Rheology of Rice Starch‐Sucrose Composites

The effect of sucrose at different concentrations (0, 10, 20 and 30%) on rheological properties of rice starch pastes (5% w/w) was investigated in steady and dynamic shear. The steady shear properties of rice starch‐sucrose composites were determined from rheological parameters for power law and Casson flow models. At 25°C all the starch‐sucrose composites exhibited a shear‐thinning flow behavior (n=0.25–0.44). The presence of sucrose resulted in the decrease in consistency index (K), apparent viscosity (η_a,100) and yield stress (σ_oc). Dynamic frequency sweeps at 25°C indicated that starch‐sucrose composites exhibited weak gel‐like behavior with storage moduli (G′) higher than loss moduli (G′′). G′ and G′′ values decreased with the increase in sucrose concentration. The dynamic (η*) and steady‐shear (η_a) viscosities at various sucrose concentrations did not follow the Cox‐Merz superposition rule. G′ values as a function of aging time (10 h) at 4°C showed a pseudoplateau region at long aging times. In general, the values of G′ and G′′ in rice starch‐sucrose composites were reduced in the presence of sucrose and depended on sucrose concentration.     

Rheological Properties of Rice Starch Dispersions in Dimethyl Sulfoxide

The steady and dynamic shear rheological properties of rice starches dispersed in dimethyl sulfoxide (DMSO) solution (90% DMSO‐10% water) were evaluated at various concentrations (7, 8, 9 and 10%, w/w). Rice starch dispersions in DMSO solution at 25°C showed a shear‐thinning flow behavior (n=0.44–0.60) and their consistency index (K) and apparent viscosity (η_a,100) increased with the increase in concentration. The apparent viscosity over the temperature range of 25–70°C obeyed the Arrhenius temperature relationship, indicating that the magnitudes of activation energy (E_a) were in the range of 11.7–12.7 kJ/mol. The Carreau model provided better fit on the shear rate‐apparent viscosity data than the Cross model. Dynamic frequency sweep test showed that both storage modulus (G′) and loss modulus (G′′) of rice starch dispersions increased with the increase in concentration. G′′ showed a higher dependence on frequency (ω) compared to G′ due to the higher G′′ slopes. All rice starch dispersions showed the plateau of G′ at high frequencies. Intrinsic viscosity of rice starch dispersions in DMSO was 104.1 mL/g.     

Steady and Dynamic Shear Rheology of Rice Starch‐Galactomannan Mixtures

Rheological properties of rice starch‐galactomannan mixtures (5%, w/w) at different concentrations (0, 0.2, 0.4, 0.6 and 0.8%, w/w) of guar gum and locust bean gum (LBG) were investigated in steady and dynamic shear. Rice starch‐galactomannan mixtures showed high shear‐thinning flow behaviors with high Casson yield stress. Consistency index (K), apparent viscosity (η_a,100) and yield stress (σ_oc) increased with the increase in gum concentration. Over the temperature range of 20–65°C, the effect of temperature on apparent viscosity (η_a,100) was described by the Arrhenius equation. The activation energy values (E_a = 4.82–9.48 kJ/mol) of rice starch‐galactomannan mixtures (0.2–0.8% gum concentration) were much lower than that (E_a = 12.8 kJ/mol) of rice starch dispersion with no added gum. E_a values of rice starch‐LBG mixtures were lower in comparison to rice starch‐guar gum mixtures. Storage (G′) and loss (G′′) moduli of rice starch‐galactomannan mixtures increased with the increase in frequency (ω), while complex viscosity (η*) decreased. The magnitudes of G′ and G′′ increased with the increase in gum concentration. Dynamic rheological data of ln (G′, G′′) versus ln frequency (ω) of rice starch‐galactomannan mixtures have positive slopes with G′ greater than G′′ over most of the frequency range, indicating that their dynamic rheological behavior seems to be a weak gel‐like behavior.     

Dynamic Rheology of Rice Starch‐Galactomannan Mixtures in the Aging Process

The effect of galactomananns (guar gum and locust bean gum) at different concentrations (0, 0.2, 0.4, 0.6 and 0.8%, w/w) on the dynamic rheological properties of aqueous rice starch dispersions (5%, w/w) was investigated by small‐deformation oscillatory measurements during aging. Magnitudes of storage (G′) and loss (G′′) moduli measured at 4°C before aging increased with the increase in gum concentration in the range of 0.2–0.8%. G′ and G′′ values of rice starch‐locust bean gum (LBG) mixtures, in general, were higher than those of rice starch‐guar gum mixtures. G′ values of rice starch‐guar gum mixtures as a function of aging time (10 h) at 4°C increased rapidly at initial stage and then reached a plateau region at long aging times. However, G′ values of rice starch‐LBG mixtures increased steadily without showing a plateau region. Increasing the guar gum concentration resulted in an increase in plateau values. The rate constant (K) for structure development during aging was described by first‐order kinetics. K values in rice starch‐guar gum mixtures increased with the increase in guar gum concentration. G′ values of rice starch‐galactomannan mixtures after aging were greater than those before aging.     

Rheological and thermal effects of galactomannan addition to acorn starch paste

Effect of galactomannans (guar gum and locust bean gum) at different concentrations on rheological and thermal properties of acorn starch pastes was examined. Steady and dynamic shear rheological tests indicated that the magnitudes of consistency index (K), apparent viscosity (η_a,100), Casson yield stress (σ_oc), dynamic moduli (G′, G″), and complex viscosity (η∗) of acorn starch-galactomannan mixtures were much higher than those of the control (0 g/100 g gum concentration), and that these values also increased with an increase in gum concentration. At temperatures ranging from 25 to 70 °C, the effect of temperature on η_a,100 was well described by the Arrhenius equation. In addition, DSC studies showed that the presence of galactomannans resulted in an increase in the transition temperatures (T_o, T_p, and T_c) and a decrease of the gelatinization enthalpy (ΔH). In general, these results suggest that the presence of galactomannans in acorn starch modifies the rheological and thermal properties, but that these modifications are dependent on the gum type and gum concentration.     

Steady and dynamic shear rheology of glutinous rice flour dispersions

The steady and dynamic shear rheological properties of Korean glutinous rice flour dispersions were evaluated at different concentrations (4, 5, 6, 7 and 8%). Glutinous rice flour dispersions at 25 °C showed a shear‐thinning behaviour (n = 0.487–0.522) with low magnitudes of Casson yield stresses (σ_oc = 0.056–0.339 Pa). The magnitudes of σ_oc, consistency index (K) and apparent viscosity (η_a,100) increased with the increase in concentration. The power law model was found to be more suitable than the exponential model in expressing the relationship between concentration and apparent viscosity. The apparent viscosity over the temperature range of 25–70 °C obeyed the Arrhenius temperature relationship, with high determination coefficients (R² = 0.982–0.998), indicating that the magnitudes of activation energies (E_a) were in the range of 9.05–11.89 kJ mol^?1. A single equation, combining the effects of temperature and concentration on η_a,100, was used to describe the flow behaviour of glutinous rice flour dispersions. Magnitudes of storage (G′) and loss (G′′) moduli increased with the increase in concentration and frequency. Magnitudes of G′ were higher than those of G′′ over most of the frequency range.     

Effects of cross‐linking on the rheological and thermal properties of sweet potato starch

Sweet potato starches were modified with three different concentrations of phosphorus oxychloride (POCl₃) (0.01, 0.02, and 0.03%, based on dry weight of starch) as a cross‐linking agent. The effects of crosslinking on rheological and thermal properties of sweet potato starch (SPS) pastes were evaluated. Cross‐linking considerably reduced the swelling power, consistency index (K), apparent viscosity (η_a), and yield stress (σ_oc) values of SPS, which significantly decreased with increase in POCl₃ concentration. The gelatinization temperature (T_p) and enthalpy (ΔH) values of the cross‐linked SPS, which were determined using differential scanning calorimetry, were higher than those of native SPS. Storage modulus (G′), loss modulus (G″), and complex viscosity (η*) of the cross‐linked SPS pastes determined using small deformation oscillatory rheometry, were higher than native starch, and they also decreased with increase in POCl₃ concentration from 0.01 to 0.03%. The tan δ (ratio of G″/G′) values (0.15–0.19) of the cross‐linked SPS samples were much lower than that (0.37) of the native SPS, indicating that the elastic properties of the SPS pastes were strongly influenced by modifications from cross‐linking. Finally, Cox–Merz plots showed that η* was much higher than η_a for the cross‐linked SPS pastes.     

Rheological behaviors of hydroxypropylated sweet potato starches influenced by guar,locust bean,and xanthan gums

This study examined the steady flow and dynamic rheological behaviors of hydroxypropylated sweet potato starch (HPSPS) pastes mixed with guar gum (GG), locust bean gum (LBG), and xanthan gum (XG) at different concentrations (0, 0.3, and 0.6%). The HPSPS–gum mixtures had higher shear‐thinning fluid characteristics than the control (0% gum) at 25°C. The addition of the gums resulted in an increase in the consistency index (K) and apparent viscosity (η_a,100). The dynamic moduli (G′, G″) and complex viscosity (η*) values of the HPSPS–gum mixtures were higher than those of the control, and they increased with an increase in gum concentration. In particular, the presence of XG at 0.6% in the HPSPS–gum mixture systems gave rise to the greatest viscoelastic properties among the gums examined at different concentrations. The tan δ (ratio of G″/G′) values (0.35–0.57) of the HPSPS–GG and HPSPS–XG mixtures were much lower than those of the control (0.82) and HPSPS–LBG (0.88–1.06), indicating that the elastic properties in the HPSPS–gum mixture systems were strongly affected by the additions of GG and XG. These steady flow and dynamic rheological parameters indicated there were synergistic interactions between the HPSPS and gums. The synergistic effects of the gums and modified starch were hypothesized by considering the molecular incompatibility and molecular interactions between the gums and HPSPS.     

Rheological properties of polysaccharides from Pholiota nameko with different temperature extraction: Concentration,pH, temperature,and saltion

Cold and hot water extracted polysaccharides (CW-PNPs and HW-PNPs) were isolated from Pholiota nameko. The rheological properties of PNPs were investigated by steady shear and oscillatory rheological measurements. The PNPs exhibited typical non-Newtonian and shear-thinning behavior, which are affected by PNP concentration, temperature, pH value, salt ion, and concentration. Specifically, the apparent viscosity of the two PNPs solutions at concentration of 1% (w/w) was shown as HW-PNPs > CW-PNPs. The apparent viscosity of PNPs decreases under acidic and alkaline conditions and when the temperature rises; K⁺ and Na⁺ cause the apparent viscosity of CW-PNPs to decrease, while Ca²⁺ and Al³⁺ are opposite. The addition of four different salt ions all caused the apparent viscosity of the HW-PNPs to decrease. The results of dynamic rheological experiments show that G′ and G″ showed slightly frequency dependency with G′ exceeding G″ throughout the accessible range of frequency for CW-PNPs and HW-PNPs.     

Measurement of dynamic rheology during ageing of gelatine–sugar composites

The effect of sugars (sucrose, glucose and xylose) at different concentrations (0, 10, 20, 30, 40 and 50%) on the dynamic rheological properties of gelatine (2% w/w) was investigated during ageing. Storage moduli (G′), when measured at 5 °C, decreased with increasing concentration of added sugar. Xylose was found to induce the greatest reduction in the values of G′. G′ values, measured as a function of ageing time (10 h) at 5 °C, increased rapidly at the initial stage and then reached a pseudoplateau region after long ageing times. Increasing the sugar concentration resulted in a decrease in the pseudoplateau values. The rate constant (K) for structure development of gelatine during ageing was described by apparent first‐order kinetics. G′ and K values in gelatine–sugar composites increased in the following order: xylose < glucose < sucrose. The magnitudes of G′ at the end of ageing were much greater than those of G′′, showing a small dependence (slope = 0.005–0.088) on frequency (ω).     

Buckwheat and Millet Affect Thermal,Rheological, and Gelling Properties of Wheat Flour

Buckwheat (BF) and millet (MF) are recommended as healthy foods due to their unique chemical composition and health benefits. This study investigated the thermal and rheological properties of BF‐WF (wheat flour) and MF‐WF flour blends at various ratios (0:100 to 100:0). Increasing BF or MF concentration led to higher cold paste viscosity and setback viscosity of pasting properties gel adhesiveness, storage modulus (G′) and loss modulus (G″) of dynamic oscillatory rheology, and yield stress (σ₀) of flow curve of WF. BF and MF addition decreased peak viscosity and breakdown of pasting, gel hardness, swelling volume, and consistency coefficient (K) of flow curve of WF. Thermal properties of the blends appeared additive of that of individual flour. Nonadditive effects were observed for some property changes in the mixtures, and indicated interactions between flour components. This may provide a physicochemical basis for using BF and MF in formulating novel healthy products.     

Physicochemical and Gelatinization Properties of Starches Separated from Various Rice Cultivars

Morphological, viscoelastic, hydration, pasting, and thermal properties of starches separated from 10 different rice cultivars were investigated. Upon gelatinization, the G′ values of the rice starch pastes ranged from 37.4 to 2057 Pa at 25 °C, and remarkably, the magnitude depended on the starch varieties. The rheological behavior during gelatinization upon heating brought out differences in onset in G′ and degree of steepness. The cultivar with high amylose content (Goami) showed the lowest critical strain (γ_c), whereas the cultivars with low amylose content (Boseokchal and Shinseonchal) possessed the highest γ_c. The amylose content in rice starches affected their pasting properties; the sample possessing the highest amylose content showed the highest final viscosity and setback value, whereas waxy starch samples displayed low final viscosity and setback value. The onset gelatinization temperatures of the starches from 10 rice cultivars ranged between 57.9 and 64.4 °C. The amylose content was fairly correlated to hydration and pasting properties of rice starches but did not correlate well with viscoelastic and thermal characteristics. The combined analysis of hydration, pasting, viscoelastic, and thermal data of the rice starches is useful in fully understanding their behavior and in addressing the processability for food applications.     

Dynamic Rheological and Thermal Properties of Acetylated Sweet Potato Starch

Dynamic rheological and thermal properties of acetylated sweet potato starch (SPS) pastes (5%, w/w) were evaluated as a function of the degree of substitution (DS). The transition temperatures (T_o, T_p and T_c) and enthalpy of gelatinization (ΔH) of acetylated SPS, which were determined using differential scanning calorimetry, were lower than those of native starch, and significantly decreased with an increase in DS. Magnitudes of storage modulus (G′), loss modulus (G′′) and complex viscosity (η*) of acetylated SPS pastes were determined using a small‐deformation oscillatory rheometer. Dynamic moduli (G′, G′′ and η*) values of acetylated SPS pastes except for 0.123 DS were higher than those of native starch, and they also decreased with an increase in DS. The tan δ (ratio of G′′/G′) values (0.37–0.39) of acetylated SPS samples were lower than that (0.44) of native starch and no significant differences were found among acetylated SPS samples, indicating that the elastic properties of SPS pastes were affected by acetylation but did not depend on DS. The G′ values of acetylated SPS during aging at 4°C for 10 h were much lower than those of native starch, showing that the addition of acetyl groups produced a pronounced effect on the retrogradation properties of SPS.     

Effect of hydroxypropylation on physical and rheological properties of sweet potato starch

Sweet potato starches (SPS) were hydroxypropylated to evaluate the effect of molar substitution (MS, 0.042-0.153) on the rheological properties, thermal properties, freeze-thaw stability, paste clarity, and gel strength of hydroxypropylated sweet potato starches (HPSPS). The swelling power and solubility values of HPSPS were higher than those of native sweet potato starch (SPS) and increased with an increase in MS. The transition temperatures (T_o, T_p, and T_c), and enthalpy (ΔH) of gelatinization of HPSPS were lower than those of native SPS, and significantly decreased with an increase in MS.Rheological properties of HPSPS pastes were measured under the conditions of steady and dynamic shear. Their consistency index (K), apparent viscosity (η_a,100), Casson yield stress (σ_oc), complex viscosity (η*), and dynamic moduli (G′ and G″) values decreased with an increase in MS, while their flow behavior index (n) and tan δ (ratio of G″/G′) values increased. The dependence of apparent viscosity on temperature followed the Arrhenius model for all samples. The paste clarity of HPSPS paste was more pronounced with increasing MS of hydroxypropyl groups. The HPSPS gels showed lower gel strength and also better freeze-thaw stability with a significant decrease in syneresis (g/100 g) compared to native SPS.     

Influence of guar gum addition on physicochemical,microbial, rheological and sensory properties of stirred yoghurt

This study investigated the effects of adding guar gum (0, 0.6 and 0.8 g/100 mL) on the physicochemical, microbial, rheological and sensory properties of stirred yoghurt. Incorporation of guar gum into the yoghurt significantly affected the pH and colour, but did not significantly influence the lactic acid bacteria counts. The magnitudes of apparent viscosity (η_a,100), consistency index (K), yield stress (σ_oc), storage modulus (G′) and loss modulus (G″) for yoghurt samples containing guar gum (0.6–0.8 g/100 mL) were significantly greater than those for the control (without guar gum), indicating that guar gum can improve the steady and dynamic shear rheological properties of yoghurt.     

The Effects of Different Gums and Their Interactions on the Rheological Properties of a Dairy Dessert: A Mixture Design Approach

In this study, the steady and dynamic rheological properties of the dairy dessert samples (puddings) containing carrageenan, alginate, guar and xanthan gums and their combinations were investigated in a model system, and mixture design was utilized to observe the effects of the gums and their interactions. The flow behaviour of the pudding samples fitted to the Ostwald de Waele model (R ²?>?0.98). All the samples exhibited a gel structure with their higher G′ (storage modulus) values than the G″ (loss modulus) values. Carrageenan was the most effective hydrocolloid on both the steady and dynamic rheological parameters of the dairy dessert samples. On the other hand, alginate had relatively smaller effect. Furthermore, 30 pudding samples containing different gum or gum combinations were classified into two groups (A and B) by using principal component analysis (PCA). Samples containing more than 33% carrageenan in their formulations made up the group A which positively correlated to K (consistency index), η ₅₀ (apparent viscosity at shear rate 50 s^?1), G′, G″, G* (complex modulus) and η* (complex viscosity) values.     

APPLICATION OF WLF AND ARRHENIUS KINETICS TO RHEOLOGY OF SELECTED DARK-COLORED HONEY

The rheological properties of Common Black Horehound, Globe Thistle, and Squill types of dark‐colored Jordanian honey were examined. The types of honey used were identified via assessing the source of nectar using pollen analysis (Melissopalynology). The apparent viscosity, η, was measured as a function of the shear rate, γ. In addition, the apparent viscosity was measured, at constant shear rate (6.12 s^?1), as a function of shearing time. Newton's law of viscosity (i.e., τ=ηγ) was found to adequately (R²～ 0.99) describe the flow behavior of honey samples. The apparent viscosity was found to decrease with temperature, and the temperature dependence of viscosity was contrasted versus both Arrhenius model (η=η_oe^Ea/RT) and WLF model (η/η_G= 10 (C₁(T–T)/C₂+(T–T_G))). Although Arrhenius kinetics may fit the viscosity versus temperature data for the examined types of honey, nevertheless, it gives a relatively high value of activation energy that is quite comparable with, if not even larger than, that of a typical chemical reaction. On the other hand, WLF‐model was found to adequately describe the data while at the same time it gives quite reasonable values of both T_G and η_G, which are in agreement with those cited in literature.     

Rheology of Mixed Systems of Sweet Potato Starch and Galactomannans

The effect of galactomannans (guar gum and locust bean gum) at different concentrations (0, 0.2, 0.4 and 0.6%, w/w) on rheological properties of sweet potato starch (SPS) was studied. The flow behaviors of SPS‐galactomannan mixtures were determined from the rheological parameters of power law and Casson models. The SPS‐galactomannan mixtures had high shear‐thinning fluid characteristics (n = 0.30‐0.36) exhibiting yield stress at 25°C. The presence of galactomannans resulted in the increase in consistency index (K), apparent viscosity (η_a,100) and Casson yield stress (σ_oc). In the temperature range of 25‐70°C, the mixtures followed the Arrhenius temperature relationship. Dynamic rheological tests at 25°C indicated that the SPS‐galactomannan mixtures had weak gel‐like behavior with storage moduli (G′) higher than loss moduli (G") over most of the frequency range (0.63‐62.8 rad/s) with frequency dependency. The magnitudes of dynamic moduli (G′, G" and η*) of the SPS‐galactomannan mixtures were higher than those of the control (0% gum), and increased with an increase in gum concentration. The tan δ (ratio of G"/G′) values (0.41‐0.46) of SPS‐guar gum mixtures were much lower than those (0.50‐0.63) of SPS‐locust bean gum mixtures, indicating that there was a more pronounced effect of guar gum on the elastic properties of SPS.     

Rheological properties of selected gum solutions

Gums are integral ingredients in fluid foods used for controlling viscosity and mouthfeel. Advances in rheological instrumentations permits enhanced evaluations of the viscoelastic properties of fluids. Rheological properties of twelve gum solutions were investigated at concentrations of 0.05%, 0.1%, and 0.5%. The viscous (η″) and elastic (η″) components of the complex viscosity η1, elastic yield stress, and tan δ were measured as functions of oscillatory shear. Konjac exhibited the highest η′ and η″ components among all gums at 0.5% and 50 s⁻¹. Gum Arabic, methylcellulose and pectin, exhibited the least η′ and no η″ component under the same conditions. Konjac exhibited greatest elastic yield stress, whereas microcrystallinecellulose had the least. Modeling results showed that rheological properties of CMC were characterized by an exponential relationship, whereas riota-carrageenan and xanthan were described by a power type relationship. A substantial increase in tan δ was observed for most 0.5% gums solutions at shear rates beyond 10 s⁻¹, indicating a shift from a visco-elastic regime to a purely viscous one. For gums that showed substantial visco-elasticity, peak tan δ values ranged from 5.7 to 68.3.     

Steady and dynamic oscillatory shear rheological properties of ketchup-processed cheese mixtures: Effect of temperature and concentration

The steady and dynamic shear properties of ketchup-processed cheese (K-PC) mixtures were investigated at different temperatures (10-50 °C) and PC concentrations (0-30%). The K-PC mixtures showed a shear-thinning behavior with low magnitudes of yield stress. The consistency coefficient (K) and apparent viscosity (η₅₀) decreased with increase in temperature and concentration. The mixtures followed the Arrhenius temperature relationship, indicating that the magnitudes of activation energies (E_a) were in the range of 8.83-17.16 kJ mol⁻¹. Storage (G′), loss (G′′) and complex (G∗) modulus increased with increase in frequency while complex viscosity (η∗) decreased. The K-PC mixtures at concentrations of 0-15% exhibited weak gel-like behavior. Increase in the PC concentration resulted in a decrease in G∗, G′, G′′ and η∗ up to the 15% of PC concentration, showing a plateau value between 0% and 30% concentrations. Cox-Merz rule was not applicable to K-PC mixtures.