The Interaction Between Surfactants and 2‐Hydroxy‐3‐(N,N‐dimethyl‐N‐dodecylammonium)‐propyloxy Starches

The phase behavior of temperature‐responsive hydrophobically modified starches and the interaction between oxidized potato amylose and hydrophobically modified potato amylopectin have been investigated by rheology, turbidity measurements and differential scanning calorimetry. When oxidized amylose was mixed with hydrophobically modified amylopectin, a viscosity peak was observed, indicative of a guest‐host interaction between the oxidized amylose and the hydrophobically modified amylopectin. A series of oxidized and hydrophobically modified potato starches were investigated in the presence of an anionic and cationic surfactant. A coil‐helix transition of the investigated starches was observed in the presence of surfactant, with the exception of a cationic surfactant combined with a hydrophobically modified zwitterionic starch of high positive net charge. The destabilizing mechanism (the phase separation) of the hydrophobically modified starches was studied as well as the difference in stabilizing capacity between the investigated cationic and anionic surfactants.     

Reversible Regulation of Gelatinization of Potato Starch with Poly(ε‐lysine) and Amino Acids

Poly(ε‐lysine) (PL), lysine (Lys), monosodium glutamate (GluNa), glycine (Gly), alanine (Ala), and leucine (Leu) were used to regulate the characteristic gelatinization behavior of potato starch. As determined by differential scanning calorimetry, PL, Lys, and GluNa with positive or negative net charge elevated the gelatinization temperature with increasing amount added as compared with the small effect of Gly, Ala, and Leu with zero net charge. The peak viscosity evaluated by a Rapid Viscoanalyser was markedly decreased by adding PL, Lys, and GluNa, whereas Gly and Ala had no effect on the peak viscosity. The swelling was also decreased by added PL, Lys, and GluNa, whereas it was unchanged by added Gly, Ala, and Leu. Potato starch immersed in PL or amino acid solution released most of the retained PL and amino acids by the subsequent washing with water. The increased gelatinization temperature of the PL‐treat­ed potato starch returned to the original value by washing with water. It is thus considered that the regulatory effects of PL and amino acids on the gelatinization behavior of potato starch were substantially reversible.     

Turbidity potentials of single long‐chain fatty acids and gelatinised starch in synthetic lautering wort

The turbidity potentials of long‐chain fatty acids as well as gelatinised starch were investigated in synthetic lautering wort to determine their contribution to turbidity according to concentration. Synthetic wort proved to be a standardised and reproducible model solution. Concentration series of gelatinised starch and single long‐chain fatty acids as pure substances showed high correlations between concentrations and turbidity levels of turbidity 11° and turbidity 90° measurements. Gelatinised barley starch has the turbidity potential of 0.04 EBC/(mg L^?1) on turbidity 11° levels. Regarding long‐chain fatty acids, saturated fatty acids showed distinctly higher turbidity potentials on turbidity 11° (≥0.32 EBC/(mg L^?1) and turbidity 90° (≥0.15 EBC/(mg L^?1) than unsaturated fatty acids. The turbidity potential of the saturated fatty acids corresponded with their chain lengths, with stearic acid (18:0) showing the highest turbidity potential. However, the impact on turbidity is primarily determined by concentration and not by turbidity potential.     

Synergetically Acting new Flocculants on the Basis of Starch‐graft‐Poly(acrylamide)‐co‐Sodium Xanthate

A synergetically acting new flocculant on the basis of starch‐graft‐poly(acrylamide)‐co‐sodium xanthate (CSAX) was synthesized by grafting copolymerization of crosslinked corn starch, acrylamide (AM), and sodium xanthate, using epichlorohydrin (EPI) as cross‐linking agent and ceric ammonium nitrate (CAN) as polymerization initiator in aqueous solution. The effects of some factors, such as crosslinker, initiator, AM, NaOH, on the %Tr (turbidity removal rate), %Trd (turbidity removal rate of a water sample which has both turbidity and heavy metal ions %Hr (heavy metal ion removal rate) and %Hrd (heavy metal ions removal rate of water which has both heavy metal ions and turbidity), are investigated. As proven by FTIR and elemental analysis, the CSAX can be successfully synthesized and can remove both turbidity‐causing substances and heavy metal ions from aqueous solutions. Under optimum synthesis conditions CSAX exhibits excellent performance, i.e. %Tr = 98%, %Trd = 98.4%, %Hrd = 99% and %Hr = 91.6%, respectively.     

A Novel Copolymer: Starch‐g‐Polyvinylpyrrolidone

In this study, graft copolymerization of N‐vinylpyrrolidone (N‐VP) onto starch was carried out in an aqueous medium using azobisisobutyronitrile (AIBN) as initiator. The variables affecting the graft copolymerization, such as monomer and initiator concentrations, reaction time and temperature, were thoroughly examined. In general, grafting of N‐vinylpyrrolidone onto starch increased with the increase in time and monomer concentration up to a certain value and then leveled off. Similarly, increase both in initiator concentration and temperature first favored and than impeded the grafting reaction. Optimum conditions established for grafting were as follows: N‐VP = 0.7 M, AIBN = 1.5×10^‐3 M, T = 70°C and t = 5 h. Structural changes of the grafted starch were followed by FTIR, intrinsic viscosity and water absorption capacity studies.     

Heat‐induced gels of soy protein and κ‐carrageenan at different pH values

Heat‐induced (90 °C/30 min) gelling of soy protein isolate (SPI) and κ‐carrageenan (κ‐CR) systems at pH values of 6.7 and 5.7 was evaluated. κ‐CR addition, increase in protein concentration and reduction in pH led to decreases in the initial gel structure forming temperature. Self‐supporting gels were not formed at concentrations of 8% (w/w) SPI or at concentrations below 0.3% (w/w) κ‐CR, but an increase in the concentration of SPI and κ‐CR led to an increase in the stress at rupture without influencing the deformability. Gel properties were a consequence of a simultaneous process of gelling and phase separation during heating. The non‐linear parameter of the Blatz, Sharda and Tschoegl (BST) rheological model allowed for the evaluation of the structural characteristics that in general corresponded to strain hardening behaviour. Strain weakening behaviour was observed at high biopolymer concentrations and at pH 6.7, which was associated with accentuated phase separation and a more discontinuous gel network.     

Physicochemical,crystallinity, pasting and thermal properties of heat‐moisture‐treated pinhão starch

The effect of heat‐moisture treatment (HMT) on the properties of pinhão starches under different moisture and heat conditions was investigated. The starches were adjusted to 15, 20 and 25% moisture levels and heated to 100, 110 and 120°C for 1 h. The X‐ray diffractograms, swelling power, solubility, gel hardness, pasting properties and thermal properties of the native and HMT pinhão starches were evaluated. Compared to native starch, there was an increase in the X‐ray intensity and gel hardness of HMT starches, with the exception of the 25% moisture‐treated and 120°C heat‐treated starch. HMT reduced the swelling power and solubility of the pinhão starches when compared to native starch. There was an increase in the pasting temperature, final viscosity and setback and a decrease in the peak viscosity and breakdown of HMT pinhão starches compared to native starch. HMT increases the gelatinisation temperature of native pinhão starch and reduces gelatinisation enthalpy.     

N,N‐Bis(2‐hydroxyethyl)formamide as a New Plasticizer for Thermoplastic Starch

N,N‐Bis(2‐hydroxyethyl)formamide (BHF) was synthesized efficiently and used as a new plasticizer for corn starch to prepare thermoplastic starch (TPS). The hydrogen bond interaction between BHF and starch was proven by Fourier‐transform infrared (FT‐IR) spectroscopy. As detected by scanning electron microscopy (SEM), starch granules were completely disrupted and a continuous phase was obtained. The crystallinity of corn starch and BHF‐plasticized TPS (BTPS) was characterized by X‐ray diffraction (XRD). The thermal behavior of glycerol‐plasticized TPS (GTPS) and BTPS was investigated by differential scanning calorimetry (DSC). The water resistance of BTPS was better than that of GTPS. Generally, at low relative humidity (RH), the tensile strength of BTPS was higher than that of GTPS. At high RH, the elongation at break of BTPS was higher than that of GTPS.     

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.     

Rheological and calorimetric properties of corn‐, wheat‐, and cassava‐ starches and soybean protein concentrate composites

The effect of soy protein concentrate (SPC) on the rheological and calorimetric properties of corn, wheat, and cassava starches was assessed. SPC increased T_o values and decreased the ΔH of all tested starches, which could be related to lower availability of water for starch gelatinization and/or to the interactions between SPC and amorphous regions of starch granules. SPC and sugar addition modified the viscosity parameters (obtained through a rapid visco‐analyser) of starch pastes, which was attributed to an increase in solid content and to the interaction of proteins with the starch dispersed phase. Frequency sweeps were carried out with a rheometer on gels containing starch, SPC, and sucrose. SPC raised storage and loss modulus, producing more consistent starch gels. Besides, penetration tests showed that SPC steadily increased starch gel firmness. Scanning electron micrographs showed that protein concentrate produced gels with closer structures. Summarizing, the starch and SPC in the gels obtained were expected to be arranged in a two‐phase system. Results showed that it is possible to achieve different textures for starch dessert formulations.     

Response surface optimization and characteristics of Indica rice starch‐based fat substitute prepared by α‐amylase

Response surface methodology (RSM) was used to study the effect of enzyme to substrate ratio (11.8–23.6 U α‐amylase/g rice starch), hydrolysis temperature (90–100°C) and pH value (6.0–6.6) on the gel strength of rice starches‐based fat substitute using α‐amylase hydrolysis. The optimum conditions obtained from response surface analysis was 16.52 U/g enzyme dosage, 92°C hydrolysis temperature while the influence of pH was found insignificant in the range tested. Under these optimum conditions, the gel strength of this fat substitute was 113 g/cm², very close to the gel strength of butter of 114 g/cm², while the solubility of the substitute was 1.33 ± 0.01% and the swelling power 4.85 ± 0.02. There were no observable differences in the granular size distribution between the untreated rice starch and the hydrolyzed rice starch. Rheological properties of this rice starch‐based fat substitute implied that it is easier for the substitute to form three‐dimensional networks under 34°C.     

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.     

Desizing of untreated cotton fabric with the conventional and ultrasonic bath procedures by immobilized and native α‐amylase

In this work, starch‐sized, untreated 100% cotton plain woven fabric was treated with native and immobilized α‐amylase enzyme in two different system (conventional and ultrasonic bath procedures) and time (15 and 30 min). Weight loss, the amount of removed starch, tensile properties, contact angle, and scanning electron micrograph morphology were investigated. Sonification and treatment time enhance the desizing performance. Free enzyme, treatment time, and ultrasound brings about a significant increase in the starch‐size removal along with a decrease in the retained strength values, regardless of the used fabric. Immobilized enzyme can be use many times which enables to improve environment friendly pretreatment processes for the textile industry.     

Formulation and in vitro evaluation of κ‐carrageenan‐pregelatinized starch‐based mucoadhesive gels containing miconazole

The aim of this work was to investigate the effects of using κ‐carrageenan (κ‐Carr) with pregelatinized starch (PGS) in the improvement of swelling and erosion behaviors of mucoadhesive gels containing 2% of miconazole. Polymer blends containing carrageenan and PGS were used for the formulation, and the effect of varying polymer concentrations on the drug release was studied. The matrices were prepared using different biopolymer (starch hydrogel) concentrations. Swelling and erosion characteristics of the matrices were carried out in various media and their impact on drug release were studied. The swelling action of the gel matrix was controlled by the rate of its hydration in the medium. Release studies have showed that the swelling and erosion of matrices influence the drug release. In addition, the presence of κ‐Carr in the gel formula improves the bioadhesive properties. The release data showed a good fit into the power law or Korsmeyer–Peppas equation indicating the combined effects of diffusion and erosion mechanisms of drug release. Most of the formulations released miconazole by an anomalous (non‐Fickian) transport mechanism, except those matrices that contained PGS alone which showed zero‐order release.     

Coating of Peanuts with Edible Whey Protein Film Containing α‐Tocopherol and Ascorbyl Palmitate

ABSTRACT: Physical properties of whey protein isolate (WPI) coating solution incorporating ascorbic palmitate (AP) and α‐tocopherol (tocopherol) were characterized, and the antioxidant activity of dried WPI coatings against lipid oxidation in roasted peanuts were investigated. The AP and tocopherol were mixed into a 10% (w/w) WPI solution containing 6.7% glycerol. Process 1 (P1) blended an AP and tocopherol mixture directly into the WPI solution using a high‐speed homogenizer. Process 2 (P2) used ethanol as a solvent for dissolving AP and tocopherol into the WPI solution. The viscosity and turbidity of the WPI coating solution showed the Newtonian fluid behavior, and 0.25% of critical concentration of AP in WPI solution rheology. After peanuts were coated with WPI solutions, color changes of peanuts were measured during 16 wk of storage at 25 °C, and the oxidation of peanuts was determined by hexanal analysis using solid‐phase micro‐extraction samplers and GC‐MS. Regardless of the presence of antioxidants in the coating layer, the formation of hexanal from the oxidation of peanut lipids was reduced by WPI coatings, which indicates WPI coatings protected the peanuts from oxygen permeation and oxidation. However, the incorporation of antioxidants in the WPI coating layer did not show a significant difference in hexanal production from that of WPI coating treatment without incorporation of antioxidants.     

Modification of poovan banana (Musa AAB) starch by γ‐irradiation: effect on in vitro digestibility,molecular structure and physico‐chemical properties

This study focussed at evaluating the effect of gamma irradiation on the in vitro digestibility, molecular structure and physico‐chemical properties of poovan banana (Musa AAB) starch using γ‐rays from a ⁶⁰Co source at different doses with a dose rate of 2 kGy h^?1. Physico‐chemical properties varied significantly and exhibited strong dose‐dependent relationship. Escalating irradiation leads to decrease in amylose content, pH, swelling power of the starch granules and syneresis of the gelatinised starch, while the same led to an increase in carboxyl content, in vitro digestibility, solubility and water absorption capacity of the starch granules. The results revealed that peak, hold, final and setback viscosities were significantly reduced. X‐ray diffraction pattern remained the same upon irradiation but a decrease in relative crystallinity was observed with increasing irradiation dose. Gelatinisation temperature and enthalpy decreased significantly when the increasing the dose of gamma irradiation.     

Hydrophobic Modification of Starch by Alkali‐Catalyzed Addition of 1,2‐Epoxyalkanes

An efficient method of preparing hydrophobic α‐hydroxy starch ethers using aqueous alkaline conditions is described. α‐Hydroxy starch ethers were synthesized by addition of 1,2‐epoxyalkanes to an aqueous alkaline starch gel in the presence of sodium sulfate as a co‐catalyst. The reaction, carried out in a stirred autoclave at 140 °C and 3.9 bar, was optimized with respect to the concentrations of sodium hydroxide and 1,2‐epoxyalkane. Optimum yields and molar substitutions (MS) were obtained at molar ratios of sodium hydroxide to anhydroglucose unit (AGU) of 0.5 to 1.0. The amount of molar substitution could be controlled by 1,2‐epoxyalkane concentration. Thus, a series of α‐hydroxyoctyl starch ethers with MS from 0.7 to 2.4 were synthesized in yields up to 90% by using these conditions. Starches with different amylose contents were also converted to the corresponding ethers using a threefold excess of 1,2‐epoxyoctane and an equimolar ratio sodium hydroxide : AGU. The reaction is hardly effected by the origin of the starch and its amylose content. The influence of the 1,2‐epoxyalkane chain length was investigated by performing the conversion with a series of terminal epoxyalkanes from 1,2‐epoxyhexane to 1,2‐epoxydodecane. The results indicated that the hydrophobic character of the starch ethers increased by increasing the molar substitution and alkyl chain length. All products were insoluble in water, but soluble in mixtures of methanol and methylene chloride. Furthermore the starch ethers can be converted into shaped articles by extrusion technology without the addition of plasticizers.     

Investigation of sweet potato starch as a structural enhancer for three‐dimensional printing of Scomberomorus niphonius surimi

Three‐dimensional printing (3DP) of surimi requires a structural modifier to achieve a stable construct. This work investigated the effect of addition of sweet potato starch (0–10% wt/wt) on the physical properties (rheological properties, gel strength, water‐holding capacity [WHC], and microstructural characteristics) of surimi gels and the 3D printed behavior of these gels. The results showed that as the starch content increased, the viscosity of the starch–surimi mixture decreased facilitating the flow of the surimi out of the printer nozzle. The surimi gel with 8% sweet potato starch concentration showed good gel strength (2,021.70 g mm), WHC (82.39%), microstructural characteristics, and less cooking loss (1.95%). A comparison of the traditional surimi preparation method with 3DP showed that the surimi gel prepared by a 3D printed construct was softer in gel strength (1,398.65 g mm) and lower in hardness (945.17 g) although showing slightly higher cooking loss (6.76%) and lower WHC (72.66 g) than the conventional product. The results suggest that sweet potato starch can be effectively used as a structural enhancer for 3DP complex‐shaped surimi.     

Functional Properties and Retrogradation of Heat‐Moisture Treated Wheat and Potato Starches in the Presence of Hydroxypropyl β‐cyclodextrin

Some functional and retrogradation properties of native and heat‐moisture treated potato and wheat starches were examined in the presence of hydroxypropyl β‐cyclodextrin (HPβ‐CD). HPβ‐CD increased swelling factor, amylose leaching, and solubility of both native and heat‐moisture treated wheat starches but it had less impact on corresponding potato starches. Gelatinization enthalpy of native wheat starch was decreased in the presence of HPβ‐CD but was increased in potato starch with increasing concentration. Reduction of amylose‐lipid complex endotherm in both native and heat‐moisture treated wheat starch was observed in the presence of HPβ‐CD. Heat‐moisture treatment did not change the transition parameters of amylose‐lipid complex showing its resistance to hydrothermal treatment. HPβ‐CD greatly decreased the pasting temperature of wheat starch. Cold paste viscosity of both native and heat‐moisture treated wheat starch was increased by HPβ‐CD to a greater extent than corresponding potato starch. Amylopectin retrogradation of all the starches was unaffected in the presence of HPβ‐CD but heat‐moisture treatment slightly decreased retrogradation of potato starch. These results suggest that HPβ‐CD can disrupt the amylose‐lipid complex within the starch granule in both native and heat‐moisture treated wheat starch but has no influence on amylopectin retrogradation. However, greatly increased wheat starch setback with HPβ‐CD indicates its greater effect on wheat starch amylose retrogradation.     

In situ kinetic study of solid‐state crosslinking of potato starch

This work studies the solid‐state modification of potato starch using sodium trimetaphosphate (STMP) at elevated temperature (120°C). Kinetics for the reaction was investigated using an in situ technique based on attenuated total reflectance infrared spectroscopy for monitoring the extent of crosslinking. For tested STMP concentrations between 1.6 and 20% (w/w, dry starch basis), the degree of substitution varied between 0.015 and 0.106 mol P/mol anhydroglucose unit, respectively, within a reaction time of less than 10 min. The reaction data was found to follow a first‐order rate dependency and by examination using a phase‐boundary kinetic model was considered to be exterior diffusion limited. The extent of conversion always converged to an asymptotic value less than 100%. The inclusion of 1–2% hydrocolloidal xanthan gum were found to have no effect on the crosslinking of starch whereas 10–30% glycerol significantly lowered the rate of reaction.