Changes in nutritive quality of osmodehydrated pork meat in sugar beet molasses

The aim of this study was to examine effects of sugar beet molasses as hypertonic solution during osmotic dehydration on nutritional properties of pork meat. Samples of pork meat were dehydrated in sugar beet molasses as an osmotic agent during 5 hours, at room temperature of 22°C and atmospheric pressure. This paper presents basic chemical composition and mineral contents of fresh meat, as compared to meat osmotically treated in sugar beet molasses. It was detected that dehydrated product shows enhanced chemical composition and considerable increased mineral content, thus confirming the usefulness of molasses from a nutritive point of view. The enrichment of the meat in protein, fat, sucrose, sodium chloride and analyzed minerals (K. Na. Mg, Fe and Ca) proves their diffusion from molasses into the raw material during process

Re-use of osmotic solution

In this paper the re-use of osmotic solution after osmotic treatment has been studied. A large amount of used osmotic solution remaining after the process is one of the major unsolved problems of osmotic treatment process. This problem has both ecological and economic aspects that should be concerned. Pork meat cubes were treated in three different osmotic solutions diluted with distilled water (R1 -sugar beet molasses, R2 – solution of salt and sucrose and R3 - combination of R1 and R2 solutions in a 1:1 mass ratio). Osmotic process has been observed during 5 hours, at temperature of 35oC and atmospheric pressure. Osmotic treatment has been performed simultaneously in concentrated solutions and diluted solutions (dilutions were obtained by mixing the solution and water in the mass ratio of 7:1 and 3:1). Parameters monitored during osmotic treatment were: dry mater content (DMC), water loss (WL), solid gain (SG) and osmotic dehydration efficiency index (DEI). Maximum values of these parameters were obtained in the dehydration with concentrated solutions, while recorded values in diluted solutions were much lower. The results show that the least effect on the osmotic process efficiency, when the osmotic concentration is lowered, has been observed for solution R3. This conclusion indicates that molasses is good osmotic solution with the possibility of re-using in successive processes of osmotic dehydration, with minimal treatment of reconstitution to original values of concentration

Mass transfer and microbiological profile of pork meat dehydrated in two different osmotic solutions

The effects of osmotic dehydration on mass transfer properties and microbiological profile were investigated in order to determine the usefulness of this technique as pre-treatment for further treatment of meat. Process was studied in two solutions (sugar beet molasses, and aqueous solution of sodium chloride and sucrose), at two temperatures (4 and 22°C) at atmospheric pressure. The most significant parameters of mass transfer were determined after 300 minutes of the dehydration. The water activity (aw) values of the processed meat were determined, as well as the change of the microbiological profile between the fresh and dehydrated meat. At the temperature of 22°C the sugar beet molasses proved to be most suitable as an osmotic solution, despite the greater viscosity

CaO&CaSO4 and CaO&Al2(SO4)3 as Pectin Precipitants–Model of Overlapping Diffuse Layers

This work is concerned with the theoretical basis of novel sugar beet juice purification method using binary systems CaO&CaSO4 and CaO&Al2(SO4)3. The Gouy–Chapman–Stern (GCS) model of overlapping of diffuse layers of EDLs on pectin surface and that on Ca2+ and Al3+ ions, theoretically explains this method. The change of the zeta potential was used to quantitatively indicate overlapping of diffuse layers. For the experiment two model solutions of pectin (0.1 % w/w) were prepared, while the concentrations of CaO&CaSO4 and CaO&Al2(SO4)3 in the range of 50–500 g dm-3 were used. The greater decrease in the absolute value of zeta potential indicated greater overlapping of diffuse layers between pectin particles and Ca2+ and Al3+ ions and faster coagulation of pectin. The overlapping degree increased with increased concentration of these binary systems. Pectin with a greater surface charge and multivalent Al3+ from CaO&Al2(SO4), exerted a greater impact on the zeta potential. Optimal quantities of the applied binary mixtures were as follows: 256–640 mg g-1 pectin. This is much lower than CaO commonly used in the conventional process of sugar beet juice purification (about 9 g g-1 pectin)

Antioxidant Capacity of Nettle Leaves During Osmotic Treatment

Osmotic treatment (OT) of nettle leaves was assessed in various osmotic solutions (sugar beet molasses – SBM and ternary aqueous solution – TAS), at temperatures of 20, 35 and 50 °C, under the atmospheric pressure. The influence of the kind of utilized osmotic solution, process temperature and osmotic time on the antioxidant activity (AOC), expressed with the spectrophotometric assays (ABTS, FRAP and DPPH), as well as two direct current polarographic assays, Hydroxo Perhydroxo Mercury (II) complex assay, based on the decrease of anodic current and assay based on the decrease of a cathodic current of Hg (II) reduction. For determination of the total phenolic content Folin-Ciocalteu assay was used. The Relative Antioxidant Capacity Index (RACI), obtained by setting equal weight for every involved assay was applied in order to get an extensive comparison among analyzed samples and between the used assays. Based on these results, after the OT of nettle leaves in TAS, the AOC decreased, while the OT in SBM increased AOC values. The phenolic antioxidant coefficients (PAC), calculated as the ratio between particular AO capacity and TPC, were used to achieve a more comprehensive comparison between analysed samples, as well as applied assays. The results of RACI evaluation revealed that the most favorable osmotic treatment is the one performed for 5h at 35 °C

Structural characterisation of starch based edible films with essential oil addition

Present study investigated structure of starch based edible films with essential oil addition. Films were obtained from water solutions containing gelatinized modified starch, polyol, guar-xantan gum modified mixture and essential oil by casting it on a Petri dish and evaporating at room temperature for 72h. Both, glycerol and guar-xantan modified mixture, had role to improve film flexibility and enable better film folding and handling. Two sample groups were obtained: starch based edible films with black cumin oil addition and starch based edible films with black pepper oil addition. Both essential oils were added in three different concentrations. Starch based edible film without essential oil addition was used as blank shot. Structural properties were determined by analyzing spectra obtained by FT-IR Spectrometer in the spectral range of 4000–400 cm−1 with a 4.0 cm−1 resolution. Software Omnic 8.1. and TQ Analyst were used to operate the FTIR spectrometer, collect and present all the data. Results pointed to quantitative law dependency between added amount of essential oils and spectra absorption values for both sample groups and FTIR spectra were used to calculate coefficient of correlation

Structural characterisation of starch based edible films with essential oil addition

Present study investigated structure of starch based edible films with essential oil addition. Films were obtained from water solutions containing gelatinized modified starch, polyol, guar-xantan gum modified mixture and essential oil by casting it on a Petri dish and evaporating at room temperature for 72h. Both, glycerol and guar-xantan modified mixture, had role to improve film flexibility and enable better film folding and handling. Two sample groups were obtained: starch based edible films with black cumin oil addition and starch based edible films with black pepper oil addition. Both essential oils were added in three different concentrations. Starch based edible film without essential oil addition was used as blank shot. Structural properties were determined by analyzing spectra obtained by FT-IR Spectrometer in the spectral range of 4000–400 cm−1 with a 4.0 cm−1 resolution. Software Omnic 8.1. and TQ Analyst were used to operate the FTIR spectrometer, collect and present all the data. Results pointed to quantitative law dependency between added amount of essential oils and spectra absorption values for both sample groups and FTIR spectra were used to calculate coefficient of correlation

Comparison of methods of zeta potential and residual turbidity of pectin solutions using calcium sulphate/aluminium sulphate as a precipitant

The affinity of calcium ion binding from CaO used in the most common process of purification of sugar beet juice is relatively low. Therefore, large amounts of this compound are required. This paper presents the theoretical basis of a novel sugar beet juice purification method based on the application of the binary system CaSO4/Al2(SO4) . In order to monitor the process of coagulation and precipitation of pectin in the presence of CaSO4/Al2(SO4)3, two methods were compared: measurement of the zeta potential and of residual solution turbidity. The zeta potential of pectin solution was determined by electrophoretic method, while the residual turbidity was determined by spectrophotometry. Two model solutions of pectin (0.1 % w/w) were investigated. Studies were performed with 10 different concentrations of the binary solution CaSO4/Al2(SO4)3 (50 - 500 g dm-3). The amount of the precipitant CaSO4/Al2(SO4)3 (1:1 w/w) needed to achieve the minimum solution turbidity and charge neutralization of pectin particles (zero zeta potential) were measured and compared. Colloidal destabilization occurred before a complete neutralization of the surface charge of pectin particles (zeta potential ~ 0 mV). Optimal quantities (490 - 705 mg g-1 pectin) of the applied binary mixture, were obtained using both methods. This is much lower than the amount of CaO that is commonly used in the conventional process of sugar beet juice purification (about 9 g• g-1 pectin). The use of these precipitants could be important from both economic and environmental point of view. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. TR 31055

Aluminium and calcium ions binding to pectin in sugar beet juice: Model of electrical double layer

In sugar industry, there is a problem of the presence of undesirable macromolecules such as pectins in sugar beet juice. Separation of these compounds is done mostly by CaO. Calcium may cause undesirable process of alkalization of soil in the near environment of the sugar factory. The theoretical basis of new juice purificatin method based on the application of Al2(SO4)3, CaSO4 and their mixtures are presented. Two model solutions of pectin (0.1 % w/w) are investigated using a method of measuring zeta potential. Pure salts Al2(SO4)3 and CaSO4, showed better binding properties with the pectin than mixtures. Amount of all studied pure salts and mixtures of Al3+ and Ca2+ ions were significantly less (142 - 710 mg/gpectin) than the average amount of CaO used in classical process (about 9 g/gpectin). Mechanism of discharge of pectin macromolecules in the presence of mixtures of these ions using a model of double electric layer are suggested