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Hadronic Correlations and Fluctuations

Description: We will provide a review of some of the physics which can be addressed by studying fluctuations and correlations in heavy ion collisions. We will discuss Lattice QCD results on fluctuations and correlations and will put them into context with observables which have been measured in heavy-ion collisions. Special attention will be given to the QCD critical point and the first order co-existence region, and we will discuss how the measurement of fluctuations and correlations can help in an experimental search for non-trivial structures in the QCD phase diagram.
Date: October 9, 2008
Creator: Koch, Volker
Partner: UNT Libraries Government Documents Department

Collective phenomena in non-central nuclear collisions

Description: Recent developments in the field of anisotropic flow in nuclear collision are reviewed. The results from the top AGS energy to the top RHIC energy are discussed with emphasis on techniques, interpretation, and uncertainties in the measurements.
Date: October 20, 2008
Creator: Voloshin, Sergei A.; Poskanzer, Arthur M. & Snellings, Raimond
Partner: UNT Libraries Government Documents Department

Chapter 8: Selective Stoichiometric and Catalytic Reactivity in the Confines of a Chiral Supramolecular Assembly

Description: Nature uses enzymes to activate otherwise unreactive compounds in remarkable ways. For example, DNases are capable of hydrolyzing phosphate diester bonds in DNA within seconds,[1-3]--a reaction with an estimated half-life of 200 million years without an enzyme.[4] The fundamental features of enzyme catalysis have been much discussed over the last sixty years in an effort to explain the dramatic rate increases and high selectivities of enzymes. As early as 1946, Linus Pauling suggested that enzymes must preferentially recognize and stabilize the transition state over the ground state of a substrate.[5] Despite the intense study of enzymatic selectivity and ability to catalyze chemical reactions, the entire nature of enzyme-based catalysis is still poorly understood. For example, Houk and co-workers recently reported a survey of binding affinities in a wide variety of enzyme-ligand, enzyme-transition-state, and synthetic host-guest complexes and found that the average binding affinities were insufficient to generate many of the rate accelerations observed in biological systems.[6] Therefore, transition-state stabilization cannot be the sole contributor to the high reactivity and selectivity of enzymes, but rather, other forces must contribute to the activation of substrate molecules. Inspired by the efficiency and selectivity of Nature, synthetic chemists have admired the ability of enzymes to activate otherwise unreactive molecules in the confines of an active site. Although much less complex than the evolved active sites of enzymes, synthetic host molecules have been developed that can carry out complex reactions with their cavities. While progress has been made toward highly efficient and selective reactivity inside of synthetic hosts, the lofty goal of duplicating enzymes specificity remains.[7-9] Pioneered by Lehn, Cram, Pedersen, and Breslow, supramolecular chemistry has evolved well beyond the crown ethers and cryptands originally studied.[10-12] Despite the increased complexity of synthetic host molecules, most assembly conditions utilize self-assembly to form complex highly-symmetric structures from ...
Date: September 27, 2007
Creator: University of California, Berkeley; Laboratory, Lawrence Berkeley National; Raymond, Kenneth; Pluth, Michael D.; Bergman, Robert G. & Raymond, Kenneth N.
Partner: UNT Libraries Government Documents Department

Chapter 9: Electronics

Description: Sophisticated front-end electronics are a key part of practically all modern radiation detector systems. This chapter introduces the basic principles and their implementation. Topics include signal acquisition, electronic noise, pulse shaping (analog and digital), and data readout techniques.
Date: December 19, 2006
Creator: Grupen, Claus & Shwartz, Boris A.
Partner: UNT Libraries Government Documents Department

Biomolecular Modification of Inorganic Crystal Growth

Description: The fascinating shapes and hierarchical designs of biomineralized structures are an inspiration to materials scientists because of the potential they suggest for biomolecular control over materials synthesis. Conversely, the failure to prevent or limit tissue mineralization in the vascular, skeletal, and urinary systems is a common source of disease. Understanding the mechanisms by which organisms direct or limit crystallization has long been a central challenge to the biomineralization community. One prevailing view is that mineral-associated macromolecules are responsible for either inhibiting crystallization or initiating and stabilizing non-equilibrium crystal polymorphs and morphologies through interactions between anionic moieties and cations in solution or at mineralizing surfaces. In particular, biomolecules that present carboxyl groups to the growing crystal have been implicated as primary modulators of growth. Here we review the results from a combination of in situ atomic force microscopy (AFM) and molecular modeling (MM) studies to investigate the effect of specific interactions between carboxylate-rich biomolecules and atomic steps on crystal surfaces during the growth of carbonates, oxalates and phosphates of calcium. Specifically, we how the growth kinetics and morphology depend on the concentration of additives that include citrate, simple amino acids, synthetic Asp-rich polypeptides, and naturally occurring Asp-rich proteins found in both functional and pathological mineral tissues. The results reveal a consistent picture of shape modification in which stereochemical matching of modifiers to specific atomic steps drives shape modification. Inhibition and other changes in growth kinetics are shown to be due to a range of mechanisms that depend on chemistry and molecular size. Some effects are well described by classic crystal growth theories, but others, such as step acceleration due to peptide charge and hydrophylicity, were previously unrealized. Finally, we show that the molecular scale observations are well correlated with macroscopic growth rate data.
Date: April 27, 2007
Creator: De Yoreo, J. J.
Partner: UNT Libraries Government Documents Department

Structural Genomics of Minimal Organisms: Pipeline and Results

Description: The initial objective of the Berkeley Structural Genomics Center was to obtain a near complete three-dimensional (3D) structural information of all soluble proteins of two minimal organisms, closely related pathogens Mycoplasma genitalium and M. pneumoniae. The former has fewer than 500 genes and the latter has fewer than 700 genes. A semiautomated structural genomics pipeline was set up from target selection, cloning, expression, purification, and ultimately structural determination. At the time of this writing, structural information of more than 93percent of all soluble proteins of M. genitalium is avail able. This chapter summarizes the approaches taken by the authors' center.
Date: September 14, 2007
Creator: Kim, Sung-Hou; Shin, Dong-Hae; Kim, Rosalind; Adams, Paul & Chandonia, John-Marc
Partner: UNT Libraries Government Documents Department

The CKM quark-mixing matrix

Description: No abstract prepared.
Date: April 1, 2006
Creator: Ligeti, Zoltan; Ceccucci, Augusto; Ligeti, Zoltan & Sakai, Yoshihide
Partner: UNT Libraries Government Documents Department

Macroscopic Modeling of Polymer-Electrolyte Membranes

Description: In this chapter, the various approaches for the macroscopic modeling of transport phenomena in polymer-electrolyte membranes are discussed. This includes general background and modeling methodologies, as well as exploration of the governing equations and some membrane-related topic of interest.
Date: April 1, 2007
Creator: Weber, A.Z. & Newman, J.
Partner: UNT Libraries Government Documents Department

Automated Structure Solution with the PHENIX Suite

Description: Significant time and effort are often required to solve and complete a macromolecular crystal structure. The development of automated computational methods for the analysis, solution and completion of crystallographic structures has the potential to produce minimally biased models in a short time without the need for manual intervention. The PHENIX software suite is a highly automated system for macromolecular structure determination that can rapidly arrive at an initial partial model of a structure without significant human intervention, given moderate resolution and good quality data. This achievement has been made possible by the development of new algorithms for structure determination, maximum-likelihood molecular replacement (PHASER), heavy-atom search (HySS), template and pattern-based automated model-building (RESOLVE, TEXTAL), automated macromolecular refinement (phenix.refine), and iterative model-building, density modification and refinement that can operate at moderate resolution (RESOLVE, AutoBuild). These algorithms are based on a highly integrated and comprehensive set of crystallographic libraries that have been built and made available to the community. The algorithms are tightly linked and made easily accessible to users through the PHENIX Wizards and the PHENIX GUI.
Date: June 9, 2008
Creator: Zwart, Peter H.; Zwart, Peter H.; Afonine, Pavel; Grosse-Kunstleve, Ralf W.; Hung, Li-Wei; Ioerger, Tom R. et al.
Partner: UNT Libraries Government Documents Department

Philosophy of Mind and the Problem of FreeWill in the Light of Quantum Mechanics.

Description: Arguments pertaining to the mind-brain connection and to the physical effectiveness of our conscious choices have been presented in two recent books, one by John Searle, the other by Jaegwon Kim. These arguments are examined, and it is argued that the difficulties encountered arise from a defective understanding and application of a pertinent part of contemporary science, namely quantum mechanics.
Date: April 1, 2008
Creator: Stapp, Henry & Stapp, Henry P
Partner: UNT Libraries Government Documents Department

Cavity Microwave Searches for Cosmological Axions

Description: This chapter will cover the search for dark matter axions based on microwave cavity experiments proposed by Pierre Sikivie. We will start with a brief overview of halo dark matter and the axion as a candidate. The principle of resonant conversion of axions in an external magnetic field will be described as well as practical considerations in optimizing the experiment as a signal-to-noise problem. A major focus of this chapter will be the two complementary strategies for ultra-low noise detection of the microwave photons--the 'photon-as-wave' approach (i.e. conventional heterojunction amplifiers and soon to be quantum-limited SQUID devices), and 'photon-as-particle' (i.e. Rydberg-atom single-quantum detection). Experimental results will be presented; these experiments have already reached well into the range of sensitivity to exclude plausible axion models, for limited ranges of mass. The section will conclude with a discussion of future plans and challenges for the microwave cavity experiment.
Date: January 22, 2007
Creator: Carosi, G. & van Bibber, K.
Partner: UNT Libraries Government Documents Department

Adventures in Laser Produced Plasma Research

Description: In the UK the study of laser produced plasmas and their applications began in the universities and evolved to a current system where the research is mainly carried out at the Rutherford Appleton Laboratory Central Laser Facility ( CLF) which is provided to support the universities. My own research work has been closely tied to this evolution and in this review I describe the history with particular reference to my participation in it.
Date: January 13, 2006
Creator: Key, M.
Partner: UNT Libraries Government Documents Department

Chapter 9: Model Systems for Formation and Dissolution of Calcium Phosphate Minerals

Description: Calcium phosphates are the mineral component of bones and teeth. As such there is great interest in understanding the physical mechanisms that underlie their growth, dissolution, and phase stability. Control is often achieved at the cellular level by the manipulation of solution states and the use of crystal growth modulators such as peptides or other organic molecules. This chapter begins with a discussion of solution speciation in body fluids and relates this to important crystal growth parameters such as the supersaturation, pH, ionic strength and the ratio of calcium to phosphate activities. We then discuss the use of scanning probe microscopy as a tool to measure surface kinetics of mineral surfaces evolving in simplified solutions. The two primary themes that we will touch on are the use of microenvironments that temporally evolve the solution state to control growth and dissolution; and the use of various growth modifiers that interact with the solution species or with mineral surfaces to shift growth away from the lowest energy facetted forms. The study of synthetic minerals in simplified solution lays the foundation for understand mineralization process in more complex environments found in the body.
Date: July 29, 2006
Creator: Orme, C. A. & Giocondi, J. L.
Partner: UNT Libraries Government Documents Department

The Fidelity of Ocean Models With Explicit Eddies (Chapter 17)

Description: Current practices within the oceanographic community have been reviewed with regard to the use of metrics to assess the realism of the upper-ocean circulation, ventilation processes diagnosed by time-evolving mixed layer depth and mode water formation, and eddy heat fluxes in large-scale fine resolution ocean model simulations. We have striven to understand the fidelity of these simulations in the context of their potential use in future fine-resolution coupled climate system studies. A variety of methodologies are used to assess the veracity of the numerical simulations. Sea surface height variability and the location of western boundary current paths from altimetry have been used routinely as basic indicators of fine-resolution model performance. Drifters and floats have also been used to provide pseudo-Eulerian measures of the mean and variability of surface and sub-surface flows, while statistical comparisons of observed and simulated means have been carried out using James tests. Probability density functions have been used to assess the Gaussian nature of the observed and simulated flows. Length and time scales have been calculated in both Eulerian and Lagrangian frameworks from altimetry and drifters, respectively. Concise measures of multiple model performance have been obtained from Taylor diagrams. The time-evolution of the mixed layer depth at monitoring stations has been compared with simulated time series. Finally, eddy heat fluxes are compared to climatological inferences.
Date: August 1, 2007
Creator: McClean, J.; Jayne, S.; Maltrud, M. & Ivanova, D.
Partner: UNT Libraries Government Documents Department

Statistical Modeling of Large-Scale Scientific Simulation Data

Description: With the advent of massively parallel computer systems, scientists are now able to simulate complex phenomena (e.g., explosions of a stars). Such scientific simulations typically generate large-scale data sets over the spatio-temporal space. Unfortunately, the sheer sizes of the generated data sets make efficient exploration of them impossible. Constructing queriable statistical models is an essential step in helping scientists glean new insight from their computer simulations. We define queriable statistical models to be descriptive statistics that (1) summarize and describe the data within a user-defined modeling error, and (2) are able to answer complex range-based queries over the spatiotemporal dimensions. In this chapter, we describe systems that build queriable statistical models for large-scale scientific simulation data sets. In particular, we present our Ad-hoc Queries for Simulation (AQSim) infrastructure, which reduces the data storage requirements and query access times by (1) creating and storing queriable statistical models of the data at multiple resolutions, and (2) evaluating queries on these models of the data instead of the entire data set. Within AQSim, we focus on three simple but effective statistical modeling techniques. AQSim's first modeling technique (called univariate mean modeler) computes the ''true'' (unbiased) mean of systematic partitions of the data. AQSim's second statistical modeling technique (called univariate goodness-of-fit modeler) uses the Andersen-Darling goodness-of-fit method on systematic partitions of the data. Finally, AQSim's third statistical modeling technique (called multivariate clusterer) utilizes the cosine similarity measure to cluster the data into similar groups. Our experimental evaluations on several scientific simulation data sets illustrate the value of using these statistical models on large-scale simulation data sets.
Date: November 15, 2003
Creator: Eliassi-Rad, T.; Baldwin, C.; Abdulla, G. & Critchlow, T.
Partner: UNT Libraries Government Documents Department

Development of U.S. Regulations for the Transportation of Radioactive Materials - A Look Back Over the Past 40 Years

Description: The discussion in this Chapter is a relatively straightforward, chronological description of the development of U.S. transportation regulations for radioactive materials over the past 40 years. Although primarily based on the development of U.S. regulations for the shipment of what is now known as Type B quantities of radioactive materials, the information presented details the interactions between a number of U.S. governmental agencies, commissions, and departments, and the International Atomic Energy Agency (IAEA). For the most part, the information that follows was taken directly from the Federal Register, between 1965 and 2004, which, within the boundaries of the U.S., is considered law, or at least policy at the federal level. Starting in 1978, however, the information presented also takes a look at a series of so-called Guidance Documents, including Regulatory Guides (Reg. Guides), NUREGs, and NUREG/CRs. Developed originally by the U.S. Atomic Energy Agency (AEC), and later adapted by the U.S. Nuclear Regulatory Commission (NRC), the NUREGs and NUREG/CRs cited in this Chapter clearly specify a preferred methodology that can be used to meet the regulatory requirements of Title 10 of the Code of Federal Regulations, Part 71 (10 CFR Part 71, or, more simply, 10 CFR 71). As is appropriate for the discussion in this Chapter, the methodology preferred by the NRC, not as law but as guidance, was adapted directly from the requirements of the ASME's Boiler & Pressure Vessel Code. The information provided below is provided with little embellishment. By taking the information directly from the Federal Register, it becomes a story that tells itself. The information is self-consistent, and it provides all of the details behind the numerous policy decisions that led to the development of the U.S. regulations, as they were in their time, and as they are now.
Date: August 29, 2005
Creator: Hafner, R. S.
Partner: UNT Libraries Government Documents Department

Constraints on the Origin of Chondrules and CAIs from Short-Lived and Long-Lived Radionuclides

Description: The high time resolution Pb-Pb ages and short-lived nuclide based relative ages for CAIs and chondrules are reviewed. The solar system started at 4567.2 {+-} 0.6Ma inferred from the high precision Pb-Pb ages of CAIs. Time scales of CAIs ({le}0.1Myr), chondrules (1-3Myr), and early asteroidal differentiation ({ge}3Myr) inferred from {sup 26}Al relative ages are comparable to the time scale estimated from astronomical observations of young star; proto star, classical T Tauri star and week-lined T Tauri star, respectively. Pb-Pb ages of chondrules also indicate chondrule formation occur within 1-3 Myr after CAIs. Mn-Cr isochron ages of chondrules are similar to or within 2 Myr after CAI formation. Chondrules from different classes of chondrites show the same range of {sup 26}Al ages in spite of their different oxygen isotopes, indicating that chondrule formed in the localized environment. The {sup 26}Al ages of chondrules in each chondrite class show a hint of correlation with their chemical compositions, which implies the process of elemental fractionation during chondrule formation events.
Date: October 24, 2005
Creator: Kita, N. T.; Huss, G. R.; Tachibana, S.; Amelin, Y.; Nyquist, L. E. & Hutcheon, I. D.
Partner: UNT Libraries Government Documents Department

Deformation Behavior of Nanoporous Metals

Description: Nanoporous open-cell foams are a rapidly growing class of high-porosity materials (porosity {ge} 70%). The research in this field is driven by the desire to create functional materials with unique physical, chemical and mechanical properties where the material properties emerge from both morphology and the material itself. An example is the development of nanoporous metallic materials for photonic and plasmonic applications which has recently attracted much interest. The general strategy is to take advantage of various size effects to introduce novel properties. These size effects arise from confinement of the material by pores and ligaments, and can range from electromagnetic resonances to length scale effects in plasticity. In this chapter we will focus on the mechanical properties of low density nanoporous metals and how these properties are affected by length scale effects and bonding characteristics. A thorough understanding of the mechanical behavior will open the door to further improve and fine-tune the mechanical properties of these sometimes very delicate materials, and thus will be crucial for integrating nanoporous metals into products. Cellular solids with pore sizes above 1 micron have been the subject of intense research for many years, and various scaling relations describing the mechanical properties have been developed.[4] In general, it has been found that the most important parameter in controlling their mechanical properties is the relative density, that is, the density of the foam divided by that of solid from which the foam is made. Other factors include the mechanical properties of the solid material and the foam morphology such as ligament shape and connectivity. The characteristic internal length scale of the structure as determined by pores and ligaments, on the other hand, usually has only little effect on the mechanical properties. This changes at the submicron length scale where the surface-to-volume ratio becomes large and the ...
Date: November 28, 2007
Creator: Biener, J.; Hodge, A. M. & Hamza, A. V.
Partner: UNT Libraries Government Documents Department

Environmentally Assisted Cracking of Nickel Alloys

Description: Environmentally Assisted Cracking (EAC) is a general term that includes phenomena such as stress corrosion cracking (SCC), hydrogen embrittlement (HE), sulfide stress cracking (SSC), liquid metal embrittlement (LME), etc. EAC refers to a phenomenon by which a normally ductile metal looses its toughness (e.g. elongation to rupture) when it is subjected to mechanical stresses in presence of a specific corroding environment. For EAC to occur, three affecting factors must be present simultaneously. These include: (1) Mechanical tensile stresses, (2) A susceptible metal microstructure and (3) A specific aggressive environment. If any of these three factors is removed, EAC will not occur. That is, to mitigate the occurrence of EAC, engineers may for example eliminate residual stresses in a component or limit its application to certain chemicals (environment). The term environment not only includes chemical composition of the solution in contact with the component but also other variables such as temperature and applied potential. Nickel alloys are in general more resistant than stainless steels to EAC. For example, austenitic stainless steels (such as S30400) suffer SCC in presence of hot aqueous solutions containing chloride ions. Since chloride ions are ubiquitous in most industrial applications, the use of stressed stainless steels parts is seriously limited. On the other hand, nickel alloys (such as N10276) are practically immune to SCC in presence of hot chloride solutions and therefore an excellent alternative to replace the troubled stainless steels. Nonetheless, nickel alloys are not immune to other types of EAC. There are several environments (such as hot caustic and hot hydrofluoric acid) that may produce embrittlement in nickel alloys (Crum et al, 2000) (Table 1). The conditions where nickel alloys suffer EAC are highly specific and therefore avoidable by the proper design of the industrial components.
Date: February 6, 2004
Creator: Rebak, R. B.
Partner: UNT Libraries Government Documents Department

Development and Application of Compatible Discretizations of Maxwell's Equations

Description: We present the development and application of compatible finite element discretizations of electromagnetics problems derived from the time dependent, full wave Maxwell equations. We review the H(curl)-conforming finite element method, using the concepts and notations of differential forms as a theoretical framework. We chose this approach because it can handle complex geometries, it is free of spurious modes, it is numerically stable without the need for filtering or artificial diffusion, it correctly models the discontinuity of fields across material boundaries, and it can be very high order. Higher-order H(curl) and H(div) conforming basis functions are not unique and we have designed an extensible C++ framework that supports a variety of specific instantiations of these such as standard interpolatory bases, spectral bases, hierarchical bases, and semi-orthogonal bases. Virtually any electromagnetics problem that can be cast in the language of differential forms can be solved using our framework. For time dependent problems a method-of-lines scheme is used where the Galerkin method reduces the PDE to a semi-discrete system of ODE's, which are then integrated in time using finite difference methods. For time integration of wave equations we employ the unconditionally stable implicit Newmark-Beta method, as well as the high order energy conserving explicit Maxwell Symplectic method; for diffusion equations, we employ a generalized Crank-Nicholson method. We conclude with computational examples from resonant cavity problems, time-dependent wave propagation problems, and transient eddy current problems, all obtained using the authors massively parallel computational electromagnetics code EMSolve.
Date: May 27, 2005
Creator: White, D.; Koning, J. & Rieben, R.
Partner: UNT Libraries Government Documents Department

High Pressure Materials Research: Novel Extended Phases of Molecular Triatomics

Description: Application of high pressure significantly alters the interatomic distance and thus the nature of intermolecular interaction, chemical bonding, molecular configuration, crystal structure, and stability of solid [1]. With modern advances in high-pressure technologies [2], it is feasible to achieve a large (often up to a several-fold) compression of lattice, at which condition material can be easily forced into a new physical and chemical configuration [3]. The high-pressure thus offers enhanced opportunities to discover new phases, both stable and metastable ones, and to tune exotic properties in a wide-range of atomistic length scale, substantially greater than (often being several orders of) those achieved by other thermal (varying temperatures) and chemical (varying composition or making alloys) means. Simple molecular solids like H{sub 2}, C, CO{sub 2}, N{sub 2}, O{sub 2}, H{sub 2}O, CO, NH{sub 3}, and CH{sub 4} are bounded by strong covalent intramolecular bonds, yet relatively weak intermolecular bonds of van der Waals and/or hydrogen bonds. The weak intermolecular bonds make these solids highly compressible (i.e., low bulk moduli typically less than 10 GPa), while the strong covalent bonds make them chemically inert at least initially at low pressures. Carbon-carbon single bonds, carbon-oxygen double bonds and nitrogen-nitrogen triple bonds, for example, are among the strongest. These molecular forms are, thus, often considered to remain stable in an extended region of high pressures and high temperatures. High stabilities of these covalent molecules are also the basis of which their mixtures are often presumed to be the major detonation products of energetic materials as well as the major constituents of giant planets. However, their physical/chemical stabilities are not truly understood at those extreme pressure-temperature conditions. In fact, an increasing amount of experimental evidences contradict the assumed stability of these materials at high pressures and temperatures.
Date: May 26, 2004
Creator: Yoo, C.
Partner: UNT Libraries Government Documents Department

Laser Fusion: The First Ten Years 1962-1972

Description: This account of the beginning of the program on laser fusion at Livermore in 1962, and its subsequent development during the decade ending in 1972, was originally prepared as a contribution to the January 1991 symposium 'Achievements in Physics' honoring Professor Keith Brueckner upon his retirement from the University of San Diego at La Jolla. It is a personal recollection of work at Livermore from my vantage point as its scientific leader, and of events elsewhere that I thought significant. This period was one of rapid growth in which the technology of high-power short-pulse lasers needed to drive the implosion of thermonuclear fuel to the temperature and density needed for ignition was developed, and in which the physics of the interaction of intense light with plasmas was explored both theoretically and experimentally.
Date: July 6, 2006
Creator: Kidder, R. E.
Partner: UNT Libraries Government Documents Department

Hydrogen Outgassing from Lithium Hydride

Description: Lithium hydride is a nuclear material with a great affinity for moisture. As a result of exposure to water vapor during machining, transportation, storage and assembly, a corrosion layer (oxide and/or hydroxide) always forms on the surface of lithium hydride resulting in the release of hydrogen gas. Thermodynamically, lithium hydride, lithium oxide and lithium hydroxide are all stable. However, lithium hydroxides formed near the lithium hydride substrate (interface hydroxide) and near the sample/vacuum interface (surface hydroxide) are much less thermally stable than their bulk counterpart. In a dry environment, the interface/surface hydroxides slowly degenerate over many years/decades at room temperature into lithium oxide, releasing water vapor and ultimately hydrogen gas through reaction of the water vapor with the lithium hydride substrate. This outgassing can potentially cause metal hydriding and/or compatibility issues elsewhere in the device. In this chapter, the morphology and the chemistry of the corrosion layer grown on lithium hydride (and in some cases, its isotopic cousin, lithium deuteride) as a result of exposure to moisture are investigated. The hydrogen outgassing processes associated with the formation and subsequent degeneration of this corrosion layer are described. Experimental techniques to measure the hydrogen outgassing kinetics from lithium hydride and methods employing the measured kinetics to predict hydrogen outgassing as a function of time and temperature are presented. Finally, practical procedures to mitigate the problem of hydrogen outgassing from lithium hydride are discussed.
Date: April 20, 2006
Creator: Dinh, L. N.; Schildbach, M. A.; Smith, R. A.; Balazs, B. & McLean, W., II
Partner: UNT Libraries Government Documents Department