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At least 199 records · Page 11

Mineralization of Basalts in the CO2-H2O-SO2-O2 System

Sequestering carbon dioxide (CO2) containing minor amounts of co-contaminants in geologic formations was investigated in the laboratory through the use of high pressure static experiments. Five different basalt samples were immersed in water equilibrated with supercritical CO2 containing 1wt% sulfur dioxide (SO2) and 1wt% oxygen (O2) at reservoir conditions (~100 bar, 90°C) for 49 and 98 days. Gypsum (CaSO4) was a common precipitate, occurred early as elongated blades with striations, and served as substrates for other mineral products. Bimodal pulses of water released during dehydroxylation were key indicators along with X-ray diffraction for verifying the presences of jarosite-alunite group minerals. Well-developed pseudocubic jarosite crystals formed surface coatings, and in some instances mixtures of natrojarosite and natroalunite aggregated into spherically shaped structures measuring 100 μm in diameter. Reaction products were also characterized using infrared spectroscopy, which indicated OH and Fe-O stretching modes. The presences of jarosite-alunite group minerals were found in the lower wavenumber region from 700–400 cm-1. A strong preferential incorporation of Fe(III) into natrojarosite was attributed to the oxidation potential of O2. Evidence of CO2 was detected during thermal decomposition of precipitates, suggesting the onset of mineral carbonation.

Environmental Molecular Sciences Laboratory↗

Studying the effect of meteorological factors on the SO2 and PM10 pollution levels with refined versions of the SARIMA model

Numerous time series methods are used in environmental sciences allowing the detailed investigation of air pollution processes. The goal of this study is to present the empirical analysis of various aspects of stochastic modeling and in particular the ARIMA/SARIMA methods. The subject of investigation is air pollution in the town of Kardzhali, Bulgaria with 2 problematic pollutants – sulfur dioxide (SO2) and particulate matter (PM10). Various SARIMA Transfer Function models are built taking into account meteorological factors, data transformations and the use of different horizons selected to predict future levels of concentrations of the pollutants.

54 ENVIRONMENTAL SCIENCES↗

AmeriFlux US-SO2 Sky Oaks- Old Stand

This is the AmeriFlux version of the carbon flux data for the site US-SO2 Sky Oaks- Old Stand. Site Description - The Sky Oaks Old site is located near the Sky Oaks Field station, owned and operated by San Diego State University. Chaparral vegetation, associated with a Mediterranean climate, covers nearly half of the rough and rocky terrain. Precipitation is almost exclusively confined to the winter months. During the summer and early fall, hot and dry Santa Ana winds from the northeast bring desert heat to the site. A high intensity natural wildfire occurred in July of 2003. The stand age at the time of the wildfire was 80 years old, following an early wildfire poorly characterized. Following the 2003 wildfire, most native chaparral began to regrow from root stocks reaching a height of 1.0 m in 2008.

Oechel, Walt↗

Infrared Absorption Spectra of H2SO4, SO3, SO2, and H2O at 300C and 350C

Mid infrared absorption spectra of sulfuric acid (H2SO4), sulfur trioxide (SO3), sulfur dioxide (SO2), and water (H2O) were collected in a high temperature gas cell operating at either 300C or 350C. The spectra were collected using tunable external cavity quantum cascade lasers (ECQCLs) tuning, which were capable of operating over the wavelength range from approximately 7 microns to 9 microns, where H2SO4 and SO3 have their strongest absorption features. The spectra can be used as a library for developing gas sensors.

infrared absorption↗

Computed linewidths of SO2

Self-broadened and foreign-gas (N2 and O2) broadened linewidths of sulfur dioxide, for both type A and type B bands, have been calculated using the Anderson-Tsao-Curnutte theory of line broadening. Computed values of these linewidths at 300 K are given for all the transitions with J or = 20 and K sub minus 1 or = 15. Air-broadened linewidths have also been calculated for SO2 at 250 K and 200 K for these transitions.

Tejwani, G. D. T.↗

Work on power-plant (air) plumes involving remote sensing of SO2

Acquisition of air quality and concurrent meteorological data was used for dispersion model development and plant siting needs of the Maryland power plants. One of the major instruments in these studies was the Barringer correlation spectrometer, a remote sensor, using atmospherically scattered sunlight that was used to measure the total amount of SO2 in a cross section of the plume. Correlation spectrometer and its role in this measurement program are described.

White, C. L., Jr.↗

Safety characteristics of the lithium SO2 system

Extensive tests were conducted to quantitatively define the safety characteristics of high-rate SO2 multicell batteries under various discharge and temperature profiles, which closely simulated actual field-use conditions. The resulting behavior patters of the multicell batteries and the corrective action which can be implemented to minimize or prevent hazardous battery performance are briefly summarized.

Watson, T.↗

The stability of an SO2 atmosphere on Io

Active volcanism observed on Io could provide a continuous source of gases from Io's interior. Only a small fraction of what is coming out of Io's volcanoes is escaping; the bulk of it is being recycled. There must be an atmospheric reservoir which maintains the gases until they have had a chance to recycle. Such an atmosphere must be protected from Jupiter's corotating plasma in order to be stable. Only the dayside atmosphere is subject to escape, while the cold nightside and poles would serve as a sink for atmospheric gases. However, the scavenging of atmospheric gases is maximum at the eastern elongation and minimum at the western elongation. A stable SO2 atmosphere on Io shows promise if the volcanic activity is continuous. If the volcanoes stop erupting, the atmosphere will be depleted.

Kumar, S.↗

A kinetics study of the reaction of SO2 with CH3O2

The reaction of CH3O2 with SO2 has been studied using the flash photolysis/ultraviolet absorption technique. In contrast to previous measurements, no reaction could be detected over the temperature range 298-423 K. An upper limit of 5 x 10 to the -17th cu cm/molecule/sec has been determined for the reaction rate constant.

Sander, S. P.↗

Far-UV, visible, and near-IR reflectance spectra of frosts of H2O, CO2, NH3 and SO2

Measurements in the 0.1-2.5 micron range are presented for the reflectance spectra of the frosts of several volatiles pertinent to the study of comet nuclei. The frost spectra have distinctive features permitting their identification by spectroscopic reflectance remote sensing, notably in the far UV. It is found that: (1) H2O has a minimum at 0.16 microns and a maximum at 0.13 microns; (2) CO2 has minima near 0.21, 0.18 and 0.125 microns, with maxima at 0.19, 0.135 and 0.120 microns; (3) NH3 is bright at wavelengths longer than 0.21 microns, where reflectance drops to a value of only a few per cent at shorter wavelengths; (4) SO2 has a sharp drop at 0.32 microns, with a minimum at 0.18 microns and a maximum at 0.13 microns. The features in the frost spectra largely correspond to absorption line bands in the gas phase.

Hapke, B.↗

A theoretical investigation of gaseous absorption by water droplets from SO2-HNO3-NH3-CO2-HCl mixtures

A physical-chemical model is developed and used to investigate gaseous absorption by water droplets from trace gas mixtures. The model is an extension of that of Carmichael and Peters (1979) and includes the simultaneous absorption of SO2, NH3, HNO3, CO2, and HCl. Gas phase depletion is also considered. Presented results demonstrate that the absorption behavior of raindrops is strongly dependent on drop size, fall distance, trace gas concentrations, and the chemical and physical properties of the constituents of the mixture. In addition, when gas phase depletion is considered, the absorption rates and equilibrium values are also dependent on the precipitation rate itself. Also, the trace constituents liquid phase concentrations may be a factor of six or more lower when gas depletion is considered then when the depletion is ignored. However, the hydrogen ion concentration may be insensitive to the gas phase depletion.

Adewuyi, Y. G.↗

Reactions of NaCl with Gaseous SO3, SO2, and O2

Hot corrosion of gas turbine engine components involves deposits of Na2SO4 which are produced by reactions between NaCl and oxides of sulfur. For the present investigation, NaCl single crystals were exposed at 100 to 850 C to gaseous mixtures of SO3, SO2, and O2. The products formed during this exposure depend, primarily, on the temperatures. The four product films were: NaCl-SO3; Na2S2O7; Na2SO4; and NaCl-Na2SO4. The kinetics of the reactions were measured.

Fielder, W. L.↗

Reaction of cobalt in SO2 atmospheric at elevated temperatures

The reaction rate of cobalt in SO2 argon environments was measured at 650 C, 700 C, 750 C and 800 C. Product scales consist primarily of an interconnected sulfide phase in an oxide matrix. At 700 C to 800 C a thin sulfide layer adjacent to the metal is also observed. At all temperatures, the rapid diffusion of cobalt outward through the interconnected sulfide appears to be important. At 650 C, the reaction rate slows dramatically after five minutes due to a change in the distribution of these sulfides. At 700 C and 750 C the reaction is primarily diffusion controlled values of diffusivity of cobalt (CoS) calculated from this work show favorable agreement with values of diffusivity of cobalt (CoS) calculated from previous sulfidation work. At 800 C, a surface step becomes rate limiting.

Jacobson, N. S.↗

Production of negative ions by dissociative electron attachment to SO2

Dissociative electron attachment cross section measurements for the production of O(-), S(-), and SO(-) have been performed utilizing a crossed target SO2 molecule beam-electron beam geometry. The relative flow technique is employed to determine the absolute values of cross sections. The attachment energies corresponding to various cross section maxima are: 4.30 and 7.1 eV for O(-)/SO2; 4.0, 7.5, and 8.9 eV for S(-)/SO2, and 4.7 and 7.5 eV for SO(-)/SO2.

Orient, O. J.↗

Electron impact excitation of SO2 - Differential, integral, and momentum transfer cross sections

Electron impact excitation of the electronic states of SO2 was investigated. Differential, integral, and inelastic momentum transfer cross sections were obtained by normalizing the relative measurements to the elastic cross sections. The cross sections are given for seven spectral ranges of the energy-loss spectra extending from the lowest electronic state to near the first ionization limit. Most of the regions represent the overlap of several electronic transitions. No measurements for these cross sections have been reported previously.

Vuskovic, L.↗

Reaction of cobalt in SO2 atmospheres at elevated temperatures

The reaction rate of cobalt in SO2 argon environments was measured at 650 C, 700 C, 750 C and 800 C. Product scales consist primarily of an interconnected sulfide phase in an oxide matrix. At 700 C to 800 C, a thin sulfide layer adjacent to the metal is also observed. At all temperatures, the rapid diffusion of cobalt outward through the interconnected sulfide appears to be important. At 650 C, the reaction rate slows dramatically after five minutes due to a change in the distribution of these sulfides. At 700 C and 750 C, the reaction is primarily diffusion controlled; values of diffusivity of cobalt (CoS) calculated from this work show favorable agreement with values of diffusivity of cobalt (CoS) calculated from previous sulfidation work. At 800 C, a surface step becomes rate limiting. Previously announced in STAR as N83-35104

Jacobson, N. S.↗

Reactions of NaCl with gaseous SO3, SO2, and O2

Hot corrosion of gas turbine engine components involves deposits of Na2SO4 which are produced by reactions between NaCl and oxides of sulfur. For the present investigation, NaCl single crystals were exposed at 100 to 850 C to gaseous mixtures of SO3, SO2, and O2. The products formed during this exposure depend, primarily, on the temperatures. The four product films were: NaCl-SO3; Na2S2O7; Na2SO4; and NaCl-Na2SO4. The kinetics of the reactions were measured.

Fielder, W. L.↗

Carbon catalysis in the aqueous oxidation of SO2 by NO2 and air

Sulfur dioxide and an oxidant gas (air or NO2) were bubbled through aqueous suspensions of both washed and unwashed carbon black as well as through samples of wash water, which contained whatever soluble species were originally present on the carbon, and high-purity water. The sulfate yields obtained showed the washed and unwashed carbon to be equally catalytic for the oxidation of SO2 to sulfate by both oxidants, whereas little sulfate was generated in either the wash water or high-purity water in the absence of carbon. These results indicate that the sulfate yields produced in aqueous suspensions of the carbon studied are due to catalysis by the carbon particles rather than by soluble species dissolved from them.

Schryer, D. R.↗