Consequence assessment for Airborne Releases of SO2 from the Y-12 Pilot Dechlorination Facility

International Nuclear Information System (INIS)

Pendergrass, W.R.

1992-06-01

The Atmospheric Turbulence and Diffusion Division was requested by the Department of Energy's Oak Ridge Operations Office to conduct a consequence assessment for potential atmospheric releases of SO 2 from the Y-12 Pilot Dechlorination Facility. The focus of the assessment was to identify ''worst'' case meteorology which posed the highest concentration exposure potential for both on-site as well as off-site populations. A series of plausible SO 2 release scenarios were provided by Y-12 for the consequence assessment. Each scenario was evaluated for predictions of downwind concentration, estimates of a five-minute time weighted average, and estimate of the dimension of the puff. The highest hazard potential was associated with Scenario 1, in which a total of eight SO 2 cylinders are released internally to the Pilot Facility and exhausted through the emergency venting system. A companion effort was also conducted to evaluate the potential for impact of releases of SO 2 from the Pilot Facility on the population of Oak Ridge. While specific transport trajectory data is not available for the Pilot Facility, extrapolations based on the Oak Ridge Site Survey and climatological records from the Y-12 meteorological program does not indicate the potential for impact on the city of Oak Ridge. Steering by the local topographical features severely limits the potential impact ares. Due to the lack of specific observational data, both tracer and meteorological, only inferences can be made concerning impact zones. It is recommended tat the Department of Energy Oak Ridge Operations examine the potential for off-site impact and develop the background data to prepare impact zones for releases of hazardous materials from the Y-12 facility

Debunking the myths: Natural gas and SO2 allowance solutions

International Nuclear Information System (INIS)

Roberts, G.D. Jr.

1993-01-01

During the decade of the 1990's and beyond, natural gas is expected to be the fuel of choice for a significant portion of new generation capacity. Natural gas already enjoys a greater than 50% market share as a fuel source in the non-regulated cogeneration and Independent Power Producer market. With the new administration in Washington, increased environmental focus will likely increase the attractiveness of natural gas based capacity expansions. While these various issues may appear to contribute to making this decade, the decade for natural gas, there are a number of challenges that must be met if the natural gas and power generation industries are going to satisfy the ever increasing needs of the marketplace. These challenges include: (1) myths of natural gas supply availability, (2) transportation and operational coordination issues, (3) uncertainty of price and reliability, and (4) natural gas for NO x and SO 2 compliance. The author believes that these challenges are actively being met and that there are existing solutions already being offered and incorporated into contracts by natural gas suppliers. The focus of this paper is how electric utilities need to become comfortable with the new natural gas industry and how services can be structured to meet these challenges of serving the electric market requirements

IFPE/RISOE-II, Fuel Performance Data from Transient Fission Gas Release

International Nuclear Information System (INIS)

Turnbull, J.A.

1995-01-01

Description: The RISO National Laboratory in Denmark have carried out three irradiation programs of slow ramp and hold tests, so called 'bump tests' to investigate fission gas release and fuel microstructural changes. The second project took place between 1982 and 1986 and was called 'The RISO Transient Fission Gas Project'. The fuel used in the project was from: IFA-161 irradiated in the Halden BWR (27 to 42 MWd/kgUO 2 ) and GE BWR fuel irradiated in the Millstone 1 reactor 14 to 29 MWd/kgUO 2 . Using the re-fabrication technique, it was possible to back fill the test segment with a choice of gas and gas pressure and to measure the time dependence of fission gas release by continuous monitoring of the plenum pressure. The short length of the test segment was an advantage because, depending on where along the original rod the section was taken, burnup could be chosen variable, and during the test the fuel experienced a single power

Gas Release as a Deformation Signal

Energy Technology Data Exchange (ETDEWEB)

Bauer, Stephen J. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

2017-09-01

Radiogenic noble gases are contained in crustal rock at inter and intra granular sites. The gas composition depends on lithology, geologic history, fluid phases, and the aging effect by decay of U, Th, and K. The isotopic signature of noble gases found in rocks is vastly different than that of the atmosphere which is contributed by a variety of sources. When rock is subjected to stress conditions exceeding about half its yield strength, micro-cracks begin to form. As rock deformation progresses a fracture network evolves, releasing trapped noble gases and changing the transport properties to gas migration. Thus, changes in gas emanation and noble gas composition from rocks could be used to infer changes in stress-state and deformation. The purpose of this study has been to evaluate the effect of deformation/strain rate upon noble gas release. Four triaxial experiments were attempted for a strain rate range of %7E10-8 /s (180,000s) to %7E 10-4/s (500s); the three fully successful experiments (at the faster strain rates) imply the following: (1) helium is measurably released for all strain rates during deformation, this release is in amounts 1-2 orders of magnitude greater than that present in the air, and (2) helium gas release increases with decreasing strain rate.

Gas release from pressurized closed pores in nuclear fuels

International Nuclear Information System (INIS)

Bailey, P.; Donnelly, S.E.; Armour, D.G.; Matzke, H.

1988-01-01

Gas release from the nuclear fuels UO 2 and UN out of pressurized closed pores produced by autoclave anneals has been studied by Thermal Desorption Spectrometry (TDS). Investigation of gas release during heating and cooling has indicated stress related mechanical effects leading to gas release. This release occurred in a narrow temperature range between about 1000 and 1500 K for UO 2 , but it continued down to ambient temperature for UN. No burst release was observed above 1500 K for UO 2 . (orig.)

A new method research of monitoring low concentration NO and SO2 mixed gas

Science.gov (United States)

Bo, Peng; Gao, Chao; Guo, Yongcai; Chen, Fang

2018-01-01

In order to reduce the pollution of the environment, China has implemented a new ultra-low emission control regulations for polluting gas, requiring new coal-fired power plant emissions SO2 less than 30ppm, NO less than 75ppm, NO2 less than 50ppm, Monitoring low concentration of NO and SO2 mixed gases , DOAS technology facing new challenges, SO2 absorb significantly weaken at the original absorption peak, what more the SNR is very low, it is difficult to extract the characteristic signal, and thus cannot obtain its concentration. So it cannot separate the signal of NO from the mixed gas at the wavelength of 200 230nm through the law of spectral superposition, it cannot calculate the concentration of NO. The classical DOAS technology cannot meet the needs of monitoring. In this paper, we found another absorption spectrum segment of SO2, the SNR is 10 times higher than before, Will not be affected by NO, can calculate the concentration of SO2 accurately, A new method of segmentation and demagnetization separation technology of spectral signals is proposed, which achieves the monitoring the low concentration mixed gas accurately. This function cannot be achieved by the classical DOAS. Detection limit of this method is 0.1ppm per meter which is higher than before, The relative error below 5% when the concentration between 0 5ppm, the concentration of NO between 6 75ppm and SO2 between 6 30ppm the relative error below 1.5%, it has made a great breakthrough In the low concentration of NO and SO2 monitoring. It has great scientific significance and reference value for the development of coal-fired power plant emission control, atmospheric environmental monitoring and high-precision on-line instrumentation.

Considerations in modeling fission gas release during normal operation

International Nuclear Information System (INIS)

Rumble, E.T.; Lim, E.Y.; Stuart, R.G.

1977-01-01

The EPRI LWR fuel rod modeling code evaluation program analyzed seven fuel rods with experimental fission gas release data. In these cases, rod-averged burnups are less than 20,000 MWD/MTM, while the fission gas release fractions range roughly from 2 to 27%. Code results demonstrate the complexities in calculating fission gas release in certain operating regimes. Beyond this work, the behavior of a pre-pressurized PWR rod is simulated to average burnups of 40,000 MWD/MTM using GAPCON-THERMAL-2. Analysis of the sensitivity of fission gas release to power histories and release correlations indicate the strong impact that LMFBR type release correlations induce at high burnup. 15 refs

SO2 and NO removal from flue gas over V2O5/AC at lower temperatures - role of V2O5 on SO2 removal

International Nuclear Information System (INIS)

Ma, Jianrong; Liu, Zhenyu; Liu, Qingya; Guo, Shijie; Huang, Zhanggen; Xiao, Yong

2008-01-01

Supporting V 2 O 5 onto an activated coke (AC) has been reported to significantly increase the AC's activity in simultaneous SO 2 and NO removal from flue gas. To understand the role of V 2 O 5 on SO 2 removal, V 2 O 5 /AC is studied through SO 2 removal reaction, surface analysis, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) techniques. It is found that the main role of V 2 O 5 in SO 2 removal over V 2 O 5 /AC is to catalyze SO 2 oxidation through a VOSO 4 -like intermediate species, which reacts with O 2 to form SO 3 and V 2 O 5 . The SO 3 formed transfers from the V sites to AC sites and then reacts with H 2 O to form H 2 SO 4 . At low V 2 O 5 loadings, a V atom is able to catalyze as many as 8 SO 2 molecules to SO 3 . At high V 2 O 5 loadings, however, the number of SO 2 molecules catalyzed by a V atom is much less, due possibly to excessive amounts of V 2 O 5 sites in comparison to the pores available for SO 3 and H 2 SO 4 storage. (author)

Simultaneous absorption of SO2 and NO from flue gas with KMnO4/NaOH solutions

International Nuclear Information System (INIS)

Chu, H.; Chien, T.W.; Li, S.Y.

2001-01-01

The wet scrubbing combined SO x /NO x removal system is an advanced air pollution control device. This study attempts to understand the absorption kinetics in the system. The absorption of diluted SO 2 and simultaneous absorption of diluted SO 2 and NO, as occurs in flue gases, in a stirred tank reactor with KMnO 4 /NaOH solutions were carried out at 50C. The liquid-side and gas-side mass transfer coefficients of the system were determined. The results indicate that the absorption of SO 2 is close to completely gas-film controlled where the NaOH concentration is greater than 0.1 M or the KMnO 4 concentration is greater than 0.05 M. The increasing gas flow rate has a positive effect on the absorption rate of SO 2 . The existence of O 2 has no significant effect on the absorption rate of SO 2 . Adding SO 2 would decrease the absorption rate of NO; however, the addition of NO has no effect on the absorption rate of SO 2

A DFT study of SO2 and H2S gas adsorption on Au-doped single-walled carbon nanotubes

International Nuclear Information System (INIS)

Zhang, Xiaoxing; Dai, Ziqiang; Chen, Qinchuan; Tang, Ju

2014-01-01

Intrinsic carbon nanotubes (CNTs) show limited toxic gas detection, thus, we need to develop a method to fabricate a novel CNT sensor that has good sensitivity. In this study, density functional theory (DFT) was applied to determine the adsorption behavior of Au-doped single-walled carbon nanotubes (Au-SWCNTs) to SO 2 and H 2 S. The calculated results show that Au-SWCNTs have a high sensitivity to SO 2 and H 2 S. When SO 2 adsorbs on the surface of the nanotube, a large number of electrons transfer from the Au-SWCNT to SO 2 , which results in a decrease in the frontier orbital energy gap and an increase in electrical conductivity. On the other hand, when H 2 S adsorbs on the surface of the nanotube, the electrons transfer from H 2 S to the Au-SWCNT, the frontier orbital energy gap increases, and the electrical conductivity decreases. Thus, SO 2 and H 2 S could be detected by Au-SWCNTs. This conclusion is useful for the development of CNT-based gas sensors and provides a theoretical basis to fabricate Au-SWCNT-based gas sensors. (papers)

Aerosol formation on the flash photolysis of SO2/gas mixtures

International Nuclear Information System (INIS)

Fogel, L.D.; Sutherland, J.W.

1979-01-01

A long-lived transient absorption observed on the flash photolysis of SO 2 /gas mixtures at lambda> or =190 nm has been identified as resulting from light scattering by H 2 SO 4 aerosols. No detectable signals were monitored on photolysis at lambda> or =270 nm, indicating that the aerosol precursors originated from the promotion of SO 2 into its second singlet level and into its dissociation continuum. The SO 3 that was formed was hydrated immediately to yield H 2 SO 4 vapor in a highly supersaturated state and heteromolecular homogeneous nucleation to produce H 2 SO 4 aerosols ensued. This nucleation was quenched rapidly as the acid vapor was consumed by further nucleation, by condensation, and by vapor diffusion to the cell walls. A model was formulated in which the condensations of the H 2 SO 4 and the H 2 O vapors on the growing droplets were considered kinetically negligible and the particles grew by coagulation; simultaneously, they were lost by tranquil gravitational settling and by diffusion to the cell walls. Computer simulations demonstrated that the observed time dependence of the absorbance data (measured at a fixed wavelength) could be accounted for by this scheme. The effects of temperature, pressure, and wavelength (of the analyzing light) were also described satisfactorily by this model

Effect of gas release in hot molding on flexural strength of composite friction brake

Science.gov (United States)

Rusdja, Andy Permana; Surojo, Eko; Muhayat, Nurul; Raharjo, Wijang Wisnu

2018-02-01

Composite friction brake is a vital part of braking system which serves to reduce the speed of vehicle. To fulfill the requirement of brake performance, composite friction brake must have friction and mechanical characteristic as required. The characteristics of composite friction brake are affected by brake material formulation and manufacturing parameter. In the beginning of hot molding, intermittent hot pressing was carried out to release the gases that consist of ammonia gas and water vapor. In composite friction brake, phenolic resin containing hexamethylenetetramine (HMTA) is often used as a binder. During hot molding, the reaction of phenolic resin and HMTA forms ammonia gas. Hot molding also generates water vapor because raw materials absorb moisture from environment when they are placed in storage. The gas release in hot molding is supposed affecting mechanical properties because it avoid entrapped gas in composite, so that this research investigated effect of gas release on flexural strength. Manufacturing of composite specimen was carried out as follow: mixing of raw materials, cold molding, and hot molding. In this research, duration of intermittent hot pressing and number of gas release were varied. The flexural strength of specimen was measured using three point bending test. The results showed that flexural strength specimens that were manufactured without gas release, using 4 times gas release with intermittent hot pressing for 5 and 10 seconds were not remarkably different. Conversely, hot molding using 4 times gas release with intermittent hot pressing for 15 seconds decreased flexural strength of composite. Hot molding using 2, 4, and 8 times gas release with intermittent hot pressing for 10 seconds also had no effect on increasing flexural strength. Increasing of flexural strength of composite was obtained only by using 6 times gas release with intermittent hot pressing for 10 seconds.

Modelling isothermal fission gas release

International Nuclear Information System (INIS)

Uffelen, P. van

2002-01-01

The present paper presents a new fission gas release model consisting of two coupled modules. The first module treats the behaviour of the fission gas atoms in spherical grains with a distribution of grain sizes. This module considers single atom diffusion, trapping and fission induced re-solution of gas atoms associated with intragranular bubbles, and re-solution from the grain boundary into a few layers adjacent to the grain face. The second module considers the transport of the fission gas atoms along the grain boundaries. Four mechanisms are incorporated: diffusion controlled precipitation of gas atoms into bubbles, grain boundary bubble sweeping, re-solution of gas atoms into the adjacent grains and gas flow through open porosity when grain boundary bubbles are interconnected. The interconnection of the intergranular bubbles is affected both by the fraction of the grain face occupied by the cavities and by the balance between the bubble internal pressure and the hydrostatic pressure surrounding the bubbles. The model is under validation. In a first step, some numerical routines have been tested by means of analytic solutions. In a second step, the fission gas release model has been coupled with the FTEMP2 code of the Halden Reactor Project for the temperature distribution in the pellets. A parametric study of some steady-state irradiations and one power ramp have been simulated successfully. In particular, the Halden threshold for fission gas release and two simplified FUMEX cases have been computed and are summarised. (author)

Intercomparison of SO2 camera systems for imaging volcanic gas plumes

Science.gov (United States)

Kern, Christoph; Lübcke, Peter; Bobrowski, Nicole; Campion, Robin; Mori, Toshiya; Smekens, Jean-François; Stebel, Kerstin; Tamburello, Giancarlo; Burton, Mike; Platt, Ulrich; Prata, Fred

2015-07-01

SO2 camera systems are increasingly being used to image volcanic gas plumes. The ability to derive SO2 emission rates directly from the acquired imagery at high time resolution allows volcanic process studies that incorporate other high time-resolution datasets. Though the general principles behind the SO2 camera have remained the same for a number of years, recent advances in CCD technology and an improved understanding of the physics behind the measurements have driven a continuous evolution of the camera systems. Here we present an intercomparison of seven different SO2 cameras. In the first part of the experiment, the various technical designs are compared and the advantages and drawbacks of individual design options are considered. Though the ideal design was found to be dependent on the specific application, a number of general recommendations are made. Next, a time series of images recorded by all instruments at Stromboli Volcano (Italy) is compared. All instruments were easily able to capture SO2 clouds emitted from the summit vents. Quantitative comparison of the SO2 load in an individual cloud yielded an intra-instrument precision of about 12%. From the imagery, emission rates were then derived according to each group's standard retrieval process. A daily average SO2 emission rate of 61 ± 10 t/d was calculated. Due to differences in spatial integration methods and plume velocity determination, the time-dependent progression of SO2 emissions varied significantly among the individual systems. However, integration over distinct degassing events yielded comparable SO2 masses. Based on the intercomparison data, we find an approximate 1-sigma precision of 20% for the emission rates derived from the various SO2 cameras. Though it may still be improved in the future, this is currently within the typical accuracy of the measurement and is considered sufficient for most applications.

Fission gas release of MOX with heterogeneous structure

International Nuclear Information System (INIS)

Nakae, N.; Akiyama, H.; Kamimura, K; Delville, R.; Jutier, F.; Verwerft, M.; Miura, H.; Baba, T.

2015-01-01

It is very useful for fuel integrity evaluation to accumulate knowledge base on fuel behavior of uranium and plutonium mixed oxide (MOX) fuel used in light water reactors (LWRs). Fission gas release is one of fuel behaviors which have an impact on fuel integrity evaluation. Fission gas release behavior of MOX fuels having heterogeneous structure is focused in this study. MOX fuel rods with a heterogeneous fuel microstructure were irradiated in Halden reactor (IFA-702) and the BR-3/BR-2 CALLISTO Loop (CHIPS program). The 85 Kr gamma spectrometry measurements were carried out in specific cycles in order to examine the concerned LHR (Linear Heat Rate) for fission gas release in the CHIPS program. The concerned LHR is defined in this paper to be the LHR at which a certain additional fission gas release thermally occurs. Post-irradiation examination was performed to understand the fission gas release behavior in connection with the pellet microstructure. The followings conclusions can be made from this study. First, the concerned LHR for fission gas release is estimated to be in the range of 20-23 kW/m with burnup over 37 GWd/tM. It is moreover guessed that the concerned LHR for fission gas release tends to decrease with increasing burnup. Secondly It is observed that FGR (fission gas release rate) is positively correlated with LHR when the LHR exceeds the concerned value. Thirdly, when burnup dependence of fission gas release is discussed, effective burnup should be taken into account. The effective burnup is defined as the burnup at which the LHR should be exceed the concerned value at the last time during all the irradiation period. And fourthly, it appears that FGR inside Pu spots is higher than outside and that retained (not released) fission gases mainly exist in the fission gas bubbles. Since fission gases in bubbles are considered to be easily released during fuel temperature increase, this information is very important to estimate fission gas release behavior

Fission gas release from UO2 pellet fuel at high burn-up

International Nuclear Information System (INIS)

Vitanza, C.; Kolstad, E.; Graziani, U.

1979-01-01

Analysis of in-reactor measurements of fuel center temperature and rod internal pressure at the OECD Halden Reactor Project has led to the development of an empirical fission gas release model, which is described. The model originally derived from data obtained in the low and intermediate burn-up range, appears to give good predictions for rods irradiated to high exposures as well. PIE puncturing data from seven fuel rods, operated at relatively constant powers and peak center temperatures between 1900 and 2000 0 C up to approx. 40,000 MWd/t UO 2 , did not exhibit any burn-up enhancement on the fission gas release rate

Transient fission gas release from UO2 fuel for high temperature and high burnup

International Nuclear Information System (INIS)

Szuta, M.

2001-01-01

In the present paper it is assumed that the fission gas release kinetics from an irradiated UO 2 fuel for high temperature is determined by the kinetics of grain growth. A well founded assumption that Vitanza curve describes the change of uranium dioxide re-crystallization temperature and the experimental results referring to the limiting grain size presented in the literature are used to modify the grain growth model. Algorithms of fission gas release due to re-crystallization of uranium dioxide grains are worked out. The defect trap model of fission gas behaviour described in the earlier papers is supplemented with the algorithms. Calculations of fission gas release in function of time, temperature, burn-up and initial grain sizes are obtained. Computation of transient fission gas release in the paper is limited to the case where steady state of irradiation to accumulate a desired burn-up is performed below the temperature of re-crystallization then the subsequent step temperature increase follows. There are considered two kinds of step temperature increase for different burn-up: the final temperature of the step increase is below and above the re-crystallization temperature. Calculations show that bursts of fission gas are predicted in both kinds. The release rate of gas liberated for the final temperature above the re-crystallization temperature is much higher than for final temperature below the re-crystallization temperature. The time required for the burst to subside is longer due to grain growth than due to diffusion of bubbles and knock-out release. The theoretical results explain qualitatively the experimental data but some of them need to be verified since this sort of experimental data are not found in the available literature. (author)

Pulsed sub-microsecond dielectric barrier discharge treatment of simulated glass manufacturing industry flue gas: removal of SO2 and NOx

International Nuclear Information System (INIS)

Khacef, A; Cormier, J M

2006-01-01

Experiments were carried out to investigate the removal of SO 2 and NOx from simulated glass manufacturing industry flue gas containing O 2 , N 2 , NO, NO 2 , CO 2 , SO 2 and H 2 O using a sub-microsecond pulsed dielectric barrier discharge (DBD) at atmospheric pressure. Removal efficiencies of SO 2 and NOx (NO+NO 2 ) were achieved as a function of gas temperature for two specific energies and two initial NO, NO 2 and SO 2 concentrations. The higher SO 2 and NOx removal efficiencies were achieved in a gas stream containing 163 ppm of SO 2 , 523 ppm of NO, 49 ppm of NO 2 , 14% of CO 2 , 8% of O 2 , 16% of H 2 O and N 2 as balance. The experimental results were evaluated using the energy cost or W-value (eV/molecule removed). About 100% of SO 2 and 36% of NOx were removed at a gas temperature of 100 deg. C with an energy cost of about 45 eV/molecule removed and 36 eV/molecule removed, respectively. These results indicate that DBD plasmas have the potential to remove SO 2 and NOx from gas streams without additives

Investigation of delayed fission gas release

International Nuclear Information System (INIS)

Cayet, Nicolas

1996-05-01

The study of the fission gas release process in the high burnup rig IFA-562 has revealed a particular fuel behaviour: a delay in the fission gas release process. It appeared that an important release of gas was measured by the pressure transducers once the power had decreased, whereas, during steady-state operation, the pressure did not increase very much. After examinations, the gap size has been concluded to be the main parameter involving this delay. However the burnup could have been a potential factor, its role is mainly to close the gap by swelling. The observations of low burnup rods have shown the same delayed fission gas release, the gap being small by design and closed essentially by thermal expansion. The study of the kinetics has demonstrated the time-independency of the phenomenon. Thus the proposed mechanism driving this delayed fission gas release would involve three consecutives stages. During steady-state, the gas is released into the interlinkage network of grain boundary bubbles and cracks. Due to the closed gap, the gas is trapped in some void volumes, unable to escape the pellet. During power reduction, the gap and some old/new cracks open, immediately providing a path for the gas to the pressure transducers and explaining this delay in the fission gas release. (author)

Intercomparison of SO2 camera systems for imaging volcanic gas plumes

Science.gov (United States)

Kern, Christoph; Lübcke, Peter; Bobrowski, Nicole; Campion, Robin; Mori, Toshiya; Smekens, Jean-Francois; Stebel, Kerstin; Tamburello, Giancarlo; Burton, Mike; Platt, Ulrich; Prata, Fred

2015-01-01

SO2 camera systems are increasingly being used to image volcanic gas plumes. The ability to derive SO2 emission rates directly from the acquired imagery at high time resolution allows volcanic process studies that incorporate other high time-resolution datasets. Though the general principles behind the SO2 camera have remained the same for a number of years, recent advances in CCD technology and an improved understanding of the physics behind the measurements have driven a continuous evolution of the camera systems. Here we present an intercomparison of seven different SO2 cameras. In the first part of the experiment, the various technical designs are compared and the advantages and drawbacks of individual design options are considered. Though the ideal design was found to be dependent on the specific application, a number of general recommendations are made. Next, a time series of images recorded by all instruments at Stromboli Volcano (Italy) is compared. All instruments were easily able to capture SO2 clouds emitted from the summit vents. Quantitative comparison of the SO2 load in an individual cloud yielded an intra-instrument precision of about 12%. From the imagery, emission rates were then derived according to each group's standard retrieval process. A daily average SO2 emission rate of 61 ± 10 t/d was calculated. Due to differences in spatial integration methods and plume velocity determination, the time-dependent progression of SO2 emissions varied significantly among the individual systems. However, integration over distinct degassing events yielded comparable SO2 masses. Based on the intercomparison data, we find an approximate 1-sigma precision of 20% for the emission rates derived from the various SO2 cameras. Though it may still be improved in the future, this is currently within the typical accuracy of the measurement and is considered sufficient for most applications.

Recovery of SO2 and MgO from By-Products of MgO Wet Flue Gas Desulfurization.

Science.gov (United States)

Yan, Liyun; Lu, Xiaofeng; Wang, Quanhai; Guo, Qiang

2014-11-01

An industrial demonstration unit using natural gas as a heat source was built to calcine the by-products of MgO wet flue gas desulfurization from power plants; influencing factors on the SO 2 content in calciner gas were comprehensively analyzed; and an advantageous recycling condition of MgO and SO 2 from by-products was summarized. Results showed that the SO 2 content in the calciner gas was increased by more than 10 times under a lower excess air coefficient, a higher feed rate, a lower crystal water in by-products, and a higher feed port position. For the tests conducted under the excess air coefficient above and below one, the effect of the furnace temperature on the SO 2 content in the calciner gas was reversed. Results of activity analysis indicate that particles of MgO generated under the calcination temperature of 900-1,000°C had a high activity. In contrast, due to the slight sintering, MgO generated under the calcination temperature of 1,100°C had a low activity. To recycle SO 2 as well as MgO, a temperature range of 900-927°C for TE103 is proposed. These studies will prompt the desulfurization market diversification, reduce the sulfur's dependence on imports for making sulfuric acid, be meaningful to balance the usage of the natural resource in China, and be regarded as a reference for the development of this technology for other similar developing countries.

Finite element simulation of fission gas release and swelling in UO2 fuel pellets

International Nuclear Information System (INIS)

Denis, Alicia C.

1999-01-01

A fission gas release model is presented, which solves the atomic diffusion problem with xenon and krypton elements tramps produced by uranium fission during UO 2 nuclear fuel irradiation. The model considers intra and intergranular precipitation bubbles, its re dissolution owing to highly energetic fission products impact, interconnection of intergranular bubbles and gas sweeping by grain border in movement because of grain growth. In the model, the existence of a thermal gradient in the fuel pellet is considered, as well as temporal variations of fission rate owing to changes in the operation lineal power. The diffusion equation is solved by the finite element method and results of gas release and swelling calculation owing to gas fission are compared with experimental data. (author)

Treatment of reduced sulphur compounds and SO2 by Gas Phase Advanced Oxidation

DEFF Research Database (Denmark)

Meusinger, Carl; Bluhme, Anders Brostrøm; Ingemar, Jonas L.

2017-01-01

Reduced sulphur compounds (RSCs) emitted from pig farms are a major problem for agriculture, due to their health and environmental impacts and foul odour. This study investigates the removal of RSCs, including H2S, and their oxidation product SO2 using Gas Phase Advanced Oxidation (GPAO). GPAO...... is a novel air cleaning technique which utilises accelerated atmospheric chemistry to oxidise pollutants before removing their oxidation products as particles. Removal efficiencies of 24.5% and 3.9% were found for 461 ppb of H2S and 714 ppb of SO2 in a laboratory system (volumetric flow Q = 75 m3/h......). A numerical model of the reactor system was developed to explore the basic features of the system; its output was in fair agreement with the experiment. The model verified the role of OH radicals in initiating the oxidation chemistry. All sulphur removed from the gas phase was detected as particulate matter...

MnFe{sub 2}O{sub 4} as a gas sensor towards SO{sub 2} and NO{sub 2} gases

Energy Technology Data Exchange (ETDEWEB)

Rathore, Deepshikha, E-mail: deep.nano@gmail.com; Mitra, Supratim [Department of Natural Sciences, NIIT University, Neemrana, Rajasthan 301705 (India)

2016-05-06

The chemical co-precipitation method was used to synthesize MnFe{sub 2}O{sub 4} nanoparticles. Single cubic phase formation of nanoparticles was confirmed by X-ray diffraction technique. The average particle size of MnFe{sub 2}O{sub 4} nanoparticles was found to be 10.7 nm using Scherrer formula. The ultrafine powder of MnFe{sub 2}O{sub 4} nanoparticles was pressed to design pellet of 10 mm diameter and 1mm thickness. Copper electrodes have been deposited on the surface of pellet using silver paste in the form of capacitor. Fabricated gas sensing device of MnFe{sub 2}O{sub 4} nanoparticles was tested towards SO{sub 2} and NO{sub 2} gases. Cole-Cole plot of MnFe{sub 2}O{sub 4} was investigated with the help of electrochemical workstation. The performance of the sensors including sensitivity, response and recovery time was also determined. It was observed that the MnFe{sub 2}O{sub 4} nanoparticles are more sensible for NO{sub 2} gas as compared to SO{sub 2} gas.

Prediction of the UO/sub 2/ fission gas release data of Bellamy and Rich using a model recently developed by Combustion Engineering

International Nuclear Information System (INIS)

Freeburn, H.R.; Pati, S.R.

1983-01-01

The trend in the light water reactor industry to higher discharge burnups of UO/sub 2/ fuel rods has initiated the modification of existing fuel rod models to better account for high burnup effects. The degree to which fission gas release from UO/sub 2/ fuel is enhanced at higher burnup is being addressed in the process. Fission gas release modeling should include the separation of the individual effects of thermal diffusion and any burnup enhancement on the release. Although some modelers have interpreted the Bellamy and Rich data on fission gas release from UO/sub 2/ fuel in this fashion, they have assumed that below about 1250 0 C the gas release is not temperature-dependent, and this has led them to predict a very strong burnup enhancement of gas release above 20 MWd/kgU. More recent data, however, suggest that an appreciable amount of fission gas is released by a thermal diffusion mechanism at even lower temperatures and will add to the fission gas released due to the temperature-independent mechanisms of knockout and recoil

Experimental and simulation studies of iron oxides for geochemical fixation of CO2-SO2 gas mixtures

Science.gov (United States)

Garcia, Susana; Rosenbauer, Robert J.; Palandri, James; Maroto-Valer, M. Mercedes

2011-01-01

Iron-bearing minerals are reactive phases of the subsurface environment and could potentially trap CO2–SO2gas mixtures derived from fossil fuel combustion processes by their conversion to siderite (FeCO3) and dissolved sulfate. Changes in fluid and mineral compositions resulting from reactions, involving the co-injection of SO2 with CO2 were observed both theoretically and experimentally. Experiments were conducted with a natural hematite (α-Fe2O3) sample. A high pressure-high temperature apparatus was used to simulate conditions in geologic formations deeper than 800 m, where CO2 is in the supercritical state. Solid samples were allowed to react with a NaCl–NaOH brine and SO2-bearing CO2-dominated gas mixtures. The predicted equilibrium mineral assemblage at 100 °C and 250 bar became hematite, dawsonite (NaAl(OH)2CO3), siderite (FeCO3) and quartz (SiO2). Experimentally, siderite and dawsonite, derived from the presence of kaolinite (Al2Si2O5(OH)4) in the parent material, were present in residual solids at longer reaction time intervals, which agreed well with results from the modelling work.

Sulfate cooling effects on climate through in-cloud oxidation of anthropogenic SO2

International Nuclear Information System (INIS)

Lelieveld, J.; Heintzenberg, J.

1992-01-01

Anthropogenic SO 2 emissions may exert a significant cooling effect on climate in the Northern Hemisphere through backscattering of solar radiation by sulfate particles. Earlier estimates of the sulfate climate forcing were based on a limited number of sulfate-scattering correlation measurements from which a high sulfate-scattering efficiency was derived. Model results suggest that cloud processing of air is the underlying mechanism. aqueous phase oxidation of SO 2 into sulfate and the subsequent release of the dry aerosol by cloud evaporation render sulfate a much more efficient scatterer than through gas-phase SO 2 oxidation

Simultaneous removal of SO2, NO and Hg0 from flue gas by ferrate (VI) solution

International Nuclear Information System (INIS)

Zhao, Yi; Han, Yinghui; Guo, Tianxiang; Ma, Tianzhong

2014-01-01

Simultaneously removing SO 2 , NO and Hg 0 from flue gas was examined by ferrate (VI) solution at a bubbling reactor. The removal efficiencies of 100% for SO 2 , 64.8% for NO and 81.4% for Hg 0 were achieved respectively, under the optimum experimental conditions, in which concentration of ferrate (VI) solution was 0.25 mmol/L, solution pH was 8.0, flue gas flow rate was 1 L/min and reaction temperature was 320 K. Based on the discussions of the ferrate (VI) solution characteristics, the comparisons of the standard electrode potential (E 0 ) of ferrate (VI) solution with E 0 values of reactant, and the analysis of the reaction products, a mechanism of simultaneous removal was proposed. In the process of simultaneous removal, FeO 4 2− and HFeO 4 − as the dominant species of ferrate (VI), could rapidly oxidize SO 2 , NO, and Hg 0 into SO 4 2− , NO 3 − and Hg 2+ . - Highlights: • Prepared ferrate (VI) absorbent has excellent property of removing SO 2 , NO and Hg 0 . • 100% of SO 2 , 63.8% of NO and 83.6% of Hg 0 were simultaneously removed. • The simultaneous removal mechanism of SO 2 , NO and Hg 0 was proposed

Fission gas release behaviour in MOX fuels

International Nuclear Information System (INIS)

Viswanathan, U.K.; Anantharaman, S.; Sahoo, K.C.

2002-01-01

As a part of plutonium recycling programme MOX (U,Pu)O 2 fuels will be used in Indian boiling water reactors (BWR) and pressurised heavy water reactors (PHWR). Based on successful test irradiation of MOX fuel in CIRUS reactor, 10 MOX fuel assemblies have been loaded in the BWR of Tarapur Atomic Power Station (TAPS). Some of these MOX fuel assemblies have successfully completed the initial target average burnup of ∼16,000 MWD/T. Enhancing the burnup target of the MOX fuels and increasing loading of MOX fuels in TAPS core will depend on the feedback information generated from the measurement of released fission gases. Fission gas release behaviour has been studied in the experimental MOX fuel elements (UO 2 - 4% PuO 2 ) irradiated in pressurised water loop (PWL) of CIRUS. Eight (8) MOX fuel elements irradiated to an average burnup of ∼16,000 MWD/T have been examined. Some of these fuel elements contained controlled porosity pellets and chamfered pellets. This paper presents the design details of the experimental set up for studying fission gas release behaviour including measurement of gas pressure, void volume and gas composition. The experimental data generated is compared with the prediction of fuel performance modeling codes of PROFESS and GAPCON THERMAL-3. (author)

Reduction of prostate intrafraction motion using gas-release rectal balloons

International Nuclear Information System (INIS)

Su Zhong; Zhao Tianyu; Li Zuofeng; Hoppe, Brad; Henderson, Randy; Mendenhall, William; Nichols, R. Charles; Marcus, Robert; Mendenhall, Nancy

2012-01-01

Purpose: To analyze prostate intrafraction motion using both non-gas-release (NGR) and gas-release (GR) rectal balloons and to evaluate the ability of GR rectal balloons to reduce prostate intrafraction motion. Methods: Twenty-nine patients with NGR rectal balloons and 29 patients with GR balloons were randomly selected from prostate patients treated with proton therapy at University of Florida Proton Therapy Institute (Jacksonville, FL). Their pretreatment and post-treatment orthogonal radiographs were analyzed, and both pretreatment setup residual error and intrafraction-motion data were obtained. Population histograms of intrafraction motion were plotted for both types of balloons. Population planning target-volume (PTV) margins were calculated with the van Herk formula of 2.5Σ+ 0.7σ to account for setup residual errors and intrafraction motion errors. Results: Pretreatment and post-treatment radiographs indicated that the use of gas-release rectal balloons reduced prostate intrafraction motion along superior–inferior (SI) and anterior–posterior (AP) directions. Similar patient setup residual errors were exhibited for both types of balloons. Gas-release rectal balloons resulted in PTV margin reductions from 3.9 to 2.8 mm in the SI direction, 3.1 to 1.8 mm in the AP direction, and an increase from 1.9 to 2.1 mm in the left–right direction. Conclusions: Prostate intrafraction motion is an important uncertainty source in radiotherapy after image-guided patient setup with online corrections. Compared to non-gas-release rectal balloons, gas-release balloons can reduce prostate intrafraction motion in the SI and AP directions caused by gas buildup.

Reduction of prostate intrafraction motion using gas-release rectal balloons

Energy Technology Data Exchange (ETDEWEB)

Su Zhong; Zhao Tianyu; Li Zuofeng; Hoppe, Brad; Henderson, Randy; Mendenhall, William; Nichols, R. Charles; Marcus, Robert; Mendenhall, Nancy [Department of Radiation Oncology, University of Florida Proton Therapy Institute, Jacksonville, Florida 32206 (United States)

2012-10-15

Purpose: To analyze prostate intrafraction motion using both non-gas-release (NGR) and gas-release (GR) rectal balloons and to evaluate the ability of GR rectal balloons to reduce prostate intrafraction motion. Methods: Twenty-nine patients with NGR rectal balloons and 29 patients with GR balloons were randomly selected from prostate patients treated with proton therapy at University of Florida Proton Therapy Institute (Jacksonville, FL). Their pretreatment and post-treatment orthogonal radiographs were analyzed, and both pretreatment setup residual error and intrafraction-motion data were obtained. Population histograms of intrafraction motion were plotted for both types of balloons. Population planning target-volume (PTV) margins were calculated with the van Herk formula of 2.5{Sigma}+ 0.7{sigma} to account for setup residual errors and intrafraction motion errors. Results: Pretreatment and post-treatment radiographs indicated that the use of gas-release rectal balloons reduced prostate intrafraction motion along superior-inferior (SI) and anterior-posterior (AP) directions. Similar patient setup residual errors were exhibited for both types of balloons. Gas-release rectal balloons resulted in PTV margin reductions from 3.9 to 2.8 mm in the SI direction, 3.1 to 1.8 mm in the AP direction, and an increase from 1.9 to 2.1 mm in the left-right direction. Conclusions: Prostate intrafraction motion is an important uncertainty source in radiotherapy after image-guided patient setup with online corrections. Compared to non-gas-release rectal balloons, gas-release balloons can reduce prostate intrafraction motion in the SI and AP directions caused by gas buildup.

Deep Sludge Gas Release Event Analytical Evaluation

International Nuclear Information System (INIS)

Sams, Terry L.

2013-01-01

Long Abstract. Full Text. The purpose of the Deep Sludge Gas Release Event Analytical Evaluation (DSGRE-AE) is to evaluate the postulated hypothesis that a hydrogen GRE may occur in Hanford tanks containing waste sludges at levels greater than previously experienced. There is a need to understand gas retention and release hazards in sludge beds which are 200 -300 inches deep. These sludge beds are deeper than historical Hanford sludge waste beds, and are created when waste is retrieved from older single-shell tanks (SST) and transferred to newer double-shell tanks (DST).Retrieval of waste from SSTs reduces the risk to the environment from leakage or potential leakage of waste into the ground from these tanks. However, the possibility of an energetic event (flammable gas accident) in the retrieval receiver DST is worse than slow leakage. Lines of inquiry, therefore, are (1) can sludge waste be stored safely in deep beds; (2) can gas release events (GRE) be prevented by periodically degassing the sludge (e.g., mixer pump); or (3) does the retrieval strategy need to be altered to limit sludge bed height by retrieving into additional DSTs? The scope of this effort is to provide expert advice on whether or not to move forward with the generation of deep beds of sludge through retrieval of C-Farm tanks. Evaluation of possible mitigation methods (e.g., using mixer pumps to release gas, retrieving into an additional DST) are being evaluated by a second team and are not discussed in this report. While available data and engineering judgment indicate that increased gas retention (retained gas fraction) in DST sludge at depths resulting from the completion of SST 241-C Tank Farm retrievals is not expected and, even if gas releases were to occur, they would be small and local, a positive USQ was declared (Occurrence Report EM-RP--WRPS-TANKFARM-2012-0014, 'Potential Exists for a Large Spontaneous Gas Release Event in Deep Settled Waste Sludge'). The purpose of this technical

A fission gas release model

Energy Technology Data Exchange (ETDEWEB)

Denis, A; Piotrkowski, R [Argentine Atomic Energy Commission, Buenos Aires (Argentina)

1997-08-01

The hypothesis contained in the model developed in this work are as follows. The UO{sub 2} is considered as a collection of spherical grains. Nuclear reactions produce fission gases, mainly Xe and Kr, within the grains. Due to the very low solubility of these gases in UO{sub 2}, intragranular bubbles are formed, of a few nanometers is size. The bubbles are assumed to be immobile and to act as traps which capture gas atoms. Free atoms diffuse towards the grain boundaries, where they give origin to intergranular, lenticular bubbles, of the order of microns. The gas atoms in bubbles, either inter or intragranular, can re-enter the matrix through the mechanism of resolution induced by fission fragment impact. The amount of gas stored in intergranular bubbles grows up to a saturation value. Once saturation is reached, intergranular bubbles inter-connect and the gas in excess is released through different channels to the external surface of the fuel. The resolution of intergranular bubbles particularly affects the region of the grain adjacent to the grain boundary. During grain growth, the grain boundary traps the gas atoms, either free or in intragranular bubbles, contained in the swept volume. The grain boundary is considered as a perfect sink, i.e. the gas concentration is zero at that surface of the grain. Due to the spherical symmetry of the problem, the concentration gradient is null at the centre of the grain. The diffusion equation was solved using the implicit finite difference method. The initial solution was analytically obtained by the Laplace transform. The calculations were performed at different constant temperatures and were compared with experimental results. They show the asymptotic growth of the grain radius as a function of burnup, the gas distribution within the grain at every instant, the growth of the gas content at the grain boundary up to the saturation value and the fraction of gas released by the fuel element referred to the total gas generated

The effect of UO2 density on fission product gas release and sheath expansion

International Nuclear Information System (INIS)

Notley, M.J.F.; MacEwan, J.R.

1965-03-01

The effect of UO 2 density on fission product gas release and sheath expansion has been determined in an irradiation experiment in which the performance of fuel elements with densities between 10.42 and 10.74 g/cm 3 was compared at ∫λdθ values of 39 and 42 W/cm. The elements were irradiated as clusters of four in a pressurized water loop, hence their irradiation histories were identical. Fission product gas release and the extend of grain growth were greater for the lower density elements. Both effects can be attributed solely to the variation of the thermal conductivity of the fuel with the fractional porosity p, if λ p λ [1 - (2.6 ± 0.8) p] where λ is the thermal conductivity of fully dense UO 2 and λ p is that of the porous UO 2 . This expression is in agreement with laboratory findings. A correlation between the extent of grain growth in the UO 2 and the fractional gas release was found to exist in this test and was shown to apply in a large number of other fuel irradiations. Diametral sheath strain was lower for the low density fuel elements than for those of high density, although the former were deduced to have operated with higher central temperatures. It is supposed that the thermal expansion of the fuel can be partially accommodated by elimination of some of the original porosity. The data are consistent with the assumption that approximately half the porosity in the region of the fuel undergoing grain growth is eliminated. (author)

Noble Gas Release Signal as a Precursor to Fracture

Science.gov (United States)

Bauer, S. J.; Lee, H.; Gardner, W. P.

2017-12-01

We present empirical results of rock strain, microfracturing, acoustic emissions, and noble gas release from laboratory triaxial experiments for a granite, basalt, shale and bedded rock salt. Noble gases are released and measured real-time during deformation using mass spectrometry. The gas release represents a precursive signal to macrofracture. Gas release is associated with increased acoustic emissions indicating that microfracturing is required to release gas and create pathways for the gas to be sensed. The gas released depends on initial gas content, pore structure and its evolution during deformation, the deformation amount, matrix permeability, deformation style and the stress/strain history. Gases are released from inter and intracrystalline sites; release rate increases as strain and microfracturing increases. The gas composition depends on lithology, geologic history and age, fluids present, and radioisotope concentrations that affect radiogenic noble gas isotope (e.g. 4He,40Ar) production. Noble gas emission and its relationship to crustal processes such as seismicity and volcanism, tectonic velocities, qualitative estimates of deep permeability, age dating of groundwater, and a signature of nuclear weapon detonation. Our result show that mechanical deformation of crustal materials is an important process controlling gas release from rocks and minerals, and should be considered in techniques which utilize gas release and/or accumulation. We propose using noble gas release to signal rock deformation in boreholes, mines and waste repositories. We postulate each rock exhibits a gas release signature which is microstructure, stress, strain, and/or permanent deformation dependent. Calibration of such relationships, for example relating gas release per rock unit volume to strain may be used to quantify rock deformation and develop predictive models.Sandia National Laboratories is a multimission laboratory managed and operated by National Technology and

Non-Volcanic release of CO2 in Italy: quantification, conceptual models and gas hazard

Science.gov (United States)

Chiodini, G.; Cardellini, C.; Caliro, S.; Avino, R.

2011-12-01

Central and South Italy are characterized by the presence of many reservoirs naturally recharged by CO2 of deep provenance. In the western sector, the reservoirs feed hundreds of gas emissions at the surface. Many studies in the last years were devoted to (i) elaborating a map of CO2 Earth degassing of the region; (ii) to asses the gas hazard; (iii) to develop methods suitable for the measurement of the gas fluxes from different types of emissions; (iv) to elaborate the conceptual model of Earth degassing and its relation with the seismic activity of the region and (v) to develop physical numerical models of CO2 air dispersion. The main results obtained are: 1) A general, regional map of CO2 Earth degassing in Central Italy has been elaborated. The total flux of CO2 in the area has been estimated in ~ 10 Mt/a which are released to the atmosphere trough numerous dangerous gas emissions or by degassing spring waters (~ 10 % of the CO2 globally estimated to be released by the Earth trough volcanic activity). 2) An on line, open access, georeferenced database of the main CO2 emissions (~ 250) was settled up (http://googas.ov.ingv.it). CO2 flux > 100 t/d characterise 14% of the degassing sites while CO2 fluxes from 100 t/d to 10 t/d have been estimated for about 35% of the gas emissions. 3) The sites of the gas emissions are not suitable for life: the gas causes many accidents to animals and people. In order to mitigate the gas hazard a specific model of CO2 air dispersion has been developed and applied to the main degassing sites. A relevant application regarded Mefite d'Ansanto, southern Apennines, which is the largest natural emission of low temperature CO2 rich gases, from non-volcanic environment, ever measured in the Earth (˜2000 t/d). Under low wind conditions, the gas flows along a narrow natural channel producing a persistent gas river which has killed over a period of time many people and animals. The application of the physical numerical model allowed us to

TOXRISK, Toxic Gas Release Accident Analysis

International Nuclear Information System (INIS)

Bennett, D.E.; Chanin, D.I.; Shiver, A.W.

1993-01-01

1 - Description of program or function: TOXRISK is an interactive program developed to aid in the evaluation of nuclear power plant control room habitability in the event of a nearby toxic material release. The program uses a model which is consistent with the approach described in the NRC Regulatory Guide 1.78. Release of the gas is treated as an initial puff followed by a continuous plume. The relative proportions of these as well as the plume release rate are supplied by the user. Transport of the gas is modeled as a Gaussian distribution and occurs through the action of a constant velocity, constant direction wind. Great flexibility is afforded the user in specifying the release description, meteorological conditions, relative geometry of the accident and plant, and the plant ventilation system characteristics. Two types of simulation can be performed: multiple case (parametric) studies and probabilistic analyses. Upon execution, TOXRISK presents a menu, and the user chooses between the Data Base Manager, the Multiple Case program, and the Probabilistic Study Program. The Data Base Manager provides a convenient means of storing, retrieving, and modifying blocks of data required by the analysis programs. The Multiple Case program calculates resultant gas concentrations inside the control room and presents a summary of information that describes the event for each set of conditions given. Optimally, a time history profile of inside and outside concentrations can also be produced. The Probabilistic Study program provides a means for estimating the annual probability of operator incapacitation due to toxic gas accidents on surrounding transportation routes and storage sites. 2 - Method of solution: Dispersion or diffusion of the gas during transport is described by modified Pasquill-Gifford dispersion coefficients

Gas-phase hydrolysis of triplet SO2: A possible direct route to atmospheric acid formation

Science.gov (United States)

Donaldson, D. James; Kroll, Jay A.; Vaida, Veronica

2016-07-01

Sulfur chemistry is of great interest to the atmospheric chemistry of several planets. In the presence of water, oxidized sulfur can lead to new particle formation, influencing climate in significant ways. Observations of sulfur compounds in planetary atmospheres when compared with model results suggest that there are missing chemical mechanisms. Here we propose a novel mechanism for the formation of sulfurous acid, which may act as a seed for new particle formation. In this proposed mechanism, the lowest triplet state of SO2 (3B1), which may be accessed by near-UV solar excitation of SO2 to its excited 1B1 state followed by rapid intersystem crossing, reacts directly with water to form H2SO3 in the gas phase. For ground state SO2, this reaction is endothermic and has a very high activation barrier; our quantum chemical calculations point to a facile reaction being possible in the triplet state of SO2. This hygroscopic H2SO3 molecule may act as a condensation nucleus for water, giving rise to facile new particle formation (NPF).

Fission gas release and pellet microstructure change of high burnup BWR fuel

International Nuclear Information System (INIS)

Itagaki, N.; Ohira, K.; Tsuda, K.; Fischer, G.; Ota, T.

1998-01-01

UO 2 fuel, with and without Gadolinium, irradiated for three, five, and six irradiation cycles up to about 60 GWd/t pellet burnup in a commercial BWR were studied. The fission gas release and the rim effect were investigated by the puncture test and gas analysis method, OM (optical microscope), SEM (scanning electron microscope), and EPMA (electron probe microanalyzer). The fission gas release rate of the fuel rods irradiated up to six cycles was below a few percent; there was no tendency for the fission gas release to increase abruptly with burnup. On the other hand, microstructure changes were revealed by OM and SEM examination at the rim position with burnup increase. Fission gas was found depleted at both the rim position and the pellet center region using EPMA. There was no correlation between the fission gas release measured by the puncture test and the fission gas depletion at the rim position using EPMA. However, the depletion of fission gas in the center region had good correlation with the fission gas release rate determined by the puncture test. In addition, because the burnup is very large at the rim position of high burnup fuel and also due to the fission rate of the produced Pu, the Xe/Kr ratio at the rim position of high burnup fuel is close to the value of the fission yield of Pu. The Xe/Kr ratio determined by the gas analysis after the puncture test was equivalent to the fuel average but not to the pellet rim position. From the results, it was concluded that fission gas at the rim position was released from the UO 2 matrix in high burnup, however, most of this released fission gas was held in the porous structure and not released from the pellet to the free volume. (author)

Validation Studies of the Accuracy of Various SO2 Gas Retrievals in the Thermal InfraRed (8-14 μm)

Science.gov (United States)

Gabrieli, A.; Wright, R.; Lucey, P. G.; Porter, J. N.; Honniball, C.; Garbeil, H.; Wood, M.

2016-12-01

Quantifying hazardous SO2 in the atmosphere and in volcanic plumes is important for public health and volcanic eruption prediction. Remote sensing measurements of spectral radiance of plumes contain information on the abundance of SO2. However, in order to convert such measurements into SO2 path-concentrations, reliable inversion algorithms are needed. Various techniques can be employed to derive SO2 path-concentrations. The first approach employs a Partial Least Square Regression model trained using MODTRAN5 simulations for a variety of plume and atmospheric conditions. Radiances at many spectral wavelengths (8-14 μm) were used in the algorithm. The second algorithm uses measurements inside and outside the SO2 plume. Measurements in the plume-free region (background sky) make it possible to remove background atmospheric conditions and any instrumental effects. After atmospheric and instrumental effects are removed, MODTRAN5 is used to fit the SO2 spectral feature and obtain SO2 path-concentrations. The two inversion algorithms described above can be compared with the inversion algorithm for SO2 retrievals developed by Prata and Bernardo (2014). Their approach employs three wavelengths to characterize the plume temperature, the atmospheric background, and the SO2 path-concentration. The accuracy of these various techniques requires further investigation in terms of the effects of different atmospheric background conditions. Validating these inversion algorithms is challenging because ground truth measurements are very difficult. However, if the three separate inversion algorithms provide similar SO2 path-concentrations for actual measurements with various background conditions, then this increases confidence in the results. Measurements of sky radiance when looking through SO2 filled gas cells were collected with a Thermal Hyperspectral Imager (THI) under various atmospheric background conditions. These data were processed using the three inversion approaches

Simultaneous purifying of Hg0, SO2, and NOx from flue gas by Fe3+/H2O2: the performance and purifying mechanism.

Science.gov (United States)

Xing, Yi; Li, Liuliu; Lu, Pei; Cui, Jiansheng; Li, Qianli; Yan, Bojun; Jiang, Bo; Wang, Mengsi

2018-03-01

Hg 0 , SO 2 , and NOx result in heavily global environmental pollution and serious health hazards. Up to now, how to efficiently remove mercury with SO 2 and NOx from flue gas is still a tough task. In this study, series of high oxidizing Fenton systems were employed to purify the pollutants. The experimental results showed that Fe 3+ /H 2 O 2 was more suitable to purify Hg 0 than Fe 2+ /H 2 O 2 and Cu 2+ /H 2 O 2. The optimal condition includes Fe 3+ concentration of 0.008 mol/L, Hg 0 inlet concentration of 40 μg/m 3 , solution temperature of 50 °C, pH of 3, H 2 O 2 concentration of 0.7 mol/L, and O 2 percentage of 6%. When SO 2 and NOx were taken into account under the optimal condition, Hg 0 removal efficiency could be enhanced to 91.11% while the removal efficiency of both NOx and SO 2 was slightly declined, which was consistent to the analysis of purifying mechanism. The removal efficiency of Hg 0 was stimulated by accelerating the conversion of Fe 2+ to Fe 3+ , which resulted from the existence of SO 2 and NOx. The results of this study suggested that simultaneously purifying Hg 0 , SO 2 , and NOx from flue gas is feasible.

Mechanism of SO2 removal by carbon

Science.gov (United States)

Lizzio, Anthony A.; DeBarr, Joseph A.

1997-01-01

The reaction of SO2 with carbon (C) in the presence of O2 and H2O involves a series of reactions that leads to the formation of sulfuric acid as the final product. The rate-determining step in the overall process is the oxidation of SO2 to SO3. Three SO2 oxidation reactions are possible. Adsorbed SO2 (C−SO2) can react either with gas phase O2 or with adsorbed oxygen (C−O complex) to form sulfur trioxide (SO3), or gas phase SO2 can react directly with the C−O complex. In optimizing the SO2 removal capabilities of carbon, most studies only assume a given mechanism for SO2 adsorption and conversion to H2SO4 to be operable. The appropriate SO2 oxidation step and role of the C−O complex in this mechanism remain to be determined. The ultimate goal of this study was to prepare activated char from Illinois coal with optimal properties for low-temperature (80−150°C) removal of sulfur dioxide from coal combustion flue gas. The SO2 adsorption capacity of activated char was found to be inversely proportional to the amount of oxygen adsorbed on its surface. A temperature-programmed desorption technique was developed to titrate those sites responsible for adsorption of SO2 and conversion to H2SO4. On the basis of these results, a mechanism for SO2 removal by carbon was proposed. The derived rate expression showed SO2 adsorption to be dependent only on the fundamental rate constant and concentration of carbon atoms designated as free sites. Recent studies indicate a similar relationship exists between the rate of carbon gasification (in CO2 or H2O) and the number of reactive sites as determined by transient kinetics experiments. Utilizing the concept of active or free sites, it was possible to produce a char from Illinois coal having an SO2 adsorption capacity surpassing that of a commercial catalytic activated carbon.

Swift heavy ion irradiated SnO_2 thin film sensor for efficient detection of SO_2 gas

International Nuclear Information System (INIS)

Tyagi, Punit; Sharma, Savita; Tomar, Monika; Singh, Fouran; Gupta, Vinay

2016-01-01

Highlights: • Response of Ni"7"+ ion irradiated (100 MeV) SnO_2 film have been performed. • Effect of irradiation on the structural and optical properties of SnO_2 film is studied. • A decrease in operating temperature and increased response is seen after irradiation. - Abstract: Gas sensing response studies of the Ni"7"+ ion irradiated (100 MeV) and non-irradiated SnO_2 thin film sensor prepared under same conditions have been performed towards SO_2 gas (500 ppm). The effect of irradiation on the structural, surface morphological, optical and gas sensing properties of SnO_2 thin film based sensor have been studied. A significant decrease in operating temperature (from 220 °C to 60 °C) and increased sensing response (from 1.3 to 5.0) is observed for the sample after irradiation. The enhanced sensing response obtained for the irradiated SnO_2 thin film based sensor is attributed to the desired modification in the surface morphology and material properties of SnO_2 thin film by Ni"7"+ ions.

Fission gas and iodine release measured up to 15 GWd/t UO2 burnup

International Nuclear Information System (INIS)

Appelhans, A.D.

1983-01-01

A summary is presented of the measured release of xenon, krypton and iodine up to 15 GWd/t UO 2 burnup for fuel centerline temperatures ranging from 950 to 1800 K, at average linear heat ratings of 15 to 35 kW/m. The IFA-430 is composed of four 1.28-m-long fuel rods containing 10% enriched UO 2 pellet fuel. Two of the fuel rods are connected, top and bottom, to a gas flow system that permits the fission gases released from the fuel pellets to be swept out of the rods during irradiation and measured via gamma spectrometry. The release/burnup increased significantly between 10 and 15 GWd/t burnup. Fuel temperature did not change. Increased releases were due to physical changes in the fuel-surface area. Changes appeared to be due to higher power operation and burnup

Pilot-plant for NOx, SO2, HCl removal from flue-gas of municipal waste incinerator by electron beam irradiation

International Nuclear Information System (INIS)

Doi, Takeshi; Suda, Shoichi; Morishige, Atsushi; Tokunaga, Okihiro; Aoki, Yasushi; Sato, Shoichi; Komiya, Mikihisa; Hashimoto, Nobuo; Nakajima, Michihiro.

1992-01-01

A pilot-Plant for NO x , SO 2 and HCl removal from flue-gas of municipal waste incinerator by electron beam irradiation was designed and its construction at Matsudo City Waste Disposal Center was planned. The flue-gas of 1,000 Nm 3 /hr is guided from the waste incinerator flue-gas line of 30,000 Nm 3 /hr to the Pilot-Plant to be processed by spraying Ca(OH) 2 slurry (NKK-LIMAR Process) and irradiating high-energy electron beam of an accelerator. NO x , SO 2 and HCl are removed simultaneously from the flue-gas by the enhanced reaction with Ca(OH) 2 under irradiation. According to the basic research performed using a small size reactor at TRCRE of JAERI, the electron beam irradiation process was proved to be very effective for these harmful gases removal. Based on this result, the Pilot-Plant was designed for the demonstration of NO x , SO 2 and HCl removal performance using electron accelerator of maximum energy 0.95 MeV and maximum power 15 kW. The designing and planning were promoted by NKK in cooperation with JAERI and Matsudo City. (author)

Reversible physical absorption of SO2 by ionic liquids

DEFF Research Database (Denmark)

Huang, Jun; Riisager, Anders; Fehrmann, Rasmus

2006-01-01

Ionic liquids can reversibly absorb large amounts of molecular SO2 gas under ambient conditions with the gas captured in a restricted configuration, possibly allowing SO2 to probe the internal cavity structures in ionic liquids besides being useful for SO2 removal in pollution control....

Modelling intragranular fission gas release in irradiation of sintered LWR UO2 fuel

International Nuclear Information System (INIS)

Loesoenen, Pekka

2002-01-01

A model for the release of stable fission gases by diffuion from sintered LWR UO 2 fuel grains is presented. The model takes into account intragranular gas bubble behaviour as a function of grain radius. The bubbles are assumed to be immobile and the gas migrates to grain boundaries by diffusion of single gas atoms. The intragranular bubble population in the model at low burn-ups or temperatures consists of numerous small bubbles. The presence of the bubbles attenuates the effective gas atom diffusion coefficient. Rapid coarsening of the bubble population in increased burn-up at elevated temperatures weakens significantly the attenuation of the effective diffusion coefficient. The solution method introduced in earlier papers, locally accurate method, is enhanced to allow accurate calculation of the intragranular gas behaviour in time varying conditions without excessive computing time. Qualitatively the detailed model can predict the gas retention in the grain better than a more simple model

Apparatus and method for improving electrostatic precipitator performance by plasma reactor conversion of SO.sub.2 to SO.sub.3

Science.gov (United States)

Huang, Hann-Sheng; Gorski, Anthony J.

1999-01-01

An apparatus and process that utilize a low temperature nonequilibrium plasma reactor, for improving the particulate removal efficiency of an electrostatic precipitator (ESP) are disclosed. A portion of the flue gas, that contains a low level of SO.sub.2 O.sub.2 H.sub.2 O, and particulate matter, is passed through a low temperature plasma reactor, which defines a plasma volume, thereby oxidizing a portion of the SO.sub.2 present in the flue gas into SO.sub.3. An SO.sub.2 rich flue gas is thereby generated. The SO.sub.3 rich flue gas is then returned to the primary flow of the flue gas in the exhaust treatment system prior to the ESP. This allows the SO.sub.3 to react with water to form H.sub.2 SO.sub.4 that is in turn is absorbed by fly ash in the gas stream in order to improve the removal efficiency of the EPS.

A new mechanistic and engineering fission gas release model for a uranium dioxide fuel

International Nuclear Information System (INIS)

Lee, Chan Bock; Yang, Yong Sik; Kim, Dae Ho; Kim, Sun Ki; Bang, Je Geun

2008-01-01

A mechanistic and engineering fission gas release model (MEGA) for uranium dioxide (UO 2 ) fuel was developed. It was based upon the diffusional release of fission gases from inside the grain to the grain boundary and the release of fission gases from the grain boundary to the external surface by the interconnection of the fission gas bubbles in the grain boundary. The capability of the MEGA model was validated by a comparison with the fission gas release data base and the sensitivity analyses of the parameters. It was found that the MEGA model correctly predicts the fission gas release in the broad range of fuel burnups up to 98 MWd/kgU. Especially, the enhancement of fission gas release in a high-burnup fuel, and the reduction of fission gas release at a high burnup by increasing the UO 2 grain size were found to be correctly predicted by the MEGA model without using any artificial factor. (author)

A Green Desulfurization Technique: Utilization of Flue Gas SO2 to Produce H2 via a Photoelectrochemical Process Based on Mo-Doped BiVO4

Directory of Open Access Journals (Sweden)

Jin Han

2017-12-01

Full Text Available A green photoelectrochemical (PEC process with simultaneous SO2 removal and H2 production has attracted an increasing attention. The proposed process uses flue gas SO2 to improve H2 production. The improvement of the efficiency of this process is necessary before it can become industrial viable. Herein, we reported a Mo modified BiVO4 photocatalysts for a simultaneous SO2 removal and H2 production. And the PEC performance could be significantly improved with doping and flue gas removal. The evolution rate of H2 and removal of SO2 could be enhanced by almost three times after Mo doping as compared with pristine BiVO4. The enhanced H2 production and SO2 removal is attributed to the improved bulk charge carrier transportation after Mo doping, and greatly enhanced oxidation reaction kinetics on the photoanode due to the formation of SO32− after SO2 absorption by the electrolyte. Due to the utilization of SO2 to improve the production of H2, the proposed PEC process may become a profitable desulfurization technique.

A green desulfurization technique: utilization of flue gas SO2 to produce H2 via a photoelectrochemical process based on Mo-doped BiVO4

Science.gov (United States)

Han, Jin; Li, Kejian; Cheng, Hanyun; Zhang, Liwu

2017-12-01

A green photoelectrochemical (PEC) process with simultaneous SO2 removal and H2 production has attracted an increasing attention. The proposed process uses flue gas SO2 to improve H2 production. The improvement of the efficiency of this process is necessary before it can become industrial viable. Herein, we reported a Mo modified BiVO4 photocatalysts for a simultaneous SO2 removal and H2 production. And the PEC performance could be significantly improved with doping and flue gas removal. The evolution rate of H2 and removal of SO2 could be enhanced by almost 3 times after Mo doping as compared with pristine BiVO4. The enhanced H2 production and SO2 removal is attributed to the improved bulk charge carrier transportation after Mo doping, and greatly enhanced oxidation reaction kinetics on the photoanode due to the formation of SO32- after SO2 absorption by the electrolyte. Due to the utilization of SO2 to improve the production of H2, the proposed PEC process may become a profitable desulfurization technique.

Transient fission gas release during direct electrical heating experiments

International Nuclear Information System (INIS)

Fenske, G.R.; Emerson, J.E.; Savoie, F.E.

1983-12-01

The gas release behavior of irradiated EBR-II fuel was observed to be dependent on several factors: the presence of cladding, the retained gas content, and the energy absorbed. Fuel that retained in excess of 16 to 17 μmoles/g of fission gas underwent spallation as the cladding melted and released 22 to 45% of its retained gas, while fuel with retained gas levels below approx. 15 to 16 μmoles/g released less than approx. 9% of its gas as the cladding melted. During subsequent direct electrical heating ramps, fuel that did not spall released an additional quantity of gas (up to 4 μmoles/g), depending on the energy absorbed

Bubble development and fission gas release during rapid heating of 18 GWd/TeU UO2

International Nuclear Information System (INIS)

Small, G.J.

1985-01-01

Small samples (approximately 50 mg) of UO 2 irradiated to 18 GWd/TeU have been heated rapidly in an out-of-pile furnace. Ramp rates were in the range 10-80 deg. C.s -1 , peak temperatures varied from 1400 deg. C to 2500 deg. C and dwell times from one to fifteen min. The specimens were sealed in small capsules which were subsequently pierced to determine the total amount of fission gas ( 85 Kr) released during each test. Changes in the size and number of gas bubbles on grain boundaries were examined using SEM, TEM, replication and fractography techniques will be employed later. In this paper are reported the first series of gas release results and some metallography. The results are compared with related experiments and some qualitative conclusions are drawn regarding the mechanisms and kinetics of transient fission gas behaviour. (author)

Local Fission Gas Release and Swelling in Water Reactor Fuel during Slow Power Transients

DEFF Research Database (Denmark)

Mogensen, Mogens Bjerg; Walker, C.T.; Ray, I.L.F.

1985-01-01

Gas release and fuel swelling caused by a power increase in a water reactor fuel (burn-up 2.7–4.5% FIMA) is described. At a bump terminal level of about 400 W/cm (local value) gas release was 25–40%. The formation of gas bubbles on grain boundaries and their degree of interlinkage are the two...... factors that determine the level of fission gas release during a power bump. Release begins when gas bubbles on grain boundaries start o interlink. This occurred at r/r0 ~ 0.75. Release tunnels were fully developed at r/r0 ~ 0.55 with the result that gas release was 60–70% at this position....

The conversion of SO{sub 2} to SO{sub 3} in gas turbine engines

Energy Technology Data Exchange (ETDEWEB)

Miake-Lye, R C; Anderson, M R; Brown, R C; Kolb, C E [Aerodyne Research, Inc., Billerica, MA (United States). Center for Chemical and Environmental Physics; Sorokin, A A; Buriko, Y I [Scientific Research Center ` Ecolen` , Moscow (Russian Federation)

1998-12-31

The oxidation of fuel sulfur to S(6) (SO{sub 3}+H{sub 2}SO{sub 4}) in a supersonic (Concorde) and a subsonic (ATTAS) aircraft engine is estimated numerically. The results indicate between 2% and 10% of the fuel sulfur is emitted as S(6). It is also shown that conversion in the turbine is limited by the level of atomic oxygen at the combustor exit, resulting in a higher oxidation efficiency as the sulfur mass loading is decreased. SO{sub 2} and SO{sub 3} are the primary sulfur oxidation products, with less than 1% of fuel sulfur converted to H{sub 2}SO{sub 4}. For the Concorde, H{sub 2}SO{sub 4} was primarily formed during the supersonic expansion through the divergent nozzle. (author) 20 refs.

The conversion of SO{sub 2} to SO{sub 3} in gas turbine engines

Energy Technology Data Exchange (ETDEWEB)

Miake-Lye, R.C.; Anderson, M.R.; Brown, R.C.; Kolb, C.E. [Aerodyne Research, Inc., Billerica, MA (United States). Center for Chemical and Environmental Physics; Sorokin, A.A.; Buriko, Y.I. [Scientific Research Center `Ecolen`, Moscow (Russian Federation)

1997-12-31

The oxidation of fuel sulfur to S(6) (SO{sub 3}+H{sub 2}SO{sub 4}) in a supersonic (Concorde) and a subsonic (ATTAS) aircraft engine is estimated numerically. The results indicate between 2% and 10% of the fuel sulfur is emitted as S(6). It is also shown that conversion in the turbine is limited by the level of atomic oxygen at the combustor exit, resulting in a higher oxidation efficiency as the sulfur mass loading is decreased. SO{sub 2} and SO{sub 3} are the primary sulfur oxidation products, with less than 1% of fuel sulfur converted to H{sub 2}SO{sub 4}. For the Concorde, H{sub 2}SO{sub 4} was primarily formed during the supersonic expansion through the divergent nozzle. (author) 20 refs.

LIFAC flue gas desulfurization process an alternative SO{sub 2} control strategy

Energy Technology Data Exchange (ETDEWEB)

Patel, J.G. [Tampella Power Corp., Atlanta, GA (United States); Vilala, J. [Tampella Power Inc., Tampere (Finland)

1995-12-01

This paper discusses the results from two recently completed LIFAC flue gas desulfurization plants - 300 MW Shand lignite powered station owned by Saskatchewan Power Corporation and 60 MW Whitewater Valley high sulfur coal fired station owned by Richmond Powerand Light. LIFACis a dry FGD process in which limestone is injected into the upper regions of the boiler furnace and an activation reactor is used to humidify the unreacted limestone to achieve additional sulfur capture. The performance in both plants indicates that 70 to 80% sulfur is removed at a Ca/S ratio of 2. Cost performance data from these plants has shown that LI FAC both on construction cost and $/ton SO{sub 2} removed basis is very cost competitive compared to other SO{sub 2} control technologies. The Richmond plant has been realized under the auspices of the U.S. Department of Energy`s Clean Coal Technology program. The Shand plant is the first commercial installation in North America. The paper also discusses highlights of operating and maintenance experience, availability and handling of the solid waste product.

Screening of inorganic gases released from firework-rockets by a gas chromatography/whistle-accelerometer method.

Science.gov (United States)

Chen, Kuan-Fu; Wu, Hui-Hsin; Lin, Chien-Hung; Lin, Cheng-Huang

2013-08-30

The use of an accelerometer for detecting inorganic gases in gas chromatography (GC) is described. A milli-whistle was connected to the outlet of the GC capillary and was used instead of a classical GC detector. When the GC carrier gases and the sample gases pass through the milli-whistle, a sound is produced, leading to vibrational changes, which can be recorded using an accelerometer. Inorganic gases, including SO2, N2 and CO2, which are released from traditional Chinese firework-rockets at relatively high levels as the result of burning the propellant and explosive material inside could be rapidly determined using the GC/whistle-accelerometer system. The method described herein is safe, the instrumentation is compact and has potential to be modified so as to be portable for use in the field. It also can be used in conjunction with FID (flame ionization detector) or TCD (thermal conductivity detector), in which either no response for FID (CO2, N2, NO2, SO2, etc.) or helium gas is needed for TCD, respectively. Copyright © 2013 Elsevier B.V. All rights reserved.

[Adsorption and removal of gas-phase Hg(0) over a V2O5/AC catalyst in the presence of SO2].

Science.gov (United States)

Wang, Jun-wei; Yang, Jian-li; Liu, Zhen-yu

2009-12-01

The adsorption and removal behaviors of gas-phase Hg(0) over V2O5/AC and AC were studied under a simulated flue gas (containing N2, SO2, O2) in a fixed-bed reactor. The influences of the V2O5, loading, SO2 concentration and adsorption temperature on Hg0 adsorption were investigated. The speciation of mercury adsorbed was determined by X-ray photoelectron spectroscopy (XPS). It was found that the V2O5/AC catalyst has a much higher capability than AC for Hg(0) adsorption and removal, mainly because of the catalytic oxidation activity of V2O5. The Hg(0) adsorption capability depends on the V2O5 content of the V2O5/AC catalyst. The amounts of mercury adsorbed increase from 75.9 microg x g(-1) to 89.6 microg x g(-1) (in the absence of O2) and from 115.9 microg x g(-1) to 185.5 microg x g(-1) (in the presence of O2) as the V2O5 loading increases from 0.5% to 1.0%, which are much higher than those over AC under the same conditions (9.6 microg x g(-1) and 23.3 microg x g(-1)). SO2 in the flue gas enhances Hg(0) adsorption over the V2O5/AC catalyst, which is due to the reaction of SO2 and Hg(0) on V2O3/AC. But as the SO2 concentration increases from 500 x 10(-6) to 2000 x 10(-6), the amount of mercury adsorbed has only a slight increase. The optimal temperature for Hg(0) adsorption over the V2O5/AC catalyst is around 150 degrees C, at which the amounts of mercury adsorbed are up to 98.5 microg x g(-1) (in the absence of O2) and 187.7 microg x g(-1) (in the presence of O2). The XPS results indicate the formation of Hg(0) and HgSO4 on the surface of the V2O5/AC catalyst, which confirms the role of V2O5 and SO2.

Structural Characterization of 1,1,3,3-Tetramethylguanidinium Chloride Ionic Liquid by Reversible SO2 Gas Absorption

DEFF Research Database (Denmark)

Berg, Rolf W.; Harris, Pernille; Riisager, Anders

2013-01-01

A unique new ionic liquid−gas adduct solid state compound formed between 1,1,3,3-tetramethylguanidinium chloride ([tmgH]Cl) and sulfur dioxide has been characterized by X-ray diffraction and Raman spectroscopy. The structure contains SO2 molecules of near normal structure kept at their positions ...... with bromide and iodide are discussed. Some of these salts may prove useful as reversible absorbents of SO2 in industrial flue gases....

Validating the accuracy of SO2 gas retrievals in the thermal infrared (8-14 μm)

Science.gov (United States)

Gabrieli, Andrea; Porter, John N.; Wright, Robert; Lucey, Paul G.

2017-11-01

Quantifying sulfur dioxide (SO2) in volcanic plumes is important for eruption predictions and public health. Ground-based remote sensing of spectral radiance of plumes contains information on the path-concentration of SO2. However, reliable inversion algorithms are needed to convert plume spectral radiance measurements into SO2 path-concentrations. Various techniques have been used for this purpose. Recent approaches have employed thermal infrared (TIR) imaging between 8 μm and 14 μm to provide two-dimensional mapping of plume SO2 path-concentration, using what might be described as "dual-view" techniques. In this case, the radiance (or its surrogate brightness temperature) is computed for portions of the image that correspond to the plume and compared with spectral radiance obtained for adjacent regions of the image that do not (i.e., "clear sky"). In this way, the contribution that the plume makes to the measured radiance can be isolated from the background atmospheric contribution, this residual signal being converted to an estimate of gas path-concentration via radiative transfer modeling. These dual-view approaches suffer from several issues, mainly the assumption of clear sky background conditions. At this time, the various inversion algorithms remain poorly validated. This paper makes two contributions. Firstly, it validates the aforementioned dual-view approaches, using hyperspectral TIR imaging data. Secondly, it introduces a new method to derive SO2 path-concentrations, which allows for single point SO2 path-concentration retrievals, suitable for hyperspectral imaging with clear or cloudy background conditions. The SO2 amenable lookup table algorithm (SO2-ALTA) uses the MODTRAN5 radiative transfer model to compute radiance for a variety (millions) of plume and atmospheric conditions. Rather than searching this lookup table to find the best fit for each measured spectrum, the lookup table was used to train a partial least square regression (PLSR) model

The uptake of SO2 on Saharan dust: a flow tube study

Directory of Open Access Journals (Sweden)

J. W. Adams

2005-01-01

Full Text Available The uptake of SO2 onto Saharan mineral dust from the Cape Verde Islands was investigated using a coated wall flow tube coupled to a mass spectrometer. The rate of loss of SO2 to the dust coating was measured and uptake coefficients were determined using the measured BET surface area of the sample. The uptake of SO2, with an initial concentration between (2-40x1010molecule cm-3 (0.62-12 µTorr, was found to be strongly time dependent over the first few hundred seconds of an experiment, with an initial uptake γ0,BET of (6.6±0.8x10-5 (298 K, declining at longer times. The amount of SO2 adsorbed on the dust samples was measured over a range of SO2 concentrations and mineral dust loadings. The uptake of SO2 was found to be up to 98% irreversible over the timescale of these investigations. Experiments were also performed at 258 K, at a relative humidity of 27% and at 298 K in the presence of ozone. The initial uptake and the amount of SO2 taken up per unit area of BET dust surface was the same within error, irrespective of the conditions used; however the presence of ozone reduced the amount of SO2 released back into the gas-phase per unit area once exposure of the surface ended. Multiple uptakes to the same surface revealed a loss of surface reactivity, which did not return if the samples were exposed to gas-phase water, or left under vacuum overnight. A mechanism which accounts for the observed uptake behaviour is proposed and numerically modelled, allowing quantitative estimates of the rate and amount of SO2 removal in the atmosphere to be estimated. Removal of SO2 by mineral dust is predicted to be significant at high dust loadings.

Persistent explosive activity at Stromboli investigated with OP-FTIR and SO2 cameras

Science.gov (United States)

Burton, M. R.; La Spina, A.; Sawyer, G. M.; Harris, A. J.

2012-12-01

Stromboli volcano in Italy exhibits what is perhaps one of the most well-known examples of cyclic activity, in the form of its regular explosions, which send a few m3 of material 100-200 m into the air every 10-20 minutes. Recent developments in measurements of volatile release from Stromboli using a series of novel approaches have allowed this cyclic behaviour to be examined in detail. In particular, the use of an automated OP-FTIR has revealed unprecedented detail in the dynamics of degassing from individual craters at the summit of Stromboli. Furthermore, the variations in composition of explosive degassing from Stromboli demonstrate a deep source ~2 km for the gas slugs which produce explosions at this volcano, in contrast to the commonly-held view that gas coalescence at shallow depth is responsible for the behaviour. The SO2 camera has revealed fascinating new details on the dynamics of degassing at Stromboli, and has allowed direct quantification of the amount of gas released during explosions and through quiescent degassing. The remarkable observation that 99% of degassing takes place quiescently, and that the explosions, whilst apparently more significant, are in fact a secondary process compared with the mass and energy involved in background, quiet processes. The new insight that the explosions are actually only a relatively minor aspect of the activity (in terms of mass and energy) actually makes the regularity of the cyclic explosive activity still more remarkable. In this paper we present a detailed overview of the state of the art of our understanding of cyclic explosive activity at Stromboli volcano from the perspective of recent advances in geochemical monitoring of the gas emissions. We also report initial results from a multidisciplinary campaign on Stromboli which utilised both OP-FTIR and SO2 camera techniques.

Simulation experiments on the radial pool growth in gas-releasing melting system

International Nuclear Information System (INIS)

Farhadieh, R.; Purviance, R.; Carlson, N.

1983-01-01

Following an HCDA, molten core-debris can contact the concrete foundation of the reactor building resulting in a molten UO 2 /concrete interaction and considerable gas release. The released gas can pressurize the containment building potentially leading to radiological releases. Furthermore, directional growth of the molten core-debris pool can reduce the reactor building structural integrity. To implement design changes that insure structural integrity, an understanding of the thermal-hydraulic and mass-transfer process associated with such a growth is most desirable. Owing to the complex nature of the combined heat, mass, and hydrodynamic processes associated with the two-dimensional problem of gas release and melting, the downward and radial penetration problems have been investigated separately. The present experimental study addresses the question of sideward penetration of the molten core debris into a gas-releasing, meltable, miscible solid

Fission gas release from fuel at high burnup

International Nuclear Information System (INIS)

Meyer, R.O.; Beyer, C.E.; Voglewede, J.C.

1978-03-01

The release of fission gas from fuel pellets at high burnup is reviewed in the context of the safety analysis performed for reactor license applications. Licensing actions are described that were taken to correct deficient gas release models used in these safety analyses. A correction function, which was developed by the Nuclear Regulatory Commission staff and its consultants, is presented. Related information, which includes some previously unpublished data, is also summarized. The report thus provides guidance for the analysis of high burnup gas release in licensing situations

Conditions for a partial summation of SO2 and NO2 hazardous effect in gas emission regulations

Science.gov (United States)

Sokolov, A. K.

2017-12-01

In order to provide environmental safety, the concentrations of SO2 and SO2 in the surface layer of atmospheric air should not exceed corresponding one-time values accepted for maximum permissible concentrations (MPCs). The only document that provides a normative calculation of hazardous substance dispersion in the atmospheric air up to the present time is presented by regulations OND-86. It has established that, in taking into account the summation (unidirectionality) of hazardous action of substances (including SO2 and NO2 gases), the sum of their relative concentrations should not exceed unity. A novel standard GN 2.1.6.2326-08 stipulates that "nitrogen dioxide and sulfur dioxide have a partial summation of action; therefore the sum of their relative concentrations should not exceed 1.6." This paper is devoted to analyzing the calculation of the summation of action for SO2 and NO2 gases and proving that the condition established in GN 2.1.6.2326-08 is not quite correct. According to the condition required by standard GN 2.1.6.2326-08, it turns out that, for some combinations of concentrations, the hazardous effect of gases is not added together, but one gas compensates an effect of the other, which contradicts the points of OND-86. For example, at SO2 and NO2 concentrations amounting to 0.6 and 0.04, respectively, the condition required by standard GN 2.1.6.2326-08 is satisfied, although the concentration of SO2 exceeds a normatively fixed value of MPC = 0.5. The graphical analysis of a concentration region for SO2 and NO2 gases clearly shows the areas where the condition required by standard GN 2.1.6.2326-08 is satisfied, but the environmental safety according to OND-86 is not provided. Recommendations are proposed for the correction of requirements established by standard GN 2.1.6.2326-08.

The gas release programs to increase competition in the European gas market

International Nuclear Information System (INIS)

Clastres, Cedric

2005-01-01

Regulators have implemented asymmetric regulation measures, such as gas release programs and market share targets, because of European gas supply features and gas market specificities. Empirical experiences show in line with economic theory that these regulation measures favour entry and competition without deterring investments. If we look at impacts on competition, they are mitigated. Some positive effects result from the increase in consumption or in importation and transportation infrastructure developments. But these regulations can also encourage anti-competitive behaviours like collusion, cream-skimming, reverse cherry picking or inefficient entries. Gas release measures establish a link between the incumbent and its competitors. A system of constraints on operators capacities can also appear. Thus, pricing or quantity strategies are more complex. Equilibrium prices are more volatile and very different of competition mark-up. The incumbent, for high gas release quantities and low supplies, can increase its costs to make more profit. This Raising Rivals' Costs strategy often occur if the gas release price is closer to supply costs. This strategy does not impact on consumers surplus but decreases welfare. The regulator can restore incentives to efficiency by setting gas release proportion function of incumbent's supplies. This proportion must be high enough to have a positive impact on the market because of incumbent's incentives to efficiency and greater total quantities sold by the two operators. But, on another way, it must not be too high as it could, thus, increase the probability of Raising Rivals' Costs or favour collusive strategies. (author) [fr

Long-term stability of FeSO{sub 4} and H{sub 2}SO{sub 4} treated chromite ore processing residue (COPR): Importance of H{sup +} and SO{sub 4}{sup 2−}

Energy Technology Data Exchange (ETDEWEB)

Wang, Xin [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhang, Jingdong [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Wang, Linling, E-mail: wanglinling@mail.hust.edu.cn [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Chen, Jing, E-mail: chenjing@mail.hust.edu.cn [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Hou, Huijie; Yang, Jiakuan [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Lu, Xiaohua [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

2017-01-05

Highlights: • The long-term stability of the FeSO{sub 4}-H{sub 2}SO{sub 4} treated COPR was evaluated. • Reliable long-term stability for samples curing 400 days was achieved. • H{sub 2}SO{sub 4} significantly enhanced the stabilization efficiency of COPR using FeSO{sub 4}. • H{sup +} and SO{sub 4}{sup 2−} both reinforced Cr(VI) release from COPR core to react with Fe(II). - Abstract: In this study, the long-term stability of Cr(VI) in the FeSO{sub 4} and H{sub 2}SO{sub 4} (FeSO{sub 4}-H{sub 2}SO{sub 4}) treated chromite ore processing residue (COPR) after 400 curing days and the stabilization mechanisms were investigated. FeSO{sub 4}-H{sub 2}SO{sub 4} treatment significantly reduced toxicity characteristic leaching procedure (TCLP) and synthetic precipitation leaching procedure (SPLP) Cr(VI) concentrations to lower than the regulatory limit of 1.5 mg L{sup −1} (HJ/T 301-2007, China EPA) even for the samples curing 400 days, achieving an outstanding long-term stability. Our independent leaching tests revealed that H{sup +} and SO{sub 4}{sup 2−} have synergistic effect on promoting the release of Cr(VI), which would make Cr(VI) easier accessed by Fe(II) during stabilization. The contributions of H{sup +} and SO{sub 4}{sup 2−} to Cr(VI) release ratio were 25%–44% and 19%–38%, respectively, as 5 mol H{sub 2}SO{sub 4} per kg COPR was used. X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and alkaline digestion analyses were also employed to interpret the possible stabilization mechanism. Cr(VI) released from COPR solid was reduced to Cr(III) by Fe(II), and then formed stable Fe{sub x}Cr{sub (1−x)}(OH){sub 3} precipitate. This study provides a facile and reliable scheme for COPR stabilization, and verifies the excellent long-term stability of the FeSO{sub 4}-H{sub 2}SO{sub 4} treated COPR.

Gas retention and release behavior in Hanford single-shell waste tanks

International Nuclear Information System (INIS)

Stewart, C.W.; Brewster, M.E.; Gauglitz, P.A.; Mahoney, L.A.; Meyer, P.A.; Recknagle, K.P.; Reid, H.C.

1996-12-01

This report describes the current understanding of flammable gas retention and release in Hanford single-shell waste tanks based on theory, experimental results, and observations of tank behavior. The single-shell tanks likely to pose a flammable gas hazard are listed and described, and photographs of core extrusions and the waste surface are included. The credible mechanisms for significant flammable gas releases are described, and release volumes and rates are quantified as much as possible. The only mechanism demonstrably capable of producing large (∼100 m 3 ) spontaneous gas releases is the buoyant displacement, which occurs only in tanks with a relatively deep layer of supernatant liquid. Only the double-shell tanks currently satisfy this condition. All release mechanisms believed plausible in single-shell tanks have been investigated, and none have the potential for large spontaneous gas releases. Only small spontaneous gas releases of several cubic meters are likely by these mechanisms. The reasons several other postulated gas release mechanisms are implausible or incredible are also given

Oxidation of SO2 and formation of water droplets under irradiation of 20MeV protons in N2/H2O/SO2

DEFF Research Database (Denmark)

Tomita, Shigeo; Nakai, Yoichi; Funada, Shuhei

2015-01-01

We have performed an experiment on charged droplet formation in a humidified N2 gas with trace SO2 concentration and induced by 20MeV proton irradiation. It is thought that SO2 reacts with the chemical species, such as OH radicals, generated through the reactions triggered by N2+ production. Both...

Gas retention and release behavior in Hanford single-shell waste tanks

Energy Technology Data Exchange (ETDEWEB)

Stewart, C.W.; Brewster, M.E.; Gauglitz, P.A.; Mahoney, L.A.; Meyer, P.A.; Recknagle, K.P.; Reid, H.C.

1996-12-01

This report describes the current understanding of flammable gas retention and release in Hanford single-shell waste tanks based on theory, experimental results, and observations of tank behavior. The single-shell tanks likely to pose a flammable gas hazard are listed and described, and photographs of core extrusions and the waste surface are included. The credible mechanisms for significant flammable gas releases are described, and release volumes and rates are quantified as much as possible. The only mechanism demonstrably capable of producing large ({approximately}100 m{sup 3}) spontaneous gas releases is the buoyant displacement, which occurs only in tanks with a relatively deep layer of supernatant liquid. Only the double-shell tanks currently satisfy this condition. All release mechanisms believed plausible in single-shell tanks have been investigated, and none have the potential for large spontaneous gas releases. Only small spontaneous gas releases of several cubic meters are likely by these mechanisms. The reasons several other postulated gas release mechanisms are implausible or incredible are also given.

Effect of flue gas composition on deposit induced high temperature corrosion under laboratory conditions mimicking biomass firing. Part II: Exposures in SO2 containing atmospheres

DEFF Research Database (Denmark)

Okoro, Sunday Chukwudi; Kiamehr, Saeed; Montgomery, Melanie

2017-01-01

SO2. Scanning electron microscopy (SEM), energy dispersive X-rayspectroscopy (EDS) and X-ray diffraction (XRD) techniques werecomplimentarily applied to characterize the resulting corrosion products. Apartially molten K2SO4-layer formed on KCl coated specimens, and corrosionresulted in localized......In biomass fired power plants, the fast corrosion of superheaters is facilitatedby the presence of corrosive flue gas species, for example, SO2, which arereleased during combustion. To understand the role of the gas species on thecorrosion process, comparative laboratory exposures of deposit (KCl......)-coatedand deposit-free austenitic stainless steel (TP 347H FG) samples to gas mixturescontaining SO2 was carried out, under conditions relevant to biomass-firing.Exposures were conducted isothermally at 560 8C for 72 h, in oxidizingsulphidizing,and oxidizing-sulphidizing-chlorinating gas mixtures containing60 ppmv...

Aerosol particle charger and an SO2 reactor using energetic electrons

International Nuclear Information System (INIS)

Davis, R.H.

1984-01-01

Two properties of energetic electrons in gas, their high specific ionization and their production of radicals and other chemically active specie, have promising applications to the cleanup of flue gas from coal combustion. The copious ionization has been used in a test particle charger to electrically charge 1 and 3 μm particles for subsequent removal by electrostatic precipitation. Particle charge greater than 5 times the theoretical ionic charging value for 1 μm particles have been observed in a bi-electrode electron beam precharger in which the beam energy is matched with the electrode spacing. In another test device, pulsed streamer coronas have been used to release and to energize electrons which promote gas phase chemical reactions and remote sulfur dioxide from humid air with high efficiency. The energized electrons produce oxidant radicals and chemically active specie which convert the SO 2 into sulfuric acid mist. While reported separately here, the two applications of energetic electrons may be amenable to combination in an integrated system for the combined treatment of flue gas

SO3 tinges stack gas from scrubbed coal-fired units

International Nuclear Information System (INIS)

Jones, C.; Ellison, W.

1998-01-01

The small amount of SO 3 in flue gas creates enough problems inside the plant. New US EPA regulations on so-called air toxics are making SO 3 discharge an emission problem as well - and a visible one at that. Units that have installed wet scrubbers to control SO 2 emissions may be most affected. The article explains that SO 3 levels in coal-fired power plants are mainly increased by catalytic oxidation of SO 2 by iron oxide on the fireside surfaces of the superheater tubes. Dependence on air-heater temperature is discussed. Wet FGD systems are responsible for the formation of 'blue eye' where SO 3 causes a blue hue in the plume. Ammonia injection has been effective in reducing SO 3 vapour, as has injecting water ahead of the electrostatic precipitator. Replacement of a wet ESP with a dry ESP is also a solution. 2 figs

Emission of SO2, CO2, and H2S from Augustine Volcano, 2002-2008: Chapter 26 in The 2006 eruption of Augustine Volcano, Alaska

Science.gov (United States)

McGee, Kenneth A.; Doukas, Michael P.; McGimsey, Robert G.; Neal, Christina A.; Wessels, Rick L.; Power, John A.; Coombs, Michelle L.; Freymueller, Jeffrey T.

2010-01-01

Airborne surveillance of gas emissions from Augustine Volcano and other Cook Inlet volcanoes began in 1990 to identify baseline emission levels during noneruptive conditions. Gas measurements at Augustine for SO2, CO2, and H2S showed essentially no evidence of anomalous degassing through spring 2005. Neither did a measurement on May 10, 2005, right after the onset of low level seismicity and inflation. The following measurement, on December 20, 2005, showed Augustine to be degassing about 600 metric tons per day (t/d) of SO2, and by January 4, 2006, only 7 days before the first explosive event, SO2 emissions had climbed to ten times that amount. Maximum emission rates measured during the subsequent eruption were: 8,930 t/d SO2 (February 24, 2006), 1,800 t/d CO2 (March 9, 2006), and 4.3 t/d H2S (January 19, 2006). In total, 45 measurements for SO2 were made from December 2005 through the end of 2008, with 19 each for CO2 and H2S during the same period. Molar CO2/SO2 ratios averaged about 1.6. In general, SO2 emissions appeared to increase during inflation of the volcanic edifice, whereas CO2 emissions were at their highest during the period of deflation associated with the vigorous effusive phase of the eruption in March. High SO2 was probably associated with degassing of shallow magma, whereas high CO2 likely reflected deep (>4 km) magma recharge of the sub-volcanic plumbing system, For the 2005–6 period, the volcano released a total of about 1.5×106 tons of CO2 to the atmosphere, a level similar to the annual output of a medium-sized natural-gas-fired powerplant. Augustine also emitted about 8×105 tons of SO2, similar to that produced by the 1976 and 1986 eruptions of the volcano.

A fission gas release model for MOX fuel and its verification

International Nuclear Information System (INIS)

Koo, Y.H.; Sohn, D.S.; Strijov, P.

2000-01-01

A fission gas release model for MOX fuel has been developed based on a model for UO 2 fuel. Using the concept of equivalent cell, the model considers the uneven distribution of Pu within the fuel matrix and a number of Pu-rich particles that could lead to a non-uniform fission rate and fission gas distribution across the fuel pellet. The model has been incorporated into a code, COSMOS, and some parametric studies were made to analyze the effect of the size and Pu content of Pu-rich agglomerates. The model was then applied to the experimental data obtained from the FIGARO program, which consisted of the base irradiation of MOX fuels in the BEZNAU-1 PWR and the subsequent irradiation of four refabricated fuel segments in the Halden reactor. The calculated gas releases show good agreement with the measured ones. In addition, the present analysis indicates that the microstructure of the MOX fuel used in the FIGARO program is such that it has produced little difference in terms of gas release compared with UO 2 fuel. (author)

Fundamental Study of Disposition and Release of Methane in a Shale Gas Reservoir

Energy Technology Data Exchange (ETDEWEB)

Wang, Yifeng [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Nuclear Waste Disposal Research and Analysis; Xiong, Yongliang [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Repository Performance; Criscenti, Louise J. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Geochemistry; Ho, Tuan Ahn [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Geochemistry; Weck, Philippe F. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Storage and Transportation Technology; Ilgen, Anastasia G. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Geochemistry; Matteo, Edward [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Nuclear Waste Disposal Research and Analysis; Kruichak, Jessica N. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Nuclear Waste Disposal Research and Analysis; Mills, Melissa M. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Nuclear Waste Disposal Research and Analysis; Dewers, Thomas [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Geomechanics; Gordon, Margaret E. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States). Dept. of Materials, Devices and Energy Technologies; Akkutlu, Yucel [Texas A & M Univ., College Station, TX (United States). Dept. of Petroleum Engineering

2016-09-01

simulations also indicate that a significant fraction (3 - 35%) of methane deposited in kerogen can potentially become trapped in isolated nanopores and thus not recoverable. We have successfully established experimental capabilities for measuring gas sorption and desorption on shale and model materials under a wide range of physical and chemical conditions. Both low and high pressure measurements show significant sorption of CH₄ and CO₂ onto clays, implying that methane adsorbed on clay minerals could contribute a significant portion of gas-in-place in an unconventional reservoir. We have also studied the potential impact of the interaction of shale with hydrofracking fluid on gas sorption. We have found that the CH₄-CO₂ sorption capacity for the reacted sample is systematically lower (by a factor of ~2) than that for the unreacted (raw) sample. This difference in sorption capacity may result from a mineralogical or surface chemistry change of the shale sample induced by fluid-rock interaction. Our results shed a new light on mechanistic understanding gas release and production decline in unconventional reservoirs.

Swift heavy ion irradiated SnO{sub 2} thin film sensor for efficient detection of SO{sub 2} gas

Energy Technology Data Exchange (ETDEWEB)

Tyagi, Punit; Sharma, Savita [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India); Tomar, Monika [Department of Physics, Miranda House, University of Delhi, Delhi 110007 (India); Singh, Fouran [Inter University Accelerator Center, Aruna Asaf Ali Marg, New Delhi 110067 (India); Gupta, Vinay, E-mail: drguptavinay@gmail.com [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India)

2016-07-15

Highlights: • Response of Ni{sup 7+} ion irradiated (100 MeV) SnO{sub 2} film have been performed. • Effect of irradiation on the structural and optical properties of SnO{sub 2} film is studied. • A decrease in operating temperature and increased response is seen after irradiation. - Abstract: Gas sensing response studies of the Ni{sup 7+} ion irradiated (100 MeV) and non-irradiated SnO{sub 2} thin film sensor prepared under same conditions have been performed towards SO{sub 2} gas (500 ppm). The effect of irradiation on the structural, surface morphological, optical and gas sensing properties of SnO{sub 2} thin film based sensor have been studied. A significant decrease in operating temperature (from 220 °C to 60 °C) and increased sensing response (from 1.3 to 5.0) is observed for the sample after irradiation. The enhanced sensing response obtained for the irradiated SnO{sub 2} thin film based sensor is attributed to the desired modification in the surface morphology and material properties of SnO{sub 2} thin film by Ni{sup 7+} ions.

A microstructure-dependent model for fission product gas release and swelling in UO2 fuel

International Nuclear Information System (INIS)

Notley, M.J.F.; Hastings, I.J.

1979-06-01

A model for the release of fission gas from irradiated UO2 fuel is presented. It incorporates fission gas diffusion bubble and grain boundary movement,intergranular bubble formation and interlinkage. In addition, the model allows estimates of the extent of structural change and fuel swelling. In the latter, contributions of thermal expansion, densification, solid fission products, and gas bubbles are considered. When included in the ELESIM fuel performance code, the model yields predictions which are in good agreement with data from UO2 fuel elements irradiated over a range of water-cooled reactor conditions: linear power outputs between 40 and 120 kW/m, burnups between 10 and 300 MW.h/kg U and power histories including constant, high-to-low and low-to-high power periods. The predictions of the model are shown to be most sensitive to fuel power (temperature), the selection of diffusion coefficient for fission gas in UO2 and burnup. The predictions are less sensitive to variables such as fuel restraint, initial grain size and the rate of grain growth. (author)

GRSIS program to predict fission gas release and swelling behavior of metallic fast reactor fuel

International Nuclear Information System (INIS)

Lee, Chan Bock; Lee, Byung Ho; Nam, Cheol; Sohn, Dong Seong

1999-03-01

A mechanistic model of fission gas release and swelling for the U-(Pu)-Zr metallic fuel in the fast reactor, GRSIS (Gas Release and Swelling in ISotropic fuel matrix) was developed. Fission gas bubbles are assumed to nucleate isotropically from the gas atoms in the metallic fuel matrix since they can nucleate at both the grain boundaries and the phase boundaries which are randomly distributed inside the grain. Bubbles can grow to larger size by gas diffusion and coalition with other bubbles so that they are classified as three classes depending upon their sizes. When bubble swelling reaches the threshold value, bubbles become interconnected each other to make the open channel to the external free space, that is, the open bubbles and then fission gases inside the interconnected open bubbles are released instantaneously. During the irradiation, fission gases are released through the open bubbles. GRSIS model can take into account the fuel gap closure by fuel bubble swelling. When the fuel gap is closed by fuel swelling, the contact pressure between fuel and cladding in relation to the bubble swelling and temperature is calculated. GRSIS model was validated by comparison with the irradiation test results of U-(Pu)-Zr fuels in ANL as well as the parametric studies of the key variable in the model. (author). 13 refs., 1 tab., 22 figs

GRSIS program to predict fission gas release and swelling behavior of metallic fast reactor fuel

Energy Technology Data Exchange (ETDEWEB)

Lee, Chan Bock; Lee, Byung Ho; Nam, Cheol; Sohn, Dong Seong

1999-03-01

A mechanistic model of fission gas release and swelling for the U-(Pu)-Zr metallic fuel in the fast reactor, GRSIS (Gas Release and Swelling in ISotropic fuel matrix) was developed. Fission gas bubbles are assumed to nucleate isotropically from the gas atoms in the metallic fuel matrix since they can nucleate at both the grain boundaries and the phase boundaries which are randomly distributed inside the grain. Bubbles can grow to larger size by gas diffusion and coalition with other bubbles so that they are classified as three classes depending upon their sizes. When bubble swelling reaches the threshold value, bubbles become interconnected each other to make the open channel to the external free space, that is, the open bubbles and then fission gases inside the interconnected open bubbles are released instantaneously. During the irradiation, fission gases are released through the open bubbles. GRSIS model can take into account the fuel gap closure by fuel bubble swelling. When the fuel gap is closed by fuel swelling, the contact pressure between fuel and cladding in relation to the bubble swelling and temperature is calculated. GRSIS model was validated by comparison with the irradiation test results of U-(Pu)-Zr fuels in ANL as well as the parametric studies of the key variable in the model. (author). 13 refs., 1 tab., 22 figs.

Comparison of FISGAS swelling and gas release predictions with experiment

International Nuclear Information System (INIS)

Ostensen, R.W.

1979-01-01

FISGAS calculations were compared to fuel swelling data from the FD1 tests and to gas release data from the FGR39 test. Late swelling and gas release predictions are satisfactory if vacancy depletion effects are added to the code. However, early swelling predictions are not satisfactory, and early gas release predictions are very poor. Explanation of these discrepancies is speculative

Fission gas release from the sintered UO{sub 2} fuel; Oslobadjanje fisionih gasova iz goriva od sinterovanog UO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Sigulinski, F; Stevanovic, M [Institute of Nuclear Sciences Boris Kidric, Vinca, Beograd (Yugoslavia)

1966-11-15

This paper shoes the phenomena which control fission gases release from the sintered UO{sub 2} dependent of the burnup rate: ejection, release, diffusion, increased fission gas accumulation causing structural changes in the fuel. release of fission gases from the fuel for power reactors was studied as well. The influence of factors as temperature, characteristics of fuel, burnup rate and burnup level was analyzed. Prikazani su mehanizmi koji kontrolisu izdvajanje fisionih gasova iz sinterovanog UO{sub 2} pri razlicitim brzinama izgaranja: izletanje, izbijanje, difuzija, povecano izdvajanje fisionih gasova koje prati strukturne promene u gorivu. Razmatrano je proucavanje izdvajanja fisionih gasova iz goriva za reaktore snage. Analiziran je uticaj faktora kao sto su temperatura, karakteristike goriva, brzina i stepen izgaranja (author)

Calculations of Fission Gas Release During Ramp Tests Using Copernic Code

Energy Technology Data Exchange (ETDEWEB)

Tong, Liu [Nuclear Fuel R and D Center, China Nuclear Power Technology Research Institute (CNPRI) (China)

2013-03-15

The report performed under IAEA research contract No.15951 describes the results of fuel performance evaluation of LWR fuel rods operated at ramp conditions using the COPERNIC code developed by AREVA. The experimental data from the Third Riso Fission Gas Project and the Studsvik SUPER-RAMP Project presented in the IFPE database of the OECD/NEA has been utilized for assessing the code itself during simulation of fission gas release (FGR). Standard code models for LWR fuel were used in simulations with parameters set properly in accordance with relevant test reports. With the help of data adjustment, the input power histories are restructured to fit the real ones, so as to ensure the validity of FGR prediction. The results obtained by COPERNIC show that different models lead to diverse predictions and discrepancies. By comparison, the COPERNIC V2.2 model (95% Upper bound) is selected as the standard FGR model in this report and the FGR phenomenon is properly simulated by the code. To interpret the large discrepancies of some certain PK rods, the burst effect of FGR which is taken into consideration in COPERNIC is described and the influence of the input power histories is extrapolated. In addition, the real-time tracking capability of COPERNIC is tested against experimental data. In the process of investigation, two main dominant factors influencing the measured gas release rate are described and different mechanisms are analyzed. With the limited predicting capacity, accurate predictions cannot be carried out on abrupt changes of FGR during ramp tests by COPERNIC and improvements may be necessary to some relevant models. (author)

Role of fission gas release in reactor licensing

International Nuclear Information System (INIS)

1975-11-01

The release of fission gases from oxide pellets to the fuel rod internal voidage (gap) is reviewed with regard to the required safety analysis in reactor licensing. Significant analyzed effects are described, prominent gas release models are reviewed, and various methods used in the licensing process are summarized. The report thus serves as a guide to a large body of literature including company reports and government documents. A discussion of the state of the art of gas release analysis is presented

Experience of iodine, caesium and noble gas release from AGR failures

International Nuclear Information System (INIS)

Chapman, C.J.; Harris, A.M.; Phillips, M.E.

1985-01-01

In the event of a fuel failure in an Advanced Gas Cooled Reactor (AGR), the quantity of fission products available for release to the environment is determined by the transport of fission products in the UO 2 fuel, by the possible retention of fission products in the fuel can interspace and by the deposition of fission products on gas circuit surfaces ('plate-out'). The fission products of principal radiological concern are radioactive caesium (Cs-137 and Cs-134) and iodine (principally I-131). Results are summarised of a number of experiments which were designed to study the release of these fission products from individual fuel failures in the prototype AGR at Windscale. Results are also presented of fission product release from failures in commercial AGRs. Comparisons of measured releases of caesium and iodine relative to the release of the noble gas fission products show that, for some fuel failures, there is a significant retention of caesium and iodine within the fuel can interspace. Under normal conditions circuit deposition reduces caesium and iodine gas concentrations by several orders of magnitude. Differing release behaviour of caesium and iodine from the failures is examined together with subsequent deposition within the sampling equipment. These observations are important factors which must be considered in developing an understanding of the mechanisms involved in circuit deposition. (author)

High-Temperature Corrosion of AlCrSiN Film in Ar-1%SO2 Gas

Directory of Open Access Journals (Sweden)

Poonam Yadav

2017-03-01

Full Text Available AlCrSiN film with a composition of 29.1Al-17.1Cr-2.1Si-51.7N in at. % was deposited on a steel substrate by cathodic arc ion plating at a thickness of 1.8 μm. It consisted of nanocrystalline hcp-AlN and fcc-CrN, where a small amount of Si was dissolved. Corrosion tests were carried out at 800 °C for 5–200 h in Ar-1%SO2 gas. The major corrosion reaction was oxidation owing to the high oxygen affinity of Al and Cr in the film. The formed oxide scale consisted primarily of (Al,Cr2O3, within which Fe, Si, and S were dissolved. Even after corrosion for 200 h, the thickness of the scale was about 0.7–1.2 μm, indicating that the film had good corrosion resistance in the SO2-containing atmosphere.

Conversion degree of SO{sub 2} into SO{sub 3} and SO{sub x} emissions in steam generators; Grado de conversion de SO{sub 2} en SO{sub 3} y emisiones de SO{sub x} en generadores de vapor

Energy Technology Data Exchange (ETDEWEB)

Espinoza Garza, Jesus; Penna Garcia, Adriana; Huerta Espino, Mario [Instituto de Investigaciones Electricas, Cuernavaca (Mexico)

1996-12-31

A large part of the electric energy produced in this country is obtained burning fossil fuels as primary energy source. These fuels are mainly coal, fuel oil, and natural gas. The first two have high percentages of sulfur, therefore producing and emitting to the air different amounts of sulfur dioxide (SO{sub 2}) and sulfur trioxide (SO{sub 3}). The relationship between this two contaminants varies depending on the type of steam generator, the rated capacity, and most of all on the sulfur content in the fuel and on the combustion system operating conditions. [Espanol] Una gran parte de la energia electrica generada en el pais se obtiene utilizando combustibles fosiles como fuente primaria de energia. Estos combustibles son principalmente carbon, combustoleo y gas natural. Los dos primeros tienen altos porcentajes de azufre, con lo cual se producen y emiten a la atmosfera diferentes cantidades de dioxido de azufre (SO{sub 2}) y trioxido de azufre (SO{sub 3}). La relacion entre estos dos contaminantes varia dependiendo del tipo de generador de vapor, la capacidad nominal y, sobre todo, de la concentracion de azufre en el combustible y de las condiciones de operacion del sistema de combustion.

Conversion degree of SO{sub 2} into SO{sub 3} and SO{sub x} emissions in steam generators; Grado de conversion de SO{sub 2} en SO{sub 3} y emisiones de SO{sub x} en generadores de vapor

Energy Technology Data Exchange (ETDEWEB)

Espinoza Garza, Jesus; Penna Garcia, Adriana; Huerta Espino, Mario [Instituto de Investigaciones Electricas, Cuernavaca (Mexico)

1997-12-31

A large part of the electric energy produced in this country is obtained burning fossil fuels as primary energy source. These fuels are mainly coal, fuel oil, and natural gas. The first two have high percentages of sulfur, therefore producing and emitting to the air different amounts of sulfur dioxide (SO{sub 2}) and sulfur trioxide (SO{sub 3}). The relationship between this two contaminants varies depending on the type of steam generator, the rated capacity, and most of all on the sulfur content in the fuel and on the combustion system operating conditions. [Espanol] Una gran parte de la energia electrica generada en el pais se obtiene utilizando combustibles fosiles como fuente primaria de energia. Estos combustibles son principalmente carbon, combustoleo y gas natural. Los dos primeros tienen altos porcentajes de azufre, con lo cual se producen y emiten a la atmosfera diferentes cantidades de dioxido de azufre (SO{sub 2}) y trioxido de azufre (SO{sub 3}). La relacion entre estos dos contaminantes varia dependiendo del tipo de generador de vapor, la capacidad nominal y, sobre todo, de la concentracion de azufre en el combustible y de las condiciones de operacion del sistema de combustion.

[Effect of SO2 volume fraction in flue gas on the adsorption behaviors adsorbed by ZL50 activated carbon and kinetic analysis].

Science.gov (United States)

Gao, Ji-xian; Wang, Tie-feng; Wang, Jin-fu

2010-05-01

The influence of SO2 dynamic adsorption behaviors using ZL50 activated carbon for flue gas desulphurization and denitrification under different SO2 volume fraction was investigated experimentally, and the kinetic analysis was conducted by kinetic models. With the increase of SO2 volume fraction in flue gas, the SO2 removal ratio and the activity ratio of ZL50 activated carbon decreased, respectively, and SO2 adsorption rate and capacity increased correspondingly. The calculated results indicate that Bangham model has the best prediction effect, the chemisorption processes of SO2 was significantly affected by catalytic oxidative reaction. The adsorption rate constant of Lagergren's pseudo first order model increased with the increase of inlet SO, volume fraction, which indicated that catalytic oxidative reaction of SO2 adsorbed by ZL50 activated carbon may be the rate controlling step in earlier adsorption stage. The Lagergren's and Bangham's initial adsorption rate were deduced and defined, respectively. The Ho's and Elovich's initial adsorption rate were also deduced in this paper. The Bangham's initial adsorption rate values were defined in good agreement with those of experiments. The defined Bangham's adsorptive reaction kinetic model can describe the SO2 dynamic adsorption rate well. The studied results indicated that the SO2 partial order of initial reaction rate was one or adjacent to one, while the O2 and water vapor partial order of initial reaction rate were constants ranging from 0.15-0.20 and 0.45-0.50, respectively.

Relative Release-to-Birth Indicators for Investigating TRISO Fuel Fission Gas Release Models

International Nuclear Information System (INIS)

Harp, Jason M.; Hawari, Ayman I.

2008-01-01

TRISO microsphere fuel is the fundamental fuel unit for Very High Temperature Reactors (VHTR). A single TRISO particle consists of an inner kernel of uranium dioxide or uranium oxycarbide surrounded by layers of pyrolytic carbon and silicon carbide. If the silicon carbide layer fails, fission products, especially the noble fission gases Kr and Xe, will begin to escape the failed particle. The release of fission gas is usually quantified by measuring the ratio of the released activity (R) to the original birth activity (B), which is designated as the R/B ratio. In this work, relative Release-to-Birth indicators (I) are proposed as a technique for interpreting the results of TRISO irradiation experiments. By implementing a relative metric, it is possible to reduce the sensitivity of the indicators to instrumental uncertainties and variations in experimental conditions. As an example, relative R/B indicators are applied to the interpretation of representative data from the Advanced Gas Reactor-1 TRISO fuel experiment that is currently taking place at the Advanced Test Reactor of Idaho National Laboratory. It is shown that the comparison of measured to predicted relative R/B indicators (I) gives insight into the physics of release and helps validate release models. Different trends displayed by the indicators are related to the mechanisms of fission gas release such as diffusion and recoil. The current analysis shows evidence for separate diffusion coefficients for Kr and Xe and supports the need to account for recoil release. (authors)

Modeling of the fluid dynamics and SO{sub 2} absorption in a gas-liquid reactor

Energy Technology Data Exchange (ETDEWEB)

Marocco, L. [Alstom Power Italy, Milan (Italy)

2010-08-01

This paper illustrates a computational fluid dynamic (CFD) model of a counter-current Open Spray Tower desulphurisation reactor and its application in the simulation of a full-scale industrial equipment. The raw flue gas flows upward while a suspension of water and limestone is sprayed downward from different heights. Thereby sulfur dioxide is washed out of the gas. The two-phase gas-liquid flow inside the equipment has been simulated with an Euler-Lagrange approach using a commercial CFD code, while a model for the SO{sub 2} absorption has been developed and implemented in the software through dedicated modules. Physical absorption is modeled using dual-film theory and appropriate empirical and semi-empirical correlations. The aqueous phase chemistry accounts for the instantaneous equilibrium reactions of eight dissolved species into a slurry droplet. The model is used to simulate an industrial plant at different operating conditions. The numerical results are in good agreement with the measured values of pressure drop and sulphur removal efficiency.

Future prices and market for SO2 allowances

International Nuclear Information System (INIS)

Sanghi, A.; Joseph, A.; Michael, K.; Munro, W.; Wang, J.

1993-01-01

The expected price of SO 2 emission allowances is an important issue in energy and integrated resource planning activities. For example, the expected price of SO 2 allowances in needed in order to evaluate alternative strategies for meeting SO 2 provisions of the Clean Air Act Amendments of 1990. In addition, the expected SO 2 allowance price is important to state public utility regulators who must provide guidance on rate-making issues regarding utility compliance plans which involve allowance trading and direct investment of SO 2 control technologies. Last but not the least, the expected SO 2 allowance price is an important determinant of the future market for natural gas and low sulfur coal. The paper develops estimates of SO 2 allowance prices over time by constructing national supply and demand curves for SO 2 reductions. Both the supply and demand for SO 2 reductions are based on an analysis of the sulfur content of fuels burned in 1990 by utilities throughout the United States; and on assumptions about plant retirements, the rate of new capacity growth, the types of new and replacement plants constructed, the costs of SO 2 reduction measures and legislation by midwest states to maintain the use of high sulfur coal to protect local jobs. The paper shows that SO 2 allowance prices will peak around the year 2000 at about $500 per ton, and will eventually fall to zero by about the year 2020. A sensitivity analysis indicates that the price of SO 2 allowances is relatively insensitive to assumptions regarding the availability of natural gas or energy demand growth. However, SO 2 allowance prices tend to be quite sensitive to assumptions regarding regulations which may force early retirement of existing power plants and possible legislation which may reduce CO 2 emissions

Towards a mechanistic understanding of transient fission gas release

International Nuclear Information System (INIS)

Matthews, J.R.; Small, G.J.

1989-01-01

Recent experimental results on transient fission gas release from oxide fuels are briefly reviewed. These together with associated microstructural observations are compared with the main models for fission gas behaviour. Single gas atom diffusion, bubble migration, heterogeneous percolation and grain boundary sweeping are examined as possible release mechanisms. The role of gas trapping in bubbles and re-solution by irradiation and thermal processes are included in the comparison. As much of the data, and the main range of interest for light water reactor fuels, is for release during mild transients in fuel with a burn-up below 4%, the role of gas retention on grain boundaries is very important and in some cases dominant. The grain boundaries are found to respond very differently to various gas arrival rates and to local temperature conditions. This can lead to early interlinkage and release in some cases, but retention with accompanying large swelling in others. The role of fission products and the local oxygen content of the fuel are found to be important. The effective fuel stoichiometry is likely to change significantly during transients with substantial effects on the transport processes controlling fission gas behaviour. The results of the evaluation of the models are summarized in mechanism maps for intragranular and grain boundary behaviour. (author). 36 refs, 8 figs

A prediction of the UO2 fission gas release data of Bellamy and Rich using a model recently developed by combustion engineering

International Nuclear Information System (INIS)

Freeburn, H.R.; Pati, S.R.

1983-01-01

The trend in the Light Water Reactor industry to higher discharge burnups of UO 2 fuel rods has initiated the modification of existing fuel rod models to better account for high burnup effects. A model recently developed by Combustion Engineering, Inc. (C-E) for fission gas release from UO 2 fuel recognizes the separate effects of temperature-dependent and temperature-independent release mechanisms. This model accounts for a moderate burnup enhancement that is based on a concept of a saturation inventory existing for the intra- and inter-grannular storage of fission gas within the fuel pellet. The saturation inventory, as modelled, is strongly dependent on the local temperature and the changing grain size of the fuel with burnup. Although the fitting constants of the model were determined solely from more current gas release data from fuel more typical of the C-E product line, the model, nonetheless, provides an excellent prediction of the Bellamy and Rich data over the entire burnup range represented by the data (+-1.6% gas release at a 1σ level). The ability to obtain a good comparison with this data base provides additional support for the use of the particular separation of the effects of thermal diffusion and burnup enhancement on fission gas release that is embodied in the model. Furthermore, the degree of burnup enhancement in the model is believed to be moderate enough to suggest that this high burnup effect should not impede the extension of discharge burnup limits associated with current design fuel rods for Pressurized Water Reactors

The effects of fission gas release on PWR fuel rod design and performance

International Nuclear Information System (INIS)

Leech, W.J.; Kaiser, R.S.

1980-01-01

The purpose of this investigation was to determine the effects of fission gas release on PWR fuel rod design and performance. Empirical models were developed from fission gas release data. Fission gas release during normal operation is a function of burnup. There is little additional fission gas release during anticipated transients. The empirical models were used to evaluate Westinghouse fuel rod designs. It was determined that fission gas release is not a limiting parameter for obtaining rod average burnups in the range of 50,000 to 60,000 MWD/MTU. Fission gas release during anticipated transients has a negligible effect on the margins to rod design limits. (author)

Fission gas release from fuels at high burnup

International Nuclear Information System (INIS)

Kauffmann, Yves; Pointud, M.L.; Vignesoult, Nicole; Atabek, Rosemarie; Baron, Daniel.

1982-04-01

Determinations of residual gas concentrations by heating and by X microanalysis were respectively carried out on particles (TANGO program) and on sections of fuel rods, perfectly characterized as to fabrication and irradiation history. A threshold release temperature of 1250 0 C+-100 0 C was determined irrespective of the type of oxide and the irradiation history in the 18,000-45,000 MWdt -1 (U) specific burnup field. The overall analyses of gas released from the fuel rods show that, in the PWR operating conditions, the fraction released remains less than 1% up to a mean specific burnup of 35000 MWdt -1 (U). The release of gases should not be a limiting factor in the increase of specific burnups [fr

Simultaneous absorption of NO and SO2 into hexamminecobalt(II)/iodide solution.

Science.gov (United States)

Long, Xiang-Li; Xiao, Wen-De; Yuan, Wei-kang

2005-05-01

An innovative catalyst system has been developed to simultaneously remove NO and SO2 from combustion flue gas. Such catalyst system may be introduced to the scrubbing solution using ammonia solution to accomplish sequential absorption and catalytic oxidation of both NO and SO2 in the same reactor. When the catalyst system is utilized for removing NO and SO2 from the flue gas, Co(NH3)(6)2+ ions act as the catalyst and I- as the co-catalyst. Dissolved oxygen, in equilibrium with the residual oxygen in the flue gas, is the oxidant. The overall removal process is further enhanced by UV irradiation at 365 nm. More than 95% of NO is removed at a feed concentration of 250-900 ppm, and nearly 100% of SO2 is removed at a feed concentration of 800-2500 ppm. The sulfur dioxide co-existing in the flue gas is beneficial to NO absorption into hexamminecobalt(II)/iodide solution. NO and SO2 can be converted to ammonium sulfate and ammonium nitrate that can be used as fertilizer materials. The process described here demonstrates the feasibility of removing SO2 and NO simultaneously only by retrofitting the existing wet ammonia flue-gas-desulfurization (FGD) scrubbers.

Uptake of SO/sub 2/ and NO/sub 2/ by the isolated upper airways

Energy Technology Data Exchange (ETDEWEB)

Yokoyama, E

1968-01-01

SO/sub 2/ and NO/sub 2/ concentrations were measured above and below isolated tracheas of 2 dogs and 3 rabbits. Air--gas mixtures were pumped through nose to upper trachea for 10 to 15 min at rates of 3.5 and 0.75 liters/min, respectively. Gas concentrations ranged from 7 to 87 ppM SO/sub 2/ and from 4 to 41 ppM NO/sub 2/. The rate of uptake for the isolated airways was a generally constant 93.7% for SO/sub 2/ and 42.1% for NO/sub 2/, a significant difference.

Microbial reduction of SO[sub 2] and NO[sub x] as a means of by- product recovery/disposal from regenerable processes for the desulfurization of flue gas

Energy Technology Data Exchange (ETDEWEB)

Sublette, K.L.

1992-01-01

Based on the work described simultaneous SO[sub 2]/No[sub x] removal from flue gas based on direct contact of the gas with SRB and T. denitrificans co-cultures or cultures-in-series has been eliminated as a viable process concept at this time. The technical reasons are as follows: (1) NO inhibition of SO[sub 2] reduction by D. desulfuricans - Although the NO concentrations used in the experiments described above are somewhat higher than that found in a typical flue gas, it is quite possible that at lower NO concentrations (or partial pressures) the inhibiting effects will simply take longer to become apparent. (2) Nitrate suppression of NO removal - As noted previously, the cultivation of T. denitrificans in a microbial flue gas treatment system (either one or two stages) would require sulfide-limiting conditions. Therefore, the electron acceptor must be in excess, requiring nitrate in the T. denitrificans process culture. As shown in experiments described above, nitrate significantly suppresses the removal of NO from a feed gas making simultaneous SO[sub 2]/NO[sub x] removal impractical by microbial means. (3) O[sub 2] inhibition of SO[sub 2] and NO reduction - It has been demonstrated that D. desulfuricans working cultures are tolerant of up to 1.7% O[sub 2] in the feed gas. However, further increases in the O[sub 2] partial pressure in the feed gas resulted in O[sub 2] inhibition of SO[sub 2] reduction. These inhibiting levels of O[sub 2] are comparable to those concentrations found in flue gases (3). Therefore, in any process in which raw flue gas contacts a D. desulfuricans culture marginal stability at best can be expected.

Rapid preparation of ultrafine BaSO{sub 3} by SO{sub 2} storage material

Energy Technology Data Exchange (ETDEWEB)

Zhang, Fei; Sha, Feng; Qiao, Xian Shu; Zhao, Tian Xiang; Guo, Bo; Zhang, Jian Bin [College of Chemical Engineering, Inner Mongolia University of Technology, Huhhot (Korea, Republic of)

2017-01-15

In this work, a green and efficient process was developed for the preparation of ultrafine BaSO{sub 3} with layered nanostructure surface via the reaction of BaCl{sub 2} with a SO{sub 2} storage material (SO{sub 2}SM) at room temperature. The absorption of SO{sub 2} with equimolar ethylenediamine (EDA) and ethylene glycol (EG) afforded SO{sub 2}SM, which not only offered alkyl sulfite but also released EDA and EG that served as efficient surfactants to promote the formation of BaSO{sub 3} with spherical morphology and porous structure in the process of synthesis of ultrafine BaSO{sub 3}. The factors affecting the morphology and size of BaSO{sub 3} particle were assessed by investigating the effects of SO{sub 2}SM concentration, BaCl{sub 2} concentration, stirring time and speed. It was found that a higher SO{sub 2}SM concentration led to a higher degree of supersaturation, and the particle size of BaSO{sub 3} could be reduced by increasing SO{sub 2}SM concentration. Moreover, under the identified optimal reaction conditions, ultrafine BaSO{sub 3} was obtained with an average diameter of 450 nm. In addition, a plausible formation process of BaSO{sub 3} was proposed to explain the observed reaction results. Overall, the developed process in this work provides an efficient method for the capture, utilization, and conversion of SO{sub 2} into a valuable chemical.

Gas retention and release behavior in Hanford double-shell waste tanks

Energy Technology Data Exchange (ETDEWEB)

Meyer, P.A.; Brewster, M.E.; Bryan, S.A. [and others

1997-05-01

This report describes the current understanding of flammable gas retention and release in Hanford double-shell waste tanks AN-103, AN-104, AN-105, AW-101, SY-101, and SY-103. This knowledge is based on analyses, experimental results, and observations of tank behavior. The applicable data available from the void fraction instrument, retained gas sampler, ball rheometer, tank characterization, and field monitoring are summarized. Retained gas volumes and void fractions are updated with these new data. Using the retained gas compositions from the retained gas sampler, peak dome pressures during a gas burn are calculated as a function of the fraction of retained gas hypothetically released instantaneously into the tank head space. Models and criteria are given for gas generation, initiation of buoyant displacement, and resulting gas release; and predictions are compared with observed tank behavior.

Gas retention and release behavior in Hanford double-shell waste tanks

International Nuclear Information System (INIS)

Meyer, P.A.; Brewster, M.E.; Bryan, S.A.

1997-05-01

This report describes the current understanding of flammable gas retention and release in Hanford double-shell waste tanks AN-103, AN-104, AN-105, AW-101, SY-101, and SY-103. This knowledge is based on analyses, experimental results, and observations of tank behavior. The applicable data available from the void fraction instrument, retained gas sampler, ball rheometer, tank characterization, and field monitoring are summarized. Retained gas volumes and void fractions are updated with these new data. Using the retained gas compositions from the retained gas sampler, peak dome pressures during a gas burn are calculated as a function of the fraction of retained gas hypothetically released instantaneously into the tank head space. Models and criteria are given for gas generation, initiation of buoyant displacement, and resulting gas release; and predictions are compared with observed tank behavior

Effect of Na2SO3 concentration to drug loading and drug release of ascorbic acid in chitosan edible film as drug delivery system membrane

Directory of Open Access Journals (Sweden)

Kistriyani Lilis

2018-01-01

Full Text Available Chitosan is a type of carbohydrate compounds produced from waste marine products, in particular the class of shrimp, crabs and clams. Chitosan is often process into edible films and utilized for food packaging also has potential as a membrane for drug delivery system. Drug loading and drug release can be controlled by improve the characteristics of the membrane by adding crosslinker. The purpose of this research is to study the effect of addition of crosslinker to the rate of loading and release of ascorbic acid in the chitosan edible film. Na2SO3 was used as crosslinker. Two grams of chitosan was dissolved into 100 ml of distilled water. Acetic acid and plasticizer were added in the solution then heated at 50°C. Na2SO3 solution with mass various of Na2SO3 dissolved, 01026 0.3; and 0.5 grams were added about 30 mL to make edible film. The analysis include of drug loading, drug release and tensile strength. The result showed that the loading of edible film with crosslinker 0.15 g; 0.3 g; and 0.5 g respectively were 60.98 ppm; 52.53 ppm; and 40.88 ppm, meanwhile for the release with crosslinker 0.15 g; 0.3 g; and 0.5 g respectively were 3.78 ppm; 5.72 ppm; and 5.97 ppm.

A Discussion of SY-101 Crust Gas Retention and Release Mechanisms

International Nuclear Information System (INIS)

Mendoza, D.P.; Mahoney, L.A.; Gauglitz, P.A.; Rassat, S.D.; Caley, S.M.

1999-01-01

The flammable gas hazard in Hanford waste tanks was made an issue by the behavior of double-shell Tank (DST) 241-SY-101 (SY-101). Shortly after SY-101 was filled in 1980, the waste level began rising periodically, due to the generation and retention of gases within the slurry, and then suddenly dropping as the gases were released. An intensive study of the tank's behavior revealed that these episodic releases posed a safety hazard because the released gas was flammable, and, in some cases, the volume of gas released was sufficient to exceed the lower flammability limit (LFL) in the tank headspace (Alleinann et al. 1993). A mixer pump was installed in SY-101 in late 1993 to prevent gases from building up in the settled solids layer, and the large episodic gas releases have since ceased (Allemann et al. 1994; Stewart et al. 1994; Brewster et al. 1995). However, the surface level of SY-101 has been increasing since at least 1995, and in recent months the level growth has shown significant and unexpected acceleration. Based on a number of observations and measurements, including data from the void fraction instrument (VFI), we have concluded that the level growth is caused largely by increased gas retention in the floating crust. In September 1998, the crust contained between about 21 and 43% void based on VFI measurements (Stewart et al. 1998). Accordingly, it is important to understand the dominant mechanisms of gas retention, why the gas retention is increasing, and whether the accelerating level increase will continue, diminish or even reverse. It is expected that the retained gas in the crust is flammable, with hydrogen as a major constituent. This gas inventory would pose a flammable gas hazard if it were to release suddenly. In May 1997, the mechanisms of bubble retention and release from crust material were the subject of a workshop. The evaluation of the crust and potential hazards assumed a more typical void of roughly 15% gas. It could be similar to

A Discussion of SY-101 Crust Gas Retention and Release Mechanisms

Energy Technology Data Exchange (ETDEWEB)

SD Rassat; PA Gauglitz; SM Caley; LA Mahoney; DP Mendoza

1999-02-23

The flammable gas hazard in Hanford waste tanks was made an issue by the behavior of double-shell Tank (DST) 241-SY-101 (SY-101). Shortly after SY-101 was filled in 1980, the waste level began rising periodically, due to the generation and retention of gases within the slurry, and then suddenly dropping as the gases were released. An intensive study of the tank's behavior revealed that these episodic releases posed a safety hazard because the released gas was flammable, and, in some cases, the volume of gas released was sufficient to exceed the lower flammability limit (LFL) in the tank headspace (Allemann et al. 1993). A mixer pump was installed in SY-101 in late 1993 to prevent gases from building up in the settled solids layer, and the large episodic gas releases have since ceased (Allemann et al. 1994; Stewart et al. 1994; Brewster et al. 1995). However, the surface level of SY-101 has been increasing since at least 1995, and in recent months the level growth has shown significant and unexpected acceleration. Based on a number of observations and measurements, including data from the void fraction instrument (VFI), we have concluded that the level growth is caused largely by increased gas retention in the floating crust. In September 1998, the crust contained between about 21 and 43% void based on VFI measurements (Stewart et al. 1998). Accordingly, it is important to understand the dominant mechanisms of gas retention, why the gas retention is increasing, and whether the accelerating level increase will continue, diminish or even reverse. It is expected that the retained gas in the crust is flammable, with hydrogen as a major constituent. This gas inventory would pose a flammable gas hazard if it were to release suddenly. In May 1997, the mechanisms of bubble retention and release from crust material were the subject of a workshop. The evaluation of the crust and potential hazards assumed a more typical void of roughly 15% gas. It could be similar to

Spray process for the recovery of CO.sub.2 from a gas stream and a related apparatus

Science.gov (United States)

Soloveichik, Grigorii Lev; Perry, Robert James; Wood, Benjamin Rue; Genovese, Sarah Elizabeth

2014-02-11

A method for recovering carbon dioxide (CO.sub.2) from a gas stream is disclosed. The method includes the step of reacting CO.sub.2 in the gas stream with fine droplets of a liquid absorbent, so as to form a solid material in which the CO.sub.2 is bound. The solid material is then transported to a desorption site, where it is heated, to release substantially pure CO.sub.2 gas. The CO.sub.2 gas can then be collected and used or transported in any desired way. A related apparatus for recovering carbon dioxide (CO.sub.2) from a gas stream is also described herein.

Modelling of fission gas release in rods from the International DEMO-RAMP-II Project at Studsvik

International Nuclear Information System (INIS)

Malen, K.

1983-01-01

The DEMO-RAMP-II rods had a burn-up of 25-30 MWd/kg U. They were ramped to powers in the range 40-50 kW/m with hold times between 10 s and 4.5 minutes. In spite of the short hold times the fission gas release at the higher powers was more than 1%. With these short hold times it is natural to assume that mixing of released gas with plenum gas is limited. Modelling has been performed using GAPCONSV (a modified GAPCON-THERMAL-2) both with and without mixing of released gas with plenum gas. In particular for the high power-short duration ramps only the ''no mixing'' modelling yields release fractions comparable to the experimental values. (author)

Interaction of SO2 with the Surface of a Water Nanodroplet.

Science.gov (United States)

Zhong, Jie; Zhu, Chongqin; Li, Lei; Richmond, Geraldine L; Francisco, Joseph S; Zeng, Xiao Cheng

2017-11-29

We present a comprehensive computational study of interaction of a SO 2 with water molecules in the gas phase and with the surface of various sized water nanodroplets to investigate the solvation behavior of SO 2 in different atmospheric environments. Born-Oppenheimer molecular dynamics (BOMD) simulation shows that, in the gas phase and at a temperature of 300 K, the dominant interaction between SO 2 and H 2 O is (SO 2 ) S···O (H 2 O) , consistent with previous density-functional theory (DFT) computation at 0 K. However, at the surface of a water nanodroplet, BOMD simulation shows that the hydrogen-bonding interaction of (SO 2 ) O···H (H 2 O) becomes increasingly important with the increase of droplet size, reflecting a marked effect of the water surface on the SO 2 solvation. This conclusion is in good accordance with spectroscopy evidence obtained previously (J. Am. Chem. Soc. 2005, 127, 16806; J. Am. Chem. Soc. 2006, 128, 3256). The prevailing interaction (SO 2 ) O···H (H 2 O) on a large droplet is mainly due to favorable exposure of H atoms of H 2 O at the air-water interface. Indeed, the conversion of the dominant interaction in the gas phase (SO 2 ) S···O (H 2 O) to the dominant interaction on the water nanodroplet (SO 2 ) O···H (H 2 O) may incur effects on the SO 2 chemistry in atmospheric aerosols because the solvation of SO 2 at the water surface can affect the reactive sites and electrophilicity of SO 2 . Hence, the solvation of SO 2 on the aerosol surface may have new implications when studying SO 2 chemistry in the aerosol-containing troposphere.

Degassing, gas retention and release in Fe(0) permeable reactive barriers.

Science.gov (United States)

Ruhl, Aki S; Jekel, Martin

2014-04-01

Corrosion of Fe(0) has been successfully utilized for the reductive treatment of multiple contaminants. Under anaerobic conditions, concurrent corrosion leads to the generation of hydrogen and its liberation as a gas. Gas bubbles are mobile or trapped within the irregular pore structure leading to a reduction of the water filled pore volume and thus decreased residence time and permeability (gas clogging). With regard to the contaminant transport to the reactive site, the estimation of surface properties of the reactive material indicated that individual gas bubbles only occupied minor contact areas of the reactive surface. Quantification of gas entrapment by both gravimetrical and tracer investigations revealed that development of preferential flow paths was not significant. A novel continuous gravimetrical method was implemented to record variations in gas entrapment and gas bubble releases from the reactive filling. Variation of grain size fractions revealed that the pore geometry had a significant impact on gas release. Large pores led to the release of comparably large gas amounts while smaller volumes were released from finer pores with a higher frequency. Relevant processes are explained with a simplified pictorial sequence that incorporates relevant mechanisms. Copyright © 2014 Elsevier B.V. All rights reserved.

Combined effects Na and SO{sub 2} in flue gas on Mn-Ce/TiO{sub 2} catalyst for low temperature selective catalytic reduction of NO by NH{sub 3} simulated by Na{sub 2}SO{sub 4} doping

Energy Technology Data Exchange (ETDEWEB)

Zhou, Aiyi [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing 210023 (China); Yu, Danqing [School of Chemical Engineering and Technology, Wuhan University of Science and Technology, Wuhan 430081 (China); Yang, Liu [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing 210023 (China); Sheng, Zhongyi, E-mail: 09377@njnu.edu.cn [Department of Environmental Science and Engineering, Nanjing Normal University, Nanjing 210023 (China); Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing 210023 (China)

2016-08-15

Highlights: • Sodium sulfate (Na{sub 2}SO{sub 4}) was deposited on Mn-Ce/TiO{sub 2} catalyst to simulate the co-existing of sodium and SO{sub 2} in the flue gas. • Na{sub 2}SO{sub 4} had strong and fluctuant influence on Mn-Ce/TiO{sub 2} catalyst’s performance in SCR of NOx with NH{sub 3}, due to the combined effect of the deactivation of sodium salts and the enhanced performance of ceria with surface sulfation. • The changes of the surface chemical species and acid sites on the Na{sub 2}SO{sub 4} deposited catalysts could be considered as the main reasons for the fluctuation changes with the catalytic activity. - Abstract: A series of Mn-Ce/TiO{sub 2} catalysts were synthesized through an impregnation method and used for low temperature selective catalytic reduction (SCR) of NOx with ammonia (NH{sub 3}). Na{sub 2}SO{sub 4} was added into the catalyst to simulate the combined effects of alkali metal and SO{sub 2} in the flue gas. Experimental results showed that Na{sub 2}SO{sub 4} had strong and fluctuant influence on the activity of Mn-Ce/TiO{sub 2}, because the effect of Na{sub 2}SO{sub 4} included pore occlusion and sulfation effect simultaneously. When Na{sub 2}SO{sub 4} loading content increased from 0 to 1 wt.%, the SCR activities of Na{sub 2}SO{sub 4}-doped catalysts decreased greatly. With further increasing amount of Na{sub 2}SO{sub 4}, however, the catalytic activity increased gradually. XRD results showed that Na{sub 2}SO{sub 4} doping could induce the crystallization of MnOx phases, which were also confirmed by TEM and SEM results. BET results showed that the surface areas decreased and a new bimodal mesoporous structure formed gradually with the increasing amount of Na{sub 2}SO{sub 4}. XPS results indicated that part of Ce{sup 4+} and Mn{sup 3+} were transferred to Ce{sup 3+} and Mn{sup 4+} due to the sulfation after Na{sub 2}SO{sub 4} deposition on the surface of the catalysts. When the doped amounts of Na{sub 2}SO{sub 4} increased, NH{sub 3

Research progress of SO2 removal from flue gas by functionalized ionic liquids

Directory of Open Access Journals (Sweden)

Xinle SHI

2017-02-01

Full Text Available Functionalized ionic liquids are receiving increasing attention in the field of flue gas desulfurization due to its unique physical and chemical properties. Research progress on the field of SO2 removal by ionic liquids (ILs including guanidinium-based, amines-based and ether-based ILs is summarized. Industrial application of polymerization ILs and loaded ILs to desulfurization is reviewed. Relevant suggestions on industrial application of ionic liquids based on fundamental research are put forward. The first thing is to develop functional ionic liquid for desulfurization,and thus investigate and propose its desulfurization mechanism and model; the second is to carry out the research work on immobilized ionic liquid, and explore its recycling properties, thus prolonging its service life.

Technical and economical aspects of SO2 and NOx removal from flue gas by electron beam irradiation

International Nuclear Information System (INIS)

Turhan, S.; Karadeniz, S.; Tugluoglu, N.; Eken, M.; Oktar, O.; Ercan, I.

2001-01-01

The emission of sulfur dioxide (SO 2 , also SO 3 ) and nitrogen oxides (NO, NO 2 , called NO x ) from fossil fuel burning power and industrial plants is one of the major sources of environmental pollution. These pollutants are named as acid gases causing acid rain and also indirect greenhouse gases contributing greenhouse effect. Acid rain damages forest, agriculture fields and flora, and cause public health concerns in regions having a number of industrial plants. Today, many countries have started to impose industrial emission limits and this movement has generated renewed interest in finding viable and cost effective solutions to SO 2 and NO x pollution control. The conventional technologies, wet scrubbing de-SO 2 and de-NO x , now reached their full potential therefore these methods are not expected to provide further improvements in terms of efficiency or reduction in construction costs. However, new technologies are being investigated for industrial scale commercial viability. One of them is electron beam process, which is dry scrubbing process and simultaneously removes SO 2 and NO x , and useful by-product for agriculture fertilizer. In this study, the economical and technical aspects of electron beam flue gas treatment process are discussed. Because an electron accelerator facility with electron beam energy of 500 KeV and electron beam current of 20 mA will be installed at ANRTC in TURKEY

Numerical simulation of flue gas purification from NOx, SO2 by electron beam

International Nuclear Information System (INIS)

Morgunov, V.V.; Shkilko, A.M.; Fainchtein, O.L.

2011-01-01

Complete text of publication follows. The paper is devoted to numerical simulation of radiation-chemical processes in gas phase, which are take place during electron beam (EB) treatments of flue gases. A mathematical model of EB processes in gas phase was created. Also, a computer code which numerically simulates radiation-chemical processes during EB treatment of flue gases was created. The needed data such as chemical species, radiation-chemical yields and rate constants of the chemical reactions were collected and putted into database. The computer code allows do following: 1. The following technological parameters: irradiation dose, temperature, initial composition of the flue gases, time of irradiation (time which flue gases spend in an irradiation zone), one- or two-stage irradiation can be defined by the user in the code shell; 2. In accordance with the initial composition of flue gases selects chemical species from database of the chemical species (total amount of species in database is 522) which took part in simulation taking into account species that are formed due to irradiation; 3. In accordance with the selected chemical species selects chemical and radiation-chemical reactions from the database of reactions (total amount of chemical and radiation-chemical reaction is 2275) which are took part in the simulation; 4. Creates a stiff system of ordinary differential equations (ODEs) which describes chemical and radiation-chemical reactions; 5. Solves the received system of ODEs by backward differentiation formula (Gear's method); 6. Creates plots of dependencies: concentrations of chemical species versus time of irradiation under different parameters of modeled EB-processes. The received results. For the following technological parameters: irradiation dose is 8.0 kGy; two stage irradiation; initial temperature is 353 deg K; time of the irradiation - 4 s; initial composition of the flue gases - typical for power plant, following removal efficiencies were

Fission gas release from oxide fuels at high burnups (AWBA development program)

International Nuclear Information System (INIS)

Dollins, C.C.

1981-02-01

The steady state gas release, swelling and densification model previously developed for oxide fuels has been modified to accommodate the slow transients in temperature, temperature gradient, fission rate and pressure that are encountered in normal reactor operation. The gas release predictions made by the model were then compared to gas release data on LMFBR-EBRII fuels obtained by Dutt and Baker and reported by Meyer, Beyer, and Voglewede. Good agreement between the model and the data was found. A comparison between the model and three other sets of gas release data is also shown, again with good agreement

Analysis of fuel centre temperatures and fission gas release data from the IFPE Database

International Nuclear Information System (INIS)

Schubert, A.; Lassmann, K.; Van Uffelen, P.; Van de Laar, J.; Elenkov, D.; Asenov, S.; Boneva, S.; Djourelov, N.; Georgieva, M.

2003-01-01

The present work has continued the analysis of fuel centre temperatures and fission gas release, calculated with standard options of the TRANSURANUS code. The calculations are compared to experimental data from the International Fuel Performance Experiments (IFPE) database. It is reported an analysis regarding UO 2 fuel for Western-type reactors: Fuel centre temperatures measured in the experiments Contact 1 and Contact 2 (in-pile tests of 2 rods performed at the Siloe reactor in Grenoble, France, closely simulating commercial PWR conditions); Fission gas release data derived from post-irradiation examinations of 9 fuel rods belonging to the High-Burnup Effects Programme, task 3 (HBEP3). The results allow for a comparison of predictions by TRANSURANUS for the mentioned Western-type fuels with those done previously for Russian-type WWER fuel. The comparison has been extended to include fuel centre temperatures as well as fission gas release. The present version of TRANSURANUS includes a model that calculates the production of Helium. The amount of produced Helium is compared to the measured and to the calculated release of the fission gases Xenon and Krypton

Continuation of Global NO2 and SO2 Monitoring with Suomi NPP OMPS

Science.gov (United States)

Yang, K.; Zhang, H.; Wang, J.; Ge, C.; Wang, Y.

2017-12-01

We have produced high-quality NO2 and SO2 standard products (named NMNO2 and NMSO2 respectively) from the SNPP OMPS-NM daily global observations. These OMPS standard products have been archived and publicly released at NASA Goddard Earth Sciences Data and Information Services Center (https://daac.gsfc.nasa.gov/information/news/595e9675624016d1af392c73/omps-nm-no- 2-and-so-2-l-2-data-products-released). Analyses and comparisons have demonstrated that the qualities of these OMPS standard products match or surpass those of the corresponding OMI products, enabling the continuity and extension of these two key standard Earth System Data Records (ESDRs) that begun with NASA's EOS Aura mission using the SNPP observations. In this presentation, we summarize the new techniques and algorithm advances that improve the accuracy and consistency of these ESDRs from satellite observations, and highlight the regional changes in NO2 and SO2 detected from half a decade of SNPP OMPS observations.

Understanding SO2 Capture by Ionic Liquids.

Science.gov (United States)

Mondal, Anirban; Balasubramanian, Sundaram

2016-05-19

Ionic liquids have generated interest for efficient SO2 absorption due to their low vapor pressure and versatility. In this work, a systematic investigation of the structure, thermodynamics, and dynamics of SO2 absorption by ionic liquids has been carried out through quantum chemical calculations and molecular dynamics (MD) simulations. MP2 level calculations of several ion pairs complexed with SO2 reveal its preferential interaction with the anion. Results of condensed phase MD simulations of SO2-IL mixtures manifested the essential role of both cations and anions in the solvation of SO2, where the solute is surrounded by the "cage" formed by the cations (primarily its alkyl tail) through dispersion interactions. These structural effects of gas absorption are substantiated by calculated Gibbs free energy of solvation; the dissolution is demonstrated to be enthalpy driven. The entropic loss of SO2 absorption in ionic liquids with a larger anion such as [NTf2](-) has been quantified and has been attributed to the conformational restriction of the anion imposed by its interaction with SO2. SO2 loading IL decreases its shear viscosity and enhances the electrical conductivity. This systematic study provides a molecular level understanding which can aid the design of task-specific ILs as electrolytes for efficient SO2 absorption.

Effect of SO 2 on CO 2 Capture Using Liquid-like Nanoparticle Organic Hybrid Materials

KAUST Repository

Lin, Kun-Yi Andrew

2013-08-15

Liquid-like nanoparticle organic hybrid materials (NOHMs), consisting of silica nanoparticles with a grafted polymeric canopy, were synthesized. Previous work on NOHMs has revealed that CO2 capture behaviors in these hybrid materials can be tuned by modifying the structure of the polymeric canopy. Because SO2, which is another acidic gas found in flue gas, would also interact with NOHMs, this study was designed to investigate its effect on CO2 capture in NOHMs. In particular, CO2 capture capacities as well as swelling and CO2 packing behaviors of NOHMs were analyzed using thermogravimetric analyses and Raman and attenuated total reflectance (ATR) Fourier transform infrared (FTIR) spectroscopies before and after exposure of NOHMs to SO2. It was found that the SO2 absorption in NOHMs was only prominent at high SO2 levels (i.e., 3010 ppm; Ptot = 0.4 MPa) far exceeding the typical SO2 concentration in flue gas. As expected, the competitive absorption between SO2 and CO2 for the same absorption sites (i.e., ether and amine groups) resulted in a decreased CO2 capture capacity of NOHMs. The swelling of NOHMs was not notably affected by the presence of SO 2 within the given concentration range (Ptot = 0-0.68 MPa). On the other hand, SO2, owing to its Lewis acidic nature, interacted with the ether groups of the polymeric canopy and, thus, changed the CO2 packing behaviors in NOHMs. © 2013 American Chemical Society.

Effect of SO 2 on CO 2 Capture Using Liquid-like Nanoparticle Organic Hybrid Materials

KAUST Repository

Lin, Kun-Yi Andrew; Petit, Camille; Park, Ah-Hyung Alissa

2013-01-01

Liquid-like nanoparticle organic hybrid materials (NOHMs), consisting of silica nanoparticles with a grafted polymeric canopy, were synthesized. Previous work on NOHMs has revealed that CO2 capture behaviors in these hybrid materials can be tuned by modifying the structure of the polymeric canopy. Because SO2, which is another acidic gas found in flue gas, would also interact with NOHMs, this study was designed to investigate its effect on CO2 capture in NOHMs. In particular, CO2 capture capacities as well as swelling and CO2 packing behaviors of NOHMs were analyzed using thermogravimetric analyses and Raman and attenuated total reflectance (ATR) Fourier transform infrared (FTIR) spectroscopies before and after exposure of NOHMs to SO2. It was found that the SO2 absorption in NOHMs was only prominent at high SO2 levels (i.e., 3010 ppm; Ptot = 0.4 MPa) far exceeding the typical SO2 concentration in flue gas. As expected, the competitive absorption between SO2 and CO2 for the same absorption sites (i.e., ether and amine groups) resulted in a decreased CO2 capture capacity of NOHMs. The swelling of NOHMs was not notably affected by the presence of SO 2 within the given concentration range (Ptot = 0-0.68 MPa). On the other hand, SO2, owing to its Lewis acidic nature, interacted with the ether groups of the polymeric canopy and, thus, changed the CO2 packing behaviors in NOHMs. © 2013 American Chemical Society.

Assessing and Projecting Greenhouse Gas Release due to Abrupt Permafrost Degradation

Science.gov (United States)

Saito, K.; Ohno, H.; Yokohata, T.; Iwahana, G.; Machiya, H.

2017-12-01

Permafrost is a large reservoir of frozen soil organic carbon (SOC; about half of all the terrestrial storage). Therefore, its degradation (i.e., thawing) under global warming may lead to a substantial amount of additional greenhouse gas (GHG) release. However, understanding of the processes, geographical distribution of such hazards, and implementation of the relevant processes in the advanced climate models are insufficient yet so that variations in permafrost remains one of the large source of uncertainty in climatic and biogeochemical assessment and projections. Thermokarst, induced by melting of ground ice in ice-rich permafrost, leads to dynamic surface subsidence up to 60 m, which further affects local and regional societies and eco-systems in the Arctic. It can also accelerate a large-scale warming process through a positive feedback between released GHGs (especially methane), atmospheric warming and permafrost degradation. This three-year research project (2-1605, Environment Research and Technology Development Fund of the Ministry of the Environment, Japan) aims to assess and project the impacts of GHG release through dynamic permafrost degradation through in-situ and remote (e.g., satellite and airborn) observations, lab analysis of sampled ice and soil cores, and numerical modeling, by demonstrating the vulnerability distribution and relative impacts between large-scale degradation and such dynamic degradation. Our preliminary laboratory analysis of ice and soil cores sampled in 2016 at the Alaskan and Siberian sites largely underlain by ice-rich permafrost, shows that, although gas volumes trapped in unit mass are more or less homogenous among sites both for ice and soil cores, large variations are found in the methane concentration in the trapped gases, ranging from a few ppm (similar to that of the atmosphere) to hundreds of thousands ppm We will also present our numerical approach to evaluate relative impacts of GHGs released through dynamic

Simultaneous absorption of NO and SO{sub 2} into hexamminecobalt(II)/iodide solution

Energy Technology Data Exchange (ETDEWEB)

Long, X.L.; Xiao, W.D.; Yuan, W.K. [East China University of Science & Technology, Shanghai (China)

2005-05-01

An innovative catalyst system has been developed to simultaneously remove NO and SO{sub 2} from combustion flue gas. Such catalyst system may be introduced to the scrubbing solution using ammonia solution to accomplish sequential absorption and catalytic oxidation of both NO and SO{sub 2} in the same reactor. When the catalyst system is utilized for removing NO and SO{sub 2} from the flue gas, Co(NH{sub 3}){sub 6}{sup 2+} ions act as the catalyst and I{sup -} as the co-catalyst. Dissolved oxygen, in equilibrium with the residual oxygen in the flue gas, is the oxidant. The overall removal process is further enhanced by UV irradiation at 365 nm. More than 95% of NO is removed at a feed concentration of 250-900 ppm, and nearly 100% of SO{sub 2} is removed at a feed concentration of 800-2500 ppm. The sulfur dioxide co-existing in the flue gas is beneficial to NO absorption into hexamminecobalt(II)/iodide solution. NO and SO{sub 2} can be converted to ammonium sulfate and ammonium nitrate that can be used as fertilizer materials. The process described here demonstrates the feasibility of removing SO{sub 2} and NO simultaneously only by retrofitting the existing wet ammonia flue-gas-desulfurization (FGD) scrubbers.

Emission control of SO2 and NOx by irradiation methods

International Nuclear Information System (INIS)

Radoiu, Marilena T.; Martin, Diana I.; Calinescu, Ioan

2003-01-01

Microwave discharges at 2.45 GHz frequency and accelerated electron beams operated at atmospheric pressure in synthetic gas mixtures containing N 2 , O 2 , CO 2 , SO 2 , and NO x are investigated experimentally for various gas mixture constituents and operating conditions, with respect to their ability to purify exhaust gases. An original experimental unit easily adaptable for both separate and simultaneous irradiation with microwaves and electron beams was set up. The simultaneous treatment with accelerated electron beams and microwaves was found to increase the removal efficiency of NO x and SO 2 and also helped to reduce the total required dose rate with ∼30%. Concomitant removal of NO x (∼80%) and SO 2 (>95%) by precipitation with ammonia was achieved

Sulfur Release from Cement Raw Materials during Solid Fuel Combustion

DEFF Research Database (Denmark)

Nielsen, Anders Rooma; Larsen, Morten B.; Glarborg, Peter

2011-01-01

During combustion of solid fuels in the material inlet end of cement rotary kilns, local reducing conditions can occur and cause decomposition of sulfates from cement raw materials. Decomposition of sulfates is problematic because it increases the gas-phase SO2 concentration, which may cause...... deposit formation in the kiln system. SO2 release from cement raw materials during combustion of solid fuels has been studied experimentally in a high temperature rotary drum. The fuels were tire rubber, pine wood, petcoke, sewage sludge, and polypropylene. The SO2 release from the raw materials...

SO2 - An indirect source of energy

DEFF Research Database (Denmark)

Kriek, R.J.; Van Ravenswaay, J.P.; Potgieter, M.

2013-01-01

-related processes 12.8 Mt. As a well-known gaseous pollutant, SO2 is not per se known as a source of energy. However, in the presence of water SO2 can be electro-oxidized at the anode of an electrolyser to produce hydrogen ions, which in turn can be reduced at the cathode of the electrolyser to produce hydrogen gas......Global sulphur dioxide (SO2) emissions peaked around the mid- 1970s, after which they declined. However, with the growth of specifically China, emissions are on the rise again. In 2008, global anthropogenic SO2 emissions totalled 127 Mt, with energy production accounting for 63.2 Mt and metal....... Gaseous emissions of SO2 can therefore be cleaned up with the simultaneous production of hydrogen, an energy store or carrier, which provides an economic offset to the overall cost of this potential remediation process. This process forms part of the Hybrid Sulfur (HyS) cycle as well as the once...

Ultrahigh and Selective SO2 Uptake in Inorganic Anion-Pillared Hybrid Porous Materials.

Science.gov (United States)

Cui, Xili; Yang, Qiwei; Yang, Lifeng; Krishna, Rajamani; Zhang, Zhiguo; Bao, Zongbi; Wu, Hui; Ren, Qilong; Zhou, Wei; Chen, Banglin; Xing, Huabin

2017-07-01

The efficient capture of SO 2 is of great significance in gas-purification processes including flue-gas desulfurization and natural-gas purification, but the design of porous materials with high adsorption capacity and selectivity of SO 2 remains very challenging. Herein, the selective recognition and dense packing of SO 2 clusters through multiple synergistic host-guest and guest-guest interactions by controlling the pore chemistry and size in inorganic anion (SiF 6 2- , SIFSIX) pillared metal-organic frameworks is reported. The binding sites of anions and aromatic rings in SIFSIX materials grasp every atom of SO 2 firmly via S δ+ ···F δ- electrostatic interactions and O δ- ···H δ+ dipole-dipole interactions, while the guest-guest interactions between SO 2 molecules further promote gas trapping within the pore space, which is elucidated by first-principles density functional theory calculations and powder X-ray diffraction experiments. These interactions afford new benchmarks for the highly efficient removal of SO 2 from other gases, even if at a very low SO 2 concentration. Exceptionally high SO 2 capacity of 11.01 mmol g -1 is achieved at atmosphere pressure by SIFSIX-1-Cu, and unprecedented low-pressure SO 2 capacity is obtained in SIFSIX-2-Cu-i (4.16 mmol g -1 SO 2 at 0.01 bar and 2.31 mmol g -1 at 0.002 bar). More importantly, record SO 2 /CO 2 selectivity (86-89) and excellent SO 2 /N 2 selectivity (1285-3145) are also achieved. Experimental breakthrough curves further demonstrate the excellent performance of these hybrid porous materials in removing low-concentration SO 2 . © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Continuous desulfurization and bacterial community structure of an integrated bioreactor developed to treat SO2 from a gas stream.

Science.gov (United States)

Lin, Jian; Li, Lin; Ding, Wenjie; Zhang, Jingying; Liu, Junxin

2015-11-01

Sulfide dioxide (SO2) is often released during the combustion processes of fossil fuels. An integrated bioreactor with two sections, namely, a suspended zone (SZ) and immobilized zone (IZ), was applied to treat SO2 for 6months. Sampling ports were set in both sections to investigate the performance and microbial characteristics of the integrated bioreactor. SO2 was effectively removed by the synergistic effect of the SZ and IZ, and more than 85% removal efficiency was achieved at steady state. The average elimination capacity of SO2 in the bioreactor was 2.80g/(m(3)·hr) for the SZ and 1.50g/(m(3)·hr) for the IZ. Most SO2 was eliminated in the SZ. The liquid level of the SZ and the water content ratio of the packing material in the IZ affected SO2 removal efficiency. The SZ served a key function not only in SO2 elimination, but also in moisture maintenance for the IZ. The desired water content in IZ could be feasibly maintained without any additional pre-humidification facilities. Clone libraries of 16S rDNA directly amplified from the DNA of each sample were constructed and sequenced to analyze the community composition and diversity in the individual zones. The desulfurization bacteria dominated both zones. Paenibacillus sp. was present in both zones, whereas Ralstonia sp. existed only in the SZ. The transfer of SO2 to the SZ involved dissolution in the nutrient solution and biodegradation by the sulfur-oxidizing bacteria. This work presents a potential biological treatment method for waste gases containing hydrophilic compounds. Copyright © 2015. Published by Elsevier B.V.

The Effect of Deposit Temperature on the Catalytic SO2-to-SO3 Conversion in a Copper Flash Smelting Heat Recovery Boiler

Science.gov (United States)

Lehmusto, Juho; Vainio, Emil; Laurén, Tor; Lindgren, Mari

2018-02-01

The aim of the work was to study the catalytic role of copper flash smelter deposit in the SO2-to-SO3 conversion. In addition, the effect of process gas temperature at 548 K to 1173 K (275 °C to 900 °C) on the amount of SO3 formed was addressed both in the absence and presence of genuine copper flash smelter deposit. The SO3 conversion rate changed as a function of process gas temperature, peaking at 1023 K (750 °C). A dramatic increase in the SO2-to-SO3 conversion was observed when process dust was present, clearly indicating that process dust catalyzes the SO2-to-SO3 conversion. Based on these results, the catalytic ability of the deposit may lead to sulfuric acid dew point corrosion.

Acoustic mapping of shallow water gas releases using shipborne multibeam systems

Science.gov (United States)

Urban, Peter; Köser, Kevin; Weiß, Tim; Greinert, Jens

2015-04-01

Water column imaging (WCI) shipborne multibeam systems are effective tools for investigating marine free gas (bubble) release. Like single- and splitbeam systems they are very sensitive towards gas bubbles in the water column, and have the advantage of the wide swath opening angle, 120° or more allowing a better mapping and possible 3D investigations of targets in the water column. On the downside, WCI data are degraded by specific noise from side-lobe effects and are usually not calibrated for target backscattering strength analysis. Most approaches so far concentrated on manual investigations of bubbles in the water column data. Such investigations allow the detection of bubble streams (flares) and make it possible to get an impression about the strength of detected flares/the gas release. Because of the subjective character of these investigations it is difficult to understand how well an area has been investigated by a flare mapping survey and subjective impressions about flare strength can easily be fooled by the many acoustic effects multibeam systems create. Here we present a semi-automated approach that uses the behavior of bubble streams in varying water currents to detect and map their exact source positions. The focus of the method is application of objective rules for flare detection, which makes it possible to extract information about the quality of the seepage mapping survey, perform automated noise reduction and create acoustic maps with quality discriminators indicating how well an area has been mapped.

Identification of tropospheric emissions sources from satellite observations: Synergistic use of HCHO, NO2, and SO2 trace gas measurements

Science.gov (United States)

Marbach, T.; Beirle, S.; Khokhar, F.; Platt, U.

2005-12-01

We present case studies for combined HCHO, NO2, and SO2 satellite observations, derived from GOME measurements. Launched on the ERS-2 satellite in April 1995, GOME has already performed continuous operations over 8 years providing global observations of the different trace gases. In this way, satellite observations provide unique opportunities for the identifications of trace gas sources. The satellite HCHO observations provide information concerning the localization of biomass burning (intense source of HCHO). The principal biomass burning areas can be observed in the Amazon basin region and in central Africa Weaker HCHO sources (south east of the United States, northern part of the Amazon basin, and over the African tropical forest), not correlated with biomass burning, could be due to biogenic isoprene emissions. The HCHO data can be compared with NO2 and SO2 results to identify more precisely the tropospheric sources (biomass burning events, human activities, additional sources like volcanic emissions). Biomass burning are important tropospheric sources for both HCHO and NO2. Nevertheless HCHO reflects more precisely the biomass burning as it appears in all biomass burning events. NO2 correlate with HCHO over Africa (grassland fires) but not over Indonesia (forest fires). In south America, an augmentation of the NO2 concentrations can be observed with the fire shift from the forest to grassland vegetation. So there seems to be a dependence between the NO2 emissions during biomass burning and the vegetation type. Other high HCHO, SO2, and NO2 emissions can be correlated with climatic events like the El Nino in 1997, which induced dry conditions in Indonesia causing many forest fires.

Free energy study of H2O, N2O5, SO2, and O3 gas sorption by water droplets/slabs

Science.gov (United States)

Li, Wentao; Pak, Chi Yuen; Tse, Ying-Lung Steve

2018-04-01

Understanding gas sorption by water in the atmosphere is an active research area because the gases can significantly alter the radiation and chemical properties of the atmosphere. We attempt to elucidate the molecular details of the gas sorption of water and three common atmospheric gases (N2O5, SO2, and O3) by water droplets/slabs in molecular dynamics simulations. The system size effects are investigated, and we show that the calculated solvation free energy decreases linearly as a function of the reciprocal of the number of water molecules from 1/215 to 1/1000 in both the slab and the droplet systems. By analyzing the infinitely large system size limit by extrapolation, we find that all our droplet results are more accurate than the slab results when compared to the experimental values. We also show how the choice of restraints in umbrella sampling can affect the sampling efficiency for the droplet systems. The free energy changes were decomposed into the energetic ΔU and entropic -TΔS contributions to reveal the molecular details of the gas sorption processes. By further decomposing ΔU into Lennard-Jones and Coulombic interactions, we observe that the ΔU trends are primarily determined by local effects due to the size of the gas molecule, charge distribution, and solvation structure around the gas molecule. Moreover, we find that there is a strong correlation between the change in the entropic contribution and the mean residence time of water, which is spatially nonlocal and related to the mobility of water.

On-line mass spectrometry measurement of fission gas release from nuclear fuel submitted to thermal transients

International Nuclear Information System (INIS)

Guigues, E.; Janulyte, A.; Zerega, Y.; Pontillon, Y.

2013-06-01

The work presented in this paper has been performed in the framework of a joint research program between Aix-Marseille University and CEA Cadarache. The aim is to develop a mass spectrometer (MS) device for the MERARG facility. MERARG is devoted to the study of fission gas release measurement, from nuclear fuels submitted to annealing tests in high activity laboratory such as LECA-STAR, thanks to gamma spectrometry. The mass spectrometer will then extend the measurement capability from the γ-emitters gases to all the gases involved in the release in order to have a better understanding of the fission gas release dynamics from fuel during thermal transients. Furthermore, the mass spectrometer instrument combines the capabilities and performances of both on-line (for release kinetic) and off-line implementations (for delayed accurate analysis of capacities containing total release gas). The paper deals with two main axes: (1) the modelling of gas sampling inlet device and its performance and (2) the first MS qualification/calibration results. The inlet device samples the gas and also adapts the pressure between MERARG sweeping line at 1.2 bar and mass spectrometer chamber at high vacuum. It is a two-stage device comprising a capillary at inlet, an intermediate vacuum chamber, a molecular leak inlet and a two-stage pumping device. Pressure drops, conductance and throughputs are estimated both for mass spectrometer operation and for exhaust gas recovery. Possible gas segregation is also estimated and device modification is proposed to attain a more accurate calibration. First experimental results obtained from a standard gas bottle show that the quantitative analysis at a few ppm level can be achieved for all isotopes of Kr and Xe, as well as masses 2 and 4 u. (authors)

Source strength and dispersion of CO2 releases from high-pressure pipelines: CFD model using real gas equation of state

International Nuclear Information System (INIS)

Liu, Xiong; Godbole, Ajit; Lu, Cheng; Michal, Guillaume; Venton, Philip

2014-01-01

Highlights: • Validated CFD models for decompression and dispersion of CO 2 releases from pipelines. • Incorporation of real gas EOS into CFD code for source strength estimation. • Demonstration of better performance of SST k–ω turbulence model for jet flow. • Demonstration of better performance of real gas EOS compared to ideal gas EOS. • Demonstration of superiority of CFD models over a commercial risk assessment package. - Abstract: Transportation of CO 2 in high-pressure pipelines forms a crucial link in the ever-increasing application of Carbon Capture and Storage (CCS) technologies. An unplanned release of CO 2 from a pipeline presents a risk to human and animal populations and the environment. Therefore it is very important to develop a deeper understanding of the atmospheric dispersion of CO 2 before the deployment of CO 2 pipelines, to allow the appropriate safety precautions to be taken. This paper presents a two-stage Computational Fluid Dynamics (CFD) study developed (1) to estimate the source strength, and (2) to simulate the subsequent dispersion of CO 2 in the atmosphere, using the source strength estimated in stage (1). The Peng–Robinson (PR) EOS was incorporated into the CFD code. This enabled accurate modelling of the CO 2 jet to achieve more precise source strength estimates. The two-stage simulation approach also resulted in a reduction in the overall computing time. The CFD models were validated against experimental results from the British Petroleum (BP) CO 2 dispersion trials, and also against results produced by the risk management package Phast. Compared with the measurements, the CFD simulation results showed good agreement in both source strength and dispersion profile predictions. Furthermore, the effect of release direction on the dispersion was studied. The presented research provides a viable method for the assessment of risks associated with CCS

Reactivity of micas and cap-rock in wet supercritical CO_2 with SO_2 and O_2 at CO_2 storage conditions

International Nuclear Information System (INIS)

Pearce, Julie K.; Dawson, Grant K.W.; Law, Alison C.K.; Biddle, Dean; Golding, Suzanne D.

2016-01-01

Seal or cap-rock integrity is a safety issue during geological carbon dioxide capture and storage (CCS). Industrial impurities such as SO_2, O_2, and NOx, may be present in CO_2 streams from coal combustion sources. SO_2 and O_2 have been shown recently to influence rock reactivity when dissolved in formation water. Buoyant water-saturated supercritical CO_2 fluid may also come into contact with the base of cap-rock after CO_2 injection. Supercritical fluid-rock reactions have the potential to result in corrosion of reactive minerals in rock, with impurity gases additionally present there is the potential for enhanced reactivity but also favourable mineral precipitation. The first observation of mineral dissolution and precipitation on phyllosilicates and CO_2 storage cap-rock (siliciclastic reservoir) core during water-saturated supercritical CO_2 reactions with industrial impurities SO_2 and O_2 at simulated reservoir conditions is presented. Phyllosilicates (biotite, phlogopite and muscovite) were reacted in contact with a water-saturated supercritical CO_2 containing SO_2, or SO_2 and O_2, and were also immersed in the gas-saturated bulk water. Secondary precipitated sulfate minerals were formed on mineral surfaces concentrated at sheet edges. SO_2 dissolution and oxidation resulted in solution pH decreasing to 0.74 through sulfuric acid formation. Phyllosilicate dissolution released elements to solution with ∼50% Fe mobilized. Geochemical modelling was in good agreement with experimental water chemistry. New minerals nontronite (smectite), hematite, jarosite and goethite were saturated in models. A cap-rock core siltstone sample from the Surat Basin, Australia, was also reacted in water-saturated supercritical CO_2 containing SO_2 or in pure supercritical CO_2. In the presence of SO_2, siderite and ankerite were corroded, and Fe-chlorite altered by the leaching of mainly Fe and Al. Corrosion of micas in the cap-rock was however not observed as the pH was

A simple operational gas release and swelling model. Pt. 1

International Nuclear Information System (INIS)

Wood, M.H.; Matthews, J.R.

1980-01-01

A new and simple model of fission gas release and swelling has been developed for oxide nuclear fuel under operational conditions. The model, which is to be incorporated into a fuel element behaviour code, is physically based and applicable to fuel at both thermal and fast reactor ratings. In this paper we present that part of the model describing the behaviour of intragranular gas: a future paper will detail the treatment of the grain boundary gas. The results of model calculations are compared with recent experimental observations of intragranular bubble concentrations and sizes, and gas release from fuel irradiated under isothermal conditions. Good agreement is found between experiment and theory. (orig.)

On the SO2 problem in power engineering

International Nuclear Information System (INIS)

Boyadjiev, C.

2011-01-01

The presented theoretical analysis shows, that the low SO2 concentration in the waste gases of the thermal power plants needs an irreversible chemical reactions of SO2 with alkaline reagents in the liquid phase in case of gas-liquid dispersion system. For the purification of huge amounts of waste gases must be used inexpensive reagents (CaCO 3 suspension). The presence of the active component in the absorbent as both a solution and solid phase leads to an increase of the absorption capacity of the absorbent, but the introduction of a new process (the dissolution of the solid phase) creates conditions for a variation of the absorption mechanism (interphase mass transfer through two interphase surfaces - gas/liquid and liquid/solid). At these conditions the mass transfer resistance is distributed in the both phases, i.e. the convection-diffusion equations of SO2 (in gas and liquid phases) and CaCO 3 (in liquid phase) must be solved together. The impossibility for the solution of the convection-diffusion equations in gas-liquid dispersion system leads to the necessity of using a diffusion type of models, where the velocity and concentration distributions in column apparatuses are replaced by the average values of the velocity and concentration over the cross-sectional area of the column. The parameters in these type of models replace the effects, the radial non-uniformities of the velocity and the concentration distributions at the cross-sectional area of the column. They can be obtained, using experimental data

Considerations on abatement of SO2 pollution

International Nuclear Information System (INIS)

Ataman, E.

1992-01-01

The paper brings into focus the problems related to the SO 2 environmental pollution, to the emission standards, stress being laid on the possibilities of SO 2 emissions reduction resulting from the man-made stationary sources. A comparative estimation is made concerning the necessary investments for the desulfurization plants in accordance with the process employed and with the size of the boiler, as well as, of the operating costs brought about by desulfurization. The paper concludes with the prospects of flue gas reduction in thermal power plants. (author). 5 tabs., 21 refs

Recent status of purging SO2 and NOx in flue gas by EB and R and D of electron accelerator in China

International Nuclear Information System (INIS)

Liu Zhenhao

2005-01-01

The main energy resource is coal in China. Flue gas from burning coal is the most fearful pollution. Chinese Government pays more attention to reduction of SO 2 in flue gas from 1990's. Various technical facilities of reducing SO 2 have been imported from developed countries especially from Japanese companies. For example, A largest project is that Chongqing-luohuang electric power station imported limestone-gypsum process FGD technology and facility from Mitsubishi of Japan in 1980s for 300 MW generator spending 36.4 million US$ and 27.3 million RMB. Recently an example is EBA technology in Chengdu thermal plant. Some of Chinese institute is going to improve the technology to treat larger amount of flue gas from one generator such as 200 - 300 MW generator. And an R and D program of manufacturing higher voltage accelerator is being implemented. Otherwise, electron accelerator of industry application has been successfully made from 20 kW - 100 kW with 2.5 MeV energy in China. (author)

Adsorption of SO{sub 2} on activated carbon for low gas concentrations

Energy Technology Data Exchange (ETDEWEB)

Zhang, P.; Wanko, H.; Ulrich, J. [Martin-Luther-Universitaet Halle-Wittenberg, Zentrum fuer Ingenieurwissenschaften, Verfahrenstechnik/TVT, Halle (Saale) (Germany)

2007-05-15

Adsorption experiments of SO{sub 2} on activated carbon has been carried out for low concentrations (about 100 ppm) at room temperature (15 to 33 C) with varying humidity in the air. The breakthrough curves show that at high relative humidity or relative higher SO{sub 2} concentration, the load capacity increases with respect to temperature. The humidity of the air is also of benefit to the load capacity of SO{sub 2}. When an adsorption process is interrupted and the activated carbon is kept closed for a while, the SO{sub 2} concentration at the exit of a fixed-bed adsorber is similar to that of the fresh activated carbon and begins at a very low value. It appears that the sorption potential has been refreshed after the storage period. Analysis of desorption experiments by simultaneous thermal analysis combined with mass spectrometry (MS) after loading, shows that the physisorbed SO{sub 2} and H{sub 2}O are desorbed at low temperatures. At higher temperatures, the MS peak of SO{sub 2} and H{sub 2}O occur at the same time. Compared with desorption immediately after loading, after one day, the desorption peak due to the physisorbed SO{sub 2} disappears. From this, it can be concluded that the refreshment of the loading capacity of the activated carbon after storage is mainly due to a change in the nature of the SO{sub 2} from a physisorbed state to a chemisorbed form. The same mechanism leads to a continuous refreshment of the sorption potential by means of a chemical reaction during the adsorption process. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

SPEAR-BETA fuel-performance code system: fission-gas-release module. Final report

International Nuclear Information System (INIS)

Christensen, R.

1983-03-01

The original SPEAR-BETA general description manual covers both mechanistic and statistical models for fuel reliability, but only mechanistic modeling of fission gas release. This addendum covers the SPEAR-BETA statistical model for fission gas release

Oxidation of SO{sub 2} and formation of water droplets under irradiation of 20 MeV protons in N{sub 2}/H{sub 2}O/SO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Tomita, Shigeo [Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Nakai, Yoichi, E-mail: nakaiy@riken.jp [Radioactive Isotope Physics Laboratory, RIKEN Nishina Center, Wako, Saitama 351-0198 (Japan); Funada, Shuhei; Tanikawa, Hideomi; Harayama, Isao [Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki 305-8573 (Japan); Kobara, Hitomi [National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8569 (Japan); Sasa, Kimikazu [Tandem Accelerator Complex, University of Tsukuba, Tsukuba, Ibaraki 305-8577 (Japan); Pedersen, Jens Olaf Pepke [National Space Institute, Technical University of Denmark, DK-2800 Kgs. Lyngby (Denmark); Hvelplund, Preben [Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C (Denmark)

2015-12-15

We have performed an experiment on charged droplet formation in a humidified N{sub 2} gas with trace SO{sub 2} concentration and induced by 20 MeV proton irradiation. It is thought that SO{sub 2} reacts with the chemical species, such as OH radicals, generated through the reactions triggered by N{sub 2}{sup +} production. Both droplet number and droplet size increased with SO{sub 2} consumption for the proton irradiation. The total charged droplet numbers entering the differential mobility analyzer per unit time were proportional to the 0.68 power of the SO{sub 2} consumption. These two findings suggest that coagulation among the small droplets contributes to the formation of the droplets. The charged droplet volume detected per unit time is proportional to the SO{sub 2} consumption, which indicates that a constant amount of sulfur atoms is contained in a unit volume of droplet, regardless of different droplet-size distributions depending on the SO{sub 2} consumption.

GRASS-SST, Fission Products Gas Release and Fuel Swelling in Steady-State and Transients

International Nuclear Information System (INIS)

Zawadzki, S.

2001-01-01

1 - Description of program or function: GRASS-SST is a comprehensive, mechanistic model for the prediction of fission-gas behaviour in UO 2 -base fuels during steady-state and transient conditions. GRASS-SST treats fission-gas release and fuel swelling on an equal basis and simultaneously treats all major mechanisms that influence fission-gas behaviour. Models are included for intra- and inter-granular fission-gas bubble behaviour as well as a mechanistic description of the role of grain-edge inter-linked porosity on fission-gas release and swelling. GRASS-SST calculations include the effects of gas production from fissioning uranium atoms, bubble nucleation, a realistic equation of state for xenon, lattice bubble diffusivities based on experimental observations, bubble migration, bubble coalescence, re-solution, temperature and temperature gradients, inter-linked porosity, and fission-gas interaction with structural defects (dislocations and grain boundaries) on both the distribution of fission-gas within the fuel and on the amount of fission-gas released from the fuel. GRASS-SST includes the effects of the degree of nonequilibrium in the UO 2 lattice on fission-gas bubble mobility and bubble coalescence and also accounts for the observed formation of grain-surface channels. GRASS-SST also includes mechanistic models for grain-growth/grain boundary sweeping and for the behaviour of fission gas during liquefaction/dissolution and fuel melting conditions. 2 - Method of solution: A system of coupled equations for the evolution of the fission-gas bubble-size distributions in the lattice, on dislocations, on grain faces, and grain edges is derived based on the GRASS-SST models. Given a set of operating conditions, GRASS-SST calculates the bubble radii for the size classes of bubbles under consideration using a realistic equation of state for xenon as well as a generalised capillary relation. 3 - Restrictions on the complexity of the problem: Maxima of : 1 axial section

Thermal ramp rate effects on mixed-oxide fuel swelling/gas release

International Nuclear Information System (INIS)

Hinman, C.A.; Randklev, E.H.

1979-01-01

Macroscopic swelling behavior of PNL-10 was compared to that of PNL-2 fuel and it was found that the swelling-threshold behavior is similar for similar thermal conditions. Transient fission gas release for the PNL-10 fuel is very similar to that observed for the PNL-2 fuel for similar thermal conditions

East Asian SO2 pollution plume over Europe – Part 2: Evolution and potential impact

Directory of Open Access Journals (Sweden)

A. Stohl

2009-07-01

Full Text Available We report on the first observation-based case study of an aged East Asian anthropogenic SO2 pollution plume over Europe. Our airborne measurements in that plume detected highly elevated SO2 mole fractions (up to 900 pmol/mol between about 5000 and 7000 m altitude. Here, we focus on investigations of the origin, dispersion, evolution, conversion, and potential impact of the observed excess SO2. In particular, we investigate SO2 conversion to gas-phase sulfuric acid and sulfuric acid aerosols. Our FLEXPART and LAGRANTO model simulations, along with additional trace gas measurements, suggest that the plume originated from East Asian fossil fuel combustion sources and, 8–7 days prior to its arrival over Europe, ascended over the coast region of central East Asia to 9000 m altitude, probably in a cyclonic system with an associated warm conveyor belt. During this initial plume ascent a substantial fraction of the initially available SO2 must have escaped from removal by cloud processes. Hereafter, while mostly descending slowly, the plume experienced advection across the North Pacific, North America and the North Atlantic. During its upper troposphere travel, clouds were absent in and above the plume and OH-induced gas-phase conversion of SO2 to gas-phase sulfuric acid (GSA was operative, followed by GSA nucleation and condensation leading to sulfuric acid aerosol formation and growth. Our AEROFOR model simulations indicate that numerous large sulfuric acid aerosol particles were formed, which at least tempora-rily, caused substantial horizontal visibility degradation, and which have the potential to act as water vapor condensation nuclei in liquid water cloud formation, already at water vapor supersaturations as low as about 0.1%. Our AEROFOR model simulations also indicate that those fossil fuel combustion generated soot particles, which have survived cloud induced removal during the initial plume ascent, have experienced extensive H2SO4/H2O

Amino-Functionalized Luminescent Metal-Organic Framework Test Paper for Rapid and Selective Sensing of SO2 Gas and Its Derivatives by Luminescence Turn-On Effect.

Science.gov (United States)

Wang, Meng; Guo, Lin; Cao, Dapeng

2018-03-06

Rapid and selective sensing of sulfur dioxide (SO 2 ) gas has attracted more and more attention because SO 2 not only causes environmental pollution but also severely affects the health of human beings. Here we report an amino-functionalized luminescent metal-organic framework (MOF) material (i.e., MOF-5-NH 2 ) and further investigate its sensing property for SO 2 gas and its derivatives as a luminescent probe. The results indicate that the MOF-5-NH 2 probe can selectively and sensitively sense SO 2 derivatives (i.e., SO 3 2- ) in real time by a luminescence turn-on effect with a lower detection limit of 0.168 ppm and a response time of less than 15 s. Importantly, the luminescence turn-on phenomenon can be observed by the naked eye. We also assembled MOF-5-NH 2 into a test paper to achieve the aim of portable detection, and the lower-limit concentration of the test paper for sensing SO 2 in real time was found to be about 0.05 ppm. Moreover, MOF-5-NH 2 also shows good anti-interference ability, strong luminescence stability, and reusability, which means that this material is an excellent sensing candidate. The amino functionalization may also provide a modification strategy to design luminescent sensors for other atmospheric pollutants.

A global catalogue of large SO2 sources and emissions derived from the Ozone Monitoring Instrument

Directory of Open Access Journals (Sweden)

V. E. Fioletov

2016-09-01

Full Text Available Sulfur dioxide (SO2 measurements from the Ozone Monitoring Instrument (OMI satellite sensor processed with the new principal component analysis (PCA algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr−1 to more than 4000 kt yr−1 of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources; power plants (297; smelters (53; and sources related to the oil and gas industry (65. The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005–2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30 % of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80 % over the 2005–2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr−1 and not detected by OMI.

A Global Catalogue of Large SO2 Sources and Emissions Derived from the Ozone Monitoring Instrument

Science.gov (United States)

Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

2016-01-01

Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr(exp -1) to more than 4000 kt yr(exp -1) of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005- 2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30% of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80% over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr(exp -1) and not detected by OMI.

Gas Release Behavior of Cu-TiH2 Composite Powder and Its Application as a Blowing Agent to Fabricate Aluminum Foams with Low Porosity and Small Pore Size

Science.gov (United States)

Cheng, Ying; Li, Yanxiang; Chen, Xiang; Liu, Zhiyong; Zhou, Xu; Wang, Ningzhen

2018-03-01

Compared to traditional pore structure with high porosity (≥ 80 pct) and large pore size (≥ 3 mm), aluminum foams with low porosity (60 to 70 pct) and small pore size (≤ 2 mm) possess higher compressive property and formability. In order to achieve the goal of reducing pore size, Cu-TiH2 composite powder prepared by ball milling preoxidized TiH2 with Cu powder was used as a blowing agent. Its gas release behavior was characterized by thermogravimetric analysis and differential scanning calorimetry. The results show that the ball milling treatment can advance the gas release process and slow the gas release rate at the same time. All these changes are favorable to the reduction of porosity and pore size. Such Cu-TiH2 composite powder provides an alternative way to fabricate aluminum foams with low porosity and small pore size.

Gas Release Behavior of Cu-TiH2 Composite Powder and Its Application as a Blowing Agent to Fabricate Aluminum Foams with Low Porosity and Small Pore Size

Science.gov (United States)

Cheng, Ying; Li, Yanxiang; Chen, Xiang; Liu, Zhiyong; Zhou, Xu; Wang, Ningzhen

2018-06-01

Compared to traditional pore structure with high porosity (≥ 80 pct) and large pore size (≥ 3 mm), aluminum foams with low porosity (60 to 70 pct) and small pore size (≤ 2 mm) possess higher compressive property and formability. In order to achieve the goal of reducing pore size, Cu-TiH2 composite powder prepared by ball milling preoxidized TiH2 with Cu powder was used as a blowing agent. Its gas release behavior was characterized by thermogravimetric analysis and differential scanning calorimetry. The results show that the ball milling treatment can advance the gas release process and slow the gas release rate at the same time. All these changes are favorable to the reduction of porosity and pore size. Such Cu-TiH2 composite powder provides an alternative way to fabricate aluminum foams with low porosity and small pore size.

The footprint of CO2 leakage in the water-column: Insights from numerical modeling based on a North Sea gas release experiment

Science.gov (United States)

Vielstädte, L.; Linke, P.; Schmidt, M.; Sommer, S.; Wallmann, K.; McGinnis, D. F.; Haeckel, M.

2013-12-01

Assessing the environmental impact of potential CO2 leakage from offshore carbon dioxide storage sites necessitates the investigation of the corresponding pH change in the water-column. Numerical models have been developed to simulate the buoyant rise and dissolution of CO2 bubbles in the water-column and the subsequent near-field dispersion of dissolved CO2 in seawater under ocean current and tidal forcing. In order to test and improve numerical models a gas release experiment has been conducted at 80 m water-depth within the Sleipner area (North Sea). CO2 and Kr (used as inert tracer gas) were released on top of a benthic lander at varying gas flows (impact of such leakage rates is limited to the near-field bottom waters, due to the rapid dissolution of CO2 bubbles in seawater (CO2 is being stripped within the first two to five meters of bubble rise). In particular, small bubbles, which will dissolve close to the seafloor, may cause a dangerous low-pH environment for the marine benthos. However, on the larger scale, the advective transport by e.g. tidal currents, dominates the CO2 dispersal in the North Sea and dilutes the CO2 peak quickly. The model results show that at the small scales (impact on the marine environment, thereby reducing pH substantially (by 0.4 units) within a diameter of less than 50 m around the release spot (depending on the duration of leakage and the current velocities). Strong currents and tidal cycles significantly reduce the spreading of low-pH water masses into the far-field by efficiently diluting the amount of CO2 in ambient seawater.

Investigation of nucleation kinetics in H2SO4 vapor through modeling of gas phase kinetics coupled with particle dynamics

Science.gov (United States)

Carlsson, Philip T. M.; Zeuch, Thomas

2018-03-01

We have developed a new model utilizing our existing kinetic gas phase models to simulate experimental particle size distributions emerging in dry supersaturated H2SO4 vapor homogeneously produced by rapid oxidation of SO2 through stabilized Criegee-Intermediates from 2-butene ozonolysis. We use a sectional method for simulating the particle dynamics. The particle treatment in the model is based on first principles and takes into account the transition from the kinetic to the diffusion-limited regime. It captures the temporal evolution of size distributions at the end of the ozonolysis experiment well, noting a slight underrepresentation of coagulation effects for larger particle sizes. The model correctly predicts the shape and the modes of the experimentally observed particle size distributions. The predicted modes show an extremely high sensitivity to the H2SO4 evaporation rates of the initially formed H2SO4 clusters (dimer to pentamer), which were arbitrarily restricted to decrease exponentially with increasing cluster size. In future, the analysis presented in this work can be extended to allow a direct validation of quantum chemically predicted stabilities of small H2SO4 clusters, which are believed to initiate a significant fraction of atmospheric new particle formation events. We discuss the prospects and possible limitations of the here presented approach.

SO2 oxidation catalyst model systems characterized by thermal methods

DEFF Research Database (Denmark)

Hatem, G; Eriksen, Kim Michael; Gaune-Escard, M

2002-01-01

The molten salts M2S2O7 and MHSO4, the binary molten salt Systems M2S2O7-MHSO4 and the molten salt-gas systems M2S2O7 V2O5 and M2S2O7-M2SO4 V2O5 (M = Na, K, Rb, Cs) in O-2, SO2 and At atmospheres have been investigated by thermal methods like calorimetry, Differential Enthalpic Analysis (DEA) and...... to the mechanism Of SO2 oxidation by V2O5 based industrial catalysts....

Defect trap model of gas behaviour in UO2 fuel during irradiation

International Nuclear Information System (INIS)

Szuta, A.

2003-01-01

Fission gas behaviour is one of the central concern in the fuel design, performance and hypothetical accident analysis. The report 'Defect trap model of gas behaviour in UO 2 fuel during irradiation' is the worldwide literature review of problems studied, experimental results and solutions proposed in related topics. Some of them were described in details in the report chapters. They are: anomalies in the experimental results; fission gas retention in the UO 2 fuel; microstructure of the UO 2 fuel after irradiation; fission gas release models; defect trap model of fission gas behaviour; fission gas release from UO 2 single crystal during low temperature irradiation in terms of a defect trap model; analysis of dynamic release of fission gases from single crystal UO 2 during low temperature irradiation in terms of defect trap model; behaviour of fission gas products in single crystal UO 2 during intermediate temperature irradiation in terms of a defect trap model; modification of re-crystallization temperature of UO 2 in function of burnup and its impact on fission gas release; apparent diffusion coefficient; formation of nanostructures in UO 2 fuel at high burnup; applications of the defect trap model to the gas leaking fuel elements number assessment in the nuclear power station (VVER-PWR)

An innovative process for simultaneous removal of CO2 and SO2 from flue gas of a power plant by energy integration

International Nuclear Information System (INIS)

Yu, Y.S.; Li, Y.; Li, Q.; Jiang, J.; Zhang, Z.X.

2009-01-01

With the fast development of the society, the amount of carbon dioxide has been increased enormously in the atmosphere all over the world, which has already endangered the survival of human being. More and more people or organizations are studying new technologies to reduce the cost of capturing CO 2 . The recovery and sequestration of CO 2 from flue gas of the power plant is regarded as a feasible way to mitigate the greenhouse gas emissions. Therefore, the process of recovering carbon dioxide by chemical absorption with monoethanolamine (MEA) in industry was emphatically described in this paper. Based on energy integration, a coupled process was proposed which included MEA absorption of CO 2 and SO 2 , and the heat recovery from the flue gas's waste heat recovery unit and compressor inter-stage cooling unit. Compared the innovative process with an original process, 9% of thermal energy could be reduced in the new flowsheet. Meanwhile decarbonization and desulphurization could be carried on in the absorber simultaneously without the usual wet flue gas desulphurization (FGD) system. An exergy analysis model was established and validated by the literature data with a deviation less than 5.40%. The exergy results indicated that the exergy loss of the improved process was 15.48-20.75% less than that of the original one, which proved that the innovative process was reasonable and effective from the perspective of energy utilization.

Novel Solid Encapsulation of Ethylene Gas Using Amorphous α-Cyclodextrin and the Release Characteristics.

Science.gov (United States)

Ho, Binh T; Bhandari, Bhesh R

2016-05-04

This research investigated the encapsulation of ethylene gas into amorphous α-cyclodextrins (α-CDs) at low (LM) and high (HM) moisture contents at 1.0-1.5 MPa for 24-120 h and its controlled release characteristics at 11.2-52.9% relative humidity (RH) for 1-168 h. The inclusion complexes (ICs) were characterized using X-ray diffractometry (XRD), nuclear magnetic resonance spectroscopy (CP-MAS (13)C NMR), and scanning electron microscopy (SEM). Ethylene concentrations in the ICs were from 0.45 to 0.87 mol of ethylene/mol CD and from 0.42 to 0.54 mol of ethylene/mol CD for LM and HM α-CDs, respectively. Ethylene gas released from the encapsulated powder at higher rates with increasing RH. An analysis of release kinetics using Avrami's equation showed that the LM and HM amorphous α-CDs were not associated with significant differences in release constant k and parameter n for any given RH condition. NMR spectra showed the presence of the characteristic carbon-carbon double bond of ethylene gas in the encapsulated α-CD powder.

Diffusion and release of noble gas and halogen fission products with several days half-life in UO2 particle

International Nuclear Information System (INIS)

Fang Chao

2013-01-01

The exact solutions of diffusion and release model of noble gas and halogen fission products in UO 2 particle of HTGR were built under the conditions of adsorption effect and other physical processes. The corresponding release fractions (F(t)) and the ratio of release and productive amounts (R(t)/B (t)) of fission products were also derived. Furthermore, the F(t) and R(t)/B(t) of 131 I, 131 IXe m , 133 Xe and 133 Xe m whose half-lifes are several days in UO 2 particle with the exact solutions, approximate solutions and corresponding numerical solutions under different temperature histories of reactor core were investigated. The results show that the F(t) and R(t)/B(t) are different in numerical values unless the time of release is long enough. The properties of conservation of exact solutions are much more reasonable than the ones of approximate solutions. It is also found that the results of exact solutions approach the actual working conditions more than the approximate and numerical solutions. (author)

The application of release models to the interpretation of rare gas coolant activities

International Nuclear Information System (INIS)

Wise, C.

1985-01-01

Much research is carried out into the release of fission products from UO 2 fuel and from failed pins. A significant application of this data is to define models of release which can be used to interpret measured coolant activities of rare gas isotopes. Such interpretation is necessary to extract operationally relevant parameters, such as the number and size of failures in the core and the 131 I that might be released during depressurization faults. The latter figure forms part of the safety case for all operating CAGRs. This paper describes and justifies the models which are used in the ANAGRAM program to interpret CAGR coolant activities, highlighting any remaining uncertainties. The various methods by which the program can extract relevant information from the measurements are outlined, and examples are given of the analysis of coolant data. These analyses point to a generally well understood picture of fission gas release from low temperature failures. Areas of higher temperature release are identified where further research would be beneficial to coolant activity analysis. (author)

Safety barriers to prevent release of hydrocarbons during production of oil and gas

OpenAIRE

Sklet, Snorre; Hauge, Stein

2004-01-01

This report documents a set of scenarios related to release of hydrocarbons during production on oil and gas platforms. For each release scenario, initiating events, barrier functions aimed to prevent loss of containment, and barrier systems that realize these barrier functions are identified and described. Safety barriers to prevent release of hydrocarbons during production of oil and gas

Steady-state and transient fission gas release and swelling model for LIFE-4

International Nuclear Information System (INIS)

Villalobos, A.; Liu, Y.Y.; Rest, J.

1984-06-01

The fuel-pin modeling code LIFE-4 and the mechanistic fission gas behavior model FASTGRASS have been coupled and verified against gas release data from mixed-oxide fuels which were transient tested in the TREAT reactor. Design of the interface between LIFE-4 and FASTGRASS is based on an earlier coupling between an LWR version of LIFE and the GRASS-SST code. Fission gas behavior can significantly affect steady-state and transient fuel performance. FASTGRASS treats fission gas release and swelling in an internally consistent manner and simultaneously includes all major mechanisms thought to influence fission gas behavior. The FASTGRASS steady-state and transient analysis has evolved through comparisons of code predictions with fission-gas release and swelling data from both in- and ex-reactor experiments. FASTGRASS was chosen over other fission-gas behavior models because of its availability, its compatibility with the LIFE-4 calculational framework, and its predictive capability

Experimental study on removals of SO2 and NOX using adsorption of activated carbon/microwave desorption.

Science.gov (United States)

Ma, Shuang-Chen; Yao, Juan-Juan; Gao, Li; Ma, Xiao-Ying; Zhao, Yi

2012-09-01

Experimental studies on desulfurization and denitrification were carried out using activated carbon irradiated by microwave. The influences of the concentrations of nitric oxide (NO) and sulfur dioxide (SO 2 ), the flue gas coexisting compositions, on adsorption properties of activated carbon and efficiencies of desulfurization and denitrification were investigated. The results show that adsorption capacity and removal efficiency of NO decrease with the increasing of SO 2 concentrations in flue gas; adsorption capacity of NO increases slightly first and drops to 12.79 mg/g, and desulfurization efficiency descends with the increasing SO 2 concentrations. Adsorption capacity of SO 2 declines with the increasing of O 2 content in flue gas, but adsorption capacity of NO increases, and removal efficiencies of NO and SO 2 could be larger than 99%. Adsorption capacity of NO declines with the increase of moisture in the flue gas, but adsorption capacity of SO 2 increases and removal efficiencies of NO and SO 2 would be relatively stable. Adsorption capacities of both NO and SO 2 decrease with the increasing of CO 2 content; efficiencies of desulfurization and denitrification augment at the beginning stage, then start to fall when CO 2 content exceeds 12.4%. The mechanisms of this process are also discussed. [Box: see text].

Fission gas release at high burn-up: beyond the standard diffusion model

International Nuclear Information System (INIS)

Landskron, H.; Sontheimer, F.; Billaux, M.R.

2002-01-01

At high burn-up standard diffusion models describing the release of fission gases from nuclear fuel must be extended to describe the experimental loss of xenon observed in the fuel matrix of the rim zone. Marked improvements of the prediction of integral fission gas release of fuel rods as well as of radial fission gas profiles in fuel pellets are achieved by using a saturation concept to describe fission gas behaviour not only in the pellet rim but also as an additional fission gas path in the whole pellet. (author)

Fission Gas Release in LWR Fuel Rods Exhibiting Very High Burn-Up

DEFF Research Database (Denmark)

Carlsen, H.

1980-01-01

Two UO2Zr BWR type test fuel rods were irradiated to a burn-up of about 38000 MWd/tUO2. After non-destructive characterization, the fission gas released to the internal free volume was extracted and analysed. The irradiation was simulated by means of the Danish fuel performance code WAFER-2, which...

2D Hybrid Nanomaterials for Selective Detection of NO2 and SO2 Using "Light On and Off" Strategy.

Science.gov (United States)

Chen, Aimin; Liu, Rui; Peng, Xiao; Chen, Qiaofen; Wu, Jianmin

2017-10-25

In order to distinguish NO 2 and SO 2 gas with one sensor, we designed a paper chip assembled with a 2D g-C 3 N 4 /rGO stacking hybrid fabricated via a layer-by-layer self-assembly approach. The g-C 3 N 4 /rGO hybrid exhibited a remarkable photoelectric property due to the construction of a van der Waals heterostructure. For the first time, we have been able to selectively detect NO 2 and SO 2 gas using a "light on and off" strategy. Under the "light off" condition, the g-C 3 N 4 /rGO sensor exhibited a p-type semiconducting behavior with a low detection limit of 100 ppb of NO 2 , but with no response toward SO 2 . In contrast, the sensor showed n-type semiconducting behavior which could detect SO 2 at concentration as low as 2 ppm under UV light irradiation. The effective electron transfer among the 2D structure of g-C 3 N 4 and rGO nanosheets as well as highly porous structures could play an important role in gas sensing. The different sensing mechanisms at "light on and off" circumstances were also investigated in detail.

Safety barriers on oil and gas platforms. Means to prevent hydrocarbon releases

Energy Technology Data Exchange (ETDEWEB)

Sklet, Snorre

2005-12-15

/operational safety barriers are considered. The initiating events are divided into five main categories; (1) human and operational errors, (2) technical failures, (3) process upsets, (4) external events, and (5) latent failures from design. The development of the hydrocarbon release scenarios has generated new knowledge about causal factors of hydrocarbon releases and safety barriers introduced to prevent the releases. Collectively, the release scenarios cover the most frequent initiating events and the most important safety barriers introduced to prevent hydrocarbon releases. BORA-Release is a new method for qualitative and quantitative risk analysis of the hydrocarbon release frequency on oil and gas platforms. BORA-Release combines use of barrier block diagrams/event trees, fault trees, and risk influence diagrams in order to analyse the risk of hydrocarbon release from a set of hydrocarbon release scenarios. Use of BORA-Release makes it possible to analyse the effect on the hydrocarbon release frequency of safety barriers introduced to prevent hydrocarbon releases. Further, BORA-Release may be used to analyse the effect on the barrier performance of platform specific conditions of technical, human, operational, and organisational risk influencing factors. Thus, BORA-Release may improve today's quantitative risk analyses on two weak points; i) analysis of causal factors of the initiating event hydrocarbon release (loss of containment), and ii) analysis of the effect on the risk of human and organisational factors. The main focus of this thesis is safety barriers introduced to prevent hydrocarbon releases on offshore oil and gas production platforms. Thus, the results are primarily useful for the oil and gas industry in their effort to control and reduce the risk of hydrocarbon releases. The Norwegian oil and gas industry can use the results in their work to fulfil the requirements to safety barriers and risk analyses from the Petroleum Safety Authority. However, the concepts

Adsorption of radioactive I2 gas onto fly-ash aerosol

International Nuclear Information System (INIS)

Noguchi, Hiroshi; Murata, Mikio; Suzuki, Katsumi.

1988-01-01

The adsorption of radioactive elemental iodine (I 2 ) gas onto fly-ash aerosol has been studied to provide basic data for the realistic and precise assessment of dose to the general public from radioiodine released from nuclear facilities. A mixture of fly-ash aerosol and 131 I 2 gas was passed through a cylindrical glass vessel so that particulate iodine was formed by adsorption of I 2 onto aerosol. Then the concentrations of I 2 and particulate iodine were measured. It was found that the adsorption reached an equilibrium state between 5 and 12 min and that the proportion of iodine which was adsorbed on the aerosol decreased with increasing initial I 2 concentration ranging over 10 -13 to 10 -9 g/cm 3 . The adsorption isotherm of the aerosol for I 2 gas approximately followed Freundlich isotherm. Using the adsorption isotherm, a theoretical equation was derived to explain the adsorption on the basis of FUCHS' theory on the evaporation of droplets. A sticking probability in the equation decreased with increasing adsorbed amount. The calculated results were in good agreement with the experimental ones. (author)

Simulation of pellet-cladding thermomechanical interaction and fission gas release

International Nuclear Information System (INIS)

Denis, A.; Soba, A.

2001-01-01

This paper summarizes the present status of a computer code that describes some of the main phenomena occurring in a nuclear fuel element throughout its life. Temperature distribution, thermal expansion, elastic and plastic strains, creep, mechanical interaction between pellet and cladding, fission gas release, swelling and densification are modelized. The code assumes an axi-symmetric rod and hence, cylindrical finite elements are employed for the discretization. Due to the temperature dependence of the thermal conductivity, the heat conduction problem is non-linear. Thermal expansion gives origin to elastic or plastic strains, which adequately describe the bamboo effect. Plasticity renders the stress-strain problem non linear. The fission gas inventory is calculated by means of a diffusion model, which assumes spherical grains and uses a finite element scheme. In order to reduce the calculation time, the rod is divided into five cylindrical rings where the temperature is averaged. In each ring the gas diffusion problem is solved in one grain and the results are then extended to the whole ring. The pressure, increased by the released gas, interacts with the stress field. Densification and swelling due to solid and gaseous fission products are also considered. Experiments, particularly those of the FUMEX series, are simulated with this code. A good agreement is obtained for the fuel center line temperature, the inside rod pressure and the fractional gas release. (author)

Fission gas release behavior of MOX fuels under simulated daily-load-follow operation condition. IFA-554/555 test evaluation with FASTGRASS code

International Nuclear Information System (INIS)

Ikusawa, Yoshihisa; Ozawa, Takayuki

2008-03-01

IFA-554/555 load-follow tests were performed in HALDEN reactor (HBWR) to study the MOX fuel behavior under the daily-load-follow operation condition in the framework of ATR-MOX fuel development in JAEA. IFA-554/555 rig had the instruments of rod inner pressure, fuel center temperature, fuel stack elongation, and cladding elongation. Although the daily-load-follow operation in nuclear power plant is one of the available options for economical improvement, the power change in a short period in this operation causes the change of thermal and mechanical irradiation conditions. In this report, FP gas release behavior of MOX fuel rod was evaluated under the daily-load-follow operation condition with the examination data from IFA-554/555 by using the computation code 'FASTGRASS'. From the computation results of FASTGRASS code which could compute the FP gas release behavior under the transient condition, it could be concluded that FP gas was released due to the relaxation of fuel pellet inner stress and pellet temperature increase, which were caused by the cyclic power change during the daily-load-follow operation. In addition, since the amount of released FP gas decreased during the steady operation after the daily-load-follow, it could be mentioned that the total of FP gas release at the end of life with the daily-load-follow is not so much different from that without the daily-load-follow. (author)

Gas chromatography/sniffing port analysis evaluated for aroma release from rehydrated French beans (Phaseolus vulgaris).

NARCIS (Netherlands)

Ruth, van S.M.; Roozen, J.P.; Cozijnsen, J.L.

1996-01-01

The technique of gas chromatography/sniffing port analysis was evaluated for studying the release of aroma compounds from rehydrated diced French beans. The aroma compounds 2-—methylbutanal and hexanal were released at a constant rate over time. An identical selection of odour active compounds was

Microbial reduction of SO{sub 2} and NO{sub x} as a means of by-product recovery/disposal from regenerable processes for the desulfurization of flue gas. Technical progress report, September 11, 1992--December 11, 1992

Energy Technology Data Exchange (ETDEWEB)

Sublette, K.L.

1992-12-31

With the continual increase in the utilization of high sulfur and high nitrogen containing fossil fuels, the release of airborne pollutants into the environment has become a critical problem. The fuel sulfur is converted to SO{sub 2} during combustion. Fuel nitrogen and a fraction of the nitrogen from the combustion air are converted to nitric oxide and nitrogen dioxide, NO{sub x}. For the past five years Combustion Engineering (now Asea Brown Boveri or ABB) and, since 1986, the University of Tulsa (TU) have been investigating the oxidation of H{sub 2}S by the facultatively anaerobic and autotrophic bacterium Thiobacillus denitrificans and have developed a process, concept for the microbial removal of H{sub 2}S from a gas stream the simultaneous removal of SO{sub 2} and NO by D. desulfuricans and T. denitrificans co-cultures and cultures-in-series was demonstrated. These systems could not be sustained due to NO inhibition of D. desulfuricans. However, a preliminary economic analysis has shown that microbial reduction of SO{sub 2} to H{sub 2}S with subsequent conversion to elemental sulfur by the Claus process is both technically and economically feasible if a less expensive carbon and/or energy source can be found. It has also been demonstrated that T. denitrificans can be grown anaerobically on NO(g) as a terminal electron acceptor with reduction to elemental nitrogen. Microbial reduction of NO{sub x} is a viable process concept for the disposal of concentrated streams of NO{sub x} as may be produced by certain regenerable processes for the removal of SO{sub 2} and NO{sub x} from flue gas.

Removal kinetics for gaseous NO and SO2by an aqueous NaClO2solution mist in a wet electrostatic precipitator

KAUST Repository

Park, Hyun-Woo

2016-07-26

Removal kinetics for NO and SO2 by NaClO2 solution mist were investigated in a wet electrostatic precipitator. By varying the molar concentrations of NO, SO2, and NaClO2, the removal rates of NO and SO2 confirmed to range from 34.8 to 72.9 mmol/m3 s and 36.6 to 84.7 mmol/m3 s, respectively, at a fixed gas residence time of 0.25 s. The rate coefficients of NO and SO2 were calculated to be 0.679 (mmol/m3)−0.33 s−1 and 1.401 (mmol/m3)−0.1 s−1 based on the rates of the individual removal of NO and SO2. Simultaneous removal of NO and SO2 investigated after the evaluation of removal rates for their individual treatment was performed. At a short gas residence time, SO2 gas removed more quickly by a mist of NaClO2 solution than NO gas in simultaneous removal experiments. This is because SO2 gas, which has a relatively high solubility in solution, was absorbed more rapidly at the gas–liquid interface than NO gas. NO and SO2 gases were absorbed as nitrite (Formula presented.) and sulfite (Formula presented.) ions, respectively, by the NaClO2 solution mist at the gas–liquid interface. Then, (Formula presented.) and (Formula presented.) were oxidized to nitrate (Formula presented.) and sulfate (Formula presented.), respectively, by reactions with (Formula presented.), ClO2, HClO, and ClO in the liquid phase. © 2016 Informa UK Limited, trading as Taylor & Francis Group

Preventing Buoyant Displacement Gas Release Events in Hanford Double-Shell Waste Tanks

Energy Technology Data Exchange (ETDEWEB)

Meyer, Perry A.; Stewart, Charles W.

2001-01-01

This report summarizes the predictive methods used to ensure that waste transfer operations in Hanford waste tanks do not create waste configurations that lead to unsafe gas release events. The gas release behavior of the waste in existing double-shell tanks has been well characterized, and the flammable gas safety issues associated with safe storage of waste in the current configuration are being formally resolved. However, waste is also being transferred between double-shell tanks and from single-shell tanks into double-shell tanks by saltwell pumping and sluicing that create new wastes and waste configurations that have not been studied as well. Additionally, planning is underway for various waste transfer scenarios to support waste feed delivery to the proposed vitrification plant. It is critical that such waste transfers do not create waste conditions with the potential for dangerous gas release events.

High-throughput technology for novel SO2 oxidation catalysts

International Nuclear Information System (INIS)

Loskyll, Jonas; Stoewe, Klaus; Maier, Wilhelm F

2011-01-01

We review the state of the art and explain the need for better SO 2 oxidation catalysts for the production of sulfuric acid. A high-throughput technology has been developed for the study of potential catalysts in the oxidation of SO 2 to SO 3 . High-throughput methods are reviewed and the problems encountered with their adaptation to the corrosive conditions of SO 2 oxidation are described. We show that while emissivity-corrected infrared thermography (ecIRT) can be used for primary screening, it is prone to errors because of the large variations in the emissivity of the catalyst surface. UV-visible (UV-Vis) spectrometry was selected instead as a reliable analysis method of monitoring the SO 2 conversion. Installing plain sugar absorbents at reactor outlets proved valuable for the detection and quantitative removal of SO 3 from the product gas before the UV-Vis analysis. We also overview some elements used for prescreening and those remaining after the screening of the first catalyst generations. (topical review)

Ash partitioning during the oxy-fuel combustion of lignite and its dependence on the recirculation of flue gas impurities (H{sub 2}O, HCl and SO{sub 2})

Energy Technology Data Exchange (ETDEWEB)

Facun Jiao; Juan Chen; Lian Zhang; Yajuan Wei; Yoshihiko Ninomiya; Sankar Bhattacharya; Hong Yao [Monash University, Clayton, Vic. (Australia). Department of Chemical Engineering

2011-06-15

Oxy-fuel combustion of a brown coal (i.e. lignite) has been carried out at 1000{sup o}C to experimentally examine the vaporisation of organically bound metals and the agglomeration of ash particles as a function of the concentration of gaseous impurities including H{sub 2}O, HCl and SO{sub 2} in about 27% O{sub 2} balanced with CO{sub 2}. The properties of bulk ash and individual metals were investigated intensively. Particularly, attention was paid to Na which is notorious for fouling and to organically bound Al which has been less studied. The results indicate that, the organically bound metals, although possessing a very low content in the raw coal, are vital for the agglomeration of ash particles, which are also highly sensitive to the loading of gas impurities in flue gas. HCl recirculation is the most crucial factor promoting the vaporisation of metals via chlorination. Apart from alkali metals, the organically bound Al and Ti were also vaporised noticeably. Recirculation of SO{sub 2} promoted the sulfation of Na to condense into liquid droplet which increased fine ash yield. Co-existence of bulk HCl and SO{sub 2} played a synergetic role in the sulfation of Na via an initial chlorination of the char-bound Na. In contrast, co-existence of steam with HCl and SO{sub 2} favored the formation of Na alumino-silicates, which are favorable for ash agglomeration. 34 refs., 15 figs., 3 tabs.

Effect of axial diffusional delays on the overall fission gas release

International Nuclear Information System (INIS)

Pedersen, N.K.

1983-01-01

In fission gas release modeling, it is normally assumed that any locally released gas mixes instantly and perfectly with other gases throughout the internal rod void volume. The present work investigates the consequences of the assumption that perfect mixing is dependent on diffusion, although the subassumption is maintained that pressure equilibrium is instantly achieved. In other words, when a burst of gas release occurs at any axial location, sufficient local accommodation takes place throughout the rod to eliminate any pressure gradients, but due to the narrowness of the passages through fuel cracks and fuel-cladding gap, concentration gradients may still prevail. Diffusion coefficients for the subsequent concentration equilibration are derived from classical theories. Application of one-dimensional diffusion theory is straightforward, but the lack of knowledge of the effective width of the axial passage introduces an uncertainty

Characterization of the gas releasing behaviors of catalytic pyrolysis of rice husk using potassium over a micro-fluidized bed reactor

International Nuclear Information System (INIS)

Liu, Yuan; Wang, Yan; Guo, Feiqiang; Li, Xiaolei; Li, Tiantao; Guo, Chenglong; Chang, Jiafu

2017-01-01

Highlights: • Releasing propensity of CO, CO 2 , CH 4 and H 2 was studied in a micro-fluidized bed. • Gas releasing pattern was influenced by temperature and potassium concentration. • Variations in gas forming E a are indicative of catalytic performance of potassium. - Abstract: Influence of potassium on the gas releasing behaviors during rice husk high-temperature pyrolysis was investigated under isothermal conditions in a two stage micro-fluidized bed reactor. Reaction kinetics for generating H 2 , CO, CO 2 and CH 4 was investigated based on the Friedman and model-fitting approaches. Results indicated that different gas species had different times to start and end the gas release process, particularly at 600 °C, representing different chemical routes and mechanics for generating these gas components. The resulting apparent activation energies for H 2 , CO, and CO 2 decreased from 23.10 to 12.00 kJ/mol, 15.48 to 14.03 kJ/mol and 10.14 to 7.61 kJ/mol respectively with an increase in potassium concentration from 0 to 0.5 mol/kg, while that for CH 4 increased from 16.85 to 19.40 kJ/mol. The results indicated that the addition of potassium could promote the generation reactions of H 2 , CO and CO 2 while hinder the generation reactions of CH 4 . The pyrolysis reaction was further found to be subject to the three-dimensional diffusion model for all the samples.

Monitoring of the release of gaseous and aerosol-bound radioactive materials. Pt. 2

International Nuclear Information System (INIS)

1992-01-01

KTA 1503 contains requirements on technical installations and supplementary organizational measures considered necessary in order to monitor the release of gaseous and aerosol-bound radioactive materials. It consists of part 1: Monitoring of the release of radioactive materials together with stack gas during normal operation; part 2: Monitoring of the release of radioactive materials together with stack gas in the event of incidents; part 3: Monitoring of radioactive materials not released together with stack gas. The concept on which this rule is based is to ensure that in the case of incidents during which the result of effluent monitoring remains meaningful, such monitoring can be reliably performed. (orig./HSCH) [de

Simplified model of SO2 removal from industrial gas in e-beam process

International Nuclear Information System (INIS)

Bouzyk, J.; Sowinski, M.

1997-01-01

The analysis of SO 2 and, on the part, NO x removal mechanism by e-beam process has been discussed. It is estimated that radiation contribution to SO 2 removal amounts to 40% while in the case of NO x it appears to reach about 70%. Taking into account the main reactions responsible for SO 2 oxidation as well as the assumption presented in our previous paper an algorithm has been developed to describe linear kinetics of the process. The principal assumption referred to depends on OH radical concentration to be nearly stable. The concept of an extended model of NO x /SO 2 removal has been presented and the literature data have been used to check the suggested model. On that basis the general idea has been proposed for controlling SO 2 /NO x removal which comprises both the simplified and extended pathway. (author)

On-Line Fission Gas Release Monitoring System in the High Flux Reactor Petten

International Nuclear Information System (INIS)

Laurie, M.; Fuetterer, M. A.; Appelman, K.H.; Lapetite, J.-M.; Marmier, A.; Knol, S.; Best, J.

2013-06-01

For HTR fuel irradiation tests in the HFR Petten a specific installation was designed and installed dubbed the 'Sweep Loop Facility' (SLF). The SLF is tasked with three functions, namely temperature control by gas mixture technique, surveillance of safety parameters (temperature, pressure, radioactivity etc.) and analysis of fission gas release for three individual capsules in two separate experimental rigs. The SLF enables continuous and independent surveillance of all gas circuits. The release of volatile fission products (FP) from the in-pile experiments is monitored by continuous gas purging. The fractional release of these FP, defined as the ratio between release rate of a gaseous fission isotope (measured) to its instantaneous birth rate (calculated), is a licensing-relevant test for HTR fuel. The developed gamma spectrometry station allows for higher measurement frequencies, thus enabling follow-up of rapid and massive release transients. The designed stand-alone system was tested and fully used through the final irradiation period of the HFR-EU1 experiment which was terminated on 18 February 2010. Its robustness allowed the set up to be used as extra safety instrumentation. This paper describes the gas activity measurement technique based on HPGe gamma spectrometry and illustrates how qualitative and quantitative analysis of volatile FP can be performed on-line. (authors)

Iron triggers λSo prophage induction and release of extracellular DNA in Shewanella oneidensis MR-1 biofilms.

Science.gov (United States)

Binnenkade, Lucas; Teichmann, Laura; Thormann, Kai M

2014-09-01

Prophages are ubiquitous elements within bacterial chromosomes and affect host physiology and ecology in multiple ways. We have previously demonstrated that phage-induced lysis is required for extracellular DNA (eDNA) release and normal biofilm formation in Shewanella oneidensis MR-1. Here, we investigated the regulatory mechanisms of prophage λSo spatiotemporal induction in biofilms. To this end, we used a functional fluorescence fusion to monitor λSo activation in various mutant backgrounds and in response to different physiological conditions. λSo induction occurred mainly in a subpopulation of filamentous cells in a strictly RecA-dependent manner, implicating oxidative stress-induced DNA damage as the major trigger. Accordingly, mutants affected in the oxidative stress response (ΔoxyR) or iron homeostasis (Δfur) displayed drastically increased levels of phage induction and abnormal biofilm formation, while planktonic cells were not or only marginally affected. To further investigate the role of oxidative stress, we performed a mutant screen and identified two independent amino acid substitutions in OxyR (T104N and L197P) that suppress induction of λSo by hydrogen peroxide (H2O2). However, λSo induction was not suppressed in biofilms formed by both mutants, suggesting a minor role of intracellular H2O2 in this process. In contrast, addition of iron to biofilms strongly enhanced λSo induction and eDNA release, while both processes were significantly suppressed at low iron levels, strongly indicating that iron is the limiting factor. We conclude that uptake of iron during biofilm formation triggers λSo-mediated lysis of a subpopulation of cells, likely by an increase in iron-mediated DNA damage sensed by RecA. Copyright © 2014, American Society for Microbiology. All Rights Reserved.

Emission of gas and atmospheric dispersion of SO2 during the December 2013 eruption at San Miguel volcano (El Salvador)

Science.gov (United States)

Salerno, Giuseppe G.; Granieri, Domenico; Liuzzo, Marco; La Spina, Alessandro; Giuffrida, Giovanni B.; Caltabiano, Tommaso; Giudice, Gaetano; Gutierrez, Eduardo; Montalvo, Francisco; Burton, Michael; Papale, Paolo

2016-04-01

San Miguel volcano, also known as Chaparrastique, is a basaltic volcano along the Central American Volcanic Arc (CAVA). Volcanism is induced by the convergence of the Cocos Plate underneath the Caribbean Plate, along a 1200-km arc, extending from Guatemala to Costa Rica and parallel to the Central American Trench. The volcano is located in the eastern part of El Salvador, in proximity to the large communities of San Miguel, San Rafael Oriente, and San Jorge. Approximately 70,000 residents, mostly farmers, live around the crater and the city of San Miguel, the second largest city of El Salvador, ten km from the summit, has a population of ~180,000 inhabitants. The Pan-American and Coastal highways cross the north and south flanks of the volcano.San Miguel volcano has produced modest eruptions, with at least 28 VEI 1-2 events between 1699 and 1967 (datafrom Smithsonian Institution http://www.volcano.si.edu/volcano.cfm?vn=343100). It is characterized by visible milddegassing from a summit vent and fumarole field, and by intermittent lava flows and Strombolian activity. Since the last vigorous fire fountaining of 1976, San Miguel has only experienced small steam explosions and gas emissions, minor ash fall and rock avalanches. On 29 December 2013 the volcano erupted producing an eruption that has been classified as VEI 2. While eruptions tend to be low-VEI, the presence of major routes and the dense population in the surrounding of the volcano increases the risk that weak explosions with gas and/or ash emission may pose. In this study, we present the first inventory of SO2, CO2, HCl, and HF emission rates on San Miguel volcano, and an analysis of the hazard from volcanogenic SO2 discharged before, during, and after the December 2013 eruption. SO2 was chosen as it is amongst the most critical volcanogenic pollutants, which may cause acute and chronicle disease to humans. Data were gathered by the geochemical monitoring network managed by the Ministerio de Medio Ambiente

Fission gas release in LWR fuel measured during nuclear operation

International Nuclear Information System (INIS)

Appelhans, A.D.; Skattum, E.; Osetek, D.J.

1980-01-01

A series of fuel behavior experiments are being conducted in the Heavy Boiling Water Reactor in Halden, Norway, to measure the release of Xe, Kr, and I fission products from typical light water reactor design fuel pellets. Helium gas is used to sweep the Xe and Kr fission gases out of two of the Instrumented Fuel Assembly 430 fuel rods and to a gamma spectrometer. The measurements of Xe and Kr are made during nuclear operation at steady state power, and for 135 I following reactor scram. The first experiments were conducted at a burnup of 3000 MWd/t UO 2 , at bulk average fuel temperatures of approx. 850 K and approx. 23 kW/m rod power. The measured release-to-birth ratios (R/B) of Xe and Kr are of the same magnitude as those observed in small UO 2 specimen experiments, when normalized to the estimated fuel surface-to-volume ratio. Preliminary analysis indicates that the release-to-birth ratios can be calculated, using diffusion coefficients determined from small specimen data, to within a factor of approx. 2 for the IFA-430 fuel. The release rate of 135 I is shown to be approximately equal to that of 135 Xe

Pilot scale-SO{sub 2} control by dry sodium bicarbonate injection and an electrostatic precipitator

Energy Technology Data Exchange (ETDEWEB)

Pliat, M.J.; Wilder, J.M. [University of Washington, Seattle, WA (United States). Dept. of Civil & Environmental Engineering

2007-10-15

A 500 actual cubic feet gas per minute (acfm) pilot-scale SO{sub 2} control study was undertaken to investigate flue gas desulfurization (FGD) by dry sodium sorbents in 400{sup o}F (204.5{sup o}C) flue gases emitted from a coal fired boiler with flue gas concentrations between 350 and 2500 ppm SO{sub 2}. Powdered sodium alkaline reagents were injected into the hot flue gas downstream of the air preheater and the spent reagents were collected using an electrostatic precipitator. Three different sorbents were used: processed sodium bicarbonate of two particle sizes; solution mined sodium bicarbonate, and processed sodium sesquicarbonate. SO{sub 2} concentrations were measured upstream of the reagent injection, 25-ft (7.62 m) downstream of the injection point, and downstream of the electrostatic precipitator. SO{sub 2} collection efficiencies ranged from 40 to 80% using sodium bicarbonate stoichiometric ratios from 0.5 to 3.0. Much of the in-duct SO{sub 2} removal occurred during the first second of reagent reaction time, indicating that the sulfur dioxide-sodium reaction rates may be faster than have been measured for fixed bed measurements reported in the literature.

Experimental study on removals of SO2 and NO(x) using adsorption of activated carbon/microwave desorption.

Science.gov (United States)

Ma, Shuang-Chen; Yao, Juan-Juan; Gao, Li; Ma, Xiao-Ying; Zhao, Yi

2012-09-01

Experimental studies on desulfurization and denitrification were carried out using activated carbon irradiated by microwave. The influences of the concentrations of nitric oxide (NO) and sulfur dioxide (SO2), the flue gas coexisting compositions, on adsorption properties of activated carbon and efficiencies of desulfurization and denitrification were investigated. The results show that adsorption capacity and removal efficiency of NO decrease with the increasing of SO2 concentrations in flue gas; adsorption capacity of NO increases slightly first and drops to 12.79 mg/g, and desulfurization efficiency descends with the increasing SO2 concentrations. Adsorption capacity of SO2 declines with the increasing of O2 content in flue gas, but adsorption capacity of NO increases, and removal efficiencies of NO and SO2 could be larger than 99%. Adsorption capacity of NO declines with the increase of moisture in the flue gas, but adsorption capacity of SO2 increases and removal efficiencies of NO and SO2 would be relatively stable. Adsorption capacities of both NO and SO2 decrease with the increasing of CO2 content; efficiencies of desulfurization and denitrification augment at the beginning stage, then start to fall when CO2 content exceeds 12.4%. The mechanisms of this process are also discussed. The prominent SO2 and NOx treatment techniques in power plants are wet flue gas desulfurization (FGD) and the catalytic decomposition method like selective catalytic reduction (SCR) or nonselective catalytic reduction (NSCR). However, these processes would have some difficulties in commercial application due to their high investment, requirement of expensive catalysts and large-scale equipment, and so on. A simple SO2 and NOx reduction utilizing decomposition by microwave energy method can be used. The pollutants control of flue gas in the power plants by the method of microwave-induced decomposition using adsorption of activated carbon/microwave desorption can meet the

Removal of SO2 and NO/sub x/ from flue gas by means of a spray dryer/electron beam combination: a feasibility study

International Nuclear Information System (INIS)

Helfritch, D.J.; Feldman, P.L.; Ray, A.B.; Morgan, J.R.; Hildreth, G.A.

1982-04-01

This study examines the feasibility of adding an electron beam between the spray dryer and the fabric filter of dry scrubber flue gas desulfurization (FGD) systems. The beam promises effective removal of nitrogen oxides (NO/sub x/) and sulfur dioxide (SO 2 ), even at higher coal-sulfur levels than usually economic for dry scrubbers. The beam excites gas molecules, promoting reactions that convert SO 2 and NO/sub x/ to acids that then react with calcium compounds and are removed by the filter. Concerns examined here are feasibility and waste disposal. The cost findings are promising for both manufacture and operation. The system uses commercially available components. The relatively low temperatures and high humidity downstream of the spray dryer favor economic beam operation. The beam removes SO 2 , so the dryer can be run for economy, not high removal. The beam's incidental heating effect reduces reheat cost. Safe landfilling of the nitrate-rich waste appears practical, with leachate carrying no more nitrate than natural rain and dustfall. We expect natural pozzolanic reactions between alumina-silica compounds in the fly ash and lime compounds from the spray dryer to form an impermeable concrete-like material within 10 days after landfilling. Dry scrubber with electron beam appears competitive with commercial FGD systems, and we recommend a pilot scale operation

Sulphur dioxide (SO2) electrotransfer in electric field generated by corona discharge

International Nuclear Information System (INIS)

Wang, Zu-wu; Guo, Jia; Zeng, Han-cai; Ge, Chun-liang; Yu, Jiang

2007-01-01

The mechanism of the forming SO 2 negative ions and their electrotransfer in the corona discharge electric field was investigated in this paper. The experimental results showed that SO 2 electrotransfer occurred in the electric field with corona discharge, which had potential applications in removal of SO 2 of the flue gas from coal-fired power plants by electrotransfer. SO 2 electrotransfer was enhanced by higher electric-field intensity or a larger discharging area. Assistant uniform electric field after the corona discharge electric field would improve SO 2 electrotransfer. The increment of the desulphurization efficiency by SO 2 electrotransfer might reach as high as 50%. (author)

Rate-based modelling of combined SO2 removal and NH3 recycling integrated with an aqueous NH3-based CO2 capture process

International Nuclear Information System (INIS)

Li, Kangkang; Yu, Hai; Qi, Guojie; Feron, Paul; Tade, Moses; Yu, Jingwen; Wang, Shujuan

2015-01-01

Highlights: • A rigorous, rate-based model for an NH 3 –CO 2 –SO 2 –H 2 O system was developed. • Model predictions are in good agreement with pilot plant results. • >99.9% of SO 2 was captured and >99.9% of slipped ammonia was reused. • The process is highly adaptable to the variations of SO 2 /NH 3 level, temperatures. - Abstract: To reduce the costs of controlling emissions from coal-fired power stations, we propose an advanced and effective process of combined SO 2 removal and NH 3 recycling, which can be integrated with the aqueous NH 3 -based CO 2 capture process to simultaneously achieve SO 2 and CO 2 removal, NH 3 recycling and flue gas cooling in one process. A rigorous, rate-based model for an NH 3 –CO 2 –SO 2 –H 2 O system was developed and used to simulate the proposed process. The model was thermodynamically and kinetically validated by experimental results from the open literature and pilot-plant trials, respectively. Under typical flue gas conditions, the proposed process has SO 2 removal and NH 3 reuse efficiencies of >99.9%. The process is strongly adaptable to different scenarios such as high SO 2 levels in flue gas, high NH 3 levels from the CO 2 absorber and high flue gas temperatures, and has a low energy requirement. Because the process simplifies flue gas desulphurisation and resolves the problems of NH 3 loss and SO 2 removal, it could significantly reduce the cost of CO 2 and SO 2 capture by aqueous NH 3

Multispectral Observations of Explosive Gas Emissions from Santiaguito, Guatemala

Science.gov (United States)

Carn, S. A.; Watson, M.; Thomas, H.; Rodriguez, L. A.; Campion, R.; Prata, F. J.

2016-12-01

Santiaguito volcano, Guatemala, has been persistently active for decades, producing frequent explosions from its actively growing lava dome. Repeated release of volcanic gases contains information about conduit processes during the cyclical explosions at Santiaguito, but the composition of the gas phase and the amount of volatiles released in each explosion remains poorly constrained. In addition to its persistent activity, Santiaguito offers an exceptional opportunity to investigate lava dome degassing processes since the upper surface of the active lava dome can be viewed from the summit of neighboring Santa Maria. In January 2016 we conducted multi-spectral observations of Santiaguito's explosive eruption plumes and passive degassing from multiple perspectives as part of the first NSF-sponsored `Workshop on Volcanoes' instrument deployment. Gas measurements included open-path Fourier-Transform infrared (OP-FTIR) spectroscopy from the Santa Maria summit, coincident with ultraviolet (UV) and infrared (IR) camera and UV Differential Optical Absorption Spectroscopy (DOAS) from the El Mirador site below Santiaguito's active Caliente lava dome. Using the OP-FTIR in passive mode with the Caliente lava dome as the source of IR radiation, we were able to collect IR spectra at high temporal resolution prior to and during two explosions of Santiaguito on 7-8 January, with volcanic SO2 and H2O emissions detected. UV and IR camera data provide constraints on the total SO2 burden in the emissions (and potentially the volcanic ash burden), which coupled with the FTIR gas ratios provides new constraints on the mass and composition of volatiles driving explosions at Santiaguito. All gas measurements indicate significant volatile release during explosions with limited degassing during repose periods. In this presentation we will present ongoing analysis of the unique Santiaguito gas dataset including estimation of the total volatile mass released in explosions and an

Integrated biomass gasification using the waste heat from hot slags: Control of syngas and polluting gas releases

International Nuclear Information System (INIS)

Sun, Yongqi; Seetharaman, Seshadri; Liu, Qianyi; Zhang, Zuotai; Liu, Lili; Wang, Xidong

2016-01-01

In this study, the thermodynamics of a novel strategy, i.e., biomass/CO 2 gasification integrated with heat recovery from hot slags in the steel industry, were systemically investigated. Both the target syngas yield and the polluting gas release were considered where the effect of gasifying conditions including temperature, pressure and CO 2 reacted was analyzed and then the roles of hot slags were further clarified. The results indicated that there existed an optimum temperature for the maximization of H 2 production. Compared to blast furnace slags, steel slags remarkably increased the CO yield at 600–1400 °C due to the existence of iron oxides and decreased the S-containing gas releases at 400–700 °C, indicating potential desulfurizing ability. The identification of biomass/CO 2 gasification thermodynamics in presence of slags could thus provide important clues not only for the deep understanding of biomass gasification but also for the industrial application of this emerging strategy from the viewpoint of syngas optimization and pollution control. - Highlights: • Biomass/CO 2 gasification was integrated with the heat recovery from hot slags. • Both syngas yield and polluting gas release during gasification were determined. • There existed an optimum temperature for the maximization of H 2 production. • Steel slags increased CO yield at 600–1400 °C due to the existence of iron oxides. • Steel slags remarkably decreased the releases of S-containing gas at 400–700 °C.

Concurrent removal of elemental mercury and SO2 from flue gas using a thiol-impregnated CaCO3-based adsorbent: a full factorial design study.

Science.gov (United States)

Balasundaram, Karthik; Sharma, Mukesh

2018-03-22

Mercury (Hg) emitted from coal-based thermal power plants (CTPPs) can accumulate and bio-magnify in the food chain, thereby posing a risk to humans and wildlife. The central idea of this study was to develop an adsorbent which can concurrently remove elemental mercury (Hg 0 ) and SO 2 emitted from coal-based thermal power plants (CTPPs) in a single unit operation. Specifically, a composite adsorbent of CaCO 3 impregnated with 2-mercaptobenimidazole (2-MBI) (referred to as modified calcium carbonate (MCC)) was developed. While 2-MBI having sulfur functional group could selectively adsorb Hg 0 , CaCO 3 could remove SO 2 . Performance of the adsorbent was evaluated in terms of (i) removal (%) of Hg 0 and SO 2 , (ii) adsorption mechanism, (iii) adsorption kinetics, and (iv) leaching potential of mercury from spent adsorbent. The adsorption studies were performed using a 2 2 full factorial design of experiments with 15 ppbV of Hg 0 and 600 ppmV of SO 2 . Two factors, (i) reaction temperature (80 and 120 °C; temperature range in flue gas) and (ii) mass of 2-MBI (10 and 15 wt%), were investigated for the removal of Hg 0 and SO 2 (as %). The maximum Hg 0 and SO 2 removal was 86 and 93%, respectively. The results of XPS characterization showed that chemisorption is the predominant mechanism of Hg 0 and SO 2 adsorption on MCC. The Hg 0 adsorption on MCC followed Elovich kinetic model which is also indicative of chemisorption on heterogeneous surface. The toxicity characteristic leaching procedure (TCLP) and synthetic precipitation leaching procedure (SPLP) leached mercury from the spent adsorbent were within the acceptable levels defined in these tests. The engineering significance of this study is that the 2-MBI-modified CaCO 3 -based adsorbent has potential for concurrent removal of Hg 0 and SO 2 in a single unit operation. With only minor process modifications, the newly developed adsorbent can replace CaCO 3 in the flue-gas desulfurization (FGD) system.

The Cs2SO4-Ce2(SO4)3-H2SO4-H2O system at 150 and 200 deg C

International Nuclear Information System (INIS)

Bondar', S.A.; Belokoskov, V.I.; Trofimov, G.V.

1982-01-01

Solubility in the system Cs 2 SO 4 -Ce 2 (SO 4 ) 3 -H 2 SO 4 -H 2 O using the isothermal method at 150 and 200 deg C at molar ratios Cs 2 SO 4 :Ce 2 (SO 4 ) 3 =1:5 and conditions of sulfate crystallization Cs 2 SO 4 xCe 2 (SO 4 ) 3 , Ce 2 (SO 4 ) 3 x0.5H 2 SO 4 xnH 2 O (n=2-3) and Ce 2 (SO 4 ) 3 x3H 2 SO 4 are determined. Double sulfate Cs 2 SO 4 xCe 2 (SO 4 ) 3 is studied using the methods of crystallooptical, thermal, X-ray phase analyses and IR spectroscopy

Analysis of fission gas release-to-birth ratio data from the AGR irradiations

International Nuclear Information System (INIS)

Einerson, Jeffrey J.; Pham, Binh T.; Scates, Dawn M.; Maki, John T.; Petti, David A.

2016-01-01

A series of advanced gas reactor (AGR) irradiation tests is being conducted in the advanced test reactor (ATR) at Idaho National Laboratory (INL) in support of development and qualification of tristructural isotropic (TRISO) fuel used in the High temperature gas-cooled reactor (HTGR). Each AGR test consists of multiple independent capsules containing fuel compacts placed in a graphite cylinder shrouded by a steel shell. These capsules are instrumented with thermocouples (TC) embedded in the graphite enabling temperature control. For AGR-1, the first US irradiation of modern TRISO fuel completed in 2009, there were no particle failures detected. For AGR-2, a few exposed kernels existed in the fuel compacts based upon quality control data. For the AGR-3/4 experiment, particle failures in all capsules were expected because of the use of designed-to-fail (DTF) fuel particles whose kernels are identical to the driver fuel kernels and whose coatings are designed to fail under irradiation. The release-rate-to-birth-rate ratio (R/B) for each of krypton and xenon isotopes is calculated from release rates measured by the germanium detectors used in the AGR fission product monitoring (FPM) system installed downstream from each irradiated capsule. Birth rates are calculated based on the fission power in the experiment and fission product generation models. Thus, this R/B is a measure of the ability of fuel particle coating layers and compact matrix to retain fission gas atoms preventing their release into the sweep gas flow. The major factors that govern gaseous diffusion and release processes are found to be fuel material diffusion coefficient, temperature, and isotopic decay constant. To compare the release behavior among the AGR capsules and historic experiments, the R/B per failed particle is used. HTGR designers use this parameter in their fission product behavior models. For the U.S. TRISO fuel, a regression analysis is performed to establish functional relationships

Analysis of Fission Gas Release-to-Birth Ratio Data from the AGR Irradiations

International Nuclear Information System (INIS)

Einerson, Jeffrey J.; Pham, Binh T.; Scates, Dawn M.; Maki, John T.; Petti, David A.

2014-01-01

A series of Advanced Gas Reactor (AGR) irradiation tests is being conducted in the Advanced Test Reactor (ATR) at Idaho National Laboratory (INL) in support of development and qualification of tristructural isotropic (TRISO) fuel used in the High Temperature Gas-cooled Reactor (HTGR). Each AGR test consists of multiple independent capsules containing fuel compacts placed in a graphite cylinder shrouded by a steel shell. These capsules are instrumented with thermocouples (TC) embedded in the graphite enabling temperature control. For AGR-1, the first US irradiation of modern TRISO fuel completed in 2009, there were no particle failures detected. For AGR-2, a few exposed kernels existed in the fuel compacts based upon quality control data. For the AGR-3/4 experiment, particle failures in all capsules were expected because of the use of designed-to-fail (DTF) fuel particles whose kernels are identical to the driver fuel kernels and whose coatings are designed to fail under irradiation. The release-rate-to-birth-rate ratio (R/B) for each of krypton and xenon isotopes is calculated from release rates measured by the germanium detectors used in the AGR Fission Product Monitoring (FPM) System installed downstream from each irradiated capsule. Birth rates are calculated based on the fission power in the experiment and fission product generation models. Thus, this R/B is a measure of the ability of fuel particle coating layers and compact matrix to retain fission gas atoms preventing their release into the sweep gas flow. The major factors that govern gaseous diffusion and release processes are found to be fuel material diffusion coefficient, temperature, and isotopic decay constant. To compare the release behavior among the AGR capsules and historic experiments, the R/B per failed particle is used. HTGR designers use this parameter in their fission product behavior models. For the U.S. TRISO fuel, a regression analysis is performed to establish functional relationships

Analysis of fission gas release-to-birth ratio data from the AGR irradiations

Energy Technology Data Exchange (ETDEWEB)

Einerson, Jeffrey J., E-mail: jeffrey.einerson@inl.gov; Pham, Binh T.; Scates, Dawn M.; Maki, John T.; Petti, David A.

2016-09-15

A series of advanced gas reactor (AGR) irradiation tests is being conducted in the advanced test reactor (ATR) at Idaho National Laboratory (INL) in support of development and qualification of tristructural isotropic (TRISO) fuel used in the High temperature gas-cooled reactor (HTGR). Each AGR test consists of multiple independent capsules containing fuel compacts placed in a graphite cylinder shrouded by a steel shell. These capsules are instrumented with thermocouples (TC) embedded in the graphite enabling temperature control. For AGR-1, the first US irradiation of modern TRISO fuel completed in 2009, there were no particle failures detected. For AGR-2, a few exposed kernels existed in the fuel compacts based upon quality control data. For the AGR-3/4 experiment, particle failures in all capsules were expected because of the use of designed-to-fail (DTF) fuel particles whose kernels are identical to the driver fuel kernels and whose coatings are designed to fail under irradiation. The release-rate-to-birth-rate ratio (R/B) for each of krypton and xenon isotopes is calculated from release rates measured by the germanium detectors used in the AGR fission product monitoring (FPM) system installed downstream from each irradiated capsule. Birth rates are calculated based on the fission power in the experiment and fission product generation models. Thus, this R/B is a measure of the ability of fuel particle coating layers and compact matrix to retain fission gas atoms preventing their release into the sweep gas flow. The major factors that govern gaseous diffusion and release processes are found to be fuel material diffusion coefficient, temperature, and isotopic decay constant. To compare the release behavior among the AGR capsules and historic experiments, the R/B per failed particle is used. HTGR designers use this parameter in their fission product behavior models. For the U.S. TRISO fuel, a regression analysis is performed to establish functional relationships

Impacts of Four SO2 Oxidation Pathways on Wintertime Sulfate Concentrations

Science.gov (United States)

Sarwar, G.; Fahey, K.; Zhang, Y.; Kang, D.; Mathur, R.; Xing, J.; Wei, C.; Cheng, Y.

2017-12-01

Air quality models tend to under-estimate winter-time sulfate concentrations compared to observed data. Such under-estimations are particularly acute in China where very high concentrations of sulfate have been measured. Sulfate is produced by oxidation of sulfur dioxide (SO2) in gas-phase by hydroxyl radical and in aqueous-phase by hydrogen peroxide, ozone, etc. and most air quality models employ such typical reactions. Several additional SO2 oxidation pathways have recently been proposed. Heterogeneous reaction on dust has been suggested to be an important sink for SO2. Oxidation of SO2 on fine particles in presence of nitrogen dioxide (NO2) and ammonia (NH3) at high relative humidity has been implicated for sulfate formation in Chinese haze and London fog. Reactive nitrogen chemistry in aerosol water has also been suggested to produce winter-time sulfate in China. Specifically, high aerosol water can trap SO2 which can be subsequently oxidized by NO2 to form sulfate. Aqueous-phase (in-cloud) oxidation of SO2 by NO2 can also produce sulfate. Here, we use the hemispheric Community Multiscale Air Quality (CMAQ) modeling system to examine the potential impacts of these SO2 oxidation pathways on sulfate formation. We use anthropogenic emissions from the Emissions Database for Global Atmospheric Research and biogenic emissions from Global Emissions InitiAtive. We performed simulations without and with these SO2 oxidation pathways for October-December of 2014 using meteorological fields obtained from the Weather Research and Forecasting model. The standard CMAQ model contains one gas-phase chemical reaction and five aqueous-phase chemical reactions for SO2 oxidation. We implement four additional SO2 oxidation pathways into the CMAQ model. Our preliminary results suggest that the dust chemistry enhances mean sulfate over parts of China and Middle-East, the in-cloud SO2 oxidation by NO2 enhances sulfate over parts of western Europe, oxidation of SO2 by NO2 and NH3 on

Influence of additives and impurities in sweep gas and solid tritium release behaviour from lithium ceramics (review)

International Nuclear Information System (INIS)

Tanaka, Satoru

1991-01-01

Tritium release from solid breeding material is affected by small amounts of additives or impurities in the sweep gas or solid itself. Addition of hydrogen or water vapor to the sweep gas is reported to enhance the surface reaction of tritium release. Doping to solid breeder with elements of different valence from lithium has a possibility to improve tritium diffusion in the solid. Surface reaction and migration behavior in bulk are believed to be also affected by impurities in the sweep gas and in the solid. In order to model tritium release behavior in the blanket of fusion reactor, the mechanism of interaction with these additives or impurities must be quantitatively formulated. However, the mechanism of these remains to be elucidated. In this paper effects of these additives and impurities on tritium migration are reviewed. The mechanism of surface reaction for He+H 2 sweep gas is also discussed. (orig.)

Specialists' meeting on fission product release and transport in gas-cooled reactors. Summary report

Energy Technology Data Exchange (ETDEWEB)

NONE

1985-07-01

The purpose of the Meeting on Fission Product Release and Transport in Gas-Cooled Reactors was to compare and discuss experimental and theoretical results of fission product behaviour in gas-cooled reactors under normal and accidental conditions and to give direction for future development. The technical part of the meeting covered operational experience and laboratory research, activity release, and behaviour of released activity.

Specialists' meeting on fission product release and transport in gas-cooled reactors. Summary report

International Nuclear Information System (INIS)

1985-01-01

The purpose of the Meeting on Fission Product Release and Transport in Gas-Cooled Reactors was to compare and discuss experimental and theoretical results of fission product behaviour in gas-cooled reactors under normal and accidental conditions and to give direction for future development. The technical part of the meeting covered operational experience and laboratory research, activity release, and behaviour of released activity

Predictions of PuO2 and tracer compound release from ISV melts

International Nuclear Information System (INIS)

Cronenberg, A.W.; Callow, R.A.

1992-04-01

Two field tests were conducted at the Idaho National Engineering Laboratory (INEL) to assess in situ vitrification (ISV) suitability for long-term stabilization of buried radioactive waste. Both tests contained rare-earth oxide tracers (DY 2 O 3 , Yb 2 O 3 , and Tb 4 O 7 ) to simulate the presence of plutonium in the form of PuO 2 . In the first test, Intermediate Field Test (IFT)-l, approximately 4-% release of tracer material occurred during soil melting and associated off-gassing, while essentially nil release was observed for the second experiment (IFT-2) for which off-gassing was much reduced. This report presents an evaluation of the IFT test data in terms of governing release processes. Prediction of tracer release during ISV melting centered on an assessment of three potential transport mechanisms, (a) tracer diffusion through stagnant pool, (b) tracer transport by convective currents, and (c) tracer carry-off by escaping gas bubbles. Analysis indicates that tracer release by escaping gas is the dominant release mechanism, which is consistent with video records of gas bubble escape from the ISV melt surface. Quantitative mass transport predictions were also made for the IFT-I test conditions, indicating similarity between the 4-% release data and calculational results at viscosities of ∼ poise and tracer diffusivities of ∼10 -6 CM 2 /s. Since PuO 2 has similar chemical and transport (diffusivity) properties as the rare-earth tracers used in the rare earth tracers used in the IFT experiments, release of PuO 2 is predicted for similar off-gassing conditions. Reduced off-gassing during ISV would thus be expected to improve the overall retention of heavy-oxides within vitrified soil

SO2 frost - UV-visible reflectivity and Io surface coverage

Science.gov (United States)

Nash, D. B.; Fanale, F. P.; Nelson, R. M.

1980-01-01

The reflectance spectrum in the range 0.24-0.85 microns of SO2 frost is measured in light of the discovery of SO2 gas in the atmosphere of Io and the possible discovery of the frost on its surface. Frost deposits up to 1.5 mm thick were grown in vacuum at 130 K and bi-directional reflectance spectra were obtained. Typical SO2 frost is found to exhibit very low reflectivity (2-5%) at 0.30 microns, rising steeply at 0.32 microns to attain a maximum reflectivity (75-80%) at 4.0 microns and uniformly high reflectivity throughout the visible and near infrared. Comparison with the full disk spectrum of Io reveals that no more than 20% of the surface can be covered with optically thick SO2 frost. Combinations of surface materials including SO2 frost which can produce the observed spectrum are indicated.

Formation of Nanodroplets in N₂/H₂O/SO₂ under Irradiation of Fast Proton Beams

DEFF Research Database (Denmark)

Nakai, Youchi; Shigeoka, Tomita; Funada, Shuhei

of the droplet growth in thebinary nucleation process of water and H2SO4.We have performed irradiation of proton beam on the gas mixture of N2/H2O/SO2 andAir/H2O/SO2. The reduction of SO2 concentration by beam irradiation was monitored usingan SO2 meter and the size distributions of generated droplets were...

Delignification and Enhanced Gas Release from Soil Containing Lignocellulose by Treatment with Bacterial Lignin Degraders.

Science.gov (United States)

Rashid, Goran M M; Duran-Pena, Maria Jesus; Rahmanpour, Rahman; Sapsford, Devin; Bugg, Timothy D H

2017-04-10

The aim of the study was to isolate bacterial lignin-degrading bacteria from municipal solid waste soil, and to investigate whether they could be used to delignify lignocellulose-containing soil, and enhance methane release. A set of 20 bacterial lignin degraders, including 11 new isolates from municipal solid waste soil, were tested for delignification and phenol release in soil containing 1% pine lignocellulose. A group of 7 strains were then tested for enhancement of gas release from soil containing 1% lignocellulose in small-scale column tests. Using an aerobic pre-treatment, aerobic strains such as Pseudomonas putida showed enhanced gas release from the treated sample, but four bacterial isolates showed 5-10 fold enhancement in gas release in an in situ experiment under microanaerobic conditions: Agrobacterium sp., Lysinibacillus sphaericus, Comamonas testosteroni, and Enterobacter sp.. The results show that facultative anaerobic bacterial lignin degraders found in landfill soil can be used for in situ delignification and enhanced gas release in soil containing lignocellulose. The study demonstrates the feasibility of using an in situ bacterial treatment to enhance gas release and resource recovery from landfill soil containing lignocellulosic waste. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

The ternary system K2SO4MgSO4CaSO4

Science.gov (United States)

Rowe, J.J.; Morey, G.W.; Silber, C.C.

1967-01-01

Melting and subsolidus relations in the system K2SO4MgSO4CaSO4 were studied using heating-cooling curves, differential thermal analysis, optics, X-ray diffraction at room and high temperatures and by quenching techniques. Previous investigators were unable to study the binary MgSO4CaSO4 system and the adjacent area in the ternary system because of the decomposition of MgSO4 and CaSO4 at high temperatures. This problem was partly overcome by a novel sealed-tube quenching method, by hydrothermal synthesis, and by long-time heating in the solidus. As a result of this study, we found: (1) a new compound, CaSO4??3MgSO4 (m.p. 1201??C) with a field extending into the ternary system; (2) a high temperature form of MgSO4 with a sluggishly reversible inversion. An X-ray diffraction pattern for this polymorphic form is given; (3) the inversion of ??-CaSO4 (anhydrite) to ??-CaSO4 at 1195??C, in agreement with grahmann; (1) (4) the melting point of MgSO4 is 1136??C and that of CaSO4 is 1462??C (using sealed tube methods to prevent decomposition of the sulphates); (5) calcium langbeinite (K2SO4??2CaSO4) is the only compound in the K2SO4CaSO4 binary system. This resolved discrepancies in the results of previous investigators; (6) a continuous solid solution series between congruently melting K2SOP4??2MgSO4 (langbeinite) and incongruently melting K2SO4??2CaSO4 (calcium langbeinite); (7) the liquidus in the ternary system consists of primary phase fields of K2SO4, MgSO4, CaSO4, langbeinite-calcium langbeinite solid solution, and CaSO4??3MgSO4. The CaSO4 field extends over a large portion of the system. Previously reported fields for the compounds (K2SO4??MgSO4??nCaSO4), K2SO4??3CaSO4 and K2SO4??CaSO4 were not found; (8) a minimum in the ternary system at: 740??C, 25% MgSO4, 6% CaSO4, 69% K2SO4; and ternary eutectics at 882??C, 49% MgSO4, 19% CaSO4, 32% K2SO4; and 880??, 67??5% MgSO4, 5% CaSO4, 27??5% K2SO4. ?? 1967.

submitter Thermodynamics of the formation of sulfuric acid dimers in the binary (H2SO4–H2O) and ternary (H2SO4–H2O–NH3) system

CERN Document Server

Kürten, A; Rondo, L; Bianchi, F; Duplissy, J; Jokinen, T; Junninen, H; Sarnela, N; Schobesberger, S; Simon, M; Sipilä, M; Almeida, J; Amorim, A; Dommen, J; Donahue, N M; Dunne, E M; Flagan, R C; Franchin, A; Kirkby, J; Kupc, A; Makhmutov, V; Petäjä, T; Praplan, A P; Riccobono, F; Steiner, G; Tomé, A; Tsagkogeorgas, G; Wagner, P E; Wimmer, D; Baltensperger, U; Kulmala, M; Worsnop, D R; Curtius, J

2015-01-01

Sulfuric acid is an important gas influencing atmospheric new particle formation (NPF). Both the binary $(H_2SO_4–H_2O)$ system and the ternary system involving ammonia $(H_2SO_4–H_2O–NH_3)$ may be important in the free troposphere. An essential step in the nucleation of aerosol particles from gas-phase precursors is the formation of a dimer, so an understanding of the thermodynamics of dimer formation over a wide range of atmospheric conditions is essential to describe NPF. We have used the CLOUD chamber to conduct nucleation experiments for these systems at temperatures from 208 to 248 K. Neutral monomer and dimer concentrations of sulfuric acid were measured using a chemical ionization mass spectrometer (CIMS). From these measurements, dimer evaporation rates in the binary system were derived for temperatures of 208 and 223 K. We compare these results to literature data from a previous study that was conducted at higher temperatures but is in good agreement with the present study. For the ternary sys...

Cs2SO4-Pr2(SO4)3-H2O and NiSO4-Pr2(SO4)3-H2O systems at 75 deg C

International Nuclear Information System (INIS)

Onishchenko, M.K.; Skorikov, V.M.; Shevchuk, V.G.; AN SSSR, Moscow. Inst. Obshchej i Neorganicheskoj Khimii)

1979-01-01

To investigate physico-chemical properties of equilibrium saturated solutions and to elucidate the chemical changes under way, the aqueous systems of cesium, nickel and praseodymium (3) sulfates are studied. The method of isothermal saturation of salts at 75 deg C is used. It has been found that in the system Cs 2 SO 4 -Pr 2 (SO 4 ) 3 -H 2 O in a wide concentration range the soluble binary salt Cs 2 SO 4 xPr 2 (SO 4 ) 3 csytallizes in a congruent way. For the system NiSO 4 -Pr 2 (SO 4 ) 3 -H 2 O a solubility curve of the eutonic type is obtained, there being no chemical interaction between the components. The solubility isotherms for the system are given

On the fission gas release from oxide fuels during normal grain growth

International Nuclear Information System (INIS)

Paraschiv, M.C.; Paraschiv, A.; Glodeanu, F.

1997-01-01

A mathematical formalism for calculating the fission gas release from oxide fuels considering an arbitrary distribution of fuel grain size with only zero boundary condition for gas diffusion at the grain boundary is proposed. It has also been proved that it becomes unnecessary to consider the grain volume distribution function for fission products diffusion when the grain boundary gas resolution is considered, if thermodynamic forces on grain boundaries are only time dependent. In order to highlight the effect of the normal grain growth on fission gas release from oxide fuels Hillert's and Lifshitz and Slyozov's theories have been selected. The last one was used to give an adequate treatment of normal grain growth for the diffusion-controlled grain boundary movement in oxide fuels. It has been shown that during the fuel irradiation, the asymptotic form of the grain volume distribution functions given by Hillert and Lifshitz and Slyozov models can be maintained but the grain growth rate constant becomes time dependent itself. Experimental results have been used to correlate the two theoretical models of normal grain growth to the fission gas release from oxide fuels. (orig.)

In-pile observation of gas release from sodium-joint carbide pins irradiated in Osiris

International Nuclear Information System (INIS)

Colin, M.; Faugere, J.L.; Rouault, J.

1978-01-01

Gas release is studied in three sodium-joint carbide pins irradiated in the reactor Osiris at a nominal linear power of 900 W/cm to burn-ups ranging from 4 to 13%. The overall activity, stable gases and radioactive gases are measured. It is found that most of the gas is released in busts, that the release of stable gases speeds up sharply after an incubation time, that the initial bursts are very large and that for each mode of release observed and for each class of nuclide the radioactive gases follow a law R/B=A/lambda.n. An attempt is made to interpret the results in terms of either the formation of gas bubbles in the sodium joint, the existence of a large bubble above the fissile column or the simultaneous release of a large number of smaller bubbles [fr

The effect of gas release on column separator

NARCIS (Netherlands)

Kranenburg, C.

1974-01-01

A mathematical model has been considered in which the influence of gas release on transient cavitating flow and column separation in pipel ines is taken into account. A rei iable numerical method has been developed for the computation of the wave propagation and cavitation phenomena following pump

Increasing of MERARG experimental performances: on-line fission gas release measurement by mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Pontillon, Y.; Capdevila, H.; Clement, S. [CEA, DEN, DEC, SA3C, LAMIR, F-13108 Saint Paul lez Durance, (France); Guigues, E.; Janulyte, A.; Zerega, Y.; Andre, J. [Aix-Marseille Universite, LISA EA 4672, 13397 MARSEILLE cedex 20, (France)

2015-07-01

The MERARG device - implemented at the LECASTAR Hot Laboratory, at the CEA Cadarache - allows characterizing nuclear fuels with respect to the behaviour of fission gases during thermal transients representative of normal or off normal operating nuclear power plant conditions. The fuel is heated in order to extract a part or the total gas inventory it contains. Fission Gas Release (FGR) is actually recorded by mean of both on-line gamma spectrometry station and micro gas chromatography. These two devices monitor the quantity and kinetics of fission gas release rate. They only address {sup 85}Kr radioactive isotope and the elemental quantification of Kr, Xe and He (with a relatively low detection limit in the latter case, typically 5-10 ppm). In order to better estimate the basic mechanisms that promote fission gas release from irradiated nuclear fuels, the CEA fuel study department decided to improve its experimental facility by modifying MERARG to extend the studies of gamma emitter fission gases to all gases (including Helium) with a complete isotopic distribution capability. To match these specifications, a Residual Gas Analyser (RGA) has been chosen as mass spectrometer. This paper presents a review of the main aspects of the qualification/calibration phase of the RGA type analyser. In particular, results recorded over three mass ranges 1-10 u, 80-90 u and 120-140 u in the two classical modes of MERARG, i.e. on-line and off-line measurements are discussed. Results obtained from a standard gas bottle show that the quantitative analysis at a few ppm levels can be achieved for all isotopes of Kr and Xe, as well as masses 2 and 4 u. (authors)

Accelerated Reduction in \\(SO_2\\) Emissions from the U.S. Power Sector Triggered by Changing Prices of Natural Gas

OpenAIRE

Wu, Gang; McElroy, Michael Brendon; Lu, Xi; Nielsen, Chris

2012-01-01

Emissions of sulfur dioxide (\\(SO_2\\)) from the U.S. power sector decreased by 24% in 2009 relative to 2008. The Logarithmic Mean Divisia Index (LMDI) approach was applied to isolate the factors responsible for this decrease. It is concluded that 15% of the decrease can be attributed to the drop in demand for electricity triggered by the economic recession, and 28% can be attributed to switching of fuel from coal to gas responding to the decrease in prices for the latter. The largest factor i...

Partial discharge early-warning through ultraviolet spectroscopic detection of SO2

International Nuclear Information System (INIS)

Zhao, Yu; Wang, Xianpei; Dai, Dangdang; Dong, Zhengcheng; Huang, Yunguang

2014-01-01

Surveillance of SF 6  decomposition products is significant for detection of partial discharge (PD) in gas insulation switchgear (GIS). As a basis in on-site detection and diagnosis, PD early-warning aims to quickly find the abnormalities using a simple and cheap device. In this paper, SO 2  is chosen as a feature product and detected through ultraviolet spectroscopy. The derivative method is employed for baseline correction and spectral enhancement. The standard gases of the main decomposition products are qualitatively and quantitatively detected. Then decomposition experiments with different defects are designed to further verify the feasibility. As a stable decomposition product under PD, SO 2  is proved to be applicable for PD early-warning in the field. By selecting the appropriate wavelength range, namely 290–310 nm, ultraviolet derivative spectroscopy is sensitive enough to the trace SO 2  in the decomposed gas and the interference of other products can be avoided. Fast Fourier transform could be used for feature extraction in qualitative detection. Concentrations of SO 2  and other by-products increase with increasing discharge time and could be affected by the discharge energy and PD type. Ultraviolet detection based on SO 2  is effective for PD early-warning but the threshold should still be carefully selected in practice. (paper)

The release code package REVOLS/RENONS for fission product release from a liquid sodium pool into an inert gas atmosphere

International Nuclear Information System (INIS)

Starflinger, J.; Scholtyssek, W.; Unger, H.

1994-12-01

For aerosol source term considerations in the field of nuclear safety, the investigation of the release of volatile and non-volatile species from liquid surfaces into a gas atmosphere is important. In case of a hypothetical liquid metal fast breeder reactor accident with tank failure, primary coolant sodium with suspended or solved fuel particles and fission products may be released into the containment. The computer code package REVOLS/RENONS, based on a theoretical mechanistic model with a modular structure, has been developed for the prediction of sodium release as well as volatile and non-volatile radionuclide release from a liquid pool surface into the inert gas atmosphere of the inner containment. Hereby the release of sodium and volatile fission products, like cesium and sodium iodide, is calculated using a theoretical model in a mass transfer coefficient formulation. This model has been transposed into the code version REVOLS.MOD1.1, which is discussed here. It enables parameter analysis under highly variable user-defined boundary conditions. Whereas the evaporative release of the volatile components is governed by diffusive and convective transport processes, the release of the non-volatile ones may be governed by mechanical processes which lead to droplet entrainment from the wavy pool surface under conditions of natural or forced convection into the atmosphere. The mechanistic model calculates the liquid entrainment rate of the non-volatile species, like the fission product strontium oxide and the fuel (uranium dioxide) from a liquid pool surface into a parallel gas flow. The mechanistic model has been transposed into the computer code package REVOLS/RENONS, which is discussed here. Hereby the module REVOLS (RElease of VOLatile Species) calculates the evaporative release of the volatile species, while the module RENONS (RElease of NON-Volatile Species) computes the entrainment release of the non-volatile radionuclides. (orig./HP) [de

Ultrasound-induced Gas Release from Contrast Agent Microbubbles

NARCIS (Netherlands)

Postema, M.A.B.; Postema, Michiel; Bouakaz, Ayache; Versluis, Michel; de Jong, N.

2005-01-01

We investigated gas release from two hard-shelled ultrasound contrast agents by subjecting them to high-mechanical index (MI) ultrasound and simultaneously capturing high-speed photographs. At an insonifying frequency of 1.7 MHz, a larger percentage of contrast bubbles is seen to crack than at 0.5

Experimental study on the mechanism of SO2 emission and calcium-based desulfurization in the coal oxygen-enriched combustion

International Nuclear Information System (INIS)

Tian, Luning; Chen, Hanping; Yang, Haiping; Wang, Xianhua; Zhang, Shihong

2010-01-01

Full text: The emission of SO 2 , CO 2 brings serious harm to the ecological environment, human health and the global climate change. The largest source of SO 2 , CO 2 is the combustion of fossil fuels for power generation. So developing the new technology for controlling pollutants emissions from coal combustion was imperative. Oxygen-enriched combustion technology is such a new technology which can realize CO 2 zero emission, enhance the combustion efficiency and reduce pollutants emission. Due to the high concentration of CO 2 , it has many different aspects in the SO 2 emission and calcium-based desulfurization compare with the conventional combustion. In this article, experiments have been done to investigate the behavior and mechanism of SO 2 emissions and removal in oxygen-enriched combustion. First, in TGA and fixed bed reactor, the SO 2 emission characteristics were investigated under various bed temperature, particle size and O 2 / CO 2 concentration. It was observed that SO 2 released faster and the emission peak was higher than air atmosphere. SO 2 emission concentration increased with the reaction temperature increasing. Simultaneously, the mechanism of SO 2 emission was obtained by analyzing the sulfur compounds in the gas products and solid products in different reaction times. Then, the impacts of reaction temperature, particle size, O 2 / CO 2 concentration and SO 2 concentration etc. on the efficiency of SO 2 removal were analyzed. The phase analysis, pore diameter distribution and microstructure of the solid product were investigated. The experimental results showed that the sulphur capture takes place by direct sulphation reaction at high CO 2 concentration which attributes to light sinter, better porous structure, higher optimal desulfurization temperature and high desulfurization efficiency of calcium-based sorbent. (author)

Atmospheric SO{sub 2}. Global measurements using aircraft-based CIMS

Energy Technology Data Exchange (ETDEWEB)

Fiedler, V.

2008-06-27

Aircraft based measurements of tropospheric sulfur dioxide, SO{sub 2}, have been carried out during four campaigns in South America (TROCCINOX), Australia (SCOUT-O3), Europe (INTEX/MEGAPLUME) and Africa (AMMA). SO{sub 2} has been measured by chemical ionization mass spectrometry (CIMS), permanently online calibrated with isotopically labelled SO{sub 2}. The measurement method is described thoroughly in this work and the measured data are presented. Moreover, the data of the different regions are compared in general and typical air mass situations with SO{sub 2} enhancement are shown. A detailed analysis of four SO{sub 2} pollution plume cases emphasizes the main features: long-range transport, SO{sub 2} from metal smelters/volcanoes or from biomass burning. The SO{sub 2} measurements are analyzed in the light of simultaneously measured trace gas, particle and meteorological data. Air mass trajectory models (FLEXPART or HYSPLIT) are employed for a determination of the pollution origin. Further going evaluations with the aerosol model AEROFOR complete the analyses and point out, that the measured SO{sub 2} mole fractions are sufficient to explain new particle formation and growth. Finally, a first comparison of the measured SO{sub 2} to results from a global circulation model (ECHAM) with implemented sulfur chemistry showed a significant underestimation of the measured SO{sub 2} mole fraction by the model in the free troposphere. (orig.)

Development of Novel CO2 Adsorbents for Capture of CO2 from Flue Gas

Energy Technology Data Exchange (ETDEWEB)

Fauth, D.J.; Filburn, T.P. (University of Hartford, West Hartford, CT); Gray, M.L.; Hedges, S.W.; Hoffman, J.; Pennline, H.W.; Filburn, T.

2007-06-01

Capturing CO2 emissions generated from fossil fuel-based power plants has received widespread attention and is considered a vital course of action for CO2 emission abatement. Efforts are underway at the Department of Energy’s National Energy Technology Laboratory to develop viable energy technologies enabling the CO2 capture from large stationary point sources. Solid, immobilized amine sorbents (IAS) formulated by impregnation of liquid amines within porous substrates are reactive towards CO2 and offer an alternative means for cyclic capture of CO2 eliminating, to some degree, inadequacies related to chemical absorption by aqueous alkanolamine solutions. This paper describes synthesis, characterization, and CO2 adsorption properties for IAS materials previously tested to bind and release CO2 and water vapor in a closed loop life support system. Tetraethylenepentamine (TEPA), acrylonitrile-modified tetraethylenepentamine (TEPAN), and a single formulation consisting of TEPAN and N, N’-bis(2-hydroxyethyl)ethylenediamine (BED) were individually supported on a poly (methyl methacrylate) (PMMA) substrate and examined. CO2 adsorption profiles leading to reversible CO2 adsorption capacities were obtained using thermogravimetry. Under 10% CO2 in nitrogen at 25°C and 1 atm, TEPA supported on PMMA over 60 minutes adsorbed ~3.2 mmol/g{sorbent} whereas, TEPAN supported on PMMA along with TEPAN and BED supported on PMMA adsorbed ~1.7 mmol/g{sorbent} and ~2.3 mmol/g{sorbent} respectively. Cyclic experiments with a 1:1 weight ratio of TEPAN and BED supported on poly (methyl methacrylate) beads utilizing a fixed-bed flow system with 9% CO2, 3.5% O2, nitrogen balance with trace gas constituents were studied. CO2 adsorption capacity was ~ 3 mmols CO2/g{sorbent} at 40°C and 1.4 atm. No beneficial effect on IAS performance was found using a moisture-laden flue gas mixture. Tests with 750 ppmv NO in a humidified gas stream revealed negligible NO sorption onto the IAS. A high SO2

A review of selected aspects of the effect of water vapor on fission gas release from uranium oxycarbide

International Nuclear Information System (INIS)

Myers, B.F.

1994-04-01

A selective review is presented of previous measurements and the analysis of experiments on the effect of water vapor on fission gas release from uranium oxycarbide. Evidence for the time-dependent composition of the uranium oxycarbide fuel; the diffusional release of fission gas; and the initial, rapid and limited release of stored fission gas is discussed. In regard to the initial, rapid release of fission gas, clear restrictions on mechanistic hypotheses can be deduced from the experimental data. However, more fundamental experiments may be required to establish the mechanism of the rapid release

A Study on the Evaluation of Real Gas vs. Ideal Gas for its Application to the CO2 Leak Flow Model

International Nuclear Information System (INIS)

Jung, Hwa-Young; Lee, Jeong Ik

2015-01-01

The leak can cause various mechanical and thermal problems. Moreover, CO 2 also reacts with sodium by producing some solid reaction products (i.e. Na 2 CO 3 , Na 2 O, etc.), toxic gas (i.e. CO) and heat. Prior to applying the S-CO 2 Brayton cycle to the SFRs, the important safety issues that can occur in the Na-CO 2 heat exchanger should be evaluated. For this, it is essential to predict a CO 2 leak mechanism when the pressure boundary fails. The degree of sodium-CO 2 reaction is determined by several factors; a crack or rupture size, the interfacial area between sodium and CO 2 , the amount of released CO 2 , and so on. In order to simulate more reasonable and realistic CO 2 leak flow, one needs to evaluate and improve some limitations found from the previous studies. The dynamic response in the CO 2 side should be considered for varying mass flux at the nozzle exit over time. Thus, it is necessary to investigate more practical flow model to evaluate the system condition change and its consequences during the CO 2 leak. For the flow modeling, it is obvious that a real gas effect and friction force should be considered. However, due to its complexity and difficulty, it is generally assumed that CO 2 behaves as an ideal gas, and an isentropic critical flow without considering the friction force was applied for the analysis so far. In this paper, before incorporating the real gas effect and friction force to the model, gas properties are evaluated as the first step. The fluid properties of CO 2 is studied to observe how strong the real gas effect can be under SFR operating conditions. From this result, it is determined that which gas model is applicable to the CO 2 leak flow model for simulating the accident scenario in the given conditions of Na-CO 2 heat exchanger. The ideal gas law and the isentropic critical flow model are generally applied to predict the state and the flow rate of CO 2 leak in the Na-CO 2 heat exchanger previously. However, to simulate a

Macroscopic calculational model of fission gas release from water reactor fuels

International Nuclear Information System (INIS)

Uchida, Masaki

1993-01-01

Existing models for estimating fission gas release rate usually have fuel temperature as independent variable. Use of fuel temperature, however, often brings an excess ambiguity in the estimation because it is not a rigorously definable quantity as a function of heat generation rate and burnup. To derive a mathematical model that gives gas release rate explicitly as a function of design and operational parameters, the Booth-type diffusional model was modified by changing the character of the diffusion constant from physically meaningful quantity into a mere mathematical parameter, and also changing its temperature dependency into power dependency. The derived formula was found, by proper choice of arbitrary constants, to satisfactorily predict the release rates under a variety of irradiation histories up to a burnup of 60,000 MWd/t. For simple power histories, the equation can be solved analytically by defining several transcendental functions, which enables simple calculation of release rate using graphs. (author)

Aura OMI Observations of Global SO2 and NO2 Pollution from 2005 to 2013

Science.gov (United States)

Krotkov, Nickolay; Li, Can; Lamsal, Lok; Celarier, Edward; Marchenko, Sergey; Swartz, William H.; Bucsela, Eric; Fioletov, Vitali; McLinden, Chris; Joiner, Joanna;

The present status of rare gas release control

International Nuclear Information System (INIS)

Yamamoto, Hiroshi

1974-01-01

Of the rare gases Ar, Kr and Xe released from nuclear facilities, the problem of release control can be confined to 41 Ar, 85 Kr and 133 Xe. The cases of the latter two are described, as 41 Ar is not much significant. 133 Xe, having relatively short half-life, can be dealt sufficiently by holding-up in case of light water reactors. 85 Kr of long half-life must be removed : the methods are low temperature adsorption, liquefaction distillation, absorption and diaphragm method. As for future problem, there is disposal of concentrated rare gas. (Mori, K.)

Gas release during salt well pumping: model predictions and comparisons to laboratory experiments

International Nuclear Information System (INIS)

Peurrung, L.M.; Caley, S.M.; Bian, E.Y.; Gauglitz, P.A.

1996-09-01

The Hanford Site has 149 single-shell tanks (SSTs) containing radioactive wastes that are complex mixes of radioactive and chemical products. Some of these wastes are known to generate mixtures of flammable gases, including hydrogen, nitrous oxide, and ammonia. Nineteen of these SSTs have been placed on the Flammable Gas Watch List (FGWL) because they are known or suspected, in all but one case, to retain these flammable gases. Salt well pumping to remove the interstitial liquid from SSTs is expected to cause the release of much of the retained gas, posing a number of safety concerns. Research at the Pacific Northwest National Laboratory (PNNL) has sought to quantify the release of flammable gases during salt well pumping operations. This study is being conducted for Westinghouse Hanford Company as part of the PNNL Flammable Gas Project. Understanding and quantifying the physical mechanisms and waste properties that govern gas release during salt well pumping will help to resolve the associated safety issues

Manufacturing and test of a low cost polypropylene bag to reduce the radioactive gas released by a radiopharmaceutical production facility

Energy Technology Data Exchange (ETDEWEB)

Tavares, Jose Carlos Freitas; Lacerda, Marco Aurelio de Sousa, E-mail: jcft@cdtn.b, E-mail: masl@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (SEPRA/ CDTN/CNEN-MG) Belo Horizonte, MG (Brazil). Servico de Protecao Radiologica; Nascimento, Leonardo Tafas Constantino do; Silva, Juliana Batista da, E-mail: ltcn@cdtn.b, E-mail: silvajb@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (SECPRA/ CDTN/CNEN-MG) Belo Horizonte, MG (Brazil). Secao de Producao de Radiofarmacos

2011-07-01

The main objective of this work was to evaluate the efficiency of a plastic gas storage bag to reduce the radioactive gas released by the chimney of a radiopharmaceutical production facility during the 2-[{sup 18}F]fluoro-2- deoxy-D-glucose ({sup 18}FDG) synthesis. The studied facility was the Development Centre of Nuclear Technology (CDTN/CNEN) in Belo Horizonte, Brazil. The bag was manufactured utilizing foils of polypropylene of 360 x 550 x 0.16 mm and disposable components of the cassette of the synthesizer. Two synthesis of {sup 18}FDG were done using the same hot cell and synthesizer to evaluate the efficiency of the bag. The manufactured bag was put in the gas exit of the synthesizer and the activity reported by the online radiation monitoring system in the first synthesis. These results were compared to the activity released in a synthesis performed without the bag. We observed when the bag was used the amount released was about 0.2% in 270 minutes. The second synthesis was performed without the bag, about 7,1% of the input activity was released by the exhaust of the facility in the same time interval. The bag presented a very good efficiency in the reducing of the radioactive gas released by the chimney of the radiopharmaceutical production facility. (author)

Manufacturing and test of a low cost polypropylene bag to reduce the radioactive gas released by a radiopharmaceutical production facility

International Nuclear Information System (INIS)

Tavares, Jose Carlos Freitas; Lacerda, Marco Aurelio de Sousa; Nascimento, Leonardo Tafas Constantino do; Silva, Juliana Batista da

2011-01-01

The main objective of this work was to evaluate the efficiency of a plastic gas storage bag to reduce the radioactive gas released by the chimney of a radiopharmaceutical production facility during the 2-[ 18 F]fluoro-2- deoxy-D-glucose ( 18 FDG) synthesis. The studied facility was the Development Centre of Nuclear Technology (CDTN/CNEN) in Belo Horizonte, Brazil. The bag was manufactured utilizing foils of polypropylene of 360 x 550 x 0.16 mm and disposable components of the cassette of the synthesizer. Two synthesis of 18 FDG were done using the same hot cell and synthesizer to evaluate the efficiency of the bag. The manufactured bag was put in the gas exit of the synthesizer and the activity reported by the online radiation monitoring system in the first synthesis. These results were compared to the activity released in a synthesis performed without the bag. We observed when the bag was used the amount released was about 0.2% in 270 minutes. The second synthesis was performed without the bag, about 7,1% of the input activity was released by the exhaust of the facility in the same time interval. The bag presented a very good efficiency in the reducing of the radioactive gas released by the chimney of the radiopharmaceutical production facility. (author)

Effects of Operating Conditions on Gas Release Thermal ...

African Journals Online (AJOL)

The gas release rates and the flame length of the potential jet fires were initially estimated using Simplex Source Term Models which pay limited attention to operating conditions. Finally a more detailed follow-up study, accounting for a range of practical factors was conducted. A number of useful risk management metrics ...

Tritium release reduction and radiolysis gas formation

Energy Technology Data Exchange (ETDEWEB)

Batifol, G.; Douche, Ch.; Sejournant, Ch. [CEA Valduc, 21 - Is-sur-Tille (France)

2008-07-15

At CEA Valduc, the usual tritiated waste container is the steel drum. It allows good release reduction performance for middle activity waste but in some cases tritium outgassing from the waste drums is too high. It was decided to over-package each drum in a tighter container called the over-drum. According to good safety practices it was also decided to measure gas composition evolution into the over-drum in order to defect hydrogen formation over time. After a few months, a significant release reduction was observed. Additionally there followed contamination reduction in the roof storage building rainwater. However hydrogen was also observed in some over-drums, in addition to other radiolysis products. Catalyst will be added to manage the hydrogen risk in the over-drums. (authors)

Flammable gas tank safety program: Technical basis for gas analysis and monitoring

International Nuclear Information System (INIS)

Sherwood, D.J.

1995-01-01

Flammable gases generated in radioactive liquids. Twenty-five high level radioactive liquid waste storage tanks located underground at the Hanford Site are on a Flammable Gas Watch List because they contain waste which tends to retain the gases generated in it until rather large quantities are available for sudden release to the tank head space; if a tank is full it has little dome space, and a flammable concentration of gases could be produced--even if the tank is ventilated. If the waste has no tendency to retain gas generated in it then a continual flammable gas concentration in the tank dome space is established by the gas production rate and the tank ventilation rate (or breathing rate for unventilated tanks); this is also a potential problem for Flammable Gas Watch List tanks, and perhaps other Hanford tanks too. All Flammable Gas Watch List tanks will be fitted with Standard Hydorgen Monitoring Systems so that their behavior can be observed. In some cases, such as tank 241-SY-101, the data gathered from such observations will indicate that tank conditions need to be mitigated so that gas release events are either eliminated or rendered harmless. For example, a mixer pump was installed in tank 241-SY-101; operating the pump stirs the waste, replacing the large gas release events with small releases of gas that are kept below twenty-five percent of the lower flammability limit by the ventilation system. The concentration of hydrogen measured in Hanford waste tanks is greater than that of any other flammable gas. Hydrogen levels measured with a Standard Hydrogen Monitoring System in excess of 0.6 volume percent will cause Westinghouse Hanford Company to consider actions which will decrease the amount of flammable gas in the tank

Thermodynamic modeling of NH_3-CO_2-SO_2-K_2SO_4-H_2O system for combined CO_2 and SO_2 capture using aqueous NH_3

International Nuclear Information System (INIS)

Qi, Guojie; Wang, Shujuan

2017-01-01

Highlights: • A new application of aqueous NH_3 based combined CO_2 and SO_2 process was proposed. • A thermodynamic model simulated the heat of absorption and the K_2SO_4 precipitation. • The CO_2 content can be regenerated in a stripper with lower heat of desorption. • The SO_2 content can be removed by K_2SO_4 precipitation from the lean NH_3 solvent. - Abstract: A new application of aqueous NH_3 based post-combustion CO_2 and SO_2 combined capture process was proposed to simultaneously capture CO_2 and SO_2, and remove sulfite by solid (K_2SO_4) precipitation method. The thermodynamic model of the NH_3-CO_2-SO_2-K_2SO_4-H_2O system for the combined CO_2 and SO_2 capture process was developed and validated in this work to analyze the heat of CO_2 and SO_2 absorption in the NH_3-CO_2-SO_2-H_2O system, and the K_2SO_4 precipitation characteristics in the NH_3-CO_2-SO_2-K_2SO_4-H_2O system. The average heat of CO_2 absorption in the NH_3-CO_2-H_2O system at 40 °C is around −73 kJ/mol CO_2 in 2.5 wt% NH_3 with CO_2 loading between 0.2 and 0.5 C/N. The average heat of SO_2 absorption in the NH_3-SO_2-H_2O system at 40 °C is around −120 kJ/mol SO_2 in 2.5 wt% NH_3 with SO_2 loading between 0 and 0.5 S/N. The average heat of CO_2 absorption in the NH_3-CO_2-SO_2-H_2O system at 40 °C is 77, 68, and 58 kJ/mol CO_2 in 2.5 wt% NH_3 with CO_2 loading between 0.2 and 0.5 C/N, when SO_2 loading is 0, 0.1, 0.2 S/N, respectively. The solubility of K_2SO_4 increases with temperature, CO_2 and SO_2 loadings, but decreases with NH_3 concentration in the CO_2 and SO_2 loaded aqueous NH_3. The thermodynamic evaluation indicates that the combined CO_2 and SO_2 capture process could employ the typical absorption/regeneration process to simultaneously capture CO_2 and SO_2 in an absorber, thermally desorb CO_2 in a stripper, and feasibly remove sulfite (oxidized to sulfate) content by precipitating K_2SO_4 from the lean NH_3 solvent after the lean/rich heat exchanger.

Modelling of trona based spray dry scrubbing of SO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

N. Erdol-Aydin; G. Nasun-Saygili [Istanbul Technical University, Istanbul (Turkey). Chemical and Metallurgical Engineering Faculty

2007-02-15

The paper presents a model of the reaction between SO{sub 2} and trona based slurries. Experimental findings relevant to the desulfurisation in a spray dryer were compared with the proposed mathematical model and were found in good agreement. It is observed that at high stoichiometric ratios, the diffusion of SO{sub 2} from the gas bulk to the droplet interface is dominant for absorption and with decreasing stoichiometric ratio the absorption efficiency decreases. An increase in the temperature also causes a decrease in absorption efficiency. At the stoichiometric ratio (Na/S = 2), SO{sub 2} removal efficiency was found to be around 90%.

Multi-decadal satellite measurements of passive and eruptive volcanic SO2 emissions

Science.gov (United States)

Carn, Simon; Yang, Kai; Krotkov, Nickolay; Prata, Fred; Telling, Jennifer

2015-04-01

Periodic injections of sulfur gas species (SO2, H2S) into the stratosphere by volcanic eruptions are among the most important, and yet unpredictable, drivers of natural climate variability. However, passive (lower tropospheric) volcanic degassing is the major component of total volcanic emissions to the atmosphere on a time-averaged basis, but is poorly constrained, impacting estimates of global emissions of other volcanic gases (e.g., CO2). Stratospheric volcanic emissions are very well quantified by satellite remote sensing techniques, and we report ongoing efforts to catalog all significant volcanic SO2 emissions into the stratosphere and troposphere since 1978 using measurements from the ultraviolet (UV) Total Ozone Mapping Spectrometer (TOMS; 1978-2005), Ozone Monitoring Instrument (OMI; 2004 - present) and Ozone Mapping and Profiler Suite (OMPS; 2012 - present) instruments, supplemented by infrared (IR) data from HIRS, MODIS and AIRS. The database, intended for use as a volcanic forcing dataset in climate models, currently includes over 600 eruptions releasing a total of ~100 Tg SO2, with a mean eruption discharge of ~0.2 Tg SO2. Sensitivity to SO2 emissions from smaller eruptions greatly increased following the launch of OMI in 2004, but uncertainties remain on the volcanic flux of other sulfur species other than SO2 (H2S, OCS) due to difficulty of measurement. Although the post-Pinatubo 1991 era is often classified as volcanically quiescent, many smaller eruptions (Volcanic Explosivity Index [VEI] 3-4) since 2000 have injected significant amounts of SO2 into the upper troposphere - lower stratosphere (UTLS), peaking in 2008-2011. We also show how even smaller (VEI 2) tropical eruptions can impact the UTLS and sustain above-background stratospheric aerosol optical depth, thus playing a role in climate forcing on short timescales. To better quantify tropospheric volcanic degassing, we use ~10 years of operational SO2 measurements by OMI to identify the

Microbial reduction of SO{sub 2} and NO{sub x} as a means of by- product recovery/disposal from regenerable processes for the desulfurization of flue gas. Technical progress report, June 11, 1992--September 11, 1992

Energy Technology Data Exchange (ETDEWEB)

Sublette, K.L.

1992-12-31

Based on the work described simultaneous SO{sub 2}/No{sub x} removal from flue gas based on direct contact of the gas with SRB and T. denitrificans co-cultures or cultures-in-series has been eliminated as a viable process concept at this time. The technical reasons are as follows: (1) NO inhibition of SO{sub 2} reduction by D. desulfuricans - Although the NO concentrations used in the experiments described above are somewhat higher than that found in a typical flue gas, it is quite possible that at lower NO concentrations (or partial pressures) the inhibiting effects will simply take longer to become apparent. (2) Nitrate suppression of NO removal - As noted previously, the cultivation of T. denitrificans in a microbial flue gas treatment system (either one or two stages) would require sulfide-limiting conditions. Therefore, the electron acceptor must be in excess, requiring nitrate in the T. denitrificans process culture. As shown in experiments described above, nitrate significantly suppresses the removal of NO from a feed gas making simultaneous SO{sub 2}/NO{sub x} removal impractical by microbial means. (3) O{sub 2} inhibition of SO{sub 2} and NO reduction - It has been demonstrated that D. desulfuricans working cultures are tolerant of up to 1.7% O{sub 2} in the feed gas. However, further increases in the O{sub 2} partial pressure in the feed gas resulted in O{sub 2} inhibition of SO{sub 2} reduction. These inhibiting levels of O{sub 2} are comparable to those concentrations found in flue gases (3). Therefore, in any process in which raw flue gas contacts a D. desulfuricans culture marginal stability at best can be expected.

Problems of cleaning of gas releases from heat generating facilities

International Nuclear Information System (INIS)

Tret'yakov, V.; Burdejnaya, T.

2000-01-01

The paper deals with the problem of flue gases cleaning in the situation of a significant increasing use of fossil fuels in the Russian energy production. Information is given about the methods used in TPPs in different countries for cleaning of the gases released to the atmosphere from SO 2 and NO x . The main ways for solving the problem of decreasing of air pollution are outlined

Simulation of pellet-cladding thermomechanical interaction and fission gas release

International Nuclear Information System (INIS)

Denis, Alicia; Soba, Alejandro

2003-01-01

This paper summarizes the present status of a computer code that describes some of the main phenomena occurring in a nuclear fuel rod throughout its life. Temperature distribution, thermal expansion, elastic and plastic strains, creep, mechanical interaction between pellet and cladding, fission gas release, gas mixing, swelling, and densification are modeled. The modular structure of the code allows for the incorporation of models to simulate different phenomena and material properties. Collapsible rods can be also simulated. The code is bidimensional, assumes cylindrical symmetry for the rod and uses the finite element method to integrate the differential equations. The stress-strain and heat conduction problems are nonlinear due to plasticity and to the temperature dependence of the thermal conductivity. The fission gas inventory is calculated with a diffusion model, assuming spherical grains and using a one-dimensional finite element scheme. Pressure increase, swelling and densification are coupled with the stress field. Good results are obtained for the simulation of the irradiation tests of the first argentine prototypes of MOX fuels, where the bamboo effect is clearly observed, and of the FUMEX series for the fuel centerline temperature, the inside rod pressure and the fractional gas release.

Analysis of UO2 fuel structure for low and high burn-up and its impact on fission gas release

International Nuclear Information System (INIS)

Szuta, M.; El-Koliel, M.S.

1999-01-01

During irradiation, uranium dioxide (UO 2 ) fuel undergo important restructuring mainly represented by densification and swelling, void migration, equiaxed grain growth, grain subdivision, and the formation of columnar grains. The purpose of this study is to obtain a comprehensive picture of the phenomenon of equiaxed grain growth in UO 2 ceramic material. The change of the grain size in high-density uranium dioxide as a function of temperature, initial grain size, time, and burnup is calculated. Algorithm of fission gas release from UO 2 fuel during high temperature irradiation at high burnup taking into account grain growth effect is presented. Theoretical results are compared with experimental data. (author)

Fission gas behaviour in UO2 under steady state and transient conditions

International Nuclear Information System (INIS)

Zimmermann, H.

1980-01-01

Fission gas behaviour in UO 2 is determined by the limited capacity of the fuel to retain fission gas. This capacity depends primarily on temperature, but also on fission rate, pressure loading, and fuel microstructure. Under steady state irradiation conditions fission gas behaviour can be described qualitatively as follows: At the beginning of the irradiation most of the fission gas remains in the grains in irradiation-induced solution. With increasing gas content in the grains the gas transport to the grain boundaries increases, too. The fission gas release from the grain boundaries occurs primarily by interlinkage of inter-granular bubbles. The fission gas release without noticeable fuel swelling during the short-term heating in the LOCA tests and the powdering of the high burnup UO 2 in the annealing tests can only be accounted for by formation of inter-granular separations, which are caused by the fission gas accumulated in the grain boundaries. Besides this short-term effect there are diffusion-controlled long-term effects, such as growth and coalescence of bubbles and formation of inter-connected porosity, which result in time-dependent fission gas release and fuel swelling

H₂ production through electro-oxidation of SO₂

DEFF Research Database (Denmark)

Kriek, Roelof J.; Rossmeisl, Jan; Siahrostami, Samira

2014-01-01

one volt lower than that of a regular water electrolyser. In taking this technology forward the greatest improvement to be made is in developing a suitable electrocatalyst, which is also the 'lowest hanging fruit' in that very limited research and development has been conducted on the electrocatalyst....... The electrolysis of aqueous solutions of dissolved SO2 holds huge environmental potential in that SO2 is converted to sulphuric acid (H2SO4) and at the same time hydrogen gas is produced. A further benefit or incentive is that a sulphur depolarised electrolyser (SDE) operates at an applied potential that is about...... are found to scale with the surface reactivity (measured as the adsorption of OH). Irrespective of the pathway water needs to be activated and reduction of SO2 to elemental sulphur must be avoided. This requirement alone calls for an electrode potential of at least 0.7-0.8 V for all the investigated...

SO2 EMISSION MEASUREMENT BY DOAS (DIFFERENTIAL OPTICAL ABSORPTION SPECTROSCOPY AND COSPEC (CORRELATION SPECTROSCOPY AT MERAPI VOLCANO (INDONESIA

Directory of Open Access Journals (Sweden)

Hanik Humaida

2010-06-01

Full Text Available The SO2 is one of the volcanic gases that can use as indicator of volcano activity. Commonly, SO2 emission is measured by COSPEC (Correlation Spectroscopy. This equipment has several disadvantages; such as heavy, big in size, difficulty in finding spare part, and expensive. DOAS (Differential Optical Absorption Spectroscopy is a new method for SO2 emission measurement that has advantages compares to the COSPEC. Recently, this method has been developed. The SO2 gas emission measurement of Gunung Merapi by DOAS has been carried out at Kaliadem, and also by COSPEC method as comparation. The differences of the measurement result of both methods are not significant. However, the differences of minimum and maximum result of DOAS method are smaller than that of the COSPEC. It has range between 51 ton/day and 87 ton/day for DOAS and 87 ton/day and 201 ton/day for COSPEC. The measurement of SO2 gas emission evaluated with the seismicity data especially the rockfall showed the presence of the positive correlation. It may cause the gas pressure in the subsurface influencing instability of 2006 eruption lava.   Keywords: SO2 gas, Merapi, DOAS, COSPEC

Evaluation of SO2 compliance strategies at Virginia Power

International Nuclear Information System (INIS)

Presley, J.V.; Tomlinson, M.; Ulmer, R.H.

1992-01-01

This paper will address the process undertaken by Virginia Power to assess SO 2 control strategies available for complying with the Revised Clean Air Act. In April 1990, in anticipation of the passage of an amended Clean Air Act, Virginia Power assembled a task force of personnel from a wide cross section of the company. This task force was given the responsibility of providing an assessment of the requirements of the new legislation, evaluating compliance alternatives and providing recommendations for implementation of the least cost alternative. Twenty-four potential SO 2 compliance options were identified for evaluation for Phase I. These options included various levels of coal switching, gas co-firing and scrubbing. Each option was evaluated and compared to a base case which assumed no SO 2 control. As a result of our evaluations, the lowest cost and least risk approach to Phase I SO 2 compliance for Virginia Power appears to be to construct a scrubber for one unit (550 MW g ) at our Mt. Storm Power Station

OMS, OM(η2-SO), and OM(η2-SO)(η2-SO2) molecules (M = Ti, Zr, Hf): infrared spectra and density functional calculations.

Science.gov (United States)

Liu, Xing; Wang, Xuefeng; Wang, Qiang; Andrews, Lester

2012-07-02

Infrared spectra of the matrix isolated OMS, OM(η(2)-SO), and OM(η(2)-SO)(η(2)-SO(2)) (M = Ti, Zr, Hf) molecules were observed following laser-ablated metal atom reactions with SO(2) during condensation in solid argon and neon. The assignments for the major vibrational modes were confirmed by appropriate S(18)O(2) and (34)SO(2) isotopic shifts, and density functional vibrational frequency calculations (B3LYP and BPW91). Bonding in the initial OM(η(2)-SO) reaction products and in the OM(η(2)-SO)(η(2)-SO(2)) adduct molecules with unusual chiral structures is discussed.

THE DETERMINATION THE POLLUTION EMISSIONS OF SO2, NOX, CO, CO2 AND O2 FROM THE CHANNELS OF BURNT GAS ON BOILER OF 420 T/H - STEAM, IN THE SIGHT APPLICATION PROCEEDING TO REDUCE OF THESE

Directory of Open Access Journals (Sweden)

Valentin Nedeff

2007-03-01

Full Text Available The work present the results obtained after dynamic analyze the pollution emissions of SO2, NOx, CO, CO2 and O2 on evacuation channels of burnt gas on boiler of 420 t/h steam, having right the basic combustible the lignite, and auxiliary combustible the fuel oil and the natural gas. The values of pollution emission was analyze beside the admissible maxims values required by European legislation for Romania in the year 2005. The conclusion elaborated it adverted to: the values of oxides azoth, carry they frame in the limits provide in Environmental Authorization, under 60 mg/Nmc on 6% oxygen, the concentration values of SO2 which was bigger in report with one authorized comprised between 3500-3900 mg/Nmc confronted by 3400 mg/Nm. For integration in the foresee Government Decision 541/2003 aren't sufficient just proceeding of below reduce SO2, must take and another measures such as: get the fuel with quantity of sulphur 0.5% and with a content of ash below 35%.

Sulfur Release during Alternative fuels Combustion in Cement Rotary Kilns

DEFF Research Database (Denmark)

Cortada Mut, Maria del Mar

fuel with the bed material, heating up of a particle, 5 iv devolatilization, char combustion, the reactions between CaSO 4 and the different reducing agents, and the oxidation of the volatiles gases in the free board. The main reducing agents are CO, CH 4 and H 2 , which are introduced under the bed...... are of high importance for SO 2 release because it is shown that introducing the same total amount of gas, the highest reducing agent concentration fo r a short period released a higher total SO 2 amount compared to the lowest concentration during a long period. A mathematical reaction based model...... but the effect of sulfur content in the bed cannot be predicted. Further development regarding particle motion according to the rotational speed may be needed. Furthermore, a model for predicting the tendency of build-ups for a kiln system is developed based on the prediction of SO 3 and Cl concentrations...

Modeling of Oceanic Gas Hydrate Instability and Methane Release in Response to Climate Change

Energy Technology Data Exchange (ETDEWEB)

Reagan, Matthew; Reagan, Matthew T.; Moridis, George J.

2008-04-15

Paleooceanographic evidence has been used to postulate that methane from oceanic hydrates may have had a significant role in regulating global climate, implicating global oceanic deposits of methane gas hydrate as the main culprit in instances of rapid climate change that have occurred in the past. However, the behavior of contemporary oceanic methane hydrate deposits subjected to rapid temperature changes, like those predicted under future climate change scenarios, is poorly understood. To determine the fate of the carbon stored in these hydrates, we performed simulations of oceanic gas hydrate accumulations subjected to temperature changes at the seafloor and assessed the potential for methane release into the ocean. Our modeling analysis considered the properties of benthic sediments, the saturation and distribution of the hydrates, the ocean depth, the initial seafloor temperature, and for the first time, estimated the effect of benthic biogeochemical activity. The results show that shallow deposits--such as those found in arctic regions or in the Gulf of Mexico--can undergo rapid dissociation and produce significant methane fluxes of 2 to 13 mol/yr/m{sup 2} over a period of decades, and release up to 1,100 mol of methane per m{sup 2} of seafloor in a century. These fluxes may exceed the ability of the seafloor environment (via anaerobic oxidation of methane) to consume the released methane or sequester the carbon. These results will provide a source term to regional or global climate models in order to assess the coupling of gas hydrate deposits to changes in the global climate.

Unit mechanisms of fission gas release: Current understanding and future needs

Energy Technology Data Exchange (ETDEWEB)

Tonks, Michael; Andersson, David; Devanathan, Ram; Dubourg, Roland; El-Azab, Anter; Freyss, Michel; Iglesias, Fernando; Kulacsy, Katalin; Pastore, Giovanni; Phillpot, Simon R.; Welland, Michael

2018-06-01

Gaseous fission product transport and release has a large impact on fuel performance, degrading fuel properties and, once the gas is released into the gap between the fuel and cladding, lowering gap thermal conductivity and increasing gap pressure. While gaseous fission product behavior has been investigated with bulk reactor experiments and simplified analytical models, recent improvements in experimental and modeling approaches at the atomistic and mesoscales are being applied to provide unprecedented understanding of the unit mechanisms that define the fission product behavior. In this article, existing research on the basic mechanisms behind the various stages of fission gas release during normal reactor operation are summarized and critical areas where experimental and simulation work is needed are identified. This basic understanding of the fission gas behavior mechanisms has the potential to revolutionize our ability to predict fission product behavior during reactor operation and to design fuels that have improved fission product retention. In addition, this work can serve as a model on how a coupled experimental and modeling approach can be applied to understand the unit mechanisms behind other critical behaviors in reactor materials.

Modelling of oceanic gas hydrate instability and methane release in response to climate change

International Nuclear Information System (INIS)

Reagan, M.T.; Moridis, G.J.

2008-01-01

Methane releases from oceanic hydrates are thought to have played a significant role in climatic changes that have occurred in the past. In this study, gas hydrate accumulations subjected to temperature changes were modelled in order to assess their potential for future methane releases into the ocean. Recent ocean and atmospheric chemistry studies were used to model 2 climate scenarios. Two types of hydrate accumulations were used to represent dispersed, low-saturation deposits. The 1-D multiphase thermodynamic-hydrological model considered the properties of benthic sediments; ocean depth; sea floor temperature; the saturation and distribution of the hydrates; and the effect of benthic biogeochemical activity. Results of the simulations showed that shallow deposits undergo rapid dissociation and are capable of producing methane fluxes of 2 to 13 mol m 3 per year over a period of decades. The fluxes exceed the ability of the anaerobic sea floor environment to sequester or consume the methane. A large proportion of the methane released in the scenarios emerged in the gas phase. Arctic hydrates may pose a threat to regional and global ecological systems. It was concluded that results of the study will be coupled with global climate models in order to assess the impact of the methane releases in relation to global climatic change. 39 refs., 5 figs

Environmental risks due to radionuclide releases Environmental Risks Due To Radionuclide Releases From The Oil And Gas Industry

International Nuclear Information System (INIS)

Steinhausler, F.

2005-01-01

Full text : Exploration and transport in the oil- and gas industry result in the release of elevated levels of natural radioactivity into the environment. This has the following impact: Due to the large volumes of water needed during the extraction of gas and oil the resulting waste water can contain increased concentration of natural radionuclides, such as radium (Ra 226) and its decay products; At the oil/water interface waste water and sludge precipitate and form scalings, containing elevated levels of radium (Ra 226); At oil- and gas extraction sites tanks and equipment can be coated with long-lived radon (Rn 222) decay products; Along oil- and gas pipelines (e.g., at compressor stations) radon (Rn 222) decay products can be deposited internally on metal surfaces, such as valves. Typical U 238-series concentration values in production water range from 8 to 42 kBq/ m3, respectively in scale from 1 to 1 000 kBq/kg. In addition, oil- and gas extraction results in significant releases of natural radionuclides to the atmosphere (Rn 222) and to the water (Th 228, Ra 226, Rn 222, Pb 210, Po 210); for example, about 0.15 GBq/a of Rn 222 are released to the atmosphere per 106 m3 of oil extracted. The disposal of large amounts of contaminated wastes (scales, sludges) represents an environmental problem for the scrap metal industry (recycling of steel pipes containing scales) and the housing industry (use of sludge for landfill below a residential area). Using data from the oil- and gas industry in Latin America, Europe and the Asia-Pacific region, the various exposure pathways are reviewed. Furthermore, the current efforts in defining a suitable regulatory framework are discussed

The influence of cladding on fission gas release from irradiated U-Mo monolithic fuel

Energy Technology Data Exchange (ETDEWEB)

Burkes, Douglas E., E-mail: Douglas.Burkes@pnnl.gov; Casella, Amanda J.; Casella, Andrew M.

2017-04-01

The monolithic uranium-molybdenum (U-Mo) alloy has been proposed as a fuel design capable of converting the world's highest power research reactors from use of high enriched uranium to low enriched uranium. However, a zirconium (Zr) diffusion barrier must be used to eliminate interactions that form between the U-Mo monolith and aluminum alloy 6061 (AA6061) cladding during fabrication and are enhanced during irradiation. One aspect of fuel development and qualification is to demonstrate an appropriate understanding of the extent of fission product release from the fuel under anticipated service environments. An exothermic reaction has previously been observed between the AA6061 cladding and Zr diffusion layer. In this paper, two fuel segments with different irradiation history were subjected to specified thermal profiles under a controlled atmosphere using a thermogravimetric/differential thermal analyzer coupled with a mass spectrometer inside a hot cell. Samples from each segment were tested with cladding and without cladding to investigate the effect, if any, that the exothermic reaction has on fission gas release mechanisms. Measurements revealed there is an instantaneous effect of the cladding/Zr exothermic reaction, but not necessarily a cumulative effect above approximately 973 K (700 °C). The mechanisms responsible for fission gas release events are discussed. - Highlights: •Complementary fission gas release events are reported for U-Mo fuel with and without cladding. •Exothermic reaction between Zr diffusion layer and cladding influences fission gas release. •Mechanisms responsible for fission gas release are similar, but with varying timing and magnitude. •Behavior of samples is similar after 800 °C signaling the onset of superlattice destabilization.

Absorption of SO2 and NO through an integrative process with a cost-effective aqueous oxidant

Directory of Open Access Journals (Sweden)

Chelluboyana Vaishnava Raghunath

2016-09-01

Full Text Available Due to the substantial influence on the environment and health, there has been an intensifying environmental concern on sulfur dioxide (SO2 and nitrogen oxide (NO discharge to the atmosphere all over the world. Flue gas of coal-fired power stations is major leading source for the emission of SO2 and NO. Cost-effective and balanced technologies for the reduction of these pollutants from flue gas have become increasingly essential at the present time. The preliminary experimental attributes were retrieved in a batch scale agitating bubbling reactor for instantaneous absorption of SO2 and NO using aqueous oxidant. The prime conditions for instantaneous absorption examined were including absorbent concentration, reaction temperature, and pH in the fabricated flue gas system. Removal efficiencies of 99% for SO2 and 85% for NO were acquired, respectively under absorbent concentration 5 g/100 ml, reaction temperature 313 K, and pH 5.6.

Utilization of ''CONTACT'' experiments to improve the fission gas release knowledge in PWR fuel rods

Energy Technology Data Exchange (ETDEWEB)

Charles, M; Abassin, J J; Bruet, M; Baron, D; Melin, P

1983-03-01

The CONTACT experiments, which were carried out by the French CEA, within the framework of a CEA-FRAMATOME collaboration agreement, bear on the behaviour of in-pile irradiated PWR fuel rods. We will focus here upon their results dealing with fission gas release. The experimental device is briefly described, then the following results are given: the kinetics of stable fission gas release for various linear ratings; the instantaneous fractional release rates of radioactive gases versus their decay constant in the range 1.5 10/sup -6/-3.6 10/sup -3/s/sup -1/, for various burnups, as also the influence of fuel temperature. Moreover, the influence of the nature and the pressure of the filling gas upon the release is presented for various linear ratings. The experimental results are discussed and analysed with the purpose to model various physical phenomena involved in the release (low-temperature mechanisms, diffusion).

Utilization of ''CONTACT'' experiments to improve the fission gas release knowledge in PWR fuel rods

International Nuclear Information System (INIS)

Charles, M.; Abassin, J.J.; Bruet, M.

1983-01-01

The CONTACT experiments, which were carried out by the French CEA, within the framework of a CEA-FRAMATOME collaboration agreement, bear on the behaviour of in-pile irradiated PWR fuel rods. We will focus here upon their results dealing with fission gas release. The experimental device is briefly described, then the following results are given: the kinetics of stable fission gas release for various linear ratings; the instantaneous fractional release rates of radioactive gases versus their decay constant in the range 1.5 10 -6 -3.6 10 -3 s -1 , for various burnups, as also the influence of fuel temperature. Moreover, the influence of the nature and the pressure of the filling gas upon the release is presented for various linear ratings. The experimental results are discussed and analysed with the purpose to model various physical phenomena involved in the release (low-temperature mechanisms, diffusion)

OMI measurements of SO2 pollution over Eastern China in 2005-2008

Science.gov (United States)

Krotkov, N.; Pickering, K.; Witte, J.; Carn, S.; Yang, K.; Carmichael, G.; Streets, D.; Zhang, Q.; Wei, C.

2009-05-01

The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. OMI seasonal to multi-year average images clearly show the world-highest consistent SO2 pollution in northeast China. China is the world's largest SO2 emitter, mostly due to the burning of high-sulfur coal in its many coal-fired power plants, which lack the technology used in many other countries to remove sulfur from smoke stack emissions. China's government has instituted nationwide measures to control SO2 emissions through the adoption of flue-gas desulfurization technology on new power plants; and even greater measures were adopted in the Beijing area in anticipation of the Olympic Games. To study the environmental effects of the emission controls we compared OMI SO2 time series over eastern China for 2005 through 2008. The time series have been done as 7-day running means of the cloud-free daily observations. By mid-March we started to see substantial periods of lower SO2 values in 2008 compared to 2007, and by mid June the 2008 values were consistently lower than 2007 and prior years. The decline is widespread with highest SO2 typically located to the south and southwest of Beijing in regions with large clusters of power plants and also around Shanghai. The decline also lasted beyond the Olympic season. We do not yet know to what extent the economic downturn in China (and reduced industrial production) contributed to lower SO2 levels in the fall of 2008. We have also compared the observed and modeled fields using University of Iowa STEM model for the period June - September 2008. The model provided SO2 vertical distributions as well as aerosol vertical profiles that were used to correct OMI operational SO2 retrievals and improve the comparisons. The OMI SO2 changes in 2008 have also been compared with the estimated changes in SO2 emissions

LOFC fission product release and circulating activity calculations for gas-cooled reactors

International Nuclear Information System (INIS)

Apperson, C.E. Jr.; Carruthers, L.M.; Lee, C.E.

1977-01-01

The inventories of fission products in a gas-cooled reactor under accident and normal steady state conditions are time and temperature dependent. To obtain a reasonable estimate of these inventories it is necessary to consider fuel failure, a temperature dependent variable, and radioactive decay, a time dependent variable. Using arbitrary radioactive decay chains and published fuel failure models for the High Temperature Gas-Cooled Reactor (HTGR), methods have been developed to evaluate the release of fission products during the Loss of Forced Circulation (LOFC) accident and the circulating and plateout fission product inventories during steady state non-accident operation. The LARC-2 model presented here neglects the time delays in the release from the HTGR due to diffusion of fission products from particles in the fuel rod through the graphite matrix. It also neglects the adsorption and evaporation process of metallics at the fuel rod-graphite and graphite-coolant hole interfaces. Any time delay due to the finite time of transport of fission products by convection through the coolant to the outside of the prestressed concrete reactor vessel (PCRV) is also neglected. This model assumes that all fission products released from fuel particles are immediately deposited outside the PCRV with no time delay

Molecular Dynamics Investigation of Efficient SO2 Absorption by ...

Indian Academy of Sciences (India)

ANIRBAN MONDAL

J. Chem. Sci. Vol. 129, No. 7, July 2017, pp. 859–872. c Indian Academy of Sciences. ... Ionic liquids are appropriate candidates for the absorption of acid gases such as SO2. Six anion- ... nificant number of task-specific ILs were designed and used to ...... investigation of a pilot-scale jet bubbling reactor for wet flue gas ...

Management of gas releases with greenhouse effect: which economical tools?; Maitriser les emissions de gaz a effet de serre: quels instruments economiques?

Energy Technology Data Exchange (ETDEWEB)

Lepeltier, Serge [Senat, Paris (France)

2000-06-09

The climatic change represents the most severe danger to the durable world development, public health and future prosperity. This document concerning the gas releases with greenhouse effect is a report of the Senate Planning delegation regarding the economic and fiscal tools envisaging abatement of releases of gases with greenhouse effect. These issues are presented in four chapters titled as follows: 1. Since the scientific evidencing, requirement of managing the releases of gas with greenhouse effect has been unanimously recognized at the summits of Rio (1992) and Kyoto (1997); 2. The economic theory suggests instruments for reducing the gas releases with greenhouse effect at a minimum cost; 3. Challenges and ways of international cooperation in the field of climatic change; 4. Joining the political will with the pragmatic use of the economic instruments at national scale. The document contains a synthesis of proposals directed towards the following goals: international negotiations relating to climatic change; creating the community framework of managing the gas releases resulting in greenhouse effect; establishing national measures for managing the gas releases leading to greenhouse effect; actions to be undertaken by the territorial collectivities.

Fate of SO(sub 2) During Plasma Treatment of Diesel Engine Exhaust

International Nuclear Information System (INIS)

Brusasco, R.M.; Merritt, B.T.; Vogtlin, G.E.

1999-01-01

Several catalytic aftertreatment technologies rely on the conversion of NO to NO(sub 2) to achieve efficient reduction of NO(sub x) and particulates in diesel engine exhaust. These technologies require low sulfur fuel because the catalyst component that is active in converting NO to NO(sub 2) is also active in converting SO(sub 2) to SO(sub 3). A non-thermal plasma can be used for the selective partial oxidation of NO to NO(sub 2) in the gas-phase under diesel engine exhaust conditions. This paper discusses how a non-thermal plasma can efficiently oxidize NO to NO(sub 2) without oxidizing SO(sub 2) to SO(sub 3). It is shown that the presence of hydrocarbons in the plasma is essential for enhancing the selective partial oxidation of NO and suppressing the oxidation of SO(sub 2)

Operational experience in mitigating flammable gas releases from Hanford Site Tank 241-SY-101

International Nuclear Information System (INIS)

Lentsch, J.W.; Babad, H.; Kirch, N.W.

1995-01-01

Flammable gases consisting of hydrogen, nitrous oxide, ammonia, and methane are periodically released from Hanford Site waste tank 241-SY-101 at concentrations above the flammable limit. A large mixer pump installed in the tank in 1993 has effectively mitigated this problem by continuously releasing small amounts of the flammable gases at the rate they are generated. Tank 241-SY-101 is also equipped with multiple high-sensitivity gas monitoring systems and level detection systems to measure the quantity of gas that is retained in and released from the waste

Gas generation in SFL 3-5 and effects on radionuclide release

International Nuclear Information System (INIS)

Skagius, K.; Lindgren, M.; Pers, K.

1999-12-01

A deep repository, SFL 3-5, is presently planned for disposing of long-lived low- and intermediate-level waste. In this study the amounts of gas that can be generated in the waste packages and in the vaults are estimated. The potential gas pressure build-up, the displacement of contaminated water and the consequences on radionuclide release from the engineered barriers in the repository are also addressed. The study is focussed on the repository design and waste inventory that was defined for the prestudy of SFL 3-5. Since the reporting of the prestudy the design of the repository has been modified and the waste inventory has been updated and a preliminary safety assessment of the repository has been carried out based on the new design and updated waste inventory. The implications on gas generation and release of these modifications in design and waste inventory are briefly addressed in this study

Gas generation in SFL 3-5 and effects on radionuclide release

Energy Technology Data Exchange (ETDEWEB)

Skagius, K.; Lindgren, M.; Pers, K. [Kemakta Konsult AB, Stockholm (Sweden)

1999-12-01

A deep repository, SFL 3-5, is presently planned for disposing of long-lived low- and intermediate-level waste. In this study the amounts of gas that can be generated in the waste packages and in the vaults are estimated. The potential gas pressure build-up, the displacement of contaminated water and the consequences on radionuclide release from the engineered barriers in the repository are also addressed. The study is focussed on the repository design and waste inventory that was defined for the prestudy of SFL 3-5. Since the reporting of the prestudy the design of the repository has been modified and the waste inventory has been updated and a preliminary safety assessment of the repository has been carried outbased on the new design and updated waste inventory. The implications on gas generation and release of these modifications in design and waste inventory are briefly addressed in this study.

New discoveries enabled by OMI SO2 measurements and future missions

Science.gov (United States)

Krotkov, Nickolay

2010-05-01

The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. This talk highlights most recent science results enabled by using OMI SO2 data. OMI daily contiguous volcanic SO2 data continue 25+ climatic record by its predecessors (Total Ozone mapping Spectrometers 1978-2005), but higher SO2 sensitivity allows measuring volcanic plumes for a longer time as well as measuring passive volcanic degassing from space. New algorithm development allows direct estimating of SO2 plume heights to refine SO2 tonnages in largest volcanic plumes important for climate applications. Quantitatively, anthropogenic SO2 is more difficult to measure from space, since ozone absorption and Rayleigh scattering reduce sensitivity to pollutants in the lower troposphere. OMI data first enabled daily detection of SO2 burdens from individual smelters as well as observed SO2 pollution lofting from boundary layer and long-range transport in free troposphere. Interplay between volcanic and anthropogenic SO2 emissions resulted in highly variable SO2 pollution levels in Peru and Mexico City. We have updated our copper smelter analysis, which showed interesting new trends. Combining OMI data with trajectory models and aerosol/cloud measurements by A-train sensors (MODIS, CALIPSO) allowed tracking long-range transport of volcanic and anthropogenic aerosol/SO2 plumes. These studies placed new constraints on conversion rates of SO2 to sulfate at different heights from free troposphere to the lower stratosphere. We describe new techniques for spatial and time averaging that have been used to determine the global distribution of anthropogenic SO2 burdens, and the efficacy of abatement strategies. OMI seasonal to multi-year average images clearly show the world-highest consistent SO2 pollution in eastern China, mostly due to the burning of high

Acoustic sensor for in-pile fuel rod fission gas release measurement

International Nuclear Information System (INIS)

Fourmentel, D.; Villard, J. F.; Ferrandis, J. Y.; Augereau, F.; Rosenkrantz, E.; Dierckx, M.

2009-01-01

We have developed a specific acoustic sensor to improve the knowledge of fission gas release in Pressurized Water Reactor (PWR) fuel rods when irradiated in materials testing reactors. In order to perform experimental programs related to the study of the fission gas release kinetics, the CEA (French Nuclear Energy Commission) acquired the ability to equip a pre-irradiated PWR fuel rod with three sensors, allowing the simultaneous on-line measurements of the following parameters: - fuel temperature with a centre-line thermocouple type C, - internal pressure with a specific counter-pressure sensor, - fraction of fission gas released in the fuel rod with an innovative acoustic sensor. The third detector is the subject of this paper. This original acoustic sensor has been designed to measure the molar mass and pressure of the gas contained in the fuel rod plenum. For in-pile instrumentation, the fraction of fission gas, such as Krypton and Xenon, in Helium, can be deduced online from this measurement. The principle of this acoustical sensor is the following: a piezoelectric transducer generates acoustic waves in a cavity connected to the fuel rod plenum. The acoustic waves are propagated and reflected in this cavity and then detected by the transducer. The data processing of the signal gives the velocity of the acoustic waves and their amplitude, which can be related respectively to the molar mass and to the pressure of the gas. The piezoelectric material of this sensor has been qualified in nuclear conditions (gamma and neutron radiations). The complete sensor has also been specifically designed to be implemented in materials testing reactors conditions. For this purpose some technical points have been studied in details: - fixing of the piezoelectric sample in a reliable way with a suitable signal transmission, - size of the gas cavity to avoid any perturbation of the acoustic waves, - miniaturization of the sensor because of narrow in-pile experimental devices

Fireside Corrosion Behaviors of Super304H and HR3C in Coal Ash/Gas Environment with Different SO2 Contents at 650 °C

Science.gov (United States)

Lu, Jintao; Yang, Zhen; Li, Yan; Huang, Jinyang; Zhou, Yongli; Zhao, Xinbao; Yuan, Yong

2018-05-01

The corrosion behaviors of Super304H and HR3C used for USC boiler applications were investigated in simulated coal ash/gas environments with 0.1 and 1.5% of SO2 at 650 °C for 500 h. The results indicated that the increase in SO2 accelerated the corrosion rate and the spalling tendency of the corrosion layer in both tested alloys. Fe2O3, Cr2O3 and FeCr2O4 main peaks were revealed by XRD on Super304H, but on HR3C only the Cr2O3 peak showed a high intensity. The SO2 content did not affect the corrosion product composition of any of the alloys, but accelerated the inner sulfidation and the spallation on Super304H. No obvious internal sulfidation was observed on HR3C in either SO2 content. Based on the experimental results, the alloy corrosion mechanism and the influence of sulfur content on the corrosion process were discussed.

Application of DBD and DBCD in SO2 removal

International Nuclear Information System (INIS)

Sun Yanzhou; Henan Polytechnic Univ., Jiaozuo; Qiu Yuchang; Yuan Xingcheng; Yu Fashan

2004-01-01

The dielectric barrier corona discharge (DBCD) in a wire-cylinder configuration and the dielectric barrier discharge (DBD) in a coaxial cylinder configuration are studied. The discharge current in DBD has a higher pulse amplitude than in DBCD. The dissipated power and the gas-gap voltage are calculated by analyzing the measured Lissajous figure. With the increasing applied voltage, the energy utilization factor for SO 2 removal increases in DBCD but decreases in DBD because of the difference in their electric field distribution. Experiments of SO 2 removal show that in the absence of NH 3 the energy utilization factor can reach 31 g/k Wh in DBCD and 39 g/kWh in DBD. (authors)

Supported polytertiary amines: highly efficient and selective SO2 adsorbents.

Science.gov (United States)

Tailor, Ritesh; Abboud, Mohamed; Sayari, Abdelhamid

2014-01-01

Tertiary amine containing poly(propyleneimine) second (G2) and third (G3) generation dendrimers as well as polyethyleneimine (PEI) were developed for the selective removal of SO2. N-Alkylation of primary and secondary amines into tertiary amines was confirmed by FTIR and NMR analysis. Such modified polyamines were impregnated on two nanoporous supports, namely, SBA-15PL silica with platelet morphology and ethanol-extracted pore-expanded MCM-41 (PME) composite. In the presence of 0.1% SO2/N2 at 23 °C, the uptake of modified PEI, G2, and G3 supported on SBA-15PL was 2.07, 2.35, and 1.71 mmol/g, respectively; corresponding to SO2/N ratios of 0.22, 0.4, and 0.3. Under the same conditions, the SO2 adsorption capacity of PME-supported modified PEI and G3 was significantly higher, reaching 4.68 and 4.34 mmol/g, corresponding to SO2/N ratios of 0.41 and 0.82, respectively. The working SO2 adsorption capacity decreased with increasing temperature, reflecting the exothermic nature of the process. The adsorption capacity of these materials was enhanced dramatically in the presence of humidity in the gas mixture. FTIR data before SO2 adsorption and after adsorption and regeneration did not indicate any change in the materials. Nonetheless, the SO2 working capacity decreased in consecutive adsorption/regeneration cycles due to evaporation of impregnated polyamines, rather than actual deactivation. FTIR and (13)C and (15)N CP-MAS NMR of fresh and SO2 adsorbed modified G3 on PME confirmed the formation of a complexation adduct.

Numerical algorithms for intragranular diffusional fission gas release incorporated in the Transuranus code

International Nuclear Information System (INIS)

Lassmann, K.

2002-01-01

Complicated physical processes govern diffusional fission gas release in nuclear fuels. In addition to the physical problem there exists a numerical problem, as some solutions of the underlying diffusion equation contain numerical errors that by far exceed the physical details. In this paper the two algorithms incorporated in the TRANSURANUS code, the URGAS and the new FORMAS algorithm are compared. The previously reported deficiency of the most elegant and mathematically sound FORMAS algorithm at low release could be overcome. Both algorithms are simple, fast, without numerical problems, insensitive to time step lengths and well balanced over the entire range of fission gas release. They can be made available on request as FORTRAN subroutines. (author)

Detection of transient infrared absorption of SO3 and 1,3,2-dioxathietane-2,2-dioxide [cyc-(CH2)O(SO2)O] in the reaction CH2OO+SO2

Science.gov (United States)

Wang, Yi-Ying; Dash, Manas Ranjan; Chung, Chao-Yu; Lee, Yuan-Pern

2018-02-01

We recorded time-resolved infrared absorption spectra of transient species produced on irradiation at 308 nm of a flowing mixture of CH2I2/O2/N2/SO2 at 298 K. Bands of CH2OO were observed initially upon irradiation; their decrease in intensity was accompanied by the appearance of an intense band at 1391.5 cm-1 that is associated with the degenerate SO-stretching mode of SO3, two major bands of HCHO at 1502 and 1745 cm-1, and five new bands near >1340, 1225, 1100, 940, and 880 cm-1. The band near 1340 cm-1 was interfered by absorption of SO2 and SO3, so its band maximum might be greater than 1340 cm-1. SO3 in its internally excited states was produced initially and became thermalized at a later period. The rotational contour of the band of thermalized SO3 agrees satisfactorily with the reported spectrum of SO3. These five new bands are tentatively assigned to an intermediate 1,3,2-dioxathietane-2,2-dioxide [cyc-(CH2)O(SO2)O] according to comparison with anharmonic vibrational wavenumbers and relative IR intensities predicted for this intermediate. Observation of a small amount of cyc-(CH2)O(SO2)O is consistent with the expected reaction according to the potential energy scheme predicted previously. SO3+HCHO are the major products of the title reaction. The other predicted product channel HCOOH+SO2 was unobserved and its branching ratio was estimated to be <5%.

Hot Experiment on Fission Gas Release Behavior from Voloxidation Process using Spent Fuel

International Nuclear Information System (INIS)

Park, Geun Il; Park, J. J.; Jung, I. H.; Shin, J. M.; Cho, K. H.; Yang, M. S.; Song, K. C.

2007-08-01

Quantitative analysis of the fission gas release characteristics during the voloxidation and OREOX processes of spent PWR fuel was carried out by spent PWR fuel in a hot-cell of the DFDF. The release characteristics of 85 Kr and 14 C fission gases during voloxidation process at 500 .deg. C is closely linked to the degree of conversion efficiency of UO 2 to U 3 O 8 powder, and it can be interpreted that the release from grain-boundary would be dominated during this step. Volatile fission gases of 14 C and 85 Kr were released to near completion during the OREOX process. Both the 14 C and 85 Kr have similar release characteristics under the voloxidation and OREOX process conditions. A higher burn-up spent fuel showed a higher release fraction than that of a low burn-up fuel during the voloxidation step at 500 .deg. C. It was also observed that the release fraction of semi-volatile Cs was about 16% during a reduction at 1,000 .deg. C of the oxidized powder, but over 90% during the voloxidation at 1,250 .deg. C

Emission of NO and SO{sub 2} in a 300 kW pilot scale O{sub 2}/RFG Combustion

Energy Technology Data Exchange (ETDEWEB)

Zhang, Tai; Liu, Zhaohui; Huang, Xiaohong; Liu, Jingzhang; Wang, Dingbang; Zheng, Chuguang [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion