The thesis focuses on the synthesis and characterization of mesoporous SiO$_2$ materials with additives for pore size tuning. Due to their unique properties, such as large specific surface area and ordered pore structure, mesoporous materials are suitable for various applications, including catalysis, adsorption, drug delivery and application in sensoring. The main objective of the research was to study the impact of different additives, such as 1,3,5-trimethylbenzene (TMB) and fatty acid salts with varying alkyl chain lengths, on the size and order of the pores.
The materials were synthesized using the sol-gel method in the presence of a surfactant that acted as a structure-directing agent. We varied synthesis conditions, such as the temperature and pH of the reaction mixture, and the type and concentration of the additives for pore size tuning, such as TMB and fatty acid salts with different alkyl chain lengths. In addition to varying the synthesis conditions, we also examined the effect of post-synthesis hydrothermal treatment on the selected samples and the influence of different techniques for removing the structure-directing agent. We studied the impact of extraction, thermal treatment (calcination), and a combination of both techniques on the pore size and order.
The synthesized materials were characterized using nitrogen adsorption, providing data on specific surface area and porosity. The ordering of the porous matrix was analyzed by low-angle X-ray powder diffraction. The morphology and particle size were examined by electron microscopy and dynamic light scattering analysis.
The results show that by adding TMB and fatty acids, the pore size in mesoporous SiO$_2$ materials can be effectively controlled, which opens up possibilities for tailoring these materials to meet the specific needs of various applications.
The second part of the research focused on a potential application of the materials for use as drug delivery systems. Ibuprofen was adsorbed into the porous matrix as a model molecule. I found that the release rate of adsorbed ibuprofen is faster than the dissolution rate of non-adsorbed ibuprofen.
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