Microstructure of acid–induced skim milk–locust bean gum–xanthan gels

The microstructure of acid skim milk gels (14% w/w milk protein low heat powder) with or without addition of locust bean gum (LBG), xanthan gum (XG) and LBG/XG blends was determined by transmission electron microscopy (TEM), phase-contrast light microscopy (PCLM) and scanning electron microscopy (SEM). Three polysaccharide concentrations (0.001%, 0.02% and 0.1%, w/w) were used for binary mixtures. In the case of ternary mixtures, three LBG/XG weight ratios were used (4/16, 11/9 and 16/4) at 0.02% total polysaccharide concentration. Control acid skim milk gels were structured by a homogeneous network of casein particles (0.1–0.7 μm in diameter) and clusters immobilizing whey in small pores (1–5 μm in diameter). Filamentous structures and small aggregates were observed at the surface of casein particles. Low concentration of LBG or XG (0.001% w/w) did not affect markedly the microstructure of acid skim milk gels. Conversely, LBG or XG at 0.02 or 0.1% concentration and LBG/XG blends at the three ratios selected had a great influence on the gel microstructure. Although the size and surface structure of the casein particles were not modified by the presence of polysaccharides, the primary casein network appeared very compact with a decrease of pore size and a large increase in the porosity of the network at the supramolecular level (sponge-like morphology). The effect is stronger for gels containing LBG and XG used at higher concentration and less apparent for gels containing LBG/XG blends. Skim milk/XG gels were highly organized into fibrous structures whereas skim milk/LBG gels were more heterogeneous. These structures were discussed in the light of volume-exclusion effects (demixing) and specific interactions between casein micelles and polysaccharides. At the three weight ratios, skim milk/LBG/XG gels displayed both jagged “coral-like”, “veil-like” and filamentous structures. These structures could originate from a secondary network constituted by the known LBG/XG synergistic interactions.     

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.     

Stability and rheological behaviour of salad dressing obtained with whey and different combinations of stabilizers

In this work the stability and the rheological behaviour of salad dressing containing 'Minas Frescal' whey cheese was studied. The salad dressing was stabilised by xanthan gum (XG), propylene glycol alginate (PGA) and carboxymethylcellulose (CMC). All samples were stable for a period of 4 months. The rheological model of Ostwald-de-Waelle (Power-Law) was used in order to fit the data and to obtain the rheological parameters of flow behaviour index ( n ), consistency coefficient and apparent viscosity (η_ap). All formulations showed a pseudoplastic behaviour and the PGA contributed to increase the values of flow behaviour index. Consistency coefficient was similarly affected by XG and PGA fractions. Apparent viscosity was highly influenced by the hydrocolloid CMC, with higher values of apparent viscosity in the proportion of 0.25/0.25/0.5% (PGA/XG/CMC). Hydrocolloid association (ternary mixtures) was statistically significant, resulting in an increase of K and η_ap parameters. The results show that salad dressing with whey as aqueous phase and stabilised by a ternary combination of XG, PGA and CMC can be a technological alternative to the food industry.     

Droplet characterization and stability of soybean oil/palm kernel olein O/W emulsions with the presence of selected polysaccharides

Droplet characteristics, flow properties and stability of egg yolk-stabilized oil-in-water (O/W) emulsions as affected by the presence of xanthan gum (XG), carboxymethyl cellulose (CMC), guar gum (GG), locust bean gum (LBG) and gum Arabic (AG) were studied. The dispersed phase (40%) of the emulsions was based on soybean oil/palm kernel olein blend (70:30) that partially crystallized during extended storage at 5 °C. In freshly prepared emulsions, the presence of XG, CMC, GG and LBG had significantly decreased the droplet mean diameters. XG, LBG, GG and CMC emulsions exhibited a shear-thinning behavior but AG emulsion exhibited a Bingham plastic behavior and control (without gum) emulsion almost exhibited a Newtonian behavior. Both control and AG emulsions exhibited a severe phase separation after storage (30 days, 5 °C). The microstructure of stored XG emulsion showed the presence of partially coalesced droplets, explaining a large increase in its droplet mean diameters. Increases in droplet mean diameters and decreases in flow properties found for stored GG and LBG emulsions were attributed to droplet coalescence. Nevertheless, the occurrence of droplet coalescence in these emulsions was considered to be small as no free oil could be separated under centrifugation force. Increases in flow properties and excellent stability towards phase separation found for stored CMC emulsion suggested that CMC could retard partial coalescence. Thus, the results support the ability of CMC, GG and LBG in reducing partial coalescence either by providing a sufficiently thick continuous phase or by acting as a protective coating for oil droplets.     

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.     

琼脂-刺槐豆胶协同作用及其凝胶骨架材料缓释性能

对由琼脂与刺槐豆胶组成的复合胶液进行了流变性能,旋光性能测试,对其形成的凝胶进行了力学性能与负载盐酸二甲双胍药物的缓释性能测试。测试结果表明:随着复合胶液温度的降低,琼脂分子与刺槐豆胶分子发生了相互作用;随着复合胶液中刺槐豆胶含量的增加,复合胶液的表观黏度明显增大,温度降低过程中表观黏度突增时温度点移向高温区;复合胶液的旋光度值在降温过程中明显增大;复合凝胶的硬度、耐咀性明显降低,内聚性增大,凝胶骨架结构网孔更加致密细小,药物突释现象减弱,药物缓释效果更加明显。其中样品25/75(琼/刺)效果最佳,5h达到最大溶胀率,溶胀过程吸水率可达22倍,其载药率为16.59%,载药样品的缓释过程符合一级动力学模型,T50时间为88min,整个缓释过程可持续5h以上。     

Effect of gums on the multi-scale characteristics and 3D printing performance of potato starch gel

This research investigated the multi-scale characteristics of potato starch gel (PSG) with different addition ratios of xanthan gum (XG) and locust bean gum (LBG). These characteristics are closely related and had significant impacts on 3D printing performance. Both xanthan gum and locust bean gum were able to increase the apparent viscosity, storage modulus (G′) and loss modulus (G″) of the blended gel system to varying degrees. Large amplitude oscillation shear (LAOS) was used to detect slight rheological differences led by microstructure changes. The critical strain values of the blended gel system rose as the addition ratio of locust bean gum increased. At the same time, the elastic and viscous Lissajous curves could characterize the viscoelastic changes under large strains. Fourier transforms infrared spectroscopy (FT-IR) illustrated that locust bean gum could strengthen the hydrogen bonds so that the gel had stronger mechanical properties compared with the addition of xanthan gum. Scanning electron microscopy (SEM) could observe the changes in the microstructure of the blended gel systems with addition of different addition ratios of gums. From the perspectives of 3D printing results and data analysis, the appropriate amount of xanthan gum improved the fineness and fluidity of the gels by virtue of its lubricating and coating characteristics, while the locust bean gum enabled them to have stronger shape retention abilities and better performances of resisting compressed deformation.     

Relationship between sensory saltiness intensity and added oil in low-viscosity and high-viscosity polymer solutions

Generally, the foods we usually eat are not only aqueous solutions, but also viscous solutions and solids. Therefore, it is interesting for us to explore how taste components are perceived in a viscous polymer solution. The relationship between the sensory evaluation of saltiness intensity, amount of added oil, and apparent viscosity was clarified in low-viscosity and high-viscosity polymer solutions. The study was conducted using samples containing corn oil, sodium chloride, and [xanthan gum] or [xanthan gum + locust bean gum] as a thickener. Oil was added to the viscous polymer solutions regardless of whether they were low- or high-viscosity, and saltiness intensity was evaluated as compared with a reference solution. The low-viscous polymer solutions with [xanthan gum] were perceived to be saltier than the high-viscous polymer solutions with [xanthan gum + LBG] as the amount of oil increased. The shear stress value gradually increased as the amount of oil increased in both the low-viscosity and the high-viscosity polymer solutions, as derived from the fluid constitutive equation. There was a correlation between saltiness intensity and apparent viscosity in both high- and low-viscosity polymer solutions. A coefficient of determination (R²) of 0.918 was obtained between saltiness intensity and “apparent viscosity” for the samples using [xanthan gum] and that of 0.683 between saltiness intensity and “apparent viscosity” for the samples using [xanthan gum+LBG]. The low-viscosity polymer solutions showed a saltier intensity as the amount of oil increased and a greater correlation with apparent viscosity, as compared with the high-viscosity polymer solutions.     

Adsorption-isotherm and Effect of Gum Blends on Viscosity and Microstructure of Oat Gum (β-D-Glucan)

Interactions of oat β-glucan/oat gum (OG) in binary mixtures with other gums [xanthan (XG), locust bean (LBG), and guar (GG)] were studied by viscometry at ratios (50/50, 60/40, and 80/20) and concentrations (0.5 and 0.75%). Physical structure changes due to interactions were examined by scanning electron microscopy (SEM). Equilibrium moisture contents (EMC) were observed at relative humidities (RH), 10.5%, 22%, 33%, 44%, 76% and 93%. Water and oil uptake were determined. Viscosity enhancement occurred in OG/LBG (50/50 and 60/40; 0.5%) and OG/XG (60/40; 0.5%) blends, suggesting synergism. Micrographs depicted microstructural homogeneity (single bulk phase) in OG/LBG and OG/XG blends. EMC of OG and GG were 26.1 and 31.6%, respectively, at 93% RH for 2 wk. LBG showed high mold growth at 93% RH. Uptake of water and oil by OG were 2.6 and 2.0 mL/g, respectively.     

THE INFLUENCE OF DIFFERENT TOTAL SOLID, STABILIZER AND OVERRUN LEVELS IN INDUSTRIAL ICE CREAM PRODUCTION USING COCONUT OIL

The purpose of this research was to explain the combined effects of different total solid (TS) contents (20, 30 and 40%), stabilizer types (guar gum [GG], locust bean gum [LBG], carboxymethyl cellulose [CMC]) and overrun rates (OR) (30, 60 and 90%) on mix viscosity, melting time and hardness properties, which are the most important quality characteristics on industrial ice cream production. According to the investigation parameters; GG gave significantly less viscosity to the mix than LBG and CMC. In other words, LBG and CMC may be preferred to increase the viscosity of the mix or to limit the growth rate of ice crystals during recrystallization. Softness of ice creams and melting rapidity were linearly proportional to the increase of TS and ORs.

PRACTICAL APPLICATIONS

The most important parameters affected ice cream structure and quality are total solid, overrun and stabilizers. In many researches, the investigators have been focused of these parameters on only one or rarely two. In this research, the combined effects of different total solids (20, 30 and 40%), stabilizer types (guar gum, locust bean gum, carboxymethyl cellulose) and overrun levels (30, 60 and 90%) were investigated together in same mix and in industrial production conditions.     

Effect of single and integrated emulsifier-stabiliser on soy-ice confection

Soy-ice confections were prepared incorporating locust bean gum (LBG), guar gum (GG), sodium carboxymethylcellulose (CMC) and alginate as single stabilisers with glyceromonostearate (GMS) as an emulsifier. The integrated emulsifier-stabiliser (IBS) used was Sherex (mixture of mono-di glycerides, LBG, GG and carrageenan). All confections were analysed for viscosity, foam and texture properties, meltdown and shape factor, glass transition temperature (Tg), melting temperature (Tm) and sensory properties. Sherex imparted highest viscosity (8.88 Pa.s) to the confection mix. LBG, CMC and Sherex gave better foaming properties, with LBG providing the best air incorporation. All samples exhibited desirable melting characteristics. Sherex influenced the shape factor more than other stabilisers, with a highest score (125.3%). The Sherex-incorporated confection showed the highest Tg (−29.64 °C) and Tm (2.59 °C). Sherex, LBG and alginate provided good sensory attributes to the confection. It was concluded that an IBS, such as Sherex, enhanced viscosity in the product mix, and hence could produce a soy-ice confection with improved quality as shown by better foaming and textural properties as well as better sensory attributes.     

The effect of shear rate on the viscosity of solutions of guar gum and locust bean gum

The apparent viscosities of aqueous solutions of guar gum and locust bean gum have been measured over a range of shear rates from 14 to 1142 s^?1. Comparable measurements were also made on gum solutions to which glucose, sucrose or glucose syrup had been added. For all the solutions the variation of relative viscosity with shear rate fits a power law equation. Addition of sugar has no effect on the non-Newtonian behaviour of the gum solutions. The relative viscosity of the gum in the sugar solutions is lower than in water. The ratios of the relative viscosities closely correspond with the ratios of the intrinsic viscosities. This is interpreted in terms of a smaller extension of the gum molecule in the sugar solution.     

黄原胶与魔芋胶混胶黏度的影响因素研究

黄原胶和魔芋胶都是非凝胶多糖，二者在一定条件下共混可以出现强烈的协同效应。本文研究当黄原胶和魔芋胶以5／5的配比共混，总浓度为1％，温度，柠檬酸，蔗糖和功能型甜味对混胶多糖黏度的影响。结果表明：升高温度使混胶的黏度降低；当柠檬酸的使用量大于0．2％时，混胶的黏度下降；40℃时甜味剂的加入使得混胶的黏度升高。     

The role of characteristic times in rheological description of structure forming food additives

The work is focused on the interpretation of flow curves obtained at two different temperatures for water solutions of xanthan and guar gum, and pastes of oxidized corn starch and starch phosphate. Based on exponential state equations for shear thinning and shear thickening systems characteristic times distributions were estimated using Tikhonov regularization method. Values of time constants and their intensities were strongly associated with the composition of the examined mixtures. Food thickeners such as GG or XG form solutions of very high viscosity. Characteristic times determined from De Kee equation take large values (0.1–1 s). This could be connected with a predominance of viscous behavior during shear. Starch pastes with GG or XG show very complex rheological behavior resulting from synergistic effects. This is reflected in the form of distributions of time constants, which have two peaks. One of them is specific to the non-starch hydrocolloid and corresponds to the characteristic time of approximately 1 s. Global maximum is located at the time of 0.001 s and is associated with the presence of starch and its gel structure. The differences in rheological characteristic times for various structure forming agents reflect their technological functions.     

Viscosity of solutions of xanthan/locust bean gum mixtures

Xanthan and locust bean gums are polysaccharides able to produce aqueous solutions with high viscosity and non‐Newtonian behaviour. When these solutions are mixed a dramatic increase on viscosity is observed, much greater than the combined viscosity of the separated polysaccharide solutions. In this work the influences of different variables on the viscosity of solutions of mixtures of xanthan/locust bean gum have been studied. Total polysaccharide concentration, xanthan and locust bean ratio on mixture and temperature at which the gum was dissolved (dissolution temperature) for both xanthan and locust bean gums have been considered. Under these different operational mixture conditions shear rate and time have also been considered to describe the rheological behaviour of the solutions studied. The high viscosity increase observed in these mixtures is due to the interaction between xanthan gum and locust bean gum molecules. This interaction takes place between the side chains of xanthan and the backbone of the locust bean gum. Both xanthan molecule conformation in solution – tertiary structure – and locust bean gum structure show great influence on the final viscosity of the solution mixtures. Xanthan conformation changes with temperature, going from ordered structures to disordered or chaotic ones. Locust bean gum composition changes with dissolution temperature, showing a dissolved galactose/mannose ratio reduction when temperature increases, ie the smooth regions – zones without galactose radicals – are predominantly dissolved. The highest viscosity was obtained for the solution mixture with a total polysaccharide concentration of 1.5 kg m⁻³ and a xanthan/locust ratio of 2:4 (w/w) and when xanthan gum and locust bean gum were dissolved at 40°C and 80°C, respectively. © 1999 Society of Chemical Industry     

Effect of hydrocolloids on the rheological, microscopic, mass transfer characteristics during frying and quality characteristics of puri

Effect of hydrocolloids such as guar gum (GG), arabic gum (AG), carrageenan (CG), locust bean gum (LBG), xanthan gum (XN), hydroxypropyl methylcellulose (HPMC) and carboxymethylcellulose (CMC) at 0.5% w/w level on rheological and quality parameters of puri from whole wheat flour was studied. Hydrocolloids like CMC, XN and HPMC increased the water absorption of puri dough, while it decreased in all other samples. The dough development time and mixing tolerance index values increased, while dough stability did not get affected. On addition of hydrocolloid, there was a reduction in the pasting temperature, while the peak viscosity, hot paste viscosity and cold paste viscosity values increased. Hardness, cohesiveness and adhesiveness properties of the puri dough increased with the addition of hydrocolloids. All the hydrocolloids used in general helped in retention of moisture in the puri and hence remained softer and pliable, while there was a significant reduction in the oil content of puri samples containing hydrocolloids. Among the different hydrocolloids used, addition of guar gum at 0.5% w/w level led to puris having improved quality characteristics to a greater extent with respect to moisture retention, lowering of oil content upon frying with softer and pliable texture and better keeping quality. The mass transfer studies confirmed that the mass transfer co-efficient values for moisture loss and oil uptake were lower in puris with guar gum than control.     

NONMEAT INGREDIENTS FOR LOW-FAT GROUND BEEF PATTIES

Nine ground beef treatments were evaluated to compare chemical, physical and sensory characteristics of low-fat ground beef patties containing various water binders. Treatments 1–5 contained a blend of iota and kappa carrageenans having various viscosity and gelling characteristics (SD389, Viscarin SD 389; ME389, Viscarin ME 389; GP379, Gelcarin GP379; ME389/GP379, 50/50 ME389 & GP379; and ME621, Gelcarin ME621), and treatments 6–9 contained other water binders (XG/LBG, xanthan/locust bean gum; PF, pea flour; ALG, algin; and LB. Lean Bind^TMmodified food starch). Treatment 1, which contained carrageenan (SD389), served as the control. Algin patties were rated lowest in flavor intensity. Algin and LB patties were highest in sensory tenderness and had the lowest shear force values. The patties manufactured from ME389/GP379 and XG/LBG received higher overall acceptability scores than the control SD389 patties.     

LINEAR AND NONLINEAR VISCOELASTIC BEHAVIOR OF OIL-IN-WATER EMULSIONS STABILIZED WITH POLYSACCHARIDES

The rheological behavior and stability of oil-in-water emulsions stabilized by different thickening agents were analyzed. Food emulsions were prepared with commercial sunflower oil (40% w/w oil-in-water) and stabilized with 1% emulsifier. The tested thickeners were: (1) 1% w/w xanthan gum (XG), (2) 5% w/w potato starch (PS), (3) 5% PS + 0.5% XG, (4) 1% w/w guar gum (GG), and (5) 0.5% XG + 0.5% GG. Mean droplet size and droplet size distribution (DSD) of emulsions were determined by static light scattering. Steady flow (viscosity versus shear rate), transient flow (viscosity versus time) and oscillatory shear tests (linear viscoelasticity) were performed. The addition of thickening agents improved the stability of the emulsions, the effect was less marked in systems containing only GG. DSD was not significantly modified in emulsions containing starch or hydrocolloids. Microscopic observations showed that all the tested emulsions were flocculated due to the presence of hydrocolloids. The observed shear thinning behavior was attributed to the molecular structure of the polysaccharides and to the flocculation/deflocculation process; viscosity data were satisfactorily fitted to the Cross model. Frequency sweeps showed that emulsions with PS or XG have a weak gel structural network (G' > G); those with GG correspond to a polymeric solution where G' and G" curves intersect within the range of tested frequencies. The viscoelastic linear behavior was described according to the Maxwell generalized model. The discrete relaxation spectrum and relaxation times were estimated from the experimental values of G' and G" for emulsions with PS, PS + XG, and XG. Nonlinear viscoelasticity was also studied from stress relaxation curves at different shear strains. The damping function was calculated and the Soskey-Winter parameters were determined. Transient flow viscosities at different shear rates were comparable to the values estimated from stress relaxation measurements.     

Rheological Properties of Solutions and Emulsions Stabilized with Xanthan Gum and Propylene Glycol Alginate

The rheological effects of propylene glycol alginate (PGA) added to solutions and model emulsions containing xanthan gum (XG) were studied using controlled stress rheometry with concentrations appropriate for salad dressings. For samples with XG and XG + PGA blends, solutions and emulsions showed a Newtonian plateau at low shear stresses. The Newtonian plateau of a solution accurately predicted (r²= 1.00) the Newtonian plateau for an emulsion of equivalent gum concentration. Addition of PGA to constant levels of XG showed a more than additive increase in the Newtonian plateau viscosity for solutions and emulsions. For XG aqueous solutions, pseudoplasticity decreased upon addition of PGA. Storage and loss moduli increased with addition of PGA to XG for solutions and emulsions, although G’ for solutions of PGA alone were negligible.     

RHEOLOGICAL CHARACTERIZATION OF CARBOXYMETHYLCELLULOSE SOLUTION UNDER ASEPTIC PROCESSING CONDITIONS

The rheology of Carboxymethylcellulose (CMC) solutions, which are widely used as carrier fluids in aseptic processing simulations, was studied. Effects such as time dependency, recovery, and viscoelasticity were studied. A model was developed to determine the apparent viscosity of CMC solutions as a function of shear rate, temperature, and concentration. The model can be used in process design from both a fluid mechanics standpoint and a heat transfer standpoint. It was found that the solutions behaved as pseudoplastic fluids that were irreversibly thixotropic and also viscoelastic.