Evidence of an equimolar C2H2-CO2 reaction in the synthesis of carbon nanotubes.
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Biomedical subjects
Publications and source records attributed to Arnaud Magrez.
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The cellular toxicity of carbon-based nanomaterials was studied as a function of their aspect ratio and surface chemistry. These structures were multiwalled carbon nanotubes, carbon nanofibers, and carbon nanoparticles. Their toxicity was tested in vitro on lung tumor cells. Our work clearly indicated that these materials are toxic while the hazardous effect is size-dependent. Moreover, cytotoxicity is enhanced when the surface of the particles is functionalized after an acid treatment.
NaNbO(3) powders with various particle sizes (ranging from 30 nm to several microns) and well-controlled stoichiometry were obtained through microemulsion-mediated synthesis. The effect of particle size on the phase transformation of the prepared NaNbO(3) powders was studied using X-ray powder diffraction, Raman spectroscopy, and nuclear site group analysis based on these spectroscopic data. Coarsened particles exhibit an orthorhombic Pbcm (D(2h)(11), no. 57) structure corresponding to the bulk structure, as observed for single crystals or powders prepared by conventional solid-state reaction. The crystal symmetry of submicron powders was refined with the space group Pmc2(1) (C(2v)(2), no. 26). The reduced perovskite cell volumes of these submicron powders were most expanded compared to all the other structures. Fine particles with a diameter of less than 70 nm as measured from SEM observations showed an orthorhombic Pmma (D(2h)(5), no. 51) crystal symmetry. The perovskite formula cell of this structure was pseudocubic and was the most compact one. A possible mechanism of the phase transformation is suggested.
Multiwalled carbon nanotubes (MWCNTs) were grown by chemical vapor deposition by applying C(2)H(2) fluxed over Fe(1)(-x)Co(x) catalyst supported by alkaline earth carbonate. Detailed investigations of the chemical process occurring prior and during the growth allowed us a significant improvement of the nanotube production rate and quality. We observed a strong influence of the catalyst stoichiometry on the carbon deposition rate and the nanotube characteristics. We also found evidence for the active role of the support in the growth process, which is explained by the decomposition of the carbonate at the growth temperature. Using the optimized parameters obtained from our study performed in a fixed bed furnace, we could improve the production rate to about 500 g/day of purified MWCNTs in our large-scale rotary tube furnace.