A new model of water sorption isotherm is developed on the basis of Raoult's law. It is assumed that water present in food occurs in two states, as free water with properties of the bulk water and as water of hydration. Hydrated molecules are considered as new entities with molecular weights larger than those of non-hydrated molecules. Hydration reduces the free concentration of water and thus affects water activity in solution. Application of the developed equation to food sorption data showed that it gives approximation of sorption isotherms much better than that offered by the GAB model. Moreover, it predicts infinite adsorption at a(w)=1, the property which is not offered by the GAB equation. The new equation makes it possible to interpolate isotherms at high water activities close to one. The probability that the new equation will fit the food isotherm with small RMS is higher than 90% and substantially exceeds that found for the GAB model. As a two-parameter model it makes substantial improvement over the three-parameter GAB equation.

This study was carried out to evaluate the effects of power ultrasound (US) on the molecular weight and rheological properties of a food polysaccharide, konjac glucomannan (KGM). Upon the exposure of KGM solution (1% w/v in water) to US at a relatively high power intensity (50 W/cm2), the apparent viscosity decreased rapidly from about 50 Pa s to a negligible level within 10–20 min. The intrinsic viscosity ([η]) of KGM solution decreased gradually during the US exposure with a time course closely fitted to the first-order polymer degradation kinetics (random chain scission). The US treatment also caused a significant reduction of particle size (Zavg) of KGM aggregates and changes in the rheological properties including the decrease of storage modulus (G′) and loss modulus (G″), and the increase in phase angle (tan δ = G″/G′). Nevertheless, no change in primary structure was detected by Fourier transformation infrared (FT-IR) analysis. The results suggested that high intensity US was an effective means for KGM degradation without significant structural destruction.

This research paper presents the results of tests on the colligative properties of konjac gum chains in water solutions. For this purpose, the measurements of osmotic pressure and intrinsic viscosity of aqueous solutions, in the function of konjac gum concentration and temperature were carried out. The applied methods allowed for the determination of the second osmotic virial coefficients B2, which raised with the increase of temperature. It indicate that increase of temperature causes higher affinity of polysaccharide’s chains to water. It was determined, that the osmotic average molecular mass of the konjac gum in non-purified solutions increases with temperature (1.07×105–3.80×105g×mol−1). Values of the reduced viscosity linearly increased in range 18–29dL×g for all temperatures. Received values of the Huggins constant (0.81–1.72) lead that water is poor solvent for konjac gum. The theta (θ) conditions were extrapolated for non-purified solutions − 325K (52°C), and interpolated for purified solutions − 307K (34°C). Based on the results of tests using the dynamic light scattering, the values of two main relaxation times (fast − 0.4–1.8ms and slow components − 4300–5500ms) were determined (the Kohlrausch-Williams-Watts). The obtained autocorrelation functions were characteristic for sol type systems or these which indicate a gel-like structure.

The potential isolation of bio-active polysaccharides from bay tree pruning waste was studied using sequential subcritical water extraction using different time-temperature combinations. The extracted polysaccharides were highly enriched in pectins while preserving their high molecular mass (10–100 kDa), presenting ideal properties for its application as additive in food packaging. Pectin-enriched chitosan films were prepared, improving the optical properties (≥95% UV-light barrier capacity), antioxidant capacity (˃95% radical scavenging activity) and water vapor permeability (≤14 g·Pa⁻¹·s⁻¹·m⁻¹·10⁻⁷) in comparison with neat chitosan-based films. Furthermore, the antimicrobial activity of chitosan was maintained in the hybrid films. Addition of 10% of pectins improved mechanical properties, increasing the Young's modulus 12%, and the stress resistance in 51%. The application of pectin-rich fractions from bay tree pruning waste as an additive in active food packaging applications, with triple action as antioxidant, barrier, and antimicrobial has been demonstrated.

Compatibility of CNF with three polysaccharides having different surface charges and backbones (chitosan, methyl cellulose, and carboxymethyl cellulose) was investigated. Chitosan (CH) incorporation reduced water absorption (WA) of CNF films (P < 0.05). CH molecular weight (Mw) (68, 181, 287 kDa) and amount (10 and 20 g/100 g CNF in dry basis) impacted moisture barrier, mechanical, antibacterial, thermal, and structural properties of CNF films. Regardless of Mw, CH incorporation (20 g/100 g CNF) decreased (P < 0.05) WA of CNF films, and high Mw (287 kDa) CH (20 g/100 g CNF) incorporation resulted in lower film water solubility while increasing film water vapor permeability compared with low Mw CH (68 kDa) incorporation (P < 0.05). CNF film with low Mw CH (20 g/100 g CNF) exhibited antibacterial activity against L. innocua and E. coli. Interaction mechanisms between CH and CNF were investigated through thermal, structural, and morphology analyses using DSC, FTIR, and SEM, respectively. CNF films with low or high Mw CH incorporation (20 g/100 g CNF) were further validated as surface contact films for fresh beef patties, showing effectiveness to prevent moisture transfer between the layered patties. This study demonstrated the potential of using CNF-CH composite films as water resistant and antibacterial packaging for foods with high moisture surfaces.

Options were explored for fulfilling the legally required safety assessment for a widely applied epoxy/amine coating used for restoring corroded domestic drinking water supply systems. The coating was made up of two components mixed shortly before application, the first mainly consisting of bisphenol A diglycidyl ether (BADGE), the second of various amines. The analytically identified starting substances were all authorised, but only constituted a small proportion of the low molecular mass material left after curing and potentially migrating into water. Reaction products synthesised from constituents of the starting components (expected oligomers) could not be eluted from GC even after derivatisation, indicating that standard GC-MS screening would miss most potential migrants. They were detectable by size exclusion chromatography (SEC) after acetylation. HPLC with MS or fluorescence detection was possible for constituents including a BADGE moiety, but phenalkamines could not be detected with adequate sensitivity. Possibilities for determining long-term migration relevant for chronic toxicity are discussed. Analysis in water shortly after application of the coating overestimates migration if migration decreases over time and requires detection limits far out of reach. Analysis of a solvent extract of the coating is easier and provides an upper estimate of what could migrate into the drinking water over the years. However, to satisfy the regulatory requirements, components of the complex mixture need to be identified at lower proportions than those accessible. In vitro testing of the whole mixture for genotoxicity is expected to fail because of the required sensitivity and the glycidyl functions probably wrongly resulting in positive tests. The difficulties in dealing with this situation are discussed.