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At least 127 records · Page 7Linked to original sources

Mechanism of SO2 removal by carbon

The reaction of SO 2 with carbon (C) in the presence of O 2 and H 2 O involves a series of reactions that leads to the formation of sulfuric acid as the final product. The rate-determining step in the overall process is the oxidation of SO 2 to SO 3 . Three SO 2 oxidation reactions are possible. Adsorbed SO 2 (C−SO 2 ) can react either with gas phase O 2 or with adsorbed oxygen (C−O complex) to form sulfur trioxide (SO 3 ), or gas phase SO 2 can react directly with the C−O complex. In optimizing the SO 2 removal capabilities of carbon, most studies only assume a given mechanism for SO 2 adsorption and conversion to H 2 SO 4 to be operable. The appropriate SO 2 oxidation step and role of the C−O complex in this mechanism remain to be determined. The ultimate goal of this study was to prepare activated char from Illinois coal with optimal properties for low-temperature (80−150°C) removal of sulfur dioxide from coal combustion flue gas. The SO 2 adsorption capacity of activated char was found to be inversely proportional to the amount of oxygen adsorbed on its surface. A temperature-programmed desorption technique was developed to titrate those sites responsible for adsorption of SO 2 and conversion to H 2 SO 4 . On the basis of these results, a mechanism for SO 2 removal by carbon was proposed. The derived rate expression showed SO 2 adsorption to be dependent only on the fundamental rate constant and concentration of carbon atoms designated as free sites. Recent studies indicate a similar relationship exists between the rate of carbon gasification (in CO 2 or H 2 O) and the number of reactive sites as determined by transient kinetics experiments. Utilizing the concept of active or free sites, it was possible to produce a char from Illinois coal having an SO 2 adsorption capacity surpassing that of a commercial catalytic activated carbon.

Energy and Fuels↗

Adsorption of SO 2 on bituminous coal char and activated carbon fiber

The SO 2 adsorption behaviors of activated carbons produced from Illinois coal and of commercially prepared activated carbon fibers (ACFs) were compared. There was no relation between surface area of coal-based carbons and SO 2 adsorption, whereas adsorption of SO 2 on the series of ACFs was inversely proportional to N 2 BET surface area. Higher surface area ACFs had wider pores and adsorbed less SO 2 ; thus, pore size distribution is thought to play a significant role in SO 2 adsorption for these materials. Oxidation with HNO 3 and/or H 2 SO 4 , followed by heat treatment at 700−925°C to remove carbon−oxygen complexes, resulted in increased SO 2 adsorption for both coal chars and ACFs. This behavior was explained by an increase in the available number of free sites, previously occupied by oxygen and now available for SO 2 adsorption. The use of nitrogen-containing functional groups on ACFs of proper pore size shows promise for further increasing SO 2 adsorption capacities. Knowledge of the relationship among the number of free sites, pore size, and surface chemistry on corresponding SO 2 adsorption should lead to the development of more efficient adsorbents prepared from either coal or ACFs.

Energy and Fuels↗

Adsorbed natural gas storage with activated carbons made from Illinois coals and scrap tires

Activated carbons for natural gas storage were produced from Illinois bituminous coals (IBC-102 and IBC-106) and scrap tires by physical activation with steam or CO 2 and by chemical activation with KOH, H 3 PO 4 , or ZnCl 2 . The products were characterized for N 2 -BET area, micropore volume, bulk density, pore size distribution, and volumetric methane storage capacity ( V m / V s ). V m / V s values for Illinois coal-derived carbons ranged from 54 to 83 cm 3 /cm 3 , which are 35−55% of a target value of 150 cm 3 /cm 3 . Both granular and pelletized carbons made with preoxidized Illinois coal gave higher micropore volumes and larger V m / V s values than those made without preoxidation. This confirmed that preoxidation is a desirable step in the production of carbons from caking materials. Pelletization of preoxidized IBC-106 coal, followed by steam activation, resulted in the highest V m / V s value. With roughly the same micropore volume, pelletization alone increased V m / V s of coal carbon by 10%. Tire-derived carbons had V m / V s values ranging from 44 to 53 cm 3 /cm 3 , lower than those of coal carbons due to their lower bulk densities. Pelletization of the tire carbons increased bulk density up to 160%. However, this increase was offset by a decrease in micropore volume of the pelletized materials, presumably due to the pellet binder. As a result, V m / V s values were about the same for granular and pelletized tire carbons. Compared with coal carbons, tire carbons had a higher percentage of mesopores and macropores.

Energy and Fuels↗

Polycrystalline methane hydrate: Synthesis from superheated ice, and low-temperature mechanical properties

We describe a new and efficient technique to grow aggregates of pure methane hydrate in quantities suitable for physical and material properties testing. Test specimens were grown under static conditions by combining cold, pressurized CH 4 gas with granulated H 2 O ice, and then warming the reactants to promote the reaction CH 4 (g) + 6H 2 O(s→l) → CH 4 ·6H 2 O (methane hydrate). Hydrate formation evidently occurs at the nascent ice/liquid water interface on ice grain surfaces, and complete reaction was achieved by warming the system above the ice melting point and up to 290 K, at 25−30 MPa, for approximately 8 h. The resulting material is pure, cohesive, polycrystalline methane hydrate with controlled grain size and random orientation. Synthesis conditions placed the H 2 O ice well above its melting temperature while reaction progressed, yet samples and run records showed no evidence for bulk melting of the unreacted portions of ice grains. Control experiments using Ne, a non-hydrate-forming gas, showed that under otherwise identical conditions, the pressure reduction and latent heat associated with ice melting are easily detectable in our fabrication apparatus. These results suggest that under hydrate-forming conditions, H 2 O ice can persist metastably to temperatures well above its ordinary melting point while reacting to form hydrate. Direct observations of the hydrate growth process in a small, high-pressure optical cell verified these conclusions and revealed additional details of the hydrate growth process. Methane hydrate samples were then tested in constant-strain-rate deformation experiments at T = 140−200 K, P c = 50−100 MPa, and ε = 10 - 4 −10 - 6 s - 1 . Measurements in both the brittle and ductile fields showed that methane hydrate has measurably different strength than H 2 O ice, and work hardens to an unusually high degree compared to other ices as well as to most metals and ceramics at high homologous temperatures. This work hardening may be related to a changing stoichiometry under pressure during plastic deformation; X-ray analyses showed that methane hydrate undergoes a process of solid-state disproportionation or exsolution during deformation at conditions well within its conventional stability field.

Energy and Fuels↗

Gas hydrate formation in the deep sea: In situ experiments with controlled release of methane, natural gas, and carbon dioxide

We have utilized a remotely operated vehicle (ROV) to initiate a program of research into gas hydrate formation in the deep sea by controlled release of hydrocarbon gases and liquid CO 2 into natural sea water and marine sediments. Our objectives were to investigate the formation rates and growth patterns of gas hydrates in natural systems and to assess the geochemical stability of the reaction products over time. The novel experimental procedures used the carrying capacity, imaging capability, and control mechanisms of the ROV to transport gas cylinders to depth and to open valves selectively under desired P − T conditions to release the gas either into contained natural sea water or into sediments. In experiments in Monterey Bay, California, at 910 m depth and 3.9 °C water temperature we find hydrate formation to be nearly instantaneous for a variety of gases. In sediments the pattern of hydrate formation is dependent on the pore size, with flooding of the pore spaces in a coarse sand yielding a hydrate cemented mass, and gas channeling in a fine-grained mud creating a veined hydrate structure. In experiments with liquid CO 2 the released globules appeared to form a hydrate skin as they slowly rose in the apparatus. An initial attempt to leave the experimental material on the sea floor for an extended period was partially successful; we observed an apparent complete dissolution of the liquid CO 2 mass, and an apparent consolidation of the CH 4 hydrate, over a period of about 85 days.

Energy and Fuels↗

Preparation and evaluation of coal-derived activated carbons for removal of mercury vapor from simulated coal combustion flue fases

Coal-derived activated carbons (CDACs) were tested for their suitability in removing trace amounts of vapor-phase mercury from simulated flue gases generated by coal combustion. CDACs were prepared in bench-scale and pilot-scale fluidized-bed reactors with a three-step process, including coal preoxidation, carbonization, and then steam activation. CDACs from high-organicsulfur Illinois coals had a greater equilibrium Hg0 adsorption capacity than activated carbons prepared from a low-organic-sulfur Illinois coal. When a low-organic-sulfur CDAC was impregnated with elemental sulfur at 600 ??C, its equilibrium Hg0 adsorption capacity was comparable to the adsorption capacity of the activated carbon prepared from the high-organicsulfur coal. X-ray diffraction and sulfur K-edge X-ray absorption near-edge structure examinations showed that the sulfur in the CDACs was mainly in organic forms. These results suggested that a portion of the inherent organic sulfur in the starting coal, which remained in the CDACs, played an important role in adsorption of Hg0. Besides organic sulfur, the BET surface area and micropore area of the CDACs also influenced Hg0 adsorption capacity. The HgCl2 adsorption capacity was not as dependent on the surface area and concentration of sulfur in the CDACs as was adsorption of Hg0. The properties and mercury adsorption capacities of the CDACs were compared with those obtained for commercial Darco FGD carbon.

Energy and Fuels↗

Correlating N2 and CH4 adsorption on microporous carbon using a new analytical model

A new pore size distribution (PSD) model is developed to readily describe PSDs of microporous materials with an analytical expression. Results from this model can be used to calculate the corresponding adsorption isotherm to compare the calculated isotherm to the experimental isotherm. This aspect of the model provides another check on the validity of the model's results. The model is developed on the basis of a 3-D adsorption isotherm equation that is derived from statistical mechanical principles. Least-squares error minimization is used to solve the PSD without any preassumed distribution function. In comparison with several well-accepted analytical methods from the literature, this 3-D model offers a relatively realistic PSD description for select reference materials, including activated-carbon fibers. N2 and CH4 adsorption is correlated using the 3-D model for commercial carbons BPL and AX-21. Predicted CH4 adsorption isotherms at 296 K based on N2 adsorption at 77 K are in reasonable agreement with experimental CH4 isotherms. Use of the model is also described for characterizing PSDs of tire-derived activated carbons and coal-derived activated carbons for air-quality control applications.

Energy and Fuels↗

Sorption and modeling of mass transfer of toxic chemical vapors in activated-carbon fiber-cloth adsorbers

A new activated-carbon fiber-cloth (ACFC) adsorber coupled with an electrothermal regenerator and a cryogenic condenser was designed and developed to efficiently capture and recover toxic chemical vapors (TCVs) from simulated industrial gas streams. The system was characterized for adsorption by ACFC, electrothermal desorption, and cryogenic condensation to separate acetone and methyl ethyl ketone from gas streams. Adsorption dynamics are numerically modeled to predict system characteristics during scale-up and optimization of the process in the future. The model requires diffusivities of TCVs into an activated-carbon fiber (ACF) as an input. Effective diffusivities of TCVs into ACFs were modeled as a function of temperature, concentration, and pore size distribution. Effective diffusivities for acetone at 65 °C and 30−60 ppmv were measured using a chromatography method. The energy factor for surface diffusion was determined from comparison between the experimental and modeled effective diffusivities. The modeled effective diffusivities were used in a dispersive computational model to predict mass transfer zones of TCVs in fixed beds of ACFC under realistic conditions for industrial applications.

Energy and Fuels↗

Front Range Infrastructure Resources Project; energy resources activities

Oil, natural gas, and coal (energy resources) have been produced from rocks in the Front Range of Colorado and Wyoming for more than a century, and significant quantities of oil and gas continue to be developed in the study area of the U.S. Geological Survey (USGS) Front Range Infrastructure Resources Project (fig. 1). As an infrastructure resource, energy resources helped to fuel past development of (1) urban areas in the Front Range as well as (2) some of the manufacturing and mining upon which the urban centers were built and thrived. At present, much of the oil and gas extracted from rocks beneath the Front Range urban corridor is used locally; the people living in the urban area provide a need and viable marketplace for these commodities.

Colorado, Wyoming↗

X-ray Computed Tomography Observation of Methane Hydrate Dissociation

Deposits of naturally occurring methane hydrate have been identified in permafrost and deep oceanic environments with global reserves estimated to be twice the total amount of energy stored in fossil fuels. The fundamental behavior of methane hydrate in natural formations, while poorly understood, is of critical importance if the economic recovery of methane from hydrates is to be accomplished. In this study, computed X-ray tomography (CT) scanning is used to image an advancing dissociation front in a heterogeneous gas hydrate/sand sample at 0.1 MPa. The cylindrical methane hydrate and sand aggregate, 2.54 cm in diameter and 6.3 cm long, was contained in a PVC sample holder that was insulated on all but one end. At the uninsulated end, the dissociated gas was captured and the volume of gas monitored. The sample was initially imaged axially using X-ray CT scanning within the methane hydrate stability zone by keeping the sample temperature at 77??K. Subsequently, as the sample warmed through the methane hydrate dissociation point at 194??K and room pressure, gas was produced and the temperature at the bottom of the sample plug was monitored while CT images were acquired. The experiment showed that CT imaging can resolve the reduction in density (as seen by a reduction in beam attenuation) of the hydrate/sand aggregate due to the dissociation of methane hydrate. In addition, a comparison of CT images with gas flow and temperature measurements reveals that the CT scanner is able to resolve accurately and spatially the advancing dissociation front. Future experiments designed to better understand the thermodynamics of hydrate dissociation are planned to take advantage of the temporal and spatial resolution that the CT scanner provides.

Conference Paper↗

Impacts to wildlife of wind energy siting and operation in the United States

Electricity from wind energy is a major contributor to the strategy to reduce greenhouse gas emissions from fossil fuel use and thus reduce the negative impacts of climate change. Wind energy, like all power sources, can have adverse impacts on wildlife. After nearly 25 years of focused research, these impacts are much better understood, although uncertainty remains. In this report, we summarize positive impacts of replacing fossil fuels with wind energy, while describing what we have learned and what remains uncertain about negative ecological impacts of the construction and operation of land-based and offshore wind energy on wildlife and wildlife habitat in the U.S. Finally, we propose research on ways to minimize these impacts. TO SUMMARIZE: 1 Environmental and other benefits of wind energy include near-zero greenhouse gas emissions, reductions of other common air pollutants, and little or no water use associated with producing electricity from wind energy. Various scenarios for meeting U.S. carbon emission reduction goals indicate that a four- to five-fold expansion of land-based wind energy from the current 97 gigawatts (GW) by the year 2050 is needed to minimize temperature increases and reduce the risk of climate change to people and wildlife. 2 Collision fatalities of birds and bats are the most visible and measurable impacts of wind energy production. Current estimates suggest most bird species, especially songbirds, are at low risk of population-level impacts. Raptors as a group appear more vulnerable to collisions. Population-level impacts on migratory tree bats are a concern, and better information on population sizes is needed to evaluate potential impacts to these species. Although recorded fatalities of cave-dwelling bat species are typically low at most wind energy facilities, additional mortality from collisions is a concern given major declines in these species due to white-nose syndrome (WNS). Assessments of regional and cumulative fatality impacts for birds and bats have been hampered by the lack of data from areas with a high proportion of the nation’s installed wind energy capacity. Efforts to expand data accessibility from all regions are underway, and this greater access to data along with improvements in statistical estimators should lead to improved impact assessments. 3 Habitat impacts of wind energy development are difficult to assess. An individual wind energy facility may encompass thousands of acres, but only a small percentage of the landscape within the project area is directly transformed. If a project is sited in previously undisturbed habitat, there is concern for indirect impacts, such as displacement of sensitive species. Studies to date indicate displacement of some species, but the long-term population impacts are unknown. 4 Offshore wind energy development in the U.S. is just beginning. Studies at offshore wind facilities in Europe indicate some bird and marine mammal species are displaced from project areas, but substantial uncertainty exists regarding the individual or population-level impacts of this displacement. Bird and bat collisions with offshore turbines are thought to be less common than at terrestrial facilities, but currently the tools to measure fatalities at offshore wind energy facilities are not available. The wind energy industry, state and federal agencies, conservation groups, academia, and scientific organizations have collaborated for nearly 25 years to conduct the research needed to improve our understanding of risk to wildlife and to avoid and minimize that risk. Efforts to reduce the uncertainty about wildlife risk must keep up withthe pace and scale of the need to reduce carbon emissions. This will require focusing our research priorities and increasing the rate at which we incorporate research results into the development and validation of best practices for siting and operating wind energy facilities.

Issues in Ecology↗

From Projectile Points to Microprocessors - The Influence of Some Industrial Minerals

In the language of economic geology, Earth materials are classified as metallic ores, fuel minerals, gemstones, and industrial minerals. Most people know that metallic ores yield shiny, conductive, ductile elements such as copper, iron, or gold. Most understand that energy-producing coals constitute a fuel mineral. Likewise, dazzling rubies and rare sapphires are universally recognized as gemstones. The fourth group, industrial minerals, is largely unknown to the general public, even though industrial minerals are as essential to daily life as metals and fuel minerals. This report examines the occurrence and practical uses of nine important industrial minerals - constituting just a few of the more than 50 industrial minerals that shape human culture.

Circular↗

The Global food‐energy‐water nexus

Water availability is a major factor constraining humanity's ability to meet the future food and energy needs of a growing and increasingly affluent human population. Water plays an important role in the production of energy, including renewable energy sources and the extraction of unconventional fossil fuels that are expected to become important players in future energy security. The emergent competition for water between the food and energy systems is increasingly recognized in the concept of the “food‐energy‐water nexus.” The nexus between food and water is made even more complex by the globalization of agriculture and rapid growth in food trade, which results in a massive virtual transfer of water among regions and plays an important role in the food and water security of some regions. This review explores multiple components of the food‐energy‐water nexus and highlights possible approaches that could be used to meet food and energy security with the limited renewable water resources of the planet. Despite clear tensions inherent in meeting the growing and changing demand for food and energy in the 21st century, the inherent linkages among food, water, and energy systems can offer an opportunity for synergistic strategies aimed at resilient food, water, and energy security, such as the circular economy.

Reviews of Geophysics↗

Fundamental challenges to methane recovery from gas hydrates

The fundamental challenges, the location, magnitude, and feasibility of recovery, which must be addressed to recover methane from dispersed hydrate sources, are presented. To induce dissociation of gas hydrate prior to methane recovery, two potential methods are typically considered. Because thermal stimulation requires a large energy input, it is less economically feasible than depressurization. The new data will allow the study of the effect of pressure, temperature, diffusion, porosity, tortuosity, composition of gas and water, and porous media on gas-hydrate production. These data also will allow one to improve existing models related to the stability and dissociation of sea floor hydrates. The reproducible kinetic data from the planned runs together with sediment properties will aid in developing a process to economically recover methane from a potential untapped hydrate source. The availability of plentiful methane will allow economical and large-scale production of methane-derived clean fuels to help avert future energy crises.

Topics in Catalysis↗

Land status and federal mineral ownership in the Powder River basin, Wyoming and Montana; a digital data set for geographic information systems

As the Nation's energy resources continue to be examined for development, it is critical that a digital database exist that contains location data for all Federal land and mineral resources. The U.S. Geological Survey (USGS), in cooperation with the Bureau of Land Management (BLM), is collecting these ownership files and compiling them in Environmental Systems Research Institute, Inc. (ESRI) ARC/INFO coverages, to form a standardized data library. A coverage is a digital version of a map in the form of vector data storage. These coverages are combined with models of coal deposits from the USGS National Coal Resource Assessment project, a five-year effort to identify and characterize the coal beds and coal zones that will provide fuel for the Nation’s energy needs during the first quarter of the twenty-first century. Geographic and geologic data layers are integrated in a Geographic Information System (GIS) to answer complex geo-spatial questions concerning coal resource occurrence.

Montana, Wyoming↗

The history and development of FETAX (ASTM standard guide, E-1439 on conducting the frog embryo teratogenesis Assay-Xenopus)

The energy crisis of the 1970's and 1980's prompted the search for alternative sources of fuel. With development of alternate sources of energy, concerns for biological resources potentially adversely impacted by these alternative technologies also heightened. For example, few biological tests were available at the time to study toxic effects of effluents on surface waters likely to serve as receiving streams for energy-production facilities; hence, we began to use Xenopus laevis embryos as test organisms to examine potential toxic effects associated with these effluents upon entering aquatic systems. As studies focused on potential adverse effects on aquatic systems continued, a test procedure was developed that led to the initial standardization of FETAX. Other .than a limited number of aquatic toxicity tests that used fathead minnows and cold-water fishes such as rainbow trout, X. laevis represented the only other aquatic vertebrate test system readily available to evaluate complex effluents. With numerous laboratories collaborating, the test with X. laevis was refined, improved, and developed as ASTM E-1439, Standard Guide for the Conducting Frog Embryo Teratogenesis Assay-Xenopus (FETAX). Collabrative work in the 1990s yielded procedural enhancements, for example, development of standard test solutions and exposure methods to handle volatile organics and hydrophobic compounds. As part of the ASTM process, a collaborative interlaboratory study was performed to determine the repeatability and reliability of FETAX. Parallel to these efforts, methods were also developed to test sediments and soils, and in situ test methods were developed to address "lab-to-field extrapolation errors" that could influence the method's use in ecological risk assessments. Additionally, a metabolic activation system composed of rat liver microsomes was developed which made FETAX more relevant to mammalian studies.

Conference Paper↗

Variation in foraging patterns as reflected by floral resources used by male vs female bees of selected species at Badlands National Park, SD

Female and male bees forage for different reasons: females provision nests with pollen appropriate for larval development and consume nectar for energy while males need only fuel their own energetic requirements. The expectation, therefore, is that females should visit fewer floral resource species than males, due to females’ focus on host plant species and their tie to the nest location. We used pollen collected from bees’ bodies and the flowers they were collected on to infer floral resource use in 2010-2012 at Badlands National Park, SD, USA. We collected bees on 24 1-ha plots centered on particular plant species. We compared number of floral species and families (1) associated with individual female and male bees (via generalized linear mixed models) and (2) accumulated by each sex (using rarefaction); and (3) effect of variation between sexes in plant-bee interactions via modularity analyses. Analyses were restricted to bee species with > 5 individuals per sex. Contrary to expectation, female and male bees differed infrequently in the number of floral resources they had visited, both on single foraging bouts and collectively when accumulated across all males and females of a species. When males and females did differ, males visited fewer floral species than females. Generalist and specialist bee species did not differ markedly in floral resource use by females and males. When separated by sex, seven of eleven species occupied different modules than they did when analyzed as a species; most of the bee species were connectors, thus important for stability of the network during perturbations.

South Dakota↗