Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 4

Liczba wyników na stronie
first rewind previous Strona / 1 next fast forward last
Wyniki wyszukiwania
Wyszukiwano:
w słowach kluczowych:  MCM-41 porous silica
help Sortuj według:

help Ogranicz wyniki do:
first rewind previous Strona / 1 next fast forward last
EN
Nanoparticles of manganese ferrite were obtained by the impregnation of highly ordered mesoporous MCM-41 silica support. The investigated sample contained 20% wt. Fe. The obtained nanocrystallites were strongly dispersed in silica matrix and their size was about 2 nm. The sample annealing at 500°C led to increase of particle size to about 5 nm. The Mössbauer spectroscopy investigations performed at room temperature show on occurrence of MnFe2O4 nanoparticle in superparamagnetic state for the sample annealed in all temperatures. The coexistence of superparamagnetic and ferromagnetic phase was observed at liquid nitrogen temperature. The sample annealed at 400°C and 500 °C has bigger manganese ferrite particle and better crystallized structure. One can assign them the discrete hyperfi ne magnetic field components.
EN
Fe1.xCox/MCM-41 nanocomposite materials were prepared by wet impregnation of the silica mesoporous support with aqueous solution of iron and cobalt salt mixtures. Samples, after calcination, were reduced at 573 K in order to obtain homogeneous distribution of (Fe-Co)3O4 oxide species over the MCM-41 support. Bimetallic systems were achieved through high temperature reduction, carried out at 1073 K. The temperature-programmed reduction studies indicated complex nature of the oxide species. The phase analysis of the obtained samples after low temperature reduction process carried out by means of X-ray diffraction method and using 57Fe Mossbauer spectroscopy revealed the presence of nanostructured magnetite- and maghemite-like phases. The samples with higher cobalt contents (x . 0.2) contained additionally bimetallic phases. The complete transformation of oxide phases to bimetallic Fe-Co systems occurred during reduction process in hydrogen at 1073 K. It was observed that high temperature processing caused partial transformation of highly dispersed iron oxide nanocrystallites into fayalite species embedded in the silica walls.
EN
Iron-molybdenum silica mesoporous materials were obtained by the application of direct hydrothermal method. Four samples with different metal contents relative to silica were investigated. Incorporation of iron and molybdenum ions in the synthesis stage led to structural changes of the MCM-41 support. With an increasing metals content, cylindrical pores of silica initially transformed into bottle-ink type pores, and then into the slit-like ones. Mössbauer spectroscopy investigations indicated that Fe ions were embedded in the silica walls and then formed nanosized crystallites in the pores. Superparamagnetic phase was observed at liquid nitrogen temperature.
EN
The subject of investigation were the samples obtained by impregnation of MCM-41 template with an aqueous solution prepared from Fe(NO3)3ź9H2O. As a result of such a procedure, iron oxides deposits on MCM-41 were formed. The Mössbauer studies revealed an occurrence of Fe3O4 nanocrystallites in the both ferri- and superparamagnetic states. Almost 80% small particles exist in a paramagnetic state. The positron annihilation lifetime spectroscopy (PALS) spectra were measured in air or in vacuum. The long-lived ortho-positronium (o-Ps) components and their intensities are time dependent due to air molecules interaction with iron oxide nanocrystallites and silica walls surfaces. The adsorption of air on the nanocrystallites surface causes a total screening of their surface and a raise of the o-Ps lifetime values. Observed anti-quenching effect is a result of competition of two phenomena: practically switching off a pick-off mechanism related to interaction of o-Ps with magnetite nanoparticles and considerably weaker usual quenching by paramagnetic oxygen molecules.
first rewind previous Strona / 1 next fast forward last
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.