Hordein electrospun ultra-thin fibers are unstable in an aqueous environment. Chitosan was added to improve their water resistance. With increasing chitosan concentration, the viscosity and conductivity of the biopolymer blends increased, and the surface tensions remained almost constant. The structure and morphology of composite biopolymer fiber membranes showed that the average fiber diameter varied with chitosan concentration. ATR-FTIR spectra showed that the C–H stretching band changed or disappeared with increased chitosan. X-ray diffraction showed that chitosan was distributed in hordein fibers without crystallites. Compared with the hordein nanofibers, thermogravimetric analysis and derivative thermogravimetry curves showed that hordein/chitosan electrospun fibers had slightly decreased thermal stability. In conclusion, a low chitosan content improved the water resistance and other properties of hordein fibers, without changing their morphology or structure.

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 micrometers 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.

Unheated and heat-aggregated β-lactoglobulin (β-lg) solutions were used to stabilize clove oil-in-water emulsion and limonene-in-water emulsion prepared by microchannel (MC) emulsification. The size of the MC array plate was 15 × 15 mm2 consisting of 100 parallel MCs fabricated on each side of the plate. The channels were 4 μm depth, 71 μm length, and 8.2 μm width, with the terrace length of 29.1 μm. Unheated and heat-aggregated β-lg effectively stabilized clove oil-in-water and limonene-in-water emulsions during production using MC emulsification. The emulsion droplets were steadily produced by the channels. The average diameter of clove oil droplets was around 17 μm, with both unheated and heat-aggregated β-lg, regardless of the concentration of β-lg. The average diameter of the limonene droplets was 18–26 μm depending on the conditions (unheated or heat-aggregated) and the concentration of β-lg. The coefficient of variation for all average droplet diameters was ≤8%, which was an indication of monodisperse droplets. Clove oil-in-water emulsion droplets became polydisperse within 2 h observation, whilst limonene-in-water emulsion droplets remained monodisperse over time. The stability of the oil droplets over time related to the solubility of the oil phases rather than the effects of β-lg as the surfactant. In addition, the droplet sizes at different surfactant concentrations seemed to relate to the viscosity ratio between the dispersed phase and the continuous phase rather than the effects of the surfactant.

Zein electrospun nanofibers have poor water resistance, which restricts its applications in food preservation. To improve the water resistance of nanofibers, zein/ethyl cellulose (EC) hybrid nanofibers were prepared at different ratios. Besides, we also encapsulated cinnamon essential oil (CEO) into electrospun fibers for Agaricus bisporus preservation. As the weight ratio of EC increased from 0% (ZE-10) to 100% (ZE-01), the viscosity of electrospinning solutions gradually increased from 80.33 ± 19.23 mPa·s to 756.78 ± 22.48 mPa·s, resulting in sufficient chain entanglement for the preparation of uniform fibers. The average diameters of ZE-01, ZE-12, ZE-11, ZE-21, and ZE-10 nanofibers were 326 ± 53 nm, 267 ± 31 nm, 237 ± 51 nm, 292 ± 45 nm, and 362 ± 70 nm, respectively. The hydrogen bonds between the hydroxyl groups of ethyl cellulose and the amino groups of zein decreased the amount of free hydrophilic group, thus improving water resistance of nanofibers. Food packaging potential was evaluated using Agaricus bisporus. The zein/EC nanofibers loaded CEO significantly decreased weight loss and maintained the firmness of the Agaricus bisporus, and improved the quality of the Agaricus bisporus during storage.

The problem of the wall slip in steady-state flow measurements of oil-in-water (o/w) food emulsions has been investigated for different sensor system geometries and surface profiles. Experimental results demonstrated that slip effects are strongly dependent on the type of emulsion studied. This may be related to the emulsion microstructure. Thus, for instance, a highly structured gel-like continuous phase dampens wall slip effects, as opposed to emulsions in which creaming appears as a mechanism of instability, because of the formation of particulate flocs. The occurrence of wall slip is more clearly observed if the flow curves are obtained from stress sweep experiments. Although the recovery of the steady-state viscosity of a presheared sample is generally complete (similar values at low and high shear rates), the appearance of slip effects may be favoured by emulsion preshearing.

A green, switchable water dispersive liquid–liquid microextraction (SWDLL-ME) method is introduced for the first time as a preconcentration/separation tool for measuring trace levels of cadmium (Cd) in real water and food samples. In the present study, a switchable aqueous solution of polar organic solvent (acetonitrile) was reversibly switched (on and off) from miscible monophasic to immiscible biphasic in aqueous medium by exposure to an anti-solvent trigger (CO₂). The developed SWDLL-ME was successfully applied as an extraction method for the extraction of a Cd–PAN complex (1-(2-pyridylazo)-2-naphthol) in polar organic solvent (PS). The solvent enriched phase containing Cd–PAN was separated from the switchable water (SW) and treated with 200 μL of 0.1 mol L⁻¹ HNO₃ with ethanol (1 : 1, v/v) in order to reduce its viscosity, and it was then easily injected into a GFAAS for analysis. The SW was reused for the next assay after the removal of CO₂. The switching phenomenon of the SW from low to high polarity was confirmed by FTIR spectroscopy and conductivity measurements. The enrichment factor and limit of detection of the proposed method were 22 and 0.38 ng L⁻¹, respectively. Validation of the developed method was carried out by analyzing certified reference materials (SLRS-4 Riverine water and NIST SRM 1515 Apple leaves).

This research paper presents the results of tests on the colligative properties of konjac gum chains in water solutions. For this purpose, the measurements of osmotic pressure and intrinsic viscosity of aqueous solutions, in the function of konjac gum concentration and temperature were carried out. The applied methods allowed for the determination of the second osmotic virial coefficients B2, which raised with the increase of temperature. It indicate that increase of temperature causes higher affinity of polysaccharide’s chains to water. It was determined, that the osmotic average molecular mass of the konjac gum in non-purified solutions increases with temperature (1.07×105–3.80×105g×mol−1). Values of the reduced viscosity linearly increased in range 18–29dL×g for all temperatures. Received values of the Huggins constant (0.81–1.72) lead that water is poor solvent for konjac gum. The theta (θ) conditions were extrapolated for non-purified solutions − 325K (52°C), and interpolated for purified solutions − 307K (34°C). Based on the results of tests using the dynamic light scattering, the values of two main relaxation times (fast − 0.4–1.8ms and slow components − 4300–5500ms) were determined (the Kohlrausch-Williams-Watts). The obtained autocorrelation functions were characteristic for sol type systems or these which indicate a gel-like structure.

Microemulsions based on five-component mixtures for food applications and improved oil solubilization have been studied. The compositions included water, oil phase [such as R(+)-limonene and medium-chain triglycerides (MCT)], short-chain alcohols (such as ethanol), polyols (propylene glycol and glycerol), and several surfactants and their corresponding mixtures (nonionic, such as ethoxylated sorbitan esters, polyglycerol esters, sugar ester, and anionic, such as phosphatidylcholine). The phase behavior of these systems is discussed with respect to the influence of polyols and short-chain alcohols on the degree of solubilization of oils in the aqueous phase. The alcohol and polyols modify the interfacial spontaneous curvature and the flexibility of the surfactant film, enhancing the oil solubilization capacity of the microemulsions. The solubilization of R(+)-limonene was dramatically improved in the presence of the alcohol and polyols, whereas the improvement of solubilization for triglycerides containing MCT was less pronounced. In some systems high oil solubilization was achieved, and some of them can be easily diluted to infinity both with the aqueous phase and with the oil phase. Viscosity measurements along selected dilution lines [characterized by a single continuous microemulsion region starting from a pseudo binary solution (surfactant/oil phase) to the microemulsion (water/polyol corner)] indicate that at a certain composition the system inverts from a W/O to an O/W microemulsion.