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.     

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 rheological properties of sweet potato flour dispersions

Korean sweet potato flour dispersions at different concentrations (6, 7, 8, 9, and 10%) were evaluated for their steady and dynamic shear rheological properties. The steady shear rheological properties showed that sweet potato flour dispersions at 25 °C showed a shear-thinning fluid (n=0.31–0.41) exhibiting a yield stress. The magnitudes of Casson yield stress (σ_oc), consistency index (K) and apparent viscosity (η_a,100) increased with an increase in concentration. Within the temperature range of 25–70 °C, the apparent viscosity obeyed the Arrhenius temperature relationship with high determination coefficient (R ²=0.97–0.99) with activation energies (Ea) ranging 0.015–0.024 KJ/mol. Both power law and exponential type models were used to establish the relationship between concentration and apparent viscosity (η_a). Magnitudes of G′ and G″ increased with an increase in concentration. G′ values were higher than G″ over the most of the frequency range (0.63–63 rad/s), being frequency dependent. The sweet potato flour dispersions did not closely follow the Cox–Merz rule at concentrations lower than 10%.     

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.     

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.     

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.     

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.     

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.     

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.     

COMPLEX VISCOSITY-TEMPERATURE MASTER CURVE OF CORNSTARCH DISPERSION DURING GELATINIZATION

Complex viscosity (η*) of 8% cornstarch dispersion during gelatinization at oscillatory frequencies (ω): 0.63–47.12 (rad s^?1) was independent of the heating rates: 1.6–6.0 (°C min^?1) when temperature was the independent variable. The influence of ω on η* was scaled by a frequency shift factor resulting in reduced complex viscosity (η*_R) versus temperature (60–95C) master curve. Similar η*_R master curves were derived for data on 6% and 3.5% dispersions. A modified Cox-Merz rule correlated the complex and apparent viscosity data, and a power law model described the effect of concentration of the gelatinized structures.     

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.     

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.     

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.     

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.     

Effect of pH on Apparent Viscosity of Wholemeal Oat Flour Water Dispersions

Research was undertaken to determine the effects of pH (1.5–12), stabilization time (1–3 h), and shear rate (200–1200 s^?1) on the apparent viscosity of wholemeal oat flour—water dispersions (10% w/w). Six oat cultivars, with different content of dietary fibre, especially of (1–3) (1–4) β-D-glucans, were used in this study. The study demonstrated instability of apparent viscosity of wholemeal oat flour dispersions. An increase of viscosity was observed with the increase in stabilization time. The range of viscosity changes was related with the dispersion pH level—the greatest range of changes was noted for dispersion with pH 9.5. Wholemeal oat flour dispersions, irrespective of the pH level, displayed pseudoplastic flow behaviour. A moderate to high significant linear correlations (Pearson, p ≤ 0.05) existed between the apparent viscosity and the (1–3) (1–4) β-D-glucans, soluble dietary fibre and total dietary fibre content. Measurements of apparent viscosity of wholemeal oat flour water dispersions can be used for the estimation of particular dietary fibre fractions content, especially of (1–3) (1–4) β-D glucans. With the application of suitable measurement conditions, the content of (1→3) (1→4) β—D glucans can be explained by the apparent viscosity of the oat flour dispersion (R² = 0.97–0.98).     

Effects of oligosaccharides on phase transition temperatures and rheological characteristics of waxy rice starch dispersion

BACKGROUND: The creation of starch‐based foods incorporated with functional ingredients such as probiotics is of great current interest in the food industry. This study aimed to investigate the effects of prebiotic oligosaccharides on the phase transition temperatures and rheological characteristics of waxy rice starch dispersions. Four oligosaccharides were applied to the rice starch dispersions: chitooligosaccharides, fructooligosaccharides, isomaltooligosaccharides and xylooligosaccharides. RESULTS: The addition of 125 g kg^?1 oligosaccharides elevated the onset and peak temperatures for gelatinisation of 200–400 g kg^?1 waxy rice starch dispersions. The temperature of the storage modulus (G′) for gelatinisation increased markedly on adding fructooligosaccharides to 200–300 g kg^?1 waxy rice starch. For gelatinisation of 300 g kg^?1 rice starch dispersion the effectiveness of the oligosaccharides in changing the above parameters was as follows: chitooligosaccharides > fructooligosaccharides > isomaltooligosaccharides > xylooligosaccharides. Moreover, their effectiveness was dependent on the amylose content, as illustrated by comparing waxy and non‐waxy rice starches (amylose contents 9–256 g kg^?1). Importantly, the logarithmic G′₉₅ change was linearly and negatively correlated with amylose content. CONCLUSION: The results suggest that oligosaccharide‐containing rice starch dispersions may potentially be used for the formulation of oligosaccharide‐containing starchy functional foods owing to the rheological changes of these starch dispersions. Copyright © 2011 Society of Chemical Industry     

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.     

Pasting Properties of Non‐waxy Rice Starch‐Hydrocolloid Mixtures

The swelling and pasting properties of non‐waxy rice starch‐hydrocolloid mixtures were investigated using commercial and laboratory‐generated hydrocolloids. The swelling power of the rice starch‐hydrocolloid mixtures was generally depressed at low concentration of hydrocolloids (0–0.05%), but increased directly with increasing hydrocolloid concentrations (0.05–0.1%). In gellan gum dispersion, the swelling power at 100°C was higher than that of control. The rice starch‐hydrocolloids mixtures showed shear‐thinning flow behavior (n = 0.26–0.49). Hydrocolloids except the exopolysaccharide from S. chungbukensis (EPS‐CB) increased apparent viscosity and consistency index (K) of rice starch dispersions, but decreased the n value. Hydrocolloids enhanced the trough and final viscosity of rice starch dispersions but EPS‐CB reduced the viscosity of rice starch pastes. Hydrocolloids lowered peak viscosity but addition of guar gum resulted in high peak viscosity, apparent viscosity, and consistency index of rice starch dispersions. Total setback viscosity appeared to be not affected by hydrocolloids at low concentration (0.05%). The hot and cold paste of the starch‐gellan gum mixture exhibited the highest viscosity values in the Brookfield viscometer.     

Rheological flow models of banana peel pectin jellies as affected by sugar concentration

In the present study, peel pectin jellies (PPJ) were isolated from banana peel Musa acuminata Colla (AAA, cv ‘Berangan’) varieties using water bath extraction; five jellies were produced, namely, PPJ_68%, PPJ_70%, PPJ_71%, PPJ_72%, and PPJ_76%. The effect of sugar content on the rheology of the PPJ and commercial fruit jelly was conducted at 25°C within 0.05–100 s^?1 shear rate. Flow behaviour was evaluated on the test dispersions while frequency sweeps (E_a) to obtain the viscoelastic (G’ and G”) were performed on the jellies. PPJ dispersion showed shear thinning flow behaviour, a good fit to the Casson model. Sugar concentration does not affect Casson parameters (K_c, K_oc, ?_ca, and σ_oc). Frequency sweep decreased as viscosity increased which revealed high dependence for both G’ and G”. Tan δ for PPJ was more than unity which showed that jelly has less elastic properties. PPJ with the lowest sugar concentration, PPJ_68%, conducted at a high shear rate showed it was compatible with validation of the Cox–Merz rule.     

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.