The present investigation deals with analyzing the validity of GAB model for isotherms of different food products. The model was found satisfactory for different food products with different shapes of of isotherms under widely varying conditions (temperature: 4-140 C; moisture %D.B.:2-71; activity: 0.059-0.99). The present study covered a wide range of food products from green vegetables, fruits, cereals and nuts to casein, pectin and protein. Food products with complex molecular structure and high sugar contents were also included. A non linear regression method was applied to evaluate the six parameters of the GAB model. The Guggenheim constant, factor for multilayer molecules and the monolayer moisture were assumed to follow an Arrhenius type relationship with temperature variation. The values of net isosteric heat of sorption obtained by GAB model and Clausius Clapeyron equation were compatible. Monolayer moisture values for food products obtained by GAB model were in agreement with values reported in the literature.

In food packaging systems, moisture content influences chemical and physical film properties, also determining processes such as food spoilage, and properties of food texture and crispiness level. The study of water permeation and sorption processes of new materials intended to be used as packaging is very important to determine the best application conditions and to predict the film behavior under different moisture conditions inside and/or outside the packaging. In order to determine the suitable temperature and water activity (aw) application conditions for whey protein isolate (WPI)/polyvinyl alcohol (PVOH) blends as food flexible packaging, water permeation and water sorption thermodynamic behavior of these materials were evaluated. WPI/PVOH films and blends had solubility preponderant over the diffusion on the water permeation process. Water sorption experimental data were well described by the GAB model, and curves showed a more expressive increase of water sorption at aw > 0.75, with lower equilibrium moistures (Ye) at room than at chilled temperatures. Differential enthalpy decreased and differential entropy increased by the Ye gain, and the occurrence of enthalpy-entropy compensation was confirmed with enthalpy driving the sorption process. The addition of PVOH to the WPI matrix made the water sorption process more spontaneous. Water sorption thermodynamic analysis indicates that the application of WPI/PVOH blends as packaging is best suitable for foods and external environments with aw below 0.75 and at room temperature.

Humans and animals can be exposed to mixtures of chemicals from food and water, especially during disasters such as extended droughts, hurricanes and floods. Drought stress facilitates the occurrence of mycotoxins such as aflatoxins B₁ (AfB₁) and zearalenone (ZEN), while hurricanes and floods can mobilize toxic soil and sediments containing important pesticides (such as glyphosate). To address this problem in food, feed and water, we developed broad-acting, clay-based enterosorbents that can reduce toxin exposures when included in the diet. In this study, we processed sodium and calcium montmorillonite clays with high concentrations of sulfuric acid to increase surface areas and porosities, and conducted equilibrium isothermal analyses and dosimetry studies to derive binding parameters and gain insight into: (1) surface capacities and affinities, (2) potential mechanisms of sorption, (3) thermodynamics (enthalpy) of toxin/surface interactions and (4) estimated dose of sorbent required to maintain toxin threshold limits. We have also used a toxin-sensitive living organism (Hydra vulgaris) to predict the safety and efficacy of newly developed sorbents. Our results indicated that acid processed montmorillonites were effective sorbents for AfB₁, ZEN and glyphosate, with high capacity and tight binding, and effectively protected hydra against individual toxins, as well as mixtures of mycotoxins.

The aim of this study was to determine thermal properties of pseudoplastic polysaccharides (guar gum, κ-carrageenan and xanthan gum) which find many applications as food hydrocolloids in food industry. There was an obvious relationship between thermal dependency of heats of fusion of hydrocolloids in powder form and activation parameters of hydrodynamic flow in solutions, respectively. Results of thermal analysis confirmed, that powder samples of hydrocolloids as typical foodstuffs of low moisture content less than 15 w% after room conditioning, exhibited varying ability to bind water as depending on their molecular structure. The peak temperature of the endothermic polysaccharide order-disorder phase transition process was found in the temperature range of 50–85 °C. It was influenced simultaneously by the applied heating rate and the samples moisture content. Studied samples moisture content was ranging between 9–40 w.% as was obtained after different conditioning. Observed reaction enthalpy (ΔH) associated with phase transition and water evaporation (proved by appropriate weight loss of the samples Δmw) was ranging from 140 to 670 J/g. Activation energy (Eₐ) of this process in powder samples was calculated from the kinetic parameters using three kinetic models developed by Friedman, Kissinger and model-free kinetics. The latter kinetic models were compared with the Arrhenius model, which was used to determine Eₐ of polysaccharide solutions on reflecting sensitivity of their molecular structure to the temperature and the solvent. According to the Arrhenius model, there were obtained the highest values of Eₐ for κ-carrageenan solutions, indicating the highest resistance of their molecular structure to temperature. This fact can be related to the observed the lowest value of the reaction enthalpy in the case of powder samples, suggesting that energy obtained during the order-disorder transition to change the carrageenan powder structure is limited. On the other hand, xanthan gum was the least temperature dependent sample; activation energy of xanthan solutions was only in the range of 2–6 kJ/mol. Concurrently, ΔH of xanthan powder was determined as the largest of all samples under study. In general, there was found an indirect relationship between activation energy of the solutions determined by viscometry and reaction enthalpy of the powders determined by thermal analysis. Results of the Arrhenius model also indicate that the energy necessary to promote viscous flow of solutions is higher for hydrocolloids in distilled water rather than in 0.07 M KCl aqueous solutions, suggesting the suppression of the polyelectrolyte effect. In both cases, Eₐ was substantially reduced by application of higher shear rate.

Few data are available on the thermophysical properties of high porosity foodstuff in the freezing domain. This paper presents some data obtained with a cellulose sponge used as a model food. The fraction of unfreezable water was obtained from differential scanning calorimetry data, using two different methods with a very good agreement. Water activity was experimentally determined at positive temperature. Experimental data were modeled by the Guggenheim-Anderson-de Boer (GAB) model, and a model deduced from the Clausius-Clapeyron equation. The GAB model was used to extrapolate these data in the subzero domain. It showed a good agreement until a water activity of 0.9, whereas the second model is usable only up to the value of 0.75.

BACKGROUND: Partition coefficients give an indication of the retention of aroma compounds by the food matrix. Data in the literature are obtained by various methods, under various conditions and expressed in various units, and it is thus difficult to compare the results. The aim of the present study was first to obtain gas/water and gas/matrix partition coefficients of selected aroma compounds, at different temperatures, in order to calculate thermodynamic parameters and second to compare the retention of these aroma compounds in different food matrices.RESULTS: Yogurts containing lipids and proteins induced a higher retention of aroma compounds than model gel matrices. The observed effects strongly depend on hydrophobicity of aroma compounds showing a retention for ethyl hexanoate and a salting out effect for ethyl acetate. A small but noticeable decrease in enthalpy of affinity is observed for ethyl butyrate and ethyl hexanoate between water and food matrices, suggesting that the energy needed for the volatilization is lower in matrices than in water.CONCLUSION: The composition and complexity of a food matrix influence gas/matrix partition coefficients or aroma compounds in function of their hydrophobicity and to a lower extent enthalpy of vaporization.