Mangosteen Oil-In-Water Emulsions: Rheology, Creaming, and Microstructural Characteristics during Storage

The rheological properties and physical stability of mangosteen (Garcinia mangostana L.) extract in oil-in-water (MIO/W) emulsions were investigated. Rheological study on the emulsions exhibited Newtonian flow behavior. The 20?wt.% emulsion showed higher apparent viscosity than 10?wt.% MIO/W sample. The effects of salt (NaCl) concentration (0, 50, 100, and 200?mM) and heat treatment (70?°C) on the stability of the emulsions were also examined. Heat (70?°C)- and NaCl (100 and 200?mM)-treated emulsions showed creaming and droplet aggregation on storage for a period of 60?days. The 10?wt.% MIO/W emulsions stored at 4?°C showed a homogeneous distribution of oil droplets with good stability to creaming and viscosity independent of shear stress (i.e., a Newtonian liquid).     

Effect of xanthan and guar gums on the formation and stability of soy soluble polysaccharide oil-in-water emulsions

The incorporation of relevant amounts of non-adsorbing hydrocolloids to oil-in-water (O/W) emulsions is a suitable alternative to reduce creaming. The effect of incorporating xanthan gum (XG) or guar gum (GG) in soy soluble polysaccharide (SSPS) stabilized oil-in-water (O/W) emulsions was studied. The emulsions contained 6 wt.% of SSPS, 20 wt.% Perilla seed oil (PSO), an omega-3 vegetable oil, and variable amounts of XG or GG ranging from 0.03 to 0.3 wt.%. The presence of minute amounts of XG or GG in fresh emulsions significantly decreased the emulsion droplet size (EDS) although such low concentrations did not provide enough continuous phase viscosity to arrest creaming. Emulsion microstructure indicated the presence of flocculation even at high concentrations of XG or GG caused by a depletion mechanism. All emulsions with XG or GG exhibited pseudoplastic behavior while the control emulsions showed an almost Newtonian behavior. Emulsion droplet polydispersion generally decreased with increase in the continuous phase viscosity indicating the importance of continuous phase viscosity in the dissipation of shear energy throughout the emulsion during homogenization. The characteristics of the emulsions were closely related to the rheological changes of the continuous phase.     

Structuring of lipid phases using controlled heteroaggregation of protein microspheres in water-in-oil emulsions

The effect of heteroaggregation of oppositely charged protein microspheres dispersed within a liquid oil phase on the microstructure and rheological properties of water-in-oil (W/O) emulsions was evaluated. The aqueous phase of the initial W/O emulsions contained either 10% β-lactoglobulin or 10% lactoferrin (pH 7, 100 mM NaCl). At this pH, β-lactoglobulin (BLG) is negatively charged while lactoferrin (LF) is positively charged. The oil phase consisted of a lipophilic non-ionic surfactant (8% polyglycerol polyricinoleate, PGPR) dispersed within soybean oil. Three 40% W/O emulsions were formed containing different types of protein microspheres: (i) BLG: 100% BLG droplets; (ii) LF: 100% LF droplets; and (iii) Mixed: 50% BLG droplets and 50% LF droplets. Prior to heating, the mixed emulsions had a higher shear viscosity, yield stress, and shear modulus than the BLG or LF emulsions, which suggested that electrostatic attraction led to the formation of a three-dimensional network of aggregated droplets. All three W/O emulsions underwent an irreversible fluid-to-solid transition when they were heated above ≈70 °C. This phenomenon was attributed to thermal denaturation of the globular BLG and LF molecules within the aqueous phase promoting aggregation and network formation of the protein microspheres. After heating, the mixed emulsions had a higher shear viscosity, yield stress and shear modulus than the BLG or LF emulsions, suggesting that a stronger droplet network was formed due to electrostatic attraction. Shear rheology measurements of the W/O emulsions showed that the lipid phases formed after heating were non-ideal plastics characterized by a yield stress and shear thinning behavior. These results may facilitate the design of semi-solid or solid foods with reduced saturated- or trans-fat contents suitable for use in commercial products.     

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.     

蜂乳的触变性研究

针对蜂乳所表现出的流变性质,用旋转型粘度计,测定蜂乳在不同剪切速率下的剪切应力和表观粘度。通过回归分析,建立蜂乳在触变条件下的流变模型方程,探讨温度和剪切速率对蜂乳触变性的影响以及蜂乳的表观粘度随着剪切时间的变化规律。     

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.     

Characterization of commercial Spanish hummus formulation: Nutritional composition,rheology, and structure

Nutritional composition, rheological behavior, and structure of a commercial Spanish hummus were analyzed. The hummus is “high in fiber,” and Fe (1.9 ± 0.02 mg/100 g), Ca (65.7 ± 10.9 mg/100 g), Mg (66.8 ± 1.0 mg/100 g), P (164.9 ± 4.6 mg/100 g), and especially, K (250.7 ± 11.6 mg/100 g) are present in it. The hummus, with dispersion index of 4.14, behaved like a weak gel and exhibited hysteresis loops, and the Herschel-Bulkley model described its steady time-independent flow behavior. Complex viscosity and apparent viscosity at similar frequency and shear rate failed to follow the Cox-Merz rule.     

Viscosity change in oil/water food emulsions prepared using a membrane emulsification system

This paper reports viscosity measurements of oil/water (O/W) monodispersed emulsions of different droplet diameters obtained in a membrane emulsification system. Hydrophilic microporous glass membranes of different pore diameters were used to prepare O/W emulsions. The results showed that the droplet diameter of the emulsions varied with the average pore diameter of the membrane. The average droplet diameter was found to be about five times greater than the average membrane pore diameter. A correlation was found for the relationship between the average droplet diameter and the emulsion viscosity. As the dispersed droplet size became smaller, the total surface area of the droplets increased. Therefore, the emulsion viscosity and the relative viscosity increased. Few studies have reported the viscosity of O/W emulsions with droplet diameter of 5 μm or more and an oil phase concentration of 10 vol% or less. In the present study a correlation between the droplet diameter and the emulsion viscosity was statistically established. ©     

Water/Oil Emulsions Prepared by the Membrane Emulsification Method and Their Stability

We developed and tested a simple method to measure dispersed droplet size of W/O emulsions. Then, using a microporous glass membrane treated with oil phase, we produced a W/O emulsion with high water content (40% w/w) at a high emulsification rate by the membrane emulsification method, and assessed its stability. In comparison with emulsions by the stirring methods, variations in dispersed droplet size and viscosity of emulsions by membrane method were small and the emulsions were more stable. Droplet size was not related to the stability of the W/O emulsion prepared by membrane emulsification.     

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.     

The characterization of the semi-solid W/O/W emulsions with low concentrations of the primary polymeric emulsifier

Semi-solid multiple W/O/W emulsions with low concentrations (0.8, 1.6 and 2.4% w/w) of lipophilic polymeric primary emulsifier PEG-30-dipolyhydroxystearate (PDHS) have been formulated. Both emulsions, primary and multiple, were prepared with high content of inner phase (Phi1 = Phi2 = 0.8). All the formulations differ only in the lipophilic emulsifier concentration. Evaluating several parameters such as macroscopic and microscopic aspect, droplet size, accelerated stability under centrifugation and flow and oscillatory rheological behaviour, assessed the multiple systems. It is possible to formulate the semi-solid W/O/W multiple emulsions with low concentrations of PDHS as the primary emulsifier. It appeared that the highest long-term stable multiple emulsion with the lowest droplet size, the highest apparent viscosity and highest elastic characteristic, was the sample with the highest concentration (2.4% w/w) of the primary emulsifier.     

Rheological properties of corn oil emulsions stabilized by commercial micellar casein and high pressure homogenization

The rheological behavior of corn oil emulsions prepared by high pressure homogenization (HPH) was investigated. Coarse emulsions of corn oil (10-30 g oil/100 g emulsion) in casein dispersions containing 0.5-3.5 g micellar casein/100 g casein dispersion in an oil-free basis were homogenized at 0-300 MPa. Flow behavior under continuous increasing (0-150 s⁻¹) or decreasing (150-0 s⁻¹) shear rate was tested. Emulsions that showed macroscopic change in consistency were tested for viscoelasticity (G′). Homogenization of emulsions with low oil concentration (10 g/100 g) resulted in Newtonian behavior for all treatment pressures. The rheological behavior of emulsions with higher oil concentration (30 g/100 g) was dependent on casein concentration in the aqueous phase and varied from Newtonian to shear thinning. Homogenization pressures between 20 and 100 MPa induced the formation of a gel-like structure possibly through pressure-induced interactions between caseins surrounding adjacent droplets.     

Effect of heat treatment on the properties of soy protein‐stabilised emulsions

The effect of heat treatment on the properties of soy protein‐stabilised emulsions was investigated. Emulsions were prepared with unheated and heat‐treated soy protein (NSP and HSP) dispersions. Heating on soy protein dispersions at 95 °C for 30 min resulted in smaller average oil droplet size, lower tendency for oil droplet flocculation, higher protein adsorption and lower viscosity. The properties of emulsions were significantly influenced by the protein concentration. The sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE) profiles showed that the heat treatment on soy protein dispersions increased the protein adsorption at O/W interface. The viscosity of all samples at low shear rate was inversely proportional to the d₃₂, suggesting a positive relation to the total interfacial area per unit volume. Emulsions showed shear‐thinning behaviour. The relaxation time was found to increase with aqueous phase viscosity determined by the Cross viscosity model.     

EFFECT OF POLYSORBATE-60 ON THE STABILITY OF O/W EMULSIONS STABILIZED BY PROPYLENE GLYCOL ALGINATE AND XANTHAN GUM

The effect of polysorbate-60 in improving the stability of model oil-in-water emulsions formulated with xanthan gum and propylene glycol alginate was studied at two levels of the surfactant; 0.15% and 0.30%. Creep measurements and steady shear measurements as well as surface tension and oil droplet size measurements were conducted to relate rheological and surface properties to improved stability. Higher polysorbate-60 concentration resulted in lower surface tension values which shifted the oil droplet size distribution to a smaller size range; this distribution was a function of aging time at 0.15% weight concentration PS-60. The decay in rheological parameters, particularly Newtonian viscosity, was slower at 0.30% surfactant concentration.     

Influence of chitosan concentration on the stability,microstructure and rheological properties of O/W emulsions formulated with high-oleic sunflower oil and potato protein

Relatively concentrated (40 wt%) O/W emulsions formulated with high-oleic sunflower oil as disperse phase, potato protein isolate as emulsifier and chitosan as stabiliser were prepared by rotor–stator/high-pressure valve/rotor–stator homogenization. The influence of chitosan concentration on the physical stability of emulsions was studied in (0.25–1) wt% range by visual inspection, rheological and microstructural techniques. Steady shear flow curves were sensitive to the occurrence of creaming upon the rise of zero-shear viscosity values. The effect of increasing concentration of chitosan on the zero-shear viscosity turned out to be dependent on emulsion ageing and always resulted in a stepwise increase of the critical shear rate for the onset of shear thinning flow. The critical oscillatory shear stress for the onset of non-linear viscoelastic behaviour was more sensitive than the critical shear rate to detect creaming in emulsions. Mechanical spectra are definitely demonstrated to be the most powerful tool to detect not only creaming but also oil droplet flocculation on account of changes in the plateau relaxation zone. CSLM micrographs supported the interpretation of dynamic viscoelastic results, especially when flocculation as well as coalescence took place. Cryo-SEM micrographs evidenced the formation of increasingly denser protein–polysaccharide networks with chitosan concentration and the fact that the latter governs the microstructure of the emulsion when reaches 1 wt% concentration promoting enhanced physical stability.     

Emulsifying properties of pea protein/guar gum conjugates and mayonnaise application

Modified plant protein may be used as a healthy and more functional emulsifier in food products. The objective of this study was to evaluate the emulsifying properties of functionally enhanced pea protein (i.e. pea protein conjugated with guar gum, G-PPI) and its potential application to mayonnaise, compared with unmodified pea protein. Emulsions containing G-PPI were prepared at different pH, salt concentrations, protein concentrations and oil/water ratios. Mayonnaise samples were prepared using the pea proteins or egg yolk powder. Various characteristics of the emulsions, including droplet size, apparent viscosity, viscoelasticity and microstructure, were analysed. The emulsions with G-PPI had significantly increased stability of up to 89.4% and apparent viscosity of up to 48.62 mPa.s. The G-PPI emulsion had a smaller average droplet size of 934.4 nm at pH 7 compared with the PPI emulsion (stability 62.7%, apparent viscosity 22.8 mPa.s and droplet size 1664.8 nm). The pH, NaCl concentration, protein concentration and oil/water ratio greatly affected the emulsifying properties. The G-PPI mayonnaise at higher protein concentrations (6 or 8%) exhibited excellent emulsifying and rheological properties. The modified pea protein through the green modification process with natural polysaccharides could be used as a safe and functional emulsifier in different emulsified foods.     

玉米醇溶蛋白/乳清蛋白纤维核复合纳米粒稳定 Pickering乳液的制备与性质

以玉米醇溶蛋白和乳清蛋白为原料,利用反溶剂共沉淀法制备玉米醇溶蛋白/乳清蛋白纤维核复合纳米粒,并与玉米油高速剪切制备Pickering乳液。探究了复合纳米粒在不同pH下的乳化性,以及复合纳米粒添加量对Pickering乳液粒径、微观形貌、储藏稳定性及流变学特性的影响。结果表明：玉米醇溶蛋白与乳清蛋白纤维核复合后乳化性显著提高,制备的Pickering乳液类型为水包油型;随着复合纳米粒添加量的增加,Pickering乳液粒径先减小后稍增大,添加量大于3 g（100 mL玉米油）后无显著性差异;在复合纳米粒添加量为4 g（100 mL玉米油）时,Pickering乳液油滴大小均一,储藏稳定性最好;Pickering乳液为假塑性流体,随复合纳米粒添加量的增加,表观黏度先减小后增大。     

再生纤维素凝胶对乳清分离蛋白预乳化液稳定性的影响

利用再生纤维素（regenerated cellulose,RC）凝胶改善蛋白质预乳化液的乳化稳定性。考察添加量分别为0%、0.4%、0.8%、1.2%、1.6%的RC对乳清分离蛋白（whey protein isolate,WPI）-橄榄油预乳化液乳化稳定性、乳化活性、粒度大小、微观结构、流变特性的影响。结果表明,添加RC可以显著提高WPI预乳化液的乳化稳定性及乳化活性（P＜0.05）,RC添加量为0.8%时可以有效抑制乳化液的分层现象;随着RC添加量的增加,乳化液粒度大小及絮凝程度显著降低（P＜0.05）;乳化液流变学特性显示RC具有很好的增稠作用和凝胶性能。结果表明RC的添加对于WPI-预乳化液稳定性有很大影响,预乳化液中添加1.2% RC,可以有效增加乳化液黏度,获得较强的凝胶网络结构,显著降低粒度,改善乳化液稳定性。     

球磨-酯化复合改性槟榔芋淀粉对Pickering乳液形成的影响

为了提高淀粉颗粒的乳化能力,以球磨-酯化复合改性槟榔芋淀粉为颗粒乳化剂,大豆油为油相,制备水包油型Pickering乳液.采用激光粒度仪、研究级正置显微镜、流变仪等对Pickering乳液外观、液滴粒径、显微形态及动态流变特性进行表征,考察淀粉颗粒质量浓度(1、5、10、20、30 mg/mL)和油相体积分数(10％、...     

Effects of ultrasound power on the properties of non-salt chicken myofibrillar protein emulsions

The present study was designed to investigate the effects of different ultrasonic powers (0–600 W) on the storage stability, rheological properties and microstructure of non-salt chicken myofibrillar protein (MP) emulsions. The Turbiscan stability index (TSI) values, storage modulus (G′) values, loss modulus (G″) values, viscosity values and droplet size of the MP emulsions first increased and then decreased with an increase in ultrasonic power. The results of the creaming index and TSI values showed that ultrasonic treatment effectively improved the storage stability of the emulsions compared with non-ultrasonic treatment. Meanwhile, sonication decreased the oil droplet size and the contact angles accompanied by an increase in G′ and G″ values and the viscosity. The oil droplets became smaller and more uniform distribution observed through the different kinds of microscopic analysis. The physical stability of non-salt MP emulsions treated with different ultrasonic powers was significantly enhanced, and ultrasonic treatment with 450 W power had the optimal efficiency for the stability of the emulsions.