Novel Organochlorinated Xerogels: From Microporous Materials to Ordered Domains.
Guillermo Cruz-QuesadaMaialen Espinal-ViguriMaría Victoria López RamónJulián J GarridoPublished in: Polymers (2021)
Hybrid silica xerogels combine the properties of organic and inorganic components in the same material, making them highly promising and versatile candidates for multiple applications. They can be tailored for specific purposes through chemical modifications, and the consequent changes in their structures warrant in-depth investigation. We describe the synthesis of three new series of organochlorinated xerogels prepared by co-condensation of tetraethyl orthosilicate (TEOS) and chloroalkyltriethoxysilane (ClRTEOS; R = methyl [M], ethyl [E], or propyl [P]) at different molar ratios. The influence of the precursors on the morphological and textural properties of the xerogels was studied using 29Si NMR (Nuclear Magnetic Resonance), FTIR (Fourier-Transform Infrared Spectroscopy), N2, and CO2 adsorption, XRD (X-ray Diffraction), and FE-SEM (Field-Emission Scanning Electron Microscopy). The structure and morphology of these materials are closely related to the nature and amount of the precursor, and their microporosity increases proportionally to the molar percentage of ClRTEOS. In addition, the influence of the chlorine atom was investigated through comparison with their non-chlorinated analogues (RTEOS, R = M, E, or P) prepared in previous studies. The results showed that a smaller amount of precursor was needed to detect ordered domains (ladders and T8 cages) in the local structure. The possibility of coupling self-organization with tailored porosity opens the way to novel applications for this type of organically modified silicates.
Keyphrases
- electron microscopy
- magnetic resonance
- high resolution
- solid state
- smoking cessation
- room temperature
- aqueous solution
- optical coherence tomography
- drinking water
- water soluble
- molecular docking
- contrast enhanced
- magnetic resonance imaging
- ionic liquid
- gas chromatography
- case control
- polycyclic aromatic hydrocarbons
- electron transfer
- drug induced
- tandem mass spectrometry
- simultaneous determination
- liquid chromatography