Spectrophotometric Determination of Trace Nitrite with Brilliant Cresyl Blue Using β-Cyclodextrin as a Sensitizer

A simple and sensitive spectrophotometric method for determination of nitrite has been described. The method is based on the oxidation of brilliant cresyl blue (BCB) by nitrite in acidic medium, which results in the decrease in absorbance at 636 nm. The decrease in absorbance is directly proportional to nitrite concentration obeying Beer’s law. The sensitivity is largely enhanced in the presence of β-cyclodextrin (β-CD) because of inclusion complexation. It was calculated that β-CD and BCB could form 1:1 inclusion complexation with a formation constant of 546.6 L/mol. Linear calibration graphs were obtained for 0.02 × 10⁻³–0.8 × 10⁻³ g/L sodium nitrite at 636 nm. The detection limit for the analytical procedure was 4.0 × 10⁻⁶ g/L sodium nitrite. The relative standard deviation for determination of 0.1 × 10⁻³ g/L and 0.5 × 10⁻³ g/L sodium nitrite were 0.69% and 0.38%, for ten determinations, respectively. Twenty-two coexistent ions or species were examined, and no serious interference for most of ions was observed. The method has been applied to determine nitrite in water and vegetable samples with satisfactory results.     

Effects of Characteristics Changes of Collagen on Meat Physicochemical Properties of Beef Semitendinosus Muscle during Ultrasonic Processing

Low-frequency and high-power ultrasound (40 kHz, 1,500 W) was tested for its effects on the characteristics of intramuscular heat-insoluble collagen and meat quality and textural properties of beef semitendinosus muscle. Meat steaks (2.5 × 5.0 × 5.0 cm, 100 ± 5 g) were sonicated for 10, 20, 30, 40, 50, and 60 min, respectively. Characteristics changes of collagen and meat quality and texture were estimated. The results indicated that ultrasound treatment had no significant (P > 0.05) effects on L* (lightness) and a* (redness) values but decreased b* (yellowness) value significantly when sonicated for 30 min (minimum 6.98). Ultrasound treatment significantly (P < 0.01) reduced the muscle fiber diameter and filtering residues but had no significant effects on the content of heat-insoluble collagen. Significant differences (P < 0.05) in β-galactosidase and β-glucuronidase activity were found between ultrasound treated for 10 min (reached the minimum were 5.2 × 10⁻³ and 1.6 × 10⁻³ umol∙ml⁻¹∙min⁻¹, respectively) and control samples. Thermal characteristics analysis of collagen suggested that ultrasound treatment weaken the average stability of collagen. After ultrasound treatment, collagenous fibers were disordered and staggered significantly; fiber arrangement became loose; and the denaturing, granulation, and aggregation of collagen fiber appeared in the extracellular space. Those changes on collagen characteristics had significant effects on meat textural properties. The results suggested that low-frequency and high-power sonication had a significant effect on collagen characters and meat textural properties.     

Evaluation of Protease-producing Ability of Fish Gut Isolate Bacillus cereus for Aqua Feed

Extracellular protease production by Bacillus cereus isolated from the intestine of fish Mugil cephalus has been investigated in shake-flask experiment using different preparations of tuna-processing waste such as raw fish meat, defatted fish meat, alkali hydrolysate, and acid hydrolysate as nitrogen source. Among the tuna preparations tested, defatted fish meat supported the maximum protease production (134.57 ± 0.47 U ml⁻¹), and 3% concentration of the same was found to be optimum for maximizing the protease production (178.50 ± 0.28 U ml⁻¹). Effect of carbon sources on protease production in the optimized concentration of defatted tuna fish meat revealed that galactose aided the higher protease production (259.83 ± 0.04 U ml^–1) than the other tested carbon sources and a concentration of 1.5% galactose registered as optimum to enhance the protease production (289.40 ± 0.16 U ml⁻¹). The halotolerancy of B. cereus for protease production indicated that 3% of sodium chloride was optimum to yield maximum protease (301.63 ± 0.20 U ml⁻¹). Among the surfactants tested, protease production was high in Triton X 100-added medium (298.63 ± 0.12 U ml⁻¹) when compared to other surfactants, and its optimum concentration recorded was 0.8% (320.57 ± 0.17 U ml⁻¹) for more protease production. Partial characterization of crude enzyme revealed that pH 7.0 (278.90 ± 0.08 U ml⁻¹) and 60°C temperature (332.37 ± 0.18 U ml⁻¹) were optimum for better protease activity by B. cereus.     

A Sensitive, Selective New Analytical Reagent, 2, 6-Diacetylpyridine bis-4-phenyl-3-thiosemicarbazone for Extractive Spectrophotometric Determination of Mo(VI) in Food Samples

Synthesized a new reagent 2, 6-Diacetylpyridine bis-4-phenyl-3-thiosemicarbazone (2, 6-DAPBPTSC) characterized and is proposed as a sensitive and selective analytical reagent for the extractive spectrophotometric determination of molybdenum(VI) at pH 3.5 to form a yellowish orange colored 1:1 chelate complex. The absorbance was measured at a maximum wavelength, 500 nm. This method obeys Beer’s law in the concentration range 0.90–9.00 μg mL⁻¹ and the correlation coefficient of Mo(VI)–2,6-DAPBPTSC complex is 0.954, which indicates an adequate linearity between the two variables with good molar absorptivity and Sandell’s sensitivity, 1.212 × 10⁴ L mol⁻¹cm⁻¹, 0.0079 μg cm⁻², respectively. The precision and accuracy of the method is checked with calculation of relative standard deviation (n = 5), 0.894% and the detection limit value is 0.0056 μg mL⁻¹. The instability constant of the method has been calculated by Asmus’ method as 6.476 × 10^–5, at room temperature. The interfering effect of various cations and anions has also been studied. The method was successfully applied for the determination of Mo(VI) in food and water samples. The validity of the present method was evaluated in terms of Student ‘t’ test and Variance ‘f’ test, which indicates the significance of the present method an inter comparison of the experimental values, using atomic absorption spectrometer.     

Effect of Acetic Acid and Commercial Protease Pretreatment on Salting and Characteristics of Salted Duck Egg

Salting of duck egg pretreated with 5% acetic acid and different commercial proteases (flavourzyme, protamex, alcalase, and neutrase) was studied. After 2 weeks of salting, duck eggs soaked in 5% acetic acid for 30 min, followed by soaking in 5% (w/v) flavourzyme and neutrase had the highest hardening ratio (90.14 ± 2.43%, 90.25 ± 1.23%) with the coincidental increase in salt content in egg white and decrease in moisture content of yolk, compared with those from other treatments (p < 0.05). However, similar hardening ratio of the sample treated with alcalase was obtained to that of sample treated with either flavourzyme or neutrase (P > 0.05). After 1 week of salting, protamex showed the similar effect on hardening ratio to other proteases (p > 0.05). When eggs were pretreated with neutrase at different concentrations (0.25%, 0.5%, and 0.75%, w/v) for different times (30, 60, and 90 min), those pretreated with 0.25% (w/v) neutrase for 90 min had the shorter salting time, while soaking time did not have the impact on hardening ratio for egg treated with 0.5% and 0.75% neutrase (P > 0.05). The oil exudation of egg treated with 0.25% neutrase had the higher oil exudates than the control at week 2 and 3 of salting (P < 0.05). Treatment of neutrase had no impact on viscosity of egg white, regardless of salting time (P > 0.05). Microstructure study revealed that shell of salted egg pretreated with acetic acid had rough and porous surfaces when compared with control, whereas no changes in microstructure and FTIR spectra of shell membrane were found. Therefore, pretreatment of egg with 5% acetic acid for 30 min, followed by 0.25% neutrase for 90 min prior to salting could expedite the salting process and yielded egg yolk with hardening ratio and oil exudates, comparable to the traditionally salted egg.     

Electrochemical Determination of Phenothrin in Agricultural Formulations, Vegetables, and Storage Bags of Wheat and Rice by Differential Pulse Adsorptive Stripping Voltammetry (DP-AdSV)

An electroanalytical method has been developed for the determination of the pesticide phenothrin by differential pulse adsorptive stripping voltammetry on a hanging mercury drop electrode in universal buffer as supporting electrolyte. The best adsorption conditions were found to be pH 6.0, an accumulation potential of −0.6 V, and an accumulation time of 75 s. Effects of stirring rate, scan rate, pulse amplitude, and purge time were examined for the optimization of instrumental conditions. Calibration curve is linear in the range 2 × 10⁻⁹ to 2 × 10⁻⁷ mol l⁻¹ with a detection limit of 1.9 × 10⁻¹⁰ mol l⁻¹. The correlation coefficient and relative standard deviation were 0.995% and 1.1%. The method is applied to the determination of the phenothrin in agricultural formulations, vegetables, and storage bags of wheat and rice under Food Corporation of India’s storage system.     

Application of Catalytic Hydrogen Evolution in the Presence of Neonicotinoid Insecticide Clothianidin

Clothianidin, a new generation of pesticide, was determined in spiked tap water, apple juice, and soil by square-wave adsorptive stripping voltammetry. The method of determination is based on the hydrogen evolution reaction catalyzed by clothianidin at the hanging mercury drop electrode. The optimal signal was detected at −1.4 V versus Ag/AgCl in citrate buffer at pH 2.2. Various parameters such as pH, buffer concentration, frequency, amplitude, step potential, accumulation time, and potential were investigated to enhance the sensitivity of the determination. The optimal results were recorded at an accumulation potential of −0.35 V, accumulation time of 7 s, amplitude of 100 mV, frequency of 200 Hz, and step potential of 7 mV. The mechanism of catalytic hydrogen evolution was considered under experimental and theoretical conditions. This electroanalytical procedure enabled to determine clothianidin in the concentration range 9 × 10⁻⁹–4 × 10⁻⁶ mol L⁻¹ in supporting electrolyte and tap water, 1 × 10⁻⁷–4 × 10⁻⁶ mol L⁻¹ in diluted apple juice, and 2 × 10⁻⁷–1 × 10⁻⁶ mol L⁻¹ in soil. The detection and quantification limits in supporting electrolyte and diluted apple juice were found to be 2.6 × 10⁻⁹, 8.6 × 10⁻⁹ and 3 × 10⁻⁸, and 1 × 10⁻⁷ mol L⁻¹, respectively. A standard addition method was successfully used to determine clothianidin in spiked tap water, spiked apple juice, and spiked soil.     

Water Diffusion and Concentration Profiles During Osmodehydration and Storage of Apple Tissue

The objective of this work was to study the mobility of water and sucrose during osmotic dehydration and storage of apple tissue and to conduct an analysis of the behavior of the effective diffusion coefficients determined from concentration profiles. Osmotic dehydration (OD) of apple was carried out at 40°C for 1 h, and the solution: sample ratio was 20:1 (w/w). Samples of 20-mm diameter were extracted from the dehydrated apple immediately after the OD process and after 4 and 24 h of storage at 25 °C. Moisture of these samples and soluble solids content were analyzed. Our results showed, after 1 h of OD, the outer layer of the apple sample lost 0.37 kg water/kg apple and gained 0.30 kg sucrose/kg apple. These values decreased toward the internal layers of the apple. A fine layer of greatly dehydrated cells was formed on the surface around the sample, which determined the mass transfer rate in the whole tissue. Smaller mass transport rates were observed in the development of concentration profiles during storage. Diffusion coefficients obtained for the outer layer after 1 h of OD were 1.53 × 10⁻¹⁰ and 1.05 × 10⁻¹⁰ m²/s for water and sucrose, respectively. The analysis of compositional profiles developed during osmodehydration was a useful tool to get a better understanding of the changes in the water activity of the outer layer of the apple tissue.     

Kinetics of Mass Transfer in Microwave Precooked and Deep-Fat Fried Ostrich Meat Plates

The aim of this study was to evaluate the effect of microwave precooking on mass transfer during deep-fat frying of ostrich meat plates. The influence of microwave power level, frying temperature, and time on mass transfer was determined. Among all treatments, the plates being precooked at 5.23 W/g of microwave power and then deep-fat fried at 135 °C had the minimum fat content. The effective moisture diffusivity ranged between 1.47 × 10⁻⁸ and 4.17 × 10⁻⁸ m²/s. Fat transfer rate constant was in the range of 0.024 and 19.708 s⁻¹. The activation energy obtained from Arrhenius plot for the effective moisture diffusivity ranged between 38.84 and 51.07 kJ/mol.     

Polysaccharide/Protein Nanomultilayer Coatings: Construction,Characterization and Evaluation of Their Effect on ‘Rocha’ Pear (<Emphasis Type="Italic">Pyrus communis</Emphasis> L.) Shelf-Life

Nanolayered coatings of κ-carrageenan, a polysaccharide with good gas barrier properties, and lysozyme, a protein with antimicrobial action, were in a first stage assembled on aminolysed/charged polyethylene terephthalate (PET) pieces, which acted as a support, by alternate five-layer deposition. This was performed to allow the characterization of the nanomultilayer system. PET aminolysis was confirmed by Fourier transform infrared spectroscopy and contact angle, and the subsequent layer adsorption on aminolysed PET surface was confirmed by absorbance, contact angle and SEM images. The water vapour permeability and the oxygen permeability (O₂P) of the five layers were found to be 0.013 ± 0.003 × 10⁻¹¹ and 0.1 ± 0.01 × 10⁻¹⁴ g m⁻¹ s⁻¹ Pa⁻¹, respectively. The nanomultilayer system was subsequently applied (without PET support) directly on ‘Rocha’ (Pyrus communis L.) fresh-cut pears and whole pears. Uncoated fresh-cut pears and whole pears presented higher mass loss, higher total soluble solids (TSS) and lower titratable acidity when compared with coated fresh-cut pears and whole pears. Uncoated fresh-cut pears also presented a darker colour. These results showed that the nanolayered coating assembled on the fruits’ surface has a positive effect on fruit quality and contributed to extend the shelf-life.     

Study of the diffusion coefficients of diphenylbutadiene and triclosan into and within meat

The migration of two chemicals, diphenylbutadiene and triclosan, was the target of this paper. Pork meat with different fat contents was prepared to study the influence of this parameter in the migration levels and to study the rate of diffusion of these migrants into the whole plastic/foodstuffs system and within the foodstuff. The whole system plastic/foodstuff diffusion coefficient (effective D) was calculated according to an equation based on the Fick’s Second Law, and D within the foodstuff (D _F) was calculated according to the Moisan equation. At 5 °C, D _F was 1.6 × 10⁻⁷ and 1.7 × 10⁻⁷ cm²/s for DPBD and triclosan, respectively. At 25 °C, D _F was 3.7 × 10⁻⁷ and 3.9 × 10⁻⁷ cm²/s for DPBD and triclosan, respectively. As expected, D within the pork meat is faster than the whole system D, which means that the interface plastic/foodstuff may be the limiting step for the mass transport of chemicals from the packaging to the foodstuff.     

Stability and Degradation Kinetics of Bioactive Compounds and Colour in Strawberry Jam during Storage

The effect of storage time and temperature on degradation of bioactive compounds such as ascorbic acid, anthocyanins, total phenols, colour and total antioxidant capacity of strawberry jam were investigated. The results indicated that lightness (L) value decreased significantly (p < 0.05) over 28 days of storage at 4 and 15 °C, with lower values measured at higher temperatures. Anthocyanins, ascorbic acid and colour degradation followed first-order kinetics where the rate constant increased with an increase in the temperature. The reaction rate constant (k) increased from 0.95 × 10⁻² day⁻¹ to 1.71 × 10⁻² day⁻¹ at 4 and 15 °C for anthocyanins. Similarly, k increased from 2.08 × 10⁻² day⁻¹ to 4.54 × 10⁻² day⁻¹ at 4 and 15 °C for ascorbic acid. In general, total antioxidant activity for strawberry jam samples stored for 28 days at 4 and 15 °C exhibited lower values as compared to control (day 0). The results showed greater stability of nutritional parameters at 4 °C compared to 15 °C.     

Determination of Rosmarinic Acid by High-Performance Liquid Chromatography and Its Application to Certain Salvia Species and Rosemary

This study describes a method development for the determination of rosmarinic acid (RA) by using a gradient high-performance liquid chromatography (HPLC) and its application to certain plant materials. The analysis was performed by utilizing a two solvents system [A: methanol/water/formic acid (10:88:2; v:v:v); B: methanol/water/formic acid (90:8:2; v:v:v)] on a reverse-phase column. The flow rate and injection volume were 1 ml min⁻¹ and 10 μl, respectively. Signals were detected at 280 nm. In addition, an internal standard (IS) technique was applied for the analysis of RA to increase precision, and propylparaben was employed for this purpose. The repeatability results as RSD% were 1.66, 1.17 and 1.26 for intra-day and 1.38 was for inter-day with the employment of (3.67 × 10⁻⁵ M) RA. A limit of linearity (LOL) was observed in a wide (1.13 × 10⁻⁵–5.65 × 10⁻⁴ M) concentration range. Linearity parameters were also examined in the range of 5.95 × 10⁻⁶–7.14 × 10⁻⁵ M RA, and very good correlation was observed. The limit of detection (LOD) and limit of quantification (LOQ) (for inter-day) were 1.60 × 10⁻⁶ M (signal/noise [S/N] = 3.3) and 4.80 × 10⁻⁶ M (S/N = 10), respectively. The method was applied to the extracts of certain Lamiaceae plants (Salvia candidissima Vahl. subsp. candidissima, S. sclarea L., S. verticillata L. subsp. verticillata and R. officinalis L.), and reasonable results were obtained.     

Co-production of Lactic Acid and <Emphasis Type="Italic">Lactobacillus rhamnosus</Emphasis> Cells from Whey Permeate with Nutrient Supplements

Lactic acid and cell production from whey permeate by Lactobacillus rhamnosus with different nutrient supplements were investigated in this study. Yeast extract was identified as the most effective nutrient affecting lactic acid production. Increase in inoculum size from 0.05% to 1% (v/v) resulted in a substantial increase in lactic acid productivity from 0.66 to 0.83 g L⁻¹ h⁻¹ (P < 0.001). The optimal temperature for lactic acid production was 37 °C, while the highest cell production was obtained at 42 °C. When whey permeate and yeast extract concentrations were 6.8% (w/v) and 3 g L⁻¹, respectively, lactic acid productivity reached 0.85 g L⁻¹ h⁻¹ after 48-h cultivation, which is 3.40 times of those without nutrient supplements.     

Benzyloxybenzaldehydethiosemicarbazone: Extractive Spectrophotometric Reagent for the Determination of Cu(II) in Food and Water Samples

Benzyloxybenzaldehydethiosemicarbazone (BBTSC) was prepared and developed a new method for the simple, highly selective, and extractive spectrophotometric determination of copper(II) with BBTSC at wavelength 370 nm. The metal ion formed a bluish green colored complex with BBTSC in acetate buffer of pH 5.0, which was easily extractable into n-butanol with 1:1(metal/ligand) composition. The method obeys Beer’s law in the range of 0.5–5.2 ppm. The molar absorptivity and Sandell’s sensitivity were found to be 1.5 × 10⁴ l mol⁻¹ cm⁻¹ and 0.00412 g cm⁻², respectively. The correlation coefficient of the Cu(II)–BBTSC complex was 0.998, which indicated an excellent linearity between the two variables. The repeatability of the method was checked by finding the relative standard deviation (RSD; n = 10), which was 0.377% and its detection limit 0.0204 μg ml⁻¹. The interfering effect of various cations and anions were also studied. The proposed method was successfully applied to the determination of copper(II) in food and water samples. Comparing the results with those obtained using an atomic absorption spectrophotometer tested the validity of the method.     

A Rapid Spectrophotometric Method for Trace Determination of Zinc

A simple, sensitive, and highly selective method is proposed for the determination of zinc(II) using a bis-azo dye, 2,6-bis(1-hydroxy-2-naphthylazo)pyridine as spectrophotometric reagent. At pH 7.8, in 50% (v/v) ethanol–water medium, the complex is found to obey Beer’s law up to 1.3 mg/L with an optimum concentration range between 0.19 and 1.0 mg/L. Sandell’s sensitivity of the color reaction was calculated to be 0.0011 μg cm⁻² with molar absorptivity of 6.0 × 10⁴ L mol⁻¹ cm⁻¹ at 560 nm. The optimum conditions for the determination of Zn(II) with the reagent were ascertained. The complexation at different pH was studied in water–ethanol medium. The composition of the complex is 1:2. The action of some interfering ions was verified, and the developed method applied successfully for the estimation of zinc levels in food and milk samples, and the results were then compared with those obtained by using AAS.     

Kinetics Modeling of Mass Transfer Using Peleg’s Equation During Osmotic Dehydration of Seedless Guava (<Emphasis Type="Italic">Psidium guajava</Emphasis> L.): Effect of Process Parameters

Peleg’s equation was used to study the effect of process parameters on kinetics of mass transfer in terms of solids gain and water loss during osmotic dehydration using 30–50% (w/w) sucrose solution at 30, 40 and 50 °C. The experimental data were successfully fitted employing Peleg’s equation with the coefficient of determination (R ²) higher than 0.88, the root mean square error, and the mean relative percentage deviation modulus (E) of less than 0.003% and 6.40% for all treatments, respectively. In all cases, initial mass transfer rate parameter (K ₁) decreased significantly (p < 0.05) as the solution concentration and solution temperature increased suggesting a corresponding increase in the initial mass transfer rate. Initial mass transfer rate followed an Arrhenius relationship which showed that solids gain had the highest temperature sensitivity (E _a = 21.93–33.84 kJ mol⁻¹) during osmotic dehydration. Equilibrium mass transfer parameter (K ₂) decreased significantly (p < 0.05) as solution concentration increased demonstrating that the equilibrium solid and water contents increased with increase in solution concentration. The equilibrium solid and water contents were also estimated adequately using Peleg’s equation (R ² > 0.78). The results of this work allow estimating the kinetics of mass transfer during osmotic dehydration in order to obtain products with determined solid and water contents.     

Shelf Life of Pretreated Dried Tomato

Determining the shelf life has become a factor of major importance in the development of foods designed to meet consumer demands in terms of quality and safety. The goal of the present study was to investigate the shelf life of vacuum-packed dried tomatoes, stored at both room and refrigeration temperature (4 °C) for a period of 180 days. The following determinations were performed during the storage period studied: microbiological analysis, instrumental color, lycopene, and ascorbic acid. Sorption isotherms were determined at both temperatures (room temperature and 4 °C). The microbiological quality of vacuum-packed dried tomatoes remained unchanged during 180 days for the refrigerated samples and 90 days for the samples stored at room temperature. The rate constant (k) of lycopene degradation of the refrigerated samples and the samples stored at room temperature was 3.209 × 10⁻⁵ and 12.994 × 10⁻⁵/day, respectively. The rate constant (k) of ascorbic acid degradation was 3.339 × 10⁻⁴/day for cold storage and 76.655 × 10⁻⁴/day for storage at room temperature. The tomatoes stored at room temperature were subjected to analysis over 90 days of storage, period after which both the appearance and sensory characteristics of the product fell below the levels of consumer acceptability. As for the tomatoes stored at refrigeration temperature, the original sensory characteristics were maintained throughout the entire storage period of 180 days.     

Estimation of the antioxidative properties of tocopherols – an electrochemical approach

The electrochemical behaviour of tocopherols on solid platinum electrodes, using cyclic voltammetry, linear sweep voltammetry and differential pulse voltammetry, in non-aqueous media, was studied. D-α-, D-γ-, and D-δ-tocopherol (E vitamins) provided well-defined voltammograms, each of them exhibiting a characteristic peak (respectively 0.550 V, 0.700 V and 0.750 V vs. a silver, silver chloride/chloride reference electrode). The differential pulse voltammograms were suitable for the electroanaytical determination, in the respective concentration ranges of (2 ×10⁻⁸÷1×10⁻⁵) mol l⁻¹, (2.2×10⁻⁸÷1.4×10⁻⁶) mol l⁻¹ and (2.2×10⁻⁸÷3.31×10⁻⁵) mol l⁻¹, of α-, γ-, δ- tocopherol. An electrochemical estimation of the tocopherols' antioxidative properties, related to the free radical 2,2′diphenyl-1-pycrilhydrazil was made. The maximum value of the characteristic peak of tocopherol decreased with DPPH concentration. Received: 26 July 1999 / Revised version: 1 October 1999     

Thin Layer Drying of African Breadfruit (Treculia africana) Seeds: Modeling and Rehydration Capacity

African breadfruit (ABF) seeds are underutilized plant resources, which have been reported to have high potential for novel food and industrial uses. The kinetics of moisture removal during air drying of the whole (WS) and dehulled (DS) seeds was studied at temperatures of 40–70 °C. Five empirical models were tested for predicting the experimental data. Drying of ABF seeds followed an exponential decay pattern, while drying predominantly took place during the falling rate periods. All the drying models predicted the experimental data above 90% accuracy while the Henderson–Pabis model gave the best fit (0.95 < r ² < 0.99) at most of the experimental conditions. Effective moisture diffusivity, D _eff, ranged from 3.65 to 7.15 × 10⁻⁹ m²/s and 3.95 to 6.10 × 10⁻⁹ m²/s for WS and DS, respectively. D _eff showed significant dependence on the moisture content (p < 0.01). Rehydration capacity of DS was not significantly affected by drying temperature while that of WS increased with drying temperature.