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.     

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.     

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 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.     

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     

Functional and dynamic rheological properties of acetylated starches from two cultivars of cassava

The starches derived from two different cultivars of cassava were modified with acetic anhydride. The increase in swelling power and solubility of the cassava starch (CS) pastes treated with different acetic anhydride concentration could be attributed to easier hydration, resulting from reduction of interaction between starch chains due to the substitution. The transition temperatures (T_o, T_p and T_c) and enthalpy of gelatinisation (ΔH) of acetylated CS, were determined. The values were lower than those of native starches. Rheological properties of CS pastes (5% w/w) as a function of the degree of substitution were evaluated in dynamic shear force measurements. Magnitude of storage modulus (G′), loss modulus (G′′) and complex viscosity (Eta*) of acetylated CS pastes were determined also. Dynamic moduli (G′, G′′ and Eta*) values of acetylated sweet cultivar pastes were generally higher than those of native starch whereas the acetylated samples of the bitter cultivar were lower than those of native starch. The magnitudes of G′ were greater than those of G′′ and Eta* at all frequencies (ω). The fact that all the tan δ (ratio G′′/G′) values (0.7–0.48 and 0.25–0.44) were less than one is an indication that the samples are more elastic than viscous. The acetylated starches could find promising industrial uses in food products like Lemon curd and Mayonnaise and other non‐food applications.     

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.     

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 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.     

Rheological properties of starches from grain amaranth and their relationship to starch structure

Amaranth starch (Amaranthus cruentus L. and Amaranthus hypochondriacus L.) in this investigation possessed a relatively small and uniform granule size of a type “A” pattern obtained by X‐ray diffraction, with the degree of crystallinity ranging from 24.5 to 27.9%. This was followed by work on steady and dynamic rheological properties on shear of seven native amaranth starches. Aqueous pastes (5% solids) exhibited shear‐thinning behavior, and the flow behavior was fitted with the Herschel–Bulkley equation (regression coefficients were over 0.99). Cultivar V69 showed much higher G′ (storage modulus) and G″ (loss modulus) than the other samples and produced a solid‐like gel, which could be attributed to the high amylose content of its network. Correlation analysis revealed that amylose content was positively correlated with G′ and negatively with the loss tangent (tan δ) of the material.     

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.     

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.     

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.     

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.     

VISCOELASTIC AND THERMAL CHARACTERISTICS OF VEGETABLE PUREE-BASED BABY FOODS

Viscoelastic properties of three commercial vegetable puree‐based baby foods (pea, corn and wax bean) were evaluated in the temperature range of 20 to 80C using dynamic oscillatory viscometry, and the thermal properties were evaluated using a standard differential scanning calorimeter (DSC) (?10 to 100C). Test samples behaved like viscoelastic fluids with consistently higher magnitudes of storage modulus (G′) as compared to loss modulus (G″) in an oscillatory frequency (ω) range between 0.628 and 62.800 rad/s. Both G′ and G″ versusωdata were well fitted by a power‐type relationship at all temperatures employed in the study. However, the derived power‐law parameters of G′ and G″ showed no consistent trends with temperature. Both pea and wax bean purees exhibited similar viscoelastic patterns with an increase in both G′ and G″ at 50C, somewhat coinciding with the initiation of starch gelatinization. However, the corn puree exhibited a stronger elastic characteristic with starch gelatinization occurring around 80C. The rheological measurements were well supported by the calorimetric data from the DSC.     

Effect of extraction conditions on composition,surface activity and rheological properties of protein isolates from flaxseed (Linum usitativissimum L)

Flaxseed protein isolates were prepared by micellisation (FM) and isoeletric precipitation (FI). The influence of preparation conditions on composition and functional properties was investigated. Contents of 0.6% phytic acid and 2.3% pentosans were found for FI, whereas FM was almost phytic acid‐free and had a low content of pentosans (0.6%). Chromatography and electrophoresis identified the 11S globulin (linin) as the main protein fraction in both isolates. Protein solubility, water‐ and oil‐binding capacities, emulsification and rheological properties of dispersions and gels were measured at pH 8 and 3. For the latter, interactions of protein with phytic acid and pentosans are highly probable. FI possesses a lower solubility (about 40–50%) and an overall higher water‐binding capacity than FM. For FI dispersions a higher storage modulus G′ than loss modulus G″ was measured, clearly pointing to the formation of protein networks. Moreover, FI formed stronger gels than FM (G′ about fivefold). The emulsifying activity, however, was distinctly lower for FI. These results point to enhanced complexation and aggregation of the isoelectric‐precipitated protein isolate. © 2002 Society of Chemical Industry     

RETENTION OF IODINE IN FORTIFIED PARBOILED RICE AND ITS PASTING CHARACTERISTICS DURING STORAGE

Iodine fortification, as potassium iodide (KI) or potassium iodate (KIO₃), in parboiled milled rice was investigated. The fortified parboiled milled rice (9–10% moisture content) contained 11.6 × 10^?2 mol KI per 100‐g salt or 9 × 10^?2 mol KIO₃ per 100‐g salt. The iodine‐fortified parboiled milled rice after dialysis retained 80.50–84.87% iodine, while the milled rice retained 97–100% iodine in the samples. Test on in vitro starch digestion showed that most iodine was released within 15 min of starch digestion. The iodine‐fortified and nonfortified parboiled milled rice showed significant higher pasting temperature, peak time and setback viscosity than normal milled rice. After storage for 5 months, iodine content in fortified parboiled milled rice decreased significantly (P ≤ 0.01), while iodine content in milled rice did not change during storage. For the rice stored at ambient temperature, the rapid visco‐analyzer amylograph viscosity (peak viscosity, trough viscosity and final viscosity) increased during the first 2 months and decreased during storage. Iodine did not affect these attributes of parboiled milled rice.