P-CC) or autoclaving-cooling (A-CC) combined with pullulanase debranching to determine changes in resistant starch (RS) content, digestibility, rheological properties and microstructure. Native buckwheat starch had 11.9 g/kg of RS, while the highest RS content (58.7 g/kg) was reached after A-CC and 6 h of pullulanase treatment. Among the P-CC samples, the highest RS content (43.3 g/kg) was obtained after treatment with 600 MPa/9 min and 6 h pullulanase debranching. The digestibility of the starch samples was negatively correlated with RS content and its highest values were noted for native and P-CC 200 MPa preparations subjected to 2 and 16 h of pullulanase treatment (95.18–95.35%). Buckwheat starch A-CC preparations after 6 h of pullulanase treatment exhibited the lowest digestibility (85.87%). Rheological analysis of 6% starch pastes showed that all investigated samples demonstrated a non-Newtonian flow, pseudoplastic properties and thixotropy. The Ostwald de Waele rheological model was very well fitted to the flow curves of the investigated pastes (R2 >0.98). Both P-CC and A-CC reduced the consistency coeffi cient (K) and thixotropy values, while the flow behavior index (n) was increased only after P-CC treatment. The P-CC and A-CC treatment resulted in starch granule breakdown and porous gel structure formation, differing in surface properties.
Starch is a cheap and abundant polysaccharide, which is found in nature as water insoluble semicry- stalline granules with sizes in the range of 0.5-70 µm. Although starch is easily gelatinised or dissolved in water, it is not possible to obtain stable suspensions or colloidal systems from native starches. This inherent disadvantage of starch has limited its applications. In this study potato starches were processed to obtain fully biodegradable microparticles, which behave as microgels or colloids in aqueous suspensions. The synthesis process is based on the unique combination of gelatinization and cross-linking performed in water-oil emulsions. The obtained starches are very stable in water and show an interesting shear-thinning behaviour even at high solid contents. In particular, the rheological behaviour of the new starches is unique. The starches offer new possibilities for preparing starch colloids with a range of properties. A range of starch microparticles was obtained opening the door to numerous food and non-food markets (paints and coatings, inks and pigments, super- absorbent polymers, food additives, personal care products, pharmaceuticals, ceramics, paper additives, adhesives, thickeners, emulsifiers, ....). In order to make a wide-scale industrial use of these new materials possible, it is necessary to acquire detailed knowledge about the structure and properties of the prepared particles. By a multidisciplinary approach, a start was made on their process-structure-property relationships. The final goal of this work is to establish the relationships between synthesis parameters and the structural, colloidal and rheological features. Particles were prepared using epichlorohydrin and trisodium trimetaphosphate as cross-linkers. In this paper important reaction parameters, such as temperature, time and composition of the reactants (starch, cross-linker, hydroxide), which influence the structure of the microparticles during synthesis, were identified. Using Bohlin reometry the formation of the starch network structure was studied. Particle sizes of the microgels are in the range of 60 nm up to 10 µm. The synthesised particles were slightly negative (in the range of - 5 to - 45 mV). Features such as size and charge of the particles depended on the type and amount of cross-linker used. Descriptions of the rheological properties of starch-based microparticles in aqueous suspensions, both in dilute and concentrated systems, were given. The microgel-type particles showed a behaviour that is typical for (slightly) charged materials or polyelectrolytes.
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