Texture Changes During the Ripening of Port Salut Argentino Cheese in 2 Sampling Zones

ABSTRACT: Texture changes during ripening of Port Salut Argentino cheese for different sampling zones were studied. Compression relaxation tests were performed and results were analyzed using both Maxwellian and Peleg's models. Elastic equilibrium modulus obtained from the Maxwellian model decreased from 1.22 to 0.11 10⁴Pa during ripening. The constants derived from Peleg's model, k₁ and k₂, diminished with ripening time from 1.18 to 0.71 min and from 1.27 to 1.12, respectively. Asymptotic equilibrium modulus from Peleg's model decreased from 0.95 to 0.07 10⁴Pa during ripening. Rate parameters derived from a 1st order kinetics applied to both equilibrium moduli showed that the decrease was faster in the external zone (0.0846 d⁻¹) than in the central zone (0.0368 d⁻¹). The correlation between equilibrium moduli, salt concentration, moisture content, and maturation indexes was obtained with a determination coefficient of 0.76.     

Prediction of the diffusion coefficients in multicomponent liquid refrigerant solutions

Immersion chilling and freezing (ICF) consist of soaking foods in a low freezing point liquid medium maintained at a low temperature that are considered secondary refrigerants. Data related to transport properties for the refrigerating media used in ICF processes are scarce, particularly for ternary and higher order systems. The objective of this work was to develop a model for the prediction of diffusion coefficients for systems of interest for ICF processes. The generalized Maxwell-Stefan equations were used in the model development. Data obtained from literature corresponding to Fick diffusion coefficients of the binary systems NaCl-H₂O and KCl-H₂O, and the ternary system NaCl-KCl-H₂O, were compared with predicted values. Results were satisfactory, errors of the main diffusion coefficients less than 13.5% being obtained. These results may be extended to the typical range of conditions of ICF, where no data are available in literature to date.     

Fast headspace-enantioselective GC-mass spectrometric-multivariate statistical method for routine authentication of flavoured fruit foods

This study describes a rapid total analysis system (TAS) to detect the authenticity of fruit-flavoured foods and beverages by on-line combining headspace solid phase microextraction (HS-SPME) with enantioselective GC-MS (Es-GC-MS) and statistical multivariate methods (PCA, HCA). Peach, coconut, apricot, raspberry, as fruits mainly characterised by γ- and δ-lactones as chiral markers, strawberry (α-ionone, linalool, nerolidol, ethyl 2-methylbutyrate, 2-methylbutyric acid and γ-lactones) and melon (ethyl 2-methylbutyrate and 2-methylbutanol) were investigated. The system was developed by (a) optimising non-equilibrium HS-SPME sample preparation, (b) speeding-up ES-GC using cyclodextrin derivatives as chiral selectors with conventional and narrow-bore columns and (c) elaborating data by multivariate methods. The resulting TAS affords a reduction of the time needed for the whole analytical process from about 150 min to 20-50 min (67-87% of the current routine method) depending on matrix, sampling and analysis conditions and Es-GC columns.     

Temperature dependency of linear viscoelastic properties of a commercial low-fat soft cheese after frozen storage

The temperature dependency of linear viscoelastic properties of a commercial low-fat soft cheese containing microparticulated whey protein as fat replacer was studied considering the effect of freezing. After thawing, cheeses were held at 6 °C during 48 days for ripening. Refrigerated cheeses (stored at 6 °C for 48 days) were used as control samples. Frequency sweeps (0.01-10 Hz) in the linear viscoelastic region at 10, 20, 30, 40, and 50 °C were performed. Activation energies for complex viscosity at 1 Hz were obtained from an Arrhenius-type equation. Also, the time-temperature superposition method, the modified Cole-Cole analysis and the weak gel model for foods were used to compare the behavior of frozen and refrigerated cheeses. The results obtained in this work indicated that the viscoelastic properties of the studied cheeses obtained at different temperatures were influenced by freezing.     

Effect of freezing on the viscoelastic behaviour of whey protein concentrate suspensions

The effect of freezing on viscoelastic behaviour of whey protein concentrate (WPC) suspensions was studied. Suspensions with total protein content of 5% and 9% w/v were prepared from a commercial WPC (unheated suspensions). A group of unheated suspensions was treated at two temperatures (72.5 and 77.5 °C) during selected times to obtain 60% of soluble protein aggregates (heat-treated suspensions). Unheated suspensions and heat-treated suspensions were frozen at −25 °C (frozen unheated and frozen heat-treated suspensions). Frequency sweeps (0.01–10 Hz) were performed in the region of linear viscoelasticity at 10, 20, 30, 40, and 50 °C. Mechanical spectra of all studied suspensions at 20 °C were similar to viscoelastic fluids and complex viscosity increased with the frequency (ω). Elastic (G′) and viscous (G″) moduli were modelled using power law equations (G′ = aω^x, G″ = bω^y), using fitted parameters a, x, b, and y for statistical analysis. Exponent y was the most influenced by freezing, indicating the existence of a higher degree of arrangement in frozen unheated suspensions and a lower degree of arrangement in frozen heat-treated suspensions. Only characteristic relaxation times (inverse of the crossover frequency) of suspensions with 5% w/v of total protein content were significantly influenced by freezing. Time–temperature superposition was satisfactory applied in unheated whey protein concentrate suspensions only in the range of high temperatures (30–50 °C). However, this principle failed over the complete temperature range in most of the frozen suspensions. It is possible that freezing produced an increase in the susceptibility to morphological changes with temperature during the rheological measurements.     

Combined ab initio and experimental study of A2 + L21 coherent equilibria in the Fe–Al–X (X = Ti,Nb, V) systems

A combined theoretical and experimental study of ordering and phase separation in α-Fe alloys in the Fe–Al–X (X = Ti, Nb, V) systems is presented. The theoretical part is dedicated to the assessment of the BCC-based phase equilibrium diagram in the iron-rich zone of the ternary systems via a truncated cluster expansion, through the combination of Full-Potential-Linear augmented Plane Wave (FP-LAPW) electronic structure calculations and of Cluster Variation Method (CVM) thermodynamic calculations in the irregular tetrahedron approximation. The stability and the solid solubility of Al in the Fe₂X Laves phases are also included in the discussion of the ternary BCC ground state diagrams. The approach was employed in order to explore particular vertical sections of the ternary systems where a coherent two-phase microstructure can be generated with an optimal combination of volume fraction of Fe₂AlX (L2₁) Heusler type precipitates and Al content in the α-Fe (A2) matrix. The results indicate that in the Fe–Al–Ti and Fe–Al–V systems there are two kinds of phase separations of the BCC phase, (A2+ L2₁) and (B2 (FeAl structure) + L2₁). A tie-line separates both two-phase fields that shrinks and moves toward the Fe-X binary system while its direction remains almost parallel as the temperature increases. Selected experiments were performed on three alloys of the Fe–Al–Ti system belonging to vertical sections that contain this tie-line. The microstructure and composition of the matrix and precipitate phases were characterized by transmission electron microscopy (TEM) and Energy Dispersive Spectroscopy (EDS), the theoretical predictions were borne out.     

Study of milk/κ-carrageenan mixtures by atomic force microscopy

Structural characteristics of milk components and milk/κ-carrageenan mixtures were studied by atomic force microscopy (AFM). Samples were adsorbed on highly ordered pyrolytic graphite (HOPG) and mica substrates. Sample attachment by physisorption and imaging in air by AFM resulted in a very promising technique to investigate structures and interactions between biological macromolecules under “near-native” conditions. Differences in adsorption of casein micelles on HOPG and mica surfaces were observed. Casein micelles were adsorbed satisfactorily on HOPG while poor adsorption was obtained on mica surface. Topographical images of casein micelles adsorbed on HOPG denoted pseudo-spherical structures forming aggregates which were polydisperse in size and shape. In the case of milk/κ-carrageenan mixtures, it was observed that as κ-carrageenan concentration increased, the amount of casein micelles attached on HOPG surface decreased. An opposite behavior was observed when samples were adsorbed on mica. Hydrophobic and hydrophilic interactions between samples and substrates helped in improving the understanding of the interactions between the macromolecules studied. Our findings agreed with previous studies suggesting a surface level interaction between casein micelles and κ-carrageenan, the structures observed being dependent on polysaccharide concentration. It can also be concluded that mica may be a suitable substrate for imaging milk/κ-carrageenan mixtures.     

Casein Degradation of Fynbo Cheese Salted with NaCl/KCl Brine and Ripened at Various Temperatures

ABSTRACT: Effect of temperature and salt substitution on casein degradation of Fynbo cheese was studied. Fynbo cheeses, salted in solutions of 190 g NaCl/L and of 100 g NaCl/L and 100 g KCl/L and ripened at 5, 12, and 16 °C, were sampled at 1, 5, 10, 20, 30, 60, and 90 d of ripening, at central and external zones. Samples were analyzed for moisture and chloride contents, maturation index, and casein degradation by urea‐polyacrylamide gel electrophoresis. NaCl replacement by KCl did not affect any of the parameters studied. Total salt concentration and ripening temperature affected proteolysis significantly. First‐order kinetics constants for α_s1‐casein degradation were in the range of 0.002 to 0.016 day^‐1 and the activation energy of the reaction was approximately 26 kcal/gmol.     

Effect of freezing on physical properties of whey protein emulsion films

The objective of this work was to study the effect of the freezing process on physical properties of whey protein emulsion films with different beeswax content dried at 5 °C. Thickness, microstructure, water vapour permeability, solubility in water, sorption isotherms and mechanical properties were measured in Control and Frozen films. The freezing process did not cause fractures or perforations in films, but films with beeswax showed a change in the appearance of the lipids after freezing. Only films with 40% of beeswax showed a significant increase in the water vapour permeability after freezing. The freezing process did not affect film solubility in water but produced small differences in the equilibrium moisture content values. In the puncture test, the freezing process increased puncture strength and deformation of films without beeswax but those parameters were not affected in films with beeswax. In tensile test, tensile strength and elastic modulus decreased, but elongation was not affected by freezing process. Principal component analysis accomplished an adequate condensation of the date grouping samples according to film formulation and treatment (Control and Frozen films). Indeed, the relationships of sample grouping and measured parameters were enlightened by principal component analysis. In conclusion, whey protein emulsion films were resistant to the freezing process (freezing, frozen storage and thawing) and could be a good alternative as a treatment to preserve the quality of frozen foods.