Role of silanol groups and hydrothermal rehydroxylation on the functionalization of SBA-15 with APTES for CO2 capture
Year: 2025
Type: article
Abstract: In order to find the best initial characteristics of an APTES-functionalized SBA-15 material, a group of SBA-15 materials was synthesized. Firstly, to remove the template, two methods were employed: i) water and ethanol washing method, and ii) calcination method where three calcination temperatures were explored (350, 450 and 550 °C), all carried out in a constant air flow. The purpose of avoiding calcination of the material is to prevent the loss of silanol groups, which are involved in chemical modification with amino groups. And secondly, a portion of these materials were subjected to a hydrothermal process to improve the amount of surface silanol groups, groups on which APTES molecules are anchored. In this way, 8 materials were obtained that were then functionalized with APTES. Based on the nitrogen adsorption isotherms, an increase in pore size was observed when the material is rehydroxylated, which demonstrates the formation of silanol groups. And when the materials are functionalized, the average pore size decreases by about 1.0 nm, indicating the probability of the formation of new bonds between the surface silanol groups with the ethoxy groups of the APTES molecule. The CO2 uptake capacity showed interesting results for most of the materials, with the uncalcined materials presenting the highest values, 2.52 and 2.32 mmol g-1 at 1 bar and 25 ºC for S15WC-F and S15WC-FR, respectively.
Language: English
Subfield: Mechanical Engineering
Field: Engineering
Domain: Physical Sciences
SDG: Climate action
Open Access status: hybrid
Estimated APC paid: $3,970
Funders: Tecnológico Nacional de México, Federación Española de Enfermedades Raras, Consejo Nacional de Ciencia y Tecnología, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Universidad Autónoma Metropolitana, Secretaría de Ciencia, Tecnología e Innovación del Distrito Federal, Agencia Estatal de Investigación
Awards: G1258750515, G5144134635
OpenAlex ID: W4408305789
