Non-hydrolytic sol-gel synthesis of amine-functionalized silica: Template- and catalyst-free preparation of mesoporous catalysts for CO2 valorization
| Authors | |
|---|---|
| Year of publication | 2025 |
| Type | Article in Periodical |
| Magazine / Source | Microporous and Mesoporous Materials |
| MU Faculty or unit | |
| Citation | |
| web | https://www.sciencedirect.com/science/article/pii/S1387181124003937?via%3Dihub |
| Doi | http://dx.doi.org/10.1016/j.micromeso.2024.113371 |
| Keywords | Non-aqueous condensation; Silsesquioxane; Tertiary amine; Heterogeneous catalysis; Carbon dioxide; Epoxide; Cyclic carbonate |
| Description | Carbon dioxide utilization presents an important and topical research topic. However, the performance of catalysts needed for CO2 transformations does not achieve the necessary levels for their widespread application. To this end, we decided to study non-aqueous condensations providing amine-functionalized silica catalysts, possibly active in CO2-epoxide cycloaddition reaction. While non-hydrolytic sol-gel method is well-known for its efficiency in providing highly porous Lewis and Br & oslash;nsted acid metallosilicates, here we show for the first time its application for the preparation of silica-based catalysts containing basic groups. First, the reaction conditions were screened to reproducibly obtain porous materials with preserved amine moieties. These were identified as follows: silicon tetraacetate and bridging tertiary amine silanes as precursors, toluene as a solvent, and temperature between 160 and 180 degrees C. In such a way, materials with up to 776 m(2) g(-1) and 1.58 cm(3) g(-1) were obtained in one-step process, without any template, after conventional drying step. Next, the amine-functionalized materials were tested in CO2-epoxide coupling providing cyclic organic carbonates with high selectivity (>99 %) and moderate activity (up to 86 % epichlorohydrin conversion after 1 h at 120 degrees C and 10 bar CO2). The characterization of spent catalysts revealed a presence of cyclic organic carbonates at the catalyst surface as well as conversion of tertiary amine groups to quaternary ammonium moieties. |
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