38 research outputs found
Production of Gelatin Nanoparticles by Solvent Dissolution Method for Use as Food-grade
Introduction
Gelatin is one of the most widely used colloidal proteins, which has unique hydrocolloidal property. Gelatin is derived from collagen by changing the thermal nature. This product is widely used in food, pharmaceutical, biomedical, cosmetic and photography industries. Global gelatin demand for food and non-food products is increasing. Two important properties of nanoparticles are: Increasing the surface-to-volume ratio of nanoparticles causes the atoms on the surface to have a much greater effect on their properties than the atoms within the particle volume. The effects of quantum size, which is the second feature. Methods for preparing nanoparticles from natural macromolecules: In general, two major methods for making protein nanoparticles have been reported Emulsion-solvent evaporation method and sedimentation or phase separation method in aqueous medium. Numerous methods have been reported for the preparation of nanoparticles from natural macromolecules. The first method is based on emulsification and the second method is based on phase separation in aqueous medium. In the first method, due to the instability of the emulsion, it is not possible to prepare nanoparticles smaller than 500 nm with a narrow particle size distribution. Therefore, coagulation method or anti-solvent method which is based on phase separation was proposed to prepare nanoparticles from natural macromolecules.
Materials and Methods
Type B (cow) gelatin was purchased from processing company with Bloom 260-240 food and pharmaceutical Iran solvent gelatin solution of 25% aqueous acetate glutaraldehyde from Iran Neutron Company. Two-stage anti-solvent method was used to produce gelatin nanoparticles. Then, to form nanoparticles, acetone was added dropwise while stirring until the dissolved acetone begins to change color and eventually turns white, which indicates the formation of nanoparticles. Finally, glutaraldehyde solution was added for cross-linking and finally centrifuged.
Results and Discussion
The results showed that with increasing gelatin concentration, nanoparticle size and PDI increased significantly. According to the announced results, the solvent has a direct effect on the size. Therefore, the best mixing speed is determined to achieve the smallest particle size. Zeta potential is the best indicator for determining the electrical status of the particle surface and a factor for the stability of the potential of the colloidal system because it indicates the amount of charge accumulation in the immobile layer and the intensity of adsorption of opposite ions on the particle surface. If all the particles in the suspension are negatively or positively charged, the particles tend to repel each other and do not tend to accumulate. The tendency of co-particles to repel each other is directly related to the zeta potential. Fabricated gelatin nanoparticles have a stable structure, and are heat resistant. These nanoparticles are ready to be used to accept a variety of aromatic substances, compounds with high antioxidant properties, a variety of vitamins and heat-sensitive substances.
Conclusion
The results of this study showed that the optimal conditions for the production of a particle of 88.6 nm at 40 ° C, the volume of acetone consumption was 15 ml, concentration 200 mg and speed 1000 rpm, and the morphology of gelatin nanoparticles have resistant, spherical polymer structure and mesh with a smooth surface that can be clearly seen under an electron microscope
Monitoring geometric characteristics of rice during processing by image analysis system and micrometer measurement
Improvements in gelatin cold water solubility after electrospinning and associated physicochemical, functional and rheological properties
A major limitation of gelatin feedstocks for industrial food and pharmaceutical applications is the lack of solubility at room temperature, necessitating use of drum/dry blending processes, combined with additives. Herein, electrospinning is investigated as an alternative route for producing cold water soluble 100% gelatin feedstock in place of powders. The physicochemical, rheological and functional properties of electrospun gelatin and an industrially available gelatin powder feedstocks were compared. Optimal conditions for producing gelatin nanofiber sheets were found to be 25% (w/v) polymer concentration in a binary solvent system of acetic acid: water (3:1 v/v), a spinning voltage of 25 kV, a flow rate of 0.5 ml/h and a tip-to-collector distance of 150 mm. The production of nanofibers from gelatin powder did not change the nature of the material. The glass transition temperature of gelatin nanofibers was lower than gelatin powder. Conversion of gelatin powder into nanofiber sheets also increased the dissolution rate in water at ambient temperature and promoted emulsion and foam forming ability, as well as increasing foam stability. Loss tangent measurements revealed that the gel formed by the gelatin nanofibers could be characterized as a weak gel. No difference was observed in the Young's modulus of samples made from gelatin nanofibers and powder, and the 0.2% (w/v) gelatin nanofiber sample yielded a higher viscosity than the 0.1% (w/v) concentration. Gelatin nanofibers have promising potential to be used as feedstock in food technology when cold water solubility and improved control of physical, functional and textural properties are required
Solvothermal synthesis of nanoporous TiO2: the impact on thin-film composite membranes for engineered osmosis application
In the current study, the impact of self-synthesized nanoporous titanium oxide (NT) on the morphology, performance and fouling of a polyamide (PA) thin-film composite (TFC) membrane was investigated when the membrane was applied for engineering osmosis (EO). The nanoporous structure and the spindle-like shape of NT were revealed through transmission electron microscopy (TEM), while the AATPS modification of NT was verified by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. The results of x-ray photoelectron spectroscopy (XPS) and x-ray diffraction (XRD) confirmed the presence of modified NT (mNT) in the PA dense active layer of the TFC membrane. The outgrowth of the 'leaf-like' structure, upon mNT loading, at the surface of the PA layer was observed by field-emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM). The TFC membrane prepared with 0.05 wt% mNT loading in the organic phase showed the water flux of 26.4 l m-2 h-1 when tested in the forward osmosis (FO) mode using 0.5M and 10 mM NaCl solution as the draw and feed solution, respectively. Moreover, the TFC-mNT membrane also demonstrated an intensified antifouling property against organic foulant during FO application and it was possible to retrieve the initial water flux almost completely with a simple water-rinsing process
Surface modification of thin film composite membrane by nanoporous titanate nanoparticles for improving combined organic and inorganic antifouling properties
In this study, nanoporous titanate (NT) nanoparticle synthesized by the solvothermal method was used to modify polyamide layer of thin film composite membranes with the aim of improving membrane resistances against organic and inorganic fouling. Thin film nanocomposite membranes (NMs) were synthesized by adding mNTs (modified nanoparticles) into polyamide selective layer followed by characterization using different analytical instruments. The results of XPS and XRD confirmed the presence of mNTs in the polyamide layer of NMs, while FESEM, AFM, zeta potential and contact angle measurement further supported the changes in physical and chemical properties of the membrane surface upon mNTs incorporation. Results of fouling showed that NM1 (the membrane incorporated with 0.01 w/v% mNTs) always demonstrated lower degree of flux decline compared to the control membrane when membranes were tested with organic, inorganic and multicomponent synthesized water, brackish water or seawater. Besides showing greater antifouling resistance, the NM also displayed significantly higher water flux compared to the control M membrane. The findings of this work confirmed the positive impact of mNTs in improving the properties of NM with respect to fouling mitigation and flux improvement
Microstructural evaluation and thermal oxidation behaviors of YSZ/NiCoCrAlYTa coatings deposited by different thermal techniques
In this paper, two coating techniques, the high velocity oxy-fuel (HVOF) and air plasma spray (APS) techniques, were used to deposit a bond coat of NiCoCrAlYTa on the Inconel 625 substrate, followed by applying a topcoat of yttria-stabilized zirconia (YSZ). The samples were preoxidized in an argon-controlled furnace at a temperature of 1000 °C for 12 and 24 h to characterize the microstructure of a thermally grown oxide (TGO) using the two coating techniques. The most suitable preoxidized samples were further tested for isothermal oxidation at 1000 °C for up to 120 h, and a hot corrosion test was performed at 1000 °C for up to 52 h or until spalling occurred. As-sprayed and oxidized samples prepared with different coating techniques were evaluated in terms of their microstructure using different characterization methods, such as field emission scanning electron microscopy (FESEM), variable pressure scanning electron microscopy (VPSEM), energy dispersive X-ray spectroscopy (EDS) equipped with energy dispersive X-ray and X-ray diffraction (XRD) analyses. In addition, the mechanical properties of these samples were evaluated using adhesion tests. The results show that the YSZ/NiCoCrAlYTa coating applied with the HVOF technique forms a more thin and continuous layer of TGO than that obtained when applying a YSZ/NiCoCrAlYTa coating using the APS technique, indicating that a severe brittle oxidation interface exists between the two layers. The results also indicate that the mechanical strength obtained from the adhesion test of the coated samples is observably affected by the oxidation behaviors obtained with the different deposition techniques chosen