Synthesis of a Nanofibrous Manganese Oxide Octahedral Molecular Sieve with Co(NH3)63+ Complex Ions as a Template via a Reflux Method
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文摘
Todorokite-type manganese oxide octahedral molecular sieves (OMS-1) have been extensively studied due to their potential applications as materials. In this study, a nanofibrous todorokite-type, tunnel structure, manganese oxide molecular sieve material was successfully synthesized from a layered precursor with Co(NH3)63+ complex ions as a template director by a refluxing method (namely, Co(N)-todorokite). X-ray photoelectron spectroscopy (XPS) indicates that complex ions are located in the tunnel of the Co(N)-todorokite in the form of [Co(NH3)x]3+ (4 < x < 6) ions, while keeping the trivalence of the cobalt ions. Scanning electron microscopic (SEM) and high resolution transmission electron microscopic (HRTEM) images reveal that this material has a fibrous morphology with a thickness of 20−40 nm, and a lattice fringe spacing of 0.96 nm, corresponding to the (100) plane of the todorokite structure. The [010] HRTEM fringe images show that the tunnels contained a constant triple-chain width (3 × 3) along the c and a axes. The Co(N)-todorokite consists of a chemical composition of Co0.11N0.48H1.39MnO1.99·H2Ox. Thermogravity analysis (TGA) indicates that these nanofibers are thermally stable up to 400 °C. The Brunauer−Emmett−Teller (BET) surface area for Co(N)-todorokite is 98.2 m2/g, which is higher than that of bulk todorokite materials. The Horvath−Kawazoe (HK) plot shows a major pore size distribution peak centered at 0.71 nm for Co(N)-todorokite.

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