Immobilizing particles on beads, fibers or filaments, when only one side is exposed to the reaction medium and therefore can be selectively functionalized, is a scalable and easy to control strategy for the fabrication of amphiphilic Janus particles. Here we describe a new, robust method for the fabrication of amphiphilic Janus particles based on immobilization of polymethylsilsesquioxane (PMSQ) particles on polycarbonate (PC), a high impact-resistance polymer with superior mechanical properties. The immobilization of the particles on the PC microspores is preformed via inverse solvent displacement method. PMSQ particles are added to a PC solution in tetrahydrofuran (THF), a good solvent for PC. The solution is then precipitated by the introduction of aqueous surfactant solution (anti solvent for PC) under an ultrasonic field. It is important to note that THF and water are miscible and do not form emulsion. During precipitation, PMSQ particles are assembled onto the surface of the PC spherical precipitates/microspheres. The exposed hemispheres of the PMSQ particles are then selectively silanized by (3-Aminopropyl)triethoxysilane (APTES) to introduce amine groups on their surface. To increase the polarity of the functionalized hemispheres, the amine groups are further modified to introduce carboxyl groups. SEM characterization confirms the fine embedment of PMSQ particles onto the PC microspheres. Covalent attachment of silica nanoparticles (NPs) to the functionalized hemispheres of the resulting particles along with fluorescent confocal microscopy conclusively proof the successful fabrication of amphiphilic Janus particles. The immobilization of particles onto highly rigid polymeric microspheres such as PC may pave the way to the development of a robust fabrication procedure with high resistance to temperature fluctuations and harsh mixing conditions that can arise during preparation. This method can be implemented toward a large variety of other synthetic commercial polymers such as polyamide, polyether sulfones, Polyether ether ketone or similar.

This work studied sorption regularities and assessed thermal stability and resistance to microbial degradation of humic acid as a result of 3 sorption cycles on bentonite clay, kaolinite, and muscovite using TGA/DSC, XRD, hydrophobic chromatography, light and electron microscopy, etc. The experiment revealed that kaolinite sorbed more humic acids (HAs) in terms of unit surface area (1.03 × 10-3 C, g/m2) compared to bentonite (0.35 × 10-3 C, g/m 10-3 g/m2). Sorption at pH 4.5 was accompanied by HA fractionation in amphiphilicity and chemical composition. HA was sorbed mainly due to hydrophobic components on the surface of all sorbents. HA was not intercalated into the interlayer spaces of montmorillonite during sorption. Sorption due to hydrophilic interactions was mostly performed on muscovite and bentonite than on kaolinite. Sorption was followed by a change in the chemical composition of HA and decreased C/N compared to free HA, indicating selective sorption of nitrogen-containing compounds which is most characteristic of muscovite. Only a relatively thermolabile HA fraction was adsorbed on all minerals while its thermal stability increased compared to that before the experiment. Thermal stability and ratio of the Exo2/Exo1 peak areas on the DSC curves of sorbed HA increased with each subsequent sorption cycle. Thermal stability and resistance to microbial oxidation of sorbed HA showed the following relationship: the higher the thermal stability, the less available is sorbed HA for utilization by microorganisms.