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At least 307 records · Page 17Linked to original sources

Influence of dissolved and free gases on iodine release and cell killing by shock waves in vitro.

Exposure of a potassium iodide solution to lithotripter shock waves resulted in formation of iodine with the amount of iodine depending on the gas dissolved in the solution. Iodine yield was higher with O2 and Ar, as compared to CO2 and N2O; degassed solution revealed the lowest iodine yield. Exposure of L1210 mouse leukemia cells to shock waves reduced the number of viable cells with no difference between O2-, Ar-, or N2O-equilibrated and degassed conditions. CO2 equilibration resulted in a more pronounced reduction. The difference between chemical and biological effects argues against the involvement of free radicals in cell killing by shock waves. In additional experiments, gas bubbles of various sizes were introduced into the test vials. Addition of a 10 microL gas bubble revealed an over 10-fold increase in iodine yield from degassed potassium iodide solution with all gases. Addition of a gas bubble also reduced the number of viable cells again with no difference between the gases. It is suggested that shock wave-gas bubble interaction is an important mediator of iodine release and cell killing by shock waves.

Animals↗

Single-breath inhalation or rebreathing of gases labelled with positron emitters: some technical aspects of dispensing and waste gas management.

A simple and reliable system for the single-breath inhalation and for short-term rebreathing of radioactive gases used in positron emission tomography is described. It comprises a collection- and radioactivity measurement-device, an inhalation bag for single-breath application, a modified anaesthetic system for rebreathing and a patient exhaled gas management system. The system is mainly used with 15O-labelled gases, but allows also the use of longer lived tracers such as methyl fluoride labelled with 18F or 11C.

Administration, Inhalation↗

Determination of the energy potential of gases produced in the pyrolysis processes of the vegetal carbon manufacture industry.

In this work, a pyrolysis plant located in Valverde de Leganes, Badajoz (SW Spain) was studied. At present, only the solid phase obtained by pyrolysis finds an application as domestic fuel. In order to analyze the feasibility of a further energetic exploitation of the plant under study, the gases flowing through the chimneys were collected at different times throughout the pyrolysis process. Next, they were characterized and quantified by gas chromatography, the energy potential of each of the gases being determined. According to the results obtained in this study, a total energy potential of 5.6 x 10(7) MJ (i.e., 1.78 MW(t)) might be generated yearly. Hence, considering an overall process yield equal to 20%, up to 358 KW(e) would be produced. This power would supply enough electric energy to the industry, the remaining being added to the common electric network.

Bioelectric Energy Sources↗

Cosorption effect in gas chromatography: flow fluctuations caused by adsorbing carrier gases.

Adsorbing carrier gases have a number of advantages in analytical and preparative gas chromatography, such as clearer detector signals and higher column efficiencies. This work shows that adsorbing carrier gases also may be useful because they cause the mobile phase flow rate to become unsteady after injecting a small amount of sample. This work shows that a 100 microL sample of helium can liberate enough carbon dioxide carrier gas from a zeolite 5A packed column at 373 K, that the departure from the steady-state flow rate had an upper lobe area of 586 microL of carrier gas. This was confirmed by coupling a modified Langmuir kinetic model with the Ergun equation.

Adsorption↗

Chemical coupling between ammonia, acid gases, and fine particles.

The concentrations of inorganic aerosol components in the fine particulate matter (PM(fine)< or =2.5 microm) consisted of primarily ammonium, sodium, sulfate, nitrate, and chloride are related to the transfer time scale between gas to particle phase, which is a function of the ambient temperature, relative humidity, and their gas phase constituent concentrations in the atmosphere. This study involved understanding the magnitude of major ammonia sources; and an up-wind and down-wind (receptor) ammonia, acid gases, and fine particulate measurements; with a view to accretion gas-to-particle conversion (GTPS) process in an agricultural/rural environment. The observational based analysis of ammonia, acid gases, and fine particles by annular denuder system (ADS) coupled with a Gaussian dispersion model provided the mean pseudo-first-order k(S-1) between NH(3) and H(2)SO(4) aerosol approximately 5.00 (+/-3.77)x10(-3) s(-1). The rate constant was found to increase as ambient temperature, wind speed, and solar radiation increases, and decreases with increasing relative humidity. The observed [NH(3)][HNO(3)] products exceeded values predicted by theoretical equilibrium constants, due to a local excess of ammonia concentration.

Aerosols↗

Flammability of gas mixtures. Part 2: influence of inert gases.

Ternary systems, which contain flammable gas, inert gas and air, were studied in order to give the user an evaluation of the ISO 10156 calculation method for the flammability of gas mixtures. While in Part 1 of this article the fire potential of flammable gases was the focal point, the influence of inert gases on the flammability of gas mixtures was studied in Part 2. The inerting capacity of an inert gas is expressed by the dimensionless K value, the so-called "coefficient of nitrogen equivalency". The experimental determination of K values is demonstrated by using explosion diagrams. The objective of this study was to compare the estimated results, given by ISO 10156, with measurements of explosion ranges based on the German standard DIN 51649-1, given by CERN and CHEMSAFE. The comparison shows that ISO 10156, Table 1, supplies conservative K values, which can be regarded as safe in all cases. Nevertheless, in a number of cases ISO underestimates the inerting capacity, so that non-flammable gas mixtures are considered flammable.

Explosions↗

Gas chromatography for in situ analysis of a cometary nucleus. II. Analysis of permanent gases and light hydrocarbons with a carbon molecular sieve porous layer open tubular column.

Considering the severe constraints of space instrumentation, a great improvement for the in situ gas chromatographic (GC) determination of permanent and noble gases in a cometary nucleus is the use of a new carbon molecular sieve porous layer open tubular (PLOT) column called Carbobond. No exhaustive data dealing with this column being available, studies were carried out to entirely characterize its analytical performances, especially when used under the operating conditions of the cometary sampling and composition (COSAC) experiment of the European Space Agency (ESA) Rosetta space mission to be launched in 2003 for a rendezvous with comet 46 P/Wirtanen in 2011. The high efficiency and speed of analysis of this column at both atmospheric and vacuum outlet column pressure is demonstrated, and the kinetic mass transfer contribution of this carbon molecular sieve adsorbent is calculated. Besides, differential adsorption enthalpies of several gases and light hydrocarbons were determined from the variation of retention volume with temperature. The data indicate close adsorption behaviors on the Carbobond porous layer adsorbent and on the carbon molecular sieve Carboxen support used to prepare the packed columns. Moreover, taking into account the in situ operating conditions of the experiment, a study of two columns with different porous layer thicknesses allowed one to optimize the separation of the target components and to select the column parameters compatible with the instrument constraints. Comparison with columns of similar selectivity shows that these capillary columns are the first ones able to perform the same work as the packed and micro-packed columns dedicated to the separation of this range of compounds in GC space exploration.

Adsorption↗

Potential of electrophilic epoxide reactions for the monitoring of acid gases in the environment.

Mineral and short-chain carboxylic acid vapours and NO(x) gases were reacted with cyclohexene oxide (1,2-epoxycyclohexane) to quantitatively produce specific, thermally stable cyclohexyl derivatives. Subsequent analysis of these derivatives by gas chromatography with mass spectroscopy and flame ionisation detection afforded a multi analyte method for the assay of these gaseous acidic atmospheric species. Derivatisation was found to be quantitative for the derivatives tested and the method highly sensitive (to 0.3 mg/m3 for a 30 l sample), accurate, precise and free from apparent interferences. The technique has been applied to "acid stack gases" and a number of other acid rich atmospheres and the results obtained show good agreement with the single analyte wet chemical determinations indicating that the approach has considerable potential as a routine analytical method for measuring such atmospheric pollutants. The high specificity of the reaction mechanism and its potential for the analysis of analyte mixtures is illustrated in the assay of nitric acid and its acid anhydride, dinitrogen pentoxide.

Acids↗

Effects of dissolved gases and an echo contrast agent on apoptosis induced by ultrasound and its mechanism via the mitochondria-caspase pathway.

Human histiocytic lymphoma U937 cells were exposed to continuous 1-MHz ultrasound (US) for therapeutic use, (0 approximately 6.5 W/cm(2) (I(SPTA)). Apoptosis and its related end points were examined by flow cytometry. Fraction of cells with low mitochondria membrane potential were observed after sonication and significant superoxide and peroxide formation, increased activity of caspase-3, and DNA fragmentation revealed biochemically, were also found. The fraction of early apoptosis and secondary necrosis increased with the incubation time after sonication. Early apoptosis observed at 6 h after sonication reached its maximum at 2 min of sonication and gradually decreased. On the other hand, secondary necrosis increased with the duration of sonication. When the effects of dissolved gases, Ar, N(2), O(2), air, N(2)O and CO(2), on free radical formation due to inertial cavitation were investigated by electron spin resonance (ESR) spin trapping, formation of hydroxyl radicals and hydrogen atoms was found in solutions saturated with Ar, N(2), O(2) and air, but not with N(2)O and CO(2). Apoptosis induced by US was also dependent on the dissolved gases in the order Ar = N(2) = O(2) = air >> N(2)O = CO(2) approximately 0. These results suggest that US-induced apoptosis, which is mitochondria-caspase dependent, was linked to inertial cavitation. However, quantities of free radicals did not influence the fraction of early apoptosis and secondary necrosis. When the cells were sonicated in the presence of an echo contrast agent, Levovist; synergistic enhancement of secondary necrosis induced by US was observed at concentrations of more than 20 mg/mL. In contrast, an additive increase of early apoptosis was observed in the combined treatments. These results suggest that Levovist; acting as cavitation nuclei, enhances secondary necrosis induced by US due to an increase in the membrane damage.

Apoptosis↗

Simultaneous control of acid gases and PAHs using a spray dryer combined with a fabric filter using different additives.

The purpose of this research was to simultaneously evaluate the removal efficiency of acid gases and PAHs from the flue gas emitted by a laboratory incinerator. This flue gas contained dust, acid gases, organics and heavy metals. A spray dryer combined with a fabric filter was used as the air pollution control device (APCD) in this study. The operating conditions investigated included different feedstock additives (polyvinyl chloride (PVC) and NaCl) and spray dryer additives (SiO2, CaCl2 and NaHCO3). The removal efficiency for SO2 could be enhanced by adding inorganic additives, such as SiO2, CaCl2 and NaHCO3. The presence of PVC in the incinerator feedstock also increased the removal efficiency of SO2in the spray dryer. The improved removal of PAHs could be attributed to the addition of feedstock additives (PVC and NaCl) and spray dryer additives (SiO2, CaCl2 and NaHCO3).

Acids↗

Theoretical calculation of heat of formation and heat of combustion for several flammable gases.

Heats of formation have been calculated by the Gaussian-2 (G2) and/or G2MP2 method for a number of flammable gases. As a result, it has been found that the calculated heat of formation for compounds containing, such atoms as fluorine and chlorine tends to deviate from the observed values more than calculations for other molecules do. A simple atom additivity correction (AAC) has been found effective to improve the quality of the heat of formation calculation from the G2 and G2MP2 theories for these molecules. The values of heat of formation thus obtained have been used to calculate the heat of combustion and related constants for evaluating the combustion hazard of flammable gases.

Fires↗

Volatile metals and metalloids in hydrothermal gases.

Volatile metals and metalloids were sampled from hot springs, fumaroles, and a hydrothermally influenced wetland in Yellowstone National Park. The sampling was based on diffusion through gas sampling chambers. Collected gases were stabilized by dissolution and oxidation in 1:100 diluted NaOCl. Special procedures were developed to analyze the oxidized samples by GF-AAS and HG-AAS. For ICP-MS, samples had to be blank-corrected for polyatomic isotope interferences, especially by 23Na35Cl+ and 23Na37Cl+ on 58Ni and 60Ni and by 40Ar23Na+ on 63Cu. From the concentrations trapped in solution, net diffusion rates were calculated by Fick's first law. The highest concentrations reached a maximum of 8 g/m3 for volatile silicon. Volatile nickel, tungsten, zinc, copper, and molybdenum, previously only known from anthropogenic sources, occurred naturally in the hydrothermal gases in ranges of tens to hundreds of microg/m3. Replicate measurements indicated significant temporal variations in concentrations, probably the result of complex changes in the hydrothermal regime as well as varying microbial activity. Global correlations between gaseous and superficial aqueous phases were missing.

Air Pollutants↗

Electronic fluctuations in nanotube circuits and their sensitivity to gases and liquids.

The temperature-dependent noise of individual, single-walled carbon nanotubes is measured here in a variety of different gases and liquids. The ambient environment is found to have only a weak relationship with device noise, even in cases where adsorption significantly changes the dc resistance. Correspondingly, a 450 K degassing procedure typically reduces the device noise by only 1 order of magnitude. An important exception to this finding is a pronounced, 100-fold increase in noise observed near gas-liquid phase transitions of the ambient. Wide-range temperature scans clearly identify the condensation of N(2), H(2), and CH(4) onto metallic nanotubes, but not the sublimation of CO(2). The observations suggest that nanotube devices can directly transduce ambient density fluctuations, though without an inherent gas specificity. Even so, the method is a particularly sensitive characterization of nanotube chemical interactions, one which is successful even for the extreme case of inert gases adsorbed on metallic nanotubes.

Carbon Dioxide↗

Diffusion in binary gas mixtures studied by NMR of hyperpolarized gases and molecular dynamics simulations.

The dependence of the individual mean square displacement of rare gases in binary mixtures is studied by a combined experimental and theoretical approach. We show that the diffusion constant can be varied in a considerable range by changing the molar fractions of the mixtures. On the experimental side, NMR diffusion measurements are done on hyperpolarized 3He and 129Xe, mixed with several inert buffer gases, in the presence of a magnetic field gradient. The results are compared to diffusion coefficients obtained from atomistic molecular dynamics simulations based on Lennard-Jones type potentials of the corresponding gas mixtures, and to appropriate analytical expressions, yielding very good mutual agreement. This study is the first quantitative validation of the effects of the mutual interactions between gas particles on the individual diffusion properties. It is shown that the dependency of gas phase diffusion properties on the local chemical environment may not be neglected, e.g. in diffusion-controlled chemical reactions.

Complex Mixtures↗

Fullerenes: an extraterrestrial carbon carrier phase for noble gases.

In this work, we report on the discovery of naturally occurring fullerenes (C60 to C400) in the Allende and Murchison meteorites and some sediment samples from the 65 million-year-old Cretaceous/Tertiary boundary layer (KTB). Unlike the other pure forms of carbon (diamond and graphite), fullerenes are extractable in an organic solvent (e.g., toluene or 1,2,4-trichlorobenzene). The recognition of this unique property led to the detection and isolation of the higher fullerenes in the Kratschmer/Huffmann arc evaporated graphite soot and in the carbon material in the meteorite and impact deposits. By further exploiting the unique ability of the fullerene cage structure to encapsulate and retain noble gases, we have determined that both the Allende and Murchison fullerenes and the KTB fullerenes contain trapped noble gases with ratios that can only be described as extraterrestrial in origin.

Carbon↗

An internal dose model for interspecies extrapolation of immediate incapacitation risk from inhalation of fire gases.

A quantitative mathematical model assesses incapacitation risk in humans from toxic gas inhalation. A body-mass-normalized internal dose for each gas is calculated from an inhalation equation in which ventilation is a function of species, activity, and the gases inhaled. Uptake in the dead space considers U.S. Environmental Protection Agency (EPA) gas categories. The probability of incapacitation is a function of normalized internal dose and follows a cumulative distribution curve whose parameters are found from small-animal incapacitation data. No internal interaction of gases is modeled, and probabilities are combined independently. The model compares favorably with combined gas and large-animal incapacitation data.

Acute Disease↗

An internal dose model of incapacitation and lethality risk from inhalation of fire gases.

A mathematical model for estimating the likelihood of incapacitation and lethality from the inhalation of toxic gases is presented. The model computes an internal dose, equal to retained toxic gas per body mass, which is used to extrapolate outcomes across species. Account is taken for ventilation changes due to species, activity, and chemical response. The internal dose is correlated with each outcome using a cumulative, log-normal, probability distribution, which allows the estimation of tolerances for any population incidence. No internal interactions of gases are modeled and probabilities are combined independently. The model compares favorably with combined gas and large animal data.

Acrolein↗

Free radical formation and cell lysis induced by ultrasound in the presence of different rare gases.

The effect of varying the temperature of cavitation bubbles in aqueous solutions of different rare gases on free radical formation and shearing stress induced by ultrasound was investigated. After sonication with 50kHz ultrasound the yield of hydroxyl radicals was measured by spin trapping with 5,5-dimethyl-1-pyrroline-N-oxide and the cell lysis of cultured mammalian cells was investigated. The hydroxyl radical yields were in the order Xe greater than Kr greater than Ar greater than Ne greater than He, in accord with the higher temperatures of the cavitation bubbles. However, cell lysis induced by shearing stress was the same for all of the rare gases, and independent of their thermal conductivity and the temperature of the cavitation bubbles.

Animals↗