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1

A novel mechanism and kinetic model to explain enhanced xylose yields from dilute sulfuric acid compared to hydrothermal pretreatment of corn stover  

E-Print Network [OSTI]

significant poten- tial as a feedstock for conversion to liquid fuels such as ethanol and biodiesel (Kadam to be limited. However, dilute sulfuric acid pretreatment has proven to be a very effective in recov- ering most of these pretreatments to corn stover include dilute-sulfuric acid in a high-solids percola- tion reactor (Zhu et al

California at Riverside, University of

2

The Effect of Flow Rate of Very Dilute Sulfuric Acid on Xylan, Lignin, and Total Mass Removal from Corn Stover  

E-Print Network [OSTI]

The Effect of Flow Rate of Very Dilute Sulfuric Acid on Xylan, Lignin, and Total Mass Removal from mass, xylan, and lignin and increases cellulose digestibility compared to batch operations at otherwise in corn stover at 180 °C. A flow rate of 10 mL/min in a 3.8-mL reactor enhanced xylan removal by about 25

California at Riverside, University of

3

Reversion and dehydration reactions of glucose during the dilute sulfuric acid hydrolysis of cellulose  

SciTech Connect (OSTI)

The inaccessibility of all glycosidic bonds necessitates industrial conversion schemes which employ a dilute acid catalyst at high temperatures. Process conditions also promote further reactions of glucose via the reversion and dehydration pathways. Quantitative determination of the yields of the major reversion and dehydration products is important for understanding and predicting the amounts of these materials expected under envisioned industrial operating conditions. Microcrystalline cellulose (Avicel) was hydrolyzed with sulfuric acid (0.0-1.25 wt.%), at high temperatures (160-250/sup 0/C), and at a 3:1 liquid-to-solid ratio. The hydrolysis was monitored by evaluating the amount of cellulose remaining and the yields of glucose, solid humin, levulinic acid, formic acid, hydroxymethylfurfural (HMF), and reversion products as a function of the aforementioned reaction conditions. Analysis of the reversion products required the development of a technique for the quantitation of trace carbohydrates in complex mixtures and led to the development of a reduction/permethylation gas chromatographic procedure. Cellulose hydrolysis followed pseudo-homogeneous first-order kinetics. Glucose yield was adequately described as consecutive first-order reactions. Anhydrosugars formed via reversion followed equilibrium reaction kinetics whereas the disaccharides did not. Total reversion product yields approached 10% at 250/sup 0/C. Quantitative determination of the major dehydration products provided important information concerning the destruction of glucose. HMF was produced in up to 12% yields based on the theoretical amount of glucose available, and furfural was detected in up to 5% yields. A carbon mass balance based on the determined product yields revealed that approximately 90% of all carbon was accounted for at maximum glucose yields.

Helm, R.F.

1987-01-01T23:59:59.000Z

4

Corrosion resistance and behavior of construction materials exposed to dilute sulfuric acid at elevated temperatures under static conditions  

SciTech Connect (OSTI)

Laboratory investigation has been undertaken to determine the electrochemical behavior and corrosion resistance of various construction materials in a simulated hydrolysis environment (5 wt % sulfuric acid) at temperatures ranging from 90 to 220C. Tests were performed in an autoclave-type electrochemical cell. The corrosion behavior of the test materials was determined using computer-controlled DC potentiodynamic polarization. Corrosion rates of the test materials were determined using AC impedance techniques. Among the stainless steels tested, only alloy N08026 (Carpenter 20Mo-6) performed satisfactory up to a temperature of 100C. The alloy passivated spontaneously in the environment and corroded at a rate of less than 2 mpy. None of the stainless steels tested could be used at 120{degrees}C or above. A number of nickel-based alloys tested had good corrosion resistance up to 100C, but their corrosion rate exceeded 2 mpy at higher temperatures. Zirconium alloys were satisfactory up to 180C. Only tantalum and a tantalum-niobium alloy were satisfactory up to 220C.

Nguyen, D.T.

1994-10-01T23:59:59.000Z

5

Heat Transfer Characteristics of Sulfur and Sulfur Diluted with Hydrogen Sulfide Flowing Through Circular Tubes  

E-Print Network [OSTI]

is called the pumping-power advantage factor, and has the value 2. 5 x 10 for sodium. The only metals having a higher value of H are 13 lithium 7 and bismuth. Lithium 7 comprises 92. 5% of natural lithium, but the cost of separating it from lithium 6...-section for thermal neutrons being 0. 130 barns. For comparison, water has an absorption cross-section of 0. 58 barns for thermal neutrons (2) . Sulfur is not activated by exposure to neutron flux in such a way as to produce a radioactive isotope which...

Stone, Porter Walwyn

1960-01-01T23:59:59.000Z

6

High Xylose Yields from Dilute Acid Pretreatment of Corn Stover Under Process-Relevant Conditions  

SciTech Connect (OSTI)

Pretreatment experiments were carried out to demonstrate high xylose yields at high solids loadings in two different batch pretreatment reactors under process-relevant conditions. Corn stover was pretreated with dilute sulfuric acid using a 4-l Steam Digester and a 4-l stirred ZipperClave{reg_sign} reactor. Solids were loaded at 45% dry matter (wt/wt) after sulfuric acid catalyst impregnation using nominal particle sizes of either 6 or 18 mm. Pretreatment was carried out at temperatures between 180 and 200 C at residence times of either 90 or 105 s. Results demonstrate an ability to achieve high xylose yields (>80%) over a range of pretreatment conditions, with performance showing little dependence on particle size or pretreatment reactor type. The high xylose yields are attributed to effective catalyst impregnation and rapid rates of heat transfer during pretreatment.

Weiss, N. D.; Nagle, N. J.; Tucker, M. P.; Elander, R. T.

2009-01-01T23:59:59.000Z

7

Integrated boiler, superheater, and decomposer for sulfuric acid decomposition  

DOE Patents [OSTI]

A method and apparatus, constructed of ceramics and other corrosion resistant materials, for decomposing sulfuric acid into sulfur dioxide, oxygen and water using an integrated boiler, superheater, and decomposer unit comprising a bayonet-type, dual-tube, counter-flow heat exchanger with a catalytic insert and a central baffle to increase recuperation efficiency.

Moore, Robert (Edgewood, NM); Pickard, Paul S. (Albuquerque, NM); Parma, Jr., Edward J. (Albuquerque, NM); Vernon, Milton E. (Albuquerque, NM); Gelbard, Fred (Albuquerque, NM); Lenard, Roger X. (Edgewood, NM)

2010-01-12T23:59:59.000Z

8

Martinez Sulfuric Acid Regeneration Plt Biomass Facility | Open Energy  

Open Energy Info (EERE)

Martinez Sulfuric Acid Regeneration Plt Biomass Facility Martinez Sulfuric Acid Regeneration Plt Biomass Facility Jump to: navigation, search Name Martinez Sulfuric Acid Regeneration Plt Biomass Facility Facility Martinez Sulfuric Acid Regeneration Plt Sector Biomass Facility Type Non-Fossil Waste Location Contra Costa County, California Coordinates 37.8534093°, -121.9017954° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":37.8534093,"lon":-121.9017954,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

9

High pressure sulfuric acid decomposition experiments for the sulfur-iodine thermochemical cycle.  

SciTech Connect (OSTI)

A series of three pressurized sulfuric acid decomposition tests were performed to (1) obtain data on the fraction of sulfuric acid catalytically converted to sulfur dioxide, oxygen, and water as a function of temperature and pressure, (2) demonstrate real-time measurements of acid conversion for use as process control, (3) obtain multiple measurements of conversion as a function of temperature within a single experiment, and (4) assess rapid quenching to minimize corrosion of metallic components by undecomposed acid. All four of these objectives were successfully accomplished. This report documents the completion of the NHI milestone on high pressure H{sub 2}SO{sub 4} decomposition tests for the Sulfur-Iodine (SI) thermochemical cycle project. All heated sections of the apparatus, (i.e. the boiler, decomposer, and condenser) were fabricated from Hastelloy C276. A ceramic acid injection tube and a ceramic-sheathed thermocouple were used to minimize corrosion of hot liquid acid on the boiler surfaces. Negligible fracturing of the platinum on zirconia catalyst was observed in the high temperature decomposer. Temperature measurements at the exit of the decomposer and at the entry of the condenser indicated that the hot acid vapors were rapidly quenched from about 400 C to less than 20 C within a 14 cm length of the flow path. Real-time gas flow rate measurements of the decomposition products provided a direct measurement of acid conversion. Pressure in the apparatus was preset by a pressure-relief valve that worked well at controlling the system pressure. However, these valves sometimes underwent abrupt transitions that resulted in rapidly varying gas flow rates with concomitant variations in the acid conversion fraction.

Velasquez, Carlos E; Reay, Andrew R.; Andazola, James C.; Naranjo, Gerald E.; Gelbard, Fred

2005-09-01T23:59:59.000Z

10

Cellulase Accessibility of Dilute-Acid Pretreated Corn Stover  

SciTech Connect (OSTI)

The conclusions of this presentation are: (1) The dilute-acid pretreatment reduces xylan content in corn stover. This reduction in xylan content appears to render the substrate less recalcitrant. Below {approx}8%, xylan content is no longer the dominant factor in biomass recalcitrance. (2) Decreasing xylan content of corn stover also created more binding sites for Cel7A, but no strong correlation with actual xylan content. (3) We found no correlation between bound Cel7A concentration and lignin content. Maybe lignin is blocking the way for Cel7A? The contribution of lignin to biomass recalcitrance requires further investigation.

Jeoh, T.; Johnson, D. K.; Adney, W. S.; Himmel, M. E.

2005-01-01T23:59:59.000Z

11

FURNACE INJECTION OF ALKALINE SORBENTS FOR SULFURIC ACID CONTROL  

SciTech Connect (OSTI)

This document summarizes progress on Cooperative Agreement DE-FC26-99FT40718, Furnace Injection of Alkaline Sorbents for Sulfuric Acid Control, during the time period April 1, 2001 through September 30, 2001. The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. The coincident removal of hydrochloric acid and hydrofluoric acid is also being determined, as is the removal of arsenic, a known poison for NO{sub x} selective catalytic reduction (SCR) catalysts. EPRI, the Tennessee Valley Authority (TVA), FirstEnergy Corporation, and the Dravo Lime Company are project co-funders. URS Corporation is the prime contractor. During the current period, American Electric Power (AEP) joined the project as an additional co-funder and as a provider of a host site for testing. This is the fourth reporting period for the subject Cooperative Agreement. During this period, two long-term sorbent injection tests were conducted, one on Unit 3 at FirstEnergy's Bruce Mansfield Plant (BMP) and one on Unit 1 at AEP's Gavin Station. These tests determined the effectiveness of injecting alkaline slurries into the upper furnace of the boiler as a means of controlling sulfuric acid emissions from these units. The alkaline slurries tested included commercially available magnesium hydroxide slurry (Gavin Station), and a byproduct magnesium hydroxide slurry (both Gavin Station and BMP). The tests showed that injecting either the commercial or the byproduct magnesium hydroxide slurry could achieve up to 70 to 75% sulfuric acid removal. At BMP, the overall removal was limited by the need to maintain acceptable electrostatic precipitator (ESP) particulate control performance. At Gavin Station, the overall sulfuric acid removal was limited because the furnace injected sorbent was less effective at removing SO{sub 3} formed across the SCR system installed on the unit for NO{sub x} control than at removing SO{sub 3} formed in the furnace. Balance of plant impacts, primarily on the ESP particulate control device, were also determined during both tests. These results are presented and discussed in this report.

Gary M. Blythe

2001-11-06T23:59:59.000Z

12

SULFURIC ACID REMOVAL PROCESS EVALUATION: SHORT-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. Sulfuric acid controls are becoming of increasing interest to utilities with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species, a precursor to acid aerosol/condensable emissions, and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of SCR for NOX control on some coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project is testing the effectiveness of furnace injection of four different calcium- and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents have been tested during four one- to two-week tests conducted on two FirstEnergy Bruce Mansfield Plant units. One of the sorbents tested was a magnesium hydroxide slurry produced from a wet flue gas desulfurization system waste stream, from a system that employs a Thiosorbic{reg_sign} Lime scrubbing process. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles into the front wall of upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests. The longer-term tests are being conducted to confirm the effectiveness of the sorbents tested over extended operation and to determine balance-of-plant impacts. This reports presents the results of the short-term tests; the long-term test results will be reported in a later document. The short-term test results showed that three of the four reagents tested, dolomite powder, commercial magnesium hydroxide slurry, and byproduct magnesium hydroxide slurry, were able to achieve 90% or greater removal of sulfuric acid compared to baseline levels. The molar ratio of alkali to flue gas sulfuric acid content (under baseline conditions) required to achieve 90% sulfuric acid removal was lowest for the byproduct magnesium hydroxide slurry. However, this result may be confounded because this was the only one of the three slurries tested with injection near the top of the furnace across from the pendant superheater platens. Injection at the higher level was demonstrated to be advantageous for this reagent over injection lower in the furnace, where the other slurries were tested.

Gary M. Blythe; Richard McMillan

2002-03-04T23:59:59.000Z

13

SULFURIC ACID REMOVAL PROCESS EVALUATION: SHORT-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. Sulfuric acid controls are becoming of increasing interest to utilities with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species, a precursor to acid aerosol/condensable emissions, and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of SCR for NO{sub x} control on some coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project is testing the effectiveness of furnace injection of four different calcium- and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents have been tested during four one- to two-week tests conducted on two First Energy Bruce Mansfield Plant units. One of the sorbents tested was a magnesium hydroxide slurry produced from a wet flue gas desulfurization system waste stream, from a system that employs a Thiosorbic{reg_sign} Lime scrubbing process. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles into the front wall of upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests. The longer-term tests are being conducted to confirm the effectiveness of the sorbents tested over extended operation and to determine balance-of-plant impacts. This reports presents the results of the short-term tests; the long-term test results will be reported in a later document. The short-term test results showed that three of the four reagents tested, dolomite powder, commercial magnesium hydroxide slurry, and byproduct magnesium hydroxide slurry, were able to achieve 90% or greater removal of sulfuric acid compared to baseline levels. The molar ratio of alkali to flue gas sulfuric acid content (under baseline conditions) required to achieve 90% sulfuric acid removal was lowest for the byproduct magnesium hydroxide slurry. However, this result may be confounded because this was the only one of the three slurries tested with injection near the top of the furnace across from the pendant superheater platens. Injection at the higher level was demonstrated to be advantageous for this reagent over injection lower in the furnace, where the other slurries were tested.

Gary M. Blythe; Richard McMillan

2002-02-04T23:59:59.000Z

14

SULFURIC ACID REMOVAL PROCESS EVALUATION: LONG-TERM RESULTS  

SciTech Connect (OSTI)

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. The project is being co-funded by the U.S. DOE National Energy Technology Laboratory, under Cooperative Agreement DE-FC26-99FT40718, along with EPRI, the American Electric Power Company (AEP), FirstEnergy Corp., the Tennessee Valley Authority, and Dravo Lime, Inc. Sulfuric acid controls are becoming of increasing interest to power generators with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of selective catalytic reduction (SCR) for NO{sub x} control on many coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project previously tested the effectiveness of furnace injection of four different calcium-and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents were tested during four one- to two-week tests conducted on two FirstEnergy Bruce Mansfield Plant (BMP) units. One of the sorbents tested was a magnesium hydroxide byproduct slurry produced from a modified Thiosorbic{reg_sign} Lime wet flue gas desulfurization system. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles inserted through the front wall of the upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests on two different units. The longer-term tests were conducted to confirm the effectiveness of the sorbents tested over extended operation on two different boilers, and to determine balance-of-plant impacts. The first long-term test was conducted on FirstEnergy's BMP, Unit 3, and the second test was conducted on AEP's Gavin Plant, Unit 1. The Gavin Plant testing provided an opportunity to evaluate the effects of sorbent injected into the furnace on SO{sub 3} formed across an operating SCR reactor. This report presents the results from those long-term tests. The tests determined the effectiveness of injecting commercially available magnesium hydroxide slurry (Gavin Plant) and byproduct magnesium hydroxide slurry (both Gavin Plant and BMP) for sulfuric acid control. The results show that injecting either slurry could achieve up to 70 to 75% overall sulfuric acid removal. At BMP, this overall removal was limited by the need to maintain acceptable electrostatic precipitator (ESP) particulate control performance. At Gavin Plant, the overall sulfuric acid removal was limited because the furnace injected sorbent was less effective at removing SO{sub 3} formed across the SCR system installed on the unit for NOX control than at removing SO{sub 3} formed in the furnace. The long-term tests also determined balance-of-plant impacts from slurry injection during the two tests. These include impacts on boiler back-end temperatures and pressure drops, SCR catalyst properties, ESP performance, removal of other flue gas species, and flue gas opacity. For the most part the balance-of-plant impacts were neutral to positive, although adverse effects on ESP performance became an issue during the BMP test.

Gary M. Blythe; Richard McMillan

2002-07-03T23:59:59.000Z

15

Production of levulinic acid from glucosamine by dilute-acid catalyzed hydrothermal process  

Science Journals Connector (OSTI)

Abstract Glucosamine is a basic unit of the chitin/chitosan structure, which is derived from crustacean (e.g. crab, shrimp) and insect shells. In this study, the production of levulinic acid (LA) from glucosamine via dilute-acid-catalyzed hydrothermal hydrolysis was investigated. Among the reaction conditions, reaction temperature, reaction time, and substrate concentration were more effective than catalyst concentration. The optimal conditions for LA production, as determined by the response-surface methodology (RSM), were as follows: 188C reaction temperature, 4wt% catalyst concentration, 49min reaction time, 120g/L substrate concentration. Under these conditions, the LA yield was 30.3g/L (25.3wt%), while the 5-HMF concentration was zero. These results might provide basic knowledge essential to the production of valuable chemicals derivable from renewable marine resources and utilizable as fuel additives and polymer building blocks.

Gwi-Taek Jeong

2014-01-01T23:59:59.000Z

16

Evidence for a Plasma Core during Multibubble Sonoluminescence in Sulfuric Acid  

E-Print Network [OSTI]

.g., SOx, trace amounts of H2S, and elemental sulfur)7 are either highly soluble or solids. Prior MBSL to be problematic. These volatile products can have limited solubility in the liquid and therefore accumulate for the generation of higher temperatures during cavitation. Sulfuric acid is one such liquid because it has a very

Suslick, Kenneth S.

17

Unusual refinery boiler tube failures due to corrosion by sulfuric acid induced by steam leaks  

SciTech Connect (OSTI)

Corrosion by sulfuric acid in boilers is a low probability event because gas temperature and metal temperature of boiler tubes are high enough to avoid the condensation of sulfuric acid from flue gases. This degradation mechanism is frequently considered as an important cause of air preheaters materials degradation, where flue gases are cooled by heat transfer to the combustion air. Corrosion is associated to the presence of sulfuric acid, which condensates if metal temperature (or gas temperature) is below of the acid dew point. In economizer tubes, sulfuric acid corrosion is an unlikely event because flue gas and tube temperatures are normally over the acid dewpoint. In this paper, the failure analysis of generator tubes (similar to the economizer of bigger boilers) of two small oil-fired subcritical boilers is reported. It is concluded that sulfuric acid corrosion was the cause of the failure. The sulfuric acid condensation was due to the contact of flue gases containing SO{sub 3} with water-steam spray coming from leaks at the interface of rolled tube to the drum. Considering the information gathered from these two cases studied, an analysis of this failure mechanism is presented including a description of the thermodynamics condition of water leaking from the drum, and an analysis of the factors favoring it.

Lopez-Lopez, D.; Wong-Moreno, A. [Instituto de Investigaciones Electricas, Cuernavaca (Mexico)

1998-12-31T23:59:59.000Z

18

Changes in lignocellulosic supramolecular and ultrastructure during dilute acid pretreatment of Populus and switchgrass  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

lignocellulosic lignocellulosic supramolecular and ultrastructure during dilute acid pretreatment of Populus and switchgrass Marcus Foston, Art J. Ragauskas* BioEnergy Science Center, School of Chemistry and Biochemistry, Institute of Paper Science and Technology, Georgia Institute of Technology, 500 10th St., Atlanta, GA 30332, USA a r t i c l e i n f o Article history: Received 23 March 2009 Received in revised form 17 July 2010 Accepted 23 July 2010 Available online xxx Keywords: Dilute acid pretreatment Cellulose Supramolecular structure Populus Switchgrass a b s t r a c t Dilute acid pretreatment (DAP) is commonly employed prior to enzymatic deconstruction of cellulose to increase overall sugar and subsequent ethanol yields from downstream bioconversion processes. Typically optimization of pretreatment is evaluated by deter- mining hemicellulose removal, subsequent reactivity towards

19

ENERGY EFFICIENCY LIMITS FOR A RECUPERATIVE BAYONET SULFURIC ACID DECOMPOSITION REACTOR FOR SULFUR CYCLE THERMOCHEMICAL HYDROGEN PRODUCTION  

SciTech Connect (OSTI)

A recuperative bayonet reactor design for the high-temperature sulfuric acid decomposition step in sulfur-based thermochemical hydrogen cycles was evaluated using pinch analysis in conjunction with statistical methods. The objective was to establish the minimum energy requirement. Taking hydrogen production via alkaline electrolysis with nuclear power as the benchmark, the acid decomposition step can consume no more than 450 kJ/mol SO{sub 2} for sulfur cycles to be competitive. The lowest value of the minimum heating target, 320.9 kJ/mol SO{sub 2}, was found at the highest pressure (90 bar) and peak process temperature (900 C) considered, and at a feed concentration of 42.5 mol% H{sub 2}SO{sub 4}. This should be low enough for a practical water-splitting process, even including the additional energy required to concentrate the acid feed. Lower temperatures consistently gave higher minimum heating targets. The lowest peak process temperature that could meet the 450-kJ/mol SO{sub 2} benchmark was 750 C. If the decomposition reactor were to be heated indirectly by an advanced gas-cooled reactor heat source (50 C temperature difference between primary and secondary coolants, 25 C minimum temperature difference between the secondary coolant and the process), then sulfur cycles using this concept could be competitive with alkaline electrolysis provided the primary heat source temperature is at least 825 C. The bayonet design will not be practical if the (primary heat source) reactor outlet temperature is below 825 C.

Gorensek, M.; Edwards, T.

2009-06-11T23:59:59.000Z

20

Laboratory studies of 2H evaporator scale dissolution in dilute nitric acid  

SciTech Connect (OSTI)

The rate of 2H evaporator scale solids dissolution in dilute nitric acid has been experimentally evaluated under laboratory conditions in the SRNL shielded cells. The 2H scale sample used for the dissolution study came from the bottom of the evaporator cone section and the wall section of the evaporator cone. The accumulation rate of aluminum and silicon, assumed to be the two principal elemental constituents of the 2H evaporator scale aluminosilicate mineral, were monitored in solution. Aluminum and silicon concentration changes, with heating time at a constant oven temperature of 90 deg C, were used to ascertain the extent of dissolution of the 2H evaporator scale mineral. The 2H evaporator scale solids, assumed to be composed of mostly aluminosilicate mineral, readily dissolves in 1.5 and 1.25 M dilute nitric acid solutions yielding principal elemental components of aluminum and silicon in solution. The 2H scale dissolution rate constant, based on aluminum accumulation in 1.5 and 1.25 M dilute nitric acid solution are, respectively, 9.21E-04 6.39E-04 min{sup -1} and 1.07E-03 7.51E-05 min{sup -1}. Silicon accumulation rate in solution does track the aluminum accumulation profile during the first few minutes of scale dissolution. It however diverges towards the end of the scale dissolution. This divergence therefore means the aluminum-to-silicon ratio in the first phase of the scale dissolution (non-steady state conditions) is different from the ratio towards the end of the scale dissolution. Possible causes of this change in silicon accumulation in solution as the scale dissolution progresses may include silicon precipitation from solution or the 2H evaporator scale is a heterogeneous mixture of aluminosilicate minerals with several impurities. The average half-life for the decomposition of the 2H evaporator scale mineral in 1.5 M nitric acid is 12.5 hours, while the half-life for the decomposition of the 2H evaporator scale in 1.25 M nitric acid is 10.8 hours. Based on averaging the two half-lives from the 2H scale acid dissolution in 1.25 and 1.5 M nitric acid solutions, a reasonable half-live for the dissolution of 2H scales in dilute nitric acid is 11.7 1.3 hours. The plant operational time for chemically cleaning (soaking) the 2H evaporator with dilute nitric acid is 32 hours. It therefore may require about 3 half-lives or less to completely dissolve most of the scales in the Evaporator pot which come into contact with the dilute nitric acid solution. On a mass basis, the Al-to-Si ratio for the scale dissolution in 1.5 M nitric acid averaged 1.30 0.20 and averaged 1.18 0.10 for the 2H scale dissolution in 1.25 M nitric acid. These aluminum-to-silicon ratios are in fairly good agreement with ratios from previous studies. Therefore, there is still more aluminum in the 2H evaporator scales than silicon which implies that there are no significant changes in scale properties which will exclude nitric acid as a viable protic solvent for aluminosilicate scale buildup dissolution from the 2H evaporator. Overall, the monitoring of the scale decomposition reaction in 1.25 and 1.5 M nitric acid may be better ascertained through the determination of aluminum concentration in solution than monitoring silicon in solution. Silicon solution chemistry may lead to partial precipitating of silicon with time as the scale and acid solution is heated.

Oji, L.

2014-09-23T23:59:59.000Z

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21

THE EFFECT OF ANOLYTE PRODUCT ACID CONCENTRATION ON HYBRID SULFUR CYCLE PERFORMANCE  

SciTech Connect (OSTI)

The Hybrid Sulfur (HyS) cycle (Fig. 1) is one of the simplest, all-fluids thermochemical cycles that has been devised for splitting water with a high-temperature nuclear or solar heat source. It was originally patented by Brecher and Wu in 1975 and extensively developed by Westinghouse in the late 1970s and early 1980s. As its name suggests, the only element used besides hydrogen and oxygen is sulfur, which is cycled between the +4 and +6 oxidation states. HyS comprises two steps. One is the thermochemical (>800 C) decomposition of sulfuric acid (H{sub 2}SO{sub 4}) to sulfur dioxide (SO{sub 2}), oxygen (O{sub 2}), and water. H{sub 2}SO{sub 4} = SO{sub 2} + 1/2 O{sub 2} + H{sub 2}O. The other is the SO{sub 2}-depolarized electrolysis of water to H{sub 2}SO{sub 4} and hydrogen (H{sub 2}), SO{sub 2} + 2 H{sub 2}O = H{sub 2}SO{sub 4} + H{sub 2}, E{sup o} = -0.156 V, explaining the 'hybrid' designation. These two steps taken together split water into H{sub 2} and O{sub 2} using heat and electricity. Researchers at the Savannah River National Laboratory (SRNL) and at the University of South Carolina (USC) have successfully demonstrated the use of proton exchange membrane (PEM) electrolyzers (Fig. 2) for the SO{sub 2}-depolarized electrolysis (sulfur oxidation) step, while Sandia National Laboratories (SNL) successfully demonstrated the high-temperature sulfuric acid decomposition (sulfur reduction) step using a bayonet-type reactor (Fig. 3). This latter work was performed as part of the Sulfur-Iodine (SI) cycle Integrated Laboratory Scale demonstration at General Atomics (GA). The combination of these two operations results in a simple process that will be more efficient and cost-effective for the massive production of hydrogen than alkaline electrolysis. Recent developments suggest that the use of PEMs other than Nafion will allow sulfuric acid to be produced at higher concentrations (>60 wt%), offering the possibility of net thermal efficiencies around 50% (HHV basis). The effect of operation at higher anolyte concentrations on the flowsheet, and on the net thermal efficiency for a nuclear-heated HyS process, is examined and quantified.

Gorensek, M.; Summers, W.

2010-03-24T23:59:59.000Z

22

EFFECTIVENESS OF USING DILUTE OXALIC ACID TO DISSOLVEHIGH LEVEL WASTE IRON BASED SLUDGE SIMULANT  

SciTech Connect (OSTI)

At the Savannah River Site (SRS), near Aiken South Carolina, there is a crucial need to remove residual quantities of highly radioactive iron-based sludge from large select underground storage tanks (e.g., 19,000 liters of sludge per tank), in order to support tank closure. The use of oxalic acid is planned to dissolve the residual sludge, hence, helping in the removal. Based on rigorous testing, primarily using 4 and 8 wt% oxalic acid solutions, it was concluded that the more concentrated the acid, the greater the amount of residual sludge that would be dissolved; hence, a baseline technology on using 8 wt% oxalic acid was developed. In stark contrast to the baseline technology, reports from other industries suggest that the dissolution will most effectively occur at 1 wt% oxalic acid (i.e., maintaining the pH near 2). The driver for using less oxalic acid is that less (i.e., moles) would decrease the severity of the downstream impacts (i.e., required oxalate solids removal efforts). To determine the initial feasibility of using 1 wt% acid to dissolve > 90% of the sludge solids, about 19,000 liters of representative sludge was modeled using about 530,000 liters of 0 to 8 wt% oxalic acid solutions. With the chemical thermodynamic equilibrium based software results showing that 1 wt% oxalic acid could theoretically work, simulant dissolution testing was initiated. For the dissolution testing, existing simulant was obtained, and an approximate 20 liter test rig was built. Multiple batch dissolutions of both wet and air-dried simulant were performed. Overall, the testing showed that dilute oxalic acid dissolved a greater fraction of the stimulant and resulted in a significantly larger acid effectiveness (i.e., grams of sludge dissolved/mole of acid) than the baseline technology. With the potential effectiveness confirmed via simulant testing, additional testing, including radioactive sludge testing, is planned.

Ketusky, E

2008-07-11T23:59:59.000Z

23

Infrared Optical Constants of Highly Diluted Sulfuric Acid Solution Droplets at Cirrus Temperatures  

Science Journals Connector (OSTI)

The data evaluation procedure, previously developed for open-path TDLAS measurements in combustion processes,(28) water sprays,(29) and on stratospheric balloon platforms,(30) ensured a precise correction of the broadband optical scattering losses caused by the aerosol and cloud particles along the absorption path, as well as the pressure and temperature changes during the expansion. ...

Robert Wagner; Stefan Benz; Helmut Bunz; Ottmar Mhler; Harald Saathoff; Martin Schnaiter; Thomas Leisner; Volker Ebert

2008-10-22T23:59:59.000Z

24

Impact of Recycling Stillage on Conversion of Dilute Sulfuric Acid Pretreated Corn Stover to Ethanol (Poster)  

SciTech Connect (OSTI)

A description of methods and results from an experiment designed to assess the impact of process water recycle on corn stover-to-ethanol conversion process performance.

Mohagheghi, A.; Schell, D. J.

2009-11-01T23:59:59.000Z

25

Kinetic evaluation of the esterification of fatty acids to biodiesel  

Science Journals Connector (OSTI)

The free fatty acids of cotton seed oil were processed with methanol and ethanol into the corresponding alkyl fatty esters in the presence of diluted sulfuric acid. The products characterized as biodiesels pre...

Frederico A. D. Arajo; Sonia V. Pereira

2012-10-01T23:59:59.000Z

26

Resistance of biofilm-covered mortars to microbiologically influenced deterioration simulated by sulfuric acid exposure  

SciTech Connect (OSTI)

Following the reported success of biofilm applications on metal surfaces to inhibit microbiologically influenced corrosion, effectiveness and sustainability of E. coli DH5? biofilm on mortar surface to prevent microbiologically influenced concrete deterioration (MICD) are investigated. Experiments simulating microbial attack were carried out by exposing incrementally biofilm-covered mortar specimens to sulfuric acid solutions with pH ranging from 3 to 6. Results showed that calcium concentration in control reactors without biofilm was 2347% higher than the reactors with biofilm-covered mortar. Formation of amorphous silica gel as an indication of early stages of acid attack was observed only on the control mortar specimens without biofilm. During acidification, the biofilm continued to grow and its thickness almost doubled from ? 30 ?m before acidification to ? 60 ?m after acidification. These results demonstrated that E. coli DH5? biofilm was able to provide a protective and sustainable barrier on mortar surfaces against medium to strong sulfuric acid attack. -- Highlights: Effectiveness of E.coli DH5? biofilm to prevent MICD was studied. Conditions that lead to MICD were simulated by chemical acidification. Biofilm-covered mortar specimens were exposed to sulfuric acid solutions. The presence of biofilm helped reduce the chemically-induced mortar deterioration. Biofilm remained alive and continued to grow during the acidification process.

Soleimani, Sahar, E-mail: ssoleima@connect.carleton.ca; Isgor, O. Burkan, E-mail: burkan_isgor@carleton.ca; Ormeci, Banu, E-mail: banu_ormeci@carleton.ca

2013-11-15T23:59:59.000Z

27

Refined understanding of sulfur amino acid nutrition in hybrid striped bass, Morone chrysops (male symbol) x M. saxatilis (female symbol)  

E-Print Network [OSTI]

to methionine supported the lowest responses. Inclusion of MHA or AlimetTM did not affect TAN excretion of HSB. These findings will aid in refining diet formulations for HSB to ensure adequate sulfur amino acid nutrition....

Kelly, Mark Christopher

2005-08-29T23:59:59.000Z

28

Active/passive behavior of copper in strong sulfuric acid  

SciTech Connect (OSTI)

A combination of thermodynamic analyses and potentiodynamic polarization tests have been used to study the anodic behavior of Cu in strong H{sub 2}SO{sub 4} solutions in the concentration range 1--10 M. The studies were supplemented by chemical analyses of surface films. It was found that concentration-dependent changes in the activity of water played a major role in determining the anodic behavior and relative stability of corrosion product films. The anodic Tafel slope decreased from {approximately} 41 to {approximately} 31 mV with increasing acid concentration. The onset of limiting current and active-passive behaviors at higher potentials was determined by the formation of films of hydrated copper sulfate, CuSO{sub 4} {center_dot} xH{sub 2}O, and not by formation of oxides. Limiting current behavior was observed in 1 M solutions, where the degree of hydration was x = 5. Well-developed passivity occurred in 10 M solutions where x = 1. The results are relevant to industrial electrorefining operations for Cu and indicate that chloride contamination, if present in sufficient amounts, could cause the premature onset of limiting current behavior (anode passivity) during refining.

Tromans, D.; Ahmed, T. [Univ. of British Columbia, Vancouver, British Columbia (Canada). Dept. of Metals and Materials Engineering

1998-02-01T23:59:59.000Z

29

Effects of Dilute Acid Pretreatment on Cellulose DP and the Relationship Between DP Reduction and Cellulose Digestibility  

SciTech Connect (OSTI)

The degree of polymerization(DP) of cellulose is considered to be one of the most important properties affecting the enzymatic hydrolysis of cellulose. Various pure cellulosic and biomass materials have been used in a study of the effect of dilute acid treatment on cellulose DP. A substantial reduction in DP was found for all pure cellulosic materials studied even at conditions that would be considered relatively mild for pretreatment. The effect of dilute acid pretreatment on cellulose DP in biomass samples was also investigated. Corn stover pretreated with dilute acid under the most optimal conditions contained cellulose with a DPw in the range of 1600{approx}3500, which is much higher than the level-off DP(DPw 150{approx}300) obtained with pure celluloses. The effect of DP reduction on the saccharification of celluloses was also studied. From this study it does not appear that cellulose DP is a main factor affecting cellulose saccharification.

Wang, W.; Chen, X.; Tucker, M.; Himmel, M. E.; Johnson, D. K.

2012-01-01T23:59:59.000Z

30

Impacts of Deacetylation Prior to Dilute Acid Pretreatment on the Bioethanol Process  

SciTech Connect (OSTI)

Dilute acid pretreatment is a promising pretreatment technology for the biochemical production of ethanol from lignocellulosic biomass. During dilute acid pretreatment, xylan depolymerizes to form soluble xylose monomers and oligomers. Because the xylan found in nature is highly acetylated, the formation of xylose monomers requires two steps: (1) cleavage of the xylosidic bonds, and (2) cleavage of covalently bonded acetyl ester groups. Results: In this study, we show that the latter may be the rate limiting step for xylose monomer formation. Furthermore, acetyl groups are also found to be a cause of biomass recalcitrance and hydrolyzate toxicity. While the removal of acetyl groups from native corn stover by alkaline de-esterification prior to pretreatment improves overall process yields, the exact impact is highly dependent on the corn stover variety in use. Xylose monomer yields in pretreatment generally increases by greater than 10%. Compared to pretreated corn stover controls, the deacetylated corn stover feedstock is approximately 20% more digestible after pretreatment. Finally, by lowering hydrolyzate toxicity, xylose utilization and ethanol yields are further improved during fermentation by roughly 10% and 7%, respectively. In this study, several varieties of corn stover lots were investigated to test the robustness of the deacetylation-pretreatment-saccharification-fermentation process. Conclusions: Deacetylation shows significant improvement on glucose and xylose yields during pretreatment and enzymatic hydrolysis, but it also reduces hydrolyzate toxicity during fermentation, thereby improving ethanol yields and titer. The magnitude of effect is dependent on the selected corn stover variety, with several varieties achieving improvements of greater than 10% xylose yield in pretreatment, 20% glucose yield in low solids enzymatic hydrolysis and 7% overall ethanol yield.

Chen, X.; Shekiro, J.; Franden, M. A.; Wang, W.; Johnson, D. K.; Zhang, M.; Kuhn, E.; Tucker, M. P.

2011-12-01T23:59:59.000Z

31

Combined Dilute Acid and Solvent Based Pretreatment of Agricultural Wastes for Efficient Lignocellulosic Fractionation and Biofuels Production  

SciTech Connect (OSTI)

A true biorefinery for processing lignocellulosic biomass should achieve maximum utilization of all major constituents (cellulose, hemicellulose, & lignin) within the feedstock. In this work a combined pretreatment process of dilute acid (DA) and N-methyl morpholine N-oxide (NMMO) is described that allows for both fractionation and subsequent complete hydrolysis of the feedstocks (corn stover and sugarcane bagasse). During this multi-step processing, the dilute acid pretreatment solubilizes the majority (>90%) of the hemicellulosic fraction, while the NMMO treatment yields a cellulosic fraction that is completely digestible within 48 hours at low enzyme loadings. With both the cellulosic and hemicellulosic fractions being converted into separate, dissolved sugar fractions, the remaining portion is nearly pure lignin. When used independently, DA and NMMO pretreatments are only able to achieve ~80% and ~45% cellulosic conversion, respectively. Mass balance calculations along with experimental results are used to illustrate the feasibility of separation and recycling of NMMO.

Brodeur, G.; Ramakrishnan, S.; Wilson, C.; Telotte, J.; Collier, J.; Stickel, J.

2013-01-01T23:59:59.000Z

32

Adequacy of low-sulfur coal supplies for meeting acid rain requirements  

SciTech Connect (OSTI)

As we have shown, acid rain legislation would create a large demand for low-sulfur bituminous coals. These coals are primarily found in Central Appalachia and in parts of the West, and would displace much of the highersulfur coal production now coming from the Midwest and Northern Appalachia. The magnitude of the related shifts in coal production are potentially huge. Previously, it has been assumed that these shifts in demands could be met by the industry. This paper has tried to highlight possible difficulties in actually meeting such demands. In the near-term, these difficulties concern the ability of the industry to develop mines and of the transportation industry to ship the coal. In the longer-term, questions can be raised regarding the amount, the quality, and the mineability of low-sulfur bituminous coal reserves. These potential difficulties in coal supply could affect attainment of the legislative goals. If not addressed and resolved in a timely fashion, the results could be a higher cost to meeting legislative goals and/or a longer time required to meet them.

Klein, D.E.

1983-06-01T23:59:59.000Z

33

Effects of Fuel Dilution with Biodiesel on Lubricant Acidity, Oxidation and Corrosion  

Broader source: Energy.gov [DOE]

In-cylinder fuel injection to produce rich exhaust for regeneration of lean NOx trap catalyst and diesel particulate filter results in substantial fuel dilution of lubricating oil cause changes of lubricating oil properties and scuffing of engine components.

34

Efficient Conversion of Thermal Energy into Hydrogen: Comparing Two Methods to Reduce Exergy Losses in a Sulfuric Acid Decomposition Reactor  

Science Journals Connector (OSTI)

Efficient Conversion of Thermal Energy into Hydrogen: Comparing Two Methods to Reduce Exergy Losses in a Sulfuric Acid Decomposition Reactor ... The first design uses optimal control theory to obtain a more uniform distribution of the entropy production. ... This optimized design is found to perform the best, but it requires significant changes in the heating equipment in order to approximately realize the optimal temperature profiles. ...

Leen V. van der Ham; Joachim Gross; Ad Verkooijen; Signe Kjelstrup

2009-08-06T23:59:59.000Z

35

Effects of Nitrogen and Sulfur Fertilization on Free Amino Acids, Sugars, and Acrylamide-Forming Potential in Potato  

Science Journals Connector (OSTI)

In this study, 13 varieties of potato were grown in a field trial in 2010 and treated with different combinations of N and S. Potatoes were analyzed immediately after harvest to show the effect of N and S fertilization on concentrations of free asparagine, other free amino acids, sugars, and acrylamide-forming potential. ... (4-7) With respect to potato, De Wilde et al. showed that concentrations of sugars in tubers rose in response to N deprivation by up to 100% compared with adequately fertilized potatoes,(8) and Kumar et al. similarly reported that plants adequately fertilized with N had lower reducing sugar concentration at harvest. ... To examine how sulfur deprivation may affect acrylamide formation in cooked potatoes, three varieties of potato were grown under conditions of either severe sulfur deprivation or an adequate supply of sulfur. ...

Nira Muttucumaru; Stephen J. Powers; J. Stephen Elmore; Donald S. Mottram; Nigel G. Halford

2013-06-15T23:59:59.000Z

36

E-Print Network 3.0 - aqueous sulfuric acid Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

TRACE ATMOSPHERIC CONSTITUENTS Summary: . Reactions of Sulfur(IV) with Transition-Metal Ions in Aqueous Solutions Robert E. Huie and Norman C... . Peterson 3. Catalytic...

37

Corrosion rate and anodic dissolution behavior of a B2-iron aluminide alloy in sulfuric acid  

SciTech Connect (OSTI)

An electrochemical investigation was conducted to evaluate the corrosion behavior of an iron aluminide (B2-FeAl) alloy (with 24 wt% Al) in sulfuric acid (H{sub 2}SO{sub 3}) under potentiodynamic polarization conditions. Corrosion rates were determined using the polarization resistance (R{sub p}) technique, in which simultaneous computations of the Tafel slopes were obtained by a curve-fitting procedure. The corrosion rate of B2-FeAl was comparable to high-purity iron at the beginning of immersion but increased noticeably with time, showing significantly diminished corrosion resistance after several hours of immersion. At small anodic overpotentials, the polarization curve showed an active dissolution region, with the anodic current dependent upon potential and pH, which suggested an anodic process under iron dissolution control. Active corrosion of B2-FeAl was believed to follow an initial selective dissolution of the aluminum constituent. The rate-determining step of the process was the charge-transfer reaction of iron, similar to that for iron-chromium alloys. However, a significant difference between aluminum and chromium existed in the poorer performance of aluminum as an alloying element in inhibiting active dissolution of iron-based alloys.

Frangini, S. [ENEA Centro Ricerche Energie, Rome (Italy). Div. Nuovi Materiali

1999-01-01T23:59:59.000Z

38

Comparison of Optimal Thermodynamic Models of the Tricarboxylic Acid Cycle from Heterotrophs, Cyanobacteria, and Green Sulfur Bacteria  

Science Journals Connector (OSTI)

Comparison of Optimal Thermodynamic Models of the Tricarboxylic Acid Cycle from Heterotrophs, Cyanobacteria, and Green Sulfur Bacteria ... The ability to evaluate the thermodynamics of metabolic pathways allows one to understand the relationship between coupling of energy and material gradients in the environment and the self-organization of stable biological systems, and it is shown that each cycle operates in the direction expected due to its environmental niche. ...

Dennis G. Thomas; Sebastian Jaramillo-Riveri; Douglas J. Baxter; William R. Cannon

2014-11-19T23:59:59.000Z

39

Amphiphilic Maleic Acid-Containing Alternating Copolymers--2. Dilute Solution Characterization by Light  

E-Print Network [OSTI]

polyelectrolyte. The copolymer of maleic acid­sodium salt and di-isobutylene (DIBMA-Na) has a similar salting

Colby, Ralph H.

40

ADVANCED SULFUR CONTROL CONCEPTS  

SciTech Connect (OSTI)

Conventional sulfur removal in integrated gasification combined cycle (IGCC) power plants involves numerous steps: COS (carbonyl sulfide) hydrolysis, amine scrubbing/regeneration, Claus process, and tail-gas treatment. Advanced sulfur removal in IGCC systems involves typically the use of zinc oxide-based sorbents. The sulfides sorbent is regenerated using dilute air to produce a dilute SO{sub 2} (sulfur dioxide) tail gas. Under previous contracts the highly effective first generation Direct Sulfur Recovery Process (DSRP) for catalytic reduction of this SO{sub 2} tail gas to elemental sulfur was developed. This process is currently undergoing field-testing. In this project, advanced concepts were evaluated to reduce the number of unit operations in sulfur removal and recovery. Substantial effort was directed towards developing sorbents that could be directly regenerated to elemental sulfur in an Advanced Hot Gas Process (AHGP). Development of this process has been described in detail in Appendices A-F. RTI began the development of the Single-step Sulfur Recovery Process (SSRP) to eliminate the use of sorbents and multiple reactors in sulfur removal and recovery. This process showed promising preliminary results and thus further process development of AHGP was abandoned in favor of SSRP. The SSRP is a direct Claus process that consists of injecting SO{sub 2} directly into the quenched coal gas from a coal gasifier, and reacting the H{sub 2}S-SO{sub 2} mixture over a selective catalyst to both remove and recover sulfur in a single step. The process is conducted at gasifier pressure and 125 to 160 C. The proposed commercial embodiment of the SSRP involves a liquid phase of molten sulfur with dispersed catalyst in a slurry bubble-column reactor (SBCR).

Apostolos A. Nikolopoulos; Santosh K. Gangwal; William J. McMichael; Jeffrey W. Portzer

2003-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Conversion of the Common Food Constituent 5-Hydroxymethylfurfural into a Mutagenic and Carcinogenic Sulfuric Acid Ester in the Mouse in Vivo  

Science Journals Connector (OSTI)

Conversion of the Common Food Constituent 5-Hydroxymethylfurfural into a Mutagenic and Carcinogenic Sulfuric Acid Ester in the Mouse in Vivo ... 5-Hydroxymethylfurfural (HMF), formed by acid-catalyzed dehydration and in the Maillard reaction from reducing sugars, is found at high levels in numerous foods. ... Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources ...

Bernhard H. Monien; Heinz Frank; Albrecht Seidel; Hansruedi Glatt

2009-04-22T23:59:59.000Z

42

The structure of a copper adlayer at a solid-liquid interface, Au(III) in sulfuric acid  

SciTech Connect (OSTI)

A stable adlayer of copper can be deposited electrochemically on gold from sulfuric acid solutions at potentials positive of the thermodynamically reversible potential, so called underpotential deposition. On the Au(III) surface, Cu underpotentially deposits in two stages, the structures of which are controversial even though they have been examined ex situ using LEED and RIIEED, and in situ using STM, AFM, and EXAFS. New surface ESAFS data and simultaneous charge and mass coverage data obtained with an oscillating quartz crystal microbalance demonstrates that copper deposition is complicated by sulfate (or bisulfate) coadsorption and that the Cu coverage at the first stage is high than the 1/3 coverage of a {radical}3 x {radical}3 arrangement of Cu atoms deduced from the STM pictures. The authors believe the first stage structure is more complex and will discuss possible models. The data is consistent with a 1 x 1 Cu adlayer for the second stage.

Gordon, J.G.; Melroy, O.; Borges, G.L.; Kanazawa, K.K. [IBM Research Division, San Jose, CA (United States); Richer, J. [Atomic Energy of Canada, Ontario (Canada)

1993-12-31T23:59:59.000Z

43

Equilibrium surface composition of sulfuric acid films in contact with various atmospheric gases (HNO{sub 3}, CO{sub 2}, CH{sub 2}O, Cl{sub 2}, NO, NO{sub 2})  

SciTech Connect (OSTI)

Differentially pumped X-ray photoelectron spectroscopy has been used to study the surface composition of sulfuric acid (H{sub 2}SO{sub 4}) and sulfuric acid/water mixtures in equilibrium with various atmospheric species. Nitric acid uptake in sulfuric acid solutions was observed below {approx}220 K. Compared to the theoretically predicted bulk composition, a significant enrichment of nitrogen was observed at the interface. The uptake of background water in sulfuric acid below 200 K was responsible for the reversible uptake of CO{sub 2}, moderated through the formation of carbonic acid (H{sub 2}CO{sub 3}). For CH{sub 2}O, Cl{sub 2}, NO, and NO{sub 2}, no observable surface species were observed over the temperature range studied ({approx}180--298 K).

Fairbrother, D.H.; Somorjai, G.A.

2000-05-18T23:59:59.000Z

44

Why sequence Alkaliphilic sulfur oxidizing bacteria for sulfur pollution  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Alkaliphilic sulfur oxidizing Alkaliphilic sulfur oxidizing bacteria for sulfur pollution remediation? Burning sulfur-containing fuels, such as coal, oil, and natural gas, contributes significantly to global environmental problems, such as air pollution and acid rain, besides contributing to the loss of the ozone layer. One method of managing sulfur compounds released as byproducts from industrial processes is to scrub them out using chemical treatments and activated charcoal beds. A lower-cost solution relies on incorporating alkaliphic sulfur-oxidizing bacteria into biofilters to convert the volatile and toxic compounds into insoluble sulfur for easier removal. Discovered in the last decade, these bacteria have been found to thrive in habitats that span the full pH range. The bacteria could have applications

45

Process Design and Economics for Biochemical Conversion of Lignocellulosic Biomass to Ethanol: Dilute-Acid Pretreatment and Enzymatic Hydrolysis of Corn Stover  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Biochemical Conversion of Biochemical Conversion of Lignocellulosic Biomass to Ethanol Dilute-Acid Pretreatment and Enzymatic Hydrolysis of Corn Stover D. Humbird, R. Davis, L. Tao, C. Kinchin, D. Hsu, and A. Aden National Renewable Energy Laboratory Golden, Colorado P. Schoen, J. Lukas, B. Olthof, M. Worley, D. Sexton, and D. Dudgeon Harris Group Inc. Seattle, Washington and Atlanta, Georgia Technical Report NREL/TP-5100-47764 May 2011 NREL is a national laboratory of the U.S. Department of Energy, Office of Energy Efficiency & Renewable Energy, operated by the Alliance for Sustainable Energy, LLC. National Renewable Energy Laboratory 1617 Cole Boulevard Golden, Colorado 80401 303-275-3000 * www.nrel.gov Contract No. DE-AC36-08GO28308

46

Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbons: Dilute-Acid and Enzymatic Deconstruction of Biomass to Sugars and Biological Conversion of Sugars to Hydrocarbons  

Broader source: Energy.gov [DOE]

This report describes one potential conversion process to hydrocarbon products by way of biological conversion of lingnocellulosic-dervied sugars. The process design converts biomass to a hydrocarbon intermediate, a free fatty acid, using dilute-acid pretreatement, enzymatic saccharification, and bioconversion. Ancillary areas--feed handling, hydrolysate conditioning, product recovery and upgrading (hydrotreating) to a final blendstock material, wastewater treatment, lignin combusion, and utilities--are also included in the design.

47

Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbons: Dilute-Acid and Enzymatic Deconstruction of Biomass to Sugars and Biological Conversion of Sugars to Hydrocarbons  

SciTech Connect (OSTI)

This report describes one potential conversion process to hydrocarbon products by way of biological conversion of lingnocellulosic-dervied sugars. The process design converts biomass to a hydrocarbon intermediate, a free fatty acid, using dilute-acid pretreatement, enzymatic saccharification, and bioconversion. Ancillary areas--feed handling, hydrolysate conditioning, product recovery and upgrading (hydrotreating) to a final blendstock material, wastewater treatment, lignin combusion, and utilities--are also included in the design.

Davis, R.; Tao, L.; Tan, E. C. D.; Biddy, M. J.; Beckham, G. T.; Scarlata, C.; Jacobson, J.; Cafferty, K.; Ross, J.; Lukas, J.; Knorr, D.; Schoen, P.

2013-10-01T23:59:59.000Z

48

Solvent Extraction Behavior of Neptunium (IV) Ions between Nitric Acid and Diluted 30% Tri-butyl Phosphate in the Presence of Simple Hydroxamic Acids  

SciTech Connect (OSTI)

Formo- and aceto-hydroxamic acids are very effective reagents for stripping tetravalent actinide ions such as Np(IV) and Pu(IV) ions from a tri-butyl phosphate phase into nitric acid. Distribution data for Np(IV) in the presence of these hydroxamate ions have now been accumulated and trends established. Stability constants for aceto-hydroxamate complexes of Np(IV) and Np(V) ions have also been determined in a perchlorate medium, and these reaffirm the affinity of hydroxamate ligands for actinide (IV) ions over actinyl (V,VI) ions.

Taylor, Robin J.; Sinkov, Sergey I.; Choppin, Gregory R.; May, Iain

2008-01-15T23:59:59.000Z

49

Effects of dilution conditions on diesel particle size distribution and filter mass measurements in case of marine fuels  

Science Journals Connector (OSTI)

Abstract Particle emission characteristics were studied from heavy-duty diesel engine operating on fuels with sulfur levels relevant to marine operation, i.e. 0.05% S and 3% S respectively. Effects of primary dilution temperature (PDT) and primary dilution ratio (PDR) were investigated together with effect of filter media and time of filter conditioning. PDT increase was found slowing down nucleation rate due to increase of saturation vapor pressures of volatile species. In turn, increasing PDR reduces partial pressure of exhaust species and hence weakens both homogeneous and heterogeneous nucleation. All these effects are amplified by high sulfur content in marine fuels which increases available amount of nucleation-prone vapor-phase semivolatile compounds. At the same time, water condensation artifact was observed at PDR=3. No filter type was found to be overwhelmingly superior as certain positive and/or negative measurement artifacts are inherently associated with all filter materials. The filter conditioning time was also found to cause substantial PM mass variation, as control over VOC take up from (or lost to) laboratory air and hydration of sulfuric acid is required. The standard 24hour conditioning time was found insufficient to reach complete PM mass equilibrium, so longer time is required when measuring from high-sulfur fuels.

Sergey Ushakov; Harald Valland; Jrgen B. Nielsen; Erik Hennie

2014-01-01T23:59:59.000Z

50

Process Design and Economics for Biochemical Conversion of Lignocellulosic Biomass to Ethanol: Dilute-Acid Pretreatment and Enzymatic Hydrolysis of Corn Stover  

Broader source: Energy.gov [DOE]

This report describes one potential biochemical ethanol conversion process, conceptually based upon core conversion and process integration research at NREL. The overarching process design converts corn stover to ethanol by dilute-acid pretreatment, enzymatic saccharification, and co-fermentation. Building on design reports published in 2002 and 1999, NREL, together with the subcontractor Harris Group Inc., performed a complete review of the process design and economic model for the biomass-to-ethanol process. This update reflects NREL's current vision of the biochemical ethanol process and includes the latest research in the conversion areas (pretreatment, conditioning, saccharification, and fermentation), optimizations in product recovery, and our latest understanding of the ethanol plant's back end (wastewater and utilities). The conceptual design presented here reports ethanol production economics as determined by 2012 conversion targets and 'nth-plant' project costs and financing. For the biorefinery described here, processing 2,205 dry ton/day at 76% theoretical ethanol yield (79 gal/dry ton), the ethanol selling price is $2.15/gal in 2007$.

51

Sulfur: its clinical and toxicologic aspects  

Science Journals Connector (OSTI)

Although there is no known dietary requirement for inorganic sulfur, it is an essential element for all animal species in as much as they all require the sulfur-containing amino acid methionine. There are three predominate forms of organic sulfur in animals and humans: 1) the thiomethyl of methionine residues in protein; 2) the sulfhydryl disulfides of protein; and 3) the compounds containing ester or amide bound sulfates of glycosaminoglycans, steroids, and many xenobiotic metabolites. Thus, sulfur becomes an important constituent of amino acids, proteins, enzymes, vitamins and other biomolecules. Unlike mammalian species, plants can use inorganic sulfur and synthesize methionine from which are synthesized all the other important sulfur compounds. Hence, sulfur deficiency occurs mainly when plants are grown in sulfur-depleted soils and when humans and animals consume low-protein diets. In recent times, however, the increasing prevalence of refining petroleum and smelting sulfur compounds of metallic minerals into free metals are having a large impact on the balance of sulfur in the environment. Sulfur toxicity is associated mainly with high levels of the element and its toxic volatile substances in the environment. Sulfur dioxide (SO2), a major air pollutant, may adversely affect animal and human health by causing bronchitis, bronchoconstriction, and increased pulmonary resistance.

Lioudmila A Komarnisky; Robert J Christopherson; Tapan K Basu

2003-01-01T23:59:59.000Z

52

Comparative Study of Corn Stover Pretreated by Dilute Acid and Cellulose Solvent-Based Lignocellulose Fractionation: Enzymatic Hydrolysis, Supramolecular Structure, and Substrate Accessibility  

SciTech Connect (OSTI)

Liberation of fermentable sugars from recalcitrant biomass is among the most costly steps for emerging cellulosic ethanol production. Here we compared two pretreatment methods (dilute acid, DA, and cellulose solvent and organic solvent lignocellulose fractionation, COSLIF) for corn stover. At a high cellulase loading [15 filter paper units (FPUs) or 12.3 mg cellulase per gram of glucan], glucan digestibilities of the corn stover pretreated by DA and COSLIF were 84% at hour 72 and 97% at hour 24, respectively. At a low cellulase loading (5 FPUs per gram of glucan), digestibility remained as high as 93% at hour 24 for the COSLIF-pretreated corn stover but reached only {approx}60% for the DA-pretreated biomass. Quantitative determinations of total substrate accessibility to cellulase (TSAC), cellulose accessibility to cellulase (CAC), and non-cellulose accessibility to cellulase (NCAC) based on adsorption of a non-hydrolytic recombinant protein TGC were measured for the first time. The COSLIF-pretreated corn stover had a CAC of 11.57 m{sup 2}/g, nearly twice that of the DA-pretreated biomass (5.89 m{sup 2}/g). These results, along with scanning electron microscopy images showing dramatic structural differences between the DA- and COSLIF-pretreated samples, suggest that COSLIF treatment disrupts microfibrillar structures within biomass while DA treatment mainly removes hemicellulose. Under the tested conditions COSLIF treatment breaks down lignocellulose structure more extensively than DA treatment, producing a more enzymatically reactive material with a higher CAC accompanied by faster hydrolysis rates and higher enzymatic digestibility.

Zhu, Z.; Sathitsuksanoh, N.; Vinzant, T.; Schell, D. J.; McMillian, J. D.; Zhang, Y. H. P.

2009-07-01T23:59:59.000Z

53

Why Sequence Sulfur-Oxidizing Bacteria?  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Sulfur-Oxidizing Bacteria? Sulfur-Oxidizing Bacteria? Several environmental problems, such as acid rain, biocorrosion, etc., are caused by sulfur compounds, such as sulfur dioxide (SO2) and hydrogen sulfide (H2S). A sustainable process to remove these sulfur compounds is the production of elemental sulfur from H2S-containing gas streams by the use of sulfide-oxidizing bacteria. In this process, H2S is absorbed into the alkaline solution in the scrubber unit, followed by the biological oxidation of H2S to elemental sulfur and the recycling of water. With this two-step process, a variety of gas streams (i.e., natural gas, synthesis gas, biogas, and refinery gas) can be treated. For the treatment of sulfate-containing waste streams, an extra step has to be introduced: the transformation of sulfate into H2S by sulfate-reducing bacteria. In

54

Amino acid nutrition of the red drum (Sciaenops ocellatus): development of an improved test diet and determination of the total sulfur amino acid requirement  

E-Print Network [OSTI]

(1985) also found a significant correlation (r=0. 96) between dietary amino acid requirements and whole-body amino acid composition of channel catfish. However, a lower correlation (r-0. 68) was observed between dietary requirements and amino acid... fed amino acid test diets for six weeks1 Diet Weight gain Feed efficiency Survival designation ('/o of initial weight) (g gain/ g feed) (%%d) PM C G/AA CG RDM R D M/A A 210 c 227 c 68 1116 507 b 0. 40c 0. 41 c 0. 17d 0. 81 a 0. 67...

Moon, Hae Young

2012-06-07T23:59:59.000Z

55

Sulfur minimization in bacterial leaching  

SciTech Connect (OSTI)

The production of sewage biosolids in Ontario in 1989 was estimated to be 7 million m{sup 3} of wet sludge per year. Of this amount, land application accounts for between 20 and 30% of the total. Unfortunately, the use of sewage biosolids on agricultural land is often prohibited because of heavy metal contamination of the biosolids. High cost and operational problems have made chemical methods of metal extraction unattractive. Consequently, microbiological methods of leaching of heavy metals have been studied for over a decade. A relatively simple microbiological process has been investigated in recent years in flask level experiments and recently in a semicontinuous system. The process exploits nonacidophilic and acidophilic indigenous thiobacilli to extract heavy metals from sewage biosolids. These thiobacilli use elemental sulfur as the energy source, producing sulfuric acid. However, the resulting decontaminated biosolids can cause environmental problems like acidification of the soil, when acid is generated from the residual sulfur in the biosolids. The present study examines the possibility of reducing the amount of sulfur added in batch and semicontinuous bacterial leaching systems, and maximizing sulfur oxidation efficiency, thereby reducing the residual sulfur in leached biosolids.

Seth, R.; Prasad, D.; Henry, J.G. [Univ. of Toronto, Ontario (Canada). Dept. of Civil Engineering

1996-11-01T23:59:59.000Z

56

Particle size distributions from heavy-duty diesel engine operated on low-sulfur marine fuel  

Science Journals Connector (OSTI)

Particulate matter (PM) emission characteristics of a four-stroke diesel engine were investigated while operating on low-sulfur marine gas oil. PM size distributions appeared to be unimodal (accumulation mode) with fairly constant count median diameter (CMD) of 5565nm for all test modes at maximum engine speed. The slightly bigger CMD of around 76nm for unimodal particle size distributions at 1080rpm at medium- and high-load conditions was observed. The bimodal size distribution was registered only at very low load with nuclei CMD being below 15nm, accumulation CMD of around 82nm and percentage of nanoparticles of around 65%. The study of primary dilution air temperature (PDT) effect revealed a significant reduction in total particle number for all operating conditions when PDT was increased from 30C to 400C. This also had an effect on particle CMD values and is believed to be due to evaporation of sulfuric acid with bound water and certain organic fractions that were formed during dilution process (at PDT=30C). At very low load intermediate speed conditions, the heating of dilution air had a very little effect on the nucleation mode, which could suggest that it primarily consists of heavy hydrocarbons associated with lubrication oil.

Sergey Ushakov; Harald Valland; Jrgen B. Nielsen; Erik Hennie

2013-01-01T23:59:59.000Z

57

Instrument Development and Measurements of the Atmospheric Pollutants Sulfur Dioxide, Nitrate Radical, and Nitrous Acid by Cavity Ring-down Spectroscopy and Cavity Enhanced Absorption Spectroscopy  

E-Print Network [OSTI]

A. , A method of nitrogen dioxide and sulphur dioxidedetermination of nitrogen dioxide and sulfur dioxide in theDOAS) have measured nitrogen dioxide (NO 2 ), nitrate

Medina, David Salvador

2011-01-01T23:59:59.000Z

58

On the Subject of Analyzing Iron and Sulfur Bearing Minerals from Three Extreme Environments| Geological Carbon Sequestration, Acid Mine Drainage, and Mars.  

E-Print Network [OSTI]

?? The global iron and sulfur cycles are linked to some of the most ancient metabolisms on our planet, and, therefore, possibly other planetary bodies. (more)

Sklute, Elizabeth Christ

2014-01-01T23:59:59.000Z

59

Thermodynamics of dilute solutions  

Science Journals Connector (OSTI)

Thermodynamics of dilute solutions ... The development of the necessary thermodynamic equations directly in terms of molality is not common ... ...

Gabor Jancso; David V. Fenby

1983-01-01T23:59:59.000Z

60

Surface-enhanced Raman scattering and atomic force microscopy of brass electrodes in sulfuric acid solution containing benzotriazole and chloride ion  

SciTech Connect (OSTI)

Three different methods were used to roughen brass (Cu/Zn = 67/33) electrodes in 0.5 M H[sub 2]SO[sub 4] containing 1.0 mM benzotriazole (BTAH): (1) polarization at +0.05 V vs. saturated calomel for 5 min; (2) immersion in the above solution for six hours; and (3) oxidation-reduction cycling in the presence of chloride ion. The surfaces prepared by the first two methods exhibited surface-enhanced Raman scattering (SERS) spectra of the polymeric complex [Cu(I)BTA][sub s]. The SERS spectrum obtained from electrodes prepared by the third method is very similar to that of [Cu(I)CIBTAH][sub 4]. Examination of the electrodes by atomic force microscopy (AFM) showed that a large number of grain boundary sites are formed by the roughening processes. This effect is attributed to the loss of zinc, which occurs during corrosion of the mirror-like, polished brass electrode surface in the sulfuric acid solution. 11 refs., 5 figs.

Rubim, J.C.; Kim, J.; Henderson, E.; Cotton, T.M. (Instituto de Quimica da Universidade de Sao Paulo (Brazil) Ames Lab., IA (United States) Iowa State Univ., Ames (United States))

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

CATALYST EVALUATION FOR A SULFUR DIOXIDE-DEPOLARIZED ELECTROLYZER  

SciTech Connect (OSTI)

Thermochemical processes are being developed to provide global-scale quantities of hydrogen. A variant on sulfur-based thermochemical cycles is the Hybrid Sulfur (HyS) Process which uses a sulfur dioxide depolarized electrolyzer (SDE) to produce the hydrogen. Testing examined the activity and stability of platinum and palladium as the electrocatalyst for the SDE in sulfuric acid solutions. Cyclic and linear sweep voltammetry revealed that platinum provided better catalytic activity with much lower potentials and higher currents than palladium. Testing also showed that the catalyst activity is strongly influenced by the concentration of the sulfuric acid electrolyte.

Hobbs, D; Hector Colon-Mercado, H

2007-01-31T23:59:59.000Z

62

Performance and cost models for the direct sulfur recovery process. Task 1 Topical report, Volume 3  

SciTech Connect (OSTI)

The purpose of this project is to develop performance and cost models of the Direct Sulfur Recovery Process (DSRP). The DSRP is an emerging technology for sulfur recovery from advanced power generation technologies such as Integrated Gasification Combined Cycle (IGCC) systems. In IGCC systems, sulfur present in the coal is captured by gas cleanup technologies to avoid creating emissions of sulfur dioxide to the atmosphere. The sulfur that is separated from the coal gas stream must be collected. Leading options for dealing with the sulfur include byproduct recovery as either sulfur or sulfuric acid. Sulfur is a preferred byproduct, because it is easier to handle and therefore does not depend as strongly upon the location of potential customers as is the case for sulfuric acid. This report describes the need for new sulfur recovery technologies.

Frey, H.C. [North Carolina State Univ., Raleigh, NC (United States); Williams, R.B. [Carneigie Mellon Univ., Pittsburgh, PA (United States)

1995-09-01T23:59:59.000Z

63

CRADA Final Report For CRADA NO. CR-12-006 [Operation and Testing of an SO{sub 2}-depolarized Electrolyzer (SDE) for the Purpose of Hydrogen and Sulfuric Acid Production  

SciTech Connect (OSTI)

Over the past several years, Savannah River National Laboratory (SRNL) has led a team of collaborators under the Department of Energys (DOE) nuclear hydrogen production program to develop the Hybrid Sulfur (HyS) Process. HyS is a 2-step water-splitting process consisting of high temperature decomposition of sulfuric acid to generate SO{sub 2}, followed by the electrolysis of aqueous SO{sub 2} to generate hydrogen and sulfuric acid. The latter is fed back into the high temperature reactor. SRNL designed and built an SO{sub 2}-depolarized electrolyzer (SDE) and a test facility. Over 40 SDEs were tested using different catalysts, membranes and other components. SRNL demonstrated that an SDE could be operated continuously for approximately 200 hours under certain conditions without buildup of sulfur at the SDEs cathode, thus solving a key technical problem with SDE technology. Air Products and Chemicals, Inc. (APCI) is a major supplier of hydrogen production systems, and they have proprietary technology that could benefit from the SDE developed by SRNS, or some improved version thereof. However, to demonstrate that SRNLs SDE is a truly viable approach to the electrolyzer design, continuous operation for far greater periods of time than 200 hours must be demonstrated, and the electrolyzer must be scaled up to greater hydrogen production capacities. SRNL and Air Products entered into a Cooperative Research and Development Agreement with the objective of demonstrating the effectiveness of the SDE for hydrogen and sulfuric acid production and to demonstrate long-term continuous operation so as to dramatically increase the confidence in the SDE design for commercial operation. SRNL prepared a detailed technical report documenting previous SDE development, including the current SDE design and operating conditions that led to the 200-hour sulfurfree testing. SRNL refurbished its single cell SDE test facility and qualified the equipment for continuous operation. A new membrane electrode assembly (MEA) was fabricated and installed in the single cell electrolyzer (60 cm{sup 2} active cell area). Shakedown testing was conducted, and several modifications were made to the test facility equipment. Seven different MEAs were used during testing. Beginning on May 20, 2013, SRNL was able to test the SDE continuously for 1200 hours, including 1000 hours under power to generate hydrogen at an average rate of 10.8 liters per hour. The SDE was not removed or repaired during the 50-day test and was successfully restarted after each shutdown. The test was intentionally stopped after 1200 hours (1000 hours of hydrogen production) due to funding constraints. Post-test examination of the MEA using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Microanalysis (EDAX) showed no elemental sulfur deposits or sulfur layer inside the cell, thus successfully achieving the test goals. The results demonstrated that the SDE could be operated for extended periods without major performance degradation or the buildup of sulfur inside the MEA. Air Products conducted an assessment of the economic viability of the SDE based on the as tested design. The results indicated that the SDE faces significant economic obstacles in its current state. Further development and scale-up are necessary before the SDE is ready for commercialization.

Summers, W. A.; Colon-Mercado, H. R.; Steimke, J. L.; Zahn, Steffen

2014-02-24T23:59:59.000Z

64

Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbons: Dilute-Acid and Enzymatic Deconstruction of Biomass to Sugars and Biological Conversion of Sugars to Hydrocarbons  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Process Design and Economics Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbons: Dilute-Acid and Enzymatic Deconstruction of Biomass to Sugars and Biological Conversion of Sugars to Hydrocarbons R. Davis, L. Tao, E.C.D. Tan, M.J. Biddy, G.T. Beckham, and C. Scarlata National Renewable Energy Laboratory J. Jacobson and K. Cafferty Idaho National Laboratory J. Ross, J. Lukas, D. Knorr, and P. Schoen Harris Group Inc. Technical Report NREL/TP-5100-60223 October 2013 NREL is a national laboratory of the U.S. Department of Energy Office of Energy Efficiency & Renewable Energy Operated by the Alliance for Sustainable Energy, LLC. This report is available at no cost from the National Renewable Energy Laboratory (NREL) at www.nrel.gov/publications.

65

Chemical repair of base lesions, AP-sites, and strand breaks on plasmid DNA in dilute aqueous solution by ascorbic acid  

SciTech Connect (OSTI)

Highlights: We report a novel mechanism of radiation protection of DNA by chemical activity of ascorbic acid. The chemical repair of DNA damage was revealed using biochemical assay and chemical kinetics analysis. We found that ascorbic acid significantly repairs precursors of nucleobase lesions and abasic sites. However, ascorbic acid seldom repairs precursors of DNA-strand breaks. -- Abstract: We quantified the damage yields produced in plasmid DNA by ?-irradiation in the presence of low concentrations (10100 ?M) of ascorbic acid, which is a major antioxidant in living systems, to clarify whether it chemically repairs radiation damage in DNA. The yield of DNA single strand breaks induced by irradiation was analyzed with agarose gel electrophoresis as conformational changes in closed circular plasmids. Base lesions and abasic sites were also observed as additional conformational changes by treating irradiated samples with glycosylase proteins. By comparing the suppression efficiencies to the induction of each DNA lesion, in addition to scavenging of the OH radicals derived from water radiolysis, it was found that ascorbic acid promotes the chemical repair of precursors of AP-sites and base lesions more effectively than those of single strand breaks. We estimated the efficiency of the chemical repair of each lesion using a kinetic model. Approximately 5060% of base lesions and AP-sites were repaired by 10 ?M ascorbic acid, although strand breaks were largely unrepaired by ascorbic acid at low concentrations. The methods in this study will provide a route to understanding the mechanistic aspects of antioxidant activity in living systems.

Hata, Kuniki [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan) [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Advanced Science Research Center, Japan Atomic Energy Agency, 2-4 Shirakatashirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Urushibara, Ayumi; Yamashita, Shinichi; Shikazono, Naoya; Yokoya, Akinari [Advanced Science Research Center, Japan Atomic Energy Agency, 2-4 Shirakatashirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan)] [Advanced Science Research Center, Japan Atomic Energy Agency, 2-4 Shirakatashirane, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Katsumura, Yosuke, E-mail: katsu@n.t.u-tokyo.ac.jp [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan) [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan); Nuclear Professional School, School of Engineering, The University of Tokyo, 2-22 Shirakatashirane, Tokai-mura, Naka-gun, Ibaraki 319-1188 (Japan)

2013-05-03T23:59:59.000Z

66

Offshore Sulfur Comes In  

Science Journals Connector (OSTI)

Offshore Sulfur Comes In ... "The deposit is a major new source of sulfur," say Hines H. Baker, president of Humble Oil, and Langbourne M. Williams, president of Freeport Sulphur. ... Humble's deposit, known as Grand Isle (Block 18), was discovered in the course of offshore oil exploration and it ranks among the most important sulfur discoveries of recent years. ...

1956-10-01T23:59:59.000Z

67

An Aerosol Condensation Model for Sulfur Trioxide  

SciTech Connect (OSTI)

This document describes a model for condensation of sulfuric acid aerosol given an initial concentration and/or source of gaseous sulfur trioxide (e.g. fuming from oleum). The model includes the thermochemical effects on aerosol condensation and air parcel buoyancy. Condensation is assumed to occur heterogeneously onto a preexisting background aerosol distribution. The model development is both a revisiting of research initially presented at the Fall 2001 American Geophysical Union Meeting [1] and a further extension to provide new capabilities for current atmospheric dispersion modeling efforts [2]. Sulfuric acid is one of the most widely used of all industrial chemicals. In 1992, world consumption of sulfuric acid was 145 million metric tons, with 42.4 Mt (mega-tons) consumed in the United States [10]. In 2001, of 37.5 Mt consumed in the U.S., 74% went into producing phosphate fertilizers [11]. Another significant use is in mining industries. Lawuyi and Fingas [7] estimate that, in 1996, 68% of use was for fertilizers and 5.8% was for mining. They note that H{sub 2}SO{sub 4} use has been and should continue to be very stable. In the United States, the elimination of MTBE (methyl tertiary-butyl ether) and the use of ethanol for gasoline production are further increasing the demand for petroleum alkylate. Alkylate producers have a choice of either a hydrofluoric acid or sulfuric acid process. Both processes are widely used today. Concerns, however, over the safety or potential regulation of hydrofluoric acid are likely to result in most of the growth being for the sulfuric acid process, further increasing demand [11]. The implication of sulfuric acid being a pervasive industrial chemical is that transport is also pervasive. Often, this is in the form of oleum tankers, having around 30% free sulfur trioxide. Although sulfuric acid itself is not a volatile substance, fuming sulfuric acid (referred to as oleum) is [7], the volatile product being sulfur trioxide. Sulfate aerosols and mist may form in the atmosphere on tank rupture. From chemical spill data from 1990-1996, Lawuyi02 and Fingas [7] prioritize sulfuric acid as sixth most serious. During this period, they note 155 spills totaling 13 Mt, out of a supply volume of 3700 Mt. Lawuyi and Fingas [7] summarize information on three major sulfuric acid spills. On 12 February 1984, 93 tons of sulfuric acid were spilled when 14 railroad cars derailed near MacTier, Parry Sound, Ontario. On 13 December 1978, 51 railroad cars derailed near Springhill, Nova Scotia. One car, containing 93% sulfuric acid, ruptured, spilling nearly its entire contents. In July 1993, 20 to 50 tons of fuming sulfuric acid spilled at the General Chemical Corp. plant in Richmond, California, a major industrial center near San Francisco. The release occurred when oleum was being loaded into a nonfuming acid railroad tank car that contained only a rupture disk as a safety device. The tank car was overheated and this rupture disk blew. The resulting cloud of sulfuric acid drifted northeast with prevailing winds over a number of populated areas. More than 3,000 people subsequently sought medical attention for burning eyes, coughing, headaches, and nausea. Almost all were treated and released on the day of the spill. By the day after the release, another 5,000 people had sought medical attention. The spill forced the closure of five freeways in the region as well as some Bay Area Rapid Transit System stations. Apart from corrosive toxicity, there is the additional hazard that the reactions of sulfur trioxide and sulfuric acid vapors with water are extremely exothermic [10, 11]. While the vapors are intrinsically denser than air, there is thus the likelihood of strong, warming-induced buoyancy from reactions with ambient water vapor, water-containing aerosol droplets, and wet environmental surface. Nordin [12] relates just such an occurrence following the Richmond, CA spill, with the plume observed to rise to 300 m. For all practical purposes, sulfur trioxide was the constituent released from the heated tank

Grant, K E

2008-02-07T23:59:59.000Z

68

Can Delignification Decrease Cellulose Digestibility in Acid Pretreated Corn Stover?  

SciTech Connect (OSTI)

It has previously been shown that the improved digestibility of dilute acid pretreated corn stover is at least partially due to the removal of xylan and the consequent increase in accessibility of the cellulose to cellobiohydrolase enzymes. We now report on the impact that lignin removal has on the accessibility and digestibility of dilute acid pretreated corn stover. Samples of corn stover were subjected to dilute sulfuric acid pretreatment with and without simultaneous (partial) lignin removal. In addition, some samples were completely delignified after the pretreatment step using acidified sodium chlorite. The accessibility and digestibility of the samples were tested using a fluorescence-labeled cellobiohydrolase (Trichoderma reesei Cel7A) purified from a commercial cellulase preparation. Partial delignification of corn stover during dilute acid pretreatment was shown to improve cellulose digestibility by T. reesei Cel7A; however, decreasing the lignin content below 5% (g g{sup -1}) by treatment with acidified sodium chlorite resulted in a dramatic reduction in cellulose digestibility. Importantly, this effect was found to be enhanced in samples with lower xylan contents suggesting that the near complete removal of xylan and lignin may cause aggregation of the cellulose microfibrils resulting in decreased cellulase accessibility.

Ishizawa, C. I.; Jeoh, T.; Adney, W. S.; Himmel, M. E.; Johnson, D. K.; Davis, M. F.

2009-01-01T23:59:59.000Z

69

Diluted Graphene Antiferromagnet  

Science Journals Connector (OSTI)

We study RKKY interactions between local magnetic moments for both doped and undoped graphene. In the former case interactions for moments located on definite sublattices fall off as 1/R2, whereas for those placed at interstitial sites they decay as 1/R3. The interactions are primarily (anti)ferromagnetic for moments on (opposite) equivalent sublattices, suggesting that at low temperature dilute magnetic moments embedded in graphene can order into a state analogous to that of a dilute antiferromagnet. In the undoped case we find no net magnetic moment in the ground state, and demonstrate numerically this effect for ribbons, suggesting the possibility of an unusual spin-transfer device.

L. Brey; H. A. Fertig; S. Das Sarma

2007-09-12T23:59:59.000Z

70

Helium dilution refrigeration system  

DOE Patents [OSTI]

A helium dilution refrigeration system operable over a limited time period, and recyclable for a next period of operation. The refrigeration system is compact with a self-contained pumping system and heaters for operation of the system. A mixing chamber contains .sup.3 He and .sup.4 He liquids which are precooled by a coupled container containing .sup.3 He liquid, enabling the phase separation of a .sup.3 He rich liquid phase from a dilute .sup.3 He-.sup.4 He liquid phase which leads to the final stage of a dilution cooling process for obtaining low temperatures. The mixing chamber and a still are coupled by a fluid line and are maintained at substantially the same level with the still cross sectional area being smaller than that of the mixing chamber. This configuration provides maximum cooling power and efficiency by the cooling period ending when the .sup.3 He liquid is depleted from the mixing chamber with the mixing chamber nearly empty of liquid helium, thus avoiding unnecessary and inefficient cooling of a large amount of the dilute .sup.3 He-.sup.4 He liquid phase.

Roach, Patrick R. (Darien, IL); Gray, Kenneth E. (Naperville, IL)

1988-01-01T23:59:59.000Z

71

Sulfur@Carbon Cathodes for Lithium Sulfur Batteries > Research...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrode Channel Flow DEMS Cell Sulfur@Carbon Cathodes for Lithium Sulfur Batteries Better Ham & Cheese: Enhanced Anodes and Cathodes for Fuel Cells Epitaxial Single...

72

Sulfur-Graphene Oxide Nanocomposite Cathodes for Lithium/Sulfur...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Advanced Materials Advanced Materials Find More Like This Return to Search Sulfur-Graphene Oxide Nanocomposite Cathodes for LithiumSulfur Cells Lawrence Berkeley National...

73

Effects of Sulfur Dioxide on Formation of Fishy Off-Odor and Undesirable Taste in Wine Consumed with Seafood  

Science Journals Connector (OSTI)

Effects of Sulfur Dioxide on Formation of Fishy Off-Odor and Undesirable Taste in Wine Consumed with Seafood ... These results suggest that sulfur dioxide in wine participated in degradation of unsaturated fatty acids, causing an increase in undesirable taste and fishy off-odor in wine and seafood pairings. ... Wine; seafood; fishy off-odor; undesirable taste; unsaturated fatty acids; sulfur dioxide ...

Akiko Fujita; Atsuko Isogai; Michiko Endo; Hitoshi Utsunomiya; Shigeyoshi Nakano; Hiroshi Iwata

2010-03-10T23:59:59.000Z

74

Elemental sulfur recovery process  

DOE Patents [OSTI]

An improved catalytic reduction process for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides combined high activity and selectivity for the reduction of SO[sub 2] to elemental sulfur product with carbon monoxide or other reducing gases. The reaction of sulfur dioxide and reducing gas takes place over certain catalyst formulations based on cerium oxide. The process is a single-stage, catalytic sulfur recovery process in conjunction with regenerators, such as those used in dry, regenerative flue gas desulfurization or other processes, involving direct reduction of the SO[sub 2] in the regenerator off gas stream to elemental sulfur in the presence of a catalyst. 4 figures.

Flytzani-Stephanopoulos, M.; Zhicheng Hu.

1993-09-07T23:59:59.000Z

75

Chapter 11 - Sulfur Recovery  

Science Journals Connector (OSTI)

Abstract Sulfur is present in many raw industrial gases and in natural gas in the form of hydrogen sulfide. Sulfur removal facilities are located at the majority of oil and gas processing facilities throughout the world. The sulfur recovery unit does not make a profit for the operator but it is an essential processing step to allow the overall facility to operate, as the discharge of sulfur compounds to the atmosphere is severely restricted by environmental regulations. Concentration levels of H2S vary significantly depending upon their source. H2S produced from absorption processes, such as amine treating of natural gas or refinery gas, can contain 5075% H2S by volume or higher. This chapter provides information about fundamentals of sulfur removal facilities in the natural gas industry.

Alireza Bahadori

2014-01-01T23:59:59.000Z

76

E-Print Network 3.0 - absorbing sulfur dioxide Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

provides some chemicals which are incompatible with other compounds. Summary: Potassium carbon tetrachloride, carbon dioxide, water Potassium chlorate sulfuric and other acids...

77

E-Print Network 3.0 - ambient sulfur dioxide Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

provides some chemicals which are incompatible with other compounds. Summary: Potassium carbon tetrachloride, carbon dioxide, water Potassium chlorate sulfuric and other acids...

78

Flue-gas sulfur-recovery plant for a multifuel boiler  

SciTech Connect (OSTI)

In October 1991, a Finnish fluting mill brought on stream a flue-gas desulfurization plant with an SO{sub 2} reduction capacity of 99%. The desulfurization plant enabled the mill to discontinue the use of its sulfur burner for SO{sub 2} production. The required makeup sulfur is now obtained in the form of sulfuric acid used by the acetic acid plant, which operates in conjunction with the evaporating plant. The mill`s sulfur consumption has decreased by about 6,000 tons/year (13.2 million lb/year) because of sulfur recycling.

Miettunen, J. [Tampella Power Inc., Tampere (Finland); Aitlahti, S. [Savon Sellu Oy, Kuopio (Finland)

1993-12-01T23:59:59.000Z

79

Helium dilution refrigeration  

E-Print Network [OSTI]

. 1875" OD exchanger Qu ID copper cap Fig. 6. Assembled view of 3He - He dilution refrigerator. 26 The joint thru the tubing wall and the joining of the two sizes of capillary were silver soldered (35/ silver content). A 0. 250" OD tube... the inert atmosphere inside the refrigerator. After removal from the nitrogen atmosphere the graphite support, was 'attached to the still and mixing chamber using Stycast 2850 GT with catalyst g9 ). The mass of the graphite 26 support 1s 11. 62 grams...

McKee, Thomas Raymond

2012-06-07T23:59:59.000Z

80

Bacterial Sulfur Storage Globules  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

by I. J. Pickering and G. N. George by I. J. Pickering and G. N. George Sulfur is essential for all life, but it plays a particularly central role in the metabolism of many anaerobic microorganisms. Prominent among these are the sulfide-oxidizing bacteria that oxidize sulfide (S2-) to sulfate (SO42-). Many of these organisms can store elemental sulfur (S0) in "globules" for use when food is in short supply (Fig. 1). The chemical nature of the sulfur in these globules has been an enigma since they were first described as far back as 1887 (1); all known forms (or allotropes) of elemental sulfur are solid at room temperature, but globule sulfur has been described as "liquid", and it apparently has a low density – 1.3 compared to 2.1 for the common yellow allotrope a-sulfur. Various exotic forms of sulfur have been proposed to explain these properties, including micelles (small bubble-like structures) formed from long-chain polythionates, but all of these deductions have been based upon indirect evidence (for example the density was estimated by flotation of intact cells), and many questions remained.

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Synthesis and development of processes for the recovery of sulfur from acid gases. Part 1, Development of a high-temperature process for removal of H{sub 2}S from coal gas using limestone -- thermodynamic and kinetic considerations; Part 2, Development of a zero-emissions process for recovery of sulfur from acid gas streams  

SciTech Connect (OSTI)

Limestone can be used more effectively as a sorbent for H{sub 2}S in high-temperature gas-cleaning applications if it is prevented from undergoing calcination. Sorption of H{sub 2}S by limestone is impeded by sintering of the product CaS layer. Sintering of CaS is catalyzed by CO{sub 2}, but is not affected by N{sub 2} or H{sub 2}. The kinetics of CaS sintering was determined for the temperature range 750--900{degrees}C. When hydrogen sulfide is heated above 600{degrees}C in the presence of carbon dioxide elemental sulfur is formed. The rate-limiting step of elemental sulfur formation is thermal decomposition of H{sub 2}S. Part of the hydrogen thereby produced reacts with CO{sub 2}, forming CO via the water-gas-shift reaction. The equilibrium of H{sub 2}S decomposition is therefore shifted to favor the formation of elemental sulfur. The main byproduct is COS, formed by a reaction between CO{sub 2} and H{sub 2}S that is analogous to the water-gas-shift reaction. Smaller amounts of SO{sub 2} and CS{sub 2} also form. Molybdenum disulfide is a strong catalyst for H{sub 2}S decomposition in the presence of CO{sub 2}. A process for recovery of sulfur from H{sub 2}S using this chemistry is as follows: Hydrogen sulfide is heated in a high-temperature reactor in the presence of CO{sub 2} and a suitable catalyst. The primary products of the overall reaction are S{sub 2}, CO, H{sub 2} and H{sub 2}O. Rapid quenching of the reaction mixture to roughly 600{degrees}C prevents loss Of S{sub 2} during cooling. Carbonyl sulfide is removed from the product gas by hydrolysis back to CO{sub 2} and H{sub 2}S. Unreacted CO{sub 2} and H{sub 2}S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H{sub 2} and CO, which recovers the hydrogen value from the H{sub 2}S. This process is economically favorable compared to the existing sulfur-recovery technology and allows emissions of sulfur-containing gases to be controlled to very low levels.

Towler, G.P.; Lynn, S.

1993-05-01T23:59:59.000Z

82

The adsorption of gold, palladium and platinum from acidic chloride solutions on mesoporous carbons.  

SciTech Connect (OSTI)

Studies on the adsorption characteristics of gold, palladium and platinum on mesoporous carbon (CMK-3) and sulfur-impregnated mesoporous carbon (CMK-3/S) evaluated the benefits/drawbacks of the presence of a layer of elemental sulfur inside mesoporous carbon structures. Adsorption isotherms collected for Au(III), Pd(II) and Pt(IV) on those materials suggest that sulfur does enhance the adsorption of those metal ions in mildly acidic environment (pH 3). The isotherms collected in 1 M HCl show that the benefit of sulfur disappears due to the competing influence of large concentration of hydrogen ions on the ion-exchanging mechanism of metal ions sorption on mesoporous carbon surfaces. The collected acid dependencies illustrate similar adsorption characteristics for CMK-3 and CMK-3/S in 1-5 M HCl concentration range. Sorption of metal ions from diluted aqueous acidic mixtures of actual leached electronic waste demonstrated the feasibility of recovery of gold from such liquors.

Peter Zalupski; Rocklan McDowell; Guy Dutech

2014-10-01T23:59:59.000Z

83

Direct determination of organic and inorganic sulfur in coal by controlled oxidation  

SciTech Connect (OSTI)

The overall objective of this project is to develop an analytical method to directly measure the forms of organic sulfur in coal. The method will provide a route to monitor the effectiveness of coal preparation research directed toward removal of organic sulfur in coal. The approach involves subjecting diluted coal samples simultaneously to an oxygen flow and a linear increase in temperature. Distinctive sulfur dioxide evolution patterns are observed among coals of different rank and between raw and treated coals. Assignments have been made relating each specific sulfur dioxide evolution to the non-aromatic organic, aromatic organic, and inorganic sulfur present in coals and treated coals. Work is progressing on schedule to optimize experimental conditions and to improve the efficiency of the controlled-atmosphere programmed-temperature oxidation (CAPTO) method by developing a multiple sample instrumental system.

LaCount, R.B.

1992-01-01T23:59:59.000Z

84

Direct determination of organic and inorganic sulfur in coal by controlled oxidation  

SciTech Connect (OSTI)

The overall objective of this project is to develop an analytical method to directly measure the forms of organic sulfur in coal. The method will provide a route to monitor the effectiveness of coal preparation research directed toward removal of organic sulfur in coal. The approach involves subjecting diluted coal samples simultaneously to an oxygen flow and a linear increase in temperature. Distinctive sulfur dioxide evolution patterns are observed among coals of different rank and between raw and treated coals. Assignments have been made relating each specific sulfur dioxide evolution to the non-aromatic organic, aromatic organic, and inorganic sulfur present in coals and treated coals. Work is progressing on schedule to optimize experimental conditions and to improve the efficiency of the controlled-atmosphere programmed-temperature oxidation (CAPTO) method by developing a multiple sample instrumental system.

LaCount, R.B.

1992-12-31T23:59:59.000Z

85

Freeport Begins Offshore Sulfur Plant  

Science Journals Connector (OSTI)

Freeport Begins Offshore Sulfur Plant ... Discovered by Humble Oil & Refining, the sulfur deposit off Grand Isle is believed by industry observers to be one of the largest discovered in recent years. ...

1958-07-07T23:59:59.000Z

86

In situ Observation of Sulfur in Living Mammalian Cells: Uptake of Taurine  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

In situ Observation of Sulfur in Living In situ Observation of Sulfur in Living Mammalian Cells: Uptake of Taurine into MDCK Cells Sulfur is essential for life. It plays important roles in the amino acids methionine and cysteine, and has a structural function in disulfide bonds. As a component of iron-sulfur clusters it takes part in electron and sulfur transfer reactions.1 Glutathione, a sulfur-containing tripeptide, is an important part of biological antioxidant systems.2 Another example for the biological relevance of sulfur is the amino acid taurine, which is present in high concentrations in algae and the animal kingdom. Taurine has been implicated in a range of physiological phenomena, but its osmolytic role in cell volume regulation has been studied in greatest detail.3 In situ information on sulfur is rare despite its important biological role. This is due to the fact that sulfur is not easily accessible with most biophysical techniques. In recent years, sulfur x-ray absorption spectroscopy (XAS) has become increasingly important in the study of sulfur species in biological systems.4 The near-edge region of the XAS spectrum is a sensitive probe of electronic structure and hence chemical form.5

87

SULFUR POLYMER ENCAPSULATION.  

SciTech Connect (OSTI)

Sulfur polymer cement (SPC) is a thermoplastic polymer consisting of 95 wt% elemental sulfur and 5 wt% organic modifiers to enhance long-term durability. SPC was originally developed by the U.S. Bureau of Mines as an alternative to hydraulic cement for construction applications. Previous attempts to use elemental sulfur as a construction material in the chemical industry failed due to premature degradation. These failures were caused by the internal stresses that result from changes in crystalline structure upon cooling of the material. By reacting elemental sulfur with organic polymers, the Bureau of Mines developed a product that successfully suppresses the solid phase transition and significantly improves the stability of the product. SPC, originally named modified sulfur cement, is produced from readily available, inexpensive waste sulfur derived from desulfurization of both flue gases and petroleum. The commercial production of SPC is licensed in the United States by Martin Resources (Odessa, Texas) and is marketed under the trade name Chement 2000. It is sold in granular form and is relatively inexpensive ({approx}$0.10 to 0.12/lb). Application of SPC for the treatment of radioactive, hazardous, and mixed wastes was initially developed and patented by Brookhaven National Laboratory (BNL) in the mid-1980s (Kalb and Colombo, 1985; Colombo et al., 1997). The process was subsequently investigated by the Commission of the European Communities (Van Dalen and Rijpkema, 1989), Idaho National Engineering Laboratory (Darnell, 1991), and Oak Ridge National Laboratory (Mattus and Mattus, 1994). SPC has been used primarily in microencapsulation applications but can also be used for macroencapsulation of waste. SPC microencapsulation has been demonstrated to be an effective treatment for a wide variety of wastes, including incinerator hearth and fly ash; aqueous concentrates such as sulfates, borates, and chlorides; blowdown solutions; soils; and sludges. It is not recommended for treatment of wastes containing high concentrations of nitrates because of potentially dangerous reactions between sulfur, nitrate, and trace quantities of organics. Recently, the process has been adapted for the treatment of liquid elemental mercury and mercury contaminated soil and debris.

KALB, P.

2001-08-22T23:59:59.000Z

88

RECENT ADVANCES IN THE DEVELOPMENT OF THE HYBRID SULFUR PROCESS FOR HYDROGEN PRODUCTION  

SciTech Connect (OSTI)

Thermochemical processes are being developed to provide global-scale quantities of hydrogen. A variant on sulfur-based thermochemical cycles is the Hybrid Sulfur (HyS) Process, which uses a sulfur dioxide depolarized electrolyzer (SDE) to produce the hydrogen. In the HyS Process, sulfur dioxide is oxidized in the presence of water at the electrolyzer anode to produce sulfuric acid and protons. The protons are transported through a cation-exchange membrane electrolyte to the cathode and are reduced to form hydrogen. In the second stage of the process, the sulfuric acid by-product from the electrolyzer is thermally decomposed at high temperature to produce sulfur dioxide and oxygen. The two gases are separated and the sulfur dioxide recycled to the electrolyzer for oxidation. The Savannah River National Laboratory (SRNL) has been exploring a fuel-cell design concept for the SDE using an anolyte feed comprised of concentrated sulfuric acid saturated with sulfur dioxide. The advantages of this design concept include high electrochemical efficiency and small footprint compared to a parallel-plate electrolyzer design. This paper will provide a summary of recent advances in the development of the SDE for the HyS process.

Hobbs, D.

2010-07-22T23:59:59.000Z

89

METHOD TO PREVENT SULFUR ACCUMULATION INSIDE MEMBRANE ELECTRODE ASSEMBLY  

SciTech Connect (OSTI)

HyS is conceptually the simplest of the thermochemical cycles and involves only sulfur chemistry. In the HyS Cycle hydrogen gas (H{sub 2}) is produced at the cathode of the electrochemical cell (or electrolyzer). Sulfur dioxide (SO{sub 2}) is oxidized at the anode to form sulfuric acid (H{sub 2}SO{sub 4}) and protons (H{sup +}) as illustrated below. A separate high temperature reaction decomposes the sulfuric acid to water and sulfur dioxide which are recycled to the electrolyzers, and oxygen which is separated out as a secondary product. The electrolyzer includes a membrane that will allow hydrogen ions to pass through but block the flow of hydrogen gas. The membrane is also intended to prevent other chemical species from migrating between electrodes and undergoing undesired reactions that could poison the cathode or reduce overall process efficiency. In conventional water electrolysis, water is oxidized at the anode to produce protons and oxygen. The standard cell potential for conventional water electrolysis is 1.23 volts at 25 C. However, commercial electrolyzers typically require higher voltages ranging from 1.8 V to 2.6 V [Kirk-Othmer, 1991]. The oxidation of sulfur dioxide instead of water in the HyS electrolyzer occurs at a much lower potential. For example, the standard cell potential for sulfur dioxide oxidation at 25 C in 50 wt % sulfuric acid is 0.29 V [Westinghouse, 1980]. Since power consumption by the electrolyzers is equal to voltage times current, and current is proportional to hydrogen production, a large reduction in voltage results in a large reduction in electrical power cost per unit of hydrogen generated.

Steimke, J.; Steeper, T.; Herman, D.; Colon-Mercado, H.; Elvington, M.

2009-06-22T23:59:59.000Z

90

Assessing Potential Acidification of Marine Archaeological Wood Based on Concentration of Sulfur Species  

SciTech Connect (OSTI)

The presence of sulfur in marine archaeological wood presents a challenge to conservation. Upon exposure to oxygen, sulfur compounds in waterlogged wooden artifacts are being oxidized, producing sulfuric acid. This speeds the degradation of the wood, potentially damaging specimens beyond repair. Sulfur K-edge x-ray absorption spectroscopy was used to identify the species of sulfur present in samples from the timbers of the Mary Rose, a preserved 16th century warship known to undergo degradation through acidification. The results presented here show that sulfur content varied significantly on a local scale. Only certain species of sulfur have the potential to produce sulfuric acid by contact with oxygen and seawater in situ, such as iron sulfides and elemental sulfur. Organic sulfurs, such as the amino acids cysteine and methionine, may produce acid but are integral parts of the wood's structure and may not be released from the organic matrix. The sulfur species contained in the sample reflect the exposure to oxygen while submerged, and this exposure can differ greatly over time and position. A better understanding of the species pathway to acidifications required, along with its location, in order to suggest a more customized and effective preservation strategy. Waterlogged archaeological wood, frequently in the form of shipwrecks, is being excavated for historical purposes in many countries around the world. Even after extensive efforts towards preservation, scientists are discovering that accumulation of sulfate salts results in acidic conditions on the surfaces of the artifacts. Sulfuric acid degrades structural fibers in the wood by acid hydrolysis of cellulose, accelerating the decomposition of the ship timbers. Determining the sulfur content of waterlogged wood is now of great importance in maritime archaeology. Artifact preservation is often more time consuming and expensive than the original excavation; but it is key to the availability of objects for future study as well as maintaining the integrity of historical data and preserving the value of museum pieces. Sulfur occurs in a wide number of oxidation states from -2 to +6, and appears in numerous organic and inorganic compounds in nature. However, it is a very minor component of wood. Sulfur K-edge x-ray absorption spectroscopy (XAS) is a valuable technique because it has the ability to detect very low concentrations of sulfur in the specimen. XAS is also sensitive to differences in oxidation states, as well as long and short range order in molecules.

Not Available

2011-06-22T23:59:59.000Z

91

E-Print Network 3.0 - acid alkyl esters Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Nitric Acid 34. Sulfuric acid... .5 will not be accepted through this program. Heavy metal, toxic, acidic (without solvents) and basic wastes should... . Mercaptans 4. ......

92

acid  

Office of Legacy Management (LM)

Acid/Pueblo Canyon, New Mexico, Site is Acid/Pueblo Canyon, New Mexico, Site is located near the town of Los Alamos, New Mexico, approximately 25 miles northwest of Santa Fe and 60 miles north-northeast of Albuquerque. The site is accessible from Canyon Road, which runs just south of the former waste treatment plant. The plant was situated on a mesa that forms the south rim of Acid Canyon. Acid Canyon is a small tributary near the head

93

Sulfur dioxide oxidation and plume formation at cement kilns  

SciTech Connect (OSTI)

Results of source sampling at the Glens Falls cement kiln in Glens Falls, N.Y., are reported for sulfur oxides, ammonia, hydrochloric acid, oxygen, and moisture content. The origin of a detached, high-opacity, persistent plume originating from the cement kiln stack is investigated. It is proposed that this plume is due to ammonium salts of SOx and sulfuric acid that have been formed in condensed water droplets in the plume by the pseudocatalytic action of ammonia. (1 diagram, 1 graph, 22 references, 7 tables)

Dellinger, B.; Grotecloss, G.; Fortune, C.R.; Cheney, J.L.; Homolya, J.B.

1980-10-01T23:59:59.000Z

94

It's Elemental - The Element Sulfur  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Phosphorus Phosphorus Previous Element (Phosphorus) The Periodic Table of Elements Next Element (Chlorine) Chlorine The Element Sulfur [Click for Isotope Data] 16 S Sulfur 32.065 Atomic Number: 16 Atomic Weight: 32.065 Melting Point: 388.36 K (115.21°C or 239.38°F) Boiling Point: 717.75 K (444.60°C or 832.28°F) Density: 2.067 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 3 Group Number: 16 Group Name: Chalcogen What's in a name? From the Sanskrit word sulvere and the Latin word sulphurium. Say what? Sulfur is pronounced as SUL-fer. History and Uses: Sulfur, the tenth most abundant element in the universe, has been known since ancient times. Sometime around 1777, Antoine Lavoisier convinced the rest of the scientific community that sulfur was an element. Sulfur is a

95

Why sequence purple sulfur bacteria?  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

purple sulfur bacteria? purple sulfur bacteria? The process by which plants and some bacteria can convert light energy to sugar, or photosynthesis, is crucial to global food webs, and complicated. Very little is known about the photosynthetic bacteria in the purple sulfur bacteria group, which may represent one of the most primitive photosynthetic organisms and are capable of carbon fixation and sequestration in both light and dark conditions with the help of sulfur compounds. Purple sulfur bacteria are autotrophic and can synthesize organic compounds from inorganic sources. Researchers hope to learn more by sequencing nine type strains of purple sulfur bacteria that are found in freshwater, brackish and marine systems. The information would lead to a better understanding of the process of photosynthesis as well as the global

96

acid  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Acid/Pueblo Canyon, New Mexico, Site. Acid/Pueblo Canyon, New Mexico, Site. This site is managed by the U.S. Department of Energy Office of Legacy Management. Site Description and History The Acid/Pueblo Canyon, New Mexico, Site is located near the town of Los Alamos, New Mexico, approximately 25 miles northwest of Santa Fe and 60 miles north-northeast of Albuquerque. The site is accessible from Canyon Road, which runs just south

97

Microbial transformations of sulfur compounds  

Science Journals Connector (OSTI)

Oct 13, 1978 ... tains a large part of the chemical energy transferred ... ical energy is partly preserved in the bio- mass of .... ethanol to remove elemental sulfur.

2000-01-10T23:59:59.000Z

98

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur.  

SciTech Connect (OSTI)

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1997-06-01T23:59:59.000Z

99

Studying Cellulose Fiber Structure by SEM, XRD, NMR and Acid...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Studying Cellulose Fiber Structure by SEM, XRD, NMR and Acid Hydrolysis. Abstract: Cotton linters were partially hydrolyzed in dilute acid and the morphology of remaining...

100

COMPONENT DEVELOPMENT NEEDS FOR THE HYBRID SULFUR ELECTROLYZER  

SciTech Connect (OSTI)

Fiscal year 2008 studies in electrolyzer component development have focused on the characterization of membrane electrode assemblies (MEA) after performance tests in the single cell electrolyzer, evaluation of electrocatalysts and membranes using a small scale electrolyzer and evaluating the contribution of individual cell components to the overall electrochemical performance. Scanning electron microscopic (SEM) studies of samples taken from MEAs testing in the SRNL single cell electrolyzer test station indicates a sulfur-rich layer forms between the cathode catalyst layer and the membrane. Based on a review of operating conditions for each of the MEAs evaluated, we conclude that the formation of the layer results from the reduction of sulfur dioxide as it passes through the MEA and reaches the catalyst layer at the cathode-membrane interface. Formation of the sulfur rich layer results in partial delamination of the cathode catalyst layer leading to diminished performance. Furthermore we believe that operating the electrolyzer at elevated pressure significantly increases the rate of formation due to increased adsorption of hydrogen on the internal catalyst surface. Thus, identification of a membrane that exhibits much lower transport of sulfur dioxide is needed to reduce the quantity of sulfur dioxide that reaches the cathode catalyst and is reduced to produce the sulfur-rich layer. Three candidate membranes are currently being evaluated that have shown promise from preliminary studies, (1) modified Nafion{reg_sign}, (2) polybenzimidazole (PBI), and (3) sulfonated Diels Alder polyphenylene (SDAPP). Testing examined the activity for the sulfur dioxide oxidation of platinum (Pt) and platinum-alloy catalysts in 30 wt% sulfuric acid solution. Linear sweep voltammetry showed an increase in activity when catalysts in which Pt is alloyed with non-noble transition metals such as cobalt and chromium. However when Pt is alloyed with noble metals, such as iridium or ruthenium, the kinetic activity decreases. We recommend further testing to determine if these binary alloys will provide the increased reaction kinetic needed to meet the targets. We also plan to test the performance of these catalyst materials for both proton and sulfur dioxide reduction. The latter may provide another parameter by which we can control the reduction of sulfur dioxide upon transport to the cathode catalyst surface. A small scale electrolyzer (2 cm{sup 2}) has been fabricated and successfully installed as an additional tool to evaluate the effect of different operating conditions on electrolyzer and MEA performance. Currently this electrolyzer is limited to testing at temperatures up to 80 C and at atmospheric pressure. Selected electrochemical performance data from the single cell sulfur dioxide depolarized electrolyzer were analyzed with the aid of an empirical equation which takes into account the overpotential of each of the components. By using the empirical equation, the performance data was broken down into its components and a comparison of the potential losses was made. The results indicated that for the testing conditions of 80 C and 30 wt% sulfuric acid, the major overpotential contribution ({approx}70 % of all losses) arise from the slow reaction rate of oxidation of sulfur dioxide. The results indicate that in order to meet the target of hydrogen production at 0.5 A/cm{sup 2} at 0.6 V and 50 wt% sulfuric acid, identification of a better catalyst for sulfur dioxide oxidation will provide the largest gain in electrolyzer performance.

Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

2008-05-30T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

E-Print Network 3.0 - acid ammonium glycyrrhizate Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

liquids, chlorates, nitrites, sulfur, finely... hypochlorite, all oxidizing agents Carbon tetrachloride Sodium Chlorates Ammonium salts, acids, powdered metals... Ammonium...

102

E-Print Network 3.0 - acidic transition metals Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

liquids, chlorates, nitrites, sulfur, finely... hypochlorite, all oxidizing agents Carbon tetrachloride Sodium Chlorates Ammonium salts, acids, powdered metals... , copper,...

103

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Final report  

SciTech Connect (OSTI)

This project has investigated new metal oxide catalysts for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as CO. Significant progress in catalyst development has been made during the course of the project. We have found that fluorite oxides, CeO{sub 2} and ZrO{sub 2}, and rare earth zirconates such as Gd{sub 2}Zr{sub 2}O{sub 7} are active and stable catalysts for reduction Of SO{sub 2} by CO. More than 95% sulfur yield was achieved at reaction temperatures about 450{degrees}C or higher with the feed gas of stoichiometric composition. Reaction of SO{sub 2} and CO over these catalysts demonstrated a strong correlation of catalytic activity with the catalyst oxygen mobility. Furthermore, the catalytic activity and resistance to H{sub 2}O and CO{sub 2} poisoning of these catalysts were significantly enhanced by adding small amounts of transition metals, such as Co, Ni, Co, etc. The resulting transition metal-fluorite oxide composite catalyst has superior activity and stability, and shows promise in long use for the development of a greatly simplified single-step sulfur recovery process to treat variable and dilute SO{sub 2} concentration gas streams. Among various active composite catalyst systems the Cu-CeO{sub 2} system has been extensively studied. XRD, XPS, and STEM analyses of the used Cu-CeO{sub 2} catalyst found that the fluorite crystal structure of ceria was stable at the present reaction conditions, small amounts of copper was dispersed and stabilized on the ceria matrix, and excess copper oxide particles formed copper sulfide crystals of little contribution to catalytic activity. A working catalyst consisted of partially sulfated cerium oxide surface and partially sulfided copper clusters. The overall reaction kinetics were approximately represented by a first order equation.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1995-06-01T23:59:59.000Z

104

A method of cobalt ion concentration from dilute aqueous solutions  

SciTech Connect (OSTI)

The liquid membrane technique is very useful for metal ions recovery from dilute solutions. Co{sup 2+} ions can be removed and concentrated from wastewaters with an emulsion liquid membrane. The paper describes the permeation of Co{sup 2+} using naphthenic acids as the carrier and kerosene as the membrane material. The inner phase is a HCl 3.162 x 10{sup -4} solution. The extraction yield is more than 96%.

Amanatidou, E. [Technological Education Inst., Kila Kozanis (Greece); Stefanut, M.N.; Grozav, A. [Institute for Chemical and Technological Sciences, Timisoara (Romania)

1996-03-01T23:59:59.000Z

105

Graphene-sulfur nanocomposites for rechargeable lithium-sulfur battery electrodes  

SciTech Connect (OSTI)

Rechargeable lithium-sulfur batteries having a cathode that includes a graphene-sulfur nanocomposite can exhibit improved characteristics. The graphene-sulfur nanocomposite can be characterized by graphene sheets with particles of sulfur adsorbed to the graphene sheets. The sulfur particles have an average diameter less than 50 nm..

Liu, Jun; Lemmon, John P; Yang, Zhenguo; Cao, Yuiliang; Li, Xiaolin

2014-06-17T23:59:59.000Z

106

HYBRID SULFUR ELECTROLYZER DEVELOPMENT FY09 SECOND QUARTER REPORT  

SciTech Connect (OSTI)

The primary objective of the DOE-NE Nuclear Hydrogen Initiative (NHI) is to develop the nuclear hydrogen production technologies necessary to produce hydrogen at a cost competitive with other alternative transportation fuels. The focus of the NHI is on thermochemical cycles and high temperature electrolysis that can be powered by heat from high temperature gas reactors. The Savannah River National Laboratory (SRNL) has been tasked with the primary responsibility to perform research and development in order to characterize, evaluate and develop the Hybrid Sulfur (HyS) thermochemical process. This report documents work during the first quarter of Fiscal Year 2009, for the period between January 1, 2009 and March 31, 2009. The HyS Process is a two-step hybrid thermochemical cycle that is part of the 'Sulfur Family' of cycles. As a sulfur cycle, it uses high temperature thermal decomposition of sulfuric acid to produce oxygen and to regenerate the sulfur dioxide reactant. The second step of the process uses a sulfur dioxide depolarized electrolyzer (SDE) to split water and produce hydrogen by electrochemically reacting sulfur dioxide with H{sub 2}O. The SDE produces sulfuric acid, which is then sent to the acid decomposer to complete the cycle. The DOE NHI program is developing the acid decomposer at Sandia National Laboratory for application to both the HyS Process and the Sulfur Iodine Cycle. The SDE is being developed at SRNL. During FY05 and FY06, SRNL designed and conducted proof-of-concept testing for a SDE using a low temperature, PEM fuel cell-type design concept. The advantages of this design concept include high electrochemical efficiency, small footprint and potential for low capital cost, characteristics that are crucial for successful implementation on a commercial scale. During FY07, SRNL extended the range of testing of the SDE to higher temperature and pressure, conducted a 100-hour longevity test with a 60-cm{sup 2} single cell electrolyzer, and designed and built a larger, multi-cell stack electrolyzer. During FY08, SRNL continued SDE development, including development and successful testing of a three-cell electrolyzer stack with a rated capacity of 100 liters per hour. The HyS program for FY09 program will address improving SDE performance by focusing on preventing or minimizing sulfur deposition inside the cell caused by SO{sub 2} crossover, reduction of cell voltage for improved efficiency, an extension of cell operating lifetime. During FY09 a baseline technology development program is being conducted to address each of these issues. Button-cell (2-cm{sup 2}) and single cell (60-cm{sup 2}) SDEs will be fabricated and tested. A pressurized button-cell test facility will be designed and constructed to facilitate addition testing. The single cell test facility will be upgraded for unattended operation, and later for operation at higher temperature and pressure. Work will continue on development of the Gas Diffusion Electrode (GDE), or Gap Cell, as an alternative electrolyzer design approach that is being developed under subcontract with industry partner Giner Electrochemical Systems. If successful, it could provide an alternative means of preventing sulfur crossover through the proton exchange membrane, as well as the possibility for higher current density operation based on more rapid mass transfer in a gas-phase anode. Promising cell components will be assembled into membrane electrode assemblies (MEAs) and tested in the single cell test facility. Upon modification for unattended operation, test will be conducted for 200 hours or more. Both the button-cell and modified single cell facility will be utilized to demonstrate electrolyzer operation without sulfur build-up limitations, which is a Level 1 Milestone.

Herman, D; David Hobbs, D; Hector Colon-Mercado, H; Timothy Steeper, T; John Steimke, J; Mark Elvington, M

2009-04-15T23:59:59.000Z

107

E-Print Network 3.0 - acid complex films Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

doping acid during the formation of thin films. Both the electrical switching and electrochromic... and forms sulfuric acid within the PBZT film. The ... Source: Guo, John Zhanhu...

108

Controlling acid rain  

E-Print Network [OSTI]

High concentrations of sulfuric and nitric acid in raTn fn the northeastern USA are caused by the large scale combustion of fossil fuels within this region. Average precipitation acidity is pH 4.2, but spatial and temporal ...

Fay, James A.

1983-01-01T23:59:59.000Z

109

Sulfur capture in combination bark boilers  

SciTech Connect (OSTI)

A review of sulfur dioxide emission data for eight combination bark boilers in conjunction with the sulfur contents of the fuels reveals significant sulfur capture ranging from 10% to over 80% within the solid ash phase. Wood ash characteristics similar to activated carbon as well as the significant wood ash alkali oxide and carbonate fractions are believed responsible for the sulfur capture. Sulfur emissions from combination bark-fossil fuel firing are correlated to the sulfur input per ton of bark or wood residue fired.

Someshwar, A.V.; Jain, A.K. (National Council of the Paper Industry for Air and Stream Improvement, Gainesville, FL (United States))

1993-07-01T23:59:59.000Z

110

FY08 MEMBRANE CHARACTERIZATION REPORT FOR HYBRID SULFUR ELECTROLYZER  

SciTech Connect (OSTI)

This report summarizes results from all of the membrane testing completed to date at the Savannah River National Laboratory (SRNL) for the sulfur dioxide-depolarized electrolyzer (SDE). Several types of commercially-available membranes have been analyzed for ionic resistance and sulfur dioxide transport including perfluorinated sulfonic acid (PFSA), sulfonated polyether-ketone-ketone (SPEKK), and polybenzimidazole membranes (PBI). Of these membrane types, the poly-benzimidazole membrane, Celtec-L, exhibited the best combination of characteristics for use in an SDE. Several experimental membranes have also been analyzed including hydrated sulfonated Diels-Alder polyphenylenes (SDAPP) membranes from Sandia National Laboratory, perfluorosulfonimide (PFSI) and sulfonated perfluorocyclobutyl aromatic ether (S-PFCB) prepared by Clemson University, hydrated platinum-treated PFSA prepared by Giner Electrochemical Systems (GES) and Pt-Nafion{reg_sign} 115 composites prepared at SRNL. The chemical stability, SO{sub 2} transport and ionic conductivity characteristics have been measured for several commercially available and experimental proton-conducting membranes. Commercially available PFSA membranes such as the Nafion{reg_sign} series exhibited excellent chemical stability and ionic conductivity in sulfur dioxide saturated sulfuric acid solutions. Sulfur dioxide transport in the Nafion{reg_sign} membranes varied proportionally with the thickness and equivalent weight of the membrane. Although the SO{sub 2} transport in the Nafion{reg_sign} membranes is higher than desired, the excellent chemical stability and conductivity makes this membrane the best commercially-available membrane at this time. Initial results indicated that a modified Nafion{reg_sign} membrane incorporating Pt nanoparticles exhibited significantly reduced SO{sub 2} transport. Reduced SO{sub 2} transport was also measured with commercially available PBI membrane and several experimental membranes produced at SNL and Clemson. These membranes also exhibit good chemical stability and conductivity in concentrated sulfuric acid solutions and, thus, serve as promising candidates for the SDE. Therefore, we recommend further testing of these membranes including electrolyzer testing to determine if the reduced SO{sub 2} transport eliminates the formation of sulfur-containing films at the membrane/cathode interface. SO{sub 2} transport measurements in the custom built characterization cell identified experimental limitations of the original design. During the last quarter of FY08 we redesigned and fabricated a new testing cell to overcome the previous limitations. This cell also offers the capability to test membranes under polarized conditions as well as test the performance of MEAs under selected electrolyzer conditions.

Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

2008-09-01T23:59:59.000Z

111

Hydrogen and Sulfur Production from Hydrogen Sulfide Wastes  

E-Print Network [OSTI]

HYDROGEN AND SULFUR PRODUCTION FROM HYDROGEN SULFIDE WASTES? John B.L. Harkness and Richard D. Doctor, Argonne National Laboratory, Argonne. IL ABSTRACT A new hydrogen sulfide waste-treatment process that uses microwave plasma... to be economically competitive. In addition, the experiments show-that. typical refinery acid-gas streams are compatible with the plasma process and that all by-products can be treated with existing technology. BACKGROUND In 1987, Argonne staff found the first...

Harkness, J.; Doctor, R. D.

112

Molecular Structures of Polymer/Sulfur Composites for Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long Cycle Life. Molecular Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long...

113

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of LithiumSulfur Battery  

Science Journals Connector (OSTI)

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of LithiumSulfur Battery ... An amylopectin wrapped graphene oxide-sulfur composite was prepared to construct a 3-dimensionally cross-linked structure through the interaction between amylopectin and graphene oxide, for stabilizing lithium sulfur batteries. ...

Weidong Zhou; Hao Chen; Yingchao Yu; Deli Wang; Zhiming Cui; Francis J. DiSalvo; Hctor D. Abrua

2013-09-05T23:59:59.000Z

114

Two stage sorption of sulfur compounds  

DOE Patents [OSTI]

A two stage method for reducing the sulfur content of exhaust gases is disclosed. Alkali- or alkaline-earth-based sorbent is totally or partially vaporized and introduced into a sulfur-containing gas stream. The activated sorbent can be introduced in the reaction zone or the exhaust gases of a combustor or a gasifier. High efficiencies of sulfur removal can be achieved.

Moore, William E. (Manassas, VA)

1992-01-01T23:59:59.000Z

115

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur. Fifth quarterly technical progress report, December 1996  

SciTech Connect (OSTI)

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1996-12-01T23:59:59.000Z

116

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur. Sixth quarterly technical progress report, January - March 1997  

SciTech Connect (OSTI)

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1997-03-01T23:59:59.000Z

117

Dilute Clean Diesel Combustion Achieves Low Emissions and High...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Dilute Clean Diesel Combustion Achieves Low Emissions and High Efficiency While Avoiding Control Problems of HCCI Dilute Clean Diesel Combustion Achieves Low Emissions and High...

118

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print Wednesday, 29 November 2006 00:00...

119

Biodiesel Impact on Engine Lubricant Oil Dilution | Department...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Impact on Engine Lubricant Oil Dilution Biodiesel Impact on Engine Lubricant Oil Dilution Heavy-duty engine and light-duty vehicle experiments were conducted to investigate the...

120

Biodiesel Impact on Engine Lubricant Oil Dilution  

Broader source: Energy.gov (indexed) [DOE]

Impact on Engine Lubricant Oil Dilution Xin He, Aaron M. Williams, Earl D. Christensen, Jonathan L. Burton, Robert L. McCormick National Renewable Energy Laboratory October 5, 2011...

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Chain elongation with reactor microbiomes: upgrading dilute ethanol to medium-chain carboxylates  

E-Print Network [OSTI]

through a reversed b-oxidation pathway.6­8 This bacterium uses ethanol as a source of carbon, energy for elongation by C. kluyveri, one molecule of ethanol is oxidized to acetic acid for metabolic energy.6 OpenChain elongation with reactor microbiomes: upgrading dilute ethanol to medium-chain carboxylates

Angenent, Lars T.

122

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries 2011 DOE...

123

Improve reformer operation with trace sulfur removal  

SciTech Connect (OSTI)

Modern bimetallic reforming catalysts typically have feed specifications for sulfur of 0.5 to 1 wppm in the reformer naphtha carge. Sulfur in the raw naphtha is reduced to this level by naphtha hydrotreating. While most naphtha hydrotreating operations can usually obtain these levels without substantial problems. It is difficult to obtain levels much below 0.5 to 1 wppm with this process. Revamp of a constrained existing hydrotreater to reduce product sulfur slightly can be extremely costly typically entailing replacement or addition of a new reactor. At Engelhard the authors demonstrated that if the last traces of sulfur remaining from hydrotreating can be removed, the resulting ultra-low sulfur feed greatly improves the reformer operation and provides substantial economic benefit to the refiner. Removal of the remaining trace sulfur is accomplished in a simple manner with a special adsorbent bed, without adding complexity to the reforming operation.

McClung, R.G.; Novak, W.J.

1987-01-01T23:59:59.000Z

124

Measurement of Porosity in Dilute Acid Pretreated Corn Stover  

SciTech Connect (OSTI)

The conclusions of this report are: (1) pretreated corn stover appeared to have more accessible pore volume than raw corn stover; (2) solute exclusion method--differences in the pore volume were not detectable due to the high variability of the measurements; (3) thermoporosimetry--differences in pore volume between pretreated samples were not observed despite the low variability of the measurement and a good correction was found between unfrozen water at 240K and xylan content; and (4) porosity measurements showed no correlation between ethanol yields and the volume accessible to an enzyme size probe, for this sample set.

Ishizawa, C.; Davis, M. F.; Johnson, D. K.

2005-01-01T23:59:59.000Z

125

Redistribution of Lignin Caused by Dilute Acid Pretreatment of Biomass  

SciTech Connect (OSTI)

Research conducted at NREL has shown that lignin undergoes a phase transition during thermochemical pretreatments conducted above its glass transition temperature. The lignin coalesces within the plant cell wall and appears as microscopic droplets on cell surfaces. It is clear that pretreatment causes significant changes in lignin distribution in pretreatments at all scales from small laboratory reactors to pilot scale reactors. A method for selectively extracting lignin droplets from the surfaces of pretreated cell walls has allowed us to characterize the chemical nature and molecular weight distribution of this fraction. The effect of lignin redistribution on the digestibility of pretreated solids has also been tested. It is clear that removal of the droplets increases the digestibility of pretreated corn stover. The improved digestibility could be due to decreased non-specific binding of enzymes to lignin in the droplets, or because the droplets no longer block access to cellulose.

Johnson, D. K.; Donohoe, B. S.; Katahira, R.; Tucker, M. P.; Vinzant, T. B.; Himmel, M. E.

2012-01-01T23:59:59.000Z

126

Effects of Fuel Dilution with Biodiesel on Lubricant Acidity...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Affecting Fuel Economy and Engine Wear Reducing Lubricant Ash Impact on Exhaust Aftertreatment with a Oil Conditioning Filter Development of High Performance Heavy Duty Engine Oils...

127

Contribution of isotopologue self-shielding to sulfur mass-independent fractionation during sulfur dioxide photolysis  

E-Print Network [OSTI]

Signatures of sulfur mass-independent fractionation (S-MIF) are observed for sulfur minerals in Archean rocks, and for modern stratospheric sulfate aerosols (SSA) deposited in polar ice. Ultraviolet light photolysis of ...

Lyons, J. R.

128

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

SciTech Connect (OSTI)

The following report summarizes work conducted during the Phase I program Hydrocarbon and Sulfur Sensors for SOFC Systems under contract No. DE-FC26-02NT41576. For the SOFC application, sensors are required to monitor hydrocarbons and sulfur in order to increase the operation life of SOFC components. This report discusses the development of two such sensors, one based on thick film approach for sulfur monitoring and the second galvanic based for hydrocarbon monitoring.

A.M. Azad; Chris Holt; Todd Lesousky; Scott Swartz

2003-11-01T23:59:59.000Z

129

Sulfur-Free Selective Pulping  

E-Print Network [OSTI]

Technoeconomic Appraisal," December 1991. 5. DOE Annual Report on Contract No. AC02-83CH10093, Bozell, J. J., Hames, B., Chum, H. L., Dimmel, D. R, Althen, E., Caldwell, P. L., Daube, Oxidation ;; Diels-Alder .. I I -Methanol .. ~ 5 I 3 (C~O) OCH... - Hydrogen 3 (Q-IP) # Q-I 3 o o ~ o 1 2 ~ (H) Lignin DMBQ =two OCH3 groups Anthraquinone MMBQ =one OCH3 group A. K, and Kuroda, K-I.,"Sulfur-free Selective Pulping," March 1992. 6. DOE Annual Report on Contrac No. DE-AC02-83CH10093, Bozell, J. J...

Dimmel, D. R.; Bozell, J. J.

130

The determination of potential acidity in overburden sediments  

E-Print Network [OSTI]

Weathered Overburden Samples. Determination of Total Sulfur by LECO. Determination of Non-Sulfate Sulfur by LECO. Pyritic Iron Using the ASTM Method Potential Acidity Using a Rapid Oxidation Technique - Original Method. Potential Acidity Using a Rapid... the Sample. The Addition of Excess H 02. Catalysing the Decomposition of Excess H202. Leaching the Oxidized Sample with CaC12. Comparison of Potential Acidity Methods. F and T Tests. Potential Acidity of Weathered vs. Unweathered Samples. Total S...

O'Shay, Tracey Ann

2012-06-07T23:59:59.000Z

131

Sulfurization of a carbon surface for vapor phase mercury removal II: Sulfur forms and mercury uptake  

E-Print Network [OSTI]

promote the formation of organic sulfur and the presence of H2S during the cooling process increased in the presence of H2S was very effective towards Hg uptake in nitrogen. Corre- lation of mercury uptake capacitySulfurization of a carbon surface for vapor phase mercury removal ­ II: Sulfur forms and mercury

Borguet, Eric

132

Phase boundary detection for dilution refrigerators  

SciTech Connect (OSTI)

We describe a device to conveniently measure the positions of the phase boundaries in a dilution refrigerator. We show how a simple modification of a standard capacitive level gauge (segmentation of one of the electrodes) permits a direct calibration of the capacitance versus phase boundary position. We compare this direct calibration with the indirect procedure that must be adopted for a conventional capacitive level gauge. The device facilitates the correct adjustment of the {sup 3}He/{sup 4}He fraction in the dilution refrigerator.

Haar, E. ter; Martin, R.V. [DFMT, Instituto de Fisica, Universidade de Sao Paulo, C.P. 66.318, 05315-970 Sao Paulo, SP (Brazil)

2004-09-01T23:59:59.000Z

133

Viscosity Oscillations and Hysteresis in Dilute Emulsions  

Science Journals Connector (OSTI)

We show that the viscosity of a dilute emulsion exhibits oscillations and hysteresis as a function of the shear rate. This results from breaking up of droplets in response to the shear flow. The new phenomena we describe are generic and do not depend on a specific choice of model. The interesting dependence of the basic properties of a dilute emulsion on the shear rate results from the fact that the immersed droplets must break when the shear rate applied to the system is large enough.

Yiftah Navot and Moshe Schwartz

1997-12-15T23:59:59.000Z

134

Diluted magnetic semiconductor nanowires exhibiting magnetoresistance  

DOE Patents [OSTI]

A method for is disclosed for fabricating diluted magnetic semiconductor (DMS) nanowires by providing a catalyst-coated substrate and subjecting at least a portion of the substrate to a semiconductor, and dopant via chloride-based vapor transport to synthesize the nanowires. Using this novel chloride-based chemical vapor transport process, single crystalline diluted magnetic semiconductor nanowires Ga.sub.1-xMn.sub.xN (x=0.07) were synthesized. The nanowires, which have diameters of .about.10 nm to 100 nm and lengths of up to tens of micrometers, show ferromagnetism with Curie temperature above room temperature, and magnetoresistance up to 250 Kelvin.

Yang, Peidong (El Cerrito, CA); Choi, Heonjin (Seoul, KR); Lee, Sangkwon (Daejeon, KR); He, Rongrui (Albany, CA); Zhang, Yanfeng (El Cerrito, CA); Kuykendal, Tevye (Berkeley, CA); Pauzauskie, Peter (Berkeley, CA)

2011-08-23T23:59:59.000Z

135

Graphene-wrapped sulfur nanospheres with ultra-high sulfur loading for high energy density lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithiumsulfur (LiS) battery with high theoretical energy density is one of the most promising energy storage systems for electric vehicles and intermittent renewable energy. However, due to the poor conductivity of the active material, considerable weight of the electrode is occupied by the conductive additives. Here we report a graphene-wrapped sulfur nanospheres composite (S-nanosphere@G) with sulfur content up to 91wt% as the high energy density cathode material for LiS battery. The sulfur nanospheres with diameter of 400500nm are synthesized through a solution-based approach with the existence of polyvinylpyrrolidone (PVP). Then the sulfur nanospheres are uniformly wrapped by conductive graphene sheets through the electrostatic interaction between graphene oxide and PVP, followed by reducing of graphene oxide with hydrazine. The design of graphene wrapped sulfur nanoarchitecture provides flexible conductive graphene coating with void space to accommodate the volume expansion of sulfur and to minimize polysulfide dissolution. As a result, the S-nanosphere@G nanocomposite with 91wt% sulfur shows a reversible initial capacity of 970mAhg?1 and an average columbic efficiency>96% over 100 cycles at a rate of 0.2C. Taking the total mass of electrode into account, the S-nanosphere@G composite is a promising cathode material for high energy density LiS batteries.

Ya Liu; Jinxin Guo; Jun Zhang; Qingmei Su; Gaohui Du

2015-01-01T23:59:59.000Z

136

Heterogeneous Reactions of Epoxides in Acidic Media  

E-Print Network [OSTI]

on sulfuric acid using Ion drift-Chemical Ionization Mass Spectrometry (ID-CIMS) showed an irreversible uptake of epoxides at room temperature resulting in the formation of less volatile products like diols, organosulfates and acetals. However, at lower...

Lal, Vinita

2012-02-14T23:59:59.000Z

137

High-Sulfur Coal for Generating Electricity  

Science Journals Connector (OSTI)

High-Sulfur...FLUIDIZED-BED COMBUSTORS, COMBUSTION...MAY FLUE GAS DES S E...1971 ). High-sulfur...was brief. Natural gas became...overdependent on natural gas and oil to...elevated pressure with a downward...coals of high ash-fusion...

James T. Dunham; Carl Rampacek; T. A. Henrie

1974-04-19T23:59:59.000Z

138

E-Print Network 3.0 - acidic sulfate aerosols Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

18 6, 116, 2006 Hygroscopicity of Summary: phase sulfuric acid is in the form of10 ammoniated sulfate clusters. Hence, these compounds are expected... sulfate particles was...

139

E-Print Network 3.0 - actual acid sulfate Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

16 6, 116, 2006 Hygroscopicity of Summary: phase sulfuric acid is in the form of10 ammoniated sulfate clusters. Hence, these compounds are expected... particles either as...

140

E-Print Network 3.0 - acidic sulfate solutions Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

26 6, 116, 2006 Hygroscopicity of Summary: phase sulfuric acid is in the form of10 ammoniated sulfate clusters. Hence, these compounds are expected... growth of ammoniated...

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

E-Print Network 3.0 - acid potassium glycyrrhetinate Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

provides some chemicals which are incompatible with other compounds. Summary: Potassium carbon tetrachloride, carbon dioxide, water Potassium chlorate sulfuric and other acids...

142

Two-dimensional kinetics of binary nucleation in sulfuric acidwater mixtures  

E-Print Network [OSTI]

. INTRODUCTION Binary homogeneous nucleation is a mechanism for gas- to-particle conversion that can result in significant rates of new particle formation even if both components are under- saturated in the gas phase. An important example is the at- mospheric production of sulfuric acid in the presence of am- bient water vapor

143

The complete genome sequence of Staphylothermus marinus reveals differences in sulfur metabolism among heterotrophic Crenarchaeota  

SciTech Connect (OSTI)

Staphylothermus marinus is an anaerobic, sulfur-reducing peptide fermenter of the archaeal phylum Crenarchaeota. It is the third heterotrophic, obligate sulfur reducing crenarchaeote to be sequenced and provides an opportunity for comparative analysis of the three genomes. The 1.57 Mbp genome of the hyperthermophilic crenarchaeote Staphylothermus marinus has been completely sequenced. The main energy generating pathways likely involve 2-oxoacid:ferredoxin oxidoreductases and ADP-forming acetyl-CoA synthases. S. marinus possesses several enzymes not present in other crenarchaeotes including a sodium ion-translocating decarboxylase likely to be involved in amino acid degradation. S. marinus lacks sulfur-reducing enzymes present in the other two sulfur-reducing crenarchaeotes that have been sequenced - Thermofilum pendens and Hyperthermus butylicus. Instead it has three operons similar to the mbh and mbx operons of Pyrococcus furiosus, which may play a role in sulfur reduction and/or hydrogen production. The two marine organisms, S. marinus and H. butylicus, possess more sodium-dependent transporters than T. pendens and use symporters for potassium uptake while T. pendens uses an ATP-dependent potassium transporter. T. pendens has adapted to a nutrient-rich environment while H. butylicus is adapted to a nutrient-poor environment, and S. marinus lies between these two extremes. The three heterotrophic sulfur-reducing crenarchaeotes have adapted to their habitats, terrestrial vs. marine, via their transporter content, and they have also adapted to environments with differing levels of nutrients. Despite the fact that they all use sulfur as an electron acceptor, they are likely to have different pathways for sulfur reduction.

Anderson, iain J.; Dharmarajan, Lakshmi; Rodriguez, Jason; Hooper, Sean; Porat, Iris; Ulrich, Luke E.; Elkins, James G.; Mavromatis, Kostas; Sun, Hui; Land, Miriam; Lapidus, Alla; Lucas, Susan; Barry, Kerrie; Huber, Harald; Zhulin, Igor B.; Whitman, William B.; Mukhopadhyay, Biswarup; Woese, Carl; Bristow, James; Kyrpides, Nikos

2008-09-05T23:59:59.000Z

144

Method of removal of sulfur from coal and petroleum products  

DOE Patents [OSTI]

A method for the removal of sulfur from sulfur-bearing materials such as coal and petroleum products using organophosphine and organophosphite compounds is provided.

Verkade, John G. (Ames, IA); Mohan, Thyagarajan (Ames, IA); Angelici, Robert J. (Ames, IA)

1995-01-01T23:59:59.000Z

145

Investigation of Sulfur Deactivation on Cu/Zeolite SCR Catalysts...  

Broader source: Energy.gov (indexed) [DOE]

of Sulfur Deactivation on CuZeolite SCR Catalysts in Diesel Application Investigation of Sulfur Deactivation on CuZeolite SCR Catalysts in Diesel Application Investigation of...

146

Additives and Cathode Materials for High-Energy Lithium Sulfur...  

Broader source: Energy.gov (indexed) [DOE]

Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries 2013 DOE Hydrogen and Fuel Cells...

147

Manipulating the Surface Reactions in Lithium Sulfur Batteries...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode Structures. Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode...

148

Analyzing organic sulfur in coal/char: Integrated mild degradation/XANES methods. Final technical report, September 1, 1993--November 30, 1994  

SciTech Connect (OSTI)

The overall goal of this study is to improve the understanding of sulfur in coals/chars via the use of combined advanced nondestructive and advanced destructive methods of sulfur analysis. This study combines selective oxidation, analytical pyrolysis, and sulfur X-ray Absorption Near Edge Structure Spectroscopy (XANES) analysis. Samples with a wide variety of sulfur contents, (0.63%--4.40%) have been prepared for use in this study. This includes steam gasification chars, oxidized coals and desulfurized coals as well of the original unaltered coals. Mild pyrolysis and XANES data shows that the sulfur chemistry of gasification chars is significantly different from that of the original coals. Mild pyrolysis of the samples that were oxidized with peroxyacetic acid showed that the level of simple thiophene structures observed in the pyrolysis products declines with increasing levels of oxidation. Sulfur XANES spectra of treated samples showed various effects depending on the treatment severity. The XANES spectra of less severely treated samples were similar, although not identical, to the untreated coal spectra. XANES of gasification chars indicated conversion of pyrite to pyrrhotite, removal of organic sulfide sulfur and dissolution of soluble inorganic sulfur species during gasification. Mild oxidation with peroxyacetic acid results in preferential oxidation of sulfide forms before thiophene forms but increasing oxidation severity leads to virtually all sulfur species being oxidized. Good agreement between W-band EPR and XANES data for aromatic sulfur contents were obtained. The TPR analysis of coal indicated that organic sulfur was present as alkyl-aryl sulfide, aryl-aryl sulfides, simple thiophenes and condensed thiophenes. TPR shows that non-thiophenic compounds are removed by PAA oxidation, and that the longer the oxidation is performed the greater is the removal of non-thiophenic sulfur structures.

Palmer, S.R. [Southern Illinois Univ., Carbondale, IL (United States); Huffman, G.P. [Univ. of Kentucky, Lexington, KY (United States)

1994-12-31T23:59:59.000Z

149

Sulfur nanocrystals anchored graphene composite with highly improved electrochemical performance for lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract Two kinds of graphenesulfur composites with 50wt% of sulfur are prepared using hydrothermal method and thermal mixing, respectively. Transmission Electron Microscopy (TEM) and Energy Dispersive X-ray Spectra mapping show that sulfur nanocrystals with size of ?5nm dispersed on graphene sheets homogeneously for the sample prepared by hydrothermal method (NanoS@G). While for the thermal mixed graphenesulfur composite (SG mixture), sulfur shows larger and uneven size (50200nm). X-ray Photoelectron Spectra (XPS) reveals the strong chemical bonding between the sulfur nanocrystals and graphene. Comparing with the SG mixture, the NanoS@G composite shows highly improved electrochemical performance as cathode for lithiumsulfur (LiS) battery. The NanoS@G composite delivers an initial capacity of 1400mAhg?1 with the sulfur utilization of 83.7% at a current density of 335mAg?1. The capacity keeps above 720mAhg?1 over 100 cycles. The strong adherence of the sulfur nanocrystals on graphene immobilizes sulfur and polysulfides species and suppressed the shuttle effect, resulting higher coulombic efficiency and better capacity retention. Electrochemical impedance also suggests that the strong bonding enabled rapid electronic/ionic transport and improved electrochemical kinetics, therefore good rate capability is obtained. These results demonstrate that the NanoS@G composite is a very promising candidate for high-performance LiS batteries.

Jun Zhang; Zimin Dong; Xiuli Wang; Xuyang Zhao; Jiangping Tu; Qingmei Su; Gaohui Du

2014-01-01T23:59:59.000Z

150

Infinitely Dilute Partial Molar Properties of Proteins from Computer Simulation  

Science Journals Connector (OSTI)

A detailed understanding of temperature and pressure effects on an infinitely dilute proteins conformational equilibrium requires knowledge of the corresponding infinitely dilute partial molar properties. Established molecular dynamics methodologies ...

Elizabeth A. Ploetz; Paul E. Smith

2014-10-17T23:59:59.000Z

151

Catalyst for elemental sulfur recovery process  

DOE Patents [OSTI]

A catalytic reduction process is described for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides high activity and selectivity, as well as stability in the reaction atmosphere, for the reduction of SO[sub 2] to elemental sulfur product with carbon monoxide or other reducing gases. The reaction of sulfur dioxide and reducing gas takes place over a metal oxide composite catalyst having one of the following empirical formulas: [(FO[sub 2])[sub 1[minus]n](RO)[sub n

Flytzani-Stephanopoulos, M.; Liu, W.

1995-01-24T23:59:59.000Z

152

Sulfur-graphene oxide material for lithium-sulfur battery cathodes  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Sulfur-graphene oxide material for lithium-sulfur battery cathodes Sulfur-graphene oxide material for lithium-sulfur battery cathodes Theoretical specific energy and theoretical energy density Scanning electron micrograph of the GO-S nanocomposite June 2013 Searching for a safer, less expensive alternative to today's lithium-ion batteries, scientists have turned to lithium-sulfur as a possible chemistry for next-generation batteries. Li/S batteries have several times the energy storage capacity of the best currently available rechargeable Li-ion battery, and sulfur is inexpensive and nontoxic. Current batteries using this chemistry, however, suffer from extremely short cycle life-they don't last through many charge-discharge cycles before they fail. A research team led by Elton Cairns and Yuegang Zhang has developed a new

153

Phosphazene groups modified sulfur composites as active cathode materials for rechargeable lithium/sulfur batteries  

Science Journals Connector (OSTI)

A novel phosphazene groups modified sulfur composites cathode [triphosphazene sulfide composite (PS) or nitroanilinetriphosphazene disulfide composite (NPS)] which can give good affinity with electrolytes was...

J. D. Liu; S. Q. Zhang; S. B. Yang; Z. F. Shi; S. T. Zhang; L. K. Wu

2013-11-01T23:59:59.000Z

154

Sulfur Dioxide Crossover during the Production of Hydrogen and Sulfuric Acid in a PEM Electrolyzer  

E-Print Network [OSTI]

and must be resup- plied. For example, researchers at the Savannah River National Laboratory SRNL have

Weidner, John W.

155

Involvement of Intermediate Sulfur Species in Biological Reduction of Elemental Sulfur under Acidic, Hydrothermal Conditions  

E-Print Network [OSTI]

, Hydrothermal Conditions Eric S. Boyd,a Gregory K. Druschelb Department of Chemistry and Biochemistry, Montana in size, a rate which was influenced by the pH of the me- dium and the presence of organic carbon. Thus, S to serve as a growth-promoting TEA for A. sulfurireducens. Terrestrial and hydrothermal spring source

Ahmad, Sajjad

156

Energy Levels in Sulfur Nuclei  

Science Journals Connector (OSTI)

A study has been made of the proton groups from the reaction of 3.22-Mev deuterons with sulfur in the form, primarily, of H2S gas. The following Q values have been assigned to the reaction S32(dp)S33:6.48,5.69,4.58,4.31,3.63,3.33,2.60,2.33,2.06,1.78,1.37,0.85,and0.18 Mev, corresponding to the ground state and twelve excited states of S33. Four of these groups have been investigated for proton gamma-ray coincidences to confirm this assignment. The yield as a function of deuteron energy has been observed for the six highest energy groups and indication of the presence of some broad resonances found. A qualitative measurement of the variation with angle of relative yields of the groups has indicated a proton intensity distribution that is symmetric for some groups and asymmetric for others. The cross section for the reaction for 90 observation has been found to be 1.2 barns. The mass difference S33-S32 has been calculated to be 0.99963 mass unit.Two low intensity, high energy groups have been assigned to the reaction S33(dp)S34 with Q values of 8.67 and 7.85 Mev. This, together with the above observation, leads to a value of 1.99691 for the mass difference S34-S32.

Perry W. Davison

1949-03-01T23:59:59.000Z

157

Steam reforming utilizing sulfur tolerant catalyst  

SciTech Connect (OSTI)

This patent describes a steam reforming process for converting hydrocarbon material to hydrogen gas in the presence of sulfur which consists of: adding steam to the hydrocarbon material and passing the steam and hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity, sulfur tolerant catalyst of platinum supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina. It also describes a steam process for converting hydrocarbon material to hydrogen gas in the presence of sulfur which consists of steam to the hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity, sulfur tolerant catalysts consisting essentially of iridium supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina. In addition a steam reforming process is described for converting hydrocarbon material to hydrogen gas in the presence of sulfur comprising adding steam to the hydrocarbon material and passing the steam and hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity sulfur tolerant catalysts consisting essentially of palladium supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina.

Setzer, H.J.; Karavolis, S.; Bett, J.A.S.

1987-09-15T23:59:59.000Z

158

THE DISTRIBUTION OF COPPER IN TROPICAL SEAWATER  

Science Journals Connector (OSTI)

Loss of Cu to PVC sampler (counts corrected for decay). Bottle No. .... sulfuric acid mixture ( 1 + 1). Heat to dense fumes of sulfuric acid. Cool and dilute to 1 liter...

159

Aerosol acidity in rural New England: Temporal trends and source region analysis  

E-Print Network [OSTI]

the dissociation of sulfuric acid (H2SO4) that condenses after forming via the gas phase oxidation of sulfur; accepted 9 January 2007; published 26 April 2007. [1] Data from 24-hour bulk filter samples collected by the AIRMAP program were used to estimate aerosol acidity at a site in New England. The sampling site

Fischer, Emily V.

160

Central Appalachia: Production potential of low-sulfur coal  

SciTech Connect (OSTI)

The vast preponderance of eastern US low sulfur and 1.2-lbs SO{sub 2}/MMBtu compliance coal comes from a relatively small area composed of 14 counties located in eastern Kentucky, southern West Virginia and western Virginia. These 14 counties accounted for 68% of all Central Appalachian coal production in 1989 as well as 85% of all compliance coal shipped to electric utilities from this region. A property-by-property analysis of total production potential in 10 of the 14 counties (Floyd, Knott, Letcher, Harlan, Martin and Pike in Kentucky and Boone, Kanawha, Logan and Mingo in West Virginia) resulted in the following estimates of active and yet to be developed properties: (1) total salable reserves for all sulfur levels were 5.9 billion tons and (2) 1.2-lbs. SO{sub 2}/MMBtu compliance'' reserves totaled 2.38 billion tons. This potential supply of compliance coal is adequate to meet the expanded utility demand expected under acid rain for the next 20 years. Beyond 2010, compliance supplies will begin to reach depletion levels in some areas of the study region. A review of the cost structure for all active mines was used to categorize the cost structure for developing potential supplies. FOB cash costs for all active mines in the ten counties ranged from $15 per ton to $35 per ton and the median mine cost was about $22 per ton. A total of 47 companies with the ability to produce and ship coal from owned or leased reserves are active in the ten-county region. Identified development and expansion projects controlled by active companies are capable of expanding the region's current production level by over 30 million tons per year over the next twenty years. Beyond this period the issue of reserve depletion for coal of all sulfur levels in the ten county region will become a pressing issue. 11 figs., 12 tabs.

Watkins, J. (Hill and Associates, Inc., Annapolis, MD (United States))

1991-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

The reaction kinetics of gasoline sulfur compounds: Catalytic mechanisms for sulfur reduction  

SciTech Connect (OSTI)

One of the key elements of reformulated gasoline is the reduction of the sulfur compounds produced by fluid catalytic cracking. This paper probes the reaction kinetics of refractory gasoline-range thiophene derivatives (thiophene, tetrahydrothiophene, and alkylthiophenes) in an effort to determine the mechanisms of sulfur compound cracking in the FCC unit. The gasoline-range sulfur compounds were analyzed using gas chromatography with an atomic emission detector. The authors` results show that the FCC catalysts affects the cracking of sulfur compounds through both hydrogen transfer and zeolite pore restriction mechanisms. An experimental FCC catalyst is shown to reduce gasoline sulfur content in the Davidson Circulating Riser (DCR{sup TM}) pilot unit. Model compound tests show that the activity of the catalyst is due to both its catalytic and adsorptive properties. Tetrahydrothiophene, which is produced from thiophenes by hydrogen transfer, is completely removed by the experimental catalyst.

Harding, R.H.; Gatte, R.R.; Albro, T.G.; Wormsbecher, R.F. [W.R. Grace & Co. Conn, Columbia, MD (United States)

1993-12-31T23:59:59.000Z

162

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

& Publications Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries...

163

Safety considerations for the use of sulfur in sulfur-modified pavement materials  

E-Print Network [OSTI]

on the surround1ng environment. As sulfur-modified paving materials were being developed, there was a corresponding concern for studying the amounts of gaseous emiss1ons that were generated. The Texas Trans- portat1on Inst1tute (TTI) was one of the first... organizations in the United States to become 1nvolved in the research and development of sulfur-modified pavements, Throughout 1ts laboratory stud1es TTI cont1nually mon1tored hydrogen sulf1de (H25) and sulfur d1oxide (502) em1ssions produced during mix...

Jacobs, Carolyn Yuriko

2012-06-07T23:59:59.000Z

164

Dilute Oxygen Combustion - Phase 3 Report  

SciTech Connect (OSTI)

Dilute Oxygen Combustion (DOC) burners have been successfully installed and operated in the reheat furnace at Auburn Steel Co., Inc., Auburn, NY, under Phase 3 of the Dilute Oxygen Combustion project. Two new preheat zones were created employing a total of eight 6.5 MMBtu/hr capacity burners. The preheat zones provide a 30 percent increase in maximum furnace production rate, from 75 tph to 100 tph. The fuel rate is essentially unchanged, with the fuel savings expected from oxy-fuel combustion being offset by higher flue gas temperatures. When allowance is made for the high nitrogen level and high gas phase temperature in the furnace, measured NOx emissions are in line with laboratory data on DOC burners developed in Phase 1 of the project. Burner performance has been good, and there have been no operating or maintenance problems. The DOC system continues to be used as part of Auburn Steel's standard reheat furnace practice. High gas phase temperature is a result of the high firing density needed to achieve high production rates, and little opportunity exists for improvement in that area. However, fuel and NOx performance can be improved by further conversion on furnace zones to DOC burners, which will lower furnace nitrogen levels. Major obstacles are cost and concern about increased formation of oxide scale on the steel. Oxide scale formation may be enhanced by exposure of the steel to higher concentrations of oxidizing gas components (primarily products of combustion) in the higher temperature zones of the furnace. Phase 4 of the DOC project will examine the rate of oxide scale formation in these higher temperature zones and develop countermeasures that will allow DOC burners to be used successfully in these furnace zones.

Riley, Michael F.

2000-05-31T23:59:59.000Z

165

Dilute Oxygen Combustion Phase 3 Final Report  

SciTech Connect (OSTI)

Dilute Oxygen Combustion (DOC) burners have been successfully installed and operated in the reheat furnace at Auburn Steel Co., Inc., Auburn, NY, under Phase 3 of the Dilute Oxygen Combustion project. Two new preheat zones were created employing a total of eight 6.5 MMBtu/hr capacity burners. The preheat zones provide a 30 percent increase in maximum furnace production rate, from 75 tph to 100 tph. The fuel rate is essentially unchanged, with the fuel savings expected from oxy-fuel combustion being offset by higher flue gas temperatures. When allowance is made for the high nitrogen level and high gas phase temperature in the furnace, measured NOx emissions are in line with laboratory data on DOC burners developed in Phase 1 of the project. Burner performance has been good and there have been no operating or maintenance problems. The DOC system continues to be used as part of Auburn Steel?s standard reheat furnace practice. High gas phase temperature is a result of the high firing density needed to achieve high production rates, and little opportunity exists for improvement in that area. However, fuel and NOx performance can be improved by further conversion of furnace zones to DOC burners, which will lower furnace nitrogen levels. Major obstacles are cost and concern about increased formation of oxide scale on the steel. Oxide scale formation may be enhanced by exposure of the steel to higher concentrations of oxidizing gas components (primarily products of combustion) in the higher temperature zones of the furnace. Phase 4 of the DOC project will examine the rate of oxide scale formation in these higher temperature zones and develop countermeasures that will allow DOC burners to be used successfully in these furnace zones.

Riley, M.F.; Ryan, H.M.

2000-05-31T23:59:59.000Z

166

Fact #824: June 9, 2014 EPA Sulfur Standards for Gasoline  

Broader source: Energy.gov [DOE]

Sulfur naturally occurs in gasoline and diesel fuel, contributing to pollution when the fuel is burned. Beginning in 2004, standards were set on the amount of sulfur in gasoline (Tier 2 standards)....

167

Development of a new FGD process that converts sulfur dioxide to salable ammonium phosphate fertilizer  

SciTech Connect (OSTI)

Rich mineral resources have enabled Chinese coal output and energy consumption to rank second and third in the world, respectively. In 1992, up to 70 percent of the country`s electric power was generated by the combustion of some 300 million tons of coal. Although the average sulfur content level in Chinese coals is only about 0.8 percent, the share of high- sulfur coals with 2 percent or more sulfur content is as high as 18 percent. As a result, air pollution accompanied by acid rain now occurs over most of the country, especially in southwestern China. Currently, the area comprising Guangdong, Guangxi, the Sichuan Basin, and the greater part of Gueizhou, where the sulfur content in coal is between 2 and 7 percent and the average pH values of rain water are between 4 and 5 per annum, has become one of the three biggest acid rain-affected areas in the world. In 1992, the national installed coal-fired electricity generation capacity exceeded 100,000 MWe. By the year 2000, it is expected to reach as much as 200,000 MWe, according to a new scheduled program. Environmental pollution caused by large-scale coal combustion is a very important issue that needs to be considered in the implementation of the program. To ensure that the effects of coal-fired power generation on the environment can be properly controlled in the near future, TPRI (Thermal Power Research Institute), the sole thermal power engineering research institution within the Ministry of Electric Power Industry (MOEPI), has conducted a long-term research program to develop sulfur emission control technologies suitable to the special conditions prevalent in China since the early 1970s. The details are summarized. The objective of this chapter is to describe the fundamental concept and major pilot test results and present an economic evaluation of a new process combining flue gas desulfurization (FGD) and ammonium phosphate fertilizer production.

Ji-lu Chen

1993-12-31T23:59:59.000Z

168

Can Sulfur Spectroscopy the Vasa?  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Title Title by Magnus Sandström*, Farideh Jalilehvand, Ingmar Persson, Ulrik Gelius and Patrick Frank The famous 17th-century Swedish warship Vasa has been on display in the Vasa Museum since 1990 (Figure 1). The Vasa sank on its maiden voyage in 1628, and was recovered in 1961 after 333 years in the cold brackish water of Stockholm harbor. After extensive conservation treatment, the oaken Vasa appeared in good condition (1). Figure 1. The Vasa on display in the Vasa Museum, Stockholm, Sweden. Dimensions: length 61 m (69 m including bowsprit), maximum width 11.7 m, stern castle 19.3 m high, displacement 1210 tons. (photo by Hans Hammarskiöld at the Vasa Museum). Reproduced by permission, (http://www.nature.com/). However, high acidity and a rapid spread of sulfate salts and elemental

169

ORIGINAL ARTICLE Sulfur oxidizers dominate carbon fixation  

E-Print Network [OSTI]

). Methylotrophs and iron oxidizers were also active in plume waters and expressed key proteins for methane by bacteria (especially, alpha-, gamma- and epsilon-proteobacteria) that likely participate in the oxidationORIGINAL ARTICLE Sulfur oxidizers dominate carbon fixation at a biogeochemical hot spot in the dark

Hansell, Dennis

170

High-Sulfur Coal for Generating Electricity  

Science Journals Connector (OSTI)

...amounts of coal, because...Director-Mineral Re-sources...of Gas from Coal through a...on coals of high ash-fusion temperature...per ton of high-sulfur coal burned. Absorp-tion...particulate matter as well as...capable of remov-ing up to...

James T. Dunham; Carl Rampacek; T. A. Henrie

1974-04-19T23:59:59.000Z

171

Short communication Influence of molybdenum and sulfur on copper  

E-Print Network [OSTI]

Short communication Influence of molybdenum and sulfur on copper metabolism in sheep: comparison of molybdenum able to trigger the copper sulfur molybdenum interference in sheep was measured with either only) and 4 increasing molybdenum doses. The sulfur-molybdenum-copper interference was quantified

Paris-Sud XI, Université de

172

A novel lithium/sulfur battery based on sulfur/graphene nanosheet composite cathode and gel polymer electrolyte  

Science Journals Connector (OSTI)

A novel sulfur/graphene nanosheet (S/GNS) composite was prepared ... ball milling of sulfur with commercial multi-layer graphene nanosheet, followed by a heat treatment. ... of irregularly interlaced nanosheet-li...

Yongguang Zhang; Yan Zhao; Zhumabay Bakenov

2014-03-01T23:59:59.000Z

173

A simple approach to synthesize nanosized sulfur/graphene oxide materials for high-performance lithium/sulfur batteries  

Science Journals Connector (OSTI)

We report on a simple and facile synthesis route for the sulfur/graphene oxide composite via ultrasonic mixing of the nano-sulfur and graphene oxide aqueous suspensions followed by a low-temperature heat treat...

Yongguang Zhang; Yan Zhao; Zhumabay Bakenov

2014-07-01T23:59:59.000Z

174

Investigation of Ultrafine Particle Formation during Diesel Exhaust Dilution  

Science Journals Connector (OSTI)

Investigation of Ultrafine Particle Formation during Diesel Exhaust Dilution ... In on-road exhaust studies with a heavy duty diesel vehicle and in laboratory studies with two gasoline-fueled passenger cars, we found that ... ... Analyses of Turbulent Flow Fields and Aerosol Dynamics of Diesel Engine Exhaust Inside Two Dilution Sampling Tunnels Using the CTAG Model ...

Ji Ping Shi; Roy M. Harrison

1999-09-16T23:59:59.000Z

175

Dilution and microsegregation in dissimilar metal welds between super austenitic  

E-Print Network [OSTI]

Dilution and microsegregation in dissimilar metal welds between super austenitic stainless steel the weld will also signi® cantly affect the corrosion resistance. Dissimilar metal welds between a super dissimilar weld. The dilution level was found to decrease as the ratio of volumetric ® ller metal feedrate

DuPont, John N.

176

Graphene-Wrapped Sulfur Particles as a Rechargeable LithiumSulfur Battery Cathode Material with High Capacity and Cycling Stability  

Science Journals Connector (OSTI)

Graphene-Wrapped Sulfur Particles as a Rechargeable LithiumSulfur Battery Cathode Material with High Capacity and Cycling Stability ... The resulting graphenesulfur composite showed high and stable specific capacities up to ?600 mAh/g over more than 100 cycles, representing a promising cathode material for rechargeable lithium batteries with high energy density. ...

Hailiang Wang; Yuan Yang; Yongye Liang; Joshua Tucker Robinson; Yanguang Li; Ariel Jackson; Yi Cui; Hongjie Dai

2011-06-24T23:59:59.000Z

177

Method to prevent sulfur accumulation in membrane electrode assembly  

DOE Patents [OSTI]

A method of operating a hybrid sulfur electrolyzer to generate hydrogen is provided that includes the steps of providing an anolyte with a concentration of sulfur dioxide, and applying a current. During steady state generation of hydrogen a plot of applied current density versus concentration of sulfur dioxide is below a boundary line. The boundary line may be linear and extend through the origin of the graph with a slope of 0.001 in which the current density is measured in mA/cm2 and the concentration of sulfur dioxide is measured in moles of sulfur dioxide per liter of anolyte.

Steimke, John L; Steeper, Timothy J; Herman, David T

2014-04-29T23:59:59.000Z

178

(Acid rain workshop)  

SciTech Connect (OSTI)

The traveler presented a paper entitled Susceptibility of Asian Ecosystems to Soil-Mediated Acid Rain Damage'' at the Second Workshop on Acid Rain in Asia. The workshop was organized by the Asian Institute of Technology (Bangkok, Thailand), Argonne National Laboratory (Argonne, Illinois), and Resource Management Associates (Madison, Wisconsin) and was sponsored by the US Department of Energy, the United Nations Environment Program, the United Nations Economic and Social Commission for Asia and the Pacific, and the World Bank. Papers presented on the first day discussed how the experience gained with acid rain in North America and Europe might be applied to the Asian situation. Papers describing energy use projections, sulfur emissions, and effects of acid rain in several Asian countries were presented on the second day. The remaining time was allotted to discussion, planning, and writing plans for a future research program.

Turner, R.S.

1990-12-05T23:59:59.000Z

179

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. We have conducted adsorption, phase behavior, interfacial tension (IFT) and wettability studies. Alfoterra-38 (0.05 wt%), Alfoterra-35 (0.05 wt%), SS-6656 (0.05 wt%), and DTAB (1 wt%) altered the wettability of the initially oil-wet calcite plate to an intermediate/water-wet state. Low IFT ({approx}10{sup -3} dynes/cm) is obtained with surfactants 5-166, Alfoterra-33 and Alfoterra-38. Plans for the next quarter include conducting wettability and mobilization studies.

Kishore K. Mohanty

2003-10-01T23:59:59.000Z

180

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. We have acquired field oil and core samples and field brine compositions from Marathon. We have conducted preliminary adsorption and wettability studies. Addition of Na{sub 2}CO{sub 3} decreases anionic surfactant adsorption on calcite surface. Receding contact angles increase with surfactant adsorption. Plans for the next quarter include conducting adsorption, phase behavior and wettability studies.

Kishore K. Mohanty

2003-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Dilute Surfactant Methods for Carbonate Formations  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Anionic surfactants (Alfoterra 35, 38) recover more than 40% of the oil in about 50 days by imbibition driven by wettability alteration in the core-scale. Anionic surfactant, Alfoterra-68, recovers about 28% of the oil by lower tension aided gravity-driven imbibition in the core-scale. Residual oil saturation showed little capillary number dependence between 10{sup -5} and 10{sup -2}. Wettability alteration increases as the number of ethoxy groups increases in ethoxy sulfate surfactants. Plans for the next quarter include conducting mobilization, and imbibition studies.

Kishore K. Mohanty

2004-03-31T23:59:59.000Z

182

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Anionic surfactants (SS-6656, Alfoterra 35, 38, 63,65,68) have been identified which can change the wettability of the calcite surface to intermediate/water-wet condition as well or better than the cationic surfactant DTAB with a West Texas crude oil in the presence of Na{sub 2}CO{sub 3}. All the carbonate surfaces (Lithographic Limestone, Marble, Dolomite and Calcite) show similar behavior with respect to wettability alteration with surfactant 4-22. Anionic surfactants (5-166, Alfoterra-33 and Alfoterra-38 and Alfoterra-68), which lower the interfacial tension with a West Texas crude oil to very low values (<10{sup -2} nM/m), have also been identified. Plans for the next quarter include conducting wettability, mobilization, and imbibition studies.

Kishore K. Mohanty

2004-01-01T23:59:59.000Z

183

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Simulation studies indicate that both wettability alteration and gravity-driven flow play significant role in oil recovery from fractured carbonates. Anionic surfactants (Alfoterra 35, 38) recover about 55% of the oil in about 150 days by imbibition driven by wettability alteration and low tension in the core-scale. Anionic surfactant, Alfoterra-68, recovers about 40% of the oil by lower tension aided gravity-driven imbibition in the core-scale. Cationic surfactant, DTAB recovers about 35% of the oil. Plans for the next quarter include conducting simulation and imbibition studies.

Kishore K. Mohanty

2004-10-01T23:59:59.000Z

184

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. We have conducted adsorption, phase behavior, interfacial tension (IFT) and wettability studies. Addition of Na{sub 2}CO{sub 3} decreases IFT with a minimum at about 0.2 M. Addition of surfactant decreases IFT further. In the absence of surfactant the minerals are oil-wet after aging with crude oil. Addition of surfactant solution decreases the contact angle to intermediate-wet for many surfactants and water-wet for one surfactant. Addition of Na{sub 2}CO{sub 3} decreases anionic surfactant adsorption on calcite surface. Plans for the next quarter include conducting core adsorption, phase behavior, wettability and mobilization studies.

Kishore K. Mohanty

2003-07-01T23:59:59.000Z

185

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Laboratory imbibition tests show that imbibition rate is not very sensitive to the surfactant concentration (in the range of 0.05-0.2 wt%) and small amounts of trapped gas saturation. It is however very sensitive to oil permeability and water-oil-ratio. Less than 0.5 M Na2CO3 is needed for in situ soap generation and low adsorption; NaCl can be added to reach the necessary total salinity. The simulation result matches the laboratory imbibition experimental data. Small fracture spacing and high permeability would be needed for high rate of recovery.

Kishore K. Mohanty

2005-07-01T23:59:59.000Z

186

DILUTE SURFACTANT METHODS FOR CARBONATE FORMATIONS  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the only hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Laboratory imbibition tests show about 61% oil recovery in the case of Alf-38 and 37% in the case of DTAB. A numerical model has been developed that fits the rate of imbibition of the laboratory experiment. Field-scale fracture block simulation shows that as the fracture spacing increases, so does the time of recovery. Plans for the next quarter include simulation studies.

Kishore K. Mohanty

2005-04-01T23:59:59.000Z

187

Dilute Surfactant Methods for Carbonate Formations  

SciTech Connect (OSTI)

There are many carbonate reservoirs in US (and the world) with light oil and fracture pressure below its minimum miscibility pressure (or reservoir may be naturally fractured). Many carbonate reservoirs are naturally fractured. Waterflooding is effective in fractured reservoirs, if the formation is water-wet. Many fractured carbonate reservoirs, however, are mixed-wet and recoveries with conventional methods are low (less than 10%). Thermal and miscible tertiary recovery techniques are not effective in these reservoirs. Surfactant flooding (or huff-n-puff) is the best hope, yet it was developed for sandstone reservoirs in the past. The goal of this research is to evaluate dilute (hence relatively inexpensive) surfactant methods for carbonate formations and identify conditions under which they can be effective. Laboratory-scale surfactant brine imbibition experiments give high oil recovery (35-62% OOIP) for initially oil-wet cores through wettability alteration and IFT reduction. Core-scale simulation results match those of the experiments. Initial capillarity-driven imbibition gives way to a final gravity-driven process. As the matrix block height increases, surfactant alters wettability to a lesser degree, or permeability decreases, oil production rate decreases. The scale-up to field scale will be further studied in the next quarter.

Kishore K. Mohanty

2005-10-01T23:59:59.000Z

188

Safety Slide 1 Hydrofluoric (HF) Acid Hazards http://www.emsworld.com/web/online/Education/Hydrofluoric-Acid-/5$12949  

E-Print Network [OSTI]

Safety Slide 1 ­ Hydrofluoric (HF) Acid Hazards http://www.emsworld.com/web may be delayed for up to 24 hours, even with dilute solutions. HF burns affect deep tissue layers

Cohen, Robert E.

189

sulfur dioxide emissions | OpenEI  

Open Energy Info (EERE)

sulfur dioxide emissions sulfur dioxide emissions Dataset Summary Description Emissions from energy use in buildings are usually estimated on an annual basis using annual average multipliers. Using annual numbers provides a reasonable estimation of emissions, but it provides no indication of the temporal nature of the emissions. Therefore, there is no way of understanding the impact on emissions from load shifting and peak shaving technologies such as thermal energy storage, on-site renewable energy, and demand control. Source NREL Date Released April 11th, 2011 (3 years ago) Date Updated April 11th, 2011 (3 years ago) Keywords buildings carbon dioxide emissions carbon footprinting CO2 commercial buildings electricity emission factors ERCOT hourly emission factors interconnect nitrogen oxides

190

Special dilution refrigerator systems of Milli-Kelvin detector experiments  

SciTech Connect (OSTI)

Several hundred ultra low temperature systems have been designed and built for a variety of applications. One common application is the refrigeration of low temperature detectors. Although many of the requirements are satisfied by standard designs, Oxford Instruments has often built special refrigerators to suit specific detector requirements. A few of the most interesting of these systems will be discussed. (1) dilution refrigerators to cool gravitational wave antennae to 65 mK; (2) rotating dilution refrigerator for cosmic ray detector experiments; (3) compact dilution refrigerator to cool large bolometer arrays within the SCUBA telescope; (4) side access systems for beam line experiments

Batey, G.; Balshaw, N. (Oxford Instruments Ltd., Old Station Way (United Kingdom))

1993-11-01T23:59:59.000Z

191

Dilute Oxygen Combustion Phase I Final Report  

SciTech Connect (OSTI)

A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NOx) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NOx through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NOx production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature (~1366 K) oxidant (7-27% O2 vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d+ scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d+ scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW (~0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric arrangement, firing rate, and fuel injection velocity. NOx emissions increased with increasing furnace nitrogen content and furnace temperature, but remained relatively insensitive to variations in fuel injection velocity and firing rate. NOx emissions below 5-10-3 g/MJ (10 ppm-air equivalent at 3% O2 dry) were obtained for furnace temperatures below 1533 K (2300°F) and furnace nitrogen levels between 1 and 40%. CO emissions were typically low (<35 ppm). Detailed in-furnace species measurements revealed the importance of the interior furnace circulation patterns, as influenced by fuel and oxidant injection schemes, on pollutant emissions. The combustion stability traits of several DOC burner arrangements were ascertained through furnace pressure measurements, wit6h increased stability occurring as furnace temperature increased and as the separation distance between fuel and oxidant inputs decreased. Based on current market conditions, oxy-fuel conversion of batch steel reheat furnaces with a DOC burner is justified on the basis of lower utility costs alone. However, conversion of continuous steel reheat furnaces, which are responsible for most steel production, required additional economic incentives, such as further fuel savings, increased furnace productivity, or emission credits.

Ryan, H.M.; Riley, M.F.; Kobayashi, H.

1997-10-31T23:59:59.000Z

192

Dilute Oxygen Combustion Phase 2 Final Report  

SciTech Connect (OSTI)

A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NOx) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NOx through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NOx production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature (~1366 K) oxidant (7-27% O2 vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d+ scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d+ scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW (~0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric arrangement, firing rate, and fuel injection velocity. NOx emissions increased with increasing furnace nitrogen content and furnace temperature, but remained relatively insensitive to variations in fuel injection velocity and firing rate. NOx emissions below 5-10-3 g/MJ (10 ppm-air equivalent at 3% O2 dry) were obtained for furnace temperatures below 1533 K (2300?F) and furnace nitrogen levels between 1 and 40%. CO emissions were typically low (<35 ppm). Detailed in-furnace species measurements revealed the importance of the interior furnace circulation patterns, as influenced by fuel and oxidant injection schemes, on pollutant emissions. The combustion stability traits of several DOC burner arrangements were ascertained through furnace pressure measurements, wit6h increased stability occurring as furnace temperature increased and as the separation distance between fuel and oxidant inputs decreased. Based on current market conditions, oxy-fuel conversion of batch steel reheat furnaces with a DOC burner is justified on the basis of lower utility costs alone. However, conversion of continuous steel reheat furnaces, which are responsible for most steel production, required additional economic incentives, such as further fuel savings, increased furnace productivity, or emission credits.

Ryan, H.M.; Riley, M.F.; Kobayashi, H.

2005-09-30T23:59:59.000Z

193

Dilute oxygen combustion. Phase I report  

SciTech Connect (OSTI)

A novel burner, in which fuel (natural gas) and oxidant (oxygen or air) are separately injected into a furnace, shows promise for achieving very low nitrogen oxide(s) (NO{sub x}) emissions for commercial furnace applications. The dilute oxygen combustion (DOC) burner achieves very low NO{sub x} through in-furnace dilution of the oxidant stream prior to combustion, resulting in low flame temperatures, thus inhibiting thermal NO{sub x} production. The results of a fundamental and applied research effort on the development of the DOC burner are presented. In addition, the results of a market survey detailing the potential commercial impact of the DOC system are disclosed. The fundamental aspects of the burner development project involved examining the flame characteristics of a natural gas turbulent jet in a high-temperature ({approximately}1366 K) oxidant (7-27% O{sub 2} vol. wet). Specifically, the mass entrainment rate, the flame lift-off height, the velocity field and major species field of the jet were evaluated as a function of surrounding-gas temperature and composition. The measured entrainment rate of the fuel jet decreased with increasing oxygen content in the surrounding high-temperature oxidant, and was well represented by the d{sup +} scaling correlation found in the literature. The measured flame lift-off height decreased with increasing oxygen content and increasing temperature of the surrounding gas. An increase in surrounding-gas oxygen content and/or temperature inhibited the velocity decay within the jet periphery as a function of axial distance as compared to isothermal turbulent jets. However, the velocity measurements were only broadly represented by the d{sup +} scaling correlation. Several DOC burner configurations were tested in a laboratory-scale furnace at a nominal firing rate of 185 kW ({approximately}0.63 MMBtu/h). The flue gas composition was recorded as a function of furnace nitrogen content, furnace temperature, burner geometric arrangement, firing rate, and fuel injection velocity. NO{sub x} emissions increased with increasing furnace nitrogen content and furnace temperature, but remained relatively insensitive to variations in fuel injection velocity and firing rate. NO{sub x} emissions below 5{times}10{sup -3} g/MJ (10 ppm-air equivalent at 3% O{sub 2} dry) were obtained for furnace temperatures below 1533 K (2300{degree}F) and furnace nitrogen levels between 1 and 40%. CO emissions were typically low (<35 ppm). Detailed in- furnace species measurements revealed the importance of the interior furnace circulation patterns, as influenced by fuel and oxidant injection schemes, on pollutant emissions. The combustion stability traits of several DOC burner arrangements were ascertained through furnace pressure measurements, with increased stability occurring as furnace temperature increased and as the separation distance between fuel and oxidant inputs decreased. Based on current market conditions, oxy-fuel conversion of batch steel reheat furnaces with a DOC burner is justified on the basis of utility costs alone. However, conversion of continuous steel reheat furnaces, which are responsible for most steel production, requires additional economic incentives, such as further fuel savings, increased furnace productivity, or emission credits.

NONE

1997-10-01T23:59:59.000Z

194

Paramagnetic Relaxation in Dilute Potassium Ferricyanide  

Science Journals Connector (OSTI)

Paramagnetic relaxation times have been measured for the ground-state doublet of iron present as a dilute substitutional impurity in potassium cobalt cyanide. Measurements were carried out over the temperature range 1.25 to 4.5K and over a range of Fe/Co concentrations 0.24 to 3.5 at.%. Two frequencies were used, 1.8 and 8.5 Gc/sec, to provide a direct test of the frequency variation of the relaxation time. The "fast-passage-recovery" technique was employed, and a description of the apparatus is included. At 0.24% the 1.8-Gc/sec times are found to be well fitted by a Raman rate 1T1=4.310-3 T9 sec-1 over the entire temperature range and over five decades of time. At 8.5 Gc/sec this rate is augmented by a direct rate 1T1=3.1 T. At 0.5% the X-band direct rate is the same, but the Raman rate appears slightly higher; and the L-band rates are substantially faster. All relaxation rates increase with further increases in concentration, but the effect is stronger at 1.8 Gc/sec, so that the rates at both frequencies become equal at 1.7%. Still higher concentrations give rise to behavior not describable by a simple relaxation rate.For low concentration, the theoretical fourth-power frequency dependence of the direct relaxation process is not verified directly because the low frequency rates are always dominated by the Raman process; however, the frequency dependence must be as at least the third power to be consistent with the data. Some attempts are made to interpret the concentration dependence in terms of cross relaxation between single ions and coupled pairs.

Andreas Rannestad and Peter E. Wagner

1963-09-01T23:59:59.000Z

195

Sulfur-isotope separation by distillation  

SciTech Connect (OSTI)

Sulfur-isotope separation by low-temperature distillation of hydrogen sulfide was studied in an 8-m, 25-mm diameter distillation column. Column temperature was controlled by a propane-propylene heat pipe. Column packing HETP was measured using nitric oxide in the column. The column was operated at pressures from 45 to 125 kPa. The relative volatility of S-32 vs. S-34 varied from 1.0008 to 1.0014.

Mills, T.R.

1982-01-01T23:59:59.000Z

196

Comparison of modified sulfur cement and hydraulic cement for encapsulation of radioactive and mixed wastes  

SciTech Connect (OSTI)

The majority of solidification/stabilization systems for low-level radioactive waste (LLW) and mixed waste, both in the commercial sector and at Department of Energy (DOE) facilities, utilize hydraulic cement (such as portland cement) to encapsulate waste materials and yield a monolithic solid waste form for disposal. A new and innovative process utilizing modified sulfur cement developed by the US Bureau of Mines has been applied at Brookhaven National Laboratory (BNL) for the encapsulation of many of these problem'' wastes. Modified sulfur cement is a thermoplastic material, and as such, it can be heated above it's melting point (120{degree}C), combined with dry waste products to form a homogeneous mixture, and cooled to form a monolithic solid product. Under sponsorship of the DOE, research and development efforts at BNL have successfully applied the modified sulfur cement process for treatment of a range of LLWs including sodium sulfate salts, boric acid salts, and incinerator bottom ash and for mixed waste contaminated incinerator fly ash. Process development studies were conducted to determine optimal waste loadings for each waste type. Property evaluation studies were conducted to test waste form behavior under disposal conditions by applying relevant performance testing criteria established by the Nuclear Regulatory Commission (for LLW) and the Environmental Protection Agency (for hazardous wastes). Based on both processing and performance considerations, significantly greater waste loadings were achieved using modified sulfur cement when compared with hydraulic cement. Technology demonstration of the modified sulfur cement encapsulation system using production-scale equipment is scheduled for FY 1991. 12 refs., 8 figs., 3 tabs.

Kalb, P.D.; Heiser, J.H. III; Colombo, P.

1990-01-01T23:59:59.000Z

197

Sulfur/three-dimensional graphene composite for high performance lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract A sulfur/graphene composite is prepared by loading elemental sulfur into three-dimensional graphene (3D graphene), which is assembled using a metal ions assisted hydrothermal method. When used as cathode materials for lithiumsulfur (LiS) batteries, the sulfur/graphene composite (S@3D-graphene) with 73wt % sulfur shows a significantly enhanced cycling performance (>700mAhg?1 after 100 cycles at 0.1C rate with a Coulombic efficiency>96%) as well as high rate capability with a capacity up to 500mAhg?1 at 2C rate (3.35Ag?1). The superior electrochemical performance could be attributed to the highly porous structure of three-dimensional graphene that not only enables stable and continue pathway for rapid electron and ion transportation, but also restrain soluble polysulfides and suppress the shuttle effect. Moreover, the robust structure of 3D graphene can keep cathode integrity and accommodate the volume change during high-rate charge/discharge processes, making it a promising candidate as cathode for high performance LiS batteries.

Chunmei Xu; Yishan Wu; Xuyang Zhao; Xiuli Wang; Gaohui Du; Jun Zhang; Jiangping Tu

2015-01-01T23:59:59.000Z

198

Development of the Hybrid Sulfur Thermochemical Cycle  

SciTech Connect (OSTI)

The production of hydrogen via the thermochemical splitting of water is being considered as a primary means for utilizing the heat from advanced nuclear reactors to provide fuel for a hydrogen economy. The Hybrid Sulfur (HyS) Process is one of the baseline candidates identified by the U.S. Department of Energy [1] for this purpose. The HyS Process is a two-step hybrid thermochemical cycle that only involves sulfur, oxygen and hydrogen compounds. Recent work has resulted in an improved process design with a calculated overall thermal efficiency (nuclear heat to hydrogen, higher heating value basis) approaching 50%. Economic analyses indicate that a nuclear hydrogen plant employing the HyS Process in conjunction with an advanced gas-cooled nuclear reactor system can produce hydrogen at competitive prices. Experimental work has begun on the sulfur dioxide depolarized electrolyzer, the major developmental component in the cycle. Proof-of-concept tests have established proton-exchange-membrane cells (a state-of-the-art technology) as a viable approach for conducting this reaction. This is expected to lead to more efficient and economical cell designs than were previously available. Considerable development and scale-up issues remain to be resolved, but the development of a viable commercial-scale HyS Process should be feasible in time to meet the commercialization schedule for Generation IV gas-cooled nuclear reactors.

Summers, William A.; Steimke, John L

2005-09-23T23:59:59.000Z

199

Alaska has 4. 0 trillion tons of low-sulfur coal: Is there a future for this resource  

SciTech Connect (OSTI)

The demand for and use of low-sulfur coal may increase because of concern with acid rain. Alaska's low-sulfur coal resources can only be described as enormous: 4.0 trillion tons of hypothetical onshore coal. Mean total sulfur content is 0.34% (range 0.06-6.6%, n = 262) with a mean apparent rank of subbituminous B. There are 50 coal fields in Alaska; the bulk of the resources are in six major fields or regions: Nenana, Cook Inlet, Matanuska, Chignik-Herendeen Bay, North Slope, and Bering River. For comparison, Carboniferous coals in the Appalachian region and Interior Province have a mean total sulfur content of 2.3% (range 0.1-19.0%, n = 5,497) with a mean apparent rank of high-volatile A bituminous coal, and Rocky Mountain and northern Great Plains Cretaceous and Tertiary coals have a mean total sulfur content of 0.86% (range 0.02-19.0%, n = 2,754) with a mean apparent rank of subbituminous B. Alaskan coal has two-fifths the total sulfur of western US coals and one-sixth that of Carboniferous US coals. Even though Alaska has large resources of low-sulfur coal, these resources have not been developed because of (1) remote locations and little infrastructure, (2) inhospitable climate, and (3) long distances to potential markets. These resources will not be used in the near future unless there are some major, and probably violent, changes in the world energy picture.

Stricker, G.D. (Geological Survey, Denver, CO (USA))

1990-05-01T23:59:59.000Z

200

Treatment of acid mine wastewaters  

SciTech Connect (OSTI)

Acid mine drainage often results from the oxidation sulfide minerals to form sulfuric acid. As a consequence, high concentrations of metals in the both the suspended and dissolved state result from the low pH water. This paper discusses several of the more common treatment methods for acid mine drainage including the use of chemical precipitation agents, pH correction agents, filtration methods, and biodegradation methods. Advanced treatment technologies are also briefly described and include microfiltration, reverse osmosis, ion exchange, and electrodialysis.

Hayward, D.; Barnard, R.

1993-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Addressing Complexity In Laboratory Experiments- The Scaling Of Dilute  

Open Energy Info (EERE)

source source History View New Pages Recent Changes All Special Pages Semantic Search/Querying Get Involved Help Apps Datasets Community Login | Sign Up Search Page Edit History Facebook icon Twitter icon » Addressing Complexity In Laboratory Experiments- The Scaling Of Dilute Multiphase Flows In Magmatic Systems Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Addressing Complexity In Laboratory Experiments- The Scaling Of Dilute Multiphase Flows In Magmatic Systems Details Activities (0) Areas (0) Regions (0) Abstract: The kinematic and dynamic scaling of dilute multiphase mixtures in magmatic systems is the only guarantee for the geological verisimilitude of laboratory experiments. We present scaling relations that can provide a more complete framework to scale dilute magmatic systems because they

202

Separation processes using expulsion from dilute supercritical solutions  

DOE Patents [OSTI]

A process is described for separating isotopes as well as other mixtures by utilizing the behavior of dilute repulsive or weakly attractive elements of the mixtures as the critical point of the solvent is approached.

Cochran, H.D. Jr.

1993-04-20T23:59:59.000Z

203

A lattice Boltzmann method for dilute polymer solutions  

Science Journals Connector (OSTI)

...Succi and Stefano Ubertini A lattice Boltzmann method for dilute polymer solutions...560064, India We present a lattice Boltzmann approach for the simulation...Fokker-Planck equation|lattice Boltzmann method|finitely extensible...

2011-01-01T23:59:59.000Z

204

Fully portable, highly flexible dilution refrigerator systems for neutron scattering  

E-Print Network [OSTI]

775 Fully portable, highly flexible dilution refrigerator systems for neutron scattering P. A systems developed specifically for neutron scattering environ- ments. The refrigerators are completely relatively recently however, the lowest temperatures available in almost all neutron scattering laboratories

Boyer, Edmond

205

Contraction/expansion flow of dilute elastic solutions in microchannels  

E-Print Network [OSTI]

An experimental study is conducted on the nature of extensional flows of mobile dilute polymer solutions in microchannel. By observing such fluids on the microscale it is possible to generate large strain rates ([approximately] ...

Scott, Timothy Peter, 1980-

2004-01-01T23:59:59.000Z

206

Translation of dilution tolerance for gasoline SI engine  

E-Print Network [OSTI]

There are a variety of fuel improvement strategies being developed for spark ignition engines which use dilution. Many of these technologies use a combination of different diluents. It is impractical in optimizing these ...

Niekamp, Troy S. (Troy Steven)

2013-01-01T23:59:59.000Z

207

Waste acid recycling via diffusion dialysis  

SciTech Connect (OSTI)

Inorganic acids are commonly used for surface cleaning and finishing of metals. The acids become unuseable due to contamination with metals or diluted and weakened. Diffusion dialysis has become a way to recover the useable acid and allow separation of the metals for recovery and sale to refineries. This technique is made possible by the use of membranes that are strong enough to withstand low ph and have long service life.

Steffani, C.

1995-05-26T23:59:59.000Z

208

Acid-catalytic decomposition of peracetic acid in the liquid phase  

SciTech Connect (OSTI)

This paper elucidates the kinetic relationships of peracetic acid (PAA) decomposition in the presence of mineral acids and their heterogeneous analogs, polystyrene-di-vinylbenzene cation-exchangers, differing in physicochemical and morphological parameters. It is shown that the thermal decomposition of PAA in acetic acid is an acid-catalyzed reaction. The controlling step of the reaction is protonation of the substrate with formation of an active intermediate form. Sulfonated cation-exchangers are twice as effective as sulfuric acid in this process. Polystyrene-divinylbenzene sulfonated cation-exchangers can be used with success as acid catalysts in oxidation processes involving PAA, because of their high effectiveness, stability, and availability.

Kharchuk, V.G.; Kolenko, I.P.; Petrov, L.A.

1985-12-01T23:59:59.000Z

209

Anatomy of symmetry energy of dilute nuclear matter  

E-Print Network [OSTI]

The symmetry energy coefficients of dilute clusterized nuclear matter are evaluated in the $S$-matrix framework. Employing a few different definitions commonly used in the literature for uniform nuclear matter, it is seen that the different definitions lead to perceptibly different results for the symmetry coefficients for dilute nuclear matter. They are found to be higher compared to those obtained for uniform matter in the low density domain. The calculated results are in reasonable consonance with those extracted recently from experimental data.

J. N. De; S. K. Samaddar; B. K. Agrawal

2010-09-23T23:59:59.000Z

210

Dilute Oxygen Combustion Phase IV Final Report  

SciTech Connect (OSTI)

Novel furnace designs based on Dilute Oxygen Combustion (DOC) technology were developed under subcontract by Techint Technologies, Coraopolis, PA, to fully exploit the energy and environmental capabilities of DOC technology and to provide a competitive offering for new furnace construction opportunities. Capital cost, fuel, oxygen and utility costs, NOx emissions, oxide scaling performance, and maintenance requirements were compared for five DOC-based designs and three conventional air5-fired designs using a 10-year net present value calculation. A furnace direct completely with DOC burners offers low capital cost, low fuel rate, and minimal NOx emissions. However, these benefits do not offset the cost of oxygen and a full DOC-fired furnace is projected to cost $1.30 per ton more to operate than a conventional air-fired furnace. The incremental cost of the improved NOx performance is roughly $6/lb NOx, compared with an estimated $3/lb. NOx for equ8pping a conventional furnace with selective catalytic reduction (SCCR) technology. A furnace fired with DOC burners in the heating zone and ambient temperature (cold) air-fired burners in the soak zone offers low capital cost with less oxygen consumption. However, the improvement in fuel rate is not as great as the full DOC-fired design, and the DOC-cold soak design is also projected to cost $1.30 per ton more to operate than a conventional air-fired furnace. The NOx improvement with the DOC-cold soak design is also not as great as the full DOC fired design, and the incremental cost of the improved NOx performance is nearly $9/lb NOx. These results indicate that a DOC-based furnace design will not be generally competitive with conventional technology for new furnace construction under current market conditions. Fuel prices of $7/MMBtu or oxygen prices of $23/ton are needed to make the DOC furnace economics favorable. Niche applications may exist, particularly where access to capital is limited or floor space limitations are critical. DOC technology will continue to have a highly competitive role in retrofit applications requiring increases in furnace productivity.

Riley, M.F.

2003-04-30T23:59:59.000Z

211

Process for production of synthesis gas with reduced sulfur content  

DOE Patents [OSTI]

A process for the partial oxidation of a sulfur- and silicate-containing carbonaceous fuel to produce a synthesis gas with reduced sulfur content which comprises partially oxidizing said fuel at a temperature in the range of 1800.degree.-2200.degree. F. in the presence of a temperature moderator, an oxygen-containing gas and a sulfur capture additive which comprises an iron-containing compound portion and a sodium-containing compound portion to produce a synthesis gas comprising H.sub.2 and CO with a reduced sulfur content and a molten slag which comprises (i) a sulfur-containing sodium-iron silicate phase and (ii) a sodium-iron sulfide phase. The sulfur capture additive may optionally comprise a copper-containing compound portion.

Najjar, Mitri S. (Hopewell Junction, NY); Corbeels, Roger J. (Wappingers Falls, NY); Kokturk, Uygur (Wappingers Falls, NY)

1989-01-01T23:59:59.000Z

212

Sulfide catalysts for reducing SO2 to elemental sulfur  

DOE Patents [OSTI]

A highly efficient sulfide catalyst for reducing sulfur dioxide to elemental sulfur, which maximizes the selectivity of elemental sulfur over byproducts and has a high conversion efficiency. Various feed stream contaminants, such as water vapor are well tolerated. Additionally, hydrogen, carbon monoxide, or hydrogen sulfides can be employed as the reducing gases while maintaining high conversion efficiency. This allows a much wider range of uses and higher level of feed stream contaminants than prior art catalysts.

Jin, Yun (Peking, CN); Yu, Qiquan (Peking, CN); Chang, Shih-Ger (El Cerrito, CA)

2001-01-01T23:59:59.000Z

213

Lithium/Sulfur Batteries Based on Doped Mesoporous Carbon - Energy...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Materials Advanced Materials Find More Like This Return to Search LithiumSulfur Batteries Based on Doped Mesoporous Carbon Oak Ridge National Laboratory Contact ORNL About...

214

Analyses of sulfur-asphalt field trials in Texas  

E-Print Network [OSTI]

128 LIST OF FIGURES FIGURE PAGF Layout of SNPA sulfur bitumen binder pavem nt test ? U. S. Highway 69, Lufkin, Texas 15 Col 1oi d mi 1 1 furnished by SNPA for preparation of sul fur-asphalt emulsions View of mixing station showing sulfur... designed to investigate the advantage of using a colloid mill to prepare sulfur-asphalt binders as compared to comingling the asphalt and molten sulfur in a pipeline leading directly to the pug mill. After only six months of testing, the results...

Newcomb, David Edward

1979-01-01T23:59:59.000Z

215

Development of sulfur cathode material for Li-S batteries.  

E-Print Network [OSTI]

??M.S. Efforts were taken to fabricate a cathode material having Sulfur as the active material. First step is composed of identifying potential ways of fabricating (more)

Dharmasena, Ruchira Ravinath, 1984-

2014-01-01T23:59:59.000Z

216

Project Profile: Baseload CSP Generation Integrated with Sulfur...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Related Links FAQs Contact Us Offices You are here Home Concentrating Solar Power Project Profile: Baseload CSP Generation Integrated with Sulfur-Based...

217

SULFUR-TOLERANT CATALYST FOR THE SOLID OXIDE FUEL CELL.  

E-Print Network [OSTI]

??JP-8 fuel is easily accessible, transportable, and has hydrogen content essential to solid oxide fuel cell (SOFC) operation. However, this syngas has sulfur content which (more)

Bozeman, Joe Frank, III

2010-01-01T23:59:59.000Z

218

Fundamental Studies of Lithium-Sulfur Cell Chemistry  

Broader source: Energy.gov (indexed) [DOE]

Studies of Lithium-Sulfur Cell Chemistry PI: Nitash Balsara LBNL June 17, 2014 Project ID ESS224 This presentation does not contain any proprietary, confidential, or otherwise...

219

Abatement of Air Pollution: Control of Sulfur Compound Emissions  

Broader source: Energy.gov (indexed) [DOE]

Abatement of Air Pollution: Control of Sulfur Compound Emissions Abatement of Air Pollution: Control of Sulfur Compound Emissions (Connecticut) Abatement of Air Pollution: Control of Sulfur Compound Emissions (Connecticut) < Back Eligibility Agricultural Commercial Construction Fed. Government Fuel Distributor General Public/Consumer Industrial Installer/Contractor Institutional Investor-Owned Utility Local Government Low-Income Residential Multi-Family Residential Municipal/Public Utility Nonprofit Residential Retail Supplier Rural Electric Cooperative Schools State/Provincial Govt Systems Integrator Transportation Tribal Government Utility Program Info State Connecticut Program Type Environmental Regulations Provider Department of Energy and Environmental Protection These regulations set limits on the sulfur content of allowable fuels (1.0%

220

Sulfur removal and comminution of carbonaceous material  

DOE Patents [OSTI]

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product. 2 figs.

Narain, N.K.; Ruether, J.A.; Smith, D.N.

1987-10-07T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Sulfur removal and comminution of carbonaceous material  

DOE Patents [OSTI]

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product.

Narain, Nand K. (Bethel Park, PA); Ruether, John A. (McMurray, PA); Smith, Dennis N. (Herminie, PA)

1988-01-01T23:59:59.000Z

222

Sulfur isotopes in coal constrain the evolution of the Phanerozoic sulfur cycle  

Science Journals Connector (OSTI)

...obviously influence the average isotope values. For the other data, samples...pp 87105 . 19 Price FT Casagrande DJ ( 1991 ) Sulfur...coals. Geology of Fossil Fuels, Proc 30th Int Geol Congress...Jersey Pinelands and its effect on stream water chemistry...223 248 . 29 Price FT Shieh YN ( 1979 ) Fractionation...

Donald E. Canfield

2013-01-01T23:59:59.000Z

223

SYNTHESIS OF SULFUR-BASED WATER TREATMENT AGENT FROM SULFUR DIOXIDE WASTE STREAMS  

SciTech Connect (OSTI)

We propose a process that uses sulfur dioxide from coal combustion as a raw material to synthesize polymeric ferric sulfate (PFS), a water treatment agent. The process uses sodium chlorate as an oxidant and ferrous sulfate as an absorbent. The major chemical mechanisms in this reaction system include oxidation, hydrolysis, and polymerization. Oxidation determines sulfur conversion efficiency while hydrolysis and polymerization control the quality of product. Many factors, including SO{sub 2} inlet concentration, flow rate of simulated flue gas, reaction temperature, addition rate of oxidant and stirring rate, may affect the efficiencies of SO{sub 2} removal. Currently, the effects of SO{sub 2} inlet concentration, the flow rate of simulated flue gas and addition rate of flue gas on removal efficiencies of SO{sub 2}, are being investigated. Experiments shown in this report have demonstrated that the conversion efficiencies of sulfur dioxide with ferrous sulfate as an absorbent are in the range of 60-80% under the adopted process conditions. However, the conversion efficiency of sulfur dioxide may be improved by optimizing reaction conditions to be investigated. Partial quality indices of the synthesized products, including Fe{sup 2+} concentration and total iron concentration, have been evaluated.

Robert C. Brown; Maohong Fan

2001-12-01T23:59:59.000Z

224

Lithiumsulfur batteries: Influence of C-rate, amount of electrolyte and sulfur loading on cycle performance  

Science Journals Connector (OSTI)

Abstract In the past four years major improvement of the lithium sulfur battery technology has been reported. Novel carbon cathode materials offer high sulfur loading, sulfur utilization and cycle stability. An often neglected aspect is that sulfur loading and amount of electrolyte strongly impact the performance. In this paper, we demonstrate how the amount of electrolyte, sulfur loading, lithium excess and cycling rate influences the cycle stability and sulfur utilization. We chose vertically aligned carbon nanotubes (VA-CNT) as model system with a constant areal loading of carbon. For a high reproducibility, decreased weight of current collector and good mechanical adhesion of the VA-CNTs we present a layer transfer technique that enables a light-weight sulfur cathode. The sulfur loading of the cathode was adjusted from 20 to 80wt.-%. Keeping the total amount of electrolyte constant and varying the C-rate, we are able to demonstrate that the capacity degradation is reduced for high rates, high amount of electrolyte and low sulfur loading. In addition idle periods in the cycling regiment and lower rates result in an increased degradation. We attribute this to the redox-reaction between reactive lithium and polysulfides that correlates with the cycling time, rather than cycle number.

Jan Brckner; Sren Thieme; Hannah Tamara Grossmann; Susanne Drfler; Holger Althues; Stefan Kaskel

2014-01-01T23:59:59.000Z

225

Using ISC & GIS to predict sulfur deposition from coal-fired power plants  

E-Print Network [OSTI]

The goal of this research project was to determine if atmospheric sources have the potential of contributing significantly to the sulfur content of grazed forage. Sulfur deposition resulting from sulfur dioxide emissions from coal- fired power...

Lopez, Jose Ignacio

2012-06-07T23:59:59.000Z

226

Formation of Colloidal Shells on Acidic Droplets Undergoing Neutralization in Marine Diesel Engine Cylinder Oils  

Science Journals Connector (OSTI)

In this study, a novel colloidal shell formation phenomenon was observed when sulfuric acid droplets underwent neutralization in marine cylinder lubricant at 1155C ... the formation of well-known deposits fo...

Miguel Garcia-Bermudes; Riccardo Rausa; Kyriakos Papadopoulos

2013-07-01T23:59:59.000Z

227

Evaluation of various sulphur amino acid compounds in the diet of red drum, Sciaenops ocellatus  

E-Print Network [OSTI]

Refinement of diet formulations to enhance the efficiency of red drum production continues to be pursued. Based on previous studies, the sulfur amino acid (SAA) requirement of red drum for methionine plus cystine appears to be most limiting, which...

Goff, Jonathan B

2003-01-01T23:59:59.000Z

228

HEALTH AND CLIMATE POLICY IMPACTS ON SULFUR EMISSION CONTROL  

E-Print Network [OSTI]

the climate and health effects of sulfate aerosol into an integrated-assessment model of fossil fuel emission warming and health simultaneously will support more stringent fossil fuel and sulfur controls control. Our simulations show that a policy that adjusts fossil fuel and sulfur emissions to address both

Russell, Lynn

229

Near-Zero Emissions Oxy-Combustion Flue Gas Purification Task 2: SOx/Nox/Hg Removal for High Sulfur Coal  

SciTech Connect (OSTI)

The goal of this project is to develop a near-zero emissions flue gas purification technology for existing PC (pulverized coal) power plants that are retrofitted with oxy-combustion technology. The objective of Task 2 of this project was to evaluate an alternative method of SOx, NOx and Hg removal from flue gas produced by burning high sulfur coal in oxy-combustion power plants. The goal of the program was not only to investigate a new method of flue gas purification but also to produce useful acid byproduct streams as an alternative to using a traditional FGD and SCR for flue gas processing. During the project two main constraints were identified that limit the ability of the process to achieve project goals. 1) Due to boiler island corrosion issues >60% of the sulfur must be removed in the boiler island with the use of an FGD. 2) A suitable method could not be found to remove NOx from the concentrated sulfuric acid product, which limits sale-ability of the acid, as well as the NOx removal efficiency of the process. Given the complexity and safety issues inherent in the cycle it is concluded that the acid product would not be directly saleable and, in this case, other flue gas purification schemes are better suited for SOx/NOx/Hg control when burning high sulfur coal, e.g. this project's Task 3 process or a traditional FGD and SCR.

Nick Degenstein; Minish Shah; Doughlas Louie

2012-05-01T23:59:59.000Z

230

Application of Cryocoolers to a Vintage Dilution Refrigerator  

SciTech Connect (OSTI)

A dilution refrigerator is required for 50mK detector operation of CDMS (Cryogenic Dark Matter Search). Besides shielding the dilution refrigerator itself, the liquid nitrogen shield and liquid helium bath in the refrigerator cool the detector cryostat heat shields and cool electronics, resulting in significant external heat loads at 80K and at 4K. An Oxford Instruments Kelvinox 400 has served this role for ten years but required daily transfers of liquid nitrogen and liquid helium. Complicating the cryogen supply is the location 800 meters below ground in an RF shielded, class 10000 clean room at Soudan, MN. Nitrogen and helium re-liquefiers using cryocoolers were installed outside the clean room and continuously condense room temperature gas and return the liquids to the dilution refrigerator through a transfer line. This paper will describe the design, installation, controls and performance of liquefaction systems.

Schmitt, Richard; Smith, Gary; Ruschman, Mark; /Fermilab; Beaty, Jim; /Minnesota U.

2011-06-06T23:59:59.000Z

231

Process of concentrating ethanol from dilute aqueous solutions thereof  

DOE Patents [OSTI]

Relatively dilute aqueous solutions of ethanol are concentrated by passage through a bed of a crystalline silica polymorph, such as silicalite, to adsorb the ethanol with residual dilute feed in contact with the bed, which is displaced by passing concentrated aqueous ethanol through the bed without displacing the adsorbed ethanol. A product concentrate is then obtained by removing the adsorbed ethanol from the bed together with at least a portion of the concentrated aqueous ethanol used as the displacer liquid. This process permits ethanol to be concentrated from dilute fermentation beers, which may contain from 6 to 10% ethanol, to obtain a concentrate product at very low energy cost having an ethanol concentration in excess of 95%, such as a concentration of from 98 to 99.5%.

Oulman, Charles S. [Ames, IA; Chriswell, Colin D. [Slater, IA

1981-07-07T23:59:59.000Z

232

Process of concentrating ethanol from dilute aqueous solutions thereof  

DOE Patents [OSTI]

Relatively dilute aqueous solutions of ethanol are concentrated by passage through a bed of a crystalline silica polymorph, such as silicalite, to adsorb the ethanol with residual dilute feed in contact with the bed, which is displaced by passing concentrated aqueous ethanol through the bed without displacing the adsorbed ethanol. A product concentrate is then obtained by removing the adsorbed ethanol from the bed together with at least a portion of the concentrated aqueous ethanol used as the displacer liquid. This process permits ethanol to be concentrated from dilute fermentation beers, which may contain from 6 to 10% ethanol, to obtain a concentrate product at very low energy cost having an ethanol concentration in excess of 95%, such as a concentration of from 98 to 99.5%. 5 figs.

Oulman, C.S.; Chriswell, C.D.

1981-07-07T23:59:59.000Z

233

EVALUATION OF PROTON-CONDUCTING MEMBRANES FOR USE IN A SULFUR-DIOXIDE DEPOLARIZED ELECTROLYZER  

SciTech Connect (OSTI)

The chemical stability, sulfur dioxide transport, ionic conductivity, and electrolyzer performance have been measured for several commercially available and experimental proton exchange membranes (PEMs) for use in a sulfur dioxide depolarized electrolyzer (SDE). The SDE's function is to produce hydrogen by using the Hybrid Sulfur (HyS) Process, a sulfur based electrochemical/thermochemical hybrid cycle. Membrane stability was evaluated using a screening process where each candidate PEM was heated at 80 C in 60 wt. % H{sub 2}SO{sub 4} for 24 hours. Following acid exposure, chemical stability for each membrane was evaluated by FTIR using the ATR sampling technique. Membrane SO{sub 2} transport was evaluated using a two-chamber permeation cell. SO{sub 2} was introduced into one chamber whereupon SO{sub 2} transported across the membrane into the other chamber and oxidized to H{sub 2}SO{sub 4} at an anode positioned immediately adjacent to the membrane. The resulting current was used to determine the SO{sub 2} flux and SO{sub 2} transport. Additionally, membrane electrode assemblies (MEAs) were prepared from candidate membranes to evaluate ionic conductivity and selectivity (ionic conductivity vs. SO{sub 2} transport) which can serve as a tool for selecting membranes. MEAs were also performance tested in a HyS electrolyzer measuring current density versus a constant cell voltage (1V, 80 C in SO{sub 2} saturated 30 wt% H2SO{sub 4}). Finally, candidate membranes were evaluated considering all measured parameters including SO{sub 2} flux, SO{sub 2} transport, ionic conductivity, HyS electrolyzer performance, and membrane stability. Candidate membranes included both PFSA and non-PFSA polymers and polymer blends of which the non-PFSA polymers, BPVE-6F and PBI, showed the best selectivity.

Hobbs, D.; Elvington, M.; Colon-Mercado, H.

2009-11-11T23:59:59.000Z

234

Metal-sulfur type cell having improved positive electrode  

DOE Patents [OSTI]

An novel metal-sulfur type cell operable at a temperature of 200.degree. C. or less with an energy density of 150 Whrs/Kg or better is disclosed characterized by an organo-sulfur cathode formed from an organic-sulfur compound having the general formula, in its charged state, of (R(S).sub.y).sub.n wherein y=1 to 6; n=2 to 20; and R is one or more different aliphatic or aromatic organic moieties having 1 to 20 carbon atoms, which may include one or more oxygen, sulfur, or nitrogen heteroatoms when R comprisises one of more aromatic rings, or one or more oxygen, sulfur, nitrogen, or fluorine atoms associtated with the chain when R comprises an aliphatic chain, wherein the aliphatic group may be linear or branched, saturated or unsaturated, and wherein either the aliphatic chain or the aromatic ring may have substituted groups thereon.

Dejonghe, Lutgard C. (Berkeley, CA); Visco, Steven J. (Berkeley, CA); Mailhe, Catherine C. (Berkeley, CA); Armand, Michel B. (St. Martin D'Uriage, FR)

1989-01-01T23:59:59.000Z

235

FISCAL YEAR 2006 REPORT ON ELECTROLYZER COMPONENT DEVELOPMENT FOR THE HYBRID SULFUR PROJECT  

SciTech Connect (OSTI)

Thermochemical processes are being developed to provide global-scale quantities of hydrogen. A variant on sulfur-based thermochemical cycles is the Hybrid Sulfur (HyS) Process which uses a sulfur dioxide depolarized electrolyzer (SDE) to produce the hydrogen. In FY05, testing at the Savannah River National Laboratory (SRNL) explored a low temperature fuel cell design concept for the SDE. The advantages of this design concept include high electrochemical efficiency and small volumetric footprint that is crucial for successful implementation on a commercial scale. A key component of the SDE is the ion conductive membrane through which protons produced at anode migrate to the cathode and react to produce hydrogen. An ideal membrane for the SDE should have both low ionic resistivity and low sulfur dioxide transport. These features allow the electrolyzer to perform at high currents with low potentials, along with preventing contamination of both the hydrogen output and poisoning of the catalysts involved. Another key component is the electrocatalyst material used for the anode and cathode. Good electrocatalysts should be chemically stable and low overpotential for the desired electrochemical reactions. This report summarizes results from activities to evaluate different membrane and electrocatalyst materials for the SDE. Several different types of commercially-available membranes were analyzed for ionic resistance and sulfur dioxide transport including perfluorinated sulfonic acid, sulfonated poly-etherketone-ketone, and poly-benzimidazole membranes. Of these membrane types, the poly-benzimidazole (PBI) membrane, Celtec-L, exhibited the best combination of characteristics for use in an SDE. Testing examined the activity and stability of platinum and palladium as electrocatalyst for the SDE in sulfuric acid solutions. Cyclic and linear sweep voltammetry revealed that platinum provided better catalytic activity with much lower potentials and higher currents than palladium. Testing also showed that the catalyst activity is strongly influenced by concentration of the sulfuric acid. Various cell configurations were examined with respect to the deposition of electrocatalyst and use of conductive carbon materials such as carbon cloth and carbon paper. Findings from these evaluations and the results of the membrane and electrocatalyst testing, we prepared three different membrane electrode assemblies (MEA) for electrolyzer testing. The first MEA consisted of a Nafion{reg_sign} membrane with platinum electrocatalyst deposited on carbon cloths, which were heat pressed onto the membrane, an assembly identical to those used in proton exchange membrane fuel cells. The second MEA also used a Nafion membrane with the electrocatalysts deposited directly onto the membrane. The third MEA proved similar to the second but utilized a PBI membrane in place of the Nafion{reg_sign} membrane. Tailor of the membrane and catalysts properties for the SDE system was concluded as a required step for the technology to move forward. It was also recommended the evaluation of the tested and new developed materials at conditions closer to the SDE operating conditions and for longer period of time.

Colon-Mercado, H; David Hobbs, D; Daryl Coleman, D; Amy Ekechukwu, A

2006-08-03T23:59:59.000Z

236

Analysis of organic sulfur and nitrogen in coal via tandem degradation methods. Final technical report, 1 September 1991--31 October 1992  

SciTech Connect (OSTI)

With the recent increase in concern for environmental issues and the implication of sulfur and nitrogen in coal combustion preducts as prime causes of acid rain, it has become clear that there is an urgent need for alternative methods for determining the nature of organic sulfur and nitrogen compounds in coal. The principal impediment to the molecular characterization of organic sulfur and nitrogen forms in coal is the polymeric nature of coal`s molecular structure, rendering coal insoluble and impossible to analyze by the necessary gas chromatographic (GC) methods. In our research, we apply mild chemical degradation techniques in order to render coal soluble in common organic solvents and thus amenable to standard GC characterization. The study also seeks to apply the degradative techniques to coal asphaltenes, since they are believed to be polymeric structures similar to the whole coal, but smaller and more readily analyzed. Of the degradation techniques used to date, oxidation by sodium dichromate provides the best chemical structure information. A variety of major sulfur compounds were detected in the dichromate oxidation products of demineralized IBC101 coal, including thiazoles (compounds which contains both sulfur and nitrogen) and a series of isomers of C{sub 2}-, C{sub 3}- and C{sub 4}-alkylthiophene derivatives. Precise agreement between GC-MS and sulfur-selective GC-FPD data was obtained for these compounds, which probably originated as short alkyl chains on exterior portions of the original peat macromolecular structure that were sulfurized shortly after burial by H{sub 2}S. The results were further confirmed by the analysis of a non-Illinois Basin coal with nearly twice the organic sulfur content of IBC101.

Kruge, M.A.; Palmer, S.R. [Southern Illinois Univ., Carbondale, IL (United States)

1992-12-31T23:59:59.000Z

237

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

May 2011 CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries "This presentation does not contain any proprietary, confidential, or otherwise...

238

E-Print Network 3.0 - amoco sulfur recovery process Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

and Medicine 80 Sulfur and oxygen isotope composition of the atmosphere in Saxony (Germany) Tichomirowa et al. Summary: ? a) Mixing processes 12;Sulfur and oxygen isotope...

239

Determination of americium and curium by isotope dilution  

SciTech Connect (OSTI)

The authors propose a method for the determination of americium and curium in solutions of spent fuels from water cooled and moderated reactors that is based on isotope dilution with Am 241 and Cm 244 combined with extraction chromatography of americium and curium and alpha spectroscopy of the labels.

Yablochkin, A.V.; Krapivin, M.I.; Fedotov, S.N.; Yudina, V.G.; Yakobson, A.A.

1987-11-01T23:59:59.000Z

240

Dry Dilution Refrigerator with He-4 Precool Loop  

E-Print Network [OSTI]

He-3/He-4 dilution refrigerators (DR) are very common in sub-Kelvin temperature research. We describe a pulse tube precooled DR where a separate He-4 circuit condenses the He-3 of the dilution loop. Whereas in our previous work the dilution circuit and the He-4 circuit were separate, we show how the two circuits can be combined. Originally, the He-4 loop with a base temperature of ~ 1 K was installed to make an additional cooling power of up to 100 mW available to cool cold amplifiers and electrical lines. In the new design, the dilution circuit is run through a heat exchanger in the vessel of the He-4 circuit so that the condensation of the He-3 stream of the DR is done by the He-4 stage. A much reduced condensation time (factor of 2) of the He-3/He-4 gas mixture at the beginning of an experiment is achieved. A compressor is no longer needed with the DR as the condensation pressure remains below atmospheric pressure at all times; thus the risk of losing expensive He-3 gas is small. The performance of the DR ...

Uhlig, K

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Computational Modelling of Particle Degradation in Dilute Phase Pneumatic Conveyors  

E-Print Network [OSTI]

, GU2 7XH, UK {h.abou-chakra, u.tuzun}@surrey.ac.uk c The Wolfson Centre for Bulk Solids Handling Technology, University of Greenwich, Wellington Street, Woolwich, London, SE18 6PF, UK {i.bridle, m degradation during dilute phase pneumatic conveying. A numerical procedure, based on a matrix representation

Christakis, Nikolaos

242

Automated control and data acquisition for a small dilution refrigerator  

Science Journals Connector (OSTI)

An automatic temperature controller and data acquisition system for use with a dilution refrigerator is described. The unit is controlled by a 16?bit home microcomputer and operates and reads a resistance bridge capacitance bridge and temperature controller. Interfacing is achieved with common components and minimum additional wiring. Flexibility is retained in the software to allow application to several types of measurements.

David G. Haase

1981-01-01T23:59:59.000Z

243

HYBRID SULFUR ELECTROLYZER DEVELOPMENT, NHI WORK PACKAGE N-SR07TC0301, FY07 FIRST QUARTER REPORT  

SciTech Connect (OSTI)

The proof of concept of SO2 electrolysis for the hybrid sulfur (HyS) process is the second priority research target of the DOE Nuclear Hydrogen Initiative's thermochemical program for FY07. The proof of concept of the liquid-phase option must be demonstrated at the single cell level for an extended run times (>100 hours). The rate of development of HyS will depend on the identification of a promising membrane or an alternative means for controlling sulfur formation. Once successful long-duration operation has been demonstrated, SRNL will develop a multi-cell stack that can be connected to the H2SO4 decomposer being developed by SNL for the S-I ILS for a Hybrid Sulfur Integrated Laboratory-Scale Experiment during FY 2008. During the first quarter of FY07, SRNL continued the component development and membrane development activities with the goal of identifying and characterizing improved electrodes, electrocatalysts, membranes and MEA configurations which could then be tested at larger scale in the SDE test facility. A modified glass cell was fabricated to allow measurements of sulfur dioxide (SO2) transport across membrane samples at elevated temperatures (up to 70 C). This testing also includes evaluating SO2 transport in different sulfuric acid concentrations (30-70 wt%). A new potentiostat/frequency analyzer was installed for determining ionic conductivity of membranes. This instrument enhances our capabilities to characterize membrane, electrocatalyst and MEA properties and performance. Continuing work from FY06, evaluations were preformed on various commercial and experimental membranes and electrocatalyst materials for the SDE. Several different types of commercially-available membranes were analyzed for sulfur dioxide transport as a function of acid strength including perfluorinated sulfonic acid (PFSA), sulfonated polyetherketone-ketone, and poly-benzimidazole (PBI) membranes. Experimental membranes from the sulfonated diels-alder polyphenylenes (SDAPP) and modified Nafion{reg_sign} 117 were evaluated for SO{sub 2} transport as well. These membranes exhibited reduced transport coefficient for SO{sub 2} transport without the loss in ionic conductivity.

Summers, W

2006-12-20T23:59:59.000Z

244

Terpolymerization of ethylene, sulfur dioxide and carbon monoxide  

DOE Patents [OSTI]

This invention relates to a high molecular weight terpolymer of ethylene, sulfur dioxide and carbon monoxide stable to 280.degree. C. and containing as little as 36 mol % ethylene and about 41-51 mol % sulfur dioxide; and to the method of producing said terpolymer by irradiation of a liquid and gaseous mixture of ethylene, sulfur dioxide and carbon monoxide by means of Co-60 gamma rays or an electron beam, at a temperature of about 10.degree.-50.degree. C., and at a pressure of about 140 to 680 atmospheres, to initiate polymerization.

Johnson, Richard (Shirley, NY); Steinberg, Meyer (Huntington Station, NY)

1981-01-01T23:59:59.000Z

245

Low Temperature Sorbents for removal of Sulfur Compounds from fluid feed Streams  

SciTech Connect (OSTI)

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjan

1999-09-30T23:59:59.000Z

246

Low Temperature Sorbents for Removal of Sulfur Compounds from Fluid Feed Streams  

DOE Patents [OSTI]

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjani

2004-06-01T23:59:59.000Z

247

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents [OSTI]

A system for adding sulfur to a reformate stream feeding a fuel cell stack, having a sulfur source for providing sulfur to the reformate stream and a metering device in fluid connection with the sulfur source and the reformate stream. The metering device injects sulfur from the sulfur source to the reformate stream at a predetermined rate, thereby providing a conditioned reformate stream to the fuel cell stack. The system provides a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish; Haltiner, Jr., Karl J; Weissman, Jeffrey G

2013-08-13T23:59:59.000Z

248

Diesel Emissions Control-Sulfur Effects (DECSE) Program Status  

SciTech Connect (OSTI)

Determine the impact of fuel sulfur levels on emission control systems that could be implemented to lower emissions of NO{sub x} and PM from on-highway trucks in the 2002-2004 time frame.

None

1999-06-29T23:59:59.000Z

249

Hybrid Microfabricated Device for Field Measurement of Atmospheric Sulfur Dioxide  

Science Journals Connector (OSTI)

It is also now generally agreed that forthcoming major volcanic eruptions will sensitively monitored for increasing sulfur gas emissions as indicated by increasing seismic activity. ... (12)?Fish, B. R.; Durham, J. L. Environ. ...

Shin-Ichi Ohira; Kei Toda; Shin-Ichiro Ikebe; Purnendu K. Dasgupta

2002-10-10T23:59:59.000Z

250

Sulfur meter for blending coal at Plant Monroe: Final report  

SciTech Connect (OSTI)

An on-line sulfur analyzer, installed at the Detroit Edison, Monroe Power station, was placed into service and evaluated for coal blending optimization to minimize the cost of complying with changing stack gas sulfur dioxide regulations. The project involved debugging the system which consisted of an /open quotes/as-fired/close quotes/ sampler and nuclear source sulfur analyzer. The system was initially plagued with mechanical and electronic problems ranging from coal flow pluggages to calibration drifts in the analyzer. Considerable efforts were successfully made to make the system reliable and accurate. On-line testing showed a major improvement in control of sulfur dioxide emission rates and fuel blending optimization equivalent to as much as $6 million in fuel costs at the time of the evaluation. 7 refs., 14 figs., 12 tabs.

Trentacosta, S.D.; Yurko, J.O.

1988-04-01T23:59:59.000Z

251

Engineering of Deinococcus radiodurans R1 for Bioprecipitation of Uranium from Dilute Nuclear Waste  

Science Journals Connector (OSTI)

...radiodurans R1 for Bioprecipitation of Uranium from Dilute Nuclear Waste Published ahead of print on 20 October 2006. Deepti...situ approach to biorecovery of uranium from dilute nuclear waste. Nuclear waste contains a variety of heavy metals, radionuclides...

Deepti Appukuttan; Amara Sambasiva Rao; Shree Kumar Apte

2006-10-20T23:59:59.000Z

252

Diluting the founder effect: cryptic invasions expand a marine invader's range  

Science Journals Connector (OSTI)

...dilute the founder effect for nonindigenous...community of a wooden ship (Yamada 2001...Diluting the founder effect: conservation implications...assemblages entrained by ships are not only species...coastal invasions via ships: effects of emerging strategies...

2006-01-01T23:59:59.000Z

253

A Novel Approach in Determining Oil Dilution Level on a DPF Equipped...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

A Novel Approach in Determining Oil Dilution Level on a DPF Equipped Vehicle as a Result of Regeneration A Novel Approach in Determining Oil Dilution Level on a DPF Equipped...

254

Feasibility of actinide separation from UREX-like raffinates using a combination of sulfur- and oxygen-donor extractants  

SciTech Connect (OSTI)

A synergistic combination of bis(o-trifluoromethylphenyl)dithiosphosphinic acid and trioctylphosphine oxide has been recently shown to selectively remove uranium, neptunium, plutonium and americium from aqueous environment containing up to 0.5 M nitric acid and 5.5 g/L fission products. Here the feasibility of performing this complete actinide recovery from aqueous mixtures is forecasted for a new organic formulation containing sulfur donor extractant of modified structure based on Am(III) and Eu(III) extraction data. A mixture of bis(bis-m,m-trifluoromethyl)phenyl)-dithiosphosphinic acid and TOPO in toluene enhances the extraction performance, accomplishing Am/Eu differentiation in aqueous mixtures up to 1 M nitric acid. The new organic recipe is also less susceptible to oxidative damage resulting from radiolysis.

Peter R. Zalupski; Dean R. Peterman; Catherine L. Riddle

2013-09-01T23:59:59.000Z

255

Feasibility of actinide separation from UREX-like raffinates using a combination of sulfur- and oxygen-donor extractants  

SciTech Connect (OSTI)

A synergistic combination of bis(o-trifluoromethylphenyl)dithios-phosphinic acid and trioctylphosphine oxide has been recently shown to selectively remove uranium, neptunium, plutonium and americium from aqueous environment containing up to 0.5 M nitric acid and 5.5 g/l fission products. Here the feasibility of performing this complete actinide recovery from aqueous mixtures is forecasted for a new organic formulation containing sulfur donor extractant of modified structure based on Am(III) and Eu(III) extraction data. A mixture of bis(bis-m,m-trifluoromethyl)phenyl)-dithios-phosphinic acid and TOPO in toluene enhances the extraction performance, accomplishing Am/Eu differentiation in aqueous mixtures up to 1 M nitric acid. The new organic recipe is also less susceptible to oxidative damage resulting from radiolysis. (authors)

Zalupski, P.R.; Peterman, D.R.; Riddle, C.L. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415 (United States)

2013-07-01T23:59:59.000Z

256

Novel Sulfur-Tolerant Anodes for Solid Oxide Fuel Cells  

SciTech Connect (OSTI)

One of the unique advantages of SOFCs over other types of fuel cells is the potential for direct utilization of hydrocarbon fuels (it may involve internal reforming). Unfortunately, most hydrocarbon fuels contain sulfur, which would dramatically degrade SOFC performance at parts-per-million (ppm) levels. Low concentration of sulfur (ppm or below) is difficult to remove efficiently and cost-effectively. Therefore, knowing the exact poisoning process for state-of-the-art anode-supported SOFCs with Ni-YSZ cermet anodes, understanding the detailed anode poisoning mechanism, and developing new sulfur-tolerant anodes are essential to the promotion of SOFCs that run on hydrocarbon fuels. The effect of cell operating conditions (including temperature, H{sub 2}S concentration, cell voltage/current density, etc.) on sulfur poisoning and recovery of nickel-based anode in SOFCs was investigated. It was found that sulfur poisoning is more severe at lower temperature, higher H{sub 2}S concentration or lower cell current density (higher cell voltage). In-situ Raman spectroscopy identified the nickel sulfide formation process on the surface of a Ni-YSZ electrode and the corresponding morphology change as the sample was cooled in H{sub 2}S-containing fuel. Quantum chemical calculations predicted a new S-Ni phase diagram with a region of sulfur adsorption on Ni surfaces, corresponding to sulfur poisoning of Ni-YSZ anodes under typical SOFC operating conditions. Further, quantum chemical calculations were used to predict the adsorption energy and bond length for sulfur and hydrogen atoms on various metal surfaces. Surface modification of Ni-YSZ anode by thin Nb{sub 2}O{sub 5} coating was utilized to enhance the sulfur tolerance. A multi-cell testing system was designed and constructed which is capable of simultaneously performing electrochemical tests of 12 button cells in fuels with four different concentrations of H{sub 2}S. Through systematical study of state-of-the-art anode-supported SOFC button cells, it is seen that the long-term sulfur poisoning behavior of those cells indicate that there might be a second-stage slower degradation due to sulfur poisoning, which would last for a thousand hour or even longer. However, when using G-18 sealant from PNNL, the 2nd stage poisoning was effectively prohibited.

Lei Yang; Meilin Liu

2008-12-31T23:59:59.000Z

257

Low temperature fracture evaluation of plasticized sulfur paving mixtures  

E-Print Network [OSTI]

May 1985 Major Subject: Civil Engineering LOW TEMPERATURE FRACTURE EVALUATION OF PLASTICIZED SULFUR PAVING MIXTURES A Thesis by KAMYAR MAHBOUB Approved as to style and content by: Dallas N. Li tie (Chai rman of Committee) Ro e . Lytto Member... modifications to the standard ASTM procedure. These modifications were required due to the nature of plasticized sulfur mixtures and asphalt cement mixtures. The J-integral version of Paris ' law was successfully used to characterize the fatigue...

Mahboub, Kamyar

2012-06-07T23:59:59.000Z

258

Recent advances in lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithiumsulfur (LiS) batteries have attracted much attention lately because they have very high theoretical specific energy (2500Whkg?1), five times higher than that of the commercial LiCoO2/graphite batteries. As a result, they are strong contenders for next-generation energy storage in the areas of portable electronics, electric vehicles, and storage systems for renewable energy such as wind power and solar energy. However, poor cycling life and low capacity retention are main factors limiting their commercialization. To date, a large number of electrode and electrolyte materials to address these challenges have been investigated. In this review, we present the latest fundamental studies and technological development of various nanostructured cathode materials for LiS batteries, including their preparation approaches, structure, morphology and battery performance. Furthermore, the development of other significant components of LiS batteries including anodes, electrolytes, additives, binders and separators are also highlighted. Not only does the intention of our review article comprise the summary of recent advances in LiS cells, but also we cover some of our proposals for engineering of LiS cell configurations. These systematic discussion and proposed directions can enlighten ideas and offer avenues in the rational design of durable and high performance LiS batteries in the near future.

Lin Chen; Leon L. Shaw

2014-01-01T23:59:59.000Z

259

Dilution calculations for determining laboratory exhaust stack heights  

SciTech Connect (OSTI)

Laboratory exhaust stacks should be designed with sufficient height and exit momentum to avoid re-entry of exhaust and possible air quality problems, and the design should be evaluated before construction. One evaluation method is presented in this paper that combines dilution prediction equations from the 1997 ASHRAE Handbook--Fundamentals (1997) and a dilution criteria of Halitsky (1988). This method is less conservative than a geometric method in the ASHRAE Handbook and is less costly than wind-tunnel modeling. The method should only be applied to relatively simple building geometries with no larger buildings adjacent to them. A planned change to the ASHRAE equations, which would result in larger stacks being necessary, is discussed. Further investigation of this change is recommended using comparisons to wind tunnel data.

Ratcliff, M.A.; Sandru, E.

1999-07-01T23:59:59.000Z

260

Polyaniline-modified cetyltrimethylammonium bromide-graphene oxide-sulfur nanocomposites with enhanced performance for lithium-sulfur batteries  

Science Journals Connector (OSTI)

Conductive polymer coatings can boost the power storage capacity of lithium-sulfur batteries. We report here on the design and ... polyaniline (PANI)-modified cetyltrimethylammonium bromide (CTAB)-graphene oxide ...

Yongcai Qiu; Wanfei Li; Guizhu Li; Yuan Hou; Lisha Zhou; Hongfei Li

2014-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Dry dilution refrigerator with He-4 precool loop  

SciTech Connect (OSTI)

He-3/He-4 dilution refrigerators (DR) are very common in sub-Kelvin temperature research. We describe a pulse tube precooled DR where a separate He-4 circuit condenses the He-3 of the dilution loop. Whereas in our previous work the dilution circuit and the He-4 circuit were separate, we show how the two circuits can be combined. Originally, the He-4 loop with a base temperature of ? 1 K was installed to make an additional cooling power of up to 100 mW available to cool cold amplifiers and electrical lines. In the new design, the dilution circuit is run through a heat exchanger in the vessel of the He-4 circuit so condensation of the He-3 stream of the DR is done by the He-4 stage. A much reduced condensation time (factor of 2) of the He-3/He-4 gas mixture at the beginning of an experiment is achieved. A compressor is no longer needed with the DR as the condensation pressure remains below atmospheric pressure at all times; thus the risk of losing expensive He-3 gas is small. The performance of the DR has been improved compared to previous work: The base temperature of the mixing chamber at a small He-3 flow rate is now 4.1 mK; at the highest He-3 flow rate of 1.2 mmol/s this temperature increases to 13 mK. Mixing chamber temperatures were measured with a cerium magnesium nitrate (CMN) thermometer which was calibrated with a superconducting fixed point device.

Uhlig, Kurt [Walther-Meissner-Institute, 85748 Garching (Germany)

2014-01-29T23:59:59.000Z

262

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electronic Structure and Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print Wednesday, 29 November 2006 00:00 The possibility of using electrons' spins in addition to their charge in information technology has created much enthusiasm for a new field of electronics popularly known as "spintronics." An intensely studied approach to obtaining spin-polarized carriers for data-storage devices is the use of diluted magnetic semiconductors created by doping ions like Mn, Fe, or Co having a net spin into a semiconducting host such as GaAs, ZnO, or GaN. The interaction among these spins leads to ferromagnetic order at low temperatures, which is necessary to create spin-polarized carriers. A research team working at ALS Beamline 4.0.2 and European Synchrotron Radiation Facility Beamline ID8 made a big leap forward in clarifying the microscopic picture of magnetism and anisotropy in Mn-doped GaAs by resolving localized and hybridized d states using angle-dependent x-ray magnetic circular dichroism (XMCD) measurements.

263

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print The possibility of using electrons' spins in addition to their charge in information technology has created much enthusiasm for a new field of electronics popularly known as "spintronics." An intensely studied approach to obtaining spin-polarized carriers for data-storage devices is the use of diluted magnetic semiconductors created by doping ions like Mn, Fe, or Co having a net spin into a semiconducting host such as GaAs, ZnO, or GaN. The interaction among these spins leads to ferromagnetic order at low temperatures, which is necessary to create spin-polarized carriers. A research team working at ALS Beamline 4.0.2 and European Synchrotron Radiation Facility Beamline ID8 made a big leap forward in clarifying the microscopic picture of magnetism and anisotropy in Mn-doped GaAs by resolving localized and hybridized d states using angle-dependent x-ray magnetic circular dichroism (XMCD) measurements.

264

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print Electronic Structure and Magnetism in Diluted Magnetic Semiconductors Print The possibility of using electrons' spins in addition to their charge in information technology has created much enthusiasm for a new field of electronics popularly known as "spintronics." An intensely studied approach to obtaining spin-polarized carriers for data-storage devices is the use of diluted magnetic semiconductors created by doping ions like Mn, Fe, or Co having a net spin into a semiconducting host such as GaAs, ZnO, or GaN. The interaction among these spins leads to ferromagnetic order at low temperatures, which is necessary to create spin-polarized carriers. A research team working at ALS Beamline 4.0.2 and European Synchrotron Radiation Facility Beamline ID8 made a big leap forward in clarifying the microscopic picture of magnetism and anisotropy in Mn-doped GaAs by resolving localized and hybridized d states using angle-dependent x-ray magnetic circular dichroism (XMCD) measurements.

265

Dry dilution refrigerator with 4He-1K-loop  

E-Print Network [OSTI]

In this article we summarize experimental work on cryogen-free 3He/4He dilution refrigerators which, in addition to the dilution refrigeration circuit, are equipped with a 4He-1K-stage. This type of DR becomes worth considering when high cooling capacities are needed at T ~ 1 K to cool cold amplifiers and heat sink cables. In our application, the motivation for the construction of this type of cryostat was to do experiments on superconducting quantum circuits for quantum information technology and quantum simulations. In other work, DRs with 1K-stage were proposed for astro-physical cryostats. For neutron scattering research, a top-loading cryogen-free DR with 1K-stage was built which was equipped with a standard commercial dilution refrigeration insert. Cooling powers of up to 100 mW have been reached with our 1K-stage, but higher refrigeration powers were achieved with more powerful pulse tube cryocoolers and higher 4He circulation rates in the 1K-loop. Several different versions of a 1K-loop have been test...

Uhlig, Kurt

2014-01-01T23:59:59.000Z

266

Crystal Fields in Dilute Rare-Earth Metals Obtained from Magnetization Measurements on Dilute Rare-Earth Alloys  

Science Journals Connector (OSTI)

Crystal field parameters of Tb, Dy, and Er in Sc, Y, and Lu are summarized. These parameters are obtained from magnetization measurements on dilute single crystals, and successfully checked by a number of different methods. The crystal field parameters vary unpredictably with the rare-earth solute. B40, B60, and B66 are similar in Y and Lu. Crystal field parameters for the pure metals Tb, Dy, and Er are estimated from the crystal fields in Y and Lu.

P. Touborg and J. Hg

1974-09-23T23:59:59.000Z

267

Hybrid Sulfur Thermochemical Process Development Annual Report  

SciTech Connect (OSTI)

The Hybrid Sulfur (HyS) Thermochemical Process is a means of producing hydrogen via water-splitting through a combination of chemical reactions and electrochemistry. Energy is supplied to the system as high temperature heat (approximately 900 C) and electricity. Advanced nuclear reactors (Generation IV) or central solar receivers can be the source of the primary energy. Large-scale hydrogen production based on this process could be a major contributor to meeting the needs of a hydrogen economy. This project's objectives include optimization of the HyS process design, analysis of technical issues and concerns, creation of a development plan, and laboratory-scale proof-of-concept testing. The key component of the HyS Process is the SO2-depolarized electrolyzer (SDE). Studies were performed that showed that an electrolyzer operating in the range of 500-600 mV per cell can lead to an overall HyS cycle efficiency in excess of 50%, which is superior to all other currently proposed thermochemical cycles. Economic analysis indicated hydrogen production costs of approximately $1.60 per kilogram for a mature nuclear hydrogen production plant. However, in order to meet commercialization goals, the electrolyzer should be capable of operating at high current density, have a long operating lifetime , and have an acceptable capital cost. The use of proton-exchange-membrane (PEM) technology, which leverages work for the development of PEM fuel cells, was selected as the most promising route to meeting these goals. The major accomplishments of this project were the design and construction of a suitable electrolyzer test facility and the proof-of-concept testing of a PEM-based SDE.

Summers, William A.; Buckner, Melvin R.

2005-07-21T23:59:59.000Z

268

ADDITIVE TESTING FOR IMPROVED SULFUR RETENTION: PRELIMINARY REPORT  

SciTech Connect (OSTI)

The Savannah River National Laboratory is collaborating with Alfred University to evaluate the potential for additives in borosilicate glass to improve sulfur retention. This preliminary report provides further background on the incorporation of sulfur in glass and outlines the experiments that are being performed by the collaborators. A simulated waste glass composition has been selected for the experimental studies. The first phase of experimental work will evaluate the impacts of BaO, PbO, and V{sub 2}O{sub 5} at concentrations of 1.0, 2.0, and 5.0 wt % on sulfate retention in simulated high level waste borosilicate glass. The second phase of experimental work will evaluate the effects of time at the melt temperature on sulfur retention. The resulting samples will be characterized to determine the amount of sulfur remaining as well as to identify the formation of any crystalline phases. The results will be used to guide the future selection of frits and glass forming chemicals in vitrifying Department of Energy wastes containing high sulfur concentrations.

Amoroso, J.; Fox, K.

2011-09-07T23:59:59.000Z

269

l-Amino Acid Transporter-1 and Boronophenylalanine-Based Boron Neutron Capture Therapy of Human Brain Tumors  

Science Journals Connector (OSTI)

...nebulizer, quartz spray chamber, and nickel cones. Calibration used matrix-matched aqueous standards prepared from boron-10-enriched boric acid. Standards and specimens to be assayed were diluted with an aqueous solution containing 2 butanol...

Allah Detta and Garth S. Cruickshank

2009-03-01T23:59:59.000Z

270

Synergistic Inhibitors for Dilute High-Level Radioactive Waste  

SciTech Connect (OSTI)

Cyclic potentiodynamic polarization scans were conducted to determine the effectiveness of various combinations of anodic inhibitors in the prevention of pitting in carbon steel exposed to dilute radioactive waste. Chromate, molybdate, and phosphate were investigated as replacements for nitrite, whose effective concentrations are incompatible with the waste vitrification process. The polarization scans were performed in non-radioactive waste simulants. Their results showed that acceptable combinations of phosphate with chromate and phosphate with molybdate effectively prevented pitting corrosion. Chromate with molybdate could not replace nitrite.

Wiersma, B.J.; Zapp, P.E.

1995-11-01T23:59:59.000Z

271

Electrical conductivity of dispersions: from dry foams to dilute suspensions  

E-Print Network [OSTI]

We present new data for the electrical conductivity of foams in which the liquid fraction ranges from two to eighty percent. We compare with a comprehensive collection of prior data, and we model all results with simple empirical formul\\ae. We achieve a unified description that applies equally to dry foams and emulsions, where the droplets are highly compressed, as well as to dilute suspensions of spherical particles, where the particle separation is large. In the former limit, Lemlich's result is recovered; in the latter limit, Maxwell's result is recovered.

K. Feitosa; S. Marze; A. Saint-Jalmes; D. J. Durian

2005-07-18T23:59:59.000Z

272

Zero sound modes of dilute Fermi gases with arbitrary spin  

Science Journals Connector (OSTI)

Motivated by the recent success of optical trapping of alkali-metal bosons, we have studied the zero sound modes of dilute Fermi gases with arbitrary spin-f, which are spin-S excitations (0<~S<~2f). The dispersion of the mode (S) depends on a single Landau parameter F(S), which is related to the scattering lengths of the system through a simple formula. Measurement of (even a subset of) these modes in finite magnetic fields will enable one to determine all the interaction parameters of the system.

S.-K. Yip and Tin-Lun Ho

1999-06-01T23:59:59.000Z

273

Why sequence Sulfur cycling in the Frasassi aquifer?  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

sulfur cycling in the Frasassi aquifer? sulfur cycling in the Frasassi aquifer? The terrestrial subsurface remains one of the least explored microbial habitats on earth, and is critical for understanding pollutant migration and attenuation, subsurface processes such as limestone dissolution (affecting porosity), and the search for life elsewhere in the solar system and beyond. The deep and sulfidic Frasassi aquifer (of Ancona, Italy) has emerged as a model system for studying sulfur cycling in the terrestrial subsurface, and this sequencing project has relevance for developing applications for wastewater treatment and capabilities relevant for radionuclide, metal and organic pollutant remediation that can be applied at environments at DOE subsurface sites. Principal Investigators: Jennifer Macalady, Penn State University

274

Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

II. Phase Equilibria II. Phase Equilibria Title Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria Publication Type Journal Article Year of Publication 1996 Authors Ridgway, Paul L., Frank R. McLarnon, and John S. Newman Journal Journal of the Electrochemistry Society Volume 143 Issue 2 Pagination 412-417 Keywords 25 ENERGY STORAGE, 36 MATERIALS SCIENCE, ALUMINIUM OXIDES, equilibrium, performance, PHASE DIAGRAMS, PHOSPHIDES, PHOSPHORUS ADDITIONS, SODIUM COMPOUNDS, SODIUM SULFIDES, SODIUM-SULFUR BATTERIES Abstract Equilibrium open-circuit cell voltage data from a sodium/{beta}{double_prime}-alumina/phosphorus-sulfur cell utilizing P/S ratios of 0, 0.143, and 0.332 and a sodium atom fraction ranging from 0 to 0.4 were interpreted to construct ternary phase diagrams of the Na-P-S ternary system at 350 and 400 C.

275

Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results  

SciTech Connect (OSTI)

A global, self-consistent estimate of sulfur dioxide emissions over the last one and a half century were estimated by using a combination of bottom-up and best available inventory methods including all anthropogenic sources. We find that global sulfur dioxide emissions peaked about 1980 and have generally declined since this time. Emissions were extrapolated to a 1{sup o} x 1{sup o} grid for the time period 1850-2000 at annual resolution with two emission height levels and by season. Emissions are somewhat higher in the recent past in this new work as compared with some comprehensive estimates. This difference is largely due to our use of emissions factors that vary with time to account for sulfur removals from fossil fuels and industrial smelting processes.

Smith, Steven J.; Andres, Robert; Conception , Elvira; Lurz, Joshua

2004-01-25T23:59:59.000Z

276

Indication of Meissner Effect in Sulfur-Substituted Strontium Ruthenates  

E-Print Network [OSTI]

Ceramic samples of Sr2RuO(4-y)Sy (y=0.03-1.2) with intended isovalent substitution of oxygen by sulfur have been synthesized and explored in the temperature range 4-300K. It is found that at a range of optimum sulfur substitution the magnetic response of ceramic samples reveals large diamagnetic signal with amplitudes approaching comparability with that of the YBCO-superconductors. Contrary to a pure ceramic Sr2RuO4, if properly optimized, the resistivity of sulfur-substituted samples has a metallic behavior except at lower temperatures where an upturn occurs. Both synthesis conditions and results of measurements are reported. The Meissner effect may point to high-temperature superconductivity.

Gulian, Armen

2011-01-01T23:59:59.000Z

277

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 6, October--December 1993  

SciTech Connect (OSTI)

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant (reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range (400--650{degree}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2} formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams. The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought ``Claus-alternative`` for coal-fired power plant applications.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1993-12-31T23:59:59.000Z

278

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 4, April--June 1993  

SciTech Connect (OSTI)

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant(reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range(400--650{degrees}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2}-formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams, The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought ``Claus-alternative`` for coal-fired power plant applications.

Liu, Wei; Flytzani-Stephanopoulos, M.; Sarofim, A.F.; Williams, R.S.

1993-12-31T23:59:59.000Z

279

Advanced byproduct recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Fourth quarterly technical progress report  

SciTech Connect (OSTI)

The team of Arthur D. Little, Tufts University and Engelhard Corporation are conducting Phase 1 of a four and a half year, two-phase effort to develop and scale-up an advanced byproduct recovery technology that is a direct, single-stage, catalytic process for converting sulfur dioxide to elemental sulfur. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. More than 95% elemental sulfur yield, corresponding to almost complete sulfur dioxide conversion, was obtained over a Cu-Ce-O oxide catalyst as part of an on-going DOE-sponsored, University Coal Research Program. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning. Tests with CO and CH{sub 4} reducing gases indicate that the catalyst has the potential for flexibility with regard to the composition of the reducing gas, making it attractive for utility use. The performance of the catalyst is consistently good over a range of SO{sub 2} inlet concentration (0.1 to 10%) indicating its flexibility in treating SO{sub 2} tail gases as well as high concentration streams.

NONE

1997-01-01T23:59:59.000Z

280

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

lignocellulosic biomass, in Enzymatic Conversion of Biomassfor biochemical conversion of lignocellulosic biomass toand expensive steps in conversion of biomass into fuels, and

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Stagewise Dilute-Acid Pretreatment and Enzyme Hydrolysis of Distillers Grains and Corn Fiber  

Science Journals Connector (OSTI)

Distillers grains and corn fiber are the coproducts of the corn dry grind and wet milling industries, respectively. Availability of distillers grains and corn fiber at the ethanol plant and their ... three-stag...

Hossein Noureddini; Jongwon Byun; Ta-Jen Yu

2009-11-01T23:59:59.000Z

282

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

16 Figure 2.4 Structure and composition of lignin (Adler,References Adler E. 1977. Lignin chemistry - past, presentRalph J, Baucher M. 2003. Lignin biosynthesis. Annual Review

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

283

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

Klass DL. 1998. Biomass for renewable energy, fuels, andNational Renewable Energy Laboratory.2003, Biomass feedstockKlass DL. 1998. Biomass for Renewable Energy, Fuels and

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

284

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

Industrial and Engineering Chemistry 37: 43-52. Saha B.production. Industrial & Engineering Chemistry Research 48:Industrial and Engineering Chemistry 37: 43-52. Saulnier L,

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

285

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

J. 2007. Ethanol for a sustainable energy future. ScienceA. 2006. Ethanol can contribute to energy and environmentalof ethanol is captured when growing new energy crops to

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

286

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

dioxide emission. Ethanol converted from celluloses andin cellulose and hemicellulose and ferment them to ethanol,cellulose fiber into glucose by enzyme and ferment the xylose and glucose to ethanol

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

287

Dilute Acid Hydrolysis of Oligomers in Hydrothermal Pretreatment Hydrolyzate into Monomers with High Yields  

E-Print Network [OSTI]

heat and electricity used by conversion process or exported to the grid.heat and power to the production facility with excess left to export to the power grid.

Tsai, Yueh-Du

2012-01-01T23:59:59.000Z

288

Direct sulfur recovery during sorbent regeneration. Final report  

SciTech Connect (OSTI)

The objective of this research project was to improve the direct elemental sulfur yields that occur during the regeneration of SO{sub 2}-saturated MgO-vermiculite sorbents (MagSorbents) by examining three approaches or strategies. The three approaches were regeneration-gas recycle, high-pressure regeneration, and catalytic reduction of the SO{sub 2} gas using a new catalyst developed by Research Triangle Institute (RTI). Prior to the project, Sorbent Technologies Corporation (Sorbtech) had developed a sorbent-regeneration process that yielded directly a pure elemental sulfur product. In the process, typically about 25 to 35 percent of the liberated S0{sub 2} was converted directly to elemental sulfur. The goal of this project was to achieve a conversion rate of over 90 percent. Good success was attained in the project. About 90 percent or more conversion was achieved with two of the approaches that were examined, regeneration-gas recycle and use of the RTI catalyst. Of these approaches, regeneration-gas recycle gave the best results (essentially 100 percent conversion in some cases). In the regeneration-gas recycle approach, saturated sorbent is simply heated to about 750{degree}C in a reducing gas (methane) atmosphere. During heating, a gas containing elemental sulfur, water vapor, H{sub 2}S, S0{sub 2}, and C0{sub 2} is evolved. The elemental sulfur and water vapor in the gas stream are condensed and removed, and the remaining gas is recycled back through the sorbent bed. After several recycles, the S0{sub 2} and H{sub 2}S completely disappear from the gas stream, and the stream contains only elemental sulfur, water vapor and C0{sub 2}.

Nelson, S.G.; Little, R.C. [Sorbent Technologies Corp., Twinsburg, OH (United States)

1993-08-01T23:59:59.000Z

289

Extraction, separation, and analysis of high sulfur coal. Final report  

SciTech Connect (OSTI)

The work described in this report studies the removal of sulfur by oxidative interaction of various cupric salts with coal and also considers the possibility of removing organic sulfur by the selective interaction of supercritical ethanol with the organic coal matrix. Either one of these methods could potentially be used to pretreat coals before burning. The primary purpose of these studies is to ascertain the nature of the chemical reactions occurring, the chemical composition of the resultant products, and information on possible reaction mechanisms. This information should allow prediction of reasonable reaction conditions for the removal of organosulfur compound from coal.

Olesik, S.V.; Pekay, L.A.; Larkins, W. Jr. [comps.

1992-05-31T23:59:59.000Z

290

Extraction, separation, and analysis of high sulfur coal  

SciTech Connect (OSTI)

The work described in this report studies the removal of sulfur by oxidative interaction of various cupric salts with coal and also considers the possibility of removing organic sulfur by the selective interaction of supercritical ethanol with the organic coal matrix. Either one of these methods could potentially be used to pretreat coals before burning. The primary purpose of these studies is to ascertain the nature of the chemical reactions occurring, the chemical composition of the resultant products, and information on possible reaction mechanisms. This information should allow prediction of reasonable reaction conditions for the removal of organosulfur compound from coal.

Olesik, S.V.; Pekay, L.A.; Larkins, W. Jr. (comps.)

1992-05-31T23:59:59.000Z

291

HYBRID SULFUR RECOVERY PROCESS FOR NATURAL GAS UPGRADING  

SciTech Connect (OSTI)

This second quarter report of 2002 describes progress on a project funded by the U.S. Department of Energy (DOE) to test a hybrid sulfur recovery process for natural gas upgrading. The process concept represents a low cost option for direct treatment of natural gas streams to remove H{sub 2}S in quantities equivalent to 0.2-25 metric tons (LT) of sulfur per day. This process is projected to have lower capital and operating costs than the competing technologies, amine/aqueous iron liquid redox and amine/Claus/tail gas treating, and have a smaller plant footprint, making it well suited to both on-shore and offshore applications. CrystaSulf (service mark of CrystaTech, Inc.) is a new nonaqueous sulfur recovery process that removes hydrogen sulfide (H{sub 2}S) from gas streams and converts it into elemental sulfur. CrystaSulf features high sulfur recovery similar to aqueous-iron liquid redox sulfur recovery processes, but differs from the aqueous processes in that CrystaSulf controls the location where elemental sulfur particles are formed. In the hybrid process, approximately 1/3 of the total H{sub 2}S in the natural gas is first oxidized to SO{sub 2} at low temperatures over a heterogeneous catalyst. Low temperature oxidation is done so that the H{sub 2}S can be oxidized in the presence of methane and other hydrocarbons without oxidation of the hydrocarbons. The project involves the development of a catalyst using laboratory/bench-scale catalyst testing, and then demonstration of the catalyst at CrystaTech's pilot plant in west Texas. Previous reports described development of a catalyst with the required selectivity and efficiency for producing sulfur dioxide from H{sub 2}S. In the laboratory, the catalyst was shown to be robust and stable in the presence of several intentionally added contaminants, including condensate from the pilot plant site. This report describes testing using the laboratory apparatus but operated at the pilot plant using the actual pilot plant gas, which contains far more contaminants than can be simulated in the laboratory. The results are very encouraging, with stable and efficient operation being obtained for a prolonged period of time.

Girish Srinivas; Steven C. Gebhard; David W. DeBerry

2002-07-01T23:59:59.000Z

292

Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results  

SciTech Connect (OSTI)

This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program`s Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

1990-08-01T23:59:59.000Z

293

Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results  

SciTech Connect (OSTI)

This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program's Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

1990-08-01T23:59:59.000Z

294

Stability Regimes of Turbulent Nitrogen-Diluted Hydrogen Jet Flames  

SciTech Connect (OSTI)

One option for combustion in zero-emission Integrated Gasification Combined Cycle (IGCC) power plants is non-premixed combustion of nitrogen-diluted hydrogen in air. An important aspect to non-premixed combustion is flame stability or anchoring, though only a few fundamental stability studies of these flames have taken place to date. The following paper presents the results of experiments investigating the effects of nitrogen diluent fraction, jet diameter, and exit velocity on the static stability limits of a turbulent hydrogen jet flame issuing from a thin-lipped tube into a quiescent atmosphere. Four different stability limits are observed: detachment from the burner lip, reattachment to the burner lip, transition from a laminar lifted flame base to blowout or to a turbulent lifted flame, and transition from a turbulent lifted flame to blowout. The applicability of existing theories and correlations to the stability results is discussed. These results are an important step in assessing the viability of a non-premixed combustion approach using hydrogen diluted with nitrogen as a fuel.

Weiland, N.T.; Strakey, P.A.

2007-03-01T23:59:59.000Z

295

Surface tension in the dilute Ising model. The Wulff construction  

E-Print Network [OSTI]

We study the surface tension and the phenomenon of phase coexistence for the Ising model on $\\mathbbm{Z}^d$ ($d \\geqslant 2$) with ferromagnetic but random couplings. We prove the convergence in probability (with respect to random couplings) of surface tension and analyze its large deviations : upper deviations occur at volume order while lower deviations occur at surface order. We study the asymptotics of surface tension at low temperatures and relate the quenched value $\\tau^q$ of surface tension to maximal flows (first passage times if $d = 2$). For a broad class of distributions of the couplings we show that the inequality $\\tau^a \\leqslant \\tau^q$ -- where $\\tau^a$ is the surface tension under the averaged Gibbs measure -- is strict at low temperatures. We also describe the phenomenon of phase coexistence in the dilute Ising model and discuss some of the consequences of the media randomness. All of our results hold as well for the dilute Potts and random cluster models.

Marc Wouts

2008-04-14T23:59:59.000Z

296

Short-Term Fates of High Sulfur Inputs in Northern California Vineyard Soils  

SciTech Connect (OSTI)

The widespread application of elemental sulfur (S{sup 0}) to vineyards may have ecosystem effects at multiple scales. We evaluated the short-term fates of applied S{sup 0} in a Napa Valley vineyard; we determined changes in soil sulfur (S) speciation (measured by X-ray absorption near-edge structure (XANES) spectroscopy), soil pH, extractable sulfate (SO{sub 4}{sup 2-}), and total S to evaluate changes in acidity and soil S within the vineyard over time. Surface soil samples were collected immediately prior to and following two applications of S{sup 0} (6.7 kg S{sup 0} ha{sup -1}), with weekly collections in the 2 weeks between applications and following the last application. XANES spectra indicated that the majority of soil S persists in the +6 oxidation state and that S{sup 0} oxidizes within 7 days following application. Soil pH and extractable SO{sub 4}{sup 2-} measurements taken at 30 min after S{sup 0} application revealed generation of acidity and an increase in extractable SO{sub 4}{sup 2-}, but by 12 days after application, soil pH increased to approximately pre-application levels. These data suggest that the major consequence of reactive S applications in vineyards may be the accumulation of soil SO{sub 4}{sup 2-} and organic S during the growing season, which can be mobilized during storm events during the dormant (wet) season. In spatially-extensive winegrowing regions where these applications are made by hundreds of individual farmers each year, it will be important to understand the long-term implications of this perturbation to the regional S cycle.

E Hinckley; S Fendorf; P Matson

2011-12-31T23:59:59.000Z

297

Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program  

Alternative Fuels and Advanced Vehicles Data Center [Office of Energy Efficiency and Renewable Energy (EERE)]

Tier 2 Vehicle and Tier 2 Vehicle and Gasoline Sulfur Program to someone by E-mail Share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Facebook Tweet about Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Twitter Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Google Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Delicious Rank Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Digg Find More places to share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on AddThis.com... More in this section... Federal State Advanced Search All Laws & Incentives Sorted by Type Tier 2 Vehicle and Gasoline Sulfur Program

298

Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite SCR System Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite SCR System effect and performance...

299

Revisit Carbon/Sulfur Composite for Li-S Batteries. | EMSL  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Revisit CarbonSulfur Composite for Li-S Batteries. Revisit CarbonSulfur Composite for Li-S Batteries. Abstract: To correlate the carbon properties e.g. surface area and porous...

300

A design strategy applied to sulfur resistant lean NOx̳ automotive catalysts  

E-Print Network [OSTI]

Catalyst poisoning due to sulfur compounds derived from fuel sulfur presents a major challenge, intractable thus far, to development of many advanced technologies for automotive catalysts such as the lean NOx, trap. Under ...

Tang, Hairong

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents [OSTI]

A system for adding sulfur to a fuel cell stack, having a reformer adapted to reform a hydrocarbon fuel stream containing sulfur contaminants, thereby providing a reformate stream having sulfur; a sulfur trap fluidly coupled downstream of the reformer for removing sulfur from the reformate stream, thereby providing a desulfurized reformate stream; and a metering device in fluid communication with the reformate stream upstream of the sulfur trap and with the desulfurized reformate stream downstream of the sulfur trap. The metering device is adapted to bypass a portion of the reformate stream to mix with the desulfurized reformate stream, thereby producing a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish (Pittsford, NY); Haltiner, Jr., Karl J (Fairport, NY); Weissman, Jeffrey G. (West Henrietta, NY)

2012-03-06T23:59:59.000Z

302

Ultra-Low Sulfur diesel Update & Future Light Duty Diesel | Department...  

Broader source: Energy.gov (indexed) [DOE]

Ultra-Low Sulfur diesel Update & Future Light Duty Diesel Ultra-Low Sulfur diesel Update & Future Light Duty Diesel Presentation given at DEER 2006, August 20-24, 2006, Detroit,...

303

HYBRID SULFUR CYCLE FLOWSHEETS FOR HYDROGEN PRODUCTION USING HIGH-TEMPERATURE GAS-COOLED REACTORS  

SciTech Connect (OSTI)

Two hybrid sulfur (HyS) cycle process flowsheets intended for use with high-temperature gas-cooled reactors (HTGRs) are presented. The flowsheets were developed for the Next Generation Nuclear Plant (NGNP) program, and couple a proton exchange membrane (PEM) electrolyzer for the SO2-depolarized electrolysis step with a silicon carbide bayonet reactor for the high-temperature decomposition step. One presumes an HTGR reactor outlet temperature (ROT) of 950 C, the other 750 C. Performance was improved (over earlier flowsheets) by assuming that use of a more acid-tolerant PEM, like acid-doped poly[2,2'-(m-phenylene)-5,5'-bibenzimidazole] (PBI), instead of Nafion{reg_sign}, would allow higher anolyte acid concentrations. Lower ROT was accommodated by adding a direct contact exchange/quench column upstream from the bayonet reactor and dropping the decomposition pressure. Aspen Plus was used to develop material and energy balances. A net thermal efficiency of 44.0% to 47.6%, higher heating value basis is projected for the 950 C case, dropping to 39.9% for the 750 C case.

Gorensek, M.

2011-07-06T23:59:59.000Z

304

Examination Of Sulfur Measurements In DWPF Sludge Slurry And SRAT Product Materials  

SciTech Connect (OSTI)

Savannah River National Laboratory (SRNL) was asked to re-sample the received SB7b WAPS material for wt. % solids, perform an aqua regia digestion and analyze the digested material by inductively coupled plasma - atomic emission spectroscopy (ICP-AES), as well as re-examine the supernate by ICP-AES. The new analyses were requested in order to provide confidence that the initial analytical subsample was representative of the Tank 40 sample received and to replicate the S results obtained on the initial subsample collected. The ICP-AES analyses for S were examined with both axial and radial detection of the sulfur ICP-AES spectroscopic emission lines to ascertain if there was any significant difference in the reported results. The outcome of this second subsample of the Tank 40 WAPS material is the first subject of this report. After examination of the data from the new subsample of the SB7b WAPS material, a team of DWPF and SRNL staff looked for ways to address the question of whether there was in fact insoluble S that was not being accounted for by ion chromatography (IC) analysis. The question of how much S is reaching the melter was thought best addressed by examining a DWPF Slurry Mix Evaporator (SME) Product sample, but the significant dilution of sludge material, containing the S species in question, that results from frit addition was believed to add additional uncertainty to the S analysis of SME Product material. At the time of these discussions it was believed that all S present in a Sludge Receipt and Adjustment Tank (SRAT) Receipt sample would be converted to sulfate during the course of the SRAT cycle. A SRAT Product sample would not have the S dilution effect resulting from frit addition, and hence, it was decided that a DWPF SRAT Product sample would be obtained and submitted to SRNL for digestion and sample preparation followed by a round-robin analysis of the prepared samples by the DWPF Laboratory, F/H Laboratories, and SRNL for S and sulfate. The results of this round-robin analytical study are the second subject of this report.

Bannochie, C. J.; Wiedenman, B. J.

2012-11-29T23:59:59.000Z

305

Sulfur Degassing From Volcanoes: Source Conditions, Surveillance, Plume Chemistry and Earth System Impacts  

E-Print Network [OSTI]

of sulfur in magmas owes much to its multiple valence states (-II, 0, IV, VI), speciation (e.g., S2, H2S, SO on the redox chemistry of sulfur: by reducing sulfur, thiosulfate, sulfite and sulfate to H2S, or oxidizing sulfur and H2S to sulfate (e.g., Takano et al. 1997; Amend and Shock 2001; Shock et al. 2010

Boyer, Edmond

306

Sulfur-deactivated steam reforming of gasified biomass  

SciTech Connect (OSTI)

The effect of hydrogen sulfide on the stream reforming of methane has been studied. Methane is the most difficult component to convert by steam reforming in the mixture of hydrocarbons, which is produced in biomass gasification. Two catalysts were subjected to hydrogen sulfide levels up to 300 ppm so as to study the effect of sulfur on their deactivation. These catalysts were the C11-9-061, from United Catalyst Inc., and the HTSR1, from Haldor Topsoee. The activation energy of the sulfur-deactivated steam-reforming reaction was calculated to be 280 and 260 kJ/mol, for each catalyst, respectively. The high values most probably originate from the fact that the degree of sulfur coverage of the nickel surface is close to 1 for these experiments. Even under these severe conditions, steam reforming of methane is possible without any carbon formation. The HTSR1 catalyst exhibits a very high sulfur-free activity, resulting in a performance in the presence of hydrogen sulfide higher than that for the C11-9-061 catalyst. By using the HTSR1 catalyst, the reactor temperature can be lowered by 60 C in order to reach comparable levels of conversion.

Koningen, J.; Sjoestroem, K. [Kungl Tekniska Hoegskolan, Stockholm (Sweden)] [Kungl Tekniska Hoegskolan, Stockholm (Sweden)

1998-02-01T23:59:59.000Z

307

Effect of sulfur on heavy duty diesel engine lubricants  

SciTech Connect (OSTI)

Diesel engine exhaust legislation has become quite onerous for heavy duty engines. Yet, these high thermal efficiency engines continue to meet lower exhaust particulate and NOx emissions limits, due to new engine designs and the complementary engine oil performance requirements of the API service categories. In addition, the EPA has mandated changes in on-highway diesel fuel to help meet particulate emissions regulations. On October 1, 1993, when the EPA outlawed high sulfur fuels for on-highway use, the development of the API CG-4 engine oil performance specification was already in progress. All the new diesel engine tests in the category were therefore designed to run with low (< 0.05% wt.) sulfur fuel. In some engine tests, this new fuel improved some lubricant performance characteristics and degraded others. An engine oil specification for low sulfur fuel brings new challenges to developing future specifications for diesel engine oils. Both higher and lower lubricant additive treat rate products, high performance single grade oils, and formulations to meet world-wide specifications become viable. This paper discusses the results of a diesel engine oil technology that performs well with the new, low sulfur fuel in both engine tests and in the field.

Hayden, T.E. [Texaco Fuels and Lubricants Research Dept., Beacon, NY (United States)

1996-12-01T23:59:59.000Z

308

Revisit Carbon/Sulfur Composite for Li-S Batteries  

SciTech Connect (OSTI)

To correlate the carbon properties e.g. surface area and porous structure, with the electrochemical behaviors of carbon/sulfur (C/S) composite cathodes for lithium-sulfur (Li-S) batteries, four different carbon frameworks including Ketjen Black (KB, high surface area and porous), Graphene (high surface area and nonporous), Acetylene Black (AB, low surface area and nonporous) and Hollow Carbon Nano Sphere (HCNS, low surface area and porous) are employed to immobilize sulfur (80 wt.%). It has been revealed that high surface area of carbon improves the utilization rate of active sulfur and decreases the real current density during the electrochemical reactions. Accordingly, increased reversible capacities and reduced polarization are observed for high surface area carbon hosts such as KB/S and graphene/S composites. The porous structure of KB or HCNS matrix promotes the long-term cycling stability of C/S composites but only at relatively low rate (0.2 C). Once the current density increases, the pore effect completely disappears and all Li-S batteries show similar trend of capacity degradation regardless of the different carbon hosts used in the cathodes. The reason has been assigned to the formation of reduced amount of irreversible Li2S on the cathode as well as shortened time for polysulfides to transport towards lithium anode at elevated current densities. This work provides valuable information for predictive selection on carbon materials to construct C/S composite for practical applications from the electrochemical point of view.

Zheng, Jianming; Gu, Meng; Wagner, Michael J.; Hays, Kevin; Li, Xiaohong S.; Zuo, Pengjian; Wang, Chong M.; Zhang, Jiguang; Liu, Jun; Xiao, Jie

2013-07-23T23:59:59.000Z

309

Workshop on sulfur chemistry in flue gas desulfurization  

SciTech Connect (OSTI)

The Flue Gas Desulfurization Workshop was held at Morgantown, West Virginia, June 7-8, 1979. The presentations dealt with the chemistry of sulfur and calcium compounds in scrubbers. DOE and EPRI programs in this area are described. Ten papers have been entered individually into EDB and ERA. (LTN)

Wallace, W.E. Jr.

1980-05-01T23:59:59.000Z

310

Auction design and the market for sulfur dioxide emissions  

E-Print Network [OSTI]

Title IV of the Clean Air Act Amendments of 1990 created a market for electric utility emissions of sulfur dioxide (SO2). Recent papers have argued that flaws in the design of the auctions that are part of this market have ...

Joskow, Paul L.

1996-01-01T23:59:59.000Z

311

Sulfur tolerant molten carbonate fuel cell anode and process  

DOE Patents [OSTI]

Molten carbonate fuel cell anodes incorporating a sulfur tolerant carbon monoxide to hydrogen water-gas-shift catalyst provide in situ conversion of carbon monoxide to hydrogen for improved fuel cell operation using fuel gas mixtures of over about 10 volume percent carbon monoxide and up to about 10 ppm hydrogen sulfide.

Remick, Robert J. (Naperville, IL)

1990-01-01T23:59:59.000Z

312

Vapor phase elemental sulfur amendment for sequestering mercury in contaminated soil  

DOE Patents [OSTI]

The process of treating elemental mercury within the soil is provided by introducing into the soil a heated vapor phase of elemental sulfur. As the vapor phase of elemental sulfur cools, sulfur is precipitated within the soil and then reacts with any elemental mercury thereby producing a reaction product that is less hazardous than elemental mercury.

Looney, Brian B.; Denham, Miles E.; Jackson, Dennis G.

2014-07-08T23:59:59.000Z

313

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase  

E-Print Network [OSTI]

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase Mercury: Sulfur was impregnated onto activated carbon fibers ACFs through H2S oxidation catalyzed by the sorbent CE Database subject headings: Activated carbon; Sulfur; Mercury; Hydrogen sulfides; Oxidation

Borguet, Eric

314

Sulfur-induced greenhouse warming on early Mars Sarah Stewart Johnson,1  

E-Print Network [OSTI]

and 500 mbar CO2 with varying abundances of H2O and sulfur volatiles (H2S and SO2 mixing ratios of 10?3Sulfur-induced greenhouse warming on early Mars Sarah Stewart Johnson,1 Michael A. Mischna,2 melting model, we obtain a high sulfur solubility, approximately 1400 ppm, in Martian mantle melts. We

Zuber, Maria

315

Evaluation of a Partial Flow Dilution System for Transient Particulate Matter Emissions  

Broader source: Energy.gov [DOE]

A commercially available partial flow dilution system was evaluated against a constant volume sampling system over a suite of transient engine dynamometer tests.

316

Scanning Hall probe microscopy of a diluted magnetic semiconductor  

SciTech Connect (OSTI)

We have measured the micromagnetic properties of a diluted magnetic semiconductor as a function of temperature and applied field with a scanning Hall probe microscope built in our laboratory. The design philosophy for this microscope and some details are described. The samples analyzed in this work are Ga{sub 0.94}Mn{sub 0.06}As films grown by molecular beam epitaxy. We find that the magnetic domains are 2-4 mum wide and fairly stable with temperature. Magnetic clusters are observed above T{sub C}, which we ascribe to MnAs defects too small and sparse to be detected by a superconducting quantum interference device magnetometer.

Kweon, Seongsoo [Materials Science and Engineering, University of Texas at Austin, Austin, Texas 78712 (United States); Samarth, Nitin [Physics Department, Penn State University, University Park, Pennsylvania 16802 (United States); Lozanne, Alex de [Materials Science and Engineering, University of Texas at Austin, Austin, Texas 78712 (United States); Department of Physics, University of Texas at Austin, Austin, Texas 78712 (United States)

2009-05-01T23:59:59.000Z

317

Vibrational Dynamics of Isotopically Dilute Nitrogen to 104 GPa  

Science Journals Connector (OSTI)

Raman studies to 104 GPa of a 14N2 host with dilute 15N2 and 14N15N isotopic species indicate an increase in vibrational coupling with pressure. The lowest frequency branch of the isotopic species 15N2 reaches a plateau around 100 GPa suggesting the onset of bond weakening for molecules located on particular sites. An unusual intensity increase is observed for the isotopic ?1 guest modes. The phase transitions above 20 GPa appear to involve an increase in the number of inequivalent sites, with possibly subtle changes in the orientational behavior of particular molecules in the pressure range 25 to 50 GPa not readily revealed in recent x-ray diffraction studies.

H. Olijnyk and A. P. Jephcoat

1999-07-12T23:59:59.000Z

318

A Rapid, Sensitive Method for the Quantitation of Specific Metabolites of Sulfur Mustard in Human Urine Using Isotope-Dilution Gas Chromatography-Tandem Mass Spectrometry  

Science Journals Connector (OSTI)

......Chemicals, remains a public health concern because it is simple...synthetic methods make HD a dangerous chemical warfare agent. In...tinued monitoringfor long-term health effects)from the wor- ried...the initial stages ofa public health re- sponse because additional......

Carrie L. Young; Doris Ash; W. Jack Driskell; Anne E. Boyer; Rodolfo A. Martinez; L.A. Silks; John R. Barr

2004-01-01T23:59:59.000Z

319

Enhanced electrochemical performance by wrapping graphene on carbon nanotube/sulfur composites for rechargeable lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract A novel graphene-wrapped carbon nanotube/sulfur structure was designed to improve the electrochemical performance of the lithiumsulfur (LiS) batteries. Owing to the introduction of the reduced graphene oxide (rGO) with the aim to restrain the polysulfide anions diffusion phenomenon, increase the overall electronic conductivity of the electrode and accommodate volume expansion between the delithiated S and lithiated Li2S phases, the resulted graphene-wrapped carbon nanotube/sulfur (S/CNT@rGO) composite makes the cycling performance of the LiS batteries better than that without rGO. The S/CNT@rGO composite showed an initial discharge capacity of ~1299mAhg?1 at 0.2C rate. After 100 cycles of charge/discharge, the S/CNT@rGO composite retained a high specific capacity of ~670mAhg?1, much higher than that without rGO (graphene-wrapped carbon nanotube/sulfur composite could be a promising cathode material for high-rate performance LiS batteries.

Yishan Wu; Chunmei Xu; Jinxin Guo; Qingmei Su; Gaohui Du; Jun Zhang

2014-01-01T23:59:59.000Z

320

Strong Sulfur Binding with Conducting Magneli-Phase TinO2n-1 Nanomaterials for Improving Lithium-Sulfur Batteries  

E-Print Network [OSTI]

will go through a series of soluble intermediate higher-order polysulfides (Li2S8, Li2S6, and Li2S4 of Li2S2, Li2S, and sulfur.6-8 In order to solve these challenges, there have been recent developmentsStrong Sulfur Binding with Conducting Magneli-Phase TinO2n-1 Nanomaterials for Improving Lithium-Sulfur

Cui, Yi

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Analysis of organic sulfur and nitrogen in coal via tandem degradation methods. [Quarterly] technical report, 1 March--31 May 1992  

SciTech Connect (OSTI)

Sporinite, vitrinite and semi-fusinite single macerals were separated from the IBC 101 coal by the density gradient technique. In addition, a gel permeation chromatography (GPC) system was assembled and the GPC column calibrated with four polystyrene molecular weight standards. A variety of sulfur compounds were identified in the dichromate oxidation products of the IBC 101 coal, including a thiazole and isomers of C2-, C3- and C4-alkyl thiophene carboxylic acids. Precise agreement between GC-MS and FPD chromatograms were obtained for these compounds. These compounds probably originated as short alkyl chains on exterior portions of the original peat macromolecular structures and were sulfurized by H{sub 2}S shortly after burial. Thus the dichromate oxidation appears useful for the characterization of sulfur compounds. Unfortunately, this treatment yields only small amounts of products, but the reaction is relatively mild. On the other hand the peroxyacetic acid gives a very good yield in only a single step, but seems to be very degradative. It was difficult to isolate the products after lithium aluminum hydride reduction of oxidation products. It is believed that this is due to the formation of polyalcohols from polycarboxyl compounds. However polyalcohols were successfully converted to their parent hydrocarbons by the LAH reduction of tosylate intermediates. This allows for much easier separation and characterization and leads to enhanced elucidation of coal structures. To test the hypothesis that asphaltenes are similar in structure to their parent coal, IBC101 asphaltenes and the extracted coal were subjected to PAA oxidation and analytical pyrolysis. The PAA products as well as the pyrolysates show very good correlation. This indicates a very strong relationship between the organic structure of the coal and that of the asphaltenes derived from them.

Kruge, M.A.; Palmer, S.R.; Baudet, N.

1992-10-01T23:59:59.000Z

322

Sulfur-tolerant anode materials for solid oxide fuel cell application  

SciTech Connect (OSTI)

This paper summarizes the degradation mechanisms for SOFC anodes in the presence of sulfur and recent developments in sulfur-tolerant anodes. There are two primary sulfur-degradation mechanisms for the anode materials: physical absorption of sulfur that blocks the hydrogen reaction sites, and chemical reaction that forms nickel sulfide. The sulfur-tolerant anodes are categorized into three kinds of materials: thiospinels and metal sulfides, metal cermets, and mixed ionic and electronic conductors. Each material has its own advantages and disadvantages, and the combined application of available materials to serve as different functional components in anodes through proper design may be effective to achieve a balance between stability and performance.

Gong, M. (West Virginia University, Morgantown, WV); Liu, X. (West Virginia University, Morgantown, WV); Trembly, J.; Johnson, C.

2007-06-01T23:59:59.000Z

323

Sulfur tolerant anode materials. Quarterly report, October 1--December 31, 1987  

SciTech Connect (OSTI)

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-02-01T23:59:59.000Z

324

Sulfur tolerant anode materials. Quarterly report, January 1--March 31, 1988  

SciTech Connect (OSTI)

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-05-01T23:59:59.000Z

325

Method of burning sulfur-containing fuels in a fluidized bed boiler  

DOE Patents [OSTI]

A method of burning a sulfur-containing fuel in a fluidized bed of sulfur oxide sorbent wherein the overall utilization of sulfur oxide sorbent is increased by comminuting the bed drain solids to a smaller average particle size, preferably on the order of 50 microns, and reinjecting the comminuted bed drain solids into the bed. In comminuting the bed drain solids, particles of spent sulfur sorbent contained therein are fractured thereby exposing unreacted sorbent surface. Upon reinjecting the comminuted bed drain solids into the bed, the newly-exposed unreacted sorbent surface is available for sulfur oxide sorption, thereby increasing overall sorbent utilization.

Jones, Brian C. (Windsor, CT)

1982-01-01T23:59:59.000Z

326

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 6, October 1993--December 1993  

SciTech Connect (OSTI)

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant (reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range(400-650 {degrees}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2}-formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams. The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought {open_quotes}Claus-alternative{close_quotes} for coal-fired power plant applications.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1996-01-01T23:59:59.000Z

327

Advanced byproduct recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly report, April 1--June 30, 1997  

SciTech Connect (OSTI)

The team of Arthur D. Little, Tufts University and Engelhard Corporation are conducting Phase 1 of a four and a half year, two-phase effort to develop and scale-up an advanced byproduct recovery technology that is a direct, single-stage, catalytic process for converting sulfur dioxide to elemental sulfur. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. More than 95% elemental sulfur yield, corresponding to almost complete sulfur dioxide conversion, was obtained over a Cu-Ce-O oxide catalyst as part of an on-going DOE-sponsored, University Coal Research Program. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning. Tests with CO and CH{sub 4} reducing gases indicate that the catalyst has the potential for flexibility with regard to the composition of the reducing gas, making it attractive for utility use. The performance of the catalyst is consistently good over a range of SO{sub 2} inlet concentration (0.1 to 10%) indicating its flexibility in treating SO{sub 2} tail gases as well as high concentration streams. The principal objective of the Phase 1 program is to identify and evaluate the performance of a catalyst which is robust and flexible with regard to choice of reducing gas. In order to achieve this goal, the authors have planned a structured program including: Market/process/cost/evaluation; Lab-scale catalyst preparation/optimization studies; Lab-scale, bulk/supported catalyst kinetic studies; Bench-scale catalyst/process studies; and Utility review. Progress is reported from all three organizations.

NONE

1997-12-31T23:59:59.000Z

328

HYBRID SULFUR RECOVERY PROCESS FOR NATURAL GAS UPGRADING  

SciTech Connect (OSTI)

This final report describes the objectives, technical approach, results and conclusions for a project funded by the U.S. Department of Energy to test a hybrid sulfur recovery process for natural gas upgrading. The process concept is a configuration of CrystaTech, Inc.'s CrystaSulf{reg_sign} process which utilizes a direct oxidation catalyst upstream of the absorber tower to oxidize a portion of the inlet hydrogen sulfide (H{sub 2}S) to sulfur dioxide (SO{sub 2}) and elemental sulfur. This hybrid configuration of CrystaSulf has been named CrystaSulf-DO and represents a low-cost option for direct treatment of natural gas streams to remove H{sub 2}S in quantities equivalent to 0.2-25 metric tons (LT) of sulfur per day and more. This hybrid process is projected to have lower capital and operating costs than the competing technologies, amine/aqueous iron liquid redox and amine/Claus/tail gas treating, and have a smaller plant footprint, making it well suited to both onshore and offshore applications. CrystaSulf is a nonaqueous sulfur recovery process that removes H{sub 2}S from gas streams and converts it to elemental sulfur. In CrystaSulf, H{sub 2}S in the inlet gas is reacted with SO{sub 2} to make elemental sulfur according to the liquid phase Claus reaction: 2H{sub 2}S + SO{sub 2} {yields} 2H{sub 2}O + 3S. The SO{sub 2} for the reaction can be supplied from external sources by purchasing liquid SO{sub 2} and injecting it into the CrystaSulf solution, or produced internally by converting a portion of the inlet gas H{sub 2}S to SO{sub 2} or by burning a portion of the sulfur produced to make SO{sub 2}. CrystaSulf features high sulfur recovery similar to aqueous-iron liquid redox sulfur recovery processes, but differs from the aqueous processes in that CrystaSulf controls the location where elemental sulfur particles are formed. In the hybrid process, the needed SO{sub 2} is produced by placing a bed of direct oxidation catalyst in the inlet gas stream to oxidize a portion of the inlet H{sub 2}S. Oxidation catalysts may also produce some elemental sulfur under these conditions, which can be removed and recovered prior to the CrystaSulf absorber. The CrystaSulf-DO process can utilize direct oxidation catalyst from many sources. Numerous direct oxidation catalysts are available from many suppliers worldwide. They have been used for H{sub 2}S oxidation to sulfur and/or SO{sub 2} for decades. It was believed at the outset of the project that TDA Research, Inc., a subcontractor, could develop a direct oxidation catalyst that would offer advantages over other commercially available catalysts for this CrystaSulf-DO process application. This project involved the development of several of TDA's candidate proprietary direct oxidation catalysts through laboratory bench-scale testing. These catalysts were shown to be effective for conversion of H{sub 2}S to SO{sub 2} and to elemental sulfur under certain operating conditions. One of these catalysts was subsequently tested on a commercial gas stream in a bench-scale reactor at CrystaTech's pilot plant site in west Texas with good results. However, commercial developments have precluded the use of TDA catalysts in the CrystaSulf-DO process. Nonetheless, this project has advanced direct oxidation catalyst technology for H{sub 2}S control in energy industries and led to several viable paths to commercialization. TDA is commercializing the use of its direct oxidation catalyst technology in conjunction with the SulfaTreat{reg_sign} solid scavenger for natural gas applications and in conjunction with ConocoPhillips and DOE for gasification applications using ConocoPhillips gasification technology. CrystaTech is commercializing its CrystaSulf-DO process in conjunction with Gas Technology Institute for natural gas applications (using direct oxidation catalysts from other commercial sources) and in conjunction with ChevronTexaco and DOE for gasification applications using ChevronTexaco's gasification technology.

Dennis Dalrymple

2004-06-01T23:59:59.000Z

329

SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

CSP Generation CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage to someone by E-mail Share SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on Facebook Tweet about SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on Twitter Bookmark SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on Google Bookmark SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on Delicious Rank SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on Digg Find More places to share SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage on

330

Integrated Process Configuration for High-Temperature Sulfur Mitigation during Biomass Conversion via Indirect Gasification  

SciTech Connect (OSTI)

Sulfur present in biomass often causes catalyst deactivation during downstream operations after gasification. Early removal of sulfur from the syngas stream post-gasification is possible via process rearrangements and can be beneficial for maintaining a low-sulfur environment for all downstream operations. High-temperature sulfur sorbents have superior performance and capacity under drier syngas conditions. The reconfigured process discussed in this paper is comprised of indirect biomass gasification using dry recycled gas from downstream operations, which produces a drier syngas stream and, consequently, more-efficient sulfur removal at high temperatures using regenerable sorbents. A combination of experimental results from NREL's fluidizable Ni-based reforming catalyst, fluidizable Mn-based sulfur sorbent, and process modeling information show that using a coupled process of dry gasification with high-temperature sulfur removal can improve the performance of Ni-based reforming catalysts significantly.

Dutta. A.; Cheah, S.; Bain, R.; Feik, C.; Magrini-Bair, K.; Phillips, S.

2012-06-20T23:59:59.000Z

331

Phase Uniqueness and Correlation Length in DilutedField Ising Models  

E-Print Network [OSTI]

Phase Uniqueness and Correlation Length in Diluted­Field Ising Models L. R. G. Fontes E. J. Neves Instituto de Matem'atica e Estat'istica, USP November 18, 1994 Abstract The Diluted­Field Ising Model 1 when the field mean is positive. Our methods involve comparisons with ordinary uniform field Ising

332

Viscosity of semi-dilute polymer solutions M. Adam and M. Delsanti  

E-Print Network [OSTI]

549 Viscosity of semi-dilute polymer solutions M. Adam and M. Delsanti Laboratoire Léon viscosity measurements on semi-dilute solutions (c* c 10 %). The viscosity variation is independent to the solvent viscosity. With concentration, the following variations were observed : 2014 for PIB-toluene, ~r

Paris-Sud XI, Université de

333

Fusion of Dilute AL Lattice Models Yu-kui Zhou1  

E-Print Network [OSTI]

Fusion of Dilute AL Lattice Models Yu-kui Zhou1 , Paul A. Pearce2 Mathematics Department The fusion procedure is implemented for the dilute AL lattice models. A fusion hierarchy of functional ansatz equations of the transfer matrices have been given. 1 Introduction The fusion procedure

Pearce, Paul A.

334

Physical mechanisms for the offshore detachment of the Changjiang Diluted Water in the East China Sea  

E-Print Network [OSTI]

Physical mechanisms for the offshore detachment of the Changjiang Diluted Water in the East China mechanisms for the summertime offshore detachment of the Changjiang Diluted Water (CDW) into the East China in the northern coastal area of the Changjiang mouth offshore over a submerged plateau that extends toward Cheju

Chen, Changsheng

335

Secondary economic impact of acid deposition control legislation in six coal producing states: Final report  

SciTech Connect (OSTI)

Among the difficult policy questions on the US environmental agenda is what to do about emissions to the earth's atmosphere of pollutants that may result in ''acid rain''. The Congress has considered several pieces of legislation spelling out potential approaches to the problem and setting goals for emission reduction, mostly emphasizing the control of oxides of sulfur and nitrogen. Significant policy concern is the dollar costs to the nation's economy of achieving the intended effects of the legislation and the potential impacts on economic activity---in particular, losses of both coal mining and secondary service sector employment in states and regions dependent on the mining of high sulfur coal. There are several direct economic effects of regulations such as the acid rain control legislation. One of the more obvious effects was the switching from high sulfur coal to low sulfur coal. This would result in increases in employment and coal business procurements in low sulfur coal mining regions, but also would result in lower employment and lower coal business procurements in high sulfur coal mining areas. The potential negative effects are the immediate policy concern and are the focus of this report. 15 refs., 1 fig., 17 tabs.

Scott, M.J.; Guthrie, S.J.

1988-12-01T23:59:59.000Z

336

Oxidation of trace amounts of transplutonium elements to the tetravalent state in solutions of mineral acids and their stabilities  

SciTech Connect (OSTI)

The behavior of trace amounts of americium(IV) in sulfuric and nitric acid solutions as a function of the mineral acid, potassium phosphotungstate, and ammonium persulfate concentrations was investigated. The stability of americium(IV) was studied. The optimal conditions and time of oxidation of trace amounts of americium to the tetravalent state were found on the basis of the experimental data obtained.

Milyukova, M.S.; Varezhkina, N.S.; Kuzovkina, E.V.; Malikov, D.A.; Myasoedov, B.F.

1989-01-01T23:59:59.000Z

337

Sulfur Lamps-The Next Generation of Efficient Light?  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

5 5 Sulfur Lamps-The Next Generation of Efficient Light? The figure above is a schematic of the system installed at the National Air and Space Museum and the DOE headquarters in Washington, D.C., Light from the sulfur lamp is focused by a parabolic reflector so that it enters the light pipe within a small angular cone. Light travels down the pipe, reflecting off the prismatic film (A) that lines the outer acrylic tube. The prismatic film reflects the light through total internal reflection (C), an intrinsically efficient process. Some of the light striking the film (at A) is not reflected and "leaks out" of the pipe walls (B), giving the pipe a glowing appearance. A light ray that travels all the way down the pipe will strike the mirror at the end (D) and return back up the pipe.

338

Cost-cutting for offshore sulfur recovery processes studied  

SciTech Connect (OSTI)

An increasing portion of future US gas supply is likely to come from offshore, primarily Gulf of Mexico. Because this gas can be sour, the industry has sought lower cost H{sub 2}S-removal/recovery processes for treating it. Usually the gas contains < 5 tons/day (tpd) of sulfur. A study to compare several emerging sulfur-removal/recovery processes against a baseline Amine/LO-CAT II process has indicated that some emerging processes, though not yet commercialized, show considerable potential for reducing costs. Specifically, the major findings were that Double Loop and CrystaSulf, developed by Radian International LLC, Austin, were the least expensive capital-cost processes by a significant margin and that Marathon Oil Co.`s Hysulf`s cost has the potential to compete with Double Loop and CrystaSulf.

Quinlan, M.P.; Echterhoff, L.W. [M.W. Kellogg Co., Houston, TX (United States); Leppin, D.; Meyer, H.S. [Gas Research Inst., Chicago, IL (United States)

1997-07-21T23:59:59.000Z

339

Method of making sulfur-resistant composite metal membranes  

DOE Patents [OSTI]

The invention provides thin, hydrogen-permeable, sulfur-resistant membranes formed from palladium or palladium-alloy coatings on porous, ceramic or metal supports. Also disclosed are methods of making these membranes via sequential electroless plating techniques, wherein the method of making the membrane includes decomposing any organic ligands present on the substrate, reducing the palladium crystallites on the substrate to reduced palladium crystallites, depositing a film of palladium metal on the substrate and then depositing a second, gold film on the palladium film. These two metal films are then annealed at a temperature between about 200.degree. C. and about 1200.degree. C. to form a sulfur-resistant, composite PdAu alloy membrane.

Way, J. Douglas (Boulder, CO) [Boulder, CO; Lusk, Mark (Golden, CO) [Golden, CO; Thoen, Paul (Littleton, CO) [Littleton, CO

2012-01-24T23:59:59.000Z

340

Availability of heavy fuel oils by sulfur level, September 1981  

SciTech Connect (OSTI)

A narrative analysis of the status of the United States' total new supply of heavy fuel oils, is given with emphasis on sulfur levels. Tables detail refinery production, stocks, and imports of residual fuel oil and No. 4 fuel oil by sulfur content. All data except stock figures are reported on a monthly and on a year-to-date basis; stock data are reported on an end-of-current-month basis. Units of measure are thousands of barrels. Stocks held, refineries and bulk terminals and refinery production are given by Petroleum Administration for Defense (PAD) and refinery Districts. Imports are given by PAD District, by country of origin, and by importing State. Waterborne movements from PAD District III to other districts are detailed for the most recent month only. This report was previously published by the Bureau of Mines in the Minerals Industries Surveys Series under the same title. Publication was discontinued with the December 1981 issue. 2 figures, 13 tables.

Wolfrey, J.

1981-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

More Economical Sulfur Removal for Fuel Processing Plants  

Broader source: Energy.gov (indexed) [DOE]

enabled TDA to develop and commercialize its direct oxidation process-a simple, catalyst-based system for removing sulfur from natural gas and petroleum-that was convenient and economical enough for smaller fuel processing plants to use. TDA Research, Inc. (TDA) of Wheat Ridge, CO, formed in 1987, is a privately-held R&D company that brings products to market either by forming internal business

342

Structure of Chemisorbed Sulfur on a Pt(111) Electrode  

Science Journals Connector (OSTI)

Contribution from the Department of Chemistry, University of Illinois and Frederick Seitz Materials Research Laboratory, 600 S. Mathews Ave., Urbana, Illinois 61801, and Dpartement de Chimie, Universit de Sherbrooke, Sherbrooke, Qubec, J1K 2R1, Canada ... Sulfur was deposited from aqueous sulfide and bisulfide media on Pt(111), and the interrogations were conducted by low electron energy diffraction (LEED), Auger electron spectroscopy (AES), and core-level electron energy loss spectroscopy (CEELS). ...

Y.-E. Sung; W. Chrzanowski; A. Zolfaghari; G. Jerkiewicz; A. Wieckowski

1997-01-08T23:59:59.000Z

343

Extraction, separation, and analysis of high sulfur coal  

SciTech Connect (OSTI)

Coal Reaction Study: The results of the reaction of aqueous cupric chloride with Illinois {number sign}6 coal are listed on page 21. These results indicate that the oxidative desulfurization of coal with cupric chloride is more complex and less effective than previously reported. Although almost all the pyritic and sulfate sulfur are removed from the coal, the organic sulfur is actually reported to have increased. This may be due to an actual increase in the organic sulfur through a side reaction of the pyrite, or it may be caused by inaccuracy of the ASTM method when large proportions of chloro substituents are present. The amount of chlorine added to the coal (from 0 to 3.18%) is quite large and counterproductive. Most importantly, the amount of non-combustible ash has increased from 15.48 to 51.21%, most likely in the form of copper. This will dramatically decrease both the efficiency of combustion in terms of altering the heat capacity of the coal as well as decrease the amount of energy produced per ton of coal. As a result, it is quite evident that this method of desulfurization needs some modification prior to further exploitation.

Olesik, S. (comp.)

1990-01-01T23:59:59.000Z

344

Removal of nitrogen and sulfur from oil-shale  

SciTech Connect (OSTI)

This patent describes a process for enhancing the removal of nitrogen and sulfur from oil-shale. The process consists of: (a) contacting the oil-shale with a sufficient amount of an aqueous base solution comprised of at least a stoichiometric amount of one or more alkali metal or alkaline-earth metal hydroxides based on the total amount of nitrogen and sulfur present in the oil-shale. Also necessary is an amount sufficient to form a two-phase liquid, solid system, a temperature from about 50/sup 0/C to about 350/sup 0/C., and pressures sufficient to maintain the solution in liquid form; (b) separating the effluents from the treated oil-shale, wherein the resulting liquid effluent contains nitrogen moieties and sulfur moieties from the oil-shale and any resulting gaseous effluent contains nitrogen moieties from the oil-shale, and (c) converting organic material of the treated oil-shale to shale-oil at a temperature from about 450/sup 0/C to about 550/sup 0/C.

Olmstead, W.N.

1986-01-28T23:59:59.000Z

345

Metal-insulator transition in dilute alkali-metal systems  

Science Journals Connector (OSTI)

The metal-insulator transition is studied for dilute systems of alkali metals. Using a spin-split self-consistent band-structure approach, we find the transition density, a strikingly enhanced magnetic susceptibility, and the electron effective mass. The critical density nc is found to be given by the simple relation rsc=r0+2.8. Here rsc=[3(4?nc)]13 and r0 is the model potential radius which is roughly the radius of the neutral atom. The Mott criterion of nc13aB?0.25 (where aB is the appropriate Bohr orbit) is found to be inadequate for describing these systems. The predicted effective mass and magnetic susceptibility enhancements are largest for Li and become systematically smaller for the heavier alkalis. We compare our results for the transition density with two sets of experiments, namely the gas-liquid critical density and the metal-insulator transition for codeposited thick films of alkali-metal and rare-gas atoms. Good agreement is found in both cases.

J. H. Rose

1981-01-15T23:59:59.000Z

346

Advanced product recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Third quarterly technical progress report  

SciTech Connect (OSTI)

More than 170 wet scrubber systems applied to 72,000 MW of US, coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed form the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. Arthur D. Little, Inc., together with its industry and commercialization advisor, Engelhard Corporation, and its university partner, Tufts, plans to develop and scale-up an advanced, byproduct recovery technology that is a direct, catalytic process for reducing sulfur dioxide to elemental sulfur. The principal objective of the Phase 1 program is to identify and evaluate the performance of a catalyst which is robust and flexible with regard to choice of reducing gas. In order to achieve this goal, they have planned a structured program including: market/process/cost/evaluation; lab-scale catalyst preparation/optimization studies; lab-scale, bulk/supported catalyst kinetic studies; bench-scale catalyst/process studies; and utility review. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning.

NONE

1996-07-01T23:59:59.000Z

347

A Novel Approach in Determining Oil Dilution Level on a DPF Equipped Vehicle as a Result of Regeneration  

Broader source: Energy.gov [DOE]

This approach can be easily adopted for developing optimum engine calibration meeting performance, emissions and oil dilution.

348

Concentrating aqueous volatile fatty acid salt solutions using a tertiary amine mixture  

E-Print Network [OSTI]

, and that reaction is difficult to reverse (Streitwieser and Heathcock, 1976; King and Poole, 1994). Tertiary amines (R, N) do not form amides but generally give lower K, values than secondary amines. For the extraction of undissociated carboxylic acids, aliphatic... by acidifying with carbon dioxide under pressure in the presence of a suitable solvent (Busche, 1988). Gregor has used electrodialysis to recover acetic acid from dilute (1-5 wt%) acetate solutions. With newer membranes, acid concentrations up to 30% were...

Gaskin, David J

1997-01-01T23:59:59.000Z

349

Evidence of magnetic isotope effects during thermochemical sulfate reduction  

E-Print Network [OSTI]

Thermochemical sulfate reduction experiments with simple amino acid and dilute concentrations of sulfate reveal significant degrees of mass-independent sulfur isotope fractionation. Enrichments of up to 13 for [superscript ...

Oduro, Harry D.

350

Inert Gas Dilution Effect on the Flammability Limits of Hydrocarbon Mixtures  

E-Print Network [OSTI]

previous one from U.S. BMs???????....69 5.3 Ethane flammability properties with dilution of nitrogen (25 ?C and 1 atm)??????????????????????..????.. 70 5.4 Propane flammability properties with dilution of nitrogen (25 ?C and 1 atm...)???????????????????????..???.. 72 5.8 Flammability properties of methane and propane at different molar radios (20 %/80%, 40%/60%, 60%/40%, and 80%/20%) with dilution of nitrogen (25 ?C and 1 atm)?..????.?..?????????73 5.9 Flammability properties of ethane and propane...

Zhao, Fuman

2012-02-14T23:59:59.000Z

351

Effect of hydrous ethanol on crankcase oil dilution  

SciTech Connect (OSTI)

Adequate lubrication is of the utmost importance in internal combustion engines. Low temperature operation with low-proof alcohol may create some operational problems if alcohol and/or water accumulates in the crankcase oil. Condensates of unburned alcohol and water maybe blown into the crankcase oil with blowby gases. These condensates may form an emulsion with the crankcase oil that may restrict the supply of oil for adequate lubrication. Three engine tests were performed to identify the effect of low-proof ethanol fueling on crankcase oil dilution and degradation. The first test was hydrous ethanol carburetion in a 2.3 liter, 4 cylinder, 1974 Ford gasoline engine. The second test was a mixture of low-proof ethanol fumigation and normal diesel fuel injection (at reduced rate) in an Allis-Chalmers Model 2900 turbocharged diesel engine. The third test was also a mixture of ethanol fumigation and diesel injection in an Allis-Chalmers Mod2800 naturally aspirated diesel engine. Independent parameters of crankcase oil temperature, engine load and speed, percent of total energy in the form of ethyl alcohol and proof of the ethyl alcohol were considered and varied. After each test the oil was sampled for determination of flash point, fire points, water by centrifuge, water by distillation, and viscosity at room temperature. Results for the first test indicate that the use of ethanol of 130 proof or less may result in accumulation of water in the crankcase oil that may be harmful to the engine. In the second and third tests although there was a decrease in fire and flash points as well as in the viscosity of the oil, no appreciable amount of water or alcohol was detected in the crankcase oil. It is important to mention that there was a maximum alcohol fuel flow rate beyond which the diesel engine starts to knock or misfire.

Khalifa, G.A.

1985-01-01T23:59:59.000Z

352

Solvent Tuning of Properties of Iron-Sulfur Clusters in Proteins  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Solvent Tuning of Properties of Solvent Tuning of Properties of Iron-Sulfur Clusters in Proteins Figure 1. Schematic repre-sentation of the common active-site iron-sulfur cluster structural motif. Proteins containing Fe4S4 iron-sulfur clusters are ubiquitous in nature and catalyze one-electron transfer processes. These proteins have evolved into two classes that have large differences in their electrochemical potentials: high potential iron-sulfur proteins (HiPIPs) and bacterial ferredoxins (Fds). The role of the surrounding protein environment in tuning the redox potential of these iron sulfur clusters has been a persistent puzzle in biological electron transfer [1]. Although HiPIPs and Fds have the same iron sulfur structural motif - a cubane-type structure - (Figure 1), there are large differences in their electrochemical

353

SunShot Initiative: Baseload CSP Generation Integrated with Sulfur-Based  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage General Atomics logo Graphic of a diagram of squares and circles connected by arrows. Sulfur-based TES can compensate for diurnal and seasonal insolation fluctuations. General Atomics, under the Baseload CSP FOA, is demonstrating the engineering feasibility of using a sulfur-based thermochemical cycle to store heat from a CSP plant and support baseload power generation. Approach There are three main project objectives under this award: Study the sulfur generating disproportionation reaction and develop it into a practical engineering process step. Carry out preliminary process components design and experimental validation. The engineering data will be used for process integration between the CSP plant, the sulfur processing and storage plant, and the electricity generation unit.

354

doi:10.1016/j.gca.2005.02.002 Sulfur diffusion in basaltic melts  

E-Print Network [OSTI]

doi:10.1016/j.gca.2005.02.002 Sulfur diffusion in basaltic melts CARMELA FREDA,1, * DON R. BAKER,1,2 February 3, 2005) Abstract--We measured the diffusion coefficients of sulfur in two different basaltic for sulfur diffusion in anhydrous basalts: D 2.19 10 4 exp 226.3 58.3 RT where D is the diffusion coefficient

Long, Bernard

355

Microsoft Word - Vapor Phase Elemental Sulfur Tech Brief DRAFT bbl 08-24.docx  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AT A GLANCE AT A GLANCE  eliminates excavation expense  applicable to large or small sites  straightforward deployment  uses heat to distribute sulfur throughout a soil  mercury reacts with sulfur to form immobile and insoluble minerals  patent applied for TechBrief Vapor Phase Elemental Sulfur Amendment for Sequestering Mercury in Contaminated Soil Scientists at the Savannah River National Laboratory (SRNL) have identified a method of targeting mercury in contaminated soil zone by use of sulfur vapor heated gas. Background Mercury contamination in soil is a common problem in the environment. The most common treatment is excavation - a method that works well for small sites where the

356

Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite...  

Broader source: Energy.gov (indexed) [DOE]

October 04, 2011 Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite SCR System DEER CONFERENCE 2011 Outline Introduction Zeolite-based SCR behavior -...

357

Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales...  

Gasoline and Diesel Fuel Update (EIA)

200 Energy Information AdministrationPetroleum Marketing Annual 1998 Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales Type, and PAD District (Cents per Gallon...

358

Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales...  

Gasoline and Diesel Fuel Update (EIA)

200 Energy Information AdministrationPetroleum Marketing Annual 1999 Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales Type, and PAD District (Cents per Gallon...

359

Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales...  

Gasoline and Diesel Fuel Update (EIA)

Energy Information Administration Petroleum Marketing Annual 1995 Table 41. No. 2 Diesel Fuel Prices by Sulfur Content, Sales Type, and PAD District (Cents per Gallon...

360

E-Print Network 3.0 - aqueous organic sulfur Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

TRACE ATMOSPHERIC CONSTITUENTS Summary: . Reactions of Sulfur(IV) with Transition-Metal Ions in Aqueous Solutions Robert E. Huie and Norman C... . Peterson 3. Catalytic...

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

E-Print Network 3.0 - ashless low-sulfur fuel Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Blendstocks for Low Sulfur Diesel Fuel in PADD III . . . . . . . . . . . . . . . . 17... markets for low ... Source: Oak Ridge National Laboratory, Center for Transportation...

362

E-Print Network 3.0 - aromatic sulfur heterocycles Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

distribution in the oil fractions obtained by thermal cracking of Jordanian El-Lajjun oil Shale Summary: . Polycyclic aromatic sulfur heterocycles IV. Determination of polycyclic...

363

Portable instrument and method for detecting reduced sulfur compounds in a gas  

DOE Patents [OSTI]

A portable real time instrument for detecting concentrations in the part per billion range of reduced sulfur compounds in a sample gas. Ozonized air or oxygen and reduced sulfur compounds in a sample gas stream react to produce chemiluminescence in a reaction chamber and the emitted light is filtered and observed by a photomultiplier to detect reduced sulfur compounds. Selective response to individual sulfur compounds is achieved by varying reaction chamber temperature and ozone and sample gas flows, and by the use of either air or oxygen as the ozone source gas.

Gaffney, J.S.; Kelly, T.J.; Tanner, R.L.

1983-06-01T23:59:59.000Z

364

Sulfur behavior in the Sasol-Lurgi fixed-bed dry-bottom gasification process  

SciTech Connect (OSTI)

This article reports on the findings of a study regarding the sulfur behavior across a Sasol-Lurgi gasifier. This was undertaken to understand the behavior of the various sulfur-bearing components in the coal, as they are exposed to the conditions in the gasifier. In this study, conventional characterization techniques were employed to monitor the behavior of sulfur-bearing mineral matter across the gasifier. It was observed from the study that the sulfur-bearing mineral (pyrite) in the coal structure undergoes various changes with pyrite being transformed to pyrrhotite and then to various oxides of iron with the subsequent loss of sulfur to form H{sub 2}S. A low proportion of the sulfur species including the organically associated sulfur was encapsulated by a melt that was formed by the interaction between kaolinite and fluxing minerals (pyrite, calcite, and dolomite/ankerite) present in the coal at elevated temperatures and pressure, thereby ending up in the ash. The remaining small proportions of sulfur-bearing mineral matter including pyrite and organically bound sulfur in the unburned carbon in the carbonaceous shales also report to the ash. 18 refs., 8 figs., 2 tabs.

M. Pat Skhonde; R. Henry Matjie; J. Reginald Bunt; A. Christien Strydom; H. Schobert [Sasol Technology R& amp; D, Sasolburg (South Africa)

2009-01-15T23:59:59.000Z

365

Status of Heavy Vehicle Diesel Emission Control Sulfur Effects (DECSE) Test Program  

SciTech Connect (OSTI)

DECSE test program is well under way to providing data on effects of sulfur levels in diesel fuel on performance of emission control technologies.

George Sverdrup

1999-06-07T23:59:59.000Z

366

Sulfur-tolerant natural gas reforming for fuel-cell applications.  

E-Print Network [OSTI]

??An attractive simplification of PEM-FC systems operated with natural gas would be the use of a sulfur tolerant reforming catalyst, but such a catalyst has (more)

Hennings, Ulrich

2010-01-01T23:59:59.000Z

367

E-Print Network 3.0 - africa sulfur isotope Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Search Powered by Explorit Topic List Advanced Search Sample search results for: africa sulfur isotope Page: << < 1 2 3 4 5 > >> 1 Geobiology (2006), 4, 191201 2006 The...

368

Sulfur barrier for use with in situ processes for treating formations  

DOE Patents [OSTI]

Methods for forming a barrier around at least a portion of a treatment area in a subsurface formation are described herein. Sulfur may be introduced into one or more wellbores located inside a perimeter of a treatment area in the formation having a permeability of at least 0.1 darcy. At least some of the sulfur is allowed to move towards portions of the formation cooler than the melting point of sulfur to solidify the sulfur in the formation to form the barrier.

Vinegar, Harold J. (Bellaire, TX); Christensen, Del Scot (Friendswood, TX)

2009-12-15T23:59:59.000Z

369

Metallurgical characterization of self catalytic structural materials for sulfuric acid decomposition  

E-Print Network [OSTI]

Eight heats of material with base alloy chemistries of Alloys 800 HT or 617 with platinum additions of 2, 5, 15, or 30 wt% have been characterized according to their microstructural features. The goals of characterization ...

Rigual, David Andrs

2005-01-01T23:59:59.000Z

370

Effect of Water Transport on the Production of Hydrogen and Sulfuric Acid in a PEM Electrolyzer  

E-Print Network [OSTI]

be developed that provides efficient production of clean hydrogen. The methods existing today for large-scale produc- tion of hydrogen typically involve hydrocarbon reforming of natural gas or coal gasification% , the overall efficiency is 40%.7 Two issues remain, however, that make the future of this technology un

Weidner, John W.

371

Source of Error in Determination of Chromic Oxide Using Perchloric-Sulfuric Acid Digestion Method  

Science Journals Connector (OSTI)

...due to prolonged digestion. KATHERINE MI. DAY Department of Agricultural...irrevo-cably homothallic." H. E. WHEELER Depairtment of Botany, Louisianta...244 (1914). :3. II. E. Wheeler, Phytopathology 44, 342...P. Chilton tand H. E. Wheeler, Am. J. Botany 36, 717...

KATHERINE M. DAY

1954-10-29T23:59:59.000Z

372

The corrosion behavior of cobalt and nickel in sulfuric acid solution containing propargylic alcohol  

SciTech Connect (OSTI)

Extrapolation of the anodic and cathodic Tafel lines of current density-potential curves was determined by potentiodynamic polarization (1 mVs/sup -1/) and galvanostatic large signal pulse polarization was applied to the corrosion potential. Polarization resistance was measured under potentiodynamic polarization (1 mVs/sup -1/) or galvanostatic small signal pulse polarization in the vicinity of the corrosion potential and applied to the Stern-Geary equation.

Aksut, A.A.

1984-08-01T23:59:59.000Z

373

Determination of boron in nuclear materials by isotope dilution technique. Part I  

Science Journals Connector (OSTI)

The application of the mass-spectrometric stable-isotope dilution technique for the determination of microgram and submicrogram quantities of boron in nuclear materials is described. An adequate...10B) is added t...

J. Marsel; D. Milivojevi?

1971-01-01T23:59:59.000Z

374

Determination of boron traces in rye grass BCR 281 by isotope dilution mass spectrometry  

Science Journals Connector (OSTI)

A method for the isotope dilution mass spectrometric (IDMS) determination of boron in rye grass at the 5 ?g...?1 level has been developed. The mass spectrometric measurements are performed using negative thermal ...

A. Lamberty; V. Holland; A. Verbruggen

1988-01-01T23:59:59.000Z

375

Engineering of Deinococcus radiodurans R1 for Bioprecipitation of Uranium from Dilute Nuclear Waste  

Science Journals Connector (OSTI)

...February 15, 2007 ERRATUM ERRATUM Engineering of Deinococcus radiodurans R1 for Bioprecipitation of Uranium from Dilute Nuclear Waste Deepti Appukuttan Amara Sambasiva Rao Shree Kumar Apte Molecular Biology Division, Bhabha Atomic Research Centre...

Deepti Appukuttan; Amara Sambasiva Rao; Shree Kumar Apte

2007-02-15T23:59:59.000Z

376

Structural, Optical and Magnetic Properties of Mn-doped CdS Diluted Magnetic Semiconductor Nanoparticles  

Science Journals Connector (OSTI)

Diluted magnetic CdS:Mn nanoparticles were synthesized by the aqueous...2+) concentrations (x...=710atom%) at room temperature in nitrogen atmosphere and capped with Thiogelycerol. The X-ray diffraction patter...

S. Salimian; S. Farjami Shayesteh

2012-08-01T23:59:59.000Z

377

New materials for methane capture from dilute and medium-concentration...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

New materials for methane capture from dilute and medium-concentration sources Previous Next List J. Kim, A. Maiti, L.-C. Lin, J. K. Stolaroff, B. Smit, and R. D. Aines, Nature...

378

An algorithm for U-Pb isotope dilution data reduction and uncertainty propagation  

E-Print Network [OSTI]

High-precision U-Pb geochronology by isotope dilution-thermal ionization mass spectrometry is integral to a variety of Earth science disciplines, but its ultimate resolving power is quantified by the uncertainties of ...

McLean, Noah Morgan

379

Dendritic cells: sensors of extreme antigen dilutions and role in immunity against Salmonella typhimurium infections  

E-Print Network [OSTI]

The intention of the work described in this thesis was to identify whether extremely high dilutions of antigen can induce changes in dendritic cell maturation and dendritic cell ability to initiate immune responses. ...

Zienkiewicz, Dimitrios Tomasz

2010-01-01T23:59:59.000Z

380

Multivariate analysis of homogeneous nucleation rate measurements. Nucleation in the p-toluic acid/sulfuric acid/water system  

E-Print Network [OSTI]

occur through various mecha- nisms of gas to particle conversion.1 Early models were lim- ited almost to be important for applications exceeds the predic- tive capability of phenomenological nucleation theories in

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Sulfur polymer cement for macroencapsulation of mixed waste debris  

SciTech Connect (OSTI)

In FY 1997, the US DOE Mixed Waste Focus Area (MWFA) sponsored a demonstration of the macroencapsulation of mixed waste debris using sulfur polymer cement (SPC). Two mixed wastes were tested--a D006 waste comprised of sheets of cadmium and a D008/D009 waste comprised of lead pipes and joints contaminated with mercury. The demonstration was successful in rendering these wastes compliant with Land Disposal Restrictions (LDR), thereby eliminating one Mixed Waste Inventory Report (MWIR) waste stream from the national inventory.

Mattus, C.H.

1998-06-01T23:59:59.000Z

382

Removal of sulfur and nitrogen containing pollutants from discharge gases  

DOE Patents [OSTI]

Oxides of sulfur and of nitrogen are removed from waste gases by reaction with an unsupported copper oxide powder to form copper sulfate. The resulting copper sulfate is dissolved in water to effect separation from insoluble mineral ash and dried to form solid copper sulfate pentahydrate. This solid sulfate is thermally decomposed to finely divided copper oxide powder with high specific surface area. The copper oxide powder is recycled into contact with the waste gases requiring cleanup. A reducing gas can be introduced to convert the oxide of nitrogen pollutants to nitrogen.

Joubert, James I. (Pittsburgh, PA)

1986-01-01T23:59:59.000Z

383

Study of Lean Premixed Methane Combustion with CO2 Dilution under Gas Turbine Conditions  

Science Journals Connector (OSTI)

In gas turbines, high air dilution is used in order to keep the turbine inlet temperature (TIT)(7) below the metallurgical temperature limit of the first turbine stages. ... It was shown that CO2 dilution could be an efficient method for increasing CO2 concentration in exhaust gas, thus making its capture easier. ... Efforts were focused on the impacts on cycle efficiency, combustion, gas turbine components, and cost. ...

Stphanie de Persis; Gilles Cabot; Laure Pillier; Iskender Gkalp; Abdelakrim Mourad Boukhalfa

2012-12-29T23:59:59.000Z

384

The effects of an ambient salinity gradient on the dilution of dense brine jets  

E-Print Network [OSTI]

THE EFFECTS OF AN AMBIENT SALINITY GRADIENT ON THE DILUTION OF DENSE BRINE JETS A Thesis by GARY WAYNE MCCULLOUGH Submitted to the Graduate College of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER... OF SCIENCE December 1986 Major Subject: Ocean Engineering THE EFFECTS OF AN AMBIENT SALINITY GRADIENT ON THE DILUTION OF DENSE BRINE JETS A Thesis by GARY NAYNE MCCULLOUGH Approved as to style and content by: Robert E. Randall (Chair of Committee...

McCullough, Gary Wayne

2012-06-07T23:59:59.000Z

385

Microcanonical simulation of the site-diluted three-dimensional Ising model  

Science Journals Connector (OSTI)

We use a microcanonical simulation to obtain the phase diagram in the temperature-concentration space of the three-dimensional site-diluted Ising model, for concentrations of magnetic atoms in the range 1?p?0.4. The temperature and concentration dependence of the magnetization, internal energy, and specific heat are calculated on 323232 lattices. The resulting phase diagram agrees well with recent Monte Carlo simulations and extends the numerical estimates up to the regime of strong dilution.

Andria A. de Alcntara, Adauto J. F. de Souza, and F. G. Brady Moreira

1994-04-01T23:59:59.000Z

386

The effect of dilution on the gas retention behavior of Tank 241-SY- 103 waste  

SciTech Connect (OSTI)

Twenty-five of the 177 underground waste storage tanks on the Hanford Site have been placed on the Flammable Gas watch list. These 25 tanks, containing high-level waste generated during plutonium and uranium processing, have been identified as potentially capable of accumulating flammable gases above the lower flammability limit (Babad et al. 1991). In the case of Tanks 241-SY-101 and 241-SY-103, it has been proposed that diluting the tank waste may mitigate this hazard (Hudson et al. 1995; Stewart et al. 1994). The effect of dilution on the ability of waste from Tank 241-SY-103 to accumulate gas was studied at Pacific Northwest National Laboratory. A similar study has been completed for waste from Tank 241-SY-101 (Bredt et al. 1995). Because of the additional waste-storage volume available in Tank 241-SY-103 and because the waste is assumed to be similar to that currently in Tank 241-SY-101, Tank 241-SY-103 became the target for a demonstration of passive mitigation through in-tank dilution. In 1994, plans for the in-tank dilution demonstration were deferred pending a decision on whether to pursue dilution as a mitigation strategy. However, because Tank 241-SY-103 is an early retrieval target, determination of how waste properties vary with dilution will still be required.

Bredt, P.R.; Tingey, S.M.

1996-01-01T23:59:59.000Z

387

ULTRA-LOW SULFUR REDUCTION EMISSION CONTROL DEVICE/DEVELOPMENT OF AN ON-BOARD FUEL SULFUR TRAP  

SciTech Connect (OSTI)

Honeywell is actively working on a 3-year program to develop and demonstrate proof-of-concept for an ''on-vehicle'' desulfurization fuel filter for heavy-duty diesel engines. Integration of the filter into the vehicle fuel system will reduce the adverse effects sulfur has on post combustion emission control devices such as NO{sub x} adsorbers. The NO{sub x} adsorber may be required to meet the proposed new EPA Tier II and ''2007-Rule'' emission standards. The proposed filter concept is based on Honeywell's reactive filtration technology and experience in liquids handling and conditioning. A regeneration and recycling plan for the spent filters will also be examined. We have chosen to develop and demonstrate this technology based on criteria set forth for a heavy duty CIDI engine system because it represents a more challenging set of conditions of service intervals and overall fuel usage over light duty systems. It is anticipated that the technology developed for heavy-duty applications will be applicable to light-duty as well. Further, technology developed under this proposal would also have application for the use of liquid based fuels for fuel cell power generation. The program consists of four phases. Phase I will focus on developing a concept design and analysis and resolution of technical barriers concerning removal of sulfur-containing species in low sulfur fuels. In Phase II we will concentrate on prototype filter design and preparation followed by qualification testing of this component in a fuel line application. Phase III will study life cycle and regeneration options for the spent filter. Phase IV will focus on efficacy and life testing and component integration. The project team will include a number of partners, with Honeywell International as the prime contractor. The partners include an emission control technology developer (Honeywell International), a fuel technology developer (Marathon Ashland Petroleum), a catalyst technology developer (Johnson Matthey), a CIDI engine manufacturer (Mack Trucks Inc.), a filter recycler (American Wastes Industries), and a low-sulfur fuel supplier (Equilon, a joint venture between Shell and Texaco).

Ron Rohrbach; Gary Zulauf; Tim Gavin

2003-04-01T23:59:59.000Z

388

Availability of heavy fuel oils by sulfur levels, February 1981  

SciTech Connect (OSTI)

This monthly report includes a narrative analysis of the status of the United States' total new supply of heavy fuel oils, with an emphasis on sulfur levels. Tables detail refinery production, stocks, and imports of residual fuel oil and No. 4 fuel oil by sulfur content. All data except stock figures are reported on a monthly and on a year-to-date basis; stock data are reported on an end-of-current-month basis. Units of measure are thousands of barrels. Stocks held at refineries and bulk terminals and refinery production are given by Petroleum Administration for Defense (PAD) and Refinery Districts. Imports are given by PAD District, by country or origin, and by importing state. Waterborne movements from PAD District III to other districts are detailed for the most recent month only. The December issue repeats the seven major tables with final data in all categories for the previous calendar year. This report was previously published by the Bureau of Mines in the Minerals Industries Surveys Series under the same title. 2 figs., 13 tabs.

Wolfrey, J.

1981-10-15T23:59:59.000Z

389

Availability of heavy fuel oils by sulfur levels, March 1981  

SciTech Connect (OSTI)

This monthly report includes a narrative analysis of the status of the United States' total new supply of heavy fuel oils, with an emphasis on sulfur levels. Tables detail refinery production, stocks, and imports of residual fuel oil and No. 4 fuel oil by sulfur content. All data except stock figures are reported on a monthly and on a year-to-date basis; stock data are reported on an end-of-current-month basis. Units of measure are thousands of barrels. Stocks held at refineries and bulk terminals and refinery production are given by Petroleum Administration for Defense (PAD) and Refinery Districts. Imports are given by PAD District, by country of origin, and by importing state. Waterborne movements from PAD District III to other districts are detailed for the most recent month only. The December issue repeats the seven major tables with final data in all categories for the previous calendar year. This report was previously published by the Bureau of Mines in the Minerals Industries Survey Series under the same title. 2 figs., 13 tabs.

Wolfrey, J.

1981-10-15T23:59:59.000Z

390

Availability of heavy fuel oils by sulfur level, August 1981  

SciTech Connect (OSTI)

A narrative analysis of the status of the United States' total new supply of heavy fuel oils, is given with emphasis on sulfur levels. Tables detail refinery production, stocks, and imports of residual fuel oil and No. 4 fuel oil by sulfur content. All data except stock figures are reported on a monthly and on a year-to-date basis; stock data are reported on an end-of-current-month basis. Units of measure are thousands of barrels. Stocks held at refineries and bulk terminals and refinery production are given by Petroleum Administration for Defense (PAD) and Refinery Districts. Imports are given by PAD District, by country of origin, and by importing State. Waterborne movements from PAD District III to other districts are detailed for the most recent month only. This report was previously published by the Bureau of Mines in the Minerals Industries Surveys Series under the same title. Publication was discontinued with the December 1981 issue. 1 figure, 14 tables.

Wolfrey, J.

1981-01-01T23:59:59.000Z

391

Availability of heavy fuel oils by sulfur level, October 1981  

SciTech Connect (OSTI)

A narrative analysis of the status of the United States' total new supply of heavy fuel oils, is given with emphasis on sulfur levels. Tables detail refinery production, stocks, and imports of residual fuel oil and No. 4 fuel oil by sulfur content. All data except stock figures are reported on a monthly and on a year-to-date basis; stock data are reported on an end-of-current-month basis. Units of measure are thousands of barrels. Stocks held at refineries and bulk terminals and refinery production are given by Petroleum Administration for Defense (PAD) and refinery Districts. Imports are given by PAD District, by country of origin, and by importing State. Waterbone movements from PAD District III to other districts are detailed for the most recent month only. This report was previously published by the Bureau of Mines in the Minerals Industries Surveys Series under the same title. Publication was discontinued with the December 1981 issue. 1 figure, 14 tables.

Wolfrey, J.

1981-01-01T23:59:59.000Z

392

Extracellular iron-sulfur precipitates from growth of Desulfovibrio desulfuricans  

SciTech Connect (OSTI)

The authors have examined extracellular iron-bearing precipitates resulting from the growth of Desulfovibrio desulfuricans in a basal medium with lactate as the carbon source and ferrous sulfate. Black precipitates were obtained when D. desulfuricans was grown with an excess of FeSO{sub 4}. When D. desulfuricans was grown under conditions with low amounts of FeSO{sub 4}, brown precipitates were obtained. The precipitates were characterized by iron K-edge XAFS (X-ray absorption fine structure), {sup 57}Fe Moessbauer-effect spectroscopy, and powder X-ray diffraction. Both were noncrystalline and nonmagnetic (at room temperature) solids containing high-spin Fe(III). The spectroscopic data for the black precipitates indicate the formation of an iron-sulfur phase with 6 nearest S neighbors about Fe at an average distance of 2.24(1) {angstrom}, whereas the brown precipitates are an iron-oxygen-sulfur phase with 6 nearest O neighbors about Fe at an average distance of 1.95(1) {angstrom}.

Antonio, M. R.; Tischler, M. L.; Witzcak, D.

1999-12-20T23:59:59.000Z

393

Demonstration of Mixed Waste Debris Macroencapsulation Using Sulfur Polymer Cement  

SciTech Connect (OSTI)

This report covers work performed during FY 1997 as part of the Evaluation of Sulfur Polymer Cement Fast-Track System Project. The project is in support of the ``Mercury Working Group/Mercury Treatment Demonstrations - Oak Ridge`` and is described in technical task plan (TTP) OR-16MW-61. Macroencapsulation is the treatment technology required for debris by the U.S. Environmental Protection Agency Land Disposal Restrictions (LDR) under the Resource Conservation and Recovery Act. Based upon the results of previous work performed at Oak Ridge, the concept of using sulfur polymer cement (SPC) for this purpose was submitted to the Mixed Waste Focus Area (MWFA). Because of the promising properties of the material, the MWFA accepted this Quick Win project, which was to demonstrate the feasibility of macroencapsulation of actual mixed waste debris stored on the Oak Ridge Reservation. The waste acceptance criteria from Envirocare, Utah, were chosen as a standard for the determination of the final waste form produced. During this demonstration, it was shown that SPC was a good candidate for macroencapsulation of mixed waste debris, especially when the debris pieces were dry. The matrix was found to be quite easy to use and, once the optimum operating conditions were identified, very straightforward to replicate for batch treatment. The demonstration was able to render LDR compliant more than 400 kg of mixed wastes stored at the Oak Ridge National Laboratory.

Mattus, C.H.

1998-07-01T23:59:59.000Z

394

Acid-producing potential of the various lithic units associated with the mining of coal. Technical completion report  

SciTech Connect (OSTI)

A collection of the seven different potentially toxic lithotypes encountered in the mining of coal were collected for five coals in 18 mines over a 5 county area in northern West Virginia for a total of 89 samples. Each sample was subjected to total sulfur analysis and to the soxhlet extraction/oven reoxidation procedure devised by the authors for the evaluation of an acid-production rate constant, alpha. The data show that the samples with the lowest sulfur contents have the highest acid production rate constants.

Renton, J.J.; Stiller, A.H.

1986-01-01T23:59:59.000Z

395

Chemical and radiation stability of poly (ethylene terephthalate)-polyacrylic acid graft copolymers  

SciTech Connect (OSTI)

The authors have studied variations of the deformation and strength properties of PETP graft copolymers with various PAA contents under the influence of hydrochloric and sulfuric acid solutions of various concentrations, and of Co 60 gamma radiation. It is shown that graft PETP-PAA copolymers are stable in aqueous hydrochloric and sulfuric acid solutions and, therefore, they can be regenerated by acid treatment when used as cation-exchangers. There is a correlation between the degree of retention of the deformation and strength properties of graft PETP-PAA fibers under the influence of acids and ionizing radiations and the energy of molecular interaction of the macromolecular chains in the amorphous PETP phase.

Osipenko, I.F.; Martinovich, V.I.; Prokopchuk, N.P.

1986-09-01T23:59:59.000Z

396

Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis  

E-Print Network [OSTI]

The oxidation of SO[subscript 2] to sulfate is a key reaction in determining the role of sulfate in the environment through its effect on aerosol size distribution and composition. Sulfur isotope analysis has been used to ...

Harris, E.

397

A composite material of uniformly dispersed sulfur on reduced graphene oxide: Aqueous one-pot synthesis, characterization and excellent performance as the cathode in rechargeable lithium-sulfur batteries  

Science Journals Connector (OSTI)

Sulfur-reduced graphene oxide composite (SGC) materials with uniformly dispersed sulfur on reduced graphene oxide sheets have been prepared by a ... the simultaneous oxidation of sulfide and reduction of graphene

Hui Sun; Gui-Liang Xu; Yue-Feng Xu; Shi-Gang Sun; Xinfeng Zhang

2012-10-01T23:59:59.000Z

398

Separation and Detection of Sulfur-Containing Anions Using Single-Column Ion Chromatography  

Science Journals Connector (OSTI)

......principal sulfur-containing anions in oil shale retort by-product waters are separated...electrochemical detection in some of the oil shale retort by-product water matrices...principal sulfur-containing anions in oil shale retort by-product waters are separated......

Richard E. Poulson; Harry M. Borg

1987-09-01T23:59:59.000Z

399

Quantitative Determination of Aliphatic Sulfur-Containing Additives by Pyrolysis-Gas Chromatography  

Science Journals Connector (OSTI)

......pyrolysis (7), infrared (8), combustion to SO4 = with subsequent determination...Drushel. The Analytical Chemistry of Sulfur and Its Compounds...London, p. 358. Sulfur in Coal and Coke by the Bomb Washing...organic materials by oxygen bomb combustion. Anal. Chem. 33:1760......

J.W. Sinclair; L. Schall; N.T. Crabb

1980-01-01T23:59:59.000Z

400

The sulfur content of volcanic gases on Mars Fabrice Gaillard, a  

E-Print Network [OSTI]

principles, we model here the likely sulfur contents of (1) the martian and terrestrial mantles and (2 a denser atmosphere are shown to be dominated by CO ± CO2 and H2 ± H2O species, depending on fO2, sulfur by H2S, which should have favored the acidification of any persistent water layer. The calculated

Boyer, Edmond

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Toxicology Studies on Lewisite and Sulfur Mustard Agents: Subchronic Toxicity of Sulfur Mustard (HD) In Rats Final Report  

SciTech Connect (OSTI)

Occupational health standards have not been established for sulfur mustard [bis(2- chlorethyl)-sulfide], a strong alkylating agent with known mutagenic properties. Seventytwo Sprague-Dawley rats of each sex, 6-7 weeks old, were divided into six groups (12/group/ sex) and gavaged with either 0, 0.003 , 0.01 , 0.03 , 0.1 or 0.3 mg/kg of sulfur mustard in sesame oil 5 days/week for 13 weeks. No dose-related mortality was observed. A significant decrease (P ( 0.05) in body weight was observed in both sexes of rats only in the 0.3 mg/kg group. Hematological evaluations and clinical chemistry measurements found no consistent treatment-related effects at the doses studied. The only treatment-related lesion associated with gavage exposure upon histopathologic evaluation was epithelial hyperplasia of the forestomach of both sexes at 0.3 mg/kg and males at 0.1 mg/kg. The hyperplastic change was minimal and characterized by cellular disorganization of the basilar layer, an apparent increase in mitotic activity of the basilar epithelial cells, and thickening of the epithelial layer due to the apparent increase in cellularity. The estimated NOEL for HD in this 90-day study is 0.1 mg/kg/day when administered orally.

Sasser, L. B.; Miller, R. A.; Kalkwarf, D, R.; Buschbom, R. L.; Cushing, J. A.

1989-06-30T23:59:59.000Z

402

Population, Economy and Energy Uses Influence on Sulfur Emissions in the United States Since 1900  

E-Print Network [OSTI]

This paper seeks to identify how changes in population, economic activity, and energy use have influenced sulfur emissions during this century. A linear model is presented which characterizes sulfur emissions as the product of these driving forces...

Kissock, J. K.; Husar, R. B.

403

Nitrous oxide as a substitute for sulfur hexafluoride in the ANSI/ASHRAE 110 Method of hood performance evaluation  

E-Print Network [OSTI]

The ANSI/ASHRAE 110 Method is the standard test for laboratory hood containment performance. Sulfur hexafluoride is specified as the gas most suitable for this test and is most commonly used. Sulfur hexafluoride use has ...

Guffey, Eric J. (Eric Jemison)

2011-01-01T23:59:59.000Z

404

Conversion of biomass to organic acid using the rumen bacteria Bacteroides succinogenes  

E-Print Network [OSTI]

of MASTER OF SCIENCE August 1992 Major Subject: Agricultural Engineering CONVERSION OF BIOMASS TO ORGANIC ACID USING THE RUMEN BACTERIA Bacreroi des succi nogenes A thesis by TSUEY-ER LO Approved as to style and content by: lbert G ta I (Chair... concentration (A) glucose analyzer phenol-sulfuric acid method glucose concentration (B) total sugar concentration cellobiose concentration (B-A) xylose concentration (T-B) Fig. 8: Sugar analysis scheme for sorghum samples. 33 0, 6, 24, and 48...

Lo, Tsuey-er

2012-06-07T23:59:59.000Z

405

DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur  

Broader source: Energy.gov (indexed) [DOE]

DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur Distillate DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur Distillate February 1, 2011 - 12:00pm Addthis Washington, DC - The current inventory of the Northeast Home Heating Oil Reserve will be converted to cleaner burning ultra low sulfur distillate to comply with new, more stringent fuel standards by some Northeastern states, the U.S. Department of Energy (DOE) said today. The State of New York and other Northeastern states are implementing more stringent fuel standards that require replacement of high sulfur (2,000 parts per million) heating oil to ultra low sulfur fuel (15 parts per million). As a result, DOE will sell the current inventory of the Northeast

406

DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur  

Broader source: Energy.gov (indexed) [DOE]

Will Convert Northeast Home Heating Oil Reserve to Ultra Low Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur Distillate DOE Will Convert Northeast Home Heating Oil Reserve to Ultra Low Sulfur Distillate February 1, 2011 - 12:00pm Addthis Washington, DC - The current inventory of the Northeast Home Heating Oil Reserve will be converted to cleaner burning ultra low sulfur distillate to comply with new, more stringent fuel standards by some Northeastern states, the U.S. Department of Energy (DOE) said today. The State of New York and other Northeastern states are implementing more stringent fuel standards that require replacement of high sulfur (2,000 parts per million) heating oil to ultra low sulfur fuel (15 parts per million). As a result, DOE will sell the current inventory of the Northeast Home Heating Oil Reserve, a total of approximately 2 million barrels, and

407

Effect of Sulfur Compounds and Higher Homologues of Methane on Hydrogen Cyanide Production by the Andrussow Method  

Science Journals Connector (OSTI)

The influence of sulfur compounds, higher homologues of methane on the parameters ofoxidative ammonolysis of methane was studied.

N. V. Trusov

2001-10-01T23:59:59.000Z

408

Sulfur dioxide and nitrogen dioxide levels inside and outside homes and the implications on health effects research  

Science Journals Connector (OSTI)

Sulfur dioxide and nitrogen dioxide levels inside and outside homes and the implications on health effects research ...

John D. Spengler; Benjamin G. Ferris Jr.; Douglas W. Dockery; Frank E. Speizer

1979-10-01T23:59:59.000Z

409

Optical spacing effect in organic photovoltaic cells incorporating a dilute acceptor layer  

SciTech Connect (OSTI)

The addition of spacing layers in organic photovoltaic cells (OPVs) can enhance light absorption by optimizing the spatial distribution of the incident optical field in the multilayer structure. We explore the optical spacing effect in OPVs achieved using a diluted electron acceptor layer of C{sub 60}. While optical spacing is often realized by optimizing buffer layer thickness, we find that optical spacing via dilution leads to cells with similar or enhanced photocurrent. This is observed despite a smaller quantity of absorbing molecules, suggesting a more efficient use of absorbed photons. In fact, dilution is found to concentrate optical absorption near the electron donor-acceptor interface, resulting in a marked increase in the exciton diffusion efficiency. Contrasting the use of changes in thickness to engineer optical absorption, the use of dilution does not significantly alter the overall thickness of the OPV. Optical spacing via dilution is shown to be a viable alternative to more traditional optical spacing techniques and may be especially useful in the continued optimization of next-generation, tandem OPVs where it is important to minimize competition for optical absorption between individual sub-cells.

Menke, S. Matthew; Lindsay, Christopher D.; Holmes, Russell J. [Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455 (United States)

2014-06-16T23:59:59.000Z

410

Extraction, separation, and analysis of high sulfur coal  

SciTech Connect (OSTI)

The work completed this past quarter has centered around the further study and characterization of the selective desulfurization of coal through the oxidative interaction of aqueous copper chloride. The reaction of the CuCl{sub 2} with the particular model compounds is conducted at a series of reaction times and reaction temperatures. The reaction times studied were 1, 3, 6, 12, and 24 hours. The reaction temperatures studied were 50, 130, 210, and 295{degree}C. After the reaction, the organic compounds were extracted with methylene chloride. These products were then analyzed via GC/IRD/MS and SFC/SCD (sulfur chemiluminescence detector). Model Coal Compounds reacted include: tetrahydrothiophene, methyl p-tolyl sulfide, cyclohexyl mercaptan, and thiophenol. At 130{degree}C, in addition to these compounds reacting, reactions were also detected for phenyl sulfide and benzo(b)thiophene. 14 figs.

Olesik, S. (comp.)

1990-01-01T23:59:59.000Z

411

Process for sequestering carbon dioxide and sulfur dioxide  

DOE Patents [OSTI]

A process for sequestering carbon dioxide, which includes reacting a silicate based material with an acid to form a suspension, and combining the suspension with carbon dioxide to create active carbonation of the silicate-based material, and thereafter producing a metal salt, silica and regenerating the acid in the liquid phase of the suspension.

Maroto-Valer, M. Mercedes (State College, PA); Zhang, Yinzhi (State College, PA); Kuchta, Matthew E. (State College, PA); Andresen, John M. (State College, PA); Fauth, Dan J. (Pittsburgh, PA)

2009-10-20T23:59:59.000Z

412

Persistence of magnons in a site-diluted dimerized frustrated antiferromagnet  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Persistence of magnons in a site-diluted dimerized frustrated antiferromagnet Persistence of magnons in a site-diluted dimerized frustrated antiferromagnet This article has been downloaded from IOPscience. Please scroll down to see the full text article. 2011 J. Phys.: Condens. Matter 23 416003 (http://iopscience.iop.org/0953-8984/23/41/416003) Download details: IP Address: 128.219.49.9 The article was downloaded on 17/10/2011 at 17:07 Please note that terms and conditions apply. View the table of contents for this issue, or go to the journal homepage for more Home Search Collections Journals About Contact us My IOPscience IOP PUBLISHING JOURNAL OF PHYSICS: CONDENSED MATTER J. Phys.: Condens. Matter 23 (2011) 416003 (9pp) doi:10.1088/0953-8984/23/41/416003 Persistence of magnons in a site-diluted dimerized frustrated antiferromagnet M B Stone 1 , A Podlesnyak 1 , G Ehlers

413

Evaluation of feeds for melt and dilute process using an analytical hierarchy process  

SciTech Connect (OSTI)

Westinghouse Savannah River Company was requested to evaluate whether nuclear materials other than aluminum-clad spent nuclear fuel should be considered for treatment to prepare them for disposal in the melt and dilute facility as part of the Treatment and Storage Facility currently projected for construction in the L-Reactor process area. The decision analysis process used to develop this analysis considered many variables and uncertainties, including repository requirements that are not yet finalized. The Analytical Hierarchy Process using a ratings methodology was used to rank potential feed candidates for disposition through the Melt and Dilute facility proposed for disposition of Savannah River Site aluminum-clad spent nuclear fuel. Because of the scoping nature of this analysis, the expert team convened for this purpose concentrated on technical feasibility and potential cost impacts associated with using melt and dilute versus the current disposition option. This report documents results of the decision analysis.

Krupa, J.F.

2000-03-22T23:59:59.000Z

414

MOBILE SYSTEMS FOR DILUTION OF HIGHLY ENRICHED URANIUM AND URANIUM CONTAINING COMPONENTS  

SciTech Connect (OSTI)

A mobile melt-dilute (MMD) module for the treatment of aluminum research reactor spent fuel is being developed. The process utilizes a closed system approach to retain fission products/gases inside a sealed canister after treatment. The MMD process melts and dilutes spent fuel with depleted uranium to obtain a fissile fraction of less than 0.2. The final ingot is solidified inside the sealed canister and can be stored safely either wet or dry until final disposition or reprocessing. The MMD module can be staged at or near the research reactor fuel storage sites to facilitate the melt-dilute treatment of the spent fuel into a stable non-proliferable form.

Adams, T

2007-05-02T23:59:59.000Z

415

Three-Dimensional Flower-Shaped Activated Porous Carbon/Sulfur Composites as Cathode Materials for LithiumSulfur Batteries  

Science Journals Connector (OSTI)

After the active sulfur impregnation, both the FESEM images (Figure 1e,f) and TEM images (Figure 2c) of the FA-PC/S composite demonstrate a flower-shaped 3D superstructure similar to the original FA-PC material. ... Early on, carbonaceous materials dominated the anode and hence most of the possible improvements in the cell were anticipated at the cathode terminal; on the other hand, major developments in anode materials made in the last portion of the decade with the introduction of nanocomposite Sn/C/Co alloys and Si-C composites have demanded higher capacity cathodes to be developed. ... The photodecompn. of methyl orange indicates that such ZnO superstructures possess excellent photocatalytic activity. ...

Lan Zhou; Tao Huang; Aishui Yu

2014-09-19T23:59:59.000Z

416

Coexistence of Ising cluster excitations and intracluster excitations in diluted Ising magnets  

Science Journals Connector (OSTI)

To elucidate magnetic excitations in diluted Ising magnets over the entire magnetic concentration, we performed neutron inelastic-scattering experiments on two-dimensional diluted Ising magnets Rb2CocMg1-cF4, (c=0.1,0.2,0.3,0.4,0.5,0.58), whose magnetic concentration was below the percolation threshold. We found that Ising cluster excitations and intracluster excitations coexist over the entire concentration region, and that the scattering intensities from these different origins change with the concentration.

Hironobu Ikeda and Kenji Ohoyama

1992-04-01T23:59:59.000Z

417

Prompt neutron decay constants in uranium diluted with matrix material systems  

SciTech Connect (OSTI)

Rossi-Alpha measurements were performed on uranium diluted with matrix material systems to determine the prompt neutron decay constants. These constants represent an eigenvalue characteristic of these particular critical assemblies, which can be experimentally measured by the Rossi-Alpha or pulse neutron source techniques and calculated by a deterministic or Monte Carlo method. In the measurements presented in this summary, highly enriched foils diluted in various X/{sup 235}U ratios with polyethylene and SiO{sub 2}, and polyethylene and aluminum were assembled to a high multiplication and the prompt neutron decay constants were obtained by the Rossi-Alpha technique.

Sanchez, R. G. (Rene G.); Loaiza, D. J. (David J.); Brunson, G. S. (Glenn S.)

2001-01-01T23:59:59.000Z

418

Long-Range Order of Dilute Rare-Earth Spin Ensemble Revealed with Cavity QED  

E-Print Network [OSTI]

This work demonstrates strong coupling regime between an Erbium ion spin ensemble and Hybrid Cavity-Whispering Gallery Modes in a Yttrium Aluminium Garnet dielectric crystal. Coupling strengths of $220$~MHz and mode quality factors in excess of $10^6$ are demonstrated. The spin ensemble exhibits memory effects as well as remnant magnetisation. A qualitative change of system magnetic field response between 190 and 445mK is interpreted as a phase transition. This work is the first observation of the long range order in an ensemble of dilute Rare-Earth impurities similar to the phenomenon of dilute ferromagnetism in semiconductors.

W. G. Farr; M. Goryachev; J. M. le Floch; P. Bushev; M. E. Tobar

2014-11-29T23:59:59.000Z

419

Galvanic corrosion of structural aluminum coupled with mild steel in a dilute sodium dichromate electrolyte  

E-Print Network [OSTI]

or the requirement for' the deqr, e of MASTER OF SCIl-NCI= Jaruary IgiO Major Sub ect: Civii I. ngineering GALVANIC CORROSION GF STRUCTURAI. ALUMINUM COUPLED WITH MILD STI:EL IN A DILUTE SODIUii DICIIROMA1'E ELECTROLTTE A Thesis ROBERT FRANKLIN FORD, JR.... Approved as to style and content by: + ~J Co-Chairman of Commii:t C Co-Chair n of Committe~e Member+ I Head of D=p rtm t) Januar; IDIO ABSTRACT Calvanic Corrosion of Structural Aluminum Coup'led with Mild Steel in a Dilute Sodium Dichromate...

Ford, Robert Franklin

2012-06-07T23:59:59.000Z

420

Method for Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Sequestering Carbon Dioxide and Sulfur Dioxide Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 7,922,792 entitled "Method for Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams." Disclosed in this patent is the invention of a neutralization/sequestration method that concomitantly treats bauxite residues from aluminum production processes, as well as brine wastewater from oil and gas production processes. The method uses an integrated approach that coincidentally treats multiple industrial waste by-product streams. The end results include neutralizing caustic

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Method of making a current collector for a sodium/sulfur battery  

DOE Patents [OSTI]

This specification is directed to a method of making a current collector for a sodium/sulfur battery. The current collector so-made is electronically conductive and resistant to corrosive attack by sulfur/polysulfide melts. The method includes the step of forming the current collector for the sodium/sulfur battery from a composite material formed of aluminum filled with electronically conductive fibers selected from the group of fibers consisting essentially of graphite fibers having a diameter up to 10 microns and silicon carbide fibers having a diameter in a range of 500--1,000 angstroms. 2 figs.

Tischer, R.P.; Winterbottom, W.L.; Wroblowa, H.S.

1987-03-10T23:59:59.000Z

422

The effect of sulfate sulfur on the yield and chemical composition of oats, vetch, and turnips  

E-Print Network [OSTI]

with sulfur and gypsum applications to alfalfa in Washington and Oregon. Subsequent vork showed that a large part of the ali'alfa land in Oregon vas deficient in sulfur. Experiments conducted over a period of several years on various soil types in southern... Oregon showed that, yields of ali'alf'a and cover crops could be increased from 50 percent to 1000 percent by the use of various fertilissrs containing sulfur (35). Other workers in Oregon ob- tained similar results with crops other than legumes...

Gipson, Jack Rogers

2012-06-07T23:59:59.000Z

423

Energy Dispersive X-ray Fluorescence Analysis of Sulfur in Biomass  

Science Journals Connector (OSTI)

An energy dispersive X-ray fluorescence (ED-XRF) spectroscopy method was developed to analyze low ppm level sulfur (S) in biomass feedstocks and in subsequent residues from pretreatment reactions. ... Representative biomass feedstocks and pretreatment residues were analyzed for S. ... The goal of this project was to determine whether an energy dispersive X-ray fluorescence (ED-XRF) spectroscopy method is effective in conducting sulfur analysis of woody biomass feedstocks at an appropriately useful sensitivity, especially when used to effectively monitor the extent of sulfur removal after biomass pretreatment reactions. ...

J. Michael Robinson; Staci R. Barrett; Kevin Nhoy; Rajesh K. Pandey; Joseph Phillips; Oscar M. Ramirez; Richard I. Rodriguez

2009-03-06T23:59:59.000Z

424

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents [OSTI]

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, John E. (Woodridge, IL); Jalan, Vinod M. (Concord, MA)

1984-01-01T23:59:59.000Z

425

High-temperature sorbent method for removal of sulfur-containing gases from gaseous mixtures  

DOE Patents [OSTI]

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorbtion capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, J.E.; Jalan, V.M.

1982-07-07T23:59:59.000Z

426

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents [OSTI]

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, J.E.; Jalan, V.M.

1984-06-19T23:59:59.000Z

427

Update on Transition to Ultra-Low-Sulfur Diesel Fuel (released in AEO2006)  

Reports and Publications (EIA)

On November 8, 2005, the Environmental Protection Agency (EPA) Administrator signed a direct final rule that will shift the retail compliance date for offering ultra-low sulfur diesel (ULSD) for highway use from September 1, 2006, to October 15, 2006. The change will allow more time for retail outlets and terminals to comply with the new 15 parts per million (ppm) sulfur standard, providing time for entities in the diesel fuel distribution system to flush higher sulfur fuel out of the system during the transition. Terminals will have until September 1, 2006, to complete their transitions to ULSD. The previous deadline was July 15, 2006.

2006-01-01T23:59:59.000Z

428

Definition: Lead-acid battery | Open Energy Information  

Open Energy Info (EERE)

Definition Definition Edit with form History Facebook icon Twitter icon » Definition: Lead-acid battery Jump to: navigation, search Dictionary.png Lead-acid battery A type of battery that uses plates made of pure lead or lead oxide for the electrodes and sulfuric acid for the electrolyte.[1] View on Wikipedia Wikipedia Definition Related Terms Battery, electrolyte References ↑ http://www1.eere.energy.gov/solar/solar_glossary.html Retr LikeLike UnlikeLike You like this.Sign Up to see what your friends like. ieved from "http://en.openei.org/w/index.php?title=Definition:Lead-acid_battery&oldid=487934" Category: Definitions What links here Related changes Special pages Printable version Permanent link Browse properties 429 Throttled (bot load) Error 429 Throttled (bot load)

429

COARSENING AND SELF-ORGANIZATION IN DILUTE DIBLOCK COPOLYMER MELTS AND MIXTURES  

E-Print Network [OSTI]

COARSENING AND SELF-ORGANIZATION IN DILUTE DIBLOCK COPOLYMER MELTS AND MIXTURES KARL GLASNER RUSTUM, on the other hand, is responsible for producing self-organized patterns. We construct approximations based upon incompatible [9]. Block copoly- mers, on the other hand, are inhomogeneous chain molecules composed of two

Glasner, Karl B.

430

Viscosity and longest relaxation time of semi-dilute polymer solutions. I. Good solvent  

E-Print Network [OSTI]

1185 Viscosity and longest relaxation time of semi-dilute polymer solutions. I. Good solvent M expliqués par un modèle de reptation classique. Abstract. 2014 The zero shear viscosity and longest concentration (4 c/c* 70), we find that : 2014 both the relative viscosity ~r and the longest relaxation time TR

Paris-Sud XI, Université de

431

Solvation Phenomena in Dilute Solutions: Formal, Experimental Evidence, and Modeling Implications  

SciTech Connect (OSTI)

We review the fundamentals underlying a general molecular-based formalism for the microscopic interpretation of the solvation phenomena involving sparingly soluble solutes in compressible media, an approach that hinges around the unambiguous splitting of the species correlation function integrals into short-(finite) and long-ranged (diverging) contributions at infinite dilution, where this condition is taken as the reference system for the derivation of composition expansions. Then, we invoke the formalism (a) to illustrate the well-behaved nature of the solvation contributions to the mechanical partial molecular properties of solutes at infinite dilution, (b) to guide the development of, and provide molecular-based support to, the macroscopic modeling of high-temperature dilute aqueous-electrolyte solutions, (c) to study solvation effects on the kinetic rate constants of reactions in near-critical solvents in an attempt to understand from a microscopic perspective the macroscopic evidence regarding the thermodynamic pressure effects, and (d) to interpret the microscopic mechanism behind synergistic solvation effects involving either co-solutes or co-solvents, and provide a molecular argument on the unsuitability of the van der Waals one-fluid (vdW-1f) mixing rules for the 2 description of weakly attractive solutes in compressible solvents. Finally, we develop thermodynamically consistent perturbation expansions, around the infinite dilution reference, for the species residual properties in binary and ternary mixtures, and discuss the theoretical and modeling implications behind ad hoc first-order truncated expansions.

Chialvo, Ariel A [ORNL

2013-01-01T23:59:59.000Z

432

Henry's law, surface tension, and surface adsorption in dilute binary mixtures  

E-Print Network [OSTI]

Henry's law, surface tension, and surface adsorption in dilute binary mixtures Akira Onukia. The solute partitioning between gas and liquid Henry's law and the surface tension change are discussed fraction X and the temperature-derivative / T cx,p of the surface tension at fixed pressure p

433

hal00272925, SURFACE TENSION IN THE DILUTE ISING MODEL. THE WULFF  

E-Print Network [OSTI]

hal­00272925, version 1 ­ 14 Apr 2008 SURFACE TENSION IN THE DILUTE ISING MODEL. THE WULFF CONSTRUCTION. MARC WOUTS Abstract. We study the surface tension and the phenomenon of phase coexistence in probability (with respect to random couplings) of surface tension and analyze its large deviations : upper

Paris-Sud XI, Université de

434

Impact of N2 dilution on combustion and emissions in a spark ignition CNG engine  

Science Journals Connector (OSTI)

Abstract In order to reduce \\{NOx\\} (nitrogen oxides) emissions, N2 (nitrogen) was introduced as dilution gas to dilute mixture with a specially-designed injection device. The impacts of varying N2 DR (dilution ratio) on the combustion and the exhaust emissions were investigated, including engine heat release rate, indicator diagram, NOx, CO (carbon monoxide), THC (total hydrocarbon) emissions and so on. For this study, a modified 6.6L CNG (compressed natural gas) engine was tested and N2 was injected into the end of intake manifold by a specially-designed device. The results showed that N2 dilution has a significant influence on the combustion and the exhaust emissions. With the rise of N2 DR, the maximum of pressure in cylinder and the maximum of heat release rate exhibited decrease trends, the centre of heat release curve showed a moving backward tendency. Higher N2 DR exhibited lower \\{NOx\\} (1781%) emissions, but higher emissions of THC (378%) and CO (128%). The change of BSFC (brake specific fuel consumption) can be ignored with N2 DR no more than 167%. Satisfactory results can be obtained, with lower \\{NOx\\} (31%) emissions, lower BSFC (0.5%), and relatively higher THC (6%) and CO (1%) emissions, when N2 DR is 67%.

Zhongshu Wang; Hongbin Zuo; Zhongchang Liu; Weifeng Li; Huili Dou

2014-01-01T23:59:59.000Z

435

Modeling dilute sediment suspension using large-eddy simulation with a dynamic mixed model  

E-Print Network [OSTI]

Modeling dilute sediment suspension using large-eddy simulation with a dynamic mixed model Yi Transport of suspended sediment in high Reynolds number channel flows Re=O 600 000 is simulated using large-eddy simulation along with a dynamic-mixed model DMM . Because the modeled sediment concentration is low

Fringer, Oliver B.

436

Spin-polarized current oscillations in diluted magnetic semiconductor multiple quantum wells Manuel Bejar,1  

E-Print Network [OSTI]

. The transport properties of Mn-based heterostructures have been studied10 including miniband transportSpin-polarized current oscillations in diluted magnetic semiconductor multiple quantum wells Manuel. The spin polarization oscillates in both magnetic and nonmagnetic quantum wells and the time average

Sánchez, David

437

Tuning the optical properties of dilute nitride site controlled quantum dots  

SciTech Connect (OSTI)

We show that deterministic control of the properties of pyramidal site-controlled quantum dots (QD) could be achieved by exposing the QD layer to nitrogen precursor unsymmetrical dimethylhydrazine (UDMHy). The properties that could be tuned include an expected emission reduction in dilute nitride materials, excitonic pattern (biexciton binding energy) and improved carrier confinement potential symmetry (reduced fine-structure splitting)

Juska, G.; Dimastrodonato, V.; Mereni, L. O.; Gocalinska, A.; Pelucchi, E. [Tyndall National Institute, University College Cork, Lee Maltings, Cork (Ireland)

2013-12-04T23:59:59.000Z

438

Storage of Dressed Chinook Salmon, Oncorhynchus tshawytscha, in Refrigerated Freshwater, Diluted Seawater, Seawater, and in Ice  

E-Print Network [OSTI]

Storage of Dressed Chinook Salmon, Oncorhynchus tshawytscha, in Refrigerated Freshwater, Diluted Seawater, Seawater, and in Ice M. N. BRONSTEIN, R. J. PRICE, E. M. STRANGE, E. F. MELVIN, C. M. DEWEES mixtures of seawater and freshwater, refrigerated seawater, and chilled mixtures of seawater and ice

439

Noise-Induced Intermittency in a Convecting Dilute Solution of He3 in Superfluid He4  

Science Journals Connector (OSTI)

Measurements on a convecting dilute He3-superfluid-He4 solution show a transition from periodic to chaotic behavior via intermittency. In a region near but below the onset of intermittency, injection of external noise greater than some threshold value induces chaos.

H. Haucke; R. E. Ecke; Y. Maeno; J. C. Wheatley

1984-11-26T23:59:59.000Z

440

The effect of iron dilution on strength of nickel/steel and Monel/steel welds  

SciTech Connect (OSTI)

The weld strength, as a function of iron content, for nickel/steel and Monel/steel welds was determined. Samples were prepared using a Gas Metal Arc (GMAW) automatic process to weld steel plate together with nickel or Monel to produce a range of iron contents typical of weld compositions. Tensile specimens of each iron content were tested to obtain strength and ductility measurements for that weld composition. Data indicate that at iron contents of less than 20% iron in a nickel/steel weld, the weld fails at the weld interface, due to a lack of fusion. Between 20% and 35% iron, the highest iron dilution that could be achieved in a nickel weld, the welds were stronger than the steel base metal. This indicates that a minimum amount of iron dilution (20%) is necessary for good fusion and optimum strength. On the other hand for Monel/steel welds, test results showed that the welds had good strength and integrity between 10% and 27% iron in the weld. Above 35% iron, the welds have less strength and are more brittle. The 35% iron content also corresponds to the iron dilution in Monel welds that has been shown to produce an increase in corrosion rate. This indicates that the iron dilution in Monel welds should be kept below 35% iron to maximize both the strength and corrosion resistance. 2 refs., 6 figs., 3 tabs.

Fout, S.L.; Wamsley, S.D.

1983-03-28T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

Secondary Capture of Chlorine and Sulfur during Thermal Conversion of Biomass  

Science Journals Connector (OSTI)

Secondary Capture of Chlorine and Sulfur during Thermal Conversion of Biomass ... Six biomasses with different chemical compositions ... ... Therefore, different types of woody biomass and biomass residues (shells) were thermochemically converted in an atmospheric flow ... ...

Jacob N. Knudsen; Peter A. Jensen; Weigang Lin; Kim Dam-Johansen

2005-02-10T23:59:59.000Z

442

Structural analysis of sulfur in natural rubber using X-ray absorption near-edge spectroscopy  

Science Journals Connector (OSTI)

The opportunity to employ X-ray absorption near-edge spectroscopy techniques to investigate the alteration of the structural properties of sulfur in various vulcanized rubber sheets is presented.

Pattanasiriwisawa, W.

2008-07-11T23:59:59.000Z

443

Cost-benefit analysis of ultra-low sulfur jet fuel  

E-Print Network [OSTI]

The growth of aviation has spurred increased study of its environmental impacts and the possible mitigation thereof. One emissions reduction option is the introduction of an Ultra Low Sulfur (ULS) jet fuel standard for ...

Kuhn, Stephen (Stephen Richard)

2010-01-01T23:59:59.000Z

444

Table 17. U.S. No. 2 Diesel Fuel Prices by Sulfur Content and...  

Gasoline and Diesel Fuel Update (EIA)

EIA-782B, "Resellers'Retailers' Monthly Petroleum Product Sales Report." 17. U.S. No. 2 Diesel Fuel Prices by Sulfur Content and Sales Type Energy Information Administration ...

445

E-Print Network 3.0 - aromatic sulfur compounds Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

distribution in the oil fractions obtained by thermal cracking of Jordanian El-Lajjun oil Shale Summary: . It has been also shown that most of the sulfur compounds in oil shale are...

446

Infrared and Raman Spectra of a Sulfur-resistant Methanation Catalyst  

Science Journals Connector (OSTI)

The infrared and Raman spectra of a sulfur-resistant NiO/Cr2O3/MgSiO3 methanation catalyst are presented and compared to the spectra of the catalyst...

Stencel, J M; Bradley, E B; Brown, Fred R

1980-01-01T23:59:59.000Z

447

Diesel Emission Control -- Sulfur Effects (DECSE) Program; Phase I Interim Data Report No. 1  

SciTech Connect (OSTI)

The Diesel Emission Control-Sulfur Effects (DECSE) is a joint government/industry program to determine the impact of diesel fuel sulfur levels on emission control systems whose use could lower emissions of nitrogen oxides (NO{sub x}) and particulate matter (PM) from on-highway trucks in the 2002--2004 model years. Phase 1 of the program was developed with the following objectives in mind: (1) evaluate the effects of varying the level of sulfur content in the fuel on the emission reduction performance of four emission control technologies; and (2) measure and compare the effects of up to 250 hours of aging on selected devices for multiple levels of fuel sulfur content. This interim data report summarizes results as of August, 1999, on the status of the test programs being conducted on three technologies: lean-NO{sub x} catalysts, diesel particulate filters and diesel oxidation catalysts.

DOE; ORNL; NREL; EMA; MECA

1999-08-15T23:59:59.000Z

448

The variability of methane, nitrous oxide and sulfur hexafluoride in Northeast India  

E-Print Network [OSTI]

High-frequency atmospheric measurements of methane (CH[subscript 4]), nitrous oxide (N[subscript 2]O) and sulfur hexafluoride (SF[subscript 6]) from Darjeeling, India are presented from December 2011 (CH[subscript 4])/March ...

Chatterjee, A.

449

Effective hydrogen generation and resource circulation based on sulfur cycle system  

SciTech Connect (OSTI)

For the effective hydrogen generation from H{sub 2}S, it should be compatible that the increscent of the photocatalytic (or electrochemical) activities and the development of effective utilization method of by-products (poly sulfide ion). In this study, system integration to construct the sulfur cycle system, which is compatible with the increscent of the hydrogen and or electron energy generation ratio and resource circulation, is investigated. Photocatalytic hydrogen generation rate can be enhanced by using stratified photocatalysts. Photo excited electron can be transpired to electrode to convert the electron energy to hydrogen energy. Poly sulfide ion as the by-products can be transferred into elemental sulfur and/or industrial materials such as rubber. Moreover, elemental sulfur can be transferred into H{sub 2}S which is the original materials for hydrogen generation. By using this system integration, the sulfur cycle system for the new energy generation can be constructed.

Takahashi, Hideyuki; Mabuchi, Takashi; Hayashi, Tsugumi; Yokoyama, Shun; Tohji, Kazuyuki [Graduate School of Environmental Studies, Tohoku University 6-6-20, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan)

2013-12-10T23:59:59.000Z

450

Project Profile: Baseload CSP Generation Integrated with Sulfur-Based Thermochemical Heat Storage  

Broader source: Energy.gov [DOE]

General Atomics, under the Baseload CSP FOA, is demonstrating the engineering feasibility of using a sulfur-based thermochemical cycle to store heat from a CSP plant and support baseload power...

451

Electronic Transitions in Sulfur-Centered Radicals by Means of MSX? Calculations  

Science Journals Connector (OSTI)

Highly reactive sulfur-centered radicals, which play an important role in air pollution and in biological systems, are usually idientified by their UV/visible absorption and/or ESR spectra. Spectral informatio...

Maurizio Guerra

1990-01-01T23:59:59.000Z

452

Magnetic quenching of time-reversed light in photorefractive diluted magnetic semiconductors M. Dinu, I. Miotkowski, and D. D. Nolte  

E-Print Network [OSTI]

Magnetic quenching of time-reversed light in photorefractive diluted magnetic semiconductors M 47907-1396 Received 18 February 1998 Magnetic fields selectively quench phase conjugation during photorefractive four-wave mixing experiments in the diluted magnetic semiconductor Cd1 xMnxTe. Phase conjugation

Nolte, David D.

453

Physicochemical aspects of the adsorption of sulfur dioxide by carbon adsorbents  

Science Journals Connector (OSTI)

Literature data on the chemistry of the adsorption of sulfur dioxide on carbon adsorbents are surveyed and described systematically. The influence of various factors (the nature of the carbon matrix, the activation method, the chemistry of the adsorbent surfaces, temperature, the composition of the gas stream, etc.) on the sorption of SO2 by activated carbons and semicokes is examined. The possible ways in which sulfur dioxide interacts with the carbon surface are discussed. The bibliography includes 128 references.

Sergey A Anurov

1996-01-01T23:59:59.000Z

454

Sulfur resistance of Group VIII transition metal promoted nickel catalysts for synthesis gas methanation  

E-Print Network [OSTI]

SULFUR RESISTANCE OF GROUP VIII TRANSITION METAL PROMOTED NICKEL CATALYSTS FOR SYNTHESIS GAS METHANATION A Thesis by KELLEE HALL HAMLIN Submitted to the Graduate College of Texas AgrM University in partial fulfillment of the requirement...: Aydin Akger n (Chairman of Co 'ttee) Ahme M. Gadalla (Member) Michael . Rosynek (Member) aries D. Holland . ( ead of Department) May 1986 ABSTRACT Sulfur Resistance of Group VIII Transition Metal Promoted Nickel Catalysts For Synthesis Gas...

Hamlin, Kellee Hall

2012-06-07T23:59:59.000Z

455

A Mathematical Model for a LithiumSulfur Cell Karthikeyan Kumaresan,a,  

E-Print Network [OSTI]

S8 l is reduced to S2- in steps. For example, S8 l is reduced to S8 2- , then to S6 2- , S4 2- , S2,4 Figure 1 presents a typical experimental discharge profile at a C/50 rate C = 2.5 Ah . The lithium/sulfur Development The schematic of the lithium/sulfur cell modeled in this work is shown in Fig. 2. The cell is made

456

Development of Efficient Flowsheet and Transient Modeling for Nuclear Heat Coupled Sulfur Iodine Cyclefor Hydrogen Production  

SciTech Connect (OSTI)

The realization of the hydrogen as an energy carrier for future power sources relies on a practical method of producing hydrogen in large scale with no emission of green house gases. Hydrogen is an energy carrier which can be produced by a thermochemical water splitting process. The Sulfur-Iodine (SI) process is an example of a water splitting method using iodine and sulfur as recycling agents.

Shripad T. Revankar; Nicholas R. Brown; Cheikhou Kane; Seungmin Oh

2010-05-01T23:59:59.000Z

457

Experimental and computational investigations of sulfur-resistant bimetallic catalysts for reforming of biomass gasification products  

SciTech Connect (OSTI)

A combination of density functional theory (DFT) calculations and experimental studies of supported catalysts was used to identify H{sub 2}S-resistant biomass gasification product reforming catalysts. DFT calculations were used to search for bimetallic, nickel-based (1 1 1) surfaces with lower sulfur adsorption energies and enhanced ethylene adsorption energies. These metrics were used as predictors for H{sub 2}S resistance and activity toward steam reforming of ethylene, respectively. Relative to Ni, DFT studies found that the Ni/Sn surface alloy exhibited enhanced sulfur resistance and the Ni/Ru system exhibited an improved ethylene binding energy with a small increase in sulfur binding energy. A series of supported bimetallic nickel catalysts was prepared and screened under model ethylene reforming conditions and simulated biomass tar reforming conditions. The observed experimental trends in activity were consistent with theoretical predictions, with observed reforming activities in the order Ni/Ru > Ni > Ni/Sn. Interestingly, Ni/Ru showed a high level of resistance to sulfur poisoning compared with Ni. This sulfur resistance can be partly explained by trends in sulfur versus ethylene binding energy at different types of sites across the bimetallic surface.

Rangan, Meghana; Yung, Matthew M.; Medlin, J. William (NREL); (Colorado)

2011-11-17T23:59:59.000Z

458

Comparison of Comprehensive Two-Dimensional Gas Chromatography Coupled with Sulfur-Chemiluminescence Detector to Standard Methods for Speciation of Sulfur-Containing Compounds in Middle Distillates  

Science Journals Connector (OSTI)

......in seconds). The general elution profile was...sulfur-specific analysis of diesel oils. Comparison...different types of diesel oils by XRF and GC...and LCO, light cycle gasoil. Figure 2...components in a light cycle oil of catalytic...compounds in gasoline and diesel range process streams......

Rosario Ruiz-Guerrero; Colombe Vendeuvre; Didier Thibaut; Fabrice Bertoncini; Didier Espinat

2006-10-01T23:59:59.000Z

459

Hydrogenase of the hyperthermophile Pyrococcus furiosus is an elemental sulfur reductase or sulfhydrogenase: evidence for a sulfur-reducing hydrogenase ancestor  

Science Journals Connector (OSTI)

...polysulfide reduction/geothermal biolog/evolution...appears to be an energy-conserving reaction...The publication costs of this article...sulfur-rich, geothermal environ- ments...fact, represent an energy- conserving reaction...the Department of Energy (FG09-88ER13901...

K Ma; R N Schicho; R M Kelly; M W Adams

1993-01-01T23:59:59.000Z

460

Comparison of Comprehensive Two-Dimensional Gas Chromatography Coupled with Sulfur-Chemiluminescence Detector to Standard Methods for Speciation of Sulfur-Containing Compounds in Middle Distillates  

Science Journals Connector (OSTI)

......discussed later (16,19). For straight-run samples (SR1 and SR2, Figures...identification of C4 and C5DBTs). For straight-run samples (SR1 and SR2), the...analysis of sulfur com- pounds in gasoline range petroleum products with......

Rosario Ruiz-Guerrero; Colombe Vendeuvre; Didier Thibaut; Fabrice Bertoncini; Didier Espinat

2006-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "dilute sulfuric acid" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Acidic dissolution behavior of U containing ZrO2MgO ceramics  

SciTech Connect (OSTI)

This study explores the possibility of dissolving zirconia-magnesia inert matrix fuel containing uranium oxide as a fissile material and plutonium homolog and erbium oxide as a burnable poison with nitric and sulfuric acid as a potential first step in a reprocessing scheme. The progress of the dissolution is followed by monitoring the amount of material in solution by inductively coupled plasma-atomic emission spectroscopy, assessing the speciation of the material by time resolved laser fluorescence spectroscopy, and determining and quantifying the crystalline phases present in the remaining residue by X-ray diffraction. This study has shown a linear incongruent dissolution of the cubic zirconia phase in concentrated nitric acid under certain chemical compositions, while the magnesium oxide phase is completely soluble. In sulfuric acid uranium, erbium, and magnesium are soluble to different extents while zirconium forms a colloidal suspension that conglomerates and settles out of solution. The feasibility of the dissolution of zirconia-magnesia inert matrix fuel with nitric and sulfuric acid for reprocessing is discussed.

Kiel Holliday; Nicholas Smith; Thomas Hartmann; Gary Cerefice; Ken Czerwinski

2011-11-01T23:59:59.000Z

462

Sulfur Content, Weighted Average Refinery Crude Oil Input Qualities  

U.S. Energy Information Administration (EIA) Indexed Site

(Percent) (Percent) Type: Sulfur Content API Gravity Period: Monthly Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes Show Data By: Type Area Apr-13 May-13 Jun-13 Jul-13 Aug-13 Sep-13 View History U.S. 1.43 1.38 1.41 1.43 1.47 1.42 1985-2013 PADD 1 0.75 0.73 0.69 0.68 0.73 0.68 1985-2013 East Coast 0.67 0.66 0.61 0.63 0.66 0.57 1985-2013 Appalachian No. 1 2.0 1.72 1.52 1.40 1.55 1.74 1985-2013 PADD 2 1.42 1.34 1.44 1.46 1.61 1.49 1985-2013 Ind., Ill. and Ky. 1.45 1.36 1.47 1.56 1.75 1.67 1985-2013 Minn., Wis., N. Dak., S. Dak. 2.33 2.11 2.18 2.03 2.01 1.69 1985-2013 Okla., Kans., Mo. 0.89 0.89 0.92 0.82 0.87 0.85 1985-2013 PADD 3 1.54 1.48 1.51 1.52 1.54 1.48 1985-2013

463

Isotope shift in the sulfur electron affinity: Observation and theory  

SciTech Connect (OSTI)

The sulfur electron affinities {sup e}A(S) are measured by photodetachment microscopy for the two isotopes {sup 32}S and {sup 34}S (16 752.975 3(41) and 16 752.977 6(85) cm{sup -1}, respectively). The isotope shift in the electron affinity is found to be more probably positive, {sup e}A({sup 34}S)- {sup e}A({sup 32}S) =+0.0023(70) cm{sup -1}, but the uncertainty allows for the possibility that it may be either ''normal''[{sup e}A({sup 34}S) > {sup e}A({sup 32}S)] or ''anomalous''[{sup e}A({sup 34}S) < {sup e}A({sup 32}S)]. The isotope shift is estimated theoretically using elaborate correlation models, monitoring the electron affinity and the mass polarization term expectation value. The theoretical analysis predicts a very large specific mass shift (SMS) that counterbalances the normal mass shift (NMS) and produces an anomalous isotope shift {sup e}A({sup 34}S)- {sup e}A({sup 32}S) =-0.0053(24) cm{sup -1}, field shift corrections included. The total isotope shift can always be written as the sum of the NMS (here +0.0169 cm{sup -1}) and a residual isotope shift (RIS). Since the NMS has nearly no uncertainty, the comparison between experimental and theoretical RIS is more fair. With respective values of -0.0146(70) cm{sup -1} and -0.0222(24) cm{sup -1}, these residual isotope shifts are found to agree within the estimated uncertainties.

Carette, Thomas; Scharf, Oliver; Godefroid, Michel [Chimie Quantique et Photophysique, Universite Libre de Bruxelles - CP160/09, B-1050 Brussels (Belgium); Drag, Cyril; Blondel, Christophe; Delsart, Christian [Laboratoire Aime-Cotton, CNRS, Universite Paris-sud, F-91405 Orsay cedex (France); Froese Fischer, Charlotte [National Institute of Standards and Technology Gaithersburg, Maryland 20899-8420 (United States)

2010-04-15T23:59:59.000Z

464

The solubility of sulfur hexafluoride in water and seawater  

Science Journals Connector (OSTI)

The concentration of sulfur hexafluoride (SF6) in the atmosphere has been rapidly increasing during the past several decades. This long-lived compound enters the surface ocean by airsea gas exchange and is potentially a very useful transient tracer for studying ocean circulation and mixing. SF6 has also been directly injected into the ocean at a minimal number of locations as a part of deliberate tracer release experiments to study gas exchange and sub-surface mixing rates. In this study, laboratory measurements of the solubility of SF6 in water and seawater were made over the temperature range of ??0.5C to 40C. Volumes of water and seawater held at constant temperature in glass chambers were equilibrated with a gas mixture containing SF6 and CFC-12 (CF2Cl2) at parts-per-trillion levels in nitrogen. Small volume water samples were analyzed by electron capture gas chromatography. Using the method of least squares, equations previously used in describing gas solubility as a function of temperature and salinity were fit to the SF6 and CFC-12 measurements. The CFC-12 results were in good agreement with previous work, while substantial differences were found between these SF6 results and those reported in earlier studies. The mean error for the analytical measurements is estimated to be ?0.5%. Based on errors in the fits and the analytical errors, we estimate the overall accuracy of the SF6 solubility function to be of the order of 2%. The results from this work should be useful in determining equilibrium concentrations for SF6 in ocean observation and modeling studies.

John L Bullister; David P Wisegarver; Frederick A Menzia

2002-01-01T23:59:59.000Z

465

Topographical differences in soil N transformation using15N dilution method along a slope in a conifer plantation forest in Japan  

Science Journals Connector (OSTI)

Soil N transformation was investigated using15N dilution method along a slope on a conifer plantation forest. Although there was no significant difference in...15N dilution method showed a distinct difference not...

Naoko Tokuchi; Muneto Hirobe; Keisuke Koba

2000-02-01T23:59:59.000Z

466

The use of ethanol to remove sulfur from coal. Final report, September 1991--December 1992; Revision  

SciTech Connect (OSTI)

The initial technical goal in the project was to develop a chemical method for the cost effective removal of both inorganic and organic sulfur from Ohio coals. Verifying and using a process of reacting ethanol vapors with coal under conditions disclosed in U.S. Patent 4,888,029, the immediate technical objectives were to convert a small scale laborative batch process to a larger scale continuous process which can serve as the basis for commercial development of the technology. This involved getting as much information as possible from small scale batch autoclave or fluid bed laboratory reactors for use in pilot plant studies. The laboratory data included material balances on the coal and sulfur, temperature and pressure ranges for the reaction, minimum reaction times at different conditions, the effectiveness of different activators such as oxygen and nitric oxide, the amount and nature of by-products such as sulfur dioxide, hydrogen sulfide and acetaldehyde, the effect of coal particle size on the speed and completeness of the reaction, and the effectiveness of the reaction on different Ohio coals. Because the laboratory experiments using the method disclosed in U.S. 4,888,029 were not successful, the objective for the project was changed to develop a new laboratory process to use ethanol to remove sulfur from coal. Using copper as a catalyst and as an H{sub 2}S scavenger, a new laboratory procedure to use ethanol to remove sulfur from coal has been developed at Ohio University and a patent application covering this process was filed in March, 1993. The process is based on the use of copper as a catalyst for the dehydrogenation of ethanol to produce nascent hydrogen to remove sulfur from the coal and the use of copper as a scavenger to capture the hydrogen sulfide formed from the sulfur removed from coal.

Savage, R.L.; Lazarov, L.K.; Prudich, M.E.; Lange, C.A.; Kumar, N.

1994-03-10T23:59:59.000Z

467

Comparison of the processes induced by nitrogen dilution on the photodissociation of silane and disilane at 193 nm  

Science Journals Connector (OSTI)

We compare the influence of the dilution of silane and disilane in nitrogen during laser photodissociation to produce silicon at 193nm, at room temperature in a static reaction chamber. The experimental results show that the conversion of the reactant gas and its deposition yield can be controlled by varying adequately the extent of dilution. So, two total pressure regions have been observed, independent of the dilution: below 4050Torr, the variations of stable species concentration are very important but above these values the variation in the dilution rate has practically no effects on their concentrations. In the first region, during the silane photodissociation at the initial reactant pressure below 5Torr, the conversion of silane increases with increasing dilution, and at higher initial reactant pressure the conversion of silane tends to rise only a little. In contrast, at any initial reactant pressure, the conversion of disilane during its photodecomposition decreases with increasing dilution. In the second region, the concentration of each stable gaseous species tends to reach a pressure stationary-state. For both the silane and disilane photodissociation, the deposition yield of silicon increases with decreasing the initial reactant gas pressure and it reaches a pressure stationary-state above 50% dilution; but in all the cases, it is greater in disilane photolysis than that of silane. A simple kinetic model is proposed for which the computed results predict the time-evolution of gas composition and amount of silicon deposited.

B. Aka; E. Boch

2002-01-01T23:59:59.000Z

468

Effects of Fuel Sulfur Content and Diesel Oxidation Catalyst on PM Emitted from Light-Duty Diesel Engine  

Science Journals Connector (OSTI)

This work aims at the particle number concentrations and size distributions, sulfate and trace metals emitted from a diesel engine fueled with three different sulfur content fuels, operating with and without DOC. ... Figure 2. Sulfate emission rate and fuel consumption as a function of sulfur content at engine speed of 2690 rpm. ... Thus, the use of low metal fuels and lubricating oil is as important to the environment and human health as low sulfur fuels, especially for engines with after-treatment devices. ...

Hong Zhao; Yunshan Ge; Xiaochen Wang; Jianwei Tan; Aijuan Wang; Kewei You

2010-01-05T23:59:59.000Z

469

TUDE DE L'ABSORPTION ULTRAVIOLETTE DU SULFURE DE CARBONE Par Mlles ODETTE AMIOT et HENRIETTE MARSAC.  

E-Print Network [OSTI]

dilué de plus en plus le sulfure de carbone dans un solvant inactif. Nous avons choisi l'hexane, liquide montage par autocollimation. 2. Purification du sulfure de carbone et prépa- ration des solutions. - On sait que le sulfure de car- bone est un liquide altérable et qu'il se décompose à la lumière avec

Boyer, Edmond

470

Structure of finite-RSB asymptotic Gibbs measures in the diluted spin glass models  

E-Print Network [OSTI]

We suggest a possible approach to proving the M\\'ezard-Parisi formula for the free energy in the diluted spin glass models, such as diluted K-spin or random K-sat model at any positive temperature. In the main contribution of the paper, we show that a certain small modification of the Hamiltonian in any of these models forces all finite-RSB asymptotic Gibbs measures in the sense of the overlaps to satisfy the M\\'ezard-Parisi ansatz for the distribution of spins. Unfortunately, what is still missing is a description of the general full-RSB asymptotic Gibbs measures. If one could show that the general case can be approximated by finite-RSB case in the right sense then one could a posteriori remove the small modification of the Hamiltonian to recover the M\\'ezard-Parisi formula for the original model.

Dmitry Panchenko

2014-06-18T23:59:59.000Z

471

Effects of Inert Dilution and Preheating Temperature on Lean Flammability Limit of Syngas  

Science Journals Connector (OSTI)

Lean flammability limits (LFL) of syngas mixtures were measured at different levels of inert dilution and unburned gas preheating temperatures using a counter-flow flame burner. ... The syngas and air are then premixed within a mixing chamber before being injected into the counter-flow burners. ... (45) Multicomponent transport was used in the calculation to account for the Soret effect, which generally enhance the burning intensity of lean syngas flame. ...

Suhui Li; Yang Zhang; Xiaolong Qiu; Bo Li; Hai Zhang

2014-04-24T23:59:59.000Z

472

Aerosol dilution and dispersion at the Nuclear Science Center confinement building  

E-Print Network [OSTI]

Experiments Release 4 1, Reactor Pool Area Release tt' 2, Irradiation CelL Release 4 3. Beam Port 4 Flow Rate Measurements. CHAPTER III SAMPLING SYSTEM CALIBRATION Introduction Equipment Air Sampler. GMA Chemical Cartridge Efficiency Determination... 52 LIST OF TABLES TABLE Page 2. 1 Flow Rate Measurements. 22 3. 1 Efficiency Calibration. The statistical counting error at the 90% confidence level is given for each determination. 33 4. 1 Reactor Bridge Dilution Factors. The statistical...

Contreras Gonzalez, Yenny Rose

2012-06-07T23:59:59.000Z

473

Semiclassical Approximation for Non-Abelian Field Strength Correlators in the Instanton Dilute Gas Model  

E-Print Network [OSTI]

Field strength correlators are semi-classically evaluated in the dilute gas model of non-Abelian sources (instantons) and compared with lattice data for QCD at zero temperature. We show that one of the Euclidean invariant, tensorial structures vanishes for configurations being purely selfdual or anti-selfdual. We compute the invariant functions contributing to the correlators within the two lowest orders in an instanton density expansion. Fitting instanton size and density for quenched and full QCD, we obtain a reasonable description.

E. -M. Ilgenfritz; B. V. Martemyanov; S. V. Molodtsov; M. Mller--Preussker; Yu. A. Simonov

1997-12-26T23:59:59.000Z