Preparation of Thermosensitive Microcapsules Containing Water Soluble Powder by Melting Dispersion Cooling Method

It was tried to prepare the thermosensitive microcapsules containing the water soluble solid powder by the melting dispersion cooling method and to establish the optimum preparation conditions. As a model water soluble solid powder, sodium hydrogen carbonate was adopted in order to generate carbon dioxide gas and as a thermosensitive shell material, olefin resin with the melting point of ca. 40°C was used. In the experiment, the concentration of olefin resin in the shell material solution was mainly changed together with the concentrations of the oil soluble surfactant species and the α-tocopherol as a modifier of shell. Addition of α-tocopherol into the shell material solution could prevent the core from breaking away during the microencapsulation process and result in the higher microencapsulation efficiency, because the dispersion stability of solid powder in the shell material solution could be increased due to the increase in affinity between the shell material solution and solid powder. Also, the microencapsulation efficiency increased with the concentration of olefin resin, became maximum at 50 wt% and then, decreased. The microcapsules were found to begin melting at 36°C and to generate carbon dioxide gas.

Preparation of Microcapsules Containing Phase Change Material and Silicon Carbide Powder with Interfacial Polycondensation Reaction Method

The fundamental experiments were performed to establish the operational conditions required to prepare the microcapsules containing paraffin wax as a phase change material (PCM) and SiC powder with the interfacial polycondensation reaction. It was investigated how SiC powder affected a few characteristics of microcapsules such as the diameters of microcapsules, latent heat storage density, thermal responsibility and supercooling. In the experiment, the concentration of oil soluble surfactant, the revolution speed of impeller for preparing the (O/W) emulsion and the added weight of SiC powder were changed stepwise. The microcapsules containing PCM in which SiC powder was dispersed could be prepared well and characterized. The diameters of microcapsules increased by containing SiC powder and the content of SiC powder could be increased by performing surface modification of SiC powder. Latent heat storage density decreased with the content of SiC powder. Supercooling of PCM and thermal responsibility could be improved to some degree by containing SiC powder.

Preparation of Microcapsules Containing Camellia Oil with Heterocoagulation between Chitosan and Oleic Acid

It was tried to microencapsulate camellia oil using heterocoagulation between fatty acid dissolved in camellia oil and chitosan dissolved in the continuous water phase. Oleic acid as a fatty acid was dissolved in camellia oil in order to certainly form the microcapsule shell made from oleic acid and chitosan. The microcapsules were observed with optical microscope and characterized about the diameters, ζ-potential, FTIR analysis and adhesion feature on human hair. Microcapsules with the mean diameter in the range from ca. 1.5 μm to 4.5 μm could be prepared with the preparation method presented in this study. The oil droplets of camellia oil charged negatively to be -54.6 mV and the microcapsules charged positively to be 59.6 mV. The microcapsules adhered well on the negatively charged human hair and were kept stably before and after drying at room temperature for 24 h and blowing.

Preparation of Microcapsules Containing Dye Aqueous Solution and Investigation of Release Feature According to Preparation Method

Microcapsules containing the dye aqueous solution were prepared with three kinds of preparation methods and the release feature of microcapsules with each preparation method was mainly investigated. As a dye tried to microencapsulate, methylene blue was adopted, because methylene blue aqueous solution was changed in color with light irradiation and utilized in order to check the degree of river pollution. Microencapsulation using multiple emulsion was performed with the suspension polymerization method, the inverse interfacial polycondensation method and the suspension polymerization in parallel with the interfacial polymerization method, respectively. The release feature of microcapsules prepared with each preparation method was estimated with the solute permeability coefficient. It was found that the release feature of dye aqueous solution was different according to the preparation method and could be delicately controlled by microencapsulating with the suspension polymerization in parallel with interfacial polycondensation reaction and forming the polyurethane shell on the surface of the dye aqueous solution droplets.

Preparation of Microcapsules Containing Grape Polyphenol with the Spray Drying Method Followed by the Layer-by-Layer Method

It was tried to prepare the microcapsules containing grape polyphenol with the spray drying method followed by the layer-by-layer method. As grape polyphenol was water soluble, the spray drying method was adopted to obtain the higher content. As the shell material of the first microcapsules prepared by the spray drying method, palmitic acid with the melting point of 60&degC was adopted in order to prevent grape polyphenol from dissolution into water. As the shell material of the second microcapsules prepared by the layer-by-layer method, chitosan was used to coat the first microcapsules and to give the microcapsules alcohol resistance. In the experiment, the spray drying conditions such as the inlet temperature and the spraying pressure, the oil soluble surfactant species and the chitosan concentration were changed. The mean diameters of microcapsules could be controlled in the range from 5 μm to 35 μm by changing the spraying pressure and the inlet temperature. The yield of microcapsules and the microencapsulation efficiency over 50% could be obtained under the conditions of P = 1.0 kgf/cm2 and Tin = 100&degC. Furthermore, the microencapsulation efficiency could be increased by adding the oil soluble surfactant with the larger HLB value. Coating with chitosan could considerably increase alcohol resistance.

Preparation of Microcapsules Containing Artificial Diet for Tropical Fishes with Spray Gelling Method

The microcapsules containing the artificial diet for tropical fishes were prepared with the spray gelling method in order to prevent water environmental pollution. The carboxymethyl cellulose sodium aqueous solution, in which α-tocopherol droplets containing the powdery artificial diet were dispersed, was dropped or sprayed into the chitosan aqueous solution. Microcapsules were prepared by forming polyionic complex shell made from chitosan and carboxymethyl cellulose sodium. In the experiment, the concentration of carboxymethyl cellulose sodium (CMCNa) was mainly changed to investigate the effect on the diameters of microcapsules, the content and the microencapsulation efficiency. The microcapsules couldn’t be prepared with the concentration of carboxymethyl cellulose sodium less than 3.0 wt%. The microcapsules were the core-shell type. The diameters of microcapsules were increased with the concentration of CMCNa and the microencapsulation efficiency of ca. 100% could be obtained by the preparation method presented in this study. The microcapsules were found to be eaten well by tropical fishes and to prevent water environmental pollution.

Preparation of Polymer Composite Particles by Phase Separation Followed by Suspension Polymerization

The novel method for preparing the polymer composite particles has been developed. It was tried to prepare polymer composite particles composed of polystyrene and carbon black with the phase separation method followed by suspension polymerization. In order to prepare the polymer composite particles with the more uniform diameter, the styrene monomer droplets containing carbon black were formed with phase separation emulsification in which ethyl alcohol and water were used as the good solvent and the poor solvent for styrene monomer, respectively. In the experiment, the surfactant species and their concentrations, the pouring velocity of water and the weight ratio of carbon black to styrene monomer were mainly changed. Water was poured at the given pouring velocity into ethyl alcohol in which styrene monomer and an initiator were dissolved and carbon black was dispersed beforehand. The spherical polymer composite particles containing carbon black were prepared with Tween 20 and Tween 80 of nonionic surfactants and the irregular polymer composite particles were prepared with PVA, SDS and Kotamine. The diameters of polymer composite particles increased with the pouring velocity of water and with the weight ratio of carbon black to styrene monomer.

Microencapsulation of Sodium Hydrogen Carbonate to Generate Carbon Dioxide with Thermal Responsible Shell Material

This paper tried to develop the optimum procedure for microencapsulating water soluble solid powder with the thermal responsible material by the melting dispersion cooling method. Sodium hydrogen carbonate was adopted as a water soluble solid powder instead of microencapsulating carbon dioxide gas. The shell material was composed of olefin wax and α-tocopherol. In the experiment, the concentration of oil soluble surfactant and the water soluble surfactant species were changed. Sodium hydrogen carbonate was treated in the aqueous solution dissolving the water soluble surfactant to form the finer sodium hydrogen carbonate powder and to increase the content. The microencapsulation efficiency could be increased with the concentration of oil soluble surfactant and considerably increased by treating sodium hydrogen carbonate with the water soluble surfactant. Sodium hydrogen carbonate was protected well from environmental water. The microcapsules showed the thermal responsibility to generate carbon dioxide.

Preparation of Microcapsules Containing Aqueous Solution of Azur B with Melting Dispersion Cooling Method and Application to DNA Amplification Detector

Microcapsules containing the aqueous solution of Azur B of a water soluble dye were prepared with the melting dispersion cooling method and applied to the amplification detector of plant DNA. Paraffin wax with melting temperature of 75°C was used as the shell material. In the experiment, the aqueous solution (W) of Azur B as the core material was dispersed in the melted paraffin wax (O) to form the (W/O) emulsion and then, the (W/O) emulsion was dispersed in the silicon oil (O’) as the continuous phase to form the (W/O)/O’ emulsion at 85°C. After formation of the (W/O)/O’ emulsion, the microcapsules were prepared by cooling the (W/O)/O’ emulsion to 50°C. The microcapsules were prepared by changing the concentration of oil soluble surfactant in the (W/O) emulsion and the volume of the (W/O) emulsion in the (W/O)/O’ emulsion. The microencapsulation efficiency increased with the concentration of oil soluble surfactant and finally became 100% under the optimum conditions. Furthermore, the microcapsules were melted down at temperature of 85°C to reveal the sharp thermal responsibility and to release the aqueous solution of Azur B. As a result, it was found that the microcapsules were able to be applied to the amplification detector of plant DNA by utilizing the reaction between DNA and Azur B.

Preparation of Microcapsules Containing Water and Effect of Water Content on Expansion Behavior

The research work was conducted in order to establish the optimum conditions for preparing the expanded polystyrene beads without harmful substances and was aimed at the preparation of the microcapsules containing water and investigation of the effect of the water content on the expansion behavior of microcapsules. Microcapsules were prepared with the suspension polymerization method and the suspension polymerization in parallel with interfacial polycondensation method using the multiple emulsion (W/O)/W and adding a few additives. With increasing the crosslinking agent concentration in the suspension polymerization method, the water content increased from R = 5.8 wt% (CT = 0) to R = 8.2 wt% (CT = 4 wt%) and then, decreased to R = 7.5 wt% (CT = 9.0 wt%), while the expansion ratio increased from E = 1.01 (CT = 0) to E = 2.20 (CT = 4 wt%) and then, decreased to E = 1.01 (CT = 7.0 wt%). With increasing the added amount of wax in the suspension polymerization method, the water content gradually increased from R = 2.5 wt% to R = 8.0 wt%, while the expansion ratio increased from E = 1.01 to E = 1.5 and then, decreased. The water content and the expansion ratio could be increased by conducting suspension polymerization in parallel with interfacial polycondensation reaction from R = 5.0 wt % to R = 8.0 wt % and from E = 1.01 to E = 1.3, respectively. The maximum expansion ratio of E = 2.58 in this work was obtained under the conditions of crosslinking agent concentration of CT = 4.0 wt %, the added amount of wax of 3.0 g, addition of Agarose and the expansion temperature of T = 150°C.