A General Chelate-Assisted Co-Assembly to Metallic Nanoparticles-Incorporated Ordered Mesoporous Carbon Catalysts for Fischer–Tropsch Synthesis

Citations Over TimeTop 10% of 2012 papers

Abstract

The organization of different nano objects with tunable sizes, morphologies, and functions into integrated nanostructures is critical to the development of novel nanosystems that display high performances in sensing, catalysis, and so on. Herein, using acetylacetone as a chelating agent, phenolic resol as a carbon source, metal nitrates as metal sources, and amphiphilic copolymers as a template, we demonstrate a chelate-assisted multicomponent coassembly method to synthesize ordered mesoporous carbon with uniform metal-containing nanoparticles. The obtained nanocomposites have a 2-D hexagonally arranged pore structure, uniform pore size (~4.0 nm), high surface area (~500 m(2)/g), moderate pore volume (~0.30 cm(3)/g), uniform and highly dispersed Fe(2)O(3) nanoparticles, and constant Fe(2)O(3) contents around 10 wt %. By adjusting acetylacetone amount, the size of Fe(2)O(3) nanoparticles is readily tunable from 8.3 to 22.1 nm. More importantly, it is found that the metal-containing nanoparticles are partially embedded in the carbon framework with the remaining part exposed in the mesopore channels. This unique semiexposure structure not only provides an excellent confinement effect and exposed surface for catalysis but also helps to tightly trap the nanoparticles and prevent aggregating during catalysis. Fischer-Tropsch synthesis results show that as the size of iron nanoparticles decreases, the mesoporous Fe-carbon nanocomposites exhibit significantly improved catalytic performances with C(5+) selectivity up to 68%, much better than any reported promoter-free Fe-based catalysts due to the unique semiexposure morphology of metal-containing nanoparticles confined in the mesoporous carbon matrix.

Related Papers

• → The role of tautomerization in acetylacetone as a complexing agent: Theoretical perspectives(2010)3 cited
• → Comparative study of the O···H···O proton transfer in the enol form of a single acetylacetone molecule and acetylacetone incorporated in β-cyclodextrin: a theoretical investigation(2013)2 cited
• → An NMR Study of Metal Complexes Containing Acetylacetone and Related Compounds. I. The Preparation, Halogenation and NMR Spectra of Cobalt(III) Complexes Containing Acetylacetone and Bis(acetylacetone)ethylenediimine(1970)16 cited
• Calculation of Gibbs free energy of iron acetylacetone hydrogenating reaction by density functional theory(2009)
• → A study on the aryla,. zo coupling reaction of bis-(acetylacetone)ethylenediaminocopper(II) and bis(acetylacetone)ethylenediaminonickei(II)(2006)