Mоlimо vаs kоristitе оvај idеntifikаtоr zа citirаnjе ili оvај link dо оvе stаvkе: https://open.uns.ac.rs/handle/123456789/12452
Nаziv: Thermally activated iron containing layered double hydroxides as potential catalyst for N <inf>2</inf>O abatement
Аutоri: Vulic T.
Reitzmann A.
Lázár K.
Dаtum izdаvаnjа: 1-окт-2012
Čаsоpis: Chemical Engineering Journal
Sažetak: Layered double hydroxides (LDHs) and derived mixed oxides with different Mg/Al/Fe contents were investigated. Two super-saturation precipitation methods were used for the synthesis of LDHs with general formula [Mg 1-xM(III) x(OH) 2](CO 3) x/2{dot operator}mH 2O where M(III) presents Al and/or Fe. The content of trivalent ions x=M(III)/[M(II)+M(III)], was varied between 0.15<x<0.7. Such a wide range of trivalent ions was chosen with the aim to induce the formation of different multiphase mixed oxides. Iron was introduced as constituent metal in order to obtain redox properties. LDHs and their derived mixed oxides were characterized with respect to their crystalline structure (XRD), thermal stability (TG/DTA), textural (N 2 adsorption), redox (H 2 TPR) and acid properties (NH 3 TPD) as well as the nature of the iron species (Mössbauer spectroscopy). Catalytic behavior was studied in two test reactions: N 2O decomposition and reduction with NH 3. It has been demonstrated that extended M(III) substitution influences the structure and surface properties of Mg-Al-Fe LDHs and derived mixed oxides, weakens Mg-Al-Fe-O interactions and improves catalytic behavior correlated with the presence of Fe-O-Fe-O-Fe entities providing possibility for facilitated extraction of oxygen with simultaneous redox Fe 3+Fe 2+ conversion. The catalytic behavior is mainly determined by redox properties, nature of iron species in mixed oxides and by structural properties of initial LDHs. The best catalytic results were obtained when the amount of M(III) was near the limit for the incorporation into LDH matrix. © 2012 Elsevier B.V.
URI: https://open.uns.ac.rs/handle/123456789/12452
ISSN: 13858947
DOI: 10.1016/j.cej.2012.06.152
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