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Highly Active Ruthenium Catalyst Supported on Magnetically Separable Mesoporous Organosilica Nanoparticles
| Content Provider | MDPI |
|---|---|
| Author | Omar, Suheir Abu-Reziq, Raed |
| Copyright Year | 2020 |
| Description | A facile and direct method for synthesizing magnetic periodic mesoporous organosilica nanoparticles from pure organosilane precursors is described. Magnetic ethylene- and phenylene-bridged periodic mesoporous organosilica nanoparticles (PMO NPs) were prepared by nanoemulsification techniques. For fabricating magnetic ethylene- or phenylene-bridged PMO NPs, hydrophobic magnetic nanoparticles in an oil-in-water (o/w) emulsion were prepared, followed by a sol–gel condensation of the incorporated bridged organosilane precursor (1,2 bis(triethoxysilyl)ethane or 1,4 bis(triethoxysilyl)benzene), respectively. The resulting materials were characterized using high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray (EDX) spectroscopy, powder X-ray diffraction (XRD), solid-state NMR analysis, and nitrogen sorption analysis (N2-BET). The magnetic ethylene-bridged PMO NPs were successfully loaded using a ruthenium oxide catalyst by means of sonication and evaporation under mild conditions. The obtained catalytic system, termed Ru@M-Ethylene-PMO NPS, was applied in a reduction reaction of aromatic compounds. It exhibited very high catalytic behavior with easy separation from the reaction medium by applying an external magnetic field. |
| Starting Page | 5769 |
| e-ISSN | 20763417 |
| DOI | 10.3390/app10175769 |
| Journal | Applied Sciences |
| Issue Number | 17 |
| Volume Number | 10 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2020-08-20 |
| Access Restriction | Open |
| Subject Keyword | Applied Sciences Inorganic Chemistry Periodic Mesoporous Organosilica Nanoparticles Magnetic Nanoparticles Ruthenium Nanoparticles Catalysis Hydrogenation of Aromatic Compounds |
| Content Type | Text |
| Resource Type | Article |