Effect of the electron energy distribution on the measurement of the atom concentration by optical actinometry

The oxygen and hydrogen atom concentrations in the hollow cathode discharge with water vapor additives are determined using small argon and xenon additives as optical actinometers. The problem of the rejection of measurements of the electron plasma component parameters is discussed.     

A review of catalyst-enhanced magnesium hydride as a hydrogen storage material

Magnesium hydride remains an attractive hydrogen storage material due to the high hydrogen capacity and low cost of production. A high activation energy and poor kinetics at practical temperatures for the pure material have driven research into different additives to improve the sorption properties. This review details the development of catalytic additives and their effect on the activation energy, kinetics and thermodynamic properties of magnesium hydride.     

Burning velocity of methane-hydrogen mixtures at elevated pressures and temperatures

The effect of the initial pressure, temperature, and equivalence ratio on a number of combustion characteristics of methane-air mixtures with hydrogen additives in a closed vessel is experimentally studied. Experiments are conducted at 1, 5, and 10 atm and temperatures from 22 to 300°C. The hydrogen content in the fuel is 0, 10, and 20 vol %. The fuel equivalence ratio varies from 0.6 to 1.0. The limitations imposed by buoyancy on measurements of the laminar burning velocity by the constant-volume bomb method with recording of pressure-time histories are analyzed. It is shown that the laminar burning velocity can be appreciably increased by adding no less than 20 vol % of hydrogen to the fuel.     

周期自洽的充氢溴化亚铜激光动力学模型

建立了一个比较完整的、周性性自洽的充氢溴化亚铜激光动力学模型,获得了激光工作物质粒子数、激光光强、电子温度、电子密度等一系列参量的时空分布与变化,并与实验值作了比较. 关键词：     

Effects of additives on hydrogen absorption and desorption characteristics of Nd(Fe,Mo)12 alloys

Effects of such additives as Co, Zr, Nb or Ga on hydrogen absorption and desorption characteristics of Nd(Fe,Mo)₁₂ alloys are investigated. It is found that Zr or Nb addition increases the disproportionation temperature of Nd(Fe,Mo)₁₂ alloys, and Co or Ga addition decreases the recombined temperature of its disproportionated products. This shows that Zr or Nb addition retards the disproportionation, while Co or Ga addition is effective for improving the recombination, which is similar to the effects of the additives on the hydrogen absorption and desorption characteristics of Nd₂Fe₁₄B alloys. However, according to X-ray diffraction (XRD) investigations for the magnetic-oriented samples, the final hydrogenation disproportiontation desorption recombination (HDDR) NdFe_10.5−XM_XMo_1.5 (M=Co, Zr, Nb or Ga) products are isotropic. The effects of additives on hydrogen absorption and desorption characteristics of Nd₂Fe₁₄B and Nd(Fe,Mo)₁₂ alloys are very similar, but the magnetic anisotropy of the final two HDDR products are different. In order to investigate this, similarities and differences of the two alloy systems and their corresponding HDDR phenomena are further studied. The results show that the formation of anisotropic powders may be related to the disproportionated products and crystal growth direction of the Nd₂Fe₁₄B and Nd(Fe,Mo)₁₂ system.     

Hydrogen dissociation on oxide covered MgH2 by catalytically active vacancies

MgH₂ is an important ingredient in modern reactive hydride composites to be used as hydrogen storage materials. The surface composition and chemical state of ball-milled MgH₂ is studied during hydrogen desorption by means of X-ray photoelectron spectroscopy. Simultaneously, the desorption rate of hydrogen is monitored, which is compared to dissociative properties of the surface investigated by hydrogen-deuterium exchange experiments. It is found that MgH₂ is also oxide covered during desorption demonstrating that MgO is able to recombine atomic hydrogen. The corresponding catalytic sites are associated with low coordinated surface vacancies on the oxide. The maximum surface concentration of these vacancies is very small, which is countered by a very high turnover frequency due to a small activation energy for dissociation of hydrogen of 0.1 eV on the single vacancy. The study provides insight into the catalytic role played by the oxide additives in MgH₂, which are superior catalysts for hydrogen sorption even when compared to 3d-metals.     

Dehydrogenation kinetics and reversibility of LiAlH4–LiBH4 doped with Ti-based additives and MWCNT

Dehydrogenation kinetics and reversibility of LiAlH₄–LiBH₄ doped with Ti-based additives (TiCl₃ and Ti-isopropoxide), multiwall carbon nanotubes (MWCNT), and MWCNT impregnated with Ti-based additives are proposed. Reduction of dehydrogenation temperature as well as improvements of kinetics and reversibility, especially decomposition of thermodynamically stable hydride (LiBH₄) is obtained from the samples doped with Ti-isopropoxide and MWCNT. This can be due to the fact that the formations of Li_xAl_(1−x)B₂ and LiH-Al containing phase during dehydrogenation favor decomposition of LiH, leading to increment of hydrogen capacity, and stabilization of boron in solid state, resulting in improvement of reversibility. Besides, the curvatures and thermal conductivity of MWCNT benefit hydrogen diffusion and heat transfer during de/rehydrogenation. Nevertheless, deficient hydrogen content reversible is observed in all samples due to the irreversible of LiAlH₄ and/or Li₃AlH₆ as well as the formation of stable phase (Li₂B₁₂H₁₂) during de/rehydrogenation.     

Modeling the plasma kinetics mechanisms of CuBr laser with neon–hydrogen additives

A mathematical model describing the discharge kinetics and lasing characteristics of copper bromide vapor laser with neon and hydrogen additives has been developed. The suggested model is based on a “zero-dimensional” model and offers simple mechanisms to explain discharge kinetics mechanisms, different physical processes and hydrogen additive effects on the copper bromide vapor laser.The model estimates the temporal evolution of discharge voltage and current, population densities, laser beam density, electron temperature and radial distribution of pressure and buffer gas temperature. The suggested mechanism assumes that the electron detachment from negative hydrogen ions does not contribute to the copper ionization process.Numerical solutions of a nonlinear rate equation system predict the generation of nanosecond pulses. The calculated maximum values of discharge voltage, current, average output laser power, electron temperature, etc. are in good agreement with other reported calculated and experimental data.     

Enhancement of sonochemical degradation of phenol using hydrogen atom scavengers

Sonochemical degradation of phenol was found to be enhanced in the presence of the volatile hydrogen atom scavengers CCl4 and perfluorohexane. The non-volatile hydrogen atom scavenger iodate did not enhance phenol degradation. The first order rate constant for aqueous phenol degradation in separate experiments using different sonochemical probes increased in the presence of 150 microM CCl4 from 0.014 to 0.031 min(-1) (probe 1) and from 0.022 to 0.061 min(-1) (probe 2). In the presence of <1.5 microM C6H14, the first order rate constant increased from 0.014 to 0.032 min(-1) (probe 1). Hydroquinone was the major observed reaction intermediate both in the presence and absence of hydrogen atom scavengers. Hydroquinone yields were substantially higher in the presence of hydrogen atom scavengers, suggesting that hydroxyl radical pathways for phenol degradation were enhanced by the hydrogen atom scavengers. These additives may be useful in improving pollutant degradation efficiency or improving synthetic processes that rely on hydroxyl radical as a key intermediate.     

Review on the roles of carbon materials in lead-carbon batteries

Lead-acid battery (LAB) has been in widespread use for many years due to its mature technology, abound raw materials, low cost, high safety, and high efficiency of recycling. However, the irreversible sulfation in the negative electrode becomes one of the key issues for its further development and application. Lead-carbon battery (LCB) is evolved from LAB by adding different kinds of carbon materials in the negative electrode, and it has effectively suppressed the problem of negative irreversible sulfation of traditional LAB. Different carbon materials play different roles in LCB, including construction of conductive network, double-layer capacitance storage effect, formation of porous structure and steric effect. Moreover, research on composite material additives (such as Pb-C composite materials and polymer-C composite materials) and Pb-C composite electrode have become a research focus in the past few years; it has been another effective way to improve the performance of the negative electrode. On the other hand, due to the relatively low overpotential of carbon materials, the hydrogen evolution reaction (HER) will be aggravated in LCB, which affects its electrochemical performance. It is necessary to modify carbon additives or add other additives to inhibit the HER. This paper will attempt to summarize the roles of carbon additives in the negative electrode made by previous research and illustrate the effect of composite material additives and Pb-C composite electrode on the negative electrode. Moreover, we will also sum up the method for solving the HER by reviewing previous research.     

Fumes generated during laser processing of polyvinyl chloride (PVC)

An approach to the assessment of fumes produced in laser material processing is presented. The subsequent design of the fume containment system and sampling strategy is detailed. Polyvinyl chloride (PVC) has been selected for investigation and the complexity resulting from the plethora of additives is discussed. Qualitative results from the preliminary studies of CO₂ laser cutting of PVC are presented together with an appraisal of the problems involved in extending this to quantitative analysis. Benzene, hydrogen chloride (HCl) and methyl methacrylate were found to be the dominant emissions.     

Formation of noble metal particles by ultrasonic irradiation

It was found that sonochemically prepared metal particles such as Ag, Pd, Au, Pt and Rh are of nanometer size with a fairly narrow distribution (e.g., about 5 nm for Pd particles obtained from a 1.0 mM Pd(II) in polyethylene glycol monostearate solution). We have suggested three different reduction pathways under sonication: (i) reduction by H atoms, (ii) reduction by secondary reducing radicals formed by hydrogen abstraction from organic additives with OH radicals and H atoms, (iii) reduction by radicals formed from pyrolysis of the additives at the interfacial region between cavitation bubbles and the bulk solution. The reduction of Ag(I) and Pt(II) mainly proceeds through reaction pathway (ii). In the cases of Pd(II) and Au(III), the reductions mainly proceed through reaction pathway (iii). The reduction of Rh(III) was not achieved under the same conditions; however, by the addition of sodium formate, reduction occurred and the preparation of Rh particles succeeded.     

Quantum chemical study of the ground-state alcoholic complexation of selected dual luminescent compounds

The ground- and excited-state features of dual luminescent molecules are strongly influenced by the presence of alcoholic additives. Selected ground-state properties of methanol and 1,1,1,3,3,3-hexafluoro-propan-2-ol complexes of 4-aminobenzonitrile, 4-aminopyridine and aniline derivatives were obtained by quantum chemical calculations. The formation enthalpies of the complexes are the most exothermic when the cyano or ring nitrogen interacts with the hydroxyl group of the alcohols. The binding energies are almost doubled when the fluorinated reactant is the hydrogen bond donor. Parallel to the enhancement of the stabilization of the complex, the ground-state dipole moment also increases notably with complex formation. In principle, consideration of this increase is essential in interpretation of the solvatochromatic behaviour of the complexed species.     

Electrochemical performance of lead acid battery using ammonium hydrogen sulphate with different alkyl groups

In this work, the application of ionic liquids (ILs)??mono-, bicycyclohexyl, monohexyl and tetrahexyl ammonium hydrogen sulphate??as electrolyte additives on the electrochemical performance of lead acid batteries is proposed. The electrochemical behaviour of Pb?C1.66% Sb?C0.24% Sn alloy in sulphuric acid solution is investigated in the presence of the mentioned ILs with different numbers of alkyl or cycloalkyl chains. Particularly, the hydrogen and oxygen evolution potential and anodic layer characteristics were studied using cyclic and linear sweep voltammetric methods. The obtained results indicate that hydrogen evolution overpotential of Pb/Sb/Sn alloy in the presence of ILs increases. This overpotential mainly depends on the concentration of ILs and the number of alkyl and cycloalkyl chains on the cations. Also, the difference between the oxygen oxidation potential in anodic and cathodic scans (?E) decreases using different ILs.     

The kinetics of methane ignition in fuel-rich HCCI engines: DME replacement by ozone

Fuel-rich combustion of methane in a homogeneous-charge compression-ignition (HCCI) engine can be used as a polygeneration process producing work, heat, and useful chemicals like syngas. Due to the inertness of methane, additives such as dimethyl ether (DME) are needed to achieve ignition at moderate inlet temperatures and to control combustion phasing. Because significant concentrations of DME are then needed, a considerable part of the fuel energy comes from DME. An alternative ignition promotor known from fuel-lean HCCI is ozone (O₃). Here, a combined experimental and modelling study on the ignition of fuel-rich partial oxidation of methane/air mixtures at Φ = 1.9 with ozone and DME as additives in an HCCI engine is conducted. Experimental results show that ozone is a suitable additive for fuel-rich HCCI, with only 75 ppm ozone reducing the fuel-fraction of DME needed from 11.0% to 5.3%. Since ozone does not survive until the end of the compression stroke, the reaction paths are analyzed in a single-zone model. The simulation shows that different ignition precursors or buffer molecules are formed, depending on the additives. If only DME is added, hydrogen peroxide (H₂O₂) and formaldehyde (CH₂O) are the most important intermediates, leading to OH formation and ignition around top dead center (TDC). With ozone addition, methyl hydroperoxide (CH₃OOH) becomes very important earlier in the compression stroke under these fuel-rich conditions. It is then later converted to CH₂O and H₂O₂. Thus, ozone is a very effective additive not only for fuel-lean, but also for fuel-rich combustion. However, the mechanism differs between both regimes. Because less of the expensive additives are needed, ozone could help improving the economics of a polygeneration process with fuel-rich operated HCCI engines.     

Pulsed barium vapor laser with hydrogen additive and interactive circuit

A small-size discharge heated barium vapor laser with an axial temperature controller was designed and made. The operational characteristics of the laser with different hydrogen additives and two excitation circuits were experimentally investigated and compared. The results indicate that the addition of a small ratio (1.5%) of hydrogen to neon and the interactive circuit (IC) can greatly increase the laser output power. The maximum average laser power of 3.5 watts and a record specific power of 117.3 mW/cm³ at a 1.5 μm wavelength were obtained under optimal discharge conditions. Some possible mechanisms were suggested to explain the enhanced effect of the hydrogen additive and IC to the laser output performances. PACS 42.55.Lt; 42.60.Lh; 52.80.Tn     

High spatial intensity 10 W-CuBr laser with hydrogen additives

High beam quality output has been demonstrated from a single medium-scale (2 cm dia. × 50 cm) CuBr laser with hydrogen additives. The addition of hydrogen leads to beam divergence reduction and laser power lift-up finally yielding 5-fold increase in laser power spatial intensity compared with the case of no hydrogen added. With a simple positive-branch unstable resonator practical (pulse-average) divergence of 80 rad is achieved. The easy-feasible sealed-off version of CuBr laser makes it an attractive source for many high-quality laser beam applications.     

Mechanically alloyed metal hydride systems

Mechanosynthesis of metal hydrides is a new field in which important progress has been reported. In this paper, we present recent developments in mechanosynthesis of magnesium-based hydrides for storage applications. The effect of intense milling on magnesium and magnesium hydrides is presented. The influence of various additives on hydrogen-sorption properties is discussed with special emphasis on nanocomposite MgH₂+5 at. % V, where hydrogen-storage characteristics, cycling properties and the mechanism of hydrogen desorption are presented. The production of novel nanocrystalline porous structures by mechanical alloying followed by a leaching technique is discussed. Hot ball-milling, as a new method for rapid synthesis of alloys, is also presented. Finally, two other methods of production of metal hydrides are discussed. One is reactive milling where metal hydrides are synthesized by mechanical alloying under hydrogen pressure, while the other is milling elemental hydrides to produce complex hydrides. Received: 15 August 2000 / Accepted: 6 November 2000 / Published online: 9 February 2001     

Effect of addition of a non-equidiffusional reactant to an equidiffusional diffusion flame

A Burke–Schumann (flame-sheet) formulation is developed for diffusion flames between a fuel and oxidiser with Lewis numbers of unity, subject to addition to the fuel and/or oxidiser stream of a different reactant for which the Lewis number differs from unity. This formulation is applied to laminar counterflow diffusion-flame experiments, reported here, in which hydrogen was added to either methane–nitrogen mixtures or oxygen–nitrogen mixtures at normal atmospheric pressure, with both feed streams at normal room temperature. Experimental conditions were adjusted to fix selected values of the stoichiometric mixture fraction and the adiabatic flame temperature, and the strain rate was increased gradually, maintaining the momentum balance of the two streams, until extinction occurred. At the selected sets of values, the strain rate at extinction was measured as a function of the hydrogen concentration in the fuel or oxidiser stream. The ratio of the fraction of the oxidiser flux that consumes hydrogen to the fraction that consumes fuel was calculated from the new Burke–Schumann formulation, and it was found that, within experimental uncertainty, the ratio of the extinction strain rate with hydrogen addition to that without was the same at any given value of this oxygen flux ratio, irrespective of whether the hydrogen was added on the fuel or oxidiser side. This experimental result was also in close agreement with computational predictions employing detailed chemistry. These results imply that differences in detailed hydrogen concentration profiles within the reaction zone have little or no influence on the chemical kinetics of extinction when the stoichiometric mixture fraction, the adiabatic flame temperature, and the proportion of oxygen that consumes the added fuel are fixed. This same correspondence may be expected to apply for other fuels and additives.     

An updated overview of diamond-like carbon coating in tribology

During the last two decades, the industry (including scientists) has focused on diamond-like carbon (DLC) coating because of its wide range of application in various fields. This material has numerous applications in mechanical, electrical, tribological, biomedical, and optical fields. Severe friction and wear in some machine parts consumes high amount of energy, which makes the process energy inefficient. Thus, DLC coating can be an effective means to lower the friction and wear rate. Some important process variables that affect the tribological characteristics of DLC coating are adhesion promoter intermediate layer, substrate surface roughness, hydrogen incorporation or hydrogen non involvement, and coating deposition parameters (e.g., bias voltage, etching, current, precursor gas, time, and substrate temperature). Working condition of DLC-coated parts also affects the tribological characteristics, such as temperature, sliding speed and load, relative humidity, counter surface, and lubrication media (DLC additive interaction). Different types of lubricated oils and additives are used in engine parts to minimize friction and wear. DLC can be coated to the respective engine parts; however, DLC does not behave accordingly after coating because of lubricant oil and additive interaction with DLC. Some additive interacts positively and some behave negatively because of the tribochemical reactions between DLC coating and additives. Numerous conflicting views have been presented by several researchers regarding this coating additive interaction, resulting in unclear determination of true mechanism of such interaction. However, lubricant additive has been established to be more inert to DLC coating compared with uncoated metal surface because the additive is fabricated in such a way that it can react with metal surfaces. In this article, the tribological characteristics of different types of DLC coating in dry and lubricated conditions will be presented, and their behavior will be discussed in relation to working condition and processing parameters.