Synthesis, characterization, and stability of Fe-MCM-41 for production of carbon nanotubes by acetylene pyrolysis

Fe-substituted MCM-41 molecular sieves with ca. 1, 2, and 3 wt % Fe were synthesized hydrothermally using different sources of colloidal silica (HiSil and Cab-O-Sil) and characterized by ICP, XRD, N2 physisorption, UV-vis, EPR, TPR, and X-ray absorption. Catalysts synthesized from Cab-O-Sil showed higher structural order and stability than those from HiSil. The local environment of Fe in the mesoporous material as studied by UV-vis reveals the dominance of framework Fe in all the as-synthesized Fe-MCM-41 samples. Dislodgement of some Fe species to extraframework location occurs upon calcination, and this effect is more severe for Fe-MCM-41 (2 wt %) and Fe-MCM-41 (3 wt %), as confirmed by EPR and X-ray absorption. These materials have been used as catalytic templates for the production of carbon nanotubes (CNTs) by acetylene pyrolysis at atmospheric pressure. A relationship between the Fe loading in MCM-41 and the carbon species produced during this reaction has been established. Using our optimized conditions for this system, Fe-MCM-41 with ca. 2 wt % Fe showed the best results with particularly high selectivity for single-wall carbon nanotube (SWNT) production. This catalyst was selective for carbon nanotubes with a low amount of amorphous carbon for a narrow range of temperatures from 1073 to 1123 K. To account for the different selectivity of these catalysts for CNTs production, the local environment and chemical state of Fe in the used catalyst was further probed by X-band EPR.     

Lyotropic self-assembly of high-aspect-ratio semiconductor nanowires of single-crystal ZnO

Lyotropic nanowire dispersions are attractive precursors for semiconductor device fabrication because they permit the alignment control of active nanomaterials. The reliable production of nanowire-based mesophases, however, is very challenging in practice. We show that appropriately functionalized high-aspect-ratio nanowires of single-crystal ZnO spontaneously form nematic phases in organic and aqueous media. These systems show isotropic, biphasic, and nematic phases on increasing concentration, in reasonable agreement with Onsager's theory for rigid rods interacting via excluded volume. Suspensions were readily processed to produce films with large-area monodomains of aligned nanowires. Imprints of the director field in quiescently dried films display a propensity for bend deformation in the organic mesophase versus splay deformation in the aqueous case, suggesting that system elasticity may be tuned via surface functionalization. These results provide critical insight for the utilization of semiconductor nanowires as novel mesogens and further enable the use of solution-based routes for fabricating optoelectronic devices.     

Sooting tendencies of nonvolatile aromatic hydrocarbons

We have measured sooting tendencies of 72 nonvolatile aromatic hydrocarbons, only five of which have been previously reported in the literature. The tested compounds include long-chain alkylbenzenes up to tridecylbenzene, methyl-substituted benzenes, naphthalenes, biaryls, and polycyclic aromatic hydrocarbons (PAH) with up to four rings. Sooting tendency was defined as the maximum soot concentration f_v,max in a methane/air coflow nonpremixed flame with 5-80 ppm of the aromatic added to the fuel. The f_v,max were converted into Yield Sooting Indices (YSI’s) by the equation YSI = C^∗f_v,max + D, where C and D are constants chosen so that YSI-2-heptanone = 17 and YSI-phenanthrene = 191. The aromatics were dissolved in 2-heptanone and added to the fuel mixture with a syringe pump. Soot concentrations were measured with laser-induced incandescence (LII). The burner and fuel lines were heated; time-resolved soot measurements verified that all of the test compounds were quantitatively transmitted to the flame without losses to the walls. The uncertainties in the results range from ±3 to ±10%.     

Decomposition and hydrocarbon growth processes for esters in non-premixed flames

Biomass fuels are a promising renewable energy source, and so, the mechanisms that may produce toxic oxygenated byproducts and aromatic hydrocarbons from oxygenated hydrocarbons are of interest. Esters have the form R-(C=O)-O-R' and are components of biodiesel fuels. The five specific esters studied here are isomers of C5H10O2. The experiments were performed in atmospheric pressure coflowing methane/air non-premixed flames. A series of flames were generated by separately doping the fuel mixture with 5,000 ppm of each ester. This concentration is sufficiently large to produce measurable changes in intermediate hydrocarbon concentrations, yet small enough to not disturb the overall flame structure. Since the overall structure is not perturbed, the measured changes in the intermediate hydrocarbons can be directly attributed to the reactions of the esters. Analysis of these changes reveals that unimolecular six-centered dissociation is the primary decomposition pathway for the three esters with molecular arrangements capable of undergoing that mechanism. The remaining two esters exhibited decomposition rates and products that are consistent with simple fission as the dominant decomposition mechanism, though we do not exclude other pathways from playing a significant role in their decomposition. All of the esters produce aromatic hydrocarbons at higher rates than the undoped fuel, and the molecular arrangement of the ester isomers plays a role in the degree of aromatic formation. Isomer variations also influence the type and quantity of toxic oxygenates that are produced in the flames.     

Two-dimensional electrophoretic analysis of Corynebacterium glutamicum membrane fraction and surface proteins

An improved protocol for the two-dimensional analysis of proteins of the Corynebacterium glutamicum cytoplasmic membrane fraction is described. By use of increased 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate (CHAPS) concentrations (2-4%) and an optimized electrophoresis protocol, horizontal streaking of proteins of the cytoplasmic membrane fraction was almost completely avoided. More important, in contrast to a previously published method, both a sample tray and IPG-phor isoelectric focusing unit can be used for the in-gel application of proteins. The described protocol was also found to be suitable for hydrophilic cytoplasmic proteins. Additionally, the preparation and analysis of C. glutamicum cell surface proteins is described. Proteins were extracted with lauroyl sarcosinate and 100-120 spots were separated on two-dimensional (2-D) gels in comparison to 18-20 spots observed previously by standard sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). C. glutamicum proteins can now be separated into three distinct fractions resembling different functional units of the bacterial cell.     

X-ray absorption spectroscopic investigation of partially reduced cobalt species in Co-MCM-41 catalysts during synthesis of single-wall carbon nanotubes

Chemometric tools were employed to analyze the in-situ dynamic X-ray absorption spectroscopy data to probe the state of Co-MCM-41 catalysts during reduction in pure hydrogen and under single-wall carbon nanotube synthesis reaction conditions. The use of the progressive correlation analysis established the sequence in which changes in the spectral features near the Co K edge occurred, and the evolving factor analysis provided evidence for the formation of an intermediate Co(1+) ionic species during reduction of the Co-MCM-41 catalyst in pure hydrogen up to 720 degrees C. This intermediate species preserves the tetrahedral environment in the silica framework and is resistant to complete reduction to the metal in H(2). While the Co(2+) species is resistant to reduction in pure CO, the intermediate Co(1+) species is more reactive in CO most likely forming cobalt carbonyl-like compounds with high mobility in the MCM-41. These mobile species are the precursors of the metallic clusters growing carbon nanotubes. Controlling the rates of each step of this two-stage reduction process is key to controlling the size of the metallic Co clusters formed in Co-MCM-41 catalysts.     

(n,m) Abundance evaluation of single-walled carbon nanotubes by fluorescence and absorption spectroscopy

A methodology that takes into account the (n,m) structure of single-walled carbon nanotubes (SWNTs), through an exciton-exciton resonance model and an electron-phonon interaction model, was employed in order to evaluate the semiconducting (n,m) abundance of two SWNT samples (i.e., Co-MCM-41 and HiPco). This was based on photoluminescence and near-infrared absorption data obtained on aqueous suspensions of individually dispersed SWNTs. In the absence of known (n,m) abundance SWNT samples, we resorted to determining the diameter distribution curves for both samples, which were found to obey an unsymmetrical log-normal distribution, typical for vapor-phase particle growth. Using this log-normal function, we reconstructed the near-infrared E S11 absorption spectrum of the narrow diameter distribution Co-MCM-41 SWNT sample, which in turn enabled us to assess the predictions of these two theoretical models. High spectral reconstruction accuracy was obtained from the electron-phonon interaction model when considering (11,0) and (10,0) zigzag nanotubes, along with (n,m) line widths inversely proportional to their extinction coefficients.     

Multiple periodic solutions for a nonlinear suspension bridge equation

We investigate nonlinear oscillations in a fourth-order partialdifferential equation which models a suspension bridge. Previouswork establishes multiple periodic solutions when a parameterexceeds a certain eigenvalue. In this paper, we use Leray-Schauderdegree theory to prove that if the parameter is increased further,beyond a second eigenvalue, then additional solutions are created.     

Proteome analysis of Corynebacterium glutamicum.

By the use of different Corynebacterium glutamicum strains more than 1.4 million tons of amino acids, mainly L-glutamate and L-lysine, are produced per year. A project was started recently to elucidate the complete DNA sequence of this bacterium. In this communication we describe an approach to analyze the C. glutamicum proteome, based on this genetic information, by a combination of two-dimensional (2-D) gel electrophoresis and protein identification via microsequencing or mass spectrometry. We used these techniques to resolve proteins of C. glutamicum with the aim to establish 2-D protein maps as a tool for basic microbiology and for strain improvement. In order to analyze the C. glutamicum proteome, methods were established to fractionate the C. glutamicum proteins according to functional entities, i.e., cytoplasm, membranes, and cell wall. Protein spots of the cytoplasmic and membrane fraction were identified by N-terminal sequencing, immunodetection, matrix assisted laser desorption/ionization-time of flight-mass spectrometry (MALDI-TOF-MS) and electrospray ionization-mass spectrometry (ESI-MS). Additionally, a protocol to analyze proteins secreted by C. glutamicum was established. Approximately 40 protein spots were observed on silver-stained 2-D gels, 12 of which were identified.