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.     

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.     

Effects of yellow mustard mucilage on functional and rheological properties of buckwheat and pea starches

The effects of yellow mustard mucilage (YMM) on the functional and rheological properties of buckwheat and pea starch were studied. Addition of YMM resulted in a marked increase of peak viscosity for both buckwheat and pea starches. Dynamic oscillation measurements showed that the storage modulus (G′), loss modulus (G″) and dynamic viscosity (η*) of buckwheat and pea starches were increased but tangent δ was decreased by addition of YMM. The gel textures of both starches were markedly changed by the presence of YMM, which resulted in an increase of hardness, adhesiveness and chewiness but a decrease of resilience. Differential scanning calorimetry showed that the presence of YMM slightly increased melting enthalpy (ΔH) and the phase transition temperature range (T_c–T_o) of buckwheat starch but these did not change much for pea starch. Addition of YMM–locust bean gum mixture (9:1) similarly increased the viscosity of buckwheat and pea starches but decreased gel hardness. The swelling powers of both starches and solubility of buckwheat starch were slightly decreased in the presence of YMM. Addition of YMM slowed the syneresis of buckwheat and pea starch gels.     

Influence of modified starches on properties of gluten-free dough and bread. Part I: Rheological and thermal properties of gluten-free dough

The aim of this study was to analyze the influence of chemically modified starches (HDP and ADA) and high amylose corn starch (HACS) on the rheological and thermal properties of gluten-free dough based on corn and potato starches with pectin and guar gum. The results indicate that the dough with the addition of modified starch behaves as weak gel, the value of storage modulus G′ significantly depends on the frequency and the values of tan δ = G″/G′ range from 0.32 to 0.49. Significant influence of hydroxypropylated distarch phosphate (HDP) on the viscoelastic properties of dough was observed. The share of modified starch in the system caused a decrease of the instantaneous and viscoelastic compliance. It also influenced the retardation time and zero shear viscosity. The application of modified starches (HDP and ADA) for dough preparation did not have much impact on the pasting characteristics. However, significant reduction of the onset and end viscosities were found for high amylose starch (HACS). Thermograms obtained for individual dough systems were characterized by the presence of two peaks, associated with the existence of two different starches in the system. No significant effect of modified starch on the onset temperature (T_O) and only a slight effect of HACS starch on gelatinization enthalpy were observed. However, the level of addition of individual starch affected peak and end (T_E) temperatures, depending on the type of preparation.     

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.     

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 cross‐linking on some properties of potato (Solanum tuberosum L.) starches

Starches separated from different potato cultivars were modified using two different cross‐linking agents: epichlorohydrin (EPI) and phosphoryl chloride (POCl₃) at different concentrations (1.0 and 2.0 g kg^?1 POCl₃; 2.5, 5.0 and 10 g kg^?1 EPI). Differential scanning calorimetry, rheological and retrogradation measurements were performed to characterise the influence of cross‐linking on the properties of potato starches. Cross‐linking considerably reduced swelling power, solubility, water‐binding capacity and paste clarity. The decrease became greater as the reagent concentration increased. The starches treated with 1.0 g kg^?1 POCl₃ exhibited exceptionally higher swelling power than their counterpart native starches. Neither cross‐linking agent caused any change in morphology of the starch granules. Studies on the phase transitions associated with the gelatinisation showed significantly higher values for the onset temperature (T_o), peak temperature (T_p), conclusion temperature (T_c) and enthalpy of gelatinisation (ΔH_gel) for the cross‐linked starches than the native starches. Starches treated with both the reagents showed lower peak storage modulus (G′) and loss modulus (G″) than their native counterparts. The tendency of the starch pastes towards retrogradation increased considerably with increases in storage duration. However, the starches treated with 1 g kg^?1 POCl₃ exhibited much lower syneresis than the other cross‐linked starches. Copyright © 2006 Society of Chemical Industry     

Physicochemical properties of Pinhão (Araucaria angustifolia, Bert, O. Ktze) starch phosphates

Physicochemical properties of pinhão (seeds of Paraná pine) starch phosphates were evaluated and compared to corn starch phosphates. The phosphorylation process used yielded starch phosphates with three different degrees of substitution (DS): low (0.015), medium (0.07) and high (?0.12). Medium and high DS starch phosphates had higher cold water binding capacity, swelling power, and paste clarity, but lower paste syneresis (at 5 °C and after freeze-thaw cycles) than native starches (P<0.05). Low, medium, and high DS corn starches had higher solubility than native starches (3.8-, 8-, and 6-fold higher; P<0.05), but the solubility of pinhão starch increased only in medium DS starch phosphates (3-fold higher; P<0.05). Low DS starch phosphates had viscosity curves similar to native starches. In contrast, medium and high DS starch pastes had peak viscosity at room temperature, reached the minimum viscosity when heated to 95 °C, and had low setback.     

Starch–cassia gum interactions: A microstructure – Rheology study

We present for the first time the interactions of starch and cassia gum – a novel galactomannan recently approved for use in food processing. Viscoelastic, pasting and microstructural characterization of various starches (waxy; high amylose; normal; cross-linked waxy corn starch; potato starch) containing different levels of the cassia gum was carried out. Significant changes were observed in the morphology of granule remnants formed during gelatinization in the starch pastes prepared with and without the addition of cassia gum. The freeze-dried starch–cassia gum pastes presented a shrunken and tight arrangement of the starch granule remnants, when studied by scanning electron microscopy. A significant reduction in the granule remnant size was also calculated using laser diffraction particle size analysis. The extent of interaction with cassia gum differed significantly among the various starch types. All the unmodified corn starches recorded an increase in peak viscosity at all levels of the cassia gum addition. An increase in the final viscosity of these starches was also observed by the addition of cassia gum, with high amylose and normal corn starch showing the maximum. Similarly, the extent of breakdown and setback viscosity also differed among the different starch types. Ranges of dynamic rheological measurements (temperature, time and frequency sweeps) were performed within the viscoelastic zones. Rheological parameters, such as storage modulus (G′), loss modulus (G″) and the gelatinization temperature (T_gel), of the corn starches during the heating cycle were observed to increase, when cassia gum was present at lower levels. The starch–gum systems also exhibited higher tan δ values during both the heating and the cooling cycles, indicating the dominance of the viscous modulus. The G′ and G″ of all the corn starch gels containing cassia gum showed higher values throughout the frequency sweep range. However, the increase in G′ and G″ of different starches was not always consistent with the increase in cassia gum levels. The changes in rheological behaviour during storage of the starch gels, aged on the plate of the rheometer and then studied through time sweeps at 5 °C and frequency sweeps at 25 °C, suggested that the starch gels containing cassia gum had less pronounced changes in the rheological parameters than had their control counterparts.     

Steady and dynamic shear rheology of sweet potato starch–xanthan gum mixtures

The effect of xanthan gum at different concentrations (0.2–0.6% w/w) on the rheological properties of sweet potato starch (SPS) pastes was evaluated under steady and dynamic shear conditions. The presence of xanthan resulted in an increase in the consistency index and vane yield stress of SPS. The effect of temperature on the apparent viscosity of SPS–xanthan mixtures is well described by the Arrhenius equation. Dynamic moduli (G′, G″, and η^*) values of the mixtures increased with an increase in xanthan concentration while the tan δ values decreased. The addition of xanthan appeared to contribute to the elastic properties of the weak network of the SPS pastes. The structure development rate constant (k) of gelation during ageing was strongly influenced by the presence of xanthan. This suggests that the phase separation process caused by the incompatibility phenomena between the amylose component in starch and xanthan can increase the elastic characteristics of the SPS–xanthan mixtures.     

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.     

A comparison of native and oxidized normal and waxy corn starches: Physicochemical, thermal, morphological and pasting properties

The effect of sodium hypochlorite on the physicochemical and functional properties of normal and waxy corn starches was investigated in this study. It was found that both carboxyl and carbonyl contents of oxidized starches from normal corn were higher than those of waxy corn. The introduction of carboxyl and carbonyl groups resulted in lower amylose content and swelling power. Both amylose and amylopectin were oxidized and degraded during oxidation but amylose was more susceptible to oxidation. Studies conducted on paste clarity revealed that the percentage transmittance increased after oxidation. The morphology of the starches was not altered after oxidation. Thermal properties measured by differential scanning calorimeter, showed that oxidation reduced transition temperatures (onset temperature, T_o; peak temperature, T_p; and conclusion temperature, T_c), gelatinization and retrogradation enthalpies of both normal and waxy corn starches. The retrogradation tendency was reduced after oxidation both in normal and waxy corn starches. Oxidation produced waxy starch with significantly higher peak (P_V), trough (T_V), breakdown (B_V), final (F_V), and setback viscosity (S_V) as demonstrated by using a rapid visco analyzer. Oxidation reduced the pasting temperature of both normal and waxy corn starches. Also, the principal component analysis (PCA) study was conducted to find the overall variations among the oxidized starches studied. Together, the first two components represent 88.7 g/100 g of the total variability.     

Hydroxypropylation of pigeon pea (Cajanus cajan) starch: Preparation, functional characterizations and enzymatic digestibility

Hydroxypropyl starch derivatives were prepared from pigeon pea starch (NPPS) which is an unconventional starch source. Functional parameters and characterization of both native and modified starches were carried out. The starch granules appeared oval or elliptical in shape with sizes ranging from 7 to 40 μm in width and 10 − 30 μm in length. Hydroxypropylation did not alter the shape of the starch granules in a pronounced way. Generally, the x-ray diffractograms of native pigeon pea starch showed the “A” pattern. However, slight reductions in the diffraction intensity of starches after modification were observed. At all temperatures studied (30-90 °C), swelling and solubility of hydroxypropylated starches were higher than the NPPS. Progressive increases in swelling capacity and solubility were observed as the molar substitution (MS) increased among the hydroxypropylated starches. Hydroxypropylation reduced starch paste turbidity on storage. Also, studies showed that syneresis reduced after hydroxypropylation. In addition, syneresis reduced as the MS of the hydroxypropyl starches increased. The results indicate that pasting temperature and peak temperature reduced after modification but peak viscosity increased in hydroxypropylated starch derivatives compared with the native starch. Setback reduced in hydroxypropylated starches compared with the native starch. Enthalpy of gelatinization and percentage retrogradation reduced after hydroxypropylation and progressive reductions were observed as the MS increased among the starch derivatives. Hydroxypropylation increased enzymatic digestibility.     

Ultrasound-treated starch: SEM and TEM imaging,and functional behaviour

Potato, wheat, corn and rice starch granules were suspended in water or ethanol and sonicated at frequency of 20 KHz and power 170 W for 30 min. The effect of ultrasonic treatment on starch structure was assessed on the basis of blue value (BV), A₆₈₀/A₅₄₅ ratio and λ_max determinations. The results showed that modification of starches in both solvents led to the reduction of all parameters connected with the starch–iodine complex. However, depolymerization of starch was higher when it was sonicated in water than in ethanol (e.g. BVs for potato starch: native and sonicated in water and ethanol were equal, respectively, 0.306, 0.275, and 0.279). Starch granules were also observed under scanning and transmission electron microscopes. The main effects of ultrasonic action were cracks and depressions on the surface of granules, which were especially well seen in the case of potato and wheat starches. Ultrasonic treatment, especially in water, influenced functional properties of starch causing an increase of fat and water absorption, least gelling concentration (except potato starch), solubility and swelling power, and a decrease of starch paste viscosity. Effect of ultrasounds on clarity of pastes was rather small, except potato starch for which its value increased from 70.3 to 82.5% after sonication in water.     

Some properties of potatoes and their starches II. Morphological,thermal and rheological properties of starches

The physico-chemical, morphological, thermal and rheological properties of the starches separated from different potato cultivars (Kufri Jyoti, Kufri Badshah and Pukhraj) were studied. The starches separated from the mealier cultivars (Kufri Jyoti and Kufri Badshah) showed lower transition temperatures (T_o; T_p and T_c), peak height indices (PHI), and higher gelatinization temperature range (R) and enthalpies of gelatinization (ΔH_gel) than the starch from the least mealy cultivar (Pukhraj). Swelling power, solubility, amylose content and transmittance values were observed to be higher for Kufri Jyoti and Kufri Badshah potato starches, while turbidity values were lower for these starches. The rheological properties of starches, measured using a dynamic rheometer, showed significant variation in the peak G′, G″ and peak tan δ values. Kufri Badshah and Kufri Jyoti starches showed higher peak G′, G″ and lower peak tan δ values than Pukhraj starch during heating and cooling cycles. Kufri Jyoti and Kufri Badshah starches showed higher breakdown in G′ than starch from the Pukhraj potato cultivar. The large-sized granules of the starches from Kufri Badshah and Kufri Jyoti appeared to be associated with higher values of peak G′ and G″ and consistency coefficient. Starch from the least mealy cultivar (Pukhraj) showed higher retrogradation, which increased progressively during storage at 4 °C for 120 h.     

A comparison of native and acid thinned normal and waxy corn starches: Physicochemical, thermal, morphological and pasting properties

The starches isolated from normal and waxy corn varieties were hydrolyzed with hydrochloric acid (0.14 mol equivalent/L) and evaluated for physicochemical and functional properties. Acid thinning decreased the amylose content and swelling power but increased the solubility. The light transmittance of acid thinned (AT) starch pastes was higher than those of their native starches after similar storage intervals. The scanning electron microscopic observation demonstrated that the acid thinning did not cause any disruption of the granular crystalline structure. Native normal corn starches showed lower onset temperature (T_o) and peak temperature (T_p) as compared to their counterpart AT starches, whereas the reverse was observed for waxy corn starch. Enthalpy of gelatinization (ΔH_gel) was lower in AT normal and waxy starches as compared to their native starches. The percentage of retrogradation (%R) was significantly higher for native corn starches as compared to their AT starches. A significant reduction in peak—(P_V), trough—(T_V), breakdown—(B_V), final—(F_V), and setback viscosity (S_V) was observed by acid thinning, and the reduction was more pronounced in AT waxy starches. Among AT starches, AT waxy starch showed the lowest values of P_V, T_V, B_V, F_V and S_V.     

Mathematical approach for two component modeling of salep–starch mixtures using central composite rotatable design: Part II. Dynamic oscillatory shear properties and applicability of Cox–Merz rule

Dynamic shear rheological properties of salep–corn starch mixture (SCSM), salep–wheat starch mixture (SWSM) and salep–potato starch mixture (SPSM) samples were determined using a 2-factor-5-level Central Composite Rotatable Design (CCRD). Salep increased loss modulus (G″) values, and decreased loss tangent (tan δ) values of only SCSM; however, all starch types increased the storage (G′), loss (G″), complex (G^∗) modulus, complex viscosity (η^*) values and decreased tan δ values. At various salep and starch combination levels, a remarkable synergistic effect was observed in the dynamic shear properties. Potato starch exhibited completely different rheological performance in terms of G′, G″ and η^∗ values. Salep did not obey the Cox–Merz rule; however, a modified Cox–Merz rule was applicable for SCSM and SPSM samples. The ridge analysis revealed that maximum G′, G″, η^* and G^∗ values for the SCSM, SWSM and SPSM samples would occur at salep = 0.54% and 0.26%, respectively, and each starch type = 2.83%.     

普通玉米杂交种间原淀粉与羟丙基淀粉糊化性质关系的研究

本文采用湿法在实验室的条件下提取了17种普通玉米杂交种淀粉，并制取了羟丙基淀粉。采用快速粘度测定仪（RVA）测定了所有淀粉的糊化性质参数。结果表明：羟丙基淀粉提高了所有原淀粉的峰值和破损值；降低了所有原淀粉的谷值、终粘度、回生值、出峰时间和成糊温度；原淀粉和羟丙基淀粉的糊化性质参数在普通玉米杂交种间均达到了极显著相关水平，表明了羟丙基淀粉并没有改变原淀粉在普通玉米杂交种间的糊化性质差异性。羟丙基淀粉的糊化性质参数间的相关性显著水平发生了明显的变化，表明了不同的普通玉米杂交种的羟丙基淀粉的糊化性质参数的变化幅度是不同的。但是，羟丙基和原淀粉的相同糊化性质参数间的相关性都达到极显著的正相关水平，说明了羟丙基淀粉与原淀粉的糊化性质参数间存在密切关系，二者的糊化性质又存在着一致性。     

The Reactivity of Porcine Pancreatic alpha-Amylase Towards Native,Defatted and Heat-moisture Treated Potato Starches Before and After Hydroxypropylation

Potato starch was defatted (hot 75% n-propanol) and heat-moisture treated (100°C, 30% moisture) for various time intervals. The results showed that the above treatments increased the susceptibility of potato starch granules (heat-moisture treated > defatted) towards hydrolysis by porcine pancreatic α-amylase. These differences can be accounted for by the structural changes that occur within the amorphous and crystalline regions of the starch granule during defatting and heat-moisture treatment. Native, defatted (7 h) and heat-moisture treated (100°C, 30% moisture, 16 h) potato starches were hydroxypropylated (to different levels of molar substitution [MS]) with propylene oxide (2 → 20 %). The results showed that the alkaline reagents (NaOH and Na₂SO₄) used during hydroxypropylation increased the susceptibility of the above starches (native > defatted > heat-moisture treated) towards hydrolysis by α-amylase. Addition of propylene oxide to alkali treated starches, further enhanced their susceptibility, towards α-amylase. However, granule susceptibility towards α-amylase did not increase exponentially with increase in MS. The extent of hydrolysis began to decrease at MS levels of 0.29 (native), 0.28 (heat-moisture treated) and 0,26 (defatted).