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.     

Stability and Rheological Properties of Egg Yolk Granule Stabilized Emulsions with Pectin and Guar Gum

The effects of pectin and guar gum on rheology, microstructure and creaming stability of 1% (w/v) egg yolk granule stabilized emulsions were investigated. While the addition of low amount of pectin (0.1% (w/v)) had no effect on the emulsion viscosity, the addition of 0.5% (w/v) pectin greatly increased the viscosity. Granule-stabilized emulsion without hydrocolloids reflects the pseudoplastic behavior (shear-thinning behavior with flow behavior index, n < 1.0). Hydrocolloids, especially at high concentrations, affected the viscoelastic behavior of the emulsions and both storage (G′) and loss modulus (G′′) were regarded as frequency dependent. Emulsions behaved like a liquid with G′′ > G′ at lower frequencies, and like an elastic solid with G′ > G′′ at higher frequencies. Emulsion microstructure indicated that the presence of hydrocolloids induced flocculation. Creaming stability of emulsions was enhanced by the presence of hydrocolloids and increasing hydrocolloid concentration decreased the creaming by restricting the movement of oil droplets.     

不同黏度多糖阿拉伯胶和瓜尔胶对肌原纤维蛋白乳化性质的影响

选取两种分子质量相近、黏度相差较大的天然高分子多糖阿拉伯胶（arabic gum,AG）和瓜尔胶（guar gum,GG）分别与肌原纤维蛋白（myofibrillarprotein,MP）进行复合,研究不同多糖添加量（0.1%～0.5%）对MP-多糖复合物乳液性质的影响规律。结果表明,AG和GG均可以显著改善MP的乳化性质,其中AG对乳化活性的改善效果较好,而GG更有利于乳液的稳定性。随着多糖质量分数增加,乳化活性指数和稳定性指数均呈先升高后降低趋势,AG和GG添加量分别为0.3%和0.2%时,乳化活性指数和稳定性指数达到最大值。界面蛋白含量测定结果显示,AG和GG均会导致界面蛋白含量下降,尤其是GG的作用更明显。随着AG和GG添加量增加,乳液粒径逐渐减小,且尺寸分布更加均一,添加量超过0.3%后,GG组乳液出现少量絮凝现象。同一添加量下,GG组乳液粒径明显小于AG组。流变学分析证实,所有乳液均为假塑性流体,表现出弱凝胶性质。AG添加量较少（≤0.3%）时会降低乳液黏度,并明显提高乳液的储能模量,而GG的添加使乳液表观黏度和储能模量均显著提高,与AG相比,高黏度GG制备的乳液拥有更高的...     

NaCl浓度、多糖以及小分子乳化剂对全蛋粉乳化性质的影响

以全蛋粉(WEP)为乳化剂制备水包油型乳状液,以乳化活性(EAI)和乳化稳定性(ESI)为乳化性质的指标,研究盐、多糖以及小分子乳化剂对全蛋粉乳化性质的影响以及不同乳状液在高温下的耐热性。单因素试验表明:全蛋粉乳化性质分别在NaCl、黄原胶以及单甘酯的添加量为0.5 mol/L、0.08%、0.06%时达到最大值。正交试验结果表明:各因素对全蛋粉乳化性质影响的主次关系为,黄原胶>单甘酯>盐浓度。在优化组合条件下全蛋粉的乳化活性和乳化稳定性分别提高了0.49倍和14.43倍;并且添加黄原胶和复合物后的乳状液耐热性显著提高。     

Characterization of emulsions prepared by egg yolk phosvitin with pectin,glycerol and trehalose

Effect of pectin (34–40% esterification), glycerol and trehalose at two concentrations (0.1% and 0.5%, wt./wt%) on physicochemical and emulsifying properties of phosvitin (Pv) was investigated under the mild conditions (oil volume fraction, 0.25; protein concentration, 5 mg/mL; 10 mM sodium phosphate buffer, pH 7.0). Pv showed better emulsifying properties than sodium caseinate (Sc). Glycerol (0.5%) significantly increased the emulsifying activity index (EAI) of Pv from 19.8 to 20.9 and the emulsion stability index (ESI) from 67.6 to 75.1. The higher ESI of Pv was also obtained by 0.1% pectin and 0.5% trehalose. The results obtained from circular dichroism (CD) spectra indicated that all the tested additives displayed slight effect on the unfolded structure of Pv. Furthermore, fluorescence pattern demonstrated that glycerol and trehalose increased the hydrophobicity of Pv, while pectin displayed an opposite effect. All emulsions exhibited a shear-thinning behavior and the flow behavior was fitted to the power law model. Frequency sweeps of the emulsions illustrated that they behaved like a viscous liquid.     

瓜尔豆胶对大豆分离蛋白乳浊液稳定性的影响

研究了不同pH值条件下瓜尔豆胶对大豆分离蛋白乳浊液乳析稳定性和絮凝稳定性的影响。研究结果表明 ,在瓜尔豆胶浓度低于 0 0 4%时 ,随着瓜尔豆胶浓度的增加 ,乳浊液的稳定性逐渐增加。当多糖浓度高于 0 0 4%时 ,液滴发生排斥絮凝 ,体系的稳定性急剧下降 ,更高浓度的瓜尔豆胶因与乳浊液液滴间的热力学不相容性而导致体系发生各向同性和各向异性相分离。     

Emulsifying properties of sweet potato protein: Effect of protein concentration and oil volume fraction

The effect of protein concentrations (0.1, 0.25, 0.5, 1.0, 1.5 and 2.0% w/v) and oil volume fractions (5, 15, 25, 35 and 45% v/v) on properties of stabilized emulsions of sweet potato proteins (SPPs) were investigated by use of the emulsifying activity index (EAI), emulsifying stability index (ESI), droplet size, rheological properties, interfacial properties and optical microscopy measurements at neutral pH. The protein concentration or oil volume fraction significantly affected droplet size, interfacial protein concentration, emulsion apparent viscosity, EAI and ESI. Increasing of protein concentration greatly decreased droplet size, EAI and apparent viscosity of SPP emulsions; however, there was a pronounced increase in ESI and interfacial protein concentration (P < 0.05). In contrast, increasing of oil volume fraction greatly increased droplet size, EAI and emulsion apparent viscosity of SPP emulsions, but decreased ESI and interfacial protein concentration significantly (P < 0.05). The rheological curve suggested that SPP emulsions were shear-thinning non-Newtonian fluids. Optical microscopy clearly demonstrated that droplet aggregates were formed at a lower protein concentration of <0.5% (w/v) due to low interfacial protein concentration, while at higher oil volume fractions of >25% (v/v) there was obvious coalescence. In addition, the main components of adsorbed SPP at the oil–water interface were Sporamin A, Sporamin B and some high-molecular-weight aggregates formed by disulfide linkage.     

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.     

Effects of the proteinaceous moiety on the emulsifying properties of sugar beet pectin

The role of the proteinaceous moiety in emulsifying was investigated using pectin from sugar beet as a model polysaccharide. Physicochemical and macromolecular characteristics of sugar beet pectin were examined with or without an enzymatic modification using multiple acid-proteinases. The enzymatic modification decreased the total protein content from 1.56±0.15% to 0.13±0.02% by the Bradford method without significant change in ferulic acid or most constitutional sugars. It also decreased the weight-average molecular weight (M_w) from 517±28 to 254±20 kg/mol and the z-average root-mean-square radius of gyration from 43.6±0.8 to 35.0±0.6 nm. Emulsifying properties of the polysaccharide with or without the enzymatic modification were evaluated by emulsion droplet size and creaming stability of O/W emulsions (pH 3.0) containing 15 w/w% middle-chain triglyceride and 1.5 w/w% sugar beet pectin as main constituents. The modification increased the average diameter (d_3,2) of emulsion droplets from 0.56±0.04 to 3.00±0.25 μm immediately after the preparation, suggesting a decrease in the emulsifying activity. It caused the creaming of the emulsions during incubation at 60 °C, which was in line with the finding that macroscopic phase separation occurred only in the presence of the modified pectin after storage at 20 °C for a day, suggesting a decrease in the emulsion stabilizing ability. The modification also decreased significantly the amount of the pectin fraction that adsorbed onto the surface of emulsion droplets from 14.58±2.21% to 1.22±0.03% and the interfacial concentration of the polysaccharide from 1.42±0.23 to 0.45±0.05 mg/m², where the proteinaceous materials in the pectin molecules activated the oil-water interface. Results from the present study suggest an important role of the proteinaceous moiety to explain the emulsifying properties of sugar beet pectin as in the case of gum arabic and soy soluble polysaccharide.     

Study of emulsions stabilized with Phaseolus vulgaris or Phaseolus coccineus with the addition of Arabic gum, locust bean gum and xanthan gum

The properties of o/w emulsions stabilized with 1%w/v common bean (Phaseolus vulgaris L.), V or scarlet runner bean (P. coccineus L.), Coc extracted by isoelectric precipitation or ultrafiltration, at pH 7.0 and 5.5, with the addition of Arabic gum, locust bean gum, xanthan gum and a mixture of xanthan gum–locust bean gum (0.1 %w/v and 0.25 %w/v) are studied. The stability of emulsions was evaluated on the basis of oil droplet size, creaming, viscosity and protein adsorption measurements. The addition of Arabic gum, caused an increase in D[4,3] values and a decrease in the amount of protein adsorbed at the interface. The addition of locust bean gum in some emulsions reduced the amount of protein adsorbed. The addition of xanthan and to a less extend of the polysaccharide mixture, promoted a decrease in D[4,3]. So, emulsion stability was affected by the polysaccharide nature. Differences were also observed with respect to the protein nature, the method of its preparation and emulsion's pH. All polysaccharides enhanced the emulsions viscosity with xanthan and xanthan–locust bean gum exhibiting the higher values. V isolates and isoelectricaly precipitated isolates of both V, Coc showed higher viscosity values. The stability was enhanced by the increase of the viscosity of the continuous phase and the creation of a network, which prevents the oil droplets from coalescence.     

Thermal denaturation and functional properties of egg proteins in the presence of hydrocolloid gums

The aim of this study was to investigate the thermal stability, foaming and emulsifying properties of egg white and egg yolk constituents (egg yolk plasma and egg yolk granule) in the presence of hydrocolloid gums. Differential scanning calorimetry was used to examine the thermal stability of proteins. Heat denaturation of proteins were not influenced from the presence of anionic pectin and i-carrageenan and neutral guar gum. The residual denaturation enthalpy was observed to decrease as a result of protein aggregation. Thermal treatment have been observed to be detrimental to foaming capacity of egg white, while foam stability was improved. The foam stability was enhanced in the presence of pectin which may provide a strong viscoelastic film together with protein. Emulsifying activity and stability and of egg yolk granule and plasma were reduced after heat treatment. The presence of guar gum improved the emulsifying properties, while both pectin and guar gum reduced the rate and extend of creaming of egg yolk protein – stabilized proteins after heat treatment.     

The effect of chitosan on the properties of emulsions stabilized by whey proteins

The influence of the cationic amino polysaccharide chitosan content (0–0.5%) on particle size distribution, creaming stability, apparent viscosity, and microstructure of oil-in-water emulsions (40% of rapeseed oil) containing whey protein isolate (WPI) (4%) at pH 3 was investigated. The emulsifying properties, apparent viscosity and phase separation behaviour of aqueous WPI/chitosan mixture at pH 3 were also studied. The interface tension data showed that WPI/chitosan mixture had a slightly higher emulsifying activity than had whey protein alone. An increase in chitosan content resulted in a decreased average particle size, higher viscosity and increased creaming stability of emulsions. The microstructure analysis indicated that increasing concentration of chitosan resulted in the formation of a flocculated droplet network. This behaviour of acidic model emulsions containing WPI and chitosan was explained by a flocculation phenomenon.     

EFFECT OF FLAXSEED GUM ON QUALITY AND STABILITY OF A MODEL SALAD DRESSING1

Flaxseed gum was evaluated for its application as a stabilizer for salad dressing. It was found that for stabilization to occur the concentration of gum had to be higher than 0.45% (w/w). Solvent quality affected the stability of model oil‐in‐water emulsions. Flaxseed gum stabilized emulsions were stable at pHs greater than 2.8. Lower values caused the polysaccharide to have a compact configuration or caused cleavage of the polymer creating instability. Larger mean droplet size and creaming were observed when the pH was too low or the gum concentration was not sufficient for coverage. Salt addition greatly affected the rheological properties of the polysaccharide; however, the electrolyte improved the emulsifying capabilities of the egg yolk protein. Aging weakened the polymer network structure as shown by a decrease in Newtonian viscosity with a corresponding increase in phase angle confirming the transformation to a more fluid system.     

Assessing the potential of flaxseed protein as an emulsifier combined with whey protein isolate

The potential use of flaxseed protein isolate (FPI) as an emulsifying agent was studied in combination with whey protein isolate (WPI) or alone. All the FPI and WPI–FPI emulsions were kinetically unstable. The increase of FPI concentration (0.7% w/v) led to a higher creaming stability of the FPI emulsions due partly to a reduction in interfacial tension between aqueous and oil phases, but mainly to the gel network formation. However at this same high FPI concentration, WPI–FPI emulsions showed a decrease in droplet size and creaming stability, which could be due to the presence of flaxseed gum in the protein isolate enhancing depletion effects. A protein excess was verified in the mixed systems (0.14 or 0.7% (w/v) FPI) and the increase of FPI concentration led to an even greater surface protein content. Increasing homogenization conditions (pressure and number of passes), the creaming stability of the FPI systems increased, mainly at higher concentration (0.7% w/v). Meanwhile, in the mixed systems, the creaming stability of the emulsions containing 0.7% (w/v) FPI decreased even more, but was improved for the emulsions with 0.14% (w/v) FPI. Thus, it was observed that systems containing only FPI at higher concentration were stabilized by gel formation, while in WPI–FPI systems there was a competition by interface between biopolymers with a consequent depletion process. As a result, more stable systems were obtained with WPI addition at lower FPI concentration (0.14% w/v) and using higher homogenization pressure and number of passes (60 MPa, two passes).     

Emulsifying characteristics of commercial canola protein–hydrocolloid systems

Emulsifying properties of commercial canola protein isolate (CPI)–hydrocolloid-stabilized emulsions were evaluated under varied conditions (CPI, salt and hydrocolloid concentrations; pH, denaturants). Emulsifying activity index (EAI) and emulsion stability (ES) were determined by turbidimetric testing. The results showed that under complexing conditions (at pH 6), the addition of 1% (w/v) κ-carrageenan (κ-CAR) increased the EAI of CPI-stabilized emulsions from 162 to 201 m²/g and ES from 68% to 95%. Under conditions promoting incompatibility (at pH 10), the use of 1% (w/v) guar gum increased the EAI of CPI-stabilized emulsions from 68 to 177 m²/g and ES from 66% to 100%. The lower EAI and ES values observed in CPI–hydrocolloid-stabilized emulsions treated with sodium salts and denaturants support the involvement of hydrophobic interactions, hydrogen bonds and disulfide linkages in the emulsification of these systems. Interfacial properties of CPI–hydrocolloid mixtures were improved by electrostatic complexing and incompatibility, making these systems suitable for stabilizing food emulsions.     

Development of multiple emulsions based on the repulsive interaction between sodium caseinate and LBG

The stability of oil-in-water, water-in-water and multiple emulsions containing sodium caseinate (Na-CN) and/or locust bean gum (LBG) at pH 5.5 was investigated with different compositions using a visual analysis (creaming and/or phase separation), optical microscopy and rheological measurements. Oil-in-water emulsions (O/W) were produced by high pressure homogenization, which promoted the formation of very small droplets (∼0.4 μm) and hindered the destabilization process. In the second step of this study, a visual phase diagram was constructed in order to identify the concentrations of sodium caseinate (Na-CN) and locust bean gum (LBG) that led to phase separation at pH 5.5. A mixed solution composed of 3% (w/v) Na-CN and 0.3% (w/v) LBG was chosen to produce the water-in-water and multiple emulsions. After centrifugation, the solution was separated into an upper phase rich in polysaccharide (PS) and a bottom phase rich in protein (PR), which were mixed in different proportions (1:3, 1:1, 3:1), forming the water-in-water (W/W) emulsions. The stability, microstructure and rheological properties of the W/W emulsions depended strongly on the composition of the biopolymers. An increase in the polysaccharide concentration in the W/W emulsions led to the production of more viscous and stable systems. Multiple emulsions with different characteristics were prepared and also depended on the biopolymer composition. The system with the highest polysaccharide content was the only one that showed an O/W/W structure, while the others presented the microstructure of an O/W-W/W emulsion.     

Influence of xanthan gum on the formation and stability of sodium caseinate oil-in-water emulsions

Studies have been made of the changes in droplet sizes, surface coverage and creaming stability of emulsions formed with 30% (w/w) soya oil, and aqueous solution containing 1 or 3% (w/w) sodium caseinate and varying concentrations of xanthan gum. Addition of xanthan prior to homogenization had no significant effect on average emulsion droplet size and surface protein concentration in all emulsions studied. However, addition of low levels of xanthan (≤0.2 wt%) caused flocculation of droplets that resulted in a large decrease in creaming stability and visual phase separation. At higher xanthan concentrations, the creaming stability improved, apparently due to the formation of network of flocculated droplets. It was found that emulsions formed with 3% sodium caseinate in the absence of xanthan showed extensive flocculation that resulted in very low creaming stability. The presence of xanthan in these emulsions increased the creaming stability, although the emulsion droplets were still flocculated. It appears that creaming stability of emulsions made with mixtures of sodium caseinate and xanthan was more closely related to the structure and rheology of the emulsion itself rather than to the rheology of the aqueous phase.     

Steady and Dynamic Shear Rheological Properties,and Stability of Non-Flocculated and Flocculated Beverage Cloud Emulsions

Rheological properties of single-phase, and emulsions containing modified starch and gum arabic as surface active hydrocolloids, as well as xanthan and tragacanth gums as stabilizers were evaluated under steady and dynamic shear testing conditions using a control stress rheometer. Emulsions were formed by 9% and 14% gum concentrations with oil concentration maintained at 9% thus giving a 1:1 and 1.5:1 surface active agent to oil ratio, respectively. The rates of droplet coalescence and creaming, for a total of 8 emulsions, as a function storage time before and after dilution in a simulated fruit beverage were then investigated. Steady shear (flow curve) were well described by the Carreau model at shear stress ranging from 0.01 to 100 Pa. All prepared water phases indicated a zero-shear viscosity plateau followed by shear thinning behavior with flow behavior index (n) ranging from 0.51 to 0.79 for 14% starch-0.3% xanthan and 14% gum arabic-0.8% tragacanth stabilized emulsions, respectively. The water phase flow property data were well fitted by the Einstein equation and its expansions. The dynamic rheological properties of water phase and emulsions were also evaluated for G′(ω) and G″(ω) from 1 to 50 rad/s. Similar curves were obtained with varying degrees of deviations (G′ from G″) for different emulsions. Starch-xanthan emulsion and associated water phase at 1.5/1 agent to oil ratio demonstrated viscoelastic behavior (G′ ≥ G″) with lower droplet coalescence and creaming rates. On the other hand, gum arabic-xanthan emulsion at 1:1 agent to oil ratio showed the highest rate of droplet coalescence and a greater degree of creaming. It was speculated that the lower stability of gum arabic-xanthan emulsion could be related to the denaturation of proteinaceous part in the gum and loss of emulsification capacity due to lower pH and pasteurization.     

Thermally stable hydrogels from enzymatically oxidized polysaccharides

Polysaccharides guar galactomannan (guar gum), locust bean galactomannan (locust bean gum) and tamarind galactoxyloglucan were selectively oxidized by galactose oxidase. The degrees of oxidation of the products were 18-28% for guar galactomannan, 10-16% for locust bean galactomannan and 12-14% for tamarind galactoxyloglucan, calculated from the ratio of oxidized galactose units and total carbohydrates. The rheological properties of the unoxidized and oxidized polysaccharide solutions were investigated by determining their viscosities, storage and loss moduli, and temperature dependence of moduli from 20 °C to 90 °C. All the studied oxidized polysaccharides formed hydrogels throughout the entire temperature range. Concentration (0.2-1% w/v) and degree of oxidation had an effect on the gel formation. The oxidized galactomannans formed stable gels already in low concentrations, such as 0.2-0.4% w/v, while oxidized galactoxyloglucan required a concentration of 0.8% w/v to be stable up to 90 °C. The oxidized polysaccharide hydrogels are highly potential materials for food and medical applications requiring thermal stability.     

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.