Resistant starch and thermal,morphological and textural properties of heat‐moisture treated rice starches with high‐, medium‐ and low‐amylose content

This study investigated the effects of heat‐moisture treatment (HMT) on the resistant starch content and thermal, morphological, and textural properties of rice starches with high‐, medium‐ and low‐amylose content. The starches were adjusted to 15, 20 and 25% moisture levels and heated at 110°C for 1 h. The HMT increased the resistant starch content in all of the rice starches. HMT increased the onset temperature and the gelatinisation temperature range (T_finish–T_onset) and decreased the enthalpy of gelatinisation of rice starches with different amylose contents. This reduction increased with the increase in the moisture content of HMT. The morphology of rice starch granules was altered with the HMT; the granules presented more agglomerated surface. The HMT affected the textural parameters of rice starches; the high‐ and low‐amylose rice starches subjected to 15 and 20% HMT possessed higher gel hardness.     

Influence of Heat‐Moisture Treatment and Acid Modifications on Physicochemical,Rheological, Thermal and Morphological Characteristics of Indian Water Chestnut (Trapa natans) Starch and its Application in Biodegradable Films

Water chestnut starch was subjected to acid modification and heat‐moisture treatment. Hydrochloric acid was used for acid modification at three different concentrations (0.25 M, 0.5 M and 1 M) for 2 h. Modifications did not alter the granule morphology. Heat‐moisture treatment (HMT) resulted in slight reduction in the granular size of the starch granules. Acid modification lowered the amylose content, swelling power, water‐ and oil‐binding capacity but improved the solubility of starch to a considerable level. Light transmittance of acid‐modified (AM) starches improved significantly. A significant reduction in peak, trough, final and setback viscosity was observed by acid‐thinning. In case of heat‐moisture treated starch the final viscosity (F_v) was found to be even higher than the peak viscosity (P_v). Native water chestnut starch exhibited a lower onset temperature (T_o) and peak temperature (T_p) of gelatinization than the corresponding acid‐treated starches. Starch films prepared from native starch exhibited excellent pliability, whereas those prepared from AM and HMT starches showed good tensile strength. Starch films prepared from acid‐treated starches provided better puncture and tensile strength.     

Effect of Osmotic Pressure on Starch: New Method of Physical Modification of Starch

A new method of physical modification of starch in the presence of high concentrated salt solution is presented, called “Osmotic Pressure Treatment” (OPT). OPT was introduced in order to produce the same physically modified products as obtained by conventional heat‐moisture treatment (HMT) of starch. Potato starch was selected for the comparative study of the two methods. For the OPT method, potato starch was suspended in a saturated solution of sodium sulfate and heated in an autoclave at 105°C and 120°C ,which corresponded to the calculated osmotic pressures of 328 and 341 atm (332 and 345 bar, respectively) (assuming sodium sulfate dissociates completely) for 15, 30 and 60 min, respectively. For the HMT method, starch with 20% moisture content was placed in a Duran bottle, then the same heat treatment method in the autoclave was applied. Light and scanning electron microscopy (SEM) showed that OPT of starch changed the shape of the starch granules to a folded structure, while the starches remained unchanged after HMT. The RVA viscogram for the OPT starch exhibited a decrease in the peak viscosity without a breakdown and an increase of the pasting temperature when increasing the temperature and time, which was in an agreement with the viscosity patterns for the HMT starches. X‐ray diffraction patterns were altered from B to A+B for the HMT and from B to A type for the OPT starch when treated at 120°C. After OPT, the gelatinization temperatures (T_o, T_p, and T_c) of the starch increased significantly with increasing temperature and time, whereas only the T_c of starch increases after HMT. The biphasic broadening of the peaks (high T_c‐T_o) can be explained by an inhomogeneous heat transfer during HMT. Narrow peaks in the DSC curve can be an indication for a better homogeneity of the OPT samples. However, both methods provide a similar decrease in the gelatinization enthalpy (ΔH). The amylose‐amylopectin ratio calculated from the HPSEC patterns was strongly increased for HMT starches at 105°C for 60 min and 120°C for 30 min and decreased after treatment at 120°C for 60 min. For OPT starches the ratio was strongly increased at 120°C for 15 min and decreased after prolong heating. The OPT provides a uniform heat distribution in the starch suspension. This allows the modified starch to be produced on a larger scale.     

Microstructural and physicochemical properties of heat-moisture treated waxy and normal starches

Starches from normal rice (21.72% amylose), waxy rice (1.64% amylose), normal corn (25.19% amylose), waxy corn (2.06% amylose), normal potato (28.97% amylose) and waxy potato (3.92% amylose) were heat-treated at 100 °C for 16 h at a moisture content of 25%. The effect of heat-moisture treatment (HMT) on morphology, structure, and physicochemical properties of those starches was investigated. The HMT did not change the size, shape, and surface characteristics of corn and potato starch granules, while surface change/partial gelatinization was found on the granules of rice starches. The X-ray diffraction pattern of normal and waxy potato starches was shifted from B- to C-type by HMT. The crystallinity of the starch samples, except waxy potato starch decreased on HMT. The viscosity profiles changed significantly with HMT. The treated starches, except the waxy potato starch, had higher pasting temperature and lower viscosity. The differences in viscosity values before and after HMT were more pronounced in normal starches than in waxy starches, whereas changes in the pasting temperature showed the reverse (waxy > normal). Shifts of the gelatinization temperature to higher values and gelatinization enthalpy to lower values as well as biphasic endotherms were found in treated starches. HMT increased enzyme digestibility of treated starches (except waxy corn starch); i.e., rapidly and slowly digestible starches increased, but resistant starch decreased. Although there was no absolute consistency on the data obtained from the three pairs of waxy and normal starches, in most cases the effects of HMT on normal starches were more pronounced than the corresponding waxy starches.     

Effect of Amylose Content on Gelatinization,Retrogradation and Pasting Properties of Flours from Different Cultivars of Thai Rice

Presently, rice cultivars are categorized according to amylose content into three groups: low, medium and high amylose content cultivars. The correlation of amylose content with gelatinization properties, retrogradation, and pasting properties of eleven cultivars of Thai rice were investigated. Rice flour was prepared from milled rice by the wet grinding process. Onset (T_o), peak (T_p) and conclusion (T_c) temperatures of gelatinization, (determined by DSC) were found to be highly positively correlated with amylose levels. This correlation could be used for prediction of amylose content of rice flour. Low amylose starch could also be characterized by low degree of retrogradation (%R). The data obtained from RVA‐viscograms (peak viscosity, breakdown, setback, and pasting temperature) can be used only for characterization of the group of low amylose starches (waxy rice). It was demonstrated that low amylose rice starch provided the highest peak viscosity and breakdown and the lowest setback and pasting temperature among the groups investigated.     

Effect of Heat-Moisture Treatment and Acid Modification on Rheological, Textural, and Differential Scanning Calorimetry Characteristics of Sweetpotato Starch

Sweetpotato starches were characterized to understand the changes upon modification by acid and heat‐moisture treatment (HMT) in the rheological, differential scanning calorimetry (DSC), and textural characteristics of starch isolated from the sweetpotato variety PSP‐21 and to compare these findings with those of commercially available arrowroot starch. The native sweetpotato starch had a Type A pasting profile characterized by a high peak viscosity (PV) (741.5 rapid viscoanalyzer unit [rvu]), with a high breakdown (378.8 rvu) and low cold paste viscosity (CPV) (417.6 rvu). After HMT, there was a marked decrease in the PV (639.1), a very slight breakdown (113.5 rvu) and an increase in CPV (759.5 rvu), more like a Type C pasting profile. However, acid modification did not notably change the pasting profile of native sweetpotato starch. The DSC characteristics were also affected significantly after modifications. The gelatinization temperature parameter to onset (T_o) decreased significantly after HMT and acid modification. The gelatinization enthalpy decreased during HMT from 15.98 to 14.42 J/g. The gel strength of acid‐modified starch was the highest compared with that of HMT and native sweetpotato and arrowroot starches.     

Structural Transformation of Sago Starch by Heat‐Moisture and Osmotic‐Pressure Treatment

Sago starch was modified by osmotic‐pressure treatment (OPT) and heat‐moisture treatment (HMT) and physicochemical characteristics were compared. In OPT, sago starch was suspended in saturated sodium sulfate solution and heated for 1 h at 100, 110 and 120°C, corresponding to a calculated osmotic pressure of 32,728, 33,640 and 34,552 kPa (assuming sodium sulfate dissociates completely), respectively, and in HMT, sago starch with 20% moisture content was used. Change of X‐ray diffraction pattern from C‐type to A‐type was obtained for OPT and HMT starch at 110°C and 120 °C, respectively. RVA viscograms of both OPT and HMT starch exhibited a decrease of peak and breakdown viscosity but increase of final viscosity and pasting temperature. Onset (T_o), peak (T_p), and conclusion temperature (T_c) of gelatinization of both OPT and HMT starch increased significantly with increase of treatment temperature. Biphasic broadening of T_p was observed for HMT starch indicating an inhomogeneous heat transfer during HMT. The observed narrow peaks of DSC curves indicated better homogeneity of OPT. These properties suggest that OPT starch is more suitable for large‐scale production.     

Interaction of wheat and rice starches with yellow mustard mucilage

The effect of yellow mustard mucilage (YMM) on gelatinization and retrogradation of wheat and rice starches were studied. Considerable interactions were observed between YMM and wheat and rice starches which were accompanied by a marked increase in viscosity. DSC studies showed that the presence of YMM did not affect peak gelatinization temperature (T_p) of wheat and rice starches, but slightly increased melting enthalpy (ΔH) and the phase transition temperature range (T_c−T₀). Addition of YMM markedly changed wheat and rice starch gel textures by increasing hardness, adhesiveness, chewiness and springiness. The addition of YMM–locust bean gum (LBG) mixture (9:1) similarly increased the viscosity of wheat and rice starches but decreased gel hardness. The swelling power as well as solubilized starch and amylose were decreased for both starches in the presence of YMM. Syneresis in wheat and rice starches was also decreased by the presence of YMM.     

Fine Structure,Thermal and Viscoelastic Properties of Starches Separated from Indica Rice Cultivars

Starches were separated from indica rice cultivars (PR‐113, Basmati‐370, Basmati‐386, PR‐115, IR‐64, and PR‐103) and evaluated using gel permeation chromatography (GPC), X‐ray diffraction, differential scanning calorimetry (DSC) and dynamic viscoelasticity . Debranching of starch with isoamylase and subsequent fractionation by GPC revealed 9.7–28.3% apparent amylose content, 3.7–5.0% intermediate fraction (mixture of short amylose and long side‐chains of amylopectin), 20.6–26.6% long side‐chains of amylopectin and 45.8–59.4% short side‐chains of amylopectin). IR‐64 starch with the highest crystallinity had the highest gelatinization temperatures and enthalpy, T_o, T_p, T_c, and ΔH_gel being 71.8, 75.9, 82.4°C and 5.1 J/g, respectively, whereas PR‐113 starch with lower crystallinity showed the lowest gelatinization temperatures (T_o, T_p, T_c, of 60.8, 65.7 and 72.2°C, respectively). Basmati‐386 starch exhibited two endotherms during heating, the first and second endotherm being associated with the melting of crystallites and amylose‐lipid complexes, respectively. T_o, T_p, T_c and ΔH_gel of the second endotherm of Basmati‐386 starch were 99.0, 100.1, 101.1°C and 2.0 J/g, respectively. During cooling, Basmati‐386 also showed an exotherm at a peak temperature of 87°C. PR‐113 starch with the highest amylose content and the lowest content of short side‐chains of amylopectin had the highest peak storage modulus (G′= 1.6×10⁴ Pa). The granules of PR‐113 starch were the least disintegrated after heating. The effects of heating starch suspensions at different temperatures (92°C, 130°C and 170°C) on intrinsic viscosity [η], transmittance and viscoelasticity were also studied to evaluate the extent of breakdown of the molecular structure. The intrinsic viscosity of starch suspensions heated at 92, 130 and 170°C ranged between 103–114, 96–110 and 28–93 mL/g. Transmittance value of starches cooked at 92°C decreased with increase in storage duration. All starches except PR103, cooked at 130°C also showed decrease in transmittance during storage, however, at lower rate. PR103 starch heated at 130°C did not show any change in transmittance up to a storage time of 48 h. The changes in viscoelasticity of starch pastes cooked at different temperatures during cooling and reheating were also evaluated. G′ and G′′ increased with decrease in temperature during cooling cycle. Starches heated at 130°C with apparent amylose content ≤ 21.2% showed an improvement in G′ and G′′ in comparison to the corresponding starches heated at 92°C, this improvement was observed to be higher in starches with lower amylose content. All starches heated at 170°C had a higher proportion of breakdown in molecular structure as indicated by lower G′ and G′′ than the same starches heated at 130 and 92°C.     

Effect of heat-moisture treatment on the formation and physicochemical properties of resistant starch from mung bean (Phaseolus radiatus) starch

Mung bean starch was subjected to a range of heat-moisture treatments (HMT) based on different moisture contents (15%, 20%, 25%, 30%, and 35%) all heated at 120 °C for 12 h. The impact on the yields of resistant starch (RS), and the microstructure, physicochemical and functional properties of RS was investigated. Compared to raw starch, the RS content of HMT starch increased significantly, with the starch treated at 20% moisture having the highest RS content. After HMT, birefringence remained at the periphery of the granules and was absent at the center of some granules. The shape and integrity of HMT starch granules did not change but concavity was observed under scanning electronic microscopy. Apparent amylose contents of HMT starch increased and the HMT starch was dominated by high molecular weight fraction. Both the native and HMT starches showed A-type X-ray diffraction pattern. Relative crystallinity increased after HMT. The gelatinization temperatures (To, Tp, and Tc), gelatinization temperature range (Tc–To) and enthalpies of gelatinization (ΔH) increased significantly in HMT starch compared to native starch. The solubility increased but swelling power decreased in HMT starches. This study clearly shows that the HMT exhibited thermal stability and resistance to enzymatic hydrolysis owing to stronger interactions of starch chains in granule.     

Structure and Viscoelastic Properties of Starches Separated from Different Legumes

A comparison between the morphological, structural, thermal and viscoelastic properties of starches separated from pigeon pea, chickpea, field pea, kidney bean and blackgram was made. The shape of the starch granules in the different legumes varied from oval to elliptical or spherical. X-ray diffraction of the legume starches indicated a typical C-pattern (mixture of A- and B-type). Granules of blackgram and pigeon pea starch had a higher degree of crystallinity than those of field pea and kidney bean starches. Apparent amylose content of field pea, kidney bean, chickpea, blackgram and pigeon pea starch was 37.9%, 36.0%, 34.4-35.5%, 32.9-35.6% and 31.8%, respectively. Distribution of isoamylase-branched materials among the starches revealed that the proportions of long and short side chains of amylopectin ranged between 13.6-18.5% and 41.7-46.5%, respectively. Field pea and kidney bean starch had the highest apparent amylose content and the lowest amount of long side chains of amylopectin, respectively. Blackgram and pigeon pea starch possessed higher proportions of both long and short side chains of amylopectin than field pea and chickpea starches. The onset, peak and conclusion temperatures of gelatinization (T_o T_p and T_c, respectively) were determined by differential scanning calorimetry. T_o and T_c ranged from 59.3 to 77.3°C, 66.8 to 79.6°C, 55.4 to 67.6°C and 68.3 to 69.3°C, respectively, for chickpea, blackgram, field pea and kidney bean starch. The enthalpy of gelatinization (ΔH_gel) of field pea, kidney bean, chickpea, blackgram and pigeon pea starches was 3.6, 3.0, 2.6-4.2, 1.6-1.7 and 2.6 J/g, respectively. Pastes of blackgram and pigeon pea starches showed lower storage and loss shear moduli G′ than field pea, kidney bean and chickpea starches. The changes in moduli during 10 h at 10°C revealed retrogradation in the order of: field pea> kidney bean> chickpea> blackgram> pigeon pea starch. In blackgram and pigeon pea starches, the lower proportion of amylose plus intermediate fraction and higher proportion of short and long side chains of amylopectin are considered responsible for the higher crystallinity, gelatinization temperature and enthalpy of gelatinization.     

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.     

Thermal Behavior of Selected Starches in Presence of Other Food Ingredients Studied by Differential Scanning Calorimetery (DSC)–Review

ABSTRACT: This review article highlights the thermal behaviors of selected starches that were studied using differential scanning calorimetery (DSC) with data shown in various research publications. The starches of sago, potato, sweet potato, cassava, yam, and corn are included in this overview. Our examinations indicate that thermal properties are highly affected by the type of starch, its amylose/amylopectin content, and the presence of other food ingredients such as sugar, sodium chloride, water, milk, hydrocolloids, and meat. When the heating temperatures of the starches were increased, the DSC measurements also showed an increase in the temperatures of the gelatinization (onset [T_o], peak [T_p], and conclusion [T_c]). This may be attributed to the differences in the degree of crystallinity of the starch, which provides structural stability and makes the granule more resistant to gelatinization.     

Digestibility and Pasting Properties of Rice Starch Heat‐Moisture Treated at the Melting Temperature (Tm )

Non‐waxy and waxy rice starches adjusted to 20% moisture (wet based, w.b.) were heated in a differential scanning calorimeter to determine the optimum parameters for producing slowly digestible starch (SDS). Starches heated to the temperature of melting (T_m) and held for 60 min in the calorimeter showed a slow digestibility compared to unheated samples. Digestibility decreased by 25 and 10%, respectively, for non‐waxy and waxy rice starches relative to non‐treated starches. Heat‐moisture treatment of waxy corn, non‐waxy corn and wheat starches at the T_m determined for non‐waxy rice starch did not result in significant decreases in digestibility. For waxy rice starches heat‐treated in microwave or conventional ovens at the T_m , there were slight but significant increases in digestibility of the treated starches compared to non‐treated starches at all incubation times. Digestibility was higher for starches heated for 30 min than for 60 min. Non‐waxy rice starches did not show any significant changes in digestibility. Heat‐moisture treatment at the T_m and the holding time of sample at that temperature in a differential scanning calorimeter were found to be significant to the formation of slowly digestible heat‐moisture treated starch.     

Amylopectin structure of heat–moisture treated starches

The effects of heat–moisture treatment (HMT; moisture content of 25%, at 100°C for 24 h) on starch chain distribution and unit chain distribution of amylopectin in normal rice, waxy rice, normal corn, waxy corn, normal potato, and waxy potato starches were investigated. After HMT, starch chain distribution (amylose and amylopectin responses) of waxy corn and potato starches were identical to those of untreated starches, whereas the chromatographic response of waxy rice starch showed a slight decrease, but with a slight increase in peak tailing. This result indicated that HMT had no (or very limited) effect on the degradation of amylopectins. Analysis of unit chain distribution of amylopectins revealed that waxy characteristics affected the molecular structure of amylopectin in untreated starches, i.e., the CL of normal‐type starches was greater than that of waxy‐type starches. After HMT, the CL and unit chain distribution of all starches were no different than those of untreated starches. The results implied that changes in the physico‐chemical properties of HMT starches would be due to other phenomena rather than the degradation of amylopectin molecular structure. However, the thermal degradation of amylopectin molecules of waxy starches could occur by HMT at higher treatment temperatures (120 and 140°C).     

Physicochemical,morphological, and thermal properties of starches separated from bulbs of four Chinese lily cultivars

The starches separated from bulbs of four different lily cultivars (Lanzhou, Pinglu, Yixing‐1, and Yixing‐2) were investigated for physicochemical, morphological, crystalline, and thermal properties. AM content of lily bulbs starches from different cultivars ranged from 19.46 to 25.17%. The swelling power of starches ranged between 14.4 and 21.3 g/g, and the solubility ranged from 8.92 and 16.6% at the temperature of 85°C. Four cultivars of lily starches paste had excellent transparency and the transmittance value of Lanzhou lily as high as 54.7%. The transmittance of the gelatinized aqueous starch suspensions, from all lily cultivars, decreased with increase in storage period. The shape of starch granules varied from triangular to cylindrical and XRD of four lily starches all showed B‐type pattern. The transition temperatures and enthalpy of gelatinization (ΔH_gel) were determined using DSC. T_p varied from 62.52 to 65.25°C. Pinglu lily starch showed the highest ΔH_gel and gelatinization range (T_c–T_o) index among starches from four different lily cultivars.     

Gelatinization Transitions of Acid‐modified Tapioca Starches by Differential Scanning Calorimetry (DSC)

Tapioca starch was partially hydrolyzed by 6 % and 12 % hydrochloric acid (w/v) at room temperature for various length of time. The gelatinization transitions of the acid‐modified tapioca starches were studied using Differential Scanning Calorimetry. Starch suspensions (67 % moisture) were heated at 5 °C/min to follow melting transition of amylopectin. As the hydrolysis time increased, onset (T_o), peak (T_p) and conclusion (T_c) temperatures of gelatinization have been observed to increase, in the same order of relative crystallinity, until reaching some critical values, then decreased with the large broadening of the endotherms. The increasing of the transition temperatures corresponded to the retrogradation of the remaining partially hydrolyzed amylose followed by a decrease of these parameters corresponding to the reduction of the length of the chains of double helices amylopectin.     

A comparative study of Indian rice starches using different modification model solutions

Starches extracted from rice flour from broken kernels of three rice cultivars (PUSA-44, PR-106 and PR-114) have been selected for modification studies due to their varied amylose content. Model solutions with different types and concentrations of modifying agents were prepared for comparative study of effect of amylose variation among the varieties and also individual and combined effect of modifying agents used. There was an increase in hot paste viscosity at 90 °C in modified starches whereas, cold paste viscosity decreased upon modification. A greater effect was observed with in dual modification of starches. The total set back was significantly lower in modified starches indicating the decreased retro-gradation of starch gels upon modification. The DSC results showed decreases in ΔH, T_o, T_p, and T_c, indicating that hydroxypropylation cross-linking and acetylation affect the structure of starches granules, requiring less heat for gelatinization. Pasting and thermal properties of PUSA-44 were significantly different from those of PR-106 and PR-114, probably due to relative higher amylose contents in the former. As observed in this study, bi-functional modifying agents can reduce the extent of cross-linking. Acetylation modified the morphology of the starch. However, hydroxypropylation cross-linking and dual modification retained the original structure with little modification.     

Physicochemical properties of waxy and normal corn starches treated in different anhydrous alcohols with hydrochloric acid

Corn starches (25 g, d. b.) were treated in anhydrous methanol, ethanol, 2-propanol or 1-butanol (100 ml) with 1 ml 36% hydrochloric acid at 45 °C for 1 h, the molecular weight and chain length distributions of starch were examined by high-performance size-exclusion chromatography (HPSEC), and the granule size, granular structure, λ_max, blue value, solubility and gelatinization thermal properties of starch were also examined. Results showed the recovery yields of the treated starch were higher than 96%, and the granule sizes of treated starches were slightly lower than their counterpart native starch. Starches after acid-alcohol treated showed internal fissures or cavities in some granules, and the number of granule with fissures or cavities increased with the increasing carbon number of alcohol. The weight average degree of polymerization and relative content of F1 fraction of starch after treated profoundly decreased, and the amylose and long chain of amylopectin of starch were preferentially degraded. The degradation extent of molecules after acid-alcohol treatment was found directly related to the alternation of internal structure of starch granule. The λ_max and blue value of both waxy and normal corn starches after treated also obviously decreased with the increasing carbon number of alcohol, while the solubility of starch profoundly increased after treated. The gelatinization onset temperature (T_o) of acid-alcohol treated waxy corn starch decreased with the increasing carbon number of alcohol, but the treated normal corn starches showed similar T_o values. Despite the alcohol used, the solubility of treated waxy corn starch linearly correlated (r²=0.983) with T/T_o value (T was the measuring temperature used for solubility determination). Whereas, normal corn starch treated in different alcohols showed distinct relations between T/T_o and solubility.     

Studies on the properties of citrate derivatives of cassava (Manihot esculenta Crantz) starch synthesized by microwave technique

Cassava starch citrates with degree of substitution (DS) ranging from 0.005 to 0.063 were synthesized by the microwave‐assisted reaction of cassava starch with citric acid. A response surface small composite design was used to study the effect of different reaction conditions, viz. time, temperature and reagent concentration. All these variables significantly affected the substitution level in the modified starches. The DS increased with increase in the time of reaction and temperature. However, reagent concentration had a negative effect on the DS. The modified starches showed higher viscosity with lower breakdown, lower setback and higher final viscosities in comparison to native starch. Differential scanning calorimetry showed that the modified starches exhibited a decrease in gelatinization temperatures, T_o, T_p, T_e, in comparison to native starch. However, the heat of gelatinization was not significantly affected. The citrate derivatives exhibited reduced swelling volume and enhanced water binding capacities. They were found to be less susceptible to enzyme hydrolysis than native starch. Copyright © 2007 Society of Chemical Industry