Fe/Co Alloys for the Catalytic Chemical Vapor Deposition Synthesis of Single- and Double-Walled Carbon Nanotubes (CNTs). 2. The CNT−Fe/Co−MgAl2O4 System

A detailed 57Fe Mössbauer study of the Mg(0.8)Fe(0.2-y)Co(y)Al2O4 (y = 0, 0.05, 0.1, 0.15, 0.2) solid solutions and of the CNT-Fe/Co-MgAl2O4 nanocomposite powders prepared by reduction in H2-CH4 has allowed characterization of the different iron phases involved in the catalytic process of carbon nanotube (CNT) formation and to correlate these results with the carbon and CNT contents. The oxide precursors consist of defective spinels of general formulas (Mg(1-x-y)(2+)Fe(x-3alpha)(2+)Fe(2alpha)(3+)[symbol: see text](alpha)Co(y)(2+)Al2(3+))O4(2-) . The metallic phase in the CNT-Fe/Co-MgAl2O4 nanocomposite powders is mostly in the form of the ferromagnetic alpha-Fe/Co alloy with the desired composition. For high iron initial proportions, the additional formation of Fe3C and gamma-Fe-C is observed while for high cobalt initial proportions, the additional formation of a gamma-Fe/Co-C phase is favored. The higher yield of CNTs is observed for postreaction alpha-Fe(0.50)Co(0.50) catalytic particles, which form no carbide and have a narrow size distribution. Alloying is beneficial for this system with respect to the formation of CNTs

From ceramic–matrix nanocomposites to the synthesis of carbon nanotubes

The selective reduction in H2 of oxide solid solutions produces nanocomposite powders in which transition metal nanoparticles are dispersed inside and on the surface of the oxide matrix grains. When using a H2/CH4 reducing atmosphere, the metal nanoparticles that form on the surface of the oxide grains act as catalysts for the CH4 decomposition and, because of their small size at high temperatures (>800○C), favor the in-situ nucleation and growth of single-wall and thin multiwall carbon nanotubes. This article reviews our results on the synthesis and characterization of M-MgAl2O4 (M=Fe, Fe/Co, Fe/Ni) nanocomposite powders, without and with carbon nanotubes, emphasizing the information that can be derived from Mössbauer spectroscopy as a complement to other characterization techniques

Characterization by Mossbauer spectroscopy of Fe phases in highly weathered serpentinitic soil from southern Cameroon

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Mössbauer spectroscopy study of MgAl2O4-matrix nanocomposite powders containing carbon nanotubes and iron-based nanoparticles

Materials involved in the catalytic formation of carbon nanotubes are for the first time systematically studied by Mössbauer spectroscopy between 11 K and room temperature. Mg1−xFexAl2O4 (x=0.1, 0.2, 0.3, 0.4) solid solutions are transformed into carbon nanotubes–Fe/Fe3C–MgAl2O4 composite powders by reduction in a H2–CH4 gas mixture. The oxides are defective spinels of general formulae (Mg1−x2+Fex−3α2+Fe2α3+□αAl23+)O42−. Ferromagnetic α-Fe, ferromagnetic Fe3C and a γ-Fe form, the latter possibly corresponding to a γ-Fe–C alloy, are detected in the composite powders. An attempt is made to correlate these results with the microstructure of the powder. It seems that the nanoparticles, which catalyze the formation of the carbon nanotubes, are detected as Fe3C in the post-reaction Mössbauer spectroscopy analysis

High-resolution in vivo imaging of xylem-transported CO2 in leaves based on real-time 11C-tracing

Plant studies using the short-lived isotope C-11 to label photosynthate via atmospheric carbon dioxide (CO2), have greatly advanced our knowledge about the allocation of recent photosynthate from leaves to sinks. However, a second source for photosynthesis is CO2 in the transpiration stream, coming from respiration in plant tissues. Here, we use in vivo tracing of xylem-transported (CO2)-C-11 to increase our knowledge on whole plant carbon cycling.We developed a newmethod for in vivo tracing of xylem-transported CO2 in excised poplar leaves using C-11 in combination with positron emission tomography (PET) and autoradiography. To show the applicability of both measurement techniques in visualizing and quantifying CO2 transport dynamics, we administered the tracer via the cut petiole and manipulated the transport by excluding light or preventing transpiration. Irrespective of manipulation, some tracer was found in main and secondary veins, little of it was fixed in minor veins or mesophyll, while most of it diffused out the leaf. Transpiration, phloem loading and CO2 recycling were identified as mechanisms that could be responsible for the transport of internal CO2. Both C-11-PET and autoradiography can be successfully applied to study xylem-transported CO2, toward better understanding of leaf and plant carbon cycling, and its importance in different growing conditions

DC-SIGN and DC-SIGNR Bind Ebola Glycoproteins and Enhance Infection of Macrophages and Endothelial Cells

AbstractEbola virus exhibits a broad cellular tropism in vitro. In humans and animal models, virus is found in most tissues and organs during the latter stages of infection. In contrast, a more restricted cell and tissue tropism is exhibited early in infection where macrophages, liver, lymph node, and spleen are major initial targets. This indicates that cellular factors other than the broadly expressed virus receptor(s) modulate Ebola virus tropism. Here we demonstrate that the C-type lectins DC-SIGN and DC-SIGNR avidly bind Ebola glycoproteins and greatly enhance transduction of primary cells by Ebola virus pseudotypes and infection by replication-competent Ebola virus. DC-SIGN and DC-SIGNR are expressed in several early targets for Ebola virus infection, including dendritic cells, alveolar macrophages, and sinusoidal endothelial cells in the liver and lymph node. While DC-SIGN and DC-SIGNR do not directly mediate Ebola virus entry, their pattern of expression in vivo and their ability to efficiently capture virus and to enhance infection indicate that these attachment factors can play an important role in Ebola transmission, tissue tropism, and pathogenesis