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Thermochemistry of nanodiamond terminated by oxygen containing functional groups
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Localized orbital corrections for density functional calculations on transition metal containing systems
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Spontaneous collapse of palmitic acid films on an alkaline buffer containing calcium ions
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Direct in-situ observation of early age void evolution in sustainable cement paste containing fly ash or limestone
This paper uses fast X-ray Computed Tomography (fCT) to study the change in air-filled voids during hydration of portland cement pastes of different water to cement ratios and with fly ash and limestone additives between 30 min and 12 h of hydration with deionized and de-aired water. For the deionized samples, the total volume of the air-filled voids increased during the induction period and decreased as the acceleration period began and finally stayed constant. The samples with 20% replacement of fly ash and 20% replacement of limestone showed the same trends as the OPC samples but with a reduction in the observed air-filled void formation. The air-filled void distribution in these samples changed from a limited number of large voids at the beginning of the measurements to a system with a significantly greater number of uniformly distributed smaller voids. The changes in the air-filled voids were not significant in pastes made with 50% fly ash or with de-aired water in the same testing condition. This might be explained by differences in pore solution chemistry and a reduced amount of dissolved air in the mixing water. A mechanism is proposed for a change in ionic concentration in solution to cause release of the dissolved air within the mixing water.
Rhamnose-Containing Cell Wall Polymers Suppress Helical Plant Growth Independently of Microtubule Orientation
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Electrochemical Corrosion of Ultra-high Strength Carbon Steel in Alkaline Brines Containing Hydrogen Sulfide
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Transformation of Ni-containing birnessite to tectomanganate: Influence and fate of weakly bound Ni(II) species
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Enhancing safety of hydrogen containment components through materials testing under in-service conditions
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The YcnI protein from Bacillus subtilis contains a copper-binding domain
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Structure of an Electric Double Layer Containing a 2:2 Valency Dimer Electrolyte
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Thermochemical properties of U(VI) hybrid materials containing uranyl tetrachloride anions
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Component effects on crystallization of RE-containing aluminoborosilicate glass
Lanthanide-aluminoborosilicate (LABS) glass is one option for immobilizing rare earth (RE) oxide fission products generated during reprocessing of pyroprocessed fuel. This glass system can accommodate a high loading of RE oxides and has excellent chemical durability. The present study describes efforts to model equilibrium crystallinity as a function of glass composition and temperature as well as liquidus temperature (TL) as a function of glass composition. The experimental method for determining TL was ASTM C1720-11. Typically, three crystalline phases were formed in each glass: Ce-borosilicate (Ce 3 BSi 2 O 10 ), mullite (Al 10 Si 2 O 19 ), and corundum (Al 2 O 3 ). Cerianite (CeO 2 ) was a common minor crystalline phase and Nd-silicate (Nd 2 Si 2 O 7 ) occurred in some of the glasses. In the composition region studied, TL decreased as SiO 2 and B 2 O 3 fractions increased and strongly increased with increasing fractions of RE oxides; Al 2 O 3 had a moderate effect on the TL but, as expected, it strongly affected the precipitation of Alcontaining crystals.
Local atomic structure of Pd and Ag in the SiC containment layer of TRISO fuel particles fissioned to 20% burn-up
The structure and speciation of fission products within the SiC barrier layer of tristructural-isotropic (TRISO) fuel particles irradiated to 19.6% fissions per initial metal atom (FIMA) burnup in the Advanced Test Reactor (ATR) at Idaho National Laboratory (INL) was investigated. As-irradiated fuel particles, as well as those subjected to simulated accident scenarios, were examined. The TRISO particles were characterized using synchrotron X-ray absorption fine-structure spectroscopy (XAFS) at the Materials Research Collaborative Access Team (MRCAT) beamline at the Advanced Photon Source. The TRISO particles were produced at Oak Ridge National Laboratory under the Advanced Gas Reactor Fuel Development and Qualification Program and sent to the ATR for irradiation. XAFS measurements on the palladium and silver K-edges were collected using the MRCAT undulator beamline. Analysis of the Pd edge indicated the formation of palladium silicides of the form Pd x Si (2 ≤ x ≤ 3). In contrast, Ag was found to be metallic within the SiC shell safety tested to 1700 °C. To the best of our knowledge, this is the first result demonstrating metallic bonding of silver from fissioned samples. Knowledge of these reaction pathways will allow for better simulations of radionuclide transport in the various coating layers of TRISO fuels for next generation nuclear reactors. In conclusion, they may also suggest different ways to modify TRISO particles to improve their fuel performance and to mitigate potential fission product release under both normal operation and accident conditions.