RESUMEN
Small-pore zeolites such as chabazite (CHA) are excellent candidates for the selective separation of CO2 ; however, the current synthesis involves several steps and the use of organic structure-directing agent (OSDA), increasing their cost and energy requirements. We report the synthesis of small-pore zeolite crystals (aluminosilicate) with CHA-type framework structure by direct synthesis in a colloidal suspension containing a mixture of inorganic cations only (Na+ , K+ , and Cs+ ). The location of CO2 molecules in the host structure was revealed by 3D electron diffraction (3D ED). The high sorption capacity for CO2 (3.8â mmol g-1 at 121â kPa), structural stability and regenerability of the discreate CHA zeolite nanocrystals is maintained for 10 consecutive cycles without any visible degradation. The CHA zeolite (Si:Al=2) reaches an almost perfect CO2 storage capacity (8 CO2 per unit cell) and high selectivity (no CH4 was adsorbed).
RESUMEN
All fields of today's technology are concerned with multifunctional materials, the subject of constantly expanding research. Among them, metal transition oxides occupy a strategic place because of the properties directly correlated with metal valence linked with oxygen stoichiometry. To enhance or induce new properties, knowledge of the relationships between the structural and physical characteristics is of prime importance, but a design at low scale also appears to be a powerful tool to increase the chemical reactivity and stabilize new compounds. Herein, an unexpected reaction is reported that associates the exchange of copper and iron in a 3D ludwigite lattice with the huge release of oxygen (14% by weight) at moderate temperature (<450 °C). Annealing of Cu2FeBO5 in a reducing atmosphere leads to the extrusion of copper and the formation of Fe3BO5, the micro/nanostructural state of which facilitates the partial Cu2FeBO5 recovery associated with the capture of oxygen in oxidizing conditions.