Synthesis and Physicochemical Characterization of Mesoporous S

There exists a knowledge gap in understanding potential toxicity of mesoporous silica nanoparticles. A critical step in assessing toxicity of these particles is to have a wide size range with different chemistries and physicochemical properties. There are several challenges when synthesizing mesoporous silica nanoparticles over a wide range of sizes including (1) nonuniform synthesis protocols using the same starting materials, (2) the low material yield in a single batch synthesis (especially for particles below 60–70 nm), and (3) morphological instability during surfactant removal process and surface modifications. In this study, we synthesized a library of mesoporous silica nanoparticles with approximate particle sizes of 25, 70, 100, 170, and 600 nm. Surfaces of the silica nanoparticles were modified with hydrophilic-CH2–(CH2)2–COOH and relatively hydrophobic-CH2–(CH2)10–COOH functional groups. All silica nanoparticles were analysed for morphology, surface functionality, surface area/pore volume, surface organic content, and dispersion characteristics in liquid media. Our analysis revealed the synthesis of a spectrum of monodisperse bare and surface modified mesoporous silica nanoparticles with a narrow particle size distribution and devoid of cocontaminants critical for toxicity studies. Complete physicochemical characterization of these synthetic mesoporous silica nanoparticles will permit systematic toxicology studies for investigation of structure-activity relationships

Long-Term Effect of Steam Exposure on CO₂ Capture Performance of Amine-Grafted Silica

This study investigates the hydrothermal stability of triamine-grafted CO₂ adsorbent based on a commercial-grade silica (CARiACT, P10). Grafting was conducted in dry and wet conditions at 85 °C. At optimum grafting conditions using 0.2 cm³ water and 1.5 cm³ aminosilane per gram of silica, the highest CO₂ uptake of 1.93 mmol/g at 50 °C was obtained. This material was exposed to steam at 120 °C for up to 360 h. It was observed that increasing the duration of steam exposure from 3 to 24 h reduced adsorption uptake at 25 °C by 56%. However, the CO₂ uptake reduction was much less severe at higher adsorption temperatures, reaching 21% at 50 °C and only 4% at 75 °C. Conducting steam treatment for 360 h reduced adsorption uptake at 25, 50, and 75 °C by 83, 61, and 26%, respectively. For this extreme steaming experiment, the decrease in CO₂ uptake at all adsorption temperatures was attributed to the reduction of the sorbent average pore width, increasing diffusional mass transfer resistance. The results revealed that steam exposure did not reduce the amine loading or deactivate the amine groups; however, increasing exposure time decreased the average pore width, until partial collapse of material structure. Nevertheless, the large average pore width (21 nm) of the P10 silica led to higher hydrothermal stability of the amine-grafted sorbent compared to those with ordered pore structure supports, such as SBA-15 silica