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.     

The viscosity of dilute solutions of x-carrageenan and sodium carboxymethylcellulose

The apparent viscosities of dilute solutions of _K-carrageenan and sodium carboxymethylcellulose have been measured and the intrinsic viscosities calculated. Added glucose, sucrose and glucose syrup increase the apparent viscosities of the solutions but give lower values for the intrinsic viscosity. In the presence of glucose syrup the macromolecules exhibit the behaviour associated with neutral macromolecules. This is attributed to the presence of inorganic cations in the glucose syrup which, by interaction with the polyanion, prevent dissociation of the ionic groups in the polysaccharides.     

The viscosity of dilute solutions of guar gum and locust bean gum with and without added sugars

The apparent viscosities of dilute solutions of guar and locust bean gums have been measured. The intrinsic viscosity [n] of guar gum solution is greater than that of locust bean gum solution, but the interaction coefficient k of guar gum solutions is less than that of locust bean gum. Addition of glucose, sucrose, or glucose syrup increases the apparent viscosity of the gum solution. The intrinsic viscosity of the gum solution is decreased but the interaction coefficient is increased.     

Effect of κ-carrageenan on milk protein polysaccharide mixtures

The effect of κ-carrageenan (0, 0.025, 0.05%) on phase separation between polysaccharides (0.36% of locust bean gum (LBG), guar gum, or xanthan gum) and milk proteins (from 10.5% skim milk powder) in solution was studied. Xanthan gum was seen to be the most incompatible with milk proteins, followed by guar gum and LBG. Casein micelles were more incompatible with all polysaccharides than whey proteins. Whereas at either concentration κ-carrageenan inhibited visual phase separation, it was seen by transmission electron microscopy that samples with κ-carrageenan showed microscopic phase separation. Samples with 0.05% κ-carrageenan and either LBG or guar gum and all samples with xanthan gum could be described rheologically as weak gels, while those with no or 0.025% κ-carrageenan and either LBG or guar gum could be described as concentrated solutions. Thus, no correlation was seen between the inhibition of macroscopic phase separation by κ-carrageenan and the formation of a weak gel in solution.     

Effect of hydrocolloid type and concentration on flow behaviour and sensory properties of milk beverages model systems

Formulation of low-calorie flavoured milk beverages involves the use of hydrocolloids to obtain an acceptable mouthfeel. Sodium alginate and κ-carrageenan are the most commonly used. In this paper, the rheological behaviour of model solutions containing either of these two hydrocolloids, with or without the addition of sucrose, in water or milk, has been studied. All solutions fitted well to the Ostwald de Waele model. The analyses of variance showed that in κ-carrageenan solutions, the effect of the medium–hydrocolloid interaction on both flow index (n) and apparent viscosity at 1 s⁻¹ (η₁) was significant. Milk-based solutions were more pseudoplastic and more viscous than the aqueous solutions, due to the well known κ-carrageenan–casein molecular interaction. In alginate solutions, the medium–hydrocolloid interaction was also significant but the differences in both n and η₁ values were of less entity. Sensory viscosity differences of more viscous chocolate milk model systems were well explained by apparent viscosity values at low shear rate (10 s⁻¹), while for less viscous samples apparent viscosity at higher shear rate (300 s⁻¹) values were appropriate. At similar viscosity, κ-carrageenan systems showed better flavour-releasing properties than alginate.     

Sweetening power of aspartame in hydrocolloids gels: Influence of texture

Equivalent sweetness of aspartame relative to two sucrose concentrations (10% and 20% w/w) were determined in water and in hydrocolloids gels. The influence of the texture of three hydrocolloids gelled systems—gellan gum, κ-carrageenan, and κ-carrageenan/locust bean gum (LBG)—at two gums concentrations (0.3% and 1.2% w/w) on the equivalent sweetness of aspartame were then studied. For the three gelled systems, the increase in hydrocolloid concentration produced a significant increase in the true rupture stress and in the deformability modulus values. For both κ-carrageenan and mixed gels the true rupture strain values increased when increasing hydrocolloid concentration while for gellan gels, decreased. For the same hydrocolloid concentrations the κ-carrageenan/LBG gels showed the largest strain at rupture and gellan gels the smallest (most brittle). For both soft (0.3% gum) and hard (1.2% gum) gellan gels and κ-carrageenan gels, the concentrations of aspartame needed to deliver a sweetness intensity equivalent to that of gels with 10% sucrose (0.079–0.087% w/w) were similar to those obtained for aqueous solutions (0.084% w/v). For hard κ-carrageenan/LBG gels the corresponding concentration of aspartame was slightly lower. For all gelled systems the concentrations of aspartame needed to deliver a sweetness intensity equivalent to that of gels with 20% sucrose were higher for soft gels than for hard gels.     

RHEOLOGICAL PROPERTIES OF HYDROCOLLOIDS IN THE PRESENCE OF SUCROSE AND MILK

Apparent viscosities of guar gum, locust bean gum, and sodium carboxymethylcellulose were measured at shear rates of 16-2620s^-1 in water, sucrose, milk, and sucrose/milk solutions. The effect of different heat treatments was also studied. For all solutions, a power law equation described the variation of relative viscosity with shear rate allowing comparison of their non-Newtonian behaviour. With the neutral hydrocolloids, the hydration was limited by the presence of sucrose and milk which reduced the effective length of the polymer molecules. The behaviour of the polyanionic hydrocolloid, Na CMC, although influenced by milk and sucrose separately, was controlled by milk in a milk/sucrose mixture. This is due to milk salts which reduced the intramolecular repulsions along the polyanion and substantially lowered its effective hydrated length.     

The effect of pH,salts and sugars on the rheological properties of cress seed (Lepidium sativum) gum

Effect of shear rate (15–600 s^?1), gum concentration (1–2%), pH (3–9), sucrose (10–40%), lactose (5–15%), NaCl (100–300 mm ) and CaCl₂ (5–50 mm ) was evaluated on apparent viscosity (η_a), flow behaviour index (n), consistency coefficient (K) and yield stress (τ₀) indices of cress seed gum (CSG) solutions. Different rheological models were used to fit the experimental data, although the Herschel–Bulkley model was found the best model. An increase in gum concentration led to an increase in τ₀, η_a, and k and a decrease in n values. The addition of salts lowered the k value; however, the n value showed slight significant change. The presence of sugar resulted in the enhancement of n, k, τ₀ and η_ap values. The existence of yield stress and pseudoplastic behaviour of CSG, its stability against salts, wide range of pH and synergic effect of sugar make it a good thickener and stabiliser in food formulations.     

Rheological characterization of experimental dairy creams formulated with locust bean gum (LBG) and λ-carrageenan combinations

The influence of the locust bean gum (LBG)–λ-carrageenan stabilizer combination on the rheology of dairy creams was analyzed. A central composite factorial design was used to choose the LBG–λ-carrageenan ratio, the weight fraction of each gum ranging from 0 to 0.1 g per 100 g cream. Cross’ rheological model was closely fitted to describe the flow curves of the samples and Cross parameters were correlated with gum concentrations. The rheological behaviour of model aqueous gum solutions, with the same pH, ionic strength, and competitive solute concentration as the cream serum, was also examined to analyze gum interactions. Strong interaction of λ-carrageenan with cream components, probably with caseins, may be anticipated based on a great increase in viscosity. The functional role of LBG seems to be associated with an increase in the emulsion shear stability.     

Enhancement effect on apparent viscosity of aqueous tragacanth gum dispersions promoted by sugars

Flow curves of aqueous dispersions of tragacanth gum (T) with sucrose and glucose at different temperatures were determined using a controlled‐stress rheometer. The effect of sodium chloride without or with sucrose (at the highest content) on the rheology of T dispersions was evaluated. The presence of sucrose and glucose promoted a noticeable enhancement impact on the apparent viscosity of aqueous T dispersions, which depended on sugar type/content, shear rate and temperature. In all cases, the glucose addition led to the largest enhanced viscosities at low shear rates (<10 s^?1) and temperature. The joint action of sugar and salt exhibited a notable effect on apparent viscosity at low shear rates, softening the strong shear‐thinning behaviour of T samples. Flow curves of T in the presence of sugars were satisfactorily described by the Cross‐Williamson model, being semi‐empirical correlations of the model parameters with ingredients content and temperature stablished.     

Mechanical properties of κ-carrageenan in high concentration of sugar solutions

While the mechanism of gelation of carrageenan in an aqueous environment, via a coil–helix transition followed by aggregation, is well accepted, its behaviour in highly concentrated sugar is still not well understood. Therefore, the effect of biopolymer and salt concentration on the gelling properties of κ-carrageenans in the presence of high concentrations of sugars was investigated rheologically. A solution of 1% κ-carrageenan in the presence of 10 mM KCl and 87.5% corn syrup did not form a measurable network whereas 1% κ-carrageenan in the presence of 10 mM KCl in aqueous solution forms a gel. Gelation was again observed as KCl concentration was increased to 40 mM KCl. An increase of κ-carrageenan concentration from 1 to 2% with 10 mM KCl present did not restore the capacity for gelation. The effect of type of the sugar solution was also investigated by substituting a corn syrup/glucose syrup mixture for the original corn syrup. In the presence of corn syrup/glucose syrup mixture and salt at concentrations higher than 40 mM KCl, a different gelation behaviour was observed: a gel structure was already present at high temperature and a glass transition was measurable at the lowest temperatures. We believe this study gives new insights into the molecular state of carrageenan in the presence of high concentrations of sugars.     

The effect of casein on the viscosity of solutions of hydrocolloids

The apparent viscosities of aqueous solutions of guar gum, locust bean gum, sodium carboxymethylcellulose and k-carrageenan have been measured over a range of shear rates from 14 to 1142 s^?1. Comparable measurements were made on solutions to which different quantities of casein (10-40 g litre^?1) had been added. For all the solutions a power law equation describes the variation of relative viscosity with shear rate. Addition of casein has no effect on the solutions of guar and locust bean gum, but does affect the rheology of solutions of sodium carboxymethylcellulose and k-carrageenan. The behaviour of k-carrageenan indicates a dependence on the polyanion:casein ratio, reaching a maximum at a concentration ratio of 1:4. The only significant solute-solute interactions in the hydrocolloid-casein solutions are electrostatic in nature.     

Flow properties of fruit fillings

The flow properties of the fluid portion of fruit fillings were assessed to investigate the effects of gums. Results indicated that the shear rate–shear stress relations of the fluid portion of commercial fruit fillings and the model fillings made of waxy corn starch, fructose, citrate buffer, and a gum which could be guar gum, locust bean gum, CMC, xanthan gum or κ-carrageenan, fit well into the Herschel–Bulkley equation for pseudoplastic fluids. The fluid portion of the commercial fruit fillings was characterized with a yield stress between 39–51 Pa, a consistency index between 52–104 Pa·sⁿ, and a flow index (n) around 0.4. In addition, the shear rate–shear stress relations could be fitted into a modified Herschel–Bulkley equation with a flow index fixed at 0.4. Addition of guar gum, locust bean gum and CMC increased while xanthan gum and κ-carrageenan decreased the consistency and flow indices in the modified Herschel–Bulkley equation. The effect of gum addition on the apparent viscosity of model fillings varies with the type of gum, amount of addition, and shear rate.     

Rheological Properties of Leucaena glauca Gum in Aqueous Solutions

The flow properties of Leucaena glauca gum solutions were studied in the range of shear rates 1.5 to 1310 s⁻¹, using a rotational viscometer Rheotest 2. The flow behaviour of aqueous solutions of the polysaccharide is pseudoplastic, and transition from Newtonian to pseudoplastic behaviour occurs in the low shear rate range at concentrations of interest to the industry. The flow of polysaccharide solutions is described by equation of state proposed by M. M. Cross. The basic rheological parameters, like zero shear rate viscosity (η_o), infinite shear rate viscosity (ηα) and a constant associated with the rupture of linkages (α) were calculated applying simple and established relations. The effect of concentration and temperature on rheological parameters have been studied. The Cross equation is found to be applicable to the data with a good degree of accuracy over a wide range of shear rates.     

Steady-shear flow of semidilute guar gum solutions with sucrose, glucose and sodium chloride at different temperatures

Steady-shear flow curves of aqueous solutions of guar gum at 0.22% at different temperatures (5-65 °C), guar gum (0.22%) with sugars (sucrose or glucose) at different sugar/water ratio (0.10, 0.20 and 0.40) at 5 °C, guar-sugar (at 0.40 sugar/water ratio) at different temperatures (5-65 °C) and guar gum and guar-sucrose (0.40 sucrose/water ratio) with NaCl (1%) at 5 °C, were determined using a controlled-stress rheometer over a wide range of shear rate (1-1000 s⁻¹). Apparent viscosity increased with decreasing temperature and increasing sugar content independent of sugar type. Synergic effect on apparent viscosity due to sugar addition was found and was correlated with sugar content. Salt addition decreased slightly the apparent viscosity and increased the shear-thinning behaviour of the guar gum solution. Steady-shear flow curves were satisfactorily described by the Cross model. Semi-empirical correlations of Cross model parameters with sugar content and temperature were obtained.     

Effects of Fat Replacers and Sweeteners on the Time-Dependent Rheological Characteristics and Emulsion Stability of Low-Calorie Pistachio Butter: A Response Surface Methodology

The effect of three fat replacers (xanthan gum, Reihan seed gum, and Balangu seed gum) and two sweeteners (sucrose and isomalt) on time-dependent rheological properties of low-calorie pistachio butter were analyzed using response surface methodology. The steady shear behavior of all samples was shear thinning (n = 0.156–0.6175), and power law model was fitted the upward and downward curves properly (R ² = 0.847–0.998). Balangu seed gum (0.01–0.04 wt.%), Reihan seed gum (0.01–0.023 wt.%), xanthan gum (0.06–0.1 wt.%), isomalt (0–1 wt.%), and sucrose (0.25–1 wt.%) were the levels investigated. A central composite design was used to develop models for the responses. The obtained experimental data were fitted to a second-order polynomial equation and also analyzed by appropriate statistical methods. In most cases, increasing the sweetener level led to a significant decrease in consistency coefficients. However, the effect on the flow behavior index was not significant. The effect of gum concentration on the rheological parameters was not significant (p ≤ 0.1), except for formulas prepared using Balangu seed gum. All formulas studied were stable on shelf.     

Rheological properties and gel strength of Phaseolus lunatus protein/carboxymethylated flamboyant gum systems

The rheological behaviour and gel strength of hydrocolloid mixture systems (HMSs) of carboxymethylated flamboyant gum (CFG) with protein hydrolysates (PHs) of Phaseolus lunatus were examined to evaluate the influence of the protein/polysaccharide ratio (2:1 and 3:1), pH (3 and 9) and concentration of solids, according to a 2³ factorial design. The protein concentrate of P. lunatus was hydrolysed with pepsin–pancreatin enzymes. The flow curve results were fitted to the Ostwald–de Waele model. The flow behaviour index (0.66–0.78) for all conditions studied was indicative of the shear‐thinning behaviour. For the HMS, the consistency index (k) values ranged from 0.4 Pa sⁿ to 1.2 Pa sⁿ. The analyses of variance showed that the ratio of PH/CFG and pH were the main variables that had significant effect on k values (P < 0.05). Only PH system presented a weak gel‐like viscoelastic behaviour. Both functional properties were affected by the protein degree of hydrolysis (DH).     

Mass transfer kinetics and mathematical modelling of the osmotic dehydration of orange‐fleshed honeydew melon in corn syrup and sucrose solutions

A simple mathematical model to predict dehydration and impregnation process during osmotic dehydration of orange‐fleshed honeydew in sucrose and corn syrup solutions was proposed. Results showed low dispersion and a good fitting capability for WL and SG kinetics. Diffusivity values for WL ranged from 0.96 × 10^?10 to 2.22 × 10^?10 and 1.04 × 10^?10 to 3.10 × 10^?10 m² s^?1 in corn syrup and sucrose solutions, respectively. For SG, the obtained range was 0.72 × 10^?10 to 2.35 × 10^?10 and 0.71 × 10^?10 to 2.46 × 10^?10 m² s^?1 in corn syrup and sucrose solutions, respectively. The half‐life of dehydration rates (t_1/2) was from 30.9 to 71.2 min and from 19.4 to 57.5 min in corn syrup and sucrose solutions, respectively. Diffusivities values obtained according to the proposed model were close to the ones observed from diffusive model; t_1/2 was a promising criterion for the process time definition.     

Effects of bacterial cellulose on glucose metabolism in an in vitro chyme model and its rheological evaluation

Hyperglycaemia affects the health of people worldwide. The study investigated the effects of bacterial cellulose (BC) on glucose metabolism using an in vitro chyme model, including glucose adsorption, glucose diffusion, kinetics model of glucose and rheological properties of BC. The results indicated that BC exhibited significant inhibition of α-amylase in a dose-dependent manner (IC₅₀ = 7.86 mg mL⁻¹) and could significantly adsorb glucose by binding to the glucose molecules (4.11 ± 0.18 mmol g⁻¹) (P < 0.05). The BC chyme system was a non-Newtonian fluid showing shear thinning and has the characteristics of elastic solid. The diffusion behaviour of glucose in the BC chyme system conformed to first-order release kinetics model, indicating its inhibition of glucose diffusion by changing the rheological properties of chyme. This study provides a theoretical basis for dietary intervention and nutritional support for patients with hyperglycaemia.     

Compression resistance,sweetener's diffusion and sweetness of hydrocolloids gels

The effects of the type and concentration of two hydrocolloids—κ-carrageenan and gellan gum—and of the type and concentration of two sweeteners—sucrose and aspartame—on the gel resistance to compression, on the sweetener diffusion and on the intensity of the gel sweetness and the relationships between the gel physical properties and their perceived sweetness were studied. The gels true rupture stress increased with hydrocolloid concentration, this increase being higher for gellan gels. Gellan gels showed lower true rupture strain values, which in contrast with carrageenan gels, decreased on increasing hydrocolloid concentration. The addition of sucrose produced a bigger increase in gel strength at the higher hydrocolloid concentration. The main effect detected on the sweeteners’ diffusion constant was the higher value observed in low concentration (3 g L⁻¹) κ-carrageenan gels. Gellan gels were perceived as sweeter than κ-carrageenan gels. The decrease in sweetness due to an increase in hydrocolloid concentration was greater in gellan than in carrageenan gels. Variations in sweetener concentration, true rupture strain, and deformability modulus values explained 93% of the variability in sweetness for gels with sucrose and 94% for gels with aspartame.