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.     

Effect of Molar Substitution on Rheological Properties of Hydroxypropylated Rice Starch Pastes

The steady and dynamic shear rheological properties of hydroxypropylated rice starch pastes (5%, w/w) were evaluated at different molar substitution (MS, 0.030‐0.142). The swelling power (35.5‐52.8 g/g) and solubility (8.19‐10.7%) values of the hydroxyproylated rice starches were higher than those of native rice starch (26.6 g/g and 7.78%) and increased with an increase in MS. The hydroxypropylated starch pastes at 25°C showed a pronounced shear‐thinning behavior (n = 0.33‐0.40) with Casson yield stress (σ_oc = 15.9‐31.7 Pa). The consistency index (K) and yield stress (σ_oc) values of the hydroxypropylated starch pastes were lower than those of the native starch, and increased progressively with an increase in MS. The apparent viscosity (η_a,500) obeyed the Arrhenius temperature relationship over the temperature range of 10‐55°C; the activation energies (E_a) of the hydroxypropylated starch pastes were in the range of 14.8‐18.5 kJ/mol, i.e. higher than that (14.1 kJ/mol) of the native starch. Storage (G′) and loss moduli (G′′) of hydroxypropylated starch pastes increased with an increase in MS, while tan δ (G′′/G′) values decreased, indicating that G′ rose more strongly than G′′ with increased MS.     

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 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 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.     

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.     

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).     

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 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.     

Characterization of the Pasting,Flow and Rheological Properties of Native and Phosphorylated Rice Starches

Phosphorylation of rice starch and its effects on the physiochemical properties of the starch were investigated. Phosphorylation was conducted using the oven heating method by heating mixtures of rice starch and monosodium dihydrogenphosphate at 120‐150°C for 0.5‐2 h, and the pasting, flow and rheological properties of the resulting starch phosphates were analyzed. Phosphorylation with substitution degrees of up to 0.12 was achieved by raising the reaction temperature to 140°C, but further increase in the temperature to 150°C caused a marked reduction in the degree of substitution. Phosphorylation resulted in significant declines in pasting temperature and setback, but increases in peak viscosity and breakdown. Suspensions of rice native starch and starch phosphates were shown to be non‐Newtonian, pseudoplastic fluids, exhibiting typical shear thinning. They also exhibited yield stress, the magnitude of which increased with the degree of phosphate substitution. Dynamic testing showed that phosphorylation resulted in a decrease in the temperature at which storage and loss moduli (G′ and G″) reached a peak during heating and a reduction in G′ during cooling. These results appeared to indicate that phosphorylation improved the shear stability of rice starch pastes and enhanced swelling of starch granules, but impeded starch retrogradation.     

Effect of resistant starch (RS3) addition on rheological properties of wheat flour

The rheological properties of wheat flour (WF) mixed with RS type 3 at different concentrations of RS (0, 5, 10, 15, and 20%) were examined. Steady and dynamic shear rheological tests indicated that the magnitudes of consistency index (K), apparent viscosity (η_a,100), dynamic modulus (G′ and G″), and complex viscosity (η*) of the WF–RS mixtures decreased with an increase in the mixing concentration of RS. G′ values of WF–RS mixture samples except for 5% RS as a function of aging time (14 h) at 5°C increased rapidly at initial stage and then reached a plateau region at long aging times. Increasing the RS concentration resulted in the decrease in plateau values. In general, these results suggest that the presence of RS in WF modifies the rheological properties, and that these modifications are dependent on the concentration of RS. The most pronounced changes of viscoelastic properties were observed for WF mixed with 20% RS.     

Comparison of the effect of sugars on the viscoelastic properties of sweet potato starch pastes

Viscoelastic properties of sweet potato starch (SPS) pastes (5% w/w) were studied in the presence of various sugars (sucrose, glucose, fructose, and xylose) at different concentrations (0, 10 and 20%) by small‐deformation oscillatory measurements. Dynamic frequency sweeps at 20 °C indicated that all SPS–sugar mixtures were more elastic than viscous with storage moduli (G′) higher than loss moduli (G′′) at all values of frequency with a frequency dependency. Dynamic moduli (G′ and G′′) values increased with the increase in sugar concentration from 10 to 20%. Changes in the dynamic moduli were more pronounced with xylose in comparison to the control (no sugar) and other sugars. G′ values as a function of ageing time (10 h) at 4 °C continuously increased with time during ageing without a plateau region. In general, G′ values of SPS–sugar mixtures during ageing decreased in the following order: pentose (xylose) > hexose (glucose and fructose) > control > disaccharide (sucrose), indicating that the xylose had the greatest ability in retarding retrogradation of SPS.     

Effect of Octenylsuccinylation on Rheological Properties of Corn Starch Pastes

Rheological properties of corn starch octenylsuccinate (OSA starch) pastes (5%, w/w), at different 1‐octenylsuccinic anhydride (OSA) contents (0, 1.0, 1.5, 2.0 and 2.5%, w/w) were evaluated in steady and dynamic shear. The OSA starch pastes had high shear‐thinning behaviors and their flow behaviors were described by power law, Casson, and Herschel‐Bulkley models. Magnitudes of consistency index (K, K_h) and yield stress (σ_oc, σ_h) increased with the increase in OSA content and the decrease in temperature. Over the temperature range of 10–50°C, the effect of temperature on apparent viscosity (η_a,100) was described by the Arrhenius equation. The activation energy values (E_a = 10.7–13.9 kJ/mol) of OSA starches were lower than that (E_a = 15.9 kJ/mol) of native starch. Dynamic frequency sweep test showed that both storage modulus (G′) and loss modulus (G′′) of OSA starch pastes increased with the increase in OSA content. Dynamic (η^*) and steady shear (η_a) viscosities of OSA starch pastes at various OSA contents did not follow the Cox‐Merz superposition rule.     

Dynamic rheological properties of rice flour‐starch blends

The dynamic rheological properties of blends of rice flour (RF) with six different commercial starches (sweet potato starch, potato starch, tapioca starch, waxy corn starch, hydroxypropylated potato starch, and hydroxypropylated tapioca starch) were evaluated. The magnitudes of storage modulus (G′) of all blend samples were higher than those of loss modulus (G′′) over most of the frequency range (0.63–62.8 rad · s⁻¹). In general, the dynamic moduli results of all blend samples showed that changes in G′ values were relatively greater than changes in G″ values after adding the starches when compared to RF. tan δ (ratio of G′′/G′) values (0.21–0.22) of the RF‐potato starch and RF‐hydroxypropylated potato starch blends were much lower than those (0.25–0.33) of other blends and RF, indicating that there is a more pronounced synergistic effect on the elastic properties of RF‐starch blend systems in the presence of potato starches.     

Rheological properties of batter systems containing different combinations of flours and hydrocolloids

The rheological properties of batters formulated using different combinations of wheat, corn, and rice flours with two types of hydrocolloids, namely methylcellulose (0.5%, 1% and 1.5%) or xanthan gum (0.2%), were studied. Control samples were formulated with combinations of flours without the added hydrocolloids. The effects of hydrocolloids on rheological characteristics of the batter systems were measured using a controlled stress rheometer at a temperature of 15 °C. The effects of hydrocolloids on dynamic viscoelastic parameters as functions of temperatures were evaluated. All the batters showed shear thinning behaviour with flow behaviour indices in the range 0.34–0.67. Addition of xanthan gum lowered the flow index values, imparting a higher degree of pseudoplasticity to the batter samples compared to methylcellulose. The consistency index of the control batter samples varied from 0.46 to 69.2 Pa sⁿ. Addition of xanthan gum or methylcellulose significantly increased the batter consistency index value. The gums changed the onset temperature of structure development, and the storage (G′_max) and loss moduli (G″_max) of the batter systems. However, no statistically significant effects were observed on the peak temperature of batter systems in which the G′ reached a maximum value. Xanthan gum increased both G′_max and G″_max, whereas at higher concentrations methylcellulose increased G′_max but lowered G″_max. Copyright © 2007 Society of Chemical Industry     

The rheological behaviour of low fat soy‐based salad dressing

Low fat soy‐based salad dressings were formulated with different oil levels (3%, 13% and 23%) and emulsifiers (whey protein concentrate, soy‐lecithin and sodium caseinate) using either blender or ultra‐turrax (UT) homogeniser. Results showed that the rheological behaviour of these samples were highly dependent on the oil content, emulsifiers and blending methods. The UT method produced samples with better viscosity and have droplet size of 2–100 μm. Samples containing higher oil level have higher viscosity, smaller droplet size, larger G′ and G″ values. All samples show a shear‐thinning effect and larger G′ than G″, indicating the elastic nature of the samples. A quantity Q(t)% was applied to estimate the elasticity and the values were found to be in the range 22.8–85.2%. G′ and G″ were found to decrease with increased temperature. However, tan δ increased slightly with temperature; the values ranged from 0.2 to 0.4 at 5 °C to 0.3–0.5 at 25 °C. Current results demonstrated that the formulated samples have good stability compared with commercial products.     

Rheological properties of cereal starch gels and Mesona Blumes gum mixtures

The effect of Mesona Blumes gum (MBG) was examined on steady and dynamic shear of MBG/rice starch and MBG/wheat starch gels. In addition, stress relaxation and creep tests were performed for two types of cereal starch gels. The flow curves of both MBG/starch gels exhibited pseudoplastic behavior at shear rates between 0.01 and 10 s⁻¹, and the data were fitted into the power law model (R² = 0.91–0.98). Dynamic mechanical spectrum showed that all gels were strong gels in frequency between 0.1 and 10 Hz. Stress relaxation data at different strains indicated a strain‐softening phenomenon for both gels. Data were fitted into Maxwell model (R² = 0.91–0.98). Creep curves were conducted at the shear stress 6.4 Pa within linear viscoelastic region of both MBG/starch gels. Data were fitted into Burgers model (R² = 0.91–0.98). Apparent viscosity η, storage moduli G′, equilibrium stress relaxation modulus G_e and zero apparent viscosity η₀ of MBG/rice starch gels decreased in the following order: 6/0>6/0.5>6/0.35>6/0.1 (starch/gum w/w). Whereas η, G′, G_e, and η₀ of MBG/wheat starch gels increased gradually along side the increase of MBG contents. The stress relaxation time λ of MBG/rice starch gels increased in the following order: 6/0<6/0.5<6/0.35<6/0.1 (starch/gum w/w) while λ of MBG/wheat starch gels decreased gradually with the increase of MBG level. The influence of MBG on two examined cereal starch is totally opposite.     

Dynamic rheology of wheat flour dough. II. Assessment of dough strength and bread‐making quality

Controlled stress rheometry revealed that differences in wheat flour dough strengths could be observed by means of dynamic rheological measurements in the region of higher stress amplitude (ie >100 Pa). At lower stress amplitude (τ_o) the values of elastic modulus G′ for weak doughs were higher than those for strong doughs, but they decreased substantially beyond 100 Pa stress amplitude (τ_o), such that the G′ values for strong doughs crossed over the G′ values for weak doughs. Beyond a critical value of stress amplitude (ie 100 Pa), true differences in dough strengths could be seen on the basis of their elastic characteristics, because at large deformations protein–protein interactions played a more dominant role in the rheological behaviour of flour doughs. Dynamic rheological analysis demonstrated a very weak inverse relationship (R² = 0.16) between the G′ values of flour doughs and loaf volume data for 12 wheat cultivars of diverse bread‐making performance. However, the G′ values of glutens showed significant positive relationships with bread‐making performance, explaining 73% of the variation in loaf volume. © 2002 Society of Chemical Industry     

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.     

Viscoelastic behavior of reconstituted Aloe vera hydrogels as a function of concentration and temperature

Viscoelastic properties for reconstituted A. vera hydrogels were evaluated in different ranges of concentration (0.2–1.6%, w/v) and temperature (30–60°C). The storage (G′) and loss (G″) moduli were well described by power function of the frequency (R² > 0.92). The combined effect of concentration and temperature was optimized for reconstituted gel formation, targeting maximum viscoelastic moduli (G₀′ and G′′₀) and minimum slope (n′ and n″) values using response surface methodology. The optimum condition selected was 1.6%, w/v at 30°C having higher gel strength [G′₀ (47.8 Pa.s^n′) and G″₀ (27.4 Pa.s^n′)], as well as minimum slope values [n′ (0.24) and n″ (0.08)]. Further, the effect of initial aging time on the viscoelastic moduli of optimized sample (1.6%, w/v at 30 ± 1°C) was noticed by fitting the intermediate creep ringing data to rheological models. The viscoelastic moduli (G′_J and G′_K) increased with aging time (0–180 min) for optimized A. vera hydrogel, as confirmed by Jeffrey’s and Kelvin-Voigt models. The obtained results suggested that optimized conditions for reconstituted A. vera gel formation could be useful to improve the gel strength which could be useful for various food applications.