Effect of ozonation on the rheological and colour characteristics of hydrocolloid dispersions

The effect of ozonation on the rheological and colour characteristics of guar, carboxyl methyl cellulose (CMC), and pectin dispersions was investigated. Guar 1%, CMC 1% and pectin 2% (w/v) dispersions were ozonated at varying ozone concentrations of 2.4%, 4.0%, 5.6% and 7.8% (w/w) for 3, 5, 7 and 10 min processing times at 20 ± 1.0 °C. Flow and dynamic rheological properties together with Hunter colour parameters (L^*, a^*, b^*) were measured for control and treated samples. Significant differences were observed in the rheological characteristics and colour of all ozonated hydrocolloid dispersion studied. No recovery was observed in the structure breakdown after a 24 h storage period. This study indicates that ozonation has a significant effect on both the rheology and colour of hydrocolloid dispersions and that due attention should be given before incorporating these hydrocolloids in food formulations which are subsequently ozonated in food processing and preservation processes.     

Rheological properties of gluten-free bread formulations

In this study, the rheological properties of rice bread dough containing different gums with or without emulsifiers were determined. In addition, the quality of rice breads (volume, firmness and sensory analysis) was evaluated. Different gums (xanthan gum, guar gum, locust bean gum (LBG), hydroxyl propyl methyl cellulose (HPMC), pectin, xanthan–guar, and xanthan–LBG blend) and emulsifiers (Purawave^™ and DATEM) were used to find the best formulation for gluten-free breads. Rice dough and wheat dough containing no gum and emulsifier were used as control formulations. The rice dough containing different gums with or without emulsifiers at 25 °C showed shear-thinning behavior with a flow behavior index (n) ranging from 0.33–0.68 (except pectin containing samples) and consistency index (K) ranging from 2.75–61.7 Pa sⁿ. The highest elastic (G′) and loss (G″) module were obtained for rice dough samples containing xanthan gum, xanthan–guar and xanthan–LBG blend with DATEM. When Purawave^™ was used as an emulsifier, dough samples had relatively smaller consistency index and viscoelastic moduli values compared to DATEM. The viscoelastic parameters of rice dough were found to be related to bread firmness. Addition of DATEM improved bread quality in terms of specific volume and sensory values.     

Rheological behaviour of pullulanase-treated guar galactomannan on co-gelation with xanthan

The present study involves the use of non-specific enzyme pullulanase (from Bacillus acidopullulyticus) to remove galactose residues from guar galactomannan to obtain modified guar galactomannan mimicking the functional properties of locust bean gum. The modified guar galactomannan blended with xanthan exhibited the rheological behaviour of elastic modulus (G′) greater than viscous modulus (G″) with a decrease in tan δ value similar to locust bean gum/xanthan blend. Also a twofold increase in the magnitude of elasticity compared to xanthan alone suggested the synergistic interaction with formation of three dimensional networks. The modified guar galactomannan with galactose content of 21% and M:G ratio 1:3.8, almost akin to locust bean gum, showed a better interaction with xanthan. Dynamic stress sweep study of modified guar galactomannan/xanthan blend with increased yield stress of 800 dynes/cm² also indicated the synergistic behaviour. Modified guar galactomannan also revealed the maximum synergistic interaction with xanthan at a mixing temperature of 60 °C than at 20 °C, 30 °C, 40 °C and 50 °C, respectively. Modification of guar galactomannan by pullulanase is an alternative route to produce galactose-depleted guar galactomannan with enhanced rheological functionalities on co-gelation with xanthan, as a cost effective replacement to locust bean gum.     

Steady shear flow properties of wild sage (Salvia macrosiphon) seed gum as a function of concentration and temperature

The steady shear flow properties of dispersions of a new potential hydrocolloid, sage seed gum (SSG), were determined as a function of concentration (0.5–2% w/w), and temperature (20–50 °C). SSG dispersions exhibited strong shear-thinning behavior at all conditions tested, which was even more pronounced than commercial hydrocolloids like xanthan, guar gum and locust bean gum. Different time-independent rheological models were used to fit the experimental data, although the Herschel–Bulkley model (H–B) was found the best model to describe steady shear flow behavior of SSG. An increase in gum concentration led to a large increase in yield stress and consistency coefficient values, whereas there was no definite trend with an increase in temperature. On the other hand, the above-mentioned increases in concentration and temperature did not yield a clear evolution of the shear-thinning characteristics of SSG dispersions. An Arrhenius-type model was also used to describe the effect of temperature. The activation energy (E_a) appeared in the range of 3949–16384 J/mol, as concentration increased from 0.5 to 2%, at a shear rate of 100 s⁻¹. The yield stress values estimated by viscoplastic rheological models were much higher than the data determined by stress ramp method. Apparent viscosity of SSG surpassed many commercial hydrocolloids such as guar gum, locust bean gum, Tara gum, fenugreek gum and konjac gum at the same conditions, which suggest it as a very good stabilizer in food formulations.     

Effects of pectin and guar gum on creaming stability, microstructure and rheology of egg yolk plasma-stabilized emulsions

The influence of pectin and guar gum on the creaming stability, microstructure and rheological properties of 1.0% (w/v) egg yolk plasma (EYP)-stabilized 25.0% (v/v) soybean oil-in-water emulsions was studied at pH 7.0. Addition of pectin/guar gum decreased creaming percentage, and no creaming was detected in the presence of 0.5% (w/v) pectin/guar gum as a result of increasing viscosity. At the end of 10 h, creaming percentage decreased from 61 to 57% with the addition of 0.05% (w/v) guar gum and to 39% with the addition of 0.2% (w/v) guar gum. Microscopic observations represented the droplet aggregation arising from the presence of nonabsorbing biopolymers. At \mathop g^. \mathop \gamma \limits^{.}  = 10 s⁻¹, a tenfold increase in viscosity was observed in the presence of 0.5% (w/v) guar gum compared to the presence of 0.1% guar gum due to the thickening effect of polysaccharide. Increasing gum concentrations enhanced the viscosity and hence the consistency index. All emulsions, except for those containing 0.5% (w/v) guar gum, reflect the near-Newtonian behaviour with flow behaviour index, n, of 0.9–1.0. All emulsions exhibited a liquid-like behaviour at low frequencies (<7.0 Hz) where G″ values were higher than G′. Both G′ and G″ showed a frequency dependency and these two moduli crossed each other at higher frequencies (>7.0 Hz), G′ became greater than G″ and the system behaved like an elastic solid. Addition of pectin at all levels cause no significant change in G′ and G″ values, whereas addition of guar gum, especially at a concentration of 0.5% (w/v), significantly improved these values.     

Rheological interactions between Lallemantia royleana seed extract and selected food hydrocolloids

BACKGROUND: Lallemantia royleana (Balangu) is a mucilaginous endemic plant which is grown in different regions of world. The flow behaviour of Balangu seed extract (BSE) and its mixture with xanthan, guar and locust bean gums at 1:3, 1:1 and 3:1 ratios, in addition to control samples (0% BSE), were evaluated. To describe the rheological properties of samples, the power law model was fitted on apparent viscosity–shear rate data. To evaluate the interaction between BSE and selected hydrocolloids in dilute solutions, the relative viscosity was also investigated. RESULTS: There was no significant difference between the consistency coefficient of guar and locust bean solutions and their blends substituted with 250 g kg^?1 BSE. The BSE–xanthan mixture at 1:3 and 1:1 ratios had consistency index equal to xanthan solution. BSE–locust bean gum at all ratios, BSE–xanthan at 1:3 ratio and BSE–guar gum at 1:1 and 3:1 ratios indicated relative viscosity lower than values calculated assuming no interaction. The intrinsic viscosity value of BSE was determined 3.50 dL g^?1. CONCLUSION: The apparent viscosities of BSE, selected hydrocolloids and their blends were the same at a shear rate of 293 s^?1 and the commercial gums can be substituted by 250 g kg^?1 and 500 g kg^?1 BSE. Copyright © 2011 Society of Chemical Industry     

Rheological properties of whey protein isolate stabilized emulsions with pectin and guar gum

Dynamic oscillatory and steady-shear rheological tests were carried out to evaluate the rheological properties of whey protein isolate (WPI) stabilized emulsions with and without hydrocolloids (pectin and guar gum) at pH 7.0. Viscosity and also consistency index of emulsions increased with hydrocolloid concentration. At γ = 20 s⁻¹, the value of viscosity of the emulsion with 0.5% (w/v) pectin was about fivefold higher than that of the emulsion without pectin. Flow curves were analyzed using power law model through a fitting procedure. Flow behaviour index of all emulsions except for containing 0.5% (w/v) guar gum was approximately in the range of 0.9–1.0, which corresponds to near-Newtonian behaviour. The shear thinning behaviour of emulsions containing 0.5% (w/w) guar gum was confirmed by flow behaviour index, n, of 0.396. Both storage (G′) and loss modulus (G″) increased with an increase in frequency. Emulsions behaved like a liquid with G″ > G′ at lower frequencies; and like an elastic solid with G′ > G″ at higher frequencies. Effect of guar gum was more pronounced on dynamic properties. Phase angle values decreased from 89 to <10° with increasing frequency and indicated the viscoelasticity of WPI-stabilized emulsions with and without pectin/guar gum.     

On the heat stability of whey protein: Effect of sodium hexametaphosphate

Despite a growing demand for whey protein‐based drinks, their instability and lack of solubility during thermal processing is a major challenge for food product formulators. In the present study, the effects of different hydrocolloids and sodium hexametaphosphate (SHMP) on the heat stability, rheological properties, microstructure and sensory characteristics of whey protein concentrate (WPC) dispersions were evaluated. The results indicated that at pH 4, xanthan, k‐carrageenan, low methoxyl pectin (LMP) and guar stabilised WPC dispersion without heat treatment, all maintained stability during pasteurisation but not sterilisation. For pH 7, for the same set of hydrocolloids, a similar trend was also observed, albeit at different concentrations. However, by adding optimum ratios of SHMP protein denaturation was retarded, particularly in the case of LMP and i‐carrageenan. The highest and lowest apparent viscosities were exhibited by samples containing 0.01% and 0.15% w/w SHMP, respectively. This study highlights the potential capability of SHMP in the prevention of protein denaturation. An exact plausible stability mechanism still needs further more detailed investigation.     

Ultrasonic processing influences rheological and optical properties of high-methoxyl pectin dispersions

The effect of high-intensity ultrasound on the rheological and optical properties of high-methoxyl pectin dispersions was studied. Pectin solutions (1.15 wt% pectin, 41.4 wt% sucrose) were treated with high-intensity ultrasound at intensity levels ranging from 0 to 40 W cm⁻² for various times (0–60 min). Samples were adjusted to pH 1.5 to initiate gelation and their dynamic rheological properties (G′, G″) were recorded as a function of time using a rotational rheometer. Ultrasonically pretreated pectin dispersions formed weaker gels with increasing sonication power and time. After 4 h, log G′ of the pectin dispersion that was pretreated at the highest intensity level (40 W cm⁻² and 30 min) was approximately five times lower than log G′ of the untreated dispersion. The change in phase angle [arctan (G′/G″)] with time indicated that the rate of gelation decreased as ultrasonic intensity and application time increased. The turbidity of ultrasonically pretreated pectin dispersions decreased by 50% yielding more transparent gels. Results were attributed to an overall reduction in the average molecular weight of pectin due to cavitational effects. A power law model was fitted to the flow curves of ultrasonically pretreated pectin dispersions to determine both flow behavior index n and consistency coefficient K. With increased sonication power and application time, n increased from 0.6 to 0.97 indicating that the flow behavior changed from viscoelastic to Newtonian.     

Viscosity of guar gum and xanthan/guar gum mixture solutions

The viscosity of diluted guar gum solutions and the viscosity of xanthan and guar gum mixture solutions have been studied. Guar gum solutions showed pseudoplastic behaviour. Apparent viscosity increased with gum concentration and decreased with the temperature at which viscosity was measured. A maximum in the plot of viscosity versus increasing dissolution temperature was observed at 60 °C. This behaviour was related to differences in molecular structure of the polymers solved at different temperatures. Mixtures of xanthan and guar gum showed a higher combined viscosity than that occurring in each separate gum. This synergistic interaction was affected by the gum ratio in the mixture and dissolution temperature of both gums. The effect of polysaccharide concentration (1.0, 1.5 and 2.0 kg m⁻³), xanthan/guar gum ratio (1/5, 4/2, 3/3, 4/2 and 5/1) and dissolution temperature (25, 40, 60 and 80 °C for both gums) on the viscosity of solutions of mixtures were studied. The highest viscosities were observed when 2.0 kg m⁻³ gum concentration was used together with a ratio of xanthan/guar gum of 3/3 (w/w) and dissolution temperature of 40 and 80 °C for xanthan and guar gum, respectively. © 2000 Society of Chemical Industry     

Optimization of Gum Combination in Prebiotic Instant Hot Chocolate Beverage Model System in Terms of Rheological Aspect: Mixture Design Approach

Mixture design was used to investigate the effects of four different gums (xanthan gum, guar gum, alginate and locust bean gum) and their combinations on the rheological properties of a prebiotic model instant hot chocolate beverage (including 3.5% inulin) and to determine their interactions in the model beverage. Simplex centroid mixture design was applied to predict the physicochemical (soluble solids, pH, colour properties) and rheological parameters (consistency index (K), flow behaviour index (n) and apparent viscosity (η ₅₀)) of the samples. In the model, the optimum gum combination was found by simplex centroid mixture design as 59% xanthan gum and 41% locust bean gum, and the highest K value was 33.56 Pa s ⁿ . The increase of guar gum and alginate in the gum mixture caused a decrease in the K value of the sample.     

Pectin–sucrose–Ca2+ interactions: effects on rheological properties

The effects of varying concentrations of pectin (4.5–6.5%, w/w), sucrose (40–60%, w/w) and calcium (20–60 mg/g pectin) on the viscoelastic properties of pectin dispersions at pH 3.0 were investigated. Pectin samples used were extracted from pomelo fruit peels (Citrus grandis) grown in Malaysia. The dynamic rheological parameters (G′, G″, δ and η*) of pectin–sucrose–calcium dispersion were determined at 1.5% strain from 90–20°C at a cooling rate of 3°C min⁻¹. Plots of G′ and G″ against frequency (rad s⁻¹) showed G″>G′ throughout the frequency range with no occurrence of crossover for most of the pectin dispersions. In addition both storage (G′) and loss (G″) moduli of the dispersions increase on cooling. Increasing pectin, sucrose and calcium concentrations increased G′ and G″ with pectin having the greatest effect. Interactions amongst the three factors were also studied. At lower pectin concentrations, addition of Ca²⁺ increased G′ at all temperatures. This effect was also observed at higher pectin concentrations at 20°C but not at 90°C. The opposite effect was observed with the addition of sucrose, i.e. addition of sucrose at a higher pectin concentration increased G′ whereas at a lower pectin concentration no effect was observed. Interaction between calcium and sucrose gave rise to an increase in G′ when Ca²⁺ was added at high sucrose concentrations, but a decrease in G′ was evident at low sucrose concentrations. Dispersions of pectin alone or in combination with sucrose exhibited a more liquid-like behaviour with G″>G′. However, in the presence of Ca²⁺, mechanical spectra of G′>G″ were obtained.     

Determination of the fruit content of cherry fruit preparations by gravimetric quantification of hemicellulose

A method recently developed for the determination of the fruit content of strawberry fruit preparations by gravimetric quantification of hemicellulose was extended to cherry fruit preparations. Isolation of the alcohol-insoluble residue (AIR) and sequential fractionation of the cell wall compounds from cherries (Prunus cerasus L. cv. ‘Oblacinska’) was performed yielding the amount of fresh cherries per gram hemicellulose. Cherry fruit preparations with varying fruit contents (30–40%) were produced using different hydrocolloid systems (pectin, starch, guar gum, xanthan gum, carrageenan, and combinations thereof). After separation of the hydrocolloids by enzymatical digestion and successive extraction, the fruit preparations were subjected to AIR isolation. The AIR was fractionated to yield the hemicellulose fraction, which was quantified gravimetrically for the calculation of the fruit content. Compared to strawberries, modifications including additional extraction steps for the sequential fractionation were required to separate the pectin of the cherries exhaustively. Calculated and initial fruit contents were in good agreement for the single hydrocolloid components pectin and starch as well as for the combinations pectin/xanthan gum and pectin/carrageenan (26.8% vs. 30%, 38.6% vs. 40%, 42.5% vs. 40%, 37.6% vs. 40%, and 41.2% vs. 40%), whereas the preparations produced with more complex hydrocolloid systems (pectin/xanthan gum/guar gum and starch/xanthan/guar gum) showed larger deviations in their contents (46.2% vs. 40%, 49.6% vs. 40%). It is concluded that the novel method is generally suitable for the determination of the fruit content of fruit preparations, but steps of sample preparation need to be individually adapted to the different fruit matrices.     

Effect of protein–polysaccharide mixtures on the continuous manufacturing of foamed food products

The aim of this work is to understand the effects of protein and polysaccharide interactions on the physicochemical properties of highly viscous Newtonian model foods and their impact on continuous foaming operation in laminar flow conditions. Model foods consisted of modified glucose syrups. Foaming was carried out at constant gas-to-liquid flow rate ratio as a function of rotation speed. Overrun, mean bubble diameter d₃₂ and stability over time were used to characterize foams. Results showed that blow-by occurred during foaming of models including either 0.1% guar or xanthan without proteins, while 0.1% pectin allowed a total incorporation of the gas phase with large bubbles. For proteins, models with 2% whey protein isolate (WPI) were able to form foams with the desired overrun and small bubbles, while foaming was less effective with 2% Na-caseinates. With WPI, guar addition did not improve significantly foam properties. Overrun was reduced in WPI–xanthan mixtures, probably because the matrix exhibited viscoelastic trends even though xanthan decreased d₃₂. WPI–pectin mixtures provided abundant and stable foams with the smallest d₃₂ and the best stability because WPI reinforced the time-dependent behaviour of pectin recipes. However, blow-by was observed with 0.1% pectin when WPI was replaced by Na-caseinates, which demonstrates the key role of specific protein–polysaccharide interactions on overrun. Conversely, bubble diameters in foams were governed by process parameters and could be adequately described using a laminar Weber number based on foam viscosity measured during foaming for all model foods that provided stable foams.     

Experimental Analysis of Structural Change and Rheological Behavior of Macromolecular Solutions with Guar and Xanthan Gums in Crossflow Microfiltration Processing

The present paper reports on the structural change and rheological behavior of mixtures of macromolecular suspensions (guar and xanthan gums) in crossflow microfiltration processing. Mixtures in suspension of guar and xanthan gums at low concentrations (1,000 ppm) and different proportions were processed by microfiltration with membrane of nominal pore size of 0.4 μm. The rheological behavior of the mixtures was investigated in rotational viscometers at two different temperatures, 25 and 40 °C, at the beginning and at the end of each experiment. The shear stress (τ) in function of the shear rate (γ) was fitted and analyzed with the power-law model. All the mixtures showed flow behavior index values (n) lower than 1, characterizing non-Newtonian fluids (pseudoplastic). The samples of both mixtures and permeates were also analyzed by absorbency spectroscopy in infrared radiation. The absorbency analysis showed that there is good synergism between xanthan and guar gums without structure modifications or gel formation in the concentration process by microfiltration.     

The rheological behaviors and morphological characteristics of different food hydrocolloids ground to sub-micro particles: in terms of temperature and particle size

Temperature sweep tests and steady shear properties of five different food hydrocolloids (guar gum, xanthan gum, carboxymethylcellulose, pectin and carrageenan) in two different particle sizes groups have been determined at 25, 40, 60 and 80 °C in 1% aqueous solution. Also, the Scanning Electron Microscopy (SEM) images of gums were taken to investigate the morphological properties of the samples. The particle size and processing temperature significantly affected all rheological parameters of the hydrocolloid solutions. The flow behavior of the samples was fitted to Ostwald de Waele model (R²?=?0.959). The highest n value was recorded at 60 °C for all samples. The most drastic changes in consistency coefficient (K) values of the samples were observed in carrageenan solution and it was ranged from 0.013 to 1.774 Pa.sⁿ before the size reduction and from 0.007 to 0.337 Pa.sⁿ after the size reduction process. As the consistency coefficient (K) and apparent viscosity (η₅₀) decreased with the temperature, the flow behavior index increased in both group of samples. As a result, it was concluded that the increase in processing temperature and size reduction process caused a decrease in resistance of hydrocolloid solutions subjected to the deformation, which is a very important factor affecting the quality and good mouth-feel of products.     

亲水胶体对胡柚饮料稳定性的影响

以胡柚饮料为研究对象,以离心沉淀率和混浊稳定性为考察指标,探讨了添加黄原胶、羧甲基纤维素（CMC）、瓜尔豆胶和果胶4种亲水胶体对胡柚饮料稳定性的影响。结果表明：随着亲水胶体添加量的增加,胡柚饮料的稳定性呈上升趋势,其适宜的添加量为0.15%～0.2%,亲水胶体的稳定性顺序为：果胶〉CMC〉瓜尔豆胶〉黄原胶;黄原胶与果胶复配比为1∶2～3,添加量为0.15%～0.2%时,胡柚饮料稳定性最好,口感最佳。     

Small-deformation rheology investigation of rehydrated cell wall particles–xanthan mixtures

The rheological behaviour and microstructural properties of rehydrated cell wall particle (CWP) dispersions and CWP–xanthan mixtures were investigated using small-deformation rheology and confocal laser scanning microscopy. Dispersions with two different CWP particle sizes were used. CWP dispersions were found to be elastic with a weak-gel type behaviour. The elastic modulus was a function of the CWP concentration c_p and depended on the particle size of the CWP. The addition of xanthan to the CWP dispersions was found to affect the rheological behaviour of the CWP–xanthan mixtures at low CWP concentration (c_p ≤ 1 wt%), due to the increase in the viscoelastic properties of the continuous phase. At high CWP concentrations (c_p ≥ 3%), the effect of xanthan on the rheological behaviour of the CWP–xanthan mixtures was marginal, as the viscoelastic behaviour of the mixtures was dominated by the CWP particle network, with xanthan molecules entrapped in the interstitial voids. However, at intermediate CWP volume fractions (e.g. at a CWP concentration c_p = 2%) both xanthan and CWP phases contributed to the viscoelastic behaviour of the CWP–xanthan mixtures.     

Effects of different types and concentrations of thickeners on yoghurt protein bioaccessibility by an in vitro dynamic gastrointestinal digestive model

This study analysed the protein bioaccessibility of yoghurt containing different concentrations of pectin, acid-resistant carboxymethylcellulose (CMC), guar gum and xanthan gum before and during in vitro gastrointestinal digestion, respectively. Soluble protein contents and protein digestion rates of yoghurt with 0.2% (m/v) guar gum, CMC and xanthan gum were significantly higher and faster, whereas other thickeners had slower rates than control yoghurt during gastric digestion phase. In addition, the contents of small peptides and amino acids were higher in yoghurt with 0.2% (m/v) thickeners than those with 1.0% (m/v) thickeners during simulated intestinal digestion in most of the samples.