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 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Nanostructured Pt functionalized multiwalled carbon nanotubes (MWNTs) produced by catalytic chemical vapor deposition are good room-temperature hydrogen sensors. MWNTs have been synthesized by catalytic chemical vapor deposition of acetylene using a fixed-bed catalytic reactor over hydrides of Mm(0.2)Tb(0.8)CO2 obtained through hydrogen decrepitation technique. Purified and chemically treated MWNTs have been functionalized by Pt resulting in nanostructured dispersion of Pt on CNTs. Structural, morphological, and vibrational characterizations have been carried out using XRD, SEM, TEM, HRTEM, Raman spectroscopy, and FTIR spectroscopy, respectively. Dispersion of Pt on MWNTs was confirmed by elemental analysis using EDX. Systematic investigations of hydrogen sensing properties of Pt-MWNT ensembles have been carried out. The Pt-MWNTs thin films are stable after several cycles of adsorption and desorption. The change in electrical resistance due to hydrogen adsorption is reversible, with increases to saturation on exposure to hydrogen gas. The result demonstrates that the Pt-MWNTs are p-type semiconductor materials, and chemically treated MWNTs functionalized with Pt show the better hydrogen sensing response at room temperature.
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PMID:Nanostructured Pt functionlized multiwalled carbon nanotube based hydrogen sensor. 1677 99

A porous beta-Ga2O3 photocatalyst has been successfully prepared. The photocatalyst was characterized by XRD, N2 adsorption-desorption, TEM, UV/vis, and FTIR techniques. The photocatalytic activity of the sample was evaluated by the decomposition of benzene in air under UV light illumination and was compared with that of the commercial titania (Degussa P25) and Pt/P25. Results revealed that the synthesized Ga2O3 was porous beta-Ga2O3 and was highly photoactive for mineralizing benzene and its derivatives (e.g., toluene and ethylbenzene) to CO2 under ambient conditions. The photocatalytic conversion of benzene over beta-Ga2O3 was about 1 order of magnitude higher than that over P25, and no obvious deactivation of beta-Ga2O3 was observed during the prolonged operation of 80 h. The high activity and long-term stability of the Ga2O3 have been ascribed to its stronger oxidative capability and higher specific surface area in comparison with P25.
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PMID:Efficient decomposition of benzene over a beta-Ga2O3 photocatalyst under ambient conditions. 1700 43

Total oxidation of ethyl acetate on supported copper oxide catalysts was investigated. The catalysts have been prepared by wet impregnation method and characterized by XRD, TEM and XPS. Among the catalysts with the supports of TiO2, CeO2/TiO2 and CeO2-ZrO2/TiO2, CeO2-ZrO2 solid solutions doped TiO2 supported catalyst gives the highest catalytic activity. Catalyst with the composition of 5 wt.% CuO/10 wt.% CeO2-ZrO2-TiO2 shows the total oxidation of ethyl acetate at about 270 degrees C with the 100% CO2 selectivity. The characterization studies of supported copper oxide catalysts showed that the highly dispersed CuO is one of the active phase which contacts intimately with the support, the action of the interface between the components was not be ignored.
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PMID:Catalytic combustion of ethyl acetate on supported copper oxide catalysts. 1700

We present the synthesis and characterization of Fe-doped carbon aerogels (CAs) and demonstrate the ability to grow carbon nanotubes directly on monoliths of these materials to afford novel carbon aerogel-carbon nanotube composites. Preparation of the Fe-doped CAs begins with the sol-gel polymerization of the potassium salt of 2,4-dihydroxybenzoic acid with formaldehyde, affording K+-doped gels that can then be converted to Fe2+- or Fe3+-doped gels through an ion exchange process, dried with supercritical CO2, and subsequently carbonized under an inert atmosphere. Analysis of the Fe-doped CAs by TEM, XRD, and XPS revealed that the doped iron species are reduced during carbonization to form metallic iron and iron carbide nanoparticles. The sizes and chemical composition of the reduced Fe species were related to pyrolysis temperature as well as the type of iron salt used in the ion exchange process. Raman spectroscopy and XRD analysis further reveal that, despite the presence of the Fe species, the CA framework is not significantly graphitized during pyrolysis. The Fe-doped CAs were subsequently placed in a thermal CVD reactor and exposed to a mixture of CH4 (1000 sccm), H2 (500 sccm), and C2H4 (20 sccm) at temperatures ranging from 600 to 800 degrees C for 10 min, resulting in direct growth of carbon nanotubes on the aerogel monoliths. Carbon nanotubes grown by this method appear to be multiwalled (approximately 25 nm in diameter and up to 4 microm long) and grow through a tip-growth mechanism that pushes catalytic iron particles out of the aerogel framework. The highest yield of CNTs was grown on Fe-doped CAs pyrolyzed at 800 degrees C treated at CVD temperatures of 700 degrees C.
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PMID:Iron-doped carbon aerogels: novel porous substrates for direct growth of carbon nanotubes. 1738 Nov 46

A novel method to synthesize single-wall carbon nanotube (SWNT)/poly(methyl methacrylate) (PMMA) nanocomposite by in-situ polymerization in supercritical CO2 is presented. The surfaces of the SWNT bundles were first functionalized with amino ethyl methacrylate (AEMA) followed by co-polymerization with methyl methacrylate. Supercritical fluid enhanced the diffusivity of monomer and facilitated the growth of tethered PMMA chains near the entanglement area and the interstitial space of the SWNT bundles. Partial debundling and disentanglement of the SWNT bundles and an enhanced dispersion in the polymer matrix were observed under SEM and TEM. After the removal of the polymer matrix physically attached to the nanotubes, it is found that the nanotubes were covered by tethered PMMA chains, which were a few nanometers in thickness. This work creates a route for improving impregnation and dispersion in SWNT composites; the same process can be extended to other vinyl polymers.
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PMID:Polymeric nanocomposites of functionalized carbon nanotubes synthesized in supercritical CO2. 1745 Aug 65

A CO2 laser (lambda = 10.6 microm) was used to heat a solution of water and alcohol saturated by Zn(AcAc)2 on a fused quartz substrate in open air. After only a few seconds of irradiation, various zinc oxide (ZnO) nanostructures including nanorods and nanowires are formed near the center of the irradiated zone, surrounded by a porous thin film of ZnO nanoparticles. The type of structures produced and their localization on the substrate can be varied by selecting adequate irradiation time and laser power ranges. The deposits have been analyzed using SEM, TEM, EDS, XRD, and Raman spectroscopy, revealing that the nanorods (aspect ratio ~6) and nanowires (aspect ratio ~94) are single-crystalline structures which grow along the c axis of wurtzite ZnO. The nanoparticles are also single-crystalline and have an average diameter of 16 nm. A qualitative model for nanostructure growth is proposed, based on previous studies of aqueous solution and hydrothermal processing.
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PMID:Fast synthesis of ZnO nanostructures by laser-induced decomposition of zinc acetylacetonate. 1802 27

The OXA-1 beta-lactamase is one of the few class D enzymes that has an aspartate residue at position 66, a position that is proximal to the active-site residue Ser(67). In class A beta-lactamases, such as TEM-1 and SHV-1, residues adjacent to the active-site serine residue play a crucial role in inhibitor resistance and substrate selectivity. To probe the role of Asp(66) in substrate affinity and catalysis, we performed site-saturation mutagenesis at this position. Ampicillin MIC (minimum inhibitory concentration) values for the full set of Asp(66) mutants expressed in Escherichia coli DH10B ranged from < or =8 microg/ml for cysteine, proline and the basic amino acids to > or =256 microg/ml for asparagine, leucine and the wild-type aspartate. Replacement of aspartic acid by asparagine at position 66 also led to a moderate enhancement of extended-spectrum cephalosporin resistance. OXA-1 shares with other class D enzymes a carboxylated residue, Lys(70), that acts as a general base in the catalytic mechanism. The addition of 25 mM bicarbonate to Luria-Bertani-broth agar resulted in a > or =16-fold increase in MICs for most OXA-1 variants with amino acid replacements at position 66 when expressed in E. coli. Because Asp(66) forms hydrogen bonds with several other residues in the OXA-1 active site, we propose that this residue plays a role in stabilizing the CO2 bound to Lys(70) and thereby profoundly affects substrate turnover.
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PMID:The role of OXA-1 beta-lactamase Asp(66) in the stabilization of the active-site carbamate group and in substrate turnover. 1803 Dec 91

Calcium carbonate biomineralization uses complex assemblies of macromolecules that control the nucleation, growth, and positioning of the mineral with great detail. To investigate the mechanisms involved in these processes, for many years Langmuir monolayers have been used as model systems. Here, we descibe the use of cryogenic transmission electron microscopy in combination with selected area electron diffraction as a quasi-time-resolved technique to study the very early stages of this process. In this way, we assess the evolution of morphology, polymorphic type, and crystallographic orientation of the calcium carbonate formed. For this, we used a self-assembled Langmuir monolayer of a valine-based bisureido surfactant (1) spread on a CaCl2-containing subphase and deposited on a holey carbon TEM grid. In a controlled environment, the grid is exposed to an atmosphere containing NH3 and CO2 (the (NH4)2CO3 diffusion method) for precisely determined periods of time (reaction times 30-1800 s) before it was plunged into melting ethane. This procedure allows us to observe amorphous calcium carbonate (ACC) particles growing from a few tens of nanometers to hundreds of nanometers and then crystallizing to form [00.1] oriented vaterite. The vaterite in turn transforms to yield [10.0] oriented calcite. We also performed the reaction in the absence of monolayer or in the presence of a nondirective monolayer of surfactant containing an oligo(ethylene oxide) 2 head group. Both experiments also showed the formation of a transient amorphous phase followed by a direct conversion into randomly oriented calcite crystals. These results imply the specific though temporary stabilization of the (00.1) vaterite by the monolayer. However, experiments performed at higher CaCl2 concentrations show the direct conversion of ACC into [10.0] oriented calcite. Moreover, prolonged exposure to the electron beam shows that this transformation can take place as a topotactic process. The formation of the (100) calcite as final product under different conditions shows that the surfactant is very effective in directing the formation of this crystal plane. In addition, we present evidence that more than one type of ACC is involved in the processes described.
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PMID:A quasi-time-resolved CryoTEM study of the nucleation of CaCO3 under langmuir monolayers. 1830 94

The objective of this study isto develop a novel supported nano-NiO catalyst for tar removal in biomass gasification/pyrolysis, to significantly enhance the quality of the produced gases. For this purpose, the supported nano-NiO/gamma-Al2O3 catalyst was prepared by deposition-precipitation (DP) method. Different analytical approaches such as XRD, BET, TEM and SEM/EDX were used to characterize the synthesized catalysts. The results showed thatthe prepared nano-NiO/gamma-Al2O3 catalysts had a coated structure with a loading of NiO in catalysts over 12 wt %, and they had also a higher BET surface area over commercial nickel based catalysts. The active components of catalyst were spherical NiO nanoparticles coated on the surface of supports with a size range of 12-18 nm. Furthermore, the activity of the catalysts to remove tar in the process of biomass pyrolysis was also investigated using a bench-scale combined fixed bed reactor. The experiments demonstrated that the tar yield after addition of the catalyst was reduced significantly; the tar removal efficiency reached to 99% for catalytic pyrolysis at 800 degrees C, and the gas yield after addition of the catalyst increased markedly. The compositions of gas products before and after addition of the catalyst in the process also changed significantly. The percentages of CO2 and CH4 in the product gas after addition of the catalysts were obviously reduced, while those of the valuable H2 and CO strongly increased. Therefore, using the prepared NiO/gamma-Al2O3 catalyst in biomass gasification/pyrolysis can significantly improve the quality of the produced gas and meanwhile efficiently eliminate the tar generation.
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PMID:Development of nano-niO/Al2O3 catalyst to be used for tar removal in biomass gasification. 1876 91

Postsynthesis processing of nanoparticles to obtain mesoscale hierarchal nanostructures is the key for the development of nanotechnology and smart composites/coatings from these materials. We have utilized gas-expanded liquid deposition of alkyl-coated gold nanoparticles to study the effects of variable process flowrates, variable flow oscillation and variable interaction potential of the substrate on nanoparticle array quality. Array quality is measured here as completeness of area surface coverage of approximately a monolayer of nanoparticles. Quantitative values for surface coverage are averages obtained from multiple TEM photomicrographs using Image J digital analysis. The process was modified using higher CO2 addition rate outside of the pressure range necessary for deposition, and this modified process produced an excellent film quality while reducing overall processing time by 45%. The effects of pressure oscillation during deposition appeared to anneal the film at the lower flow rates, 0.5 and 1.0 mL/min, but a reduction in area coverage was observed with pressure oscillation at 3.0 mL/min. Pressure oscillation has emerged as a useful tool for researchers to tune the film uniformity and therefore the surface roughness. Calculations based on Hamaker theories for surface-particle interactions on various substrates were performed, and better surface coverage was predicted for C-based surfaces compared to Si3N4 and SiO2 surfaces. Indeed, experimental studies verified this general ordering, indicating that if surface interactions with the particles are strong deposition directly on the surface rather than on pre-existing nanoparticle islands may govern uniform deposition.
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PMID:Gold nanoparticle deposition using CO2 expanded liquids: effect of pressure oscillation and surface-particle interactions. 1882 23


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