Hydrogen Atmosphere (hydrogen + atmosphere)

Distribution by Scientific Domains


Selected Abstracts


Synthesis of NaAlH4 -Based Hydrogen Storage Material Using Milling under Low Pressure Hydrogen Atmosphere.

CHEMINFORM, Issue 21 2007
Nico Eigen
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]


Pd/CaCO3 in Liquid Poly(ethylene glycol) (PEG): An Easy and Efficient Recycle System for Partial Reduction of Alkynes to cis-Olefins under a Hydrogen Atmosphere.

CHEMINFORM, Issue 25 2004
S. Chandrasekhar
Abstract For Abstract see ChemInform Abstract in Full Text. [source]


Application of supercritical fluid extraction to regenerate spent Pd-active carbon catalyst

ENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 4 2007
Lidia D
Abstract Pd-active carbon-type catalysts are used in a wide variety of processes, typical examples of which are liquid-phase hydrogenation reactions. In the case of these catalysts, a loss of their catalytic activity is observed. The aim of the present work was to assess the possibility of regenerating spent Pd/AC catalysts using supercritical fluid extraction. The following Pd/AC catalyst samples were investigated and compared: a commercial 10 wt % Pd catalyst (Aldrich) (denoted by CC), a spent catalyst (SC), SC subjected to supercritical fluid,CO2 extraction (SC/SFE/C), SC subjected to supercritical fluid,CO2,ethanol extraction (SC/SFE/C-Et), and SC subjected to supercritical fluid,ethane,propane extraction (SC/SFE/E-P). The last three catalysts were additionally subjected to heating in a hydrogen atmosphere at 410 K for 3 h. These were denoted by SC/SFE/C/H, SC/SFE/C-Et/H, and SC/SFE/E-P/H, respectively. The spent Pd/AC catalyst (SC) consists of mixed CC samples used in the reduction with hydrogen of various organic compounds. The catalysts CC, SC/SFE/C, SC/SFE/C/H, SC/SFE/C-Et/H, and SC/SFE/E-P/H were tested in the reduction of octanoylbenzene with hydrogen. The activity of the catalysts was estimated by measuring the reaction time and also the amount of hydrogen used in relation to the theoretical quantity required for the reaction. XPS and XRD methods were used to evaluate the changes occurring in the form of the palladium present on the Pd/AC catalyst surface during the regeneration processes. It was found that supercritical fluid-CO2 extraction followed by heating in a hydrogen atmosphere is the most effective method for regenerating that catalyst. The results of our investigations indicate that regeneration of a spent Pd/AC catalyst, irrespective of the reaction in which it has been used, should be based on the complete removal of byproducts, the purification of the catalyst surface, and the restoration of the original form of the palladium. The procedure proposed in this paper, i.e. SFE (CO2) and heating in H2, fulfils both the conditions mentioned above. © 2007 American Institute of Chemical Engineers Environ Prog, 2007 [source]


The effect of overload on the fatigue crack growth behaviour of 304 stainless steel in hydrogen

FATIGUE & FRACTURE OF ENGINEERING MATERIALS AND STRUCTURES, Issue 1 2001
M. H. Kelestemur
Fatigue crack growth (FCG) behaviour and its characteristics following tensile overloads were investigated for AISI 304 stainless steel in three different atmospheres; namely dry argon, moist air and hydrogen. The FCG tests were performed by MTS 810 servohydraulic machine. CT specimens were used for the tests and crack closure measurements were made using an extensometer. FCG rates of 304 stainless steel at both dry argon and moist air atmospheres have shown almost the same behaviour. In other words, the effect of moisture on FCG of this material is very small. However, in a hydrogen atmosphere, the material showed considerably higher crack growth rate in all regimes. In general, for all environments, the initial effect of overloads was to accelerate the FCG rate for a short distance (less than a mm) after which retardation occurred for a considerable amount of time. The main causes for retardation were found as crack blunting and a long reinitiation period for the fatigue crack. Regarding the environmental effect, the overload retardation was lowest in a hydrogen atmosphere. This low degree of retardation was explained by a hydrogen embrittlement mechanism. In a general sense, hydrogen may cause a different crack closure mechanism and hydrogen induced crack closure has come in to the picture. Scanning electron microscope and light microscope examinations agreed well with the above results. [source]


Identification of the effective distribution function for determination of the distributed activation energy models using the maximum likelihood method: Isothermal thermogravimetric data

INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 1 2009
Bojan Jankovi
The new procedure for identification of the effective distribution function for determination of the distributed activation energy models, which is based on use the maximum likelihood method (MLM), was established. The five different continuous probability functions (exponential, logistic, normal, gamma, and Weibull probability functions (the extended set of distributions)) were used for searching the best reactivity model for two heterogeneous processes: (a) the isothermal reduction process of nickel oxide under hydrogen atmosphere and (b) the isothermal degradation process of bisphenol-A polycarbonate (Lexan) under nitrogen atmosphere. The MLM showed that for both processes, the most suitable reactivity model represents the Weibull distribution model. It was concluded that the values of Arrhenius parameters (ln A and Ea), evaluated from the Weibull distribution model, represent the effective kinetic values for both considered processes. This procedure enables identification the suitable distribution model for considered process only from the experimental data (based on the shapes of obtained integral kinetic curves), and this fact represents the advantage of established analysis. The established mathematical procedure, which is based on the MLM, can be applied as the preliminary analysis for evaluating the distribution of activation energies for complex heterogeneous processes. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 41: 27,44, 2009 [source]


Time-resolved polarization-sensitive measurements of the electric field in a sliding discharge by means of dc field-induced coherent Raman scattering

JOURNAL OF RAMAN SPECTROSCOPY, Issue 3 2001
S. N. Tskhai
We investigated the properties of the IR signal generated through coherent Raman scattering involving the Q(1) transition (v = 0, J = 1,v = 1, J = 1) of a hydrogen molecule in the presence of the quasi-static electric field of the sliding discharge propagating along a ferrite surface in a hydrogen atmosphere. The results of time-resolved polarization-sensitive measurements performed on this signal were employed to determine the parameters of the electric field in the sliding discharge. These measurements showed, in particular, that the propagation of the discharge leader along the ferrite surface is accompanied by the rotation of the vector of the quasi-static electric field. Copyright © 2001 John Wiley & Sons, Ltd. [source]


Sintering of Transparent Yttria Ceramics in Oxygen Atmosphere

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2010
Yihua Huang
A novel method is reported for the preparation of transparent polycrystalline yttria ceramics in oxygen atmosphere. Zirconia and other additives were added to control the grain growth. Pores can be eliminated clearly at a temperature <1650°C with the grain size around 1 ,m. The grain growth kinetics and the mechanisms controlling grain growth were studied. Sintering in oxygen atmosphere is beneficial for making samples with a big size at low cost and avoiding the posttreatment of samples sintered in vacuum or hydrogen atmosphere. [source]


Synthesis and Characterization of Magnetic Nanocontainers

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2008
Christos Tapeinos
Magnetic hollow spheres were synthesized through a two-step process and were evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy, super quantum interference device, vibrating sample magnetometry and Mössbauer spectroscopy methods. First, polystyrene spheres (PS) were produced using emulsion polymerization. Second, the PS spheres were coated via the sol,gel method to form an iron oxide layer. The size of the PS spheres was controlled by the concentration of the monomer (styrene), the initiator (potassium persulfate), and the emulsifier (sodium dodecylsulfate). The sol,gel coatings were prepared by controlled hydrolysis of aqueous solutions of FeCl3 in the presence of PS latex, polyvinylpyrrolidone, and hydrochloric acid. The composite was treated in air to burn off the PS latex. Temperature treatments were optimized after extensive differential thermal analysis and thermo gravimetric analysis characterization of the samples. Treatments under hydrogen atmosphere at various temperatures gave control over the formation and extend of magnetic phases in the nanocontainers such as a Fe, hematite (Fe2O3), and magnetite (Fe3O4). The size of the containers ranged between 300 and 400 nm. [source]


Mechanically Stable Monoclinic Zirconia,Nickel Composite

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2002
José S. Moya
A dense (>98% theoretical density), residual-stress-free m-ZrO2/40 vol% nickel composite with K IC, 5.4 MPa·m1/2 and ,f, 225 MPa has been obtained using a simple wet processing route and subsequent sintering at 1430°C in a 90% argon/10% hydrogen atmosphere. The mechanism for release of internal stresses by the composite developed during the t , m transformation on cooling is explained in terms of plastic flow in the infinite nickel cluster formed at the percolation threshold. [source]


Near-infrared spectroscopy of the very low mass companion to the hot DA white dwarf PG 1234+482

MONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, Issue 4 2007
P. R. Steele
ABSTRACT We present a near-infrared spectrum of the hot (Teff, 55 000 K) hydrogen atmosphere (DA) white dwarf PG 1234+482. We confirm that a very low mass companion is responsible for the previously recognized infrared photometric excess. We compare spectra of M and L dwarfs, combined with an appropriate white dwarf model, to the data to constrain the spectral type of the secondary. We find that uncertainties in the Two-Micron All-Sky Survey HK photometry of the white dwarf prevent us from distinguishing whether the secondary is stellar or substellar, and assign a spectral type of L0±1 (M9,L1).Therefore, this is the hottest and youngest (,106 yr) DA white dwarf with a possible brown dwarf companion. [source]


First principles study of the decomposition processes of AlN in a hydrogen atmosphere

PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 9 2008
U. Panyukova
Abstract The growth of AlN films by the hydrogen vapor phase epitaxy method is generally carried out at a high temperature over a hydrogen atmosphere. The difficulties concerned with the decomposition processes on the surface during the film growth result in necessity of computer modelling of that processes. First principles calculations of the decomposition processes of AlN in a hydrogen atmosphere are reported. The mechanism of desorption of atoms from the surface was determined. Al atoms desorb as AlH from (0001) surface and as Al from (000-1) surface of AlN. And N atoms desorb as NH3 from (0001) surface and as NH from (000-1) surface of AlN. The desorption of Al atoms is a rate limiting reaction. The calculation results correspond well with the experimental date published earlier. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


A Mononuclear Cyclopentadiene,Iron Complex Grafted in the Supercages of HY Zeolite: Synthesis, Structure, and Reactivity

CHEMISTRY - A EUROPEAN JOURNAL, Issue 28 2007
Jinlin Long
Abstract The reaction of ferrocene with the acidic hydroxy groups in the supercages of zeolite HY dehydrated at 673,K and the reactivity of the resultant surface species towards CO and O2 were investigated by temperature-programmed decomposition (TPD) and reduction (TPR) and IR, X-ray absorption fine structure analysis (XAFS), and X-ray photoelectron (XP) spectroscopy. In situ FTIR, TPD, TPR, and chemical analysis reveal that the Cp2Fe molecule adsorbed on the zeolite surface loses one cyclopentadienyl group under vacuum at 423,K, which leads to the formation of a well-defined mononuclear surface Fe-C5H6 complex grafted to two acidic sites and one (Si-O-Si) unit, as confirmed by the lack of Fe,Fe contributions in the EXAFS spectra. Each iron atom is coordinated, on average, to three oxygen atoms of the zeolite surface with a FeO distance of 2.00,Å and to five carbon atoms with a FeC distance of 2.09,Å. IR spectra indicate that the cyclopentadiene,iron species grafted on the surface of the zeolite is quite stable in vacuo or under an inert or hydrogen atmosphere below 423,K, and is also relatively stable under oxygen at room temperature. However, the cyclopentadiene ligand readily reacts with CO to form a compound containing carbonyl at 323,K, and even at room temperature. The single carbonyl band in the IR spectra provides evidence for the nearly uniform formation of a cyclopentadiene,iron species on the surface of the zeolite. [source]