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Biomedical subjects

J B Nagy

Publications and source records attributed to J B Nagy.

11 recordsLinked to original sources
PubMed2006

Mechanism of formation of inorganic and organic nanoparticles from microemulsions.

This chapter essentially deals with the preparation of nanoparticles using microemulsions. The preparation of inorganic nanoparticles--Ni2B, Pt, Au, Pt-Au, AgX--and the synthesis of organic nanoparticles--cholesterol, rhovanil, rhodiarome--are systematically studied as a function of the concentration of the precursor molecules, the size of the inner water cores, and the manner of mixing the various solutions. Two different behaviors are observed in the various systems. The first case shows a dependence of the nanoparticle size on the various physicochemical parameters. Either a monotonous increase of the size or the presence of a minimum is observed as a function of the concentration of the precursor molecules. This case can be easily explained following the LaMer diagram, where the nucleation of the nanoparticles is separated from the particle growth. The second case does not show any dependence of the nanoparticle size on the physicochemical parameters. The size remains constant in all experimental conditions. The constant character of the size can be explained only by thermodynamic stabilization, where particles with a certain size are better stabilized. It should be emphasized that the size distribution is small in all the cases studied. Finally, the aging of the nanoparticles was also checked, especially for the organic nanoparticles. It is concluded that these particles remain stable for months in the microemulsion.

Journal Article↗
PubMed2006

Dispersion of carbon nanotubes using organic solvents.

Phenyl ethyl alcohol was used for fast and stable dispersion of carbon nanotubes. This solvent, more effective than ethanol and toluene, allows easy dispersion of carbon nanotubes for TEM characterization. For TEM grids prepared at high dilution, it is possible to observe each tube separately. Applying that solvent, it was possible to measure the length, the diameter and the solubility of different carbon nanotubes samples.

Colloids↗
PubMed2005

129Xe NMR study of Xe adsorption on multiwall carbon nanotubes.

129Xe NMR spectroscopy has been used to study the adsorption of Xe on multi-wall carbon nanotubes (MWCNT). The results obtained have shown the 129Xe NMR ability to probe the intercrystalline (aggregate) and the inner porosity of CNT. In particular, the effects on porosity of tubes openings by hydrogen exposure and of ball milling were examined. Dramatic changes observed in the 129Xe NMR spectra after moderate ball milling of MWCNTs were attributed to the destruction of the initial intercrystalline pore structure and to the Xe access inside the nanotubes. To examine the exchange dynamics the mixture of as-made and milled MWCNTs was studied with one- and two-dimensional (1D and 2D) 129Xe NMR. The exchange between the interior of milled nanotubes and the aggregate pores of as-made MWCNTs was fast on the NMR acquisition time scale. The Xenon exchange between the interior of the as-made MWCNTs and the large aggregate pores occurred on a longer time scale of 10 ms, as was established by 2D 129Xe NMR exchange spectroscopy. Variable temperature 129Xe NMR data were also discussed and analyzed in terms of the fast exchange approximation.

Journal Article↗
PubMed2004

On the growth mechanism of single-walled carbon nanotubes by catalytic carbon vapor deposition on supported metal catalysts.

A comprehensive kinetic study was performed to throw light on the formation mechanism of single walled carbon nanotubes (SWNTs) in chemical vapor deposition processes. SWNTs were synthesized by catalytic decomposition of methane or ethylene on supported transition metal catalysts. Kinetic curves (the amount of SWNT as a function of time) were obtained as a function of the nature and the preparation of the supported catalysts, temperature, the fluxes of the gases (the reagent hydrocarbon and the carrying gas), and the partial pressure of the hydrocarbon. The final products were characterized by transmission electron microscopy, Raman spectroscopy, chemical analysis, and thermogravimetric measurements. The fundamental factors determining the SWNT formation are discussed in detail, taking into consideration several observations from the literature as well.

Carbon↗
PubMed2004

Hydrocarbon decomposition in alumina membrane: an effective way to produce carbon nanotubes bundles.

Carbon nanotubes were synthesised within the pores of an alumina membrane. The membrane had 200 nm diameter pores and 60 microm thickness, and ethylene was used as carbon source. Membrane dissolution by HF results in a bundle of parallel open tubes, aligned without macroscopic defects. The external diameter of the tubes is uniform and there is no evidence of any amorphous carbon. Wall thickness control was obtained by varying the reaction time, length by the thickness of alumina membrane, and external tube diameter by the membrane pore size. Scanning (SEM) and transmission (TEM) electron microscopy, atomic force microscopy (AFM), X-ray diffraction, thermogravimetric analysis (TG) and surface area evaluation by nitrogen adsorption were used for the characterization of membrane and nanotubes.

Adsorption↗
PubMed2000

Continuous-flow optical pumping NMR in a closed circuit system.

In a typical continuous-flow optical pumping setup, the chemical shift of xenon in the adsorbed phase depends on the gas flow rate due to warming of the sample surface by the gas stream. Calibration of the system using the (207)Pb resonance of solid lead nitrate is necessary to determine the actual sample temperature. Optimum pulse repetition rates are strongly affected by gas flow and spin-lattice relaxation rates. The interplay of flow and pulse repetition rate alters signal intensity ratios and may lead to the complete suppression of signals.

Lead↗
PubMed1995

Spin relaxation studies of pyrene by 13C nuclear magnetic resonance spectroscopy.

The effect of the repetition and contact times on the intensity of the magic-angle spinning (MAS) spectra of pyrene has been studied. Pyrene, like a great number of fused polyaromatic compounds, has a very large 13C longitudinal relaxation time (T1Z). When using the cross-polarization (CP) MAS technique, the optimum repetition time is 800 s. The simulation of the central line of the pyrene CP-MAS spectra allowed us to determine the chemical shift of each carbon in the solid state. As the T1Z (13C of the total spectrum) of pyrene was observed to be 1780 s, attempts have been made to relax it by the addition of chromium(III) acetylacetonate or by supporting it on a carrier of gamma-Al2O3: the mixing of chromium(III) acetylacetonate to pyrene by solid mixing, or solution mixing followed by evaporation of the solvent, has no effect on its relaxation time; the Haldor Topsøe TK551 catalyst, a gamma-alumina supported Ni-Mo-P catalyst, has been found to be a very efficient spin relaxation agent for the products adsorbed on it. For example, at 25 degrees C, the 10 wt.-% pyrene-TK551 catalyst is 3 x 10(4) times more relaxed than pure pyrene.

Adsorption↗
PubMed1980

A multifaceted approach to the study of the side-chain conformation in beta-lactamase-resistant penicillins.

The resistance of some penicillins to beta-lactamase enzymes was previously attributed to the nature of their C(6) side chain. In order to find explicitly the influence of the conformation of this side chain in the enzymatic mechanism, we have analyzed by experimental and theoretical methods (X-ray diffraction, NMR, IR, PCILO) the molecular structure of six resistant penicillins and derivatives: oxacillin, cloxacillin, dicloxacillin, flucloxacillin, methicillin, nafcillin, cloxacillin sulfoxide, and oxacillinpenicilloic acid. X-ray crystallography of flucloxacillin and nafcillin is fully described. We observe that the side chains of these penicillins have no influence on the electronic properties of the penam nucleus but are much more rigid than in the sensitive ones. The molecular conformations are mostly governed by the nonbonded Van der Waals interactions and, in the oxacillins, partly by the conjugation between exocyclic groups. The lack of flexibility could result in a distorting effect on the structure of the active site of the beta-lactamase, leading to the deactivation of the enzyme.

Chemical Phenomena↗
PubMedDate not supplied

Synthesis of monodisperse nimesulide nanoparticles in microemulsions E170/isopropyl myristate/water/n-butanol (or isopropanol).

Nanoparticles of nimesulide have been synthesized in two systems of microemulsion: E170/isopropyl myristate/water/n-butanol (or isopropanol). Nanoparticles are monodisperse. In the two microemulsions, the size of the nanoparticles is comprised between 45 and 60 A and also seems to be independent of the factor R ([water]/[E170]) and of the concentration of the nimesulide solubilized in chloroform. The constancy of the size suggests that the size is controlled by thermodynamic stabilization of the nanoparticles with the surfactant. The nature of the cosurfactant does not have an obvious influence on the nanoparticle size. The nanoparticles are instantaneously formed and stay stable during a long period of time (several months).

2-Propanol↗