Cluster Variation Approach to the Random-Anisotropy Blume-Emery-Griffiths Model

The random--anisotropy Blume--Emery--Griffiths model, which has been proposed to describe the critical behavior of $^3$He--$^4$He mixtures in a porous medium, is studied in the pair approximation of the cluster variation method extended to disordered systems. Several new features, with respect to mean field theory, are found, including a rich ground state, a nonzero percolation threshold, a reentrant coexistence curve and a miscibility gap on the high $^3$He concentration side down to zero temperature. Furthermore, nearest neighbor correlations are introduced in the random distribution of the anisotropy, which are shown to be responsible for the raising of the critical temperature with respect to the pure and uncorrelated random cases and contribute to the detachment of the coexistence curve from the $\lambda$ line.Comment: 14 pages (plain TeX) + 12 figures (PostScript, appended), Preprint POLFIS-TH.02/9

Characterization of vanadium/silica and copper/silica aerogel catalysts

Vanadium/silica and copper/silica aerogels have been prepared using the sol-gel method followed by CO{sub 2} exchange and supercritical extraction. Structural properties of samples supercritically dried, oxidized and used in reactions studies conducted with a feed representing the average composition of automobile exhaust from a lean burn engine were investigated using laser Raman spectroscopy and temperature-programmed reduction. No evidence of crystalline V{sub 2}O{sub 5} was found for the vanadium/silica aerogel, freshly extracted, oxidized or following exposure to reaction conditions using these techniques. However, results obtained for the copper/silica sample indicate that changes in the structure of the copper species had occurred as the sample was oxidized and exposed to reaction conditions

Anisotropic Aerogels for Studying Superfluid 3^3He

It may be possible to stabilize new superfluid phases of $^{3}$He with anisotropic silica aerogels. We discuss two methods that introduce anisotropy in the aerogel on length scales relevant to superfluid $^{3}$He. First, anisotropy can be induced with uniaxial strain. A second method generates anisotropy during the growth and drying stages. We have grown cylindrical $\sim$98% aerogels with anisotropy indicated by preferential radial shrinkage after supercritical drying and find that this shrinkage correlates with small angle x-ray scattering (SAXS). The growth-induced anisotropy was found to be $\sim90^\circ$ out of phase relative to that induced by strain. This has implications for the possible stabilization of superfluid phases with specific symmetry.Comment: 6 pages, 4 figures, submitted to Quantum Fluids and Solids (QFS) conference 200

Method for acquiring, storing and analyzing crystal images

A system utilizing a digital computer for acquiring, storing and evaluating crystal images. The system includes a video camera (12) which produces a digital output signal representative of a crystal specimen positioned within its focal window (16). The digitized output from the camera (12) is then stored on data storage media (32) together with other parameters inputted by a technician and relevant to the crystal specimen. Preferably, the digitized images are stored on removable media (32) while the parameters for different crystal specimens are maintained in a database (40) with indices to the digitized optical images on the other data storage media (32). Computer software is then utilized to identify not only the presence and number of crystals and the edges of the crystal specimens from the optical image, but to also rate the crystal specimens by various parameters, such as edge straightness, polygon formation, aspect ratio, surface clarity, crystal cracks and other defects or lack thereof, and other parameters relevant to the quality of the crystals

Determination of Soil Contaminant Transport Parameters Using Time Domain Reflectometry

Proceedings of the 1993 Georgia Water Resources Conference, April 20-21, 1993, Athens, Georgia.A recent study of rural shallow drinking wells found that 4.6% of the wells in the Piedmont region of Georgia had nitrate levels above the EPA recommended level of 10 ppm nitrate nitrogen (Tyson and Issac, 1991). The most likely sources of this nitrate are septic systems, fertilizers, and manures. Nitrate transport models such as LEACHN (Wagenet and Hutson, 1989) can be used to investigate the contributions of these sources to groundwater contamination, but the models require soil transport parameters that are difficult to measure. Another problem is that we are interested in predicting nitrate transport at the field scale, but transport parameters are usually measured on a much smaller soil volume.Sponsored and Organized by: U.S. Geological Survey, Georgia Department of Natural Resources, The University of Georgia, Georgia State University, Georgia Institute of TechnologyThis book was published by the Institute of Natural Resources, The University of Georgia, Athens, Georgia 30602 with partial funding provided by the U.S. Department of Interior, Geological Survey, through the Georgia Water Research Institute as authorized by the Water Resources Research Act of 1984 (P.L. 98-242). The views and statements advanced in this publication are solely those of the authors and do not represent official views or policies of the University of Georgia or the U.S. Geological Survey or the conference sponsors

Separation of Minor Actinides from Lanthanides by Dithiophosphinic Acid Extractants

The selective extraction of the minor actinides (Am(III) and Cm(III)) from the lanthanides is an important part of advanced reprocessing of spent nuclear fuel. This separation would allow the Am/Cm to be fabricated into targets and recycled to a reactor and the lanthanides to be dispositioned. This separation is difficult to accomplish due to the similarities in the chemical properties of the trivalent actinides and lanthanides. Research efforts at the Idaho National Laboratory have identified an innovative synthetic pathway yielding new regiospecific dithiophosphinic acid (DPAH) extractants. The synthesis provides DPAH derivatives that can address the issues concerning minor actinide separation and extractant stability. For this work, two new symmetric DPAH extractants have been prepared. The use of these extractants for the separation of minor actinides from lanthanides will be discussed

Measuring scarce water saving from interregional virtual water flows in China

Trade of commodities can lead to virtual water flows between trading partners. When commodities flow from regions of high water productivity to regions of low water productivity, the trade has the potential to generate water saving. However, this accounting of water saving does not account for the water scarcity status in different regions. It could be that the water saving generated from this trade occurs at the expense of the intensified water scarcity in the exporting region, and exerts limited effect on water stress alleviation in importing regions. In this paper, we propose an approach to measure the scarce water saving associated with virtual water trade (measuring in water withdrawal/use). The scarce water is quantified by multiplying the water use in production with the water stress index. We assessed the scarce water saving/loss through interprovincial trade within China using a multi-region input-output table from 2010. The results show that interprovincial trade resulted in 14.2 km3 of water loss without considering water stress, but only 0.4 km3 scarce water loss using the scarce water concept. Among the 435 total connections of virtual water flows, 254 connections contributed to 20.2 km3 of scarce water saving. Most of these connections are virtual water flows from provinces with lower water stress index (WSI) to that with higher both water scarcity status and water productivity across regions. Identifying key connections of scarce water saving is useful in guiding interregional economic restructuring towards water stress alleviation, a major goal of China’s sustainable development strategy

DIAMIDE DERIVATIVES OF DIPICOLINIC ACID AS ACTINIDE AND LANTHANIDE EXTRACTANTS IN A VARIATION OF THE UNEX PROCESS

The Universal Extraction (UNEX) process has been developed for simultaneous extraction of cesium, strontium, and actinides from acidic solutions. This process utilizes an extractant consisting of 0.08 M chlorinated cobalt dicarbollide (HCCD), 0.007-0.02 M polyethylene glycol (PEG-400), and 0.02 M diphenyl-N,N-di-n-butylcarbamoylmethylphosphine oxide (Ph2CMPO) in the diluent trifluoromethylphenyl sulfone (CF3C6H5SO2, designated FS-13) and provides simultaneous extraction of Cs, Sr, actinides, and lanthanides from HNO3 solutions. The UNEX process is of limited utility for processing acidic solutions containing large quantities of lanthanides and/or actinides, such as dissolved spent nuclear fuel solutions. These constraints are primarily attributed to the limited concentrations of CMPO (a maximum of ~0.02 M) in the organic phase and limited solubility of the CMPO-metal complexes. As a result, alternative actinide and lanthanide extractants are being investigated for use with HCCD as an improvement for waste processing and for applications where higher concentrations of the metals are present. Our preliminary results indicate that diamide derivatives of dipicolinic acid may function as efficient actinide and lanthanide extractants. The results to be presented indicate that, of the numerous diamides studied to date, the tetrabutyldiamide of dipicolinic acid, TBDPA, shows the most promise as an alternative actinide/lanthanide extractant in the UNEX process

Interfacial Chemistry in Al/CuO Reactive Nanomaterial and Its Role in Exothermic Reaction.

Interface layers between reactive and energetic materials in nanolaminates or nanoenergetic materials are believed to play a crucial role in the properties of nanoenergetic systems. Typically, in the case of Metastable Interstitial Composite nanolaminates, the interface layer between the metal and oxide controls the onset reaction temperature, reaction kinetics, and stability at low temperature. So far, the formation of these interfacial layers is not well understood for lack of in situ characterization, leading to a poor control of important properties. We have combined in situ infrared spectroscopy and ex situ X-ray photoelectron spectroscopy, differential scanning calorimetry, and high resolution transmission electron microscopy, in conjunction with firstprinciples calculations to identify the stable configurations that can occur at the interface and determine the kinetic barriers for their formation. We find that (i) an interface layer formed during physical deposition of aluminum is composed of a mixture of Cu, O, and Al through Al penetration into CuO and constitutes a poor diffusion barrier (i.e., with spurious exothermic reactions at lower temperature), and in contrast, (ii) atomic layer deposition (ALD) of alumina layers using trimethylaluminum (TMA)produces a conformal coating that effectively prevents Al diffusion even for ultrathin layer thicknesses (∼0.5 nm), resulting in better stability at low temperature and reduced reactivity. Importantly, the initial reaction of TMA with CuO leads to the extraction of oxygen from CuO to form an amorphous interfacial layer that is an important component for superior protection properties of the interface and is responsible for the high system stability. Thus, while Al e-beam evaporation and ALD growth of an alumina layer on CuO both lead to CuO reduction, the mechanism for oxygen removal is different, directly affecting the resistance to Al diffusion. This work reveals that it is the nature of the monolayer interface between CuO and alumina/Al rather than the thickness of the alumina layer that controls the kinetics of Al diffusion, underscoring the importance of the chemical bonding at the interface in these energetic materials