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Polysaccharides hydration

Delayed Crosslinking Additives. Glyoxal [458,460,461] is effective as a delay additive within a certain pH range. It bonds chemically with both boric acid and the borate ions to limit the number of borate ions initially available in solution for subsequent crosslinking of a hydratable polysaccharide (e.g., galactomannan). The subsequent rate of crosslinking of the polysaccharide can be controlled by adjusting the pH of the solution. [Pg.255]

Oxygen Availability in Degrading Films. A major difference between natural materials and starch-plastic or cellulose-plastic blends is that the hydrophilic and relatively permeable matrix of materials like wood and hydrated polysaccharide films allows diffusion of O2 and release of nutrients from sites at a distance from the invasion site. As colonization proceeds, pore enlargement occurs when the pore walls are degraded (8) or as the polymer matrix of amylose or PVA films is hydrolyzed (10.12). In contrast, the LDPE matrix supplies no nutrients, hinders diffusion of water and O2, and the pore diameter cannot be increased. The consequence of impermeability is that the sole means of obtaining O2 and nutrients is by diffusion through water-filled pores. [Pg.81]

Water, occasionally modified by ethanol and salt, is the universal food solvent. Vj and vm are maximum in pure water and minimum in pure ethanol. Without hydration, polysaccharides cannot perform as plasticizers, thickeners, texturizers, stabilizers, crystallization inhibitors, and bulking and gelling agents. Crosslinking holds vm constant, irrespective of the solvent. All water relationships with solute theoretically disappear at 0. [Pg.29]

Water-soluble polysaccharides are commonly used in food related applications as thickeners due to their increase in viscosity when hydrated. Polysaccharides can also constitute edible films, an important quality since these polymers are of natural origin and... [Pg.1083]

Table 7 shows results obtained when data were fit to Cross model,. The upper Newtonian plateau was, as usually, inaccessible. Structural relaxation times, , showed that hydrated polysaccharides constituted a network which relaxed after attainment of its corresponding onset value. [Pg.1340]

Over the years, the term gums has been used to denote a wide range of compounds including polysaccharides, terpenes, proteins, and synthetic polymers. In the 1990s, the term more specifically denotes a group of industrially useful polysaccharides or their derivatives that hydrate in hot or cold water to form viscous solutions, dispersions, or gels (1). [Pg.430]

Water-Holding Capacity (WHC). AU polysaccharides are hydrophilic and hydrogen bond to variable amounts of water. HydratabUity is a function of the three-dimensional stmcture of the polymer (11) and is kifluenced by other components ki the solvent. Fibrous polymers and porous fiber preparations also absorb water by entrapment. The more highly crystalline fiber components are more difficult to hydrate and have less tendency to sweU. Stmctural features and other factors, including grinding, that decrease crystallinity or alter stmcture, may iacrease hydratioa capacity and solubUity. [Pg.70]

The amount of water boimd to the proteins and polysaccharides depends primarily on the ratio of water to the biopolymer in the investigated system The two extreme cases are the dry biopolymer (water content tend to zero) and highly diluted aqueous solutions of the biopolymers. The dry biopolymer undergoes hydration if is exposed to the water vapor of increased vapor pressure. The extent of hydration can be determined y measuring the... [Pg.95]

The same methods (chemicals, enzymes, physical treatments) can be also applied on the cell wall materials not with the aim of extracting polysaccharides but with the aim of obtaining modified fibres. New properties concerning for exemple fermentability, ratio soluble/insoluble dietary fibre, hydration., can be obtained (1). [Pg.426]

Other techniques to promote complete polymer hydration include vigorous mixing and slow addition of the polysaccharide. Specially designed mixing devices have been used to promote rapid particle dispersion ( 1). Adding already prepared dispersions of guar, HPG, and HEC in nonaqueous media is another means of promoting rapid... [Pg.18]

Figure 4.21 An illustration of how the configuration of glycosidic bonds determine polysaccharide structure and function. The P-1-4 linkages in cellulose favourize straight chains, optimal for structural purposes, whereas the a-1-4 linkages are favourable to bent structures, better adapted to storage in a hydrated form. Figure 4.21 An illustration of how the configuration of glycosidic bonds determine polysaccharide structure and function. The P-1-4 linkages in cellulose favourize straight chains, optimal for structural purposes, whereas the a-1-4 linkages are favourable to bent structures, better adapted to storage in a hydrated form.
Carbohydrates are literally hydrates of carbon, containing only the elements carbon, oxygen, and hydrogen. In the human diet, they are considered macronutrients, along with proteins and fats (triacylglycerols). The three types of carbohydrates are monosaccharides, disaccharides, and polysaccharides. [Pg.465]

X-ray fiber diffraction can be used to visualize highly hydrated polymer specimens at atomic resolution. An essential part of such an analysis is the inclusion of reliable stereochemical information to supplement the diffraction data. Structure determination involves modelling and refinement of putative structures, and adjudication amongst the optimized models. This technique has been successfully applied to a number of polysaccharides. The precision of resulting structures is often sufficient to identify the critical interactions within and between molecules, that are responsible for the unique properties of these materials. [Pg.330]


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See also in sourсe #XX -- [ Pg.29 , Pg.69 ]




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