Electrosprayed Ethyl Cellulose Core-Shell Microcapsules for the Encapsulation of Probiotics

Electrosprayed ethyl cellulose core–shell microcapsules were produced for the encapsulation of probiotic Bifidobacterium animalis subsp. lactis (Bifido). Ethyl cellulose (ETC) was used as a shell material with different core compounds (concentrated Bifido, Bifido–maltodextrin and Bifido–glycerol). The core–shell microcapsules have an average diameter between 3 µm and 15 µm depending on the core compounds, with a distinct interface that separates the core and the shell structure. The ETC microcapsules displayed relatively low water activity (aw below 0.20) and relatively high values of viable cells (109–1011 CFU/g), as counted post-encapsulation. The effect of different core compounds on the stability of probiotics cells over time was also investigated. After four weeks at 30 °C and 40% RH the electrospray encapsulated samples containing Bifido–glycerol in the core showed a loss in viable cells of no more than 3 log loss CFU/g, while the non-encapsulated Bifido lost about 7.57 log CFU/g. Overall, these results suggest that the viability of the Bifido probiotics encapsulated within the core–shell ETC electrosprayed capsules can be extended, despite the fact that the shell matrix was prepared using solvents that typically substantially reduce their viability.

Microencapsulation of Paraffin Wax in Melamine-Formaldehyde for use in Thermal Management Study

Melamine formaldehyde microcapsules containing paraffin wax as phase change material (PCM) were synthesized. Free space was generated in-situ inside microcapsules. These were characterized by FTIR Spectrophotometer, Scanning electron microscope (SEM), Differential Scanning colorimeter (DSC), and optical microscope. It was confirmed that PCM was successfully encapsulated inside the shell material. Encapsulated PCM showed good phase change properties during heating and cooling. Enthalpy value of about 100 J/g was observed. The shape of the microcapsule, showing rough morphology is expected to help during processing and crystallization. It has been experimentally confirmed that no leakage occurs during the melting of PCM. Effectiveness in temperature control in a hot environment was also found to be satisfactory.

Highly Efficient and Controllable Methodology of the Cd0.25Zn0.75Se/ZnS Core/Shell Quantum Dots Synthesis

The surface of any binary or multi-component nanocrystal has imperfections and defects. The number of surface defects depends both on the nature of the nanomaterial and on the method of its preparation. One of the possibilities to confine the number of surface defects is the epitaxial growth of the shell, which leads to a change in the physical properties while maintaining the morphology of the core. To form a shell of the desired thickness, an accurate calculation of the amount of its precursors is substantial to avoid the appearance of individual crystals consisting of the shell material. This study aimed to develop an effective calculation method for the theoretical amount of precursors required for the formation of a ZnS shell on the surface of a Cd0.25Zn0.75Se core, followed by the practical implementation of theoretical calculations and characterization of the prepared nanomaterials. This method allows the complete control of the masses and volumes of the initial reagents, which will in turn prevent undesirable nucleation of nuclei consisting of the shell material. In the synthesis of Cd0.25Zn0.75Se/ZnS core/shell quantum dots (QDs), the sources of chalcogens were substituted seleno- and thioureas, which are capable of not only supplanting modern toxic sources of sulfur and selenium but also allowing one to perform the controlled synthesis of highly photoluminescent QDs with a low number of surface defects. The result of this shell overcoating method was an impetuous augmentation in the photoluminescence quantum yield (PL QY up to 83%), uniformity in size and shape, and a high yield of nanomaterials. The developed synthetic technique of core/shell QDs provides a controlled growth of the shell on the core surface, which makes it possible to transfer this method to an industrial scale.

Synthesis of Urea-Formaldehyde Microcapsule Containing Fluororesin and Its Effect on Performances of Waterborne Coatings on Wood Surface

In order to self-repair the cracks of waterborne coatings on Basswood at room temperature, with fluororesin and waterborne coatings embedded in the shell structure of urea formaldehyde (UF) resin, the microcapsules were fabricated via in-situ polymerization, and the effect of microcapsules on the chroma, gloss, mechanics and repair effect for waterborne coatings on wood was discussed. The results indicated that the coating effect was the most significant when the ratio value of the core materials to the shell material of microcapsules in mass was 0.75, and the agglomeration of particles was the least and the surface was the smoothest when the content of microcapsules was 1.0%. It was negative between the gloss of the film and microcapsule content. The ratio value of the core materials to the shell material in mass and the amount of microcapsules had great influence on the film hardness and adhesion, but had little effect on the impact resistance. When the ratio value of the core materials to the shell material of microcapsules in mass was 0.65 and the addition amount was 4.0–10.0%, the aging resistance of the film was improved most significantly. When the ratio value of the core materials to the shell material of microcapsules in mass was 0.65 and the addition amount was 7.0%, the overall properties of topcoat film on Basswood board was the most significant. It is for the application of fluororesin microcapsules possessing self-repairing effect in waterborne coating on Basswood board that a technical groundwork is provided by this study.

Microencapsulation of Thermochromic Material by Silicon Oxide Nanoparticles

This study is mainly focused on the fabrication of SiO2 as an inorganic shell material encapsulated an organic thermochromic (TC) core material comprises of either the (i) three-component as-synthesized blue dyes [BDTCM@SiO2] or (ii) off-the-shelf (commercial) black dyes [CDTCM@SiO2]. Both the SiO2 encapsulated thermochromic systems have successfully demonstrated the color transition at around 31 °C. For the three-component thermochromic microcapsules, we have used the crystal violet lactone (CVL) as a leuco dye, bisphenol-A (BPA) as a color developer, and 1-tetradecanol (TD) as a solvent. Different ratios of the thermochromic dye and the metal oxide were prepared to examine the effect of the core@shell ratio on the microstructural and thermal properties of the encapsulated microcapsules. The mean particles sizes of the BDTCM@SiO2 are below 100 nm, whereas, the CDTCM@SiO2 samples exhibited the mean particle sizes varied in a range of 100-1000 nm. The endothermic phase transition due to melting and in general, the thermal stabilities of these SiO2 encapsulated TCMs have been explored for the purpose of deploying these systems for thermal energy savings or storage applications.