Ignition of a combustible gas mixture by a high-current electric discharge in a closed volume

Results are presented from experimental studies and numerical calculations of the ignition of a stoichiometric CH₄: O₂ gas mixture by a high-current gliding discharge. It is shown that this type of discharge generates an axially propagating thermal wave (precursor) that penetrates into the gas medium and leads to fast gas heating. This process is followed by an almost simultaneous ignition of the gas mixture over the entire reactor volume.     

Ignition of a combustible gas mixture by a laser spark excited in the reactor volume

Ignition of a stoichiometric CH₄: O₂ mixture by a laser spark excited in the reactor volume is studied experimentally. It is found that the spark initiates a feebly radiating incomplete-combustion wave, which is much faster than the combustion wave, but is substantially slower than the detonation wave. With a time delay of 500–700 μs, a bright optical flash occupying the entire chamber volume is observed, which indicates fast (involving branching chain reactions) ignition of the gas mixture. A conclusion is drawn regarding the common nature of the process of ignition of a combustible gas mixture by a laser spark excited in the reactor volume and the previously investigated initiation of combustion by laser sparks excited at solid targets, high-power microwave discharges, and high-current gliding discharges.     

Long-lived plasmoids as initiators of combustion of gas mixtures

A slipping surface discharge excited along a multielectrode metal-dielectric system in a chemically active (combustible) CH₄-O₂ mixture has been studied experimentally. Results obtained with the help of high-speed hotography, shadowgraphy, optical spectroscopy, and piezoelectric measurements are presented. It is hown that the slipping surface discharge is a source of high-temperature, thermally equilibrium metal plasmoids hose lifetime is much longer than the plasma recombination time (long-lived plasmoids). The experimental investigation of the evolution of plasmoids introduced into a combustible gaseous medium allows one to conclude that the medium significantly increases the lifetime of plasmoids and that plasmoids, in turn, play an important role in the initiation of gas-mixture combustion.     

Nonsputtering impulse magnetron discharge

Experiments with quasi-steady high-current discharges in crossed E × B fields in various gases (Ar, N₂, H₂, and SF₆) and gas mixtures (Ar/SF₆ and Ar/O₂) at pressures from 10⁻³ to 5 Torr in discharge systems with different configurations of electric and magnetic fields revealed a specific type of stable low-voltage discharge that does not transform into an arc. This type of discharge came to be known as a high-current diffuse discharge and, later, a nonsputtering impulse magnetron discharge. This paper presents results from experimental studies of the plasma parameters (the electron temperature, the plasma density, and the temperature of ions and atoms of the plasma-forming gas) of a high-current low-pressure diffuse discharge in crossed E × B fields.     

Effect of a pulsed high-current discharge on hydrogen-air mixtures

A self-consistent model describing the influence of a pulsed discharge on H₂-air mixtures is developed. The model includes the processes of ionization, dissociation, and excitation of the gas molecules by electron impacts; a set of ion-molecular reactions determining the time evolution of the charged particle densities; the processes involving electronically excited atoms and molecules; and a set of reactions describing the ignition of hydrogen-oxygen mixtures. Results are presented from simulations of the oxidation dynamics of hydrogen molecules in a stoichiometric H₂-air mixture and the ignition of such a mixture under the action of a pulsed high-current discharge. The simulation results are compared with available experimental data and calculations performed by other authors.     

Scanning calorimetry measurements of the gas temperature in an RF-discharge fluorine-containing plasma

The neutral-gas temperature in a low-pressure (50 Pa) capacitive RF discharge in a CF₄+O₂ mixture is determined from the heating kinetics of a gallium arsenide single crystal, which is chemically inert to any radicals in a fluorine-containing plasma. Experimental methods are discussed that make it possible to confirm the absence of heat sources capable of additional heating of the calorimeter in the discharge. The features and applicability limits of the method of non-steady-state gas thermometry in a weakly ionized nonequilibrium plasma are discussed. The method proposed is compared with conventional steady-state methods based on measurements of the established temperature of a thermal probe in the discharge. Temperature scanning makes it possible to study dependences that cannot be investigated by steady-state methods, in particular, the temperature dependence of the calorimeter heating power, which is very important for diagnosing the processes of plasma-surface heat transfer.     

Dynamics of dissolved O2, CO2, CH4, and N2O in a tropical coastal swamp in southern Thailand

We studied the distribution of dissolved O₂, CO₂, CH₄, and N₂O in a coastal swamp system in Thailand with the goal to characterize the dynamics of these gases within the system. The gas concentrations varied spatially and seasonally in both surface and ground waters. The entire system was a strong sourcefor CO₂ and CH₄, and a possible sink for atmospheric N₂O. Seasonal variation in precipitation primarily regulated the redox conditions in the system. However, distributions of CO₂, CH₄, and N₂O in the river that received swamp waters were not always in agreement with redox conditions indicated by dissolvedO₂ concentrations. Sulfate production through pyriteoxidation occurred in the swamp with thin peat layerunder aerobic conditions and was reflected by elevatedSO ₄ ^2– /Cl^– in the river water. When SO ₄ ^2– /Cl^– was high, CO₂ and CH₄ concentrations decreased, whereas the N₂O concentration increased. The excess SO ₄ ^2– in the river water was thus identified as a potential indicator for gas dynamics in this coastal swamp system.     

Long-lived plasmoids generated by surface microwave discharges in chemically active gases

The generation of long-lived microplasmoids is observed during the irradiation of a metal-dielectric surface with a high-power microwave beam in a chemically active gas mixture (H₂ + O₂; CH₄ + O₂). The lifetime of these plasmoids substantially exceeds the characteristic recombination and cooling times of plasmoids arising at the target surface in a chemically inactive medium.     

Kinetics of the reactions involving CF2 and CF in a pure tetrafluoromethane plasma: II. Production and loss of CF2 and CF in the processes of fluorocarbon polymerization

Mechanisms for the production and loss of CF₂ and CF radicals in a glow discharge in pure CF₄ are investigated by the time-resolved laser-induced fluorescence method. The fluorocarbon polymerization processes are shown to contribute significantly to the production of radicals both in the plasma volume and on the surface of the discharge tube. The effective frequencies of both the volume and surface processes of radical production and loss are determined. An analysis of these frequencies allowed us to study the polymerization mechanism in a CF₄ plasma at a high relative concentration of F atoms and low ion energy. It is shown that, at elevated pressures, when the density of C_xF_y polymer particles in the plasma volume becomes comparable with the density of simple fluorocarbon radicals, the electron-impact dissociation of these particles is the main channel for the production of CF₂ and CF radicals. Another source of CF₂ and CF radicals is related to the reactions of C_nF_2m+1 unsaturated fluorocarbon particles both in the plasma volume and on the surface of a fluorocarbon film arising on the discharge tube wall. The C_xF_y fluorocarbon polymer particles form both in the discharge volume and on the fluorocarbon filmsurface also in the course of the film destruction. At lowered pressures, the main channel for the production of CF₂ and CF is the direct electron-impact dissociation of CF₄ molecules, whereas the loss of these radicals at the tube wall is the main loss channel. The probabilities of the heterogeneous losses of CF₂ and CF radicals on the heavily fluorinated surface of the fluorocarbon film at low ion energies are determined. Under these conditions, the surface recombination of the Fch chemisorbed fluorine atoms and CF _x ^ph physisorbed radicals with the production of an activated complex is shown to be the most probable mechanism for the heterogeneous losses of CF₂ and CF. The approximate activation energies for the production of F_ch · CF ₂ ^ph and F_ch · CF^ph surface complexes are found to be 750±70 K and 1030±100 K, respectively.     

Decomposition of toluene in a steady-state atmospheric-pressure glow discharge

Results are presented from experimental studies of decomposition of toluene (C₆H₅CH₃) in a polluted air flow by means of a steady-state atmospheric pressure glow discharge at different water vapor contents in the working gas. The experimental results on the degree of C₆H₅CH₃ removal are compared with the results of computer simulations conducted in the framework of the developed kinetic model of plasma chemical decomposition of toluene in the N₂: O₂: H₂O gas mixture. A substantial influence of the gas flow humidity on toluene decomposition in the atmospheric pressure glow discharge is demonstrated. The main mechanisms of the influence of humidity on C₆H₅CH₃ decomposition are determined. The existence of two stages in the process of toluene removal, which differ in their duration and the intensity of plasma chemical decomposition of C₆H₅CH₃ is established. Based on the results of computer simulations, the composition of the products of plasma chemical reactions at the output of the reactor is analyzed as a function of the specific energy deposition and gas flow humidity. The existence of a catalytic cycle in which hydroxyl radical OH acts a catalyst and which substantially accelerates the recombination of oxygen atoms and suppression of ozone generation when the plasma-forming gas contains water vapor is established.     

Simulation of the ignition of a methane-air mixture by a high-voltage nanosecond discharge

The ignition dynamics of a CH₄: O₂: N₂: Ar = 1: 4: 15: 80 mixture by a high-voltage nanosecond discharge is simulated numerically with allowance for experimental data on the dynamics of the discharge current and discharge electric field. The calculated induction time agrees well with experimental data. It is shown that active particles produced in the discharge at a relatively low deposited energy can reduce the induction time by two orders of magnitude. Comparison of simulation results for mixtures with and without nitrogen shows that addition of nitrogen to the mixture leads to a decrease in the average electron energy in the discharge and gives rise to new mechanisms for accumulation of oxygen atoms due to the excitation of nitrogen electronic states and their subsequent quenching in collisions with oxygen molecules. Acceleration of the discharge-initiated ignition is caused by a faster initiation of chain reactions due to the production of active particles, first of all oxygen atoms, in the discharge.     

Circadian methane oxidation in the root zone of rice plants

In the root zone of rice plants aerobic methanotrophic bacteria catalyze the oxidation of CH₄ to CO₂, thereby reducing CH₄ emissions from paddy soils to the atmosphere. However, methods for in situ quantification of microbial processes in paddy soils are scarce. Here we adapted the push–pull tracer-test (PPT) method to quantify CH₄ oxidation in the root zone of potted rice plants. During a PPT, a test solution containing CH₄ ± O₂ as reactant(s), Cl^? and Ar as nonreactive tracers, and BES as an inhibitor of CH₄ production was injected into the root zone at different times throughout the circadian cycle (daytime, early nighttime, late nighttime). After a 2-h incubation phase, the test solution/pore-water mixture was extracted from the same location and rates of CH₄ oxidation were calculated from the ratio of measured reactant and nonreactive tracer concentrations. In separate rice pots, O₂ concentrations in the vicinity of rice roots were measured throughout the circadian cycle using a fiber-optic sensor. Results indicated highly variable CH₄ oxidation rates following a circadian pattern. Mean rates at daytime and early nighttime varied from 62 up to 451 μmol l^?1 h^?1, whereas at late nighttime CH₄ oxidation rates were low, ranging from 13 to 37 μmol l^?1 h^?1. Similarly, daytime O₂ concentration in the vicinity of rice roots increased to up to 250% air saturation, while nighttime O₂ concentration dropped to below detection (<0.15% air saturation). Our results suggest a functional link between root-zone CH₄ oxidation and photosynthetic O₂ supply.     

Simulation of toluene decomposition in a pulse-periodic discharge operating in a mixture of molecular nitrogen and oxygen

The kinetic model of toluene decomposition in nonequilibrium low-temperature plasma generated by a pulse-periodic discharge operating in a mixture of nitrogen and oxygen is developed. The results of numerical simulation of plasma-chemical conversion of toluene are presented; the main processes responsible for C₆H₅CH₃ decomposition are identified; the contribution of each process to total removal of toluene is determined; and the intermediate and final products of C₆H₅CH₃ decomposition are identified. It was shown that toluene in pure nitrogen is mostly decomposed in its reactions with metastable N₂(A₃?? _u ⁺ ) and N₂(a??¹?? _u ^? ) molecules. In the presence of oxygen, in the N₂ : O₂ gas mixture, the largest contribution to C₆H₅CH₃ removal is made by the hydroxyl radical OH which is generated in this mixture exclusively due to plasma-chemical reactions between toluene and oxygen decomposition products. Numerical simulation showed the existence of an optimum oxygen concentration in the mixture, at which toluene removal is maximum at a fixed energy deposition.     

Electrical and chemical properties of XeCl*(308 nm) exciplex lamp created by a dielectric barrier discharge

The aim of this work is to highlight, through numerical modeling, the chemical and the electrical characteristics of xenon chloride mixture in XeCl* (308 nm) excimer lamp created by a dielectric barrier discharge. A temporal model, based on the Xe/Cl₂ mixture chemistry, the circuit and the Boltzmann equations, is constructed. The effects of operating voltage, Cl₂ percentage in the Xe/Cl₂ gas mixture, dielectric capacitance, as well as gas pressure on the 308-nm photon generation, under typical experimental operating conditions, have been investigated and discussed. The importance of charged and excited species, including the major electronic and ionic processes, is also demonstrated. The present calculations show clearly that the model predicts the optimal operating conditions and describes the electrical and chemical properties of the XeCl* exciplex lamp.     

Hydrodynamic model of a dielectric-barrier discharge in pure chlorine

A one-dimensional hydrodynamic model of a dielectric-barrier discharge (DBD) in pure chlorine is developed, and the properties of the discharge are modeled. The discharge is excited in an 8-mm-long discharge gap between 2-mm-thick dielectric quartz layers covering metal electrodes. The DBD spatiotemporal characteristics at gas pressures of 15–100 Torr are modeled for the case in which a 100-kHz harmonic voltage with an amplitude of 8 kV is applied to the electrodes. The average power density deposited in the discharge over one voltage period is 2.5–5.8 W/cm³. It is shown that ions and electrons absorb about 95 and 5% of the discharge power, respectively. In this case, from 67 to 97% of the power absorbed by electrons is spent on the dissociation and ionization of Cl₂ molecules. Two phases can be distinguished in the discharge dynamics: the active (multispike) phase, which follows the breakdown of the discharge gap, and the passive phase. The active phase is characterized by the presence of multiple current spikes, a relatively high current, small surface charge density on the dielectrics, and large voltage drop across the discharge gap. The passive phase (with no current spikes) is characterized by a low current, large surface charge density on the dielectrics, and small voltage drop across the discharge gap. The peak current density in the spikes at all pressures is about 4 mA/cm². In the multispike phase, there are distinct space charge sheaths with thicknesses of 1.5–1.8 mm and a mean electron energy of 4.3–7 eV and the central region of quasineutral plasma with a weak electric field and a mean electron energy of 0.8–3 eV. The degree of ionization of chlorine molecules in the discharge is ~0.02% at a pressure of 15 Torr and ~0.01% at 100 Torr. The DBD plasma is electronegative due to the fast attachment of electrons to chlorine atoms: e + Cl₂ → Cl + Cl^–. The most abundant charged particles are Cl ₂ ⁺ and Cl^? ions, and the degree of ionization during current spikes in the active phase is (4.1–5.5) × 10^–7. The mechanism of discharge sustainment is analyzed. The appearance of a series of current spikes in the active phase of the discharge is explained.     

Effect of temperature on ion content, ion fluxes and energy metabolism in Chara corallina

Abstract Effects of temperature on the ionic relations and energy metabolism of Chara corallina were investigated. Measurements were made of the ionic content, tracer ion fluxes, and photosynthetic and dark CO₂ fixation in isolated cells, and of O₂ exchange in photosynthesis and respiration in isolated shoot apices. The total intracellular concentration of K⁺, Na⁺ and Cl^? was the same in cells held for 5 days in non-growing medium at 15°C (the growth temperature) as in those held at 25°C or 5°C. The tracer influx in the light of all ions tested (Rb⁺, Na⁺, CH₃NH₃⁺, Cl^? and H₂PO₄^?) was lower at 5°C than at 15°C in experiments in which cells were subjected to 5°C for less than 24 h in toto. The influx at 25°C was greater than that at 15°C for H₂PO^?₄, there was no difference between the two temperatures for Na⁺, while the influx at 25°C was less than that at 15°C for Cl^?, Rb⁺ and CH₃NH₃⁺ For Cl^? and H₂PO^?₄ similar results were found in later experiments with cells grown at 20—23°C. Photosynthetic CO₂ fixation and O₂ evolution, and respiratory O₂ uptake, are greater at 25°C, and lower at 5°C, than they are at the growth temperature of 15°C. In longer-term pretreatments at the different temperatures, tracer Cl^? influx at 15°C and particularly at 25°C were lower than in short-term experiments, while the influx at 5°C was higher. It was concluded from these experiments, and from previous data on H⁺ free energy differences across the plasmalemma, that (1) the maintenance of internal ion concentrations involves a close balancing of influx and efflux of K⁺, Na⁺ and Cl^? at all experimental temperatures; (2) the regulation of the tracer fluxes of the ions is kinetic rather than thermodynamic and (3) that the tracer fluxes at low temperatures are not restricted by the rate at which respiration or photosynthesis can supply energy to them.     

Characterization of inhibitory effects of NH2OH and its N-methyl derivatives on the O2-evolving complex of Photosystem II

Inorganic cofactors (Mn, Ca²⁺ and Cl^-) are essential for oxidation of H₂O to O₂ by Photosystem II. The Mn reductants NH₂OH and its N-methyl derivatives have been employed as probes to further examine the interactions between these species and Mn at the active site of H₂O oxidation. Results of these studies show that the size of a hydroxylamine derivative regulates its ability to inactivate O₂ evolution activity, and that this size-dependent inhibition behavior arises from the protein structure of Photosystem II. A set of anions (Cl^-, F^- and SO₄ ^2-) is able to slow NH₂OH and CH₃NHOH inactivation of intact Photosystem II membranes by exerting a stabilizing influence on the extrinsic 23 and 17 kDa polypeptides. In contrast to this non-specific anion effect, only Cl^- is capable of attenuating CH₃NHOH and (CH₃)₂NOH inhibition in salt-washed preparations lacking the 23 and 17 kDa polypeptides. However, Cl^- fails to protect against NH₂OH inhibition in salt-washed membranes. These results indicate that the attack by NH₂OH and its N-methyl derivatives on Mn occurs at different sites in the O₂-evolving complex. The small reductant NH₂OH acts at a Cl^--insensitive site whereas the inhibitions by CH₃NHOH and (CH₃)₂NOH involve a site that is Cl^- sensitive. These findings are consistent with earlier studies showing that the size of primary amines controls the Cl^- sensitivity of their binding to Mn in the O₂-evolving complex.Abbreviation MES 4-morpholinoethanesulfonic acid - PS II Photosystem II     

Synthesis of fluoroalkoxide trirhenium(III) clusters

The cluster Re₃(μ-Cl)₃Cl₆(THF)₃ reacted at room temperature in THF with 5 equivalents of NaOCMe(CF₃)₂ to give [Na(THF)₂][Re₃(μ-Cl)₃Cl₂{OCMe(CF₃)₂}₅]. The salt [Na(THF)₂][Re₃(μ-Cl)₃Cl₂{OCMe(CF₃)₂}₅] reacted with a large excess of pyridine to produce Re₃(μ-Cl)₃Cl₂[OCMe(CF₃)₂]₄(py)₂, which was isolated as a crystalline mixture of two isomers. The mono-pyridine adduct Re₃(μ-Cl)₃Cl₂[OCMe(CF₃)₂]₄(py) was observed as a side product in reactions between the salt and pyridine. The mono-pyridine adduct Re₃(μ-Cl)₃Cl₂[OCMe(CF₃)₂]₄(py) and one of the two isomers of the di-pyridine adduct Re₃(μ-Cl)₃Cl₂[OCMe(CF₃)₂]₄(py)₂ were characterized by X-ray crystallography. The other isomer of Re₃(μ-Cl)₃Cl₂[OCMe(CF₃)₂]₄(py)₂ and [Na(THF)₂][Re₃(μ-Cl)₃Cl₂{OCMe(CF₃)₂}₅] were identified by X-ray crystallography but the structures were not fully refined.     

Reduction in hypoxia-reoxygenation-induced myocardial mitochondrial damage with exogenous methane

Albeit previous experiments suggest potential anti-inflammatory effect of exogenous methane (CH₄) in various organs, the mechanism of its bioactivity is not entirely understood. We aimed to investigate the potential mitochondrial effects and the underlying mechanisms of CH₄ in rat cardiomyocytes and mitochondria under simulated ischaemia/reperfusion (sI/R) conditions. Three-day-old cultured cardiomyocytes were treated with 2.2% CH₄-artificial air mixture during 2-hour-long reoxygenation following 4-hour-long anoxia (sI/R and sI/R + CH₄, n = 6-6), with normoxic groups serving as controls (SH and SH + CH₄; n = 6-6). Mitochondrial functions were investigated with high-resolution respirometry, and mitochondrial membrane injury was detected by cytochrome c release and apoptotic characteristics by using TUNEL staining. CH₄ admixture had no effect on complex II (CII)-linked respiration under normoxia but significantly decreased the complex I (CI)-linked oxygen consumption. Nevertheless, addition of CH₄ in the sI/R + CH4 group significantly reduced the respiratory activity of CII in contrast to CI and the CH₄ treatment diminished mitochondrial H₂O₂ production. Substrate-induced changes to membrane potential were partially preserved by CH₄, and additionally, cytochrome c release and apoptosis of cardiomyocytes were reduced in the CH₄-treated group. In conclusion, the addition of CH₄ decreases mitochondrial ROS generation via blockade of electron transport at CI and reduces anoxia-reoxygenation-induced mitochondrial dysfunction and cardiomyocyte injury in vitro.     

Preparation of an unusual fluoroalkyl phosphinoyl chelate complex, {k-P,C,P,k-O-(CF3)2PCH2C6H3CH2P(CF3)O}2Pt2

Electron poor cationic complexes [(^CF₃PCP)Pt(L)]⁺ (where L = CO, NC₅F₅, or acetone) react with H₂O in polar solvents via selective hydrolysis of a single P-CF₃ substituent to afford the spectroscopically-characterized phosphinoyl-bridged complex {k³-P,C,P,k¹-O-(CF₃)₂PCH₂C₆H₃CH₂P(CF₃)O}₂Pt₂ (1) in good yield. X-ray diffraction confirms the presence of a six-member Pt-P-O-Pt-P-O ring in a chair conformation. The presumed intermediate aqua complex, (^CF₃PCP)Pt(H₂O)⁺, is stable in dichloromethane, but when dissolved in more polar solvents readily converts to 1.