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It is important to control outdoor airflow rates into HVAC systems in terms of energy conservation and healthy indoor environment. Technologies are being developed to measure outdoor air (OA) flow rates through OA intake louvers on a real time basis. The purpose of this paper is to investigate the airflow characteristics through an OA intake louver numerically in order to provide suggestions for sensor installations. Airflow patterns are simulated with and without electronic air velocity sensors within cylindrical probes installed between louver blades or at the downstream face of the louver. Numerical results show quite good agreements with experimental data, and provide insights regarding measurement system design. The simulations indicate that velocity profiles are more spatially uniform at the louver outlet relative to between louver blades, that pressure drops imposed by the sensor bars are smaller with sensor bars at the louver outlet, and that placement of the sensor bars between louver blades substantially increases air velocities inside the louver. These findings suggest there is an advantage to placing the sensor bars at the louver outlet face.

A head-end processing step, termed DEOX for its emphasis on decladding via oxidation, is being developed for the treatment of spent oxide fuel by pyroprocessing techniques. The head-end step employs high temperatures to oxidize UO2 to U3O8 resulting in the separation of fuel from cladding and the removal of volatile fission products. Development of the head-end step is being performed in collaboration with the Korean Atomic Energy Research Institute (KAERI) through an International Nuclear Energy Research Initiative. Following the initial experimentation for the removal of volatile fission products, an off-gas treatment system was designed in conjunction with KAERI to collect specific fission gases. The primary volatile species targeted for trapping were iodine, technetium, and cesium. Each species is intended to be collected in distinct zones of the off-gas system and within those zones, on individual filters. Separation of the volatile off-gases is achieved thermally as well as chemically given the composition of the filter media. A description of the filter media and a basis for its selection will be given along with the collection mechanisms and design considerations. In addition, results from testing with the off-gas treatment system will be presented.

We have performed a new combined set of evaluations for 90–96Zr, including new resolved resonance parameterizations from Said Mughabghab for 90,91,92,94,96Zr and fast region calculations made with EMPIRE-3.1. Because 90Zr is a magic nucleus, stable Zr isotopes are nearly spherical. A new soft-rotor optical model potential is used allowing calculations of the inelastic scattering on low-lying coupled levels of vibrational nature. A soft rotor model describes dynamical deformations of the nucleus around the spherical shape and is implemented in EMPIRE/OPTMAN code. The same potential is used with rigid rotor couplings for odd-A nuclei. This then led to improved elastic angular distributions, helping to resolve improper leakage in the older ENDF/B-VII.1β evaluation in KAPL proprietary, ZPR and TRIGA benchmarks. Another consequence of 90Zr being a magic nucleus is that the level densities in both 90Zr and 91Zr are unusually low causing the (n,el) and (n,tot) cross sections to exhibit large fluctuations above the resolved resonance region. To accommodate these fluctuations, we performed a simultaneous constrained generalized least-square fit to (n,tot) for all isotopic and elemental Zr data in EXFOR, using EMPIRE's TOTRED scaling factor. TOTRED rescales total cross sections so that the optical model calculations are unaltered by the rescaling and the correct competition between channels is maintained. In this fit, all (n,tot) data in EXFOR was used for Ein>100keV, provided the target isotopic makeup could be correctly understood, including spectrum averaged data and data with broad energy resolution. As a result of our fitting procedure, we will have full cross material and cross reaction covariance for all Zr isotopes and reactions.

In this study, we attempted to evaluate relative significance of the factors that have been proposed to affect the electrochemical reaction of coals in a direct carbon fuel cell (DCFC). In the pres...

AbstractA molecular dyad and triad, comprised of a known photosensitizer, BF2‐chelated dipyrromethane (BDP), covalently linked to its structural analog and near‐IR emitting sensitizer, BF2‐chelated tetraarylazadipyrromethane (ADP), have been newly synthesized and the photoinduced energy and electron transfer were examined by femtosecond and nanosecond laser flash photolysis. The structural integrity of the newly synthesized compounds has been established by spectroscopic, electrochemical, and computational methods. The DFT calculations revealed a molecular‐clip‐type structure for the triad, in which the BDP and ADP entities are separated by about 14 Å with a dihedral angle between the fluorophores of around 70°. Differential pulse voltammetry studies have revealed the redox states, allowing estimation of the energies of the charge‐separated states. Such calculations revealed a charge separation from the singlet excited BDP (1BDP*) to ADP (BDP.+‐ADP.−) to be energetically favorable in nonpolar toluene and in polar benzonitrile. In addition, the excitation transfer from the singlet BDP to ADP is also envisioned due to good spectral overlap of the BDP emission and ADP absorption spectra. Femtosecond laser flash photolysis studies provided concrete evidence for the occurrence of energy transfer from 1BDP* to ADP (in benzonitrile and toluene) and electron transfer from BDP to 1ADP* (in benzonitrile, but not in toluene). The kinetic study of energy transfer was measured by monitoring the rise of the ADP emission and revealed fast energy transfer (ca. 1011 s−1) in these molecular systems. The kinetics of electron transfer via 1ADP*, measured by monitoring the decay of the singlet ADP at λ=820 nm, revealed a relatively fast charge‐separation process from BDP to 1ADP*. These findings suggest the potential of the examined ADP–BDP molecules to be efficient photosynthetic antenna and reaction center models.

Modeling of Coupled Thermodynamic and Geomechanical Performance of Underground Compressed Air Energy Storage (CAES) in Lined Rock Caverns Jonny Rutqvist 1 , Hyung-Mok Kim 2 , Dong-Woo Ryu 2 , Joong-Ho Synn 2 , Won-Kyong Song 2 Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA 94720 U.S.A. Korea Institute of Geoscience and Mineral Resources (KIGAM), Daejeon, 305-350 Korea ACKNOWLEDGMENTS This research was supported by the Basic Research Project of the Korea Institute of Geoscience and Mineral Resources (KIGAM, GP2009-019) funded by the Ministry of Knowledge and Economy of Korea, and funding from KIGAM for Dr. Jonny Rutqvist and Berkeley Lab was provided through the U.S. Department of Energy Contract No. DE-AC02-05CH11231. Technical review by Dr. Curtis Oldenburg and editorial review by Dan Hawkes, both at Berkeley Lab are greatly appreciated.

Abstract Aquifer microcosms were used to determine how ethanol and methyl-tert-butyl ether (MtBE) affect monoaromatic hydrocarbon degradation under different electron-accepting conditions commonly found in contaminated sites experiencing natural attenuation. Response variability was investigated by using aquifer material from four sites with different exposure history. The lag phase prior to benzene, toluene, ethylbenzene, and xylenes (BTEX) and ethanol degradation was typically shorter in microcosms with previously contaminated aquifer material, although previous exposure did not always result in high degradation activity. Toluene was degraded in all aquifer materials and generally under a broader range of electron-accepting conditions compared to benzene, which was degraded only under aerobic conditions. The MtBE was not degraded within 100 d under any condition, and it did not affect BTEX or ethanol degradation patterns. Ethanol was often degraded before BTEX compounds and had a variable effect on BTEX degradation as a function of electron-accepting conditions and aquifer material source. An occasional enhancement of toluene degradation by ethanol occurred in denitrifying microcosms with unlimited nitrate; this may be attributable to the fortuitous growth of toluene-degrading bacteria during ethanol degradation. Nevertheless, experiments with flow-through aquifer columns showed that this beneficial effect could be eclipsed by an ethanol-driven depletion of electron acceptors, which significantly inhibited BTEX degradation and is probably the most important mechanism by which ethanol could hinder BTEX natural attenuation. A decrease in natural attenuation could increase the likelihood that BTEX compounds reach a receptor as well as the potential duration of exposure.

The ability to generate microorganisms that can produce biofuels similar to petroleum-based transportation fuels would allow the use of existing engines and infrastructure and would save an enormous amount of capital required for replacing the current infrastructure to accommodate biofuels that have properties significantly different from petroleum-based fuels. Several groups have demonstrated the feasibility of manipulating microbes to produce molecules similar to petroleum-derived products, albeit at relatively low productivity (e.g. maximum butanol production is around 20 g/L). For cost-effective production of biofuels, the fuel-producing hosts and pathways must be engineered and optimized. Advances in metabolic engineering and synthetic biology will provide new tools for metabolic engineers to better understand how to rewire the cell in order to create the desired phenotypes for the production of economically viable biofuels.