Ionic Liquid Mediated Sol-Gel Synthesis in the Presence of Water or Formic Acid: Which Synthesis for Which Material?
Source abstract
Abstract
Sol-gel syntheses involving either neutral water or formic acid as a reactant have been investigated (1) to determine the best conditions to confine a maximum of ionic liquid (IL) inside silica-based matrixes and (2) to reach the highest porosity after removing the IL from the ion gels (washed gels). Several sets of ionogels were prepared from various 1-butyl-3-methylimidazolium ILs and various silica or organosilica sources. The study evidenced a critical effect of the anion on the morphology (monolith, powder) and texture of the resulting washed gels. Particularly, tetrafluoroborate anion led to monolith ionogels by a simple hydrolytic method, affording highly condensed mesoporous silicas with some fluorinated surface sites. Such sites have never been reported before and were evidenced by 19 F NMR. On the other hand, formic acid solvolysis turned out to be the only method to get non-exuding, crack-free, and transparent monoliths from ILs containing bis(trifluoromethylsulfonyl)imide [NTf 2 ] anion, with promising applications in photochemistry or photosensing. With bulky imidazolium and pyridinium cations, removal of the IL led to highly porous silicas with pore diameters and pore volumes as high as 10–15 nm and 3 cm 3 g –1, respectively. These silicas could find applications as supports for immobilizing bulky molecules.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ionic liquids properties and applications · Aerogels and thermal insulation · Mesoporous Materials and Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institut Charles Gerhardt de Montpellier, UMR 5253 CNRS-UM2-ENSCM-UM1, Université Montpellier 2, CC 1701, F34095 Montpellier, France
Institute of Materials Chemistry; Vienna University of Technology, 1060 Wien, Austria
Laboratoire Charles Coulomb, UMR CNRS 5521, Université Montpellier 2, 34095 Montpellier Cédex 5, France
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