Abstract
Functionalized mesoporous silica particles offer excellent chemical and morphological properties, making them ideal adsorbents or drug carriers. However, their synthesis involves several energy- and resource-intensive steps, resulting in high economic and environmental costs. In this study, we report a strategy for the direct design of mesoporous silica with ordered mesopores densely functionalized by polyacid chains. The aqueous process relies on polyion complex micelles acting as pH-responsive multifunctional agents. They are first associated to direct the mesostructure of silica, and are then dissociated by a change in pH to reveal the material's mesoporosity and yield functional pores. Ordered mesoporous particles with controlled structure and particle size were obtained, showing dense functionalization of up to 2.1 mmol.gSiO2−1 of carboxylic acid functions, which were fully accessible to ionic exchange in aqueous solution. These highly functionalized materials were then evaluated as reversible adsorbents for the removal of a cationic dye (auramine O). The results revealed high dye uptakes, from 130 to 237 mg.gSiO2−1, which were up to 193 % higher than those achieved with non-functional calcined mesoporous silica particles. These uptakes correlated with the mesoporous volume of the materials, with an average density of around one auramine molecule per nm3 of pore. In addition, the materials exhibited excellent dye adsorption/desorption cyclability by pH stimuli in aqueous solutions under mild conditions, with an average desorption efficiency of 96 % in just 30 min. These results therefore represent an attractive strategy for the design of efficient and sustainable adsorbents for water purification.